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: 0993577
Sex: F
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/17/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: bumps that were flesh/skin tone, not red, on her hands/she developed bumps on her palms and fingers; bumps on her palms and fingers; This is a spontaneous report from a contactable nurse (patient). A 52-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK5730) on 08Jan2021 at single dose for COVID-19 immunisation (to prevent COVID). Medical history and concomitant medication were none. patient received vaccine on 08Jan2021 and 9 days later (17Jan2021) developed "bumps that were flesh/skin tone, not red, on her hands", she asked if this has been associated with the product. Patient sked if there have been any reports of coxsackievirus (Hand-foot-mouth disease) with the vaccine. It was also reported she says got the first vaccine 08Jan and 9 days later she developed bumps on her palms and fingers, it happened this Sunday. She doesn't know if it might be work related she works with cleaning supplies and wearing gloves in the hospital but she did get the vaccine so she is wondering if that is a side effect that anyone else has called about. She clarifies the bumps are not red they are skin color, they are only red if she scratches them. When they started out she only had about 3 now she has about 20. Patient was not recovered from the events. It was a non-serious report.

Other Meds:

Current Illness:

ID: 0993578
Sex: F
Age:
State: VA

Vax Date: 01/14/2021
Onset Date: 01/16/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: felt a strong pain in the chest; injection site was color purple; injection site was color red, swollen and with pain; injection site was color red, swollen and with pain; injection site was color red, swollen and with pain; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot number not reported, via an unspecified route of administration from 14Jan2021 to 14Jan2021 as SINGLE DOSE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated that 2 days after the administration, the injection site was color red, swollen and with pain; 3 days after the administration the injection site was color purple; and 4 days after the administration she felt a strong pain in the chest. The outcome of the events was unknown. Information on lot/batch has been requested.

Other Meds:

Current Illness:

ID: 0993579
Sex: F
Age:
State:

Vax Date: 12/29/2020
Onset Date: 01/11/2021
Rec V Date: 02/02/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Vax Site:

Lab Data:

Allergies:

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

Symptoms: received first dose of the vaccine on 29Dec2020 and tested positive for COVID on 11Jan2021; received first dose of the vaccine on 29Dec2020 and tested positive for COVID on 11Jan2021; 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 provided), via an unspecified route of administration on 29Dec2020 at SINGLE DOSE for COVID-19 immunisation. Patient's medical history and concomitant medications were not reported. It was reported that the patient received first dose of the vaccine on 29Dec2020 and tested positive for COVID on 11Jan2021. Patient was scheduled for her second dose this week and stated she is trying to figure out what to do. Patient asked if there are side effects if she get is earlier that the suggested 90 days. Patient also asked if there is a recommendation on what to do if it ended up running out of the vaccine before she gets her second dose. The patient underwent lab tests and procedures which included sars-cov-2 test with result of positive on 11Jan2021. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events Drug ineffective and COVID-19 cannot be totally excluded. The case will be reassessed if additional information becomes available.

Other Meds:

Current Illness:

ID: 0993580
Sex: F
Age:
State: IL

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: dizziness; aches; fever; sniffles; pain at injection site; This is a spontaneous report from a contactable health care professional (patient). A 72-year-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number requested) via an unspecified route of administration on 13Jan2021 at 07:00 PM on the left arm at a single dose for COVID-19 immunization. Medical history included hypothyroidism and allergies to eggs both from an unknown date and unknown if ongoing. Concomitant medication included levothyroxine sodium (SYNTHROID). The patient did not have COVID-19 prior to vaccination. It was reported that on 14Jan2021 at 07:00 AM, 12 hours after the vaccine, the patient experienced dizziness, aches, fever, sniffles and pain at injection site. The outcome of the events was recovered on an unspecified date in Jan2021. The patient did not receive any treatment for the events. The patient has not been tested for COVID-19 post vaccination. Information on the lot/batch number has been requested.

Other Meds: SYNTHROID

Current Illness:

ID: 0993581
Sex: M
Age:
State: NC

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

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

Lab Data:

Allergies:

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

Symptoms: Has some injection site pain/ Pain injection site; Body Aches; Pain in the opposite shoulder/the pain in the right Shoulder; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer, the patient. A 69-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EL3248) solution for injection intramuscular in the left arm on 18Jan2021 (at the age of 69-years-old) as a single dose for COVID-19 vaccination. Medical history included rotator cuff surgery (1.5 years ago, moving the shoulder around freely time to time and then it flares up time to time) and positive Covid test on 17Mar2020. There were no concomitant medications. On 18Jan2021, the patient experienced has some injection site pain/pain injection site and body aches. In Jan2021, the patient experienced pain in the opposite shoulder/the pain in the right shoulder. The outcome of the events injection site pain and body aches was recovering. The outcome of the event shoulder pain was unknown.

Other Meds:

Current Illness:

ID: 0993582
Sex: F
Age:
State: MD

Vax Date: 12/31/2020
Onset Date: 01/12/2021
Rec V Date: 02/02/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Vax Site:

Lab Data:

Allergies:

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

Symptoms: Left eye being swollen almost shut with some clear discharge; Left eye being swollen almost shut with some clear discharge; Half of the right side of her face was swelling and being numb; Half of the right side of her face was swelling and being numb; On and off chills; Sweating; Headache; Fever; This is a spontaneous report from a contactable healthcare professional (patient). A non-pregnant 27-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EJ1685), via an unspecified route of administration in left arm, on 31Dec2020 at 09:30, at a single dose, for COVID-19 immunization. The patient's medical history included enlarged thyroid (normal for her), painful menstruations, allergies to cats, dogs, and dust, seasonal allergies, and birth control. The patient's concomitant medication included ethinylestradiol/ norethisterone acetate (JUNEL) as birth control. The patient was not diagnosed with COVID-19 prior vaccination. No other vaccine was administered in four weeks. The vaccine was administered in a hospital facility. On 12Jan2021 at 06:15 AM, the patient woke up from sleep with her left eye being swollen almost shut with some clear discharge and half of the right side of her face was swelling and being numb. This persisted for about 3 days with on and off chills, sweating, headache, and a fever on 12Jan2021 (06:15). The symptoms completely dissipated on 22Jan2021. The adverse events resulted in doctor or other healthcare professional office or clinic visit. No treatment was received for the events. The patient got a COVID-19 test on 13Jan2021 just to be safe which came back as negative. The patient recovered from the events on 22Jan2021.

Other Meds: JUNEL

Current Illness:

ID: 0993583
Sex: F
Age:
State: ID

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 02/02/2021
Hospital:

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

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: sore arm; joint pain that started in the left elbow and moved down to the wrist/hand and eventually joint pai; body aches all over; This is a spontaneous report from a contactable nurse (patient). A 26-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL0140, expiration date was not reported), intramuscular in left arm on 18Dec2020 12:00 at a single dose for COVID-19 immunization. Medical history included headaches of an unknown origin from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient was not pregnant. She did no receive any other vaccine four weeks prior covid vaccine. She did not have covid prior to vaccination. She was not tested for covid post vaccination. She had no known allergies. The patient reported adverse events for the first shot: Sore arm, joint pain that started in the left elbow and moved down to the wrist/hand and eventually joint pain; and body aches all over for the next 2 days. The events' onset was on 18Dec2020 at 07:00 PM. Outcome recovered for events 'Sore arm, joint pain that started in the left elbow and moved down to the wrist/hand and eventually joint pain' was recovered in Dec2020, while body aches all over was recovered on 20Dec2020.No treatment received for the events.

Other Meds:

Current Illness:

ID: 0993584
Sex: F
Age:
State: MA

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

Vax Type:
Manufacturer:
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Lot:
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Vax Site:

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Tiredness; chills; fever; This is a spontaneous report from a contactable nurse. A 55-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand: Pfizer, lot unknown: True, lot unknown reason: not available/provided to reporter at the time of report completion) intramuscularly at right arm on 18Jan2021 at 12:00 PM at a single dose for COVID-19 immunization. Medical history included known allergies: penicillin. Other medical history was reported as none. No other vaccine in four weeks. Other concomitant medications were unknown. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand: Pfizer) intramuscularly at right arm on 28Dec2020 at 01:00 PM at a single dose for COVID-19 immunization. Facility type vaccine was at Hospital. The patient was not pregnant. The patient experienced adverse events included tiredness, chills, fever; with start date on 19Jan2021 at 04:30 AM. No treatment received for events. The outcome of events was resolving. No COVID prior vaccination and no COVID tested post vaccination. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993585
Sex: F
Age:
State: AZ

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Prolonged fever (102); shaking chills; body aches; headache; nausea; lightheadedness; fatigue; This is a spontaneous report from a contactable physician reported for herself. A 39-year-old female patient (not pregnant) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EK9231, on 18Jan2021 11:30 at single dose in left arm for covid-19 immunization. Medical history was not reported. Concomitant medication included Prenatal vitamins. The patient previously had allergies to Spironolactone. The patient previously received first dose of BNT162B2 lot number EK5730 on 28Dec2020 11:30 AM in left arm at the age of 39-year-old. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced Prolonged fever (102), shaking chills, body aches, headache, nausea, lightheadedness, fatigue on 18Jan2021 21:00. Treatment received for all events included Tylenol. The patient was not diagnosed with COVID-19 Prior to vaccination. The patient had not been tested for COVID-19 Since the vaccination. The outcome of all events was resolving.

Other Meds: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS

Current Illness:

ID: 0993586
Sex: M
Age:
State: PA

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: dizziness; His head felt like it was too heavy; threw up; flu like symptoms; discomfort in his neck; nausea; tiredness; This is a spontaneous report from a contactable consumer (patient). A 49-year-old male patient received BNT162B2 (lot number: EL3249, expiration date: May2021) first dose on 13Jan2021 15:10 to 15: 20 intramuscular injection in right arm at single dose for covid-19 immunization. Medical history included Type II diabetes mellitus, High cholesterol and Blood pressure, all diagnosed about 15 years ago and ongoing. Concomitant medications included insulin glargine (LANTUS) for diabetes, insulin aspart (NOVOLOG) for diabetes, metformin for diabetes, lisinopril for High cholesterol and pravastatin to control blood pressure, all ongoing. None History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available. None Additional Vaccines Administered on Same Date of the Pfizer Suspect. Prior Vaccinations (within 4 weeks) was none. AE(s) following prior vaccinations was None. He is supposed to get second dose on 04Feb2021. He sat for 15 minutes after getting the shot and he had no reaction. About an hour or two into his shift for work he started having nausea, tiredness, and his neck was killing him, like something was on his neck, a discomfort in his neck. He worked through his shift. He was going through discomfort flu-like symptoms through Friday (15Jan2021). He thought he was ok as of Sunday. He went to work yesterday and his shift started at 6am, he was ok and then through breakfast, the room started to spin and he was experiencing dizzy spells (18Jan2021), nausea and his neck was extremely uncomfortable. His head felt like it was too heavy. He went to his supervisor to ask to go to the back and he threw up once and then he threw up again. He had to leave work around 12-12:30. He was told to go home. He is to go back to work tomorrow. He is hoping that he feels better tomorrow. Treatment: He took Tylenol. He took a lift home and he stayed in bed all day yesterday. His wife gave him some soup last night. He is not experiencing tiredness, nausea, discomfort in his neck as of now since he is laying down and not on his feet. He feels ok and he is not really experiencing anything of the events mentioned right now since he is laying down and trying to rest. Events not require a visit to Emergency Room or Physician Office. The outcome of the events was unknown.

Other Meds: LANTUS; NOVOLOG; METFORMIN; LISINOPRIL; PRAVASTATIN

Current Illness: Blood pressure abnormal (diagnosed about 15 years ago); High cholesterol (diagnosed about 15 years ago); Type II diabetes mellitus (diagnosed about 15 years ago)

ID: 0993587
Sex: F
Age:
State: NY

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

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

Lab Data:

Allergies:

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

Symptoms: Chills; Upset stomach; Severe headache; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient 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 as vaccine. Medical history included SARS-Cov-2 in Mar2020. Concomitant medications were not reported. The patient was experiencing chills, upset stomach and severe headache on unspecified dates. She took extra strength Tylenol. She asked if she should receive second dose and about efficacy without second dose. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993588
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Tenderness at injection sight, severe enough to awaken during the night; Tenderness at injection sight, severe enough to awaken during the night; The day after the injection, I broke out in sweats to the point that my shirt was wet; This is a spontaneous report from a non-contactable nurse reported for herself. A currently 50-year-old (reported age at vaccination was 50) female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular at left arm on 11Jan2021 at single dose for covid-19 immunization in Hospital. Medical history was not reported. Patient is not pregnant at the time of vaccination. Not allergies to medications, food, or other products. Concomitant medications were not reported. the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient previously took first dose of bnt162b2 on 22Dec2020 via Intramuscular at left arm at single dose for covid-19 immunization. Patient experienced tenderness at injection sight, severe enough to awaken during the night (12Jan2021); relieved with ibuprofen. Lasted about one week. The day after the injection, patient broke out in sweats to the point that my shirt was wet. This occurred multiple times but resolved about 24 hours post injection. the patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. treatment received for the events included OTC med. Patient was recovered from the events tenderness at injection sight, severe enough to awaken during the night in Jan2021 and recovered from sweats on 13Jan2021. It was non-serious, Seriousness criteria of Results in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating and Congenital anomaly/birth defect were all no. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0993589
Sex: F
Age:
State: IL

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

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

Lab Data:

Allergies:

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

Symptoms: explosive diarrhea that was liquid and green in color; explosive diarrhea that was liquid and green in color; feeling "queasiness"/queasy abdomen; loose bowel movement; a queasy abdomen right now, kind of gurgling; This is a spontaneous report from a contactable consumer (patient) and nurse. A 75-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0140, expiration date 31Mar2021), intramuscularly at site of left arm on 18Jan2021 09:30 AM at single dose for prevent COVID. The patient medical history was not reported. There were no concomitant medications. The patient previously received flu shot in Oct2020 for immunization (she had the flu shot last year but it was not within 4 weeks, it was in the fall time around Oct2020). The patient experienced a loose bowel movement later in the day on 18Jan2021 (after the vaccine dose) and reported that on 19Jan2021 she was having explosive diarrhea that was liquid and green in color. Also reported feeling queasiness. She known about the reported side effects of the clinical trials. She asked if she could get a colonoscopy next day and she was referred to her hcp. She just had a queasy abdomen right now, kind of gurgling in Jan2021. All events were reported as non-serious. The patient did not receive any treatment from events. The outcome of event bowel movement irregularity was recovered in Jan2021, the outcome of events explosive diarrhea and greenish stool was recovered on 19Jan2021, the outcome of rest events was not recovered.

Other Meds:

Current Illness:

ID: 0993590
Sex: F
Age:
State: TX

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

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

Lab Data:

Allergies:

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

Symptoms: Chills; Body aches; A fever that has went up to 101F (also reported as 100.3); Sore throat; This is a spontaneous report from a contactable consumer (patient's husband). A 37-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL1283), via an unspecified route of administration on 18Jan2021 at 08:30 at a single dose in the left arm for COVID-19 immunization. The patient's medical history included ongoing blood pressure high, allergies, and pollen/cedar allergy. Concomitant medications were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0140) on 31Dec2020 for COVID-19 immunization .The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The husband called to report that his family got their second dose of the Covid-19 vaccine yesterday (18Jan2021). He and his daughter were okay, but his wife (patient) experienced chills, body aches, a fever that has went up to 101F (also reported as 100.3), and sore throat on 18Jan2021 at 19:00. The husband would like to know if these were normal side effects and how long should they last. The outcome of the events was not recovered.

Other Meds:

Current Illness: Hypertension

ID: 0993591
Sex: F
Age:
State: CA

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: developed two boils after getting the first dose of the COVID-19 vaccine; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received the first dose of the bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EL1284), via an unspecified route of administration in the left upper arm on 29Dec2020 at 12:00 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient developed two boils after getting the first dose of the COVID-19 vaccine (non-serious) on 29Dec2020. The patient said she had received her first dose of the COVID-19 Vaccine on 29Dec2020 at 12:00 in her left upper arm. The patient said she had developed boils since she received the COVID-19 vaccine. The patient said that she had never had boils, and now she had two boils. Therapeutic measures were taken as a result of the boils, which included antibiotics. The clinical outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0993592
Sex: M
Age:
State: AR

Vax Date: 01/17/2021
Onset Date: 01/17/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Minor soreness at injection site; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 73-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration at arm left on 17Jan2021 at 01:30 PM at a single dose for covid-19 immunization. Medical history and concomitant medications were not reported. No allergies to medications, food, or other products. 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 at doctor's office/urgent care. The patient experienced adverse event minor soreness at injection site on 17Jan2021 at 12:30 PM. The event was reported as non-serious. No treatment received for adverse event. The outcome of event was resolved in Jan2021. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993593
Sex: M
Age:
State: SC

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: increased heart rate; breathing difficulty; This is a spontaneous report from a contactable consumer. An 82-year-old male patient received first dose of BNT162B2(lot number=EK5730), via an unspecified route of administration on 15Jan2021 13:45 at single dose, left arm for covid-19 immunization. Medical history included partial obstruction in coronary artery, arthritis, allergies to pregabalin (LYRICA), levofloxacin (LEVAQUIN). Concomitant medication included cortisone. The patient experienced increased heart rate and breathing difficulty on 15Jan2021 13:45 with outcome of recovered in Jan2021. The events were non-serious. No treatment received for the adverse event. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Other Meds: CORTISONE

Current Illness:

ID: 0993594
Sex: F
Age:
State: TX

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

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: vomiting; This is a spontaneous report from a contactable consumer (reporting for his wife). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration on 18Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced vomiting on 18Jan2021. The reporter mentioned that he and his wife (patient) received the vaccine yesterday (18Jan2021). His wife has experienced vomiting since last night, earlier this morning, and 20 minutes before the call. He was asking if this was a normal side effect and for any recommendations on what they should do. His wife has been vomiting since getting the COVID-19 vaccine. He said he was trying to see if vomiting is one of the side effects of the COVID-19 vaccine. The outcome of the event was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0993595
Sex: F
Age:
State: CA

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: general feeling unwell; chills; tiredness; she was trying to do a walk but could not; pain at injection site; pain at injection site; That side was hot; headache got worse after getting the COVID 19 vaccine; joint pain; muscle pain continued to get worse; preventing her from sleeping/ she could not sleep; This is a spontaneous report from a contactable consumer (patient). A 52-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982), via an unspecified route of administration at the left arm on 18Jan2021 13:33 at a single dose for COVID-19 immunization. Medical history included back pain (a lot of time due to physical work). She had COVID in Aug2020 and she had muscle pain and was sick. The patient also had headache started initially the day before got the vaccine on 17Jan2021. The patient also has ongoing grass allergy. Concomitant medication included acetylsalicylic acid (ASPIRIN), ascorbic acid, ergocalciferol, nicotinamide, retinol, riboflavin, thiamine hydrochloride (VITAMINS) and unspecified pain medicine for back pain. She had the flu shot and Tetanus shot 2 months ago (2020) both for immunization. The patient started to notice the muscle pain on 18Jan2021 while diving back from the place she received the vaccination. She normally has muscle pain, but she thought this was something normally occurring. However, the muscle pain continued to get worse. She went to sleep, and the muscle pain continued to occur when she was trying to sleep. The muscle pain was occurring in the middle of the night and she was in so much pain it was preventing her from sleeping. She took a muscle relaxant for the pain and felt better. She noticed the pain at injection site initially around 6PM on 18Jan2021 but noticed it more when she was going to bed like 11PM. She tried to sleep on that side and it hurt. That side was hot, so she placed some ice on it. The headache started initially the day before got the vaccine 17Jan2021, but it got worse after getting the COVID 19 vaccine. It was worse on 18Jan2021, on 19Jan2021 it was better. She noticed the joint pain on 18Jan2021 but does not know really what time. She thinks it was around time noticed muscle pain. She woke up at 3AM something from the pain because she could not sleep. The chills started 4AM or 5AM on 19Jan2021. She noticed she felt tired, so tired when she woke up on 19Jan2021. She mentioned she was trying to do a walk but could not on 19Jan2021. She also mentioned she works at 1PM and would have to call out 2 hours before. She commented she needed her glasses to read the lot written on the patient card. Also was feeling unwell on an unspecified date. The events did not require Emergency Room nor Physician Office visit. The outcome of the events was recovering.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]

Current Illness: Grass allergy

ID: 0993596
Sex: M
Age:
State: WA

Vax Date:
Onset Date: 01/13/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Headache; fever; rash on forearms; tingling feeling on arms and back of neck; burning sensation on arms; irritability; General unwell feelings; Patient felt like the shot rendered his paroxetine hydrochloride useless for 5 days. Felt like he quit paroxetine hydrochloride cold turkey; This is a spontaneous report from a contactable consumer. A 50-year-old male patient to received 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EK5730), via an unspecified route of administration on 13Jan2021 13:00 at single dose on right arm for covid-19 immunisation. The patient medical history was not reported. Concomitant medication included paroxetine hydrochloride (PAXIL [PAROXETINE HYDROCHLORIDE]) at 30 mg daily for unknown indication. The patient previously took aspirin [acetylsalicylic acid] and experienced allergies. Patient experienced headache, fever, rash on forearms, tingling feeling on arms and back of neck, burning sensation on arms, irritability and general unwell feelings. Patient felt like the shot rendered his paroxetine hydrochloride useless for 5 days. Felt like he quit paroxetine hydrochloride cold turkey. All started on 13Jan2021 at 16:00. Nasal swab on 19Jan2021 was negative. No treatment was received. Outcome of the events was resolved. This case was reported as non-serious.

Other Meds: PAXIL [PAROXETINE HYDROCHLORIDE]

Current Illness:

ID: 0993597
Sex: F
Age:
State: LA

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: knot under her right arm (the side she received her vaccine) and she was assuming it was a swollen lymph node; assuming it was a swollen lymph node, it was real sore; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283), via an unspecified route of administration (reported as injection in the right arm) on 09Jan2021 at single dose for Covid-19 immunization. The patient's medical history was reported as none. There were no concomitant medications. It was reported that the patient received the first dose of the Covid vaccine and now (10Jan2021) has a knot under her right arm (the side she received her vaccine) and she was assuming it was a swollen lymph node. The patient added that it was real sore but now it is not quite as sore, it doesn't hurt. The patient asked if it could be from the vaccine and how long should it be there. She also asked if she should still get her second dose on the 30th (30Jan2021). The outcome of events was recovering.

Other Meds:

Current Illness:

ID: 0993598
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: waking up at 3 am/she was having trouble sleeping and was uncomfortable.; waking up at 3 am/she was having trouble sleeping and was uncomfortable.; headache; feeling chills; muscle soreness; a lot of fatigue; cough; her temperature was at 98.7 when it is usually at 97.2 in the morning; arm swelling, soreness and a warm feeling; arm swelling, soreness and a warm feeling; arm swelling, soreness and a warm feeling; This is a spontaneous report from a contactable consumer (patient). A 79-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number unknown), via an unspecified route of administration on 14Jan2021 11:00 at single dose for COVID-19 immunization. Medical history included covid-19 from Dec2020 to an unknown date, fatigue from Dec2020 to Jan2021 and cough from Dec2020 to an unknown date, it was reported that she further described the fatigue as the one experienced from getting COVID, 26 days prior to her injection; she mentioned that it was at day 20 post infection that she regained energy from this profound fatigue. She also mentioned that the cough she had during her infection with COVID was back. She then summarized her experience as COVID symptoms but not as severe as when she had it. The patient's concomitant medications were not reported. The patient explained waking up at 3 am, 15 hours post-injection (on 15Jan2021), not knowing how she felt but knew that she was having trouble sleeping and was uncomfortable. She added taking a sleeping pill to help her fall back asleep and woke up at 5:30am. That same day, she said that she experienced: a headache, feeling chills, muscle soreness, a lot of fatigue, and a cough. She specified that her temperature was at 98.7 when it is usually at 97.2 in the morning, as she attributed the rise of temperature to her chills. She said that her fatigue was to the point where it was an effort for her to go up and walk. She then explained that she started to feel better the evening of that first day post injection; and that by the following day, Saturday (on 16Jan2021), the headache was gone and she felt less fatigued. She added also having arm swelling, soreness and a warm feeling in Jan2021. She stated that now 5 days later, her arm was barely tender and was therefore resolving fine. The outcome of the event "having trouble sleeping and was uncomfortable, cough" was not recovered; of the event "headache" was recovered on 16Jan2021; of the events "feeling chills, muscle soreness, a lot of fatigue, arm swelling, soreness and a warm feeling" was recovering; of the rest events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993599
Sex: F
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/15/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Flu like symptoms; This is a spontaneous report from a contactable consumer reported for herself. A 68-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246), via an unspecified route of administration at Left arm on 12Jan2021 16:00 at SINGLE DOSE for covid-19 immunization. Medical history included Hypo-Thyroid and gastrooesophageal reflux disease. No known allergies, not allergies to medications, food, or other products. The patient received other medications the patient received within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced non-serious flu like symptoms three days after vaccine on 15Jan2021 at 04:00 PM, lasted for 4 days. No treatment received for the event. Prior to vaccination, the patient was not diagnosed with COVID-19. Covid (Nasal Swab) tested on 19Jan2021 post vaccination but the result was pending. The outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 0993600
Sex: F
Age:
State: NC

Vax Date: 01/15/2021
Onset Date: 01/18/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Yeast infection; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a 79-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration in right arm, on 15Jan2021, at a single dose, for COVID-19 immunization. The patient's medical history included yeast infection, braces, and facial fillers. The patient's concomitant medications were not reported. The patient got the first dose of COVID-19 vaccine on 15Jan2021 and was asking if there is any problem for her taking yeast infection medication, fluconazole (DIFLUCAN) and antibiotics. On 18Jan2021, the patient came up with the yeast infection after the vaccine injection. The patient noticed that she had yeast infection because she had those before. The patient was asking if she can take fluconazole and if there would be any interactions. Also, her dental work was scheduled after the vaccine injections. The patient could not find information if there was a problem taking antibiotic after someone got the COVID-19 vaccine. The patient had to premedicate before she has her dental work done and wanted to know if there was a problem taking antibiotics (clindamycin or doxycycline). The patient was scheduled a dental procedure and was asking for information with potential interactions with antibiotics such as doxycycline and clindamycin. The patient read that some people had sound like some bad reactions to getting fillers done even 6 months prior to getting the COVID-19 shot. The patient was thinking about getting a filler done in the first part of Feb2021 but after reading that, she thought forget it - she was not going to do that because she read that people had reactions to fillers, like this one person had a filler done 6 months before she had a COVID-19 shot and she was not the only person there were some other people, that had a swelling around the mouth. The patient was referring to facial fillers, when people get fillers done on their face and they would have reactions around their mouth. The patient assumed that it was, were they had the fillers placed on face. The patient was referring to fillers such as JUVEDERM and RESTYLANE or BOTOX. The patient was asking if there had been reactions with vaccination if people had facial fillers because her daughter was getting BOTOX done. The patient was concerned about her daughter possibly getting BOTOX based on what she has read. The patient was getting ready to have fillers done but based on what she read she will wait - what concerned her that person had her fillers done 6 months prior to COVID-19 shot. The patient has read everything. The pages that they gave her at the hospital where she had the vaccine didn't have any information about taking fluconazole. The patient was just calling to see if she could take fluconazole. The patient has some that she can take from when she had a yeast infection before. The patient doesn't think the yeast infection has anything to do with the vaccine. The patient did not have any problems with the vaccine. The patient had not recovered from the event. The causality of the event was assessed as unrelated to the suspect vaccine product. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.; Sender's Comments: Based on the available information, the event yeast infection is attributed to an intercurrent medical condition and assessed unrelated to BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE).

Other Meds:

Current Illness:

ID: 0993601
Sex: M
Age:
State: MD

Vax Date: 12/31/2020
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: initial exposure to coronavirus; COVID-19 PCR test positive; COVID-19 PCR test positive; when he woke up the next morning he had a 5 minute interval of indescribable burning sensation on the face and upper torso/being hot; This is a spontaneous report from a contactable physician from a Pfizer-sponsored program. A 28-year-old male patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine), intramuscularly on 31Dec2020 in arm at a single dose to prevent COVID. There were no medical history or no concomitant medications. He confirmed he is the physician and the primary doctor for the patient. The patient is a pharmacist and he received the first dose of the Pfizer COVID vaccine on 31Dec2020. The next day (01Jan2021), he woke up with a 5-minute interval of indiscernible burning sensation on his face and upper torso that went away after about 5 minutes. The patient reported being hot for a few seconds after taking the Pfizer COVID vaccine. The patient came in to contact with some with coronavirus and then the patient tested positive for coronavirus on 17Jan2021 with a PCR test. He had no symptoms since a week after his initial exposure to coronavirus. No adverse reactions but turned up with infection. The outcome of event burning sensation on the face and upper torso was recovered on 01Jan2021, outcome of the other events was unknown. Reporter assessed seriousness for burning sensation on face and upper torso: Medically significant. Causality between burning sensation on face and upper torso and bnt162b2 was related by Primary Source Reporter per Global Introspection. Information on the batch number/lot number has been requested.; Sender's Comments: Based on the current available information , Exposure to SARS-CoV-2 is most likely related to an intercurrent condition which is not related to the suspected drug. Based on the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of other events cannot be totally excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 0993602
Sex: F
Age:
State: DC

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

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

Lab Data:

Allergies:

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

Symptoms: mouth and tongue became itchy; mouth and tongue became itchy; tongue swelled; headache; nausea; had some trouble breathing; This is a spontaneous report from a contactable consumer (patient herself). A 65-year-old female patient (non-pregnant at the vaccination) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL1283), via an unspecified route of administration on 18Jan2021 09:45 in right arm at single dose for covid-19 immunization. Medical history included hypothyroidism, allergies: cephalosporins, cipro (ciprofloxacin), levofloxacin, penicillins, kiwi, walnuts, pineapple, certain coatings on fabrics. Concomitant medication included levothyroxine sodium (SYNTHROID), celecoxib (CELEXA), trazodone, cetirizine hydrochloride (ZYRTEK), vitamin d3. The most recent COVID-19 vaccine was administered in hospital. 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 had not been tested for COVID-19. Within a few minutes of receiving the injection, her mouth and tongue became itchy, her tongue swelled, she had a headache and nausea and had some trouble breathing on 18Jan2021. Events were reported as non-serious. Events resulted in emergency room/department or urgent care. Treatment of diphenhydramine hydrochloride (BENADRYL), famotidine (PEPCID) and an oral steroid were received for events. Outcome of events were recovering.

Other Meds: SYNTHROID; CELEXA [CELECOXIB]; TRAZODONE; ZYRTEK; VITAMIN D3

Current Illness:

ID: 0993603
Sex: F
Age:
State: NY

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: low grade fever of 99.6 Fahrenheit and 99.7 Fahrenheit. She said it was 100.1 Fahrenheit only once; chills; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program. A 74-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/lot number: EL3247) via an unspecified route of administration on the arm left on 18Jan2021 11:00 at single dose for COVID-19 immunisation. Medical history included thyroid. Concomitant medication included levothyroxine sodium (SYNTHROID) taken for thyroid and ongoing. The patient did not receive other Vaccinations within 4 weeks. The patient had low grade fever of 99.6 Fahrenheit and 99.7 Fahrenheit. She said it was 100.1 Fahrenheit only once on 19Jan2021, chills on 19Jan2021. The event did not require a visit to physician or emergency room (ER). The caller stated she took the first dose of the vaccine yesterday (18Jan2021) and today (19Jan2021) has had a low grade fever of 99.6 Fahrenheit and 99.7 Fahrenheit. She said it was 100.1 Fahrenheit only once. Fever was reported as worsened. Today 19Jan2021, she first noticed the chills, now she did not have chills but she had a fever that was going up. She is scheduled to receive the next dose of the vaccine 08Feb2021. The outcome of the event fever was not recovered, of the event chills was recovered on 19Jan2021.

Other Meds: SYNTHROID

Current Illness:

ID: 0993604
Sex: F
Age:
State: NJ

Vax Date: 12/21/2020
Onset Date:
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Right arm was sore for about 3 days; This is a spontaneous report from a contactable consumer reporting for a patient. A 57-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (brand=Pfizer), via an unspecified route of administration on 21Dec2020 at single dose for covid-19 immunization. Vaccine location was right arm and it was the first dose. Patient is not pregnant at the time of vaccination. The facility type vaccine was hospital. The patient medical history and concomitant medications were not reported. Patient was not diagnosed with COVID-19 prior to vaccination nor tested for COVID-19 since the vaccination. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced right arm was sore for about 3 days on an unspecified date with outcome of recovered. Patient didn't receive treatment for the adverse events. The event was reported as non-serious. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993605
Sex: M
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: headache; Nausea; Abdominal Cramping; This is a spontaneous report from a non-contactable physician (reporting for himself). A 68-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration (left arm) on 14Jan2021 (10:30) at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had other unspecified medications received within 2 weeks of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 14Jan2021 (20:30) the patient experienced headache, nausea and abdominal cramping. There was no treatment received for the adverse events. The outcome of events was recovered on an unspecified date. The patient has not been tested for COVID-19 since the vaccination. This case is non-serious. No follow-up attempts are not possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0993606
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 01/04/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: hallucinations; having stroke like symptoms; having intense headaches; felt exhausted; has pain in her arm; her vision affected/wavy lines throughout her eyes; numbness in her face, hands, and lips; This is a spontaneous report from contactable Nurse reporting for herself. A 65-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunisation. Patient age at time of vaccination was 65 years. The patient did not have reactions with other immunizations except a severe reaction with the measles, mumps, and rubella (MMR) vaccine when she was younger. She had seizures after receiving the MMR vaccine. The patient's concomitant medications were not reported. The patient mentioned she had a severe reaction. She described her adverse reaction by having intense headaches, having stroke-like symptoms in which she described as she cannot speak, having headaches, having numbness in her hands, face, and lips. She also felt exhausted. She also had some pain in her arm that she is not concerned about. She mentioned that she also has her vision affected, she couldn't drive, there were wavy lines all though her eyes. She started to have hallucinations such as seeing people that weren't there, seeing snow storms, and seeing things whipping throughout the wind. All the events started on 04Jan2021. She reported she was very sick in the hospital and is now getting well. However it was unknown if she was admitted to hospital (clarification pending). She wanted to know recommendations about the second shot of the COVID-19 vaccine because with her experience, she is not comfortable having the second shot of the COVID-19 vaccine. Information about lot/batch number has been requested.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events cannot be excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 0993607
Sex: F
Age:
State: AZ

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: headaches; This is a spontaneous report from a contactable consumer (patient). A 45-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on the left arm on 14Jan2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications both reported as none. The patient had no recent other vaccinations. The patient experienced headaches on 15Jan2021. She said she got the vaccine last Thursday (14Jan2021) and started having a really bad headache the next day on Friday (15Jan2021), and the headache was still there, it was not going away, nothing helps. She said she was wondering if she got that from the vaccine. She also explained that her appointment with her healthcare professional (HCP) is next Friday, and asked how to manage her symptom in the meantime. No treatment received for the event. She said that the headache had not worsened or improved, it stayed the same. The outcome of the event was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993608
Sex: F
Age:
State:

Vax Date: 01/05/2021
Onset Date:
Rec V Date: 02/02/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Nausea; Fever; neck pain; Pain/ "aces" and pains; This is a spontaneous report from a non-contactable consumer. An adult female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number and expiration date unknown), via an unspecified route of administration on 05Jan2021 at single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced nausea, fever, neck pain, aces and pains, all on an unspecified date with outcome of recovered. Prior to vaccination, the patient not diagnosed with COVID-19. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 0993609
Sex: M
Age:
State: OH

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

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

Lab Data:

Allergies:

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

Symptoms: legs hurting; This is a spontaneous report from a contactable consumer. A 92-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at SINGLE DOSE for COVID-19 vaccination. Calling on behalf of 92-year-old uncle received first dose of vaccine. The patient's medical history and concomitant medications were not reported. The patient had complaining of legs hurting on an unspecified date. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993610
Sex: F
Age:
State: MN

Vax Date: 01/12/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

Symptom List: Tremor

Symptoms: Pain injection site; short term memory problems/short term memory loss; reduction in mental clarity/feels like she has not been clear headed; scary feeling; worried; This is a spontaneous report from a contactable consumer (patient). A 57-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL0140), via an unspecified route of administration on 12Jan2021 at 13:30 at single dose to prevent Covid. The patient's medical history included ongoing blood pressure high, ongoing cholesterol, ongoing anxiety, ongoing sleep disorder, fatigue from 10Jan2021 to 10Jan2021, and spacey from 10Jan2021 to 10Jan2021. Concomitant medication included pravastatin for cholesterol, amlodipine besylate for blood pressure high, lisinopril for blood pressure high, zolpidem tartrate (AMBIEN CR) for sleep, olanzapine for anxiety, all ongoing; and naproxen sodium (ALEVE). The patient previously received the first dose of BNT162B2 (Batch/lot number: EJ1685) by injection in left arm on 22Dec2020 for COVID-19 immunization and experienced fatigue and spacey on 10Jan2021, and pain at injection site on an unspecified date. The patient experienced short term memory problems and reduction in mental clarity from 14Jan2021. The patient called and wanted to know if there were reported cases in the clinical trials that experienced "brain fog" and "memory loss" after taking the COVID 19 vaccine. The patient asked if anyone else reported spaciness, brain fog and short term memory problems after receiving the Pfizer COVID 19 vaccine. The patient reported that she received the second dose of vaccine on 12Jan2021. She reported reduction in mental clarity and short term memory loss. On 10Jan2021, the patient experienced fatigue and "spacy". The patient stated that that she has had both doses of the vaccine, she got the second dose last Tuesday. She was wondering if there were any known side effects of the product including mental clarity, or foggy brain, or memory loss, because the patient felt like she has not been clear headed. She received her 2nd dose on 12Jan2021, and has been experiencing short term memory problems and reduction in mental clarity. She stated that on 10Jan2021, she noticed feeling fatigue and spacey. The patient stated that seriousness criteria for short term memory problems and reduction in mental clarity was not serious, but stated that it was a scary feeling. She laughed and stated that she was worried, is she getting dementia or is it just the shot. She received her 2nd dose of the vaccine on 12Jan2021 at 13:30PM. Lot: EL0140, No Expiry/NDC written on card. She stated that she did get some pain at the injection site; did not clarify after which injection. She stated that she took Aleve 2 capsules as needed. The patient asked if there have been any reports of patients experiencing this after having the vaccine. It was reported that the patient works in the lab. The outcome of the events short term memory problems/short term memory loss and reduction in mental clarity/feels like she has not been clear headed was not recovered, while the outcome of the other events was unknown.

Other Meds: PRAVASTATIN; AMLODIPINE BESYLATE; LISINOPRIL; AMBIEN CR; OLANZAPINE; ALEVE

Current Illness: Anxiety; Blood cholesterol abnormal; Blood pressure high; Sleep disorder

ID: 0993611
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

Symptom List: Erythema, Pruritus

Symptoms: runny nose; itchy watery eyes, like allergies; itchy watery eyes, like allergies; fluid in her ears; allergies; only had a sore arm for a day; This is a spontaneous report from a non-contactable consumer reporting for herself. A 59-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on 14Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated she received her first Covid19 vaccine on the 14Jan2021 and everything has been great. She stated she only had a sore arm for a day, but now 5 days later (19Jan2021) she has a runny nose, itchy watery eyes, like allergies, and fluid in her ears. She stated she feels it was just allergies because she can take a Benadryl and it makes it quit. She stated Benadryl knocks her out though. She stated she would like to know if these side effects have been mentioned by others and being 5 days after given the dose. Therapeutic measures (Benadryl ) were taken as a result of runny nose, itchy watery eyes, like allergies and fluid in her ears. The outcome of the event sore arm for a day was recovered while other events were unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0993612
Sex: M
Age:
State:

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
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Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: Fever/ running temperature; felt worn out; Generally feeling like crap; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 18Jan2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient took the first dose of BNT162B2 on unspecified date for COVID-19 immunisation. The patient got the second shot of the Pfizer COVID Vaccine yesterday, 18Jan2021. On unspecified date in Jan2021, he had a running temperature and felt worn out. He had a fever and was generally feeling like crap. The temperature was almost gone. He was sure that it's a side effect. He was calling to see if he can take Advil for the fever or not. He wanted to make sure that it would not interfere with the vaccine. He says that yesterday, last night was more intense. It was almost like it was gone, but he still has a little fever. The patient asked if he can use antipyretics after vaccination with the Pfizer-BioNTech COVID-19 vaccine and how long can the symptoms last. The outcome of the event fever/ running temperature was recovering and unknown for the other events. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993613
Sex: F
Age:
State: FL

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

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Allergies:

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

Symptoms: she is having a problem with balance and dragging her right leg/balance was off; felt foggy; She has to walk very slowly; her arm started to feel funny. Patient stated it was not painful but felt numb; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL8982; expiration date: 31May2021), via an unspecified route of administration (anatomical location: Arm left) on 18Jan2021 at 14:30 at 0.3 mg, SINGLE DOSE for COVID-19 immunisation. Patient's medical history included 'hyperthyroid' from an unknown date and unknown if ongoing. Patient has no prior vaccinations within 4 weeks. There were no additional vaccines administered on the same date of Pfizer suspect. Patient has no history of previous immunizations with the Pfizer vaccine considered as suspect as this was the first dose. Concomitant medications included levothyroxine sodium (L-THYROXINE [LEVOTHYROXINE SODIUM]) for 'hyperthyroid'. The patient reported that she received her first dose of COVID vaccine yesterday (18Jan2021) afternoon at 2:30. Patient stated that at 09:00 pm last night (18Jan2021), her arm started to feel funny. Patient mentioned that it was not painful but felt numb. Patient stated that today (19Jan2021), when she woke up, she is having a problem with balance and dragging her right leg. Patient also mentioned that she also felt foggy. Patient would like to know if these are common side effects. Patient would also like to know how long the symptoms will last. Patient also stated that she has an appointment tomorrow with her HCP and she will be unable to drive in the current state she is in and will have someone else drive her to the appointment. It was also reported that patient was calling on the line calling about the Corona shot and clarified it to be the Pfizer COVID Vaccine. Patient initially stated she received her first dose around 2'oclock yesterday (18Jan2021). Patient mentioned that she is having a reaction that she does not see on the list. Patient received the injection in her left arm and her left arm feels funny which is to be expected, but her right leg is dragging. Patient also reported that her balance was off which it never was. Patient added that she also felt foggy. Patient was calling to see if this was a side effect and if it is, when will it go away. She started to notice her right leg dragging this morning around 7:30 am on 19Jan2021. She thought it would go away. Around this same time she noticed her balance was off. She has to walk very slowly. As she walks by she has to touch the wall and that is not like her at all. She is normally very active. Normally she walks for an hour as an active person. This feeling is not like her. She started to feel foggy this morning when she woke up. Patient clarified that time of vaccination was 2:30 pm. Vaccination facility type was reported as hospital. The events were assessed as non-serious. Outcome of the event 'her arm started to feel funny. Patient stated it was not painful but felt numb' was unknown, outcome of the remaining events was not recovered.

Other Meds: L-THYROXINE [LEVOTHYROXINE SODIUM]

Current Illness:

ID: 0993614
Sex: M
Age:
State: OR

Vax Date: 12/30/2020
Onset Date: 01/02/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Back pain/it hurt so bad; could not walk; This is a spontaneous report from a contactable healthcare professional reported for himself. A 60-year-old male patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), intramuscularly on 30Dec2020 13:00 at single dose, left arm for covid-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Medical history included diabetes and high blood pressure, both controlled. The patient's concomitant medications were not reported. On 02Jan2021, the patient experienced back pain, started slowly peaking on January 7 to where he could not walk, it hurt so bad. Events were non-serious. No treatment received for the adverse event. The outcome of the events was recovered. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. Test Name was Nasal Swab.

Other Meds:

Current Illness:

ID: 0993615
Sex: F
Age:
State: WA

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

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

Symptoms: Numbness noted right side of upper mouth /progressed to numbness of mouth/lips; Mild lip swelling; This is a spontaneous report from a contactable nurse (patient). A 62-year-old female nurse (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EL3246) at right arm via an unspecified route of administration on 14Jan2021 16:15 at single dose for COVID-19 immunization. Medical history included none. Concomitant medications included unspecified medications. The patient previously received the first dose of bnt162b2 (lot number: EH9899) at right arm via an unspecified route of administration on 21Dec2020 18:15 at single dose for COVID-19 immunization. The patient experienced numbness noted right side of upper mouth day after 2nd injection on 15Jan2021 16:00. It has progressed to numbness of mouth/lips 5 days post injection. Mild lip swelling on 15Jan2021 16:00. No difficulty breathing etc. Very noticeable with eating and talking in appearance like she have been to the dentist and given novocaine. The adverse events resulted in doctor or other healthcare professional office/clinic visit. It was unknown if treatment received. The reporter considered the events were non-serious. 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 did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not pregnant at the time of vaccination. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0993616
Sex: F
Age:
State: MI

Vax Date: 01/16/2021
Onset Date: 01/17/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

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

Symptoms: every bone and muscle in her body hurts, bad; every bone and muscle in her body hurts, bad; This is a spontaneous report from a contactable consumer reporting for herself. A 69-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number EL3249/expiration date: not provided), via an unspecified route of administration, on 16Jan2021 (at the age of 69 years old) as a single dose in the left arm for L121. Relevant medical history included lung cancer 10 or 11 years ago and she only has one lung that breathes well, pneumonitis due to radiation to her right lung which damaged the lining in her right lung, ongoing high cholesterol since 10 to 12 years ago, and high iron content due to simvastatin. Concomitant medication included simvastatin 20mg once daily orally since an unknown date for years, for high cholesterol. On 17Jan2021, the patient experienced every bone and muscle in her body hurts, bad and was worsened. The outcome of the events every bone and muscle in her body hurts, bad was not recovered.

Other Meds: SIMVASTATIN

Current Illness: High cholesterol

ID: 0993617
Sex: F
Age:
State: NM

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 02/02/2021
Hospital:

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Symptom List: Pain in extremity

Symptoms: left armpit and under arm became swollen and tender to the touch; left armpit and under arm became swollen and tender to the touch; arm remained somewhat sensitive to the touch; Patient was also extremely tired; This is a spontaneous report from a contactable pharmacist. A 56-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EL1284, on 06Jan2021 09:30 Intramuscular at single dose in left arm for COVID-19 immunization. Medical history included Anxiety and depression, Chronic pain in right foot, tendinopathy of right foot since 2015, Derangement of medial meniscus, Environmental allergies, Fatty liver H/O, hypothyroidism since 25Jan2013, Health care maintenance, Hyperlipidemia since May2016, thyroid nodule since 25Jan2013, Obesity, Prediabetes. Concomitant medications included salbutamol (ALBUTEROL), levothyroxine and omeprazole. The patient previously received first dose of BNT162B2 lot number=EH9899 on 16Dec2020 11:00 AM via Intramuscular at left arm at 56-year-old. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Approximately 24 hours after receiving the vaccine, left armpit and under arm became swollen and tender to the touch on 07Jan2021 08:00. Notified primary care physician during routine visit, PCP advised to notify her if symptoms did not resolve. Swelling resolved 4 days after onset, arm remained somewhat sensitive to the touch. Patient was also extremely tired for 2 days after the vaccine but otherwise fine. No treatment was received for all events. The patient was not diagnosed with COVID-19 Prior to vaccination. The patient had not been tested for COVID-19 Since the vaccination. The outcome of all events was resolved.

Other Meds: ALBUTEROL [SALBUTAMOL]; LEVOTHYROXINE; OMEPRAZOLE

Current Illness:

ID: 0993618
Sex: F
Age:
State: IN

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/02/2021
Hospital:

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

Symptoms: fever 102.9; Severe joint pain; body aches; headache; chills; weird vivid dreams; nausea; This is a spontaneous report from a contactable nurse (patient). A 55-year-old female patient started to receive the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number: EL1284/expiration date: unknown), via an unspecified route of administration, on 16Jan2021 09:45 AM (at the age of 52 years old) as a single dose on left arm for COVID-19 immunisation. Relevant medical history was none. Historical vaccine history included first dose of BNT162B2 vaccine (Pfizer product) on 26Dec2020 (lot number: EL1284) on right arm. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL), ergocalciferol (VIT D), ascorbic acid (VIT C) and Zinc. The patient did receive other vaccines within 4 weeks prior to the COVID vaccine. On 16Jan2021 05:30 PM, the patient experienced severe joint pain, body aches, headache, fever 102.9, chills, weird vivid dreams, nausea. No treatment was received. The outcome of the events severe joint pain, body aches, headache, fever 102.9, chills, weird vivid dreams, nausea was not recovered.

Other Meds: ADDERALL; VIT D; VIT C; ZINC

Current Illness:

ID: 0993619
Sex: F
Age:
State: FL

Vax Date: 01/05/2021
Onset Date: 01/09/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

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

Symptoms: Diarrhea; This is a spontaneous report from a contactable consumer (patient). An 82-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EH9899), via an unspecified route of administration in left arm, on 05Jan2021 at 13:30, at a single dose, for COVID-19 immunization. The patient's medical history included diabetes, arthritis, vitamin D, bones, gums, eye, joint pain lubrication, hair and nail growth and strength, control sugar, atrial fibrillation (Afib), heart, supplement, cholesterol, liver clean, and gastro problem. The patient's concomitant medications included apixaban (ELIQUIS) for Afib from 2019 (a year and three-fourths), metoprolol for heart from 2019 (a year and three-fourths), metformin hydrochloride (METFORMIN ER) for diabetes, berberine to control sugar, biotin from 2011 (for 10 years) for hair and nail growth and strength, Silybum marianum (MILK THISTLE) to make liver clean (two or three years), hyaluronic acid for joint pain lubrication, niacinamide for diabetes, chondroitin sulfate/ glucosamine sulfate (GLUCOSAMINE CHONDROITIN) for bones, Monascus purpureus (RED YEAST RICE) for cholesterol, colecalciferol (VITAMIN D3; UPC Number: 3373900373, Lot Number: 3162111, and Expiration Date: Jun2024) for vitamin D, probiotics for gastro problem, betacarotene for eye, ubidecarenone (COENZYME Q10) for gums, calcium/ magnesium (CALCIUM MAGNESIUM) for bones, and unspecified multivitamins as supplement and OSTEOPHASE for arthritis; all were ongoing. The patient her first dose of COVID-19 vaccine dose on 05Jan2021. The patient had experienced diarrhea ever since 09Jan2021 and is still continuing until today. The patient experienced a sudden onset of diarrhea and it has continued on and off since then; it is persisting or worse. She has seen a gastroenterologist, but they don't have any answers, sent stool cultures in Jan2021 but no results yet. The patient was asking if this is a documented adverse event. The patient is scheduled on 26Jan2021 for the second dose. With this experience, the patient was asking what to do with the second dose- if she should get the second shot. The patient had not recovered from the event.

Other Meds: ELIQUIS; METOPROLOL; METFORMIN ER; BERBERINE; BIOTIN; MILK THISTLE; HYALURONIC ACID; NIACINAMIDE; GLUCOSAMINE CHONDROITIN [CHONDROITIN SULFATE;GLUCOSAMINE]; RED YEAST RICE; VITAMIN D3; PROBIOTICS; BETACAROTENE; COENZYME Q10 [UBIDECARENONE];

Current Illness:

ID: 0993620
Sex: F
Age:
State: DC

Vax Date: 01/15/2021
Onset Date: 01/17/2021
Rec V Date: 02/02/2021
Hospital:

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

Symptoms: right side of her face was swollen and was itching; eyes swollen/puffy; puffy underneath eyes/ like bags; swelling of right side of face/ right side of her face was swollen; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL1284, expiration date: 30Apr2021) intramuscular on the right arm on 15Jan2021 at 30 ug, single for COVID-19 prophylaxis. Medical history included high cholesterol, high blood pressure, cancer survivor and allergic to walnuts. Concomitant medication included ascorbic acid, herbal nos, levoglutamide, lysine, magnesium, manganese, retinol, riboflavin, selenium, tocopherol, zinc (AIRBORNE) for supplementation therapy, HCTZ for high blood pressure, vitamins nos (MULTIVITAMIN [VITAMINS NOS]) for supplementation therapy, rosuvastatin for high cholesterol. The patient received 1st dose of vaccine on Friday and on 17Jan2021 evening, experienced the following: "swelling of right side of face, eyes swollen/puffy." She spoke with HCP office and was told to take Benadryl and Tylenol. She took the medication and the "swelling went down". She said she woke up this morning and had "puffy underneath eyes", "like bags", and "slight facial swelling." The patient ate at an Indian restaurant on 17Jan2021 at about 6:30-7:00pm and was unsure if her reaction was to the vaccine or food, since the food she ate could have been cooked with nut oil. She said that her eyes were still puffy and her face was still a little swollen. She went to see her doctor today 19Jan2021 and he was trying to figure out what could have caused this on his end. The patient said that the right side of her face was swollen and was itching. The left side did not appear to be swollen at all. Outcome of the event pruritus facial was unknown while recovering for the other events.

Other Meds: AIRBORNE; HCTZ; MULTIVITAMIN [VITAMINS NOS]; ROSUVASTATIN

Current Illness:

ID: 0993621
Sex: F
Age:
State:

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
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Allergies:

Symptom List: Vomiting

Symptoms: Diarrhea; Chills; Fever of 101.8; muscle pain; This is a spontaneous report from a non-contactable nurse (patient). A 27-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: El1283), intramuscular on 18Jan2021 00:45 at a single dose for COVID-19 immunisation. The patient's medical history included endometriosis and sulfa antibiotics allergy. Concomitant medications were not reported. The patient previously took the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on 29Dec2020 at the age of 27 years old for COVID-19 immunisation. 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 and had not been tested for COVID-19 since the vaccination. On 19Jan2021 03:45, the patient experienced diarrhea, chills, fever of 101.8 and muscle pain. No treatment was received for these adverse events. Outcome of the events diarrhea, chills, fever of 101.8 and muscle pain was not recovered. The events diarrhea, chills, fever of 101.8 and muscle pain were considered non-serious. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0993622
Sex: F
Age:
State:

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/02/2021
Hospital:

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Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Duration of diarrhea following first dose of vaccine on 16Jan2021; This is a spontaneous report from a non-contactable consumer (patient). A 70-year-old female patient received 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 16Jan2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient called and asked about duration of diarrhea following first dose of vaccine on 16Jan2021. Outcome of the event was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0993623
Sex: F
Age:
State: WA

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/02/2021
Hospital:

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

Symptoms: Tinnitus; This is a spontaneous report from a contactable consumer reported for herself. A 54-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=PFZ39), via an unspecified route of administration in left arm on 14Jan2021 19:00 at first single dose for covid-19 immunisation. Medical history included obesity, depression, hypothyroidism. Other medications the patient received within 2 weeks of vaccination included: levothyroxine sodium (SYNTHROID), bupropion hydrochloride (WELLBUTRIN) and vitamin supplements. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took demerol and experienced drug hypersensitivity. The patient experienced tinnitus on 14Jan2021 20:00 with outcome of not recovered. Since about an hour after receiving the vaccine, the patient's ears had been ringing. She had never experienced this before. It's noticeable but did not interfere with daily activities. Event was considered as non-serious. No treatment was received for the adverse event. Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds: SYNTHROID; WELLBUTRIN

Current Illness:

ID: 0993624
Sex: F
Age:
State: NV

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/02/2021
Hospital:

Vax Type:
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Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Bad headache that triggered a neuralgia attack; Bad headache that triggered a neuralgia attack; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot #: EL8982) via an unspecified route of administration on arm right on 15Jan2021 13:45 at single dose for COVID-19 immunisation. Medical history included occipital and trigeminal neuralgia, C5-C6 cervical cage, temporomandibular joint syndrome (TMJD), cerebrospinal graft. Known allergy: shellfish, walnuts, mustard, sweet potato. Concomitant medication included gabapentin, acetaminophen. The patient previously took penicillin B, phenergan and chloral hydrate (PHENERGAN), Codeine and linalool, all experienced drug allergy. 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 had not been tested for COVID-19 since the vaccination. On 16Jan2021 06:00, the patient woke up with a bad headache that triggered a neuralgia attack. It persisted for 24hrs. The events were reported as non-serious. No treatment was received for the events. The outcome of the events was recovered in Jan2021.

Other Meds: GABAPENTIN; ACETAMINOPHEN

Current Illness:

ID: 0993625
Sex: F
Age:
State: MA

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

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Allergies:

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

Symptoms: racing pounding heart rate 110-126 (normal is 60); racing pounding heart rate 110-126 (normal is 60); Very weak; chills; whole body achiness; This is a spontaneous report from a non-contactable nurse (patient). A 62-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EK4176) via an unspecified route of administration on the left arm on 18Jan2021 11:00 at a single dose for COVID-19 immunization. Medical history included coronavirus and allergies: sensitive to milk protein and gluten sensitivity. Concomitant medication included St John's Wort, colecalciferol (VITAMIN D [COLECALCIFEROL]), calcium carbonate (TUMS [CALCIUM CARBONATE]) and multivitamin. The patient previously took casein and experienced allergies. On 19Jan2021 05:00 AM, the patient experienced racing pounding heart rate 110-126 (normal is 60), very weak, chills, whole body achiness. Work the night shift, 11p-7a and symptoms started around 5am. No treatment was received for the events. Patient was not pregnant. The facility where the vaccine was administered was in a Nursing Home/Senior Living Facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Post vaccination, the patient has not been tested for COVID-19. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: ST JOHN'S WORT; VITAMIN D [COLECALCIFEROL]; TUMS [CALCIUM CARBONATE]

Current Illness:

ID: 0993626
Sex: F
Age:
State: NV

Vax Date: 12/18/2020
Onset Date: 12/19/2020
Rec V Date: 02/02/2021
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Allergies:

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

Symptoms: Lips swelling and face; Lips swelling and face; Anaphalaxis; Anaphalaxis; This is a spontaneous report from a contactable other HCP (patient). A 49-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: Eh9899) via an unspecified route of administration on 18Dec2020 18:30 at single dose in left arm for COVID-19 immunisation. She received the second dose (lot number: El1283) in right arm on 08Jan2021. Medical history included Idiopathic anaphylaxis and was allergic to penicillin, had COVID-19 from May2020 to an unknown date. Concomitant medication included unspecified birth control pills. The patient experienced anaphalaxis on 19Dec2020 06:00 AM. She talked with her doctor lips swelling and face. Treatment received for events lips swelling and face. But her question is she had an IGG antibody test and it was negative. She had COVID in May2020 and have been tracking her antibodies. She wanted to know 'does this antibody test show the same antibodies?' She had negative after the two vaccines. The patient is not pregnant. Events outcome was recovered.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events cannot be excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am