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From the 11/12/2021 release of VAERS data:

Found 2,768 cases where Vaccine is COVID19 and Symptom is COVID-19 and Patient Died

Government Disclaimer on use of this data



Case Details (Sorted by Age)

This is page 12 out of 277

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VAERS ID: 1037617 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2021-01-10
Onset:2021-01-01
Submitted: 0000-00-00
Entered: 2021-02-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Dyspnoea
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-02-01
   Days after onset: 31
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: Food allergy; Heart disorder (something to do with the valves.)
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021043788

Write-up: Contracted Covid-19 with breathing difficulties; Contracted Covid-19 with breathing difficulties; This is a spontaneous report from contactable consumer (patient) and daughter via a company representative. Patient''s daughter was a Health Care Professional. A 95-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 10Jan2021, at single dose, for COVID-19 immunization. Medical history included underlying heath issues with his heart (something to do with the valves) and was allergic to mustard. The patient''s concomitant medications were not reported. The patient contracted COVID-19 on an unspecified date, in Jan2021 and was in hospital on Friday 15Jan2021 with breathing difficulties. It was reported that he contracted COVID after the vaccine had be given. However, the patient had been self-isolating and only going to his allotment in the mornings. He did however have Christmas dinner with his family Christmas day, with his daughter and son in law who are both active paramedic. They both now also have Covid and yesterday his daughter moved in with him to take care of him and she only has mild symptoms. It could be he contracted it at Christmas but the symptoms didn''t show until this week. According to the patient''s daughter, the patient went before to have the Pfizer vaccine and was asked if he had any allergies, he said he did, he was allergic to mustard. It was reported that the patient was one of the first people to be asked to get the vaccine he even cycled to the place and when he got there, they didn''t allow him because of his allergy to mustard. Accordingly, due to that the patient was not given the vaccine at that time was told that he would be contacted when the AstaZenca one was available. He had to wait for the Astrazeneca vaccine but ended up having the Pfizer one and contracted COVID. Reporter stated that if he had it 3 weeks earlier when he was supposed to would still be alive now. The patient died on an unspecified date, in Feb2021 due to COVID-19. It was unknown if autopsy was done. Information on batch number has been request. Follow-up (25Jan2021): New information reported from a consumer (daughter) via a company representative includes: medical history (allergic to mustard and additional reporter (daughter). No follow-up attempts are possible, information about batch number cannot be obtained. Follow up (11Feb2021): New information received includes: details regarding patient''s death and event''s updated.; Reported Cause(s) of Death: COVID-19; Breathing difficult


VAERS ID: 1044967 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2020-12-31
Onset:2021-01-05
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Death, SARS-CoV-2 test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-08
   Days after onset: 3
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: Test Date: 20210105; Test Name: COVId-19 rapid test; Test Result: Positive
CDC Split Type: DEPFIZER INC2021164988

Write-up: Died/ cause of death was not reported; Corona disease/ COVId-19 rapid test positive; This is a spontaneous report from a contactable consumer based on information received by Pfizer from Biontech Manufacturer control number: 15873, license party for Comirnaty. This reporter reported similar events for 39 patients. This is the 18th of 39 reports. An approximately 90 years old patient of unspecified gender received bnt162b2 (COMIRNATY, lot number: EM0477), via unspecified route of administration on 31Dec2020 at single dose for COVID-19 vaccination. The Patient experienced Corona disease. A COVID rapid test was positive on 05Jan2021. Patient died on 08Jan2021. The patient had no symptoms. The cause of death was not reported. It was unknown if autopsy was done. The outcome of the event corona disease/ COVId-19 rapid test positive was unknown, while the other event was fatal. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-2021164939 same reporter/product, similar event, different patient; Reported Cause(s) of Death: Died/ cause of death was not reported


VAERS ID: 1044969 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2020-12-31
Onset:2021-01-07
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-22
   Days after onset: 15
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: Test Date: 20210107; Test Name: Rapid test; Test Result: Positive
CDC Split Type: DEPFIZER INC2021165016

Write-up: had a positive rapid test for COVID-19/ reported to have had COVID-19 disease; This is a spontaneous report received from a contactable consumer employee of a nursing home based on information received by Pfizer from Biontech [manufacturer control number: 15873], license party for Comirnaty. This reporter reported similar events for 39 patients. This is the 25th of 39 reports. An 87-year-old patient of unspecified gender received bnt162b2 (COMIRNATY, lot number: EM0477), via unspecified route of administration on 31Dec2020 at single dose for COVID-19 immunisation. The relevant medical history and concomitant medications were not reported. The patient was reported to have had a positive rapid test for COVID-19 on 07Jan2021. She was reported to have had COVID-19 disease. Symptoms included body temperature over 39 degrees Celsius and diarrhea. The patient died on 22Jan2021. It was not reported if the autopsy was performed. The outcome of the event was fatal. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-2021164939 same reporter/product, similar event, different patient; Reported Cause(s) of Death: had a positive rapid test for COVID-19/ reported to have had COVID-19 disease


VAERS ID: 1044970 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2020-12-31
Onset:2021-01-05
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Coronavirus test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-15
   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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210105; Test Name: Coronavirus rapid test; Test Result: Positive
CDC Split Type: DEPFIZER INC2021165112

Write-up: Coronavirus infection identified via quick test; This is a spontaneous report based on information received by Pfizer from Biontech [manufacturer control number:15873] from a non-contactable consumer, license party for Comirnaty. A patient about 91-year-old of an unspecified gender received 1st dose of bnt162b2 (COMIRNATY, lot: EM0477), via an unspecified route of administration on 31Dec2020 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had a positive COVID 19 quick test on 05Jan2021. The patient died on 15Jan2021. It was unknown if autopsy was done or not. Outcome of positive COVID 19 quick test was fatal. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-2021165108 PFIZER INC; Reported Cause(s) of Death: Coronavirus infection identified via quick test


VAERS ID: 1044977 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2020-12-31
Onset:2021-01-03
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6797 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Death, SARS-CoV-2 test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-03
   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: COVID-19 (Patient concurrent conditions included General physical health deterioration, COVID-19.); General physical health deterioration (Patient concurrent conditions included General physical health deterioration.); Living in nursing home (there was a covid-19 outbreak among several residents and staff.)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202101; Test Name: COVID-19 virus test; Test Result: Positive
CDC Split Type: DKPFIZER INC2021158646

Write-up: Death. It is not inconceivable that the total liability of Covid-19 disease and the vaccination has been fatal for the patient .; COVID-19; This is a spontaneous report received from a contactable physician downloaded from the Agency Regulatory Authority-WEB. The regulatory authority report number is DK-DKMA-WBS-0032135. A 79-years-old female patient received first dose of bnt162b2 (COMIRNATY, lot number: EJ6797), intramuscular on 31Dec2020 at single dose for covid-19 immunisation. Medical history included general physical health deterioration, COVID-19 and the patient was living in nursing home, where there was a covid-19 outbreak among several residents and staff, all ongoing. The patient''s concomitant medications were not reported. On 03Jan2021 the patient developed Death. No treatment due to the death was reported. Reported causes of death: death and of/with COVID-19. Only normal confirmation of death was performed post mortem. The patient underwent lab tests and procedures which included COVID-19 virus test: positive on Jan2021. The patient died on 03Jan2021. An autopsy was not performed. The reporter stated that it was not inconceivable that the total liability of Covid-19 disease and the vaccination had been fatal for the patient. Sender Comment: Comment from Agency: Version 001 has not been submitted to Regulatory Authority. Health Authority should therefore consider version 2 as the initial report. No follow-up attempts possible. No further information expected.; Reported Cause(s) of Death: COVID-19; Death


VAERS ID: 1044978 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2020-12-31
Onset:2021-01-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6797 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Drug ineffective, SARS-CoV-2 test
SMQs:, Lack of efficacy/effect (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-22
   Days after onset: 21
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: COVID-19; General physical health deterioration; Living in nursing home
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202101; Test Name: COVID-19 virus test; Test Result: Positive
CDC Split Type: DKPFIZER INC2021158635

Write-up: Death. It is not inconceivable that the total liability of Covid-19 disease and the vaccination has been fatal for the patient; Death. It is not inconceivable that the total liability of Covid-19 disease and the vaccination has been fatal for the patient; This is a spontaneous report from a non-contactable physician downloaded from the Agency Regulatory Authority-WEB DK-DKMA-WBS-0032140. An 85-year-old male patient received first dose of bnt162b2 (COMIRNATY, lot number: EJ6797), via intramuscular on 31Dec2020 at single dose for COVID-19 immunisation. The relevant medical history included living in nursing home, COVID-19, general physical health deterioration, all from unspecified dates and ongoing. Concomitant medications were not reported. The physician reported the occurrence of death. It was not inconceivable that the total liability of Covid-19 disease and the vaccination had been fatal for the patient. No treatment due to the event was reported. On 22Jan2021 the patient died. The reported cause of death was of/with COVID-19. The autopsy was not performed. Only usual confirmation of death was performed post-mortem. No findings were reported. The patient underwent lab test included COVID-19 virus test which showed positive in Jan2021. The outcome of the event was fatal. No follow-up attempts are needed. No further information is expected.; Reported Cause(s) of Death: Death. It is not inconceivable that the total liability of Covid-19 disease and the vaccination has been fatal for the patient; Death. It is not inconceivable that the total liability of Covid-19 disease and the vaccination has been fatal for the pat


VAERS ID: 1045000 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2020-12-29
Onset:2021-01-05
   Days after vaccination:7
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-25
   Days after onset: 20
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: Test Date: 20210105; Test Name: COVID-19; Test Result: Positive
CDC Split Type: ESPFIZER INC2021163688

Write-up: COVID-19; This is a spontaneous report from a contactable consumer. This report was downloaded from Medicines Agency (MA) regulatory authority-WEB and received via Regulatory Authority ES-AEMPS-735202. An elderly (over 65 years old) male patient received the 1st dose bnt162b2 (COMIRNATY) , via an unspecified route of administration on 29Dec2020 at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced covid-19 (positive for COVID-19) on 05Jan2021 with outcome of fatal. The patient died on 25Jan2021. It was not reported if an autopsy was performed. The cause of death was covid-19. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: COVID-19


VAERS ID: 1045017 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2021-01-19
Onset:2021-01-20
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-02-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6788 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, SARS-CoV-2 test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-30
   Days after onset: 10
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: Chronic bronchitis; Living in nursing home
Allergies:
Diagnostic Lab Data: Test Date: 20210120; Test Name: PCR SARS-COV 2; Test Result: Positive
CDC Split Type: FRPFIZER INC2021159140

Write-up: COVID-19 aggravated/Fever/ PCR test which turns out to be positive/ suspicion of bronchitis/ deterioration of the patient''s condition; This is a spontaneous report from a contactable other HCP from the Medicines Agency (MA) regulatory authority-WEB FR-AFSSAPS-LY20210485. An 88-year-old male patient received first dose of bnt162b2 (COMIRNATY, lot number: EJ6788), intramuscularly on 19Jan2021 at single dose, for covid-19 immunisation. Medical history included chronic bronchitis, autonomy: GIR 1, and living in nursing home from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. Usual treatment not known. On 19Jan2021, in the morning, 1st injection of bnt162b2, after pre-vaccination consultation. At this time, no symptoms. Stable state of health throughout the day. On 20Jan2021, faced with the presence of a fever at the end of the day, he benefits from a PCR test which turns out to be positive (but the result will not be discovered by the nursing home until 23Jan2021). On 21Jan2021, prescription of antibiotics on suspicion of bronchitis. In the following days, deterioration of the patient''s condition, with several trips to / from the hospital with return to nursing home as soon as the patient''s condition stabilizes. On 28Jan2021, hospitalization. On 30Jan2021, death. COVID-19 cluster in the facility. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 20Jan2021. The outcome of the event was fatal. The patient died on 30Jan2021. It was not reported if an autopsy was performed. No follow-up attempts possible. No further information expected.; Reported Cause(s) of Death: COVID-19 aggravated/Fever/ PCR test which turns out to be positive/ suspicion of bronchitis/ deterioration of the patient''s condition


VAERS ID: 1048262 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2020-12-31
Onset:2021-01-12
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Coronavirus test, Drug ineffective
SMQs:, Lack of efficacy/effect (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-22
   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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210112; Test Name: coronavirus rapid test; Test Result: Positive
CDC Split Type: DEPFIZER INC2021164941

Write-up: patient contracted Coronavirus/coronavirus rapid test: positive on 12Jan2021/symptoms were reported as loss of appetite and weakened; patient contracted Coronavirus/coronavirus rapid test: positive on 12Jan2021/symptoms were reported as loss of appetite and weakened; This is a spontaneous report from a non-contactable consumer based on information received by Pfizer from Biontech [manufacturer control number: 15873], license party for Comirnaty.This consumer reported similar events for 39 reports. This is the second of the 39 reports. A 78-year-old patient of an unspecified gender received bnt162b2 (COMIRNATY) lot# EM0477, via an unspecified route of administration on 31Dec2020 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced patient contracted coronavirus on 12Jan2021,symptoms were reported as loss of appetite and weakened. The patient underwent lab tests and procedures which included coronavirus rapid test: positive on 12Jan2021. The patient died on 22Jan2021. It was unknown if an autopsy was performed. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-2021164939 same reporter, same drug, different patients, similar events; Reported Cause(s) of Death: patient contracted Coronavirus/coronavirus rapid test: positive on 12Jan2021/symptoms were reported as loss of appetite and weakened; patient contracted Coronavirus/coronavirus rapid test: positive on 12Jan2021/symptoms were reported as loss of appet


VAERS ID: 1048263 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Foreign  
Vaccinated:2020-12-31
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-02-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM0477 / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: COVID-19, Coronavirus test
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-09
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: Test Date: 20210105; Test Name: Coronavirus rapid test; Test Result: Positive
CDC Split Type: DEPFIZER INC2021164984

Write-up: patient contractred Coronavirus; This is a spontaneous report from a contactable consumer based on information received by Pfizer from Biontech [manufacturer control number: 15873], license party for Comirnaty. The reporter reported similar events for 39 patients, this is the 15th of 39 reports. A 91-year-old patient of an unspecified gender received 1st dose of bnt162b2 (COMIRNATY, lot number EM0477), via an unspecified route of administration on 31Dec2020 at single dose for covid-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient contractred coronavirus (covid-19) (death) on an unspecified date. The patient underwent lab tests and procedures which included coronavirus rapid test: positive on 05Jan2021. The patient died on 09Jan2021. It was not reported if an autopsy was performed. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Linked Report(s) : DE-PFIZER INC-2021164939 same reporter/drug, similar events, different patient; Reported Cause(s) of Death: patient contractred Coronavirus


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