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: 1261395
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 03/30/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: DISCOMFORT OF THE JAW; DISCOMFORT OF THE TEETH; ABDOMINAL PAIN; MODERATE HEADACHE; This spontaneous report received from a consumer concerned a 67 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included non smoker, and non alcoholic, and other pre-existing medical conditions included the patient had no any medical history and no drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805020, and batch number: 1805020 expiry: UNKNOWN) dose was not reported, administered on 30-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 30-MAR-2021, the subject experienced moderate headache. On 31-MAR-2021, the subject experienced abdominal pain. On 12-APR-2021, the subject experienced discomfort of the jaw. On 12-APR-2021, the subject experienced discomfort of the teeth. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from abdominal pain, was recovering from moderate headache, and the outcome of discomfort of the jaw and discomfort of the teeth was not reported. This report was non-serious. This case, from the same reporter is linked to 20210445480.

Other Meds:

Current Illness: Abstains from alcohol; Non-smoker

ID: 1261396
Sex: U
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: RINGING IN HEAD; RINGING IN EARS; VERTIGO; DIZZINESS; This spontaneous report received from a consumer concerned multiple patients of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the subject experienced ringing in head, ringing in ears, vertigo, and dizziness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the ringing in head, ringing in ears, vertigo and dizziness was not reported. This report was non-serious. This case, from the same reporter is linked to 20210407556.

Other Meds:

Current Illness:

ID: 1261397
Sex: M
Age:
State: DE

Vax Date:
Onset Date: 03/30/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: MILD HEADACHE; DISCOMFORT OF THE JAW; DISCOMFORT OF TEETH; INJECTION SITE/ ARM SORENESS; This spontaneous report received from a patient concerned a 69 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included glaucoma, alcohol user, and non smoker, and other pre-existing medical conditions included no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805020 expiry: UNKNOWN) dose was not reported, administered on 30-MAR-2021 for prophylactic vaccination. Concomitant medications included latanoprost for glaucoma. On 30-MAR-2021, the subject experienced injection site/ arm soreness. On 02-APR-2021, the subject experienced discomfort of the jaw. On 02-APR-2021, the subject experienced discomfort of teeth. On an unspecified date, the subject experienced mild headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from injection site/ arm soreness, and mild headache, and the outcome of discomfort of the jaw and discomfort of teeth was not reported. This report was non-serious. This case, from the same reporter is linked.

Other Meds: LATANOPROST

Current Illness: Alcohol use (2 beers a year.); Glaucoma; Non-smoker

ID: 1261398
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: SORE ARM; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose was not reported, administered on MAR-2021 for prophylactic vaccination. The batch number was not reported. The company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On 2021, the subject experienced sore arm. Treatment medications (dates unspecified) included: isopropanol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of sore arm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261399
Sex: M
Age:
State: CA

Vax Date:
Onset Date: 04/07/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: CHEST TIGHTNESS ON LEFT SIDE (5 TIMES WITHIN THE LAST 72 HOURS); PAIN ON THE LEFT SIDE OF CHEST (5 TIMES WITHIN THE LAST 72 HOURS); PAINFUL TO BREATHE; HEART WAS TIGHT; SORE ARM A LITTLE; This spontaneous report received from a patient concerned a 61 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included high blood pressure, alcohol user, and non smoker, and other pre-existing medical conditions included the patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 043A21A, expiry: UNKNOWN) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. Concomitant medications included acetylsalicylic acid for high blood pressure. On 07-APR-2021, the subject experienced sore arm a little. On 19-APR-2021, the subject experienced chest tightness on left side (5 times within the last 72 hours). On 19-APR-2021, the subject experienced pain on the left side of chest (5 times within the last 72 hours). On 19-APR-2021, the subject experienced painful to breathe. On 19-APR-2021, the subject experienced heart was tight. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm a little on 09-APR-2021, had not recovered from chest tightness on left side (5 times within the last 72 hours), and pain on the left side of chest (5 times within the last 72 hours), and the outcome of painful to breathe and heart was tight was not reported. This report was non-serious.

Other Meds: ASPRIN

Current Illness: Alcohol use (1-2 Beers per week); Blood pressure; Nonsmoker

ID: 1261400
Sex: F
Age:
State: RI

Vax Date:
Onset Date: 03/19/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: SORE ARM AT INJECTION SITE; This spontaneous report received from a patient concerned a 46 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included non alcohol user, and non smoker, and other pre-existing medical conditions included the patient had no known allergies and did not have any drug abuse/illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805022, expiry: UNKNOWN) dose was not reported, administered on 18-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 19-MAR-2021, the subject experienced sore arm at injection site. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm at injection site on 25-MAR-2021. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Non-smoker

ID: 1261401
Sex: F
Age:
State: OH

Vax Date:
Onset Date: 03/05/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: TENDER TO TOUCH; MILD SORENESS IN INJECTED ARM; BOTH LEG PAIN; This spontaneous report received from a patient concerned a 57 year old female. The patient's height, and weight were not reported. The patient's past medical history included stromal tumor, right thyroid removed, and total knee replacement, and concurrent conditions included brain aneurysm, reflux thickening of uterine wall, asthma, seasonal allergies, non alcohol user, non smoker, and brain tumor, and other pre-existing medical conditions included the patient had no drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1802068, expiry: UNKNOWN) dose was not reported, administered on 05-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 2021, the subject experienced both leg pain. On 05-MAR-2021, the subject experienced mild soreness in injected arm. On APR-2021, the subject experienced tender to touch. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from both leg pain on 2021, had not recovered from mild soreness in injected arm, and the outcome of tender to touch was not reported. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Aneurysm cerebral (Brain aneurysm being monitored yearly); Asthma; Brain tumor (last MRI in September (2020) was stable Brain tumor); Non-smoker; Seasonal allergy; Uterine disorder

ID: 1261402
Sex: M
Age:
State: CT

Vax Date:
Onset Date: 04/06/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: BODY PAIN / BODY ACHE; HEADACHE; FEVER; This spontaneous report received from a pharmacist concerned a 64 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included diabetes, and other pre-existing medical conditions included the patient did not have known allergies .The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 043A21A expiry: UNKNOWN) dose was not reported, administered on 05-APR-2021 for prophylactic vaccination. Concomitant medications included acetylsalicylic acid. On 06-APR-2021, the subject experienced body pain / body ache. On 06-APR-2021, the subject experienced headache. On 06-APR-2021, the subject experienced fever. Treatment medications included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, body pain / body ache, and fever. This report was non-serious.

Other Meds: ASPRIN

Current Illness: Diabetes

ID: 1261403
Sex: M
Age:
State: MI

Vax Date:
Onset Date: 04/07/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: HEADACHE; This spontaneous report received from a patient concerned a 32 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On 07-APR-2021, the subject experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from headache on 08-APR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261404
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 04/12/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: MOSQUITO LIKE BITES / BUMP; SLEPT A LOT; TIRED; This spontaneous report received from a patient concerned a 55 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 206A21A, and expiry: UNKNOWN) dose was not reported, administered on 12-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-APR-2021, the subject experienced slept a lot. On 12-APR-2021, the subject experienced tired. On 15-APR-2021, the subject experienced mosquito like bites / bump. Treatment medications (dates unspecified) included: cortisone, and ethanol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the mosquito like bites / bump, tired and slept a lot was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261405
Sex: F
Age:
State: AR

Vax Date:
Onset Date: 04/06/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: DRY MOUTH; This spontaneous report received from a patient concerned an 86 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin, and batch number were not reported) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 06-APR-2021, the subject experienced dry mouth. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of dry mouth was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261406
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: THROBBING PAIN; THROWING UP; DIARRHEA; SORE ARM / SEVERE ARM PAIN; This spontaneous report received from a patient concerned a 55 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805031, and expiry: UNKNOWN) dose was not reported, administered on 31-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the subject experienced sore arm / severe arm pain, throbbing pain, throwing up, and diarrhea. Treatment medications (dates unspecified) included: naproxen sodium, and paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the sore arm / severe arm pain, throbbing pain, throwing up and diarrhea was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261407
Sex: M
Age:
State: CA

Vax Date:
Onset Date: 04/05/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: EYE STRAIN; DEHYDRATION; FELT LETHARGIC A LITTLE BIT; DULL HEADACHE; This spontaneous report received from a patient concerned a 35 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 042A21A expiry: 21/JUN/2021) dose was not reported, administered on 03-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 05-APR-2021, the subject experienced eye strain. On 05-APR-2021, the subject experienced dehydration. On 05-APR-2021, the subject experienced felt lethargic a little bit. On 05-APR-2021, the subject experienced dull headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from eye strain, dehydration, felt lethargic a little bit, and dull headache on APR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261408
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 04/06/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: UNUSUAL FATIGUE; HEADACHE; SEVERE VERTIGO; DIZZINESS; This spontaneous report received from a patient concerned a 60 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808978, expiry: UNKNOWN) dose was not reported, administered on 05-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 06-APR-2021, the subject experienced severe vertigo. On 06-APR-2021, the subject experienced dizziness. On 10-APR-2021, treatment medications included: cortisone. On an unspecified date, the subject experienced unusual fatigue, and headache. Laboratory data (dates unspecified) included: Blood test (NR: not provided) Normal. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from severe vertigo, and had not recovered from unusual fatigue, headache, and dizziness. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261409
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: FEVER; MUSCLE ACHES RIGHT SIDE OF THE BODY/MUSCLE SORENESS; This spontaneous report received from a patient concerned a 30 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included the patient was not pregnant and not breastfeeding at the time of reporting.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805031, expiry: UNKNOWN) dose was not reported, administered on 06-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced muscle aches right side of the body/muscle soreness. On 06-APR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever on 07-APR-2021, and had not recovered from muscle aches right side of the body/muscle soreness. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261410
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: LIGHT HEADEDNESS; LACK OF COORDINATION; SEVERE HEADACHE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included connective disease, and anticardiolipin antibody. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 180898 expiry: UNKNOWN) dose was not reported, administered on 06-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced light headedness. On APR-2021, the subject experienced lack of coordination. On APR-2021, the subject experienced severe headache. Laboratory data included: CT scan (NR: not provided) non revealing, and Platelet count (NR: not provided) normal. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from light headedness, and lack of coordination on APR-2021, and the outcome of severe headache was not reported. This report was non-serious.

Other Meds:

Current Illness: Anticardiolipin antibodies; Connective tissue disorder

ID: 1261411
Sex: F
Age:
State: OH

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: NON-STOP SLEEPING; LAZINESS; SWOLLEN LEFT ARM; SORENESS IN LEFT ARM; This spontaneous report received from a patient concerned a 53 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 043A21A, expiry: UNKNOWN) dose was not reported, administered on 06-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced non-stop sleeping. On APR-2021, the subject experienced laziness. On APR-2021, the subject experienced swollen left arm. On APR-2021, the subject experienced soreness in left arm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from non-stop sleeping, soreness in left arm, laziness, and swollen left arm. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261412
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: SEVERE EAR INFECTION; URINARY TRACT INFECTION; STOMACH CRAMPS; SEVERE/WORSENING HEADACHE; This spontaneous report received from a consumer concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the subject experienced severe ear infection, urinary tract infection, stomach cramps, and severe/worsening headache. Laboratory data (dates unspecified) included: CAT scan (NR: not provided) No blood clots. Treatment medications (dates unspecified) included: cefalexin. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the severe/worsening headache, stomach cramps, severe ear infection and urinary tract infection was not reported. This report was non-serious.; Sender's Comments: V0 Medical assessment comment not required as per standard operating procedure as the case assessed as non-serious.

Other Meds:

Current Illness:

ID: 1261413
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: COULD NOT FOCUS; SKIN HARD AT INJECTION SITE; POSSIBLE SEASONAL ALLERGIES; LITTLE BIT OF STIFF NECK; NECK PAIN; LITTLE RASH AROUND INJECTION SITE; TOP SHOULDER SORE; SORE ARM; RAISED RED SPOT AT INJECTION SITE; FATIGUE; HEADACHE; NAUSEA; LIGHT SENSITIVITY; This spontaneous report received from a patient concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's past medical history included thrombocytopenia, and concurrent conditions included allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose was not reported, administered on APR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On APR-2021, the subject experienced light sensitivity. On APR-2021, the subject experienced skin hard at injection site. On APR-2021, the subject experienced possible seasonal allergies. On APR-2021, the subject experienced little bit of stiff neck. On APR-2021, the subject experienced neck pain. On APR-2021, the subject experienced little rash around injection site. On APR-2021, the subject experienced top shoulder sore. On APR-2021, the subject experienced sore arm. On APR-2021, the subject experienced raised red spot at injection site. On APR-2021, the subject experienced fatigue. On APR-2021, the subject experienced headache. On APR-2021, the subject experienced nausea. Treatment medications included: cetirizine hydrochloride, paracetamol, and rizatriptan benzoate. On 21-APR-2021, the subject experienced could not focus. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from headache, top shoulder sore, nausea, and neck pain, had not recovered from sore arm, fatigue, and light sensitivity, and the outcome of little rash around injection site, could not focus, raised red spot at injection site, skin hard at injection site, little bit of stiff neck and possible seasonal allergies was not reported. This report was non-serious.

Other Meds:

Current Illness: Allergy multiple (Patient had lot of allergies)

ID: 1261414
Sex: F
Age:
State: GA

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: PRONOUNCE THUMPING AND RINGING IN THE EAR; SQUEEZING IN THE RIGHT LOWER LEG; RIGHT EAR ACHE; This spontaneous report received from a patient via a representative concerned a 71 year old female. The patient's weight was 153 pounds, and height was 66.5 inches. The patient's concurrent conditions included mild case of high blood pressure, mild case of cholesterol, alcohol use 1 beer can a day, and non-smoker, and other pre-existing medical conditions included the patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805029, expiry: 25-MAY-2021) dose was not reported, administered on 20-MAR-2021 13:30 for prophylactic vaccination. No concomitant medications were reported. On MAR-2021, the subject experienced right ear ache. On 21-MAR-2021, the subject experienced squeezing in the right lower leg. On 30-MAR-2021, the subject experienced pronounce thumping and ringing in the ear. Treatment medications (dates unspecified) included: acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from squeezing in the right lower leg, and had not recovered from pronounce thumping and ringing in the ear, and right ear ache. This report was non-serious.

Other Meds:

Current Illness: Alcohol use; Blood pressure high; Hyperlipidemia; Non-smoker

ID: 1261415
Sex: M
Age:
State: WA

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: CHILLS; FEVER; MUSCLE ACHE; This spontaneous report received from a consumer concerned an adult male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the subject experienced chills, fever, and muscle ache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, fever, and muscle ache. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261416
Sex: F
Age:
State: WA

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: CHILLS; FEVER; MUSCLE ACHES; This spontaneous report received from a consumer concerned an adult female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The company is unable to perform follow up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the subject experienced chills, fever, and muscle aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, fever, and muscle aches. This report was non-serious. This case, from the same reporter.

Other Meds:

Current Illness:

ID: 1261417
Sex: M
Age:
State: IL

Vax Date:
Onset Date: 04/03/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: DIZZINESS; FATIGUE/TIREDNESS; This spontaneous report received from a patient concerned a 73 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included hypothyroidism, sulfa allergy, azithromycin allergy, and non-smoker. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808978, and expiry: UNKNOWN) dose was not reported, administered on 02-APR-2021 for prophylactic vaccination. Concomitant medications included levothyroxine sodium for hypothyroidism. On 03-APR-2021, the subject experienced fatigue/tiredness. On 17-APR-2021, the subject experienced dizziness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from dizziness on 18-APR-2021, and fatigue/tiredness on 04-APR-2021. This report was non-serious.

Other Meds: SYNTHROID

Current Illness: Allergic reaction to antibiotics; Allergy to antibiotic; Hypothyroidism; Non-smoker

ID: 1261418
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: FEELING INTENSE DEBILITATING PAIN AROUND LOWER STOMACH AND GROIN AREA ON RIGHT SIDE; NEW TREMOR IN HANDS; THOUGHTS JUMBLING; INTERRUPT SLEEP; UNABLE TO EXERCISE; TERRIBLE HEADACHE; TERRIBLE VOMITING; COULD TAKE NO FOOD OR MEDICATION AT ALL; INTENSE VOMITING IT CAUSED TO LOSE CONTROL OF BLADDER; This spontaneous report received from a patient via a company representative concerned a 68 year old female. The patient's height, and weight were not reported. The patient's past medical history included dental implants, and concurrent conditions included malignant neoplasm of right kidney except renal pelvis. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. Concomitant medications included axitinib, and ondansetron. On MAR-2021, the subject experienced intense vomiting it caused to lose control of bladder. On 10-MAR-2021, the subject experienced terrible vomiting. On 10-MAR-2021, the subject experienced could take no food or medication at all. On an unspecified date, the subject experienced feeling intense debilitating pain around lower stomach and groin area on right side, new tremor in hands, thoughts jumbling, interrupt sleep, unable to exercise, and terrible headache. Treatment medications (dates unspecified) included: naproxen, and codeine phosphate/paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from terrible vomiting, could take no food or medication at all, and intense vomiting it caused to lose control of bladder on 2021, and the outcome of feeling intense debilitating pain around lower stomach and groin area on right side, new tremor in hands, terrible headache, thoughts jumbling, interrupt sleep and unable to exercise was not reported. This report was non-serious.

Other Meds: INLYTA; ONDANSETRON

Current Illness: Malignant neoplasm of kidney, except pelvis

ID: 1261419
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: TINNITUS; This spontaneous report received from a patient concerned multiple patients. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the subject experienced tinnitus. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of tinnitus was not reported. This report was non-serious.; Sender's Comments: V0 Medical assessment comment not required as per standard operating procedure as the case assessed as non-serious.

Other Meds:

Current Illness:

ID: 1261421
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: TINGLING IN MOUTH; 2 BODY RASHES; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date, the subject experienced tingling in mouth, and 2 body rashes. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the 2 body rashes and tingling in mouth was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261422
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: BODY ACHES; FELT LIKE COULDN'T MOVE BODY; INTENSE CHILLS; FEVER; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On 2021, the subject experienced fever. On 2021, the subject experienced intense chills. On 2021, the subject experienced body aches. On 2021, the subject experienced felt like couldn't move body. Laboratory data included: Body temperature (NR: not provided) 103 F. The action taken with covid-19 vaccine ad26.cov2.s was not reported. The patient recovered from fever, intense chills, body aches, and felt like couldn't move body. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261423
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: ARM STIFFNESS; NUMBING PAIN; LIGHTHEADEDNESS; FATIGUE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown) dose was not reported, administered on MAR-2021 for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On MAR-2021, the subject experienced arm stiffness. On MAR-2021, the subject experienced numbing pain. On MAR-2021, the subject experienced lightheadedness. On MAR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the arm stiffness, numbing pain, lightheadedness and fatigue was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261424
Sex: F
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: NERVE PAIN; CANNOT MOVE ARM; ARM PAIN; This spontaneous report received from a patient via a company representative concerned a female of unspecified age. The patient's weight, height, and medical history were not reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date, the subject experienced nerve pain, cannot move arm, and arm pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the arm pain, nerve pain and cannot move arm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261425
Sex: U
Age:
State: MD

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: POTENTIAL TEMPERATURE EXCURSION VIALS USED TO VACCINATE PATIENTS; MEDICATION ERROR; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the subject experienced potential temperature excursion vials used to vaccinate subjects, and medication error. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the potential temperature excursion vials used to vaccinate patients and medication error was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261426
Sex: M
Age:
State: TX

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: PAIN AND BODY ACHES; ABDOMINAL DISCOMFORT; LITTLE SORE ARM; FATIGUE; NAUSEA; This spontaneous report received from a consumer concerned a 62 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805029 expiry: UNKNOWN) dose was not reported, administered on 13-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced pain and body aches. On 13-MAR-2021, the subject experienced abdominal discomfort. On 13-MAR-2021, the subject experienced little sore arm. On 13-MAR-2021, the subject experienced fatigue. On 13-MAR-2021, the subject experienced nausea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from little sore arm on 15-MAR-2021, was recovering from pain and body aches, abdominal discomfort, and nausea, and had not recovered from fatigue. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261427
Sex: M
Age:
State: CT

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: BODY ACHES; SHOULDER PAIN/FELT SYMPTOMS OF SORE JOINTS; FELT FATIGUE/EXTREMELY TIRED; This spontaneous report received from a patient concerned a 46 year old male. The patient's height, and weight were not reported. The patient's past medical history included exercise induced asthma, and concurrent conditions included occasional alcohol user, and non smoker, and other pre-existing medical conditions included the patient had no known drug allergies. The patient was previously treated with salbutamol for exercise induced asthma. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808978, and expiry: UNKNOWN) dose was not reported, administered on 01-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 01-APR-2021, the subject experienced body aches. On 01-APR-2021, the subject experienced shoulder pain/felt symptoms of sore joints. On 01-APR-2021, the subject experienced felt fatigue/extremely tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches, shoulder pain/felt symptoms of sore joints, and felt fatigue/extremely tired on 03-APR-2021. This report was non-serious.

Other Meds:

Current Illness: Non-smoker; Social alcohol drinker (Once or twice a month.)

ID: 1261428
Sex: U
Age:
State: IL

Vax Date:
Onset Date: 04/22/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: CRAMP IN UNDERARM OF RIGHT ARM; BURNING IN UNDERARM OF RIGHT ARM; This spontaneous report received from a patient concerned a 19 year old of unspecified sex. The patient's weight, height, and medical history were not reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805031, expiry: UNKNOWN) dose was not reported, administered on 02-APR-2021 14:00 for prophylactic vaccination. No concomitant medications were reported. On 22-APR-2021, the subject experienced cramp in underarm of right arm. On 22-APR-2021, the subject experienced burning in underarm of right arm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from cramp in underarm of right arm, and burning in underarm of right arm. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261429
Sex: M
Age:
State: FL

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: CHILLS; This spontaneous report received from a patient concerned a 50 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included non smoker, and abstains from alcohol, and other pre-existing medical conditions included patient had no known drug allergies. Patient had no history of illness. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: Unknown) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. Batch number was not reported and has been requested. No concomitant medications were reported. On JAN-2021, Laboratory data included: PCR (NR: not provided) NEGETIVE. On 08-APR-2021, the subject experienced chills. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills on 09-APR-2021. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Non-smoker

ID: 1261430
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: SOME OTHER SYMPTOMS; BRAIN HURTS; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, the subject experienced some other symptoms, and brain hurts. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the brain hurts and some other symptoms was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261431
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: MODERATE PAIN IN VACCINATION ARM AREA; This spontaneous report received from a consumer concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown, expiry: unknown) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date, the subject experienced moderate pain in vaccination arm area. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of moderate pain in vaccination arm area was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261432
Sex: F
Age:
State: AR

Vax Date:
Onset Date: 04/11/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: LOWER ABDOMINAL PAIN; BACK PAIN; BODY PAIN; RIGHT LEG PAIN; FEVER; This spontaneous report received from a patient concerned a 36 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included thyroid problems, and other pre-existing medical conditions included the patient had no known drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported and batch number: 206A21A expiry: UNKNOWN) dose was not reported, administered on 10-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-APR-2021, the subject experienced body pain. On 11-APR-2021, the subject experienced right leg pain. On 11-APR-2021, the subject experienced fever. On 19-APR-2021, the subject experienced back pain. On 22-APR-2021, the subject experienced lower abdominal pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body pain, right leg pain, and fever on 12-APR-2021, and had not recovered from back pain, and lower abdominal pain. This report was non-serious.

Other Meds:

Current Illness: Thyroid disorder

ID: 1261433
Sex: M
Age:
State: ME

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: TICK BITE ( BUG BITE); This spontaneous report received from a patient concerned a male of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN) dose was not reported, administered on 05-APR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On APR-2021, the subject experienced tick bite ( bug bite). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of tick bite ( bug bite) was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261434
Sex: F
Age:
State: WA

Vax Date:
Onset Date: 03/09/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: SLEEP EXCESSIVE; MALAISE; TIREDNESS/FATIGUE; SORENESS IN THE ARM; MILD HEADACHE; This spontaneous report received from a patient concerned a 76 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 09-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On MAR-2021, treatment medications included: paracetamol. On 09-MAR-2021, the subject experienced soreness in the arm. On 09-MAR-2021, the subject experienced mild headache. On 10-MAR-2021, the subject experienced sleep excessive. On 10-MAR-2021, the subject experienced malaise. On 10-MAR-2021, the subject experienced tiredness/fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sleep excessive, malaise, and tiredness/fatigue on 11-MAR-2021, soreness in the arm on 23-MAR-2021, and mild headache on 10-MAR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261435
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: HIGHER THAN NORMAL HEART RATE; VIRAL NODULES; SHORTNESS OF BREATH; KNEE PAIN; FEET PAIN; MILD HEADACHE; This spontaneous report received from a patient concerned a 51 year old female. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 22-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 23-MAR-2021, the subject experienced knee pain. On 23-MAR-2021, the subject experienced feet pain. On 23-MAR-2021, the subject experienced mild headache. On 30-MAR-2021, the subject experienced shortness of breath. On APR-2021, Laboratory data included: Diagnostic ultrasound (NR: not provided) Viral nodules. On 02-APR-2021, the subject experienced viral nodules. On 08-APR-2021, the subject experienced higher than normal heart rate. Laboratory data included: Heart rate (NR: not provided) Higher than normal heart rate. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from knee pain, and feet pain, and mild headache on 30-MAR-2021, was recovering from higher than normal heart rate, and had not recovered from shortness of breath, and viral nodules. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261436
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: 36 HOURS OF THE WORST FLU EVER; This spontaneous report received from a patient via a company representative concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's past medical history included covid-19 infection. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the subject experienced 36 hours of the worst flu ever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of 36 hours of the worst flu ever was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261437
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: SEVERE DIARRHEA; BURNING RASH; NAUSEA; FLU-LIKE SYMPTOMS; SEVERE BODY ACHES; BURNING SENSATION WHEN URINATING; 4 FALLS; FELLS LIKE SOMETHING IN THROAT; BEDRIDDEN; REDUCED ABILITY TO PERFORM DAILY ACTIVITY; MEMORY PROBLEMS; TINNITUS; This spontaneous report received from a patient concerned a 53 year old female. The patient's height, and weight were not reported. The patient's past medical history included covid-19 infection, and concurrent conditions included cancer.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose was not reported, administered on 12-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 2021, the subject experienced burning sensation when urinating. On 2021, the subject experienced 4 falls. On 2021, the subject experienced fells like something in throat. On 2021, the subject experienced bedridden. On 2021, the subject experienced reduced ability to perform daily activity. On 2021, the subject experienced memory problems. On 2021, the subject experienced tinnitus. On 12-MAR-2021, the subject experienced severe body aches. On 12-MAR-2021, the subject experienced nausea. On 12-MAR-2021, the subject experienced extreme fatigue. On 13-MAR-2021, the subject experienced severe diarrhea. On 13-MAR-2021, the subject experienced flu-like symptoms. On 13-MAR-2021, the subject experienced burning rash. Treatment medications (dates unspecified) included: bismuth subsalicylate. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from severe diarrhea on 22-APR-2021, was recovering from burning rash, and nausea, had not recovered from extreme fatigue, memory problems, flu-like symptoms, and severe body aches, and the outcome of 4 falls, burning sensation when urinating, bedridden, reduced ability to perform daily activity, fells like something in throat and tinnitus was not reported. This report was non-serious.

Other Meds:

Current Illness: Cancer

ID: 1261438
Sex: M
Age:
State: TX

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: SMALL AMOUNT OF BLOOD IN NOSE; SMALL AMOUNT OF MUCUS IN NOSE; DRY NOSE; HARD TIME BEING HYDRATED; CRAMPING LEGS; This spontaneous report received from a consumer concerned a 50 year old male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 042A21A, expiry: UNKNOWN) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced small amount of blood in nose. On APR-2021, the subject experienced small amount of mucus in nose. On APR-2021, the subject experienced dry nose. On APR-2021, the subject experienced hard time being hydrated. On APR-2021, the subject experienced cramping legs. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the small amount of blood in nose, dry nose, hard time being hydrated, cramping legs and small amount of mucus in nose was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261439
Sex: F
Age:
State: WI

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: BURNING AT THE INJECTION SITE; This spontaneous report received from a patient concerned a 64 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included asthma, and fibromyalgia, and other pre-existing medical conditions included the patient had no known allergies .The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 2021, the subject experienced burning at the injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from burning at the injection site on APR-2021. This report was non-serious.

Other Meds:

Current Illness: Asthma; Fibromyalgia

ID: 1261440
Sex: M
Age:
State: KY

Vax Date:
Onset Date: 04/18/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: ACUTE HIVES FROM HEAD TO TOE OF BODY; This spontaneous report received from a patient concerned a 27 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included permanent lung damage, and allergies to insect. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 207A21A, and expiry: UNKNOWN) dose was not reported, administered on 12-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 18-APR-2021, the subject experienced acute hives from head to toe of body. Treatment medications (dates unspecified) included: hydrocortisone, and diphenhydramine hydrochloride. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from acute hives from head to toe of body. This report was non-serious.

Other Meds:

Current Illness: Allergy to insect sting (allergic to bees, wasps, hornets, bugs with stingers.); Lung disorder

ID: 1261441
Sex: F
Age:
State: NC

Vax Date:
Onset Date: 04/05/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: SHINGLES; This spontaneous report received from a patient concerned a 71 year old female. The patient's weight was 140 pounds, and height was 66 inches. The patient's concurrent conditions included alcohol user, and non smoker, and other pre-existing medical conditions included the patient had no known allergies.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805031, expiry: UNKNOWN) dose was not reported, administered on 09-MAR-2021 09:30 for prophylactic vaccination. No concomitant medications were reported. On 05-APR-2021, the subject experienced shingles. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from shingles. This report was non-serious.

Other Meds:

Current Illness: Alcohol use (4 times a week, glass of wine); Non-smoker

ID: 1261442
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: TOE TURNED BLUE; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown) dose was not reported, administered on APR-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On APR-2021, the subject experienced toe turned blue. Treatment medications (dates unspecified) included: acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from toe turned blue on APR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261443
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: SICK; FEVER 101; This spontaneous report received from a patient via a company representative concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's concurrent conditions included allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the subject experienced sick, and fever 101. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) 101 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sick, and fever 101. This report was non-serious.

Other Meds:

Current Illness: Allergy multiple

ID: 1261444
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: SWOLLEN LYMPH NODES; DISCOLORATION ON THE INJECTION SITE (BIG BRUISE); PAIN; VOMITING; HEADACHE; NAUSEA; FATIGUE; This spontaneous report received from a parent concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's past medical history included brain aneurysm. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805029, and expiry: UNKNOWN) dose was not reported, administered on 13-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced swollen lymph nodes. On 13-MAR-2021, the subject experienced discoloration on the injection site (big bruise). On 13-MAR-2021, the subject experienced pain. On 13-MAR-2021, the subject experienced vomiting. On 13-MAR-2021, the subject experienced headache. On 13-MAR-2021, the subject experienced nausea. On 13-MAR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, pain, vomiting, swollen lymph nodes, discoloration on the injection site (big bruise), nausea, and fatigue. This report was non-serious.

Other Meds:

Current Illness:

ID: 1261445
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 03/31/2021
Rec V Date: 04/27/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: FLU-LIKE SYMPTOMS(FEVER,ACHES,HEADACHE,PAINS); TOE CRAMPED UP; SHOOTING CRAMP PAIN BEHIND KNEE CAP AND PAIN IN CALF; This spontaneous report received from a patient concerned a female of unspecified age. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 042A21A expiry: UNKNOWN) dose was not reported, administered on 31-MAR-2021 09:00 for prophylactic vaccination. No concomitant medications were reported. On 2021, the subject experienced toe cramped up. On 2021, the subject experienced shooting cramp pain behind knee cap and pain in calf. On 31-MAR-2021, the subject experienced flu-like symptoms (fever, aches, headache, pains). Laboratory data included: Body temperature (NR: not provided) 101.2. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flu-like symptoms(fever, aches, headache, pains) on 01-APR-2021, and the outcome of shooting cramp pain behind knee cap and pain in calf and toe cramped up was not reported. This report was non-serious.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm