VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

Total Manufacturer

Incidents per State

State Total
92,076
AK1,880
AL6,345
AR4,151
AS46
AZ14,991
CA66,887
CO12,550
CT8,943
DC1,795
DE2,009
FL42,724
FM4
GA17,031
GU124
HI2,580
IA4,919
ID2,892
IL22,128
IN24,197
KS5,047
KY9,111
LA5,500
MA15,718
MD13,434
ME3,351
MH8
MI20,971
MN13,585
MO10,747
MP30
MS3,198
MT2,477
NC18,051
ND1,501
NE3,109
NH3,218
NJ20,216
NM4,218
NV4,728
NY37,667
OH20,793
OK6,692
OR9,244
PA25,607
PR2,588
QM2
RI2,163
SC7,261
SD1,282
TN10,445
TX39,890
UT4,618
VA15,980
VI67
VT1,830
WA16,071
WI12,042
WV2,571
WY926
XB5
XL1
XV2

ID: 1224804
Sex: U
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: had an anaphylactic reaction to Prevnar13; This is a spontaneous report from Pfizer sponsored program. A contactable consumer (patient) reported that a patient of unspecified age and gender received pneumococcal 13-val conj vac (dipht crm197 protein) (PREVNAR 13), via an unspecified route of administration on an unspecified date at single dose for immunization. The relevant medical history and concomitant medications were not reported. The patient had an anaphylactic reaction to Prevnar 13 on an unspecified date. The patient was skeptical about getting the Covid vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224805
Sex: M
Age:
State: VA

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Kidney disorder; Kidney disorder; missed his 2nd dose; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer (patient's wife). A male patient of an unspecified age received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on an unspecified date, as single dose, for COVID-19 immunisation. Medical history included renal transplant in 2013, ongoing renal disorder. Concomitant medications were not reported. The patient experienced kidney disorder on an unspecified date with outcome of unknown. The event caused patient's hospitalization. Due to this, the patient missed his 2nd dose. No follow-up attempts are possible; information about lot/batch number cannot be obtained..

Other Meds:

Current Illness: Kidney disorder; Kidney transplant

ID: 1224807
Sex: F
Age:
State:

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: Tired/fatigue; unable to sleep throughout the night; headache; dizziness; This is a spontaneous report from a contactable consumer (patient). A 52-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number was not reported), via an unspecified route of administration on 01Apr2021 at 10:15 (at 52-year-old) at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) at single dose for COVID-19 immunization. On 01Apr2021 in the evening, the patient became very tired and laid down for about a half an hour which seem to help around 5 PM. When she did go to bed at nine, she slept for only a few hours and then she was unable to sleep throughout the night. She was experiencing a headache, dizziness and it has continued through 01Apr2021 along with the fatigue. The time currently was 12:36. She had been drinking a lot of water this morning and that seemed to have helped a little. The outcome of the events was unknown. No follow-up attempts are possible, information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224808
Sex: M
Age:
State: NY

Vax Date: 01/13/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: tested positive for covid after both doses; tested positive for covid after both doses; This is a spontaneous report from a contactable consumer. This consumer reported for himself. This is 1 of the 3 report. This is a spontaneous report from a contactable consumer. The report is from a facility regarding 3 residents at the facility who tested positive for COVID after receiving both doses of the vaccine. This is 1 of three reports. A 86-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: E10140 and Expiry date: 31Mar2021), via ) via intramuscular route on 13Jan2021 as a SINGLE DOSE for COVID-19 immunization. Medical history includes diabetes, heart disease, hypertension and Alzheimer's disease from unspecified-to-unspecified date. The historical vaccine patient received first dose of BNT162B2 (COMIRNATY, Formulation: Solution for injection, lot number: E10140 and Expiry date: 31Mar2021) 0.3ml via intramuscular route in the right upper arm on 23Dec2020 as a COVID-19 immunization. There were no concomitant medications reported. On 30Mar2021 the patient tested positive for COVID after both doses. The patient underwent lab tests and procedures which included COVID-19 PCR test which was positive on 30Mar2021. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1224809
Sex: M
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: back pain; This is a spontaneous report from a non-contactable consumer (patient) via a Pfizer Sponsored Program. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), via an unspecified route of administration on 31Mar2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced back pain on an unspecified date with outcome of unknown. The patient received vaccine on 31Mar2021 and wanted to know if he could take Mortrin or Tyleonol for back pain. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224810
Sex: M
Age:
State: NY

Vax Date: 01/13/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: tested positive for covid after both doses; tested positive for covid after both doses; This is a spontaneous report from a contactable consumer. The report is from a facility regarding 3 residents at the facility who tested positive for COVID after receiving both doses of the vaccine. This is two of three reports. A 91-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: E10140 and Expiry date: 31Mar2021), via an unspecified route of administration on 13Jan2021 as single dose for COVID-19 immunization. Medical history included, cardiomegaly, acute kidney injury, atrial fibrillation, diabetes mellitus, hypertension, hyperlipidaemia and anaemia, all from an unknown date and unknown if ongoing. The historical vaccine first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: E10140 and Expiry date: 31Mar2021), via an unspecified route of administration on 23Dec2020 as single dose for COVID-19 immunization. There were no concomitant medications reported. On 30Mar2021 the patient tested positive for COVID after both doses. The patient underwent lab tests and procedures which included COVID-19 PCR test which was positive on 30Mar2021. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1224811
Sex: F
Age:
State: NY

Vax Date: 03/12/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: pain and swollen hands; pain and swollen hands; This is a spontaneous report from a Pfizer-sponsored program via a contactable consumer (patient). A female patient of an unspecified age received the first dose (dose 1) of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included ongoing arthritis. The patient's concomitant medications were not reported. The patient was calling because she wanted to reschedule her 2nd dose shot scheduled tomorrow (on 02Apr2021) because she would be going to her doctor today (on 01Apr2021) because of her arthritis and would have a steroid shot. According to the caller, she's experiencing pain and swollen hands on an unspecified date. She took her first shot on 12Mar2021. The patient wanted to know if it was possible reschedule her 2nd dose. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness: Arthritis

ID: 1224812
Sex: M
Age:
State: NV

Vax Date: 03/31/2021
Onset Date: 04/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: he is experiencing pain in the arm; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 1 via an unspecified route of administration on 31Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunization. The patient's medical history and concomitant medications was not reported. The patient got his 1st dose on 31Mar2021 and now he is experiencing pain in the arm on 01Apr2021. Patient also asked if he could walk around to the park to do exercise under the sun. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224813
Sex: F
Age:
State: MN

Vax Date: 03/18/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: tested positive on her COVID test; tested positive on her COVID test; This is a spontaneous report from a Pfizer sponsored program from a contactable consumer reported for herself. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 18Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient got the first dose of the Pfizer COVID-19 Vaccine last March 18 and she just got back from a trip and she was tested positive on her COVID test. She was asking if that could be the vaccine being detected or something else. The patient underwent lab tests and procedures which included sars-cov-2 test: positive in Mar2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224814
Sex: F
Age:
State: PA

Vax Date: 03/11/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: testing positive for covid; 24 hour amnesia; This is a spontaneous report from a Pfizer-sponsored program. A contactable nurse reported that a 68-year-old female patient (reporter's mother) received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number and expiry date unknown), via an unspecified route of administration on 11Mar2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported the patient had an accidental finding of COVID positive on 19Mar2021. She had blood work when she had an overnight stay at the hospital but everything was fine. The patient was completely asymptomatic other than that. It was also reported that the patient ended up having 24 hour amnesia (as reported) on an unspecified date in Mar2021. During the day of the report, 01Apr2021, the patient was due for her second shot but was not allowed to get her second shot that day and that she needed to wait at least a month. The reporter wanted to know if this was correct. The patient did not receive treatment for the events. The outcome of the events was unknown. Information on the lot/ batch number has been requested.; Sender's Comments: Based on the timing of finding a Covid positive test relative to day of vaccination, event 'Covid-19' was an intercurrent medical condition assessed not related to vaccination with BNT162B2. 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.

Other Meds:

Current Illness:

ID: 1224816
Sex: F
Age:
State:

Vax Date: 04/04/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: felt symptoms similar to pneumonia; This is a spontaneous report received from a contactable consumer (patient). A 48-year-old female patient received second dose of BNT162B2 (Pfizer Covid-19 Vaccine, Lot number was not reported), intramuscularly on 04Apr2021 at age of 48-year-old at single dose for covid-19 immunisation. The patient previously received first dose of BNT162B2 at single dose for covid-19 immunisation and felt itchy and experienced a skin rash. The patient's concomitant medications were not reported. On an unspecified date, after the second dose, the patient felt symptoms similar to pneumonia for one day. The outcome of event was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021377012

Other Meds:

Current Illness:

ID: 1224817
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Pancreas issues; This is a spontaneous report from a Pfizer-sponsored program. A non-contactable consumer (patient's wife) reported that a male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE. Lot Number and Expiration Date were not reported), via an unspecified route of administration, on an unspecified date, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient was in the hospital with pancreas issues. The patient's wife said that it was not because of vaccine that the patient was hospitalized after first dose. The patient missed the second vaccine dated 19Mar2021 and the patient's wife wanted to know if this will be at a certain location again. The outcome of the event was unknown. The event was assessed as unrelated to the suspect vaccine. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Reported event pancreatic issues is considered intercurrent and unrelated to BNT182B2.

Other Meds:

Current Illness:

ID: 1224818
Sex: M
Age:
State: NJ

Vax Date: 01/27/2021
Onset Date: 01/28/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: Heart stopped 6 times; unresponsive; soreness; felt like unwell; vomiting; Body aches; achiness; passed out 7 times; fever; chills; Left arm soreness at injection site and up back of shoulders; Left arm soreness at injection site and up back of shoulders; This is a spontaneous report from a contactable consumer.A 48-years-old male patient received second dose of bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Formulation: Solution for injection, Lot Number: EN5318), intramuscular, administered in left arm on 27Jan2021 11:00 at single dose for covid-19 immunisation. Medical history included asthma, myocarditis and allergies to Fruit or nut that grows on trees. Concomitant medication included esomeprazole magnesium (NEXIUM). The patient's heart stopped 6 times on 29Jan2021, he had a low grade fever, achiness and chills at 01:30, but they were gone the next day. Basically, at first, he took the shot and got the reactions that everyone else does, right arm soreness 01:30. On 07Jan2021 17:00, patient took the first dose of bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Formulation: Solution for injection, Lot Number: EL1042), intramuscular, administered in left arm. No prior vaccination was given within 4 weeks. He fell in the shower and passed out and hit his head at 18:00. He was not hooked up to a machine. About 18:30, his wife got him to the couch. He drank carrot juice and ate a granola bar. At 18:30 his eyes were wide open, but he was unresponsive. About every 30 minutes, he was going down. The third one came about 18:45-19:00. The pass outs lasted 15-20 seconds. and all he remembers was waking up to her screaming at him. The next one came at 19:15 and was in the ambulance on the way to the hospital and that is when he vomited in the ambulance and on the couch. Pass out number 3 was at home and 4 was in the ambulance. There was vomiting with both of them. Pass out number 5 was in the hospital when she was getting in the bed and was not hooked up in the room yet. Finally, they got him hooked up to a machine at 20:30 and into a room. They said if you feel dizzy, press the button. He found out his heart rate went from 80's down to 30's. That was the 6th pass out. This was the first time he was on a machine. His heart did not actually stop, it just went down to 30's and would come back. Then, it happened one more time on the machine and at that point, they were hooking him up to an IV and giving him medication to keep him from vomiting. He does not have the name of that medication or the dose or lot or expiration. He got stabilized but they had him hooked up shockpads in case anything happened. They recorded his heart stopping 6 times during the night and of those 6 times, he does not have the times.2 seconds was the longest time of all of the stops. He does not know how many each were. This was when he woke up on 30Jan2021. He later stated he was hospitalized 28Jan2021 at 7pm and those 6 stops occurred 29Jan2021 through the night previously. The patient was hospitalized for heart stopped 6 times from 29Jan2021 and discharged on 01Feb2021. The patient underwent lab tests and procedures which included body temperature was low grade fever, echocardiogram, brain scan and electrocardiogram shows normal,heart rate: 80 beats, heart rate was down to 30 on his heart beat. They gave shot in the leg for blood clots, nausea medication and a bunch of pills given as treatment. The outcome of heart stopped 6 times was recovered with Sequel, patient passed out 7 times, body aches, fever and chills, left arm soreness at injection site and up back of shoulders was recovering, unresponsive and soreness next day felt like unwell and vomiting was unknown, achiness was recovered. No follow-up attempts are possible. No further information is expected

Other Meds: NEXIUM [ESOMEPRAZOLE MAGNESIUM]

Current Illness:

ID: 1224819
Sex: F
Age:
State: PA

Vax Date: 01/16/2021
Onset Date: 03/31/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: she tested positive with Covid Virus; she tested positive with Covid Virus; This is a spontaneous report from a Pfizer sponsored program. A contactable female consumer (patient) of an unspecified age received second dose of BNT162B2 (Covid shot, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/lot number: Unknown, Expiry Date: Unknown), via an unspecified route of administration on 16Jan2021 at single dose for COVID-19 immunization. Patient had historical vaccine BNT162B2, first dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 31Mar2021, she tested positive with Covid virus. She got Covid-19 virus after receiving both doses. The patient underwent lab test and procedures included covid-19 test positive on 31Mar2021. The outcome of event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224820
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: having her appendix taken out.; stomach cramps; This is a spontaneous report from contactable female consumer (patient) via Pfizer sponsored program. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: not reported) an unspecified route of administration on an unknown date in 2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unknown date in 2021, the patient got her 1st dose last Wednesday and on Thursday she started with stomach cramps. By monday she was in surgery having her appendix taken out. She stated she is nervous about getting the 2nd dose and has tried to address this with HCP, but they don't have any information. Outcome of events not reported. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224821
Sex: F
Age:
State: AZ

Vax Date: 01/21/2021
Onset Date: 02/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: right sided jaw, facial, neck numbness; This is a spontaneous report received from a contactable consumer (patient). A 48-year-old female patient received second dose of BNT162B2 (FIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 21Jan2021 (Batch/Lot number was not reported) at single dose for COVID-19 immunization. Medical history included seasonal allergies. The patient's concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot # EH9899) via an unspecified route of administration at 2:00 on 28Dec2020 at single dose in left upper arm for COVID-19 immunization, and experienced neck was swollen with rash bilateral, neck palpitations and bounding pulse on 04Jan2021 at 9:00 (referred to AER#2021025542). CTA (computed tomography angiography) neck contrast showed no pulmonary embolism, no aneurysm or dissection, no pneumonia. Bilateral cartoid ultrasound on 11Jan2021 showed no mass or adenopathy or fluid detection. Post 2 weeks the patient experienced right sided jaw, facial, neck numbness and E.R visited on 05Feb2021. The outcomes of the events were unknown. Information on Lot/ Batch number has been requested.; Sender's Comments: Linked Report(s) : PFIZER INC-2021025542 same patient/drug, different dose/AE

Other Meds:

Current Illness:

ID: 1224822
Sex: U
Age:
State:

Vax Date: 03/24/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: I got rash on my arm where the vaccine is on my left arm they did the vaccine and it looks like a red little; This is a spontaneous report received from a contactable consumer (patient). A patient of unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 24Mar2021 (Batch/Lot number was not reported) at single dose at arm left for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 04Mar2021 (Batch/Lot number was not reported) at single dose for COVID-19 immunisation. "Today" all of sudden the patient got rash on patient's arm where the vaccine was on patient's left arm they did the vaccine and it looked like a red little. The action taken in response to the event for BNT162B2 was not applicable. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224823
Sex: F
Age:
State: WA

Vax Date: 01/11/2021
Onset Date: 03/29/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: COVID-19 confirmed by positive COVID-19 test; COVID-19 confirmed by positive COVID-19 test; This is a spontaneous report from a contactable nurse (patient). A 50-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (age at vaccination was 49-year-old), second dose via an unspecified route of administration on 11Jan2021 (batch/lot number was not reported) at 0.3 mL, single dose, and first dose via an unspecified route of administration on 21Dec2020 (batch/lot number: EH9899; expiration date: 31Mar2021) at 0.3 mL, single dose for COVID-19 immunization. Medical history included depression and anxiety from an unspecified date. Concomitant medication included escitalopram taken for antidepressant and antianxiety, start and stop date were not reported. The patient stated she just wanted to report that she was an ACU, Acute Care Nurse in (country name), (state name) and she received both Pfizer COVID Vaccines on December 21st and the other one January 11th (later clarified) and she got exposed to her son who had COVID, and she was positive now, and symptomatic. She further stated, so basically, she had a direct exposure outside of work. But she immediately contracted it and became symptomatic and she currently, she was positive for COVID-19 even though she was vaccinated. She stated this was her first time, her first call she tried to email but it didn't seem to go through that that's why she was calling. She stated, well actually, her son came home from college and apparently he was having symptoms at college but he didn't really let them know that. He came home from college at (university name) exposed herself and her husband. Her husband came out positive and so did she. It's just three of them in the house. When requested for clarification about husband and the son, she stated, neither of them have been vaccinated. By the way (name) was her son, he was 19. Husband was (name). She stated adverse event started with (name). For her personally, she just got tested positive test on Monday, the last past Monday which was on 29th March. Monday was when she was tested positive. Husband tested positive, it came back Sunday, 28th March. She further stated, and her son, she believes it was on Tuesday, 23rd she believes, 23rd March. Healthcare professional who administered the vaccine was the employer. It was a whole bunch, all of them got called down and they had volunteer nurses giving the vaccines. It looks like as initials, it's an RN, a nurse. The first dose was 'MD' and that looks like a K, she can't read. She further stated, her first dose was on 21Dec2021 Dec. She thought it was on 19th but actually it looks like here Dec2021, 21Dec2020. She further stated, the date of second vaccination was 11Jan2021. The first dose was on 21Dec2020 and the second dose 11Jan2021. She had no idea regarding purchase details because it was through her employer. She did not purchase it. She got it free as an employee. No lab work recently. She stated she tested positive on 29th and now she was in quarantine until April 9th. She stated she would say on Monday, like she started feeling nasal congestion, sneezing, runny nose, headache. Events were persisting, so far she was experiencing. No treatment, she just stays in home. The patient underwent lab tests and procedures which included Covid-19 test: positive on 29Mar2021. The outcome of the event was not recovered.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine can not be excluded for the reported events of COVID-19 test positive and vaccination failure due to temporal relationship. Case will be re-assessed upon the additional information provided.

Other Meds: ESCITALOPRAM

Current Illness:

ID: 1224824
Sex: U
Age:
State:

Vax Date: 01/14/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: My heart was racing; Felt really weird in my body; Right leg got kind of numb and my body was so weird after that; This is a spontaneous report received from a contactable consumer (patient). A patient of an unspecified age and gender received first single dose of bnt162b2 (Pfizer-BioNTech Covid-19 vaccine) via an unspecified route of administration on 14Jan2021 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. After taking the vaccine, patient's heart was racing and patient felt really weird in body and right leg when patient was driving in the evening on the highway, patient's right leg got kind of numb and body was weird after that. So, the patient was resisting taking the second shot. Patient asked what if he/she take the second shot after this time as it is more than two months. The patient had not decided yet and he/she want to know what is the maximum period after the first one and if so, what is the is the effect. The outcome of the reactions was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : PFIZER INC-2021377639 same drug, different patient/AE

Other Meds:

Current Illness:

ID: 1224825
Sex: F
Age:
State: MI

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: She was worried maybe they were scheduled to get the Moderna vaccine; This is a spontaneous report from manufacturer support received from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 31Mar2021 as SINGLE DOSE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was scheduled more than 21 days for their second appointment 29Apr2021. Patient knew that it should be 21 days apart to get the second dose of the vaccine. She was worried maybe they were scheduled to get the Moderna vaccine instead of Pfizer vaccine. The outcome of event was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224826
Sex: F
Age:
State: NJ

Vax Date: 03/19/2021
Onset Date: 03/29/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: positive COVID-19 test; This is a spontaneous report from a contactable consumer (patient) and from a Pfizer-sponsored program COVAX US Support. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot no. EN6207; Expiration Date: 31Jul2021), via an unspecified route of administration on 19Mar2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had first shot of vaccine on 19Mar2021 and on 29Mar2021 tested positive for Covid. Patient asked, is she need to take the second shot or is it safe to take the second shot if she had the Covid. Patient did not have any trouble with the shot, came up with the Covid after the first shot but she do not think that it was the shot. The outcome of the was unknown. Information on lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 1224827
Sex: U
Age:
State: KY

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: short red line and but it didn't feel like nothing it was just a red line there and then the patient woke up yesterday morning and it was burning; swelled up; Subcutaneous; red line going down collarbone; This is a spontaneous report from a contactable consumer (patient). A 63-years-old patient of an unspecified gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), subcutaneous in right arm on 29Mar2021 (Batch/Lot Number: Unknown) as single dose for covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient had first Pfizer COVID-19 shot (COVID-19 Vaccine), the 29Mar2021 two days ago (reported on 31Mar2021). The patient had nothing on collarbone when the patient went there and got the shot, the patient got the shot on right arm and when the patient got home the patient just had this red line going down collarbone, the short red line and but it didn't feel like nothing it was just a red line there and then the patient woke up yesterday morning and it was burning and yesterday afternoon it turn around and it swelled up and it like had a 'gas down' (not clarified) as it was seen where the red line was and it looked like it's coming down affected, so the patient put on (not clear nor clarified). It's still swollen on right side, they did right arm where the vaccine was and then it's right collarbone. It was on collarbone and now it looks like it's just an infected area, it was all puffed up and everything else (not clarified further). Outcome of the event swollen was not recovered, of other events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224828
Sex: F
Age:
State: GA

Vax Date: 02/17/2021
Onset Date: 02/18/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: Odd Joint Aches; Stomach pain; Felt like an elephant was sitting on her chest, she thought she was having a heart attack.; chest pain is not as bad but it is still ongoing off and on for the past 7 weeks/generally at night but sometimes during the day; This is a spontaneous report from a contactable consumer (patient). A 66-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot/Batch number: EN6200), dose 2 via an unspecified route of administration, administered in left arm on 17Feb2021 at 16:00 as single dose for COVID-19 immunisation. The patient medical history included tennis elbow (20 years ago). The patient previously received first dose of bnt162b2 (Lot/Batch number: EL3247) on 27Jan2021 for COVID-19 immunization and old shingles shot for shingles and experienced arm swelled up like a baseball and got really hot (it was a long time ago probably 7-10 years). The patient's concomitant medications were not reported. The patient neither had any history nor took any other products. No additional vaccines administered on same date of the pfizer suspect. The patient felt like an elephant was sitting on her chest, she thought she was having a heart attack and chest pain is not as bad but it is still ongoing off and on for the past 7 weeks/generally at night but sometimes during the day on 18Feb2021 at 02:00, stomach pain on 28Feb2021 and odd joint aches on 01Mar2021. She further clarified that her chest pain isn't as bad, it doesn't feel like she is having a heart attack. The tennis elbow is back sometimes and then she will work out and then her knee hurts and she doesn't have knee problems. States it comes and goes. The patient states it is odd because she knows 4 other people that are having same thing. States 1 had the Moderna and 2 are Pfizer, and 1 had the Johnson and Johnson. They all felt like they were having heart attacks in the middle of the night. The patient was treated with Nexium and states she can only eat oatmeal, bananas, chicken and rice. She neither visit the emergency room nor the physician office due to the events. She is very healthy and in good shape. She called her physician's office and they said to go to the ER or a cardiologist office. There was no family medical history relevant to the adverse events. The outcome of the event felt like an elephant was sitting on her chest, she thought she was having a heart attack was unknown and was not recovered for the rest of the events. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224829
Sex: U
Age:
State:

Vax Date: 03/30/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: sore shoulder; my foots swell; I got all in groin area kind of sore; rash and skinfold in groin; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 30Mar2021 (Batch/Lot Number: EN6208) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient got bnt162b2 yesterday (reported on 31Mar2021) and had sore shoulder little, foots swell and today the patient was driving car for an hour got all in groin area kind of sore and the patient had a rash and skinfold in groin. Outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224830
Sex: F
Age:
State: WA

Vax Date: 04/02/2021
Onset Date: 04/02/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: passed out from exhaustion; Fever; was unable to stand unassisted.; writhing in pain/so much pain; in and out of consciousness/passed out; tongue swelled up, making it hard to breathe and impossible to speak; tongue swelled up, making it hard to breathe and impossible to speak; tongue swelled up, making it hard to breathe and impossible to speak; sweating profusely; couldn't support her own body without tipping over.; seizure; lymph nodes in her left armpit swelled up so much that she couldn't put her arm down without extreme pain; lymph nodes in her left armpit swelled up so much that she couldn't put her arm down without extreme pain; chills; extreme muscle pain; spasms; This is a spontaneous report from a non-contactable consumer (patient herself). A 29-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine), dose 2 via an unspecified route of administration, administered in left arm on 02Apr2021 13:15 (Batch/Lot Number: ER8737) as single dose, for COVID-19 immunisation. Medical history was reported as no. Patient did not have COVID-19 prior to vaccination. Patient did not receive other vaccines within 4 weeks prior to COVID-19 vaccine. Patient's concomitant medication includes omeprazole, ethinylestradiol, levonorgestrel (MARLISSA), venlafaxine and gabapentin from unspecified dates, received within 2 weeks of vaccination, for unspecified indication. Patient historically took first dose of Pfizer BNT162B2 (Lot number: EN6204) on 13Mar2021 at 11:00 AM on the left arm for COVID-19 immunisation. Patient previously took hydrocodone bitartrate, paracetamol (VICODIN) on an unspecified date and indication and had allergy. On 02Apr2021, around 10pm, patient began having chills and extreme muscle pain and spasms, and the lymph nodes in her left armpit swelled up so much that she couldn't put her arm down without extreme pain. By midnight (03Apr2021 00:00), patient had a fever and was unable to stand unassisted. She was writhing in pain and arching uncontrollably off the bed. She believed in hindsight that this was a seizure as she went in and out of consciousness and her tongue swelled up, making it hard to breathe and impossible to speak. She was sweating profusely, and had to drink water constantly. Her husband had to help her get to the bathroom because she couldn't support her own body without tipping over. The chills and fever alternated all night, and she finally passed out from exhaustion at 03Apr2021 at 7am. The next 2 days, she was in a cycle of fever and chills again, and the fever got so bad that she seized twice more on Saturday (03Apr2021). She had to take the day off work on Monday (05Apr2021) as she was still in so much pain that she could barely leave bed except to use the bathroom. Events were reported as life-threatening, immediate risk of death from the events. Patient was not hospitalized. Treatment for the adverse events were cool baths, naproxen (ALEVE) for fever and pain, and PEDIALYTE. COVID-19 was not tested post vaccination. Vaccination facility type was at a hospital. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: OMEPRAZOLE; MARLISSA; VENLAFAXINE; GABAPENTIN

Current Illness:

ID: 1224831
Sex: F
Age:
State: FL

Vax Date: 03/24/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: This is a spontaneous report from received from contactable consumer. A 61-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EP7534), via an unspecified route of administration on 24Mar2021 via an unspecified route of administration in top of left arm as single dose for covid-19 immunization. Medical history included Salpingo-oophorectomy (resection to remove an ovary and fallopian tube) in Mar2016 and an operation in 2016 for diverticulitis. Concomitant medications were not reported. There were no allergies to medications, food, or other products. No known allergies. No, she says this is her first vaccine, she has never even had the flu vaccine. Caller clarifies she is talking about the Pfizer BioNTech vaccine. Later in the call clarified as the COVID-19 vaccination. She is calling to report that she contracted COVID. She says she is so discouraged, she did everything right and she ended up getting COVID, she was shot in the arm, her family forced her to get it, 7 days later she was sick, so sick Wednesday(31Mar2021)/Thursday(01Apr2021), positive on Saturday (03Apr2021). She says she is been googling this, it has only been only 6 months, less than 6 months in. On 30 Mar2021, patient had experienced ill, Sneezing, coughing, choking, coughing up phlegm, Fever, Chills and aches. Patient says she did not get her second shot, she is supposed to go for it on 14Apr2021 but she suspects she had to get tested before she gets the vaccine. She says she does not know what to do. She says she is isolating herself and has her own bathroom. She says her card has a patient number and an ISS number. She says she is got this vaccine for society to get this vaccine rolling so we can be whatever the word is, for social status, to be in the cool club. Patient says she had no tests since she does not have a primary. The adverse event was not resulted in emergency room. The patient was resolving from the event COVID. At the time of reporting the outcome of the events were unknown. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1224832
Sex: M
Age:
State: OH

Vax Date: 03/29/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: fever; body ache; headache; little nausea; loss of appetite; malaise and did not feel well; This is a spontaneous report from a contactable consumer. This Consumer reported for her son (Patient). A 28-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number was not reported) via an unspecified route of administration on 29Mar2021 as single dose for COVID-19 immunization. Medical history included covid-19 and nephrocalcinosis. The patient concomitant medications were not reported. Caller reported that her son developed symptoms early Monday morning, 7-8 days later, the patient experienced fever, body ache, headache, little nausea, loss of appetite, feeling unwell and malaise. Caller stated that her son wanted to get tested for covid and asked if the test would not come back negative because of the shot. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected

Other Meds:

Current Illness:

ID: 1224833
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/21/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: the patient experienced took vaccine already and tested positive for covid vaccine; COVID-19 virus test positive; This is spontaneous report received via Social Media report from by a consumer. A patient of unspecified age and gender was administered with first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: unknown), via intramuscular route of administration as a single dose for COVID-19 immunization. Patient was also administered with Creon (Pancreatin, Formulation and Lot number: were not provided) via an Intramuscular route of administration (with unknown daily dosage and Therapy dates) for Exocrine Pancreatic insufficiency(EPI) not associated with cystic fibrosis. Medical history and concomitant medication was not reported. Patient took vaccine already and tested positive for covid vaccine did not protect from getting covid with creon (pancreatin). On an unknown date, the patient experienced took vaccine already and tested positive for covid vaccine did not protect from getting covid on 21Mar2021, the patient experienced took vaccine already and tested positive for covid vaccine did not protect from getting covid. Outcome of the events was unknown. Causality for Creon (pancreotin): The reporter's causality for the event(s) of Took vaccine already and tested positive for covid vaccine did not protect from getting covid unknown onset and took vaccine already and tested positive for covid vaccine did not protect from getting covid onset 21Mar2021 was not provided. Information about lot/batch has been request.

Other Meds:

Current Illness:

ID: 1224834
Sex: M
Age:
State: FL

Vax Date: 03/17/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: tested positive for Covid; tested positive for Covid; This is a spontaneous report, received by a contactable consumer (patient). A male patient (age not provided) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number not provided), via an unspecified route of administration, on 17Mar2021 at single dose for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. Second dose was scheduled on 07Apr2021. After first shot, the patient had bad symptoms so he got a test for COVID-19 which resulted negative. He continued to have bad symptoms, so he had a test again on 30Mar2021 which resulted positive. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1224835
Sex: F
Age:
State: PA

Vax Date: 02/08/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: tested positive for Covid; tested positive for Covid; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program . A 41-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9269), via an unspecified route of administration in left deltoid on 08Feb2021 at single dose for covid-19 immunization. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: FL8982), via an unspecified route of administration on 05Jan2021. at single dose for covid-19 immunization. Medical history included anxiety, allergy, iron deficiency and bone locked. Concomitant medications included escitalopram oxalate (LEXAPRO) at a dose 20 mg one a day for anxiety, cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) at a dose of 10 mg for allergy, ethinylestradiol, norgestimate (SPRINTEC) one a day for birth control, iron tablet at a dose of 325 mg one a day for iron deficiency and calcium carbonate, colecalciferol (CALTRATE + D [CALCIUM CARBONATE; COLECALCIFEROL]) at 2 tablets a day for bone locked. The patient stated, she got both doses of the Pfizer Covid vaccine and she just tested positive for Covid today. The patient reported that she cannot find the date that she got. She was not sure. It will be January. No treatment was received. The outcome of the events was unknown.

Other Meds: LEXAPRO; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; SPRINTEC; IRON; CALTRATE + D [CALCIUM CARBONATE;COLECALCIFEROL]

Current Illness:

Date Died: 04/06/2021

ID: 1224836
Sex: M
Age:
State: FL

Vax Date:
Onset Date: 04/06/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: Guillain-Barre Syndrome; urinary incontinence; confusion; lethargy; dehydration; expired; This is a spontaneous report from a contactable physician. A 76-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot and expiry were not reported), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient received first dose of bnt162b2 on an unspecified date for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The physician reported that the patient received his second Pfizer vaccine dose and 2 weeks after receiving the vaccine he presented to her office with urinary incontinence, confusion and lethargy. He was admitted to the hospital and within a few days later, day 5, he was diagnosed with Guillain-Barre Syndrome. Following tests and a lumbar puncture. He was hospitalized x2 weeks, received IVIG x 5days. He was then transferred to a Nursing Home. He was readmitted to the hospital with dehydration and expired 2 days later (last night). The physician asked, "have you seen this type of thing before, with GBS?" The physician considered the case as non-serious. The outcome of the events was unknown except for expired. The patient died on 06Apr2021 as he expired. There was no autopsy done. Information on the lot/batch number has been requested.; Sender's Comments: Limited information precludes a medically meaningful assessment of the case. Based on the current available information, a possible contributory role of the suspect product to the development of events cannot be totally excluded. Additional information including relevant medical history, detailed clinical course, and specified concomitant medications is required to better assess the case. 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: expired

Other Meds:

Current Illness:

ID: 1224837
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: chills and muscle aches 12 hours following second shot of Pfizer covid-19; chills and muscle aches 12 hours following second shot of Pfizer covid-19; This is a spontaneous report received from a non-contactable physician. A patient with unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 on unspecified date for COVID-19 immunization. The patient experienced chills and muscle aches 12 hours following second shot of Pfizer covid-19 vaccine. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224838
Sex: F
Age:
State: MI

Vax Date: 04/01/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: develops ache; experiencing diarrhea; This is a spontaneous report received from a Pfizer sponsored program. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER BIONTECH COVID-19 mRNA Vaccine; Solution for injection; Lot number: UNKNOWN) via an unspecified route of administration on 01Apr2021. On an unknown date, the patient developed ache and diarrhea. The patient took Tylenol for aches and wants to know if she can take over-the-counter medicine like Imodium for the diarrhea. The clinical outcome for the events were captured as Unknown. It was unknown if the reporter a Healthcare Professional. It was unknown if the reporter is the prescribing HCP. It was unknown if the reporter's contact information available to you or a sub-contracted party. The patient attempted to provide #, caller says that she will just wait on queue. There was no medical Information: Customer and/or medical inquiry was NOT forwarded or referred. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224839
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: an allergic reaction.; This is a spontaneous report from a non-contactable consumer (for her mother) reported that a female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications was not reported. Patient was in an ICU. Trying to figure out if it was due to the covid vaccine and an allergic reaction. Serious criteria was hospitalization. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224840
Sex: M
Age:
State: MN

Vax Date: 12/05/2020
Onset Date: 03/18/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: anaphylaxis; This is a spontaneous report from a contactable healthcare professional (patient). A 55-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date unspecified), via an unspecified route of administration, administered in left arm on 05Dec2020 11:00 as single dose for COVID-19 immunisation; and amoxicillin, clavulanic acid (AUGMENTIN), via an unspecified route of administration from 18Mar2021 at unspecified dose for an unspecified indication. Medical history included myocardial infarction (MI), coronary artery bypass grafting (CABG), AV Nodal block, and pacemaker. The patient's concomitant medications were not reported. On 18Mar2021 20:00, the patient experienced anaphylaxis. The patient was hospitalized for 2 days on an unspecified date due to the event. The patient reported that he was on augmentin on and off for years and when he got his first vaccine. And on 18Mar2021, he began augmentin again and had anaphylaxis requiring hospitalization. The patient was asking if this was related to the vaccine, but seems to be a possibility. The event resulted in resulted in emergency room/department or urgent care, hospitalization, life threatening illness (immediate risk of death from the event). The event was treated with epinephrine, steroids, benadryl, and fluids. There was no other vaccine in 4 weeks and patient had not had Covid prior vaccination and was not Covid tested post vaccination. The action taken in response to the event for amoxicillin, clavulanic acid was unknown. Outcome of event was recovered in 2021. Information on batch/lot number was requested.; Sender's Comments: Based on available information, the event anaphylaxis is assessed as unrelated to BNT162B2. The event occurred more than 3 months after the administration of vaccine and can be attributed to augmentin based on provided information, including close temporal relationship and positive rechallenge.

Other Meds: Augmentin

Current Illness:

ID: 1224841
Sex: M
Age:
State: NY

Vax Date: 03/14/2021
Onset Date: 03/24/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: positive COVID-19 test with symptoms; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support received from a contactable consumer (patient). A male patient of an unspecified age received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on 14Mar2021 at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient had his 1st dose of BNT162b2 on 14Mar2021 and on 24Mar2021 he was not feeling well and then tested positive for Covid. He had been quarantined after that. His 2nd dose would be on 04Apr2021 and he wanted to know if what would be going to happen next. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224842
Sex: M
Age:
State: TN

Vax Date: 04/05/2021
Onset Date: 04/07/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: Right Sided Bell's Palsy; This is a spontaneous report from a contactable Other-HCP reporting for a patient. A 54-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 intramuscular, administered in Arm Right on 05Apr2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included Stargardt's Disease, Prediabetes, Low Testosterone, Chronic neck pain, and covid-19. Concomitant medication included testosterone (AXIRON). No other vaccine received in four weeks. The patient experienced right sided bell's palsy on 07Apr2021 06:00. The event resulted in Doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of right sided bell's palsy included Prednisone. Outcome of the event was not recovered. No Covid tested post vaccination. Information on the lot/batch number has been requested.; Sender's Comments: A causal association between BNT162B2 and the reported Bell's palsy cannot be excluded based on a temporal relation. 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 RAs, Ethics Committees, and Investigators, as appropriate.

Other Meds: AXIRON

Current Illness:

ID: 1224843
Sex: F
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: difficulties in breathing; This is a spontaneous report received from a contactable consumer (patient) through Pfizer-sponsored program. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COIVD-19 VACCINE; Lot number and expiry date unknown), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced difficulties in breathing on an unspecified date. The outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224844
Sex: F
Age:
State: WI

Vax Date: 04/01/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: diarrhea; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support via a contactable consumer on behalf of his wife(patient). A female patient of an unspecified age who received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 01Apr2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 12Mar2021 for covid-19 immunisation. The patient experienced diarrhea on 2021 with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224845
Sex: F
Age:
State:

Vax Date: 03/25/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: Tested positive for Covid-19; This is a spontaneous report received from a contactable consumer (patient). A 60-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: unknown), via an unspecified route of administration on 25Mar2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient stated she had the first dose of the vaccine on 25Mar2021 and is scheduled for the second dose on 15Apr2021. She has tested positive for COVID-19 since the first dose and asked if she can get the second dose? She asked if it is safe for someone to get the second dose if they have had Covid recently (she asked this multiple times). She stated she is almost symptom free now but the second dose is just a week after she recovers. She stated she doesn't think she should not get it just because she has antibodies. She also asked if she could get the second dose late because she isn't sure if it is too soon to get it after recovering. The reporter classified the event as non-serious. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224846
Sex: M
Age:
State: IN

Vax Date: 03/23/2021
Onset Date: 04/05/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: complete body went paralyzed; lost vision; throwing up; fever; This is a spontaneous report from a contactable consumer. A 41-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: En6207), dose 1 via an unspecified route of administration, administered in left arm on 23Mar2021 08:30 as single dose for covid-19 immunisation. Medical history was reported as none. There were no concomitant medications. The patient started throwing up, fever, complete body went paralyzed and lost vision all it the ER on 05Apr2021 13:00. The events were resulted in emergency room /department or urgent care. There is some treatment (saline and ondansetron) for the events. The patient did not have covid prior vaccination, did not test covid post vaccination. The patient received Covid test post vaccination via Nasal Swab on 05Apr2021, covid test result was negative. There is no known allergies, no other medical history, no other vaccine in four week, no other medications in two weeks. The outcome of the events was resloving.

Other Meds:

Current Illness:

ID: 1224847
Sex: M
Age:
State: PR

Vax Date: 03/10/2021
Onset Date: 03/14/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: severe rash in trunk area, lower back, thighs; This is a spontaneous report received from a contactable other HCP (patient). A 42-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in Arm Left on 10Mar2021 17:30 (Batch/Lot Number: EN6204) as SINGLE DOSE for covid-19 immunization. Medical history included obesity, gout, kidney stones and gastric sleeve bariatric surgery. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had no allergies to medications, food, or other products. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced severe rash in trunk area, lower back, thighs on 14Mar2021. The adverse event result in Emergency room/department or urgent care. No treatment received for the adverse event. The patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot ER2613) on 31Mar2021 at Arm Left as single dose for covid-19 immunisation. Since the vaccination, the patient has not been tested for COVID-19. The outcome was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224848
Sex: U
Age:
State: OH

Vax Date: 02/16/2021
Onset Date: 02/16/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: headache; dizziness; photophobia; Fatigue; nausea; Right arm pain; This is a spontaneous report from a non-contactable consumer. The reporter reported two reports, This is the 1st of 2 reports, for the 1st dose. A 67-years-old patient of an unspecified gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscularly, administered in Arm Right on 16Feb2021 12:15 (Lot Number: EL9267) at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced Headache, Dizziness, photophobia, fatigue and nausea on 16Feb2021 12:58, Pertinent details: patient felt to ill to work whole day migraine type HA/fatigue/nausea. Patient also experienced right arm pain on 16Feb2021. Patient recovered from Headache, Dizziness, photophobia and fatigue on 20Feb2021, recovered from nausea on unknown date, outcome for event Right arm pain was unknown. Tylenol/acetaminophen received as treatment for Right arm pain and headache orally from 16Feb2021 to 19Feb2021, also reported as ongoing as of the report. No follow-up attempts possible. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021234032 same drug/reporter/patient, different dose

Other Meds:

Current Illness:

ID: 1224849
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 04/02/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: brachycardia; Fatigue; rush through back of head that turned into headache; dizzy/lightheaded/feeling faint; This is a spontaneous report from a contactable consumer (reported for herself). A 56-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCIN, Solution for injection), via an unspecified route of administration on 02Apr2021 12:15 (Batch/Lot Number: EP7533) as SINGLE DOSE, for covid-19 immunisation. Medical history included Asthma, factor v Leiden, heart pfo/ stroke 2003 surgically closed 2004 and known allergies was due to Penicillin. Concomitant medications included mometasone furoate (ASMANEX HFA); azelastine; triamcinolone acetonide (NASACORT); acetylsalicylic acid (ECOTRIN); calcium citrate, colecalciferol (CALCIUM CITRATE + D3) all were taken for an unspecified indication. The patient previously took Bactrim and, nystatin suspension and experienced allergies. It was reported that on 02Apr2021 12:15, within minutes of the injection patient got a it rush through back of head that turned into headache that lasted 5 days, immediately got dizzy and lightheaded, which lasted 3 days and ended up in ER (Emergency room) with brachycardia and feeling faint fit 2 days. Fatigue still ongoing, day 6. Patient was hospitalized from an unknown date in APR2021 for 2 days. Patient received treatment for AE as IV fluids, heart monitoring. The patient had not been tested for COVID post vaccination. The patient did not receive any other vaccine in four weeks of vaccination. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 03Apr2021. Outcome of the events was recovering.

Other Meds: ASMANEX HFA; AZELASTINE; NASACORT; ECOTRIN; CALCIUM CITRATE + D3

Current Illness:

ID: 1224851
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: abdominal pain and cramping; This is a spontaneous report from a contactable pharmacist received from a Pfizer- sponsored program. A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were unknown), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced abdominal pain and cramping on an unspecified date and they are wondering if this is a side effect. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224852
Sex: M
Age:
State: GA

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: He had this vaccine and had a sore arm but the flu vaccine was worse.; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE, dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient previously received flu shot and stated it hurt worse. It was reported that the patient had this vaccine and had a sore arm but the flu vaccine was worse. Reporter states that he had both vaccines and he had nothing but a sore arm. States the flu shot hurt worse than that one. Event was assessed as non serious. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1224853
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: Diarrhea; This is a spontaneous report from a non-contactable consumer (patient) via the Pfizer- sponsored program COVAX US Support. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. As reported, patient wanted to reschedule second dose of COVID Vaccine due to diarrhea. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224854
Sex: F
Age:
State: MI

Vax Date: 01/11/2021
Onset Date: 02/09/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: numbness; pain and pressure in all areas of my body; This is a spontaneous report from a contactable nurse (patient). A 38-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration on 11Jan2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. Medical history included had her Covid. Historical Vaccine included first dose of BNT162B2 for COVID-19 immunisation on an unspecified date. The patient's concomitant medications were not reported. The patient experienced numbness, pain and pressure in all areas of my body; all (non-serious) on 09Feb2021. Reason for no lot number: of Covid vaccine: Other: Consumer stated, "They did not give her LOT# or anything down for her, they got her sign a paper she got at work. Patient was a nurse, they did not give her the first one but they gave her the LOT# for the second one." Additional Context: Nurse(Consumer) stated, "She had her Covid her second shot of Covid on 11Jan2021 and at 09Feb2021, she started having some symptoms and they were continuing to last and she have been have hospital visit and she was calling up the specialist and everything, they screen back negative as far as her blood work and her testing so her doctors and she was wondering if her symptoms are related to her Covid vaccine and so she was calling to know if there is any reports or any longer term side effects related to vaccine." When paraphrased the concern, nurse stated, "Right, as far as even the fact that it did not started to show up until a month after my vaccine and it is been a lot of pain and pressure in all areas of my body and numbness has been annoying." Event start date: Nurse stated, "On February 9th." (Confirmed as 09Feb2021). The outcome of events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224855
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: Bells Palsy; This is a spontaneous report from Pfizer - General Company Information received from contactable consumer reporting for himself (patient). A male patient (Age: 49; Unit: Unknown) received bnt162b2 (Lot number and expiry date were not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. Medical history included DVT (deep vein thrombosis). Concomitant medication included ongoing rivaroxaban (XARELTO) taken for DVT. The patient developed Bell's Palsy after receiving vaccination shot on an unspecified date. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds: XARELTO

Current Illness:

ID: 1224856
Sex: U
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: Bell's palsy; fever; Diarrhea; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (BNT162B2 reported as Covid Vaccine), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The reporter stated that "after I got the Covid vaccine after two day I mean after the same day like I got it I came home and I had fever for two days actually and then I have the next day diarrhea, two days and then again I experienced some fever after I experienced some Bell's palsy so my question is if I am going to take the Covid vaccine again should I take it or if I would not take it do I have the protection? So, I have this concern because I experienced Bell's palsy." The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am