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From the 11/26/2021 release of VAERS data:

Found 19,532 cases where Vaccine targets COVID-19 (COVID19) and Patient Died

Government Disclaimer on use of this data



Case Details

This is page 1281 out of 1,954

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VAERS ID: 1336363 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Agitation, Dyspnoea, Myocardial infarction
SMQs:, Anaphylactic reaction (broad), Myocardial infarction (narrow), Anticholinergic syndrome (broad), Dementia (broad), Embolic and thrombotic events, arterial (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Cardiomyopathy (broad), Hypoglycaemia (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: AUPFIZER INC2021562785

Write-up: Agitation; Dyspnoea; Myocardial infarction; This is a spontaneous report from a contactable other health professional via a regulatory authority. Regulatory authority report number is 553078. An 83-year-old female patient received BNT162B2 (COMIRNATY, solution for injection, Lot number), via an unspecified route of administration, on unknown date at single dose for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. On unknown date, the patient developed agitation, dyspnoea and myocardial infarction. The events caused patient''s death on unknown date. It was unknown if an autopsy was performed. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Agitation; Dyspnoea; Myocardial infarction


VAERS ID: 1336364 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Vision blurred
SMQs:, Anticholinergic syndrome (broad), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Hypoglycaemia (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: AUPFIZER INC2021562787

Write-up: Vision blurred; This is a spontaneous report from a contactable other health professional via the regulatory authority. Regulatory authority report number is 550666. An 89-year-old female patient received BNT162b2 (COMIRNATY) on unknown date at single dose for COVID-19 immunisation. Medical history and concomitant medications were unknown. The patient was not pregnant at the time of vaccine. On unknown date, the patient died due to vision blurred (as reported). It was unknown if an autopsy was performed. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Reported Cause(s) of Death: Vision blurred


VAERS ID: 1336365 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-18
Onset:2021-04-20
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Pneumonia aspiration
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: AUPFIZER INC2021562788

Write-up: Pneumonia aspiration; This is a spontaneous report from a contactable other healthcare professional received from the Therapeutic Goods Administration (TGA). The regulatory authority report number is 551017. A 99-year-old female patient received bnt162b2 (COMIRNATY) on 18Apr2021 at unknown, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced pneumonia aspiration on 20Apr2021. The patient died in 2021 due to the event. The outcome of the event was fatal. It was unknown if an autopsy was performed. No follow-up attempts are possible; information about lot/batch number cannot be obtained. ; Reported Cause(s) of Death: Pneumonia aspiration


VAERS ID: 1336375 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-02
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Arrhythmia
SMQs:, Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-16
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.MOD20211

Write-up: This regulatory authority case was reported by a pharmacist and describes the occurrence of ARRHYTHMIA in a 35-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) for COVID-19 vaccination. No Medical History information was reported. On 02-Feb-2021, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular) 1 dosage form. On 04-Mar-2021, received second dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced ARRHYTHMIA (seriousness criteria death and medically significant). The patient died on 16-Apr-2021. The cause of death was not reported. It is unknown if an autopsy was performed. For mRNA-1273 (COVID 19 Vaccine Moderna) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications reported by investigator. Treatment of this event was not reported. This is a case of death in a 35-year-old female subject with unknown medical history, who died one day after receiving the first dose of vaccine. Very limited information has been provided at this time. No follow up is possible.; Sender''s Comments: This is a case of death in a 35-year-old female subject with unknown medical history, who died one day after receiving the first dose of vaccine. Very limited information has been provided at this time. No follow up is possible.; Reported Cause(s) of Death: Unknown cause of death


VAERS ID: 1336380 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-28
Onset:2021-04-30
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA CNK: 4301081 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: 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? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: BEMODERNATX, INC.MOD20211

Write-up: Death; This regulatory authority case was reported by a physician and describes the occurrence of DEATH (Death) in an 80-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. CNK: 4301081) for COVID-19 vaccination. No Medical History information was reported. On 28-Apr-2021, the patient received second dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. Death occurred on 30-Apr-2021 The patient died on 30-Apr-2021. The cause of death was not reported. It is unknown if an autopsy was performed. For mRNA-1273 (COVID 19 Vaccine Moderna) (Unknown), the reporter did not provide any causality assessments. Action taken with the mRNA-1273 in response to the event is not applicable. Based on the current available information and temporal association between the use of the product and the events, a causal relationship cannot be excluded. Cause of death and patient''s history and concurrent conditions not provided confounded assessment; Reporter''s Comments: Treatment. Evolution of the ADR; Sender''s Comments: Based on the current available information and temporal association between the use of the product and the events, a causal relationship cannot be excluded. Cause of death and patient''s history and concurrent conditions not provided confounded assessment; Reported Cause(s) of Death: unknown cause of death


VAERS ID: 1336381 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2021-05-08
Onset:2021-05-08
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Sudden death
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-05-08
   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: Lymphoma
Allergies:
Diagnostic Lab Data:
CDC Split Type: BEPFIZER INC2021553628

Write-up: Sudden death; This is a spontaneous report from a contactable physician downloaded from the regulatory authority, regulatory authority number BE-FAMHP-DHH-N2021-91435. An adult male patient received first dose of bnt162b2 (COMIRNATY), on 08May2021 as 1st dose, single for covid-19 immunisation. Medical history included lymphoma. The patient''s concomitant medications were not reported. The patient experienced sudden death on 08May2021. No treatment received. The patient died on 08May2021. An autopsy was not performed. Reporter Comment: The patient died suddenly on this date. I happened to note when filling out the death certificates that he was prioritized for vaccination the same day with the first dose of Comirnaty. According to the family, the patient was recovering from lymphoma, with no active treatment at this time. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reporter''s Comments: The patient died suddenly on this date. I happened to note when filling out the death certificates that he was prioritized for vaccination the same day with the first dose of Comirnaty. According to the family, the patient was recovering from lymphoma, with no active treatment at this time.; Sender''s Comments: Information provided was so limited to prevent a meaningful or definite medical assessment for this demise. A causal relationship cannot be completely excluded between BNT162B2 injection and sudden death, due to the close chronological sequence. This case will be reassessed should additional information becomes available. 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: Sudden death


VAERS ID: 1336411 (history)  
Form: Version 2.0  
Age: 93.0  
Sex: Male  
Location: Foreign  
Vaccinated:2021-03-31
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19 pneumonia, Cardiogenic shock, SARS-CoV-2 test, Septic shock, Superinfection bacterial, Vaccination failure
SMQs:, Cardiac failure (narrow), Lack of efficacy/effect (narrow), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Toxic-septic shock conditions (narrow), Infective pneumonia (narrow), Sepsis (narrow), Opportunistic infections (broad), COVID-19 (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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Acute renal failure (Stage I); Aneurysm of ascending aorta; Atrial fibrillation paroxysmal; Dementia of the Alzheimer''s type NOS; Ischemia cerebrovascular; Lumbar pain syndrome
Allergies:
Diagnostic Lab Data: Test Name: Sars-CoV2; Test Result: Positive
CDC Split Type: CHPFIZER INC2021558877

Write-up: Exitus letalis, septic shock during COVID-19 pneumonia; suspected septic and cardiogenic shock in the setting of bacterial superinfected Covid-19 pneumonia; suspected septic and cardiogenic shock in the setting of bacterial superinfected Covid-19 pneumonia; suspected septic and cardiogenic shock in the setting of bacterial superinfected Covid-19 pneumonia; Exitus letalis, septic shock during COVID-19 pneumonia; This is a spontaneous report received from a contactable pharmacist via a regulatory authority. Regulatory authority report number CH-SM-2021-15010. A male patient of an unspecified age received bnt162b2 (COMIRNATY), dose 2 via an unspecified route of administration on 31Mar2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. Medical history included Dementia of the Alzheimer''s type NOS, Atrial fibrillation paroxysmal from 2018 to an unknown date , Aneurysm of ascending aorta, Ischemia cerebrovascularfrom 21Dec2018 to an unknown date , Lumbar pain syndrome , Acute renal failure with stage1. The patient''s concomitant medications were not reported. The patient experienced exitus letalis, septic shock during covid-19 pneumonia on an unspecified date, exitus letalis, septic shock during covid-19 pneumonia on an unspecified date. The patient underwent lab tests and procedures which included sars-cov-2 test: positive. The patient died on an unspecified date. It was not reported if an autopsy was performed. outcome of events was fatal.The 94-year-old male patient received his second vaccination dose of Comirnaty (Tozinameran; lot no. unknown) on 31Mar2021 for immunisation against COVID-19. On 19Apr2021, the patient was hospitalised and tested positive for Sars-CoV2. During the course, the patient became increasingly haemodynamically and respiratory unstable with suspected septic and cardiogenic shock in the setting of bacterial superinfected Covid-19 pneumonia. Therapy with Dexamethasone, Remdesivir, Piperacillin/Tazobactam, Amoxicillin/Clavulanic acid and Klacid (Clarithromycin) was initiated. In addition, acute renal failure stage I according to KDIGO was diagnosed. According to the presumed will of the patient, intensive medical measures such as intubation were waived and, in view of the poor prognosis, palliative therapy was initiated, under which the patient died. In addition, paroxysmal atrial fibrillation since 2018, cerebrovascular ischaemic insult in the mediastinal area on the right in a "wake-up" constellation on 21Dec2018, ectasia of the ascending aorta, dementia and lumbospondylogenic pain syndrome were known as relevant previous diseases. We have no further information on this case.A causal relationship between Comirnaty and COVID-19 Pneumonia and Vaccination Failure was assessed as being possible.This case was reported as serious (fatal outcome). Sender''s comment: a regulatory authority prescribing information for Comirnaty (tozinameran) states under Warnings/Precautions that vaccination with Comirnaty may not protect everyone who is vaccinated. There is a temporal relationship between the use of Comirnaty and COVID-19 infection (vaccine failure). In summary, we formally assess the causality between the use of Comirnaty and COVID-19 infection (vaccination failure) as possible on the basis of the temporal relationship and the documentation in the drug information. No follow-up attempts are possible, information about batch/lot number cannot be obtained.; Reported Cause(s) of Death: unknown cause of death


VAERS ID: 1336453 (history)  
Form: Version 2.0  
Age: 72.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-25
Onset:2021-05-04
   Days after vaccination:9
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-05-04
   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: DEPFIZER INC2021553648

Write-up: Unknown cause of death; This is a spontaneous report received from a non- contactable physician downloaded from the Regulatory Authority (RA)-WEB, regulatory authority number is DE-PEI-202100063186. A72-year-old female patient received BNT162B2 (COMIRNATY) at 0.3 ml single dose via an unknown route on 25Apr2021 for COVID-19 immunisation. Medical history and concomitant medication were not reported. On 04May2021 the patient experienced unknown cause of death. Autopsy was performed and result was pending. Assessment: Source of assessment: Agency; Result of Assessment: D. Unclassifiable. Information about lot/batch number cannot be obtained. No further information expected.; Reported Cause(s) of Death: Unknown cause of death


VAERS ID: 1336454 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-27
Onset:2021-05-09
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Gastrointestinal haemorrhage, Haematoma, Intracardiac thrombus, Petechiae
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Gastrointestinal haemorrhage (narrow), Ischaemic colitis (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-05-09
   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: Alcohol abuse; Anemia; Arterial hypertension; Diabetes mellitus; Hepatic cirrhosis; Mitral valve stenosis
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021553641

Write-up: Petechiae; Bleeding gastrointestinal; Intracardiac thrombus; Haematoma; This is a spontaneous report received from a non-contactable physician downloaded from the regulatory authority-WEB, regulatory authority number DE-PEI-202100064228. A 61-year-old female patient received bnt162b2 (COMIRNATY), via unspecified route of administration on 27Apr2021 (lot number: unknown) at single dose for COVID-19 immunisation. The relevant medical history included ongoing alcohol abuse, ongoing mitral valve stenosis, ongoing arterial hypertension, ongoing hepatic cirrhosis, ongoing diabetes mellitus and ongoing anemia. Concomitant medications were not reported. On 09May2021 the patient experienced intracardiac thrombus, petechiae, haematoma, bleeding gastrointestinal. The events were reported as serious due to death. The patient died on 09May2021. It was unknown if an autopsy was performed. The outcome of the events was fatal. Relatedness of drug to reaction/event (for all events), Source of assessment: regulatory authority, Result of Assessment reported as D. Unclassifiable. No follow-up attempts are possible. Information about batch/lot number cannot be obtained.; Reported Cause(s) of Death: Petechiae; Bleeding gastrointestinal; Haematoma; Intracardiac thrombus


VAERS ID: 1336455 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-12
Onset:2021-02-22
   Days after vaccination:10
Submitted: 0000-00-00
Entered: 2021-05-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Asthenia, Circulatory collapse, Intestinal infarction, Vomiting
SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Torsade de pointes, shock-associated conditions (narrow), Hypovolaemic shock conditions (narrow), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypoglycaemic and neurogenic shock conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ischaemic colitis (narrow), Hypersensitivity (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-02-23
   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:
Current Illness: Arterial hypertension; Coronary sclerosis; Gastritis
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021553647

Write-up: Cardiovascular failure due to small bowel infarction in Bridenileus; Cardiovascular failure due to small bowel infarction in Bridenileus; General debility; Vomiting; This is a spontaneous report downloaded from the Regulatory Authority. A non-contactable physician reported that a 76-year-old female patient received second dose of (COMIRNATY, Batch/Lot number was not reported), via an unspecified route of administration at the age of 76-year-old on 12Feb2021 at 0.3ml single dose for COVID-19 immunisation. Medical history included ongoing arterial hypertension, ongoing coronary sclerosis, ongoing gastritis. The patient''s concomitant medications were not reported. The patient previously received first dose of bnt162b2 (COMIRNATY) on 22Jan2021 at 0.3ml single dose for COVID-19 immunisation. The patient experienced general debility and vomiting on 22Feb2021, cardiovascular failure due to small bowel infarction in Bridenileus on unspecified date. The outcome of events was fatal. The patient died on 23Feb2021. An autopsy was performed that revealed cardiovascular failure due to small bowel infarction in bridenileus. This report was reported as serious report. The drug related to all events. No follow-up attempts are possible; information about lot/batch number cannot be obtained; Reported Cause(s) of Death: Vomiting; General debility; Autopsy-determined Cause(s) of Death: Cardiovascular failure due to small bowel infarction in Bridenileus; Cardiovascular failure due to small bowel infarction in Bridenileus


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