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: 1305792
Sex: F
Age:
State: CT

Vax Date: 04/07/2021
Onset Date: 04/19/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: seasonal allergies; I feel like I have the flu; This is a spontaneous report from a contactable consumer (patient herself). A 64-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration in left arm at age of 64-years, as single dose on 07Apr2021 (Lot number: ERW734) for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient had the first dose of Pfizer vaccine (COVID vaccine) on April 7 and she didn't have any side effect at all she felt perfectly fine and normal. But then 12 days later (on 19Apr2021) the patient felt like she had the flu. The patient took Ibuprofen dose 200 mg four times a day for the event. And for this, she took a Benadryl because she was not sure if there were also seasonal allergies happening. She didn't take any prescription medication. Event outcome was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305793
Sex: U
Age:
State: MD

Vax Date: 04/19/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Severe pain in joints, muscles and legs; legs, ankles and my knees were killing me; Severe pain in joints, muscles and legs; legs, ankles and my knees were killing me; Severe pain in joints, muscles and legs; legs, ankles and my knees were killing me; Nauseated; Under arm lymph node swollen and hurts to put it down; Sore throat; Under arm lymph node swollen and hurts to put it down; This is a spontaneous report from a contactable consumer (reported for self). This 72-year-old patient of an unspecified gender received first dose of BNT162B2 (Pfizer covid-19 vaccine, solution for injection, Lot number: EN6204 expiry date: 30Jun2021) via an unspecified route of administration in left arm on 19Apr2021, as a single dose, for covid-19 immunization. Medical history included depression and anxiety over 10 years. Concomitant medications included Clonazepam orally (in the morning and 1 or 2 at bedtime, ongoing) and BUPROPION HYDROCHLO-RIDE (Wellbutrin) 300 mg once a day orally. On an unknown date, the patient experienced Severe pain in joints, muscles and legs; legs, ankles and knees were killing. The patient had a little nauseated feeling throughout the day but that disappeared and had under arm lymph node was really swollen and it hurt. The patient took Tylenol 500mg capsule every 6 hours as a treatment, night prior to this report and it had not helped. The patient had little sore throat and swollen lymph nodes. The second shot was probably due on 10May2021. It was stated that lymph node swelling was not improving, It was swollen and it hurts and was persisting. The outcome of the events of severe pain in joints, in muscles, and in legs, ankles and knees pain was killing, nauseated feeling throughout the day, under arm lymph node was really swollen and it hurt was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds: CLONAZEPAM; WELLBUTRIN

Current Illness:

ID: 1305794
Sex: F
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: I can hardly move; sick; Bad reaction that I had from the vaccine, the second one; This is a spontaneous report from a contactable consumer (patient). The 76-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot Number: Unknown) as SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot Number: Unknown) as SINGLE DOSE for covid-19 immunization. The patient reported " i can hardly move, I have been sick from so long, bad reaction that i had from the vaccine, the second one" on an unspecified date. Reported as: Consumer stated, "I was calling because of a bad reaction that I had from the vaccine, the second one, not the first one." "I can hardly move, the side effect. I have been sick from so long."Regarding Height and weight: Consumer stated, "I used to be # feet # inches but I am shrunk down to # feet and I am about # pounds."The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305795
Sex: F
Age:
State: FL

Vax Date: 04/20/2021
Onset Date: 04/20/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Started experiencing Numbness in my left side of my face; Slow speech; This is a spontaneous report from a contactable consumer (Patient). A 36-years-old female patient received second dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine), at the age of 36-years-old, intramuscular, administered in Arm Right on 20Apr2021 (Lot Number: ER8731) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. patient received first dose of bnt162b2, at the age of 36-years-old, on 29Mar2021 4:00 PM for covid-19 immunisation. Patient went in for second dose of the COVID shot yesterday, The Pfizer COVID shot and the first 15 minutes she was fine. After she left (withheld), after about 20 minutes, she started experiencing numbness in left side of face and slightly slow speech and she was still actually experiencing the numbness in face. She didn't have numbness in face before getting the shot. Treatment for events was No. Events outcome were not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305796
Sex: M
Age:
State:

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 05/11/2021
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: Fever; Vaccination site pain; Headache; This is a solicited report from marketing program based on the information received by Pfizer from AbbVie Inc. (MFR Control No. # 21K-163-3862391-00). A contactable 48 year old male consumer (patient) reported for himself that patient started to receive first dose of BNT162B2 (BNT162B2 Solution for injection) on an unknown date via Intramuscular route of administration at SINGLE DOSE for COVID-19 immunisation. On 09Apr2021 patient received 2nd dose Covid-19 Vaccine. It was unknown if patient was enrolled in a COVID-19 vaccine trial. On an unknown date the patient received Adalimumab (HUMIRA) at Citrate Free via Subcutaneous route of administration for Crohn's disease). The patient's medical history and concomitant medications were not reported. On 09Apr2021 the patient experienced Fever Sore arm from Covid Vaccine, Headache resolved and Vaccination site pain. The events were assessed as non-serious. Fever, sore arm from Covid Vaccine and Headache with Humira(Adalimumab). Covid-19 vaccine was also considered suspect for all events. The outcome of the events was recovered. The reporter's assessment of the causal relationship of the events with the suspect products was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305797
Sex: F
Age:
State: MS

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Nausea; Tiredness; Not feeling good with the pain in my knees and my back hurts; lower back, my knees, my arms; Not feeling good with the pain in my knees and my back hurts; lower back, my knees, my arms; Not feeling good with the pain in my knees and my back hurts; lower back, my knees, my arms; Not feeling good with the pain in my knees and my back hurts; lower back, my knees, my arms; Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 42-years-old female patient received second dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine), via an unspecified route of administration, administered in Arm Left (reported as "Left shoulder") on an unspecified date (Lot Number: EW0151) as single dose for covid-19 immunisation. The patient medical history were not reported. Concomitant medication was none. patient received first dose of bnt162b2, at the age of 42-years-old, administered in Arm Left (reported as "Left shoulder") on 29Mar2021 (Lot Number: EP6955) for covid-19 immunisation and experienced chills, did not feel right and then had a headache. Patient had the Pfizer shot on Monday at 3 (unspecified) and had lots of side effects like the nausea, tiredness, not feeling good with the pain in my knees and my back hurts, lower back, my knees, my arms and had diarrhea. Consumer confirmed it was her second shot. She was trying to see if she can use some medication for the pain. Events outcome were unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305798
Sex: F
Age:
State: IL

Vax Date: 04/21/2021
Onset Date: 04/22/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Low fever; Chills; All over body soreness; Particularly down the left side where she got the shot; This is a spontaneous report from a contactable consumer (patient's father). A female patient (reporter's daughter) of an unspecified age received second dose of (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number, Expiration date: unknown) via an unspecified route of administration on 21Apr2021 for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Historical vaccine included first dose of (Solution for injection, Batch/Lot Number, Expiration date: Not available) for covid-19 immunisation. On 22Apr2021, in the morning she reported a low fever, chills and all over body soreness, particularly down the left side where she got the shot. The outcome of the events was Unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305799
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: ran a 102.5 fever; chills; joints ached horribly; nauseated; had no appetite; This is a spontaneous report received from a non-contactable consumer (Patient). A male patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient historical vaccine included first dose of BNT162B2 for COVID-19 immunization. On an unspecified date, the patient ran a 102.5 fever, chills, joints ached horribly, nauseated and had no appetite for the better part of 4 days. The patient woke up on day 5 and felt perfectly fine. The second dose of Pfizer took him out for nearly a week. The outcome for events fever, chills, joints ached horribly, nauseated and had no appetite was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305800
Sex: F
Age:
State: MS

Vax Date: 03/29/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: I did not feel right and then I had a headache; chills; I did not feel right and then I had a headache; This is a spontaneous report from a contactable consumer (patient). A 42-years-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine), at the age of 42-years-old, via an unspecified route of administration, administered in Arm Left (reported as "Left shoulder") on 29Mar2021 (Lot Number: EP6955) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported couple hours like 3-4 hours afterwards she had chills, did not feel right and then had a headache. Patient started experiencing problem at night. Events outcome were unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305801
Sex: F
Age:
State: OH

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Lymph node pain; This is a spontaneous report received from a contactable consumer (patient) reported for herself. A 46-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on an unspecified date (Batch/Lot Number: EN6198) as SINGLE DOSE for covid-19 immunisation. Historical vaccine included first dose of BNT162B2 (Batch/lot number: EL9261) on 05Feb2021 and experienced Injection site pain, Headache, Upper respiratory allergy symptoms, Shortness of breath, Chest pain, Chest tightness, Dizziness, Fatigue, Passed out, COVID induced POTS, Nausea, Throwing up, her husband thought she was having a stroke because she could not talk, I could not move, she could not breathe. The patient's medical history and concomitant medications were not reported. The patient experienced lymph node pain on an unspecified date with outcome of unknown. Consumer stated: EN6198. That one also gave her lymph node pain. The new symptom she had from second one was lymph node pain. She had new symptoms after the second dose. She lost her job a couple of weeks later. She lost 10 days of her work and she was not able to work for about a month. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305802
Sex: F
Age:
State: NY

Vax Date: 04/19/2021
Onset Date: 04/20/2021
Rec V Date: 05/11/2021
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: I got on my periods and I usually have really bad pain but this time it is like 10 times worse than really bad that I usually have; I have really bad abdominal pain; This is a spontaneous report from a contactable consumer (patient). A 27-years-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 19Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunization, at the age at vaccination of 27 years old. The patient's medical history and concomitant medications were not reported. The patient experienced she had really bad abdominal pain (non-serious) on 20Apr2021 with outcome of unknown, she got on her periods and she usually had really bad pain but this time it was like 10 times worse than really bad that she usually have (non-serious) on an unspecified date with outcome of unknown. Consumer stated, "On Monday I got the Pfizer covid vaccine and I got it like yesterday and situation was pretty bad but it likes lot worse and it is like has been stopped being like really bad. I don't know if this is like something, that was adverse side effect or what?" It was the 1st shot." Consumer stated, "Yes but that's not the concern about it is the fact that I got on my periods and I usually have really bad pain but this time it is like 10 times worse than really bad that I usually have. I don't know if I be concerned or not. I have really bad abdominal pain. It is worse than usual that I have in my period." No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305803
Sex: M
Age:
State: AL

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: severe impotence; This is a spontaneous report from a contactable consumer (patient). A 56-year-old male patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT/Batch number and expiration date unknown) via an unspecified route of administration at arm left on 29Mar2021 09:00 AM at age of 56-year-old for COVID-19 immunization. Medical history and concomitant medications were not reported. There was no known allergies. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, patient wasn't tested for COVID-19. After taking the first shot two weeks later (as reported), patient started experiencing severe impotence and he was still going through this he had never been this way before. Onset date of the event was reported as 29Mar2021. Event was reported as non-serious. No treatment was received for the event. Outcome of the event was not recovered. Information about lot/batch number was available. Further information was expected.

Other Meds:

Current Illness:

ID: 1305804
Sex: M
Age:
State: VA

Vax Date: 04/01/2021
Onset Date: 04/09/2021
Rec V Date: 05/11/2021
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: Tested positive for COVID; I had symptoms; This is a spontaneous report from a Pfizer. This is a report from a contactable consumer (self). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 01Apr2021 (Batch/Lot Number: ER8732) as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced tested positive for COVID, fever is gone 'and everything' (not clear nor clarified) but still have a cough and little bit of headache on 09Apr2021 with outcome of unknown. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 09Apr2021.

Other Meds:

Current Illness:

ID: 1305805
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: itching type of rash; Right below her neck she is have itching, irritation; Right below her neck she is have itching, irritation; This is a spontaneous report from a contactable consumer (patient's husband) reported for patient. A female patient of an unspecified age received dose 1 via an unspecified route of administration, administered in Arm Left on an unspecified date (Batch/Lot Number: Unknown) as SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced itching type of rash (non-serious) on an unspecified date with outcome of unknown, right below her neck she is have itching, irritation (non-serious) on an unspecified date with outcome of unknown. Reporter stated, "My wife had like a reaction, like itching type of rash or something few weeks after the first Covid shot and I wanted to know what she can use to get rid of that itching? She had the shot on her left arm and right below her neck she is have itching, irritation." No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305806
Sex: M
Age:
State: WA

Vax Date: 04/20/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: whole edge of my tongue all the way around turned bright red is sore kind of like burning, looked a little inflamed; tongue is hurting everywhere; whole edge of my tongue all the way around turned bright red is sore kind of like burning, looked a little inflamed; tongue is hurting everywhere; whole edge of my tongue all the way around turned bright red is sore kind of like burning, looked a little inflamed; tongue is hurting everywhere; This is a spontaneous report from a contactable consumer (patient). A male patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 20Apr2021 (Batch/Lot Number: Unknown) at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported that "four hours after I took the vaccine the whole edge of my tongue all the way around turned bright red is sore kind of like burning, looked a little inflamed. It is like you drink a hot drink and you burn you tongue but I did not even realized when I was speaking and I was like my tongue is hurting everywhere." Outcome for events was unknown. No follow-up attempts are needed. information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305807
Sex: F
Age:
State: MA

Vax Date: 04/25/2021
Onset Date: 04/26/2021
Rec V Date: 05/11/2021
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: Pulse continued body aches especially in legs making her almost immobile; Pulse continued body aches especially in legs making her almost immobile; Pulse continued body aches especially in legs making her almost immobile; Pulse continued body aches especially in legs making her almost immobile; bitter taste; This is a spontaneous report from a contactable consumer(patient). The 51-year-old female patient(not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in arm left on 25Apr2021 14:30 (Batch/Lot number was not reported) as second dose, single for covid-19 immunization. Medical history included hashimoto. Concomitant medication included collagen, peptide powder, multi vitamins. She previously received sulfur based antibiotics. Historical vaccine included first dose of BNT162B2 on 03Apr2021 09:30 AM for COVID-19 immunization and experienced bitter taste in back of throat for half day on date of administration. After second dose, the patient experienced same bitter taste for 24 hours from time of administration. Pulse continued body aches especially in legs making her almost immobile, all on 26Apr2021 06:00 with outcome of recovering. Treatment included alternated taking ibuprofen(ADVIL) and paracetamol (TYLENOL). 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 lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021466738 Same patient/drug, similar AEs, different dose

Other Meds: COLLAGEN; PEPTIDES NOS

Current Illness:

ID: 1305809
Sex: M
Age:
State: MA

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: Itchy from his trunk down to his arms; This is a spontaneous report from a contactable pharmacist. A male patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, as single dose on an unknown date (Lot number: not provided) for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient became well itchy from his trunk down to his arms and lasted about a day or so after he received his first shot. Event outcome was recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305810
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Rash on my hand; My lip was swollen; This is a spontaneous report from a non-contactable consumer (patient). A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, as single dose on an unknown date (Lot number: not provided) for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient asked that if he/she did have the rash on hand after the first dose and his/her lip was swollen, should he/she take the other one. Event outcome was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305811
Sex: F
Age:
State: PA

Vax Date: 03/10/2021
Onset Date: 03/17/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: I developed tinnitus in my left ear and some loss of hearing in my left ear.; I developed tinnitus in my left ear and some loss of hearing in my left ear.; This is a spontaneous report from a contactable consumer reporting for self. A 68-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 2 via an unspecified route of administration, administered in right arm on 10Mar2021 (Batch/Lot Number: EN6205) as a single dose for COVID-19 immunisation. Medical history included high blood pressure increased from 2001 ("for 20 years") and cancer (first time was in 2004 and then in 2008). The patient was receiving unspecified concomitant medications ("I am taking a lot of different medication"). The patient previously received first dose of BNT162B2 (Batch/lot number: EN6205) on 09Feb2021. On 17Mar2021, the patient developed tinnitus in her left ear and some loss of hearing in her left ear. The patient underwent lab tests including blood work on 14Apr2021 with normal results and MRI brain 15Apr2021 with normal result. The patient had not yet received any treatment for the events at the time of reporting. The patient states she doesn't know for sure, but she believed she had a side effect from receiving the Pfizer vaccine. The outcome of the events tinnitus in her left ear and some loss of hearing in her left ear was unknown.

Other Meds:

Current Illness:

ID: 1305812
Sex: M
Age:
State: MS

Vax Date: 04/21/2021
Onset Date: 04/21/2021
Rec V Date: 05/11/2021
Hospital:

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Allergies:

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

Symptoms: lump under his armpit; Fever; Chills; This is a spontaneous report from a contactable consumer or other non hcp. A 19-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection,Batch/Lot Number: EW0157), dose 2 via an unspecified route of administration, administered in Arm Right on 21Apr2021 10:30 as single dose for covid-19 immunisation; ibuprofen (IBUPROFEN), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at for an unspecified indication.History: She says he took ibuprofen and that they all started to have fever and chills.He took ibuprofen. She things the dose was 300mg or 400mg and he took a total of 3 doses .Prior Vaccinations within 4 weeks (List any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s)): no. The patient medical history, concomitant medications were not reported. On 21Apr2021 The patient experienced fever, chills, and on 23APr2021 lump under his armpit. The outcome of events was recovered ,On 23Apr2021 and lump under his armpit (axillary mass) was not recovered. Follow-up (23Apr2021): No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305813
Sex: U
Age:
State:

Vax Date: 04/10/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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Allergies:

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

Symptoms: Excruciating headaches; Dizziness; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on 10Apr2021 (Lot number was not reported) as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient received dose 1 for COVID-19 immunization. The patient experienced excruciating headaches, had the headache and dizziness, have all the possible symptoms. The patient did the neuro exam and got some migraine medications (Unspecified medication). The event outcome of excruciating headaches was not recovered, dizziness was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305815
Sex: F
Age:
State: AZ

Vax Date: 04/13/2021
Onset Date: 04/13/2021
Rec V Date: 05/11/2021
Hospital:

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Allergies:

Symptom List: Unevaluable event

Symptoms: Covid 19 vaccine exacerbated her chronic fatigue syndrome; Covid 19 vaccine exacerbated her chronic fatigue syndrome; atrial fibrillation; tachycardia/ heartrate got was 222 beats per minute; missing heartbeats; chills; fever; fatigue; lethargic; felt crummy; This is a spontaneous report received from a contactable consumer (patient). A 72-year-old female patient received the first dose of BNT162B2 (PFIZER COVID 19 VACCINE), via an unspecified route of administration, administered in Arm Left on 13Apr2021 15:00 (Batch/Lot number was not reported) at age of 72 years as single dose for covid-19 immunisation. Medical history included ongoing chronic fatigue syndrome at age 32 (she had been doing natural therapy and had gotten herself to a stable period but her chronic fatigue syndrome was still an issue sometimes), atrial fibrillation (had been admitted to the hospital because of it, she was not admitted to the hospital when she had atrial fibrillation after receiving her Covid 19 vaccine). The patient's concomitant medications were not reported. Historical vaccine included the first flu vaccine she every received sent her over the moon. Clarified she was in bed sick after receiving the flu vaccine. Patient was calling because she didn't do well with her first Pfizer Covid 19 vaccine. After the Covid 19 vaccine she experienced chills and fever on 13Apr2021 for a couple days. Then she had fatigue on 13Apr2021and that was a few days of her own chronic fatigue syndrome flaring up. She also had some problems with her heart like atrial fibrillation and tachycardia on 18Apr2021. She saw her cardiologist and he wanted her to do the dye stress test where she ran on the treadmill. The day her stress test was scheduled was the same day as her second Covid 19 vaccine. She was calling to find out if she can get the dye at her stress test and run on the treadmill and get the Covid 19 vaccine on the same day. Or does she need to put the stress test off for a couple weeks. She felt like the dye from the stress test and the Covid 19 vaccine might be too many chemicals in her body for one day. She felt like the Covid 19 vaccine exacerbated her chronic fatigue syndrome. She reported that something as simple as to much sugar or to much sun or exertion can also exacerbate her chronic fatigue syndrome. She was prepared in her thinking that the Covid 19 vaccine would be difficult for her because of her history with chronic fatigue syndrome. She had chills and a fever for a few days after the Covid 19 vaccine. She did not take her temperature to get a recorded number. She was lethargic and really felt crummy on 13Apr2021 for about the first 3 days. On day 4 she was better. Then the heart stuff started. Clarified, the atrial fibrillation and tachycardia started. She took medicine as needed for her atrial fibrillation and tachycardia. She had the atrial fibrillation and the tachycardia for about 3 days in a row. She reported she was stable now. She was able to monitor her heartrate on her watch. She then printed out her heart rate readings from her watch to take to her doctor. The highest her heartrate got was 222 beats per minute and that happened a couple times. Her watch only showed her heart rate as 150 beats per minute but when she printed the information it showed her true heart rate. She did see an electrophysiologist before she received her first dose of the Covid 19 vaccine. She was preparing herself for if anything was going to go wrong when she received the vaccine, she wanted to know what to do. She wanted to prepared in case the Covid 19 vaccine caused her any trouble. She was prescribed Diltiazem by her cardiologist to take as needed when she was having the tachycardia and atrial fibrillation. She was taking 15mg three times a day on the three days that she had the atrial fibrillation and tachycardia and it helped. She received her first dose of the Covid 19 vaccine on 13Apr2021 and according to her watch she started missing heartbeats on 14Apr2021. The atrial fibrillation and the really bad heart stuff started on 18Apr2021 and went on until 22Apr2021. She would say her heart issues started to resolve on the afternoon of the 22Apr2021. She was still missing heart beats according to her watch but nothing bad. She saw her cardiologist on Friday, 23Apr2021 and at that appointment she was in normal sinus rhythm. She has had some ups and downs since the 23Apr2021. Her second Covid 19 vaccine was scheduled for 04May2021 at 11:00AM. She did have a 3D echocardiogram and based on that, the doctor wanted to rule out any blocked arteries and that's why she's doing the stress test. AEs (atrial fibrillation and tachycardia) require a visit to Physician Office. Outcome of events chills, fever, lethargic, felt crummy was recovered on 17Apr2021, and the other events was unknown.

Other Meds:

Current Illness: Chronic fatigue syndrome

ID: 1305816
Sex: M
Age:
State: TX

Vax Date: 04/14/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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Allergies:

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

Symptoms: dehydration; low blood sugar; fatigued; Appetite; Pneumonia; Night sweats; Headache; Couldn't eat anything; Wheezing; migraine; Light, hacking cough; Fever/ 103.9 degrees; Chills; No more than 2-3 hours of sleep per night for 5 nights; Short of breath; This is a spontaneous report from a contactable consumer (patient). A 51-years-old male patient received the second dose of BNT162B2 (COVID-19 VACCINE), via an unspecified route of administration, administered on left arm on 14Apr2021 10:45 (Batch/Lot number was not reported) at age of 51 years as single dose. The patient medical history and concomitant medications was reported as none. Historical v for covid-19 immunisation accine included the first dose of BNT162B2 administered on left arm on 24Mar2021 at age of 51 years for covid-19 immunisation and experienced no issues. Patient reported that after the second dose of the Covid-19 vaccine, he had a fever for 8 days and was diagnosed with pneumonia on 21Apr2021. Patient reported that he was tested for both Covid-19, Influenza A, and Influenza B twice on 19Apr2021 and 21Apr2021 and tested negative for Covid-19 and influenza both times. Patient reported that he had no pre-conditions and that he was feeling great the night before he received the second dose of the Covid-19 vaccine, 13Apr2021. Patient reported that he was planning to go to work following the second dose of the Covid-19 vaccine on 14Apr2021. He began running a low-grade fever (102 degrees) on 14Apr2021 after receiving the Covid-19 vaccine and then his temperature flared up to 103.5 degrees on 15Apr2021. Fever: He received the second dose of the Covid-19 vaccine at 10:45 on 14Apr2021 and about 2:00 in afternoon on 14Apr2021 was the first fever that was significant. The last fever he had on 21Apr2021, his temperature was 103.9. He was put on antibiotics for pneumonia. He contacted the on-call nurse for his company. The on-call nurse advised him to see a doctor on Saturday, 17Apr2021.He went to the doctor on Monday, 19Apr2021. The doctor only ran a Covid-19 swab for testing and a flu swab. His doctor did not do blood work and stated that the patientwas experiencing an ill effect of the Covid-19 vaccine and sent the patient home. He went back to the doctor on Wednesday, 21Apr2021. When he went back to the doctor, the staff performed a chest X-ray and ran 4 different blood works to see what the patient had. The second Covid-19 test that he received on 22Apr2021 was performed with both the rapid test and the test that was sent off. Both Covid-19 tests came back negative. SARS test on 22Apr2021 was negative. 508-3 High Sensitivity CRP: One of his numbers that was parts per liter, 3 is considered to be high risk and he had 300 (300+) of whatever it was on 21Apr2021. He went back to the physician and was given another steroid shot an additional prescription. He had been back to the doctor 3 times since then. Fever: His fever was 103 consistently after 15Apr2021. 508-3 High sensitivity CRP: This value showed abnormal. The results said that relative risk was greater than 1 mg/liter and high was greater than 3. 1000 CBC with auto differential on 21Apr2021: The abnormal results were red blood cells measured at 4.38; hematocrit measured at 13.82; MCHC measured at 36.4; Neutrophils measured at 84; Lymphocytes measured at 12; and absolute Lymphocytes measured at 0.57. He wore a Garmin and that it recorded that he received no more than 2-3 hours of sleep per night for 5 nights. He didn't know anything about pneumonia previously and that he had specifically told his physician's office everything about what he was experiencing. He told his physician about the wheezing in his chest (on 17Apr2021), cough (on 16Apr2021), fever, and chills (on 14Apr2021). His physician told him it was a normal reaction to the Covid-19 vaccine and sent him home on 19Apr2021. He then consulted Google and started to realize that his side effect were very atypical. Wheezing: When he breathed really light, the crackling would continue. If he breathed shallow, the wheezing was audible but if he breathed deeply, it was not. The pneumonia was in the left side of his chest. He was still being treated for the pneumonia. He has his last dose of medication tomorrow, 27Apr2021, and that he was also being released to go back to work tomorrow. Cough: He had a little cough that would then go away. The cough began late Friday, 16Apr2021. It was interesting because it wasn't a main part of the illness. The cough was just kind of a hacking cough every once in awhile. The cough was not continuous like go and go and go and stop. The cough came, went away for awhile, then came again.The cough being worse was relative. He was coughing more than he did on Wednesday 21Apr2021, Thursday 22Apr2021, and Friday 23Apr2021. The cough was consistent more so at night when he laid down. He would probably say that it was a different feel towards the cough but it was still a cough. The cough was still the same volume but not the same effect. Headache (on 18Apr2021): He had been waking up with headaches in the morning and going to bed with them at night. On Wednesday, 21Apr2021, the headache was due to dehydration from the fever and night sweats. Once he got away from the dehydration headaches, the headache got better but he had woken up with a headache the last few days and had a headache at bedtime a few nights in a row. The headache was usually a frontal headache and this morning, 26Apr2021, the headache was toward the back of his head. The headaches last a few hours until he started moving around. On Saturday, 17Apr2021 he experienced a migraine that would not go away. He didn't usually get migraines. The migraine lasted hours if not for a day and that the headache was something furious. Sunday 18Apr2021 was pretty much the same thing with the headache. Because of the massive fever, he couldn't eat anything at all (17Apr2021). The headache was mostly due to low blood sugar and dehydration. Appetite: His appetite improved after his second doctor's appointment on 21Apr2021. The second provider was a lot more straightforward and advised the patient that he needed to start taking care of himself and trying to force himself to eat. He forced himself to eat on 21Apr2021 and by Thursday 22Apr2021, he had a full appetite and was craving food again. Shortness of breath (Apr2021): Patient reported that the shortness of breath was just from being fatigued. Patient reported that he got out of breath from going up and down the stairs. He was unsure when the shortness of breath began because he was moving very little, but that he noticed the shortness of breath on Monday, 19Apr2021 when he got up to go to the doctor.On Friday 16Apr2021 and Saturday 17Apr2021, he had a really good break.On Friday 16Apr2021 from 9 AM to 1 PM, he had no fever and it was like the sun was coming out, then the fever hit really hard. The same thing happened on Saturday, 17Apr2021, but the fever free period lasted maybe a little longer. His fever returned and that the afternoon of Saturday 17Apr2021 was the worst he had been the entire time. On 13Apr2021 to get away from arm soreness, he did a few laps in the pool. On 13Apr2021 he had a new best time on the 100 in freestyle in the pool and that he felt really strong going into 14Apr2021 to get his second dose of the Covid-19 vaccine. There was nothing that would have indicated that he had anything going on before getting the second dose of the Covid-19 vaccine. Up until Saturday, 17Apr2021, he had only been taking Motrin and just taking 2 tablets. He had no break in between fevers and chills and was not able to get ahead of the fever with the Motrin. There was a long stretch where the Motrin wasn't working and his temperature didn't get below 100 for several days. He tried to cycle acetaminophen in beginning Saturday 17Apr2021 to try to get the acetaminophen in between the Motrin doses. When he went back to the doctor on 21Apr2021, the provider told him that he could take 3 to 4 Motrin tablets at a time but not to exceed 4 doses per day. He never took more than 3 tablets. Motrin was generic ibuprofen. Night sweats (on 21A

Other Meds:

Current Illness:

ID: 1305817
Sex: F
Age:
State:

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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Allergies:

Symptom List: Injection site pain, Pain

Symptoms: She couldn't take anymore I had to take her to hospital; Pain; she hasn't felt like this ever before but this is like you know, very unusual; She is not well; Swelling in her stomach and just very like gut thing; Back pain; Nausea; She was throwing up; This is a spontaneous report from a contactable consumer (patient's son). A female patient of unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date unknown), via an unspecified route of administration in Apr2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Reporter was calling because his mom had getting some very strange (Incomplete sentence). 2 weeks before 25Apr2021 (in Apr2021) patient got the Pfizer vaccine and the following week which was last week in Apr2021 she started feeling like kind like swelling in her stomach and just very like gut thing, back pain, Nausea, she was throwing up. So, yesterday (24Apr2021) she couldn't take anymore reporter had to take her to hospital. Reporter was just told they need to go to the emergency room. They gave her pain killers and that was yesterday and she felt better after the pain medications (Unspecified medications) but then the pain returned today (25Apr2021) and she said she hadn't felt like this ever before but this was like very unusual. A week after she got the Pfizer vaccine. So, they were just had trying to figure out what they could do because she was not well in Apr2021. Therapeutic measures were taken as a result of back pain included pain killers. The outcome of the event Pain was not recovered, outcome of the other events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305818
Sex: F
Age:
State: SC

Vax Date: 04/14/2021
Onset Date: 04/18/2021
Rec V Date: 05/11/2021
Hospital: Y

Vax Type:
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Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: had an allergy induced asthma attack; had an allergy induced asthma attack; low grade fever; chills; fatigue/ extreme fatigue; severe hot flashes; light headed; lips began to swell; heart rate and blood pressure were up; heart rate and blood pressure were up; did not feel that she was back to her "normal" as it were before receiving the vaccine; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient received the second dose of BNT162B2 (PFIZER COVID-19 VACCINE), via an unspecified route of administration, administered in right arm on 14Apr2021 07:15 (lot number: EW0151) at age of 46 years as single dose for covid-19 immunisation. The patient medical history included known allergies: Sulfa drugs and penicillin. Concomitant medications included ascorbic acid, biotin, boron citrate, calcium pantothenate, calcium phosphate, choline bitartrate, chromium picolinate, colecalciferol, cyanocobalamin, dl-alpha tocopheryl acetate, folic acid, inositol nicotinate, potassium iodide, pyridoxine hydrochloride, retinol palmitate (VITAFUSION WOMEN'S) daily received within 2 weeks of vaccination. Patient had historical vaccine included the first dose of BNT162B2 (lot number: ER8733) via an unspecified route of administration, administered in right arm on 24Mar2021 07:15 at age of 46 years as single dose for covid-19 immunisation. Prior to vaccination, patient was not diagnosed with COVID-19. Patient was not pregnant. It started with low grade fever, chills, fatigue and severe hot flashes, within 12 hours of the shot. Then the next day, extreme fatigue and light headed. Four days later the fatigue was still coming and going and then her lips began to swell, her heart rate and blood pressure were up and she had an allergy induced asthma attack. That was when she went to the hospital. They gave her a liquid shot Pepcid and prednisone with a bag of iv fluids. And sent in prescriptions for Benadryl, prednisone and Pepcid. Patient had taken them for a week. Patient was still suffering from some fatigue that came and went with her heart rate that appeared to be elevated. Patient did not feel that she was back to her "normal" as it were before receiving the vaccine. Adverse event start date was on 18Apr2021 10:30 AM. Adverse events resulted in emergency room/department or urgent care, hospitalization. Treatment was received. Since the vaccination, patient had not been tested for COVID-19. Outcome of events was recovered/resolved with sequel.

Other Meds: VITAFUSION WOMEN'S

Current Illness:

ID: 1305819
Sex: U
Age:
State: GA

Vax Date: 04/16/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type:
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Allergies:

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

Symptoms: sores on my body, they burn; sores on my body, they burn; blisters up; they are leaving ugly black mark; allergic reaction to the vaccine; could hardly breathe; itching; rash that looks like impetigo; rash that looks like impetigo; scabies; fever; chills; muscle ache and pain; severe headache, off and on; nausea; Diarrhea; swollen lymph nodes, upon my left arm; I started not being able to take my food; This is a spontaneous report from a contactable consumer, the patient. A 41-year-old patient of an unspecified gender received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot: EW0158, Expiry: 31Jul2021), via an unspecified route of administration in the left arm on 16Apr2021 (at the age of 41-years-old) as a single dose for COVID-19 immuniztaion. Medical history included hypertension. Concomitant medications include triamterene tablet, hydrochlorothiazide (HCTZ) tablet. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot: ER2613) on 20Mar2021 (at the age of 41-years-old) for COVID-19 immunization and experienced "sore arm right in the area where the injection site was". On 16Apr2021, the afternoon after the second vaccination, the patient experienced fever, chills, muscle ache and pain, severe headache (off and on), nausea, diarrhea for 2 days, swollen lymph nodes upon the left arm for about 5 days. On 16Apr2021, the patient experienced itching, rash that looked like impetigo but the emergency room people claimed it was scabies. The patient did not think he/she had scabies. At the emergency room, the patient's temperature was 99 and above. On an unspecified date, the patient experienced a lot of sores on the body which burn and itch. The sores started to heal after the patient was given 9cc of dexamethasone (DECADRON) and methylprednisolone for 7 days, however, they left ugly/bad black marks that looked exactly like measles or chicken pox (the patient had chicken pox when younger). The sores looked like impetigo, per the patient, when it blistered up and they burned and wouldn't heal and left the black mark and were very itchy. Luckily, the patient didn't get it on the face. The patient had been taking diphenhydramine (BENADRYL) since before the emergency room visit, and paracetamol (TYLENOL) daily including the day of the vaccination (and when the patient experienced a feeling of "unwillingness"), since an unknown date and the temperature lingered between 99 and 100. The doctor prescribed more diphenhydramine that the patient had taken one every 4-6 hours, basically around the clock. The patient was in bed, could hardly breathe as of an unspecified date. On an unspecified date in Apr2021 (3 days after the vaccination) the patient was unable to take food and was still at home and just now starting to take food. Per the patient, the body reacted so bad to the shot, this was an allergic reaction to the vaccine. The patient still had itching on the lower part of the leg. The events had put the patient out of work, since the second vaccination. The clinical outcome of itching, rash that looks like impetigo, scabies, "sores on my body, they burn", "blisters up", "they are leaving ugly black mark", allergic reaction to the vaccine, could hardly breathe, "I started not being able to take my food", fever, chills, muscle ache and pain, severe headache (off and on), nausea, diarrhea, swollen lymph nodes upon the left arm was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021467186 same patient/drug, different vaccine dose/AE

Other Meds: TRIAMTERENE; HCTZ

Current Illness:

ID: 1305820
Sex: F
Age:
State: CA

Vax Date: 04/13/2021
Onset Date: 04/13/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type:
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Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Acute suicidal ideation with strong intent to hang herself; Severe body aches; Severe chills; Had cognitive side effects where she was forgetting basic facts including her date of birth; This is a spontaneous report from a contactable physician. A 38-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: ER8729), intramuscularly in left arm on 13Apr2021 at 09:00 (at the age of 38-years-old) at single dose for COVID-19 immunization. Medical history included post-traumatic stress disorder (PSTD), obsessive-compulsive disorder (OCD), attention deficit hyperactivity disorder (ADHD), premature ventricular tachycardia, hashimoto's disease, migraine, celiac disease, hysterectomy and was diagnosed with COVID-19 prior vaccination. Concomitant medications included trazodone, lisdexamfetamine mesilate (VYVANSE), venlafaxine hydrochloride (EFEXOR XR), and metoprolol (METOPROLOL XR). The patient previously took sulfamethoxazole and trimethoprim (BACTRIM) and experienced allergy. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: ER2613) intramuscularly in left arm on 23Mar2021 at 09:00 (at the age of 38-years-old) at single dose for COVID-19 immunization. Prior to vaccination, the patient was diagnosed with COVID-19, did not receive any other vaccines four weeks prior. The patient was not pregnant at the time of vaccination. On 13Apr2021 at 17:00, the patient experienced acute suicidal ideation with strong intent to hang herself and at the same time she developed severe body aches and chills. The patient also had cognitive side effects where she was forgetting basic facts including her date of birth. It was reported that, all the side effects resolved after 1.5 days. No treatment was received for the events. The patient had not been tested for COVID-19 since vaccination. The outcome of the events was recovered on 15Apr2021.; Sender's Comments: Based on the information currently available, the event Suicidal ideation is considered most likely associated with intercurrent or underlying medical conditions, appear unrelated to the suspect drug.

Other Meds: TRAZODONE; VYVANSE; EFEXOR; METOPROLOL

Current Illness:

ID: 1305821
Sex: F
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital: Y

Vax Type:
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Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Heart attack; This is a spontaneous report from a non-contactable consumer (patient). This 70-year-old female patient (not pregnant at time of vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose in right arm on an unspecified date for COVID-19 immunization. Medical history and concomitant medication were not reported. 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. Covid-19 test was negative. The patient had a heart attack four days after first vaccination. The adverse event result in emergency room/department or urgent care and received treatment. Seriousness criteria was caused/prolonged hospitalization for 4 days, not results in death, not life threatening, not disabling/incapacitating, not congenital anomaly/birth defect. The outcome of event was recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305822
Sex: F
Age:
State: MI

Vax Date: 04/21/2021
Onset Date: 04/22/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

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

Symptoms: visual hallucinations lasting 18 hrs; 102?-104? fever lasting 36 hrs; loss of sensation from waist down for 12 hrs; This is a spontaneous report from a non-contactable other hcp (patient). A 20-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EW0170), intramuscular on 21Apr2021 12:45 PM as single dose for covid-19 immunisation. Medical history not reported. Patient not pregnant at the time of vaccination and not diagnosed with COVID-19 prior to vaccination, not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient intramuscular received first dose of bnt162b2 (Lot number= EW0150) on 31Mar2021 12:45 PM. On 22Apr2021 patient experienced 102?-104? fever lasting 36 hrs, visual hallucinations lasting 18 hrs, loss of sensation from waist down for 12 hrs. The outcome of events was recovered. Patient has not been tested for COVID-19 Since the vaccination. No follow-up attempts are possible. No further information is expected.; 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 event visual hallucinations 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: 1305823
Sex: F
Age:
State:

Vax Date: 04/13/2021
Onset Date: 04/14/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Felt like was going to pass out; Diarrhea; Vomited; This is a spontaneous report from a contactable consumer report for self. A female patient of an unspecified age received first doe of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 13Apr2021 3:00PM as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient had the first dose of the covid vaccine on 13Apr2021 around 3:00PM. The next day, 14Apr2021 around 3:00PM, she started to have symptoms. She had diarrhea, vomited, and felt like she was going to pass out. She was supposed to get her second dose of the covid vaccine on 04May2021 (second dose of the covid vaccine is scheduled on 04May2021). She was wondering if she will have the same reaction for the second dose. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 1305824
Sex: F
Age:
State: NV

Vax Date: 04/07/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: She tested positive for covid; tested positive for covid; This is a spontaneous report from a Pfizer-sponsored program, from a contactable consumer (patient husband). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on 07Apr2021 (Batch/Lot number was not reported) as 1st dose, single for covid-19 immunisation. The patient medical history and patient's concomitant medications were not reported. The patient experienced she tested positive for covid on an unspecified date. Reporter stated his wife got (first) shot on 07Apr2021 that was like 3 weeks ago and she was supposed to get second shot on 28Apr2021 which is Wednesday. She tested positive for covid. Now she has Covid. Reported asked if she should go and get the shot or not go and get the shot. The event outcome for events was unknown

Other Meds:

Current Illness:

ID: 1305825
Sex: F
Age:
State: ME

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: Arm pain at jab site (couldn't sleep on right side); Very tired; This is a spontaneous report received from a contactable consumer (patient herself). A 55-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection; lot number: Not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient historical vaccination included first dose of BNT162B2 for COVID-19 Immunization. On an unspecified date, the patient experienced arm pain at jab site (couldn't sleep on right side) and very tired. Outcome of the events was reported as unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305826
Sex: F
Age:
State: MO

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: she had just a slight smell but it was so horrible; This is a spontaneous report from a contactable nurse (patient). A 80-year-old female patient received bnt162b2, via an unspecified route of administration, administered in Right Deltoid on 22Jan2021 (Lot Number: EK9231) as 1st dose, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. She had the first one 22Jan2021 and after that (22Jan2021) she had just a slight smell but it was so horrible. She thought that it was the blanket on the bed and she had passed it off a little bit. When she had her first shot she had mild side effects and then the next morning she could eat a little bit. After her first COVID vaccine she only had the horrible smell. That episode was short and by the next morning she didn't have the smell anymore. The event was reported as medically significant. The outcome of the event was recovered on 23Jan2021. The reporter considered the causality was related.; Sender's Comments: As there is limited information in the case provided, the causal association between the event parosmia and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer 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: 1305827
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Fevers; chills; This is a spontaneous report from a contactable consumer (patient) via sales representative. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced fevers and chills on an unspecified date after vaccination. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305828
Sex: F
Age:
State:

Vax Date: 04/15/2021
Onset Date: 04/15/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: body aches; headache; nausea; chills; sore arm; swelled lymph node under the arm; This is a spontaneous report from a contactable other health care professional. A 46-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date were not reported), via an unspecified route of administration on 15Apr2021(at the age of 46-year-old) at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient was not pregnant at the time of vaccination. The patient experienced body aches, headache, nausea, chills, sore arm and swelled lymph node under the arm the evening after receiving the second dose on 15Apr2021. The outcome of the events (body aches, headache, nausea, chills, sore arm) was recovered on 17Apr2021 and swelled lymph node under the arm was recovered on 22Apr2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305829
Sex: U
Age:
State: CO

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: got covid infection after the first dose.14 days from the second dose; got covid infection after the first dose.14 days from the second dose; This is a spontaneous report from a Pfizer sponsored program from a contactable consumer. A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose 0n an unspecified date for COVID-19 immunisation. Medical history and concomitant medication were not reported. Patient had 21 days recommendation inquiry for covid. Patient got covid infection after the first dose. 14 days from the second dose (as reported). Patient was inquiring timeline for second dose. Covid test was positive. The outcome of events was unknown. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305830
Sex: F
Age:
State: UT

Vax Date: 03/30/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital: Y

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

Lab Data:

Allergies:

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

Symptoms: infection; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer (patient's wife). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 30Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The caller wanted to reschedule their second dose appointment because his wife got hospitalized due to infection. They missed the second dose last 24Apr2021. They received the first dose last 30Mar2021(More than 3 weeks). The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1305831
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Tested positive for Covid after both Covid vaccines; Tested positive for Covid after both Covid vaccines; had a Covid exposure in another country; This is a spontaneous report received from a contactable physician. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, first dose on an unspecified date (Lot Number: Not Provided), second dose on an unspecified date (Lot Number: Not Provided), both at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Physician stated she had a question about whether Pfizer was interested in tracking people who tested positive for the Covid virus after having the Covid vaccine. Physician stated she was calling on behalf of her Nephew. Patient tested positive for Covid twice, after both Covid vaccines. Patient travelled and had a Covid exposure in another country. Patient had two positive Covid tests. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the event Drug ineffective, COVID-19, exposure to SARS-CoV-2 and the suspect drug BNT162B2.

Other Meds:

Current Illness:

ID: 1305832
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: tired; This is a spontaneous report from a contactable nurse. A male patient of an unspecified age received BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medication were not reported. The patient went to work afterwards, and was only tired after the administration on an unspecified date. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305833
Sex: F
Age:
State: TN

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: swelled up; had a knot, was red; had a knot, was red; This is a spontaneous report from a contactable consumer (patient). A 43-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. The patient medical history included auto-immune disease and psoriatic arthritis. Concomitant medications included guselkumab (TREMFYA). Patient stated that with the first shot that she had a delayed reaction to her right arm and it did not pop up until week later. Stated that it swelled up, had a knot, was red and then went away. There was no product complaint to report. There was request for medical information. Patient wanted to know if this is from the vaccine or if she should go to doctor. Wanted to know if others had reported it. The outcome for the event was recovered. Information about lot/batch number has been requested.

Other Meds: TREMFYA

Current Illness:

ID: 1305834
Sex: F
Age:
State: NY

Vax Date: 03/29/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Whole Leg Pain after first dose of Covid Vaccine/hurt in her thighs, knees, calves, and down into her ankles; Lower back sore intermittently/The back pain fluctuates from a pressure and mild ache to soreness; This is a spontaneous report from a contactable other nurse (patient). A 65-year-old female patient received bnt162b2 (Pfizer-BioNTech Covid-19 Vaccine), via an unspecified route of administration, administered in Deltoid Left on 29Mar2021 10:30 (Batch/Lot Number: ER8727) as First Dose; Left Deltoid for covid-19 immunization. Vaccination facility type was in pharmacy. No vaccines administered on same date of the Pfizer suspect. None prior vaccinations within 4 weeks. Family medical history relevant to AE was none. Medical history included ongoing high cholesterol diagnosed about 30 years ago (it was hereditary), ongoing Hashimoto's thyroiditis diagnosed about 20 years ago. Concomitant medications included rosuvastatin taken for blood cholesterol from about 3 years ago in 2018 to Apr2021 (a few weeks after the first dose of the vaccine); levothyroxine sodium (UNITHROID) taken for Hashimotos thyroiditis and ongoing. Patient was not on any other cholesterol medication currently. About 2 weeks after the first vaccine she started having leg pain. It was whole leg pain. It hurt in her thighs, knees, calves, and down into her ankles. She went to her doctor who did doppler studies and found no blood clots in Apr2021. Thought maybe it was the cholesterol medications that she had been on for years; so she stopped taking it. The pain in legs subsided a few days later and ended a few days before she got the second vaccine. She was a hiker and was in amazing shape. She had not done anything different, nothing that would have exacerbated this. She believed her symptoms are medically significant as she did not know for sure what was causing them. She was uncertain if her symptoms have been caused by the Covid Vaccine. The event whole leg pain after first dose of Covid Vaccine required a visit to physician office. No emergency room visited. She had issues with her back. She noticed something new. Her lower back was sometimes sore. It came and went intermittently; unlike the leg pain that was constant. The back pain fluctuates from a pressure and mild ache to soreness. This also occurred after both vaccines. The outcome of back pain was not recovered, of other event was recovered in Apr2021. The reporter (patient) was uncertain if her symptoms have been caused by the Covid Vaccine.; Sender's Comments: Based on the information currently available,The casual association between the reported event "Pain in extremity","Back pain" and suspected vaccine BNT162B2 cannot be completely excluded. 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.,Linked Report(s) : US-PFIZER INC-2021467940 same patient/drug, different vaccine dose/AE

Other Meds: ROSUVASTATIN; UNITHROID

Current Illness: Hashimoto's thyroiditis (diagnosed about 20 years ago); High cholesterol (diagnosed about 30 years ago)

ID: 1305835
Sex: U
Age:
State: UT

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Stevens-Johnson syndrome; allergic reaction; This is a spontaneous report received from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as an unspecified dose for covid-19 immunisation. The patient medical history included sulfa allergies. The patient's concomitant medications were not reported. The patient stated that 'I had an allergic reaction to the Covid vaccine. Stevens-Johnson syndrome. Due to my past experiences with it, I knew what was going on and got treatment. Doing some googling I learned that those with sulfa allergies shouldn't get the shot. I told the pharmacy about the allergies. Please educate the pharmacies. I'm not taking this anywhere, because people should get the shot if they can'. Outcome of events was unknown.

Other Meds:

Current Illness:

ID: 1305836
Sex: F
Age:
State: NY

Vax Date: 04/20/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Whole Leg Pain after second dose of Covid Vaccine; Lower back sore intermittently; This also occurred after both vaccines.; Leg pain making it hard to sleep; This is a spontaneous report from PPDi. A contactable nurse reported herself that a 65-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Deltoid Right on 20Apr2021 10:15 (Batch/Lot Number: ER8731) as 2ND DOSE, SINGLE for covid-19 immunization, with Age at Time of Vaccination at 65 years old. Medical history included ongoing blood cholesterol increased (Verbatim: High cholesterol. Stated she was diagnosed about 30 years ago. Said it was hereditary), ongoing autoimmune thyroiditis (Verbatim: Hashimoto's thyroiditis. Stated she was diagnosed about 20 years ago). Historical vaccine included first dose of Covid Vaccine (Batch/lot number: ER8727) on 29Mar2021 given at 1030, at Left Deltoid and experienced whole leg pain (about 2 weeks after the first vaccine she started having leg pain). Concomitant medications included rosuvastatin taken for blood cholesterol from an unspecified start date to Apr2021 (reported as Started medication about 3 years ago. Stopped a few weeks after the first dose of the vaccine, was not on any cholesterol medication at this time); levothyroxine sodium (UNITHROID) taken for autoimmune thyroiditis from an unspecified start date and ongoing. The patient experienced whole leg pain after second dose of covid vaccine (medically significant) on Apr2021 with outcome of not recovered, lower back sore intermittently (non-serious) on Apr2021 with outcome of not recovered, leg pain making it hard to sleep (non-serious) on Apr2021 with outcome of unknown. The patient underwent lab tests which included ultrasound doppler: no blood clots on Apr2021. Reported she went for her second vaccine and about 5 days later the leg pain came back. Said she took Tylenol and Motrin, nothing helps the pain. Said her legs have been hurting for about 4 days now. Stated that her pain seems unusual because it goes all the way down into her ankles and travels back and forth. Caller stated that she was a hiker and was in amazing shape. She had not done anything different, nothing that would have exacerbated this. Caller states she retired after being a Licensed Practical Nurse for 30 years in 2019. Caller stated that the leg pain after her first vaccine started about 2 weeks after the vaccine and lasted for about a week. Said it ended a few days before she got the second vaccine. Caller stated that her leg pain after the second vaccine was ongoing. Said that she got the vaccine on a Tuesday and her legs started to hurt again around Friday. Said that was effecting her life. Her legs hurt in every position. It was making it hard for her to sleep. Stated she believed her symptoms were medically significant as she did not know for sure what was causing them. Later in the call the caller mentioned that she had issues with her back. Said she noticed something new. Her lower back was sometimes sore. It comes and goes intermittently; unlike the leg pain that was constant. Stated the back pain fluctuates from a pressure and mild ache to soreness. This also occurred after both vaccines. Treatment received included: Tylenol and Motrin that did not offer any relief for her leg pains: Tylenol Extra Strength 500mg; P121876; Expiration Date: Sep 2023. Stated she took 2 tablets at a time. Motrin 200mg; 0GE2545A; Expiration Date: Mar 2022. Stated she took 2 tablets at a time. Causality: Stated she was uncertain if her symptoms have been caused by the Covid Vaccine. Follow-up attempts have been completed.; Sender's Comments: Based on the temporal association, there is a reasonable possibility that the administration of vaccination BNT162B2 played a contributory role in triggering the onset of the event pain in extremity. 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 Committees and Investigators, as appropriate.,Linked Report(s) : 2021467913 same patient/drug, different vaccine dose/AE

Other Meds: ROSUVASTATIN; UNITHROID

Current Illness: Hashimoto's thyroiditis (Verbatim: Hashimoto's thyroiditis. States she was diagnosed about 20 years ago.); High cholesterol (Verbatim: High cholesterol; States she was diagnosed about 30 years ago. Says it is hereditary.)

ID: 1305837
Sex: U
Age:
State: GA

Vax Date: 04/15/2021
Onset Date: 04/18/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: a lump in between my shoulder blade and my collar bone. The lump it is like size of a small grape like a very small grape; little sore right there; This is a spontaneous report from a contactable consumer (patient). A 39-years-old patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose via an unspecified route of administration, administered in left arm on 15Apr2021 (Lot Number: EW0162; Expiration Date: 31Jul2021) as single dose for covid-19 immunisation. There were no medical history and concomitant medications. Patient previously received first dose of vaccine on 25Mar2021 (lot number: EN6207) administered in left arm for COVID-19 immunization. Patient had COVID vaccine second shot on last Thursday on 15Apr2021 and on Sunday this past Sunday on 18Apr2021, patient noticed had a lump in between shoulder blade and collar bone and patient noticed it was little sore right there and started rubbing it and a little lump there. Patient stated that the lump it is like size of a small grape like a very small grape. Patient stated the lump is there and still a little sore, the soreness has improved but the lump is still there. Patient stated no treatment. No investigation assessment. The event outcome for a lump in between my shoulder blade and my collar bone. The lump it is like size of a small grape like a very small grape was not recovered, for little sore right there was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305838
Sex: M
Age:
State: PA

Vax Date: 02/03/2021
Onset Date: 04/20/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Got COVID; Got COVID; This is a spontaneous report received from a contactable consumer. A 52-years-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 03Feb2021 08:00 (Batch/Lot Number: EL9262) as single dose, dose 2 via an unspecified route of administration, administered in Arm Right on 23Feb2021 08:00 (Batch/Lot Number: EL9269) as single dose, both vaccinated at the age of 52 years old for covid-19 immunisation. The patient medical history was not reported. The patient was not diagnosed with COVID-19 prior to vaccination. Concomitant medications included adalimumab (HUMIRA) taken for an unspecified indication, start and stop date were not reported; levothyroxine taken for an unspecified indication, start and stop date were not reported. The patient got covid. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 20Apr2021. patient visited Doctor or other healthcare professional office/clinic visit. Outcome of events was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds: HUMIRA; LEVOTHYROXINE

Current Illness:

ID: 1305839
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: I broke out whit little bumps; I am itchy all over; Last night it was so bad it was burning; This is a spontaneous report from a contactable consumer (patient). A 65-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Formulation: Solution for injection) via an unspecified route of administration as single dose for covid-19 immunisation. Medical history included covid-19, patient had Covid back in December at Christmas time. Concomitant medication was not reported. On an unspecified date the patient experienced broke out with little bumps and experienced itchy all over, and last night it was so bad it was burning. Second dose was scheduled on 15, patient stated it is not contraindicated to receive the second dose based on his reaction. Therapeutic measures were taken by taking Benadryl which helping a little bit. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305840
Sex: F
Age:
State:

Vax Date: 03/09/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Tiny bit of arm hurting; This is a spontaneous report from a contactable patient. A 69-years-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 09Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation . Medical history included diabetes from 2004 and ongoing she has had diabetes since 2004. The patient's concomitant medications were not reported. The patient experienced tiny bit of arm hurting on an unspecified date with outcome of unknown. She received the first dose of the vaccine on 09Mar2021 and had no symptoms, just a tiny bit of arm hurting for a couple of days. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness: Diabetes

ID: 1305841
Sex: M
Age:
State: CA

Vax Date: 04/22/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: fever; headache; muscle pain; chills; he can't stand up very well because he feels weak; he can't stand up very well because he feels weak; This is a spontaneous report from a Pfizer received from a contactable consumer (patient). A male patient of an unspecified age received second dose of bnt162b2 (Pfizer Covid-19 Vaccine), via an unspecified route of administration on 22Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (Pfizer Covid-19 Vaccine), via an unspecified route of administration on 01Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for COVID-19 immunization. On an unspecified date of Apr2021, the patient experienced fever, headache, muscle pain, chills and also reported that he could not stand up very well because he felt weak. The outcome was unknown for the reported events. No follow-up attempts are possible; information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305842
Sex: M
Age:
State: PA

Vax Date: 04/23/2021
Onset Date: 04/23/2021
Rec V Date: 05/11/2021
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Allergies:

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

Symptoms: Experienced a headache before and after the first dose; This is a spontaneous report received from a Pfizer and medical information team. This consumer reported for her husband (patient) that a male patient of unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: Unknown), via an unspecified route of administration on 23Apr2021 as single dose for COVID-19 immunisation. The patient's medical history included headache. The concomitant medications were not reported. The reporter (patient's wife) mentioned that her husband just had the first dose today 23Apr2021 and experienced a headache before and after the first dose. The outcome of the event headache was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305843
Sex: F
Age:
State:

Vax Date: 04/01/2021
Onset Date: 04/07/2021
Rec V Date: 05/11/2021
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Allergies:

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

Symptoms: Tested positive for Covid; Sick; This is a spontaneous report from a contactable consumer (patient sister). A female patient of an unspecified age received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: UNKNOWN) via an unspecified route of administration on 01Apr2021 as single dose for COVID-19 immunization. The patients medical history and concomitant medication was not reported. It was reported that the patient had her 1st dose of Covid 19 vaccine on 01Apr2021 then on 07Apr21 the patient was really sick and then on 10Apr2021 she was tested positive for Covid and her 2nd dose was today 23Apr2021 and cannot make it. The outcome of the events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am