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
88,334
AK1,815
AL6,133
AR3,993
AS45
AZ14,539
CA64,759
CO12,159
CT8,719
DC1,747
DE1,868
FL41,499
FM3
GA16,132
GU92
HI2,477
IA4,739
ID2,763
IL21,496
IN23,655
KS4,844
KY8,414
LA5,328
MA15,281
MD13,105
ME3,277
MH8
MI20,143
MN12,873
MO10,275
MP30
MS3,073
MT2,392
NC17,450
ND1,440
NE3,023
NH3,124
NJ19,456
NM4,089
NV4,600
NY36,525
OH20,140
OK6,525
OR8,918
PA24,920
PR2,483
QM2
RI2,092
SC6,952
SD1,243
TN10,038
TX38,745
UT4,482
VA15,477
VI62
VT1,780
WA15,487
WI11,573
WV2,461
WY894
XB5
XL1
XV2

ID: 1426167
Sex: F
Age:
State:

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 06/25/2021
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Symptoms: She experienced sweats and chills; She experienced sweats and chills; She states she began having a racing heart moments after the injection.; it continued with chest soreness; This is a spontaneous report received from a contactable consumer (patient). A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 03Feb2021 1st Dose, Single for Covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient had the first dose of the Pfizer Covid 19 vaccine (last Wednesday) on 03Feb2021. On the same date, the patient began having a racing heart moments after the injection, it continued with chest soreness. On 04Feb2021, she experienced sweats and chills. The patient went back to work and it continued with chest soreness. She experienced sweats and chills the next morning on 04Feb2021 and the racing heart continued the next day. On 05Feb2021 (Friday) it was a little better but continued. Later she felt more normal and herself. She did not know what kind of reaction it was. "She asked how many people in the clinical trial reported a fast heartbeat". The patient underwent lab tests and procedures which included heart rate: racing on 03Feb2021. The outcome of the events was resolving. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426168
Sex: F
Age:
State: NC

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
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Symptoms: diarrhea; lightheadedness; dizziness; This is a spontaneous report from a contactable consumer(patient). A 93-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EN9581), via an unspecified route of administration, administered in Arm Left on 04Feb2021 at 09:45 (at the age of 93 years old) as first dose, single for covid-19 immunisation at School Health Clinic. Medical history included hypertension, hyperthyroidism, osteoarthritis from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Allergy to paper and Dairy products from an unknown date and unknown if ongoing. Concomitant medications included amlodipine (AMLODIPINE), telmisartan (MICARDIS) and levothyroxine sodium (SYNTHROID) taken for an unspecified indication, start and stop date were not reported. Patient was not received any other vaccine prior four weeks of vaccination. Patient received Amlodipine -10mg; Micardis 120mg; Synthroid 50m within two weeks of vaccination. Pfizer vaccine taken on Thursday 04Feb2021 at 09:45 and by Friday on 05Feb2021 at 14:15 afternoon had dizziness. Sunday on 07Feb2021 afternoon experienced lightheaded ness and on Monday 08Feb21 afternoon experienced dizziness and diarrhoea. Therapeutic measures were taken as a result of the events with Peptide Bismal. The outcome of the event was reported as not recovered. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds: AMLODIPINE; MICARDIS; SYNTHROID

Current Illness:

ID: 1426169
Sex: M
Age:
State: PA

Vax Date: 01/27/2021
Onset Date: 01/29/2021
Rec V Date: 06/25/2021
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Symptoms: tinnitus; This is a spontaneous report from a contactable or other health care professional (patient). A 60-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL3249), via an unspecified route of administration, administered in arm left on 27Jan2021 13:00 as dose 2, single (age at vaccination 60-years) for COVID-19 immunization. The patient's medical history included allergy to thimerasol. Concomitant medications included acetylsalicylic acid (ASPIRIN) taken for an unspecified indication. The patient did not have covid prior vaccination and was not tested covid for post vaccination. The patient did not receive any other vaccine within four weeks. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: unknown), via an unspecified route of administration, on an unspecified date as dose 1, single for COVID-19 immunization. On 29Jan2021, the patient stated that approximately 48 hours after second dose experienced constant tinnitus. Has not stopped at all for over 2 weeks. The treatment was not received for the event. The outcome of the event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: ASPIRIN

Current Illness:

ID: 1426170
Sex: F
Age:
State: NC

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 06/25/2021
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Symptoms: This is a spontaneous report received from a contactable consumer or other non hcp. A 78-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number: EM9809) via intramuscular route of administration in left arm on 05Feb2021 at 09:45 (age at vaccination 78 years old) as single dose for COVID-19 immunization. Medical history included cardiac disorder from an unknown date and unknown if ongoing Mother had heart issues, but she is passed away, ongoing panic attack the caller said that she has only had like 2 panic attacks in her life. She said that on 30Dec2021 she had a panic attack on the day of the vaccine, she had a light one on the way to get the injection, she said that she had COVID-19 previously and was diagnosed 05Jan2021 and was cleared so she took the vaccine, ongoing fatigue She said that her tiredness started during when she had COVID-19, but stated that she understands it was a symptom post COVID-19, ongoing gait disturbance She said that she may have been wobbly on her feet since she had COVID-19, but has gotten worse since the injection. There were no concomitant medications. On 05Feb2021 the patient experienced panic attack, her heart was racing/heart was racing to 132, unstable and wobbly on her feet, extremely tired and on unspecified date in February 2021 she said she feels like her eyesight has gotten worse, unstable and wobbly on her feet was reported as worsened/extremely tired was reported as worsened/she said she feels like her eyesight has gotten worse/and got very worse after vaccination. with outcome of unknown. The patient underwent lab tests and procedures which included electrocardiogram fine in 2021. The clinical outcome of the event panic attack, her heart was racing/heart was racing to 132 were recovered and unstable and wobbly on her feet, extremely tired were not recovered other events were unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Gait unsteady (She said that she may have been wobbly on her feet since she had COVID-19,.); Panic attack (The caller said that she has only had like 2 panic attacks in her life. She said that on 30Dec2021.); Tiredness (She said that her tiredness started during when she had COVID-19,)

ID: 1426171
Sex: M
Age:
State:

Vax Date: 01/10/2021
Onset Date: 01/11/2021
Rec V Date: 06/25/2021
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Symptoms: experienced injection site pain, pain at the site of injection; a mild headache; This is a spontaneous report from a contactable consumer (patient). A 77-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown) via an unspecified route of administration on 10Jan2021 as single dose and received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown) via an unspecified route of administration on 01Feb2021 as single dose for covid-19 immunization. The patient's medical history was not reported. The concomitant medications included acetaminophen for his back and cosmetic fillers. After both doses of the vaccines he experienced injection site pain, pain at the site of injection and a mild headache the next morning on 11Jan2021. He wanted to know if this was related to the vaccine and if this meant the vaccine worked. The patient had read that he should not take acetaminophen before the vaccine, but he takes a dose every morning. He wanted to know if that affected the vaccine. The outcome of events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: ACETAMINOPHEN

Current Illness:

ID: 1426172
Sex: F
Age:
State:

Vax Date: 01/28/2021
Onset Date: 01/29/2021
Rec V Date: 06/25/2021
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Symptoms: nausea; stomach pain; diarrhea; body aches; headache; This is a spontaneous report from a contactable consumer (nurse). A 75-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number and Expiration date was not reported), dose 1 via an unspecified route of administration on 28Jan2021 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 29Jan2021 02:00 She reports waking up 8 hours later at 2am the patient experienced nausea, stomach pain, diarrhea, body aches and headache. Patient wanted to know After the second dose, do people have more or less side effects than the first dose. The patient received treatment of a tylenol and gasx and went back to bed. At the time of reporting, the outcome of the events were unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426173
Sex: F
Age:
State: CA

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 06/25/2021
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Symptoms: Felt weak; Dry throat; States she has noticed she has been burping a lot and coughing harder.; States she has noticed she has been burping a lot and coughing harder.; She has a dry cough and when she coughs hard she gags until almost vomiting/ she has had some coughing where she coughs until she feels like she has to throw up; she has been having shortness of breath that started when she got the first dose of the Pfizer COVID vaccine on 27Jan2021; Chills; she just felt tired was all; pain at the injection site in her right arm so she took Tylenol that morning; This is a spontaneous report from a contactable nurse (patient). A 80-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9265) dose 1 via intramuscular route of administration in Arm Right on 27Jan2021 at 13:30(at the age of 80 years old) as single for COVID-19 immunisation. Medical history was none. There were no concomitant medications. Patient had no other vaccines on the same day as the COVID vaccine. The patient experienced as, she has been having shortness of breath that started when she got the first dose of the pfizer covid vaccine, chills, she just felt tired was all, pain at the injection site in her right arm so she took tylenol that morning on 27Jan2021, felt weak on 07Feb2021, she has noticed she has been burping a lot and coughing harder, she has a dry cough and when she coughs hard she gags until almost vomiting/ she has had some coughing where she coughs until she feels like she has to throw up, and dry throat on an unspecified date on Feb2021. Therapeutic measures were taken as a result of she just felt tired was all and pain at the injection site in her right arm so she took tylenol that morning. The patient underwent lab tests and procedures which included weight: 145-147 on an unspecified date. Therapeutic measures were taken as a result of she just felt tired was all and pain at the injection site in her right arm so she took tylenol that morning. Outcome of the event shortness of breath and chills were recovered and unknown for rest events. Information about batch/lot number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426174
Sex: M
Age:
State: NC

Vax Date: 02/01/2021
Onset Date: 02/02/2021
Rec V Date: 06/25/2021
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Symptoms: Fatigued; Lymph nodes swollen under arm pit; This is a spontaneous report received from a contactable other health care professional. A 43-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 01Feb2021 as dose 2, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (Lot: unknown) on 11Jan2020 in the Left arm for COVID-19 immunisation. Patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, was the patient did not diagnosed with COVID-19. Since the vaccination, did not patient been tested for COVID-19. The patient experienced extremely fatigued and lymph nodes swollen under arm pit. No treatment was received for the events. The outcome of the events was reported as recovering. Information about lot/batch number has been requested. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426175
Sex: M
Age:
State: NC

Vax Date:
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Rec V Date: 06/25/2021
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Symptoms: some symptoms of a throat condition that he has often; Cold like symptoms; sinus problem; throat hoarseness; This is a spontaneous report from a contactable consumer reporting for her husband. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3247, Expiration date was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date the patient experienced some symptoms of a throat condition that he has often, cold like symptoms, sinus problem, throat hoarseness reporter asking if her husband can receive his second covid vaccine dose if about 1 week ago he started to develop some symptoms of a throat condition that he has often due for their second vaccination tomorrow, but she wonders if he will get denied. She reports that he does not have a fever but asks if there are any symptoms that would disqualify him from getting the second dose. He has had a cold which is not what she would consider a symptom. It could just be a sinus problem. She has looked at every source of information and does not see any information about preventing one from getting a second dose with this and wanted to know if it would be contraindicated. He did not get the symptom after he got the first dose. He has had this a lot of times. He has throat hoarseness occasionally. It is the same type thing. The outcome of events was unknown. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426176
Sex: F
Age:
State:

Vax Date: 02/01/2021
Onset Date:
Rec V Date: 06/25/2021
Hospital:

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Symptoms: high blood pressure; fever of 101F; headache; This is a spontaneous report from a contactable consumer (patient) via Medical Information Team. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration on 01Feb2021 as single dose for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Caller got the first dose of the Pfizer vaccine on 01Feb2021. Her second dose was scheduled on 19Feb2021 which was only 18 days after. She would like to know whether there be a problem. Caller said she also experienced high blood pressure, fever of 101 F, headache from her first dose. She said that she had already reported this in DSU (possible duplicate AE). Caller was worried about her second shot of the vaccine since she had adverse events with the first shot. She wanted to know what to do. Outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426177
Sex: F
Age:
State: CA

Vax Date: 02/05/2021
Onset Date: 02/08/2021
Rec V Date: 06/25/2021
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Symptoms: Felt dizzy; Not been drinking enough water recently; Might be dehydrated; Stated she has been drinking water and her urine went to clear from yellow; Severely obese; This is a spontaneous report from a contactable consumer (patient herself) via a medical information team. A 68-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN5318), via an unspecified route of administration in left arm on 05Feb2021 (Friday) at 09:48 (at the age of 68-year-old) as a single dose for COVID-19 immunisation. The patient's medical history included ongoing blood pressure, dehydration, hospitalization. Mentioned in the past she had a hospitalization for dehydration. Concomitant medication included felodipine, orally from an unspecified date (taking for years) and ongoing at 5 mg once a day (5 mg take once daily by mouth) for blood pressure. No history of all previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations (within 4 weeks). Patient's medical history (including any illness at time of vaccination) was none. Family medical history was none. It was reported that, patient did not experience any immediate adverse event, however, today (08Feb2021) she felt dizzy, asked if: There are reports of other patients feeling dizzy days after vaccination, dizziness was usually followed by other side effects. Patient acknowledged she has not been drinking enough water recently (08Feb2021), considered the dizziness experienced may be a result of that and probably not an adverse event associated to the COVID-19 vaccine. She didn't have any side effects for three days and then she began to feel dizzy. Adds that it was not too bad as she was able to work but it was persisting. Mentioned she read that dizziness could be a severe side effect and she was asking could it come on three days later. Adds that she might be dehydrated on 08Feb2021 and stated she has been drinking water and her urine went to clear from yellow on 08Feb2021. Mentioned she didn't drink enough water on Saturday or Sunday, so she was trying to make that up today. Also asking would she have other side effects along with the dizziness if this was a side effect. Mentioned in the past she had a hospitalization for dehydration. Asking to have any of you girls heard anything about this. Mentioned that she was severely obese on an unspecified date in 2021. Adds she was scheduled to receive the second dose of the vaccine on 26Feb2021. The adverse events did not require a visit to physician or emergency room. No relevant test. No investigation assessment. The events were considered as non-serious by the consumer. The outcome of the event felt dizzy was not resolved and unknown for the other events. Follow-up attempts completed. No further information expected.

Other Meds: FELODIPINE

Current Illness: Blood pressure abnormal

ID: 1426178
Sex: M
Age:
State: NV

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
Hospital:

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Symptoms: Slightly swollen throat; This is a spontaneous report from a contactable consumer (patient). A 70-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot Number: EN53118), via an unspecified route of administration, administered in arm left on 05Feb2021 08:00 as 1st dose, single for COVID-19 immunization, (age at 70-year-old). Medical history included Gout, High Cholestrol & Enlarged Prostrate, food allergy (some Fish (not iodine). The patient previously took keflex and experienced drug allergies. The patient's concomitant medications was not reported. No other vaccine in four weeks. The patient did not receive any other vaccine prior to COVID-19 Vaccine. The patient did not test COVID-19 positive prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. On 05Feb2021 08:30, the patient experienced slightly swollen throat. Treatment medication included OTC Benadryl for the event. Outcome of the event was reported as recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426179
Sex: M
Age:
State: VA

Vax Date: 02/01/2021
Onset Date: 02/04/2021
Rec V Date: 06/25/2021
Hospital:

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Symptoms: feeling weak muscles; chills; sleep disturbance; This is a spontaneous report from a Pfizer-sponsored program via a contactable consumer (patient) reported for himself. An elderly male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: LL9262; Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 01Feb2021 at 14:00 pm (age at vaccination was unknown) as 1st dose, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient did not receive any other medications in two weeks. The facility where the most recent COVID-19 vaccine was administered was Doctor's office/urgent care. 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 received his 1st dose and after three days on 04Feb2021, the patient experienced feeling weak muscles, chills and sleep disturbance and stated that he did not know where to go after his symptoms appear. No treatment was received for the adverse event. Post the vaccination, the patient has been tested for COVID-19. The patient underwent lab tests and procedures which included SARS-COV-2 test (Nasal Swab) which was negative on 19Jan2021. The outcome of the events was resolving. Follow-up attempts completed. No further information expected. Follow-up#01 (04Feb2021) and Follow-up#02 (14MAY2021): New information received from a contactable consumer (patient) reported for himself included: Updated the age group (Elderly), vaccination details (administration date: 01Feb2021 and administration time: 14:00 pm), facility type vaccine (Doctor's office/urgent care), added new events (feeling weak muscles and sleep disturbance), outcome of the events (resolving), treatment details (no), laboratory tests (SARS-COV-2 test (Nasal Swab) and details about follow-up attempts (Follow-up attempts completed. No further information expected).

Other Meds:

Current Illness:

ID: 1426180
Sex: F
Age:
State: CA

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 06/25/2021
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Symptoms: Swelling and Soreness of Left arm; Swelling and Soreness of Left arm; This is a spontaneous report from a contactable consumer. A 26-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 23Jan2021 (Batch/Lot Number: EL9263) as single dose for COVID-19 immunisation. The patient medical history was not reported. Allergies were unknown. There were no concomitant medications. The patient did not have any other vaccine in four weeks and any other medications in two weeks. The patient had no COVID prior vaccination. The patient had no COVID tested post vaccination. On 23Jan2021, the patient experienced swelling and soreness of left arm. The patient received no treatment for AE. Outcome of the events was recovered in 2021. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426181
Sex: F
Age:
State: NY

Vax Date: 02/06/2021
Onset Date: 02/08/2021
Rec V Date: 06/25/2021
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Symptoms: her shoulder hurts again (48 hours after the second dose); This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number was not reported), dose 2 via an unspecified route of administration on 06Feb2021, as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number was not reported), administered on an unknown date, as single dose for COVID-19 immunisation and experienced shoulder was sore at the injection site. The patient previously took flu shot on an unspecified date for immunization and She had the same reaction to the flu shot. However when she went to sleep the pain was still bothering her so she called (Specialty Pharmacy name) and they told her it was okay to take Advil 24 hours after the vaccine, she took 2 Advil, after a couple of days the pain disappeared. When she received the second dose of the vaccine, the nurse told her that she should not have taken Advil. She would like to know if she should not have taken it because she reduces the effectiveness of the vaccine. After 48 hours of the second dose on 08Feb2021, the patient shoulder hurts again. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426182
Sex: F
Age:
State:

Vax Date: 02/06/2021
Onset Date: 02/07/2021
Rec V Date: 06/25/2021
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Symptoms: On my shoulder there is a large bump; circle around it; It's reddish and inflamed; itchy/The middle is solid, itchy around; Next morning developed a bump on her shoulder. It is red, swollen, and itchy; It's warm to the touch; This is a spontaneous report from a contactable consumer or other non health care professional (patient herself). A female patient (Age: 77 units: Unspecified) received bnt162b2, (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 06Feb2021 as dose 1, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated that, she had her first dose of the Pfizer vaccine on (Saturday) 06Feb2021 afternoon in her shoulder. She had an interesting reaction that appeared, next morning 07Feb2021 developed a large bump on her shoulder, circle around it. It was pretty reddish/red, inflamed, hot, swollen, and itchy. It was a little bigger, about 2.5 inches to 3 inches in diameter. It was at injection site. The middle was solid, itchy around. It was warm to the touch. It was around 2.5-4 inches. She wanted to know if the needle went in all the way. She didn't feel the vaccine, but she was pretty tough. She wanted to know if it was normal for people to get the rash and bump and asked for the second dose any contraindications on taking it. Investigation Assessment was not Provided. The outcome of the events was unknown. Description of complaint: Had a bump that was itchy and red after COVID-19 Vaccine. Concerned needle didn't go in deep enough. Caller declined to complete report. Full details not obtained. Product strength and count size dispensed and Additional lot numbers Not provided. sample of the product available to be returned, if requested as Not provided. Packaging sealed and intact was Not provided. From mail trail received in response to query sent regarding confirmation correct PRD involved in this report: Query: Please help to confirm correct PRD of attached report since "09Feb2021" provided in the source, but SRD is 08Feb2021in the processed ICSR screen. (Screen shot attached). Response: PRD is 08Feb2021(see below). Nurse is currently sending dates over to hospital format. If you have any questions around this, please contact your BT support or digital team for further information. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426183
Sex: F
Age:
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Rec V Date: 06/25/2021
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Symptoms: Nausea after receiving vaccine; This is a spontaneous report from a non-contactable consumer or Non-healthcare Professional reporting for a patient. A female patient of an unspecified age received bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced nausea after receiving vaccine. The clinical outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1426184
Sex: F
Age:
State:

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 06/25/2021
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Symptoms: Incision site pain; Joint Pains; Fatigue/Tiredness; This is a spontaneous report from a non-contactable physician. A 38-years-old non-pregnant female patient received first dose of bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number: 59267-1000-1 and Expiration date: unknown), via an intramuscular route, in left arm on 04Feb2021 at 08:30 as dose 1, single for covid-19 immunisation. Medical history included migraine headaches from an unknown date and covid-19 from an unknown date and unknown. The patient's concomitant medications were not reported. Patient has no known allergies. Patient did not receive any other vaccine in four weeks. On 04Feb2021 at 14:00, the patient experienced incision site pain for 24-48 hours, joint pains and fatigue/tiredness. Patient was not tested covid positive post vaccination. No treatment was received for events. Outcome of events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1426185
Sex: F
Age:
State: MI

Vax Date: 02/02/2021
Onset Date: 02/07/2021
Rec V Date: 06/25/2021
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Symptoms: Event: numbness in left arm was reported as worsened; feeling tingling and numbness in my left arm; feeling tingling and numbness in my left arm; This is a spontaneous report from a contactable consumer (reporting on herself). A 23-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection; Lot number and Expiry date was not reported) via an unspecified route of administration in Arm Left on 02Feb2021 as dose number unknown, single for COVID-19 immunization. The patient medical history was not reported. There were no concomitant medications. Patient got her Pfizer shot on 02Feb2021 (last Tuesday) in her left arm. 4-5 days later, on 07Feb2021 patient feeling tingling and numbness in her left arm. Is this a normal side effect. Patient dose not see it listed in the Pfizer vaccine information. Numbness in left arm. Event: numbness in left arm was reported as worsened. She was experiencing numbness in her arm that she got the injection in. She has not received treatment or seen a doctor. She was a medical sales rep, and she got it be-cause they fit patients for power wheel chairs. She was in and out of nursing homes and rehabs. The outcome of the feeling tingling and numbness in my left arm was not recovered and for event numbness in left arm was reported as worsened was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426186
Sex: F
Age:
State: NY

Vax Date: 02/06/2021
Onset Date: 02/07/2021
Rec V Date: 06/25/2021
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Symptoms: Feeling burn and itching behind the ears and under the back hair line; I have redness around those areas and a bit peeling; I have redness around those areas and a bit peeling; This is a spontaneous report from a contactable consumer (patient herself). A 23-year-old non-pregnant female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in arm left on 06Feb2021 at 18:15 (Batch/Lot number was not reported) (at the age of 23-year-old) as single for covid-19 immunisation. The vaccine facility type was others. The patient medical history and concomitant medication were not reported. Patient received birth control was received within 2 weeks of vaccination. The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. On 07Feb2021, the patient stated that "feeling burn and itching behind the ears and under the back hair line and had redness around those areas and a bit peeling". The events resulted in doctor or other healthcare professional office/clinic visit. Treatment received for the events was unknown. Post vaccination, the patient was not tested with COVID-19. The outcome of the events was resolving. Information about batch/lot number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426187
Sex: F
Age:
State: CO

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
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Symptoms: rash on both legs above the ankle and spreading upward; This is a spontaneous report from a contactable consumer (patient) or other non-healthcare professional. A 73-years-old female patient (non-pregnant) received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in right arm on 05Feb2021 at 14:00 (Batch/Lot Number: EL9261, Expiry date was not reported) as single dose covid-19 immunisation. Medical history included diabetes mellitus and adverse reaction to narcotic pain relievers. The patient's concomitant medications were not reported. The patient previously received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot Number and Expiry date was not reported) as single dose covid-19 immunisation. The patient did not experience covid prior to vaccination and covid was not tested after vaccination. On 05Feb2021, at 12:00 AM, the patient experienced rash on both legs above the ankle and spreading upward. There was no treatment received for the reported event. Outcome of the event was reported as not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426188
Sex: F
Age:
State: WA

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
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Symptoms: Sore arm; headache; sore neck muscles; intense fatigue; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 73-years-old non-pregnant female patient received 1st Dose of bnt162b2 (COMIRNATY, Solution for injection, Batch/Lot number was not reported) administered Arm Left on 04Feb2021 at 15:00 as SINGLE DOSE for an unspecified indication. Medical history included hypersensitivity to penicillin. The patient's concomitant medications were not reported. The patient did not have Covid prior to vaccination nor the patient was tested for Covid post vaccination. The patient experienced sore arm, headache, sore neck muscles, and intense fatigue on 05Feb2021 at 01:00 am. The patient did not receive any treatment for the events. The outcome of the events was resolved. Follow-up attempts completed. No further information expected. Information about Lot/Batch is requested.

Other Meds:

Current Illness:

ID: 1426189
Sex: U
Age:
State: MA

Vax Date: 02/07/2021
Onset Date: 02/08/2021
Rec V Date: 06/25/2021
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Symptoms: Fever, temp 100; Body aches; This is a spontaneous report from a non-contactable consumer. This consumer reported for a patient. A patient of unspecified age and gender received bnt162b2 (BNT162B2; PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 07Feb2021 as dose 1, single for covid-19 immunisation at Pharmacy. The patient medical history and concomitant medications were not reported. It was unknown if patient receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient diagnosed with COVID-19. Since the vaccination, it was unknown whether the patient been tested for COVID-19. On 08Feb2021, the reporter stated that a coworker of hers was experiencing symptoms after receiving a first dose of the covid vaccine, administered 07Feb2021. The patient had a fever, Temp 100, and body aches. The patient underwent lab tests and procedures which included body temperature: 100 on 08Feb2021. The outcome of the events was unknown. No follow up attempts are possible. Information on the lot/batch number could not be requested. No further information is expected.

Other Meds:

Current Illness:

ID: 1426190
Sex: F
Age:
State:

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Rec V Date: 06/25/2021
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Symptoms: feel arm pain on the injection site; This is a spontaneous report from a female patient of an unspecified age received first dose of BNT162B2 (BNT162B2, PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration, administered in arm on an unspecified date as 1st dose, single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, patient got the first dose and feel arm pain on the injection site. The outcome of the event was unknown. Information about lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426191
Sex: F
Age:
State: MI

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
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Symptoms: Flu-like symptoms; aches and pains; fatigue; chills; headache; This is a spontaneous report from a contactable Other HCP. A 37-year-old non pregnant female patient received BNT162B2 (BNT162B2, Solution for injection, Batch number and Expiry date were not reported) intramuscularly in the right arm on 05Feb2021 10:00 as SECOND DOSE, SINGLE for covid-19 immunisation. The patient medical history included allergy-induced asthma; uterine fibroids; fibrocystic breast disease; chronic sinus issues; migraines; associated with pregnancy (2017-18): pre-eclampsia and postpartum anxiety disorder; and allergy to Amoxicillin, Penicillin, CT Scan Reaction dye, Allium family when raw (onions/garlic and all relatives), dust, mold and cat dander. Concomitant medications included Amfetamine aspartate, Amfetamine sulfate, Dexamfetamine saccharate, Dexamfetamine sulfate (ADDERALL XR and ADDERALL QR), Fluticasone Furoate (FLONASE SENSIMIST); Hydroxyzine, ibuprofen and Olly women's multivitamin. Historical vaccine included first dose of BNT162b2 (BNT162B2, Solution for injection, Lot number was not reported), intramuscularly in the left arm on 11Jan2021 10:00 as FIRST DOSE, SINGLE for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Facility where the most recent COVID-19 vaccine was administered was clinic/facility. On 05Feb2021 at 10:00 PM (beginning at 12 hours after vaccine), the patient experienced 48 hours of flu-like symptoms including aches and pains, fatigue, chills and headache. No treatment was received for the events. The outcome of the events was recovered. Information on lot/batch number has been requested. Follow-up (07May2021): Follow-up attempts completed. No further information expected.

Other Meds: ADDERALL; FLONASE SENSIMIST ALLERGY RELIEF; HYDROXYZINE; IBUPROFEN

Current Illness:

ID: 1426192
Sex: F
Age:
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Rec V Date: 06/25/2021
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Symptoms: Sciaitic nerve is acting up and wants to take ibuprofen to help.; This spontaneous report from a contactable consumer via Pfizer-sponsored program. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: unknown), via an unspecified route of administration on an unspecified date as 1st dose, single for covid-19 immunisation.The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced Sciatica nerve was acting up and wants to take ibuprofen to help on an unspecified date. Patient clarified has not taken ibuprofen or anything for nerve pain and has been many years since Sciatica nerve has acted up. The outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426193
Sex: F
Age:
State:

Vax Date: 02/07/2021
Onset Date: 02/07/2021
Rec V Date: 06/25/2021
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Symptoms: neck pain radiating to my shoulder blade; she felt uncomfortable near my neck on the evening of getting vaccine; This is a spontaneous report received from a contactable consumer (patient). A 38-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EN5318 and expiration date was not reported), dose 1 via an unspecified route of administration, administered in arm left on 07Feb2021 at 09:30 as single dose (age at vaccination was 38 years) for COVID-19 immunisation. The patient was not pregnant at the time of vaccination. Medical history included hypothyroid (take daily Synthroid tablets in the morning). Concomitant medications included levothyroxine sodium (SYNTHYROID) taken for hypothyroidism, start and stop date were not reported. The patient did not receive other vaccine in four weeks. The patient had no COVID prior vaccination. The patient felt uncomfortable near her neck on the evening of getting vaccine on 07Feb2021 and experienced neck pain radiating to her shoulder blade on 08Feb2021 around 19:30. The clinical course of event was reported as: she took the vaccine on 07Feb2021 at 9:30 and on 08Feb2021 around 19:30, she started a neck pain radiating to her shoulder blade. Note that she received the shot on her left arm and the radiating pain was from her neck (right side of her neck near throat) to her right shoulder. She never had this type of pain until now. If she took a deep breath, she felt intense pain radiating from her neck to shoulder blade. She did not do anything unusual and spent her usual workday (work from home) as normal. She even took a short nap early evening too. Yesterday (as reported) she just stayed home and relaxed after getting vaccine. After getting the vaccine, she felt uncomfortable near her neck on the evening of getting vaccine (07Feb2021). She did not know if she could conclude that this was an adverse effect to the vaccine or not but as a precaution, she was reporting it. If the pain intensifies, she will visit an urgent care tomorrow (09Feb2021). The patient was not COVID tested post vaccination. No treatment received for the reported events. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: SYNTHYROID

Current Illness:

ID: 1426194
Sex: M
Age:
State: CA

Vax Date: 01/29/2021
Onset Date: 02/02/2021
Rec V Date: 06/25/2021
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Symptoms: a patient who received the 2 doses of the vaccine 4 days apart; a patient who received the 2 doses of the vaccine 4 days apart; Usual side effect of arm soreness, tenderness; Usual side effect of arm soreness, tenderness; This is a spontaneous report from a Pfizer-sponsored program. A contactable pharmacist reported that a 35-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, NDC number, Expiry Date of Pfizer COVID-19 Vaccine: unknown), via an unspecified route of administration, administered in arm on 29Jan2021 13:30 (Batch/Lot number was not reported) as 1st dose, 30 ug, single, [30mcg injection to unknown arm] and received BNT162B2 via an unspecified route of administration on 02Feb2021 09:45 (Batch/Lot number was not reported) as 2nd dose, single for covid-19 immunisation. The patient age at time of vaccination was 35 years. Medical history included ongoing depression and anxiety and looks like the patient has been getting treatment for depression and anxiety, further details unknown. Family history reported as none. Concomitant medications were not reported. HCP said that the patient had who received the 2 doses of the vaccine 4 days apart on 02Feb2021 and experienced usual side effect of arm soreness, tenderness on an unspecified date in 2021. The adverse events do not require a visit to emergency room and physician office and not hospitalized. No relevant tests performed. Prior vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccines was none. The report assessed as non-serious. Outcome of the events arm soreness, tenderness was recovered on an unspecified date in 2021. Relatedness of the events was reported as unrelated. Information about lot/batch number has been requested. The batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness: Anxiety (Looks like he has been getting treatment for anxiety, further details unknown.); Depression (Looks like he has been getting treatment for depression, further details unknown.)

ID: 1426195
Sex: F
Age:
State: TX

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
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Symptoms: Hot and sweaty within 3 minutes; Hot and sweaty within 3 minutes; SOB; nausea; tired; headache; muscle pain/weakness; muscle pain/weakness; dizziness; fever; high BP and HR; high BP and HR; throat swelled up; This is a spontaneous report from a contactable consumer (patient). A 37-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number: Unknown), via an unspecified route of administration in left arm on 05Feb2021 at 12:30 PM as SINGLE DOSE for covid-19 immunisation. Medical history was reported as very healthy, no medical problems, MDD. The patient had no known allergies. The patient received other medication in two weeks. The patient did not receive any other vaccines within four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. On 05Feb2021 at 12:45 PM, patient experienced hot and sweaty within 3 minutes, SOB, nausea, tired, headache, muscle pain/weakness, dizziness, fever, high BP and HR, throat swelled up. The events resulted in: Doctor or other healthcare professional office/clinic visit. The patient underwent lab tests and procedures which included blood pressure measurement: high, heart rate: high. The patient received treatment due to the events with exam, muscle relaxers, pain meds, Zofran. The outcome of all events was recovered with sequel on an unspecified date in 2021. Follow-up (07May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426196
Sex: F
Age:
State: NJ

Vax Date: 01/08/2021
Onset Date: 01/27/2021
Rec V Date: 06/25/2021
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Symptoms: Blood pressure was high/blood pressure at the ER was high, around 140 something over 90 something/her blood pressure has been all over the place, it has been high; Tachycardia; chronic anxiety order; panic attacks; heart rate was up to 150; overwhelming heavy feeling all over her head; eyes got blurry; her throat felt like it was closing up; got real shaky; This is a spontaneous report from a contactable consumer (Patient). A 44-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection Lot: EJ1685, Expiration Date: 31Mar2021), via intramuscular route of administration, administered in left arm on 08Jan2021 at 17:30 (at the age of 44-year-old) as single dose for preventative at hospital. The patient medical history included none except sinus infection. There were no concomitant medications. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection Lot: EJ1685) via intramuscular route of administration, administered in left arm on 18Dec2020 in the afternoon at around 14:00 for preventative. No additional Vaccines administered on same date of the Pfizer suspect. None aside from first dose of covid vaccine was received prior vaccination within 4 weeks. It was reported that, the patient wanted to report a really bad reaction to the vaccine. She had the first dose the Friday before Christmas. She always gets vaccines and never has a problem. After the first dose she did not feel anything, she did not have any of the normal side effects, she was fine. She is a surgical tech. About 9 or 10 days later, clarifies it was Sunday 27Jan2021 she was fine all day and later that evening, she thinks she was either laying in her bed or getting changed and she experienced an episode which she describes as overwhelming heavy feeling all over her head, her throat felt like it was closing up, not like an asthma feeling. Her eyes got blurry. She has never passed out before or fainted, she just felt like she was at that point and got real shaky. She went to the ER since this episode lasted for a while. Her blood pressure at the ER was high, around 140 something over 90 something. They did a lot of blood work and nothing came back. Her pulse ox was fine. They gave her Benadryl in case she was having an allergic reaction. They did blood work and a chest x-ray to make sure for covid. States everything was fine. Her blood pressure went down while she was there for 6 or 7 hours. She was not admitted to the hospital She was told to follow up with primary for hypertension. She went to her primary doctor a couple of days later and explained that the only thing different was that she got the covid vaccine. Her primary doctor diagnosed her with chronic anxiety order and panic attacks and put her on medication, Paxil 10mg and Klonopin for panic attacks. Her primary doctor did not seem concerned about her blood pressure. She bought a pulse ox and blood pressure cuff since she continued to feel these episodes, it was not constant, but she still continued to feel the episodes. Reports her blood pressure has been all over the place, it has been high. When she was last seen by her primary doctor in Mar her blood pressure was 116/68 and she normally runs low. She exercises and she has never had high blood pressure. When she went to the doctor previously, she normally went in for a sinus infection. She is looking to get information about these episodes she is experiencing. The episodes starts with that heavy feeling on her head, her throat feels like it is closing up, her eyes get blurry and she reports her blood pressure has stayed up. She also has some tachycardia. She decided to go see a cardiologist on her own. She had another bad episode this past Friday and her heart rate was up to 150. The cardiologist had her on a Holter monitor for the weekend. She has O negative blood and does not know if this has something to do with her episodes. She is going to have an echocardiogram and stress test next week. She is still experiencing the episodes. About 10 days after the second dose, she went back to ER where she had the same bad episode it was the same symptoms as reported above. They did not find anything in the bloodwork. States she had no issues prior to getting the vaccine, she did not have any panic attacks. States she had nothing like this before getting the vaccine. She works in the healthcare field and she has had all the mandatory vaccinations and has never had a problem. She was not even nervous about getting the covid vaccine, she forgot that she even got it, it was not even on her mind. She did report the episode to occupation health with her employer. It was suggested for her to get the second vaccine, so she did. She has been sent home a couple of times by her director and her doctor is taking her out of work since her blood pressure is going high. The patient underwent lab tests and procedures which included blood pressure measurement: high, around 140 something over 90 something on an unspecified date, blood test: nothing came back on an unspecified date, chest x-ray: everything was fine on an unspecified date, electrocardiogram ambulatory: unknown results on an unspecified date, heart rate: 150 on an unspecified date, oxygen saturation: pulse ox was fine on an unspecified date. Therapeutic measures were taken as a result events. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426197
Sex: F
Age:
State: CT

Vax Date: 02/01/2021
Onset Date: 02/06/2021
Rec V Date: 06/25/2021
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Symptoms: Slight cough; Chills; body aches; fatigue; migraine; Sore throat; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EL3247) via an unspecified route of administration in left arm on 01Feb2021 at 12:30 as 1st dose, single for COVID-19 immunization. Medical history included recurring sinusitis, recurring migraines, hypothyroid, anxiety. Patient had allergies with Codiene, Dillauded. Concomitant medications included thyroid (ARMOUR THYROID), guaifenesin, pseudoephedrine hydrochloride (MUCINEX D), levocetirizine dihydrochloride (XYZAL), ibuprofen, ergocalciferol (VIT D). Patient did not receive any other vaccine in four weeks. Patient was not diagnosed with covid prior to vaccination. Patient was not pregnant. On 06Feb2021 at 04:30 PM, patient experienced slight cough, chills, body aches, fatigue, migraine, sore throat. No treatment was received for the adverse events. Patient had not been tested covid post vaccination. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: ARMOUR THYROID; MUCINEX D; XYZAL; IBUPROFEN; VIT D

Current Illness:

ID: 1426198
Sex: F
Age:
State: TN

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 06/25/2021
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Symptoms: hard time walking; tiredness; foot swollen; foot hot to touch; Since receiving the vaccine she has been sleeping a lot for about 3 days; Foot pain; foot redness; This is a spontaneous report from a contactable consumer. A 77-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number: EL9261)via an unspecified route of administration, administered in Left Arm on 02Feb2021 at 12:00 (at the age of 77-years-old) as DOSE 1, SINGLE for COVID-19 immunization. The patient's medical history included parkinson's disease, transient ischaemic attack, hypersensitivity, sinus disorder, Cardiac disorder, vaginal infection, pain, incontinence, antidepressant therapy, hallucination, unspecified vitamin D deficiency. No relevant tests done. The concomitant medications included ongoing estradiol (ESTRACE VAGINAL) taken for vaginal infection from 2019, ongoing colecalciferol (VITAMIN D 3) taken for vitamin d deficiency, ongoing pimavanserin tartrate (NUPLAZID) taken for hallucination from 05Feb2021,ongoing venlafaxine (VENLAFAXINE) taken for antidepressant therapy, ongoing carbidopa, levodopa (RYTARY) taken for parkinson's disease, ongoing mirabegron (MYRBETRIQ) taken for incontinence, ongoing atorvastatin calcium (ATORVASTATIN CALCIUM) taken for cardiac disorder, ongoing aspirin [acetylsalicylic acid] (ASPIRIN [ACETYLSALICYLIC ACID]) taken for transient ischaemic attack ,ongoing clopidogrel bisulfate (CLOPIDOGREL BISULFATE) taken for transient ischaemic attack, ongoing paracetamol (ACETAMINOPHEN) taken for pain, ongoing loratadine (LORATADINE) taken for hypersensitivity, sinus disorder, ongoing ascorbic acid, biotin, calcium, colecalciferol, cyanocobalamin, dl-alpha tocopheryl acetate, folic acid, potassium iodide, pyridoxine hydrochloride, retinol acetate, zinc sulfate (CENTRUM MULTIGUMMIES WOMEN), amantadine hydrochloride (AMANTADINE HYDROCHLORIDE) taken for parkinson's disease. Since receiving the vaccine she had been sleeping a lot for about 3 days (on 03Feb2021). Caller stated she knew that was supposed to be a side effect. Adds her mother was a Parkinson's patient and usually able to walk using a walker. She was having a hard time walking (03Feb2021) and had to use the wheelchair. Clarifies her mother started sleeping quite a bit about three days after the vaccine on Friday 03Feb2021. Mentions previous to this on Wednesday after the vaccine, her mother was complaining of foot pain (on 03Feb2021) towards the side midway on the foot in the arch and on the top where you tie your shoe. It was almost like she dropped something on it but she did not. It was slightly swollen on the top and red and warm (on 03Feb2021). Friday when her mother started sleeping so much, they had resort to the wheelchair. She took her to see the nurse practitioner on Friday for the foot, who sent her to the ER for an X-ray on Saturday so they went out again on Saturday to get the foot x-ray done. The foot was not broken. They did treat her mother's foot with Cephalexin. Her foot was fully recovered now. Her mother's tiredness (on 05Feb2021) was persisting and she was having a hard time just getting up from the bed and to go across the room even though the foot was fine. Today they have a message into her neurologist. Adds today was the first day her mother started talking about needing or wanting to go to the hospital for her tiredness and not being able to walk (06Feb2021) Her mother was scheduled for the next dose 23Feb2021.The patient underwent lab tests and procedures which included x-ray limb: the foot was not broken on. Therapeutic measures were taken as a result of foot pain, foot redness, foot swollen, foot hot to touch.The outcome for the events foot pain, foot redness, foot swollen, foot hot to touch was recovered/resolved on 08Feb2021 and not recovered/not resolved for rest of the events. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected

Other Meds: ESTRACE VAGINAL; VITAMIN D 3; NUPLAZID; VENLAFAXINE; RYTARY; MYRBETRIQ; ATORVASTATIN CALCIUM; ASPIRIN [ACETYLSALICYLIC ACID]; CLOPIDOGREL BISULFATE; ACETAMINOPHEN; LORATADINE; CENTRUM MULTIGUMMIES WOMEN; AMANTADINE HYDROCHLORIDE

Current Illness:

ID: 1426199
Sex: M
Age:
State: NY

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Rec V Date: 06/25/2021
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Symptoms: Soreness of the arm; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer reported for a male patient (husband) who had received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number, Expiry Date: Unknown), via an unspecified route of administration on an unspecified date as 1ST DOSE, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Reported two AE for her and her husband. Reporter mentioned that her husband experienced soreness of the arm. The outcome of the event was unknown. This follow-up was being submitted to notify that the lot/batch number was not available despite the follow-up attempts made. Follow-up attempts had been completed and no further information was expected.

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Current Illness:

ID: 1426200
Sex: F
Age:
State: NY

Vax Date: 01/25/2021
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Rec V Date: 06/25/2021
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Symptoms: Got a good nights sleep which she usually does not get; feeling tired; dizzy; This is a spontaneous report received from a contactable consumer, the patient via Pfizer sponsored program Pfizer first connect. A female patient of an unspecified age received first dose of BNT162B2 (COMIRNAT PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9262, NDC number and Expiry Date: unknown) via an unspecified route of administration on 25Jan2021 as 1ST DOSE, SINGLE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was feeling tired and dizzy after the first shot. Patient got a good night sleep which she usually did not get. The outcome of events was unknown. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1426201
Sex: F
Age:
State: SC

Vax Date: 01/28/2021
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Rec V Date: 06/25/2021
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Symptoms: she was 80 years old and has heart issues; This is a spontaneous report from a non-contactable female consumer(patient). A 80-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, lot number: Unknown) via unknown route on 28Jan2021 as 1st dose, single for covid-19 immunisation. Medical history and concomitant medications were not reported. Patient reported that she was 80 years old and has heart issues. Patient was watching the today show and they are telling viewers that you can wait 3-6 weeks to get the 2nd dose on an unspecified date. Patient stated that she would contact the local health department in (State name) and see if they will allow her to get the 2nd dose there and go from there. She wanted to know what happens if the health department tells her no and she cannot get the 2nd dose until end of Feb. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 1426202
Sex: M
Age:
State: TN

Vax Date: 02/05/2021
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Rec V Date: 06/25/2021
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Symptoms: had a temperature of 100.4; pain in his shoulders and neck/has joint pain across his neck; he has joint pain across his shoulders and neck and that he cannot turn his head/ pain in his shoulders and neck; he has joint pain across his shoulders and neck and that he cannot turn his head; This is a spontaneous report from a contactable consumer. This 78-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number and expiry date were not reported) via unspecified route of administration on 05Feb2021 (at age 78-year-old) as single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. On an unspecified date, Caller stated that he had his first Pfizer shot Friday 05Feb2021. Stated that he had a temperature of 100.4 that went back to normal. Stated that he had pain in shoulders and neck since he got the shot. Clarified that it was for Pfizer Covid 19 shot. Stated that it may be normal or if others felt this way. Clarified that he had joint pain across his shoulders and neck and that he couldn't't turn his head. Wanted to know if this was serious. Patient underwent lab test includes body temperature for which result 100.4 was reported. The outcome of event was resolved for body temperature increased, whereas unknown for all other events. Information on lot/ batch number has been requested.

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Current Illness:

ID: 1426203
Sex: F
Age:
State:

Vax Date: 01/22/2021
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Rec V Date: 06/25/2021
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Symptoms: Chronic pain; lot of health issues; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect. A contactable female patient with (unspecified age and unit) reported that she received first dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: unknown) via an unspecified route of administration on 22Jan2021 as 1st dose, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient just read from the fact sheet not to take pain medicines. On an unspecified date, the patient experienced a lot of health issues and chronic pain. Patient had taken tylenol and motrin for pain relievers 2 nights ago as treatment. She was asking if there was any timeframe where she can take the pain reliever safely. Cold transfer to due to longer wait time (19 calls ahead). The outcome of the events lot of health issues and chronic pain was unknown. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1426204
Sex: F
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Rec V Date: 06/25/2021
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Symptoms: Daughter had covid vaccine. She had bad reaction.; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received BNT162B2 (Covid-19 Vaccine, Solution for injection) 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. No patient identifiers were provided but the reporter had first-hand knowledge of the patient and was reporting on a specific patient. Daughter had Covid vaccine. She had bad reaction. Outcome of the event was unknown. Information on lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1426205
Sex: F
Age:
State: FL

Vax Date: 01/18/2021
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Rec V Date: 06/25/2021
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Symptoms: sore reaction; neck pain; dizziness; nauseous that went away again after a few days; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), dose 1 via an unspecified route of administration on 18Jan2021 (Batch/Lot number was not reported) as 1st dose, single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, patient stated that she received her 1st shot of our vaccine last 18Jan2021 and had a sore reaction that went away after a few days. Then on the 15th day, she had neck pain, dizziness and nauseous that went away again after a few days. She was asking if this was normal. 2nd vaccine was scheduled 08Feb2021. The outcome of the events neck pain and dizziness was unknown and recovered on an unspecified date for other events. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

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Current Illness:

ID: 1426206
Sex: F
Age:
State: CA

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 06/25/2021
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Symptoms: itching; Rash; fatigue; joint pain; low blood sugar; This is a spontaneous report from a contactable consumer (patient). A 78-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EM9809/Expiry date: unknown), via an unspecified route of administration on 04Feb2021 at 11:00 AM in the left arm (at the age of 78-years-old) as single dose for COVID-19 immunization. The patient medical history included ongoing diabetes from 2000 and hysterectomy in the year 2000. The patient had received some other medications within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No pre-disposing factors was reported. Follow up received on 21Apr2021, it was confirmed that on 27Feb2021 at 10:00, the patient experienced rash, fatigue, joint pain and low blood sugar (previously reported as, 05Feb2021, 12:00 AM, the patient experienced rash, fatigue, joint pain, and low blood sugar. Adverse event resulted in Doctor or other healthcare professional office/clinic visit. The patient was given advice and reassurance for the treatment of the adverse event). The patient had received treatment for rash. No treatment medication for received for events fatigue, joint pain, and low blood sugar. The patient was not hospitalized as a resulted of these events. Patient reported that the Doctor suggested taking benadryl for itching due to rash. The patient reported that she required a virtual visit to Physician office. It was unknown if the patient had any primary infection site. No culture was performed. The patient reported that she was fine now at the time of reporting. The clinical outcome for the event itching was unknown and the outcome of other events had recovered. Information on the lot/batch number has been requested. Follow up(21Apr2021): This is a follow up-spontaneous report from a contactable consumer received in response to Non-HCP letter via follow-up letter which included: Added patient's age at vaccination, medical history, suspect drug details (Lot number, Time of vaccination), updated event details (onset date and outcome), clinical course and narrative updated accordingly. Follow-up attempts completed. No further information expected.

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Current Illness: Diabetes (verbatim: Diabetes)

ID: 1426207
Sex: F
Age:
State: MI

Vax Date: 02/03/2021
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Rec V Date: 06/25/2021
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Symptoms: To prevent soreness, the caller took Tylenol; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 03Feb2021 as 1st dose, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that she received the first dose yesterday. To prevent soreness, the patient took Tylenol 3 times yesterday. The patient stated that she read that you should not take any pain reliever afterward. The patient asked if it decrease the effectiveness of the vaccine. The clinical outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

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Current Illness:

ID: 1426208
Sex: F
Age:
State: MN

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Rec V Date: 06/25/2021
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Symptoms: effects on her bowel movements.; This is a spontaneous report received from contactable consumer (reporting on herself) via a Pfizer-sponsored program. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, lot number and Expire Date was not reported) via unspecified route of administration on an unspecified date as un-known, single for Covid-19 immunization. Medical history and concomitant medications were not reported. Patient received COVID vaccine and has inquired about its effects on her bowel movements. The outcome of event was unknown. Follow-up attempts have been completed and no further information is expected.

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Current Illness:

ID: 1426209
Sex: M
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Symptoms: skin growth; This is a spontaneous report from a Pfizer-sponsored program. A contactable male consumer (patient). A male patient an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, Formulation: Solution for injection, Lot Number was not reported), dose 1 via an unspecified route of administration on an unspecified date as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, patient had skin growth. The patient reported as his doctor prescribed him a Fluorouracil Cream for skin growth. The outcome of event was unknown. Information about Batch/Lot number has been requested. Follow-up attempts are completed. No further information is expected

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Current Illness:

ID: 1426210
Sex: F
Age:
State:

Vax Date: 02/03/2021
Onset Date: 02/01/2021
Rec V Date: 06/25/2021
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Symptoms: Said can feel a migraine coming on; I was getting migraine headache; This is a spontaneous report from a Pfizer-sponsored program. A contactable female consumer (patient herself) of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: not reported) via an unspecified route of administration on 03Feb2021 as 1st dose, single dose for COVID-19 immunization. Medical history included migraine; she suffered from migraines, clarified had migraines before getting COVID vaccine from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. It was reported that, she received first dose of COVID vaccine yesterday and said that she could feel a migraine coming on. She was getting migraine headache on unspecified date in Feb2021. She don't want to take anything but sometimes it escalates. She wanted to know if she could take something. Therapeutic measures were taken as a result of migraine coming on and headache as currently, she was on Imitrex or the generic Sumatriptan 50 mg and she enquired would that effect it or not. The outcome of events was unknown. Limited information was available over the call. Information on lot and Batch number has been requested. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1426211
Sex: M
Age:
State: MA

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 06/25/2021
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Symptoms: 2-3days after the first dose a rash appeared on his leg/ rash on my forearm too and it looks like Poison ivy; This is a spontaneous report received from a contactable consumer (patient himself) via a 59-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EK9231), via an unspecified route of administration on 13Jan2021 at 01.30 (at the age of 59-years-old and weight: 230 or 235 lbs) as 1st, dose single for COVID-19 immunization. Patient's medical history and concomitant medication were not reported. It was reported that, the patient had his first shot 2 days ago the first Pfizer shot and within two days he developed a rash on his leg that was about may be six inches long and two or three inches wide. Patient had a rash on her forearm too and it looks like Poison ivy, but he lives in the north and it was Feb now so he don't think it was Poison ivy but the rash has been gone way since he got the rash couple days after the shot. The patient just put Calamine and he had no medical treatment. The outcome of the event was recovered in 2021. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1426212
Sex: M
Age:
State:

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Rec V Date: 06/25/2021
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Symptoms: shortness of breath; headaches; This is a spontaneous report from a contactable Consumer (Patient). A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as 1st dose, single for covid-19 immunisation. The patient 's medical history and concomitant medications were not reported. Consumer stated that consumer had the COVID Vaccine on Friday and had some bad side effects. Consumer had shortness of breath and a headache and consumer had to use his inhaler. Consumer wanted to know if consumer was a candidate for the second dose of the vaccine after having a "bad reaction" to the first? The outcome of events was unknown. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1426213
Sex: F
Age:
State:

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 06/25/2021
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Symptoms: toe pain/A week later her toes are improving but is still tender to touch; redness on both feet; Her great toe on her right foot and the second toe on the left foot were red and inflamed; minor arm discomfort; This is a spontaneous report from a non-contactable consumer (patient herself) received via a sales representative. A 52-years-old female patient received BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number and Expiration date: Not reported), dose 2 via an unspecified route of administration on 06Jan2021 as 2nd dose, single for COVID-19 immunisation. The patient previously received first dose of BNT162B2 for COVID-19 immunization. Medical history included diagnosed with COVID-19 on Oct2020 with mild symptoms and recovered with no sequelae. Patient reported she has no underlying conditions and occasionally takes vitamins, she is quite active and walks several miles a day, she had not injured her feet nor purchased new shoes. This is the first time this has ever occurred. She has no history of autoimmune diseases or Raynaud's. On 06Jan2021, after vaccination patient had some minor arm discomfort but no other issues. On 28Jan2021, Patient started to experience toe pain and redness on both feet, her great toe on her right foot and the second toe on the left foot were red and inflamed (she has pictures). A week later her toes are improving but is still tender to touch. The outcome of minor arm pain was unknown and for other events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1426215
Sex: M
Age:
State: NC

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Rec V Date: 06/25/2021
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Symptoms: He believes the nurse that injected him went too deep and hit the bone. He said it hurt more than usual; He believes the nurse that injected him went too deep and hit the bone. He said it hurt more than usual; This is a spontaneous report from a contactable physician (patient) via Pfizer sales representative. A 70-year-old male patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- unknown) via an unspecified route of administration on an unspecified date as 2nd dose, single for COVID-19 immunization. Medical history and concomitant medications were not reported. Historical vaccine included BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- unknown) via an unspecified route of administration on an unspecified date as 1st dose, single for COVID-19 immunization. On an unspecified date, after the vaccination, the patient stated that he believes the nurse that injected him went too deep and hit the bone. He said it hurt more than usual. The patient was asking if the second dose of the vaccine would be effective if it did hit the bone. He wanted to know which antibody test he should get to see if he has immunity. The outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1426216
Sex: F
Age:
State: IA

Vax Date: 02/08/2021
Onset Date: 02/08/2021
Rec V Date: 06/25/2021
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Symptoms: I had a UTI; My ears feel hot./she feels her neck and ears feel different; worst last night; she still feels full; my glands when I would swollen would be super sharp. I have swollen lymph nodes; soreness in arm/I had injection pain; soreness in arm/I had injection pain; This is a spontaneous report from a contactable consumer or other non hcp. A 65-years-old female patient received first dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EN6201), via an unspecified route of administration, administered in Arm Left on 08Feb2021 11:00(age at vaccination: 65 years) as 1st dose, single for covid-19 immunisation. Medical history was reported as none. There were no concomitant medications. The patient stated that she had her first dose of vaccine at 11 AM yesterday. On 08 Feb2021, the patient experienced soreness in arm. The patient reported that throat doesn't feel sore and her ears feel hot. On 09Feb2021 at noon, the patient experienced her glands was swollen and when she swallows she had a sharp pain on one side, so right way, she ate chicken noodle soup and hot tea, and made it feel a lot better, she had swollen lymph nodes that have been a side effect as she saw it on the list, had a UTI (urinary tract infection) but was felt better and was taking a Macrobid 100mg capsule by mouth twice daily for UTI, so she thought maybe that would help, but her pharmacist said it would not help with swollen glands, but she did not know if it came from a UTI, her ears feel hot/she feels her neck and ears feel different, soreness in arm/I had injection pain, worst last night and she still feels full when she feels her neck and ears feel different. She was a massage therapist, she iced, and rubbed over it and can lift-up, last night it hurt to lift-up, she moved it around, now she can barely feel it, not like last night. It was reported that patient had no longer sharp pain. She had no thermometer, so unknown if she had a temperature, her face feels warm, but she was hot all the the time being 65. Patient was recovering from the events my glands when I would swollen would be super sharp. Patient had not recovered from the event still feels full. The outcome of the events UTI, my ears feel hot/she feels her neck and ears feel different and worst last night was reported as unknown. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

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Current Illness:

ID: 1426217
Sex: F
Age:
State:

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 06/25/2021
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Symptoms: Atrial tachycardia condition; This is a spontaneous report from a Pfizer-sponsored program a non-contactable consumer (patient, self-reported). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on an unspecified date in Jan2021, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that on an unspecified date, she had an atrial tachycardia condition, and she got the 1st vaccine 3 and a half weeks ago. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Total 2021 VAERS Injuries: 679,999

Page last modified: 03 October 2021 5:28pm