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
7,365
AK259
AL412
AR373
AS9
AZ1,195
CA4,208
CO955
CT600
DC70
DE117
FL1,964
GA946
GU8
HI163
IA433
ID242
IL1,484
IN1,848
KS507
KY565
LA331
MA1,130
MD904
ME380
MI1,203
MN736
MO680
MP5
MS207
MT391
NC869
ND133
NE353
NH288
NJ1,220
NM454
NV252
NY2,638
OH1,382
OK455
OR638
PA1,649
PR335
RI202
SC288
SD152
TN645
TX2,743
UT351
VA961
VI4
VT195
WA921
WI863
WV313
WY70
XB1

ID: 0923678
Sex: F
Age:
State: IN

Vax Date: 12/28/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: resembles a cellulitis to her/ red hot rash spreading on her left arm stated it was the same arm she got in injection; This is a spontaneous report from a contactable nurse reporting for herself. A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EK9231) via an unspecified route of administration (left arm), on 28Dec2020, single dose, for COVID-19 immunization. Relevant medical history and concomitant medications was provided as none. After the patient received the COVID shot few days ago, the patient had a cellulitis reaction to it on 30Dec2020. It resembles a cellulitis to her, a red hot rash spreading on her left arm, stated it was the same arm she got in injection. Cellulitis was reported as worsened. The patient would like to know when she gets the next vaccine if she should alternate arms and get it in the other arm. Outcome of the event was not recovered. The event was assessed by the reporter as non-serious.

Other Meds:

Current Illness:

ID: 0923679
Sex: F
Age:
State: WA

Vax Date: 12/26/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: hand was swollen and itchy on the same arm where the injection was; back of hand was swollen and itchy on the same arm where the injection was; This is a spontaneous report from a contactable nurse (patient). A 60-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EK5730), via an unspecified route of administration (Deltoid Right) from 26Dec2020 15:00 at single dose for Covid-19 immunization. The patient's medical history included chronic pain and insomnia. Concomitant medications included hydrocodone and temazepam. The patient reported, "On 26Dec2020 I got my first immunization for COVID and today (30Dec2020) I woke up and the back of my hand was swollen and itchy on the same arm where the injection was". The patient further stated "It never have happened before I don't have any reaction at the injection site but it was kind of odd that it kind of showed up on the back of my hand, it feels like an allergy kind of thing." The patient tried the Voltaren Gel to try and get the inflammation down, but it didn't help, and she took some Benadryl it doesn't seem to help much. The patient's next shot is due on "12Jan2021". The outcome of events was unknown.

Other Meds: ;

Current Illness:

ID: 0923680
Sex: F
Age:
State: SD

Vax Date: 12/30/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Feeling unwell; Headache; Tiredness; Muscle pain; Chills; Nausea; Injection site pain; had been asleep most of the whole day; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231, expiration date: Arp2021), via an unspecified route of administration on 30Dec2020 at single dose at right arm for Covid virus. Medical history included blood thinner treatment. Concomitant medication included ongoing apixaban (ELIQUIS) for blood thinner treatment. The patient previously took coumadin, warfarin. Patient received the Covid-19 vaccine yesterday. She had been asleep most of the whole day (Dec2020). She had injection site pain, headache, tiredness, muscle pain and chills. She thought she was going to work but that didn't work. She was currently taking Eliquis. She had been on coumadin and warfarin before. She looked at the different medications that needed to be reported. She would also call her physician and make her aware. The start date for "Injection site pain" was 30Dec2020. The start dates for headache, tiredness, muscle pain and chills all were 31Dec2020. The patient also experienced nausea, feeling unwell on 31Dec2020. Investigation assessment was no. The outcome of the event "Injection site pain" was not recovered. The outcome of the other events was unknown.

Other Meds: ELIQUIS

Current Illness:

ID: 0923681
Sex: F
Age:
State: CT

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Rec V Date: 01/06/2021
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Symptoms: Nausea; Fatigue; Head fog; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization. The COVID-19 vaccine was administered at Hospital. Medical history included the patient already had Covid 'more than 90 days ago'. The patient's concomitant medications were not reported. The patient experienced nausea, fatigue, head fog on an unspecified date. The outcome of the events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0923682
Sex: F
Age:
State: CT

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Dizziness; This is a spontaneous report from a contactable consumer. A 6-decade female patient in early 50's started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on Dec2020 (about 5 to 7 days before 30Dec2020) at single dose for covid-19 immunization. The facility type vaccine was hospital. The patient medical history and concomitant medications were not reported. The patient has not had Covid prior to the vaccine. The patient experienced has been experiencing dizziness on and off in Dec2020 since she was given the vaccine. The action taken in response to the event for bnt162b2 was not applicable. The outcome of event was unknown. Information on lot/batch number has been requested.

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Current Illness:

ID: 0923683
Sex: M
Age:
State:

Vax Date: 12/30/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: shivers; cold feeling; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9321), via an unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Caller was reporting on the COVID vaccine. He received the first shot yesterday (30Dec2020) and had experienced shivers and cold feeling in Dec2020. He wanted to know if this was normal. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0923684
Sex: F
Age:
State: OR

Vax Date: 12/30/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Shortness of breath; Sore arm like she got kicked in the arm by a horse. Her arm felt like this today.; Chest pain; Headache; Body aches; Fever; Chills; fatigued; feels cold; This is a spontaneous report from a contactable consumer (patient). A 38-year-old female patient received bnt162b2 (lot number: EL3246), via an unspecified route of administration, at deltoid right, on 30Dec2020 07:45, at single dose, for COVID-19 immunization. Medical history included chronic asthma from an unspecified date, stomach surgery a year and a half ago, sometimes has stomach pain that feels like chest pain since her stomach has been surgically altered. Has had asthma stuff since she was very young. Is relatively healthy. No family medical history. No relevant tests. The patient's concomitant medications were not reported. No additional vaccines administered on same date of Pfizer suspect. No prior vaccinations within 4 weeks. The patient previously took flu vaccine on 01Oct2020 and experienced fatigued, tired, and sore arm like she got kicked in the arm by a horse. It was reported that received COVID-19 vaccine yesterday (30Dec2020). Been having some chest pain. Started a couple hours after receiving the COVID-19 Vaccine. Chest pain doesn't whole heartedly go away. Gets more intense and then relaxes. Wants to know if this is common or something she just has to deal with. Doesn't know if this is stomach pain. Had stomach surgery a year and a half ago. Sometimes has stomach pain that feels like chest pain since her stomach has been surgically altered. Has been taking heartburn and gas medications. Chest pain is not going away. Wants to know if this is common. Tried to look online and only found common side effects. Her husband looked it up and two people died from a heart attach after receiving the COVID-19 Vaccine. She is getting older, but is not that old. Caller works in behavioral health. Had an instant headache. Clarified chest pain: Is always lingering in the background. Doesn't fully go away. Comes and goes in waves. Gets intense and relaxes. Chest pain was pretty sharp this morning and it made her short of breath. Doesn't know if it was the pain that took her breath away. Occurred at 10:00. Indication: Has older people she takes care of. Her mother is super frail and has dementia. Her uncle is elderly and has heart issues. Wants to do her part so she doesn't catch it. No further details provided. In regards to the two people who had heart attacks and died after COVID-19 Vaccine, caller has no patient identifiers or NDC/Lot/Exp to provide. Stated this people were in the UK and the information was just something her husband read on the internet. Also experienced body aches, fever, and chills between 14:30 and 15:00 yesterday, 30Dec2020. Is super fatigued. Doesn't know if she is febrile, hasn't checked temperature. Still feels cold and has chills today. Does not have a headache today. It was also reported that fatigued and tired with Flu Vaccine (historical vaccine). Sore arm like she got kicked in the arm by a horse. Her arm felt like this today (31Dec2020). Therapeutic measures in response to chest pain is received, treatment included heartburn and gas medications. Gas medication is Equate brand Simethicone Extra Strength Gas Relief (NDC: 49035-487-02, Lot:H22016, Exp: Sep2022) at 125mg liquid-gel. Heartburn medication is Equate brand Cimetidine 200mg tablet (NDC: 49035-820-72, Lot: Doesn't know if lot number is OJE2445C or 0JE2445C, Exp: Jun 2022). Stated writing is so tiny. Gas and heartburn medication has not helped with chest pain. The outcome of the event chest pain was not recovered, of the other events were unknown.

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Current Illness:

ID: 0923685
Sex: F
Age:
State:

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Heart rate high; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), via an unspecified route of administration in Dec2020 at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient had a question about the COVID 19 vaccine. She wanted to know if it was possible for it to cause an extremely high heart rate. She got her first dose on Monday (in Dec2020) and had to go to the emergency room for a high heart rate. After 48 hours it went back to normal. She stated she didn't think she was going to get the second shot because of this. The patient is a healthcare worker, a nursing assistant and it was (Pharmacy name) gave her the vaccine. The outcome of the event was recovered in Dec2020.

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Current Illness:

ID: 0923686
Sex: F
Age:
State: NM

Vax Date: 12/27/2020
Onset Date: 12/27/2020
Rec V Date: 01/06/2021
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Symptoms: Diarrhea; throwing up; very bad migraines; This is a spontaneous report from a contactable consumer (patient). A 27-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number: EK5730, expiration date: Mar2021), via an unspecified route of administration on 27Dec2020 at single dose shot left arm once for COVID-19 immunization in hospital. The patient's medical history and concomitant medications reported as no. Patient stated that she got her Covid vaccine on Sunday (27Dec2020) and had experienced very bad migraines on 27Dec2020, diarrhea and throwing up as well on 29Dec2020. Stated that the diarrhea was not as common as the migraines. Stated that she had not thrown up but did last night (30Dec2020) at 2 AM. Investigation Assessment reported as no. No treatment was received for the events. The outcome of event migraines was unknown, outcome of the other events was recovering.

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Current Illness:

ID: 0923687
Sex: F
Age:
State: NV

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/06/2021
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Symptoms: she started to get very sick, which continued to worsen until nowwhen she feels like she is improving; had stomach and abdominal pains; had stomach and abdominal pains/stomach is still very sensitive; loose stool; she was very tired; Pain or little discomfort in the arm she received the injection; Pain or little discomfort in the arm she received the injection; This is a spontaneous report from a contactable consumer (Patient). A 80-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, EH9896), via an unspecified route of administration to very top of right arm on 22Dec2020 at single dose for covid-19 immunization. It was the first dose. The COVID-19 vaccine was administered at Hospital. Medical history included glaucoma she had drops to take for, mostly she just has problem with her joints and her back with her age. She did not have any diseases or anything; she was not diabetic, nothing like that. There were no concomitant medications. She was administered her first dose of COVID-19 Vaccine on 22Dec2020. She reported that the pain or little discomfort she had in the arm she received the injection in disappeared by 25Dec2020. But on 24Dec2020 she started to get very sick, which continued to worsen until now when she felt like she was improving. She did not know if these events could have something to do with the COVID-19 Vaccine. Pain or little discomfort in the arm she received the injection: Right arm. Everyone warned her that the site would hurt, so she was really glad when it totally went away on 25Dec2020 and thought that it was over; any issues from the injection. Very sick: this event started to get bad on 24Dec2020, she was very tired and not very hungry, she had stomach and abdominal pains and loose stool; 25Dec2020 those symptoms were worse. It was Christmas so she cooked and thought at first maybe she got carried away baking pies; because that evening she started to have pain and did not each much. 26Dec2020 it was worse; she said she was going to work on 27Dec2020; it was terrible because she was stuck for 12 hours trying to work while very sick. She called off of work 28Dec2020 and 29Dec2020. Since then she has stayed home and still has pain but she took her ranitidine delayed release 100mg twice daily as needed for stomach pain as given to her by her doctor, and is now down to just once daily. She did not know what she would have done without the ranitidine. She did not have any more abdominal pain, but her stomach was still very sensitive. She was tired but thought she was going to be ok. She was scared to get the second scheduled dose of COVID-19 Vaccine because she thought the side effects will be more severe with the booster shot. She just needed to rest and stay home which she has been doing. She has not had any fever. She has not notified her family doctor of these events. There was nothing she did on Christmas that she could think of other than she drank a glass of champagne because she did not know her stomach was going to be so bad. The outcome of the events Pain or little discomfort in the arm she received the injection was recovered on 25Dec2020, the outcome of event sickness was recovering, the outcome of the event Abdominal pain was recovered on an unknown date in Dec2020, the outcome of event stomach pain was not recovered, the outcome of the other events was unknown.

Other Meds:

Current Illness:

ID: 0923688
Sex: F
Age:
State:

Vax Date:
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Rec V Date: 01/06/2021
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Symptoms: Injection site swelling and redness; increased warmth at injected site; Injection site swelling and redness; increased warmth at injected site; Injection site swelling and redness; increased warmth at injected site; This is a spontaneous report from a contactable consumer (patient husband). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The reporter stated he know it's one of the possible mild side effect is injection site swelling and redness and what about increased warmth at injected site. He asked if it is normal to have. He know it says injection site swelling and also Injection site redness but what about like warmth like increase warmth, heat at injection site. The action taken in response to the events for bnt162b2 was not applicable. The outcome of events was unknown. Pfizer is a marketing authorization holder of [BNT162B2] in the country of incidence or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of [BNT162B2] has submitted the same report to the regulatory authorities. Lot/batch number has been requested in follow-up.

Other Meds:

Current Illness:

ID: 0923689
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/06/2021
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Symptoms: Muscle pain in my back, legs; Hard for me to walk; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date were not provided), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Consumer stated, "I am calling for the side effects of the Vaccine, I am calling to see about it." When probed to clarify if consumer wanted to know about the side effects of COVID Vaccine, consumer stated, "Yes, because I am having muscle pain in my back, legs and it's hard for me to walk." The outcome of the events was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 0923690
Sex: F
Age:
State: NJ

Vax Date: 12/18/2020
Onset Date: 12/28/2020
Rec V Date: 01/06/2021
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Symptoms: Rash on lateral breasts/felt a bit of itching.; blotchy rashes; Itchiness on Scalp; broke out in hives/welts came up on right ear and behind neck/welts under buttocks and behind knees, welts were large and red; Slight chills; Tenderness in injection arm; was just a little cold; This is a spontaneous report from a contactable nurse (patient). A 64-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: PAA156571), via an unspecified route of administration in left deltoid on 28Dec2020 10:00 at 0.3 mL single for covid-19 immunization; sulfamethoxazole, trimethoprim (BACTRIM DS), at twice a day for 10 days for perineal cyst. The patient was on her last day of sulfamethoxazole, trimethoprim on the day she got the COVID-19 vaccine (28Dec2020). Medical history included perineal cyst, COVID-19 in Apr2020 with no problem, only had a cough. Husband had COVID-19 and had loss of taste and smell, had fever, but he was not serious. Both her and her husband got tested for antibodies and were positive. Family medical history was none. The patient had unspecified flu vaccine (Lot: UJ428AB) on 18Dec2020 injected in left deltoid in two weeks prior to COVID-19 Vaccine. Checked with three different people who stated the Flu vaccine would not interfere with COVID-19 Vaccine. Checked with two pharmacists who stated Bactrim DS would not affect her taking the COVID-19 Vaccine. She received COVID-19 Vaccine through her work in a nursing home. There were no additional vaccines administered on same date of Pfizer suspect. On 28Dec2020 about 7 to 8 hours after vaccination, patient had slight chills and tenderness in her arm: was just a little cold. Thirty-six hours after injection, midnight on 29Dec2020, her scalp itched like crazy, broke out in hives. On 30Dec2020, rash developed on both lateral sides of her breast, welts came up on right ear and behind neck. On 31Dec2020, welts under buttocks and behind knees, welts were large and red. Rash on lateral breasts: felt a bit of itching. The patient had blotchy rashes, rash up in her hair above her neck and back of ear, had intense itching; which subsided. It was a little pink on her chest, little itching on her head. Her ear was better. Symptoms were most mild because she was still able to function. Clarified as not serious. The patient was taking diphenhydramine (BENADRYL, Lot: SMF011, Exp: May2022) at 25mg every 3.5 to 4 hours, cortisone cream 10 Maximum Strength (Lot: 20K434, Exp: Sep2023) for rash and welts; and doing tepid soaks. It was tolerable and faded. Rash had subsided, but was a little red. Her greatest concern was what to do in regards to the second dose in three weeks. The reporter considered events were related with COVID-19 Vaccine. The action taken in response to the events for sulfamethoxazole, trimethoprim was unknown. The outcome of events was unknown.

Other Meds: BACTRIM DS

Current Illness: Perineal cyst

ID: 0923691
Sex: F
Age:
State: FL

Vax Date: 12/23/2020
Onset Date: 12/29/2020
Rec V Date: 01/06/2021
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Symptoms: whole family started to get sick and experiencing same things she experienced (chills, not feeling well); whole family started to get sick and experiencing same things she experienced (chills, not feeling well); This is a spontaneous report from a contactable consumer (patient's daughter). This consumer reported similar events for two patients. This is the second of two reports. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date not provided), via an unspecified route of administration on 23Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Caller reported her mom received COVID vaccine on the 23Dec2020. On the 29Dec2020, her whole family started to get sick and experiencing the same things she experienced (chills and not feeling well). The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923692
Sex: U
Age:
State:

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Really bad dizziness; Headache; This is a spontaneous report from a contactable consumer(patient). A patient of an unspecified age and gender received first dose BNT162B2, via an unspecified route of administration in Dec2020 at single dose for COVID-19 immunization. The medical history and concomitant medications were not reported. The patient got the vaccine today, the first dose, and the patient just had really bad dizziness and headache ever since in Dec2020. The patient was reading the side effects and it said that it can be a severe reaction. The patient didn't have any of the other severe side effects. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923693
Sex: F
Age:
State: MN

Vax Date:
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Rec V Date: 01/06/2021
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Symptoms: Developed UTI symptoms of burning in urination and frequency and urgency; Developed UTI symptoms of burning in urination and frequency and urgency; Developed UTI symptoms of burning in urination and frequency and urgency; Developed UTI symptoms of burning in urination and frequency and urgency; This is a spontaneous report from Pfizer-sponsored program. A contactable Other HCP reported for a nurse (patient). An adult female patient received bnt162b2 (batch/lot number and expiration date not provided), via an unspecified route of administration, first dose on an unspecified date, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The reporter has a patient and the patient is having the symptoms of UTI after the patient got the first dose of COVID-19 vaccine on Monday. The patient who is a 30 year old female (Age at the time of adverse event was not confirmed) who got her vaccine on Monday. She is a nurse and she developed urinary tract infection (UTI) symptoms of burning in urination and frequency and urgency and a urine sample was sent for evaluation, if it is positive the patient was wondering if the vaccine response would be altered by taking antibiotics for UTI. The outcome of the events was unknown Information on the lot/batch number has been requested

Other Meds:

Current Illness:

ID: 0923694
Sex: F
Age:
State: LA

Vax Date: 12/18/2020
Onset Date: 12/28/2020
Rec V Date: 01/06/2021
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Symptoms: Was diagnosed with the COVID-19 virus after receiving the COVID-19 Vaccine on 18Dec2020; Was diagnosed with the COVID-19 virus after receiving the COVID-19 Vaccine on 18Dec2020; This is a spontaneous report from a contactable Other Health Professional (patient) from a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs). A 38 years old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 18Dec2020 at single dose in Deltoid Right for COVID-19 immunization. Medical history and concomitant medications were none. After receiving the COVID-19 Vaccine, the patient was diagnosed with the COVID-19 virus on 28Dec2020. she saw Dr. at the clinic where she works to seek treatment. She stated she is supposed to receive the 2nd dose of the COVID-19 Vaccine on 08Jan2021. She asked now that she is COVID-19 positive, should she get the 2nd COVID-19 Vaccine dose. Reported she had a rapid nasal swab COVID-19 test performed. Reported she is taking Hydroxychloroquine and a bunch of vitamins for treating COVID-19. Caller stated she did not have the COVID-19 Vaccine card with her to provide the Lot Number. The patient underwent lab tests and procedures, which included COVID-19 rapid POC test with positive result. Outcome of event was unknown. Information on the Batch/Lot number has been requested.; Sender's Comments: Based on the information available, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported COVID-19 based on the known safety profile. However the short duration of 10 days since the vaccine first dose is given it is unlikely patient would have fully developed immunity.

Other Meds:

Current Illness:

ID: 0923695
Sex: F
Age:
State: TN

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: It is warm; Even up to the back of the shoulder to the neck is painful; Even up to the back of the shoulder to the neck is painful; Her whole arm is sore up to her neck and down the arm/It is very painful/it throbs; Last night she was up all night, every 3 hours; This is a spontaneous report from a contactable consumer (patient). A 59-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EL1284, expiration date Apr2021), via an unspecified route of administration at left arm on 30Dec2020 09:30 at single dose for COVID-19 immunization, at a hospital. The vaccine was not administered at military facility. The patient's medical history included ongoing asthma from 2005 (diagnosed 15 years ago) and allergies. For asthma She has ProAir rescue inhaler to use as needed. Breo inhaler she uses at night. She has been on it for 2 years. She has been on different inhalers. Family medical history relevant to events was reported as none. Concomitant medication included montelukast sodium (SINGULAIR) from 2005 (had been on it probably 15 years) and ongoing at 10 mg, daily for allergies; fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA) inhaler via resp Inhalation from 2018 (has been on it for 2 years), uses it at night, for asthma; and salbutamol sulfate (PROAIR HFA) rescue inhaler via resp Inhalation, to use as needed for asthma. The patient had no history of previous immunization with the Pfizer vaccine. For historical vaccine, the patient received Tetanus for immunization and had allergic to Tetanus, her arm swelled and she couldn't move it (which was kind of like this, but not as severe). She didn't know the brand name for the tetanus vaccine she had reaction to. She didn't have NDC, lot, or expiry. It was 40 years ago. She had the reaction when she was 18 years old. There was no vaccine administered on same date of the Pfizer suspect, and tno vaccinations within 4 weeks prior to the Pfizer suspect. It was reported that last night (30Dec2020) she was up all night, every 3 hours. She was taking Advil. Her whole arm was sore up to her neck and down the arm. She had a nurse look at it this morning (31Dec2020) and it was not red. It was warm and it throbs. No rash. It was very painful. Even up to the back of the shoulder to the neck was painful. Her arm being sore and painful was ongoing at the time of report. She had been taking Advil. The pain had stayed the same even with the Advil. The events started probably between 14:00 and 14:30, it started off sore then became more painful. At the time of reporting, she was not at home and didn't have the bottle to provide NDC, lot, and expiry for Advil. She was taking some at the office, but that was in a travel bottle and didn't have the lot, expiry, and NDC. No emergency room or physician office visit. Relevant tests was none. The outcome of the events was unknown.

Other Meds: SINGULAIR; BREO ELLIPTA; PROAIR HFA

Current Illness: Asthma (diagnosed 15 years ago)

ID: 0923696
Sex: F
Age:
State:

Vax Date: 12/31/2020
Onset Date: 12/31/2020
Rec V Date: 01/06/2021
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Symptoms: Short of breath; Heartbeat is fast; Feels like she has some swelling; This is a spontaneous report from a non-contactable consumer. This consumer reported for a 30-year-old female patient (daughter) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch unknown) via an unspecified route of administration on 31Dec2020 11:30 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the vaccine today at her place of work and at the moment she did not have any side effects. But now during the night she was feeling short of breath and her heartbeat was fast and she felt like she has some swelling and some other more severe side effects that were put on the paperwork and reporter was wondering she was not acutely ill in spite of being short of breath. But she was worried about if she could get worse. So, would it be wise for reporter to give her Benadryl if this is an allergic reaction. 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: 0923697
Sex: F
Age:
State: MN

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: Eyes were red; Tiredness and needed to sleep extra; Tiredness and needed to sleep extra; Heartbeat was fast; Felt like she had to throw up; Pain in right arm; Does not feel good; It felt like there was oil in her mouth; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received first dose of BNT162B2 via an unspecified route of administration on 30Dec2020 10:45 at single dose in right arm for COVID-19 immunization. The vaccination was given in hospital, not a military facility, at 10:45 and left hospital at 11:05 on 30Dec2020. Prior vaccinations within 4 weeks was none. Additional vaccines administered on same date of the Pfizer suspect was none. Medical history included ongoing migraine and family medical history included mother has high blood pressure and father has diabetes. Concomitant medication included verapamil from Oct2020 at 40 mg twice daily by mouth for migraine. Additional Information for concomitant products Verapamil included 1 for one week, 2 for second week 3rd week 3 and after 3 months, then came back down to 2. The patient experienced does not feel good at 11:30 on 30Dec2020. She was driving and did not feel good. She felt like she had to throw up at12:00 on 30Dec2020 and had it all night until she went to bed. Eyes were red when she woke up at 23:30 on 30Dec2020, that's when she first noticed. Heartbeat was fast around 12:30 on 30Dec2020. Tiredness and needed to sleep extra at 17:00 on 30Dec2020. Pain in right arm at 12:00 on 30Dec2020. When she went to drink something, she noticed her arm was painful. No ER or physician's office required. Received call from patient regarding the COVID vaccine. She received it on 30Dec2020 (yesterday) and was a healthcare worker. She later stated she works in patient transportation in a hospital. She did not feel good. Yesterday, she felt like she had to throw up. When she slept, she felt very tired and when she woke up, her eyes were red. She washed her face when she woke up around 11. Then she noticed her heart beat was kind of fast. She took another medication she takes all the time. Her doctor said that she can take it with it but she was not sure. She did not feel herself. Yesterday after she took it, she had to wait there for 15 minutes. It felt like there was oil in her mouth. She just drank water and came home. When she came home, her heart beat was fast. She had to sit down. She liked to eat spicy food, and she needed to sleep. Her kids said she never slept like this. Both eyes were red, red like blood. Her daughter told her to go look at them in the mirror. There was no pain or nothing in her eyes, they were just red and they improved today. If she goes to bed now, she can sleep, but she just wakes up and drinks tea and wants to wake up. She didn't want to sleep, but she felt like she could. Regarding the pain in her right arm, she had to hold her shoulder when she first woke up. It was worse then, but it's better now that she keeps moving it. She has 3 more weeks to get the next dose of the COVID Vaccine. Hopefully it will be this shot only and she can go back to work. She planned on going back to work on Saturday. She would like to know if she can continue to take Verapamil. She will call her pharmacy to find out. The outcome of the events does not feel good and tiredness and needed to sleep extra was not recovered. The outcome of the events felt like she had to throw up, eyes were red, heartbeat was fast and pain in right arm was recovering. The outcome of the other event was unknown. Information on Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 0923698
Sex: U
Age:
State: MS

Vax Date: 12/28/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Fever; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number was unknown), via an unspecified route of administration on 28Dec2020 09:00 at single dose for covid-19 immunization. The patient had no medical history. The patient's concomitant medications were not reported. The patient calling concerning the vaccination, the patient received vaccination on this past Tuesday which was 28Dec2020 and the patient had recently just recovered from Covid and the patient asked the person giving her/him the vaccination it was okay since the patient just recovered from Covid to have it. She said yes. The patient could have it. Since last Tuesday (28Dec2020) the patient got the vaccination at 9 AM in the morning. The patient did fine all during the day. That night the patient started to run fever (in Dec2020) and the patient kept on fever all of that night, yesterday (30Dec2020) and today (31Dec2020) and the patient was just curious if this was normal. Yesterday (30Dec2020) because the patient thought may be she/he should go have the test again for Covid, the patient's normal nurse practitioner, doctor said no, but the patient probably shouldn't take the second vaccine, so that's what the patient's question is and the patient what to know if there are going to have an adverse reaction. The patient underwent laboratory test included only the Covid test on an unspecified date. The outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923699
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: Headache; Sore throat; This is a spontaneous report from a contactable nurse (patient). A 47-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), via an unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunization. Medical history reported as none. There were no concomitant medications. The patient had a vaccine received this afternoon on 30Dec2020, 4 to 5 hours after, she was having a headache and had sore throat as well. The patient wanted to know if it was okay to take Tylenol. The outcome of events was unknown. No follow-up attempts are possible; Information on Lot/Batch Number cannot be obtained.

Other Meds:

Current Illness:

ID: 0923700
Sex: M
Age:
State: NJ

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Soreness at injection site; This is a spontaneous report from a contactable consumer (patient). An adult male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date unknown), via an unspecified route of administration in Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Prior to vaccination, patient was not diagnosed with COVID-19. The patient experienced soreness at injection site in Dec2020. Since the vaccination, it was unknown had patient been tested for COVID-19. The outcome of the event was unknown. The report was reported as non-serious, with seriousness criteria-Results in death: No; Life threatening: No; Caused/prolonged hospitalization: No; Disabling/Incapacitating: No; Congenital anomaly/birth defect: No. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0923701
Sex: U
Age:
State: NY

Vax Date: 12/29/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: I think it helps in my pain that I used to have; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EL0140), via an unspecified route of administration on 29Dec2020 at single dose for covid-19 immunization. Medical history included pain from an unknown date. The patient's concomitant medications were not reported. The patient got the vaccine on 29 and just at the site where patient got the needle, that is it and right now, it actually be going away, patient put hand up on it and didn't even feel it, patient was not throwing up, have no headache, no body ache. Patient was doing fine so far it is just 2 day, patient was not in any pain. Actually, patient think it help in pain that patient used to have. The occurrence date was Dec2020. The action taken in response to the event for bnt162b2 was not applicable. The outcome of event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0923702
Sex: F
Age:
State:

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: Stiff neck; soreness in my arm; severe pain in neck; squeezing on a nerve; pain came from up head, under my clavicle and down my back.; pain came from up head, under my clavicle and down my back.; pain came from up head, under my clavicle and down my back.; This is a spontaneous report from a contactable nurse. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date in Dec2020 at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. When the patient tried to turn around to speak to nurse (reporter), she complained of a stiff neck. The patient had the same symptoms as nurse (reporter). The nurse stated "I got the Covid vaccine on 18Dec2020 and had soreness in my arm that was gone by the next day. On 23Dec2020, while driving home driving home, I felt severe pain in neck. I almost felt like something went up in my neck and started squeezing on a nerve. It proceeded to get bad so I took muscle relaxants. Christmas day was horrible, I couldn't lift my head off my pillow. The pain came from up head, under my clavicle and down my back. " The outcome of events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0923703
Sex: U
Age:
State:

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/06/2021
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Symptoms: severe pain in neck; squeezing on a nerve; soreness in my arm; pain came from up head, under my clavicle and down my back; pain came from up head, under my clavicle and down my back; pain came from up head, under my clavicle and down my back; This is a spontaneous report from a contactable nurse. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date in Dec2020 at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient had the same symptoms as nurse (reporter). The nurse stated "I got the Covid vaccine on 18Dec2020 and had soreness in my arm that was gone by the next day. On 23Dec2020, while driving home driving home, I felt severe pain in neck. I almost felt like something went up in my neck and started squeezing on a nerve. It proceeded to get bad so I took muscle relaxants. Christmas day was horrible, I couldn't lift my head off my pillow. The pain came from up head, under my clavicle and down my back. " The outcome of events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0923704
Sex: F
Age:
State:

Vax Date: 12/28/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: intermittent fever; diarrhea; chills; nausea; This is spontaneous report from a non-contactable other health professional. An adult female patient (occupation: Nurse, not pregnant at the time of vaccination) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date not provided), intramuscularly at the age of 36-year-old (age at the time of vaccination) on 28Dec2020 at single dose at left arm for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Facility where the most recent COVID-19 vaccine was administered at Hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that 2 days later (30Dec2020): diarrhea, chills, nausea, intermittent fever. The events were non-serious per the reporter. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hadn't been tested for COVID-19. 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: 0923705
Sex: F
Age:
State: MA

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 01/06/2021
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Symptoms: slight shortness of breath all lasting over 1 week; Extreme chills; extreme fatigue and tiredness; whole body muscle aches; This is a spontaneous report from a contactable nurse (patient). A 41-year-old female patient received bnt162b2 (batch/lot number and expiration date not provided, not available/provided to reporter at the time of report completion), via an unspecified route of administration, at arm left, first dose on 23Dec2020 09:15, at single dose, for COVID-19 immunization. No relevant medical history. No known allergies to medications, food, or other products. There were no concomitant medications. The patient is not pregnant at the time of vaccination. 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. The patient experienced extreme chills, extreme fatigue and tiredness, whole body muscle aches, slight shortness of breath all lasting over 1 week, all from 23Dec2020 16:15. The adverse event result in doctor or other healthcare professional office/clinic visit. No treatment was received for the adverse event. Since the vaccination, the patient has been tested for COVID-19. The patient underwent lab tests and procedures which included COVID test (test type: Nasal Swab, test name: rapid test): negative, on both 27Dec2020 and 30Dec2020. The outcome of the events was not recovered. Information about Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0923706
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/06/2021
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Symptoms: arm soreness around injection site of vaccination; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route of administration on an unspecified date at single dose in the arm for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient's arm soreness around injection site of vaccination. Event took place after use of product. Outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923707
Sex: M
Age:
State: CA

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/06/2021
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Symptoms: Cough; Flu like symptoms; It hurts to walk; I have a stuffed up nose, I did not have it yesterday; Pale; I felt weak; Bones ache; Have not been feeling good; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot/Batch Number and Expiration Date unknown) via an unspecified route of administration on 28Dec2020 at single dose on arm for suppress the COVID-19 (COVID-19 immunization). The patient's medical history included blood pressure, stomach ulcer and psoriatic arthritis. The concomitant drug was reported as colecalciferol (VITAMIN D), potassium citrate, multivitamin, etanercept (ENBREL) at once a week, pen shot in stomach, omeprazole (PROTONIX) at once a day for stomach ulcer and blood pressure medications. The patient was a correction officer, patient work at the prisons in (state name) and were given vaccination of Pfizer on Monday and he did that on Monday and have been getting sick and it's getting worse everyday, so yesterday at work everything was fine and he went home at 8 'O' clock at night because he was getting pale, felt weak, bones ache and have not been feeling good and today he called it in because he woke up with the cough, flu like symptoms. And it's worse today than it was yesterday. Consumer stated today, bones ache was worsening of like weaker, it hurts to walk and bone ache was really, today was worse than yesterday for the bone. Today flu like symptoms was worse, today patient have more heavier cough, was coughing more today and have a stuffed up nose, I did not have it yesterday. Wanted to know if this was a side effect or is that normal with that vaccine. Start date of events was on 28Dec2020. When patient started feeling some symptoms that started getting progressively worse on 29Dec2020. Treatment included Tylenol for bone pain and hurts to walk. Lab test blood work done in Dec2020, once a month through psoriatic arthritis doctor. The outcome of events, weak, Bone pain, Cough, Flu like symptoms, was not recovered. The outcome of other events was unknown. Information on Lot/batch number has been requested.

Other Meds: VITAMIN D [COLECALCIFEROL]; ; ENBREL; PROTONIX [OMEPRAZOLE]

Current Illness:

ID: 0923708
Sex: M
Age:
State: MI

Vax Date: 12/29/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: Lost sense of taste; Lost sense of smell; Whole body is sore; Rapid test came back positive for COVID; Rapid test came back positive for COVID; This is a spontaneous report from a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs) via a contactable consumer (patient). A 21-year-old male patient received his first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK5730, expiration date: 31Mar2021), via intramuscular on 29Dec2020 07:40 at 0.3 mL, single dose on his left deltoid for covid-19 immunization. Medical history included allergic to wasp stings. There were no concomitant medications. The patient had no additional vaccines administrated on the same date and no prior vaccinations were received within 4 weeks. Caller on the line calling about the COVID Vaccine he received on 29Dec2020. The day after receiving it he woke up and had a loss of sense of smell on 30Dec2020 12:00. That afternoon he went to get tested and the rapid test came back positive for COIVD on 30Dec2020. He was now waiting on the other one, clarified to be the PCR test, the lab test. The next day he also lost his sense of taste on 31Dec2020 11:00 and his whole body feels sore on 30Dec2020 around noon. Transfer agent stated the caller needs to be transferred to Medical Information as he was scheduled to get the next shot on 19Jan2021 and he was calling to ask if he should proceed with that. It was reported that the patient works in a hospital (not an HCP). No emergency room was visited and no physician office was visited. The outcome of the event "rapid test came back positive for covid" was unknown, the outcome of the other events "lost sense of smell", "lost sense of taste", "whole body is sore" were not recovered.

Other Meds:

Current Illness:

ID: 0923709
Sex: F
Age:
State: WA

Vax Date:
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Rec V Date: 01/06/2021
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Symptoms: Report she had nausea 2 days after the shot; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had nausea 2 days after the shot on unknown date. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923710
Sex: U
Age:
State: SC

Vax Date:
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Rec V Date: 01/06/2021
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Symptoms: aches; chills; This is a spontaneous report from contactable nurse (patient) via a sales representative. A patient of unspecified age and gender started to receive BNT162B2 (also reported as "Pfizer COVID Vaccine"), via an unspecified route of administration from an unspecified date to an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient was given 2nd dose of the COVID vaccine and 24 hours later, the patient had aches and chills. The outcome of the events was unknown. No follow-up attempts are possible. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923711
Sex: F
Age:
State: MA

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: 10 minutes after administration, back of tongue and soft palate started feeling strange sensation with some swelling; 10 minutes after administration, back of tongue and soft palate started feeling strange sensation with some swelling; 10 minutes after administration, back of tongue and soft palate started feeling strange sensation with some swelling; Other vaccine was received on same date vaccine date 30Dec2020; This is a spontaneous report from a contactable other healthcare professional (patient). A 52-year-old female patient (not pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number: EJ1685), intramuscularly on 30Dec2020 at 12:30 PM on Right arm at single dose for COVID-19 immunization in hospital. Other vaccine was received on same date vaccine date 30Dec2020. The patient medical history included known allergies: Shellfish. Prior to vaccination, patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine, or any other medications within two weeks of vaccination. The patient experienced 10 minutes after administration on 30Dec2020 at 12:40 PM, back of tongue and soft palate started feeling strange sensation with some swelling. After 30 minutes, the sensation eased up but the swelling stayed the same, not getting any worse. Since the vaccination, patient had not been tested for COVID-19. Therapeutic measures were taken as result of the events included diphenhydramine hydrochloride (BENADRYL). The outcome of the event 'feeling strange sensation' was recovering, outcome of events 'back of tongue and soft palate swelling' was not recovered. The report was reported as non-serious, with seriousness criteria-Results in death: No; Life threatening: No; Caused/prolonged hospitalization: No; Disabling/Incapacitating: No; Congenital anomaly/birth defect: No.

Other Meds:

Current Illness:

ID: 0923712
Sex: U
Age:
State: TN

Vax Date: 12/30/2020
Onset Date:
Rec V Date: 01/06/2021
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Symptoms: Severe headaches; This is a spontaneous report from a contactable consumer from a Pfizer Sponsored Program. A patient of unspecified age and gender received bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 30Dec2020 at a single dose for immunization. The patient's medical history and concomitant medications were not reported. The patient experienced severe headaches on an unspecified date. The event outcome was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0923713
Sex: F
Age: 48
State: CA

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Allergies: Iodine

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Symptoms: Fever, dizziness / light headedness, servere muscle aches, vomiting, diarrhea, sore throat, like I got a servere flu

Other Meds: Omeprazole Metoprolol

Current Illness:

ID: 0923714
Sex: F
Age:
State: TX

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/06/2021
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Symptoms: Golf ball size swelling below the injection site. Arm is red and itchy; Golf ball size swelling below the injection site. Arm is red and itchy; Golf ball size swelling below the injection site. Arm is red and itchy; This is a spontaneous report from a contactable other-HCP (patient). This 60-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscularly on 28Dec2020 14:30 at single dose on the left arm for COVID-19 immunization. Medical history included pulmonary embolism and known allergies: penicillin. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN), vitamin b complex (VITAMIN B), ascorbic acid (VITAMIN C), colecalciferol (VITAMIN D), tocopherol (VITAMIN E), received within 2 weeks of vaccination. Facility that the most recent COVID-19 vaccine administered was in Pharmacy or Drug Store. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 28Dec2020 14:45, the patient experienced golf ball size swelling below the injection site. Arm was red and itchy. No treatment received for the adverse event. Outcome of the events was recovering. This report was assessed as non-serious. Information about Lot/batch number has been requested.

Other Meds: BABY ASPIRIN; VITAMIN B; VITAMIN C [ASCORBIC ACID]; VITAMIN D [COLECALCIFEROL]; VITAMIN E [TOCOPHEROL]

Current Illness:

ID: 0923715
Sex: F
Age: 48
State: IN

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 01/06/2021
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Allergies: None

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Symptoms: Chills/shivering, body aches, nausea, fatigue, extreme pain and tenderness at the injection site

Other Meds: LoEstrin, Synthroid, Zoloft

Current Illness: None

ID: 0923716
Sex: F
Age:
State: PA

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Rec V Date: 01/06/2021
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Symptoms: Feels sore and little swollen; Arm soreness and feeling crummy like does not feel good; Arm soreness and feeling crummy like does not feel good; Feels sore and little swollen; This is a spontaneous report from a Pfizer-sponsored program from a contactable Nurse (patient). A 34-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot #: EK9231), on an unspecified date at single dose on arm for COVID-19 immunisation. Medical history included asthma. Concomitant medication included fluticasone propionate, salmeterol xinafoate (ADVAIR), took one puff twice a day and it's 100 over 50. The patient took the Covid vaccine. Her arm was feeling sore and she feels a little crummy after the vaccine like she feel crummy like she does not feel good. She wanted to know if she could take Tylenol because of her arm soreness and feeling crummy. It feels really sore and little swollen yeah. The outcome was unknown.

Other Meds: ADVAIR

Current Illness:

ID: 0923717
Sex: F
Age:
State: NC

Vax Date: 12/17/2020
Onset Date: 12/23/2020
Rec V Date: 01/06/2021
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Symptoms: Cervical lymphadenopathy, developing over 2 weeks; This is a spontaneous report from a contactable physician reported for herself. This 27-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via Intramuscular on an 17Dec2020 12:45 PM on left arm at single dose (Lot # EX5730) for covid-19 immunisation. No other vaccine in four weeks. The patient experienced cervical lymphadenopathy on 23Dec2020, developing over 2 weeks. No treatments were received. Outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 0923718
Sex: F
Age:
State: MD

Vax Date: 12/21/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: Itching; Redness; Swelling; it felt hot; This is a spontaneous report from a contactable other Nurse(patient). The 43-year-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EJ1685), via an unspecified route of administration by injection in the right deltoid on 21Dec2020 at single dose to protect herself from getting COVID. Medical history included ongoing chronic sinusitis , ongoing seasonal allergy. Concomitant medication included ongoing cephalosporin for Chronic sinusitis from 29Dec2020 which was the only thing new that she has been taking, but she had taken it in the past many times, ongoing cetirizine hydrochloride(ZYRTEC) for seasonal allergies, ongoing fluticasone propionate (FLONASE) for seasonal allergies which had been taking this for years. She got her first dose of the COVID vaccine last Monday, the Monday before Christmas on 21Dec2020. Yesterday(30Dec2020), in the exact spot that she received it, she was getting itching, redness, and swelling. She read and was told that that could happen, she just thought it would be sooner rather than 9 days later. She was calling to get this reported. Otherwise, she is fine. She had been using antihistamines and cortisone cream as treatments. She had been taking cetirizine hydrochloride for years. She normally took at night, but because of her arm she took it this morning.Last night(30Dec2020) she also put ice to the are as it felt hot. Outcome of events was not recovered. Events(itching, redness, and swelling) were assessed as non-serious.

Other Meds: ; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; FLONASE [FLUTICASONE PROPIONATE]

Current Illness: Chronic sinusitis; Seasonal allergy

ID: 0923719
Sex: M
Age: 77
State: FL

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/06/2021
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Allergies: PCN, BRIO

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Symptoms: "Tightness in lungs/chest", stiff neck, headache

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Current Illness:

ID: 0923720
Sex: F
Age:
State: VT

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: muscle aches; eyes watering and won't stop; Neck pain; feeling tired; eyes hurt; feels very weak; headache; Nausea; left arm numbness; left arm tingling; left hand numbness/left side of face and head numb; left hand tingling; Dizziness; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot Number: EL1284), intramuscular on 30Dec2020 04:45 at single dose at left deltoid as Covid vaccine for coronavirus. Medical history was none. There were no concomitant medications. The patient stated that she had Covid vaccine. She had dizziness, headache, nausea, left arm hand numbness and tingling, feels very weak, left side of face and head numb, all on 30Dec2020, neck pain and feeling tired, muscle aches, eyes watering and won't stop, eyes hurt in the morning, all on 31Dec2020. Treatment was None. Headache, eyes watering and won't stop, feels very weak and tired, eyes hurt was reported as worsened. Outcome of Nausea, left arm numbness was recovering, of other events were not recovered.

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Current Illness:

ID: 0923721
Sex: F
Age:
State: NJ

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/06/2021
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Symptoms: a slight chill the first night; slight tenderness to arms; This is a spontaneous report from a contactable nurse reported for her identical twin sister. A 64-years-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration on 28Dec2020 at single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications included unspecified flu vaccine on 18Dec2020. The patient experienced a slight chill the first night and slight tenderness to arms on 28Dec2020 with outcome of unknown. Information about Lot/Batch number requested.

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Current Illness:

ID: 0923722
Sex: F
Age: 33
State: VA

Vax Date: 12/29/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Allergies: Morphine, Diluadid- anaphylactic reaction.

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Symptoms: 1 day post vaccine, 3inx3in raised circle hive noted to right upper arm with pain and itching. increased in size over night to at least 4x4 inches..... on 1/6 early am which is 8 days past vaccination, Arm started itching again and hive noted to be about 1x1 with increasing size and itching.

Other Meds: Prozac 20 mg, Vienva birth control. Multi vitamin, Vitamin D. Ibuprofen.

Current Illness: None

ID: 0923723
Sex: F
Age:
State: WI

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/06/2021
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Symptoms: 10 hours later severe pain in the tragus of both ears which woke me up; Headache within 5 minutes which lasted until the next day; This is Spontaneous report from a contactable Other-HCP (patient). A 57-years-old female patient (No pregnant) received first dose bnt162b2 (BNT162B2, lot: EL1284), via an unspecified route of administration on 30Dec2020 17:00 at single dose on Right arm for covid-19 immunisation. Medical history was none. Concomitant medication included celecoxib (CELEBREX), black cohosh [cimicifuga racemosa] (BLACK COHOSH [CIMICIFUGA RACEMOSA]) and multivitamins. The patient previously took erythromycin and experienced drug hypersensitivity. The patient experienced Headache within 5 minutes (30Dec2020 17:05) which lasted until the next day, then about 10 hours later (31Dec2020 03:00) severe pain in the tragus of both ears which woke her up. It felt like someone was grabbing them with pliers. Still recurs mildly from time to time. No treatment received. The events were reported as non-serious.

Other Meds: CELEBREX; BLACK COHOSH [CIMICIFUGA RACEMOSA]

Current Illness:

ID: 0923724
Sex: F
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Symptoms: made my arm really sore; fever; nervous; This is a spontaneous report from a contactable consumer (patient). A 59-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot/batch number and expiration date not reported, via an unspecified route of administration from an unspecified date as single dose for COVID-19 immunization. The patient's medical history was concomitant medications were not reported. The patient stated, "where I got my shot made my arm really sore for about three days. On the third day, I ran a low-grade fever-100F. The fever lasted 12 hrs. Now I'm fine. I was a little nervous about traveling but read that there was a side effect." The outcome of the event was unknown. Information on lot/batch number was requested.

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Current Illness:

ID: 0923725
Sex: F
Age: 53
State: PA

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/06/2021
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Allergies: sulfa allergy, no food allergies. Allergies to dust mites, cats, dogs, weeds, trees.

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Symptoms: Approx 730 the evening of the vaccine I was resting laying down with both legs up (horizontally). I suddenly felt a "snap" in my left calf which led to severe muscle pain. I can barely walk. It is still painful today. About the same time I developed chills which lasted till about 1PM today. Within 10 minutes of the shot I was dizzy and nauseous (lasted about 15 min). About 20 minutes after the shot my face turned red and lasted about 5 hours.

Other Meds: Xyzal, Jolessa, budesonide nasal spray, multivits, vit D, vit C, vit B complex, apple cider vinegar

Current Illness: none

ID: 0923726
Sex: U
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Vax Date: 12/29/2020
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Symptoms: I had the covid vaccine of 12/29 and I had a little bit of an allergic reaction; Well on 12/30 I had some peanut butter and within 5 minutes I had an extremely itchy palm of hand.; my palm was bright red and a little tingling; my palm was bright red and a little tingling; This is a spontaneous report from a contactable consumer (patient). This patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 29Dec2020 at single dose for COVID-19 immunization. The patient medical history included allergic to peanuts. The patient concomitant medications were not reported. Patient had the covid vaccine of 29Dec2020 and had a little bit of an allergic reaction. As a child patient was very allergic to peanuts but have out grown it as an adult. Well on 30Dec2020 patient had some peanut butter and within 5 minutes patient had an extremely itchy palm of hand. Patient immediately looked and palm was bright red and alittle tingling. Patient went and washed hand. It went completely way after about 30 minutes. Other then that feel fine. Outcome of the events was unknown. Information on the lot/batch number has been requested.

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Current Illness:

ID: 0923727
Sex: M
Age:
State: NY

Vax Date: 12/31/2020
Onset Date: 12/31/2020
Rec V Date: 01/06/2021
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Symptoms: left sided facial muscle soreness; Arm soreness/by injection in the left arm; This is a spontaneous report from a contactable consumer (patient). The 30-year-old male patient received BNT162B2(COVID Pfizer vaccine, Batch/lot number: EK9231), via an unspecified route of administration on 31Dec2020 at single dose by injection in the left arm for COVID-19 immunization. Medical history and concomitant medications were none. The patient stated that he just got the COVID vaccine an hour ago. Within 20 minutes he developed left sided facial muscle soreness, which was the side he got the vaccine on, and arm soreness, on 31Dec2020. There was no treatment. Outcome of events was not recovered.

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Current Illness:

Total 2021 VAERS Injuries: 48,079

Page last modified: 03 October 2021 5:28pm