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**
PLEASE CHECK BACK SOON
Download the files above while you wait.






Manufacturers

Total Manufacturer

Incidents per State

State Total
72,296
AK1,638
AL5,339
AR3,412
AS44
AZ13,316
CA58,147
CO11,002
CT7,824
DC1,626
DE1,670
FL36,235
FM3
GA13,429
GU82
HI2,195
IA4,332
ID2,473
IL19,261
IN22,568
KS4,284
KY6,945
LA4,714
MA13,886
MD11,901
ME2,997
MH8
MI17,865
MN11,345
MO8,919
MP30
MS2,676
MT2,147
NC15,401
ND1,273
NE2,732
NH2,859
NJ17,232
NM3,702
NV4,071
NY32,763
OH18,072
OK5,940
OR7,954
PA22,457
PR2,104
QM2
RI1,911
SC6,055
SD1,133
TN8,691
TX34,122
UT4,023
VA13,944
VI49
VT1,661
WA13,811
WI10,395
WV2,220
WY805
XB5
XL1
XV2

ID: 1230620
Sex: F
Age: 69
State: FL

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies: Several food, environmental, probiotic and some medications.

Symptom List:

Symptoms: Pain at injection site on day of shot, next day chills and achy which continued throughout the next day.

Other Meds: Calcium magnesium citrate, vitamin D, multivitamin. Probiotic.

Current Illness: None

ID: 1230621
Sex: F
Age: 25
State: NV

Vax Date: 04/05/2021
Onset Date: 04/14/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies: None

Symptom List:

Symptoms: Right leg numb and tingling for 3 days, headache for 1 week, stomach ache, joint pain.

Other Meds: None

Current Illness: None

ID: 1230622
Sex: M
Age: 57
State: OH

Vax Date: 03/18/2021
Onset Date: 03/19/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: Had a blood clot and a stroke and blind in right eye, and some paralysis in face. Happened day after first vaccine.

Other Meds:

Current Illness:

ID: 1230623
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/08/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: BODY ACHES; CHILLS; FEVER; HEADACHE; PAIN IN ARM AT VACCINATION SITE; 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: 1805022, and batch number: 1805022) dose was not reported, once a total administered on 08-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-MAR-2021, the subject experienced body aches. On 08-MAR-2021, the subject experienced chills. On 08-MAR-2021, the subject experienced fever. On 08-MAR-2021, the subject experienced headache. On 08-MAR-2021, the subject experienced pain in arm at vaccination site. Laboratory data included: Body temperature (NR: not provided) 102.9 (units unspecified). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches on 10-MAR-2021, chills, and fever on 08-MAR-2021, and headache on 09-MAR-2021, and was recovering from pain in arm at vaccination site. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230624
Sex: U
Age:
State: DC

Vax Date: 03/13/2021
Onset Date: 03/13/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER; NAUSEA; TIREDNESS; 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: 1805018, and batch number: 1805018 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 fever. On 13-MAR-2021, the subject experienced nausea. On 13-MAR-2021, the subject experienced tiredness. Laboratory data included: Body temperature (NR: not provided) 102.6. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the fever, nausea and tiredness was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230625
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: PAIN AT INJECTION SITE WHEN TOUCHED; 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, intramuscular, batch number: 180522, and batch number: 180522 expiry: UNKNOWN) .5 ml, administered on 12-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-MAR-2021, the subject experienced pain at injection site when touched. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of pain at injection site when touched was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230626
Sex: U
Age:
State: TX

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: A LITTLE NOSE BLEED IN ONE NOSTRIL; 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: 1805029, expiry: 05/MAY/2021) dose was not reported, administered on 13-MAR-2021 to upper left arm for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced a little nose bleed in one nostril. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from a little nose bleed in one nostril on 13-MAR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230627
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/08/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: HAIR FALLING OUT AND THINNING, CAN SEE SCALP; 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: 1805025, and batch number: 1805025 expiry: 31/MAR/2069) dose was not reported, administered on 06-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 08-MAR-2021, the subject experienced hair falling out and thinning, can see scalp. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from hair falling out and thinning, can see scalp. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230628
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: LIPS DRY; METALLIC TASTE; FATIGUE; MORE THIRSTY THAN USUAL; This spontaneous report received from a patient concerned a 59 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included alcoholic, and non smoker, and other pre-existing medical conditions included no drug abuse/ illicit drug used. The patient was previously treated with benzylpenicillin. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805022, and batch number: 1805022 expiry: UNKNOWN) 0 .5 ml, administered on 11-MAR-2021 03:00 pm for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, the subject experienced fatigue. On 11-MAR-2021, the subject experienced more thirsty than usual. On 11-MAR-2021, the subject experienced metallic taste. On 13-MAR-2021, the subject experienced lips dry. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from metallic taste on 11-MAR-2021, and had not recovered from fatigue, more thirsty than usual, and lips dry. This report was non-serious.

Other Meds:

Current Illness: Alcoholic (2-3 glasses of wine a week); Non-smoker

ID: 1230629
Sex: M
Age:
State: DC

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SLUGGISHNESS THE DAY AFTER; FEVERISH IN THE NIGHT OF VACCINATION; This spontaneous report received from a consumer via a company representative 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, intramuscular, batch number: Unknown, expiry: UNKNOWN) .5 ml, administered on 06-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On MAR-2021, the subject experienced feverish in the night of vaccination. On 07-MAR-2021, the subject experienced sluggishness the day after. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the feverish in the night of vaccination and sluggishness the day after was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230630
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: DECREASED APPETITE; TIREDNESS; TASTE PECULIAR(FUNNY TASTE IN MOUTH); CHILLS; This spontaneous report received from a patient concerned a 60 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included asthma allergies- used nasal-spray acid reflux- on nexium 20 mg twice daily chronic coughuse, alcoholic, covid-19 infection, and non smoker.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, and batch number: 1805025 expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 14:00 for prophylactic vaccination. Concomitant medications included esomeprazole magnesium for stomach -acid reflux. On DEC-2020, Laboratory data included: COVID-19 (NR: not provided) positive (units unspecified). On 11-MAR-2021, the subject experienced chills. On 12-MAR-2021, the subject experienced decreased appetite. On 12-MAR-2021, the subject experienced tiredness. On 12-MAR-2021, the subject experienced taste peculiar (funny taste in mouth). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chills, decreased appetite, tiredness, and taste peculiar(funny taste in mouth). This report was non-serious.

Other Meds: NEXIUM [ESOMEPRAZOLE MAGNESIUM]

Current Illness:

ID: 1230631
Sex: U
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: MUSCLE SPASMS IN ARM; 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. 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 muscle spasms in arm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of muscle spasms in arm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230632
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/06/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE THROAT; FELT OUT OF SORTS; SORE ARM; CHILLS; HEADACHE; FELT MILD QUEASY; This spontaneous report received from a patient via an unspecified 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: Unkown) dose was not reported, administered on 06-MAR-2021 for prophylactic vaccination. The batch number was not reported. The unspecified Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On 06-MAR-2021, the patient experienced chills, headache, felt mild queasy, sore arm. On 07-MAR-2021, the patient experienced felt out of sorts and sore throat. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, headache, felt mild queasy, sore arm, sore throat, and felt out of sorts. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230633
Sex: U
Age:
State: NC

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: HEADACHE; FEVER; FATIGUE; BUMPS ON THE HAND, FINGER AND WRIST THAT LOOK LIKE MOSQUITO BITES; ITCHY BUMPS; This spontaneous report received from 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, intramuscular, batch number: 1802070, expiry: UNKNOWN) .5 ml, administered on 11-MAR-2021 10:00 to Left Deltoid for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, the subject experienced itchy bumps. On 11-MAR-2021, the subject experienced bumps on the hand, finger and wrist that look like mosquito bites. On 12-MAR-2021, the subject experienced headache. On 12-MAR-2021, the subject experienced fever. On 12-MAR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever on 12-MAR-2021, and had not recovered from headache, itchy bumps, fatigue, and bumps on the hand, finger and wrist that look like mosquito bites. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230634
Sex: F
Age:
State: OH

Vax Date:
Onset Date: 03/10/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE ARM AT INJECTION SITE; 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, intramuscular, batch number: 1802068, expiry: not reported) .5 ml, administered on 10-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 10-MAR-2021, the subject experienced sore arm at injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from sore arm at injection site. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230635
Sex: M
Age:
State: MD

Vax Date:
Onset Date: 03/06/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: INJECTION SITE PAIN; TIRED; SLEEPINESS; FLU-LIKE SYMPTOMS; This spontaneous report received from a consumer concerned a 65 year old. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, and batch number: 1805022 expiry: 25/MAY/2021) .5 ml, administered on 06-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 06-MAR-2021, the patient experienced injection site pain. On 06-MAR-2021, the patient experienced tired. On 06-MAR-2021, the patient experienced sleepiness. On 06-MAR-2021, the patient experienced flu-like symptoms. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from injection site pain on 06-MAR-2021, and tired, sleepiness, and flu-like symptoms on 11-MAR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230636
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: PAIN IN EYE BONE; PAIN IN JAW/ HEADACHE LIKE PAIN INSIDE JAW BONES; 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, intramuscular, batch number: 1805031, and expiry: Unknown) 0.5 ml, administered on 12-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-MAR-2021, the subject experienced pain in eye bone. On 12-MAR-2021, the subject experienced pain in jaw/ headache like pain inside jaw bones. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from pain in eye bone, and pain in jaw/ headache like pain inside jaw bones. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230637
Sex: F
Age:
State: VT

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: DRY MOUTH; CHILLS; HEADACHES; BODY ACHES; FEVER 103.1; 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 alcoholic, and non-smoker, and other pre-existing medical conditions included patient have no known allergies.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805022 expiry: UNKNOWN) .5 ml, administered on 12-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 09-MAR-2021, Laboratory data included: COVID-19 virus test (NR: not provided) Negative. On 12-MAR-2021, the subject experienced chills. On 12-MAR-2021, the subject experienced headaches. On 12-MAR-2021, the subject experienced body aches. On 12-MAR-2021, the subject experienced dry mouth. On 12-MAR-2021, the subject experienced fever. Laboratory data included: Body temperature (NR: not provided) 103.1 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from chills, and had not recovered from headaches, body aches, dry mouth, and fever. This report was non-serious.

Other Meds:

Current Illness: Alcoholic; Non-smoker

ID: 1230638
Sex: F
Age:
State: NC

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: METALLIC TASTE APPEARED, WHICH PATIENT NOTICED WHEN DRINKING WATER,; FEVER; HEADACHE; FEELING OFF; BODY ACHES; CHILLS; NAUSEA; NOT BEEN ABLE TO EAT OR DRINK AS MUCH AS NORMAL; This spontaneous report received from a patient concerned a 27 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included alcohol user, non-smoker, and marijuana, 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, intramuscular, batch number: 1802070, and batch number: 1802070) dose was not reported, administered on 11-MAR-2021 09:30 for prophylactic vaccination. No concomitant medications were reported. On 01-FEB-2021, Laboratory data included: COVID-19 virus test (NR: not provided) Negative. On 11-MAR-2021, the subject experienced not been able to eat or drink as much as normal. On 11-MAR-2021, the subject experienced nausea. Laboratory data included: Body temperature (NR: not provided) 100.8 (units unspecified). On 11-MAR-2021 17:00, the subject experienced feeling off. On 11-MAR-2021 17:00, the subject experienced body aches. On 11-MAR-2021 17:00, the subject experienced chills. On 11-MAR-2021 17:00, the subject experienced fever. On 11-MAR-2021 17:00, the subject experienced headache. On 12-MAR-2021, the subject experienced metallic taste appeared, which subject noticed when drinking water. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches, chills, and fever on 12-MAR-2021, had not recovered from nausea, metallic taste appeared, which patient noticed when drinking water, and headache, and the outcome of not been able to eat or drink as much as normal and feeling off was not reported. This report was non-serious.

Other Meds:

Current Illness: Alcohol use (2-3 drinks per day.); Marijuana use; Non-smoker

ID: 1230639
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: KNOCKED ON ASS; CANNOT MOVE; ACHY; SHIVERING; RUNNING LIKE 103 FEVER; NAUSEOUS; 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 past medical history included covid 19.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: Unknown) dose was not reported, administered on MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On MAR-2020, Laboratory data included: Body temperature (NR: not provided) 103 F. On MAR-2021, the subject experienced knocked on bottom. On MAR-2021, the subject experienced cannot move. On MAR-2021, the subject experienced achy. On MAR-2021, the subject experienced shivering. On MAR-2021, the subject experienced running like 103 fever. On MAR-2021, the subject experienced nauseous. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the knocked on ass, cannot move, running like 103 fever, shivering, nauseous and achy was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230640
Sex: M
Age:
State:

Vax Date:
Onset Date: 03/14/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: CHILLS; HEADACHE; This spontaneous report received from a patient via a company representative 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, 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 14-MAR-2021, the patient experienced chills and headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the chills and headache was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230641
Sex: M
Age:
State:

Vax Date:
Onset Date: 03/14/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SORENESS AT INJECTION SITE; 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, intramuscular, batch number: Unknown) .5 ml, administered on 13-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 14-MAR-2021, the patient experienced soreness at Injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of soreness at Injection site was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230642
Sex: M
Age:
State: FL

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: BURNING ON TONGUE; SORE THROAT; 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: Unk) dose was not reported, administered on 13-MAR-2021 09:00 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 13-MAR-2021, the subject experienced burning on tongue. On 13-MAR-2021, the subject experienced sore throat. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the burning on tongue and sore throat was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230643
Sex: F
Age:
State: MO

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: BODY TWITCHING; HEADACHE; CHILLS; BODY ACHE; UPSET STOMACH; This spontaneous report received from a patient concerned a 65 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included non alcoholic, and non smoker, and other pre-existing medical conditions included the patient had no known drug or non drug allergy. the patient had no history of drug abuse or illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805018, and 1805018 expiry: UNKNOWN) dose was not reported, administered on 12-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 12-MAR-2021, the subject experienced headache. On 12-MAR-2021, the subject experienced chills. On 12-MAR-2021, the subject experienced body ache. On 12-MAR-2021, the subject experienced upset stomach. On 13-MAR-2021, the subject experienced body twitching. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, and upset stomach on 13-MAR-2021, and had not recovered from headache, body ache, and body twitching. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Non-smoker

ID: 1230644
Sex: U
Age:
State: CA

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: HEADACHE; FEVER; 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, intramuscular, batch number: 1805029, and batch number: 1805029 expiry: UNKNOWN) .5 ml, administered on 10-MAR-2021 15:00 for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021 07:00, the subject experienced headache. On 11-MAR-2021 07:00, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fever, and had not recovered from headache. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230645
Sex: F
Age:
State: OR

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: LEFT EAR ACHING; LEFT EAR THROBBING; LEFT SIDE NECK SORE; LEFT SIDE THROAT SORENESS; 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, intramuscular, batch number: 1805018, and expiry: UNKNOWN) .5 ml, administered on 12-MAR-2021 for prophylactic vaccination. Concomitant medications included paracetamol. On 12-MAR-2021, the patient experienced left ear aching, left ear throbbing, left side neck sore, and left side throat soreness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from left ear aching, left ear throbbing, left side neck sore, and left side throat soreness. This report was non-serious.

Other Meds: TYLENOL

Current Illness:

ID: 1230646
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/10/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: REDNESS AT INJECTION SITE; ITCHING AT INJECTION SITE; SWELLING 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: Unk) dose was not reported, administered on 09-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 10-MAR-2021, the subject experienced redness at injection site. On 10-MAR-2021, the subject experienced itching at injection site. On 10-MAR-2021, the subject experienced swelling at injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the redness at injection site, itching at injection site and swelling at injection site was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230647
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/10/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: VOMITING; DIFFICULTY IN SWALLOWING/ COULD NOT KEEP ANY FOOD DOWN; FACE HAS BROKEN OUT; HEADACHE; DIZZY; 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, intramuscular, batch number: Unknown) .5 ml, administered on 09-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 10-MAR-2021, the subject experienced vomiting. On 10-MAR-2021, the subject experienced difficulty in swallowing/ could not keep any food down. On 10-MAR-2021, the subject experienced face has broken out. On 10-MAR-2021, the subject experienced headache. On 10-MAR-2021, the subject experienced dizzy. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the vomiting, difficulty in swallowing/ could not keep any food down, face has broken out, headache and dizzy was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230648
Sex: U
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: ARM SORENESS; ARM REDNESS; 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, intramuscular, batch number: Unknown) .5 ml, administered on 06-OCT-2020 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date, the patient experienced arm soreness, and arm redness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the arm soreness and arm redness was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230649
Sex: F
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE ARM; FATIGUE; 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 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 an unspecified date, the subject experienced sore arm, fatigue, and headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the fatigue, headache and sore arm was not reported. This report was non-serious. This case, from the same reporter is linked to 20210326425.

Other Meds:

Current Illness:

ID: 1230650
Sex: F
Age:
State: OH

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE ARM AFTER RECEIVING THE VACCINE IN INJECTION ARM; FEVER; ACHES; CHILLS; TIRED; 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: Unk) dose was not reported, administered on 11-MAR-2021 19:00 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 12-MAR-2021, the subject experienced sore arm after receiving the vaccine in injection arm. On 12-MAR-2021, the subject experienced fever. On 12-MAR-2021, the subject experienced aches. On 12-MAR-2021, the subject experienced chills. On 12-MAR-2021, the subject experienced tired. Laboratory data included: Body temperature (NR: not provided) 100.7 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from sore arm after receiving the vaccine in injection arm, fever, aches, chills, and tired. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230651
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/14/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: CHILLS; FEVER; FATIGUE; 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, intramuscular, batch number: Unknown) .5 ml, start therapy date was 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 14-MAR-2021, the subject experienced chills. On 14-MAR-2021, the subject experienced fever. On 14-MAR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the chills, fever and fatigue was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230652
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: TREMBLING; HEADACHE; LOWER BACK PAIN; ACHING ALL OVER; CHILLS; This spontaneous report received from a patient concerned an 18 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 or non drug allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805031, expiry: UNKNOWN) .5 ml, administered on 13-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced headache. On 13-MAR-2021, the subject experienced lower back pain. On 13-MAR-2021, the subject experienced aching all over. On 13-MAR-2021, the subject experienced chills. On an unspecified date, the subject experienced trembling. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, and trembling, was recovering from aching all over, and had not recovered from headache, and lower back pain. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230653
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER TEMP UNKNOWN; 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, intramuscular, batch number: Unknown) .5 ml, start therapy date was not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 12-MAR-2021, the patient experienced fever temp unknown. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fever temp unknown. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230654
Sex: M
Age:
State: GA

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: CHILLS; This spontaneous report received from a health care professional concerned a 39 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included alcohol use, and non-smoker, and other pre-existing medical conditions included the patient had no known allergies and no history of drug abuse or illicit drug use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: Unknown) dose was not reported, administered on 11-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 11-MAR-2021, the subject experienced chills. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of chills was not reported. This report was non-serious.

Other Meds:

Current Illness: Alcohol use; Non-smoker

ID: 1230655
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: BLOTCHY RASH ON FOREARMS, BACK OF THIGHS, FOREHEAD, AND TRUNK; FLUID FILLED BUMPS ON REDDENED SKIN; CHILLS; HEADACHE; FEVER; FEELING TIRED; 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 vicodin allergy, celebrex allergy, and flagyl allergy, and concurrent conditions included seasonal allergies, alcohol consumption, and non smoker, and other pre-existing medical conditions included no drug abuse/illicit drug use. The patient experienced drug allergy when treated with celecoxib, metronidazole, and hydrocodone bitartrate/paracetamol. 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 12-MAR-2021 at 16:30 to left arm for prophylactic vaccination. No concomitant medications were reported. On 12-MAR-2021, the subject experienced blotchy rash on forearms, back of thighs, forehead, and trunk. On 12-MAR-2021, the subject experienced fluid filled bumps on reddened skin. On 12-MAR-2021, the subject experienced chills. On 12-MAR-2021, the subject experienced headache. On 12-MAR-2021, the subject experienced fever. On 12-MAR-2021, the subject experienced feeling tired. Treatment medications included: ibuprofen. On 13-MAR-2021, Laboratory data included: Body temperature (NR: not provided) 103 units unspecified. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from headache, fever, chills, feeling tired, blotchy rash on forearms, back of thighs, forehead, and trunk, and fluid filled bumps on reddened skin. This report was non-serious. This case, involving the same patient is linked to 20210330216.

Other Meds:

Current Illness:

ID: 1230656
Sex: F
Age:
State: IN

Vax Date:
Onset Date: 03/07/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: NERVES ACTING UP; THROAT FELT SWOLLEN; CHILLS; NAUSEA; ITCHING; TINGLING; BULLS-EYE RASH AND AND RAISED BUMP AROUND THE INJECTION SITE; MUSCLE ACHES; 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 migraines with nausea and blurred vision, lyme disease, pneumonia, bronchitis, anaphylactic reaction to eggs, anaphylactic reaction to red dye, penicillin allergy, alcohol user, and non smoker. The patient experienced drug allergy when treated with phenazopyridine hydrochloride, and sulfamethoxazole/trimethoprim. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 1802068 expiry: UNKNOWN) dose was not reported, administered on 06-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 07-MAR-2021, the subject experienced muscle aches. On 07-MAR-2021, the subject experienced headache. On 09-MAR-2021, the subject experienced itching. On 09-MAR-2021, the subject experienced tingling. On 09-MAR-2021, the subject experienced bulls-eye rash and and raised bump around the injection site. On 11-MAR-2021, the subject experienced nerves acting up. On 11-MAR-2021, the subject experienced throat felt swollen. On 11-MAR-2021, the subject experienced chills. On 11-MAR-2021, the subject experienced nausea. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from nerves acting up on MAR-2021, chills, nausea, and headache on 11-MAR-2021, and muscle aches on 09-MAR-2021, and was recovering from bulls-eye rash and and raised bump around the injection site, itching, tingling, and throat felt swollen. This report was non-serious.

Other Meds:

Current Illness: Alcohol use (patient takes rarely social occasions, holidays, 1-2 per month or not); Anaphylactic reaction to food; Bronchitis (over 20 years ago); Lyme disease (20 years ago); Migraine; Non-smoker; Penicillin allergy; Pneumonia (over 20 years ago); Reaction to food coloring

ID: 1230657
Sex: U
Age:
State: PA

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: DIARRHEA; 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, and batch number: JJ1805022 expiry: UNKNOWN) dose was not reported, administered on 12-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced diarrhea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of diarrhea was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230658
Sex: M
Age:
State: TX

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER; HEADACHE; ACHES; DEHYDRATION; 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, intramuscular, batch number: 1805031, and expiry: not reported) .5 ml, administered on 11-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, the subject experienced dehydration. On 12-MAR-2021, the subject experienced fever. On 12-MAR-2021, the subject experienced headache. On 12-MAR-2021, the subject experienced aches. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from dehydration on 12-MAR-2021, and had not recovered from fever, headache, and aches. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230659
Sex: U
Age:
State: CA

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SWOLLEN THROAT; 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: Unk) dose was not reported, administered on 10-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. The batch number was not reported and has been requested. On 10-MAR-2021, the patient experienced swollen throat. reporter report that after 4 days of vaccination suffering from throat swollen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of swollen throat was not reported. The reporter considered the causality between covid-19 vaccine ad26.cov2.s and swollen throat was related .Company causality between covid-19 vaccine ad26.cov2.s and swollen throat was related . This report was non-serious.

Other Meds:

Current Illness:

ID: 1230660
Sex: U
Age:
State: MA

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE ARM; 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) dose was not reported, administered on MAR-2021 at 10:00 am for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On MAR-2021, the subject experienced sore arm. 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: 1230661
Sex: M
Age:
State: NJ

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: LEFT ARM, UNDERNEATH THE ARMPIT FELT LUMP; ACHE/BODY ACHES; CHILLS; PRESSURE ON THE FOREHEAD (TIGHT FEELING); TIRED; This spontaneous report received from a patient concerned a 60 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included sleep apnea, and alcohol use, 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, intramuscular, batch number: 1805031, and expiry: not reported) .5 ml, administered on 11-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, the subject experienced tired. On 11-MAR-2021 22:00, the subject experienced ache/body aches. On 11-MAR-2021 22:00, the subject experienced chills. On 11-MAR-2021 22:00, the subject experienced pressure on the forehead (tight feeling). On 12-MAR-2021, the subject experienced left arm, underneath the armpit felt lump. On 12-MAR-2021 14:00, treatment medications included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, pressure on the forehead (tight feeling), and tired on 12-MAR-2021, was recovering from ache/body aches, and the outcome of left arm, underneath the armpit felt lump was not reported. This report was non-serious.

Other Meds:

Current Illness: Alcohol use (drinks: Occasionally during holidays (once every few months)); Sleep apnea

ID: 1230662
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: BODY ACHES; SINUS HEADACHE; CHILLS; TIREDNESS; This spontaneous report received from a consumer concerned a 63 year old female. The patient's height, and weight were not reported. The patient's past medical history included heart attack, and concurrent conditions included heart condition, no alcohol use, and non smoker, and other pre-existing medical conditions included 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: 1805031, and batch number: 1805031 expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, the subject experienced body aches. On 11-MAR-2021, the subject experienced sinus headache. On 11-MAR-2021, the subject experienced chills. On 11-MAR-2021, the subject experienced tiredness. Treatment medications included: ibuprofen. On 12-MAR-2021, treatment medications included: ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body aches, sinus headache, and chills on 12-MAR-2021, and was recovering from tiredness. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Heart disorder (Patient had heart condition (previous heart attack) and taking medications.); Non-smoker

ID: 1230663
Sex: F
Age:
State: VT

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: UNABLE TO DO ANYTHING; FEVER; BODY HURTS; WOKE UP MANY TIMES IN THE NIGHT; NAUSEA; DRY MOUTH; 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 pre-existing medical conditions included had no medical history. Patient reported healthy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805022, and expiry: UNKNOWN) dose was not reported, administered on 06-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the subject experienced body hurts. On 13-MAR-2021, the subject experienced woke up many times in the night. On 13-MAR-2021, the subject experienced nausea. On 13-MAR-2021, the subject experienced dry mouth. Treatment medications included: paracetamol. On 13-MAR-2021 18:00, the subject experienced fever. On 14-MAR-2021, the subject experienced unable to do anything. Treatment medications included: paracetamol. Laboratory data (dates unspecified) included: COVID-19 virus test negative (NR: not provided) Negative. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from fever, had not recovered from body hurts, nausea, unable to do anything, and dry mouth, and the outcome of woke up many times in the night was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230664
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 03/12/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: HEADACHE; FATIGUE; 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: 1805029, and expiry: not reported) dose was not reported, administered on 12-MAR-2021 10:00 for prophylactic vaccination. No concomitant medications were reported. On 12-MAR-2021, the subject experienced headache. On 12-MAR-2021, the subject experienced fatigue. On 12-MAR-2021, the subject experienced chills. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from chills, headache, and fatigue. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230665
Sex: M
Age:
State: CA

Vax Date:
Onset Date: 03/11/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: CHILLS; This spontaneous report received from a consumer concerned a male of unspecified age. 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 known drug allergies and no dug abuse/illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805029, and batch number: 1805029 expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 11-MAR-2021, the patient experienced chills. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from chills. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Non-smoker

ID: 1230666
Sex: F
Age:
State: OK

Vax Date:
Onset Date: 03/10/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: INJECTION SITE WARMNESS WHICH WAS DESCRIBED AS FEVER IN ARM; INJECTION SITE SWELLING WHICH WAS DESCRIBED AS ARM SWELLING; BODY ACHE; ARM SORENESS WHICH WAS DESCRIBED AS ARM PAIN; FATIGUE; INJECTION SITE REDNESS; 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: 1805029, and batch number: 1805029 expiry: UNKNOWN) dose was not reported, administered on 10-MAR-2021 17:00 to Right Arm for prophylactic vaccination. No concomitant medications were reported. On 10-MAR-2021, the subject experienced body ache. On 10-MAR-2021, the subject experienced arm soreness which was described as arm pain. On 10-MAR-2021, the subject experienced fatigue. On 10-MAR-2021, the subject experienced injection site redness. On 12-MAR-2021, the subject experienced injection site warmness which was described as fever in arm. On 12-MAR-2021, the subject experienced injection site swelling which was described as arm swelling. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body ache, and fatigue on MAR-2021, was recovering from arm soreness which was described as arm pain, and had not recovered from injection site redness, injection site swelling which was described as arm swelling, and injection site warmness which was described as fever in arm. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230667
Sex: U
Age:
State: CA

Vax Date:
Onset Date: 03/14/2021
Rec V Date: 04/19/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SWOLLEN ARM; WARM TO TOUCH; REDNESS; 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, intramuscular, batch number: 1805029 and expiry: 25-MAY-2021) dose was not reported, administered on 12-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 14-MAR-2021, the subject experienced swollen arm. On 14-MAR-2021, the subject experienced skin warm. On 14-MAR-2021, the subject experienced injection site redness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the swollen arm, injection site redness and skin warm was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230668
Sex: F
Age:
State: WA

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: FREQUENT DIARRHEA; STOMACH ACHE; FEELING HYPER; MILD ARM SORENESS; This spontaneous report received from a patient. 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, and expiry: not reported) dose was not reported, administered on 11-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the subject experienced frequent diarrhea, stomach ache, feeling hyper, and mild arm soreness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the mild arm soreness, stomach ache, frequent diarrhea and feeling hyper was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1230669
Sex: F
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: SIDE EFFECTS; 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. No concomitant medications were reported. On an unspecified date, the subject experienced side effects. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from side effects. This report was non-serious.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 599,999

Page last modified: 03 October 2021 5:28pm