VAERS 2021 Database www.vaers.hhs.gov

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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: 1245141
Sex: F
Age:
State: IL

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: FLU LIKE SYMPTOMS; SORE ARM; FEVER; NAUSEA; 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: 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 APR-2021, the subject experienced flu like symptoms. On APR-2021, the subject experienced sore arm. On APR-2021, the subject experienced fever. On APR-2021, the subject experienced nausea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the flu like symptoms, fever, nausea and sore arm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245142
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/23/2021
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: LEGS SWOLLEN FROM THE KNEE DOWN; ARMS FEEL KIND OF WEIRD; FEELING OF LEGS KIND OF DETACHING FROM THE BODY; FEELING LIKE WHEN YOU PRESS YOUR FEET AND IT'S DIFFERENT, NOT PUFFY; ARMS FEEL SWOLLEN; TINGLING IN RIGHT ARM; WHEN GOING TO SLEEP LEGS FEEL VERY HEAVY/LEGS FROM THIGHS TO FEET, ENTIRE LEG, FEELS HEAVY JUST BEFORE FALLING ASLEEP; VERY TIRED; A LITTLE BIT OF HEADACHE; FLAVOR IN HER MOUTH LIKE ORANGE OR CHERRY; This spontaneous report received from a patient concerned a 59 year old female. The patient's weight was not reported and height was 64 inches. The patient's concurrent conditions included alcohol use, and non-smoker, and other pre-existing medical conditions included patient had no known drug allergies and medical conditions. the patient did not take medication regularly. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 202A21A, and batch number: 202A21A expiry: UNKNOWN) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-APR-2021, the subject experienced flavor in her mouth like orange or cherry. On 08-APR-2021, the subject experienced very tired. On 08-APR-2021, the subject experienced a little bit of headache. On an unspecified date, the subject experienced legs swollen from the knee down, arms feel kind of weird, feeling of legs kind of detaching from the body, feeling like when you press your feet and it's different, not puffy, arms feel swollen, tingling in right arm, and when going to sleep legs feel very heavy/legs from thighs to feet, entire leg, feels heavy just before falling asleep. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flavor in her mouth like orange or cherry on 08-APR-2021, and very tired, and a little bit of headache on 09-APR-2021, and had not recovered from legs swollen from the knee down, arms feel kind of weird, when going to sleep legs feel very heavy/legs from thighs to feet, entire leg, feels heavy just before falling asleep, feeling of legs kind of detaching from the body, arms feel swollen, tingling in right arm, and feeling like when you press your feet and it's different, not puffy. This report was non-serious.

Other Meds:

Current Illness: Alcohol use (very rarely.); Non-smoker (very rarely)

ID: 1245143
Sex: M
Age:
State: NY

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/23/2021
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: LUMP AT THE INJECTION SITE WAS PURPLY COLOR; INJECTION SITE WAS WARM; SORE ARM; 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 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: 202A21A, expiry: UNKNOWN) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-APR-2021, the subject experienced lump at the injection site was purply color. On 08-APR-2021, the subject experienced sore arm. On 08-APR-2021, the subject experienced injection site was warm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm on 12-APR-2021, and was recovering from lump at the injection site was purply color, and injection site was warm. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245144
Sex: F
Age:
State: OK

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: MINOR ITCHY ON INJECTION ARM; SORENESS ON INJECTION ARM; This spontaneous report received from a patient concerned a 43 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 09-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced minor itchy on injection arm. On APR-2021, the subject experienced soreness on injection arm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the minor itchy on injection arm and soreness on injection arm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245145
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: BODY ACHES; CHILLS; FEVER; HEADACHE; FATIGUE; This spontaneous report received from a consumer concerned a 23 year old female. The patient's height, and weight were not reported. The patient's 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: 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 body aches. On APR-2021, the subject experienced chills. On APR-2021, the subject experienced fever. On APR-2021, the subject experienced headache. On APR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches, chills, fever, headache, and fatigue on APR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245146
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 04/16/2021
Rec V Date: 04/23/2021
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: SORENESS IN LEFT ARM AT INJECTION SITE; FEELING TIRED; This spontaneous report received from a patient concerned a 66 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included high blood pressure, anxiety, non alcoholic, and non smoker, and other pre-existing medical conditions included the patient had no known drug allergies. there were no drug abuse or illicit drug usage. the patient was on anxiety medication. 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 16-APR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 16-APR-2021, the subject experienced soreness in left arm at injection site. On 16-APR-2021, the subject experienced feeling tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from soreness in left arm at injection site on 19-APR-2021, and was recovering from feeling tired. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Anxiety (Patient used anxiety medications.); Blood pressure high; Non-smoker

ID: 1245147
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 04/10/2021
Rec V Date: 04/23/2021
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: FLUSHED; WATERING EYES; SUNBURN-LIKE RASH; CHILLS; LOW GRADE FEVER; This spontaneous report received from a patient concerned a 62 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included copd from 911 exposure, asthma, chronic rhinitis, thyroiditis, lipidaemia, codeine allergy, and levaquin allergy. The patient experienced drug allergy when treated with betamethasone, ciprofloxacin, and bupivacaine hydrochloride/epinephrine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported and batch number: 205A21A expiry: UNKNOWN) dose was not reported, administered on 10-APR-2021 09:30 for prophylactic vaccination. No concomitant medications were reported. On 10-APR-2021, the subject experienced flushed. On 10-APR-2021, the subject experienced watering eyes. On 10-APR-2021, the subject experienced sunburn-like rash. On 10-APR-2021, the subject experienced chills. On 10-APR-2021, the subject experienced low grade fever. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flushed, and sunburn-like rash on 11-APR-2021, and watering eyes, chills, and low grade fever on 12-APR-2021. This report was non-serious.

Other Meds:

Current Illness: Allergic reaction to antibiotics; Asthma; Chronic rhinitis; COPD; Drug allergy; Hyperlipidaemia; Thyroiditis

ID: 1245148
Sex: F
Age:
State: NC

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/23/2021
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: PAIN ON RIGHT SIDE OF BODY/HURT ALL OVER; FELT SICK; SEVERE HEADACHE; This spontaneous report received from a patient concerned a 56 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, and batch number: 043A21A expiry: UNKNOWN) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-APR-2021, the subject experienced pain on right side of body/hurt all over. On 08-APR-2021, the subject experienced felt sick. On 08-APR-2021, the subject experienced severe headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from pain on right side of body/hurt all over, and felt sick on 18-APR-2021, and was recovering from severe headache. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245149
Sex: F
Age:
State: IL

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/23/2021
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: STARTED PERIODS X 2; THROBBING ARM (CARPAL TUNNEL AREA); STOMACH PAINS; CHILLS; TENDER BREASTS; EMOTIONAL; This spontaneous report received from a patient concerned a 48 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, and expiry: 13-JUN-2021) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-APR-2021, the subject experienced tender breasts. On 08-APR-2021, the subject experienced emotional. On 08-APR-2021, the subject experienced chills. On 09-APR-2021, the subject experienced stomach pains. On 10-APR-2021, the subject experienced started periods x 2. On 10-APR-2021, the subject experienced throbbing arm (carpal tunnel area). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from stomach pains on 12-APR-2021, and chills on 08-APR-2021, was recovering from tender breasts, and the outcome of emotional, throbbing arm (carpal tunnel area) and started periods x 2 was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245150
Sex: M
Age:
State: CO

Vax Date:
Onset Date: 04/06/2021
Rec V Date: 04/23/2021
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: BODY ACHES; TIREDNESS; This spontaneous report received from a patient concerned a 54 year old male. The patient's weight was 280 pounds, and height was 65 inches. The patient's concurrent conditions included non smoker, and non alcohol user, and other pre-existing medical conditions included the patient had no known allergies. the patient have no history of 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: 042A21A, expiry: UNKNOWN) dose was not reported, administered on 06-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 06-APR-2021, the subject experienced tiredness. On 07-APR-2021, the subject experienced body aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches on 08-APR-2021, and tiredness on 07-APR-2021. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Non-smoker

ID: 1245151
Sex: M
Age:
State: VA

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: INJECTION SITE PAIN; ARM PAIN; This spontaneous report received from a consumer concerned a 72 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: 202A21A expiry: UNKNOWN) dose was not reported, administered on 09-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced arm pain. On 11-APR-2021, the subject experienced injection site pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from injection site pain, and arm pain. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245152
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: SLEEPING PROBLEM; TINNITUS; MUSCLE ACHES; NAUSEA; FATIGUE; HEADACHES; NIGHTMARES; MOVEMENTS REDUCED; WEIGHT LOSS; This spontaneous report received from a patient concerned a 51 year old female. The patient's weight was 140 pounds, and height was 69 inches. The patient's concurrent conditions included no alcohol use, and non-smoker, and other pre-existing medical conditions included patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 041A21A, and batch number: 041A21A expiry: UNKNOWN) dose was not reported, administered on 06-APR-2021 for prophylactic vaccination. Concomitant medications included ascorbic acid for drug used for unknown indication, and ascorbic acid/ergocalciferol/folic acid/nicotinamide/panthenol/retinol/riboflavin/thiamine hydrochloride for drug used for unknown indication. On APR-2021, the subject experienced weight loss. On 07-APR-2021, the subject experienced nightmares. On 07-APR-2021, the subject experienced movements reduced. On 07-APR-2021, the subject experienced muscle aches. On 07-APR-2021, the subject experienced nausea. On 07-APR-2021, the subject experienced fatigue. On 07-APR-2021, the subject experienced headaches. On 18-APR-2021, the subject experienced sleeping problem. On 18-APR-2021, the subject experienced tinnitus. Treatment medications included: cannabinoids nos/cannabis sativa. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from nightmares on 07-APR-2021, had not recovered from headaches, fatigue, nausea, muscle aches, movements reduced, and tinnitus, and the outcome of weight loss and sleeping problem was not reported. This report was non-serious.

Other Meds: MULTIVITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;FOLIC ACID;NICOTINAMIDE;PANTHENOL;RETINOL;RIBOFLAVIN;THI; ASCORBIC ACID

Current Illness: Abstains from alcohol; Non-smoker

ID: 1245153
Sex: F
Age:
State: WI

Vax Date:
Onset Date: 04/15/2021
Rec V Date: 04/23/2021
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: NEEDLE-LIKE PAIN ON SIDES OF NECK; NEEDLE-LIKE PAIN IN CALF AREA OF FRONT AND BACK OF BOTH LEGS; 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 hypertension, and concurrent conditions included iodine allergy, and shellfish allergy.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 043121A, and batch number: 043121A expiry: UNKNOWN) dose was not reported, administered on 09-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-APR-2021, the subject experienced needle-like pain in calf area of front and back of both legs. On 18-APR-2021, the subject experienced needle-like pain on sides of neck. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from needle-like pain in calf area of front and back of both legs, and needle-like pain on sides of neck. This report was non-serious.

Other Meds:

Current Illness: Iodine allergy; Shellfish allergy

ID: 1245154
Sex: F
Age:
State: MI

Vax Date:
Onset Date: 04/02/2021
Rec V Date: 04/23/2021
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: SORENESS AT THE SITE OF INJECTION; FEVER; This spontaneous report received from a consumer concerned a female of unspecified age. The patient's height, and weight were not reported. The patient's concurrent conditions included parkinson's disease, and alzheimer disease.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805018 expiry: UNKNOWN) dose was not reported, administered on 02-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 02-APR-2021, the subject experienced soreness at the site of injection. On 02-APR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from soreness at the site of injection, and fever on 02-APR-2021. This report was non-serious. This case, from the same reporter is linked to 20210410164.

Other Meds:

Current Illness: Alzheimer's disease; Parkinson's disease

ID: 1245155
Sex: U
Age:
State: AZ

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: BODY ACHES; WICKED 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: 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 wicked fever, and body aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the wicked fever and body aches was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245156
Sex: F
Age:
State: MO

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 04/23/2021
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: SORE ARM; FEVER; This spontaneous report received from a patient concerned a 72 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included pre diabetic, and pre cholesterol. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 203A21A, and expiry: 23-JUN-2021) dose was not reported, administered on 09-APR-2021 10:00 for prophylactic vaccination. No concomitant medications were reported. On 09-APR-2021, the subject experienced sore arm. On 09-APR-2021, the subject experienced fever. Laboratory data included: Body temperature (NR: not provided) 99.8 F. Treatment medications (dates unspecified) included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm, and fever. This report was non-serious.

Other Meds:

Current Illness: High cholesterol (Pre cholesterol with no medication); Pre-diabetic (Pre diabetic with no medication)

ID: 1245157
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/23/2021
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: TINGLING IN RIGHT ARM THAT LASTED 15 MINUTES AFTER INJECTION; This spontaneous report received from a patient concerned a 74 year old female. The patient's height, and weight were not reported. The patient's past medical history included hysterectomy, and concurrent conditions included congestive heart failure, diabetes, high blood pressure, allergies to tree, allergies to grass pollen, and left ventricular block. The patient was previously treated with , oral contraceptive nos for drug used for unknown indication; and experienced drug allergy and heart race when treated with hydrocodone bitartrate/paracetamol for drug used for unknown indication, drug allergy when treated with sulfamethoxazole/trimethoprim, povidone-iodine, codeine, erythromycin, and benzylpenicillin for drug used for unknown indication. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808609, and expiry: UNKNOWN) dose was not reported, administered on 23-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 23-MAR-2021, the subject experienced tingling in right arm that lasted 15 minutes after injection. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from tingling in right arm that lasted 15 minutes after injection on 23-MAR-2021. This report was non-serious.

Other Meds:

Current Illness: Blood pressure high; Congestive heart failure; Diabetes; LBBB; Pollen allergy; Seasonal allergy

ID: 1245158
Sex: F
Age:
State: TN

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/23/2021
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: TOES NUMB RIGHT FOOT; NUMBNESS IN LEFT HAND; CRAMPING RIGHT HAND; CHILLS; SLEEPY; This spontaneous report received from a consumer concerned a 67 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: 1805020 expiry: UNKNOWN) dose was not reported, administered on 08-APR-2021 09:30 for prophylactic vaccination. No concomitant medications were reported. On 08-APR-2021, the subject experienced sleepy. On 08-APR-2021, the subject experienced chills. On 13-APR-2021, the subject experienced cramping right hand. On 14-APR-2021, the subject experienced numbness in left hand. On 16-APR-2021, the subject experienced toes numb right foot. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sleepy on 17-APR-2021, numbness in left hand on 14-APR-2021, cramping right hand on 13-APR-2021, and chills on 09-APR-2021, and had not recovered from toes numb right foot. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245159
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: HOT FLASHES; EVERYTHING HURT FOR A SOLID 12 HOURS; CHILL; FEVER OVERNIGHT; 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. 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 hot flashes, everything hurt for a solid 12 hours, chill, and fever overnight. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from hot flashes, everything hurt for a solid 12 hours, chill, and fever overnight. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245160
Sex: U
Age:
State: GA

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/23/2021
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: FEELING AWFUL; BEACH ACHE; COULDN'T FUNCTION; 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 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 MAR-2021, the patient experienced couldn't function. On 12-MAR-2021, the patient experienced feeling awful. On 12-MAR-2021, the patient experienced beach ache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the feeling awful, beach ache and couldn't function was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245161
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 04/23/2021
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: SORENESS IN ARM AT INJECTION SITE; 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: 201A21A, and expiry: UNKNOWN) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-APR-2021, the subject experienced soreness in arm at injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from soreness in arm at injection site. This report was non-serious. This case, from the same reporter is linked to 20210430095.

Other Meds:

Current Illness:

ID: 1245162
Sex: U
Age:
State:

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 04/23/2021
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: NUMBNESS IN TONGUE; TINGLING IN TONGUE; MIGRAINE HEADACHE; SENSES WERE ALL HYPERSENSITIVE/ SENSE OF SMELL; This spontaneous report received from a patient concerned a 66 year old of unspecified sex. The patient's height, and weight were not reported. The patient's past medical history included migraine. The patient was previously treated with acetylsalicylic acid/caffeine/paracetamol/salicylamide for migraine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 041H21A/041A21A/041H21H expiry: UNKNOWN) dose was not reported, administered on 02-APR-2021 for prophylactic vaccination. Concomitant medications included estradiol, levothyroxine sodium, progesterone, and testosterone. On 09-APR-2021, the subject experienced numbness in tongue. On 09-APR-2021, the subject experienced tingling in tongue. On 09-APR-2021, the subject experienced migraine headache. On 09-APR-2021, the subject experienced senses were all hypersensitive/ sense of smell. Treatment medications (dates unspecified) included: acetylsalicylic acid/caffeine/paracetamol/salicylamide. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from migraine headache, and the outcome of numbness in tongue, tingling in tongue and senses were all hypersensitive/ sense of smell was not reported. This report was non-serious.

Other Meds: SYNTHROID; ESTRADIOL; PROGESTERONE; TESTOSTERONE

Current Illness:

ID: 1245163
Sex: F
Age:
State: MO

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: TINGLING SENSATION IN LEGS; VARICOSE VEINS; BRUISING; LEG PAIN; TEETH CHATTERING/ CHILLS; HEADACHE; FEELING HOT; FLU LIKE SYMPTOMS; This spontaneous report received from a patient concerned a 35 year old female. The patient's height, and weight were not reported. The patient's past medical history included anemia, and concurrent conditions included acne, amoxicillin allergy, non-smoker, and migraine. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 042A21A, and batch number: 042A21A expiry: UNKNOWN) dose was not reported, administered on 31-MAR-2021 14:30 for prophylactic vaccination. Concomitant medications included spironolactone for topical acne. On 01-APR-2021 03:00, the subject experienced feeling hot. On 01-APR-2021 03:00, the subject experienced flu like symptoms. On 01-APR-2021 03:00, the subject experienced teeth chattering/ chills. On 01-APR-2021 03:00, the subject experienced headache. On 05-APR-2021, the subject experienced tingling sensation in legs. On 05-APR-2021, the subject experienced varicose veins. On 05-APR-2021, the subject experienced bruising. On 05-APR-2021, the subject experienced leg pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from feeling hot, flu like symptoms, and teeth chattering/ chills on 02-APR-2021, and was recovering from headache, leg pain, tingling sensation in legs, varicose veins, and bruising. This report was non-serious.

Other Meds: SPIRONOLACTONE

Current Illness: Acne; Allergic reaction to antibiotics; Migraine; Non-smoker

ID: 1245164
Sex: U
Age:
State: GA

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: RASH; This spontaneous report received from a patient via a company representative 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. 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 rash. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of rash was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245165
Sex: F
Age:
State: PA

Vax Date:
Onset Date: 04/11/2021
Rec V Date: 04/23/2021
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: SHORTNESS OF BREATH (SLIGHT AND NOT ALL THE TIME); VERTIGO; FELT OFF BALANCE; PRESSURE PRIMARILY ON LEFT SIDE OF HEAD; LOCALIZED HEADACHE PRIMARILY TO THE LEFT SIDE; TIRED; ACHES AND PAIN; FOGGY; This spontaneous report received from a patient concerned a 50 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: 202A21A, and 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 aches and pain. On 11-APR-2021, the subject experienced foggy. On 11-APR-2021, the subject experienced tired. On 12-APR-2021, the subject experienced pressure primarily on left side of head. On 12-APR-2021, the subject experienced localized headache primarily to the left side. On 14-APR-2021, the subject experienced vertigo. On 14-APR-2021, the subject experienced felt off balance. On 18-APR-2021, the subject experienced shortness of breath (slight and not all the time). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from aches and pain, foggy, and tired on 11-APR-2021, and vertigo, and felt off balance on 14-APR-2021, was recovering from shortness of breath (slight and not all the time), and had not recovered from pressure primarily on left side of head, and localized headache primarily to the left side. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245166
Sex: F
Age:
State: OH

Vax Date:
Onset Date: 03/06/2021
Rec V Date: 04/23/2021
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: SLIGHT HEADACHE; SORE ARM AT SITE OF INJECTION; CRAWLING SENSATION; COLD; This spontaneous report received from a patient concerned a 62 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included sulfa allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1802068, expiry: 19/MAY/2021) dose was not reported, administered on 06-MAR-2021 13:15 for prophylactic vaccination. No concomitant medications were reported. On 06-MAR-2021, the subject experienced crawling sensation. On 06-MAR-2021, the subject experienced cold. On 06-MAR-2021, the subject experienced sore arm at site of injection. On 07-MAR-2021, the subject experienced slight headache. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from crawling sensation, and cold on 07-MAR-2021, slight headache on 08-MAR-2021, and sore arm at site of injection on MAR-2021. This report was non-serious.

Other Meds:

Current Illness: Allergic reaction to antibiotics

ID: 1245167
Sex: F
Age:
State: DE

Vax Date:
Onset Date: 04/11/2021
Rec V Date: 04/23/2021
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: INJECTION SITE ITCHY; CHILLS; PAIN/SORENESS IN LEFT ARM AFTER SHORT; This spontaneous report received from a patient concerned a 45 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included high blood pressure, thyroid problems, and seasonal allergies. The patient experienced drug allergy when treated with acetylsalicylic acid. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 202A21A, and batch number: 202A21A expiry: UNKNOWN) dose was not reported, administered on 11-APR-2021 for prophylactic vaccination. Concomitant medications included lisinopril for high blood pressure, and levothyroxine sodium for thyroid problems. On 11-APR-2021, the subject experienced pain/soreness in left arm after short. On 12-APR-2021, the subject experienced chills. On 13-APR-2021, the subject experienced injection site itchy. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pain/soreness in left arm after short, and the outcome of chills and injection site itchy was not reported. This report was non-serious.

Other Meds: LISINOPRIL; SYNTHROID

Current Illness: Blood pressure high; Seasonal allergy; Thyroid disorder

ID: 1245168
Sex: M
Age:
State: IN

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: TINGLING ON ELBOW DOWN TO FINGERS; PAIN IN ARM; This spontaneous report received from a parent concerned a 38 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: Unk) dose was not reported, administered on 12-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 tingling on elbow down to fingers. On APR-2021, the subject experienced pain in arm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the pain in arm and tingling on elbow down to fingers was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245169
Sex: F
Age:
State: MI

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 04/23/2021
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: TINY RASH; SORE ARM; This spontaneous report received from a patient concerned a 58 year old female. The patient's height, and weight were not reported. The patient's past medical history included blood transfusion, and concurrent conditions included epilepsy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 207A21A expiry: UNKNOWN) dose was not reported, administered on 09-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-APR-2021, the subject experienced sore arm. On 11-APR-2021, the subject experienced tiny rash. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from sore arm, and the outcome of tiny rash was not reported. This report was non-serious.

Other Meds:

Current Illness: Epilepsy

ID: 1245170
Sex: U
Age:
State:

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 04/23/2021
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: CHEST TIGHTNESS AND DISCOMFORT; SLIGHT SHORTNESS OF BREATH; DRY COUGH; 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, and batch number were not reported) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 09-APR-2021, the patient experienced chest tightness and discomfort. On 09-APR-2021, the patient experienced slight shortness of breath. On 09-APR-2021, the patient experienced dry cough. On 12-APR-2021, Laboratory data included: Chest X-ray (NR: not provided) Normal, Echocardiogram (NR: not provided) Normal, Electrocardiogram (NR: not provided) Normal, and Fibrin D dimer (NR: not provided) Normal. On 14-APR-2021, Laboratory data included: COVID-19 virus test (NR: not provided) Negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chest tightness and discomfort, slight shortness of breath, and dry cough. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245171
Sex: F
Age:
State: VA

Vax Date:
Onset Date: 03/26/2021
Rec V Date: 04/23/2021
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: CHILLS; FATIGUE; This spontaneous report received from a patient concerned a 59 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, and expiry: UNKNOWN) dose was not reported, administered on 26-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 26-MAR-2021, the subject experienced chills. On 26-MAR-2021, the subject experienced fatigue. On 16-APR-2021, Laboratory data included: Antibody test (NR: not provided) NEGATIVE. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, and the outcome of fatigue was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245172
Sex: M
Age:
State: TX

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: FATIGUE WORSENED; HEADACHE; SORE MUSCLES OR MUSCLE ACHE; NAUSEA; This spontaneous report received from a consumer 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: 201A21A expiry: UNKNOWN) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced nausea. On 08-APR-2021, the subject experienced headache. On 08-APR-2021, the subject experienced sore muscles or muscle ache. On 15-APR-2021, the subject experienced fatigue worsened. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from nausea on APR-2021, and had not recovered from headache, sore muscles or muscle ache, and fatigue worsened. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245173
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 04/17/2021
Rec V Date: 04/23/2021
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: NAUSEA; HEADACHE; TIREDNESS; LIGHT FEVER; BODY ACHES/PAIN; DIARRHEA; This spontaneous report received from a consumer concerned a 52 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included lupus. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808980, expiry: UNKNOWN) dose was not reported, administered on 06-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 17-APR-2021, the subject experienced diarrhea. On an unspecified date, the subject experienced body aches/pain, nausea, headache, tiredness, and light fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from body aches/pain, nausea, headache, tiredness, diarrhea, and light fever. This report was non-serious.

Other Meds:

Current Illness: Lupus erythematosus

ID: 1245174
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: DIARRHEA; NAUSEA; HEADACHE; TIRED; LIGHT FEVER; ACHES/PAINS; This spontaneous report received from a consumer concerned a 52 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: 1808980, and 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 aches/pains. On APR-2021, the subject experienced nausea. On APR-2021, the subject experienced headache. On APR-2021, the subject experienced tired. On APR-2021, the subject experienced light fever. On 17-APR-2021, the subject experienced diarrhea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from aches/pains, diarrhea, nausea, headache, tired, and light fever. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245175
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: BLOOD SUGAR INCREASE; 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 diabetic. 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 blood sugar increase. Laboratory data (dates unspecified) included: Blood glucose increased (NR: not provided) more than 400. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of blood sugar increase was not reported. This report was non-serious.

Other Meds:

Current Illness: Diabetic

ID: 1245176
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: FELT PRETTY OFF; CHILLS; FEVER; HEADACHE; TIRED; This spontaneous report received from a patient via a company representative 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. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the subject experienced felt pretty off, chills, fever, headache, and tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from felt pretty off, chills, fever, headache, and tired. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245177
Sex: U
Age:
State:

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: ERECTION FOR 16 HOURS; This spontaneous report received from a patient via a company representative 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. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On APR-2021, the subject experienced erection for 16 hours. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of erection for 16 hours was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245178
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: CHEST PAIN; 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, 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 chest pain. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of chest pain was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245179
Sex: F
Age:
State: PA

Vax Date:
Onset Date: 04/09/2021
Rec V Date: 04/23/2021
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: MALAISE; MILD DEHYDRATION; CHEST PAIN; CHILLS; GENERALIZED WEAKNESS; HEADACHE; This spontaneous report received from a physician 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: 043A21A, expiry: UNKNOWN) dose was not reported, administered on 07-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-APR-2021, the patient experienced chest pain. On 09-APR-2021, the patient experienced chills. On 09-APR-2021, the patient experienced generalized weakness. On 09-APR-2021, the patient experienced headache. On 19-APR-2021, the patient experienced mild dehydration. On 19-APR-2021, the patient experienced malaise. Laboratory data included: CT scan (NR: not provided) UNKNOWN, and EKG (NR: not provided) UNKNOWN. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache, generalized weakness, chills, chest pain, malaise and mild dehydration was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245180
Sex: M
Age:
State: NJ

Vax Date:
Onset Date: 03/31/2021
Rec V Date: 04/23/2021
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: STOMACH ACHE; LOSS OF APPETITE; DIARRHEA; NAUSEA; NUMBNESS FROM HEAD TO LEGS ON LEFT SIDE; FEVER; PAIN IN KIDNEYS; This spontaneous report received from a patient concerned a 24 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: 1808978, and batch number: 1808978 expiry: UNKNOWN) dose was not reported, administered on 31-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 2021, the subject experienced pain in kidneys. On MAR-2021, treatment medications included: paracetamol. On 31-MAR-2021, the subject experienced numbness from head to legs on left side. On 31-MAR-2021, the subject experienced fever. On APR-2021, the subject experienced stomach ache. On APR-2021, the subject experienced loss of appetite. On APR-2021, the subject experienced diarrhea. On APR-2021, the subject experienced nausea. Additional treatment medications (dates unspecified) included: calcium carbonate. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from stomach ache, loss of appetite, diarrhea, and nausea on APR-2021, numbness from head to legs on left side on 31-MAR-2021, and fever on 03-APR-2021, and the outcome of pain in kidneys was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245181
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: PAIN OF EXTREMITIES; This spontaneous report received from a patient. The patient's past medical history included numbness in hand, and pain in fingers, and concurrent conditions included osteoarthritis, no tobacco use, knee pain on and off, skin discoloration, sleep unwell, pain, paresthesia of fingers, psoriasis flare-up, bone pain, and skin breakout.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 041A24A, and expiry: UNKNOWN) dose was not reported, administered on 02-APR-2021 for prophylactic vaccination. Concomitant medications included adalimumab for psoriatic arthritis, and rheumatoid arthritis. On 2021, the subject experienced pain of extremities. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pain of extremities. This report was non-serious..

Other Meds: HUMIRA

Current Illness: Bone pain; Knee pain; Non-smoker; Osteoarthritis; Pain; Paresthesia of fingers; Psoriasis flare-up; Skin breakout; Skin discoloration; Sleep unwell

ID: 1245182
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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; SHAKES; CHILLS; 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, 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 fever, shakes, and chills. 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 outcome of the fever, shakes and chills was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245183
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: TERRIBLE BODY ACHES; FEVER; HEADACHE; 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. 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 terrible body aches, fever, and headache. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) 102. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from terrible body aches, fever, and headache. This report was non-serious. This parent/child case is linked to 20210439367.

Other Meds:

Current Illness:

ID: 1245184
Sex: F
Age:
State: VA

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 04/23/2021
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: A SLIGHT BRUISE AT INJECTION SITE; SORE ARM; 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, and batch number: 202A21A expiry: UNKNOWN) dose was not reported, administered on 09-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On APR-2021, the subject experienced sore arm. On 10-APR-2021, the subject experienced a slight bruise at injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from a slight bruise at injection site, and the outcome of sore arm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245190
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/23/2021
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: ENTIRE BODY HURT SO BAD THAT COULD NOT SIT/ STAND/LIE DOWN; ENTIRE RIGHT ARM ACHES; FEVER; A CONSTANT DULL HEADACHE; 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 entire body hurt so bad that could not sit/ stand/lie down. On MAR-2021, the subject experienced entire right arm aches. On MAR-2021, the subject experienced fever. On MAR-2021, the subject experienced a constant dull headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from a constant dull headache, and the outcome of fever, entire body hurt so bad that could not sit/ stand/lie down and entire right arm aches was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245197
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: TERRIBLE BODY ACHES; FEVER; HEADACHE; This spontaneous report received from a patient via a company representative 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: 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 terrible body aches, fever, and headache. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) 102 (unit not reported). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from terrible body aches, fever, and headache. This report was non-serious. This case, from the same reporter is linked to 20210439312.

Other Meds:

Current Illness:

ID: 1245204
Sex: F
Age:
State: OH

Vax Date:
Onset Date: 04/05/2021
Rec V Date: 04/23/2021
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: FEVER; FELT TIRED; RUNNY NOSE; This spontaneous report received from a patient concerned a 66 year old female. The patient's height, and weight were not reported. The patient was not pregnant at the time of reporting. The patient's concurrent conditions included penicillin and codeine allergy, alcohol use, and smoker, 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: 1808980, expiry: UNKNOWN) dose was not reported, administered on 03-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 05-APR-2021, the subject experienced runny nose. On 06-APR-2021, the subject experienced fever. On 06-APR-2021, the subject experienced felt tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from runny nose, fever, and felt tired. This report was non-serious.

Other Meds:

Current Illness: Alcohol use (Consumes 3-4 per month.); Smoker (Smokes black and milds); Specific allergy (drug)

ID: 1245209
Sex: F
Age:
State: VA

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: INSOMNIA; 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, 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 insomnia. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of insomnia was not reported. This report was non-serious. This case, from the same reporter is linked to 20210422203.

Other Meds:

Current Illness:

ID: 1245216
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/23/2021
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: HEADACHE; FEVER; This spontaneous report received from a patient via a company representative 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. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the subject experienced headache, and fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache and fever was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1245224
Sex: F
Age:
State: WA

Vax Date:
Onset Date: 04/08/2021
Rec V Date: 04/23/2021
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: VERY DEBILITATING; HEADACHE; DIZZY; SORE ARM; This spontaneous report received from a patient concerned a 50 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: 202A21A expiry: UNKNOWN) dose was not reported, administered on 08-APR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-APR-2021, the subject experienced dizzy. On 08-APR-2021, the subject experienced sore arm. On 20-APR-2021, the subject experienced very debilitating. On 20-APR-2021, the subject experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from dizzy, and sore arm on 09-APR-2021, and had not recovered from headache, and very debilitating. This report was non-serious.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm