VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

Total Manufacturer

Incidents per State

State Total
92,076
AK1,880
AL6,345
AR4,151
AS46
AZ14,991
CA66,887
CO12,550
CT8,943
DC1,795
DE2,009
FL42,724
FM4
GA17,031
GU124
HI2,580
IA4,919
ID2,892
IL22,128
IN24,197
KS5,047
KY9,111
LA5,500
MA15,718
MD13,434
ME3,351
MH8
MI20,971
MN13,585
MO10,747
MP30
MS3,198
MT2,477
NC18,051
ND1,501
NE3,109
NH3,218
NJ20,216
NM4,218
NV4,728
NY37,667
OH20,793
OK6,692
OR9,244
PA25,607
PR2,588
QM2
RI2,163
SC7,261
SD1,282
TN10,445
TX39,890
UT4,618
VA15,980
VI67
VT1,830
WA16,071
WI12,042
WV2,571
WY926
XB5
XL1
XV2

ID: 1253720
Sex: F
Age:
State: WI

Vax Date:
Onset Date: 03/19/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: APPEARED PALE; DIZZINESS; WEAKNESS; This spontaneous report received from a patient concerned a 32 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included arthritis, and fibromyalgia, and other pre-existing medical conditions included no allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805031, expiry: 26/MAY/2021) dose was not reported, administered on 19-MAR-2021 14:20 for prophylactic vaccination. Concomitant medications included celecoxib, cyclobenzaprine hydrochloride, lithium, and losartan. On 19-MAR-2021, Laboratory data included: Oxygen saturation (NR: not provided) Remained WNL. On 19-MAR-2021 14:35, the subject experienced appeared pale. On 19-MAR-2021 14:35, the subject experienced dizziness. On 19-MAR-2021 14:35, the subject experienced weakness. On 19-MAR-2021 14:40, Laboratory data included: Blood pressure (NR: not provided) 148/82 mmHg. On 19-MAR-2021 14:44, Laboratory data included: Blood pressure (NR: not provided) 142/86 mmHg. On 19-MAR-2021 14:46, Laboratory data included: Blood pressure (NR: not provided) 148/84 mmHg. On 19-MAR-2021 14:55, Laboratory data included: Blood pressure (NR: not provided) 142/94 mmHg. On 19-MAR-2021 15:00, Laboratory data included: Heart rate (NR: not provided) Remained WNL. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from appeared pale on MAR-2021, and dizziness, and weakness on 23-MAR-2021. This report was non-serious.

Other Meds: losartan; celebrex; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]; LITHIUM

Current Illness: Arthritis; Fibromyalgia

ID: 1253721
Sex: F
Age:
State: AZ

Vax Date:
Onset Date: 03/24/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: TROUBLE BREATHING; DIZZINESS; 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 expiry: UNKNOWN) dose was not reported, administered on 24-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2021, the subject experienced trouble breathing. On 24-MAR-2021, the subject experienced dizziness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from trouble breathing, and dizziness. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253722
Sex: U
Age:
State: MI

Vax Date:
Onset Date: 03/19/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: HEADACHE; ARM SORENESS; FELT ELECTRIFYING; FELT THE MEDICINE GOING INTO THE MUSCLE; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height, and weight were not reported. The patient's past medical history included fiber myalgia in arms. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 180525, and expiry: UNKNOWN) dose was not reported, administered on 19-MAR-2021 14:40 for prophylactic vaccination on left arm. No concomitant medications were reported. On 19-MAR-2021, the subject experienced felt electrifying. On 19-MAR-2021, the subject experienced felt the medicine going into the muscle. On 21-MAR-2021, the subject experienced arm soreness. On 24-MAR-2021, the subject experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from felt electrifying, and felt the medicine going into the muscle on 19-MAR-2021, and had not recovered from headache, and arm soreness. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253723
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: STRANGE SIDE EFFECTS; ACHEY; SORE ARM; TIRED; This spontaneous report received from a patient concerned a 68 year old female. The patient's weight, height, and medical history were not reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: UNKNOWN expiry date: UNKNOWN) dose was not reported, administered on 17-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 MAR-2021, the subject experienced strange side effects. On MAR-2021, the subject experienced achey. On MAR-2021, the subject experienced sore arm. On MAR-2021, the subject experienced tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the sore arm, achey, strange side effects and tired was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253724
Sex: F
Age:
State: OK

Vax Date:
Onset Date: 03/20/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE THROAT; HEADACHE; MUSCLE ACHE IN THIGH AND OTHER; FATIGUE; 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 non insulin dependent diabetes. The patient was previously treated with metformin for non insulin dependent diabetes. 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 19-MAR-2021to right arm for prophylactic vaccination. No concomitant medications were reported. On 20-MAR-2021, the subject experienced headache. On 20-MAR-2021, the subject experienced muscle ache in thigh and other. On 20-MAR-2021, the subject experienced fatigue. On 24-MAR-2021, the subject experienced sore throat. Treatment medications (dates unspecified) included: paracetamol, and ibuprofen. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from headache, and had not recovered from sore throat, muscle ache in thigh and other, and fatigue. This report was non-serious.

Other Meds:

Current Illness: Diabetes mellitus non-insulin-dependent

ID: 1253725
Sex: F
Age:
State: IN

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: HEART WAS RACING; BLOOD PRESSURE WAS 134/86; This spontaneous report received from a health care professional concerned a 49 year old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included patient was not pregnant at the time of reporting. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular and batch number: 1805029 expiry: UNKNOWN) dose was not reported, administered on 23-MAR-2021 on right arm for prophylactic vaccination. No concomitant medications were reported. On 23-MAR-2021, the subject experienced heart was racing. Laboratory data included: Blood pressure (NR: not provided) 134/86 mmHg, and Heart rate (NR: not provided) 85-81 bpm. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from heart was racing. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253726
Sex: F
Age:
State: MI

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: NO SLEEP; CHILLS; MUSCLES ACHES; HEADACHES; SWEATING; 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 non-smoker, and other pre-existing medical conditions included patient had no known drug allergy. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, and batch number: 1805018 expiry: UNKNOWN) dose was not reported, administered on 23-MAR-2021 for prophylactic vaccination on left arm. No concomitant medications were reported. On 23-MAR-2021, the subject experienced chills. On 23-MAR-2021, the subject experienced muscles aches. On 23-MAR-2021, the subject experienced headaches. On 23-MAR-2021, the subject experienced sweating. On an unspecified date, the subject experienced no sleep. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills, and muscles aches on 23-MAR-2021, had not recovered from headaches, and sweating, and the outcome of no sleep was not reported. This report was non-serious.

Other Meds:

Current Illness: Non-smoker

ID: 1253727
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: LACRIMATION; MUSCLE CRAMPS; JOINT ACHES; CHILLS; FEVER; HEADACHE; TIREDNESS AND FATIGUE; This spontaneous report received from a patient concerned a 63 year old female. The patient's weight, height, and medical history were not reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 23-MAR-2021 at right arm for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 23-MAR-2021, the subject experienced joint aches. On 23-MAR-2021, the subject experienced chills. On 23-MAR-2021, the subject experienced fever. On 23-MAR-2021, the subject experienced headache. On 23-MAR-2021, the subject experienced tiredness and fatigue. On 24-MAR-2021, the subject experienced lacrimation. On 24-MAR-2021, the subject experienced muscle cramps. Laboratory data (dates unspecified) included: Body temperature (NR: not provided) 101.6 F, 100.6 F. Treatment medications (dates unspecified) included: magnesium. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from muscle cramps, and headache on 24-MAR-2021, was recovering from fever, and chills, and had not recovered from joint aches, tiredness and fatigue, and lacrimation. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253728
Sex: M
Age:
State:

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: HIVES (GETTING WORSE); 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: Unknown) dose was not reported, administered on 17-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 23-MAR-2021, the subject experienced hives (getting worse). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from hives (getting worse). This report was non-serious.

Other Meds:

Current Illness:

ID: 1253729
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER; FLU LIKE SYMPTOMS; CHILLS; DIARRHEA; 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 arthritis. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1806609, expiry date: unknown) dose was not reported, administered on 19-MAR-2021 for prophylactic vaccination at left deltoid. Concomitant medications included paracetamol for arthritis. On MAR-2021, the subject experienced fever. On MAR-2021, the subject experienced flu like symptoms. On MAR-2021, the subject experienced chills. On MAR-2021, the subject experienced diarrhea. On MAR-2021, the subject experienced headache. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from flu like symptoms, chills, and diarrhea on MAR-2021, and was recovering from fever, and headache. This report was non-serious.

Other Meds:

Current Illness: Arthritis

ID: 1253730
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: SORE ARM FOR A DAY OR TWO; This spontaneous report received from a patient concerned a 71 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) 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 MAR-2021, the subject experienced sore arm for a day or two. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from sore arm for a day or two on MAR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253731
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: TINGLING; NUMBNESS; 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, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date, the subject experienced tingling, and numbness. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the tingling and numbness was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253732
Sex: U
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FEELING ACHY; SINUSES WERE CLOG; TIRED FROM NOT SLEEPING; COULDN'T GET WARM; NO SIDE EFFECTS; SHIVERING; HEADACHE; NAUSEOUS; FEVER; TIRED; 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: 1805028 expiry: UNKNOWN) dose, start therapy date were not reported for prophylactic vaccination. No concomitant medications were reported. On an unspecified date, the subject experienced feeling achy, sinuses were clog, tired from not sleeping, couldn't get warm, shivering, headache, nauseous, fever, tired and 48 hours after vaccination had no side effects. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the feeling achy, shivering, tired, couldn't get warm, fever, nauseous, sinuses were clog, headache, tired from not sleeping and no side effects was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253733
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FINGERS ARE VERY STIFF AND SORE; THE ARM IN WHICH THE VACCINE WAS INJECTED WAS SORE; 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 10-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 23-MAR-2021, the subject experienced the arm in which the vaccine was injected was sore. On 24-MAR-2021, the subject experienced fingers are very stiff and sore. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the the arm in which the vaccine was injected was sore and fingers are very stiff and sore was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253734
Sex: U
Age:
State: NM

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FLU LIKE SIDE EFFECTS; SEVERE BODY ACHES; SEVERE CHILLS; MODERATE FEVER; SEVERE TENSION IN MY HEAD; SEVERE FATIGUE; This spontaneous report received from a patient concerned a 31 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, the batch number were not reported and has been requested) dose was not reported, administered on 16-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On Mar-2021, the subject experienced flu like side effects, severe body aches, severe chills, moderate fever, severe tension in my head, and severe fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the flu like side effects, severe chills, moderate fever, severe body aches, severe tension in my head and severe fatigue was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253735
Sex: U
Age:
State:

Vax Date: 03/20/2021
Onset Date: 03/20/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: WEIRD DREAMS; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 20-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 20-MAR-2021, the subject experienced weird dreams. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of weird dreams was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253736
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 03/21/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: CLEARED SINUSES; UNEXPECTED THERAPEUTIC BENEFIT; This spontaneous report received from a patient concerned a 73 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included seasonal allergy of sinuses problem. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808609, expiry: UNKNOWN) dose was not reported, one total, administered on 21-MAR-2021 in left arm for prophylactic vaccination. No concomitant medications were reported. On 21-MAR-2021, the subject experienced cleared sinuses. On 21-MAR-2021, the subject experienced unexpected therapeutic benefit. Treatment medications (dates unspecified) included: loratadine. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the cleared sinuses and unexpected therapeutic benefit was not reported. This report was non-serious.

Other Meds:

Current Illness: Sinus disorder

ID: 1253737
Sex: M
Age:
State: CA

Vax Date:
Onset Date: 03/18/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: NECK PAIN; HEADACHE; 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: Unknown) dose was not reported, 1 total, administered on 13-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 18-MAR-2021, the subject experienced neck pain. On 18-MAR-2021, the subject experienced headache. On 18-MAR-2021, the subject experienced nausea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from headache, nausea, and neck pain. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253738
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/19/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: RAISED LESION ON CALF; NON RAISED LESION ON CALF; FATIGUE; This spontaneous report received from a patient concerned an 82 year old female. The patient's height, and weight were not reported. The patient's past medical history included hypothyroid, and hx of hyperthyroid, and concurrent conditions included seasonal tobacco allergy, does not consume alcohol, and does not smoke. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805022, and expiry: 25-MAY-2021) dose was not reported, administered on 19-MAR-2021 for prophylactic vaccination on left arm. No concomitant medications were reported. On 19-MAR-2021, the subject experienced fatigue. On 23-MAR-2021, the subject experienced raised lesion on calf. On 23-MAR-2021, the subject experienced non raised lesion on calf. Treatment medications (dates unspecified) included: bacitracin zinc/polymyxin b sulfate, povidone-iodine, and hydrogen peroxide. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from raised lesion on calf, non raised lesion on calf, and fatigue. This report was non-serious.

Other Meds:

Current Illness: Abstains from alcohol; Allergy; Non-smoker

ID: 1253739
Sex: U
Age:
State: FL

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: ACHY; CLOGGED SINUSES; SHIVERING AND COULD NOT GET WARM; TIRED; NAUSEOUS; FEVER; HEADACHE; This spontaneous report received from a patient via an unspecified 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: 1805028, expiry: UNKNOWN) dose was not reported, administered on MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On MAR-2021, the subject experienced achy. On MAR-2021, the subject experienced clogged sinuses. On MAR-2021, the subject experienced shivering and could not get warm. On MAR-2021, the subject experienced tired. On MAR-2021, the subject experienced nauseous. On MAR-2021, the subject experienced fever. On MAR-2021, the subject experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from achy, clogged sinuses, shivering and could not get warm, tired, nauseous, fever, and headache on MAR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253740
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: REACTION TO VACCINE; 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 number. No concomitant medications were reported. On an unspecified date, the subject experienced reaction to vaccine. The action taken with covid-19 vaccine ad26.cov2.s was not reported. The outcome of reaction to vaccine was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253741
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: SLEPT FOR TWO DAYS; PINCH-LIKE PAIN AT INJECTION SITE; 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 was not reported, administered on 20-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. No concomitant medications were reported. On MAR-2021, the subject experienced slept for two days. On MAR-2021, the subject experienced pinch-like pain at injection site. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the pinch-like pain at injection site and slept for two days was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253742
Sex: M
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: BODY SORENESS; FEELING BAD WHOLE SECOND DAY; FEVER; HEADACHE; 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: Unknown) 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 an unspecified date, the subject experienced body soreness, feeling bad whole second day, fever, and headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from body soreness, feeling bad whole second day, fever, and headache on 12-MAR-2021. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253743
Sex: M
Age:
State: MO

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER BLISTER ON LIP; 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) dose was not reported, administered on 22-MAR-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On MAR-2021, the subject experienced fever blister on lip. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of fever blister on lip was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253744
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FELT LIKE HIT BY A TRUCK; COULDN'T GET OUT OF BED; EVERYTHING HURT; This spontaneous report received from a patient via a company representative concerned a female of unspecified age. The patient's weight, height, and medical history were not reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose, start therapy date were not reported for prophylactic vaccination.The batch number was not reported. 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 felt like hit by a truck, couldn't get out of bed, and everything hurt. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the felt like hit by a truck, couldn't get out of bed and everything hurt was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253745
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/08/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: HAS A SORE ARM AFTER THE INJECTION FROM A FEW WEEKS AGO; 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 expiry: UNKNOWN) dose was not reported, administered on 08-MAR-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 08-MAR-2021, the subject experienced has a sore arm after the injection from a few weeks ago. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from has a sore arm after the injection from a few weeks ago. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253746
Sex: M
Age:
State: AL

Vax Date:
Onset Date: 03/22/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: CHILLS; FEVER; MILD HEADACHE; BODY ACHES AND PAINS; DIARRHEA; This spontaneous report received from a patient concerned a 47 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included familial tremors, non alcohol user, and smoker, and other pre-existing medical conditions included the patient had no known allergies and did not had drug abuse or illicit drug usage. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805025, and expiry: UNKNOWN) dose was not reported, administered on 22-MAR-2021 for prophylactic vaccination on left arm. Concomitant medications included propranolol, and venlafaxine hydrochloride. On 22-MAR-2021, the subject experienced diarrhea. On 23-MAR-2021, the subject experienced body aches and pains. On 23-MAR-2021, the subject experienced fever. On 23-MAR-2021, the subject experienced mild headache. On an unspecified date, the subject experienced chills. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from diarrhea on 22-MAR-2021, and body aches and pains, fever, and mild headache on 23-MAR-2021, and the outcome of chills was not reported. This report was non-serious.

Other Meds: VENLAFAXINE HYDROCHLORIDE; PROPRANOLOL

Current Illness: Abstains from alcohol; Familial tremor; Smoker (Pack and a half in a day (cigarettes))

ID: 1253747
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: CHILLS; LINGERING HEADACHE; This spontaneous report received from a consumer 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 chills, and lingering headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the chills and lingering headache was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253748
Sex: M
Age:
State: VT

Vax Date:
Onset Date: 03/22/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER; This spontaneous report received from a patient concerned an adult male. The patient's weight, height, and medical history were not reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported) dose was not reported, administered on 20-MAR-2021 for prophylactic vaccination. The batch number was not reported. The company is unable to perform follow-up to request batch or lot number. No concomitant medications were reported. On 22-MAR-2021, the subject experienced fever. Laboratory data included: Body temperature (NR: not provided) 101 F. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of fever was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253749
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FAST HEARTBEAT; DIARRHEA; TIRED; SICKNESS; 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 15-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 MAR-2021, the subject experienced sickness. On 19-MAR-2021, the subject experienced fast heartbeat. On 19-MAR-2021, the subject experienced diarrhea. On 19-MAR-2021, the subject experienced tired. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the tired, fast heartbeat, diarrhea and sickness was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253750
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 03/15/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER; LOW ENERGY; EXTREME FATIGUE; SLEEPLESS; SEVERE 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: 1805031 )expiry: UNKNOWN) dose was not reported, administered on 15-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 15-MAR-2021, the subject experienced severe headache. On 15-MAR-2021, the subject experienced sleepless. On 16-MAR-2021, the subject experienced extreme fatigue. On 21-MAR-2021, the subject experienced low energy. On 23-MAR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered with sequelae from sleepless on 16-MAR-2021, was recovering from severe headache, and fever, and had not recovered from extreme fatigue, and low energy. The reporter considered related causality between covid-19 vaccine ad26.cov2.s and sleepless ,severe headache, fever ,extreme fatigue, and low energy and company causality between covid-19 vaccine ad26.cov2.s and sleepless ,severe headache, fever ,extreme fatigue, and low energy was possible. This report was non-serious.; Sender's Comments: V0: Medical Assessment comment not required as per standard procedure as the case assessed as non-serious.

Other Meds:

Current Illness:

ID: 1253751
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/20/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: FELT SOMETHING DRIPPING DOWN HER ARM; NEEDLE GO IN A LITTLE BURN; 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: 1805031, and expiry: UNKNOWN) dose was not reported, administered on 20-MAR-2021 to left arm for prophylactic vaccination. No concomitant medications were reported. On 20-MAR-2021, the subject experienced felt something dripping down her arm. On 20-MAR-2021, the subject experienced needle go in a little burn. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the felt something dripping down her arm and needle go in a little burn was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253752
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: VACCINE AFFECTED HORRIBLY; 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, expiry: 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-2021, the subject experienced vaccine affected horribly. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaccine affected horribly was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253753
Sex: M
Age:
State: CT

Vax Date:
Onset Date: 03/06/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: BACK ACHE; TINGLING ON BOTH HANDS / TINGLING SENSATION; NUMBNESS IN THE JOINTS; LEFT KNEE SWELLING; LEFT LEG MUSCLE ACHE; LEFT KNEE ACHE; HEADACHE; 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 06-MAR-2021 08:30 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On 06-MAR-2021, the subject experienced back ache. On 06-MAR-2021, the subject experienced tingling on both hands / tingling sensation. On 06-MAR-2021, the subject experienced numbness in the joints. On 06-MAR-2021, the subject experienced left knee swelling. On 06-MAR-2021, the subject experienced left leg muscle ache. On 06-MAR-2021, the subject experienced left knee ache. On 06-MAR-2021, the subject experienced headache. Treatment medications (dates unspecified) included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from headache on 06-MAR-2021, and had not recovered from left knee ache, back ache, numbness in the joints, left knee swelling, left leg muscle ache, and tingling on both hands / tingling sensation. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253754
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/10/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: HEAD FEELS HEAVIER THAN USUAL; SPOTTY SORENESS ALL OVER; NOT FEELING ENERGETIC; FEVER; MILD HEADACHE; This spontaneous report received from a patient concerned a 40 year old female. The patient's height, and weight were not reported. The patient's past medical history included none, and other pre-existing medical conditions included patient have no known allergies. 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 left deltoid 09-MAR-2021 for prophylactic vaccination. The batch number was not provided and has been requested No concomitant medications were reported. On MAR-2021, Laboratory data included: Body temperature (NR: not provided) 100 F. On 10-MAR-2021, the subject experienced head feels heavier than usual. On 10-MAR-2021, the subject experienced spotty soreness all over. On 10-MAR-2021, the subject experienced not feeling energetic. On 10-MAR-2021, the subject experienced fever. On 10-MAR-2021, the subject experienced mild headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from fever, head feels heavier than usual, and mild headache, and the outcome of not feeling energetic and spotty soreness all over was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253755
Sex: F
Age:
State: CA

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: ITCHINESS ALL OVER BODY AND FOREHEAD; 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 13-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 itchiness all over body and forehead. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from itchiness all over body and forehead. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253756
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: TIRED; HEADACHE; MILD FEVER; ARM SWOLLEN AT SITE OF INJECTION; BODY ACHE; CHILLS; SORE ARM AT SITE OF INJECTION; 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: 1802070, and expiry: UNKNOWN) dose was not reported, administered on 23-MAR-2021 at left arm for prophylactic vaccination. No concomitant medications were reported. On 23-MAR-2021, the subject experienced sore arm at site of injection. On 24-MAR-2021, the subject experienced body ache. On 24-MAR-2021, the subject experienced chills. On 24-MAR-2021, the subject experienced headache. On 24-MAR-2021, the subject experienced mild fever. On 24-MAR-2021, the subject experienced arm swollen at site of injection. On 24-MAR-2021, the subject experienced tired. Laboratory data included: Body temperature (NR: not provided) 97.6 degrees F. Treatment medications included: paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache, mild fever, chills, body ache, arm swollen at site of injection, tired and sore arm at site of injection was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253757
Sex: F
Age:
State: NC

Vax Date:
Onset Date: 03/24/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: VACCINE EXPOSURE VIA BREAST MILK; This spontaneous report received from a parent concerned a 13 month old female. The patient's weight, height, and medical history were not reported.The patient's parent received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1808609, and batch number: 1808609 expiry: UNKNOWN) dose was not reported, administered on 24-MAR-2021 for an unspecified indication. No concomitant medications were reported. On 24-MAR-2021, the subject experienced vaccine exposure via breast milk. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaccine exposure via breast milk was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253758
Sex: M
Age:
State: WI

Vax Date:
Onset Date: 03/24/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: BODY ACHE; HEADACHE; FEVER; This spontaneous report received from a patient concerned a 59 year old male. The patient's weight, height, and medical history were not reported. The patient experienced drug allergy when treated with amoxicillin. 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 24-MAR-2021at left arm for prophylactic vaccination. Batch number was not reported and has been requested No concomitant medications were reported. On 24-MAR-2021, the subject experienced body ache. On 24-MAR-2021, the subject experienced headache. On 24-MAR-2021, 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, and body ache. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253759
Sex: F
Age:
State: KS

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: PAIN IN EAR; PAIN BEHIND EYES; CAN NOT FALL ASLEEP; LOW BACK PAIN; PAIN BEHIND EAR; PAIN AND BODY ACHES; EXHAUSTED; SEVER HEADACHE; JOINT PAIN; COLD HANDS AND FEET; This spontaneous report received from a patient concerned a 70 year old female. The patient's height, and weight were not reported. The patient's past medical history included covid 19 infection, and concurrent conditions included chronic pain, kidney problems, on physiotherapy, non alcoholic, and non smoker, and other pre-existing medical conditions included she had more 3 drug allergy but not remember. The patient experienced drug allergy when treated with levofloxacin, and sulfacetamide sodium/sulfadiazine/sulfadimidine/sulfamerazine. 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 23-MAR-2021 on left arm for prophylactic vaccination. Concomitant medications included gabapentin for pain, and oxycodone hydrochloride/paracetamol for pain. On MAR-2021, the subject experienced cold hands and feet. On MAR-2021, the subject experienced joint pain. Laboratory data included: Blood pressure (NR: not provided) FINE, and Renal function test (NR: not provided) BETTER. On 24-MAR-2021, the subject experienced pain in ear. On 24-MAR-2021, the subject experienced pain behind eyes. On 24-MAR-2021, the subject experienced can not fall asleep. On 24-MAR-2021, the subject experienced low back pain. On 24-MAR-2021, the subject experienced pain behind ear. On 24-MAR-2021, the subject experienced pain and body aches. On 24-MAR-2021, the subject experienced exhausted. On 24-MAR-2021, the subject experienced sever headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cold hands and feet on 24-MAR-2021, and low back pain on MAR-2021, had not recovered from sever headache, pain in ear, pain behind eyes, can not fall asleep, exhausted, pain and body aches, and joint pain, and the outcome of pain behind ear was not reported. This report was non-serious.

Other Meds: GABAPENTIN; PERCOCET

Current Illness: Abstains from alcohol; Chronic pain (On pain management.); Kidney disorder; Non-smoker; Physiotherapy (For pain)

ID: 1253760
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: BODY ACHE; SWEATING; SHIVERING; FEVER; HEADACHE; 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, the batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers) dose was not reported, administered on 23-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On 23-MAR-2021, the subject experienced body ache. On 23-MAR-2021, the subject experienced sweating. On 23-MAR-2021, the subject experienced shivering. On 23-MAR-2021, the subject experienced fever. On 23-MAR-2021, the subject experienced headache. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the fever, shivering, sweating, headache and body ache was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253761
Sex: M
Age:
State: MI

Vax Date:
Onset Date: 03/13/2021
Rec V Date: 04/24/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: CONGESTED COUGH; LOW GRADE FEVER/HIGH FEVER; BODY ACHES; 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, , and batch number: 1805020 expiry: UNKNOWN) dose was not reported, administered on 13-MAR-2021 in the left arm for prophylactic vaccination. No concomitant medications were reported. On 13-MAR-2021, the patient experienced body aches. On 13-MAR-2021, the patient experienced low grade fever Laboratory data included: Body temperature (NR: not provided) 99.6-99.7. Laboratory data included: Body temperature (NR: not provided) 100.7-101. On 21-MAR-2021, the patient experienced congested cough. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from body aches, low grade fever, congested cough, and high fever. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253762
Sex: F
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
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Symptoms: CHILLS; FEVER; This spontaneous report received from a patient via a company representative concerned a 28 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included alcohol use. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin, and batch number were not reported) dose, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, a couple hours after taking the vaccine, the subject experienced chills, and fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the fever and chills was not reported. This report was non-serious.

Other Meds:

Current Illness: Alcohol use

ID: 1253763
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/23/2021
Rec V Date: 04/24/2021
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Symptoms: ACHY LOWER BACK 6 HOURS AFTER VACCINATION; ARM SORENESS 3 HOURS AFTER VACCINATION; FULL BODY CHILLS 7 HOURS AFTER VACCINATION; SLIGHT HEADACHE 3 HOURS AFTER VACCINATION; TIREDNESS 6 HOURS AFTER VACCINATION; 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 was not reported, administered on 23-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 23-MAR-2021, the subject experienced achy lower back 6 hours after vaccination. On 23-MAR-2021, the subject experienced arm soreness 3 hours after vaccination. On 23-MAR-2021, the subject experienced full body chills 7 hours after vaccination. On 23-MAR-2021, the subject experienced slight headache 3 hours after vaccination. On 23-MAR-2021, the subject experienced tiredness 6 hours after vaccination. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the arm soreness 3 hours after vaccination, slight headache 3 hours after vaccination, tiredness 6 hours after vaccination, achy lower back 6 hours after vaccination and full body chills 7 hours after vaccination was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253764
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 03/18/2021
Rec V Date: 04/24/2021
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Symptoms: SHINGLES(LEFT EAR HOT AND THROBBING); 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 alcohol user, non smoker, penicillin allergy, and sulphur allergy, and other pre-existing medical conditions included patient on antibiotic for shingles. The patient experienced drug allergy when treated with codeine non-company. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805029, expiry: UNKNOWN) dose was not reported, administered on 14-MAR-2021 16:45 for prophylactic vaccination on left arm. No concomitant medications were reported. On 18-MAR-2021, the subject experienced shingles (left ear hot and throbbing). Treatment medications (dates unspecified) included: oxycodone/paracetamol. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from shingles (left ear hot and throbbing). This report was non-serious.

Other Meds:

Current Illness: Alcohol use (3 times a week); Non-smoker; Penicillin allergy

ID: 1253765
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/24/2021
Rec V Date: 04/24/2021
Hospital:

Vax Type:
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Symptom List:

Symptoms: HEADACHE; 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, route of admin not reported, batch number: Unk) dose was not reported, administered on 22-MAR-2021 for prophylactic vaccination. The batch number was not reported. We are unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On 24-MAR-2021, the subject experienced headache. On 24-MAR-2021, the subject experienced fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache and fatigue was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253766
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/24/2021
Hospital:

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Lot:
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Allergies:

Symptom List:

Symptoms: FLU LIKE SYMPTOMS; HEADACHE; FEVER; FATIGUE; 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 23-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 patient experienced flu like symptoms, headache, fever, and fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache, flu like symptoms, fever and fatigue was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253767
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Lab Data:

Allergies:

Symptom List:

Symptoms: FEVER; FATIGUE; 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 23-MAR-2021 for prophylactic vaccination. The batch number was not reported. The company was unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On MAR-2021, the subject experienced fatigue. On 23-MAR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from fever on MAR-2021, and had not recovered from fatigue. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253768
Sex: F
Age:
State: SC

Vax Date:
Onset Date: 03/24/2021
Rec V Date: 04/24/2021
Hospital:

Vax Type:
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Lot:
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Lab Data:

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Symptom List:

Symptoms: BODYACHE; CHILL; HEADACHE; FEVER; This spontaneous report received from a health care professional 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: 59676D58015 expiry: UNKNOWN) dose was not reported, administered on 24-MAR-2021 on left arm for prophylactic vaccination. No concomitant medications were reported. On 24-MAR-2021, the subject experienced bodyache. On 24-MAR-2021, the subject experienced chill. On 24-MAR-2021, the subject experienced headache. On 24-MAR-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the headache, bodyache, fever and chill was not reported. This report was non-serious.

Other Meds:

Current Illness:

ID: 1253769
Sex: U
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/24/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Vax Route:
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Lab Data:

Allergies:

Symptom List:

Symptoms: VACCINE ARM SORE, TENDER AND SENSITIVE; 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 was not reported, administered on 15-MAR-2021 for prophylactic vaccination. The batch number was not reported. The company was unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On MAR-2021, the subject experienced vaccine arm sore, tender and sensitive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from vaccine arm sore, tender and sensitive. This report was non-serious.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 03 October 2021 5:28pm