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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

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Case Details

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VAERS ID: 1328923 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Apathy, Dyspnoea, Investigation, Nausea, Pulmonary oedema
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (broad), Acute pancreatitis (broad), Dementia (broad), Acute central respiratory depression (broad), Psychosis and psychotic disorders (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Depression (excl suicide and self injury) (broad)

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? Yes, 7 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Cardiac failure; Cardiac fibrillation; Gout
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202102; Test Name: Investigation; Result Unstructured Data: Test Result:search for infection; Comments: in urine, lungs, unclear where it was.
CDC Split Type: SEPFIZER INC2021545053

Write-up: severe nausea the same evening as the vaccination; apathetic; Breathing difficulties; she gurgled as if the lungs were full of water; This is a spontaneous report from a contactable consumer downloaded from the Regulatory Authority-WEB, regulatory authority number SE-MPA-2021-034142. An 86-year-old female patient received first dose of BNT162B2 (COMIRNATY), via an unspecified route of administration in Feb2021 (Batch/Lot Number were not reported) as single dose for COVID-19 immunisation. Medical history included ongoing cardiac fibrillation, ongoing cardiac failure and ongoing gout. The patient''s concomitant medications were not reported. The reporter stated that in Feb2021 the patient experienced severe nausea the same evening as the vaccination. The woman was very ill about 7-8 days after the vaccination. Suddenly apathetic. Hospitalized for a week. At home for a day, sudden severe breathing difficulties. Hospitalized for two weeks, search for infection in urine, lungs, unclear where it was. The patient was sent home. Breathing difficulties for eleven days. The last day she gurgled as if the lungs were full of water. The events were serious life-threatening, caused hospitalization and the outcome was fatal. The patient died on an unspecified date. It was not reported if an autopsy was performed. No follow-up attempts are possible, information on batch number cannot be obtained.; Reported Cause(s) of Death: nausea; illness; apathetic; Breathing difficulties; she gurgled as if the lungs were full of water


VAERS ID: 1328940 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-01
Onset:2021-05-01
   Days after vaccination:30
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH UNKNOWN / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Activated partial thromboplastin time, Blood glucose, C-reactive protein, Cerebral haemorrhage, Computerised tomogram, International normalised ratio, Intraventricular haemorrhage, PCO2, PO2, Platelet count, White blood cell count
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Haemorrhagic central nervous system vascular conditions (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-05-01
   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: WARAN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Artificial cardiac pacemaker user; Atrioventricular block third degree; Chronic obstructive pulmonary disease; Chronic pulmonary embolism; Lobar pneumonia (Previous lobar pneumonia with septic image, chronic pulmonary embolism.); Oxygen therapy; Smoker
Allergies:
Diagnostic Lab Data: Test Date: 202105; Test Name: activated partial thromboplastin time; Result Unstructured Data: Test Result:63; Test Date: 202105; Test Name: Blood Glucose; Result Unstructured Data: Test Result:18.6; Test Date: 202105; Test Name: computerized tomography; Result Unstructured Data: Test Result:intraparenchymal hemorrhage; Comments: CT (computerized tomography) brain showed Large intraparenchymal hemorrhage about 50x45x 35 cm large frontal left involving basal, medial parts and operculum frontale with moderate ambient edema, ventricular rupture of the hemorrhage (blood in lateral ventricles, third ventricle, aqueduct and fourth ventricle). In the left frontal lobe can be sensed about 11 mm large round area with a little calcification, unclear genesis. The bleeding causes mass effect against the adjacent parenchyma and compresses and deviates the left lateral ventricle frontal horn and 3rd ventricle to the right side. Transfalcint pinching, narrow conditions in the left mesencephalic cistern hippocampal area. Right-sided lateral ventricle and left lateral ventricular temporal horn dilation - hydrocephalus development.; Test Date: 202105; Test Name: C-Reactive Protein; Result Unstructured Data: Test Result:44; Test Date: 202105; Test Name: PK/INR (International Normalized Ratio); Result Unstructured Data: Test Result:3,2; Test Date: 202105; Test Name: pCO2; Result Unstructured Data: Test Result:18.6; Test Date: 202105; Test Name: thrombocytes; Result Unstructured Data: Test Result:480; Test Date: 202105; Test Name: pO2; Result Unstructured Data: Test Result:6.0; Test Date: 202105; Test Name: leukocytes; Result Unstructured Data: Test Result:20.6
CDC Split Type: SEPFIZER INC2021539445

Write-up: superficial intracerebral hemorrhage in the cerebrum; intraventricular hemorrhage; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB SE-MPA-2021-037328. A 58-year-old female patient received first dose of bnt162b2 (COMIRNATY), via an unspecified route of administration on Apr2021 (Batch/Lot Number: Unknown) as single dose for covid-19 immunisation. Medical history included pneumonia from an unknown date and unknown if ongoing Previous lobar pneumonia with septic image, chronic pulmonary embolism , atrioventricular block complete from an unknown date and unknown if ongoing , pulmonary embolism from 2014 to an unknown date , tobacco user from an unknown date and unknown if ongoing, cardiac assistance device user from an unknown date and unknown if ongoing, oxygen therapy from an unknown date and unknown if ongoing, chronic obstructive pulmonary disease from an unknown date and unknown if ongoing. Concomitant medications included warfarin sodium (WARAN) taken for an unspecified indication, start and stop date were not reported. The patient experienced superficial intracerebral hemorrhage in the cerebrum (death) on May2021, intraventricular hemorrhage (death) on May2021. The patient underwent lab tests and procedures which included activated partial thromboplastin time: 63 on May2021, blood glucose: 18.6 on May2021, computerised tomogram: intraparenchymal hemorrhage on May2021 CT (computerized tomography) brain showed Large intraparenchymal hemorrhage about 50x45x 35 cm large frontal left involving basal, medial parts and operculum frontale with moderate ambient edema, ventricular rupture of the hemorrhage (blood in lateral ventricles, third ventricle, aqueduct and fourth ventricle). In the left frontal lobe can be sensed about 11 mm large round area with a little calcification, unclear genesis. The bleeding causes mass effect against the adjacent parenchyma and compresses and deviates the left lateral ventricle frontal horn and 3rd ventricle to the right side. Transfalcint pinching, narrow conditions in the left mesencephalic cistern hippocampal area. Right-sided lateral ventricle and left lateral ventricular temporal horn dilation - hydrocephalus development , c-reactive protein: 44 on May2021, international normalised ratio: 3,2 on May2021, pco2: 18.6 on May2021, platelet count: 480 on May2021, po2: 6.0 on May2021, white blood cell count: 20.6 on May2021. Therapeutic measures were taken as a result of superficial intracerebral hemorrhage in the cerebrum, intraventricular hemorrhage. The patient died on May2021. It was not reported if an autopsy was performed. The clinical course was reported as follows: Report from a physician regarding a 58-year-old female. Medical history included chronic obstructive pulmonary disease and oxygen therapy, atrioventricular block third degree. She has been a smoker and she was a cardiac assistance device user. Previous lobar pneumonia with septic image, chronic pulmonary embolism. Reported suspect vaccine was Comirnaty (covid-19 vaccines), 1:st dose. Reported suspect adverse events were superficial intracerebral hemorrhage in the cerebrum and intraventricular hemorrhage. The woman arrived at the hospital 6 days after receiving dose 1 of Comirnaty, during the day she had been alert and had talked to a relative, but suddenly she had strange breathing, was not contactable, an ambulance was called on. At arrival PK/INR (International Normalized Ratio) 3,2; APTT (activated partial thromboplastin time) 63. Routine tests without remark except leukocytes 20,6; TPK (thrombocytes 480; C-Reactive Protein 44; Blood Glucose 18,6. pO2 6,0; pCO2 18,6. CT (computerized tomography) brain showed Large intraparenchymal hemorrhage about 50x45x 35 cm large frontal left involving basal, medial parts and operculum frontale with moderate ambient edema, ventricular rupture of the hemorrhage (blood in lateral ventricles, third ventricle, aqueduct and fourth ventricle). In the left frontal lobe can be sensed about 11 mm large round area with a little calcification, unclear genesis. The bleeding causes mass effect against the adjacent parenchyma and compresses and deviates the left lateral ventricle frontal horn and 3rd ventricle to the right side. Transfalcint pinching, narrow conditions in the left mesencephalic cistern hippocampal area. Right-sided lateral ventricle and left lateral ventricular temporal horn dilation - hydrocephalus development. The woman received treatment with Konaktion, but it was assessed that there was nothing more to do, the woman was admitted to the stroke ward, for palliative care but died the same day. Assessment was massive intracerebral haemorrhage with ventricular breakthrough based on CT image and clinical course, one can possibly speculate in the underlying aneurysm. Waran (warfarin) may have contributed to a serious process. Probably not related to the given Comirnaty dose 1 week earlier. Outcome: Fatal. Report assessed as serious, death. Concomitant medications were Waran. Comirnaty LOT number: UNKNOWN. No follow-up attempts are possible, information on batch number cannot be obtained.; Reported Cause(s) of Death: intraventricular hemorrhage; Intracerebral haemorrhage


VAERS ID: 1329626 (history)  
Form: Version 2.0  
Age: 81.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-07
Onset:2021-04-10
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Cerebrovascular accident
SMQs:, 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)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-15
   Days after onset: 5
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: Atrial fibrillation
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEMODERNATX, INC.MOD20211

Write-up: This regulatory authority case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of CEREBROVASCULAR ACCIDENT in an 81-year-old female patient who received mRNA-1273 (COVID 19 Vaccine Moderna) for COVID-19 vaccination. The patient''s past medical history included Atrial fibrillation. On 07-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. On 10-Apr-2021, the patient experienced CEREBROVASCULAR ACCIDENT (seriousness criteria death, hospitalization and medically significant). The patient died on 15-Apr-2021. The reported cause of death was Stroke. It is unknown if an autopsy was performed. Concomitant product use was not provided by the reporter. No treatment information was provided. Company comment: This is a case of death in a 81-year-old female subject with a medical history of Atrial fibrillation, who died 8 days after receiving the second 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 81-year-old female subject with a medical history of Atrial fibrillation, who died 8 days after receiving the second dose of vaccine. Very limited information has been provided at this time. No follow up is possible.; Reported Cause(s) of Death: Stroke


VAERS ID: 1329702 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2021-04-08
Onset:2021-04-16
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW2239 / 2 - / OT

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

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-21
   Days after onset: 5
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Cardiac insufficiency (Chronic cardiac insufficiency)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210418; Test Name: PCR; Test Result: Positive ; Comments: (CT value 6.9)
CDC Split Type: ATPFIZER INC2021544622

Write-up: COVID-19 PCR test positive; Vaccination failure; COVID-19 pneumonia; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB AT-BASGAGES-2021-26177. An 82 years old male patient received BNT162B2 (COMIRNATY), 1st dose (Lot#EP2163) Intramuscular on 11Mar2021 at single dose, 2nd dose (Lot#EW2239) intramuscular on 08Apr2021 at single dose for COVID-19 immunization. The patient''s medical history and concurrent conditions included was Cardiac insufficiency (continuing). No concomitant medication reported. Date of death was 21Apr2021 due to COVID-19 Pneumonia. On 16Apr2021 the patient experienced vaccination failure, COVID-19 pneumonia. On 18Apr2021, COVID-19 PCR test positive (CT value 6.9). The patient''s outcome was fatal. It was unknown whether autopsy was done. No follow-up attempts needed. No further information is expected.; Reported Cause(s) of Death: COVID-19 Pneumonia; vaccination failure


VAERS ID: 1329705 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-15
Onset:2021-04-18
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Blood lactate dehydrogenase, Blood lactate dehydrogenase increased, General physical health deterioration, Hyperkalaemia, Low density lipoprotein, Low density lipoprotein increased, Renal failure, Transaminases, Transaminases increased
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Liver related investigations, signs and symptoms (narrow), Dyslipidaemia (narrow), Retroperitoneal fibrosis (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 (broad), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Chronic kidney disease (narrow), Tumour lysis syndrome (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (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: Medical History/Concurrent Conditions: Arterial hypertension; Peripheral arterial disease
Allergies:
Diagnostic Lab Data: Test Date: 20210418; Test Name: LDH; Result Unstructured Data: Test Result:significantly increased; Test Date: 20210418; Test Name: Low density lipoprotein cholesterol; Result Unstructured Data: Test Result:high; Test Date: 20210418; Test Name: Transaminases; Result Unstructured Data: Test Result:significantly increased
CDC Split Type: ATPFIZER INC2021544616

Write-up: Kidney failure; Transaminases / LDH significantly increased (shock organs?); Transaminases / LDH significantly increased (shock organs?); Hyperkalaemia; General condition worsening; Low density lipoprotein cholesterol high; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority -WEB AT-BASGAGES-2021-26820. An 89-year-old female patient received bnt162b2 (COMIRNATY, Batch/Lot Number: Unknown), via an unspecified route of administration on 15Apr2021 at single dose for COVID-19 immunisation. Medical history included arterial hypertension and peripheral arterial disease. The patient''s concomitant medications were not reported. On 18Apr2021 the patient experienced general condition worsening (general physical condition decreased), kidney failure, hyperkalaemia, transaminase value increased, Low density lipoprotein cholesterol high. Transaminases / LDH significantly increased (shock organs?). The outcome of events was fatal. The patient died on an unspecified date. It was not reported if an autopsy was performed. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Transaminases / LDH significantly increased (shock organs?); Hyperkalaemia; General condition worsening; Low density lipoprotein cholesterol high; Kidney failure; Transaminases / LDH significantly increased (shock organs?)


VAERS ID: 1329706 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-20
Onset:2021-04-21
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Blood lactic acid, Blood lactic acid increased, C-reactive protein, C-reactive protein increased, Diarrhoea, General physical health deterioration, SARS-CoV-2 test, Somnolence, Vomiting
SMQs:, Acute pancreatitis (broad), Lactic acidosis (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Anticholinergic syndrome (broad), Dementia (broad), Pseudomembranous colitis (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Hypoglycaemia (broad), COVID-19 (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: Medical History/Concurrent Conditions: Atrial fibrillation; Cardiac pacemaker insertion; Cardiomyopathy; Transcatheter aortic valve implantation
Allergies:
Diagnostic Lab Data: Test Date: 20210421; Test Name: Lactate; Result Unstructured Data: Test Result:increased; Test Date: 20210421; Test Name: CRP; Result Unstructured Data: Test Result:increased; Test Date: 20210421; Test Name: SARS-CoV-2 PCR test; Test Result: Negative
CDC Split Type: ATPFIZER INC2021544627

Write-up: Diarrhea; CRP, lactate elevated; CRP, lactate elevated; Vomiting; Somnolence; Deterioration of general condition; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB [AT-BASGAGES-2021-26825]. An 89 years old female patient received 2nd dose of BNT162B2 (COMIRNATY) on 20Apr2021 for COVID-19 immunisation. The patient''s medical history included: Transcatheter aortic valve implantation, Atrial fibrillation, Cardiac pacemaker insertion, Cardiomyopathy. Historical vaccine included 1st dose of BNT162B2 (COMIRNATY) on 30Mar2021 for COVID-19 immunisation. Concomitant drugs were not provided. On 21Apr2021 the patient experienced Deterioration of general condition, Diarrhea, Vomiting, Somnolence, CRP increased, Lactate increased. The outcome of all the events was fatal. SARS-CoV-2 PCR test was negative on 21Apr2021. No follow-up attempts are possible. No further information expected. Information on batch/lot number cannot be obtained. ; Reported Cause(s) of Death: CRP increased; Diarrhea; Lactate increased; Vomiting; Somnolence; Deterioration of general condition


VAERS ID: 1329787 (history)  
Form: Version 2.0  
Age: 70.0  
Sex: Male  
Location: Foreign  
Vaccinated:2021-05-03
Onset:2021-05-03
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EY3014 / 1 - / OT

Administered by: Other       Purchased by: ?
Symptoms: Death, Echocardiogram, Ejection fraction, Electrocardiogram ambulatory, Loss of consciousness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 2021-05-03
   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: ANOPYRIN; SPIOLTO RESPIMAT; FORMOVENT; VASOCARDIN; ATORVASTATIN; VEROSPIRON; AMLORATIO; SEDACORON; BERODUAL; EUPHYLLIN [THEOPHYLLINE]; FOSINOPRIL SODIUM; FURON [FUROSEMIDE]; NOLPAZA
Current Illness: Arterial hypertension; Chronic venous insufficiency; COPD; Double vessel disease; Ex-smoker (Stopped smoking 2 years ago); Insufficiency cardiac (NYHA (New York Heart Association) scale: 3); Ischemic heart disease; Malleolus edema; Obesity (Grade: 3); Oxygen therapy (Long-term oxygentherapy at home); Paroxysmal atrial flutter; Peripheral arterial disease; Polyposis intestinal; Renal insufficiency; Sleep apnea syndrome
Preexisting Conditions: Medical History/Concurrent Conditions: Aortic bi-femoral bypass; Aortocoronary bypass; Coronary revascularization (coronarography - Severe damage of the coronary arteries); DVT of calf (Right lower limb); Dyspnea; Inferior myocardial infarction (Inapparent); Septic shock (Caused by intestine perforation); Thrombectomy (Of the aorto-bifemoral bypass)
Allergies:
Diagnostic Lab Data: Test Date: 20210503; Test Name: Echocardiography; Result Unstructured Data: Test Result:dysfunction, aneurysm, dilatation; Comments: Mild systolic dysfunction of the left ventricule, aneurysm of the inferior wall, mild dilatation of the left atrium; Test Date: 20210503; Test Name: Ejection fraction; Test Result: 45 %; Test Date: 20210503; Test Name: Holter monitoring; Result Unstructured Data: Test Result:Sinus rhythm; Comments: Sinus rhythm, infrequent isolated ventricule extrasystoles; Test Date: 20210503; Test Name: Holter monitoring; Result Unstructured Data: Test Result:severe bradycardia with frequency of 15 beats per; Comments: severe bradycardia with frequency of 15 beats per minute was seen at first, then it passed into ventricular fibrillation, then after defibrillation it passed into an isoelectric line
CDC Split Type: CZPFIZER INC2021544637

Write-up: death; Loss of consciousness; This is a spontaneous report from a contactable physician downloaded from the Regulatory Authority-WEB [CZ-CZSUKL-21005177]. A 70-year-old male patient received first dose of bnt162b2 (COMIRNATY, Batch/lot number EY3014), via intramuscular on 03May2021 at single dose for covid-19 immunization. Medical history included ongoing ischemic heart disease, ongoing chronic cardial insufficiency NYHA III, in Feb2014 coronary revascularization, coronarography - severe damage of the coronary arteries, in 2012 aortocoronary bypass, in 2012 inapparent myocardial infarction of the inferior wall, ongoing double vessel disease, ongoing chronic obstructive pulmonary disease, long-term oxygen therapy at home since Oct2019 and ongoing, ongoing sleep apnea syndrome, ongoing paroxysmal atrial flutter, ongoing arterial hypertension, ongoing renal insufficiency, ongoing peripheral arterial disease, in 2004 aorto-bifemoral bypass, in 2004 septic shock caused by intestine perforation, in Jan2019 bypass thrombectomy (Of the aorto-bifemoral bypass), ongoing chronic venous insufficiency, ongoing chronic perimalleolar oedemas, in Jun2018 deep venous thrombosis of the right calf (Right lower limb), ongoing large intestine polyposis, grade III obesity, ongoing ex-smoker for 2 years, and long lasting mild dyspnea. Concomitant medications included acetylsalicylic acid (ANOPYRIN); olodaterol hydrochloride, tiotropium bromide monohydrate (SPIOLTO RESPIMAT); formoterol fumarate (FORMOVENT); metoprolol tartrate (VASOCARDIN); atorvastatin; spironolactone (VEROSPIRON); amlodipine besilate (AMLORATIO); amiodarone hydrochloride (SEDACORON); fenoterol hydrobromide, ipratropium bromide (BERODUAL); theophylline (EUPHYLLIN); fosinopril sodium; furosemide (FURON); pantoprazole sodium sesquihydrate (NOLPAZA). The patient lost consciousness 2 minutes after being vaccinated (life-threatening). Cardiopulmonary resuscitation was started, including intubation and artifical ventilation. On electrocardiogram severe bradycardia with frequency of 15 beats per minute was seen at first, then it passed into ventricular fibrillation, then after defibrillation it passed into an isoelectric line. During resuscitation the patient was administered 2 mg of Atropin, 3 mg of Adrenalin, two electrical discharges and 75 mg of Amiodaron. Cardiopulmonal resuscitation was started at 13:02, at 13:50 it was stopped and the patient was proclaimed dead. Cause of death was unknown. Outcome of event loss of consciousness was not recovered. Autopsy was performed and no result available. The patient underwent lab tests and procedures on 03May2021 which included echocardiography: Mild systolic dysfunction of the left ventricule, aneurysm of the inferior wall, mild dilatation of the left atrium, ejection fraction: 45 %, holter monitoring: Sinus rhythm, infrequent isolated ventricule extrasystoles. No follow-up attempts possible. No further information expected.; Reported Cause(s) of Death: death


VAERS ID: 1329796 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-04-28
Onset:2021-04-30
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EX3599 / UNK - / -

Administered by: Other       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: Medical History/Concurrent Conditions: Coronary disease; End stage COPD (COPD IV); Renal insufficiency
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021544661

Write-up: Unknown cause of death; This is a spontaneous report from a non-contactable physician downloaded from the Regulatory Authority-WEB DE-PEI-202100062331. A 75-year-old female patient received BNT162B2 (COMIRNATY, strength: 0.3ml), via an unspecified route of administration on 28Apr2021 (Batch/Lot Number: EX3599, at the age of 75-year-old) as single dose for covid-19 immunisation. Medical history included end stage chronic obstructive pulmonary disease (COPD) (COPD IV), coronary disease, renal insufficiency. The patient''s concomitant medications were not reported. On 30Apr2021, the patient experienced unknown cause of death. The patient died on 30Apr2021. An autopsy was not performed. The reporter''s assessment on the causal relationship between the suspect vaccine and the event was indeterminate. No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: Unknown cause of death


VAERS ID: 1329798 (history)  
Form: Version 2.0  
Age: 80.0  
Sex: Male  
Location: Foreign  
Vaccinated:2021-04-10
Onset:2021-04-14
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW8904 / UNK - / -

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

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-14
   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: Deep vein thrombosis leg
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021544649

Write-up: Unknown cause of death; This is a spontaneous report from a non-contactable physician downloaded from the Regulatory Authority-WEB DE-PEI-202100062953. An 80-year-old male patient received BNT162B2 (COMIRNATY), via an unspecified route of administration at the age of 80-year-old on 10Apr2021 (batch/Lot Number: EW8904) as single dose for covid-19 immunisation. Medical history included deep vein thrombosis leg. The patient''s concomitant medications were not reported. The patient experienced unknown cause of death on 14Apr2021. The patient died on 14Apr2021. An autopsy was not performed. The reporter''s assessment on the causal relationship between the suspect product Comirnaty and the event death was unclassifiable. No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: Unknown cause of death


VAERS ID: 1329812 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-08
Onset:2021-01-09
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Cerebrovascular accident, Pulmonary embolism
SMQs:, 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), Embolic and thrombotic events, venous (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-01-09
   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: Acute renal insufficiency; Coronary heart disease; Type 2 diabetes mellitus
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: DEPFIZER INC2021539568

Write-up: Cerebral circulatory disorder (stroke); Lung embolism; This is a spontaneous report downloaded from a Non-contactable Consumer from the Regulatory Authority-WEB [DE-PEI-CADR2021060275], Safety Report Unique Identifier [DE-PEI-202100052193] A 72-years-old female patient received bnt162b2 (COMIRNATY), on 08Jan2021 as UNKNOWN, SINGLE for covid-19 immunisation. Medical history included ongoing coronary artery disease , ongoing acute kidney injury , ongoing type 2 diabetes mellitus. The patient''s concomitant medications were not reported. On 09Jan2021 the patient experienced Cerebral circulatory disorder (stroke), Lung embolism. The patient''s outcome was fatal for Accident cerebrovascular, fatal for Lung embolism. The patient died on 09Jan2021. An autopsy was performed and results were not provided. No follow-up attempts are possible. Information on batch/lot number cannot be obtained.; Reported Cause(s) of Death: Accident cerebrovascular; Lung embolism


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