|
VAERS ID: |
1261766 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Male |
Location: |
Florida |
Vaccinated: |
2021-04-08 |
Onset: |
2021-04-10 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2021-04-27 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / IM |
Administered by: Unknown
Purchased by: ?
Symptoms: Body
temperature increased, Death, Seizure
SMQs:, Neuroleptic malignant syndrome (broad), Systemic
lupus erythematosus (broad), Convulsions (narrow), Noninfectious
encephalitis (broad), Noninfectious encephalopathy/delirium
(broad), Noninfectious meningitis (broad), Generalised convulsive
seizures following immunisation (narrow), Drug reaction with
eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia
(broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-10
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:
Write-up: increased
body temperature, seizure, death
|
|
VAERS ID: |
1696757 (history) |
Form: |
Version 2.0 |
Age: |
11.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2021-09-14 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
FA6780 / 1 |
LA / IM |
Administered by: Private
Purchased by: ?
Symptoms: Product
administered to patient of inappropriate age
SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: None
CDC Split Type:
Write-up: Patient
was 11 years old and 8 months at the time of vaccine No side
effects noted.
|
|
VAERS ID: |
1784945 (history) |
Form: |
Version 2.0 |
Age: |
12.0 |
Sex: |
Female |
Location: |
South Carolina |
Vaccinated: |
2021-07-11 |
Onset: |
2021-08-02 |
Days after vaccination: |
22 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0179 / 1 |
UN / SYR |
Administered by: Private
Purchased by: ?
Symptoms: Death, Respiratory
tract haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-08-02
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Trisomy 18,
Scoliosis, Closed Ventricular Septal Defect, Ectopic Kidney,
Gastrostomy Tube dependent, GERD, and Obstructive Sleep Apnea
Allergies:
Diagnostic Lab Data:
CDC Split Type:
Write-up: Blood in
airway, Death
|
|
VAERS ID: |
1406840 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2021-06-13 |
Onset: |
2021-06-14 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0217 / UNK |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Death, Influenza
like illness
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:
Write-up: Flu like
symptoms for 2 days then was found deceased
|
|
VAERS ID: |
1431289 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Male |
Location: |
Minnesota |
Vaccinated: |
2021-06-02 |
Onset: |
2021-06-19 |
Days after vaccination: |
17 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-28 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0191 / 1 |
- / IM |
Administered by: Other
Purchased by: ?
Symptoms: Angiogram
cerebral abnormal, Apnoea test
abnormal, Arteriovenous
malformation, Blood
sodium increased, Brain death, Brain
herniation, COVID-19, Cardiac
arrest, Central
nervous system lesion, Cerebellar
haemorrhage, Death, Electrocardiogram
abnormal, Endotracheal
intubation, Haemorrhage
intracranial, Hypernatraemia, Hypotension, Intensive
care, Mechanical
ventilation, Neoplasm, Resuscitation, SARS-CoV-2
test positive, Scan with
contrast, Sinus
tachycardia
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Angioedema (broad), Haemorrhage
terms (excl laboratory terms) (narrow), Neuroleptic malignant
syndrome (broad), Arrhythmia related investigations, signs and
symptoms (broad), Supraventricular tachyarrhythmias (narrow),
Haemorrhagic central nervous system vascular conditions (narrow),
Shock-associated circulatory or cardiac conditions (excl torsade
de pointes) (narrow), Congenital, familial and genetic disorders
(narrow), Embolic and thrombotic events, vessel type unspecified
and mixed arterial and venous (narrow), Acute central respiratory
depression (broad), Guillain-Barre syndrome (broad),
Cardiomyopathy (broad), Conditions associated with central nervous
system haemorrhages and cerebrovascular accidents (broad),
Respiratory failure (broad), Non-haematological tumours of
unspecified malignancy (narrow), Infective pneumonia (broad),
Dehydration (broad), Hypokalaemia (broad), Opportunistic
infections (broad), COVID-19 (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-20
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: see above. Was covid
positive on admission 6/19. Family gave a history of previous
covid infection earlier this year.
CDC Split Type:
Write-up: Date of
Admission: 6/19/2021 Date of Death: 6/20/2021 Primary Care
Physician: No primary care provider on file. REASON FOR ADMISSION:
Patient is a 13-year-old previously
healthy male who was admitted after out-of-hospital cardiac
arrest with ROSC after CPR for 15 minutes in the field, found to
be in the context of large cerebellar hemorrhage secondary to
brain lesion (AVM vs tumor). BRIEF SUMMARY OF
HOSPITALIZATION: Patient was intubated prior to arrival to the ED.
Upon arrival he was started on epinephrine and norepinephrine
drips to maintain perfusion and was administered bicarbonate x2.
Head CTA was obtained and was notable for midbrain hemorrhage and
tonsillar herniation, and no contrast enhanced blood flow in the
brain. Brain death exams were completed at 09:59 and 14:20. APNEA
test was performed at 13:30, which is the official time of brain
death. Official cause of death was brainstem herniation from
intracranial hemorrhage. Mechanical ventilation was continued to
allow family time to grieve and perform last rites. Time of
cardiac death after mechanical ventilation withdrawal was 18:36.
HOSPITAL COURSE BY PROBLEM: FEN/Renal/Endo: #Central DI He
received 1.5 L of normal saline bolus in the ED and an additional
3 L of ringers lactate bolus overnight in the ICU to maintain
perfusion and decrease heart rate. His sodium was 141 upon
presentation but reached a maximum of 160 due to central diabetes
insipidus. He was started on 0.45% normal saline at 100 mL/hr to
improve hypernatremia, which was monitored Q1h until
normonatremic. He additionally required vasopressin drip to be
started due to central DI, which was increased to a maximum of 20
mU/kg/hr. CV: At time of admission, epinephrine was running at 0.1
mcg/kg/min and norepinephrine was 0.1 mcg/kg/hr. Norepinephrine
was increased shortly thereafter to 0.12 mcg/kg/min. In the
morning after admission, he had tachycardia to the 190s, which
appeared to be narrow complex. Epinephrine and norepinephrine were
discontinued. Two doses of adenosine were administered (6 mg first
dose, 12 mg second dose) due to suspected SVT. The rate decreased
for ~4 seconds after the second dose however returned to ~180. EKG
arrived which showed sinus tachycardia so no further medications
or cardiac interventions were done. Fluid rates were increased to
2x MIVF rate and additional 500 mL bolus of LR was administered.
Norepinephrine and epinephrine were restarted and escalated due to
low blood pressures in the early afternoon.to allow family time
with patient. Both titrated to effect. Pulm: Patient was
mechanically ventilated to achieve normal pH, normocarbia, and
high arterial oxygen tension per brain death protocol. He had no
primary pulmonary disease during this admission. Neuro:
#Intraparenchymal hemorrhage #Tonsillar herniation Neurosurgery
was consulted. Mannitol x1 and hypertonic saline 23% x1 were
administered to decrease intracranial pressures. Keppra 2g was
administered for seizure prophylaxis. No sedation was needed
during patient''s hospitalization. PERTINENT STUDIES &
CONSULTS: Pediatric neurology Neurosurgery PENDING TESTS RESULTS:
None RECOMMENDATIONS AND FOLLOWUP: None No future appointments.
PHYSICAL EXAMINATION: BP 108/78 | Pulse (!) 144 | Temp 36.5 ?C
(97.7 ?F) | Resp (!) 15 | Ht 1.65 m (5'' 4.96") | Wt 46.5 kg (102
lb 8.2 oz) | SpO2 99% | BMI 17.08 kg/m? Estimated body mass index
is 17.08 kg/m? as calculated from the following: Height as of this
encounter: 1.65 m (5'' 4.96"). Weight as of this encounter: 46.5
kg (102 lb 8.2 oz). ALLERGIES No Known Drug Allergies
|
|
VAERS ID: |
1463061 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
0000-00-00 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / UNK |
- / OT |
Administered by: Unknown
Purchased by: ?
Symptoms: Death, Product
administered to patient of inappropriate age
SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212
Write-up: Died
three days after vaccine; 13 year old boy dies three days after
the Moderna vaccine; This spontaneous case was reported by a
consumer and describes the occurrence of DEATH (Died three days
after vaccine) in a 13-year-old male patient who received
mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The
occurrence of additional non-serious events is detailed below. No
Medical History information was reported. On an unknown date, the
patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine)
(unknown route) 1 dosage form. On an unknown date, the patient
experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE
(13 year old boy dies three days after the Moderna vaccine). The
patient died on an unknown date. The cause of death was not
reported. It is unknown if an autopsy was performed. At the time
of death, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (13
year old boy dies three days after the Moderna vaccine) had
resolved. The action taken with mRNA-1273 (Moderna COVID-19
Vaccine) (Unknown) was unknown. Concomitant product was not
provided by the reporter. Treatment information was unknown.
Company comment: This is a case of death in a 13-year-old male
subject with unknown medical history, who died one day after
receiving the vaccine. Very limited information has been provided
at this time. Further information has been requested.; Sender''s
Comments: This is a case of death in a 13-year-old male subject
with unknown medical history, who died one day after receiving the
vaccine. Very limited information has been provided at this time.
Further information has been requested.; Reported Cause(s) of
Death: Unknown cause of death
|
|
VAERS ID: |
1505250 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2021-07-01 |
Onset: |
2021-07-27 |
Days after vaccination: |
26 |
Submitted: |
0000-00-00 |
Entered: |
2021-07-27 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
- / - |
Administered by: Private
Purchased by: ?
Symptoms: Blood
glucose increased, Death, Full blood
count, Metabolic
function test normal, Pulseless
electrical activity, SARS-CoV-2
test negative, Ventricular
tachycardia
SMQs:, Torsade de pointes/QT
prolongation (narrow), Hyperglycaemia/new onset diabetes
mellitus (narrow), Ventricular
tachyarrhythmias (narrow), Shock-associated circulatory or
cardiac conditions (excl torsade de pointes) (narrow), Torsade de
pointes, shock-associated conditions (narrow), Cardiac
arrhythmia terms, nonspecific (narrow), COVID-19 (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-27
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: one dose of dramamine
given in the evening prior to arrival.
Current Illness: none
Preexisting Conditions: none, remote
history of asthma
Allergies: none
Diagnostic Lab Data: CBC, CMP normal
except slightly elevated glucose COVID PCR negative
CDC Split Type:
Write-up: patient
arrived in ventricular tachycardia via EMS, but responsive.
deteoriarated to pulseless ventricular tachycardia, PEA and
ultimately death.
|
|
VAERS ID: |
1655100 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
0000-00-00 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-08-30 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101091051
( AUTHOR'S NOTE: 2 Children died and
are listed on this same report.
This may have been counted as a single death)
Write-up: dead from
second dose of Pfizer Covid 19 vaccine; This is a spontaneous
report from a Pfizer-sponsored program
by a non-contactable consumer. This report
reported same event for two patients. This is the first dose
of two reports. A 13-year-old female patient received bnt162b2
(BNT162B2), dose 2 via an unspecified route of administration on
an unspecified date (Batch/Lot number was not reported) as DOSE 2,
SINGLE at the age of 13-year-old for covid-19 immunisation. The
patient medical history and concomitant medications were not
reported. The patient previously received the first dose of
bnt162b2 (BNT162B2) for covid-19 immunisation. A 13 years old
female is dead from second dose of Pfizer Covid 19 vaccine. Both
had no prior conditions with the heart and now are dead. The
patient died on an unspecified date. It was unknown if an autopsy
was performed. No follow-up attempts are possible; information
about lot/batch number cannot be obtained; Sender''s Comments:
Linked Report(s) : US-PFIZER INC-202101091793 same report/drug/AE,
different patients; Reported Cause(s) of Death: dead from second
dose of Pfizer Covid 19 vaccine
|
|
VAERS ID: |
1815096 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2021-07-11 |
Onset: |
2021-07-26 |
Days after vaccination: |
15 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-25 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0186 / 1 |
AR / IM |
Administered by: Other
Purchased by: ?
Symptoms: Alanine
aminotransferase normal, Anion gap
increased, Aspartate
aminotransferase increased, Blood
albumin decreased, Blood
alkaline phosphatase normal, Blood
bilirubin normal, Blood
chloride normal, Blood
creatinine normal, Blood
glucose increased, Blood
potassium decreased, Blood
sodium normal, Blood urea
normal, Carbon
dioxide decreased, Cardioversion, Death, Dizziness, Dyspnoea, Feeling
abnormal, Full blood
count, Haematocrit
normal, Haemoglobin
normal, Loss of
consciousness, Metabolic
function test, Nausea, Platelet
count normal, Resuscitation, SARS-CoV-2
test negative, Supraventricular
tachycardia, Unresponsive
to stimuli, Vomiting, White blood
cell count normal
SMQs:, Torsade de pointes/QT prolongation (broad), Liver
related investigations, signs and symptoms (narrow), Anaphylactic
reaction (broad), Acute pancreatitis (broad), Lactic acidosis
(broad), Hyperglycaemia/new onset diabetes mellitus (narrow),
Neuroleptic malignant syndrome (broad), Anticholinergic syndrome
(broad), Arrhythmia related investigations, signs and symptoms
(broad), Supraventricular tachyarrhythmias (narrow), Dementia
(broad), Acute central respiratory depression (broad), Pulmonary
hypertension (broad), Guillain-Barre syndrome (broad),
Noninfectious encephalitis (broad), Noninfectious
encephalopathy/delirium (broad), Noninfectious meningitis (broad),
Gastrointestinal nonspecific symptoms and therapeutic procedures
(narrow), Cardiomyopathy (broad), Vestibular disorders (broad),
Hypotonic-hyporesponsive episode (broad), Generalised convulsive
seizures following immunisation (broad), Tumour lysis syndrome
(broad), Drug reaction with eosinophilia and systemic symptoms
syndrome (broad), Hypoglycaemia (broad), Hypokalaemia (narrow),
COVID-19 (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-27
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: Asthma
Allergies: None known
Diagnostic Lab Data: Initial CBC with WBC
6.59, Hg 12.2, HCT 35.3, platelets 278. CMP with CO2 18, anion gap
22, glucose 270, Na 139, K 2.8, Cl 103, BUN 16, Creatinine 0.77,
Albumin 3.4, ALK 97, AST 152, ALT 32, bilirubin 0.3. COVID PCR not
detected.
CDC Split Type:
Write-up: Patient
received first COVID vaccine on 7/11/21. She was well until
7/26/21 when she developed nausea, vomiting, shortness of breath
and dizziness. At approximately 04:00 on 7/27/21, she woke up
feeling poorly, went into the bathroom and then lost
consciousness. EMS was called, she was in a tachycardia at 180
bpm, BP 88/64, unresponsive. EMS report states she was "in SVT and
cardioverted at 30J then 70 J. Still in SVT but becoming more
alert. HR 165 bpm, sats 98%." In ED, she was felt to be in
ventricular tachycardia, She received attempted resuscitation with
multiple rounds of CPR including chest compressions,
defibrillation for reported ventricular fibrillation, and
medications. She was unable to be resuscitated and death was
pronounced in the ED. Autopsy is pending.
|
|
VAERS ID: |
1633205 (history) |
Form: |
Version 2.0 |
Age: |
13.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-08-11 |
Onset: |
2021-08-13 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2021-08-25 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
10020A / 2 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Activated
partial thromboplastin time, Disseminated
intravascular coagulation, International
normalised ratio, Multiple
organ dysfunction syndrome, N-terminal
prohormone brain natriuretic peptide, Platelet
count, Prothrombin
time, Pulmonary
haemorrhage, Pyrexia, Septic
shock, Troponin T
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow),
Neuroleptic malignant syndrome (broad), Anticholinergic syndrome
(broad), Shock-associated circulatory or cardiac conditions (excl
torsade de pointes) (broad), Torsade de pointes, shock-associated
conditions (broad), Hypovolaemic shock conditions (broad),
Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid
shock conditions (broad), Hypoglycaemic and neurogenic shock
conditions (broad), Embolic and thrombotic events, vessel type
unspecified and mixed arterial and venous (narrow), Drug reaction
with eosinophilia and systemic symptoms syndrome (broad), Sepsis
(narrow), Opportunistic infections (broad)
Life Threatening? Yes
Birth Defect? No
Died? Yes
Date died: 2021-08-14
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical
History/Concurrent Conditions: Dysphagia; Extremely preterm (less
than 28 weeks); Hypoxic-ischaemic encephalopathy; Posthaemorrhagic
hydrocephalus; Reflux oesophagitis; Respiratory insufficiency;
Symptomatic epilepsy
Allergies:
Diagnostic Lab Data: Test Name: pTT;
Result Unstructured Data: Test Result:$g180 seconds; Test Name:
INR; Result Unstructured Data: Test Result:4.9; Test Name: proBNP;
Result Unstructured Data: Test Result:24937 pg/mL; Test Name:
Platelets; Result Unstructured Data: Test Result:min 3410x31uml;
Test Name: Quick; Result Unstructured Data: Test Result:<10;
Test Name: Troponin T; Result Unstructured Data: Test Result:1580
pg/mL
CDC Split Type: DEPFIZER INC202101072828
Write-up: Disseminated
intravascular coagulation; Lung hemorrhage; Pyrexia; Multiorgan
failure; Septic shock; This is a spontaneous report from a
non-contactable other HCP. DE-PEI-202100168078. A 13-yars-old male
patient received bnt162b2 (COMIRNATY, Formulation: Solution for
Injection, Batch/Lot Number: 10020A) dose 2 0.3 mL via an unknown
route of administration on 11Aug2021 (at the age of 13-years-old)
as dose 1, single for COVID-19 immunisation. The patient''s
medical history included extremely preterm (less than 28 weeks),
Hypoxic-ischaemic encephalopathy, posthaemorrhagic hydrocephalus,
symptomatic epilepsy, dysphagia, respiratory insufficiency, reflux
oesophagitis on an unspecified date. The patient previously
received first dose of bnt162b2 (COMIRNATY, Formulation: Solution
for Injection) dose 1, Batch/Lot number unknown) for COVID-19
immunisation on 16Jun2021. Concomitant medications were not
reported. The patient underwent lab tests and procedures which
included platelets min 3410x 31uml, Quick <10, INR$g4.9, pTT
$g180 sec, proBNP 24937 pg/ml, Trop T 1580 pg/ml on an unknown
date. The patient experienced multiorgan failure, lung hemorrhage,
disseminated intravascular coagulation, pyrexia and septic shock
on 13Aug2021. The patient died due to Unknown cause of death on
14Aug2021. Seriousness for the events was reported as death,
hospitallization and life threatening. The autopsy details were
not reported. Sender Comment: Platelets min 3410^31uml, Quick
<10, INR$g4,9; pTT $g180 sec, proBNP 24937 pg/ml, Trop T 1580
pg/ml Relatedness of drug to reaction(s)/event (s) Result of
Assessment D. Unclassifiable No follow-up attempts possible. No
further information expected.; Reported Cause(s) of Death: Unknown
cause of death
|
|
VAERS ID: |
1690103 (history) |
Form: |
Version 2.0 |
Age: |
14.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-07-27 |
Onset: |
2021-09-03 |
Days after vaccination: |
38 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW2246 / 2 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Pulmonary
oedema
SMQs:, Cardiac failure (narrow), Haemodynamic oedema,
effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-09-03
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of
non-encoded Patient Relevant History: Patient Other Relevant
History 1: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: ESPFIZER INC202101170757
Write-up: pulmonary
edema; This is a spontaneous report from a Pfizer-sponsored
program, from a contactable consumer (patent''s uncle) through the
Pfizer company doctor. A 14-year-old male patient received
bnt162b2 (COMIRNATY), 1st dose on 06Jul2021 (Lot Number: EX0893)
and 2nd dose on 27Jul2021 (Lot Number: EW2246, both via an
unspecified route of administration as single dose for COVID-19
immunization. Medical history none. Concomitant medications were
not reported. The patient experienced pulmonary edema (death) on
03Sep2021. The patient died on 03Sep2021. The autopsy revealed
that the cause of death was pulmonary edema.; Reported Cause(s) of
Death: pulmonary edema
|
|
VAERS ID: |
1187918 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Female |
Location: |
New Hampshire |
Vaccinated: |
0000-00-00 |
Onset: |
2021-04-05 |
Submitted: |
0000-00-00 |
Entered: |
2021-04-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / UNK |
- / - |
Administered by: Private
Purchased by: ?
Symptoms: Cardiac
arrest, Intensive
care
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Arrhythmia related investigations,
signs and symptoms (broad), Shock-associated circulatory or
cardiac conditions (excl torsade de pointes) (narrow), Acute
central respiratory depression (broad), Cardiomyopathy (broad),
Respiratory failure (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-06
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: levothyroxine
Current Illness:
Preexisting Conditions: Trisomey 21,
Atrioventricular canal s/p repair, hypothyroidism, asthma,
obstructive sleep apnea, cervical spine instability, hypotonia,
scoliosis, feeding difficulties, renal dysplasia, autism, chronic
constipation, bronchopulmonary dysplasia, mixed conductive and
sensorineural hearing loss, binocular vision disorder,
gastroesophgeal reflux,
Allergies: Cefdinir, Sulfa, Ex-Lax,
NSAIDS
Diagnostic Lab Data:
CDC Split Type:
Write-up: I do not
know the exact date of the first or second Moderna Vaccine. I am
the PICU attending who cared for the patient after her cardiac
arrest which we believe was about 3-4 days after her second
Moderna Vaccine
|
|
VAERS ID: |
1242573 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
Colorado |
Vaccinated: |
2021-04-18 |
Onset: |
2021-04-19 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2021-04-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 1 |
RA / IM |
Administered by: Public
Purchased by: ?
Symptoms: Cardiac
failure, Death
SMQs:, Cardiac failure (narrow), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-20
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vaccinated with
Pfizer/Biontech, died 04/20/2021, 2 days after vaccination
Current Illness: No
Preexisting Conditions: No
Allergies: Nothing
Diagnostic Lab Data:
CDC Split Type:
Write-up: Heart
failure
|
|
VAERS ID: |
1382906 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2021-05-15 |
Onset: |
2021-06-07 |
Days after vaccination: |
23 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0187 / 2 |
LA / IM |
Administered by: Other
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-07
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None known
Current Illness: none noted
Preexisting Conditions: Acne, no other
conditions noted
Allergies: None noted
Diagnostic Lab Data:
CDC Split Type:
Write-up: Unexplained
death within 48 hours
|
|
VAERS ID: |
1498080 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2021-07-18 |
Onset: |
2021-07-22 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2021-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0196 / 1 |
LA / IM |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0198 / 2 |
LA / IM |
Administered by: Pharmacy
Purchased by: ?
Symptoms: Resuscitation, Syncope, Ventricular
tachycardia
SMQs:, Torsade de pointes/QT prolongation (narrow),
Arrhythmia related investigations, signs and symptoms (broad),
Ventricular tachyarrhythmias (narrow), Shock-associated
circulatory or cardiac conditions (excl torsade de pointes)
(narrow), Torsade de pointes, shock-associated conditions
(narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode
(broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-22
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Lopressor 25mg BID
Current Illness: Diagnosed May 2021
hypertrophic cardiomyopathy
Preexisting Conditions: Diagnosed May
2021 hypertrophic cardiomyopathy
Allergies: unknown
Diagnostic Lab Data: none at this time
CDC Split Type:
Write-up: 7/22/2021
Child collapsed on soccer field while playing soccer at a local
camp. CPR was initiated immediately. EMS arrived and found patient
in vtac. Shock x 5. ACLS, intubation attempted. Transported to
Medical Center. Patient had covid in April 2021. Dx in May 2021
hypertrophic cardiomyopathy. Started on lopressor 25mg BID.
Patient had reported to parents that he had not recently taken his
medications. Patient had his second covid vaccine on Sunday
7/18/2021.
|
|
VAERS ID: |
1764974 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
New Hampshire |
Vaccinated: |
2021-06-14 |
Onset: |
2021-06-20 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Pharmacy
Purchased by: ?
Symptoms: Arthralgia, Autopsy, Drowning, Gene
sequencing, Intracardiac
mass, Myocardial
necrosis, Myocarditis, Pain, Pathology
test, SARS-CoV-2
test negative, Subgaleal
haemorrhage, Toxicologic
test normal, Ventricular
hypertrophy
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow),
Myocardial infarction (narrow), Embolic and thrombotic events,
arterial (narrow), Embolic and thrombotic events, vessel type
unspecified and mixed arterial and venous (narrow), Accidents and
injuries (narrow), Hostility/aggression (broad), Cardiomyopathy
(broad), Neonatal disorders (narrow), Arthritis (broad), Drug
reaction with eosinophilia and systemic symptoms syndrome (broad),
Immune-mediated/autoimmune disorders (broad), COVID-19 (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-20
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: Autopsy report
6/21/2021. Pertinent findings include: no external indication of
scalp injury, with small subgaleal hemorrhage over the left
occiput; normal epidural, subdural, and subarachnoid evaluations;
mildly elevated cardiac mass 420 mg; normal pericardial
appearance; normal coronary artery origins from the aorta and free
of atherosclerosis; increased left ventricular wall thickness (1.8
cm) and normal right ventricular wall thickness (0.3 cm); normal
gross appearance of the endocardium, myocardium, and cardiac
valves; small foci of myocardial inflammation of the lateral wall
of the left ventricle with myocyte necrosis; negative myocyte
disarray; negative toxicology; negative SARS-CoV-2 RT-PCR; Ambry
Genetics CardioNext analysis of 92 genes associated with inherited
cardiomyopathies and arrhythmias negative for pathologic findings,
positive for 2 variants of unknown significance.
CDC Split Type:
Write-up: He was in
his usual state of good health. 5 days after receiving the
vaccine, he complained of brief unilateral shoulder pain (unclear
to family which shoulder), which the family attributed to a
musculoskeletal source. No chest pains, shortness of breath, or
palpitations. He was playing with 2 friends at a community pond,
swinging from a rope swing, flipping in the air, and landing in
the water feet first. He surfaced, laughed, told his friends "Wow,
that hurt!", then swam toward shore, underwater as was his usual
routine. The friends became worried when he did not re-emerge. His
body was retrieved by local authorities more than an hour later.
|
|
VAERS ID: |
1592684 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Female |
Location: |
Foreign |
Vaccinated: |
2021-07-11 |
Onset: |
2021-07-11 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2021-08-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 1 |
- / OT |
Administered by: Other
Purchased by: ?
Symptoms: Asthenia, Blood
pressure increased, Body
temperature decreased, Brain death, Brain
hypoxia, C-reactive
protein, Cardiac
arrest, Coma, Computerised
tomogram, Computerised
tomogram head, Echocardiogram, Electrocardiogram, Electroencephalogram, Full blood
count, Headache, Magnetic
resonance imaging, Pain in
extremity, SARS-CoV-2
antibody test positive, Ultrasound
Doppler
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes
mellitus (broad), Neuroleptic malignant syndrome (broad),
Arrhythmia related investigations, signs and symptoms (broad),
Ischaemic central nervous system vascular conditions (narrow),
Shock-associated circulatory or cardiac conditions (excl torsade
de pointes) (narrow), Acute central respiratory depression
(broad), Guillain-Barre syndrome (broad), Noninfectious
encephalitis (broad), Noninfectious encephalopathy/delirium
(broad), Noninfectious meningitis (broad), Hypertension (narrow),
Cardiomyopathy (broad), Respiratory failure (broad),
Tendinopathies and ligament disorders (broad), Hypoglycaemia
(broad), Infective pneumonia (broad), Opportunistic infections
(broad), COVID-19 (narrow)
Life Threatening? Yes
Birth Defect? No
Died? Yes
Date died: 2021-08-07
Days after onset: 27
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Asthma; Barlow''s
syndrome; Marfan''s syndrome
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210713;
Test Name: arterial pressure; Result Unstructured Data: Test
Result:90/60 mmHg; Test Date: 20210713; Test Name: temperature
control; Result Unstructured Data: Test Result:36 Centigrade; Test
Date: 20210713; Test Name: CT scan; Result Unstructured Data: Test
Result:The ascending aorta is moderately dilated; Comments: No
aortic dissection or large vsx, no intracranial bleeding, the
super sigmoid aortography does not show any aortic insufficiency;
Test Date: 20210715; Test Name: CT scan; Result Unstructured Data:
Test Result:appearance of parenchymal parenchymal hemispherica;
Comments: appearance of parenchymal parenchymal hemispherical
hemispherical right upper cerebellar areas of ischemic appearance;
Test Date: 20210713; Test Name: brain CT scan; Result Unstructured
Data: Test Result:no bleeding; Comments: no traumatic injury; Test
Date: 20210723; Test Name: brain CT scan; Result Unstructured
Data: Test Result:stability of ischemic; Comments: lesions
appearance of cerebral edema compatible with anoxo-ischemic
lesions, put under Mannitol; Test Date: 20210727; Test Name: brain
CT scan; Result Unstructured Data: Test Result:increase in
cerebral edema; Comments: reaching almost the entire sustentorial
stage, sudden episodes of desaturation.; Test Date: 20210713; Test
Name: C-reactive protein; Result Unstructured Data: Test
Result:1.4; Test Name: Trans-thoracic echocardiography; Result
Unstructured Data: Test Result:finding a 30%; Comments: altered
left ventricular ejection fraction with kinetic disorders
suggestive of Takotsubo; Test Date: 20210713; Test Name:
Electrocardiography; Result Unstructured Data: Test Result:Not
very evocative; Comments: Respiratory rate; Test Date: 20210723;
Test Name: electroencephalogram; Result Unstructured Data: Test
Result:flat; Comments: with a few waves of intermittent activity;
Test Date: 20210727; Test Name: electroencephalogram; Result
Unstructured Data: Test Result:Pathological; Comments: Keppra
introduction; Test Date: 20210713; Test Name: complete blood
count; Result Unstructured Data: Test Result:normal; Test Date:
20210713; Test Name: cardiac magnetic resonance imaging; Result
Unstructured Data: Test Result:cardio; Comments: in favor of a
takotsubo; Test Date: 20210713; Test Name: covid; Test Result:
Positive ; Comments: (Ig G antiS and antiN and IgM), re-reading of
the entry serology concluded with a Covid infection starting at
the same time as the anti-covid vaccination; Test Date: 20210713;
Test Name: Left transcranial doppler; Result Unstructured Data:
Test Result:left more disturbed; Comments: than the right
(Vdiastolic 20 vs 40 on the right)
CDC Split Type: FRPFIZER INC202101056242
Write-up: This is a
spontaneous report from a contactable physician downloaded from
the Regulatory Authority-WEB [FR-AFSSAPS-MP20215396]. A
15-year-old female patient received bnt162b2 (COMIRNATY),
intramuscular on 11Jul2021 07:30 (Lot Number: Unknown) (at the age
of 15-year-old) as dose 1, single for COVID-19 immunization.
Medical history included ongoing asthma, ongoing Barlow''s
syndrome, ongoing Marfan''s syndrome. The patient''s concomitant
medications were not reported. In good health overall, apart from
a loss of 10kg over one year (since entering high school). During
the day (11Jul2021), asthenia and isolated arm pain. The next day
(12Jul2021), headaches yielding under Doliprane. On 13Jul2021,
around 16:30 (last moment conscious view), her mother drops her
off to her father. Father watered the garden and she cleaned the
garage to prepare for her birthday party. On 13Jul2021 17:20, her
father found her in cardio respiratory arrest, back to the ground,
next to a ladder. No flow was unknown. At 17:30 arrival of
firefighters: 2 external electric shocks were given and 1 mg of
adrenaline injected. Moderately reactive pupils. At 17:50 arrival
of Specialist mobile emergency unit: asystole (Life-threatening).
Two injections of 1 mg of adrenaline, transition to ventricular
fibrillation. 2 external electric shock, 2 ampule of Cordarone and
one ampule of Calcium Gluconate. Return to regular sinus rythme
without disturbance of repolarization and resumption of a pulse.
Orotracheal intubation (probe no 6). New: 1 external electric
shock, one ampule of Cordarone and 1 mg of adrenaline. Return of a
sinus rhythm but presence of a sub ST in infero lateral. 90/60
mmHg arterial pressure excluding sedation. Tight areactive
bilateral miosis pupils. Ventilated in Ventilator-Associated
Conditions but presence of spontaneous ventilation requiring
sedation by Hypnovel and Sufentanyl and 10 mg of Nimbex. Parallel
introduction of Noradrenaline 0.8 mg/h. No filling. In total: low
flow of 30 minutes. Recovered and transfer to intensive care.
Examinations: biology: complete blood count normal, C-reactive
protein 1.4. Coroner considered as normal no coronary dissection.
Computed tomography scan Computed tomography arterial portography:
No aortic dissection or large vsx, no intracranial bleeding, the
super sigmoid aortography does not show any aortic insufficiency.
The ascending aorta is moderately dilated. Computerised tomogram
head: no bleeding, no traumatic injury. Electrocardiogram: Not
very evocative. Respiratory rate. Maintenance of sedation,
temperature control at 36 degrees. Complicated cardiac arrest of a
Takotsubo. Trans-thoracic echocardiography finding a 30% altered
left ventricular ejection fraction with kinetic disorders
suggestive of Takotsubo (post stress?). More doubt about
intra-left ventricular thrombus. Low left ventricular filling
pressures. Integral time speed= 8. Inferior vena cava= 15.
15Jul2021 Appearance in the morning of continual clonies of the
multiple sulfatase deficiency, put under Keppra increased to
750x2. Electroencephalography results pending + Left transcranial
doppler more disturbed than the right (Vdiastolic 20 vs 40 on the
right), Control contrast enhanced computed tomography scan
superimposable at the level of large vsx, but appearance of
parenchymal parenchymal hemispherical hemispherical right upper
cerebellar areas of ischemic appearance. 20Jul2021 pathological
awakening, inhalation lung disease, myocarditis assessment in
progress (negative). 23Jul2021 no sign of wakign up flat
electroencephalogram alternating with a few waves of intermittent
activity. Computered tomography scan stability of ischemic lesions
appearance of cerebral edema compatible with anoxo-ischemic
lesions, put under Mannitol. Cardio: cardiac magnetic resonance
imaging in favor of a takotsubo, myocarditis unlikely, infective
and immunological workup negative. 27Jul2021 Pathological
electroencephalogram, Keppra introduction. Computered tomography
scan increase in cerebral edema reaching almost the entire
sustentorial stage, sudden episodes of desaturation. The COVID
serology returns positive (Ig G antiS and antiN and IgM),
re-reading of the entry serology concluded with a Covid infection
starting at the same time as the anti-covid vaccination. 30Jul2021
retro-rolandic aspect of brain death, vegetative coma. Decision to
limit therapy. Complete file no further information. The patient
died on 07Aug2021. An autopsy was not performed. Cause of Death:
Anoxia cerebral and Cardiac arrest while outcome of the other
events was unknown. No follow-up attempts are possible;
information about lot/batch number cannot be obtained. No further
information is expected.; Reported Cause(s) of Death: Cardiac
arrest; Anoxia cerebral
|
|
VAERS ID: |
1668800 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-08-09 |
Onset: |
2021-08-13 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-03 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
FF2154 / 1 |
LA / - |
Administered by: Other
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-08-13
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: JOPFIZER INC202101119141
Write-up: Death/passed
away; This is a spontaneous report from a contactable consumer or
other non HCP (parent, father of patient). A 15-year-old male
patient received the first dose of bnt162b2 (PFIZER-BIONTECH
COVID-19 VACCINE), via an unspecified route of administration in
the left arm on 09Aug2021 at 09:00 AM (at the age of 15-year-old;
lot number: FF2154) as DOSE 1, SINGLE for COVID-19 immunisation.
The patient''s medical history and concomitant medications were
not provided. The patient did not receive any other vaccines
within 4 weeks prior to the COVID vaccine. The father reported
that the patient (the son) received the dose 1 of the Pfizer
vaccine on 09Aug2021 at 9AM on left arm. Unfortunately, patient
passed away (death) on Friday 13Aug2021 at 04:30 without any
history of illness. The event resulted in Emergency
room/department or urgent care. Prior to vaccination, patient did
not diagnose with COVID-19. Since the vaccination, patient did not
test for COVID-19. Device date was 29Aug2021. No treatment
received. Outcome of the event was fatal. It was not reported if
an autopsy was performed.; Reported Cause(s) of Death:
Death/passed away
|
|
VAERS ID: |
1755460 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-09-16 |
Onset: |
2021-09-16 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-02 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
3005239 / 1 |
- / OT |
Administered by: Unknown
Purchased by: ?
Symptoms: Cerebral
haemorrhage, Cerebral
ventricular rupture
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow),
Haemorrhagic central nervous system vascular conditions (narrow),
Conditions associated with central nervous system haemorrhages and
cerebrovascular accidents (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-09-20
Days after onset: 4
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: JPMODERNATX, INC.MOD20213
Write-up: Cerebral
haemorrhage; Cerebral ventricular rupture; This case was received
via the Regulatory Authority (Reference number:
JP-TAKEDA-2021TJP095727) on 24-Sep-2021 and was forwarded to
Moderna on 27-Sep-2021. This case, initially reported to the
Regulatory Authority by a clerical work, was received via the
RA(Ref, v21128837). The patient''s underlying condition, cerebral
arteriovenous malformation, was discussed with the interviewing
physician, and the possibility of vaccination was discussed. On
16-Sep-2021, at 11:00, the patient received the 1st dose of this
vaccine. Around 20:00, the patient had a headache and vomiting, so
the patient''s family called for ambulance. At 20:50, the patient
was taken to the hospital. The patients JCS3 was 300 on arrival.
CT showed cerebral haemorrhage and cerebral ventricular rupture
from cerebral arteriovenous malformation. On 20-Sep-2021, the
patient was confirmed dead. The outcome of cerebral haemorrhage
and cerebral ventricular rupture was reported as fatal. Follow-up
investigation will be made. Company Comment: Although the events
"cerebral haemorrhage" and "cerebral ventricular rupture"
developed after the administration of COVID-19 vaccine mRNA (mRNA
1273), factors such as concurrent conditions and predisposing
factors of the patient may have also had an influence.;
Reporter''s Comments: Although the events "cerebral haemorrhage"
and "cerebral ventricular rupture" developed after the
administration of COVID-19 vaccine mRNA (mRNA 1273), factors such
as concurrent conditions and predisposing factors of the patient
may have also had an influence.; Sender''s Comments: This case
concerns a 15-year-old, male patient with medical history of
cerebral arteriovenous malformation, who experienced the
unexpected serious adverse event of special interest of cerebral
haemorrhage and unexpected serious adverse event of cerebral
ventricular rupture . The events occurred approximately 9 hours
after the first dose of Spikevax (Moderna COVID-19 vaccine) and
had fatal outcome with death occurring 3 days after following day.
The rechallenge was not applicable as the events occurred after
the first dose. The event was considered related to the vaccine
per the reporter''s assessment. The medical history of the patient
of previous cerebral arteriovenous malformation remain as a
significant confounder. The benefit-risk relationship of Spikevax
(Moderna COVID-19 vaccine) is not affected by this report.;
Reported Cause(s) of Death: Cerebral haemorrhage; Cerebral
ventricular rupture
|
|
VAERS ID: |
1845034 (history) |
Form: |
Version 2.0 |
Age: |
15.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-10-23 |
Onset: |
2021-10-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2021-11-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Autopsy, Bronchospasm, Death, Dyspnoea, Loss of
consciousness, Vaccination
site pain
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Asthma/bronchospasm (narrow),
Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic
malignant syndrome (broad), Anticholinergic syndrome (broad),
Arrhythmia related investigations, signs and symptoms (broad),
Acute central respiratory depression (broad), Pulmonary
hypertension (broad), Noninfectious encephalitis (broad),
Noninfectious encephalopathy/delirium (broad), Noninfectious
meningitis (broad), Cardiomyopathy (broad), Eosinophilic pneumonia
(broad), Hypotonic-hyporesponsive episode (broad), Generalised
convulsive seizures following immunisation (broad),
Hypersensitivity (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-10-24
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20211024;
Test Name: Autopsy; Result Unstructured Data: Test
Result:spontaneous bronchospasm; Comments: Incomplete, final
results awaited
CDC Split Type: MYPFIZER INC202101484694
Write-up: was found
unconscious; breathing difficulties; autopsy was performed on the
same day at 3:40pm and found there was spontaneous bronchospasm;
he was pronounced dead on the same day; injection site pain; This
is a spontaneous report from an Internet Source from a
non-contactable consumer via Pfizer colleague. A 15-year-old male
patient received bnt162b2 (COMIRNATY) via an unknown route of
administration on 23Oct2021 (at the age of 15-year-old) (Batch/Lot
number: Not provided), dose 2, single for COVID-19 immunization,
received at his school. The patient medical history and
concomitant medications were not reported. The patient did not
have any allergies to previous vaccines or medications and was not
known to have any chronic illness. The patient received COVID-19
Vaccine (COVID-19 Vaccine, MANUFACTURER UNKNOWN) via an unknown
route of administration on 23Oct2021 (Batch/Lot number: Not
provided), dose 1, single for COVID-19 immunization. Patient also
did not report any problems or complications after receiving the
first dose injection. The patient experienced injection site pain
(non-serious) on 23Oct2021 with outcome of unknown, breathing
difficulties (hospitalization) on 24Oct2021 09:30 with outcome of
unknown, was found unconscious (hospitalization) on 24Oct2021
09:30 with outcome of unknown, autopsy was performed on the same
day at 3:40pm and found there was spontaneous bronchospasm (death)
on 24Oct2021 10:40, he was pronounced dead on the same day (death)
on 24Oct2021 10:40. The patient was hospitalized for breathing
difficulties and was found unconscious from 24Oct2021 for 1 day.
Therapeutic measures were taken as a result of breathing
difficulties, was found unconscious. The patient died on
24Oct2021. An autopsy was performed that revealed found there was
spontaneous bronchospasm. The clinical course of events was as
follows: He was reported to have had injection site pain only.
However a day after he received his second jab, he was found to
have suffered from breathing difficulties and then was found
unconscious at his home at about 9.30am. Patient was rushed to the
private hospital here but he was pronounced dead on the same day
(24Oct2021) at 10.40am. An autopsy was performed on the same day
at 3.40pm and found there was spontaneous bronchospasm. All tissue
samples in the body were sent for further examination by a
hospital''s pathology forensic physician. The autopsy report is
categorised as still incomplete because there are still tests that
have not been received. A complete autopsy report to find out the
cause of his death, is awaited. No follow-up attempts are
possible; information about lot/batch number cannot be obtained.
No further information is expected.; Autopsy-determined Cause(s)
of Death: found there was spontaneous bronchospasm
|
|
VAERS ID: |
1225942 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2021-03-19 |
Onset: |
2021-03-28 |
Days after vaccination: |
9 |
Submitted: |
0000-00-00 |
Entered: |
2021-04-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
UNKNOWN / 1 |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Cardiac
arrest, Death, Laboratory
test, Lung assist
device therapy, Oral
contraception, Pulmonary
embolism, Resuscitation
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Arrhythmia related investigations,
signs and symptoms (broad), Shock-associated circulatory or
cardiac conditions (excl torsade de pointes) (narrow), Embolic and
thrombotic events, venous (narrow), Acute central respiratory
depression (broad), Cardiomyopathy (broad), Respiratory failure
(broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-03-30
Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Reported to be on
Drospirenone-Ethinyl Estradiol 3-0.02 MG per tab
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:
Write-up: Patient
was a 16yr female who received Pfizer vaccine 3/19/21 at vaccine
clinic and presented with ongoing CPR to the ED 3/28/21 after
cardiac arrest at home. Patient placed on ECMO and imaging
revealed bilateral large pulmonary embolism as likely etiology of
arrest. Risk factors included oral contraceptive use. Labs have
since confirmed absence of Factor V leiden or prothrombin gene
mutation. Patient declared dead by neurologic criteria 3/30/21.
|
|
VAERS ID: |
1386841 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Male |
Location: |
Georgia |
Vaccinated: |
2021-06-03 |
Onset: |
2021-06-07 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
AR / IM |
Administered by: Other
Purchased by: ?
Symptoms: Abdominal
discomfort, Condition
aggravated, Death, Headache
SMQs:, Gastrointestinal perforation, ulcer, haemorrhage,
obstruction non-specific findings/procedures (broad),
Gastrointestinal nonspecific symptoms and therapeutic procedures
(narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-07
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Adderall
Current Illness: Headache, upset stomach
Preexisting Conditions: ADHD
Allergies: NKDA
Diagnostic Lab Data: Autopsy pending
CDC Split Type:
Write-up: Prodrome
of headache and gastric upset over 2 days following second dose.
Then felt fine. Found the following day dead in bed. Autopsy
pending
|
|
VAERS ID: |
1420630 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2021-03-13 |
Onset: |
2021-04-03 |
Days after vaccination: |
21 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 1 |
UN / IM |
Administered by: Private
Purchased by: ?
Symptoms: Chest pain, Death, General
physical health deterioration, Haemophagocytic
lymphohistiocytosis, Pericardial
effusion
SMQs:, Systemic lupus erythematosus (broad),
Gastrointestinal nonspecific symptoms and therapeutic procedures
(broad), Haemodynamic oedema, effusions and fluid overload
(narrow), Cardiomyopathy (broad), Drug reaction with eosinophilia
and systemic symptoms syndrome (broad), Immune-mediated/autoimmune
disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-15
Days after onset: 73
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 32 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Artane, azithromycin,
calcium carbonate, dicyclomine, doxycycline, escitalopram,
flovent, gabapentin, lansoprazole, melatonin, ondansetron,
tedizolid,
Current Illness: disseminated
mycobacterium chelonae infection
Preexisting Conditions: ataxia
telangiectasia; EBV-associated lymphoma
Allergies: none
Diagnostic Lab Data:
CDC Split Type:
Write-up: ~4 weeks
after the 2nd dose of Pfizer, patient presented to the hospital
with chest pain; had pericardial effusion. Initially improved but
then had decompensation, prolonged hospitalization. Diagnosed with
hemophagocytic lymphohistocytosis (HLH) and ultimately died.
|
|
VAERS ID: |
1466009 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2021-04-03 |
Onset: |
2021-04-30 |
Days after vaccination: |
27 |
Submitted: |
0000-00-00 |
Entered: |
2021-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EN6207 / 1 |
LA / SYR |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
ER8734 / 1 |
LA / SYR |
Administered by: Other
Purchased by: ?
Symptoms: Autopsy, Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-30
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 8 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: He had no previous
symptoms. I was with him one hour before and my assistant saw him
20 minutes prior and he did not show any irregularities.
CDC Split Type:
Write-up: My son
died, while taking his math class on Zoom. We are waiting for the
autopsy because the doctors did not find anything. He was a
healthy boy, he had a good academic index, he wanted to be a civil
engineer. He was the best thing in my life.
|
|
VAERS ID: |
1475434 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2021-07-07 |
Onset: |
2021-07-13 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2021-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-13
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: enlarged heart
Allergies: unknown
Diagnostic Lab Data:
CDC Split Type:
Write-up: The
patient died 6 days after receiving dose #2
|
|
VAERS ID: |
1694568 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2021-03-19 |
Onset: |
2021-03-28 |
Days after vaccination: |
9 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Autopsy, Pulmonary
embolism
SMQs:, Embolic and thrombotic events, venous (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-03-30
Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: albuterol, Flovent,
doxycycline, drospirenone and ethinyl estradiol, and Zoloft
Current Illness:
Preexisting Conditions: asthma
Allergies:
Diagnostic Lab Data: autopsy
CDC Split Type:
Write-up: pulmonary
embolism
|
|
VAERS ID: |
1734141 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Male |
Location: |
Georgia |
Vaccinated: |
2021-04-19 |
Onset: |
2021-04-01 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-25 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
ER8731 / 1 |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Cardiomegaly
SMQs:, Cardiac failure (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-24
Days after onset: 23
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101177018
Write-up: killed
this young man/he died of an enlarged heart (500+ grams); The
initial case was missing the following minimum criteria:
unidentified reporter. Upon receipt of follow-up information on
20Sep2021, this case now contains all required information to be
valid. This is a spontaneous report from Pfizer sponsored Program,
via contactable consumers. A 16-year-old male patient received
BNT162B2 via an unspecified route of administration on 19Apr2021
(Lot Number: ER8731; Expiration Date: Jul2021) (at 16-year-old) as
dose 1, single for COVID-19 immunisation. The patient''s medical
history and concomitant medications were not reported. The patient
died in 24Apr2021. His father claimed he took the Pfizer vaccine
five days before (24Apr2021) he died and that he died of an
enlarged heart (500+grams) from Apr2021. It''s not reported if
autopsy performed. Follow-up attempts are completed. No further
information is expected. ; Reported Cause(s) of Death: died of an
enlarged heart
|
|
VAERS ID: |
1757635 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2021-10-02 |
Onset: |
2021-10-03 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / SYR |
Administered by: Pharmacy
Purchased by: ?
Symptoms: Death, Fatigue
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-10-03
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: unknown
Current Illness: unknown
Preexisting Conditions: none
Allergies: unknown
Diagnostic Lab Data:
CDC Split Type:
Write-up: fatigue
then death
|
|
VAERS ID: |
1823671 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Female |
Location: |
Missouri |
Vaccinated: |
0000-00-00 |
Onset: |
2021-10-13 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-28 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-10-13
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101426032
Write-up: death;
This is a spontaneous report from a contactable consumer. A
16-years-old female patient received BNT162B2 (PFIZER-BIONTECH
COVID-19 VACCINE), dose 2 via an unspecified route of
administration on an unspecified date (Batch/Lot number was not
reported) as DOSE 2, SINGLE at the age of 16-year-old for covid-19
immunisation. The patient medical history and concomitant
medications were not reported. patient previously received the
first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on
13Jul2021 at the age of 16-year-old for covid-19 immunization. The
patient experienced death on 13Oct2021. The patient died on
13Oct2021. The lot number for vaccine (BNT162B2), was not provided
and will be requested during follow-up; Reported Cause(s) of
Death: death
|
|
VAERS ID: |
1576798 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-07-15 |
Onset: |
2021-07-23 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2021-08-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EY0583 / 1 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Body
temperature, Completed
suicide
SMQs:, Suicide/self-injury (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-23
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical
History/Concurrent Conditions: ADHD; Self injurious behaviour
Allergies:
Diagnostic Lab Data: Test Date: 20210715;
Test Name: Body temperature; Result Unstructured Data: Test
Result:36.2; Comments: Before vaccination
CDC Split Type: JPPFIZER INC202101008056
Write-up: Suicide;
This is a spontaneous report from a contactable physician received
from the Regulatory Authority. Regulatory authority report number
is v21122543. The 16-year and 5-month-old male patient received
first dose of bnt162b2 (COMIRNATY) at 16-year-old on 15-JUL-2021
12:00 as dose 1, single (lot number: EY0583, expiration date:
31Oct2021) for COVID-19 immunisation. Body temperature before
vaccination was 36.2 degrees Centigrade. Medical history included
attention deficit hyperactivity disorder (ADHD) and Self injurious
behaviour. Concomitant medications and family history were not
provided. The course of the events was as follows: On 15Jul2021 at
12:00 (the day of vaccination), the patient received the first
dose of BNT162b2 (COMIRNATY, Solution for injection, Lot# EY0583,
Expiration date 31Oct2021) via an unspecified route of
administration as a single dose for COVID-19 immunization. On
23Jul2021 at 18:30 (8 days after the vaccination), the patient
experienced suicide and died. The outcome of the event was fatal.
It was not reported if an autopsy was performed. The course of the
event was as follows: On 23Jul2021, the patient jumped off the top
floor of the apartment and died. It was assumed the he killed
himself. The reporting physician classified the event as serious
(fatal) and assessed that the event was not related to BNT162b2.
Other possible cause of the event such as any other diseases was
ADHD. The reporting physician commented as follows: The patient
was prescribed oral medicines for ADHD at a psychiatry department,
but recently he had stopped taking them, and self injurious
behaviour had been noted.; Sender''s Comments: Event suicide
represents an intercurrent medical condition and unrelated to
bnt162b2 . The underlying history of attention deficit
hyperactivity disorder (ADHD) and Self injurious behavior may play
a explanation.; Reported Cause(s) of Death: Suicide
|
|
VAERS ID: |
1702154 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-08-10 |
Onset: |
2021-08-16 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
FF0843 / 1 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Blood
pressure measurement, Blood test, Body
temperature, Cardiac
arrest, Cardio-respiratory
arrest, Computerised
tomogram, Electrocardiogram, Intestinal
ischaemia, Ventricular
fibrillation
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Arrhythmia related investigations,
signs and symptoms (broad), Ventricular tachyarrhythmias (narrow),
Shock-associated circulatory or cardiac conditions (excl torsade
de pointes) (narrow), Acute central respiratory depression
(broad), Ischaemic colitis (narrow), Cardiomyopathy (broad),
Respiratory failure (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-09-01
Days after onset: 16
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of
non-encoded Patient Relevant History: Patient Other Relevant
History 1: none
Allergies:
Diagnostic Lab Data: Test Date: 20210831;
Test Name: blood pressure; Result Unstructured Data: Test
Result:decreased; Test Date: 20210816; Test Name: blood test;
Result Unstructured Data: Test Result:An obvious cause of cardiac
arrest was unknown; Comments: An obvious cause of cardiac arrest
was unknown; Test Date: 20210810; Test Name: body temperature;
Result Unstructured Data: Test Result:36.2 Centigrade; Comments:
Before vaccination; Test Date: 20210816; Test Name: CT; Result
Unstructured Data: Test Result:An obvious cause of cardiac arrest
was unknown; Comments: An obvious cause of cardiac arrest was
unknown; Test Date: 20210831; Test Name: CT; Result Unstructured
Data: Test Result:NOMI(Non-occlusive mesenteric ischaemia); Test
Date: 20210816; Test Name: electrocardiogram; Result Unstructured
Data: Test Result:An obvious cause of cardiac arrest was unknown;
Comments: An obvious cause of cardiac arrest was unknown
CDC Split Type: JPPFIZER INC202101184843
Write-up: Cardiac
arrest; cardiopulmonary arrest; NOMI(Non-occlusive mesenteric
ischaemia); ventricular fibrillation; This is a spontaneous report
from a contactable physician received from the Reglatory Agency.
Regulatory authority report number is v21126302. A 16-year-old
(also reported as 16-year and 6-month-old) male patient received
bnt162b2 (COMIRNATY, Lot Number: FF0843; Expiration Date:
31Oct2021), dose 1 via an unspecified route of administration on
10Aug2021 13:00 as single dose for covid-19 immunisation. Medical
history was none. The patient had no family history. There were no
points to be considered on the vaccine screening questionnaire
(primary diseases, allergies, vaccinations and illnesses within
the last one month, medications the patient was taking, past
adverse effect history, growth status). The patient''s concomitant
medications were not reported. Body temperature before vaccination
was 36.2 degrees Centigrade. On 10Aug2021 at 13:00 (the day of
vaccination), the patient received the first dose of BNT162b2. On
16Aug2021 at 16:40 (6 days, 3 hours and 40 minutes after the
vaccination), the patient experienced cardiac arrest. The patient
was immediately transported and admitted to the reporting
hospital. On 01Sep2021 (22 days after the vaccination), the
outcome of the event was fatal. The course of the event was as
follows: On 16Aug2021 at 16:40 (6 days, 3 hours and 40 minutes
after the vaccination), the patient was immediately transported
the reporting hospital because of cardiopulmonary arrest (CPA).
Before arrival to the hospital, automatic external defibrillator
(AED) was conducted once. After the arrival, asystole, then
VF(ventricular fibrillation) were noted. And return of spontaneous
circulation (ROSC) was achieved after the one attempt of
direct-current defibrillator (DC). The patient was hospitalized
after resuscitated from the CPA. An obvious cause of cardiac
arrest was unknown on computerised tomogram (CT), the blood test
and electrocardiogram. The patient underwent tracheal intubation,
and was managed by artificial respiration under hospitalization.
Although targeted temperature management (TTM) was performed,
there was no recovery of consciousness. On 31Aug2021 (21 days
after the vaccination), blood pressure decreased.
NOMI(Non-occlusive mesenteric ischaemia) was diagnosed through CT.
On 01Sep2021 (22 days after the vaccination), the death was
confirmed. The reporting physician classified the event as serious
(Hospitalized) and assessed that the causality between the event
and BNT162b2 as unassessable. Other possible cause of the event
such as any other diseases was not reported. The patient died on
01Sep2021. It was not reported if an autopsy was performed. The
outcome of event ventricular fibrillation was recovered on
16Aug2021, the rest of events was fatal.; Reported Cause(s) of
Death: Cardiac arrest; cardiopulmonary arrest; Non-occlusive
mesenteric ischaemia
|
|
VAERS ID: |
1732657 (history) |
Form: |
Version 2.0 |
Age: |
16.0 |
Sex: |
Female |
Location: |
Foreign |
Vaccinated: |
0000-00-00 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-24 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC202101245513
Write-up: death;
This is a spontaneous report from a contactable physician based on
information received by Pfizer from Biontech [manufacturer control
number: 88130], license party for BNT162B2 (COMIRNATY). A
16-year-old female patient received BNT162B2 (COMIRNATY, Batch/Lot
number was not reported), via an unspecified route of
administration on an unspecified date (at 16-year-old) as dose
number unknown, single for COVID-19 immunisation. The patient
medical history and concomitant medications were not reported. It
was reported that parents stated on 16 years old female patient
who received a vaccination in the morning and was found dead in
her bed in the afternoon. No further details and no cause of death
could be obtained by reporting physician. The patient died on an
unspecified date. It was not reported if an autopsy was performed.
The lot number for BNT162B2, was not provided and will be
requested during follow up.; Sender''s Comments: The information
on the circumstances of the patient''s death is too limited to
perform a meaningful company causality assessment: this event is
handled as related to the suspect product BNT162B2 as a cautionary
measure and for reporting purposes. The impact of this report on
the benefit/risk profile of the Pfizer product is evaluated as
part of Pfizer procedures for safety evaluation, including the
review and analysis of aggregate data for adverse events. Any
safety concern identified as part of this review, as well as any
appropriate action in response, will be promptly notified to
regulatory authorities, Ethics Committees, and Investigators, as
appropriate.; Reported Cause(s) of Death: death
|
|
VAERS ID: |
1199455 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2021-04-02 |
Onset: |
2021-04-10 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2021-04-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
- / - |
Administered by: Private
Purchased by: ?
Symptoms: Cardiac
arrest, Chest pain, Death, Dyspnoea
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (narrow), Arrhythmia related investigations,
signs and symptoms (broad), Shock-associated circulatory or
cardiac conditions (excl torsade de pointes) (narrow), Acute
central respiratory depression (broad), Pulmonary hypertension
(broad), Gastrointestinal nonspecific symptoms and therapeutic
procedures (broad), Cardiomyopathy (broad), Respiratory failure
(broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-10
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: fluoxetine,
fesoterodine, ortho-tricyclen, oxybutynin
Current Illness: NA
Preexisting Conditions: spina bifida,
spinal meningocele, VP shunt, scoliosis, neurogenic bladder,
constipation
Allergies: bananas, cephalexin, kiwi,
mango, pineapple, latex
Diagnostic Lab Data:
CDC Split Type:
Write-up: Patient
reported difficulty breathing and chest pain; suffered cardiac
arrest and death
|
|
VAERS ID: |
1243487 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2021-04-13 |
Onset: |
2021-04-21 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2021-04-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW010 / 1 |
LA / IM |
Administered by: Unknown
Purchased by: ?
Symptoms: Completed
suicide
SMQs:, Suicide/self-injury (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-21
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown, History of
Mental Illness
Current Illness: Mental Illness,
Preexisting Conditions: Mental Illness
Allergies: None Reported
Diagnostic Lab Data: None
CDC Split Type:
Write-up: Patient
Committed Suicide with a firearm.
|
|
VAERS ID: |
1307657 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Ohio |
Vaccinated: |
2021-04-19 |
Onset: |
2021-04-23 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2021-05-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0153 / 2 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Completed
suicide
SMQs:, Suicide/self-injury (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-23
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:
Write-up: Death by
suicide.
|
|
VAERS ID: |
1388042 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2021-05-23 |
Onset: |
2021-06-07 |
Days after vaccination: |
15 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0168 / 2 |
UN / IM |
Administered by: Private
Purchased by: ?
Symptoms: Brain
oedema, Cerebral
infarction, Computerised
tomogram head abnormal, Decompressive
craniectomy, Haemorrhage
intracranial, Intracranial
pressure increased, Intraventricular
haemorrhage, Ventricular
drainage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow),
Ischaemic central nervous system vascular conditions (narrow),
Haemorrhagic central nervous system vascular conditions (narrow),
Embolic and thrombotic events, vessel type unspecified and mixed
arterial and venous (narrow), Hyponatraemia/SIADH (broad),
Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? Yes
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Headache started around
3 weeks prior to event that delayed dose of second vaccine.
Headache was very severe and she saw PCP for it twice and it
lasted a week. It then resolved and she got her second vaccine.
Preexisting Conditions: None except
obesity with BMI 39
Allergies: None
Diagnostic Lab Data: CT scans 6/7 and 6/8
CDC Split Type:
Write-up: Patient
had massive acute intracranial hemorrhage. Was found down in
bathroom. In ED CT scan showed large intraventricular hemorrhage,
EVD placed, patient progressed to massive brain swelling and
infarctions, decompressive craniectomy, unable to control
intracranial pressure, parents agreed to DNR status and patient is
not expected to survive.
|
|
VAERS ID: |
1420762 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2021-06-17 |
Onset: |
2021-06-23 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
- / - |
Administered by: Private
Purchased by: ?
Symptoms: Autopsy, Cardiac
arrest
SMQs:, Torsade de pointes/QT prolongation (broad),
Anaphylactic reaction (broad), Arrhythmia related investigations,
signs and symptoms (broad), Shock-associated circulatory or
cardiac conditions (excl torsade de pointes) (narrow), Acute
central respiratory depression (broad), Cardiomyopathy (broad),
Respiratory failure (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-23
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Vienva 0.1-20 mg-mcg
per tablet
Current Illness: No.
Preexisting Conditions: Obesity, Family
history of clotting disorder (her workup with negative), and
depression.
Allergies: NKDA
Diagnostic Lab Data:
CDC Split Type:
Write-up: Cardiac
arrest without resuscitation. Unknown cause of cardiac arrest.
Awaiting autopsy report.
|
|
VAERS ID: |
1689212 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2021-04-17 |
Onset: |
2021-07-20 |
Days after vaccination: |
94 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / UNK |
- / IM |
Administered by: Private
Purchased by: ?
Symptoms: COVID-19, Death, SARS-CoV-2
test positive
SMQs:, Infective pneumonia (broad), Opportunistic
infections (broad), COVID-19 (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-08-29
Days after onset: 40
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 51 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: CETIRIZINE,
ERGOCALCIFEROL,
Current Illness: STAGE IV TESTICULAR
EMBRYONAL RHABDOMYOSARCOMA W/ LUNG & BONE METASTASES
Preexisting Conditions: SEE ABOVE
Allergies: VANCOMYCIN, TEMSIROLIMUS
Diagnostic Lab Data:
CDC Split Type:
Write-up: SARS COV2
POSITIVE ON 7/20; EXPIRED 8/29/2021
|
|
VAERS ID: |
1815295 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2021-06-18 |
Onset: |
2021-07-21 |
Days after vaccination: |
33 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-25 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
EW0178 / 2 |
LA / IM |
Administered by: Other
Purchased by: ?
Symptoms: Autopsy, Hyperglycaemia
SMQs:, Hyperglycaemia/new onset diabetes mellitus (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-23
Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Benadryl
Current Illness:
Preexisting Conditions: Obesity
Allergies: Orange Juice
Diagnostic Lab Data: Autopsy performed
07/27/2021
CDC Split Type:
Write-up: Acute
Hyperglycemic Crisis
|
|
VAERS ID: |
1828901 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2021-09-15 |
Onset: |
2021-10-21 |
Days after vaccination: |
36 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-29 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Unknown
Purchased by: ?
Symptoms: Angiogram
pulmonary normal, C-reactive
protein increased, COVID-19, Cardiac
arrest, Cardioversion, Chest
discomfort, Chest pain, Condition
aggravated, Death, Dyspnoea, Echocardiogram
abnormal, Ejection
fraction decreased, Electrocardiogram
ST segment elevation, Full blood
count, Inappropriate
schedule of product administration, Life
support, Malaise, Metabolic
function test, Resuscitation, SARS-CoV-2
test positive, Tachycardia, Troponin
increased, Ventricular
arrhythmia
SMQs:, Torsade de pointes/QT prolongation (broad), Cardiac
failure (narrow), Anaphylactic reaction (narrow), Neuroleptic
malignant syndrome (broad), Myocardial infarction (narrow),
Anticholinergic syndrome (broad), Arrhythmia related
investigations, signs and symptoms (broad), Ventricular
tachyarrhythmias (narrow), Shock-associated circulatory or cardiac
conditions (excl torsade de pointes) (narrow), Acute central
respiratory depression (broad), Pulmonary hypertension (broad),
Gastrointestinal nonspecific symptoms and therapeutic procedures
(broad), Cardiomyopathy (narrow), Respiratory failure (broad),
Medication errors (narrow), Infective pneumonia (broad),
Dehydration (broad), Opportunistic infections (broad), COVID-19
(narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-10-23
Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: none
Current Illness: COVID-19 August 2021
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: See above. CBC, BMP.
Troponin elevated at 20. CRP significantly elevated. CTA chest
negative for PE. EKG with ST elevations. Echocardiogram with
depressed EF 40-45%. SARS-CoV-2 positive.
CDC Split Type:
Write-up: Patient
reported symptomatic (non-severe) case of COVID-19 August 2021 and
recovered fully. She reported receiving Pfizer COVID vaccine
9/3/21 and second dose 9/15/21. She present to the emergency
department of my hospital 10/23/21 with chest pain and dyspnea for
48h. Was feeling completely well prior to onset of chest
discomfort. Symptoms were mild. No sick contacts or family
members. ED evaluation remarkable for normal exam, no hypoxia,
normal blood pressure. EKG with diffuse ST elevation. Troponin
elevated at 20. CTA chest negative for PE or pneumonia.
SARS-CoV-PCR positive but thought to be persistent positive rather
than reinfection because of lack of clinical symptoms, recent
COVID-19 and recent vaccination. Cardiologist consulted, thought
acute coronary syndrome unlikely based on age and lack of risk
factors. STAT Echo resulted depressed EF 40-45%. Simultaneously
she had become increasingly tachycardic and EKG appeared more
ischemic. Cardiac cath lab was activated and she was about to be
transported when she suffered cardiac arrest. Initial rhythm was
VT. Received ACLS protocol CPR x 65 minutes including multiple
cardioversion, amiodarone, lidocaine, magnesium and other
antiarrhythmics. Unfortunately she was not able to be resuscitated
and died. Cause of death possible acute myocarditis.
|
|
VAERS ID: |
1688720 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Female |
Location: |
Foreign |
Vaccinated: |
0000-00-00 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
UNKNOWN / 1 |
- / - |
Administered by: Other
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical
History/Concurrent Conditions: Raynaud''s syndrome
Allergies:
Diagnostic Lab Data:
CDC Split Type: BRPFIZER INC202101144750
Write-up: had a
reaction and is hospitalized in serious condition / the patient
had died; This is a spontaneous report from a contactable consumer
received through COVAES portal (firstly by logistic colleague). A
female patient of an unspecified age received first dose of
bnt162b2 (COMIRNATY, Formulation: solution for injection, Lot
number: unknown) via an unspecified route of administration on an
unspecified date (age at the vaccination: 17-years-old) as DOSE 1,
SINGLE for covid-19 immunisation. At the time of vaccination,
pregnancy was reported as unknown. Medical history included
raynaud''s phenomenon from an unknown date and unknown if ongoing.
The patient''s concomitant medications were not reported. Other
vaccine in four weeks was reported as unknown. Prior to the
vaccination, the patient was not diagnosed with COVID-19. The
reporter reported an adverse event that occurred in the school
where she worked, a student took the 1st dose of the pfizer
vaccine and she had a reaction and was hospitalized in serious
condition in the hospital. The reporter informed that the patient
had died on an unspecified date for an unspecified reason.
Treatment AE was reported as unknown. It was unknown if any
autopsy was performed.; Reported Cause(s) of Death: had a reaction
and is hospitalized in serious condition / the patient had died
|
|
VAERS ID: |
1737907 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-08-23 |
Onset: |
2021-09-01 |
Days after vaccination: |
9 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-27 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 1 |
RA / OT |
Administered by: Other
Purchased by: ?
Symptoms: Asthenia, COVID-19, Computerised
tomogram, Drug
ineffective, Hypotension, Pneumonia, Pulmonary
sepsis, Respiratory
failure, SARS-CoV-2
test, Septic
shock, Vomiting
SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis
(broad), Lack of efficacy/effect (narrow), Neuroleptic malignant
syndrome (broad), Shock-associated circulatory or cardiac
conditions (excl torsade de pointes) (broad), Torsade de pointes,
shock-associated conditions (broad), Hypovolaemic shock conditions
(broad), Toxic-septic shock conditions (narrow),
Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic
and neurogenic shock conditions (broad), Acute central respiratory
depression (narrow), Guillain-Barre syndrome (broad),
Gastrointestinal nonspecific symptoms and therapeutic procedures
(narrow), Eosinophilic pneumonia (broad), Hypersensitivity
(broad), Respiratory failure (narrow), Drug reaction with
eosinophilia and systemic symptoms syndrome (broad), Infective
pneumonia (narrow), Dehydration (broad), Hypokalaemia (broad),
Sepsis (narrow), Opportunistic infections (broad), COVID-19
(narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-09-18
Days after onset: 17
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: Pfizer, Inc. EUA
027034
Current Illness: Down''s syndrome
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210911;
Test Name: chest tomography; Result Unstructured Data: Test
Result:major pulmonary impairment; Test Date: 20210911; Test Name:
COVID-19 PCR test; Test Result: Positive
CDC Split Type: BRPFIZER INC202101233825
Write-up: vomit
with secretion; started to present severe symptoms of the disease
/ COVID-19/ fever / weakness / the reporter believes that the
patient''s fever and weakness were related to COVID-19; started to
present severe symptoms of the disease / COVID-19/ fever /
weakness / the reporter believes that the patient''s fever and
weakness were related to COVID-19; blood pressure low; weakness;
septic shock; pulmonary sepsis; unspecified pneumonia; respiratory
failure; This is a spontaneous report from two contactable
consumers (patient''s father and patient''s aunt) received through
portal. A 17-year-old male patient received bnt162b2 (COMIRNATY),
dose 1 via Intramuscular, administered in right arm on 23Aug2021
12:00 AM (Batch/Lot number was not reported) as DOSE 1, SINGLE for
covid-19 immunisation. Medical history included ongoing Down''s
syndrome (He was born with it). He did not have any medical
history, only Down''s Syndrome. Concomitant medication included
alprazolam taken for sedative therapy, start and stop date were
not reported. Prior to vaccination, the patient was not diagnosed
with COVID-19. No allergic to any medications, food or other
products. The patient did not receive any other vaccines within 4
weeks PRIOR to the COVID-19 vaccine. 13 days after taking the
vaccine, the patient started to present severe symptoms of the
disease and died in 7 days. The patient after taking the vaccine
got sick and as result of the disease he died. The causes were
written on the death certificate as follows bellow: Septic shock,
Pulmonary sepsis, Unspecified pneumonia and Covid-19. The patient
did not leave the house, did not receive visitors and his health
was very good. The house members did the tests and as per the
results, they were not infected. Reporter said that the patient
was a very healthy boy and refused to take any vaccine, but he
received the Pfizer vaccine against covid-19 on 23Aug2021. He
started to show symptoms of fever on 06Sep2021 at 01:00 AM and as
the fever did not go away and because he presented weakness (in
Sep2021) and vomiting with secretions on 10Sep2021, he was taken
to the emergency care unit on 11Sep2021. His condition was
considered serious and, on that same day, he was taken to the ICU
of the hospital. The patient underwent a PCR test on 11Sep2021 and
on 14Sep2021 he received a positive result (the reporter believes
that the patient''s fever and weakness were related to COVID-19).
On 11Sep2021, he also performed a chest tomography and the result
showed major pulmonary impairment, therefore, the patient was
intubated from 11Sep2021 on with oxygen supplementation. Oxygen
flow was decided according to the patient''s health status and the
patient received supplemental oxygen during the 7 days of
hospitalization. On the day of intubation, the patient had low
blood pressure (in Sep2021) and received norepinephrine. The
reporter does not know how the patient''s blood pressure was
during hospitalization. During intubation, the reporter had no
contact with the patient and did not talk to the medical team, so
she was unable to say if there was a worsening of the Down
Syndrome and was unable to say any exams and/or treatments
performed. The physician only commented that all the patient''s
organs were normal, with only the respiratory system being
compromised. On 18Sep2021 (date of death), the patient suffered a
respiratory arrest, respiratory failure, but the reporter was
unable to give further details. The reporter commented that she
did not know that the patient had pneumonia during
hospitalization, she only found out when she saw the
investigation. She reported that the patient used alprazolam as a
concomitant medication and was unable to say whether the patient
used it in the hospital until the date of death. The patient was
hospitalized from 11Sep2021 to 18Sep2021. The patient died on
18Sep2021. In case of death, an autopsy was performed. Autopsy
results: the medical report indicated the cause of death as
pulmonary sepsis, nonspecific pneumonia and covid-19. The reporter
said that the result of covid-19 in the final medical report had a
question mark, indicating it as inconclusive, but she believed
that the patient had COVID-19 due to the exam done on 11Sep2021,
which was positive. An autopsy was performed that revealed
pulmonary sepsis, unspecified pneumonia, covid-19, septic shock.
The outcome of events COVID-19, drug ineffective, septic shock,
pulmonary sepsis, unspecified pneumonia and respiratory failure
was fatal, vomit with secretion was recovered on 10Sep2021, blood
pressure low and weakness was unknown. Information on the
lot/batch number has been requested.; Reported Cause(s) of Death:
COVID-19; respiratory failure; Autopsy-determined Cause(s) of
Death: COVID-19; pulmonary sepsis; unspecified pneumonia; septic
shock
|
|
VAERS ID: |
1757964 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-07-20 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-04 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / UNK |
- / OT |
Administered by: Unknown
Purchased by: ?
Symptoms: Death, Myocarditis
SMQs:, Cardiomyopathy (broad), Drug reaction with
eosinophilia and systemic symptoms syndrome (broad),
Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: BEMODERNATX, INC.MOD20213
Write-up: Death;
Bilateral myocarditis; This spontaneous case was reported by a
consumer and describes the occurrence of DEATH (Death) and
MYOCARDITIS (Bilateral myocarditis) in a 17-year-old male patient
who received mRNA-1273 (Spikevax) for COVID-19 vaccination. No
Medical History information was reported. On 20-Jul-2021, the
patient received dose of mRNA-1273 (Spikevax) (unknown route) 1
dosage form. On an unknown date, the patient experienced DEATH
(Death) (seriousness criteria death and medically significant) and
MYOCARDITIS (Bilateral myocarditis) (seriousness criterion
medically significant). The patient died on an unknown date. The
cause of death was not reported. It is unknown if an autopsy was
performed. At the time of death, MYOCARDITIS (Bilateral
myocarditis) outcome was unknown. Concomitant product was not
provided. Treatment medication was not reported. Patient died at
17 was reported. Company Comment: This case concerns a 17-year-old
male patient with no reported medical history, who experienced the
unexpected, serious event of death and expected and AESI event of
myocarditis. Time to onset from vaccination was not reported. Date
of death was not reported and autopsy report is not available. The
rechallenge was not applicable, since vaccination dose number were
not specified. The benefit-risk relationship of Spikevax is not
affected by this report. Further information is expected. This
case was linked to MOD-2021-332861 (Patient Link).; Sender''s
Comments: This case concerns a 17-year-old male patient with no
reported medical history, who experienced the unexpected, serious
event of death and expected and AESI event of myocarditis. Time to
onset from vaccination was not reported. Date of death was not
reported and autopsy report is not available. The rechallenge was
not applicable, since vaccination dose number were not specified.
The benefit-risk relationship is not affected by this report.
Further information is expected.; Reported Cause(s) of Death:
Unknown cause of death
|
|
VAERS ID: |
1800410 (history) |
Form: |
Version 2.0 |
Age: |
17.0 |
Sex: |
Male |
Location: |
Foreign |
Vaccinated: |
2021-09-01 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2021-10-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
- / OT |
Administered by: Unknown
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: CAMODERNATX, INC.MOD20213
Write-up: Found
dead in the bedroom; This spontaneous case was reported by a
non-health professional and describes the occurrence of DEATH
(Found dead in the bedroom) in a 17-year-old male patient who
received mRNA-1273 (Moderna CoviD-19 Vaccine) for COVID-19
vaccination. No Medical History information was reported. In
September 2021, the patient received second dose of mRNA-1273
(Moderna CoviD-19 Vaccine) (unknown route) 1 dosage form. Death
occurred on 2021 The cause of death was not reported. It is
unknown if an autopsy was performed. No relevant concomitant
medications were reported. Treatment information was unknown.
Patient was found dead in the bedroom, few days after 2nd dose of
Moderna vaccine. Company comment: This case involves a 17-year-old
male subject with unknown medical history who experienced the
serious unlisted adverse event of death a few das after receiving
his second dose of mRNA-1273. The patient was found dead in his
bedroom. No further information is currently available on the
reason of his death or events that may have resulted in death. The
reporter declined further information on his name or address. The
benefit-risk relationship of mRNA-1273 is not affected by this
report.; Sender''s Comments: This case involves a 17-year-old male
subject with unknown medical history who experienced the serious
unlisted adverse event of death a few das after receiving his
second dose of mRNA-1273. The patient was found dead in his
bedroom. No further information is currently available on the
reason of his death or events that may have resulted in death. The
reporter declined further information on his name or address. The
benefit-risk relationship of mRNA-1273 is not affected by this
report.; Reported Cause(s) of Death: Unknown cause of death
|
|
VAERS ID: |
1078352 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2021-03-02 |
Onset: |
2021-03-05 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2021-03-06 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
010A21A / 1 |
LA / IM |
Administered by: Private
Purchased by: ?
Symptoms: Chest pain, Death, Fatigue, Headache, Pain, Unresponsive
to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad),
Neuroleptic malignant syndrome (broad), Guillain-Barre syndrome
(broad), Noninfectious encephalitis (broad), Noninfectious
encephalopathy/delirium (broad), Noninfectious meningitis (broad),
Gastrointestinal nonspecific symptoms and therapeutic procedures
(broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode
(broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-03-05
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Medical examiner
report is pending.
CDC Split Type:
Write-up: Developed
fatigue, body aches, headache 1 day after vaccination on 3/3. The
morning of 3/5 complained of chest pain. Took Tylenol at 8:30 am.
At 10:30 am his family found him unresponsive. EMS was called and
he was pronounced dead in the home.
|
|
VAERS ID: |
1105115 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Puerto Rico |
Vaccinated: |
2021-02-14 |
Onset: |
2021-02-18 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2021-03-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
UN / IM |
Administered by: Senior
Living Purchased by: ?
Symptoms: Abscess
limb, Death, Decreased
activity, Groin
abscess, Increased
upper airway secretion
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-02-28
Days after onset: 10
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Keppra 1000 mg,
Lamictal , Vimpat, Quetiapina, Lorazepam, Zyprexa, Motrin,
Vitamina K, Acido Folico, Sultato Ferroso, Multivitam?nico 365
Current Illness: None
Preexisting Conditions: Portal
hypertension (secondary to portal vein thrombosis), Leukopenia,
Thrombocytopenia, Epilepsy, Splenomegaly, Esophageal Varices,
Asthma, Pancytopenia and Severe mental retardation.
Allergies: Dilantin and aspirin
Diagnostic Lab Data: None
CDC Split Type: PR-55-21
Write-up: Resident
did not express having any symptoms, the only thing that the POC
observed abscesses in the arm, groin, thigh and knees after the
first vaccination. After the second dose, he was hypoactive. On
2/27 at about 3:30 am he asked him to turn on his side, between 4
am and 5 am POC went to the room I notice it strange, because his
head was wrapped in the sheet. When the POC removed the sheet, she
observed that her mouth and nose were full of secretions. So he
turned it and he himself did not react. He called the emergency
who certifies that he had no vital signs. (emergency arrives
within 5:45 am to 6:00 am)
|
|
VAERS ID: |
1386054 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Female |
Location: |
Ohio |
Vaccinated: |
2021-05-14 |
Onset: |
2021-06-06 |
Days after vaccination: |
23 |
Submitted: |
0000-00-00 |
Entered: |
2021-06-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
RA / - |
Administered by: Public
Purchased by: ?
Symptoms: Autopsy, Death, Thrombosis
SMQs:, Embolic and thrombotic events, vessel type
unspecified and mixed arterial and venous (narrow),
Thrombophlebitis (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-06-06
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: VANAFLAXINE BUSPIRONE
ABILIFY SPRINTEC
Current Illness: CHLAMYDIA
Preexisting Conditions: NA
Allergies: NA
Diagnostic Lab Data: AUTOPSY 6/8/21
CDC Split Type:
Write-up: DEATH
FROM BLOOD CLOT
|
|
VAERS ID: |
1446849 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Florida |
Vaccinated: |
2021-07-02 |
Onset: |
2021-07-04 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2021-07-05 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
- / 1 |
AR / - |
Administered by: Pharmacy
Purchased by: ?
Symptoms: Death
SMQs:
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-04
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Holcomb''s
disease; hypertrophic cardiomyopathy
Allergies: None
Diagnostic Lab Data: none
CDC Split Type:
Write-up: death
|
|
VAERS ID: |
1700329 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Wisconsin |
Vaccinated: |
2021-07-23 |
Onset: |
2021-08-30 |
Days after vaccination: |
38 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
UNAVAILABLE / 2 |
- / IM |
Administered by: Unknown
Purchased by: ?
Symptoms: Abdominal
pain, Activated
partial thromboplastin time prolonged, Acute
kidney injury, Acute
myocardial infarction, Acute
respiratory failure, Alanine
aminotransferase increased, Anisocytosis, Aspartate
aminotransferase normal, Base excess
abnormal, Basophil
count, Basophil
percentage decreased, Blood
albumin decreased, Blood
bicarbonate decreased, Blood
calcium decreased, Blood
chloride normal, Blood
creatinine normal, Blood
fibrinogen decreased, Blood
glucose increased, Blood
magnesium normal, Blood pH
normal, Blood
potassium normal, Blood
sodium normal, Blood urea
increased, Bronchoscopy
abnormal, Calcium
ionised decreased, Carbon
dioxide abnormal, Carbon
dioxide decreased, Cardiac
arrest, Catheterisation
cardiac abnormal, Chest X-ray
abnormal, Coronary
artery occlusion, Culture, Death, Dyspnoea, Electrocardiogram
abnormal, Endotracheal
intubation, Eosinophil
count decreased, Eosinophil
percentage decreased, Fatigue, Fibrin D
dimer, Full blood
count, Haematocrit
decreased, Haemofiltration, Haemoglobin
decreased, Haemorrhage, Hypoxia, Immature
granulocyte count increased, Intensive
care, International
normalised ratio increased, Lung assist
device therapy, Lung
opacity, Lymphocyte
count decreased, Lymphocyte
percentage decreased, Mean cell
haemoglobin concentration decreased, Mean cell
haemoglobin normal, Mean cell
volume increased, Mean
platelet volume increased, Mechanical
ventilation, Metabolic
function test, Monocyte
count, Monocyte
percentage decreased, Myocardial
infarction, Neutrophil
count increased, Oxygen
saturation decreased, PCO2
decreased, PO2
decreased, Platelet
count decreased, Prothrombin
time prolonged, Pulmonary
alveolar haemorrhage, Pulmonary
haemorrhage, Pyrexia, Red blood
cell count decreased, Red blood
cell nucleated morphology present, Red cell
distribution width increased, Right
ventricular failure, SARS-CoV-2
test negative, Sepsis, Septic
shock, Sinus
tachycardia, Tachycardia, Urine
analysis normal, Vomiting, White blood
cell count increased
SMQs:, Torsade de pointes/QT prolongation (broad),
Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow),
Cardiac failure (narrow), Liver related investigations, signs and
symptoms (narrow), Liver-related coagulation and bleeding
disturbances (narrow), Anaphylactic reaction (narrow), Acute
pancreatitis (broad), Angioedema (broad), Asthma/bronchospasm
(broad), Haematopoietic erythropenia (narrow), Haematopoietic
leukopenia (narrow), Haematopoietic thrombocytopenia (narrow),
Lactic acidosis (broad), Haemorrhage terms (excl laboratory terms)
(narrow), Haemorrhage laboratory terms (broad), Hyperglycaemia/new
onset diabetes mellitus (narrow), Interstitial lung disease
(narrow), Neuroleptic malignant syndrome (broad), Systemic lupus
erythematosus (broad), Myocardial infarction (narrow),
Anticholinergic syndrome (broad), Arrhythmia related
investigations, signs and symptoms (broad), Supraventricular
tachyarrhythmias (narrow), Retroperitoneal fibrosis (broad),
Shock-associated circulatory or cardiac conditions (excl torsade
de pointes) (narrow), Torsade de pointes, shock-associated
conditions (broad), Hypovolaemic shock conditions (broad),
Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid
shock conditions (broad), Hypoglycaemic and neurogenic shock
conditions (broad), Embolic and thrombotic events, arterial
(narrow), Acute central respiratory depression (narrow), Pulmonary
hypertension (narrow), Gastrointestinal nonspecific symptoms and
therapeutic procedures (narrow), Cardiomyopathy (broad),
Eosinophilic pneumonia (broad), Chronic kidney disease (narrow),
Hypersensitivity (broad), Tumour lysis syndrome (narrow),
Respiratory failure (narrow), Drug reaction with eosinophilia and
systemic symptoms syndrome (narrow), Infective pneumonia (broad),
Dehydration (broad), Sepsis (narrow), Opportunistic infections
(broad), COVID-19 (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-09-15
Days after onset: 16
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 15 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: ergocalciferol,
vitamin D2, 50,000 Units capsule pimecrolimus cream (ELIDEL) 1 %
cream triamcinolone ointment (KENALOG) 0.1 % ointment
Current Illness: Lupus
Preexisting Conditions: Lupus diagnosis
on 7/21/21
Allergies: Bactrim
Diagnostic Lab Data: Results for patient
9/1/2021 04:10 Arterial pH: 7.35 Arterial pCO2: 31.5 (L) Arterial
pO2: 71.6 Arterial HCO3: 16.8 (L) Arterial Total CO2: 17.8 (L)
Arterial Base Excess/Deficit: -7.6 Arterial Measured O2
Saturation: 90.0 Sodium Blood: 136 Potassium Blood: 4.4 Chloride
Blood: 114 (H) Carbon Dioxide: 17.8 (L) Glucose Blood: 241 (H)
BUN: 27 (H) Creatinine Blood: 0.82 Calcium Blood: 6.8 (L) WBC:
11.3 (H) RBC: 2.33 (L) Hemoglobin: 7.2 (L) Hematocrit: 22.8 (L)
MCV: 97.9 MCH: 30.9 MCHC: 31.6 (L) Platelet Count: 184 MPV: 11.4
(H) RDW: 17.9 (H) Nucleated RBC Automated: 0.2 (H) Differential
Type: MANUAL DIFF % Seg: 97.5 (H) % Lymphocytes: 1.0 (L) %
Monocytes: 1.0 % Meta: 0.5 (H) Absolute Neutrophils: 11.018 (H)
Abs Seg: 11.02 (H) Absolute Lymphocytes: 0.11 (L) Absolute
Monocytes: 0.11 Abs Meta: 0.06 (H) Total Cells Counted: 198
Anisocytosis: SLIGHT Results for patient 9/1/2021 13:38 Arterial
pH: 7.11 (LL) Arterial pCO2: 62.6 (HH) Arterial pO2: 70.3 Arterial
HCO3: 18.8 (L) Arterial Total CO2: 20.7 Arterial Base
Excess/Deficit: -12.7 Arterial Measured O2 Saturation: 85.2 (L)
Sodium Blood: 137 Potassium Blood: 4.7 Chloride Blood: 119 (H)
Carbon Dioxide: 20.7 (L) Glucose Blood: 226 (H) BUN: 31 (H)
Creatinine Blood: 0.89 Calcium Blood: 6.6 (L) WBC: 17.0 (H) RBC:
2.90 (L) Hemoglobin: 8.9 (L) Hematocrit: 28.7 (L) MCV: 99.0 MCH:
30.7 MCHC: 31.0 (L) Platelet Count: 187 MPV: 11.0 (H) RDW: 16.9
(H) Nucleated RBC Automated: 0.1 (H) Differential Type: AUTOMATED
DIFF % Neutrophils: 94.1 (H) % Imm Gran: 1.2 (H) % Lymphocytes:
1.1 (L) % Monocytes: 3.2 % Eosinophils: 0.0 % Basophils: 0.4
Absolute Neutrophils: 15.930 (H) Abs Imm Gran: 0.21 (H) Absolute
Lymphocytes: 0.19 (L) Absolute Monocytes: 0.55 (H) Absolute
Eosinophils: 0.00 Absolute Basophils: 0.07 Results for patient
9/4/2021 16:04 Arterial pH: 7.40 Arterial pCO2: 47.4 (H) Arterial
pO2: 60.2 (L) Arterial HCO3: 28.5 (H) Arterial Total CO2: 29.9 (H)
Arterial Base Excess/Deficit: 3.7 Arterial Measured O2 Saturation:
89.7 (L) Sodium Blood: 146 (H) Potassium Blood: 3.0 (L) Chloride
Blood: 106 Carbon Dioxide: 29.9 Glucose Blood: 176 (H) BUN: 67
(HH) Creatinine Blood: 2.53 (H) Calcium Blood: 8.3 (L) Ionized
Calcium: 4.66 Magnesium Blood: 1.9 WBC: 8.7 RBC: 2.47 (L)
Hemoglobin: 7.2 (L) Hematocrit: 21.9 (L) MCV: 88.7 MCH: 29.1 MCHC:
32.9 Platelet Count: 96 (L) MPV: 11.2 (H) RDW: 16.1 (H) Nucleated
RBC Automated: 0.6 (H) Differential Type: AUTOMATED DIFF %
Neutrophils: 93.0 (H) % Imm Gran: 1.6 (H) % Lymphocytes: 1.5 (L) %
Monocytes: 3.7 % Eosinophils: 0.0 % Basophils: 0.2 Absolute
Neutrophils: 8.120 (H) Abs Imm Gran: 0.14 (H) Absolute
Lymphocytes: 0.13 (L) Absolute Monocytes: 0.32 Absolute
Eosinophils: 0.00 Absolute Basophils: 0.02 PT Result: 16.1 (H) INR
Result: 1.25 PTT Result: 94.3 (H) TT Result: $g100.0 (H) D Dimer:
2.56 (H) Fibrinogen: 192 (L) Heparin Level.: 0.36 PREOPERATIVE
DIAGNOSIS: STEMI POSTOPERATIVE DIAGNOSIS: stemi Procedure(s): Left
heart catheterization with coronary angiography JL3 and SCR
ANESTHESIA: General ESTIMATED BLOOD LOSS: Minimal COMPLICATIONS:
None CONDITION: Critical ACCESS: 5 Fr left FA FINDINGS: Totally
occluded left anterior descending & circumflex coronary
arteries. Right coronary artery patent
CDC Split Type:
Write-up: Patient
is a 18 y.o. male patient with a past medical history significant
for lupus who presents with Pulmonary hemorrhage. About 2 days
ago, pt developed fevers and worsening shortness of breath. T max
102 F at home. He did not note anything that relieved or
exacerbated his difficulty breathing. He also reported fatigue,
abdominal pain and several episodes of NBNB emesis the week prior
to admission. No recently chest pain, diarrhea, hematuria,
dysuria, headache or neck stiffness. Pt presented to ED yesterday
and was treated with antibiotics and discharged, he came back
today due to worsening shortness of breath. Of note, pt was had 2
hospital admissions in the last 2 months, most recently for
febrile neutropenia. Completed 2 doses of COVID vaccine. At ED, pt
arrived with temp of 39.1, HR 143, RR 28, BP 117/67, SpO2 98% EKG
with sinus tachycardia, no ST elevations/depressions or other
acute ischemic changes. CXR revealed diffuse bilateral airspace
opacities without pneumothorax. CBC 10.6$g8.1/27.4<203, CMP
137/3.9/110/22/18/0.58<99, Ca 7, Alb 1.5, AST 15, ALT 86. UA
negative for infection, no protein. CXR with progressive diffuse
bilateral airspace opacity with air bronchograms, no pneumothorax.
Cultures obtained. Pt was treated with vancomycin, cefepime and
levofloxacin for sepsis and concern for pneumonia and given IV
fluids per ED sepsis protocol. He was also given Solumedrol 1g.
Less likely COVID given vaccination status and negative COVID
swab. Due to worsening tachycardia and hypoxia on oxygen, pt was
intubated and bleeding in airway was noted. Pt was admitted to the
ICU, and pulm crit care performed a bronchoscopy that revealed
diffuse alveolar hemorrhage. Repeat CXR in ICU revealed almost
complete white out of both lungs. Pt was bagged for almost an hour
due to persistent hypoxia. Pt was subsequently transferred to CW
due to concern for requiring VV ECMO. On arrival to CW CICU, pt
satting low 70s, vent settings titrated and sats improved to 90s.
He was continued on Epi, Norepi, Dexmed and Fentanyl. Rheum
history: Lupus diagnosed on renal biopsy 7/21/21, on bactrim
prophylaxis recently, recent treatment with rituximab, on daily
prednisone 30 mg BID Parents spanish speaking. Patient is a 18
y.o. male patient with a past medical history significant for
lupus who presents with acute hypoxic respiratory failure
requiring mechanical ventilation, septic shock and pulmonary
hemorrhage. It is unclear at this time if his pulmonary hemorrhage
is related to lupus vs idiopathic process. COVID negative and
fully vaccinated, making COVID pneumonia less likely. He is
maintaining his MAPs on epinephrine and arterial sats in the 90s
on SIMV PC PS. He is candidate for VV ECMO but does not require it
at this time due to decreasing vent settings. Rheumatology
consulted and large lab workup is underway. Plan to continue broad
spectrum antibiotics, close monitoring of hemodynamics and to
continue to watch for signs of recurrent pulmonary hemorrhage. Pt
requires CICU due to risk of acute cardiopulmonary decompensation.
Patient was an 18 yo man with Dx of lupus who presented to
hospital (transferred from outside hospital) in respiratory
failure due to pulmonary hemorrhage. Due to worsening hypoxemia in
spite of mechanical ventilation he was started on VV ECMO. While
on VV ECMO, he had a cardiac arrest due to right ventricular
failure and was converted to VA ECMO. He also developed acute
renal failure and was on CRRT. On 9/14, while on VA ECMO, he
developed a massive MI due to occlusion of his LAD and circumflex
coronaries. This heart injury was assessed as non recoverable and
all further care was considered futile. After given time to the
family to say their goodbyes, patient was removed from VA ECMO
support and pronounced dead with his family at the bedside on
9/15/2021 at 7:30 am
|
|
VAERS ID: |
1727443 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
Florida |
Vaccinated: |
2021-04-25 |
Onset: |
2021-07-07 |
Days after vaccination: |
73 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
ER8731, EW0167
/ 2 |
LA / IM |
Administered by: Other
Purchased by: ?
Symptoms: Death, Pulmonary
embolism
SMQs:, Embolic and thrombotic events, venous (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-07-07
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ADHD medication
Current Illness: None
Preexisting Conditions: None
Allergies: No
Diagnostic Lab Data:
CDC Split Type:
Write-up: Patient
died on July 7, 2021 of a pulmonary embolism. The clots were in
his lungs.
|
|
VAERS ID: |
1741267 (history) |
Form: |
Version 2.0 |
Age: |
18.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2021-08-26 |
Onset: |
2021-09-25 |
Days after vaccination: |
30 |
Submitted: |
0000-00-00 |
Entered: |
2021-09-28 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) /
PFIZER/BIONTECH |
FC3182 / UNK |
- / IM |
Administered by: Private
Purchased by: ?
Symptoms: Autopsy, Death, Pulmonary
embolism
SMQs:, Embolic and thrombotic events, venous (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-09-25
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: Bacterial Epiglottitis
Preexisting Conditions: Obesity
Allergies: Unknown
Diagnostic Lab Data: Autopsy 9/27/2021
CDC Split Type:
Write-up: Patient
died and preliminary autopsy revealed Massive pulmonary embolism
|