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
187,133MODERNA
33,878JANSSEN
2,321PFIZER\BIONTECH
1,091GLAXOSMITHKLINE BIOLOGICALS
983UNKNOWN MANUFACTURER
363MERCK & CO. INC.
229SEQIRUS, INC.
45DYNAVAX TECHNOLOGIES CORPORATION
41NOVARTIS VACCINES AND DIAGNOSTICS
29SANOFI PASTEUR
18EMERGENT BIOSOLUTIONS
8PAXVAX
7TEVA PHARMACEUTICALS
4PFIZER\WYETH
3BERNA BIOTECH, LTD.
2SMITHKLINE BEECHAM
2INTERCELL AG
2PROTEIN SCIENCES CORPORATION
1CSL LIMITED

Incidents per State

State Total
77,548
AK1,869
AL5,581
AR3,688
AS47
AZ14,288
CA61,984
CO11,665
CT8,149
DC1,663
DE1,807
FL37,749
FM5
GA15,058
GU120
HI2,453
IA4,625
ID2,692
IL20,334
IN24,007
KS4,615
KY7,696
LA4,887
MA14,654
MD12,514
ME3,129
MH11
MI18,739
MN12,528
MO9,710
MP29
MS2,790
MT2,375
NC16,368
ND1,356
NE2,880
NH3,100
NJ17,634
NM3,916
NV4,239
NY34,355
OH19,081
OK6,195
OR8,636
PA23,083
PR2,370
QM2
RI2,088
SC6,411
SD1,212
TN9,131
TX35,174
UT4,273
VA14,937
VI64
VT1,676
WA14,909
WI11,259
WV2,388
WY861
XB5
XL1
XV2

ID: 0976891
Sex: F
Age:
State: NY

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Fever (101.6); chills; body aches; headache; swelling and redness around injection site; redness around injection site; This is a spontaneous report from a contactable other healthcare professional (HCP) reporting for herself. A 24-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0142), intramuscular at Left arm on 05Jan2021 15:00 at single dose for covid-19 immunization. The COVID-19 vaccine was administered at Hospital. Medical history included epilepsy and prior to vaccination, the patient got COVID-19. The patient concomitant therapy was reported as Yes (patient received other medications in two weeks). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not pregnant. The patient experienced Fever (101.6), chills, body aches, headache, swelling and redness around injection site on 05Jan2021 22:30. No treatment received for the events. Since the vaccination, the patient was not been tested for COVID-19. The outcome of the events was recovered on an unknown date in Jan2021.

Other Meds:

Current Illness:

ID: 0976892
Sex: F
Age:
State: IL

Vax Date: 12/01/2020
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Headache; This is a spontaneous report received from a Pfizer Sponsored Program via a contactable Nurse (Patient). A 27-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE via an unspecified route of administration on Dec2020 07:30AM (reported as three weeks ago as of 13Jan2021) in the left arm at single dose for COVID-19 immunisation. There was no medical history. There were no concomitant medications. There was no additional vaccine administered on same date of the Pfizer suspect. There was no prior vaccination (within 4 weeks). The patient works in a hospital and wants to know if she can take Ibuprofen before the vaccine. She got her second dose and did take Ibuprofen. She received the first dose of the Pfizer COVID 19 vaccine three weeks ago. She is unsure of the date and she is driving and can't access information. The first dose was received at 07:30AM in the left arm. She received the second dose 13Jan2021, 45 minutes ago at 07:30AM in the left arm. She took the Ibuprofen for a headache this morning (13Jan2021). It was just a mild headache but she had to then drive an hour to get the location to received her second dose of the vaccine. After she took Ibuprofen, she read online that it might blunt the immune response. She is asking if that is true? The Ibuprofen took care of the headache; the headache is completely resolved and not serious. No any AE(s) required a visit to physician or ER. Event outcome of headache was recovered on 13Jan2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976893
Sex: M
Age:
State: FL

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: He has had gout at other times, but he has never had it as hard as this/awaken with pain in the middle of the night; He was awaken with pain in the middle of the night; This is a spontaneous report from a contactable consumer (wife) who reported for her husband (patient) that a 65-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EH9899) via an unspecified route of administration on 05Jan2021 08:40, at single dose for COVID-19 immunization. Medical history included gout, using timolol maleate to control the pressure in his eye. Concomitant medication included ongoing timolol maleate (5ml eye drops) to control the pressure in his eye. He uses eye drops that are prescribed. He keeps them on the counter to remember to take them. He has been using it for 3 years. Patient previously had the shingles vaccine on 14Dec2020 for immunization at the age of 65 years old. It said as long as the vaccine was given two weeks prior. The patient received COVID vaccine at outdoor park on 05Jan2021. The wife reported that the next day after the first dose of the vaccine (06Jan2021), her husband developed gout. He got it at the same time she did. He has had gout at other times, but he has never had it as hard as this. He awaked with pain in the middle of the night, it started from 06Jan2021 and is ongoing, slight improvement. She was not sure if that was reportable. Patient did not visit emergency room or physician office for any adverse events. Outcome of the events was recovering.

Other Meds: TIMOLOL MALEATE

Current Illness:

ID: 0976894
Sex: F
Age:
State:

Vax Date: 01/05/2021
Onset Date: 01/07/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Fever; chills; body pains; headache; diarrhea; nausea; vomiting; weakness; This is a spontaneous report from a non-contactable consumer (patient). A 41-year-old female patient received the first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL0142, expiration date not reported) via an unspecified route of administration on the left arm on 05Jan2021 at a single dose for COVID-19 immunization. Medical history included allergies: Penicillin, shellfish, seafood. The patient's concomitant medications were not reported. The patient experienced fever, chills, body pains, headache followed by diarrhea, nausea, vomiting and weakness on 07Jan2021 10:00 pm. Treatment was received for the events (unspecified). The events resulted in Emergency room/department or urgent care. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient underwent lab tests and procedures which included Nasal Swab on 09Jan2021: Negative. Outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0976895
Sex: U
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Soreness at the injection site; Dry / scratchy throat; Extreme fatigue; Slight nasal congestion; This is Spontaneous report from a contactable consumer. This 26-year-old consumer (patient) reported that she/he received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number was unknown) at single dose for Covid-19 immunisation on 14Jan2021. Relevant history and concomitant drugs were unknown. The patient experienced Soreness at the injection site since 3 hours after the injection (vaccination), and Dry / scratchy throat, Extreme fatigue and Slight nasal congestion since 9 hours after the injection on 14Jan2021. The outcome of event Soreness at the injection site was not resolved. The other events was resolved 8 hours after onset. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976896
Sex: M
Age:
State: TX

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

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Tachycardia at 110; chills; muscle pain; fever of 100.4; cough; fatigue; joint pain; wheeze; This is a spontaneous report from a contactable other HCP reported for self. This 38-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number unknown) via intramuscular at 12Jan2021 11:00 AM at single dose in left arm for COVID-19 immunization. The patient medical history included COVID-19 prior vaccination. The patient concomitant medication was reported as no. The patient had no known allergies. The patient experienced tachycardia at 110, chills, muscle pain, fever of 100.4, cough, fatigue, joint pain, wheeze at 12Jan2021 23:00 PM. The patient received treatment paracetamol (TYLENOL), ibuprofen (MOTRIN), diphenhydramine hydrochloride (BENADRYL). The patient was not diagnosed with COVID since the vaccination. The patient was recovering from the events. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976897
Sex: F
Age:
State: CO

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Itching, Hives to neck and back; Itching, Hives to neck and back; This is a spontaneous report from a contactable nurse (patient). A 44-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number=EK9231), via an unspecified route of administration on right arm at 08:45AM on 12Jan2021 at single dose for COVID-19 immunization. Medical history included hashimotos thyroid, mild exercise and allergy induced asthma, Allergies: Penicillin, Allergies: mold, Allergies: ragweed, Allergies: coconut, citrus. Concomitant medication included thyroid (ARMOUR THYROID), colecalciferol (VITAMIN D), vitamin c [ascorbic acid]. The patient previously received her first dose of bnt162b2 (Lot number=EK5730) at 09:00 AM on 22Dec2020 on right arm for COVID-19 immunization, PABA and experienced drug hypersensitivity. The patient experienced itching, hives to neck and back noted 25-30min after receiving vaccine at 09:15AM on 12Jan2021. Observed in vaccine clinic, vitals stable. Took Claritin 40min after vaccine. Hives resolving, no new symptoms at 90min post vaccine. Hives did return the next day when Claritin dose wore off; took another dose with Hives resolving within 2hours. Prior to vaccination, the patient was not diagnosed with COVID-19; Since the vaccination, the patient had not been tested for COVID-19. The outcome of events was recovering.

Other Meds: ARMOUR THYROID; VITAMIN D [COLECALCIFEROL]; VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 0976898
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: sore arm; This is a spontaneous report from a non-contactable healthcare professional. An adult female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history was not reported. There were no concomitant medications. The patient previously took vicodin and experienced allergy. The patient got her first shot and experienced sore arm on unspecified date, no other symptoms. The outcome of the event was unknown. The patient was not pregnant. The facility where the most recent COVID-19 vaccine was administered was in the 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 has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0976899
Sex: M
Age:
State:

Vax Date:
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: fever 102; chills; body malaise; sore arm; headache; This is a spontaneous report from a non-contactable nurse. A 33-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number= k9231) via an unspecified route of administration at single dose for COVID-19 immunisation. Patient had no COVID prior vaccination, no COVID tested post vaccination, no known allergies (NKA), none other medical history. The patient's concomitant medications were not reported. It was reported patient experienced adverse event: fever 102, chills, body malaise, sore arm, headache, all adverse event start date on 13Jan2021. No treatment for adverse event received. Outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0976900
Sex: F
Age:
State:

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Tenderness at site Low grade fever; Tenderness at site Low grade fever; This is a spontaneous report from a non-contactable Nurse(patient). A 28-years-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: unknown), via an unspecified route of administration at left arm on 12Jan2021 11:45 at single dose for covid-19 immunisation. Medical history included hypothyroidism. No COVID prior vaccination, no COVID tested post vaccination, no known allergies. Concomitant medication included levothyroxine sodium (SYNTHROID), ethinylestradiol, norgestimate (SPRINTEC). No other vaccine received in four weeks.The patient experienced tenderness at site low grade fever on 13Jan2021 04:00. Facility type vaccine was hospital. No treatment received. Outcome was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds: SYNTHROID; SPRINTEC

Current Illness:

ID: 0976901
Sex: F
Age:
State: NY

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: mild arm soreness that lasted a few days; headache; This is a spontaneous report from a contactable nurse (patient). This 45-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular on 22Dec2020 09:30 at single dose on the right arm for COVID-19 immunization. The patient's medical history included hypertension, anxiety, degenerative arthritis and allergies: sulfa. The patient's concomitant medications were none. No other vaccine received in four weeks. Facility type vaccine was workplace clinic. Patient was not pregnant. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. After first shot given at 09:30 by 12:00, patient had a headache and mild arm soreness that lasted a few days. No treatment received. Outcome of the events was recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976902
Sex: F
Age:
State: WI

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Tingling tongue; odd taste on her tongue; neck swelling; This is a spontaneous report from a contactable pharmacist. An adult female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 29Dec2020 13:00 at single dose for COVID-19 immunisation. Facility-type-vaccine was Hospital. It was unknown if pregnant at time of vaccination. The patient medical history and the concomitant medications were not reported. Patient experienced an adverse reaction to the COVID-19 vaccine on 29Dec2020 01:00 PM. Symptoms experienced: Tingling tongue, odd taste on her tongue and neck swelling. Patient stated she had her own 50 mg of Benadryl with her and had taken it at 13:05. She stated she has other reactions to medications in the past and it felt the same way. EMS arrived at 13:22 and care transferred. Patient was alert and oriented. AE-resulted-in Doctor or other healthcare professional office/clinic visit. The outcome was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976903
Sex: F
Age:
State: NY

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: arm hurts; This is a spontaneous report from a non-contactable consumer (patient). An adult female patient received bnt162b2 (BNT162B2), via an unspecified route of administration on 12Jan2021 at single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient reported arm hurts on 12Jan2021. The event outcome was recovering. No treatment for AE. No COVID prior vaccination; no COVID tested post vaccination. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0976904
Sex: F
Age:
State: NJ

Vax Date: 12/21/2020
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Shot #1-headache, nasal congestion; Shot #1-headache, nasal congestion; This is a spontaneous report from a contactable nurse. This 43-year-old female nurse (no pregnant) reported for herself, received 1st dose of BTN162B2 Intramuscular on 21Dec2020 06:15 PM on Left arm for covid-19 immunization. Medical history was allergy to Latex and Adhesive; Anxiety, migraines, palpitations. Concomitant drug included piroxicam (PAXIL), alprazolam (XANAX), multivitamin. No other vaccine in four weeks. It was reported that patient experienced headache, nasal congestion. No covid prior vaccination. No covid tested post vaccination. Outcome of the event was unknown. Information on the Batch/Lot number has been requested.

Other Meds: PAXIL [PIROXICAM]; XANAX

Current Illness:

ID: 0976905
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: sore arm; congestion; This is a spontaneous report from a non-contactable other hcp. An adult female patient of an unspecified age received their second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0140, expiry date not reported), via an unspecified route of administration on 11Jan2021 19:00 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took vicodin and experienced allergy. The patient received their first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date not reported) for COVID-19 immunization and experienced sore arm. The patient experienced sore arm and congestion on 11Jan2021 22:00. The patient recovered from the event on an unspecified date in Jan2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0976906
Sex: F
Age:
State:

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: fatigue; Chills; headache; body aches; This is a spontaneous report from a non-contactable Other HCP. A 26-year-old female patient received their second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date not reported), intramuscular on the left arm on 12Jan2021 08:30 at single dose for COVID-19 immunization. The patient medical history included allergies. Concomitant medication included unspecified medication. The patient received their first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date not reported) on 22Dec2020, intramuscular on the left arm. The patient experienced fatigue, chills, headache and body aches on 13Jan2021 06:00. The patient was recovering from the events. No treatment was received in response to the events. No follow-up attempts are possible. Information on lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 0976907
Sex: M
Age:
State: IL

Vax Date: 01/01/2021
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

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

Symptoms: Chills; weak; hung-over feeling; pain and swollen lymph node under left arm (injection arm); pain and swollen lymph node under left arm (injection arm); This is a spontaneous report from a contact consumer (patient). A 31-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EL1283), via an unspecified route of administration on Jan2021 08:00 AM at single dose for covid-19 immunization. Vaccine location was left arm. Patient received the first dose on Dec2020 10:00 AM (lot number EK5730) at left arm for covid-19 immunization. The facility type vaccine was hospital. Known allergies included Penicillin. Concomitant medication included omeprazole. Patient was not diagnosed with COVID-19 prior to vaccination nor tested for COVID-19 since the vaccination. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced Chills, weak, hung-over feeling the evening after second dose. Second day, pain and swollen lymph node under left arm (injection arm). The events onset date was reported as 13Jan2021 02:00 AM. Patient didn't receive treatment for the adverse events. The outcome of events was not recovered.

Other Meds: OMEPRAZOLE

Current Illness:

ID: 0976908
Sex: F
Age:
State: MI

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

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: extreme chills; neck is aching; right arm pain; the pain prevented her from sleeping; Itching; This is a spontaneous report from a contactable consumer report self. This 72-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular at right arm on 12Jan2021 15:30 at single dose for covid-19 immunisation. Medical history included had COVID back in Nov2020, blood cholesterol abnormal. Concomitant medication included Pravastatin for blood cholesterol and unspecified water pill. No prior vaccinations within 4 weeks. No additional vaccines administered on same date. Patient received Pfizer covid vaccine on 12Jan2021 around 15:30. Her right arms started getting in pain about 11pm and the pain prevented her from sleeping most of the night till she took an Aleve around 6am. She took another Aleve on 13Jan2021. She can barely raise her right arm and it is ok if she does not try to use it but if she tried to use her right arm then it is inoperable. At 12Jan2021 night after she got the vaccine she experienced itching, she never got a rash, the itching never got bad and it went away. She has not taken her temperature. She was having extreme chills that started around 13Jan2021 3:00 pm and she cannot get warm, she has blankets piled on her. Her neck is aching (started 13Jan2021 afternoon) and she thought this may be from tensing up since she is cold. No emergency room or physician office visit. The outcome of "Itching" was recovered, of else events was unknown. Information on the lot/batch number has been requested.

Other Meds: PRAVASTATIN

Current Illness:

ID: 0976909
Sex: M
Age:
State: IL

Vax Date: 12/30/2020
Onset Date: 12/01/2020
Rec V Date: 01/27/2021
Hospital:

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Feeling weak; Muscle pain; Chills; Not been able to work for last 3-4 days; Please specify other location: Right shoulder; Shortness of breath; Dizziness; This is a spontaneous report from a contactable consumer (patient). A 41-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EK9231, Expiry Date: 30Apr2021) via an unspecified route of administration in right shoulder on 30Dec2020 20:30 at single dose for COVID-19 immunisation. The medical history was not reported. There were no concomitant medications. The patient previously took influenza vaccine on 2020 for immunization 2-3 months before this BNT162B2 vaccine, previously took flu shot in the past for immunization and got sick from it. That was about 3 years ago (2018). The patient went and got the Pfizer BioNTech about 2 weeks ago. Wants to know if side effects can start then after the vaccine. He has had chills, muscle pain, shortness of breath, and dizziness. Got this at hospital and has not been able to go to work on Jan2021 that last 3-4 days due to feeling weak. Received the vaccine on 30Dec2020 and the dizziness and shortness of breath kind of started days after that on Dec2020. The chills started a couple of days ago, about 3 days ago (Jan2021) and has been off and on. The muscle pains started today (13Jan2021). Just got a text message about getting the second dose next Wednesday. He did not get any other vaccines that day or 4 weeks prior. He got the shot to protect himself from the virus, but feels like he has the virus or something. The events did not require a visit to emergency room, but may go to be seen tomorrow. Events outcome of chills, muscle pain, shortness of breath, dizziness, and not been able to go to work that last 3-4 days due to feeling weak was not recovered.

Other Meds:

Current Illness:

ID: 0976910
Sex: F
Age:
State: OK

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data:

Allergies:

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

Symptoms: Headache; extreme fatigue; joint and general muscle ache; joint and general muscle ache; This is a spontaneous report from a contactable Other HCP (patient). This adult female patient of unknown age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot # EC1283), intramuscular, on 11Dec2021 at 09:30 AM at single dose for COVID-19 immunisation. Vaccine location was right arm. Facility type vaccine was hospital. Medical history included seasonal allergies, pet allergies, penicillin allergy. Historical vaccine included first dose of BNT162B2 (lot # EH9899), on 21Dec2020 at 09:00 AM, intramuscular right arm, and flu vaccine. Concomitant medications included cetirizine hydrochloride (ZYRTEC), ibuprofen (ADVIL) and diphenhydramine hydrochloride (BENADRYL). On 12Jan2021 at 12:00 PM, the patient experienced headache, extreme fatigue, joint and general muscle ache. No treatment was given for the events. Outcome was not recovered.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; ADVIL [IBUPROFEN]; BENADRYL

Current Illness:

ID: 0976911
Sex: M
Age:
State: OR

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Back ache; some soreness in his arm; This is a spontaneous report from a contactable consumer (patient). A 66-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 12Jan2021 09:15 at single dose in the left arm for covid-19 immunisation. Vaccination Facility Type was Hospital. Medical history included prostate cancer from 3 years. Having aches and his back bothering him predates taking the vaccine. A while ago he blew out his knee and his shoulder and three years ago he started having trouble with his back. Family Medical History: heart disease.There were no concomitant medications. He had the flu vaccine from the VA and it can be a little bit of a thing but the last one it ached, made his shoulder worse; the ache lasted six months but it might have been the way it was administered. He has no product or information to provide NDC, lot or expiration date for the flu vaccine he received about two years ago. Mentions he swore off the flu vaccine after that. He was at the VA yesterday for some other business and they told him the shot was available to him so he had it. He is planning to get the second dose on 02Feb2021. He used to take blood thinners and he imagines, like with the blood thinners, that they wouldn't want him to stack Tylenol on top of the vaccine. He has a few aches and his back is bothering him; which is normal for him; but he would like to know if he can take Tylenol for his back. He noticed some soreness in his arm, a little, when he got home two or three hours later. His sister said to rub it to disperse the medication, so he did. Adds it is not a big deal. Recently he has not been sleeping well; which is also normal for him; so today he slept in; he may have slept too long on his back but his back is aching and he wanted to take some Tylenol for his back. The patient experienced some soreness in his arm on 12Jan2021 with outcome of recovering , back ache on 13Jan2021 with outcome of not recovered. Treatment received for the event. No additional Vaccines Administered on Same Date of the Pfizer Suspect. Prior Vaccinations (within 4 weeks) was none. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976912
Sex: F
Age:
State: VA

Vax Date: 01/08/2021
Onset Date: 01/12/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: does not have much taste/losing taste a little; Mouth dry; This is a spontaneous report from a contactable consumer (patient). A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route of administration on 08Jan2021 (last Friday of 13Jan2021) at single dose for COVID-19 immunization. Medical history and concomitant medications were not provided. The patient was calling for herself regrading side effects for the vaccine, she clarified the vaccine to be the COVID-19 Vaccine, the Pfizer one, she got the vaccine on 08Jan2021 (last Friday of 13Jan2021), she was having side effects, she was having issues with her mouth, her mouth was dry and issues with taste, she was losing it a little, she did not have much taste, she stated she had never had dry mouth before and she was trying to figure out if these are symptoms from getting the vaccine or something. The patient experienced mouth dry from 12Jan2021 and ongoing, losing taste a little on an unspecified date. She wanted to know if others had experienced these events. She stated these do not worry her too much, she then added she had heard that mouth dry is a side effect. The patient stated she did not not have a fever, no coughing, or aches. The outcome of the event mouth dry was not recovered, while unknown for the other event. Information about Lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 0976913
Sex: F
Age:
State: AZ

Vax Date:
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: fibromyalgia; muscle pain; super achy; This is a spontaneous report from a contactable nurse reporting for herself. A 65-year-old female patient received pneumococcal 13-val conj vac (dipht crm197 protein) (reported as PNEUMONIA SHOT), via an unspecified route of administration on an unspecified at single dose for immunization, influenza vaccine (INFLUENZA), via an unspecified route of administration on an unspecified date at an unspecified dose for immunization. The patient medical history and concomitant medications were not reported. In 2018, she had ovarian cancer, it came back and she was on chemotherapy then maintenance chemotherapy, she developed a complication. The patient had blood clots in her lungs so she stopped chemotherapy. She was treated to at a city. She needed to be on apixaban (ELIQUIS) 5mg twice a day and also take a diuretic because she had a blood clot. The patient had to take a shot when white cells drop, platelet drops, it correlated with ibuprofen (MOTRIN). The patient had taken influenza and pneumonia shot. She took both of those without any issues. She had fibromyalgia and had muscle pain, super achy, for a day or two after those vaccines. The outcome of the events was unknown. Pfizer is a marketing authorization holder of [Pneumococcal 13-Val Conj Vac] in the country of incidence or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of [Pneumococcal 13-Val Conj Vac] has submitted the same report to the regulatory authorities. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976914
Sex: F
Age:
State: CA

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: felt cold and chilly; can't move her arm up and down; Fever/ 101.2; body aches; mild pain in arm; This is a spontaneous report from a contactable consumer report self. This 61-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL4176), via an unspecified route of administration at left arm on 12Jan2021 14:30 at single dose for covid-19 immunization. Medical history included COVID in Nov2020 (Patient was tested for Covid on 23Nov2020 and found out the 25Nov2020 the result was positive), she just quarantined herself at a hotel (They gave her Benzonatate, but she was also taking Tylenol 500mg and Robitussin DM). Concomitant medications not reported. Patient did not get any other shots or 4 weeks prior. No problems with vaccines in past that she can remember. No additional vaccines administered on same date of the Pfizer suspect. Patient received the Pfizer BioNtech vaccine on 12Jan2021 and after that on 12Jan2021 night she didn't feel anything but mild pain in arm, it was so painful, but not as bad on 13Jan2021 even though she still has it. She can't move her arm up and down. On 13Jan2021 morning at dawn she had a fever and it is now 101.2. Has taken Tylenol 500mg (Lot number: SLA071, UPC number: 30047112, Expiry Date: Aug2024). Patient had body aches started 12Jan2021 at midnight (12:00) that is start date of 13Jan2021. She felt cold and chilly and not sure if it was the weather or her. No Emergency Room or Physician Office visit. The outcome of "felt cold and chilly" was unknown, of else events was not recovered.

Other Meds:

Current Illness:

ID: 0976915
Sex: M
Age:
State: GA

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: he got real cold and shaky and couldn't get warm; he got real cold and shaky and couldn't get warm; temperature was low at 96 degrees Fahrenheit; He got nauseous with it; He had severe fatigue; This is a spontaneous report from a contactable consumer (patient). A 52-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ELO140) via an unspecified route of administration on left arm on 11Jan2021 at 9:15 at single dose for COVID-19 immunization. The relevant medical history included Covid-19 from 17Jul2020 to 14Aug2020, he didn't get hospitalized but was pretty sick. He had circulation issues with it. He had numbing and tingling in his left three fingers (clarified left three fingers as his middle finger, index finger, and ring finger) and numbing and tingling in his toes as well. Concomitant medications included ubidecarenone (COQ-10), acetylsalicylic acid (BABY ASPIRIN), rosuvastatin and monascus purpureus (RED YEAST RICE). The patient previously received the first dose of BNT162B2 at the age of 52 years old on 23Dec2020 at single dose for COVID-19 immunization. With second dose the patient thought he would be better, but about 12 hours later he got real cold and shaky and couldn't get warm. He checked his body temperature and he didn't have a temp. His temperature was low at 96 degrees Fahrenheit. He tried to keep himself warm. He got nauseous with it. Basically he looked on line and was having them. Today he started to feel better, but still a little nauseous. He had severe fatigue. He didn't realize he could go fill out something on the website for CDC. He knew he had wanted the vaccine because he had some severe symptoms when he had COVID. He didn't want to get COVID again. His hospital frustrates him sometimes. They didn't put the date on there when he was to come back for the second dose. They didn't tell him to come back on the 13th. He had to figure the dates from the website and emails. He talked it over with his wife. He came in contact with it every night. He was taking care of people that were critical. He worked in the intensive care unit. Even the people he took care of that didn't have it, ended up with it. He wore a mask. He used hand sanitizer. He didn't want to get it again. People were shocked when he got it the first time. He did verify that he got the second dose one day sooner, instead of the three day window. He was sick with the first and was expecting to be more sick with this one. He wanted to give himself an extra day before he had to go back to work. He had a couple of emails where they discussed increasing the window to do it a day sooner. He was going to have to go an hour an half a way to get the second dose and he didn't want to do that. The patient underwent lab test included height was approximately six two, weight was about 194 lbs on an unspecified date, and body temperature showed 96 degrees Fahrenheit in Jan2021. The outcome of the event he got real cold and shaky and couldn't get warm, temperature was low at 96 degrees Fahrenheit was recovering, for the events he got nauseous with it and he had severe fatigue were not recovered.

Other Meds: COQ-10; BABY ASPIRIN; ROSUVASTATIN; RED YEAST RICE

Current Illness:

ID: 0976916
Sex: F
Age:
State:

Vax Date: 12/25/2020
Onset Date: 12/01/2020
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: left chest pain; left chest pain/It was sharp and seemed to get worse with movement so assumed it was musculoskeletal; woke up in the early morning with severe pain; pain even sitting up and especially with taking in a little larger breaths than usual; body aches; This is a spontaneous report from a non-contactable consumer reported for self. This 49-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EC1284) via unspecified route of administration on 25Dec2020 at single dose for COVID-19 immunization. The patient medical history and concomitant medication was not reported. About 18 hours after injection (Dec2020), the patient started having left chest pain when she went to sleep. It was sharp and seemed to get worse with movement so assumed it was musculoskeletal. The patient fell asleep and woke up in the early morning with severe pain. It again was worse with certain positions but was extremely painful. The patient couldn't find a comfortable position. There was pain even sitting up and especially with taking in a little larger breaths than usual. Could not pinpoint the area of pain, but it seemed anterior in the lower left chest. No other symptoms otherwise, no shortness of breath. The pain improved with paracetamol (TYLENOL), and she was able to fall back asleep. The pain continued throughout the day and then the patient developed body aches that afternoon. By the next day, symptoms improved and were nearly resolved by the following day. The patient was not diagnosed with COVID-19 prior to and since the vaccination. The patient recovered from the events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0976917
Sex: F
Age:
State: IL

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Chills; sweats; headache; myalgia; fatigue; This is a spontaneous report from a contactable other hcp reported for herself. This 41-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3302), via an unspecified route of administration at right arm on 11Jan2021 09:00 AM at single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. No COVID prior vaccination, no COVID tested post vaccination. No other vaccine in four weeks. NO other medications in two weeks. Patient received first dose of BNT162B2 (lot number= EJ1685) at right arm on 20Dec2020 07:15 PM. On 11Jan2021 08:30 PM, the patient experienced Chills, sweats, headache, myalgia, fatigue. No treatment received. The event outcome was recovered.

Other Meds:

Current Illness:

ID: 0976918
Sex: F
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: frontal and occipital headaches; hot flashes; exhaustion; This is a spontaneous report from a contactable Nurse (patient). A 39-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number=EH9899), on 11Jan2021 07:45 at SINGLE DOSE in Left arm for COVID-19 immunisation. Facility type vaccine was Hospital. Medical history included irritable bowel syndrome (IBS) , anxiety and depression. No other vaccine in four weeks. Concomitant medication in two weeks included buspirone, escitalopram. The patient previously received first dose of BNT162B2 (lot number=EH9899), on 21Dec2020 10:00 AM, at SINGLE DOSE in Left arm for COVID-19 immunisation. The patient experienced Continued frontal and occipital headaches on day 2 with no relief from Tylenol, hot flashes, and exhaustion, all on 12Jan2021 02:00 AM. The outcome was Not recovered. No treatment for hot flashes, and exhaustion. No COVID prior vaccination. Covid test post vaccination included Nasal Swab on 12Jan2021 with result of Negative.

Other Meds: BUSPIRONE; ESCITALOPRAM

Current Illness:

ID: 0976919
Sex: F
Age:
State: IL

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: severe dizziness; disorientation; Tired; muscle aches; L ear pain; chills; This is a spontaneous report from a contactable Other HCP (patient). A 38-year-old female (pregnant: No) patient received 1st dose of BNT162B2 (COVID vaccine, lot number= EK9231) on 11Jan2021 12:30 PM on Left arm for covid-19 immunization. Medical history and concomitant drug were not reported. No other vaccine in four weeks. No COVID prior vaccination. No COVID tested post vaccination. Patient experienced severe dizziness, disorientation, unable to finish any tasks. Tired, some muscle aches, L ear pain and chills (no fever) on 11Jan2021 01:00 PM. No treatment. Outcome of the event was Recovered/Resolved with Sequel. No further information is expected. Information on the Batch/Lot number has been obtained.

Other Meds:

Current Illness:

ID: 0976920
Sex: F
Age:
State: NJ

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: extreme headache; muscle aches; chills; nausea; diarrhea; sweating; tachycardia; This is a spontaneous report from a contactable nurse. This 43-year-old female nurse (patient) reported that she received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular at left arm on 11Jan2021 06:15 PM at single dose for COVID-19 immunization. Patient was not pregnant. Medical history included anxiety, migraines, palpitations and known allergies: latex, adhesive. Concomitant drugs included paroxetine hydrochloride (PAXIL), alprazolam (XANAX), and unspecified multivitamin. Historical vaccine included the first dose of BNT162B2 on 21Dec2020 06:15 PM via intramuscular at left arm for COVID-19 immunization, and patient had headache and nasal congestion. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. On 11Jan2021 09:45 PM, patient experienced extreme headache, muscle aches, chills, nausea, diarrhea, sweating, tachycardia. No treatment was received. Outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds: PAXIL [PAROXETINE HYDROCHLORIDE]; XANAX

Current Illness:

ID: 0976921
Sex: F
Age:
State: CO

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: right armpit and axilla swelling, pain in lymphnodes; right armpit and axilla swelling, pain in lymphnodes; headache; fever; fatigue; Vomit; Dizzy; rash not sure first time but within first 12 hours over chest and trunk; This is a spontaneous report from a contactable other HCP. This other HCP reported for herself that a 36-year-old female patient received second dose (lot number: Ek9231) of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 36-years, on 08Jan2021 19:00 (07:00 PM) at single dose in right arm; first dose (lot number: Eh9899) on 18Dec2020 07:00 PM at single dose; both via unspecified route of administration for COVID-19 immunisation in hospital. Medical history included thyroid issues; allergies to latex and adhesives. No COVID prior vaccination. No other vaccine in four weeks. Patient is not pregnant. Concomitant medications included formoterol fumarate, mometasone furoate (DULERA). The patient previously took thimerosal and experienced allergy to it. On 08Jan2021, the patient experienced vomit and dizzy within 1 hour of vaccine. Rash not sure first time but within first 12 hours over chest and trunk. On 09Jan2021 (next day) headache, dizzy, fever, fatigue. On 11Jan2021 (after 2 days), right armpit and axilla swelling, pain in lymphnodes. It was unknown if treatment was received or not. The events resulted in doctor or other healthcare professional office/clinic visit. Outcome of the events was not recovered. No COVID-19 tested post vaccination.

Other Meds: DULERA

Current Illness:

ID: 0976922
Sex: F
Age:
State: CA

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: chills; Sore throat; some aching, like body aches; joint tenderness; some swelling at the injection site; arm tenderness; This is a spontaneous report from a contactable consumer reported for self. This 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 12Jan2021 13:30 on Arm Left at single dose (lot: EK9231, Expiry: 30Apr2021) for covid-19 immunisation. Give her a follow up appointment for a second dose, that will be 02 Feb at 1:20 PM. Medical History included arthritis and had surgery for right knee replacement 6 years ago (2015). They are trying to figure out, she has water in her ear she has had CT scans recently trying to check for any problems that could be corrected surgically and that was all clean. She has had a mammogram, she was not sure about the mammogram yet but she thinks they would have called her if there was a problem with that. Historical vaccine included Just mild stuff with the flu vaccine for immunisation on occasion she has had similar reactions that were very mild with the flu vaccine and last year she had none of that at all. She says when she has had any other vaccine, she had no reaction other than maybe a slightly sore arm. No other products. She did have some mild side effects. She was really glad she got this shot. She said she had experienced some chilling on 13Jan2021, these are all very mild symptoms. She had a sore throat on 13Jan2021, some aching, like body aches on 13Jan2021 and joint tenderness on 13Jan2021. She just got chilled every once in a while. It was not very bad. She said the sore throat had persisted about the same, but the coffee helped. She was having some swelling at the injection site that was about the same as when it began on 13Jan2021. She was having some arm tenderness on 13Jan2021. She did not have any adverse reactions yesterday (12Jan2021) she was so excited to get it. Outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0976923
Sex: F
Age:
State: NC

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: heart palpitations; Stated that it felt like nerves on inside of her body were reacting like bugs crawling on the inside of her skin; bad headache; Sore throat; tongue swollen; tired; weak; This is a spontaneous report from a contactable consumer reported for self. This 40-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via Intramuscular on 12Jan2021 on Arm Left at single dose (lot: EK9231) for covid-19 immunisation. Med history and concomitant medications were none. The patient had injection done yesterday (12Jan2021) and wanted to report symptoms. Stated that it felt like nerves on inside of her body were reacting like bugs crawling on inside of her skin 12Jan2021 at 6:30pm which calmed down at 10:00pm, bad headache 12Jan2021 at 6:30pm, sore throat, tongue felt swollen happened on 12Jan2021 after the injection, both resolved at 10:30pm. Stated that she did do Benadryl. Stated that she took another Benadryl this morning and it feels like it is wearing off and the sensation is coming back. Stated felt tired and weak on 12Jan2021. Stated felt like having palpitations and heart going too fast on 13Jan2021. Stated that she called her primary healthcare provider and was told to call Pfizer. Wanted to know if she needed to go to her doctor. Outcome of the events sore throat, tongue felt swollen was recovered 12Jan2021 10:30pm. Outcome of other events was not recovered.

Other Meds:

Current Illness:

ID: 0976924
Sex: M
Age:
State: TX

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Mild fever 99.5F; headache; This is a spontaneous report from a non-contactable Other Health Professional. A 46-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular on 12Jan2021 at single dose on arm left for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced mild fever 99.5 F and headache, both on 13Jan2021 with outcome of unknown. Patient did not have COVID prior vaccination. Patient did not have COVID tested post vaccination. No follow-up attempts are possible. Information about Lot/Batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0976925
Sex: F
Age:
State: MN

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Body aches; Exhaustion/fatigue; Low grade fever; Headache; Foggy; This is a spontaneous report from a contactable Nurse (patient) reported for herself. A 39-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EL0142) intramuscular in Left arm on 12Jan2021 08:30 at single dose for COVID-19 immunisation. She received the first dose (lot number=EJ1685) intramuscular in left arm on 22Dec2020 08:30 AM at age of 38 years old for COVID-19 immunisation. The patient medical history was not reported. There was no known allergies. Concomitant medication included phentermine. On 12Jan2021 21:30, the patient experienced body aches, exhaustion/fatigue, low grade fever, headache, foggy. No treatment received for events. The patient was not pregnant. Events outcome was recovering.

Other Meds: PHENTERMINE

Current Illness:

ID: 0976926
Sex: F
Age:
State: WI

Vax Date: 12/21/2020
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

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

Symptoms: fever; chills; myalgias; some sensory changes to the left arm; This is a spontaneous report from a contactable pharmacist. An adult female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 21Dec2020, at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. It was unknown if patient was pregnant or not at the time of vaccination. Patient denies any history of vaccine associated reactions. Patient previously took Vancomycin and experienced allergy. Patient did not have other vaccine in four weeks. It was reported that after her first dose of the COVID vaccine she had fever, chills and myalgias as well as some sensory changes to the left arm on an unspecified date. Patient visited physician office for chills and sensory changes to the left arm, visited emergency room for myalgias. These symptoms lasted for around a day before resolving. It was unknown if patient had COVID prior vaccination or if patient tested COVID post vaccination. Outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976927
Sex: F
Age:
State: NY

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: headache; aches all over my body similar to how you feel with the flu; aches all over my body similar to how you feel with the flu; very tired for 2 days; One week after the second shot I felt dizzy on two occasions; This is a spontaneous report from a contactable nurse (patient). This 45-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 05Jan2021 at single dose on the left arm for COVID-19 immunization. The patient's medical history included hypertension, anxiety, degenerative arthritis and allergies: sulfa. The patient's concomitant medications were none. The patient previously took the first dose of BNT162B2 on 22Dec2020 09:30 at right arm for COVID-19 immunization and experienced headache and mild arm soreness. No other vaccine received in four weeks. Facility type vaccine was workplace clinic. Patient was not pregnant. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. After the second shot by 12:00, patient had a headache, in the middle of the night on 05Jan2021 patient started with aches all over her body similar to how you feel with the flu. The aches lasted for 2 days. Patient was also very tired for 2 days. One week after the second shot she felt dizzy on two occasions. No treatment received. Outcome of the events was recovered in Jan2021. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 0976928
Sex: F
Age:
State: MS

Vax Date: 12/18/2020
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: I had soreness in my arm the day after the first injectionbut no other adverse events after the first injection; This is a spontaneous report from a contactable Other-HCP (patient). This 40-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number=EH9899), via an unspecified route of administration on 18Dec2020 14:45 at single dose on the right arm for COVID-19 immunization. The patient's medical history included allergies: Cephalosporin (mild reaction of hives one time after having taken it with no issues for years). There were no concomitant medications. No other vaccine received in four weeks. Facility type vaccine was hospital. Patient was not pregnant. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. The patient had soreness in her arm the day after the first injection but no other adverse events after the first injection. No treatment received. Outcome of the event was recovered.

Other Meds:

Current Illness:

ID: 0976929
Sex: F
Age:
State: MO

Vax Date: 12/20/2020
Onset Date: 12/01/2020
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: right neck swelling; tenderness; it was a lymph node thing; right sided Neck Pain; Right sided armpit pain; arm pain; This is a spontaneous report from a contactable consumer (patient). A 33-years-old female patient received the first dose of BNT162B2 (lot number: EH9899, Expiry Date: 15Dec2021) via an unspecified route of administration in right arm on 20Dec2020 at single dose for COVID-19 immunisation. She received the second dose on 11Jan2021. There was no medical history. There were no concomitant medications. The patient got the first dose on 20Dec2020. It was after the second dose she had symptoms. The second dose was on 11Jan2021. The right sided neck and armpit pain started yesterday 12Jan2021 and she still has it at the moment. She further clarifies that she actually had this symptom on Dec2020 after the first vaccine dose also, she had the right neck swelling and tenderness, the same side as where she got the vaccine on. When she got the First Dose on 20Dec2020 she had the right sided neck pain and arm pain on Dec2020 she received the vaccine on the right side, she was going to the ear doctor asking about it, it occurred about 2 days after the first vaccine dose and hung around a long time, it lasted more than a week, she guess it was a lymph node thing. She has never been tested for COVID or had any Antibody tests. She has had no issues with vaccines in the past. The patient was not pregnant. Events outcome of right sided Neck Pain and Right sided armpit pain was not recovered, while for others was unknown.

Other Meds:

Current Illness:

ID: 0976930
Sex: M
Age:
State: NY

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: numbness in right side of face and right arm; hard time swallowing; felt foggy; dizzy; disoriented; This is a spontaneous report from a contactable consumer. A 43-year-old male patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on arm left from 11Jan2021 to 11Jan2021 at SINGLE DOSE for covid-19 immunisation. Medical history included was reported as none. There were no concomitant medications. The patient states about 24 hours later he felt foggy, disoriented, and dizzy (all three occurred on 12Jan2021), states he then woke up at 3 am this morning and had a lot of numbness on right side of face and arm and had a hard time swallowing (both occurred on 13Jan2021), states a couple hours later he went to hospital, went to ER and had to do an MRI, states the MRI of brain and neck came back clear and checked out, states doctors concluded it was an adverse reaction to vaccination. Outcome of the events was recovered on 13Jan2021. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0976931
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Vomiting; This is a spontaneous report from a contactable consumer received via a Pfizer sales representative. A 21-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number was not reported) via an unspecified route of administration on an unspecified date at a single dose as COVID-19 vaccine. Medical history included other health issues mainly being extremely underweight for a 21-year-old female. Concomitant medications were not reported. The patient experienced vomiting on an unspecified date. The event took place after use of product. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0976932
Sex: M
Age:
State: OR

Vax Date:
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Back pain; Joint pain; This is a spontaneous report from a contactable consumer (Patient) from a Pfizer-sponsored program Pfizer First Connect. A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation. Medical history included ongoing back problems. The patient's concomitant medications were not reported. The patient experienced back pain and joint pain on an unspecified date. Outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Back disorder

ID: 0976934
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: pain at the injection site; sore arm; This is a spontaneous report from a Pfizer-sponsored program Corporate (Pfizer) Social Media Platforms via a non-contactable consumer (patient) reported for herself. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient had now had both doses of the Pfizer COVID-19 vaccine. It has now been several days from the second dose. After 1st dose, she had a sore arm and some pain at the injection site for about 24hrs. Definitely sore that evening when sleeping and was difficult to sleep on that side. After 48hrs so more pain. No other symptoms! Events outcome was recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0976935
Sex: M
Age:
State: FL

Vax Date: 01/09/2021
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Tenderness at the injection site; This is a spontaneous report from a contactable consumer (patient). This consumer reported similar events for 2 patients (husband and Wife). This is 1st of 2 reports. A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 09Jan2021 at single dose for covid-19 immunisation.The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced Tenderness at the injection site on an unspecified date. Outcome of event was unknown. Information of lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021041453 same product/event/reporter, different patient

Other Meds:

Current Illness:

ID: 0976936
Sex: F
Age:
State: FL

Vax Date: 01/09/2021
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Tenderness at the injection site; This is a spontaneous report from a contactable consumer (husband). This consumer reported similar events for 2 patients (husband and wife). This is 2nd of 2 reports. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 09Jan2021 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced tenderness at the injection site on an unspecified date. Outcome of event was unknown. Information about lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021041442 same product/event/reporter, different patient

Other Meds:

Current Illness:

ID: 0976937
Sex: M
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: perfuse sweating; mild tenderness of arm; Muscle pain; Chills; Weakness; This is a spontaneous report from a contactable physician (patient). A 78-year-old male patient received the 2nd dose of bnt162b2 (BNT162B2) intramuscular at single dose at left deltoid on 11Jan2021 around 13:00 for covid-19 immunisation, administered at hospital. Medical history was none, he was basically healthy. There were no concomitant medications. No prior vaccinations (within 4 weeks), but the patient received the 1st dose of bnt162b2 (BNT162B2) at single dose exactly 3 weeks before 1st dose on 21Dec2020 for covid-19 immunisation. No additional vaccines administered on same date of bnt162b2. The patient began to have muscle pain, chills, and weakness about 8 hours or so after the 2nd vaccine on 11Jan2021. He states these symptoms have maybe gotten a little better, but have been continuing on for 2-3 days now. He is also experiencing perfuse sweating during 13Jan2021night. Right now, he was not experiencing this. Maybe a little bit, but not much. The caller experienced mild tenderness of arm on 12Jan2021: he explained when you press his arm, it hurts a little bit. No events required a visit to Emergency Room or Physician Office. The outcome of muscle pain was and perfuse sweating was unknown, of chills, weakness was recovering, of mild tenderness of arm was not recovered. The patient was his own primary doctor. The reporter considered all events as medically significant and he believed these symptoms are related to receiving the vaccine because he stated he was okay before that. No further information expected. Information about lot/batch number has been requested.; Sender's Comments: There is a reasonable possibility that the event muscle pain was related to BNT162b2 based on known drug safety profile. Based on the temporal relationship, the association between the other events with BNT162b2 can not 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.

Other Meds:

Current Illness:

ID: 0976938
Sex: U
Age:
State: MA

Vax Date: 01/03/2021
Onset Date: 01/01/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: tested positive for covid after 1st dose received on 03Jan2021; tested positive for covid after 1st dose received on 03Jan2021; This is a spontaneous report from a contactable Nurse via a Pfizer-sponsored program named Pfizer First Connect. This nurse reported similar events for 15 residents and 5 staff members. This case was for the 10th of 15 residents. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) , via an unspecified route of administration on 03Jan2021 at the first single dose for covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced tested positive for covid in Jan2021 after 1st dose received. The outcome of events was unknown. Information about batch/lot number has been requested.; Sender's Comments: A causal association between reported event and suspect BNT162B2 cannot be excluded.,Linked Report(s) : US-PFIZER INC-2021028829 same reporter, same drug/event, different patient

Other Meds:

Current Illness:

ID: 0976939
Sex: F
Age:
State: NJ

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: involuntary muscle contractions in her diaphragm; chills; cold; severe body aches; Involuntary muscle cramping; chest pain; Feels bad; severe joint aches; tremor; nausea; severe body pain in her back and knees; severe body pain in her back and knees; Weakness; Headache; This is a spontaneous report from a contactable Other HCP reported for self. This 50-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 12Jan2021 07:00 on Deltoid Left at single dose (Lot # EK9231) for covid-19 immunisation. Concomitant medications were none. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 22Dec2020 via Intramuscular at age of 50 years old on Deltoid, Left at single dose (Lot # EH9899) for covid-19 immunisation, experienced Tingling lips, Swollen lips, and the Benadryl took away the lip tingling and swelling, Tachypnea, Myalgia, Joint pain, severe headache, Weakness generalized, Nausea, she said she was really pale, so much so, that her husband was scared for her. She said the symptoms lasted for about 3 days, but the weakness lasted longer. Reported she took some Zofran disintegrating tablets for her nausea. Clarified she did have a PCR COVID-19 Virus test after she developed symptoms from receiving the first COVID-19 Vaccine dose. She said she had the PCR COVID-19 Virus test about 3 weeks ago and the test was negative. She said she thought she had the COVID-19 Virus after receiving the first COVID19 Vaccine dose because no one else she knew who had the COVID-19 Vaccine had any issues. Reported she received the second COVID-19 Vaccine dose on 12Jan2021 at 7:00AM in the left Deltoid. She said the adverse reaction she experienced after the second vaccine dose was slightly different from what she experienced with the first dose. She said about 10 hours after the COVID-19 Vaccine was administered, clarifying at around 17:00PM 12Jan2021, she started having severe body aches(disability), and involuntary muscle cramping (disability), like tetanus. She said even her diaphragm was cramping. She said she had chest pain on 12Jan2021(disability), tremors on 12Jan2021 (medically significant), and body aches, but doesn't think she had fever. She said the symptoms are still going on like with the first COVID-19 Vaccine dose, but she has more severe joint aching on 12Jan2021 (disability), weakness on 12Jan2021 (disability), and nausea on 12Jan2021 (medically significant). She said her knees feel like she was beaten severely. She said she aches so bad, it hurts having pants on. She said she does not have a headache or tremors now, but did have a headache on 12Jan2021 (medically significant) and tremors in the beginning. She said she feels the most pain in her back and knees. She said she feels really bad on 12Jan2021(disability). After the second dose on 12Jan2021, she reports severe body pain in her back and knees (disability). She reports almost feeling like she has tetanus- involuntary muscle contractions in her diaphragm on unknown date(disability), tremor, cold, chills, nausea, muscle cramps/chest pain. 'Felt like a heart attack. It was out of this world'. She still has nausea, severe pain all over my body, she can't be touched, and even wearing pants hurts. She said she is a healthy person with no chronic disease. She said she had nothing wrong with her prior to getting the COVID-19 Vaccine. Reported she hurts so bad, she can't even lift her arm. She completed a covid 19 PCR test after the first dose in Dec2020, which was negative. Treatment were received for the events severe body pain in her back and knees, involuntary muscle contractions in her diaphragm, tremor, nausea, muscle cramping, chest pain, Feels bad, more severe joint aching, severe body aches, Weakness, headache, chills, cold. Reported she has taken 1500mg of Motrin. Outcome of the severe body aches, Involuntary muscle cramping, Chest pain, severe joint aches, weakness, Nausea, Back pain, Knee pain, Feels bad was not recovered. Outcome of the event Tremor was recovered in Jan2021, Headache was recovered.; Sender's Comments: Based on temporal association, the causal relationship between BNT162B2 and the reported events cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once 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: 0976940
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: Not sleeping well; Throwing up; Hot and cold flashes; Can't eat; Hot and cold flashes; This is a spontaneous report from a contactable consumer reported for patient (father). A male patient of an unspecified age received BNT162B2 via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient has got the shot whatever it is, the vaccine. And he has got it on Sunday. And since Sunday night he has been not sleeping well, throwing up, hot and cold flashes, can't eat. Events outcome was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0976941
Sex: F
Age:
State: CA

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 01/27/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: Sore throat; nasal congestion; chills; headache; nausea; feels like the flu; This is a spontaneous report from a contactable consumer (patient) from a Pfizer Sponsored Program Pfizer First Connect. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration, in Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced sore throat, nasal congestion, chills, headache, nausea, and feels like the flu in Jan2021. The clinical outcome of sore throat, nasal congestion, chills, headache, nausea, and feels like the flu was not recovered. The batch/lot number for the vaccine, BNT162B2, was not provided and has been requested during follow up.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm