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: 1224583
Sex: F
Age:
State:

Vax Date: 03/21/2021
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: Dysphagia, Epiglottitis

Symptoms: Relative has a bladder infection; This is a spontaneous report received from a contactable consumer for her relative via Pfizer sponsored program. A female patient of unspecified age received BNT162B2 (BNT162B2, formulation: solution for injection, lot no: unknown ), via an unspecified route of administration on 21-MAR-2021 as SINGLE DOSE for covid-19 immunisation. Medical history and Concomitant medication were not reported. on unspecified date, the patient experienced bladder infection and she was prescribed Cipro. 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: 1224584
Sex: M
Age:
State:

Vax Date: 02/12/2021
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: Anxiety, Dyspnoea

Symptoms: rheumatoid arthritis; Both of his hands were swollen; face is swollen; pain was 3 to 4 from a scale of 1-10; This is a spontaneous report from a contactable consumer reported for her husband that a male patient of an unspecified age (reported as 71, no unit) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 12Feb2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) for covid-19 immunisation. Patient received both doses of the vaccine with the last one on 12Feb2021, he was 70 (no unit) when he had the shot. His wife stated his doctors were a bit flabbergasted at his symptoms and the test had not given any indication of where he should go next. He is having some issues that look like rheumatoid arthritis and he has had several tests from emergency and a primary care provider. At first, they said there was not an indication of rheumatoid arthritis and then it said it was questionable as to "ANA." Both of his hands were swollen. Initially it was little and it got to be huge. His pain was 3 to 4 from a scale of 1-10. They gave prednisone and his hands went down and then several days later they were swollen again. He had prednisone again and then it went up again. He woke up and his face was swollen. The doctors were saying cold compresses. They looked at rheumatoid arthritis positive tests online and found that one way to be positive is due to a vaccine. She wanted to know if there is any help they can be referred to or any information on this. The wife stated she has already spoke with 3 people and reported this to all 3 agents. 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: 1224585
Sex: M
Age:
State: FL

Vax Date: 03/04/2021
Onset Date: 03/08/2021
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: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: States that his symptoms are like he had a stroke; his health declined after the shot; not eating; he is not able to walk by himself; Can't stand up on his own; Mind is not working correctly/The patient was not himself/his mind goes in and out; Speech is Difficult/he was not responding to her and his speech was bad; not feeling very well/not feeling good; Tired and Sleepy; Tired and Sleepy; Noticed patient was warm but didn't take temperature; The patient didn't receive the second shot because he has been in the hospital.; This is a spontaneous report from a contactable consumer (patient's wife). An 89-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Right on 04Mar2021 14:15 (Lot Number: EN6198) at the age of 89 years, as single dose for covid-19 immunisation. Medical history included pituitary gland tumour from 2018 and ongoing (it is not growing according to tests), ongoing asthma which he had for years, and ongoing low blood pressure. His blood pressure goes up and down. He has had it for a long time but started this medication 2 years ago because it was too low. Clarified that it was not taken within 2 weeks of receiving the vaccine because his blood pressure had been too high. There were no concomitant medications. The patient previously took fludrocortisone 0.1 mg once a day. The consumer (patient's wife) stated that she called on behalf of her husband. The patient was still in the hospital. The patient received the vaccine on 04Mar2021 and by 11Mar2021, the patient was in the hospital. They have not been able to find out what was wrong with him. The patient's symptoms were like he had a stroke. The patient was 89 years old, so she took him to get the shot and his health declined after the shot and he is still under the care of the (Hospital name) in (City) (State). The reporter clarified that his symptoms were that he was feeling tired and sleepy on 08Mar2021. The patient said he was not feeling good on 08Mar2021. On 11Mar2021, he was not responding to her and his speech was bad, and now he is not able to walk by himself and can't stand up on his own. This started after he received the shot. The patient didn't receive the second shot because he has been in the hospital. He was doing fine before and now he has these issues. The patient's wife (reporter) noticed the patient was a little warm but didn't take his temperature on 08Mar2021. The reporter stated that last Thursday (11Mar2021) they called the doctor and the doctor suggested taking him to the ER at the hospital. On 11Mar2021, the patient was not himself and not eating and she doesn't know what is going on with him, but he is under care at the hospital. Reporter stated the patient is doing therapy in the hospital and they are helping him to walk but he is having difficulty. She stated they keep asking if she knows what is going on, but she has no results or medical records. Reporter stated the patient's mind is not working correctly and speech was difficult for him. She clarified that he wasn't making sense sometimes and she was not able to understand him. States the patient speaks two languages but he started speaking a third language to her. She stated that his mind goes in and out. Treatment: rest and at the hospital they are doing therapy for his legs. States she will get on update on his progress on Friday. States she can't see him because of Covid restrictions. The patient did not receive any vaccines 4 weeks prior to COVID vaccine. Outcome of the events was unknown.

Other Meds:

Current Illness: Asthma (States he has had for years.); Low blood pressure; Pituitary tumour (it is not growing according to tests)

ID: 1224586
Sex: M
Age:
State: IL

Vax Date: 03/02/2021
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: Dizziness, Fatigue, Mobility decreased

Symptoms: positive COVID-19 test with symptoms; positive COVID-19 test with symptoms; This is a spontaneous report from a contactable physician. A 75-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2nd via an unspecified route of administration on 02Mar2021 (Lot Number: EN6198) as single dose, dose 1st via an unspecified route of administration on 09Feb2021 (Lot Number: EL9269) as single dose for covid-19 immunisation. Medical history included afib, heart disease, hypothyroidism, hyperlipedemia, aortic valve disorders. Concomitant medication(s) included levothyroxine, omeprazole, rivaroxaban (XARELTO), rosuvastatin and flecainide. On 26Mar2021, the patient experienced flu like symptoms, fever, body aches, loss of smell and taste and weakness. On 31Mar2021, nasal swab test was done which showed SARS COV2 RNA as positive and for INFLUENZA A & INFLUENZA B as negative. There was no treatment given for the reported events. There was no covid prior to vaccination. The patient was tested for covid post vaccination. The outcome of the events was not recovered.; Sender's Comments: As it is reported that the patient had received both the doses of the vaccine within the required time interval yet the efficacy of the vaccine varies from patient to patient and can be affected by various factors. However, a contributory role of the usage of the vaccine BNT162B2 to the reported events vaccination failure and COVID-19 cannot be completely excluded.

Other Meds: LEVOTHYROXINE; OMEPRAZOLE; XARELTO; ROSUVASTATIN; FLECAINIDE

Current Illness:

ID: 1224587
Sex: U
Age:
State: MO

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 erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: received the Pfizer Covid vaccine and tested positive for the virus; received the Pfizer Covid vaccine and tested positive for the virus; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received 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 immunisation. The patient medical history and concomitant medications were not reported. The patient received the Pfizer Covid vaccine and tested positive for the virus. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224588
Sex: M
Age:
State: NY

Vax Date: 03/26/2021
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, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: His entire left arm was completely numb; His mouth went completely numb; His tongue is having a tingling sensation; He has headache; His vision was blurred seeing very weird things; This is a spontaneous report from a Pfizer-sponsored program. A contactable male consumer (patient). A male patient of an unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number and expiration dates were not reported), via unspecified route of administration on 26Mar2021 in the left arm at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It reported that, patient received the 1st dose of vaccine on 26Mar2021 and due to take his 2nd shot on 16Apr2021. The patient stated on an unspecified date in Mar2021 last night his entire left arm was completely numb to touch down to his fingers and he couldn't feel the things that he is touching, his mouth went completely numb and his tongue was having a tingling sensation, headache and his vision was blurred seeing very weird things. The patient wanted to know if there was a report regarding this side effects after taking the vaccine. The outcome of the patient's events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224589
Sex: F
Age:
State: NY

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: Pyrexia, White blood cell count decreased

Symptoms: arm was very heavy; dry cough; vomit; headache; chills; bones hurt; fever; right arm was swollen; feels tired; This is a spontaneous report received from a contactable consumer (patient). A 51-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on an unspecified date (yesterday at 1:00 p.m) at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced felt her arm was very heavy, at night had a lot of dry cough and about 2-3 times during the day, after which she was vomit, headache, chills, bones hurt, fever, right arm was swollen and when she does something and feels tired on an unspecified date in 2021. 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: 1224590
Sex: M
Age:
State: OH

Vax Date: 03/04/2021
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: Pharyngeal swelling

Symptoms: Possible TIA; He woke up with black clouds in both eyes surrounded by red; This is a spontaneous report from a contactable consumer (patient's son/daughter). A 75-year-old male patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT number: EN6202, expiration date unknown) via unspecified route of administration at arm left on 04Mar2021 at 11:30 AM at age of 74-year-old at single dose for COVID-19 immunisation. Medical history included traumatic brain injury (TBI) 1.5 years ago due to a horse accident. There was no known allergies. Concomitant medication was reported as none. There was no other vaccine in four weeks and no other medications in two weeks. Patient woke up with black clouds in both eyes surrounded by red. He went to an eye doctor the next day that told him not to get the next dose and to go see a doctor immediately. He did, he has still not received any real answers. The eye doctor was afraid it was a possible transient ischaemic attack (TIA). Onset date of events was 24Mar2021 at 03:30 AM. Outcome of events was not recovered. No treatment received for the events. Events resulted in doctor or other healthcare professional office/clinic visit. There was no Covid prior vaccination. Covid was not tested post vaccination.

Other Meds:

Current Illness:

ID: 1224591
Sex: F
Age:
State: CA

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: Abdominal pain, Chills, Sleep disorder

Symptoms: fainted; generally feeling fatigued; little dizzy; headache; cuts on her face and a bump on her head; This is a spontaneous report from a contactable consumer (reporting for herself). A 31-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 31Mar2021 (Batch/Lot Number: Unknown) as single dose for COVID-19 immunization. The patient's medical history was not reported. Concomitant medication included marijuana taken for an unspecified indication, start and stop date were not reported. On 01Apr2021, the patient fainted. The patient also been generally feeling fatigued and a little dizzy. The patient fainted after going to the restroom, stood up after finishing her business and blacked out and woke up on the floor with cuts on her face and a bump on her head. The patient is fine now just a little tired, dizzy and headache. The patient did not received treatment for the events. The outcome of the events was recovering. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. Information on the lot/batch number has been requested.

Other Meds: MARIJUANA

Current Illness:

ID: 1224592
Sex: F
Age:
State: GA

Vax Date: 03/16/2021
Onset Date: 03/20/2021
Rec V Date: 04/18/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Within 5 days of vaccine the patient became symptomatic with Shingles. Many years had gone by since last bout with Shingles; Within 5 days of vaccine the patient became symptomatic with Shingles. Many years had gone by since last bout with Shingles; This is a spontaneous report received from a contactable consumer (Patient). A 79-Year-old female patient (Pregnant: No) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6202), via an unspecified route of administration in right arm on 16Mar2021 at single dose for COVID-19 immunization. The relevant medical history included pre-diabetic, high Cholesterol, shingles (many years had gone by) and allergies: Penicillin, Statins, Hazelnuts, all from unspecified date. Concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (lot number: EL3247, right arm) on 15Feb2021 at the age of 79 years old for Covid-19 immunization. On 20Mar2021, within 5 days of vaccine the patient became symptomatic with Shingles. Many years had gone by since last bout with Shingles. No treatment was received for the events. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. The patient underwent lab test included nasal swab on 09Mar2021 and 10Mar2021, both showed negative. The outcome of the event was recovering. No follow up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224593
Sex: F
Age:
State: OH

Vax Date: 03/31/2021
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: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: right sided facial paralysisBell's Palsy; dizzy; headache; feeling extreme fatigue; couldn't speak; This is a spontaneous report from a contactable consumer (patient). The 50-years-old female patient (age at vaccination was 50 years old) received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Right on 31Mar2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. Medical history included kidney donor. The patient was healthy with no medical issues. Concomitant medication(s) was not reported. The patient experienced right sided facial paralysisbell's palsy, dizzy, headache, feeling extreme fatigue on an unspecified date. Reported as: Within 8 hours of receiving the dose, she said "the room got dizzy" and she developed a headache and Bell's Palsy. She states she had right sided facial paralysis, couldn't speak, and exhibited other stroke like symptoms. Was admitted to the hospital, given Plavix, and a headache "cocktail" to treat her symptoms. She underwent an MRI, CT, and echocardiogram to rule out a stroke. She is still hospitalized and states her symptoms started to resolve today, 02Apr2021, at around 8 AM. She also reports feeling extreme fatigue after receiving the vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224594
Sex: M
Age:
State: MA

Vax Date: 03/12/2021
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: Rash, Urticaria

Symptoms: tested positive with Covid; tested positive with Covid; This is a spontaneous report from a contactable consumer (patient's wife) via Pfizer Sponsored program. A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: unknown), via an unspecified route of administration on 12Mar2021 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date in Mar2021, the patient experienced tested positive with COVID. The consumer would like to cancel her and the patient's second dose schedule that was due the next day because her husband tested positive with COVID. The patient underwent lab tests and procedures which included SARS-COV-2 test: Positive on unspecified date in Mar2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224595
Sex: F
Age:
State:

Vax Date: 03/01/2021
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: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: arm soreness and more fatigue the day after the vaccine; arm soreness and more fatigue the day after the vaccine; voice hoarseness; This is a spontaneous report received from a contactable other healthcare professional and a contactable consumer (Patient)from a Pfizer Sponsored Program. A 65-year-old female patient received second dose of BNT162B2 (reported as covid vaccine), via an unspecified route of administration on Mar2021 as single dose for COVID-19 immunisation. Medical history included muscle tightness in shoulder and neck causing shoulder pain (had bone metastasis)- improved, breast cancer. Concomitant medication included palbociclib (IBRANCE, 125 mg) taken for breast cancer from 04Jan2021 and ongoing. After start of palbociclib therapy, tiredness- more tired on "third week/off week and first week of cycle''; low white blood cell count from 2.3 to 2.0. MD aware. Per MD, she was off palbociclib 2 days before and 2 days after second dose of covid vaccine (Mar2021)- had "left arm soreness and more fatigue the day after the vaccine". No other adverse effects reported while off palbociclib. Had new report of voice hoarseness at times. The action taken in response to the events for bnt162b2 was not applicable. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: IBRANCE

Current Illness:

ID: 1224596
Sex: F
Age:
State: OH

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

Symptoms: her MS symptoms exploded; head became foggy; blurred eyes; slight headache; This is a spontaneous report by contactable consumer(patient) from Pfizer Sponsored program. A 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) first dose on 17Mar2021 at single dose for COVID-19 immunization. Medical history included Multiple Sclerosis (MS) for 20 years and autoimmune disease. Concomitant medications included interferon beta-1a (AVONEX) for MS. The patient previously took Avelox for MS. Caller also states she would like to report that she has a history of Multiple Sclerosis (MS) and she goes to the clinic. Caller states since no studies were done on people with MS, she would like to report her experience. Caller states she received her first dose of the vaccine on 17Mar2021 and hours afterwards her MS symptoms exploded. Caller states she has had MS for 20 years and she doesn't even realize she has it because she is able to walk the dogs at the pound and she does 3600 steps a day and it doesn't keep her from doing anything. Caller states after the shot she has torn meniscus in her knees and her knees were so tight and she has heel spurs, and they were burning and hurt. Caller states she hurt her hand previously and her hand was tight, and it felt like it was going to explode. Caller states every injury she has ever had it felt like it was exacerbated and got worse. Caller states she was instructed by the Clinic to take Tylenol every 6 hours and these symptoms lasted for 12 days. Caller states she takes a medication called Avelox for MS once a week and she didn't take it after the shot because it is known to cause flu like symptoms, but she is back taking it now. Caller states she was working on the computer and her head became foggy and this lasted for six or seven days. The caller has MS and is on Avonex, it's a beta 1 interferon injectable that she has been taking for over 20 years. The caller's doctors told her it was okay to get the shot. Because of the caller's autoimmune disease, the caller's doctors don't know how effective the shot will be with an autoimmune disease. The caller has done well with Multiple Sclerosis; her Multiple Sclerosis was really good she was walking 3600 steps a day. The vaccine seems to have flared up everywhere the caller has been hurt. It made those spots worse. The caller had a torn meniscus and it felt like her knee was stiff like a board. The caller had a bone spur in her foot that it began to hurt where that was removed. The caller broke her left hand and then it felt like it was going to explode. The caller also had head fog and blurred eyes. It took 6-7 days for head fog to get better. The other symptoms it was 12-13 days to get better. The caller also had a slight headache. The clinic said there were no studies in someone with MS who took the covid vaccine, they only reported to them about the autoimmune disease. Someone on the thing said the second dose was 10 times worse than the first one. Then the caller was told if she gets those symptoms with the first shot then the second one will be better because your body is used to it and knows what to do. It is kind of like a trial by fire and no one knows what to expect. The caller wants to know if Pfizer had any information on Avonex interfering with MS. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds: AVONEX

Current Illness:

ID: 1224597
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: blood in her eye, like it busted; This is a spontaneous report from a non-contactable consumer reported for herself. A 56-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 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 medical history was not reported. The patient's concomitant medications were not reported. The patient got her first Pfizer covid vaccine this morning she was doing fine but when she came home and looked in the mirror, it looks like there is blood in her eye, like it busted. It doesn't hurt or anything on unknown date with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224598
Sex: M
Age:
State: CA

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

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

Lab Data:

Allergies:

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

Symptoms: Left facial Bell's Palsy; BNT162B2 subcutaneous; This is spontaneous case report from a contactable physician (patient himself). A 51-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL1283), subcutaneous, at Arm Left on 09Jan2021 (at age of 51 years old) at single dose for COVID-19 immunisation. Medical history was none. The patient's concomitant medications were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EH9899) Subcutaneous at Left Arm on 18Dec2020 18:00 (at 51 years old) at single dose for COVID-19 immunisation. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. Test Name: SARS-CoV2 RT PCR. Allergies to medications, food, or other products was None. The patient experienced Left facial Bell's Palsy on 30Jan2021. The patient underwent lab tests and procedures which included Nasal Swab: negative on 31Jan2021. The adverse event Left facial Bell's Palsy result in Emergency room/department or urgent care. Treatment (Prednisone, Acyclovir) received for the adverse event. The outcome of the events was unknown.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine can not be excluded for the reported event of Left facial Bell's Palsydue to temporal relationship and current known drug safety profile. 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. 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: 1224599
Sex: F
Age:
State: CO

Vax Date: 03/20/2021
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: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: breathing/unresponsive; seizures; blood sugar was 35/Blood sugar dropped into the 60's again; This is a spontaneous report from a contactable reporter. A 75-year-old female patient (reporter's mother) received second dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 20Mar2021 at single dose for covid-19 immunisation. Medical history included parkinson's disease from 2018 to an unknown date, the progressive type, covid-19 from Nov2020 to an unknown date (She had mild case of covid in November), she was not symptomatic, rheumatoid arthritis from 2018 to an unknown date, Heart failure from 2018 to an unknown date(which she was diagnosed in 2018 with and was being managed appropriately), spinal operation from an unknown date and unknown if ongoing PRESS (Posterior reversible encephalopathy syndrome) Complication, posterior reversible encephalopathy syndrome from an unknown date and unknown if ongoing (Complication after Back surgery). The patient's concomitant medications were not reported. The patient had the first dose of dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE) on 27Feb2021 for covid-19 immunisation. The patient experienced breathing/unresponsive but breathing on her bi-pap (hospitalization) on an unspecified date with outcome of unknown, seizures (hospitalization) on an unspecified date with outcome of recovered, blood sugar was 35/blood sugar dropped into the 60's again, blood sugar low (hospitalization) on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included lumbar puncture: proteins and white blood cells on unknown date, Presence of proteins and white blood cells, magnetic resonance imaging(MRI): something that happened with brain on unknown date, assault from something that happened with brain, white blood cell count: nothing crazy on unknown date. Therapeutic measures were taken as a result of seizures, blood sugar was 35/blood sugar dropped into the 60's again. The clinical course was reported as follows: She states, "Her mother was in a rehab facility up until the 26Mar2021, the CNA came in at noon and her mom wanted to keep sleeping. Thursday afternoon was the last time she got to talk to her. PT/OT came in at noon on Friday - found to be breathing/unresponsive. blood sugar was 35, gave her glucose, came up to 111. Still not responsive but breathing. Sent her to ER, she was breathing but still not responsive, then started she started having seizures. Blood sugar dropped into the 60's again, having seizures from Friday until Monday. managed it with Keppra and another seizure medicine and now she is in ICU. Her mother is 75 years old with degenerative Parkinson's Disease, wheelchair bound, and a history of PRES (Posterior reversible encephalopathy syndrome). She was about to be discharged but then all of this happened. The only thing that was really different is the vaccine that she received. She had mild case of covid in November, she was not symptomatic. Waited 3 months to get the covid vaccine after she had covid. The caller states that her mother received the first dose of the Pfizer COVID-19 vaccine on 27Feb2021 and the second dose on 20Mar2021. The caller would like to know if there have been any reports of low blood sugar associated with receiving the Pfizer COVID-19 vaccine. The caller wants to know if anyone has reported seizures as a side effect from receiving the Pfizer COVID-19 vaccine. Responded per page 23 of the attached EUA Prescribing Information LAB-1457-6.0 Revised: 25Feb2021: "Throughout the safety follow-up period to date, Bell's palsy (facial paralysis) was reported by four participants in the Pfizer-BioNTech COVID-19 Vaccine group. Onset of facial paralysis was Day 37 after Dose 1 (participant did not receive Dose 2) and Days 3, 9, and 48 after Dose 2. No cases of Bell's palsy were reported in the placebo group. Currently available information is insufficient to determine a causal relationship with the vaccine. There were no other notable patterns or numerical imbalances between treatment groups for specific categories of non-serious adverse events (including other neurologic or neuroinflammatory, and thrombotic events) that would suggest a causal relationship to Pfizer-BioNTech COVID-19 Vaccine. 6.2 Post Authorization Experience: The following adverse reactions have been identified during post authorization use of Pfizer-BioNTech COVID-19 Vaccine. Because these reactions are reported voluntarily, it is not always possible to reliably estimate their frequency or establish a causal relationship to vaccine exposure. Immune System Disorders: severe allergic reactions, including anaphylaxis, and other hypersensitivity reactions (e.g., rash, pruritus, urticaria, angioedema)". The caller has her best friend on the line with her in case the caller forgets something. The caller's is calling on behalf of her mother who had both doses of the covid vaccine. The patient is currently in the Intensive Care Unit. The patient was supposed to go home from a rehabilitation facility on 27Mar2021 and staff found the patient on 26Feb2021 unresponsive but breathing on her bi-pap. Prior to the patient being found like this she was tired at noon and asked the staff to hold her lunch for her because she was tired and wanted to lay down because she had been up late the previous night. When physical therapy and occupational therapy came in a couple of hours later to do therapy they found the patient unresponsive and the patient's blood sugar was 35 so they gave her glucose and the blood sugar came up to 111. Emergency medical services came and took the patient to the emergency room and then she was put in the Intensive Care Unit, this was all within 30 minutes. The glucose dropped one more time and she started having seizures. The medical staff stabilized the patient with Keppra and another seizure medicine that starts with a V on a drip. The patient has been off her sedatives since Tuesday and she has eye movement under the eyes, she withdraws from pain, and when (name withheld) was talking to the patient on speakerphone the patient moved her head towards the phone. The caller mentions that the patient was not protecting her airway when the emergency medical service showed up and so the staff placed a king airway and then the patient moved to a normal ventilator. Wednesday the patient was being weaned on the ventilator and was able to breathe on her own for 7 hours. The caller was only able to breathe on her own on the ventilator for 2 hours yesterday, split up into 2 different trials. The medical team is pressuring the caller talking about tracheostomy and peg tubes and the medical staff wants to talk about that next week if the patient is not coming around. Investigations: MRI showed basically an assault from something that happened with the brain from having a low blood sugar. The patient has no history with diabetes or low blood sugars. Maybe the patient had a seizure prior? The patient had signs of infections, her white blood cell count is nothing crazy. The patient's lumbar puncture showed proteins and white blood cells present. The caller is trying to figure out what may have caused this incident. The patient had 4 strokes on her left side and has come back from that and has been driving and fine after. The patient's outpatient neuro person said it is from the seizures. The caller is trying to rule out if there is anything weird with this vaccine that may have caused this or been reported? PRESS is a rare complication after back surgery and the patient had that. If something is super weird and rare then the patient usually has it, she usually gets weird things. Is this related to the vaccine? The caller knows it may not be likely but it was the only thing she hadn't looked into yet. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224600
Sex: M
Age:
State: WI

Vax Date: 03/25/2021
Onset Date: 03/26/2021
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: Since the vaccination, has the patient been tested for COVID-19?:Yes; Since the vaccination, has the patient been tested for COVID-19?:Yes; Fever 101-104 ongoing 8 days after vaccine; rigors; fatigue; This is a spontaneous report received from a contactable consumer (patient, self-reported). A 16-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: ER8730 and expiry dates were not reported), via unspecified route of administration in left arm on 25Mar2021 at 02:30 PM, as single dose for COVID-19 immunization. The patient's medical history includes occasional migraine and remote pneumonia. The concomitant medication included Multivitamin and Vitamin D. It reported that, on 26Mar2021 the patient experienced Fever 101-104 ongoing 8 days after vaccine, rigors and fatigue. The patient underwent lab test 24 hours post vaccine that was COVID test negative, also negative COVID Ab, increased inflammatory markers CRP, ESR, Ddimer, abnormal CBC and large platelets, mild hemolyzed blood in urine with otherwise negative UA, blood cultures x 2 negative. Vaccination facility: Pharmacy or Drug Store. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 (Nasal Swab) and after the vaccination the patient been tested for COVID-19. The patient received ongoing tx with antipyretics, monitoring ongoing as corrective treatment for the adverse event. The outcome of the patient's event drug ineffective and COVID-19 was unknown and other events (fever, rigors, and fatigue) were not recovered. Follow-up (02Apr2021): This is a follow-up spontaneous report received from a contactable physician. This physician reported for her son (Patient). The non-significant information updated. Additional information has been requested.; Sender's Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported events of COVID-19 and suspected LOE. There is limited information provided in this report. This case will be reassessed once additional information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds: VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 1224601
Sex: F
Age:
State: NY

Vax Date: 01/19/2021
Onset Date: 01/19/2021
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, Dizziness, Dysgeusia

Symptoms: headache; Total bodyache; fatigue; feeling unwell; fever; Chills; Joint pain; Fogginess of mind; This is a spontaneous report received from Pfizer-sponsored program. A contactable female consumer(patient). A female patient of an unspecified age received BNT162B2 (BNT162B2, Formulation: solution for injection, Batch/lot no: EK5730) second dose via an intramuscular administered in left arm 19Jan202 0.3ml as single dose for COVID-19 immunization. The patient family medical history Father- Deceased was Diabetic, HPN, Kidney Transplant, Dialysis. Mother- Alive-Osteoporosis, Mild Dementia. Sister-Diabetic, HPN. The patient concomitant medications were not reported. The patient experienced with second dose - 19Jan2021 - 1st Day foolness of mind,2nd day -Chills, joint pain,3rd day- Fever, 4th day- feeling unwell,5th day fatigue total body ache, 6th day -feeling unwell' 7th day then 11th day Headaches-pain score-4-5,12th day feeling back to normal about 50-90, 13th day-back to normal. First dose - 30Jan2020 - Dull Headaches for 8 Days straight starting on left side of Forhead radiating to left side of face to left jaw. 1st Dose - 30Jan2020 - Dull Headaches for 8 Days straight starting on left side of Forhead radiating to left side of face to left jaw. The outcome of the events was recovered on unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224602
Sex: F
Age:
State: MI

Vax Date: 03/24/2021
Onset Date: 03/28/2021
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 increased, Chest discomfort, Heart rate increased

Symptoms: Disabling muscle spasms in right to center neck and upper shoulder/back; This is a spontaneous report from a contactable consumer (patient). A 96-year-old non- pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at the age of 96-year-old via an unspecified route of administration, administered in Arm Right on 24Mar2021 12:00 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included High blood pressure. No known allergies. No COVID prior vaccination and no COVID tested post vaccination. No other vaccine in four weeks. Concomitant drug included unspecified other medications in two weeks. The patient experienced disabling muscle spasms in right to center neck and upper shoulder/back on unspecified date, resulted in Emergency room/department or urgent care, hospitalization and disability. Treatment was included OTC pain reliever. The outcome was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224603
Sex: U
Age:
State:

Vax Date: 03/29/2021
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: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: achy and tired; achy and tired; This is a spontaneous report from a contactable consumer. A patient of an unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), via an unspecified route of administration on 29Mar2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), as a single dose for COVID-19 immunization. It was reported that, got my second Pfizer shot yesterday (29Mar2021) and patient was achy and tired today (30Mar2021). 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: 1224604
Sex: F
Age:
State: CA

Vax Date: 04/01/2021
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: Unevaluable event

Symptoms: This is a spontaneous report from a contactable consumer (patient). A 28-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 01Apr2021 11:15 AM (Lot Number: ER8737) as SINGLE DOSE for covid-19 immunisation. Historical bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 04Mar2021 12:15 PM (Lot Number: EN6199) as SINGLE DOSE for covid-19 immunisation. Medical history included migraine, irritable bowel syndrome (IBS), attention deficit hyperactivity disorder (ADHD). No covid prior vaccination, no known allergies and no covid tested post vaccination. The patient's concomitant medications included unspecified drug and not enough space. There is no other vaccine in four weeks. Patient experienced adverse events on 02Apr2021 included Arm Pain right after 02:00 AM, Headache around 2am, Nausea around 2:15am, Fainted around 2:20am, Weak Legs around 2:30am, Tingling in hand & feet around 2:30am, ringing in ear around 2:30am, Light fever around 7am, Headache persisting until just now after getting some sleep finally from 12pm-2pm now.AE resulted in Doctor or other healthcare professional office/clinic visit. There was unknown treatment were received for adverse events. The outcome of headache was not recovered. The outcome of other events was recovering.

Other Meds:

Current Illness:

ID: 1224605
Sex: M
Age:
State: NY

Vax Date: 01/01/2021
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: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: tested positive using a Binx spit test on 31Mar2021; tested positive using a spit test on 31Mar2021; This is a spontaneous report from a contactable consumer (patient). This 65-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the 1st dose (lot number: EL9262) on Jan2021, the 2nd dose (lot number: EN6202) on 25Feb2021; both via an unspecified route of administration in the left arm at single dose for COVID-19 immunisation. Medical history included hypertension (well controlled). Concomitant medications were unknown. The patient had no other vaccine in four weeks, no other medications in two weeks. The patient tested positive using a spit test on 31Mar2021. No treatment was received for events. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1224606
Sex: F
Age:
State:

Vax Date: 03/21/2021
Onset Date: 03/28/2021
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, Pain

Symptoms: tested positive for Covid via PCR test on 28Mar2021; tested positive for Covid via PCR test on 28Mar2021; This is a spontaneous report from a Non-contactable Consumer (Patient). The female patient of an unknown age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, lot and batch number not reported), via an unspecified route of administration on 21Mar2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient previously received first single dose of bnt162b2 for Covid-19 immunization. patient received both doses of the Pfizer BioNTech Covid 19 vaccine, second dose on 21Mar2021. She then tested positive for Covid via PCR test on 28Mar2021. She was calling to see if she needs to get a booster shot. (AE due to potential lack of efficacy) (possible PQC due to potential lack of efficacy). 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: 1224607
Sex: F
Age:
State: NM

Vax Date: 03/23/2021
Onset Date: 03/23/2021
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: 12 hours after receiving the vaccination I was speaking to my husband and my neck and face started to uncontrollably move and spasm. This was painful and concerning. It got violent and much worse over; This is a spontaneous report from a contactable consumer (patient). A 28-year-old female patient started to receive second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number en2613) on 23Mar2021 11:30 at single dose in right arm for COVID-19 immunisation. Medical history included Covid-19, asthma, gastroparesis, surgeries, gastric pacemaker, allergies to Penicillin, soya. Concomitant medications included dicyclomine, sucralfate, famotidine, and ondansetron. The patient previously received cefalexin monohydrate (KEFLEX) and Amoxicillin and had drug allergy. The patient previously received first dose of BNT162B2 (Lot number: en6202) on 02Mar2021 11:30AM in right arm. 12 hours after receiving the vaccination the patient was speaking to her husband and her neck and face started to uncontrollably move and spasm. This was painful and concerning. It got violent and much worse over the next few minutes, She could not control the movements. She called emergency responders and got an ambulance to the hospital. She was given muscle relaxers and sent home. Over the next two days it got worse and more painful so she went to the ER hospital again and they did a CT and blood work and said it was dystonia. She was given ativan and it stopped the convulsions. Again she was sent home. The dystonia continued to happen all day every day. She had returned to the ER one more time and needed medical intervention to control the awful, life changing adverse reaction. This was a horrible experience. She was completely devastated. The events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient had no COVID tested post vaccination. The outcome of convulsions was resolved. The outcome of other events was not resolved.

Other Meds: DICYCLOMINE; SUCRALFATE; FAMOTIDINE; ONDANSETRON

Current Illness:

ID: 1224608
Sex: F
Age:
State: ME

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: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: tip of left ring finger turned white and numb/finger was completely white and the rest of her hands were blue and red and white and yellow; tip of left ring finger turned white and numb; her finger felt funny; Reynauds phenomenon; sore arm; fever; chills; headache; swollen lymph node in the armpit of the arm she got her Covid 19 vaccine in; swollen lymph node started with a sharp pain and it's very sore; left foot, it was pulsing and throbbing all night; feet were modeled red, blue; feet were modeled red, blue; very sick; needed her glasses trying to give her primary care doctor's phone number; has something like gout in her foot; The swollen lymph node started with a sharp pain and could be a blood clot as far as she knows; This is a spontaneous report from a contactable consumer (patient) via the medical information team. A 57-year-old female patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot: EW0150; expiry: 31Jul2021), via an unspecified route of administration in left arm on 31Mar2021 01:30 as single dose for covid-19 immunisation. The vaccination facility type was a warehouse. The vaccine was not administered at a military facility. No previous immunization with the Pfizer vaccine considered as suspect. No vaccines administered on same date with the Pfizer vaccine considered as suspect. No prior vaccinations (within 4 weeks) and no following prior vaccinations. Medical history included covid-19 in Nov2020. The patient had no concomitant medications. The patient had the first dose of bnt162b2 on 31Mar2021 and 12 hours later (on 01Apr2021), sore arm, fever, chills and headache. Got a swollen lymph node in armpit, same arm as injection left side, today tip of left ring finger turned white and numb. She thinks it was Reynauds phenomenon. The patient called and told nurse in her doctor's office and they said if it was painful, it could be a pain clot. It was painful at first, that lymph node started 24 hours later with a sharp pain, and then she just assumed it could be a lymph node. Swollen lymph node started with a sharp pain and it was very sore. The nurse told the patient to call Pfizer. The patient was fine until the tip of her finger happened. The patient said If it was painful it could be a blood clot, would need an x ray and asked if did the shot cause this. The complete ring finger left hand, the patient looked it up and it said it could happen to her feet and she looked, and her feet were modeled red, blue it was bizarre. Never happened before. The patient was not happy about getting the vaccine, she already had covid in November of last year (2020). The patient wouldn't have called if it wasn't for her finger. Not just her feet, her hands got like this too. The patient didn't want to get the second shot. The patient asked if there was any information or mandate on timing information for the second dose, should she needed to postpone it. The patient asked if what was the efficacy after first dose as she felt like she was immune because she had the virus and now the vaccine. She was very hesitant to get the Covid 19 vaccine. She thinks her body created Covid 19 antibodies. A couple days ago she was very sick. The swollen lymph node started with a sharp pain and could be a blood clot as far as she knows (in 2021). Even putting on deodorant she can tell it's there, it was very sore and there's a lump. Today (on 01Apr2021), she noticed the tip of her finger got white it was numb. She looked it up online and she thinks it was Reynaud's phenomenon. She has a picture if Pfizer needed it. The finger was on the same arm that she received her vaccine in. It was the ring finger on left hand. Once it started happening her finger felt funny and felt numb. She put her finger under warm water. She reported that the white color was maybe a third of the way down towards her knuckle. She was asking if this was normal or has this been reported. She had called her doctor today and spoke with the nurse who told her to call the CDC and report her symptoms. She needed her glasses trying to give her primary care doctor's phone number. The patient wanted to add that she has something like gout in her foot and on that side too, the left foot, it was pulsing and throbbing all night. She's had this pain in her left foot, she thinks its gout because it was all the symptoms of gout and she had it for a while, it hurts off and on but that night it was hurting and throbbing. She has not been diagnosed with gout in that left foot. She still has a headache but today she felt good except for her finger turning white and going numb. The lymph node in her armpit hurts. Her doctor's nurse told her if its painful to the touch it could be a blood clot so she was nervous about that. The tip of her finger was completely white and the rest of her hands were blue and red and white and yellow. She reported that her finger was back to normal now. She didn't want to get too inoculated since she also had the Covid 19 virus. The events did not require visit to emergency room nor physician office. The outcome of the events was unknown for thrombosis, Raynaud's phenomenon, erythema, cyanosis, illness, visual impairment, and gout while for the remaining events was recovering.

Other Meds:

Current Illness:

ID: 1224609
Sex: U
Age:
State: MN

Vax Date:
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: Nausea, Pain in extremity, Pyrexia

Symptoms: tested positive today for covid 19; tested positive today for covid 19; This is a spontaneous report from a non-contactable other hcp (Hospital worker) reported for him/herself. A patient of unspecified age and gender received series 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 immunisation. The patient medical history and concomitant medications were not reported. The patient completed Pfizer Covid vaccine series in January (as reported) and tested positive today (31Mar2021) for Covid 19, also reported that "This is my second report in two days of positive Covid post vaccination with Pfizer Covid vaccine." The outcome for the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained; Sender's Comments: Based on the information available, the reported event is possibly related to the suspect drug in terms of drug ineffective.

Other Meds:

Current Illness:

ID: 1224610
Sex: F
Age:
State: PA

Vax Date: 03/25/2021
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: Chills, Fatigue, Headache, Myalgia

Symptoms: Atrial fibrillation; This is a spontaneous report from a contactable consumer (patient). A 57-year-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 25Mar2021 10:30 (Lot Number: ER8733), at the age of 57-years at vaccination, as SINGLE DOSE for COVID-19 immunisation. Medical history included High blood pressure. The patient is not pregnant at the time of vaccination. The patient did not have COVID-19 prior vaccination. Concomitant medications included lisinopril taken for an unspecified indication, start and stop date were not reported; colecalciferol (D3) taken for an unspecified indication, start and stop date were not reported; zinc taken for an unspecified indication, start and stop date were not reported; aspirin [acetylsalicylic acid] (ASPIRIN) taken for an unspecified indication, start and stop date were not reported; fexofenadine hydrochloride (ALLEGRA) taken for an unspecified indication, start and stop date were not reported; amoxicillin taken for an unspecified indication, start and stop date were not reported. On 29Mar2021 12:15, the patient experienced atrial fibrillation 4 days after injection. The event includes emergency room visit and physician office visit. The patient underwent lab tests and procedures which included sars-cov-2 test (Nasal Swab): negative on 29Mar2021. The outcome of the event was unknown. Therapeutic measures were taken as a result of the event which includes IV medication.

Other Meds: LISINOPRIL; D3; ZINC; ASPIRIN [ACETYLSALICYLIC ACID]; ALLEGRA; AMOXICILLIN

Current Illness:

ID: 1224611
Sex: F
Age:
State: NJ

Vax Date: 03/23/2021
Onset Date: 03/24/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Lab Data:

Allergies:

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

Symptoms: dizziness; headache; fever; stomach cramps; migraine; no appetite; dry cough; fainting; stomachache; This is a spontaneous report received from a contactable consumer (patient). A non-pregnant 61-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at the age of 61 years old, administered in arm left on 23Mar2021 19:15 (Lot Number: EN6207) at single dose for covid-19 immunisation. Medical history included ongoing rheumatoid arthritis, arthrosis, osteoporosis, due to arthritis the patient couldn't eat pork because her joints get swollen. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications included etanercept (ENBREL); methotrexate sodium (METHOTREXAAT). The patient experienced fainting, stomachache, stomach cramps, migraine, no appetite, dry cough on 24Mar2021 15:30, dizziness, headache, fever on 25Mar2021. The patient stopped using Enbrel and taking Methotrexate a few days prior Pfizer's vaccine. Next day on 24Mar2021, the patient had stomachache, 3rd day (25Mar2021) started with dizziness, headache and fever. Symptoms kept going after 10 days. 5 days later the patient went to the hospital and was prescribed something for stomach cramps and migraine. But the fever continued. 3 days later doctor prescribed an antibiotic since she didn't know the reason of the fever. During the course of the fever the patient had been taking Tylenol on daily basis. Fever came and went and the patient had no appetite and keep with fainting. Doctor ordered lung rx but the patient couldn't do it. 10 days later the patient had dry cough (event onset date was also reported as 24Mar2021, 15:30). The same symptoms remained. The patient did not receive treatment for all events (except fever). Events resulted in Emergency room/department or urgent care and Doctor or other healthcare professional office/clinic visit. The outcome of the all events was reported as not recovered. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Other Meds: ENBREL; METHOTREXAAT [METHOTREXATE SODIUM]

Current Illness: Rheumatoid arthritis

ID: 1224612
Sex: F
Age:
State: PA

Vax Date: 03/16/2021
Onset Date: 03/22/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
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Lot:
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Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: unusual sensation of sharp tinny sound when she was talking/ hear someone talking nonstop causing her irritation; Tinnitus like symptoms; mild headache; mild sinus irritation; This is a spontaneous report received from a contactable consumer(patient). A 53-year-old female patient(not pregnant) received BNT162B2, dose 1 via an unspecified route of administration, administered in arm left on 16Mar2021 02:45 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was none. Concomitant medication included estradiol, progesterone (BIJUVA) taken for hormone replacement therapy. There was no covid prior vaccination, no covid tested post vaccination, no known allergies. Patient had not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 22Mar2021 15:00, She experienced tinnitus like symptoms, unusual sensation of sharp tinny sound when she was talking. First time was in a restaurant and she could hear someone talking nonstop causing her irritation and onset of a mild headache. She was also feeling mild sinus irritation. There was no treatment. Outcome of events was not recovered. Information on the lot/batch number has been requested.

Other Meds: BIJUVA

Current Illness:

ID: 1224613
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: Injection site pain

Symptoms: autoimmune issues; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient stated she experienced autoimmune issues and she had received the first dose of the Covid-19 vaccine. 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: 1224614
Sex: M
Age:
State: CT

Vax Date: 03/28/2021
Onset Date: 03/29/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Lab Data:

Allergies:

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

Symptoms: Severe Vertigo about a day after the shot; This is a spontaneous case received from two contactable consumers. An adult male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number and expiration date were not reported), via an unspecified route of administration on 28Mar2021 as single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient experienced severe vertigo about a day after the shot on 29Mar2021. It was unknown if the treatment received for the adverse event or not. The patient has not been tested for COVID-19 since the vaccination. The outcome of events was unknown. No follow up attempts are needed. information about lot/batch number can not be obtained.

Other Meds:

Current Illness:

ID: 1224615
Sex: U
Age:
State: FL

Vax Date: 01/06/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

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

Symptoms: The individual received the Pfizer vaccine on January 6th and January 27th and tested positive for Covid this week (exact date unknown).; The individual received the Pfizer vaccine on January 6th and January 27th and tested positive for Covid this week (exact date unknown).; This is a spontaneous report from a contactable other hcp. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE ), dose 1 via an unspecified route of administration on 06Jan2021 (Batch/Lot number was not reported) as SINGLE DOSE, dose 2 via an unspecified route of administration on 27Jan2021 (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 clincal curse was reported as follows: the individual received the pfizer vaccine on january 6th and january 27th and tested positive for covid in Mar2021 (reported as : this week (exact date unknown) .The patient underwent lab tests and procedures which included sars-cov-2 test: positive on Mar2021 . No follow-up attempts are needed. No further information is expected. .; Sender's Comments: Based on information provided, the events of "tested positive for covid in Mar2021" is related to bnt162b2 inherent to the therapy.

Other Meds:

Current Illness:

ID: 1224616
Sex: F
Age:
State: NC

Vax Date: 01/28/2021
Onset Date: 03/16/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
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Vax Site:

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Stroke; Headache; This is a spontaneous report from a contactable healthcare professional through a Pfizer sales representative. A 7-decade-old (60 to 61 years old) female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 28Jan2021 as a single dose, with route of administration unspecified, for COVID-19 immunization. Medical history included migraine; was COVID-19 positive from 06Dec2020 to an unspecified date; and was sick from Dec2020 to an unknown to an unspecified date. The patient's concomitant medications were not reported. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) for COVID-19 immunization. On 16Mar2021, the patient had stroke; assessed as serious (medically significant). On an unspecified date in 2021, the patient had headache. The outcome of the events was unknown. Information about lot/batch number has been requested.; Sender's Comments: Based on the information currently available, the event stroke most likely represents an intercurrent medical condition and is unrelated to Bnt162b2 vaccine. Case will be re-assessed upon the additional information provided. 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: 1224617
Sex: M
Age:
State: WI

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: Erythema, Pruritus

Symptoms: started fibrillating; This is a spontaneous report received from a contactable consumer. A male patient of an unspecified age received 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's medical history and concomitant medications were not reported. The consumer reported that the patient started fibrillating on an unspecified date. The patient got the vaccine and a couple hours later he started fibrillating and was still dealing with it. The consumer's seriousness assessment for started fibrillating was unspecified. The patient visited the doctor and the doctor adjusted his medications a bit, seems to be healing. The outcome of the event was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224618
Sex: F
Age:
State: FL

Vax Date: 03/12/2021
Onset Date: 03/26/2021
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 with symptoms; positive COVID 19 with symptoms; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot Number: EN6205) via an unspecified route of administration, administered in Arm Left, at the age of 61-year-old, on 12Mar2021 09:00, as SINGLE DOSE for covid-19 immunisation. The patient medical history was reported as none. The patient's concomitant medications were not reported. The patient had a scratchy throat on 23Mar2021; then she got a cough on 24Mar2021 and had not slept very well; she got a low grade fever of 99.9 and 100.2; then on 25Mar2021 she had a teladoc appointment because she thought she had a sinus infection. The doctor ask her to come in for tests. On 26Mar2021, she had the influenza A and B test and both were negative; and the COVID test which was positive for COVID 19 infection. By 26Mar2021, the cough had become a barking cough. Mentions she lost her taste on about the 27Apr2021 (as reported); she remembers because she was trying to eat a grilled cheese sandwich with lots of butter; adds she could just taste bitter on the edge of the tongue. Even sweet tasted bitter on the middle of her tongue. Her friend sent her something to try; she a roasted orange until it was black on the outside, and ate the warm orange mixed with brown sugar and it tasted like sweet grapefruit and then drank some water; after that her taste was there. When she got the COVID 19 test that was positive she couldn't believe it because she had had the vaccine, but her son told her the vaccine is working because you are not dead. Patient wanted to change her second dose appointment because the patient is now in quarantine and has COVID 19 infection. The events required physician office visit. The patient did not receive other vaccines the same date COVID-19 vaccine was administered and 4 weeks prior vaccination. Outcome was unknown.

Other Meds:

Current Illness:

ID: 1224619
Sex: M
Age:
State: OK

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

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

Symptoms: mind and memory depression; mind and memory depression; tired; sleepy; back pain got worse; shoulder pain; This is a spontaneous report from a contactable consumer (patient). A 65-years-old male patient received the second dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine, intramuscular in right arm on 26Feb2021 10:15, at 65 years of age, (Batch/Lot Number: EL9267) as single dose for COVID-19 immunization. Medical history included knee surgery on 23Jan2019, some tiredness, disability (reported 40% on back and 30% on mental) and mental depression since 1978 and ongoing. The patient had previously received the first dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine on 05Feb2021 at 10:15 AM (Batch/Lot number: E23247), via intramuscular route in left arm and one dose of Flu vaccine on 14Jan2021 in left arm. Concomitant medications included acetaminophen 500 mg twice daily for back pain, lithium carbonate 1 tablet 300 mg for depression and lamotrigine 25 mg 1 tablet daily for depression, all taken since an unknown date and an unspecified medicine for Disability 40% since an unknown date. On 26Feb2021, 8 hours after the second vaccine dose, the patient experienced tired and sleepy "skeleton" and back pain got worse and shoulder pain and, on an unspecified date, he experienced mind and memory depression. No treatment was administered to the patient for the reported events. The events tired and sleepy resolved on 28Feb2021, the event shoulder pain was resolving, whereas the outcome of the events back pain got worse, mind and memory depression was unknown at the time of the report.

Other Meds: ACETAMINOPHEN; LITHIUM CARBONATE; LAMOTRIGINE

Current Illness: Depression

ID: 1224620
Sex: M
Age:
State: IN

Vax Date:
Onset Date: 03/28/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
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Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: I tested positive for Covid on 28Mar 2021.; I tested positive for Covid on 28 Mar 2021.; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH mRNA COVID-19 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 medical history and concomitant medications were not reported. Patient took the first dose of the Pfizer Covid 19 vaccine and scheduled to the second dose on 7Apr2021. patient tested positive for Covid on 28Mar2021. Patient questioned can he still take the second dose even though he tested positive. Patient also questioned can he receive the vaccine if he have a current or past diagnosis of covid-19 infection. It was reported that pfizer-biontech covid-19 vaccine does not contain sars-cov-2 and cannot give you covid-19. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 28Mar2021. Outcome of the events was unknown. Information on the lot/batch number has been requested. These interim considerations also state that if you currently have a COVID-19 (either before the first dose of vaccine or in between your first and second dose of vaccine), you should wait until you have recovered from the infection, show no symptoms and completed any required isolation.

Other Meds:

Current Illness:

ID: 1224621
Sex: F
Age:
State: KY

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
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Lab Data:

Allergies:

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

Symptoms: headache; This is an initial spontaneous report from a Pfizer Sponsored Program. A contactable female consumer (patient) reported. A female patient with an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/Lot number was not reported) first dose via an unspecified route of administration as single dose for COVID-19 immunization. The patient medical history was not reported. The patient concomitant medications were not reported. Patient had first shot of vaccine. She said had a headache, but that it could be just allergies. Want to know if she can take aspirin (Excedrin). 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: 1224622
Sex: M
Age:
State:

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

Symptoms: dead arm; Feels achy; feels like he has a rash; he has Covid; This is a spontaneous report from a contactable reporter via Pfizer-sponsored program. Amale patient of unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 18Mar2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were unknown. The patient got his 1st dose on 18Mar2021 and he had no side effects until recently. In Mar2021, the patient was experiencing no fever, but felt achy and a dead arm. In Mar2021, the patient felt he has a rash but no visible rash was on the outside of the skin. The patient did get tested for Covid and it was negative in Mar2021, but it was reported that then the patient had Covid (in Mar2021, sars-cov-2 test unknown results; patient had Covid). The outcome of the events was unknown. Follow-up attempts are completed. The batch/lot number is not available despite the follow-up attempts made. No further information is expected.

Other Meds:

Current Illness:

ID: 1224623
Sex: F
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: Pain in extremity

Symptoms: Had heart flips four days after the first shot; This is a spontaneous report from a contactable consumer, reporting for herself. A 43-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date were not reported), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history was reported as none. Concomitant medications included sertraline taken for an unspecified indication, start and stop date were not reported. The patient was not pregnant at the time of vaccination. On an unspecified date, the patient had heart flips four days after the first shot, continued through the whole vaccinated month. No treatment was received. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. There were no allergies to medications, food, or other products. The outcome of the event was recovered on an unspecified date. Information on the batch/lot number has been requested.

Other Meds: SERTRALINE

Current Illness:

ID: 1224624
Sex: F
Age:
State: FL

Vax Date: 03/22/2021
Onset Date: 03/22/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Lab Data:

Allergies:

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

Symptoms: shaky inside my body; Felt like passing out; ears feel clogged; had a hard time falling asleep; unsettled stomach ( a little queasy).; Felt pressure with slight headache; Felt pressure with slight headache/felt pressure in my head; Loud Ringing in both ears; dizzy/dizzy spell; nauseated/unsettled stomach ( a little queasy)/sick to my stomach; body felt uneasy like it was fighting something inside; pain at injection site and side of left neck; pain at injection site and side of left neck; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 22Mar2021 13:00 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included vitiligo and known allergies. The patient had no COVID prior to vaccination. There were no concomitant medications. The patient has no other vaccine in four weeks. The patient was not tested for COVID post vaccination. On 22Mar2021, the patient got the shot and later (at 18:00) had pain at injection site and side of left neck. On 23Mar2021 10:30, the patient experienced loud ringing in both ears, felt dizzy and nauseated, and body felt uneasy like it was fighting something inside. On 24Mar2021, the patient was still having ringing in both ears, feel nauseated on and of lasting at least 30 seconds or so. From 25Mar2021 to 29Mar2021, ringing in ears sometimes get louder than other times, he also felt pressure with slight headache. On 30Mar2021, ringing in ears intensified and had a hard time falling asleep. The patient felt pressure in her head. She also had slight headache and an unsettled stomach (a little queasy). On 31Mar2021, ringing seems lower today; ears feel clogged. She still has pressure in head with slight headache and had one episode of dizzy spell for a few seconds only. At night, ringing in ears intensified. On 01Apr2021, lower ringing in ears noted. On 02Apr2021, the patient had pressure in head, clogged ears, sick to her stomach, shaky inside her body, and felt like passing out. Ringing was intensified at night. On 03Apr2021, headache and pressure in head were noted. The events resulted in doctor or other healthcare professional office/clinic visit but were not treated. The outcome of the events was not recovered. No follow-up attempts are possible, information about lot number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1224625
Sex: U
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: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: This is a spontaneous report received from a contactable pharmacist (other healthcare professional). A patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), as single dose for COVID-19 immunisation. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) for COVID-19 immunisation. The patient experienced sudden one sided weakness with loss of strength that occurred 2 days after 2nd dose of vaccine and resolved one own. This resulted in a hospitalization. Outcome of the event was recovered. Information on Lot/Batch number has been requested.; Sender's Comments: As there is limited information in the case provided for Hemiparesis the causal association between the event and the suspect vaccine BNT162B2 cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug 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: 1224626
Sex: M
Age:
State: NJ

Vax Date: 02/26/2021
Onset Date: 03/05/2021
Rec V Date: 04/18/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: tired; bleeding all over, over and over; He has a bad rash all over his arms, his body, his legs. He has been itching, scratching and bleeding; He has been itching; Scratching; This is a spontaneous report from a contactable consumer (the patient). An 85-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6198; Expiration Date: 30Jun2021) via an unspecified route of administration in left arm on 26Feb2021 09:30 at single dose for COVID-19 immunisation. It was not administered at Military Facility. Medical history included diabetes, allergic to penicillin, and "Thyroid, he is not sure". No prior vaccinations within 4 weeks. No relevant family medical history relevant to AEs. Concomitant medications included metformin taken for diabetes from an unspecified start date and ongoing; simvastatin (Lot and Expiry: Did not really want to provide) taken for an unspecified indication from an unspecified date; glipizide (NDC, Lot and Expiry not reported since his medications were down stairs) taken for an unspecified indication from an unspecified start date and ongoing; metoprolol tartrate taken for an unspecified indication from an unspecified start date and ongoing. The patient previously took Flu Vaccine (Vaccine name: Unknown) in Oct2020, route: Injection in left arm, 4 over the past 4 years, he has been getting them once a year for that long. No additional vaccines administered on same date of the Pfizer suspect. Lot and Expiry of metoprolol tartrate was not reported since his medications were down stairs and he did not want to go get them. Looked the patient was tired (onset date unknown) and then they moved on. The patient had a rash all over on his arms, body, legs. He has been itching, scratching and bleeding all over, over and over, he had bloody t-shirts, underwear, PJ's. It was nasty. He went to the (female) doctor twice already and next Monday, 05Apr2021, he has a follow-up from the last visit. This was for the rash all over and the scratching and bleeding. Caller reported he never had a bad rash this bad in his whole life. This was the worst experience he has had in his life. It also reported it had been difficult the last 2-3 weeks with this but it has improved but, still not clear. The events occurred on 05Mar2021 between 18:00 and 19:00. No relevant tests were taken. It also reported the patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6207; Expiration Date: 31Jul2021) via an unspecified route of administration in left arm on 19Mar2021 at single dose for COVID-19 immunisation. The outcome of the events was unknown.

Other Meds: METFORMIN; SIMVASTATIN; GLIPIZIDE; METOPROLOL TARTRATE

Current Illness:

ID: 1224627
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: Positive COVID-19 test; Positive COVID-19 test; This is a spontaneous report received from a contactable physician. A patient of unknown age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA, Solution for injection, Lot Number: Unknown) via an unspecified route of administration on an unknown date at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient had COVID and a positive test recovered. Patient received Pfizer vaccine, first dose. Reporter enquired about the need of a second dose. Outcome of the events was recovered. Information on lot/batch number has been requested.; Sender's Comments: The information currently provided is too limited to make a meaningful medical assessment. There was no vaccination timeline given relative to occurrence of event. Based solely on temporal relation, a causal relation between 'drug ineffective', 'Covid-19' and BNT162B2 vaccine cannot be totally excluded. This case will be re-assessed if relevant information is received. 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: 1224628
Sex: M
Age:
State: IN

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 04/18/2021
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Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Back Pain; This is a spontaneous report received from a contactable consumer. A 41-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), intramuscular, administered in Deltoid Left on 21Jan2021 10:00 (Batch/Lot Number: EL8982) as SINGLE DOSE for covid-19 immunization. Medical history included ongoing allergies from 2000. Concomitant medication(s) included montelukast sodium (SINGULAIR) taken for allergies from 2005 and ongoing; levocetirizine dihydrochloride (XYZAL) taken for allergies from 2009 and ongoing. The patient experienced back pain on 22Jan2021. No treatment received. The outcome was recovered. Seriousness criteria from reporter was not serious. No follow up attempts are needed no further information is expected.

Other Meds: SINGULAIR; XYZAL

Current Illness: Allergy

ID: 1224629
Sex: F
Age:
State: FL

Vax Date: 03/19/2021
Onset Date: 03/23/2021
Rec V Date: 04/18/2021
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Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: COVID-19; This is a spontaneous report received from a Pfizer sponsored program, via a contactable consumer. A 91-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 19Mar2021 at single dose (at 91-year-old) for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 23Mar2021, patient tested positive to COVID-19 virus and experienced fever. 2nd dose would be on 10Apr2021. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224630
Sex: F
Age:
State: NY

Vax Date: 03/13/2021
Onset Date: 03/18/2021
Rec V Date: 04/18/2021
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Symptom List: Injection site swelling, Limb discomfort

Symptoms: tested positive for COVID on 18Mar2021 and 29Mar2021; This is a spontaneous report received from Pfizer sponsored program Covax US Support from a contactable consumer (patient). A female patient of unspecified age received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT/Batch number and expiration date unknown) via an unspecified route of administration on 13Mar2021 at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Patient wanted to know if she can get the 2nd dose of the vaccine scheduled on 03Apr2021. She was tested positive for COVID on 18Mar2021 and 29Mar2021. 1st dose was taken on 13Mar2021. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224631
Sex: F
Age:
State: NY

Vax Date: 03/14/2021
Onset Date:
Rec V Date: 04/18/2021
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Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: After she received the 1st dose, she tested positive with the virus; After she received the 1st dose, she tested positive with the virus; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT/Batch number and expiration date unknown) via unspecified route of administration on 14Mar2021 at single dose for COVID-19 Immunization. Medical history and concomitant medications were not reported. Patient received the 1st dose of the vaccine last 14Mar2021 and she was scheduled to get the 2nd dose on 04Apr2021. After she received the 1st dose, she was tested positive with the virus. She was not sure if she should take the 2nd dose or she needs to wait. She tried to look around and she didn't find a specific answer. Patient also mentioned that she had fever for 2 days but it was gone at time of reporting. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1224632
Sex: F
Age:
State: CA

Vax Date: 01/20/2021
Onset Date: 01/23/2021
Rec V Date: 04/18/2021
Hospital:

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Allergies:

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

Symptoms: patient tested positive for COVID-19 3 days after the first dose; This is a spontaneous report from a contactable consumer from a Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 1 via an unspecified route of administration on 20Jan2021 (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. On 23Jan2021, the patient tested positive for COVID-19 3 days after the first dose (medically significant). The clinical course was reported as follows: The patient's son reported that his mother had the first dose on 20Jan2021. The patient tested positive for COVID-19 on 23Jan2021, and received an antibody shot on 24Jan2021. The patient's son reported "that's why his mother was not able to get the second dose of the vaccine." The patient underwent lab tests and procedures which included COVID-19 test: positive on 23Jan2021. Therapeutic measures were taken as a result of the event. The clinical outcome of the event, COVID-19, was unknown. The batch/lot numbers for the vaccine, bnt162b2, were not provided and will be requested during follow up.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am