VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

Total Manufacturer
199,106MODERNA
36,710JANSSEN
5,381PFIZER\BIONTECH
2,555GLAXOSMITHKLINE BIOLOGICALS
1,469UNKNOWN MANUFACTURER
897MERCK & CO. INC.
627SEQIRUS, INC.
112DYNAVAX TECHNOLOGIES CORPORATION
91SANOFI PASTEUR
75NOVARTIS VACCINES AND DIAGNOSTICS
40EMERGENT BIOSOLUTIONS
14PAXVAX
12TEVA PHARMACEUTICALS
12PROTEIN SCIENCES CORPORATION
9PFIZER\WYETH
4BERNA BIOTECH, LTD.
4SMITHKLINE BEECHAM
3INTERCELL AG
1MEDIMMUNE VACCINES, INC.
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL7,949
7,473
2,547
1,506
1,187
1,051
1,049
s0294561,043
866
IMM209861
816
UT7065MA766
657
579
U62828AA563
557
538
U6737AA516
515
S034636506
4F472471
458
P100253275449
444
276563436
429
418
4BH32414
MENVEO404
PP9L5362
UJ446AA337
319
306
290
271
49TM3270
R1B252M253
4F472179
933622147
C5763AA144
CW3116134
3Y7NL126
UNK114
113
ARBA141A105
104
103
96
300057A90
79
1F4EB73
R1B743M62
56
UJ090AA55
51
UH894AB46
45
UNK44
UNK42
42
EJ168638
Unknown36
35
34
32
32
26
el128424
24
A115A22
22
EN620222
21
UNK20
20
19
Z127A19
19
17
JEV18K95E15
12
111798PI12
10
A739088
No batch number8
3333324181078
6
6
TAR356
5
5
U6935AA5
UNK5
4
unknown4
3
2
55RB72
2
2
2
2
2
U7124AA2
JEV18A68E2
2
ABYB05BA1
1
1
1
1
AMVA436A1
1
1
TJ3521
A130A; VIS give1
1
U7140BB1
1
1
SP UP016AA1
1
1808P08802/ESV01
037K20A300,947
EL1284288,578
57,766
1,432

Incidents per State

State Total
82,750
CA62,821
FL38,209
TX36,512
NY34,921
PA23,646
IN23,622
IL20,597
MI19,590
OH19,426
NJ18,413
NC16,769
GA15,932
WA15,351
VA15,234
MA14,876
AZ14,206
MN12,940
MD12,656
CO11,908
WI11,425
MO10,240
TN9,685
OR8,768
KY8,437
CT8,300
SC6,700
OK6,293
AL5,692
LA5,025
IA4,825
KS4,821
UT4,637
NV4,374
NM3,967
AR3,807
ME3,161
NH3,096
NE2,918
MS2,859
ID2,785
WV2,469
HI2,459
PR2,417
MT2,414
RI2,076
DE1,868
AK1,830
VT1,734
DC1,715
ND1,388
SD1,269
WY866
GU118
VI69
AS47
MP29
MH8
XB6
FM4
QM3
XV2
XL1

ID: 1672817
Sex: F
Age: 69
State: FL

Vax Date: 01/04/2021
Onset Date: 08/17/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Name: Body temperature; Result Unstructured Data: high

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: no appetite; huge red blotch under vaccination site the size of a mango; which blistered and peeled; left breast red/part of right breast were all red; breasts were real itchy; 2nd dose 08Feb2021/3rd on16Aug; has no energy; On the day after her 3rd shot she woke up with a mild 99.3 fever; felt like freight train ran over her; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (felt like freight train ran over her), DECREASED APPETITE (no appetite), RASH MACULAR (huge red blotch under vaccination site the size of a mango), VACCINATION SITE VESICLES (which blistered and peeled) and ERYTHEMA (left breast red/part of right breast were all red) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002F21A, 010M20A and 012L20A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Cancer. On 04-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Aug-2021, the patient experienced FEELING ABNORMAL (felt like freight train ran over her) and PYREXIA (On the day after her 3rd shot she woke up with a mild 99.3 fever). On 20-Aug-2021, the patient experienced ASTHENIA (has no energy). On an unknown date, the patient experienced DECREASED APPETITE (no appetite), RASH MACULAR (huge red blotch under vaccination site the size of a mango), VACCINATION SITE VESICLES (which blistered and peeled), ERYTHEMA (left breast red/part of right breast were all red), PRURITUS (breasts were real itchy) and INCORRECT DOSE ADMINISTERED (2nd dose 08Feb2021/3rd on16Aug). At the time of the report, FEELING ABNORMAL (felt like freight train ran over her), DECREASED APPETITE (no appetite), RASH MACULAR (huge red blotch under vaccination site the size of a mango), VACCINATION SITE VESICLES (which blistered and peeled), ERYTHEMA (left breast red/part of right breast were all red), PRURITUS (breasts were real itchy) and PYREXIA (On the day after her 3rd shot she woke up with a mild 99.3 fever) was resolving and ASTHENIA (has no energy) and INCORRECT DOSE ADMINISTERED (2nd dose 08Feb2021/3rd on16Aug) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 99.3 (High) high. Concomitant medication were not reported. Treatment medication were not reported. Patent was a cancer survivor This case was linked to MOD-2021-293260 (Patient Link).

Other Meds:

Current Illness:

ID: 1672818
Sex: F
Age: 74
State: GA

Vax Date: 08/12/2021
Onset Date: 08/12/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Red Right Arm Injection Site (3" wide and 2.4" Long)/ Redness is getting worst and spreading to the back of the arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE ERYTHEMA (Red Right Arm Injection Site (3" wide and 2.4" Long)/ Redness is getting worst and spreading to the back of the arm) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 009C21A) for COVID-19 vaccination. Previously administered products included for an unreported indication: Tetanus (Patient had similar reaction to tetanus shot a few years ago and she was told its an allergic reaction). Past adverse reactions to the above products included Allergic reaction with Tetanus. On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Aug-2021, the patient experienced VACCINATION SITE ERYTHEMA (Red Right Arm Injection Site (3" wide and 2.4" Long)/ Redness is getting worst and spreading to the back of the arm). At the time of the report, VACCINATION SITE ERYTHEMA (Red Right Arm Injection Site (3" wide and 2.4" Long)/ Redness is getting worst and spreading to the back of the arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not provided Treatment information was not provided. Since vaccination the Right Arm became Red (3" wide and 2.4" Long), and getting worst. It looks like spreading to the back of the arm. The patient had a similar reaction to Tetanus shot a few years ago and she was told that it was an allergic reaction.

Other Meds:

Current Illness:

ID: 1672819
Sex: F
Age:
State: WA

Vax Date: 01/31/2021
Onset Date: 01/31/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Name: X-ray; Result Unstructured Data: Osteoarthritis

Allergies:

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

Symptoms: Significant reaction; patient's arm felt significantly injured around the joint/something was physically attacking area around joint; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Significant reaction) and JOINT INJURY (patient's arm felt significantly injured around the joint/something was physically attacking area around joint) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 007M20A) for COVID-19 vaccination. Concurrent medical conditions included Osteoarthritis. On 31-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Jan-2021, the patient experienced VACCINATION COMPLICATION (Significant reaction) and JOINT INJURY (patient's arm felt significantly injured around the joint/something was physically attacking area around joint). At the time of the report, VACCINATION COMPLICATION (Significant reaction) and JOINT INJURY (patient's arm felt significantly injured around the joint/something was physically attacking area around joint) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, X-ray: abnormal (abnormal) Osteoarthritis. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications was not provided by the reporter. Treatment information was not provided. This case was linked to MOD-2021-293274 (Patient Link).

Other Meds:

Current Illness: Osteoarthritis

ID: 1672820
Sex: F
Age:
State: WA

Vax Date: 01/31/2021
Onset Date: 02/28/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 2021; Test Name: X-ray; Result Unstructured Data: osteoarthritis

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: injured arm internally; osteoarthritis; This spontaneous case was reported by a consumer and describes the occurrence of LIMB INJURY (injured arm internally) and OSTEOARTHRITIS (osteoarthritis) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002A21A and 007M20A) for COVID-19 vaccination. No Medical History information was reported. On 31-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Feb-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced LIMB INJURY (injured arm internally). In 2021, the patient experienced OSTEOARTHRITIS (osteoarthritis). The patient was treated with CORTISONE from August 2021 to August 2021 for Adverse event, at an unspecified dose and frequency. At the time of the report, LIMB INJURY (injured arm internally) and OSTEOARTHRITIS (osteoarthritis) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, X-ray: osteoarthritis (abnormal) osteoarthritis. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient was not taking any concomitant medications. Patient reported that the cortisone shot did not help This case was linked to MOD-2021-293273 (Patient Link).

Other Meds:

Current Illness:

ID: 1672821
Sex: F
Age:
State:

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Shortness of breath; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (Shortness of breath) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. In March 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DYSPNOEA (Shortness of breath). At the time of the report, DYSPNOEA (Shortness of breath) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant products were reported. No treatment information provided. The patient's husband wanted to know if his wife could receive the Johnson and Johnson vaccine as the second dose. Reporter did not allow further contact

Other Meds:

Current Illness:

ID: 1672822
Sex: F
Age:
State: TN

Vax Date:
Onset Date: 08/20/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: I got I got both the Moderna Covid-19 shots. I had a sore arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (I got I got both the Moderna Covid-19 shots. I had a sore arm) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 20-Aug-2021, the patient experienced PAIN IN EXTREMITY (I got I got both the Moderna Covid-19 shots. I had a sore arm). At the time of the report, PAIN IN EXTREMITY (I got I got both the Moderna Covid-19 shots. I had a sore arm) outcome was unknown. No concomitant products were reported. No treatment information provided.

Other Meds:

Current Illness:

ID: 1672823
Sex: F
Age: 38
State:

Vax Date: 08/19/2021
Onset Date: 08/20/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Complained of a headache; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (Complained of a headache) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 002521A) for COVID-19 vaccination. No Medical History information was reported. On 19-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced HEADACHE (Complained of a headache). At the time of the report, HEADACHE (Complained of a headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. Treatment information was not provided. First Moderna Covid-19 vaccine expiration date is not provided. Patient received the Moderna Covid-19 vaccine in her left arm shoulder deltoid muscle and received her vaccine at a Pharmacy. Patient provided permission for Safety to contact her. Patient prefered to be contacted via telephone.

Other Meds:

Current Illness:

ID: 1672824
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Heavy chest tightening; Experiencing vomiting; This spontaneous case was reported by a consumer and describes the occurrence of CHEST DISCOMFORT (Heavy chest tightening) and VOMITING (Experiencing vomiting) in an 18-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced CHEST DISCOMFORT (Heavy chest tightening) and VOMITING (Experiencing vomiting). At the time of the report, CHEST DISCOMFORT (Heavy chest tightening) and VOMITING (Experiencing vomiting) outcome was unknown. The concomitant medications were not reported. The treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672825
Sex: U
Age:
State:

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: More than 35 days since first dose; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (More than 35 days since first dose) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. In January 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (More than 35 days since first dose). At the time of the report, PRODUCT DOSE OMISSION ISSUE (More than 35 days since first dose) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672826
Sex: M
Age:
State:

Vax Date:
Onset Date: 08/21/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 20210821; Test Name: Fast Heartbeat; Result Unstructured Data: Increased

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Dizziness; Weakness; Feels hungry; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), ASTHENIA (Weakness) and HUNGER (Feels hungry) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Aug-2021, the patient experienced DIZZINESS (Dizziness), ASTHENIA (Weakness) and HUNGER (Feels hungry). At the time of the report, DIZZINESS (Dizziness), ASTHENIA (Weakness) and HUNGER (Feels hungry) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 21-Aug-2021, Heart rate abnormal: increased (High) Increased. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided. Reporter did not allow further contact

Other Meds:

Current Illness:

ID: 1672827
Sex: F
Age: 63
State: TX

Vax Date: 07/22/2021
Onset Date: 08/21/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: hardly can get out of bed; strong body aches; headaches; Vomiting; This spontaneous case was reported by a consumer and describes the occurrence of MOBILITY DECREASED (hardly can get out of bed), MYALGIA (strong body aches), HEADACHE (headaches) and VOMITING (Vomiting) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. unknown) for COVID-19 vaccination. No Medical History information was reported. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 21-Aug-2021, the patient experienced MOBILITY DECREASED (hardly can get out of bed), MYALGIA (strong body aches), HEADACHE (headaches) and VOMITING (Vomiting). At the time of the report, MOBILITY DECREASED (hardly can get out of bed), MYALGIA (strong body aches), HEADACHE (headaches) and VOMITING (Vomiting) outcome was unknown. Concomitant medications were not reported. Treatment medications were not reported.

Other Meds:

Current Illness:

ID: 1672828
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: had my second shot and still not feel right including cramping and dizziness; had my second shot and still not feel right including cramping and dizziness; had my second shot and still not feel right including cramping and dizziness; still spotting; This spontaneous case was reported by a consumer and describes the occurrence of MUSCLE SPASMS (had my second shot and still not feel right including cramping and dizziness), DIZZINESS (had my second shot and still not feel right including cramping and dizziness), MALAISE (had my second shot and still not feel right including cramping and dizziness) and INTERMENSTRUAL BLEEDING (still spotting) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MUSCLE SPASMS (had my second shot and still not feel right including cramping and dizziness), DIZZINESS (had my second shot and still not feel right including cramping and dizziness), MALAISE (had my second shot and still not feel right including cramping and dizziness) and INTERMENSTRUAL BLEEDING (still spotting). At the time of the report, MUSCLE SPASMS (had my second shot and still not feel right including cramping and dizziness), DIZZINESS (had my second shot and still not feel right including cramping and dizziness) and INTERMENSTRUAL BLEEDING (still spotting) had not resolved and MALAISE (had my second shot and still not feel right including cramping and dizziness) outcome was unknown. The concomitant medication was not reported. The treatment history was not reported. This case was linked to (Patient Link).

Other Meds:

Current Illness:

ID: 1672829
Sex: F
Age: 22
State: MS

Vax Date: 08/10/2021
Onset Date: 08/13/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 20210813; Test Name: Heart rate; Result Unstructured Data: increased

Allergies:

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

Symptoms: Myalgia; chest pain; shortness of breath; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (Myalgia), CHEST PAIN (chest pain) and DYSPNOEA (shortness of breath) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 939902) for COVID-19 vaccination. No Medical History information was reported. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Aug-2021, the patient experienced MYALGIA (Myalgia), CHEST PAIN (chest pain) and DYSPNOEA (shortness of breath). At the time of the report, MYALGIA (Myalgia), CHEST PAIN (chest pain) and DYSPNOEA (shortness of breath) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-Aug-2021, Heart rate: increased (High) increased. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product was not provided by the reporter. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672830
Sex: F
Age: 53
State: AL

Vax Date: 05/17/2021
Onset Date: 08/19/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Heat on left arm Injection Site after second vaccine; Swelling on left arm Injection Site after second vaccine/Knot on left arm Injection Site after second vaccine; Redness on left arm Injection Site after second vaccine; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Heat on left arm Injection Site after second vaccine), VACCINATION SITE SWELLING (Swelling on left arm Injection Site after second vaccine/Knot on left arm Injection Site after second vaccine) and VACCINATION SITE ERYTHEMA (Redness on left arm Injection Site after second vaccine) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039C21A and 005C21A) for COVID-19 vaccination. No Medical History information was reported. On 17-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Aug-2021, the patient experienced VACCINATION SITE WARMTH (Heat on left arm Injection Site after second vaccine), VACCINATION SITE SWELLING (Swelling on left arm Injection Site after second vaccine/Knot on left arm Injection Site after second vaccine) and VACCINATION SITE ERYTHEMA (Redness on left arm Injection Site after second vaccine). At the time of the report, VACCINATION SITE WARMTH (Heat on left arm Injection Site after second vaccine), VACCINATION SITE SWELLING (Swelling on left arm Injection Site after second vaccine/Knot on left arm Injection Site after second vaccine) and VACCINATION SITE ERYTHEMA (Redness on left arm Injection Site after second vaccine) outcome was unknown. Concomitant medication were not reported. Treatment medication were not reported.

Other Meds:

Current Illness:

ID: 1672831
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: Arm is extremely sore; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Arm is extremely sore) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (Arm is extremely sore). At the time of the report, PAIN IN EXTREMITY (Arm is extremely sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product was not provided. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672832
Sex: M
Age:
State: SC

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

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

Lab Data:

Allergies:

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

Symptoms: unpunctured sitting at room temperature > 24 hours; The unpunctured vial was placed at room temperature yesterday at 3:58 pm and was administered this morning; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT STORAGE ERROR (unpunctured sitting at room temperature > 24 hours) and EXPIRED PRODUCT ADMINISTERED (The unpunctured vial was placed at room temperature yesterday at 3:58 pm and was administered this morning) in a 42-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 017E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT STORAGE ERROR (unpunctured sitting at room temperature > 24 hours) and EXPIRED PRODUCT ADMINISTERED (The unpunctured vial was placed at room temperature yesterday at 3:58 pm and was administered this morning). At the time of the report, PRODUCT STORAGE ERROR (unpunctured sitting at room temperature > 24 hours) and EXPIRED PRODUCT ADMINISTERED (The unpunctured vial was placed at room temperature yesterday at 3:58 pm and was administered this morning) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The concomitant history was not reported. The treatment details was not provided.

Other Meds:

Current Illness:

ID: 1672833
Sex: F
Age: 48
State: NY

Vax Date: 03/20/2021
Onset Date: 04/17/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: infection in her arm below the injection site; soreness at injection site/pain at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of INFECTION (infection in her arm below the injection site) and VACCINATION SITE PAIN (soreness at injection site/pain at the injection site) in a 48-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 039B21A and 046A21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Apr-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Apr-2021, the patient experienced VACCINATION SITE PAIN (soreness at injection site/pain at the injection site). On 24-Apr-2021, the patient experienced INFECTION (infection in her arm below the injection site). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Adverse event, at an unspecified dose and frequency. On 30-Apr-2021, INFECTION (infection in her arm below the injection site) had resolved. At the time of the report, VACCINATION SITE PAIN (soreness at injection site/pain at the injection site) outcome was unknown. Concomitant medications were not reported. Action taken with mRNA-1273 (Moderna COVID-19 Vaccine) was not applicable. This case was linked to MOD-2021-293234 (Patient Link).

Other Meds:

Current Illness:

ID: 1672834
Sex: F
Age:
State: NY

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: My body has edema; My body has swelling/swelling in her body; Sore arm; This spontaneous case was reported by a consumer and describes the occurrence of GENERALISED OEDEMA (My body has edema), SWELLING (My body has swelling/swelling in her body) and VACCINATION SITE PAIN (Sore arm) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. In March 2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced GENERALISED OEDEMA (My body has edema), SWELLING (My body has swelling/swelling in her body) and VACCINATION SITE PAIN (Sore arm). At the time of the report, GENERALISED OEDEMA (My body has edema), SWELLING (My body has swelling/swelling in her body) and VACCINATION SITE PAIN (Sore arm) had not resolved. The concomitant medications were not reported. The treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672835
Sex: F
Age:
State: FL

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: A little sick in the night; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (A little sick in the night) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced ILLNESS (A little sick in the night). At the time of the report, ILLNESS (A little sick in the night) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant medications were provided. No treatment medications were provided.

Other Meds:

Current Illness:

ID: 1672836
Sex: M
Age: 59
State: OH

Vax Date: 07/24/2021
Onset Date: 08/21/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Accidentally gave 2 patients a second dose from vials that were expired past the 12 hours mark this morning 21Aug2021 at 8:25am (vial was open since yesterday 20Aug2021, punctured at 1:35pm); This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Accidentally gave 2 patients a second dose from vials that were expired past the 12 hours mark this morning 21Aug2021 at 8:25am (vial was open since yesterday 20Aug2021, punctured at 1:35pm)) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 040C21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Aug-2021 at 8:25 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 21-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (Accidentally gave 2 patients a second dose from vials that were expired past the 12 hours mark this morning 21Aug2021 at 8:25am (vial was open since yesterday 20Aug2021, punctured at 1:35pm)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Accidentally gave 2 patients a second dose from vials that were expired past the 12 hours mark this morning 21Aug2021 at 8:25am (vial was open since yesterday 20Aug2021, punctured at 1:35pm)) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672837
Sex: U
Age:
State:

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

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

Lab Data: Test Name: Heart rate; Result Unstructured Data: heart bate began fluctuating from as low as 55 bpm and as high as100 bpm.

Allergies:

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

Symptoms: 5 days after receiving my 1st Moderna covid 19 vaccine my heart bate began flucuating from as low as 55 bpm and as high as100 bpm; This spontaneous case was reported by a consumer and describes the occurrence of HEART RATE ABNORMAL (5 days after receiving my 1st Moderna covid 19 vaccine my heart bate began flucuating from as low as 55 bpm and as high as100 bpm) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEART RATE ABNORMAL (5 days after receiving my 1st Moderna covid 19 vaccine my heart bate began flucuating from as low as 55 bpm and as high as100 bpm). At the time of the report, HEART RATE ABNORMAL (5 days after receiving my 1st Moderna covid 19 vaccine my heart bate began flucuating from as low as 55 bpm and as high as100 bpm) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Heart rate: abnormal (abnormal) heart bate began fluctuating from as low as 55 bpm and as high as100 bpm.. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided by the reporter. No treatment information was provided. Reporter did not allow further contact

Other Meds:

Current Illness:

ID: 1672838
Sex: F
Age:
State: OH

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

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: neighbor who is "lady down the hall, we are both very sick she has been for 7 months"; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (neighbor who is "lady down the hall, we are both very sick she has been for 7 months") in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (neighbor who is "lady down the hall, we are both very sick she has been for 7 months"). At the time of the report, VACCINATION COMPLICATION (neighbor who is "lady down the hall, we are both very sick she has been for 7 months") outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant medications was provided. No Treatment medications was provided.

Other Meds:

Current Illness:

ID: 1672839
Sex: U
Age:
State:

Vax Date: 08/05/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This spontaneous case was reported by a consumer and describes the occurrence of VERTIGO (Vertigo), HEADACHE (Headaches) and NAUSEA (Nausea) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VERTIGO (Vertigo), HEADACHE (Headaches) and NAUSEA (Nausea). At the time of the report, VERTIGO (Vertigo), HEADACHE (Headaches) and NAUSEA (Nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication details were provided. No treatment information was mentioned.

Other Meds:

Current Illness:

ID: 1672840
Sex: F
Age: 63
State: NY

Vax Date: 08/09/2021
Onset Date: 08/20/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Left side of her face felt uncomfortable; Left arm felt uncomfortable; Left side of mouth felt uncomfortable; Swelling on left side of face; Numbness on left side of face; Swelling on left side of mouth; Numbness on left side of mouth; This spontaneous case was reported by a consumer and describes the occurrence of FACIAL DISCOMFORT (Left side of her face felt uncomfortable), LIMB DISCOMFORT (Left arm felt uncomfortable), ORAL DISCOMFORT (Left side of mouth felt uncomfortable), SWELLING FACE (Swelling on left side of face) and HYPOAESTHESIA (Numbness on left side of face) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 09-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Aug-2021, the patient experienced FACIAL DISCOMFORT (Left side of her face felt uncomfortable), LIMB DISCOMFORT (Left arm felt uncomfortable), ORAL DISCOMFORT (Left side of mouth felt uncomfortable), SWELLING FACE (Swelling on left side of face), HYPOAESTHESIA (Numbness on left side of face), MOUTH SWELLING (Swelling on left side of mouth) and HYPOAESTHESIA ORAL (Numbness on left side of mouth). At the time of the report, FACIAL DISCOMFORT (Left side of her face felt uncomfortable), LIMB DISCOMFORT (Left arm felt uncomfortable), ORAL DISCOMFORT (Left side of mouth felt uncomfortable), SWELLING FACE (Swelling on left side of face), HYPOAESTHESIA (Numbness on left side of face), MOUTH SWELLING (Swelling on left side of mouth) and HYPOAESTHESIA ORAL (Numbness on left side of mouth) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The treatment history was not reported. The concomitant medication was not reported.

Other Meds:

Current Illness:

ID: 1672841
Sex: F
Age: 45
State: GA

Vax Date: 08/16/2021
Onset Date: 08/16/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Name: Heart rate; Result Unstructured Data: High (Rapid heart beat during day time); Test Date: 20210816; Test Name: Heart rate; Result Unstructured Data: Increased

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: breathing very hard; could not even go to sleep; arm was also hurting; It was very sore that night; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (breathing very hard), INSOMNIA (could not even go to sleep), PAIN IN EXTREMITY (arm was also hurting) and PAIN (It was very sore that night) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 035C21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Aug-2021, the patient experienced DYSPNOEA (breathing very hard), INSOMNIA (could not even go to sleep), PAIN IN EXTREMITY (arm was also hurting) and PAIN (It was very sore that night). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of 1 dosage form. At the time of the report, DYSPNOEA (breathing very hard), INSOMNIA (could not even go to sleep), PAIN IN EXTREMITY (arm was also hurting) and PAIN (It was very sore that night) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 16-Aug-2021, Heart rate: increased (High) Increased. On an unknown date, Heart rate: high (High) High (Rapid heart beat during day time). The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication was reported. Patient felt heart beating was very fast and breathing very hard. It lasted for a while and patient could not even go to sleep. The next night was better. Previous day, patient had rapid heartbeat during the day. Patient never had any trouble with rapid heartbeat or breathing. It was very sore that night (same day of first vaccination), and for a couple of days it continued.

Other Meds:

Current Illness:

ID: 1672842
Sex: F
Age:
State: PA

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

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

Lab Data:

Allergies:

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

Symptoms: administered Higher dose (1 ml) -than-authorized dose (0.5 Ml); This spontaneous case was reported by an other health care professional and describes the occurrence of ACCIDENTAL OVERDOSE (administered Higher dose (1 ml) -than-authorized dose (0.5 Ml)) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 ml. On an unknown date, the patient experienced ACCIDENTAL OVERDOSE (administered Higher dose (1 ml) -than-authorized dose (0.5 Ml)). At the time of the report, ACCIDENTAL OVERDOSE (administered Higher dose (1 ml) -than-authorized dose (0.5 Ml)) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Caller also stated that it was their first dose of a series for 4 out of 5 patients involved, and it was the second dose of a series for 1 patient and stated that no side effects have been reported from the patients involved. No concomitant medications were provided by reporter. No treatment medications were provided by reporter. This case was linked to MOD-2021-293191, MOD-2021-292849, MOD-2021-293520, MOD-2021-292850 (Patient Link).

Other Meds:

Current Illness:

ID: 1672843
Sex: F
Age: 65
State: FL

Vax Date: 02/25/2021
Onset Date: 03/30/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (had a tender left arm/Tender left injection site arm) and FATIGUE (patient was tired the next day after second moderna vaccine) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 037A21B and 011A21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 30-Mar-2021, the patient experienced VACCINATION SITE PAIN (had a tender left arm/Tender left injection site arm) and FATIGUE (patient was tired the next day after second moderna vaccine). At the time of the report, VACCINATION SITE PAIN (had a tender left arm/Tender left injection site arm) and FATIGUE (patient was tired the next day after second moderna vaccine) outcome was unknown. Concomitant medication not provided by reporter. Treatment information not provided by reporter. This case was linked to MOD-2021-293330, MOD-2021-293338 (Patient Link).

Other Meds:

Current Illness:

ID: 1672844
Sex: F
Age: 65
State:

Vax Date: 02/25/2021
Onset Date: 03/03/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Tender left injection site arm; patient was tired; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Tender left injection site arm ) and FATIGUE (patient was tired) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017E21A, 011A21A and 037A21B) for COVID-19 vaccination. No Medical History information was reported. On 25-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 29-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 03-Mar-2021, the patient experienced PAIN IN EXTREMITY (Tender left injection site arm ) and FATIGUE (patient was tired). At the time of the report, PAIN IN EXTREMITY (Tender left injection site arm ) and FATIGUE (patient was tired) outcome was unknown. Concomitant medication not provided by reporter. Treatment information not provided by reporter. This case was linked to MOD-2021-293330, MOD-2021-293337 (Patient Link).

Other Meds:

Current Illness:

ID: 1672845
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: Coughing; This spontaneous case was reported by a consumer and describes the occurrence of COUGH (Coughing) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COUGH (Coughing). At the time of the report, COUGH (Coughing) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient asking Is coughing a side effect . No concomitant medications were provided by reporter. No treatment details were provided by reporter. Denied to be followed by safety

Other Meds:

Current Illness:

ID: 1672846
Sex: F
Age:
State:

Vax Date: 02/12/2021
Onset Date: 03/10/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: DYSPHONIA/voice was weak; This spontaneous case was reported by a consumer and describes the occurrence of DYSPHONIA (DYSPHONIA/voice was weak) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. Co-suspect product included non-company product EDARAVONE (RADICAVA) injection for Amyotrophic lateral sclerosis. Concurrent medical conditions included Amyotrophic lateral sclerosis since August 2021 and Wheelchair user. On 12-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient started EDARAVONE (RADICAVA) (unknown route) at an unspecified dose. On 10-Mar-2021, the patient experienced DYSPHONIA (DYSPHONIA/voice was weak). At the time of the report, DYSPHONIA (DYSPHONIA/voice was weak) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant and treatment drugs were not provided This case was linked to (Patient Link). Reporter did not allow further contact

Other Meds:

Current Illness: Amyotrophic lateral sclerosis; Wheelchair user

ID: 1672847
Sex: F
Age: 72
State: TX

Vax Date: 08/13/2021
Onset Date: 08/18/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: Her muscles are still swollen 3-4 inches to the side; It broke out into a rash; Arm is still swelling; Very itchy/3 inches down from the shot site of the upper left arm; The shot location has turned kind of greenish at the injection site; It has gotten very hot; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE DISCOLOURATION (The shot location has turned kind of greenish at the injection site), VACCINATION SITE WARMTH (It has gotten very hot), MUSCLE SWELLING (Her muscles are still swollen 3-4 inches to the side), VACCINATION SITE PRURITUS (Very itchy/3 inches down from the shot site of the upper left arm) and VACCINATION SITE RASH (It broke out into a rash) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 052E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Aug-2021, the patient experienced VACCINATION SITE DISCOLOURATION (The shot location has turned kind of greenish at the injection site), VACCINATION SITE WARMTH (It has gotten very hot), VACCINATION SITE PRURITUS (Very itchy/3 inches down from the shot site of the upper left arm) and VACCINATION SITE SWELLING (Arm is still swelling). On an unknown date, the patient experienced MUSCLE SWELLING (Her muscles are still swollen 3-4 inches to the side) and VACCINATION SITE RASH (It broke out into a rash). At the time of the report, VACCINATION SITE DISCOLOURATION (The shot location has turned kind of greenish at the injection site), VACCINATION SITE WARMTH (It has gotten very hot), VACCINATION SITE PRURITUS (Very itchy/3 inches down from the shot site of the upper left arm) and VACCINATION SITE RASH (It broke out into a rash) outcome was unknown and MUSCLE SWELLING (Her muscles are still swollen 3-4 inches to the side) and VACCINATION SITE SWELLING (Arm is still swelling) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. On 22Aug2021, patient pressed the vaccination site to feel what was going on, just touched it and aggravated it more. No treatment information was provided.

Other Meds:

Current Illness:

ID: 1672848
Sex: M
Age: 33
State: OH

Vax Date: 07/22/2021
Onset Date: 08/19/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 20210819; Test Name: Body temperature; Result Unstructured Data: had fever at 103 F all night

Allergies:

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

Symptoms: Saturday Morning experienced disorientation like dizziness; real bad vision as well last Saturday Morning; Yesterday patient was still sick on the couch all day until around 6-7o'clock; Fever 103F; Chills; Violently shaking; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (Violently shaking), DISORIENTATION (Saturday Morning experienced disorientation like dizziness), VISION BLURRED (real bad vision as well last Saturday Morning), ILLNESS (Yesterday patient was still sick on the couch all day until around 6-7o'clock) and PYREXIA (Fever 103F) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 091D21A and 078C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included MULTIVITAMIN [VITAMINS NOS], ASCORBIC ACID (VITAMIN C ACID), VITAMIN D NOS and SIMVASTATIN for an unknown indication. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Aug-2021, the patient experienced TREMOR (Violently shaking), PYREXIA (Fever 103F) and CHILLS (Chills). On 20-Aug-2021, the patient experienced ILLNESS (Yesterday patient was still sick on the couch all day until around 6-7o'clock). On 21-Aug-2021, the patient experienced DISORIENTATION (Saturday Morning experienced disorientation like dizziness) and VISION BLURRED (real bad vision as well last Saturday Morning). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. At the time of the report, TREMOR (Violently shaking), DISORIENTATION (Saturday Morning experienced disorientation like dizziness), VISION BLURRED (real bad vision as well last Saturday Morning) and CHILLS (Chills) had not resolved, ILLNESS (Yesterday patient was still sick on the couch all day until around 6-7o'clock) outcome was unknown and PYREXIA (Fever 103F) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Aug-2021, Body temperature: 103 (High) had fever at 103 F all night. Patient was advised to take Tylenol and hydrate. This case was linked to MOD-2021-293388 (Patient Link).

Other Meds: MULTIVITAMIN [VITAMINS NOS]; VITAMIN C ACID; VITAMIN D NOS; SIMVASTATIN

Current Illness:

ID: 1672849
Sex: U
Age:
State: SC

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

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

Lab Data:

Allergies:

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

Symptoms: Dizziness; Afraid to drive; Experienced some issues with the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), FEAR (Afraid to drive) and VACCINATION COMPLICATION (Experienced some issues with the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DIZZINESS (Dizziness), FEAR (Afraid to drive) and VACCINATION COMPLICATION (Experienced some issues with the vaccine). At the time of the report, DIZZINESS (Dizziness), FEAR (Afraid to drive) and VACCINATION COMPLICATION (Experienced some issues with the vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not provided. Treatment medication was not provided.

Other Meds:

Current Illness:

ID: 1672850
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Terrible ringing in her right ear; This spontaneous case was reported by a consumer and describes the occurrence of TINNITUS (Terrible ringing in her right ear) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 028A21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Apr-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced TINNITUS (Terrible ringing in her right ear). At the time of the report, TINNITUS (Terrible ringing in her right ear) outcome was unknown. Treatment medication was not reported. Relevant concomitant medications were not reported. Reporter did not allow further contact

Other Meds:

Current Illness:

ID: 1672851
Sex: M
Age: 64
State: TX

Vax Date: 08/19/2021
Onset Date: 08/19/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: headache that is still going on; lot more fatigue than before; soreness in the arm a lot more; Inadvertent administration of more than two doses; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (headache that is still going on), FATIGUE (lot more fatigue than before), MYALGIA (soreness in the arm a lot more) and EXTRA DOSE ADMINISTERED (Inadvertent administration of more than two doses) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039B21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Aug-2021, the patient experienced EXTRA DOSE ADMINISTERED (Inadvertent administration of more than two doses). On an unknown date, the patient experienced HEADACHE (headache that is still going on), FATIGUE (lot more fatigue than before) and MYALGIA (soreness in the arm a lot more). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. On 19-Aug-2021, EXTRA DOSE ADMINISTERED (Inadvertent administration of more than two doses) had resolved. At the time of the report, HEADACHE (headache that is still going on) had not resolved and FATIGUE (lot more fatigue than before) and MYALGIA (soreness in the arm a lot more) outcome was unknown. Relevant concomitant medications were not reported. The treatment information was not provided. This case was linked to MOD-2021-293631, MOD-2021-293637 (Patient Link).

Other Meds:

Current Illness:

ID: 1672852
Sex: M
Age:
State: NJ

Vax Date: 02/11/2021
Onset Date: 08/19/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Off label use; I have a mild headache; body aches; I'm feeling a slight discomfort; Extra dose administered; This spontaneous case was reported by a consumer and describes the occurrence of DISCOMFORT (I'm feeling a slight discomfort), EXTRA DOSE ADMINISTERED (Extra dose administered), OFF LABEL USE (Off label use), HEADACHE (I have a mild headache) and MYALGIA (body aches) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 005C21A, 012M20A and 013A21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Aug-2021, the patient experienced EXTRA DOSE ADMINISTERED (Extra dose administered). On 20-Aug-2021, the patient experienced DISCOMFORT (I'm feeling a slight discomfort), HEADACHE (I have a mild headache) and MYALGIA (body aches). On an unknown date, the patient experienced OFF LABEL USE (Off label use). At the time of the report, DISCOMFORT (I'm feeling a slight discomfort), HEADACHE (I have a mild headache) and MYALGIA (body aches) outcome was unknown and EXTRA DOSE ADMINISTERED (Extra dose administered) and OFF LABEL USE (Off label use) had resolved. The concomitant medication was not reported. The treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672853
Sex: F
Age:
State: SC

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

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

Lab Data:

Allergies:

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

Symptoms: Great than 12 hours at room temperature; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Great than 12 hours at room temperature) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 017E21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Great than 12 hours at room temperature). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Great than 12 hours at room temperature) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product information was provided. Pharmacist states that they administered Moderna COVID-19 vaccine that has undergone a temperature excursion to 3 patients. The punctured vial was placed at room temperature yesterday at 3:58 pm and was administered this morning at 10:09am 11:17am, and 11:22am. Administered this morning 11:17am, 11:22am, 10:09am. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672854
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: side effects of the first shot of the Moderna vaccine; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (side effects of the first shot of the Moderna vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (side effects of the first shot of the Moderna vaccine). At the time of the report, VACCINATION COMPLICATION (side effects of the first shot of the Moderna vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was reported No treatment medication was reported by reporter Reporter did not allow further contact

Other Meds:

Current Illness:

ID: 1672855
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: Patient got the first vaccine on Thursday and on these past 2 days, felt all the side effects; Dizziness; Headache; Nausea; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Patient got the first vaccine on Thursday and on these past 2 days, felt all the side effects), DIZZINESS (Dizziness), HEADACHE (Headache) and NAUSEA (Nausea) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Patient got the first vaccine on Thursday and on these past 2 days, felt all the side effects), DIZZINESS (Dizziness), HEADACHE (Headache) and NAUSEA (Nausea). At the time of the report, VACCINATION COMPLICATION (Patient got the first vaccine on Thursday and on these past 2 days, felt all the side effects), DIZZINESS (Dizziness), HEADACHE (Headache) and NAUSEA (Nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication was not provided. Treatment information was not reported.

Other Meds:

Current Illness:

ID: 1672856
Sex: M
Age: 33
State: OH

Vax Date: 07/22/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Sore arm; Feeling tired; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Sore arm) and FATIGUE (Feeling tired) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Medical history was not provided by reporter. Concomitant products included MULTIVITAMINS [VITAMINS NOS], VITAMIN C [ASCORBIC ACID], VITAMIN D NOS and SIMVASTATIN for an unknown indication. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (Sore arm) and FATIGUE (Feeling tired). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Sore arm) and FATIGUE (Feeling tired) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medication also included hydrate. This case was linked to MOD-2021-293366 (Patient Link).

Other Meds: MULTIVITAMINS [VITAMINS NOS]; VITAMIN C [ASCORBIC ACID]; VITAMIN D NOS; SIMVASTATIN

Current Illness:

ID: 1672857
Sex: M
Age: 25
State: GA

Vax Date: 08/14/2021
Onset Date: 08/14/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Sore throat; Stuffy nose; Runny nose; watery eyes; coughing; lost taste; Lost smell; Chills; Fever; Headaches; Left arm pain/left arm pain went away after three days; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL PAIN (Sore throat), NASAL CONGESTION (Stuffy nose), RHINORRHOEA (Runny nose), LACRIMATION INCREASED (watery eyes) and COUGH (coughing) in a 25-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 017E21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Asthma (Respiratory asthma), Allergy NOS and Vegetable allergy (Allergic to carrots). On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 14-Aug-2021, the patient experienced OROPHARYNGEAL PAIN (Sore throat), NASAL CONGESTION (Stuffy nose), RHINORRHOEA (Runny nose), LACRIMATION INCREASED (watery eyes), COUGH (coughing), AGEUSIA (lost taste), ANOSMIA (Lost smell), CHILLS (Chills ), PYREXIA (Fever ), HEADACHE (Headaches) and VACCINATION SITE PAIN (Left arm pain/left arm pain went away after three days). The patient was treated with IBUPROFEN for Adverse event, at an unspecified dose and frequency; PARACETAMOL, PHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE (THERAFLU COLD AND FLU) for Adverse event, at an unspecified dose and frequency and IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE (VICKS ACTION) for Adverse event, at an unspecified dose and frequency. On 17-Aug-2021, VACCINATION SITE PAIN (Left arm pain/left arm pain went away after three days) had resolved. At the time of the report, OROPHARYNGEAL PAIN (Sore throat), NASAL CONGESTION (Stuffy nose), RHINORRHOEA (Runny nose), LACRIMATION INCREASED (watery eyes), COUGH (coughing), AGEUSIA (lost taste), ANOSMIA (Lost smell), CHILLS (Chills ), PYREXIA (Fever ) and HEADACHE (Headaches) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient stated that he experienced all symptoms and felt like a guinea pig. Patient occasionally uses an Asthma Inhaler (unknown name) as concomitant medication.

Other Meds:

Current Illness: Allergy NOS; Asthma (Respiratory asthma); Vegetable allergy (Allergic to carrots)

ID: 1672858
Sex: M
Age: 63
State: TX

Vax Date: 01/06/2021
Onset Date: 08/20/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 202108; Test Name: Body temperature; Result Unstructured Data: The patient's body temperature was 102.8 degrees Fahrenheit

Allergies:

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

Symptoms: Really sick; Shaking really bad; Big knot on right upper deltoid and has a little bump on itit; Felt really tired; Achy, body ache; Fever at 102.8 degrees Fahrenheit; Severe headache; Really worst reaction after the booster shot; This spontaneous case was reported by a nurse and describes the occurrence of VACCINATION COMPLICATION (Really worst reaction after the booster shot), MALAISE (Really sick), TREMOR (Shaking really bad), SKIN MASS (Big knot on right upper deltoid and has a little bump on itit) and FATIGUE (Felt really tired) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017E21A, 013M20A and 011620A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history information was reported . Concomitant products included MULTIVITAMINS [VITAMINS NOS] for an unknown indication. On 06-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Aug-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced VACCINATION COMPLICATION (Really worst reaction after the booster shot). On 21-Aug-2021, the patient experienced MALAISE (Really sick), SKIN MASS (Big knot on right upper deltoid and has a little bump on itit), FATIGUE (Felt really tired), PAIN (Achy, body ache), PYREXIA (Fever at 102.8 degrees Fahrenheit) and HEADACHE (Severe headache). 21-Aug-2021, the patient experienced TREMOR (Shaking really bad). The patient was treated with IBUPROFEN on 21-Aug-2021 for Adverse event, at an unspecified dose and frequency. On 22-Aug-2021, VACCINATION COMPLICATION (Really worst reaction after the booster shot), MALAISE (Really sick), TREMOR (Shaking really bad), PYREXIA (Fever at 102.8 degrees Fahrenheit) and HEADACHE (Severe headache) had resolved. At the time of the report, SKIN MASS (Big knot on right upper deltoid and has a little bump on itit) outcome was unknown and FATIGUE (Felt really tired) and PAIN (Achy, body ache) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In August 2021, Body temperature: 102.8 (High) The patient's body temperature was 102.8 degrees Fahrenheit. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient was unable to recall the injection site and other reactions after first both doses.

Other Meds: MULTIVITAMINS [VITAMINS NOS]

Current Illness:

ID: 1672859
Sex: M
Age:
State: NY

Vax Date:
Onset Date: 08/21/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: little dizzy; felt really fatigue; cold; chills; trembling; fever; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (little dizzy), FATIGUE (felt really fatigue), NASOPHARYNGITIS (cold), CHILLS (chills) and TREMOR (trembling) in a 24-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Aug-2021, the patient experienced DIZZINESS (little dizzy), FATIGUE (felt really fatigue), NASOPHARYNGITIS (cold), CHILLS (chills), TREMOR (trembling) and PYREXIA (fever). At the time of the report, DIZZINESS (little dizzy), FATIGUE (felt really fatigue), NASOPHARYNGITIS (cold), CHILLS (chills), TREMOR (trembling) and PYREXIA (fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Relevant concomitant medications were not provided. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672860
Sex: U
Age:
State:

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

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

Lab Data: Test Name: Body temperature; Result Unstructured Data: 101.3 Fahrenheit fever

Allergies:

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

Symptoms: 101.3 Fahrenheit fever; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (101.3 Fahrenheit fever) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PYREXIA (101.3 Fahrenheit fever). At the time of the report, PYREXIA (101.3 Fahrenheit fever) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 101.3 (High) 101.3 Fahrenheit fever. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications reported. No treatment information was reported by reporter

Other Meds:

Current Illness:

ID: 1672861
Sex: U
Age:
State:

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

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

Lab Data: Test Name: Heart rate; Result Unstructured Data: Fast heart rate was reported

Allergies:

Symptom List: Vomiting

Symptoms: Shortness of breath; Fast heartrate; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (Shortness of breath) and HEART RATE INCREASED (Fast heartrate) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DYSPNOEA (Shortness of breath) and HEART RATE INCREASED (Fast heartrate). At the time of the report, DYSPNOEA (Shortness of breath) and HEART RATE INCREASED (Fast heartrate) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Heart rate: fast (High) Fast heart rate was reported. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672862
Sex: M
Age: 77
State: TX

Vax Date: 12/30/2020
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: husband was also feeling sick after eating; arthritis is getting worse after vaccine; it's hard for him to get up and down; he has gained some weight recently; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (husband was also feeling sick after eating), CONDITION AGGRAVATED (arthritis is getting worse after vaccine), MOBILITY DECREASED (it's hard for him to get up and down) and WEIGHT INCREASED (he has gained some weight recently) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The patient's past medical history included Bypass surgery, Pacemaker insertion (cardiac), Stent placement and Heart valve replacement NOS. Concurrent medical conditions included Arthritis, Heart disorder, Cholesterol and Hypertension. On 30-Dec-2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jan-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced ILLNESS (husband was also feeling sick after eating), CONDITION AGGRAVATED (arthritis is getting worse after vaccine), MOBILITY DECREASED (it's hard for him to get up and down) and WEIGHT INCREASED (he has gained some weight recently). At the time of the report, ILLNESS (husband was also feeling sick after eating), CONDITION AGGRAVATED (arthritis is getting worse after vaccine), MOBILITY DECREASED (it's hard for him to get up and down) and WEIGHT INCREASED (he has gained some weight recently) outcome was unknown. concomitant indications are given with unspecified drugs Treatment medications were not provided

Other Meds:

Current Illness: Arthritis; Cholesterol; Heart disorder; Hypertension

ID: 1672863
Sex: F
Age:
State: NC

Vax Date: 08/11/2021
Onset Date: 08/11/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 20210811; Test Name: Heartbeat; Result Unstructured Data: fast heartbeat

Allergies:

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

Symptoms: very gassy; loose BM [bowel movement]; bothersome stomach thing; This spontaneous case was reported by a consumer and describes the occurrence of FLATULENCE (very gassy), DIARRHOEA (loose BM [bowel movement]) and ABDOMINAL DISCOMFORT (bothersome stomach thing) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On 11-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Aug-2021, the patient experienced FLATULENCE (very gassy), DIARRHOEA (loose BM [bowel movement]) and ABDOMINAL DISCOMFORT (bothersome stomach thing). At the time of the report, FLATULENCE (very gassy), DIARRHOEA (loose BM [bowel movement]) and ABDOMINAL DISCOMFORT (bothersome stomach thing) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-Aug-2021, Heart rate: fast heartbeat (High) fast heartbeat. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications was not provided by the reporter. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1672864
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Arthritis in knee; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of ARTHRITIS (Arthritis in knee) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. Co-suspect product included non-company product ATORVASTATIN for Joint pain. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form and ATORVASTATIN (unknown route) at an unspecified dose. On an unknown date, the patient experienced ARTHRITIS (Arthritis in knee). At the time of the report, ARTHRITIS (Arthritis in knee) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Treatment medications was provided.

Other Meds:

Current Illness:

ID: 1672865
Sex: F
Age: 65
State: KS

Vax Date: 07/22/2021
Onset Date: 08/12/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Vomiting; Got the second dose 21 days after the first one; This spontaneous case was reported by an other health care professional and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Got the second dose 21 days after the first one) and VOMITING (Vomiting) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 027C21A and 001C21A) for COVID-19 vaccination. Concomitant products included IBUPROFEN, TROMETHAMINE, LOSARTAN POTASSIUM, OXYBUTYNIN HYDROCHLORIDE (OXYBUTYNIN [OXYBUTYNIN HYDROCHLORIDE]), OMEPRAZOLE (PRILOSEC [OMEPRAZOLE]) and ATORVASTATIN CALCIUM for an unknown indication. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 12-Aug-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Got the second dose 21 days after the first one). On an unknown date, the patient experienced VOMITING (Vomiting). On 12-Aug-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Got the second dose 21 days after the first one) had resolved. At the time of the report, VOMITING (Vomiting) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications also included ointment plebanate propionate. Treatment information was not provided. HCP called to find out if the second dose administered to patient after 21 days of getting the first dose is a valid dose or if needed to repeat it.

Other Meds: IBUPROFEN; TROMETHAMINE; LOSARTAN POTASSIUM; OXYBUTYNIN [OXYBUTYNIN HYDROCHLORIDE]; PRILOSEC [OMEPRAZOLE]; ATORVASTATIN CALCIUM

Current Illness:

ID: 1672866
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: My husband and I had Moderna shot yesterday can he get tested for Covid if it's his first shot? He's been very sick Can he get a Covid test right after the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (My husband and I had Moderna shot yesterday can he get tested for Covid if it's his first shot? He's been very sick Can he get a Covid test right after the vaccine) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced ILLNESS (My husband and I had Moderna shot yesterday can he get tested for Covid if it's his first shot? He's been very sick Can he get a Covid test right after the vaccine). At the time of the report, ILLNESS (My husband and I had Moderna shot yesterday can he get tested for Covid if it's his first shot? He's been very sick Can he get a Covid test right after the vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. The concomitant medications were not reported. The treatment information was not provided.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am