VAERS 2021 Database www.vaers.hhs.gov

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

Total Manufacturer

Incidents per State

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

ID: 0921257
Sex: F
Age:
State: TX

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: Feeling sick; Fever of 102 degrees; Coughing; Aching; This is a spontaneous report from a Pfizer-sponsored program entitled Pfizer First Connect. A contactable consumer reported for his sister (health professional) that 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 took the COVID vaccine but she was feeling sick, had a fever of 102 degrees, she was coughing and aching from couple of days after having couple of days in Dec2020. The events outcome was unknown. The reporter mentioned if patient goes to the hospital or not, asked if they should go to the hospital and. The patient was wondering if that was normal. The information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 0921258
Sex: F
Age:
State: PA

Vax Date: 12/28/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
Hospital:

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Symptoms: tiredness; muscle ache at injection site with penny sized welt at injection site; muscle ache at injection site with penny sized welt at injection site; This is a spontaneous report from a contactable nurse (patient) via Pfizer sales representative. A female patient of unspecified age (reported as Age: 32; Unit: Unknown) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date not available), via an unspecified route of administration on 28Dec2020 at 12:30 PM at single dose for COVID-19 immunization. The patient medical history included had COVID 34 days before in 2020. The patient's concomitant medications were not reported. Currently patient was experiencing tiredness, muscle ache at injection site with penny sized welt at injection site in Dec2020. Event took place after use of product. The outcome of the events was unknown. Information on the Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 0921259
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/05/2021
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Symptoms: pain in the administration site; tired; feeling dehydrated; had a low degree fever; nostrils were stuffed or clogged; pain in the arm; went to sleep 3 hours earlier than usually did, waking up five hour later; feeling like that was about to had flu; This is a spontaneous report from a contactable consumer. This consumer reported same events for two patients (Herself and Her friend).This is the Friend report. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unknown date at single dose for covid-19 immunization. It was the second dose. The patient's medical history and concomitant medications were not reported. The Consumer reported that the same symptoms were experienced by a friend of her after the administration of the second dose of the Pfizer's COVID-19 vaccine. The same symptoms included felt only pain in the administration site, at night felt really tired, went to sleep 3 hours earlier than usually did, waking up five hour later with pain in the arm and feeling dehydrated, also feeling like that was about to had flu, had a lowdegree fever, and nostrils were stuffed or clogged. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2020518390 Same Reporter and Drug and event, different Patient.

Other Meds:

Current Illness:

ID: 0921260
Sex: M
Age:
State:

Vax Date: 12/28/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
Hospital:

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Symptoms: pain in the administration site; a strong headache; This is a spontaneous report from a contactable consumer (patient's wife). A male patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 28Dec2020 at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. Patient took his first dose of BNT162B2 for covid-19 immunization on an unspecified date. The patient was experiencing pain in the administration site, and a strong headache that has been fading away. The action taken in response to the events for BNT162B2 was not applicable. The outcome of event "strong headache" was recovering, the another event "pain in the administration site" was unknown. Information about Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0921261
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/05/2021
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Symptoms: This morning she felt bad; She has an autoimmune disease/ received BNT162B2; She has an autoimmune disease/ received BNT162B2; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2, via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. Medical history included autoimmune disease and has been under stress from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient experienced felt bad this morning on an unspecified date with outcome of unknown. Caller was a therapist, behavioral specialist and works and they are all over. It's a hospital and she was in the psychiatric phase of it as a therapist. They are offering the free COVID-19 vaccine since she was working 1 on 1 with clients and some of them are not the most reputable. She has an autoimmune disease and known she should get it, but has had so many doubts and has been under stress. Took care of a brother who was blind who recently had major shoulder surgery and her 91 years old mother who lived with her. Has been stressed and noticed her autoimmune disease was flaring up. Wanted to know was it safe for her to get the vaccine. Knows she should get the vaccine because 2 of her clients had tested positive for COVID and their parents, but when she tested she was negative and her family was also negative. No further details provided. Is so afraid to get the vaccine that she canceled her appointment at the hospital. Was scheduled today to get it. They are offering it to her free since she works there. This morning she felt bad and she had been going through the stress the last month. Mentions she didn't even get the flu this year. No further details provided and does not clarify if she didn't get the flu virus or flu shot. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921262
Sex: M
Age:
State: IL

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: Body chills; fever; headache; This is a spontaneous report from a contactable other healthcare professional (patient). A 43-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Eh9899), via an unspecified route of administration (left arm) on 29Dec2020 08:15 at single dose for Covid-19 immunization. The patient's medical history included hypertension (HTN) and high cholesterol. Concomitant medications included losartan, atorvastatin, and amlodipine. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient experienced body chills, fever, and headache on 29Dec2020 22:00 with outcome of recovering. There was no treatment received for the adverse event. The patient has not been tested for COVID-19 since the vaccination. This case is non-serious.

Other Meds: ; ;

Current Illness:

ID: 0921263
Sex: F
Age:
State: NY

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/05/2021
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Symptoms: mild headache; This is a spontaneous report from a contactable nurse (patient). This 35-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot GJ1685), via an unspecified route of administration, on 22Dec2020 (reported also as 23Dec2020, to be clarified) at 3:00 PM at single dose for COVID-19 immunisation. Vaccine location was left arm. The patient was vaccinated at Nursing Home/Senior Living Facility, age at vaccination was 35-years-old. No other vaccine was received in four weeks. Medical history and concomitant medications were unknown. On 22Dec2020 at 07:00 PM, the patient got mild headache. The event was reported as non-serious. The patient was tested for Covid post vaccination through a nasal swab in Dec2020 and was negative. Outcome was recovered on Dec2020. No treatment was received for the event.

Other Meds:

Current Illness:

ID: 0921264
Sex: F
Age:
State: TN

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/05/2021
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Symptoms: soreness in arm when using arm or to touch; This is a spontaneous report from a contactable nurse. A 56-year-old female nurse received received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date unknown) on 28Dec2020 at 12:30 PM at single dose for COVID-19 immunization on right arm.Relevant medical history included ongoing osteoarthritis and high cholesterol. Concomitant medications included atorvastatin calcium (LIPITOR ORIFARM), escitalopram oxalate (LEXAPRO) and pantoprazole. On 28Dec2020 at 07:00 PM patient started experiencing soreness in arm when using arm or to touch. At the time of the reporting the patient was recovering from the event.

Other Meds: LIPITOR ORIFARM; LEXAPRO;

Current Illness: High cholesterol; Osteoarthritis (osteoarthritis, high cholesterol)

ID: 0921265
Sex: F
Age:
State: MN

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 01/05/2021
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Symptoms: Face started to tingle then went numb roughly 45-55 minutes after receiving.; Face started to tingle then went numb roughly 45-55 minutes after receiving.; This is a spontaneous report from a contactable nurse (patient). A 45-year-old female patient received bnt162b2 (lot number: EL0140, Pfizer- BioNTech), intramuscularly at arm left, first dose on 23Dec2020 07:45, at single dose, for COVID-19 immunization. Medical history included environmental allergies, iron deficiency anemia, endometriosis, allergies to penicillin, and allergies to preservatives in flu vaccine from an unknown date. The patient is not Pregnant at the time of vaccination. Concomitant medication included ibuprofen, colecalciferol (VITAMIN D), cyanocobalamin (VITAMIN B12), magnesium, all from an unspecified date, for unspecified indication. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Age at vaccination is 45 Years old. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient experienced face started to tingle then went numb roughly 45-55 minutes after receiving (reported as from 23Dec2020, 08:30 AM). Not sure if that is an actual reaction but it occurred. The event was reported as non-serious. Therapeutic measures were taken as a result of face started to tingle then went numb roughly 45-55 minutes after receiving, treatment included BENADRYL orally taken. The outcome of the event was recovered in Dec2020.

Other Meds: ; VITAMIN D [COLECALCIFEROL]; VITAMIN B12 [CYANOCOBALAMIN];

Current Illness:

ID: 0921266
Sex: F
Age:
State:

Vax Date: 12/27/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
Hospital:

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Symptoms: She experienced soreness at the site; fatigue; numbness in the left pinky finger; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (BNT162B2), via an unspecified route of administration on 27Dec2020 at SINGLE DOSE for COVID-19 IMMUNIZATION. The patient's medical history and concomitant medications were not reported. The patient received the Pfizer Covid Vaccine at on 27Dec. She experienced soreness at the site and fatigue on 28Dec-29Dec and numbness in the left pinky finger (same arm as vaccination). She also started another med the same day, so she is unsure if the fatigue is from vaccination or the other drug. I do not know the name of that drug. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921267
Sex: F
Age:
State:

Vax Date: 12/28/2020
Onset Date:
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Symptoms: large induration; fever; Chills; vomiting; This is a spontaneous report from a contactable consumer. A 3-decade-old (precise age unknown, early-to-mid 20s) female patient received the first dose of BNT162B2 (COMIRNATY), via an unspecified route of administration on 28Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that post dose 1 of "COMIRNATY COVID-19 mRNA-based vaccine" on 28Dec2020, the patient experienced large induration, fever, chills and vomiting. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921268
Sex: F
Age:
State: TN

Vax Date: 12/28/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Symptoms: I just developed a very sore throat; This is a spontaneous report from a contactable nurse (patient herself). A 36-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), intramuscular on 28Dec2020 at a single dose for COVID-19 immunisation. Medical history was none. Concomitant medications included multivitamins (unspecified). The patient just developed a very sore throat on 29Dec2020. No therapeutic measure was taken as a result of the event. Clinical outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921269
Sex: F
Age:
State: MS

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Symptoms: Elevated heart rate, headache; Elevated heart rate, headache; This is a spontaneous report from a contactable other Healthcare Professional (HCP, patient). This 58-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EK5730), intramuscular, on 29Dec2020 at 12:30 PM at single dose for COVID-19 immunisation. Vaccine location was right arm. The patient was vaccinated at hospital, age at vaccination was 58-years-old. No other vaccine was received in four weeks. Medical history was unknown. Concomitant medications included rosuvastatin calcium (CRESTOR) and lisinopril. On 29Dec2020 at 04:00 PM, the patient experienced elevated heart rate, headache. The event was reported as non-serious. Outcome was recovered on Dec2020. No treatment was received for the event. No follow up attempts are possible. No further information is expected.

Other Meds: CRESTOR;

Current Illness:

ID: 0921270
Sex: F
Age:
State: NY

Vax Date: 12/23/2020
Onset Date: 12/24/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Symptoms: headache; constipation; This is a spontaneous report from a contactable other HCP. A 30-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EK9231), intramuscular in left arm on 23Dec2020 at a single dose for covid-19 vaccination. The vaccine was administered in the workplace clinic. The patient's medical history and concomitant medications were not reported. The patient had no known allergies. The patient was not pregnant. On 24Dec2020, the patient experienced constipation and headache since vaccine (7 days). The outcome of the events was unknown. There was no treatment for the events. ON 24Dec2020, the patient had COVID test type post vaccination=Nasal Swab with a negative result. The events were assessed as non-serious.

Other Meds:

Current Illness:

ID: 0921271
Sex: F
Age:
State: PA

Vax Date: 12/22/2020
Onset Date: 12/26/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Symptoms: Extreme fatigue, body aches, and headaches that began around day 4 post vaccine.; Extreme fatigue, body aches, and headaches that began around day 4 post vaccine.; Extreme fatigue, body aches, and headaches that began around day 4 post vaccine.; This is a spontaneous report from a contactable Other HCP reporting for herself. A 50-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EK5730), Intramuscular on 22Dec2020 17:45 at single dose for covid-19 immunisation. Vaccine administered in left arm. Medical history included Anemia and Hypothyroidism. Patient is not pregnant. Concomitant medication was not reported. Patient had allergies to Levaquin. The patient experienced extreme fatigue, body aches, and headaches that began around day 4 post vaccine on 26Dec2020. Patient has not been tested for coronavirus disease (COVID-19). Patient was not diagnosed with COVID-19. Outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 0921272
Sex: M
Age:
State: VA

Vax Date: 12/17/2020
Onset Date: 12/18/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Symptoms: Stye developed over right eyelid; This is a spontaneous report from a contactable other hcp (patient). A 52-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Ek5730) intramuscularly at left arm on 17Dec2020 14:00 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Patient experienced stye developed over right eyelid on 18Dec2020 06:00. No treatment received. The event is non-serious. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was recovered on an unspecified date in Dec2020. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0921273
Sex: F
Age:
State: IN

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Vax Name:
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Symptom List:

Symptoms: Lot of swelling at my injection site and my glands under my arms; Lot of swelling at my injection site and my glands under my arms; This is a spontaneous report from a contactable consumer (patient). The 49-years-old female patient received first dose of bnt162b2 (BNT162B2, lot number: EL1284), unknown on an unknown date in Dec2020 at single dose for COVID-19 immunisation. Medical history included Allergy and asthma. Patient also took take allergy medicine and have to use an asthma inhaler. It was reported " I got the Pfizer COVID Vaccine and I had a lot of swelling at my injection site and my glands under my arms". When talking about treatment, Consumer stated, "I did ice, I did heat, I did allergy cream (Unspecified Medication), I didn't go to the doctor where they follow up with you and check on you, the swelling got up to like 6 inches." The outcome of the events was unknown. No follow-up attempts are needed.

Other Meds:

Current Illness:

ID: 0921274
Sex: F
Age:
State: VA

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Vax Name:
Lot:
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Vax Site:

Lab Data:

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Symptom List:

Symptoms: Felt tongue tingle; had a weird sensation on tongue. At first I thought I was tasting something but I wasn't; felt a bit of nausea which is a normal side effect; This is a spontaneous report from a contactable other hcp (patient). A 37-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899) via an unspecified route of administration at left arm on 29Dec2020 09:30 at single dose for COVID-19 immunization. No medical history. No known allergies. The patient's concomitant medications were not reported. The patient felt tongue tingle and had a weird sensation on tongue. At first she thought she was tasting something but she wasn't. This lasted for about 30 mins. She also felt a bit of nausea which was a normal side effect. She was not sure what the tongue feeling was. Events onset date was 29Dec2020 10:00. No treatment received. This report is non-serious. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There were not any other medications the patient received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was recovered on an unspecified date.

Other Meds:

Current Illness:

ID: 0921275
Sex: M
Age:
State: RI

Vax Date: 12/18/2020
Onset Date: 12/28/2020
Rec V Date: 01/05/2021
Hospital:

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Symptoms: developed a circular rash at injection site/localized; This is a spontaneous report from a contactable physician. A male patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 18Dec2020 at single dose for COVID-19 immunization. Medical history and concomitant medications were unknown. The reporting physician was inquiring about information related to development of a rash at the injection site, and to report an adverse event. The patient got vaccine on 18Dec2020. 10 days later, on 28Dec2020, the patient developed a circular rash at injection site/localized (circular "like lyme disease"). Localized rash was 3cm in diameter. Per reporter, the patient was "feeling otherwise okay". The patient had been tested negative for lyme disease. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921276
Sex: F
Age:
State: MO

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: tenderness or soreness; tenderness or soreness; This is a spontaneous report from a contactable consumer (patient) from a Pfizer Sponsored Program. A 73-year-old female patient received bnt162b2 (Pfizer-Biontech Covid-19 Vaccine), via an unspecified route of administration in Dec2020 at single dose for covid-19 immunization. Medical history included lupus. Concomitant medication included hydroxychloroquine sulfate (PLAQUENIL) for lupus. The patient experienced tenderness or soreness in Dec2020. She mentioned she read the fact sheet and felt nothing, there was only tenderness or soreness but it didn't bother. The outcome was unknown. Information on Lot/Batch number has been requested.

Other Meds: PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]

Current Illness:

ID: 0921277
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/05/2021
Hospital:

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Symptoms: Absolutely no side effects other than a sore arm; This is a spontaneous report from a Pfizer-sponsored program received from a non-contactable consumer. A patient of unspecified age and gender started to receive bnt162b2 (BNT162B2; reported as Pfizer Covid-19 vaccine; unknown lot number and expiration date), via an unspecified route of administration on an unspecified date at single dose for Covid-19 vaccination. The patient's medical history and concomitant medications were not reported. It was reported that it's been a week since the patient received the Pfizer Covid-19 vaccine. There were absolutely no side effects other than a sore arm for 2ish days (unspecified date). The patient will be the first to admit that the patient was skeptical and wasn't eager to jump in line. After a few conversations with trusted colleagues and researching reliable websites, the patient decided that this was the least the patient could do. The patient was eager to see friends and family. The patient also mentioned that the patient was eager for the hospital to not be busting at the seams. Eager to not work 5 nights a week to do his/her part and eager to not see his/her friends/colleagues exhausted. The patient was also selfishly anxious to travel again. This vaccine gives us a light at the end of a very long dark tunnel. It gives us the first glimmer of hope we've had all year. The outcome of the event was unknown. No follow-up attempts are possible. Information about Lot/Batch could not be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0921278
Sex: U
Age:
State: WV

Vax Date:
Onset Date:
Rec V Date: 01/05/2021
Hospital:

Vax Type:
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Vax Name:
Lot:
Dose Series:
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Symptoms: patient receive the first dose of the vaccine and has now tested positive for Covid; patient receive the first dose of the vaccine and has now tested positive for Covid; This is a spontaneous report from a Pfizer-sponsored program. A contactable pharmacist reported a patient of unspecified age and gender received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The pharmacist reported that they had a patient receive the first dose of the vaccine and has now tested positive for Covid. He stated the patient is a week out from receiving the second dose and asks what information Pfizer can provide on receiving the second dose for someone with Covid infection. Outcome of the event was unknown. Information on the Batch/Lot number has been requested.; Sender's Comments: Based on the information currently available, a lack of efficacy with BNT162B2 in this patient might not be completely excluded.

Other Meds:

Current Illness:

ID: 0921280
Sex: F
Age:
State: TX

Vax Date: 12/22/2020
Onset Date: 12/23/2020
Rec V Date: 01/05/2021
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Symptoms: Nervous; I had two new spot on my knee; I had another one on my shoulder and on my lower back/I am getting one may be on my ear like I said they pop up and they itch a little; Red patchy hives and itchy waves of red rashes all over the body; raised red rash on my left hip; Red patchy hives and itchy waves of red rashes all over the body; raised red rash on my left hip; Red patchy hives and itchy waves of red rashes all over the body; raised red rash on my left hip; This is a spontaneous report from a Pfizer-sponsored program. A contactable 38-year-old female Nurse (patient) reported that she received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EK5730, Expiry Date: 31Mar2021) at single dose since 22Dec2020. Relevant history and concomitant drug was none. The patient excepted Covid 19 vaccine could decrease the chance of contacting Covid 19 virus, while she stated she was getting a red patchy hives and itchy waves of red rashes all over the body just after received the vaccine. The patient (nurse) stated, "I would if I can explain a little more, the day after I received the Covid vaccine I had noticed a big like what I would explain it like a red hives, like a raised red rash on my left hip it last like a day its subsided and next morning I woke up and I had a different flares that was the same on my other side of my body again went away. After a day when I woke up and I had two new spot on my knee that was the other thing, those went away on that day. This morning I woke up and I had another one on my shoulder and on my lower back. I am also thinking I am getting one may be on my ear like I said they pop up and they itch a little and they go away. I never ever experienced anything like it and I see the only thing that I have changed in my life or regimen or added to my body so I just wanted to make sure it was reported. I am nervous and curious if it is a potential side effect added if I should be careful before getting second one all those things." No treatment was received for the events. Outcome of events was unknown. When probed for the Causality, the nurse stated, "I have no idea, if it is something going on with me that is completely unrelated its just occurred right after I got the vaccine so I have no idea if this is a separate issue or not. I going to see dermatologist and physician but until then I just thought to report it to you all to see if anybody is experiencing this and to know if it is safe to go for second dose."

Other Meds:

Current Illness:

ID: 0921281
Sex: F
Age:
State: IN

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/05/2021
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Symptoms: Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; Shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of n; This is a spontaneous report from a contactable other HCP. This 36-year-old female other HCP reported for herself that that she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Intramuscular at right arm at single dose for COVID-19 immunisation on 22Dec202008:00 AM. Relevant history included Endometriosis and allergies with Keflex, Levsin. Concomitant drug included bupropion SR which received within 2 weeks of vaccination. The patient experienced shortness of breath and tightness of chest 30 minutes after vaccine, rapid heart rate, pain and swelling at injection site, heavy feeling in entire arm and up to neck, swollen lymph nodes in back of neck 4 days after vaccine. Tightness on chest was gradually improving but comes and goes daily for the past week. The events was considered as non-serious. No treatment was received. The outcome of events was reported as recovered with lasting effects. The patient did not receive any other vaccines within 4 weeks prior to the COVID. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient been tested for COVID-19 with negative result per Nasal Swab on 23Dec2020. Information on the lot/batch number has been requested.

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Current Illness:

ID: 0921282
Sex: F
Age:
State: TN

Vax Date: 12/28/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: swelling and redness in the face; swelling and redness in the face; Muscle and body aches; Muscle and body aches; shortness of breath; headache/migraine; headache/migraine; runny nose; sneezing; soreness in upper and lower left arm; swelling in left arm and in both hands; This is a spontaneous report from a contactable Other HCP (patient). This 49-year-old female patient (not pregnant at the time of vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot#: EJ1685) at single dose on 28Dec2020 at 02:00 PM on left arm for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Medical history included fibromyalgia; skin lupus; sacroiliitis; chronic migraines; allergies to Latex, TB shot skin test, several foods, environmental things (trees, grass, pollen, cockroaches, etc.). Prior to vaccination, the patient was diagnosed with COVID-19. Concomitant medication was not reported. Since the vaccination, the patient had not been tested for COVID-19. On 29Dec2020 at 06:15 AM, the patient experienced swelling and redness in the face, muscle and body aches, shortness of breath, fatigue, headache/migraine, runny nose, sneezing, swelling in left arm and in both hands. There was not treatment received for all the adverse events. All events considered non-serious as all not resulted in death, not life threatening, not caused/prolonged hospitalization, not disabling/incapacitating, not congenital anomaly/birth defect. The outcome of events was not resolved.

Other Meds:

Current Illness:

ID: 0921283
Sex: F
Age:
State: TX

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: I broke out, I was sweating; Terrible headache; Chills; My body hurt; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: EJ1685), via an unspecified route of administration on 29Dec2020 at SINGLE DOSE for COVID-19 immunization. Medical history included seasonal allergy. Concomitant medication included cetirizine hydrochloride (ZYRTEC) for seasonal allergy. On 29Dec2020 (within a few minutes), she broke out and was sweating. She had sweat at her face and sweated in her clothes. The patient also have a terrible headache, her body hurt and have chills. The patient did not receive any treatment for the events and was going to ask if she can take diphenhydramine (BENADRYL) as she do not know what to do. She doesn't know if she can take medicine because it was terrible. Outcome of the events were unknown.

Other Meds: ZYRTEC

Current Illness:

ID: 0921284
Sex: U
Age:
State:

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Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: lost my sense of smell and tested positive for Covid; lost my sense of smell and tested positive for Covid; This is a spontaneous report from a non-contactable consumer (patient) received via a Pfizer-sponsored program. A patient of unspecified age and gender received BNT162B2 via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The content of a post was noted that on Dec2020, "Got mine! And in a stroke of weird ironic awfulness, lost my sense of smell and tested positive for Covid later that day....If only a month sooner! Thank you for creating this vaccine. I know it had nothing to do with my diagnosis!". The outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. Sender's Comments: The events drug ineffective and COVID 19 are likely intercurrent and are unrelated to suspect drug BNT162B2 based on the short temporal relation between vaccination and onset of events.

Other Meds:

Current Illness:

ID: 0921285
Sex: F
Age:
State: RI

Vax Date: 12/21/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: Mild to severe headache behind her eye and sinus area; Mild to severe headache behind her eye and sinus area; This is a spontaneous report from a contactable consumer. A 52-year-old female patient received bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on 21Dec2020 at 10:15 AM, at single dose, for COVID-19 immunisation. Medical history included peanut allergy, penicillin allergy and nut allergy (unknown if ongoing). Prior to vaccination the patient was not diagnosed with COVID-19. Concomitant medications were not reported. The patient experienced mild to severe headache in Dec2020, days after the COVID-19 injection. Main complaint was headache behind her eye and sinus area. The event required physician office visit on 29Dec2020. It was unknown if the event required any treatment. The events was considered as non serious. The patient was unsure if this was related to the vaccine but informed the reporter. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0921286
Sex: F
Age:
State: SC

Vax Date: 12/21/2020
Onset Date: 12/21/2020
Rec V Date: 01/05/2021
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Symptoms: Body aches, chills and body temperature max of 101.2 F; Body aches, chills and body temperature max of 101.2 F; Body aches, chills and body temperature max of 101.2 F; she should not have taken the vaccine with us; This is a spontaneous report from a contactable nurse. A female patient of an unspecified age received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on 21Dec2020, at single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced body aches, chills and body temperature max of 101.2 F on 22Dec2020 with outcome of recovered on 23Dec2020. On 22Dec2020 she spent the day in bed. The reporting nurse stated that the patient was part of a trial study. She was vaccinated in a blind study on 28Nov2020. The patient told the reporter on 23Dec2020 that she called the intake person the week before and they told her to take the vaccine here with Pfizer. She called them back after she experienced the events and spoke with a different person who stated she should not have taken the vaccine with Pfizer. They will not un-blind her at this point either. The reporter felt certain based on her response last week that she must have received the vaccine on 28Nov2020 and not the placebo. The patient wished to drop from the study and take the 2nd Pfizer vaccine in 3 weeks. Her PCP agreed that she should do so. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921287
Sex: F
Age:
State: FL

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: she is positive that she is positive" and is having symptoms, although not yet been tested; she is positive that she is positive" and is having symptoms, although not yet been tested; This is a spontaneous report from a contactable pharmacist (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), via an unspecified route of administration on Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reportedly asking if she should keep her appointment for the second dose of the vaccine as scheduled if she thinks she was positive for COVID and having symptoms. The patient had vaccine on Tuesday (Dec2020), and husband tested positive yesterday, "she was positive that she was positive" and was having symptoms, although not yet been tested. The 2nd dose was in 2 weeks. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: Based on the information currently provided, the company considers that a causal relationship between the suspected COVID-19 and vaccination with BNT162B2 cannot be excluded.

Other Meds:

Current Illness:

ID: 0921288
Sex: F
Age:
State: TN

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/05/2021
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Symptoms: headache; Muscle aches; Chills; 102.5 fever; This is a spontaneous report from a contactable Nurse. A 49-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number EJ1685), via an unspecified route of administration on 28Dec2020 09:00 at Arm Left at single dose for COVID-19 immunisation. Medical history included Low thyroid, Covid (diagnosed with COVID-19: Yes). Concomitant medication included levothyroxine sodium (SYNTHROID). The patient experienced muscle aches, chills, headache, 102.5 fever on 28Dec2020 18:00. All events were non serious. No treatment was received. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. No allergies to medications, food, or other products. The patient underwent lab tests and procedures which included body temperature: 102.5 on 28Dec2020. The outcome of the events was resolved in Dec2020. No follow up attempts are possible. No further information is expected.

Other Meds: SYNTHROID

Current Illness:

ID: 0921289
Sex: F
Age:
State: NJ

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/05/2021
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Symptoms: deltoid muscle pain in left arm where she got the shot; Left arm feeling heavy in within 2 hours of vaccination, hard to lift up; she was feeling very tired and in day-2 she felt fatigue; This is a spontaneous report from a contactable consumer reporting for a patient. A 48-year-old female patient received first dose of BNT162B2, (Pfizer-BioNTech Covid-19 Vaccine, lot number EH9899) , via an unspecified route of administration on 28Dec2020 10:00 at single dose on left arm for COVID-19 vaccination. The patient's medical history was not reported. Concomitant medications were none. The patient experienced deltoid muscle pain in left arm where she got the shot (28Dec2020 12:00). Left arm feeling heavy in within 2 hours of vaccination, hard to lift up (28Dec2020 12:00). In the afternoon she was feeling very tired and in day-2 she felt fatigue, took Tylenol multiple times a day. On day-3 she felt perfectly fine and no pain was left. Functioning properly. No known allergies. The patient did not receive other vaccine in four weeks. No covid prior vaccination; no covid tested post vaccination. The patient was not pregnant at the time of vaccination. Therapeutic measures were taken as a result of deltoid muscle pain in left arm where she got the shot. The outcome of the events was resolved on an unspecified date.

Other Meds:

Current Illness:

ID: 0921290
Sex: F
Age:
State: NC

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: really tired; heart pounding; couldn't sleep; Headache; sore arm; She couldn't sleep because she was anxious.; almost felt like her blood pressure was up.; Her heart rate is usually 60-65 bpm, but last night it was up to 75-80 bpm; This is a spontaneous report from a contactable consumer. A 33-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number EIC9231), via an unspecified route of administration on 29Dec2020 11:30 at single dose for COVID-19 immunisation. Medical history was none. There were no concomitant medications. The patient was calling to report that she got the COVID vaccine yesterday, and she wanted to put input in on the effects she experienced last night. She is a pharmacy transition specialist. She doesn't have a prescribing doctor. A few hours after, she was really tired. She could have fallen asleep at her desk. Then, last night, her heart was like pounding but not beating fast if that makes since. Her heart rate wasn't up that much, but it felt like it was going to come out of her chest. She couldn't sleep because of it. She had a headache. She received the vaccine at 11:30. She is not as tired today. Yesterday, she could have just laid head back and went to sleep. The rest of the side effects started right after dinner. She couldn't sleep because she was anxious. Her heart rate is usually 60-65 bpm, but last night it was up to 75-80 bpm. It almost felt like her blood pressure was up. This happened right around after dinner. The headache is hanging over into today. It could be still there because she didn't sleep. Her arm is sore still. It isn't serious. The handwriting was bad on her card so it was hard for her to read the lot number. The outcome of the event Headache, sore arm was not resolved, the outcome of the event really tired was resolving, the outcome of the event heart pounding was resolved in Dec2020, while the outcome of the other events was unknown.

Other Meds:

Current Illness:

ID: 0921291
Sex: F
Age:
State: MD

Vax Date: 12/29/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: arm was hurting/very sore arm; have a really bad headache; teeth ache; muscle and joint pain; muscle and joint pain; chills; low grade fever 99.7; sore throat; congestion; This is a spontaneous report from a contactable nurse (patient). A 68-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, 3 ug/ml) Batch/lot number: EL1284, on 29Dec2020 12:33 single dose on left arm for COVID-19 immunization. Medical history included Blood pressure high which diagnosed a long time ago, probably when she was 45 years old, though it could have been when she was 42 or 43, probably earlier, 25 years ago, so put when she was 42; hemochromatosis diagnosed about 25 years ago; Arthritis; Cluster headaches; low thyroid and she didn't take medication for this, it wasn't low enough; COVID-19 in Mar2020. Concomitant medication was none. The patient received the Pfizer covid vaccine yesterday (29Dec2020) and she called the line to report the side effects today. She said she had covid around the Easter time and donated her plasma also for antibodies. She said after getting the vaccine yesterday she was feeling worse, have a really bad headache, teeth ache, arm was hurting woke up due to that in the night, really bad headache, muscle and joint pain, chills , low grade fever 99.7 , sore throat and congestion. The patient received the vaccine through work, and was not prescribed it from a provider. She had her shot at 12:33PM yesterday (29Dec2020), after lunch. Her vaccine was given to her at the hospital where she worked, which was not a military hospital. Her side effects were that she developed a headache, also her teeth were aching, and then last night around 04:00AM in the morning she woke up with a very sore arm and worse headache. She said she also had muscle and joint pains, chills, and fever. She said now she still had a headache, and still didn't feel good. Treatment received for the events included Ibuprofen and Tylenol. Ibuprofen was clarified to being generic Ibuprofen prescription in a pharmacy bottle with EXP 3 09Mar2021 and NDC: 67877032005. She said that the strength of this medication is 600mg, and she just took one last night by mouth at about four in the morning. She says she also took Tylenol before bed, 500mg, this is the name brand product. UPC/LOT/EXP: unknown, she didn't have it with her she said it was in date and was brand new, in to go packs. She said that her teeth aching was gone, she still had her headache, muscle pain, fever, and her arm hurt. She said she did take another Tylenol a half hour ago or 45 minutes ago. Her low grade fever temperature was 99.7 degrees Fahrenheit. She had COVID-19 before, she tested positive for COVID at Easter time, this was in March, they did a PCR nasal swab. She had two positive tests and then a negative test because they had to retest her to get plasma, she had to be negative before she could get plasma. She also had an antibody test a couple months after she had COVID, that showed she had 27 antibodies. She had COVID, then a couple of weeks later she gave plasma, and then a few weeks later had the antibody test that showed she had the 27 antibodies. The outcome of teeth ache was resolved. The outcome of headache, muscle pain, fever, and her arm hurt was not resolved. The outcome of other events was unknown.

Other Meds:

Current Illness:

ID: 0921292
Sex: F
Age:
State: OK

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 01/05/2021
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Symptoms: Headache, Extreme Fatigue; Headache, Extreme Fatigue; This is a spontaneous report from a contactable Other-HCP. A 66-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number Unknown), intramuscular at Left arm on 23Dec2020 10:00 at single dose for covid-19 immunisation. Medical history included Diabetes mellitus, Known allergies: penicillin. Concomitant medication included metformin. The patient experienced headache, extreme fatigue on 23Dec2020 23:00. Both events were non serious. No treatment was received. The patient was not Pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. No allergies to medications, food, or other products. The outcome of the events was resolved in Dec2020. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0921294
Sex: F
Age:
State: TN

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: eye pain; sensitivity to light; headache/Headache worsened/migraine; This is a spontaneous report from a non-contactable healthcare professional. A 40-year-old female patient received BNT162B2 on 29Dec2020 12:30 at left arm at single dose for COVID-19 immunization. Medical history included chronic kidney disease. Concomitant medications included labetalol, lisinopril, tolvaptan (JYNARQUE), calcium, and ascorbic acid/ferrous fumarate (VITRON C). Patient experienced headache the night on 29Dec2020 21:00 after took the vaccine. Slept the night without much trouble. Headache worsened in the morning, almost felt like a migraine attack with sensitivity to light and eye pain etc. on 30Dec2020. Treatment was not received for these events. Outcome of the events was not resolved. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: ; ; JYNARQUE; ; VITRON C

Current Illness:

ID: 0921295
Sex: F
Age: 31
State: CA

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Allergies: No

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Symptoms: Extreme pain in arm for 72 hrs. Continued pain for 2 more days.

Other Meds: Birth Control

Current Illness: No

ID: 0921296
Sex: F
Age:
State: OK

Vax Date: 12/28/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: chest tightness; 103.8; Fatigue; body aches; headache; nausea; This is a spontaneous report from a contactable other healthcare professional (HCP). This 52-year-old female HCP reported for herself that she received 1st dose of BNT162B2 intramuscular at left arm on 28Dec2020 08:30 AM for Covid-19 immunization. Medical history included COVID-19 and concomitant drugs were not provided. The patient did not realize vaccine should be taken 90 days after a covid infection tested positive on 12Jan2020. The patient received vaccine on 28Dec2020, she experienced 103.8, fatigue, body aches, headache, nausea, and some chest tightness on 29Dec2020 at 09:00 AM. No treatment was received. The outcome of the events was resolving. The events were reported non-serious. Information about lot/batch number has been requested.

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Current Illness:

ID: 0921297
Sex: F
Age:
State: AZ

Vax Date: 12/27/2020
Onset Date: 12/28/2020
Rec V Date: 01/05/2021
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Symptoms: 2 vesicles appeared on roof of mouth; Red bumps (rash) appeared in mouth; Left arm also very stiff/sore; Left arm also very stiff/sore; This is a spontaneous report from a contactable other healthcare professional (HCP). This 35-year-old female HCP reported for herself that she received BNT162B2 (lot number EH9899) 1st dose Intramuscular at left arm on 27Dec2020 at 12:00 PM for Covid-19 immunization. Medical history was not provided. Concomitant therapy included birth control. The patient experienced red bumps (rash) appeared in mouth, and 2 vesicles appeared on roof of mouth within 24-32 hours after receiving vaccine. Left arm also very stiff/sore for 24 hours after receiving vaccine. Event onset time was reported as 12:00 PM on 28Dec2020. No treatment was received for the events. The outcome of the event was resolving.

Other Meds:

Current Illness:

ID: 0921298
Sex: F
Age:
State: IN

Vax Date: 12/20/2020
Onset Date: 12/21/2020
Rec V Date: 01/05/2021
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Symptoms: some swelling on the underside of this same arm; This is a spontaneous report from a contactable consumer(patient). A 57-year-old female patient received her 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EJ1685) at single dose via an unknown route in her right arm on 20Dec2020 09:50 for Covid-19 immunization. Medical history and concomitant drug were not provided. Past drug history included a reaction to an antibiotic, cefadroxil (DURICEF). Patient received her initial Covid-19 vaccine in her right arm and noted some swelling on the underside of this same arm on 21Dec2020. She wanted to know if this might be associated with the vaccine. Patient stated she had that got the vaccine on 20Dec2020 at 9:50AM in the right arm, that on Monday the next day, 21Dec2020, she got this swelling under her arm. Patient stated did not know if it had anything to do with that, wanted to know if it is a side effect. Patient stated that the swelling started on Monday the next day, 21Dec2020. Patient stated the swelling has improved but she was going to the doctor to make sure everything was okay. Patient stated that years ago she had a reaction to an antibiotic, cefadroxil. She asked her doctor if she should get the shot because of that and they told her she should, states this happened like 25 years ago as of 30Dec2020, no details known. Outcome of the event was resolving.

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Current Illness:

ID: 0921299
Sex: F
Age: 50
State: MD

Vax Date: 12/28/2020
Onset Date: 12/30/2020
Rec V Date: 01/05/2021
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Allergies: dust

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Symptoms: Red face rash morning of 2 days following vaccine Dull headache, day of vaccine

Other Meds: Enalopril, 25mg Synthroid, 100 micrograms Multivitamin

Current Illness: none

ID: 0921301
Sex: F
Age:
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Vax Date: 12/22/2020
Onset Date: 12/24/2020
Rec V Date: 01/05/2021
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Symptoms: rash/legs are all rash/checked her back and told her there was a rash; itchy in back; This is a spontaneous report from a contactable healthcare professional. A 61-year-old female patient received BNT162B2 (Pfizer-Biontech Covid-19 Vaccine), via an unspecified route of administration on 22Dec2020 at left arm at single dose for COVID-19 immunisation. Medical history included ongoing diabetes from about 3-4 years before, and an allergic reaction to the dye when testing heart - couldn't remember the dye put in. She was allergic to that and sent to the ER because her throat was starting to close up about 3 years before. Concomitant medications were none. Patient received the Covid vaccine and developed rash on 24Dec2020 that was worsening and she asked if there was any recommendation on whether this was it going to get worse. Patient received the vaccine and was very worried because she was really itchy in back and her legs were all rash and in her back. She was starting to itch really bad. This was after 2 days of the vaccine (on 24Dec2020). She didn't take note until it came to her back and her friend checked her back and told her there was a rash. She asked if this could be related to the vaccine. She asked was this a severe reaction and should she receive the next dose. Her second dose was scheduled for 08Jan2021. She did not know at this time if she would get the second dose as scheduled or not. Onset of rashes started on her legs; she thought it would go away; but the rashes had worsened; they were now on her back and were getting really itchy; she had a friend look at it who told her she had patches of rashes on her back. She reported that she was going to contact her doctor about this information because she was scared about the rashes. Outcome of the events was not resolved. Lot/Batch and Expiration date has been requested.

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Current Illness: Diabetes

ID: 0921302
Sex: F
Age:
State: NC

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/05/2021
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Symptoms: Headache; Hypertension; Face flushed; Extremely tired; Slow Motion; Slurred Speech; This is a spontaneous report from a contactable healthcare professional. A 38-year-old female patient started to receive BNT162B2 (lot number: EJ1685), intramuscularly on 29Dec2020 08:00 at left arm at single dose for COVID-19 immunization. Medical history included hypertension. Concomitant medications were not reported. Patient previously took metronidazole (FLAGYL) and experienced allergy. Patient experienced headache, hypertension, face flushed, extremely tired, slow motion, and slurred speech on 29Dec2020 09:30. Treatment was not received for these events. Outcome of the events was resolving.

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Current Illness:

ID: 0921303
Sex: F
Age: 42
State: FL

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/05/2021
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Allergies: Clindamycin- causes anaphylaxis

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Symptoms: Describes feeling 'weird". dizzy, slightly SOB, felt large lump in back of throat- felt similar to when she has experienced an allergic reaction. she did not report it to observers but later reported to me after arriving home and still not feeling 100% back to baseline. she stayed in observation area for 40 minutes post vaccine. Reports that she will consult her medical provider to decide if she should take the 2nd dose.

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Current Illness: none

ID: 0921304
Sex: F
Age:
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Vax Date: 12/23/2020
Onset Date: 12/01/2020
Rec V Date: 01/05/2021
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Symptoms: I need a root canal, I have pain; a little bit of sour stomach; This is a spontaneous report from a non-contactable Other Health Professional for herself. A female patient of an unspecified age started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose number 1, via an unspecified route of administration on 23Dec2020 at single dose for covid-19 immunisation.The patient medical history and concomitant medications were not reported. Patient asked can she now take amoxicillin a week after getting first dose? Patient received the first dose on 23Dec2020. Patient though she needs a root canal, she had pain. Patient had a little bit of sour stomach after receiving the COVID 19 vaccine. Patient heard some people got more of a dose than they should have and wound up in the hospital. Action taken in response to the events for BNT162B2 was not applicable. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 0921305
Sex: F
Age:
State: LA

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 01/05/2021
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Symptoms: Rash on legs and arms developed 12-24 hours after vaccine administered. Lasted one day. Treated with OTC medication.; This is a spontaneous report from a contactable consumer. This consumer reported for a 40-year-old female patient (no pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK5730) on 23Dec2020 at single dose in left arm for covid-19 immunization. Medical history was not reported. Concomitant drug was Spironolactone in two weeks. It was reported that patient experienced Rash on legs and arms developed 12-24 hours after vaccine administered on 23Dec2020. Lasted one day with outcome was recovered. Treated with OTC medication. Patient was not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient not been tested for COVID-19. No Allergies to medications, food, or other products. No follow up attempts are needed. No further information is expected.

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Current Illness:

ID: 0921306
Sex: F
Age:
State: KS

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 01/05/2021
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Symptoms: Also c/o tingling in hands and feet; dizziness; This is a spontaneous report from a non-contactable other HCP. This other HCP reported for a 32-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EH9899) Intramuscular on 18Dec2020 at single dose in Right arm for covid-19 immunization. Medical history and concomitant drug were not reported. She was given the Pfizer vaccination in the right deltoid muscle. During her 15 minutes waiting period after the injection, the patient began to experience dizziness. Also c/o tingling in hands and feet. She denied rash, hives, difficulty breathing, difficulty swallowing, wheezing, throat tightness, hoarseness, itching and tongue swelling. This provider was notified of patient reaction and she was then assessed in the emergency bay area. Treatment included water, granola bar, and rest. Outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 0921307
Sex: F
Age: 48
State: WA

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/05/2021
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Allergies: Gentamicin

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Symptoms: Symptoms: eyelids swelling/itching, nasal/sinus swelling, nasopharyngeal swelling, circumoral swelling-around mouth and lips, not inside mouth. Administered nasal Flonase 2 pumps each nare and 50 mg Benadryl at 2230. At 0430 next morning 12/29, swelling decreased, eyelids remained swollen and minimal swelling in nasal/sinus area. Continued Benadryl 50 mg every 6 hours x 3 doses, by 1900 on 12/29 swelling resolved

Other Meds: levothyroxine .05mg/daily, pantoprazole, B-12, milk thistle, calcium, probiotic

Current Illness: respiratory symptoms (covid neg) from 12/20-12/26-mild cough, nasal congestion

ID: 0921308
Sex: F
Age:
State: TN

Vax Date: 12/26/2020
Onset Date: 12/27/2020
Rec V Date: 01/05/2021
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Symptoms: Body aches; low grade fever; chills, shivering; headache; nausea; stiff/sore arm; stiff/sore arm; This is a spontaneous report from a contactable Other Health Professional for herself. A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EJ1685) dose number 1, intramuscularly on 26Dec2020 15:30 at single dose on arm Left for COVID-19 immunization. Medical history included irritable bowel syndrome, chicken allergy and COVID-19. Concomitant medications received within 2 weeks of vaccination included clonazepam, spironolactone and melatonin, all from unknown date for unknown indication. Onset of symptoms began roughly 9hrs post vaccine. Lasted roughly 24 hours (28Dec2020). Body aches, low grade fever, chills, shivering, headache, nausea, stiff/sore arm. Adverse event start date: 27Dec2020 00:00. No treatment was received for the events. The action taken in response to the events for BNT162B2 was not applicable. Outcome of the events was resolved on 28Dec2020.

Other Meds: ; SPIRONOLACTON;

Current Illness:

ID: 0921309
Sex: F
Age:
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Symptoms: During her 15 minute waiting period after the injection, the patient began to experience dizziness, anxiety.; During her 15 minute waiting period after the injection, the patient began to experience dizziness, anxiety.; This is a spontaneous report from a non-contactable other health professional. A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EH9899) dose number 1, intramuscularly on an unspecified date at single dose on left arm (left deltoid muscle) for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. She had no history of previous hypersensitivity reactions to immunizations. During her 15 minutes waiting period after the injection, the patient began to experience dizziness, anxiety. She denied rash, hives, difficulty breathing, difficulty swallowing, throat tightness, hoarseness, itching, facial swelling and tongue swelling. This provider was notified of patient reaction and she was then assessed in the emergency. Monitored patient for severe reaction symptoms, including rapid progression of symptoms, respiratory distress with stridor, wheezing, dyspnea and increased work of breathing, vomiting and abdominal pain. Planned action included: observation, serial examination. The action taken in response to the events for BNT162B2 was not applicable. Outcome of the events was unknown. Assessment by reporter: transient anxiety associated with COVID vaccine administration. No follow-up attempts are possible. No further information is expected.

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Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 03 October 2021 5:28pm