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: 1010754
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: tingling in jaw after the vaccine; This is a spontaneous report . A non-Contactable Consumer reported information for himself and his wife. This is the first of two reports. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number unknown), on an unknown date at single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient reported that he and his wife both had tingling in jaw after the vaccine. The outcome was unknown. No follow up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021076002 Same reporter, same product, same event, different patient

Other Meds:

Current Illness:

ID: 1010755
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: tingling in jaw after the vaccine; This is a spontaneous report A non-Contactable Consumer reported information for himself and his wife. This is the second of two reports. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number unknown), on an unknown date at single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient reported that he and his wife both had tingling in jaw after the vaccine. The outcome was unknown. No follow-up attempts are possible. Information about lot/batch number could not be requested. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021075995 Same reporter, same product, same event, different patient

Other Meds:

Current Illness:

ID: 1010756
Sex: F
Age:
State: IN

Vax Date: 01/16/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: sore arm; This is a Spontaneous report . A contactable consumer (patient) reported that a female patient in her later 70s received the first dose of COVID-19 vaccine (UNSPECIFIED TRADE NAME), via an unspecified route of administration on 16Jan2021 at single dose for COVID-19 immunisation. Medical history included she had arthritis since she was in her 20's and ongoing, has severe pain in back, problems with her hips, has bone spurs in one shoulder, and her hands and fingers sometimes hurt with the arthritis. The patient's concomitant medications were not reported. The patient experienced sore arm in Jan2021. Patient had her 1st shot on 16Jan, due for her 2nd shot and was experiencing arthritic symptoms which she claimed was pre-existing and not related to the vaccine. She wanted to know if she could take Tylenol. She was currently refraining from taking Tylenol. Patient explained that the only reason she was calling was regarding a couple of post that had been going around about the Pfizer vaccine. She wanted to know if she could take Tylenol or pain killers after having the vaccine. The post said that they cause the immune system to not function with the vaccine like it was supposed to. She is in her late 70's, because of arthritis she sometimes took Tylenol or her doctor would give her a pain pill. She had the fact sheets and paperwork, she knew everything she needed to know about the vaccine except this one thing. The patient confirmed she had taken the vaccine and had no reaction other than sore arm. The patient explained she was upset and didn't feel like going through a report as she had been on the phone for 15-20 minutes just to try and get to this agent. She had no problems and just wanted to know if she could take a pain pill. If she had to hold much longer she was just gonna take and if it messes it up, then it would just have to be messed up. Patient remarked she should never have called, she thought it was a simple question but should have known nothing was simple anymore. It required a conversation and all her information just got an answer to her question. She was upset and was going to hang up, she was tired being on the phone; she was not upset at this agent but at not being able to speak with some regarding this issue. The outcome of the event sore arm was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness: Arthritis (has had arthritis since she was in her 20's)

ID: 1010757
Sex: F
Age:
State:

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: positive for Covid; positive for Covid; This is a spontaneous report from a Pfizer-sponsored program . A contactable other health care professional reported for self. A female of an unknown age received her 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose via an unknown route on 06Jan2021 for Covid-19 immunization. Medical history and concomitant drug were not provided. The patient received 1st dose of Covid vaccine on 06Jan2021 and then tested positive for Covid on an unknown date in Jan2021. She was wondering what she should do about the 2nd dose. Information on the lot/batch number has been requested.; Sender's Comments: Based on the information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the first vaccine dose and the event onset.

Other Meds:

Current Illness:

ID: 1010758
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date:
Rec V Date: 02/08/2021
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: Patient tested positive after 1st dose; Patient tested positive for Covid after 1st dose; This is a spontaneous report from a Pfizer-sponsored program. A female patient of an unspecified age received first dose of bnt162b2 (BNT162B2, batch/lot number and expiration date not provided), via an unspecified route of administration on 13Jan2021 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Reporter has patient who had 1st dose of COVID vaccine on 13Jan and then tested positive for COVID. She is calling today because her patient is scheduled for her next dose on 15Feb and she wants to make sure that date is ok. The patient underwent lab tests and procedures which included tested positive for COVID on an unspecified date. The outcome of the event was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The patient received the first dose of bnt162b2(COMIRNATY), on 13Jan2021, and COVID-19 test positive on an unspecified date. No complete effect of the suspect vaccine could be reasonably achieved from first dose to protect from the targeted infection. Further information like COVID infection date needed for a full meaningful medical assessment.

Other Meds:

Current Illness:

ID: 1010759
Sex: U
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: Very sick; This is a spontaneous report from a non-contactable other HCP. The other HCP reported same event for six patients. This is the first of six reports. A patient of unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 20Jan2021, both at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Historical Vaccine included first dose of BNT162B2 at single dose for COVID-19 immunisation. The reporter explained that 6 coworkers were very sick after the injections on Jan2021. The reporter did not share any symptoms. Rather, reporter noted that they were miserable the day after, and were all now back at work today. Event outcome was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021076652 Same drug and event, different patient;US-PFIZER INC-2021076656 Same drug and event, different patient;US-PFIZER INC-2021076654 Same drug and event, different patient;US-PFIZER INC-2021076655 Same drug and event, different patient;US-PFIZER INC-2021076653 Same drug and event, different patient

Other Meds:

Current Illness:

ID: 1010760
Sex: M
Age:
State: AZ

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/08/2021
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: he lost sense of taste and smell; he lost sense of taste and smell; legs feeling heavy and hard to move; restless sleep; This is a spontaneous report from a contactable consumer (patient). An 84-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 14Jan2021 at single dose for COVID-19 immunisation. Medical history included Patient has recently had a pacemaker implanted. Concomitant medication included potassium Once a day, hydrochlorothiazide (DIURETIC), 20 mg Twice a day, dutasteride (AVODART), Once a day, acetylsalicylic acid (ASPIRIN (E.C.) 81 mg Once a day and a multivitamin QD (Once a day). The patient had the COVID-19 vaccine administered on 14Jan2021. That evening he began waking up several times after a restless sleep approximately six times on 14Jan2021. This lasted approximately two more evenings. On 19Jan2021 he lost sense of taste and smell for approximately three days. As of 20Jan2021 he has regained some sense of taste. The patient's temperature has been normal with no fever and pulse oximetry has been approximately 96%. Lastly on 17Jan2021 patient reported his legs feeling heavy and hard to move which lasted approximately three days. The outcome was recovering. Information on the lot/batch number has been requested.

Other Meds: POTASSIUM; DIURETIC [HYDROCHLOROTHIAZIDE]; AVODART; ASPIRIN (E.C.)

Current Illness:

ID: 1010761
Sex: U
Age:
State:

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 02/08/2021
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: very sick after the injections; This is a spontaneous report from non-contactable Other-HCP. This Other-HCP reported similar events for six patients. This is second of six reports (6 coworkers). A patient of unspecified age and gender received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# unknown), via an unspecified route of administration single dose on 20Jan2021 for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient was very sick after the injections on an unspecified date. The outcome was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021076655 same reporter, same drug/event, different patient;US-PFIZER INC-2021076654 same reporter, same drug/event, different patient;US-PFIZER INC-2021076551 same reporter, same drug/event, different patient;US-PFIZER INC-2021076656 same reporter, same drug/event, different patient;US-PFIZER INC-2021076654 same reporter, same drug/event, different patient

Other Meds:

Current Illness:

ID: 1010762
Sex: U
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: 6 coworkers were very sick after the injections; This is spontaneous report from a non-contactable other HCP. This Other HCP reported similar events for 6 patients. This is 3rd of 6 reports. A patient of unspecified age and gender received the second dose of BNT162B2 via an unspecified route of administration on 20Jan2021 at single dose for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The reporter explained that 6 coworkers were very sick after the injections on Jan2021. The reporter did not share any symptoms. Rather, reporter noted that they were miserable the day after, and were all now back at work today. Event outcome was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021076551 Same drug and event, different patient

Other Meds:

Current Illness:

ID: 1010763
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: Sick; This is a spontaneous report from a non-contactable healthcare professional reporting similar events for six patients. This report is for the fourth of the six patients. A patient of an unspecified age and gender received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE lot number/expiration date: not provided), via an unspecified route of administration, on an unspecified date (reported as "as recently as 20Jan2021"), as a single dose for COVID-19 vaccination. Relevant medical history was not reported. Historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE lot number/expiration date unknown) on an unspecified date. Concomitant medication were not reported. On an unknown date, the patient was sick. The outcome of the event sick was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained. .; Sender's Comments: Linked Report(s) : US-PFIZER INC- 2021076551 Same drug and event, different patient;US-PFIZER INC- 2021076656 Same drug and event, different patient;US-PFIZER INC- 2021076655 Same drug and event, different patient;US-PFIZER INC- 2021076652 Same drug and event, different patient;US-PFIZER INC-2021076653 Same drug and event, different patient

Other Meds:

Current Illness:

ID: 1010764
Sex: U
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: sick; This is a spontaneous report from a non-contactable other HCP. The other HCP reported same event for six patients. This is the sixth of six reports. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, first dose on an unspecified date, then second dose on 20Jan2021, both at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient experienced very sick after the injection in Jan2021. Outcome of the event was not recovered/not resolved. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021076551 Same drug and event, different patient

Other Meds:

Current Illness:

ID: 1010765
Sex: M
Age:
State: FL

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: asthma and COPD and having more episodes; asthma and COPD and having more episodes; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect. A contactable male consumer (patient) with unspecified age reported that he received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 11Jan2021 at single dose for COVID-19 immunization. Medical history included asthma and COPD both ongoing (he clarified he was having episode before doing the vaccination, he had had the breathing issues for a very long time). The patient's concomitant medications were not reported. Patient had asthma and COPD and having more episodes in Jan2021 with outcome of unknown, and was given methylprednisolone (MEDROL) dose pack, he was asking if he took this would it affect the efficacy of vaccine. It was reported patient would be due for second dose of BNT162B2 on 01Feb2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Asthma (had the breathing issues for a very long time); COPD (had the breathing issues for a very long time)

ID: 1010766
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: Allergic reaction; This is a spontaneous report from a contactable consumer (patient). A patient of unknown gender and age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unknown date at single dose for COVID-19 immunisation. Medical history and concomitant medications were unknown. The patient had an allergic reaction to the COVID vaccine and she/ he was sent to the ER for treatment. The outcome of the event was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1010767
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: positive side effects; This is a spontaneous report. received from a contactable consumer (patient). A female patient of an unspecified age received 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 and concomitant medications were not reported. The patient reported that she wanted to talk to a medical professional in regard to the positive side effects that the Covid vaccine has had on her. The event details, onset date and outcome were unknown at the time of the report. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010768
Sex: M
Age:
State: NJ

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
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: 99.4 F temperature 20 hours post dose; General fatigue; local soreness; This is a spontaneous report from a contactable consumer. A 27-years-old male patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), lot number EL3247, via an unspecified route of administration, in the left arm, on 19Jan2021 at 13:45 (at the age of 27 years old) as a single dose for COVID-19 immunization. The vaccination was administered in a workplace clinic. There was no medical history and no concomitant medications were reported. The patient was not tested for COVID-19 prior to vaccination. There was no other vaccination given in 4 weeks. On 20Jan2021 at 10:00, the patient experienced a temperature of 99.4 F 20 hours post dose, general fatigue and local soreness. There was no treatment for the events. The clinical outcome of the temperature, general fatigue and local soreness was recovering. The patient was not tested for COVID-19 post-vaccination.

Other Meds:

Current Illness:

ID: 1010769
Sex: M
Age:
State: SC

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 02/08/2021
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: He felt a little lightheaded afterwards; This is a spontaneous report from a contactable registered nurse (RN) who reported for her husband. A 74-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; solution for injection; Lot#: EK9231) via an unspecified route of administration on 13Jan2021 (at the age of 74-years-old) as a single dose for COVID-19 immunization. Medical history included high blood pressure and cholesterol, both controlled with medication, both from unspecified dates and unspecified if ongoing. Concomitant medications included lisinopril taken for blood pressure at 30mg, daily, lovastatin taken for cholesterol at 40mg, daily and acetylsalicylic acid (BABY ASPIRIN) taken for an unspecified indication at 1 DF (dosage form) daily, all from unspecified dates and unspecified if ongoing. The patient experienced "he felt a little lightheaded afterwards" on 12Jan2021. It was reported that "the reporter and her husband got the vaccine at the same time. They did not put their names on the cards, but they got the same lot number. It was written small on the card. The reporter's husband felt a little lightheaded afterwards but otherwise he had been fine. He received his first dose on 13Jan2021. He sat and waited for 15 minutes and when he stood up to leave, he was lightheaded. He sat back down and was okay." The clinical outcome of the event "he felt a little lightheaded afterwards" was unknown.

Other Meds: LISINOPRIL; LOVASTATIN; BABY ASPIRIN

Current Illness:

ID: 1010770
Sex: F
Age:
State: VA

Vax Date: 01/17/2021
Onset Date: 01/18/2021
Rec V Date: 02/08/2021
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: she used to be 6'2 but she thinks she has shrunk a little; nauseous/she is still just a little queasy; tried to get out of bed, and the whole world tilted on her/everything turned upside down; sore arm; This is a spontaneous report from a contactable consumer, the patient. A 65-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number: EL1283), via an unspecified route of administration in the right arm on 17Jan2021 (at the age of 65-years-old) as a single dose for COVID-19 immunisation. Medical history included Breast cancer in 2003 or 2004, for which the patient was in three clinical trials following that time. The patient reported that she requested to have the vaccine administered into her right arm because she is a breast cancer survivor. The patient has no concomitant medications. The patient confirmed that she did not have any other vaccines on the same day as the COVID vaccine. The patient previously received Letrozole for breast cancer and provided that she has not taken letrozole or any or medications, not even vitamins, for the last three years. On 18Jan2021 the patient experienced sore arm, which was not severe per the patient. On 21Jan2021 at around 03:00, the patient was nauseous and when the patient tried to get out of bed, the patient felt like the "whole world tilted on her". The patient reported the same thing continued a few times when she tried to get up, she just couldn't because everything turned upside down. So the patient went back to sleep, and she got up at 11:00AM, and she feels much better now, and now she is just having a little bit of remaining queasiness, like she can't go on a run right now, she is not 100%. The patient inquired if these are known side effects of the product. The patient also reported that she that she used to be 6'2 but she thinks she has shrunk a little from an unknown date. The patient stated that her PCP was not aware that she received the vaccine. The clinical outcome of the sore arm was recovered on 19Jan2021. The clinical outcome of the nauseous/she is still just a little queasy, tried to get out of bed, and the whole world tilted on her, and thinks she has shrunk a little was unknown.

Other Meds:

Current Illness:

ID: 1010771
Sex: M
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
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: Joints hurt and achy; wondering if his joints hurting and achy was an allergy; body ache (muscle pain); body ache (muscle pain); This is a spontaneous report from two contactable consumers (one was the patient). A 65-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247, Expiry Date: 31May2021), via an unspecified route of administration on 20Jan2021 09:45 to at a single dose on left arm for COVID-19 immunization. Medical history included cholesterol, glaucoma, COVID-19, blood thinner, pressure, allergies, Acid Reflux/Stomach. Concomitant medication included atorvastatin calcium for cholesterol, clopidogrel for Blood thinner, amlodipine besilate for Pressure, lisinopril, flunisolide for Allergies, latanoprost for Glaucoma, famotidine for Acid Reflux/Stomach, alprazolam (XANAX). The patient previously received flu vaccine for immunization three months ago in Oct2020. Patient received the first dose of the vaccine yesterday 20Jan2021 9:45AM and between 6:00-7:00PM he started experiencing body ache (muscle pain), he's still achy and he would like to know what should he take, if he can take Tylenol. He mentioned him and his wife got the COVID Vaccine yesterday 20Jan2021. However, he is calling today because his joints hurt and achy. He initially stated he noticed his joints hurt and achy last night on 20Jan2021 around 7PM or 8PM, later stated like 6PM or 7PM. He also mentioned he told the lady yesterday a few months ago he tested positive for COVID. He was told he probably came in contact with it for a brief moment. He stated they could tell he had it in his blood and the antibodies not the first set, but second set was working. He later added, he took a blood test for COVID and was positive. He confirmed this was all prior to getting the COVID Vaccine, it was a few months ago like 3-4 months ago. He mentioned he was really calling because he is wondering if his joints hurting and achy was an allergy. He mentioned he has gone through this before with this allergy. Stated he has gone through these symptoms before. He wants to know what he can take for it. He did not do anything. He did not have a fever or anything. Stated he did not even take his nasal spray because he was unsure if he could. No treatment received for the events. The outcome of the events was not recovered. The events were assessed as non-serious. Vaccination Facility was Hospital. The adverse events did not require a visit to Emergency Room or Physician Office. No Prior vaccinations within 4 weeks.

Other Meds: ATORVASTATIN CALCIUM; CLOPIDOGREL; AMLODIPINE BESYLATE; LISINOPRIL; FLUNISOLIDE; LATANOPROST; FAMOTIDINE; XANAX

Current Illness:

ID: 1010772
Sex: F
Age:
State: NC

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: pain in her hand unable to use it for a few days; This is a spontaneous report from a non-contactable nurse reporting for herself An adult female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# unknown), via an unspecified route of administration single dose on 04Jan2021 for covid-19 immunisation. Medical history was none. Concomitant medication included ibuprofen. The patient experienced pain in her hand unable to use it for a few days on Jan2021. Therapeutic measures included tylenol. SARS-Cov-2 test nasal swab in Jan2021 was negative. The outcome was recovered Information on the lot/batch number has been requested.; Sender's Comments: Based on the current available information, a possible contributory role of the suspect product BNT162B2 to the development of event Pain in hand cannot be excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds: IBUPROFEN

Current Illness:

ID: 1010773
Sex: M
Age:
State: CO

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/08/2021
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: His heart is racing and feels like it will jump out of his chest; His blood pressure is not consistent. It goes way up and comes way down.; This is a spontaneous report from a contactable consumer. A 72-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EK4176, expiration date unspecified), via an unspecified route of administration on 16Jan2021 at single dose (left arm) for COVID-19 immunization. Medical history included back surgery and patient used to weigh 218 but lost weight due to a back surgery. This was prior to getting the vaccine. There were no concomitant medications. On 16Jan2021, the patient experienced his heart was racing and felt like it will jump out of his chest and his blood pressure was not consistent and it goes way up and comes way down. He was told by the individual who gave him the vaccine to call and report this. There was no treatment received. Patient was scheduled for the second dose on 06Feb2021. Outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 1010774
Sex: M
Age:
State: LA

Vax Date: 01/12/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
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: Covid Positive; Covid Positive; This is a spontaneous report from a contactable consumer (wife). A 72-year-old male patient received bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot Number EL1283 and Expiration Date unknown) via Intramuscular on 12Jan2021 16:30 (vaccine location: right arm ) at single dose for COVID-19 immunisation. The patient's medical history included Kidney stones and heart issues (sees a cardiologist). The concomitant medications was reported as unspecified drugs. No previous vaccine in four weeks. Patient went to urgent care this morning and had a rapid test that came back positive and had covid. Lab test included positive rapid covid test on 21Jan2021. The outcome of event was unknown.

Other Meds:

Current Illness:

ID: 1010775
Sex: F
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: Start of an ear infection; Stuffy nose; Sore throat; Headache; Muscle and joint pain; Muscle and joint pain; Chills; Dry mouth; White coating all over tongue; Nausea; Unbelievable thirst; Slight swelling at injection site; Injection site pain; Tiredness; swollen tonsils; This is a spontaneous report from a contactable consumer, the patient. A 74-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number: EL1283), via an unspecified route of administration in the right arm on 13Jan2021 (at the age of 74-years-old) as a single dose for COVID-19 immunisation. Medical history included Transverse Myelitis ongoing from 2016, neurologic lime disease ongoing from 1992 due to which the patient gets migraines (from 1992), H. Pylori in May2019 and the patient is hard of hearing, ongoing from an unknown date. The patient's concomitant medications included unspecified migraine medication. On 13Jan2021 the patient experienced injection site pain, slight swelling at injection site, tiredness, and unbelievable thirst. On 14Jan2021 the patient experienced headache, muscle and joint pain, chills (which come and go), nausea (which is off and on), dry mouth, and white coating all over tongue. On 15Jan2021 the patient experienced stuffy nose and sore throat. The patient stated she still has tonsils on her right side where she has the earache and they are swollen (from an unknown date in Jan2021). On 17Jan2021 the patient experienced start of an ear infection (earache on the right side). The patient has had no fever and no redness. The patient stated she knows injection site pain is standard for a lot of people. The patient stated on Monday, 18Jan2021 she saw her provider and went over some of this. She stated she would not think that 4 days later she would still be feeling the side effects. The patient was inquiring if this only occurs with the first dose or will it also occur with the second? She is scheduled for the second one on 05Feb2021. The patient asked what was the time frame between injections? The patient was treated for the ear infection Neomycin/Polymyxin Sulfate ear drops and for the tiredness she has been walking around and trying light exercises. The patient turned down other medication as she did not want it to have any effect with the vaccine. The patient asked if there were any recommendations for the nausea and headaches. She stated she does have her migraine medication which she is trying to use to deal with the headaches. The clinical outcome of the injection site pain and slight swelling at injection site was recovered on 14Jan2021 and the white coating all over tongue recovered on 18Jan2021. The clinical outcome of the tiredness and start of an ear infection was recovering. The clinical outcome of the headache, muscle and joint pain, chills, nausea, stuffy nose, sore throat, thirst, and dry mouth was not recovered. The clinical outcome of the swollen tonsils was unknown.

Other Meds:

Current Illness: Hard of hearing; Lyme disease (Verbatim: Neurologic lime disease); Myelitis transverse (Verbatim: Transverse Myelitis)

ID: 1010776
Sex: F
Age:
State: PA

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 02/08/2021
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: He tested positive for COVID on 13Jan2021. Since then, my 3 children have also tested positive for COVID. We did not isolate anyone once they were sick.; chills; body aches; This is a spontaneous report from a contactable consumer reporting for herself A 41-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) on 11Jan2021 at single dose via an unspecified route of administration for COVID-19 immunization. The patient received first dose of BNT162B2 on 23Dec2020. Additional medical history or concomitant medications were not reported. On 11Jan2021 the patient experienced chills and body aches. Patient also informed that her husband started with symptoms of COVID on Sunday 10Jan2021. He tested positive for COVID on 13Jan2021. Since then, my 3 children have also tested positive for COVID. We did not isolate anyone once they were sick. (We realized this was a gamble). Patient informed that she was only person in the house who has not developed symptoms. She underwent SARS-CoV-2 test on 16Jan2021 which was negative. The patient recovered from chills and body aches on 13Jan2021. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010777
Sex: F
Age:
State: SC

Vax Date: 01/15/2021
Onset Date: 01/18/2021
Rec V Date: 02/08/2021
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: feels like a muscle pull; Breathing was a little compromised; Oxygen saturation was down; Pain on left side to left breast; This is a spontaneous report from a contactable consumer. A 71-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EK5730, expiry date: Mar2021), via an unspecified route of administration on 15Jan2021 10:47 at SINGLE DOSE reported in left shoulder for covid-19 immunisation. Medical history included asthma from 1971 and ongoing Diagnosed 50 years ago, Allergies from 1971 Diagnosed 50 years ago, Sarcoids from 2008 Sarcoids, Biopsy in 2008 and that is when she was diagnosed, ongoing sinus problems, pneumonia, compromised immune status, respiratory illness, genetic /chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity. There were no concomitant medications. On 18Jan2021 07:00, on Monday, she had pain from her left side to left breast, it was a sharp pain. Monday and Tuesday, she had to sleep sitting up. Her breathing was a little compromised so she went on the breathing machine at 09:30. Her oxygen saturation went down a little. Oxygen saturation was down 09:30. Her oxygen saturation was probably at 91-92%. She thought it was Pneumonia, so they did a chest x -ray and her lungs were clear. She got it through hospital because she has higher risk. She feels like now it is better. Sometimes with deep breaths, it feels like a muscle pull on an unspecified date. She does have asthma and allergies and went on the breathing machine and she knew her oxygen levels were down. She has an oximeter that she uses to check it at home. She did not know the name of the medication she uses on the breathing machine. Today, she did not take a breathing treatment but her oximeter registered between 94-93. Usually she is at 95. She is at 94 right now. She did not have any pain at the injection site. She is unable to confirm if the injection was given intramuscularly. The breathing machine was the only medication she took. Relevant test: Chest X ray to rule out pneumonia on 20Jan2021 and it was negative. The outcome of the events Pain on left side to left breast and Breathing was a little compromised was recovering, not recovered for the event Oxygen saturation was down, while unknown for the event "feels like a muscle pull".

Other Meds:

Current Illness: Asthma (Diagnosed 50 years ago.); Sinus disorder (sinus problems)

ID: 1010778
Sex: F
Age:
State: OH

Vax Date: 01/21/2021
Onset Date: 01/25/2021
Rec V Date: 02/08/2021
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: left side of her head is hurting/the whole left side of her head hurts from her temple to her chin; in pain; migraine; This is a spontaneous report from Pfizer Sponsored program,received by a contactable consumer (patient's daughter). A 91-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route, on 21Jan2021 at a single dose for COVID-19 immunisation. Relevant medical history included some dementia. (ongoing). No relevant concomitant medications were provided. She said her mother had no side effects at the time she received the COVID-19 Vaccine. She said her mother's arm didn't even hurt. She said her mother (who lives with her) woke up this morning (25Jan2021) around 4:30AM to go to bathroom, and then went back to bed. Caller stated she, herself, had left her house around 7:00AM this morning to go shopping, and when she got back from shopping 25 minutes later, her husband said her mother was in pain, left side of her head is hurting and he gave her mother a couple of paracetamol (TYLENOL). She said her mother told her the whole left side of her head hurts from her temple to her chin. Her mother was talking fine, and her mother was able to lift both her arms up, so she didn't think her mother had a stroke. She said for the past 20 minutes her mother has been laying back down and seemed to be doing better. The reporter stated that her mother could be having a migraine. She asked if anyone has previously reported to Pfizer developing a headache 4 days after receiving the COVID-19 Vaccine. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness: Dementia

ID: 1010779
Sex: F
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: Sore arm; This is a spontaneous report from a contactable consumer (patient's mother). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's mother reported that her daughter received the vaccine and experienced a sore arm. The clinical outcome of the event was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1010780
Sex: F
Age:
State: TX

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/08/2021
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: Nausea; Elevated Heart Rate (24+Hours After); Tingling; Numbness of the arm (24+ Hours); Pain in the armpit (started approx 36 hours after the injection; Fever; Pain in hips and entire back; Pain in hips and entire back; Headache; This is a spontaneous report from a non-contactable consumer (patient). A 30-year-old female patient received second dose of bnt162b2 (Brand: Pfizer, Lot number: EJ1686), via an unspecified route of administration in left arm on 19Jan2021 15:45 at single dose for covid-19 immunization. The patient had no medical history. The patient's concomitant medications were not reported. The patient previous received first dose of bnt162b2 (Brand: Pfizer, Lot number: EK9231), via an unspecified route of administration in left arm on 29Dec2020 07:00 AM for covid-19 immunization. The patient experienced nausea, elevated heart rate (24+hours after), tingling, numbness of the arm (24+ hours), pain in the armpit (started approx 36 hours after the injection), fever, pain in hips and entire back, headache (24+ hours) all on 19Jan2021 19:30. The patient underwent lab tests and procedures which included heart rate: elevated on 19Jan2021. The outcome of events was not resolved. The adverse event was not resulted in a visit to doctor or other healthcare professional office/clinic or Emergency room/department or urgent care. No treatment received. No other vaccine in four weeks. Other medications in two weeks: Birth control. No COVID prior vaccination. No COVID tested post vaccination. Not known allergies. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1010781
Sex: M
Age:
State:

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: arm soreness - i know surprise, surprise. felt it after 4-6h mark, felt it overnight, minimal discomfort this morning; headache - mild and dull but it made me spend the evening on the couch watching tv; fatigue - definitely felt this, spent the evening watching tv and went to bed early; This is a spontaneous report from a non-contactable consumer. An adult male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) solution for injection in Jan2021 (at an unknown age) as a single dose for COVID-19 vaccination. Medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (Pfizer) in Dec2020 for COVID-19 vaccination, in left arm, dose number=1 with no reported adverse event(s). The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Prior to the vaccination, it was unknown if the patient was diagnosed with COVID-19. The patient stated, "arm soreness - I know surprise, surprise. Felt it after 4-6h mark, felt it overnight, minimal discomfort this morning (TYLENOL did the trick), headache - mild and dull but it made me spend the evening on the couch watching TV, fatigue - definitely felt this, spent the evening watching TV and went to bed early" in Jan2021. Treatment provided for the event arm soreness included acetaminophen (TYLENOL). The outcome of the events arm soreness, headache and fatigue was recovered in Jan2021. Since the vaccination, it was unknown if the patient has been tested for COVID-19. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1010782
Sex: M
Age:
State: TX

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
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: Pain where I had the vaccine; This is a spontaneous report received from a contactable consumer (patient). A 76-year-old (also reported as 72-year-old, pending clarification) male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982), via an unspecified route of administration in the left arm, on 20Jan2021 09:00, at single dose, for COVID-19 immunization, at a public health department. Medical history included diabetes, blood cholesterol abnormal (reported as cholesterol) and blood pressure high (reported as high pressure, pending clarification). The patient had no known allergies. Concomitant medication included amlodipine, atorvastatin, cyclobenzaprine, and losartan potassium (COZAAR). The patient did not have other vaccines in four weeks. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. The patient reported he had "pain where I had the vaccine" on 20Jan2021 at 14:00. No treatment was given for the events. The outcome of the event was not recovered.

Other Meds: AMLODIPINE; ATORVASTATIN; CYCLOBENZAPRINE; COZAAR

Current Illness:

ID: 1010783
Sex: F
Age:
State: CA

Vax Date: 01/17/2021
Onset Date: 01/17/2021
Rec V Date: 02/08/2021
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: First dose administered on 17Jan2021/Secodn dose administered on 23Dec2020; Headache, hypertension, tachycardia; hypertension; tachycardia; This is a spontaneous report from a contactable Pharmacist. A 35-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number EL3249), via intramuscular route on the left arm on 17Jan2021 as a single dose for COVID-19 immunization. The patient had no medical history. Concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Historical vaccine data included the firs dose of BNT162B2 (Lot Number EL0140; at the age of 35-years) via intramuscular route on the left arm on 23Dec2020 as a single dose. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Past drug history included known allergies to codeine and sulfamethoxazoletrimethoprim. On 17Jan2021, the patient experienced headache, hypertension, tachycardia. The patient was seen at the Emergency Department/ Department of urgent care. The patient was treated for the events headache, hypertension, tachycardia with acetaminophen and lorazepam. The patient was not tested for Covid-19 post vaccination. The clinical outcome of the events headache, hypertension, tachycardia was not recovered. The outcome of event, Inappropriate schedule of vaccine administered, was unknown.

Other Meds:

Current Illness:

ID: 1010784
Sex: F
Age:
State:

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
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: injection site soreness; low grade fever; whole body muscle soreness; fatigue; headache; malaise; This is a spontaneous report from a non-contactable healthcare professional. A 42-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), Lot# EK9231, via an unspecified route of administration on 19Jan2021 10:00 at a single dose in left arm (Dose 1) for COVID-19 immunization. The patient was not pregnant. The patient did not receive any other vaccine in the 4 weeks prior to COVID vaccination. Medical history included irritable bowel syndrome, herniated disc issues, and migraine. There were no known allergies. The patient was not diagnosed with COVID prior to vaccination. Concomitant medication included tramadol, colecalciferol (VITAMIN D), vitamin C, magnesium, and probiotics. On 20Jan2021 at 14:00 , the patient experienced injection site soreness, low grade fever, whole body muscle soreness, fatigue, headache, and malaise. There was no treatment received for the events. The outcome of the events injection site soreness, low grade fever, whole body muscle soreness, fatigue, headache, and malaise was recovering. The patient was not COVID tested post-vaccination. No follow up attempts are possible. No further information is expected.

Other Meds: TRAMADOL; VITAMIN D [COLECALCIFEROL]; VITAMIN C [ASCORBIC ACID]; MAGNESIUM; PROBIOTICS

Current Illness:

ID: 1010785
Sex: F
Age:
State:

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/08/2021
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: Headaches; Rigors; Extreme fatigue; left arm pain radiating up to neck and skull; left arm pain radiating up to neck and skull; chest and back pain /stabbing pain in my left chest; chest and back pain; Nausea; heart palpitations; feeling of impending doom; This is a spontaneous report from a non-contactable nurse, the patient. A 41-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration in the left arm on 18Jan2021 07:30 (at the age of 41-years) to as a single dose for Covid-19 immunization. The patient's medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Historical vaccine data included that the patient received the first dose of BNT162B2 on 28Dec2020 at 07:15 (at the age of 41-years) in the left arm for Covid-19 immunization. There were no concomitant medications. On 18Jan2021 22:30, 15 hours after second injection the patient experienced symptoms which would best be described as a cardiac event. The patient elaborated that she woke from sleep with left arm pain radiating up to neck and skull, chest and back pain, nausea and stabbing pain in my left chest. This was associated with heart palpitations and a feeling of impending doom. The episode lasted 15 minutes and happened 4 times throughout the night. On 19Jan2021 at 07:30, 24 hours after injections the patient experienced headaches and rigors began with extreme fatigue. Unable to function type of fatigue. Fatigue persisted for 48 hours post injection. The patient was now 72 hours post injection and continued with headache and nausea. The patient did not receive any treatment for the events. The patient had not been tested post vaccination. The clinical outcome of event extreme fatigue, chest and back pain, heart palpitations feeling of impending doom, left arm pain radiating up to neck and skull and rigors was recovering. The outcome of events headaches and nausea was not recovered. No follow-up attempts are possible; information about lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1010786
Sex: F
Age:
State:

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
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: muscle aches; nausea; fever, Tmax 101.7; neck ache; soreness at sight of injection; This is a spontaneous report from a non-contactable nurse. A 30-year-old female patient (not pregnant) received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL 3247), intramuscularly on 21Jan2021 at 09:15 AM in the Left arm at single dose for COVID-19 immunization in hospital. Medical history included hasimoto's, known allergies with peanuts. Prior to vaccination, patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0140), intramuscularly on 30Dec2020 at 08:15 AM in the Left arm at single dose for COVID-19 immunization at the age of 30-year-old. The patient experienced fever, Tmax 101.7, muscle aches, neck ache, soreness at sight of injection, nausea on 21Jan2021 at 23:30. Since the vaccination, patient had not been tested for COVID-19. Therapeutic measures were taken as result of the events included mefenamic acid (ADVIL). The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1010787
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: arm was very sore; This is a spontaneous report from a contactable consumer (patient's neighbor) reporting for a patient. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unknown date, as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On an unknown date the patient experienced their arm was very sore. It was reported the arm was sore, but after a couple of days, it was annoying, but it went away. The clinical outcome of the arm was very sore was recovered. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1010788
Sex: F
Age:
State: NC

Vax Date: 01/07/2021
Onset Date:
Rec V Date: 02/08/2021
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: she couldn't sit down on the commode, she was shaking/knees and legs are shaking; she couldn't sit down on the commode, she was shaking/knees and legs are shaking; This is a spontaneous report from a contactable consumer (patient's husband). A female patient of an unspecified received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), unspecified route of administration on 07Jan2021 as a single dose for COVID-19 vaccination. Medical history included walking aid user from an unknown date and unknown if ongoing, wheelchair user from an unknown date and unknown if ongoing, back surgery from an unknown date and unknown if ongoing, arthritis from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The consumer reported his wife got up this morning and went to the bathroom. His wife uses walkers and wheelchairs, but she couldn't sit down on the commode, she was shaking, and she said that she can't get up since an unspecified date. His wife can't get up now, her knees and legs are shaking, he doesn't know if this is from the vaccination or not. The clinical outcome of he couldn't sit down on the commode, she was shaking/knees and legs are shaking was unknown Information on Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 1010789
Sex: M
Age:
State: FL

Vax Date:
Onset Date: 01/12/2021
Rec V Date: 02/08/2021
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: Muscle aches; fever; chills; bones hurting; pressure on head; This is a spontaneous report from a contactable consumer. A 31-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) solution for injection (at the age of 31-years-old) as a single dose for COVID-19 vaccination. Medical history and concomitant medications were not reported. It was unknown if the patient had any known allergies. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. On 12Jan2021, the patient experienced muscle aches, fever, chills, bones hurting and pressure on head. It was unknown if treatment was provided for the events muscle aches, fever, chills, bones hurting and pressure on head. The outcome of the events muscle aches, fever, chills, bones hurting and pressure on head was recovered in Jan2021. Since the vaccination, it was unknown if the patient had been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1010790
Sex: M
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
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: bloody nose; spit from his mouth and there was blood; This is a spontaneous report from a contactable consumer (wife). A 67-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EL8982), via an injection in the left arm on 20Jan2021 at 14:00 (at the age of 67-years-old) as a single dose for Covid-19 immunization. Medical history included diabetic from 2009 and unknown if ongoing. The patient had not had any other recent vaccinations or new medications. Concomitant medications included clopidogrel bisulfate (PLAVIX) from an unknown date (taken for about 10 years) at 75mg daily for blood thinner. On 21Jan2021, the patient experienced bloody nose and he spit from his mouth and there was blood. Reporter stated that the blood was coming from his nose and dripping out. No treatment was given for the events. The clinical outcome of the epistaxis was not recovered; for mouth hemorrhage was unknown.

Other Meds: PLAVIX

Current Illness:

ID: 1010791
Sex: M
Age:
State: TN

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: sore arm; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received the first dose of bnt162b2 (BNT162B2) vaccine , via an unspecified route of administration on an unspecified date at single dose for Covid-19 immunisation . The patient medical history and concomitant medications were not reported. The patient experienced sore arm on an unspecified date with outcome of unknown. The reported event was considered non serious. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010792
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: Reaction was her arm was itchy and inflamed and red on the inside of her elbow on the arm where she received the shot; Reaction was her arm was itchy and inflamed and red on the inside of her elbow on the arm where she received the shot; Reaction was her arm was itchy and inflamed and red on the inside of her elbow on the arm where she received the shot; Pimple-like rash; Anxiety; Felt a little odd; This is a spontaneous report from a contactable nurse (patient). A 32-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3302; Expiration date was not reported) on 20Jan2021 at a single dose on the left arm, with route of administration unspecified, for COVID-19 immunization. Medical history included asthma from 1993 to an unspecified date (diagnosed when she was 5). Concomitant medication included tetanus vaccine (Lot number: U6830A; Expiration date: 17Sep2022) on 06Jan2021. On 20Jan2021 (15:00), the patient had reaction on her arm that was itchy, inflamed and red on the inside of her elbow on the arm where she received the vaccination shot. In Jan2021, the patient had pimple-like rash; anxiety; and had felt a little odd. The patient had received diphenhydramine (BENADRYL) as treatment for the events, 'reaction on her arm that was itchy, inflamed and red on the inside of her elbow on the arm where she received the vaccination shot' and 'pimple-like rash'. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1010793
Sex: M
Age:
State: NC

Vax Date: 01/19/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: husband is breaking out in cold chills, and his bones are still sore.; inflamed liver; arm is still sore; Nauseated; has no energy; sick; no appetite; he is sweating; he is tired.; husband is breaking out in cold chills, and his bones are still sore.; This is a spontaneous report from a contactable consumer. This consumer reported for a 72-year-old male patient (husband) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL3247), via an unspecified route of administration on 19Jan2021 08:00 at single dose on left arm for COVID-19 prevention. The medical history and concomitant medications were not reported. The patient got the shot on 19Jan2021. Since Jan2021, his arm was still sore, but he had been nauseated since then. He has no energy. He has had it almost four days. He was fine until he got it and his arm is sore and he is nauseated. He is usually on the go. The patient also has an inflamed liver. He has been sick since. The patient has no appetite, he is sweating, his bones are hurting, and he is tired. The consumer took her husband to his doctor, and they tested him for COVID, and it came back negative, but the consumer does not think the PA did the test right. The consumer doesn't know what to do with him, because he is still tired, and has no appetite. The patient is breaking out in cold chills, and his bones are still sore. When the patient got the vaccine, he was walking and talking, and by 11 AM that day, he was in bed. The patient had some labs done, and was being told that his liver is big, so the consumer did not know if the vaccine went to his liver. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1010794
Sex: F
Age:
State: NJ

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
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: blood pressure went up considerably; Heart racing; suddenly felt very warm; This is a spontaneous report from a contactable consumer. A 67-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscular on 21Jan2021 at 14:45 (at the age of 67-years-old) as a single dose for Covid-19 immunization. Medical history included a history of asthma. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination or additional vaccines on the same day. On 21Jan2021 around a half hour after administration (also reported as within 40 minutes) the patient started having symptoms of suddenly felt very warm, her blood pressure went up considerably and her heart was racing. The patient went to Urgent Care and Urgent Care advised to take her to the Emergency Room as they did not have an EpiPen. The patient was advised to go to the Emergency Room and was in transit to the ER. The clinical outcome of the events blood pressure increased and palpitations was not recovered; for feeling hot it was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1010795
Sex: M
Age:
State: FL

Vax Date: 01/09/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: felt a little tender where the shot was; This is a spontaneous report from a contactable consumer (patient's wife). This consumer reported for two patients (herself and her husband). This is the second of two reports. A 92-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on 09Jan2021 at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient has not had any reaction at all, maybe felt a little tender where the shot was, also reported as felt nothing except maybe a little soreness on the arm in Jan2021. The outcome of event is unknown. Information about lot/batch has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021057886 same reporter, suspect product, and event, different patient

Other Meds:

Current Illness:

ID: 1010796
Sex: U
Age:
State: MN

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: Got the first dose of the COVID Vaccine, and then tested positive for the virus; Got the first dose of the COVID Vaccine, and then tested positive for the virus/developed covid after the first dose; This is a spontaneous report from a Pfizer-sponsored program, Pfizer First Connect. A contactable pharmacist reported that a patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Pharmacist on the line calling about a patient who got the first dose of the COVID Vaccine, and then tested positive for the virus, also reported as the patient received the first dose of vaccine and then developed covid after the first dose. She was asking if it was okay for the patient to get the second dose. The outcome of the event was unknown. Information on the Lot/batch number has been requested.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors; however, a contributory role of the suspect product BNT162B2 to the reported drug ineffective and COVID-19 cannot be ruled out.

Other Meds:

Current Illness:

ID: 1010797
Sex: M
Age:
State: CT

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: felt lightheaded; a little bit of muscle pain and joint pain/ left bicep after got home had a pain in it; a little bit of muscle pain and joint pain; Took his blood pressure and it was really high like 150 something; bump at the injection; bump at the injection, it hurt if he pushed on it or bumped it; His joints felt weird. It was on the right and left which is unusual; Right forearm has slight pain in it; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer (patient). This 70-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231) in the right arm on 18Jan2021 at single dose for COVID-19 immunization. Medical history included bad arthritis in right wrist. There were no concomitant medications. When shot, patient felt lightheaded and a little bit of muscle pain and joint pain. He told the nurse there and they sent over a Physician Assistant. He took his blood pressure and it was really high like 150 something. Patient was cleared after 30 minutes. Since being home he has noticed a couple of things. Mostly muscle pain or discomfort. He had a bump at the injection, it hurt if he pushed on it or bumped it. Four days later and there is no bump or pain there. The other thing is his joints. His joints felt weird. It was on the right and left which is unusual. His left bicep after he got home had a pain in it. The right forearm has slight pain in it. He is not sure if it is the muscle or ligament. If he rubs it doesn't bother him at all. The outcome of "blood pressure 150", "bump and pain at the injection" was recovered, of other events was unknown.

Other Meds:

Current Illness:

ID: 1010798
Sex: F
Age:
State: OH

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
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: This is a spontaneous report from a contactable consumer. A 22-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL9261) at right arm, via an unspecified route of administration on 21Jan2021 at single dose for covid-19 immunisation. Medical history was none. Historical Vaccine included unspecified flu vaccine taken in Oct2020 for immunisation. The patient experienced bleeding after shot and bruise on 21Jan2021. The patient said she got her first dose last night and after the pharmacist finished and pulled the needle out there was quite a lot of blood after she pulled the needle out, and there was a bruise there. She didn't know if a blood vessel got nicked when all that happened. She would like to know if the dose was efficacious or if it is possible some of the vaccine came out with the blood. The patient said that the bleeding from the injection stopped probably within just a minute after she gave it or less, and there was no treatment given. The outcome of event bleeding after shot was recovered; of event bruise was unknown.

Other Meds:

Current Illness:

ID: 1010799
Sex: F
Age:
State: CA

Vax Date: 12/18/2020
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
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: tested positive for COVID/stuffy nose/couldn't smell; tested positive for COVID/stuffy nose/couldn't smell; This is a spontaneous report from a Pfizer-sponsored program . A contactable consumer (patient) reported that a 44-year-old female patient received first dose BNT162B2 (Pfizer BioNTech Covid 19 vaccine, Lot Number: ER5730 or EK5730), via an unspecified route of administration at Arm right on 18Dec2020 17:00 at the 44 years old at single dose for COVID-19 immunization. The medical history was none. The Family Medical History Relevant to adverse events was none. The concomitant medication was none. The patient was supposed to work the day she tested positive but had a stuffy nose on 01Jan2021. She wasn't sure if that was what it was but when she took a shower she couldn't smell the body wash and so she knew she had COVID. She had a rapid test used for the positive test for COVID on 01Jan2021. There was no hospitalization due to testing positive. The events did not require a visit to Emergency Room and Physician Office, but she did go to the urgent care to get the rapid test.There was no Prior Vaccinations (within 4 weeks). There was none additional Vaccines Administered on Same Date of the product. The patient underwent lab tests and procedures, which included tested positive for COVID on 01Jan2021. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1010800
Sex: M
Age:
State: MA

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: weeping; This is a spontaneous report from a contactable Other Health Professional. A male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose for covid-19 immunisation. Medical history, concomitant medications or past drug history were not provided. He was weeping. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010801
Sex: U
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 02/08/2021
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: tired for a couple days; This is a spontaneous report from a contactable consumer reporting for the patient. A patient of an unspecified age and gender received 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 and concomitant medications were not reported. The patient was tired for a couple days after the vaccine administration. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010802
Sex: F
Age:
State: LA

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/08/2021
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: felt flushed; This is a spontaneous report from a contactable Nurse. A 29-year-old female patient received the first dose of of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3247 with Expiration Date 31May2021), on 18Jan2021 (at 08:30) at 0.3 ml single dose on the left deltoid for COVID-19 immunisation. No relevant medical history was provided. The patient did not have relevant concomitant medications. She was vaccinated at COVID vaccine center where they are administering the Pfizer vaccine. On 18Jan2021 (at 09:05), she felt flushed. She took cetirizine hydrochloride (ZIRTEC) at home in preparation; she was given juice and cookies. At 9:20, patient was feeling better, she was monitored for 30 more minutes in observation area and stated she was feeling fine and left. The patient had recovered from the events on 18Jan2021.

Other Meds:

Current Illness:

ID: 1010803
Sex: F
Age:
State: NY

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/08/2021
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: immune system to weaken; herpes reaction; Urinary tract infection; history included multiple sclerosis and immune system weakened; history included multiple sclerosis and immune system weakened; This is a spontaneous report from a contactable consumer reported for self. This female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number not known) via an unspecified route of administration on 18Jan2021 at single dose in arm for COVID-19 immunization; and unspecified steroids via an unspecified route of administration from an unspecified date at unspecified dosage for unspecified indication. The patient medical history included multiple sclerosis and immune system weakened. The patient concomitant medications were not provided. The patient reported that she had multiple sclerosis, every time she went on steroids, her immune system was weakened, which is reported "unrelated". The patient received vaccination on 18Jan2021. When she was on steroids about 2-3 days later, she got a herpes reaction and urinary tract infection afterwards from 20Jan2021. The doctor told her it was because her immune system is weakened because of steroids. The patient was wondering if it is a normal reaction for her immune system to weaken due to the vaccine, if it is safe for her to get the second vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm