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: 1087061
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: Muscular pain; This is a spontaneous report from a Sponsored Program from a contactable consumer reported for her relative. A female patient of unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unknown date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient got the first dose and after 4 hours took Percocet due to muscular pain. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087062
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: high blood pressure; This is a spontaneous report from a Pfizer-sponsored program . A contactable consumer (patient) reported that a female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown) 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 taking the high blood pressure medication every morning ever since she took the vaccine. She was asking if it was possible to take her high blood pressure medication (hydrochlorothiazide) before she would take the second dose. The outcome of the event was unknown. Information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087063
Sex: F
Age:
State: NY

Vax Date: 02/06/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: Suffering from a migraine; Slight headache; This is a spontaneous report from a sponsored program. A contactable consumer (patient) reported that a female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 06Feb2021 at a single dose, with route of administration unspecified, for COVID-19 immunization. The patient's medical history was not reported. Concomitant medication included acetylsalicylic acid, caffeine, paracetamol (EXCEDRIN). In Feb2021, the patient was suffering from a migraine; and had a slight headache. The outcome of the events, 'migraine' and 'slight headache', was unknown. Information on lot/batch number has been requested.

Other Meds: EXCEDRIN [ACETYLSALICYLIC ACID;CAFFEINE;PARACETAMOL]

Current Illness:

ID: 1087064
Sex: F
Age:
State: FL

Vax Date: 01/27/2021
Onset Date: 02/05/2021
Rec V Date: 03/10/2021
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: I had such pain all night and I still have it. It is all around my neck and up to the top of the ears and then my right shoulder down the front and to the back and all the way down to my fingertips; I had such pain all night and I still have it. It is all around my neck and up to the top of the ears and then my right shoulder down the front and to the back and all the way down to my fingertips; I had such pain all night and I still have it. It is all around my neck and up to the top of the ears and then my right shoulder down the front and to the back and all the way down to my fingertips; I had such pain all night and I still have it. It is all around my neck and up to the top of the ears and then my right shoulder down the front and to the back and all the way down to my fingertips; torn rotator cuff; I have a slight headache in the back of my head too; This is a spontaneous report from a contactable consumer (patient). A 91-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number EL9262), via an unspecified route of administration on 27Jan2021 at single dose for COVID-19 immunization. Medical history included High blood pressure. Concomitant medication included olmesartan medoxomil for high blood pressure and pravastatin sodium. The patient stated she was 91 years old and that was why she got the first shot of the Covid19 vaccine Pfizer about 10 days ago (27Jan2021). Last night (05Feb2021) she had such pain all night and she still had it. It was all around her neck and up to the top of the ears and then her right shoulder down the front and to the back, she had a torn rotator cuff there and all the way down to her fingertips she had pain. Event onset last night, during the night. Like 9 days well, coming into the 10th day. She did not know why she have it. It was fine until last night and now it was terrible. She had a slight headache in the back of her head too on an unspecified date in 2021. She had been taking Tylenol and put some Icy Hot, you rub it on when you have pain but it did not do anything. She wanted to know will she get the same type of reaction when she get the second shot. There was no expiration date on it. There was nothing else. The outcome of the event slight headache in the back of head was unknown and the outcome of the other events was not recovered.

Other Meds: OLMESARTAN MEDOXOMIL; PRAVASTATIN SODIUM

Current Illness:

ID: 1087065
Sex: F
Age:
State: OH

Vax Date: 01/29/2021
Onset Date:
Rec V Date: 03/10/2021
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: Starting about middle of my chest up to my neck it started to get little bit bubbles on it and now it's just burning like crazy and it's starting around my ankles; It's like my chest is burned; This is a spontaneous report from a contactable consumer (patient). A 79-year-old Female patient (also the age at vaccination) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9261), via an unspecified route of administration on 29Jan2021 at SINGLE DOSE for COVID-19 immunization. Medical history included Atrial fibrillation (AFib) and back surgery (reported as: I am recovering from very serious back surgery) both from an unknown date and unknown if ongoing. Concomitant medication included methotrexate (reported as , it's a little cancer pill (Further clarification was unknown if consumer have cancer, hence cancer was not captured in medical condition), once a week), tocilizumab (ACTEMRA) (reported as I am on IV Infusions every 4 weeks and the name of it is Actemra), apixaban (ELIQUIS) (reported as I am on Eliquis because I am AFib, heart), and then another heart medicine plus all the patient's 'vitamins' (unspecified). The patient previously took oxycodone and experienced allergy (reported as I can't take any of those drugs, I am allergic to all that stuff. Yeah I can't take any of that pain medicine (Unspecified Medications)). The patient stated that: "I was calling about the, I had my first shot for the virus and on my chest, starting about middle of my chest up to my neck it started to get little bit bubbles on it and now it's just burning like crazy and it's starting around my ankles. Does that have anything to do with that shot?" The reporter confirmed that the next shot is due on 22Feb2021. The patient added that, "Actually last week they were really light, and they just keep getting worst. I was actually going to call my doctor tomorrow because I was concerned about getting this injection anyways because of my history on having reactions to medicine. I can't take any like Oxycodone or like any of those (also reported as "I can't take any of those drugs, I am allergic to all that stuff. Yeah I can't take any of that pain medicine (Unspecified Medications). No, I don't have anything like that."). I can't take any of those drugs (Unspecified Medications). And she said she thought it would be alright but I am recovering from very serious back surgery and so I have had a hard time with that. So, I thought I should call and see if I should get my second injection or if I should just let it go." It was also reported that: "Yes, it's like my chest is burned." Consumer stated for the treatment, "The only thing I put on was Benadryl cream. To keep it from 'itching'." The patient asked "Should I get the second injection?" The outcome of the events was unknown.

Other Meds: METHOTREXATE; ACTEMRA; ELIQUIS

Current Illness:

ID: 1087066
Sex: M
Age:
State:

Vax Date: 02/06/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: some arm irritation/ pain; some arm irritation/ pain; felt dazed; This is a spontaneous report from a non-contactable consumer (patient) . A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on 06Feb2021 at SINGLE DOSE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient received the vaccine yesterday (06Feb2021) and that it went well - only had some arm irritation/ pain and felt dazed on an unspecified date in Feb2021. The outcome of all the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1087067
Sex: F
Age:
State: OK

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 03/10/2021
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: diagnosed positive for COVID/ tested positive for COVID virus; This is a spontaneous report received from two contactable consumers (patient and patient's husband) via the sponsored program medical Information Team. The consumers reported similar events for 2 patients. This is the 1st of 2 reports. A 66-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration on Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's first dose was a week before his (husband), so a week before 21Jan2021, she received her vaccine at work. She did not know the exact date of her first dose. She was diagnosed positive for COVID/ tested positive for COVID virus 2 days before he was diagnosed. She was diagnosed positive on either 21Jan2021 or 22Jan2021, she also did a test in which it gave her the test results the same day. She probably had the same type of test. Her antibody infusion was a couple days before him. The case was assessed as non-serious. The outcome of event was reported as unknown. Information on lot/batch number has been requested.; Sender's Comments: Linked Report(s): 2021144363 same reporter/drug/AE, different patient.

Other Meds:

Current Illness:

ID: 1087068
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: Feeling sick/doesn't feel very well; hives (on neck and shoulder); Feverish; Achy; cannot move; This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history included "coronavirus" and allergies. The patient's concomitant medications were not reported. On an unspecified date, the patient was feeling sick and developed hives (on neck and shoulder). She wanted to know if she needs to get the second dose since she is afraid to have the side effects again. Patient was feeling feverish and achy, cannot move and doesn't feel very well on an unspecified date. She stated that the place where she received the vaccine had several sites set up. She got the first at one site. She is scheduled for her second dose at another site, but she read or heard it should be done at the same site. She wanted to know if it is safe to have the second shot. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087069
Sex: M
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 03/10/2021
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: went for the rapid test/positive/have COVID; went for the rapid test positive/have COVID; No sense of taste or smell; No sense of taste or smell; Coughing; Fatigue extreme; This is a spontaneous report from a contactable consumer. This consumer reported similar events for two patients. This is the second of two reports, reporting for the husband. A male patient of an unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 20Jan2021 to 20Jan2021 at single dose for COVID-19 immunization. Medical history included ongoing chronic fatigue syndrome. The patient's concomitant medications were not reported. The patient exhibited a lot of symptoms. And he by the way he complicated things. He got his shot, his first Pfizer shot on 20Jan2021, and then on the 24Jan2021 he left to go to (Name). He came home on the end of the week, he came on Friday. He was coughing and exhibiting extreme fatigue in Jan2021, but he also suffered from chronic fatigue syndrome and other underline situations, so he attributed to that. So he went ahead and they cohabitated and on Sunday the consumer started to get these symptoms. This past Wednesday (03Feb2021) he came to consumer and said he had no sense of taste or smell, and they knew what that meant. So, he immediately went to get a COVID test, but he had to wait. And then in the interim the consumer's situation pretty much stayed rather static, it didn't much change. Then on Thursday (04Feb2021) he said he was going for a rapid test, and consumer said wanted to go too. So, they went ahead and they went to an urgent care and they went for the rapid test and they were both been positive. They both had COVID. The event outcome was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021145196 same reporter/product, different patient, similar event

Other Meds:

Current Illness: Chronic fatigue syndrome

ID: 1087070
Sex: F
Age:
State: AZ

Vax Date: 02/03/2021
Onset Date: 02/04/2021
Rec V Date: 03/10/2021
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: chills; fever; runny nose; This is a spontaneous report from a contactable consumer from the Pfizer-sponsored program. A female patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date unknown), via an unspecified route of administration on 03Feb2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the first dose last 03Feb2021, then the next day 04Feb2021, she experienced chills, fever and runny nose. They gave her decongestant because of the runny nose. The reporter was asking if it's the side effect of the first dose. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087071
Sex: F
Age:
State: NY

Vax Date: 02/01/2021
Onset Date: 02/03/2021
Rec V Date: 03/10/2021
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: she tested COVID-19 positive; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration on 01Feb2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that received her first vaccine shot on 01Feb2021 and she tested COVID-19 positive on 03Feb2021. Her second dose schedule is on 22Feb2021. The patient asked if she should still take the second dose. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087072
Sex: F
Age:
State: LA

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: sore throat; colds; This is a spontaneous report from a contactable consumer (patient) via Pfizer-sponsored program. A female patient of an unspecified age received second single dose BNT162B2 (Pfizer Covid-19 Vaccine, Solution for injection, batch/lot number and exp date not reported), via an unspecified route of administration on 01Feb2021 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took first single dose of BNT162B2 (Pfizer Covid-19 vaccine) on an unspecified date for COVID-19 immunization.The patient received 2nd dose on a Monday and tolerated the dose she received without adverse reaction. On an unspecified date in Feb2021 (last Friday) she had a sore throat and colds and was wondering if this was due to the weather. Patient wanted to know if she should be tested for Covid-19. The outcome of events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1087073
Sex: F
Age:
State: OK

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: red rash all over her body; This is spontaneous report from a contactable consumer, the patient, via the Pfizer Sponsored Program. 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. Medical history and concomitant medications were not reported. On an unspecified date, after the vaccination, the patient had a red rash all over her body. The clinical outcome of red rash all over her body was unknown.

Other Meds:

Current Illness:

ID: 1087074
Sex: F
Age:
State: NJ

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: Hives; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient had hives after taking the first dose of the covid-19 vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087075
Sex: F
Age:
State: UT

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: mild fever after the first dose; This is spontaneous report from a contactable consumer (the patient) from a Pfizer-sponsored program. A female patient of an unspecified age received the first and second doses of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), on unspecified dates (lot numbers not provided), both via an unspecified route of administration on unspecified dates (age at vaccination unknown) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated she had a mild fever after the first dose. After her second vaccine yesterday (unspecified date), she had a very low-grade fever 99. She asked would she need to worry about contagious to anybody or was it normal? The clinical outcome of fever was unknown. Information about lot number has been requested.

Other Meds:

Current Illness:

ID: 1087076
Sex: F
Age:
State: ID

Vax Date: 02/10/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: Slight sore right arm in shot location; This is a spontaneous report from a contactable consumer, the patient. A 79-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; EL9267), via an unspecified route of administration in the right arm on 10Feb2021 at 00:30 (at the age of 79-years-old) as a single dose for COVID-19 immunization. Medical history included allergy to latex and penicillin, Afib, asthma and diabetes (under control with diet). Concomitant medications were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. On an unspecified date in Feb2021, the patient experienced a slight sore right arm in the shot location. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of slight sore right arm in shot location was unknown.

Other Meds:

Current Illness:

ID: 1087077
Sex: M
Age:
State: CA

Vax Date: 02/05/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: pain on his lower back; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a male patient of unspecified age received first dose of BNT162B2, via an unspecified route of administration on 05Feb2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient took the 1st dose on 05Feb2021. After taking the 1st dose, he experienced pain on his lower back on Feb2021 and would like to know if he can take ibuprofen. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087078
Sex: U
Age:
State: OH

Vax Date: 01/17/2021
Onset Date:
Rec V Date: 03/10/2021
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: COVID-19 confirmed by positive COVID-19 test; COVID-19 confirmed by positive COVID-19 test; This is a spontaneous report received from a contactable pharmacist through a Pfizer-sponsored program. This pharmacist reported similar events for three patients. This is the first of the three reports. A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 17Jan2021 at a single dose, with route of administration unspecified, for COVID-19 immunization. The patient's medical history and patient's concomitant medications were not reported. On an unspecified date in 2021, the patient had COVID-19 confirmed by positive COVID-19 test, and was put on isolation. The outcome of the event, 'COVID-19 confirmed by positive COVID-19 test', was unknown. The reporting pharmacist was wondering the there was a need to hold off the second dose of vaccination. Information on the lot/batch number has been requested.; Sender's Comments: The contributory role of the suspect product to the reported drug ineffective cannot be excluded as the efficacy of a drug varies individually and may be affected by different factors including drug potency.,Linked Report(s) : US-PFIZER INC-2021148567 same reporter/product/events, different patient;US-PFIZER INC-2021148568 same reporter/product/events, different patient;US-PFIZER INC-2021148567 same drug and event, different patient;US-PFIZER INC-2021148568 same drug and event, different patient

Other Meds:

Current Illness:

ID: 1087079
Sex: F
Age:
State: GA

Vax Date: 01/21/2021
Onset Date:
Rec V Date: 03/10/2021
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: laryngitis; This is a spontaneous report received from a contactable consumer (patient) via a Pfizer-sponsored program. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration, on 21Jan2021, at single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. In 2021, the patient experienced laryngitis. She was prescribed with prednisone for it, but she has not taken it yet. She was wondering if it will change the efficacy of the vaccine. The outcome of the event was unknown. Information about the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087080
Sex: F
Age:
State:

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 03/10/2021
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: Still have arm pain on the injection site; This is a spontaneous report from a non-contactable consumer. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration in the arm on 20Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient got her first shot on 20Jan2021 and still had arm pain on the injection site on an unspecified date in 2021. 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: 1087081
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: nauseous; This is a spontaneous report from a non-contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number unknown), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced nauseous on an unspecified date. 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: 1087082
Sex: U
Age:
State: OH

Vax Date: 01/17/2021
Onset Date:
Rec V Date: 03/10/2021
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: COVID-19 confirmed by positive COVID-19 test; COVID-19 confirmed by positive COVID-19 test; This is a spontaneous report from a Pfizer-sponsored program, PFIZER FIRST CONNECT. A contactable pharmacist reported similar events for three patients. This is the third of the three reports. A patient of unspecified age and gender received the first single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 17Jan2021, for COVID-19 immunization. The patient's medical history and patient's concomitant medications were not reported. On an unspecified date in 2021, after the first vaccination, the patient had COVID-19 confirmed by positive COVID-19 test and was put on isolation. The outcome of the event was unknown. The reporting pharmacist was wondering if there was a need to hold off the second dose of vaccination or if it could be administered on 07Feb2021. 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 after the first vaccine dose.,Linked Report(s) : US-PFIZER INC-2021148508 same drug and event, different patient;US-PFIZER INC-2021148568 same drug and event, different patient

Other Meds:

Current Illness:

ID: 1087083
Sex: U
Age:
State: MA

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: Brachial plexopathy; This is a spontaneous report from a sponsored program from a contactable physician (patient). A patient of an unspecified age and gender received the first dose of BNT162B2 (Pfizer-Biontech Covid-19 Vaccine) at single dose, on an unspecified date, for COVID-19 immunisation. Relevant medical history and concomitant medications were unknown. On an unspecified date, the patient experienced brachial plexopathy. It was reported that the patient did not take the second dose. Clinical outcome of the adverse event was unknown at time of this report. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087084
Sex: F
Age:
State: TX

Vax Date: 01/12/2021
Onset Date:
Rec V Date: 03/10/2021
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: Flu like symptoms; Full body rash with itching; Full body rash with itching; localized arm pain with ancillary edema x 5 days; localized arm pain with ancillary edema x 5 days; This is a spontaneous report from a contactable nurse (patient). The nurse reported 2 reports for same patient, same product. This is the second report. A 39-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=EJ3246), intramuscular in the right arm on 12Jan2021 08:30 AM at single dose for covid-19 immunisation. Known allergies included Tramadol and Lexapro. No other medical history. Concomitant medication (Other medications in two weeks) included VITAMIN B complex (B COMPLEX), collagen marine, methylsulfonylmethane (MARINE COLLAGEN PEPTIDES WITH MSM), saw palmetto [serenoa repens] and zinc. No other vaccine in four weeks. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=EJ1685, administrator route=Intramuscular, vaccine location=Left arm) on 22Dec2020 at age of 39-year-old for covid-19 immunisation and experienced general malaise with nausea and diarrhea, localized pain 3-4/10 after first dose x 5 days. The patient experienced full body rash with itching, localized arm pain with ancillary edema x 5 days. Flu like symptoms. After second dose in 2021. Treatment for events included Antihistamine. No Covid prior vaccination. The outcome of events was recovering. Unknown if Covid tested post vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021123153 same patient, same product (first dose), different events.

Other Meds: SAW PALMETTO [SERENOA REPENS]; B COMPLEX [VITAMIN B COMPLEX]; ZINC; MARINE COLLAGEN PEPTIDES WITH MSM

Current Illness:

ID: 1087085
Sex: F
Age:
State: NC

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 03/10/2021
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: I have broken out in welts all over my body and I am itching like absolute crazy; I have broken out in welts all over my body and I am itching like absolute crazy; My face is red as a bee and I even got it on my legs and my arm; all for my feet and legs are covered with white, itch spots; This is a spontaneous report from a contactable consumer (patient). An 85-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3249) at the age of 84-years-old, via an unspecified route of administration on 18Jan2021 at single dose for COVID-19 immunization. Medical history included high blood pressure, diabetes, and allergies. Concomitant medications included unspecified medications. The patient got the COVID vaccine on 18Jan2021 and she has been okay until last week. The patient has broken out in welts all over her body and was itching like absolute crazy on Jan2021. She went to her doctor on Friday but couldn't see him because he had too many people, but she asked a PA (as reported) to tell the doctor to see him. The doctor wanted to know what she has done. She mentioned that she has been at her house ever since last March because of the virus. She hasn't even been to a grocery store or anywhere. She was given ZYRTEC, PEPCID, and something to put on, it's Triamcinolone to put on twice a day. She mentioned that Triamcinolone has been helping her since Friday, but now it's not doing a thing. She was just scratching. Her face was red as a bee and she even got it on her legs and arm. It started on her hands and now, it was going up her arms. This started a week ago (Jan2021). She was suffering from the symptoms, all her feet and legs were covered with white, itch spots and they all go together. She mentioned that she was going to see another doctor tomorrow or go to the hospital or somewhere again. She couldn't stand this and added that you don't understand how serious this is. She was supposed to get the second shot tomorrow and mentioned that she was afraid to get it. The patient underwent lab test and procedure which included A1C with an unknown result on an unspecified date. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1087086
Sex: F
Age:
State: AL

Vax Date: 02/06/2021
Onset Date: 02/06/2021
Rec V Date: 03/10/2021
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: chills; congestion; tiredness; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) in left arm via an unspecified route of administration on 06Feb2021 at single dose for COVID-19 immunization. Medical history included diabetes, sleep apnea, post-traumatic stress disorder (PTSD), anxiety, herpes, vitamin d deficiency, environmental allergies, asthma, allergies to possible latex. Concomitant medications included unspecified medications in two weeks. No other vaccine in four weeks. The patient previously received the first dose of BNT162B2 on 16Jan2021 08:00 in left arm for COVID-19 immunization and experienced sore arm, slept for 17 straight hours, chills, upset stomach, upper body flushing for up to 4 days later. The patient experienced chills, congestion, tiredness, all on 06Feb2021. So far not near as bad as 1st time, but took 25mg benadryl and 1000mg of Tylenol, and a dose of pepcid just before she got the shot under advise of physician and nurse practitioner due to previous side effects. No Covid test post vaccination. The outcome of the events was recovered in Feb2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087087
Sex: F
Age:
State: CA

Vax Date: 01/15/2021
Onset Date:
Rec V Date: 03/10/2021
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: Worsened sharp headaches; jaw pain; This is a spontaneous report from a contactable healthcare professional (patient). A 32 years old non-pregnant female patient received the second single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL3246) intramuscular, in left arm, on 15Jan2021 at 09:30, for COVID-19 immunisation. The first dose of vaccine was given on 23Dec2020 at 17:30, intramuscular, in left arm (lot EJ1685), at the age of 31 years, experiencing right ear infection and right sided headaches 2 weeks after this first dose. No other vaccine was given in four weeks. Medical history included asthma, known allergies: a yellow mushroom from overwatering house plants, PCOS, eczema. The patient had no COVID prior vaccination and had not been tested for COVID post vaccination. Concomitant medication included topical triamcinolone acetonide 0.1% cream. On an unspecified date in 2021 the patient experienced worsened sharp headaches with jaw pain. Headaches became mild and jaw pain relieved when she removed ear wax. The final events outcome was unknown.

Other Meds: TRIAMCINOLONE ACETONIDE

Current Illness:

ID: 1087088
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: fatigue; achy body; This is a spontaneous report from a contactable consumer. A male 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 immunisation. The patient's medical history included ongoing psoriatic arthritis. The patient's concomitant medications were not reported. The patient experienced fatigue and achy body on an unspecified date. The outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Psoriatic arthritis

ID: 1087089
Sex: U
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: felt less tired/ increase of energy; felt less tired/ increase of energy; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender 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. Medical history included COVID-19 (last spring with severe symptoms) from an unknown date to an unknown date. The patient reported that: "I still was very tired from COVID-19. I felt less tired/ increase of energy after first Pfizer vaccine. " on an unspecified date. The patient outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1087090
Sex: U
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: Headache; body aches; Fever; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received bnt162b2 (BNT162B2) , via an unspecified route of administration from an unspecified date, as a single dose for COVID-19 immunization. Medical history included had Covid last spring with severe symptoms. Concomitant medications were not reported. The patient reported that "I still was very tired from COVID. I felt less tired after first Pfizer vaccine. I had headache fever and body aches after second one and now have even more energy. The outcome of the events was unknown. Information regarding lot number has been request.

Other Meds:

Current Illness:

ID: 1087091
Sex: F
Age:
State:

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 03/10/2021
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: mild headache; mild bodyache; This is a spontaneous report from a non-contactable consumer (patient). A 40-year-old female patient received BNT162B2 (Solution for injection, Batch/Lot: unknown) via an unspecified route of administration on 03Feb2021 at single dose for covid-19 immunisation. The patient was not pregnant at the time of vaccination. The patient's medical history and concomitant medications was not reported. Patient did not had Covid prior vaccination. Patient was not tested for Covid tested post vaccination. The patient experienced mild headache, mild body ache on 03Feb2021. Outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1087092
Sex: F
Age:
State: OR

Vax Date: 02/03/2021
Onset Date: 02/04/2021
Rec V Date: 03/10/2021
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: Headache; Slight Fever (100.4 F); Fatigue; Chills; Moderate pain at Injection Site; This is a spontaneous report received from a contactable consumer. A 34-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection) via an unspecified route of administration on 03Feb2021 15:30 to Left arm at single dose for COVID-19 immunization. Medical history included Shellfish, Tree Nuts (Migraine Trigger). Concomitant medications were not reported. Past drug included BNT162B2 (dose number:1). It was reported as on 04Feb2021 06:30 patient experienced with Slight Fever (100.4 F), Headache, Fatigue, Chills and Moderate pain at Injection Site. Treatment was not received for events. Outcome of events was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected. Information regarding Lot/Batch No. cannot be obtained.

Other Meds:

Current Illness:

ID: 1087093
Sex: F
Age:
State: SC

Vax Date: 01/30/2021
Onset Date: 02/05/2021
Rec V Date: 03/10/2021
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: 5 nights having nightmares; waking with rapid heart rate; This is a spontaneous report from a non-contactable consumer (patient). A70-year-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9265) via an unspecified route of administration in the left arm on 30Jan2021, at 14:30 (age at vaccination: 70 years) as a single dose for COVID-19 immunisation. The patient medical history included IgA blood deficiency, hypothyroidism and allergy to horse serum. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The concomitant medication included levothyroxine sodium (LEVOTHYROXIN) at 88ug daily, monascus purpureus (RED YEAST RICE), glucosamine hcl + msm (glucosamine hydrochloride;methylsulfonylmethane), calcium, fish oil, loratadine (CLARITIN), minerals nos, vitamins nos (ONE A DAY). The patient did not receive any other vaccines within four weeks prior to the vaccination. It was reported that during the 2 weeks after the first dose, the patient experienced 5 nights having nightmares and waking with rapid heart rate on 05Feb2021. The patient did not receive any treatment for the events. The events were reported as non-serious by the reporter. The outcome of the events 5 nights having nightmares and waking with rapid heart rate was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: LEVOTHYROXIN; RED YEAST RICE; GLUCOSAMINE HCl + MSM; CALCIUM; FISH OIL; CLARITIN; ONE A DAY

Current Illness:

ID: 1087094
Sex: F
Age:
State: MA

Vax Date: 12/16/2020
Onset Date: 12/16/2020
Rec V Date: 03/10/2021
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: Rash at injection site and Induration; Rash at injection site and Induration; headache; This is a spontaneous report from a non-contactable consumer or other non hcp. A 34-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot no: EH9899), on Left arm via an unspecified route of administration on 16Dec2020 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection Lot no: EL3246) on Left arm on 06Jan2021 for covid-19 immunisation and experienced 12hours after injection felt like cold, malaise, bigger rash than first dose, 1 inch induration, felt better after 48 hours with Tylenol. It was reported on 16Dec2020 due to first dose patient experienced rash at injection site and Induration, headache that lasted until day 2 after taking Tylenol. There was no COVID prior vaccination and no COVID tested post vaccination. Patient was not pregnant while vaccination. There was no known allergies. Outcome of the events was recovered on unspecified date. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1087095
Sex: F
Age:
State:

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 03/10/2021
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: 12hours after injection felt like cold; malaise; bigger rash than first dose; 1 inch induration; This is a spontaneous report from a non-contactable consumer or other non hcp. A 34-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot no:EL3246), on Left arm via an unspecified route of administration on 06Jan2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection Lot no: EH9899) on Left arm on16Dec2020 for covid-19 immunisation and experienced Rash at injection site, Induration and headache. It was reported that 12hours after injection (Jan2021) of second dose felt like cold, malaise, bigger rash than first dose, 1 inch induration, felt better after 48 hours with Tylenol. There was no COVID prior vaccination and no COVID tested post vaccination. Patient was not pregnant while vaccination. There was no known allergies. Outcome of the events was recovering. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1087096
Sex: F
Age:
State: IL

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 03/10/2021
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: Heart palpitations; sore injection site; body aches in the back; headache; This is a spontaneous report from a contactable other healthcare professional (HCP) (patient). A 58-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number: 013L20A) via an unspecified route of administration on 05Feb2021 08:45 in left arm at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. There was no other vaccine in four weeks. The patient had heart palpitations after vaccine - only lasting a few seconds, sore injection site and body aches in the back - both of which were relieved with naproxen sodium (ALEVE), small headache - went away shortly after getting out of bed. Event onset date reported as 05Feb2021 12:30. Treatment received for the events. The outcome of the event heart palpitations was recovered on 05Feb2021, of other remain events was recovered in Feb2021.

Other Meds:

Current Illness:

ID: 1087097
Sex: F
Age:
State: OH

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 03/10/2021
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: excess phlem; Exhaustion; Body aches; fever; chills; cold sweat; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number=EL3247), via an unspecified route of administration on right arm on 04Feb2021 10:00 (at age of 48 years old) at single dose for COVID-19 immunization. Medical history included spinal stenosis, liver hemangiomas, uterine fibroids, parapelvic and renal cysts, complex left ovarian cysts, PTSD (Post-traumatic stress disorder), pap smear atypical cells of undetermined significance, endometrial cells, bacterial vaginosis, HPV (Human papilloma virus infection), osteopenia, anemia, patellar tendenitis, right hip impingement, left shoulder impingement syndrome, microscopic hematuria, hiatal hernia, cricopharyngeal spasms and allergies to contrast die. Concomitant medication included pregabalin (LYRICA), sertraline hydrochloride (ZOLOFT), colecalciferol (VIT.D3) and glutathione. The patient previously received first dose of BNT162B2 (Lot number=EL3247) on 15Jan2021 at 10:45 AM on right arm for COVID-19 immunization. The patient experienced excess phlem, exhaustion, body aches, fever, chills, cold sweat on 04Feb2021 17:00. Prior to vaccination, the patient was not diagnosed with COVID-19; Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any treatment from events. The outcome of events was recovered in Feb2021.

Other Meds: LYRICA; ZOLOFT; VIT.D3; GLUTATHIONE

Current Illness:

ID: 1087098
Sex: M
Age:
State:

Vax Date: 02/05/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: he felt bad, so he took two Percocet; This is a spontaneous report from a contactable consumer. A male patient of 94(unit unknown) received the first dose of BNT162B2 (lot number unknown), via an unspecified route of administration, on 05Feb2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient (the reporter's friend) who is 94 (not clarified) and the patient had his first yesterday(05Feb2021). Then the patient went into the yard and started gardening for 5 or 6 or 7 hours. And the patient felt bad in Feb2021, so he took two Percocet. And the reporter brother-in-law is a pharmacy doctor and he, through the reporter's sister told the reporter not to take any. So, the reporter was a little worried about the patient and does it have any effect on the efficacy of the COVID-19 Vaccine. The outcome of the event was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1087099
Sex: F
Age:
State: CA

Vax Date: 01/18/2021
Onset Date: 02/02/2021
Rec V Date: 03/10/2021
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: When I swallow or when I gulp like a whole glass of water or half a glass of orange juice or something like that, my gland on the side of my neck hurts, it hurts me, it is sore; This is a spontaneous report from a contactable consumer (patient). A 81-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EL3249, on 18Jan2021 at single dose for COVID-19 immunization. Medical history was none. Concomitant medication was not reported. The patient had her first Pfizer shot and it will be three weeks, it was on 18Jan and on Monday (02Feb2021) she developed when she swallow or when gulp like a whole glass of water or half a glass of orange juice or something like that, her gland on the side of neck hurt, it hurt her, it was sore. She did not know if that was the part of the side effects. That was it and she was going to get the second shot on Monday. It happened on Monday when it started hurting. She thought it would go away. It started going away with hot, when I drink something like hot tea but it was still there, when she swallow. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1087100
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/10/2021
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: Dizzy spells/When paraphrased, consumer stated that when he/she stand up, right; not feeling good; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient had had the first shot and that was vaccination and she/he was due to have the second vaccination and she/he was having dizzy spells now (on an unspecified date), just last couple of days. She/he wanted to know if dizzy spells be coming on with His/her second vaccination and if it would that have any effect on the second vaccination at all. When paraphrased, consumer stated that when he/she stand up, right. Consumer further stated, you know he/she was not feeling good. She/he was just going to ask you if it is a serious thing or anything. The patient was just experiencing dizzy spells because she/he was going to be getting the second shot. That was all the patient wanted to know. If it is okay, that is all. The patient did not want to answer anything. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1087101
Sex: F
Age:
State: PA

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 03/10/2021
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: Headache; chills; fever; muscle aches; This is a spontaneous report from a contactable consumer. A 50-years-old female patient (not pregnant) received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EN5318), via an unspecified route of administration at arm right on 04Feb2021 11:30 at age of 50-years-old at single dose for COVID-19 immunization. The patient medical history was not reported, no known allergies. The concomitant medications in two weeks included vitamins. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The historical vaccine included 1st dose of BNT162B2 on 15Jan2021 at age of 50-years-old for COVID-19 immunization. The patient experienced headache, chills, fever, muscle aches started at 05Feb2021 20:00 and resolved within 24 hours. Reported now feeling fine on 06Feb2021, symptoms resolved. No treatment was received for the adverse events. The events outcome was recovered on 06Feb2021. No COVID prior vaccination, since the vaccination the patient hadn't been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1087102
Sex: F
Age:
State: MI

Vax Date:
Onset Date: 01/08/2021
Rec V Date: 03/10/2021
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: fever, chills, nausea, aches, joint pain; fever, chills, nausea, aches, joint pain; fever, chills, nausea, aches, joint pain; fever, chills, nausea, aches, joint pain; fever, chills, nausea, aches, joint pain; This is a spontaneous report from a contactable consumer reporting for self. A 65-years-old female patient received the second 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 covid-19. Concomitant medication included celecoxib. The patient experienced fever, chills, nausea, aches, joint pain on 08Jan2021. Outcome of events was recovered. Information on the lot/batch number has been requested.

Other Meds: CELEBREX

Current Illness:

ID: 1087103
Sex: F
Age:
State: SC

Vax Date: 01/29/2021
Onset Date: 01/30/2021
Rec V Date: 03/10/2021
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: Fever greater than 102; Swollen lips; red welt a injection site; pain at injection site; swollen injection site; chills; body aches; headache; chest pressure and tightness; This is a spontaneous report from a contactable other HCP (patient). A 24-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EL8982), intramuscular on 29Jan2021 15:00 at single dose for covid-19 immunization. Vaccine location was right arm and it was the second dose. Patient is not pregnant. The facility type vaccine was School or Student Health Clinic. Patient intramuscularly received the first dose of vaccine on 08Jan2021 04:15PM (also at age of 24 years old) at right arm with lot number EL8982 for covid-19 immunization. Medical history included chronic sinusitis from an unknown date, allergies to sulfa medications. Patient was not diagnosed with COVID-19 prior to vaccination nor tested for COVID-19 since the vaccination. The patient's concomitant medications were not reported. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine nor received any other medications within 2 weeks of vaccination. The patient experienced Fever greater than 102, Swollen lips, large red welt a injection site, pain at injection site, swollen injection site, chills, body aches, headache, chest pressure and tightness on 30Jan2021 03:00 AM. Patient didn't receive treatment for the adverse events. The outcome of events was recovered in 2021.

Other Meds:

Current Illness:

ID: 1087104
Sex: M
Age:
State: CA

Vax Date: 01/12/2021
Onset Date: 01/14/2021
Rec V Date: 03/10/2021
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: Had swelling to the right side of the neck lasting x ~6 hrs most likely the result of a swollen right lymph node.; This is a spontaneous report from a contactable Other HCP (patient). A 32-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EL3248, on 12Jan2021 20:30 at single dose in left arm for COVID-19 immunization. Medical history included Known allergies to Pumpkin seeds and Codine. Concomitant medication was none. The patient previously received first dose of BNT162B2 (Lot number EH9899) on 22Dec2020 19:30 in left arm. The patient had no other vaccine in four weeks. covid tested post vaccination. The patient had swelling to the right side of the neck lasting x ~6 hrs most likely the result of a swollen right lymph node on 14Jan2021 21:00. No treatment was received for the event. The outcome of the event was resolved on 15Jan2021.

Other Meds:

Current Illness:

ID: 1087105
Sex: F
Age:
State: FL

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 03/10/2021
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: Shortly after receiving second dose had a slight metallic taste in my mouth. Today it's 6 days later and I still have it off and on.; This is a spontaneous report from a contactable consumer (patient). A 72-years-old female patient (no pregnant) received the second dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL1283) , via an unspecified route of administration on 01Feb2021 09:30 at single dose at left arm for covid-19 immunisation. The patient previously took the first dose bnt162b2 on 11Jan2021 for covid-19 immunization. The patient medical history was not reported. Concomitant medication included sertraline. The patient experienced shortly after receiving second dose had a slight metallic taste in mouth on 01Feb2021 10:00. On 06Feb2021, it's 6 days later and patient still have it off and on. No treatment for event. The outcome of event was not recovered. No other vaccine in four weeks; No covid prior vaccination; No covid tested post vaccination.

Other Meds: SERTRALINE

Current Illness:

ID: 1087106
Sex: M
Age:
State: WA

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 03/10/2021
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: Body aches; Fatigue; headache; Chills; This is a Spontaneous report from a Contactable Consumer (patient). A 47-years-old male patient received bnt162b2 (BNT162B2; lot unknown=True, lot unknown reason=Not available/provided to reporter at the time of report completion) second dose, via an unspecified route of administration on 04Feb2021 15:00 at SINGLE DOSE for covid-19 immunization, vaccine location was Left arm. The patient's medical history and concomitant medications were not reported. No covid prior vaccination. No covid tested post vaccination. Patient had no Known allergies. Historical vaccine included first dose of BNT162B2 for covid-19 immunization on 14Jan2021. The patient experienced body aches, fatigue, headache and chills, all on 04Feb2021 20:00 with outcome of recovered. No treatment was received. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1087107
Sex: F
Age:
State: NJ

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 03/10/2021
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: Chills; achy; low grade fever; tired; Arm sore at injection site; all the patient did was sleep.; This is a spontaneous report from a contactable consumer (patient). A 63-year-old female patient (not pregnant) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EM9809) via an unspecified route of administration on 04Feb2021 16:00 in the left arm at single dose for covid-19 immunisation. Medical history included chronic obstructive pulmonary disease, COVID (prior vaccination). There was no other vaccine in four weeks. The patient received other medications in two weeks (unspecified). The patient has no COVID tested post vaccination. The patient experienced chills, achy, low grade fever, tired, arm sore at injection site, and all the patient did was sleep. Event onset date reported as 05Feb2021 06:00. Following day, feel much better. Body temperature showed low grade fever on 05Feb2021 06:00. No treatment received for the events. The outcome of the events was recovered in Feb2021.

Other Meds:

Current Illness:

ID: 1087108
Sex: M
Age:
State: IL

Vax Date: 01/30/2021
Onset Date:
Rec V Date: 03/10/2021
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: Shoulder was a little sore; arm soreness; This is a spontaneous report from a contactable consumer. This consumer reported similar events for two patients. This is the second of two reports. A male patient of an unspecified age (reported for himself) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number reported as "ELI283 or EL1283"), via an unspecified route of administration on 30Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated he heard that the second dose can cause more side effects and he stated he and his wife both experienced arm soreness after the first dose on an unspecified date. Consumer stated, first of all thank you guys for making this vaccine. He and his wife received the vaccine (unspecified vaccine) their first dose last Saturday, a week ago yesterday and had no reaction to it at all, their shoulder was a little sore but that's it. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021130328 same reporter and drug, similar events, different patient

Other Meds:

Current Illness:

ID: 1087109
Sex: F
Age:
State: WI

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 03/10/2021
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: Throwing up; Dizzy; Weakness; Headache; This is a spontaneous report from a contactable Other-HCP (patient). A 23-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EL3248, on 05Feb2021 15:30 in left arm for COVID 19. Medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (lot number EL1284) on 22Jan2021 13:30 in left arm. The patient had no other vaccine in four weeks. The patient had no COVID prior vaccination. The patient had no COVID tested post vaccination. The patient experienced Throwing up, dizzy, weakness, headache on 06Feb2021 04:00. No treatment was received for all events. The outcome of the events was not resolved.

Other Meds:

Current Illness:

ID: 1087110
Sex: F
Age:
State: TX

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 03/10/2021
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: Within 4 hours a rash between my inner thighs appeared.; This is a spontaneous report from a contactable consumer (patient). A 39-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration in the left arm on 04Feb2021 at 14:15 (02:15 PM) at a single dose for COVID-19 immunization. The vaccine was administered to the patient at a hospital. The patient had no other vaccine in four weeks. The patient's medical history included diabetes, and the patient had Covid prior to vaccination. The patient had no known allergies. Concomitant medication included ascorbic acid (VITAMIN C), colecalciferol (VITAMIN D), semaglutide (OZEMPIC), and prenatal vitamin. Within 4 hours (on 04Feb2021 at 06:30 PM) a rash between her inner thighs appeared. The event resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of the event which included steroid cream and diphenhyramin HCl (BENADRYL). The patient has not been tested for Covid post vaccination. The outcome of the event was not recovered. Information on the batch/lot number has been requested.

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

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm