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: 1315960
Sex: F
Age: 33
State: TX

Vax Date: 04/30/2021
Onset Date: 04/30/2021
Rec V Date: 05/13/2021
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Lab Data:

Allergies: Seasonal allergy, sun allergy, dust allergy

Symptom List:

Symptoms: Long lasting Rashes all over the body , some are peeling by now or obscured, but since 2 days ago I got new rashes, smaller in shape than the other ones but now in areas that I didn't have the first time (abdomen, inner tights , and glutes), and more in some areas , arms , back, chest and legs.

Other Meds: Move free, vitamin b, c and e

Current Illness: None

ID: 1342671
Sex: F
Age: 65
State: LA

Vax Date: 04/10/2021
Onset Date: 04/17/2021
Rec V Date: 05/13/2021
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Symptoms: None stated

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Current Illness:

ID: 1385451
Sex: M
Age: 65
State: WA

Vax Date: 03/22/2021
Onset Date: 04/15/2021
Rec V Date: 05/13/2021
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Allergies: NKDA

Symptom List:

Symptoms: Began having nose bleeds, progressively more frequently appx 1 month after COVID VACCINE #2.

Other Meds: Terazosin, Simvastatin, ASA, ?Saw Palmetto

Current Illness: None

ID: 1409973
Sex: F
Age: 45
State: OH

Vax Date: 04/10/2021
Onset Date: 04/17/2021
Rec V Date: 05/13/2021
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Allergies: Sulfa

Symptom List:

Symptoms: Patient seen in the office with persistent fatigue, joint pain. ANA +; Further workup shows Anti-DsNA antibody equivocal, histone Antibody positive, all other work up negative.

Other Meds: Escitalopram 10 mg-held for 3 days prior to vaccine

Current Illness: None

ID: 1409974
Sex: F
Age: 60
State: OH

Vax Date: 03/08/2021
Onset Date: 03/27/2021
Rec V Date: 05/13/2021
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Lab Data:

Allergies: Penicillin

Symptom List:

Symptoms: Severe neuropathic left flank pain gradually improving after 6 weeks.

Other Meds: Atorvastatin.B12, Lidocaine Patch. Probiotic.VitC.Vit .D

Current Illness: right leg radiculopathy

ID: 1417399
Sex: M
Age: 62
State: GA

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 05/13/2021
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Allergies: Sulfasalazine, Celebrex, statin

Symptom List:

Symptoms: After 2nd COVID-19 vaccine began having Malaise, chills, fever, polyarthralgias, myalgias Joint pain, stiffness, inflammation and tenderness in multiple Joint, tendon ruputure, DVT.

Other Meds: Ambien, Prilosec, folic acid, vit D, Cymbalta, Alfuzosh

Current Illness: N/A

ID: 1420173
Sex: M
Age: 13
State: AZ

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

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Allergies: NKDA -latex

Symptom List:

Symptoms: Several minutes after receiving vaccine patient vomited. Monitored patient and he was fine after 15 minutes

Other Meds: multivitamins

Current Illness: NO

ID: 1420231
Sex: F
Age: 20
State: WI

Vax Date: 05/13/2021
Onset Date: 05/03/2021
Rec V Date: 05/13/2021
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Allergies: NONE

Symptom List:

Symptoms: Pt felt scratchy throat, said it felt like a lump was forming in throat. Benadryl 50mg PO x1 given as precaution, Pt kept for 15 extra Min for observation

Other Meds: NONE

Current Illness: Chest & Back Pain

ID: 1315888
Sex: F
Age:
State: MA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 05/14/2021
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Symptoms: Slight left arm pain in muscle near injection site.; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 29-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Lot Number: El3247), dose 1 via an unspecified route of administration in left arm on 26Jan2021 at 13:15 (at the age of 29-years-old) 1ST DOSE SINGLE for Covid-19 immunisation. Patient's medical and concomitant medication history were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. No covid test post vaccination. No other vaccine in four weeks. The patient didn't receive other medication in two weeks. The patient experienced slight left arm pain in muscle near injection site on 26Jan2021 at 21:00. The adverse events did not require any treatment. The outcome of the event was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315889
Sex: F
Age:
State: MO

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 05/14/2021
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Symptoms: Sore arm; Tiredness; Body Aches; This is a spontaneous report from a Contactable Consumer(other Non HCP). A 20-year old non pregnant female patient started to receive first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EK9231),via intramuscular route of administration in left arm on 15Jan2021 02:15 PM as 1st dose single dose for COVID-19 immunization. The patient medical history was reported as none, No known allergies reported. Patient received medications within 2 weeks of vaccination which was Penicillin. Patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the vaccination. On 15Jan2021 at 8:00pm the patient experienced Sore arm, Tiredness, Body Aches. The patient did not receive any treatment for the adverse events. The outcome for the events were recovered/resolved on an unspecified date. Follow-up attempts are completed. No further information is expected.

Other Meds: PENICILLIN [BENZYLPENICILLIN]

Current Illness:

ID: 1315890
Sex: M
Age:
State: IN

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 05/14/2021
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Symptoms: Headache; insomnia; This is a spontaneous report from a contactable Other HCP (patient). A 24-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: unknown), via an unspecified route of administration in right arm on 25Jan2021 at 05:00 PM as 2nd dose, single for COVID-19 immunization. Patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: unknown), via an unspecified route of administration on an unspecified date as 1st dose, single for COVID-19 immunization. Medical history and concomitant medication were not reported. Facility where the most recent COVID-19 vaccine administered was hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 26Jan2021 at 07:00 PM, patient experienced headache, insomnia. No treatment was received for the adverse events. The outcome of the events was not recovered. Information on the lot/batch number has been requested. Follow-up (15Apr2021): This follow-up is being submitted to notify that the batch/lot number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1315891
Sex: F
Age:
State: SC

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 05/14/2021
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Symptoms: Severe nausea and strange taste in mouth, localized muscle pain in left arm, dizziness, headache; Severe nausea and strange taste in mouth, localized muscle pain in left arm, dizziness, headache; Severe nausea and strange taste in mouth, localized muscle pain in left arm, dizziness, headache; Severe nausea and strange taste in mouth, localized muscle pain in left arm, dizziness, headache; Severe nausea and strange taste in mouth, localized muscle pain in left arm, dizziness, headache; This is a spontaneous report from a contactable pharmacist (patient). A 34-years -old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot Number: EL9262) (non-pregnant at the time of vaccination) via unspecified route of administered in arm left on 26Jan2021 at 11:00 AM as SINGLE DOSE for COVID-19 immunisation. The patient's medical history included known allergies: sulfa antibiotics. Concomitant medications (list of any other medications the patient received within 2 weeks of vaccination) included sertraline, baclofen, tylenol, pantoprazole. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot Number: EL1284) via unspecified route of administered in arm left on 05Jan2021 at 10:30 AM as SINGLE DOSE for COVID-19 immunisation. 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 was not tested for COVID-19. On 26Jan2021, at 12:30 PM the patient had severe nausea and strange taste in mouth, localized muscle pain in left arm, dizziness, headache. It was unknown whether the patient received treatment for the events. The outcome of the events was not recovered/ not resolved. Follow-up attempts are completed. No further information was expected.

Other Meds: SERTRALINE; BACLOFEN; TYLENOL; PANTOPRAZOLE

Current Illness:

ID: 1315892
Sex: F
Age:
State: TX

Vax Date: 01/19/2021
Onset Date: 01/21/2021
Rec V Date: 05/14/2021
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Symptoms: Severe heart palpitations for two days; This is a spontaneous report received from a contactable physician (Patient) reported for herself. A 73-year-old non pregnant female received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: 123) via an unspecified route of administration in right arm on 19Jan2021 14.30 single dose for covid-19 immunisation. The patient medical history included irregular heart beat. Concomitant medication included diltiazem. Allergies to medications, food, or other products were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since vaccination. On 21Jan2021, the patient experienced severe heart palpitations for two days. No treatment was received for the adverse events. The reporter considered the event as non-serious. The outcome of events was recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: DILTIAZEM

Current Illness:

ID: 1315893
Sex: F
Age:
State: MN

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 05/14/2021
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Symptoms: Swollen and painful lymph node at base of the neck (over the clavicle) on left side (side of injection) and tender lymph nodes on the right side of the neck; Swollen and painful lymph node at base of the neck (over the clavicle) on left side (side of injection) and tender lymph nodes on the right side of the neck; This is a spontaneous report from a contactable other HCP (patient reported herself). A 22-year-old non-pregnant female patient received second dose of BNT162B2 (COVID 19, Pfizer, Solution for injection) via an unspecified route of administration to her left arm on 25Jan2021 02.00 PM as single dose for Covid-19 immunization. Facility where the most recent COVID-19 vaccine was administered: Hospital. The patient's medical history included anxiety and depression. No known allergies. Concomitant medications included iron supplements and desogestrel/ethinylestradiol (DESOGESTREL AND ETHINYL ESTRADIOL) (both received within 2 weeks of vaccination). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took BNT162B2 (COVID 19, Pfizer) via an unspecified route of administration to her left arm on 06Jan2021 03.00 PM as single dose for Covid-19 immunization. On 26Jan2021 07:00 PM, the patient experienced swollen and painful lymph node at base of the neck (over the clavicle) on left side (side of injection) and tender lymph nodes on the right side of the neck. The events were assessed as non-serious. The patient had been tested for COVID-19. Covid test type post vaccination, nasal swab in Oct2020 showed negative and saliva test in Nov2020 showed negative. She did not receive any treatment in response to the events. Outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds: DESOGESTREL & ETHINYL ESTRADIOL

Current Illness:

ID: 1315894
Sex: F
Age:
State:

Vax Date:
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Rec V Date: 05/14/2021
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Symptoms: headache; eye dryness; having trouble with my eyes; soreness; This is a spontaneous report from a contactable consumer (patient) via Medical information Team. A female patient of an unspecified age received BNT162B2 (BNT162B2, Solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/lot number: Not Provided, NDC number of Pfizer COVID 19 vaccine: Not Provided, Reason for no lot number: of Pfizer COVID 19 vaccine: Caller unwilling to complete the report, Expiry Date of Pfizer COVID 19 vaccine: Not Provided) as 1st Dose, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced headache (non-serious) on an unspecified date, eye dryness (non-serious) on an unspecified date, having trouble with my eyes (non-serious) on an unspecified date, soreness (non-serious) on an unspecified date. Consumer was calling reporting AE after receiving her first dose of Pfizer-Biontech Covid19 vaccine. She stated that she got the headache and the soreness but those "didn't bother her" she was worried about "having trouble with my eyes" specifically eye dryness, was this normal. She was due for the second shot on 09Feb2021, should she still get it. Patient stated that HA soreness but that didn't bother me- " i've been having trouble with my eyes" due for 2nd shot 09Feb2021. Trouble with her eyes being dry- SE. Should I go ahead and get the second one. Headache lasting 2-3 days. Additional Context: Received call from consumer regrading the Pfizer Covid 19 vaccine which she received a few days ago. She had a slight headache for 2-3 days, which she thought was normal. She was also having trouble with her eyes being dry and she would like to know if that is normal. She did not wish to provide an address or email. She did not wish to complete report and requested to be transferred to have her question answered. No further details provided. For events, headache, outcome was recovered on an unspecified date, eye dryness, outcome was unknown, having trouble with my eyes, outcome was unknown, soreness, outcome was unknown. Information on lot and Batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315895
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/14/2021
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Symptoms: after receiving her first vaccine dose she experienced body aches and fever; after receiving her first vaccine dose she experienced body aches and fever; sore throat; This is a spontaneous report from a Pfizer-sponsored Program. A Contactable female Pharmacist reported that: A female patient of an unspecified age received bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection;), dose 1 via an unspecified route of administration on an unspecified date as SINGLE DOSE for an unspecified indication.The patient medical history was not reported.The patient's concomitant medications were not reported. The patient experienced after receiving her first vaccine dose she experienced body aches and fever , after receiving her first vaccine dose she experienced body aches and fever , sore throat on an unspecified date Question: Warm transfer from (name) with Pfizer first connect, CEP 2191. Caller is a pharmacist, asking if it is ok to get the second dose of the covid vaccine with a recent sore throat that may or may not be strep Caller reports that she has a sore throat, she has not been tested for strep but is due to get her second vaccine dose and is asking for additional guidance During this call the caller also reported that after receiving her first vaccine dose she experienced body aches and fever but did not report it because it was consistent with the common side effects. E-transmitting for AE data capture. Caller did not report symptoms because they were consistent with the listed common side effects. Remembered AE after call end. The events were assessed as Non serious by health authority outcome of the events was sore throat was unknown. Outcome of remaining events was recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315896
Sex: F
Age:
State: PA

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 05/14/2021
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Symptoms: left arm was inflamed and in pain and she was unable to lift it; woke up with pain in my left arm from my shoulder to my wrist; her left arm was inflamed; This is a spontaneous report from a contactable consumer. A 76-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: unknown), on unspecified route of administration on unspecified date at single dose for COVID-19 immunisation. Medical history was not reported. concomitant medication included Apixban (ELIQUIS) from an unknown date. The patient had taken vaccine in right arm, but she did not have any discomfort in that arm, whereas At 3:00am her left arm was inflamed and in pain and she was unable to lift it, she had to use her right arm to move her left arm. she had taken a blood thinner right before she got her vaccination. The outcome of events was unknown. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected. Information on the Batch/Lot number has been requested.

Other Meds: ELIQUIS

Current Illness:

ID: 1315897
Sex: F
Age:
State: SC

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 05/14/2021
Hospital:

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Symptoms: cold symptoms; runny nose; cough; headache; chills; I noticed I had a rash and it was swollen on my Right Arm where the injection site was.; I noticed I had a rash and it was swollen on my Right Arm where the injection site was.; pain and itching started; pain and itching started; most of the time it is not itching, just red.; it is a flat rash, no raised areas; This is a spontaneous report from a contactable consumer. A 68-years-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Right on 13Jan2021 09:00 (Batch/Lot Number: EL0142; Expiration Date: Mar2021) as !st dodse single for covid-19 immunization.The patient's medical history concomitant medications were not reported.The patient previously took influenza vaccine and experienced slight rash, and slight rash that itched.The patient experienced I noticed i had a rash and it was swollen on my right arm where the injection site was, pain and itching started outcome of recovered, pain and itching started on 13Jan2021, cold symptoms, runny nose, cough, headache, chills on 14Jan2021, most of the time it is not itching, just red and it is a flat rash, no raised areas on Jan2021. Caller is calling about Pfizer COVID vaccine. She stated that she got the first dose and is scheduled to have 2nd on Monday. Her doctor is a little concerned about her taking the second dose. The pa-tient stated that she received the First dose of the covid vaccine on 13Jan, she didn't notice any signs and symptoms initially, She didn't have any reaction within the first 15 minutes until that evening she had the vaccine at 9am. At approximately 6pm when I was changing my clothes after work, she noticed she had a rash and it was swollen on my Right Arm where the injection site was and the past couple weeks she has felt like she had a cold with a runny nose, headache. The rash lasted about 4-5 days and now it has come back and its huge so the doctor is concerned saying He said that he wanted her to pay attention to what is happening first 4 hours after the vaccine and in that periodShe actually hadn't looked at it prior to then, she had gone back to work and wasn't hav-ing any symptoms, but that evening is when the pain and itching started. but she doesn't recall looking to check until that night. Her doctor just couldn't find anything about a rash lasting this long. Yesterday she had some chills and cold symptoms and the rash she noticed it came back, it is on the back of her arm so it is not exactly easy to see. Her doctor wanted her to call and see if anyone else has had that kind of reaction. It has kind of started to fade away and she wasn't having symp-toms so she wasn't really paying attention to it because it wasn't itching. Sometimes she looked it would look like it was almost gone but now it is back with a vengeance. Her first dose was 13Jan2021 and that same evening is when she noticed it, she noticed it when it started itching. The first 4 days were pretty bad with itching really bad, it itched for about 4 days and then the rash started to go away but now it itched slightly yesterday but now most of the time it is not itching, just red. She says it is a flat rash, no raised areas. The signs and symptoms lasted 4 days, as far as the itching and redness, by 2nd and 3rd day the itching was really bad and then the itching im-proved a little bit by the 4th day and was gone by the fifth day. The day after she had the vaccine, she also started having cold symptoms, runny nose, cough and headache. But then, she still had cold symptoms, kinda like you are coming down with a cold, nose runny, slight cough and little bit of a headache. Still having these now, not quite as bad, it seems to be getting better. Monday night this week, a week and a half after the vaccine, the rash came back in the same area the right arm, she went back to the doctor this morning. She was concerned about getting the second dose after this rash. Yesterday she had some slight chills, but no itching. Her MD wanted her to call be-cause he didnt' know if she had the rash the rash immediately following the vaccine or if the symp-toms came on later, because she didn't feel anything. He enguired if she Should get the second dose? After information was provided to caller regarding referring to Health care provider, she stated that she was hoping to see if maybe there was information in studies if anyone had similar reaction and still received the second vaccine."The outcome of the events i noticed i had a rash and it was swollen on my right arm where the injection site was, pain and itching (pain), most of the time it is not itching, just red, is a flat rash, no raised areas was unknown, outcome of pain and itching (pruritus) was recovered on unspecified date, outcome of cold symptoms, runny nose, cough, headache was recovering.

Other Meds:

Current Illness:

ID: 1315898
Sex: F
Age:
State: IN

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 05/14/2021
Hospital:

Vax Type:
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Symptoms: Headache; nausea; injection site pain; This is a spontaneous report from a contactable 43-year-old female Other HCP reported for herself that she received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/lot number: EU9231), via an unspecified route of administration on 18Jan2021 at 09:00 am in left arm as single dose for covid-19 immunization. The patient's medical history and concomitant medications not reported. Historical vaccine included bnt162b2 on 28Dec2020 (lot number=EJ1685, vaccine location-left arm, dose number-1, administration time-09:00 AM) for covid-19 immunisation. On 18Jan2021, the patient experienced headache, nausea, and injection site pain. The patient did not take treatment for the events. The outcome of the events was recovered on an unknown date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315899
Sex: F
Age:
State:

Vax Date: 01/26/2021
Onset Date: 01/01/2021
Rec V Date: 05/14/2021
Hospital:

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Symptoms: Had first dose yesterday experienced normal side effects also had diarrhea asking how long it will go; This is a spontaneous report from a contactable consumer (reported for herself). A female patient of an unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/Lot number: Not Provided) via an unknown route of administration on 26Jan2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The reporter (type of HCP the reporter was, not clarified) stated that she had the first dose on 26Jan2021 and was experiencing normal side effects and also experienced diarrhea. Reporter did not provide what the normal side effects were. Outcome of the event was not reported (unknown) Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315900
Sex: F
Age:
State: MO

Vax Date: 01/20/2021
Onset Date: 01/22/2021
Rec V Date: 05/14/2021
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Symptoms: Hands it started drying up; My skin when I washed my hand it started too turn red and felt like they were on fire; My skin when I washed my hand it started too turn red and felt like they were on fire; Body is irritated/ my hands is turning irritated; Feel itchy almost anywhere my face, neck. Arms, and legs upper back/ my legs get itchy/ itchy skin feeling; My face is irritated by the itchy skin feeling; This is a spontaneous report from a contactable Other HCP (reported for herself). A 37-years-old non pregnant female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Formulation: Solution for injection, Batch/Lot number: not reported) administered in left arm via an unknown route of administration on 20Jan2021 at 03:00 as SINGLE DOSE for covid-19 immunization. Medical history included allergies to medications, food, and other products included catfish, fish oil pills. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and medications within 2 weeks of vaccination. It was reported that On 22Jan2021 at 10:00, patient had all the side effects plus a few more as hands it started drying up patient skin when she washed hand it started to turn red and felt like they were on fire and still today a week down the road patient still having trouble with hands and body is irritated by it. Patient feel itchy almost anywhere on face, neck. Arms, and legs upper back, still is bothersome with irritation to itch cause skin is drying up or something and hands are turning irritated the most when patient get them wet and legs get itchy after wash them. patient face was irritated by the itchy skin feeling. No treatment was received for the adverse events. On an unknown date, the events were recovered with sequelae. The vaccine was administered in nursing home/senior living facility. Prior to vaccination, was the patient has not diagnosed with COVID-19. Since the vaccination, the patient has been not tested for COVID-19. No follow-up attempts were possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 1315901
Sex: M
Age:
State: MD

Vax Date: 01/27/2021
Onset Date: 01/28/2021
Rec V Date: 05/14/2021
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Symptoms: Intense Headache 7-10 of 10; Low grade fever 100.4; Significant bodyaches; cold sweats; This is a spontaneous report from a contactable other health care professional (Patient, self-reported). A 51-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL3247) via an unspecified route of administration, administered in arm left on 27Jan2021 07:30AM, as second dose, single, dose 1, (Batch/Lot Number: EJ1686), via an unspecified route of administration, administered in Arm Left on 06Jan2021 07:30AM, as first dose, single for covid-19 immunization. Reportedly other medical history was none. Patient did not have allergies to medications, food, or other products/known allergies. Concomitant medication included paracetamol (TYLENOL) and ibuprofen (MOTRIN [IBUPROFEN]) received in two weeks of vaccinations. Patient did not receive other vaccine in four weeks of vaccination. Patient was not diagnosed with COVID-19 prior vaccination. Patient has not been tested for COVID-19, post vaccination. On 28Jan2021 02:45AM, the patient experienced intense headache 7-10 of 10, low grade fever 100.4, significant body aches and cold sweats. The patient underwent lab tests and procedures which included pain assessment: 7-10 of 10 and pyrexia: 100.4 on 28Jan2021. Treatment was not received for adverse events. Outcome of the events was recovering. Follow-Up (15-Apr-2021): Follow-up attempts are completed. No further information is expected.

Other Meds: TYLENOL; MOTRIN [IBUPROFEN]

Current Illness:

ID: 1315902
Sex: F
Age:
State: UT

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 05/14/2021
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Symptoms: tenderness of arm/arm hurts; Headache; This is a spontaneous report from a contactable Consumer. An unspecified age female Consumer (patient) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number/Expiry date: not provided) via unspecified route of administration as a 2ND DOSE, SINGLE for COVID-19 immunization on 27Jan2021. The patients past medical history and concomitant medications were not reported. On an unknown date, the patient experienced tenderness of arm/arm hurts and Headache. The patient took Ibuprofen since she could not bear the pain. She had asked if it was ok to take Ibuprofen. Consumer had called about the Pfizer COVID-19 vaccine and says she got the second dose yesterday. She said she thought was stupid to report this side effect of a headache and her arm hurts. She says that she read somewhere or heard that taking Ibuprofen with COVID issues or the vaccine is not recommended so she wanted to verify this before she did that and takes Ibuprofen or Tylenol. She said that she is having a common side effect that everyone had. Caller declines to complete a report and requests to be transferred to Pfizer Medical Information for her question. No further details captured, reported, or documented at this time. The reporters contact information was available. It was unknown if the reporter was the prescribing HCP. Outcome of events was unknown. Follow-up (28Jan2021): This is a follow-up spontaneous report from a contactable Consumer. This Consumer(patient) reported new clinical information. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1315903
Sex: F
Age:
State: PA

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 05/14/2021
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Symptoms: headaches; runny nose; red, teary and painful eyes; red, teary and painful eyes; red, teary and painful eyes; She woke up with pain and swollen red watery eyes; This is a spontaneous report from a contactable consumer (patient, self-reported). A 31-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EL3248 and expiry date was not provided), via an unspecified route of administration, in Arm Left, on 27Jan2021 at 12:00 o'clock noon, as a single dose for COVID-19 immunization at local hospital. The patient was not pregnant at the time of vaccination. The patient's medical history and concomitant medications were not reported. The patient reported that she was administered with the first dose of the vaccine yesterday. On 27Jan2021, at night, around 7 pm and after that her eyes started getting red and the headache started, and also had a runny nose, red, teary and painful eyes. After midnight, either being 27Jan2021 or 28Jan2021, she had very huge pain in both eyes and swelling as well as the wateriness in the eyes. It wasn't tolerable and so she started having Tylenol. She woke up with pain and swollen red watery eyes. She started having eye drops and that helped but she was still having pain. Her headache went away last night when she slept. She did not have positive COVID test or Antibody test before the vaccine. She did not have any issues with vaccines in the past. Outcome of the event headache was recovered on an unknown date. Outcome of the event runny nose was unknown and for all other events, it was not recovered. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1315904
Sex: M
Age:
State: NV

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 05/14/2021
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Symptoms: flushed; elbow hip pain covid; elbow hip pain covid; appearing toes red swollen painful; appearing toes red swollen painful; appearing toes red swollen painful; elbow hip pain covid; This is a spontaneous report from a contactable other hcp (patient). A 77-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot Number: el3247), via an unspecified route of administration in arm left on 19Jan2021 at 08:30 AM as single dose for COVID-19 immunisation. Medical history included htn (hypertension). Patient had allergy from Indocin. Concomitant medication included (other medications the patient received within 2 weeks of vaccination) lisinopril (LISINOPRIL). The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. On 19Jan2021 at 08:30, the patient experienced flushed, elbow hip pain covid appearing toes red swollen painful still on day 8. The events were considered as non-serious. Patient reported no for seriousness criteria-results in death, seriousness criteria-life threatening, seriousness criteria-caused/prolonged hospitalization, seriousness criteria-disabling/incapacitating and seriousness criteria-congenital anomaly/birth defect. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Treatment was received for the adverse event (home care). The outcome of the events was reported as not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: LISINOPRIL

Current Illness:

ID: 1315905
Sex: F
Age:
State: TX

Vax Date: 01/21/2021
Onset Date: 01/28/2021
Rec V Date: 05/14/2021
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Symptoms: really bad headache; This is a spontaneous report from a contactable consumer (patient herself). A 66-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, lot number: EL8982 , expiry date: May2021), via an unknown route in the right arm on 21Jan2021 at 11:45 hrs as a single dose for COVID-19 vaccination. Patient's 4 weeks prior vaccination was none. The patient's medical history included allergy and headaches. The patient's concomitant medications included Benadryl for allergy and Excedrin for headache. On 28Jan2021, the patient woke up with a really bad headache. The patient was wondering whether the vaccine triggered the headache as she does get headaches before. She wanted to know if it is vaccine-related so that she could know how to take care of it. The patient didnot visit any emergency room or physician office due to the event. The outcome of the event was unknown. Follow-up (28Jan2021): This is a follow-up spontaneous report from a contactable Consumer included: Patient demographics (weight and height added, Therapy start date, time, lot number and expiry date, medical history, concomitant medications added, event onset date added. Follow-up attempts are completed. No further information is expected.

Other Meds: BENADRYL; EXCEDRIN [CAFFEINE;PARACETAMOL]

Current Illness:

ID: 1315906
Sex: F
Age:
State: OK

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 05/14/2021
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Symptoms: Headache; vertigo; nausea; body aches; chills; This is a spontaneous report from a contactable consumer (patient). A 52-years-old non-pregnant female patient who received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot: EK9261, Expiration date unknown), via an unspecified route of administration in right arm on 27Jan2021 at 12:30, 2ND DOSE, SINGLE for covid-19 immunization (at the age of 52 years). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot: EK9231, Expiration date unknown), via an unspecified route of administration in left arm on 06Jan2021 at 11:30, at a single dose for covid-19 immunization on (at the age of 52 years) in hospital. Patient's medical history included rheumatoid arthritis and fibromyalgia. Patient's concomitant medications included doxepin, pregabalin, sulfasalazine, and celecoxib (CELEBREX). The patient had penicillin allergy to medications, food, or other products. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient was not tested for COVID-19. On 27Jan2021 at 14:30, the patient experienced headache, vertigo, nausea, body aches, and chills. The patient did not receive any treatment. The outcome of events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: DOXEPIN; PREGABALIN; SULFASALAZINE; CELEBREX

Current Illness:

ID: 1315907
Sex: M
Age:
State: LA

Vax Date: 01/08/2021
Onset Date: 01/19/2021
Rec V Date: 05/14/2021
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Symptoms: lose smell and taste; lose smell and taste; Positive Rapid Covid Test; progressively fatigue; he had a headache; at night he had chills; fever with more fatigue; fever with more fatigue; This is a spontaneous report from a contactable other HCP (patient). A 48-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), (Lot number: EL3248, expiry date: 31Mar2021), via unspecified route of administration in left deltoid on 08Jan2021 as single dose for COVID-19 immunization. Patients medical history was not reported. Patient concomitant medications are Multivitamins, Zinc, colecalciferol (VITAMIN D), fexofenadine hydrochloride (ALLEGRA), Aspirin, and famotidine (PEPCID) from unspecified date and unknown still ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. On 20Jan2021, Patient underwent Rapid Covid Test (nasal swab test), tested positive for SARS-CoV-2 test positive. On 26Jan2021, Caller clarified that b he did not have any further symptoms at all, no fever, everything had resolved. Caller clarified that the reason he got tested was because he was having symptoms, on the 19Jan2021 Tuesday he became progressively fatigue at lunch he had a headache, and probably by 7-8pm at night he had chills and fever with more fatigue. He had No chest pain, No shortness of breath, and No wheezing. The symptoms improved, the headache improved Friday, he had mild lingering fatigue and low-grade temperature for next day or so, but it was Tuesday at which he had no symptoms at all. He did lose smell and taste for 24 hours, it was on Friday 22Jan2021, 100% percent couldn't even smell Vicks Menthol. His Second Dose is schedule for 29Jan2021. He enquired about contraindication to getting the second dose of the vaccine. The Outcome of events was recovering for pyrexia ,headache, fatigue The outcome of chills, loss of smell and taste was unknown. Follow-up (28Jan2021): This is a follow-up spontaneous report from a contactable other HCP (patient). New information includes clinical information. Follow-up attempts are completed. No further information is expected.

Other Meds: ZINC; VITAMIN D [COLECALCIFEROL]; ALLEGRA; ASPIRIN [ACETYLSALICYLIC ACID]; PEPCID [FAMOTIDINE]

Current Illness:

ID: 1315908
Sex: F
Age:
State: NC

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 05/14/2021
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Symptoms: nausea; sweating; body aches; swollen axillary lymph nodes; headache; fingers and ribs hurt; fingers and ribs hurt; chills; potential reaction with facial serum resulting in facial swelling; This is a spontaneous report from a contactable other healthcare professional(patient). A 33-year-old female patient received second dose of BNT162B2(PFIZER-BIONTECH COVID-19 m-RNA VACCINE, Formulation: Solution for injection, Lot number: EL0142 and Expiration date: 12Jan2021), via intramuscular route of administration in right arm, on 12Jan2021 at 10:00, as a single dose for COVID-19 immunisation. The patient previously received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 m-RNA VACCINE, Formulation: Solution for injection, Lot number: EH9899 and Expiration date was not reported), via intramuscular route of administration in left arm, on 22Dec2020 at 13:45, as a single dose for COVID-19 immunisation. The patient was not pregnant at the time of vaccination.The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. Prior to vaccination, was not the patient diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.The patient had no allergies to medications, food, or other products. The patient medical history and concomitant medications were not reported. On 13Jan2021 at 12:00, the patient experienced nausea, sweating, body aches, swollen axillary lymph nodes, headaches, fingers and ribs hurt, chills, sweating that lasted day, potential reaction with facial serum resulting in facial swelling. The adverse event resulted in in Doctor or other healthcare professional office/clinic visit. The treatment was received for events, steroid cream for face. The outcome of the events was reported as recovered on unspecified date. Follow-up (15-Apr-2021): Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1315909
Sex: F
Age:
State: WI

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 05/14/2021
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Symptoms: chills; weakness; fatigue; body aches; This is a spontaneous report from a contactable consumer. A non-pregnant female patient of an unspecified age received second dose BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL3248), via an unspecified route of administration, administered in left arm on 26Jan2021 at 14:30 as single dose for COVID-19 immunisation. The medical history included that the patient previously took penicillin and experienced allergy. The patient previously received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL1284), via an unspecified route of administration, administered in left arm on 04Jan2021 at 14:30 as single dose for COVID-19 immunisation. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other concomitant medication within 2 weeks of vaccination. On 27Jan2021 the patient experienced chills, weakness, fatigue, body aches. The patient did not receive treatment for events. The outcome of event was recovering. Follow-Up (15-Apr-2021): Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1315910
Sex: F
Age:
State: NY

Vax Date: 12/21/2020
Onset Date:
Rec V Date: 05/14/2021
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Symptoms: tiredness; muscle ache; chills; This is a spontaneous report from a contactable physician (patient, reported for herself). A 30-years-old female patient (who was not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EK5730, Expiration date: unknown), dose 1 via an unspecified route of administration, in Arm Left on 21Dec2020 15:00 (at the age of 30-years-old) as single for covid-19 immunisation. Patient also received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EL3246, Expiration date: unknown) via an unspecified route of administration, in Arm Left on 11Jan2021 15:00 ((at the age of 30-years-old) as single for covid-19 immunisation. The patient medical history included asthma. The patient concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19, Prior to vaccination. The patient has been tested for COVID-19, Since the vaccination. It was reported that after first shot of vaccination on an unknown date the patient had experienced tiredness, muscle ache and chills for about 20 hours. The patient took second shot on 11Jan2021, no adverse reactions were experienced. However, the patient had concerns in regards if Pfizer Covid vaccines were effective on her. She had an antibody testing on 27Jan2021 with SARS-CoV-2 Abbotts antibody kit and Vitalix nasal swab test with a reported IgG antibody test that has 99.63% specificity and 100% sensitivity that was completely negative at 16 days following the second dose of Pfizer COVID-19 vaccine, and she had the first dose exactly three weeks prior. She had read information from Pfizer indicating that its vaccine exhibits a robust induction of antibody response. Hence, she wanted to get advice from Pfizer on how to proceed with her concern as a health care provider who is constantly exposed to the virus and was wondering if re-vaccination would be advised. There was no treatment provided as a result of events. The patient underwent lab tests and procedures which included SARS-CoV-2 Abbotts antibody kit and Vitalix nasal swab test on 27Jan2021. The outcome of the events was unknown. The events were considered as non-serious by the reporter. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1315911
Sex: F
Age:
State: MI

Vax Date: 01/21/2021
Onset Date: 01/23/2021
Rec V Date: 05/14/2021
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Symptoms: Aching on left side of her chest/ achy on the left side of her chest; Shortness of breath where it was hard to get a deep breath; This is a spontaneous report from a contactable consumer or other non hcp (the patient reported for herself). A 66-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/ lot number: EL9261. Expiry date: UNKNOWN) via an unspecified route of administration, in the region of left arm on 21Jan2021 at 12:20 (At the age of 66-years-old) as 0.3 mL, single for COVID-19 immunisation (reported as virus protection). Medical history was not reported. History of all previous immunization with the Pfizer vaccine considered as suspect and any additional Vaccines Administered on Same Date of the Pfizer Suspect was reported as none. No Prior vaccination within 4 weeks of the vaccination. On 23JAN2021, the patient experienced aching on left side of her chest, shortness of breath where it was hard to get a deep breath. Patient was advised by her doctor to call and report the side effects that she has experienced since receiving the first dose of the Covid-19 vaccine. Patient went to the emergency room on 27Jan2021 due to the events, Aching on left side, shortness of breath. They were unable to find anything wrong with her heart. She did not have any blood clots. She also had an X-ray of her lungs. Because of these symptoms she had a COVID test on 23Jan2021 at the urgent care. The test was negative. She may have been exposed to COVID on 01Jan2021. Her next dose is 11Feb2021. She wants to get the second dose. Her doctor said she needs to speak with Pfizer for recommendations about the next dose. Both the events were reported as ongoing. The outcome of the events was reported as not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315912
Sex: M
Age:
State: MI

Vax Date: 01/25/2021
Onset Date:
Rec V Date: 05/14/2021
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Symptoms: He has a bad hip and needs to take Tylenol before he rides the bike; This is a spontaneous report received from a contactable consumer (Patient) via a Pfizer-sponsored program. CEP ID: 002191 A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown), via unspecified route of administration on 25Jan2021 at a single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date after vaccination, the patient had a bad hip and needs to take Tylenol before he rides the bike. Patient likes to ride his stationary bike. Patient read online that before getting the COVID-19 vaccine that patients were not supposed to take Tylenol or ibuprofen and wanted to know if he was okay to take the Tylenol now to ride his back or does he need to wait until the shots are over. Patient has not taken Tylenol and would not like to do a safety report. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1315913
Sex: F
Age:
State: MA

Vax Date: 01/12/2021
Onset Date: 01/17/2021
Rec V Date: 05/14/2021
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Symptoms: she had onset of a diffuse pruritic macular papular rash on arms, chest and back and mildly on her face; she had onset of a diffuse pruritic macular papular rash on arms, chest and back and mildly on her face; This is a spontaneous report from a contactable other health care professional. A 35-years-old female patient received bnt162b2 (PFIZER-BIONTECH COIVD-19 mRNA VACCINE), dose 2 intramuscular, administered in Arm Right on12Jan2021 (Batch/Lot Number: EK9231) as SINGLE DOSE for covid-19 immunisation (age at vaccination was 35years). Patient's medical history includes child asthma, since resolved.The patient previously took received bnt162b2 (PFIZER-BIONTECH COIVD-19 mRNA VACCINE), dose 1 intramuscular, administered in Arm Right on 23Dec2020 (Batch/Lot Number: EK5730) as SINGLE DOSE for covid-19 immunisation (age at vaccination was 35years). Patient was healthy and didn't take any medication. Patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.On 17Jan2021 5 days after vaccination,the patient experienced onset of a diffuse pruritic macular papular rash on arms, chest and back and mildly on her face.2 days ago, she was seen in urgent care and given prednisone and antihistamines (Triamcinolone cream, Benadryl, Tylenol and Atarax). patient has had no improvement, no mucosal involvement, no fevers or chills, no joint or body aches. Patient had no new exposures and medications. Patient was the only one in the house with the symptoms. Patient occupation was a nurse but had no known exposures. The outcomes of the all the events was recovering. Follow-up attempts are completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1315914
Sex: F
Age:
State: NY

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 05/14/2021
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Symptoms: Soreness near injection site on second day; This is a spontaneous report from a contactable consumer (patient). A 25-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3247), via an unspecified route of administration in the left arm on 19Jan2021 at 15:45 (at the age of 25-years-old) as 1ST DOSE, SINGLE for COVID-19 immunisation. The patient's had no medical history were reported. The patient's concomitant medications were reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination.The patient did not receive any other medications within two weeks prior to the vaccination.On 20Jan2021 at 12:00, the patient experienced soreness near injection site on second day. The patient did not received any treatment for the events. The outcome of the events was recovered on an unspecified date. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1315915
Sex: F
Age:
State: MN

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 05/14/2021
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Symptoms: fever of 100; 21Jan2021 6:00am woke up with bad body aches; This is a spontaneous report from a contactable Other HCP (patient). This 39-year-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number paa156051) intramuscularly on left arm on 20Jan2021 at 12:00 (at the age of 39 years) as single dose for COVID-19 immunisation. The patient had medical history asthma, depression, high cholesterol, tested positive for COVID-19 on 05Oct2020 and patient's known allergies included cephalexin, robaxin, naproxen, latex. The patient concomitant medications included cetirizine hydrochloride (ZYRTEC), venlafaxine hydrochloride (EFFEXOR), pravastatin, omeprazole taken 2 weeks prior of vaccination. Patient had no other vaccine prior to 4 weeks of vaccination. The patient had COVID prior to vaccination. On 21Jan2021 at 6:00, the patient woke up with bad body aches, which went away around 12:00. Then returned around 15:00 on/off for the day. On 22Jan2021, the patient woke up at 09:00 and felt good. At about 12:30 patient started having body aches and fever of 100, lasted all evening. Went to bed and woke up with no other symptoms on 23Jan2021. The patient received no treatment for events. The patient tested for COVID post vaccination. The outcome of the event was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; EFFEXOR; PRAVASTATIN; OMEPRAZOLE

Current Illness:

ID: 1315916
Sex: F
Age:
State: WA

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 05/14/2021
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Symptoms: low-grade fever; headache; body ache; dizzy; weak; queasy; chills; shaky; fatigue/tired another 24 hours/Third day still tired.; mild brain fog; higher fever 101.5+/couldn't get fever below 100.; This is a spontaneous report from a contactable other health care professional. A 48-year-old non pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL3247) via an unspecified route of administration in right arm on 25Jan2021 11:30 as second dose, single for COVID-19 immunization. The patient previously received first dose on 04Jan2021 11:00, (lot number: EL0142) via an unspecified route of administration in right arm as first dose, single for COVID-19 immunization. Medical history included non-Hodgkins lymphoma from 1995, invasive ductal carcinoma 2009 with breast reconstruction; phrenic nerve paralysis left side; cardiomyopathy. Concomitant medications included metoprolol 100 mg, vitamin D [COLECALCIFEROL], beclometasone dipropionate (QVAR) 80 ug. No known allergies reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was tested for COVID-19 (nasal swab, rapid test) post vaccination on 21Jan2021 test result was pending. On 25Jan2021 24:00, the patient experienced mild brain fog at 3pm; fatigue at 7pm; 11pm low-grade fever, headache, body aches; 4 am higher fever 101.5+, headache, body ache, dizzy, weak, queasy, chills, fatigue. Started ibuprofen and took every 4 hours and could not get fever below 100. Fever broke early hours the next day, but still was queasy, shaky, dizzy, achy and tired another 24 hours. Third day still tired. The patient received treatment for the events as OTC non-steroidal anti-inflammatory drugs. The events were non serious. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021007634 same patient/drug, different vaccine dose/event

Other Meds: METOPROLOL; QVAR; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1315917
Sex: M
Age:
State: NY

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Rec V Date: 05/14/2021
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Symptoms: I noticed, there is like a ball on my armpit, it's swollen and it's painful.; I noticed, there is like a ball on my armpit, it's swollen and it's painful.; I noticed, there is like a ball on my armpit, it's swollen and it's painful.; This is a spontaneous report from a contactable consumer or other non hcp. A 38-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: Unknown) via an unspecified route of administration on an unspecified date (At the age of 38-years-old) as single dose for COVID-19 immunization. The patient medical history was reported as none. The patient's concomitant medication was reported as No, just Vitamins, start and stop dates were unspecified. When probed for the concern, patient stated he received second vaccine, (today is Thursday) on Tuesday patient noticed, there was a ball like on his armpit, it's swollen and it was painful. Patient inquired whether that was normal. Regarding the lot number, the reporter stated that, he took the card home, does not have it with him. Patient stated that there were No Lab test and no Treatment was received. Patient reported he noticed it this morning(as reported), he kind of felt something but this morning it's really swollen. The outcome of the events was reported as an unknown. Information about lot and batch number was requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds: VITAMINS NOS

Current Illness:

ID: 1315918
Sex: F
Age:
State: NY

Vax Date: 01/26/2021
Onset Date: 02/03/2021
Rec V Date: 05/14/2021
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Symptoms: red rash at the site; vaccination site was itchy; This is a spontaneous report from a contactable consumer (patient, reported for herself). A 71-year-old female patient (who was not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL9262, expiry date: unknown) dose 1 via an unspecified route of administration, in left arm on 26Jan2021 09:15 AM(at the age of 71-years-old), as a single for Covid-19 immunization at Health Clinic/ Administration facility. The patient medical history was not reported, and the patient had known allergies: amoxicillin. The patient received concomitant medications in two weeks of vaccination. Patient did not receive other vaccine in four weeks of vaccination. Patient was not diagnosed with COVID, prior vaccination. Patient has not been tested for COVID, post vaccination. On 03Feb2021, day 9 following the first dose of vaccine, the patient experienced that the vaccination site was itchy. The following day there was a red rash at the site. The rash was circular and about four inches long and two inches wide. It was not a raised rash. Patient did not receive treatment for the events. The outcome of the events was not recovered. No further information was provided.

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ID: 1315919
Sex: F
Age:
State: CA

Vax Date: 02/03/2021
Onset Date: 02/05/2021
Rec V Date: 05/14/2021
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Symptoms: Rash on face, red, raised -cheeks, forehead, chin area-ongoing; Rash on face, red, raised -cheeks, forehead, chin area-ongoing; Soreness and swelling of left arm; Soreness and swelling of left arm; This is a spontaneous report from a contactable consumer. A 71-years-old female patient (not Pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9262), via an unspecified route of administration, administered in left arm on 03Feb2021 at 11:45 as 1ST dose, single for covid-19 immunization. Medical history included blood cholesterol increased, drug hypersensitivity, known_allergies of penicillin. Concomitant medication(s) within 2 weeks of vaccination included rosuvastatin, glucosamine & chondroitin; COQ10; fis. Facility where the most recent COVID-19 vaccine was administered included School or Health Clinic. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 05Feb2021, the patient experienced rash on face, red, raised -cheeks, forehead, chin area-ongoing, soreness and swelling of left arm. The events assessed as non-serious. The treatment of antihistamine, aloe vera cream received for the events. The outcome of the events soreness and swelling of left arm was recovered where the events rash on face, red, raised -cheeks, forehead, chin area was not recovered.

Other Meds: ROSUVASTATIN; GLUCOSAMINE AND CHONDROITIN; COQ10 [ASCORBIC ACID;BETACAROTENE;CUPRIC OXIDE;MANGANESE SULFATE;SELENIUM;TOCOPHERYL ACETATE;UBIDECA

Current Illness:

ID: 1315920
Sex: F
Age:
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Vax Date: 02/10/2021
Onset Date: 02/11/2021
Rec V Date: 05/14/2021
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Symptoms: feeling hot and cold and hot and cold; cough; sneeze; She had a little fever/behind her leg was 100.4F; a tiny hemorrhage in her eye; gigantic headache/very bad headache; wasn't feeling good; This is a spontaneous report from a contactable consumer. A 72-year-old female patient received the first dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine via an unspecified route of administration on 10Feb2021 (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 took diclofenac sodium. On an unspecified date in Feb2021, a couple of days before receiving her first vaccine dose, the patient took a dose of diclofenac (2 tablets, 15 mg each) and wanted to know if the vaccine will still work. Moreover she was going to receive Botox injections in between her two vaccine doses, her neurologist says that it's fine, but she wanted to have more information, if available. She also stated that she is due for her Botox injection but might postpone the shot so that it will not interfere with her COVID-19 vaccine. On an unspecified date she experienced a tiny hemorrhage in her eye that may have resulted from a cough or a sneeze; she had a rough night feeling hot and cold and hot and cold and she had a little fever stating that her infrared thermometer said that behind her leg temperature was 100.4 F (but her arm was different, along with her forehead). On 11Feb2021 the patient experienced gigantic headache/very bad headache, but she does not think the headache was caused by the vaccine, and wasn't feeling good. She wanted to know if she can take diclofenac for her headache. The patient underwent lab tests and procedures which included body temperature: 100.4 Fahrenheit on an unspecified date. At the time of the report the events outcome was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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ID: 1315921
Sex: F
Age:
State: KY

Vax Date: 02/13/2021
Onset Date: 02/13/2021
Rec V Date: 05/14/2021
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Symptoms: Upper Abdominal pain under middle to left rib cage; This is a spontaneous report from a contactable consumer (reported for herself). A 49-years-old adult non pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EM9809) administered in left arm via an unknown route of administration, on 13Feb2021 at 11:45 as SINGLE DOSE for covid-19 immunization. Medical history included autoimmune disorder, stroke. Concomitant medications within 2 weeks of vaccination included Hydroxychloroquine Sulfate (PLAQUENIL), Fish oil, Zingiber officinale (GINGER), Curcuma longa (TURMERIC) and Multivitamins. On 13Feb2021 at 12:15, the patient experienced upper abdominal pain under middle to left rib cage. The outcome of the event was not recovered.

Other Meds: PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]; FISH OIL; GINGER [ZINGIBER OFFICINALE]; TURMERIC [CURCUMA LONGA]

Current Illness:

ID: 1315922
Sex: F
Age:
State: IL

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 05/14/2021
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Symptoms: headache; Exhausted; Chills; Joint Pain; achy pain; Flu; Eye floaters; Feeling Strange; Nauseaus; Dizzy; This is a spontaneous report was received from a contactable consumer or other non hcp. A 77-year-old female patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, administered in arm right on 05Feb2021 14:00 (at the age of 77-year-old) as single dose for COVID-19 immunization. The patient's medical history included digestion problems, ongoing coeliac disease and allergy to gluten. Concomitant medications included vitamin b complex (vitamin b), zinc (zinc), vitamin c [ascorbic acid] (vitamin c [ascorbic acid]), colecalciferol (vitamin d [colecalciferol]), bifidobacterium lactis (Probiotic [bifidobacterium lactis]). The patient was not pregnant at the time of vaccination. The patient had not received other vaccine in four weeks. On 05Feb2021 at 18:00, the patient was exhausted and experienced chills, headache, joint pain started in left ankle, later she had achy pains all over and felt lousy like she had the flu. The patient had new floaters in her eyes and a strange feeling in her head and was also extremely nauseous and dizzy. The patient did not take any treatment. The patient was not tested for covid prior vaccination and post vaccination. The outcome of the events was recovered on an unspecified date in 2021. Follow up attempts are completed. No further information is expected.

Other Meds: VITAMIN B; ZINC; VITAMIN C [ASCORBIC ACID]; VITAMIN D [COLECALCIFEROL]; PROBIOTIC [BIFIDOBACTERIUM LACTIS]

Current Illness: Celiac disease

ID: 1315923
Sex: F
Age:
State: AL

Vax Date: 02/12/2021
Onset Date: 02/13/2021
Rec V Date: 05/14/2021
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Symptoms: headache; chills; fever; sore muscles; This is a spontaneous report from contactable Consumer (patient).A 77-years-old (non-pregnant) female patient received BNT162B2 (COMIRNATY, Solution for injection, Batch/Lot Number: BN5318 and expiry date was not reported) dose 2 via an unspecified route of administration in left arm on 12Feb2021 12:00 (at 77-years age) as a 2nd single dose for COVID-19 immunisation and received BNT162B2 (COMIRNATY, Solution for injection, Batch/Lot Number: EL8982 and expiry date was not reported) dose 1 via an unspecified route of administration in left arm on 22Jan2021 12:00 as a 1st single dose for COVID-19 immunisation. The patient medical history included AFib and latex allergy. Concomitant medication(s) included rivaroxaban (XARELTO); flecainide (FLECAINIDE); amlodipine (AMLODIPINE). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 13Feb2021 at 01:00 AM the patient experienced with headache, chills, fever and sore muscles. The patient had no covid tested post vaccination. The patient did not receive any treatment medication for the events. The outcome of the events was recovered.

Other Meds: XARELTO; FLECAINIDE; AMLODIPINE

Current Illness:

ID: 1315924
Sex: F
Age:
State: ME

Vax Date: 02/11/2021
Onset Date: 02/13/2021
Rec V Date: 05/14/2021
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Symptoms: ulcers; sore mouth; dryness; painful can't eat; crushing headache; Lips swollen; Lots of imflamation; This is a spontaneous report from a contactable consumer (patient, self-reported). A 75-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EN5318 and expiry date was not provided), via an unspecified route of administration, in Arm Right, on 11Feb2021 at 15:45 PM, as a single dose for COVID-19 immunization. The patient was not pregnant at the time of vaccination. The patient's medical history included known allergies-sulpha drug. Concomitant medications were not reported. The patient did not receive any vaccine in four weeks. The patient was not diagnosed with COVID prior vaccination. The patient was not tested for COVID post vaccination. The patient reported that on 13Feb2021 at 12:00 AM, within 24 to 48 hours, she had a massive sore mouth, ulcers, dryness, and so painful couldn't eat. She also woke up with crushing headache. Her lips swollen and could not stand anything hardly warm on her lips and lots of imflamation. The events resulted in emergency room/department or urgent care. The patient did not receive any treatment for the events. Outcome of the events was not recovered.

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Current Illness:

ID: 1315925
Sex: F
Age:
State: GA

Vax Date: 02/10/2021
Onset Date: 02/10/2021
Rec V Date: 05/14/2021
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Symptoms: Mild itch on face, eyes and arms. Previously reported reaction was a little more intense and it included my scalp.; Mild itch on face, eyes and arms. Previously reported reaction was a little more intense and it included my scalp.; This is a spontaneous report from a contactable consumer (Patient). A 67-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 10Feb2021 01:45 (Batch/Lot Number: EL8982) as 2ND DOSE, SINGLE for covid-19 immunisation. Medical history included high cholesterol, arthritis, glaucoma candidate, GERD, Osteopenia, lumbar radiculopathy penicillin allergy and sulfonamide allergy. Concomitant medication(s) included lovastatin (LOVASTATIN) taken for an unspecified indication, start and stop date were not reported; lansoprazole (LANSOPRAZOLE) taken for an unspecified indication, start and stop date were not reported and unspecified medications. The patient previously took Cortisone, Dexamethasone, Clindamycin, Neurontin, Gabapentin, Carbamazepine, Endocet, Metoprolol, Pamalor and experienced allergies for all medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient previously received first dose of BNT162B2), via an unspecified route of administration, administered in Arm right on 20Jan2021 02:00 PM (Batch/Lot Number: EL3246) as 1ST DOSE, SINGLE for covid-19 immunisation and expereinced mild itch on face, eyes and arms and scalp. On 10Feb2021 14:15 the patient experienced Mild itch on face, eyes and arms. Previously reported reaction was a little more intense and it included her scalp. No treatment were received for the events. The outcome of the events were recovered on an unspecified date.

Other Meds: LOVASTATIN; LANSOPRAZOLE

Current Illness:

ID: 1315939
Sex: F
Age:
State: NY

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 05/14/2021
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Symptoms: Arm pain at site of injection; This is a spontaneous report from a contactable consumer. A 60-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 23Feb2021 15:30 (Lot Number: EL9269, Expiration date: unknown, at the age of 60-years-old) as first dose, single dose for covid-19 immunisation. Medical history included ongoing hypothyroid. No known allergies. Concomitant medications included levothyroxine sodium (SYNTHROID) taken for an unspecified indication, start and stop date were not reported and supplements (vitamins). No covid prior vaccination. Covid not tested post vaccination. The patient experienced arm pain at site of injection on 23Feb2021 20:30. No treatment was received. The outcome of the event was not recovered.

Other Meds: SYNTHROID

Current Illness: Hypothyroidism (Hypothyroid was coded as Hypothyroidism.)

ID: 1315951
Sex: F
Age:
State: OH

Vax Date: 02/22/2021
Onset Date: 02/22/2021
Rec V Date: 05/14/2021
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Symptoms: Extreme whole body itching with no rash; This is a spontaneous report from a contactable consumer (patient). A 79-year-old non-pregnant female patient received second dose of bnt162b2 (BNT162B2, Solution for injection, Lot Number: EL9264), via an unspecified route of administration, administered in Arm Left on 22Feb2021 08:15 (at an age of 79-years-old) as single dose for covid-19 immunisation. Medical history included type 2 diabetes mellitus. Concomitant medications included metformin (MANUFACTURER UNKNOWN), via an unspecified route of administration from an unspecified date at 500 mg unknown frequency for unknown indication; doxycycline (MANUFACTURER UNKNOWN), via an unspecified route of administration from an unspecified date at 20 mg unknown frequency for unknown indication. The patient previously took bnt162b2 (Product=COVID 19, brand=Pfizer, lot number=EL9265, lot unknown=False, administration date=31Jan2021, administration time=08:00 AM, vaccine location=Left arm, dose number=1). On 22Feb2021 17:00, the patient experienced extreme whole body itching with no rash. The patient did not receive any treatment for the events. The clinical outcome for the extreme whole body itching with no rash was recovering.

Other Meds: METFORMIN; DOXYCYCLINE

Current Illness:

ID: 1315961
Sex: F
Age: 32
State: TN

Vax Date: 04/08/2021
Onset Date: 05/07/2021
Rec V Date: 05/14/2021
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Allergies: Allergic to morphine, levaquin, periactin, reglan

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Symptoms: Numbness, tingling and weakness / pain on right side of body that has spread to entire body neck down.

Other Meds: Zoloft

Current Illness:

ID: 1315962
Sex: M
Age: 33
State: WA

Vax Date: 05/12/2021
Onset Date: 05/13/2021
Rec V Date: 05/14/2021
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Allergies: Denies

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Symptoms: Patient post-vaccination (Pfizer/0.3ml/1st dose administered @10:23a) appeared to be seizing in his chair during observation @ 10:26a. I rushed to him, requesting aid from his colleagues to help lay him on the ground and elevate his feet. He was unresponsive and disoriented, with shallow breathing and weak pulse, so I activated EMS @ 10:26a. He appeared to seize again so I instructed two men to help roll him onto his side, at which time, an RN managing the vaccines, took over monitoring while I talked to 911. EMS was on scene @ 10:29a. RN reports he'd had a vagal response, most likely due to witnessed severe anxiety during IM injection (name /right deltoid @ 10:23a). RN gave him Gatorade and he quickly became AOx3. When EMS arrived, he was able to stand up, with assist, and be placed on the gurney. EMS monitored him for ~ 20min onsite, at which time he became hypotensive, resulting in transport to the nearest ER with O2 and IV management. Per HR representative for a business patient was discharged @ ~2p the same day, with diagnosis of severe dehydration and hypokalemia, his reaction most likely a vagal event. Unknown if medications were given outpatient.

Other Meds: Denies

Current Illness: Denies

Total 2021 VAERS Injuries: 704,237

Page last modified: 03 October 2021 5:28pm