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: 1827590
Sex: F
Age:
State: OK

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Has to take her time so that she does not fall, she can use her knees; weakness/feeling weak from her waist down/When she got ready to get in a chair she could not pull herself up; She could not use her knees; Unable to write clearly; not able to stand up; Had to crawl; This is a spontaneous report from a contactable consumer. This female consumer (patient) reported for herself that: An 87-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: ELS263, Expiry date was not reported) via an unspecified route of administration on 22Feb2021 in the left shoulder/arm left at 12:00 (at the age of 87 years old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included High blood pressure from 2000 and ongoing. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported, Expiry date was not reported) via an unspecified route of administration on 01Feb2021 (at the age of 87-years-old) as DOSE 1, SINGLE for covid-19 immunisation/ first dose was administered 3 weeks before second dose approximately 01Feb2021. There were no concomitant medications. The patient has not received any other products. On 23Feb2021 she had onset of feeling weak from her waist down; unable to write clearly (unable to write checks), was not able to stand up, had to crawl, when she got ready to get in a chair, she could not pull herself up; she could not use her knees. Patient takes her time so that she does not fall, she can use her knees on 24Feb2021. She asked for information on why these events occurred relative to the Pfizer COVID-19 Vaccine. Patient stated that there has been no emergency room visit, hospitalization or physician's office visit relative to any of the adverse events reported. Patient has not received any investigation assessment. The clinical outcome of the event has to take her time so that she does not fall, she can use her knees was recovering while other events recovered with sequel. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Blood pressure high (Verbatim: High blood pressure)

ID: 1827591
Sex: F
Age:
State: NJ

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 10/29/2021
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: Metallic taste in my mouth that will not go away; This is a spontaneous report from a contactable consumer (patient). A 46-year-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; Lot Number: EN6203) via an unspecified route of administration, on 26Feb2021 at 10:00 (age at vaccination 46 years) as DOSE 1, 0.3 ML, SINGLE for COVID-19 immunization. Medical history included sinusitis, heart murmur, mitrovalve and known allergy: nuts, treenuts, fish and shellfish. Concomitant medications included fluticasone furoate, umeclidinium bromide, vilanterol trifenatate (TRELEGY, montelukast sodium (SINGULAIR), fexofenadine hydrochloride (ALLEGRA), triamcinolone acetonide (NASACORT) and azelastine (AZELASTINE). The patient previously took Ibuprofen, Sulfa, NSAIDS and Penicillin and experienced allergies to medications. Patient had not received any other vaccine within 4 weeks. Patient was not pregnant at time of vaccination. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. On 26Feb2021 at 11:00 the patient experienced metallic taste in mouth that would not go away. The patient had a simple question since she had her first dose on 26Feb2021 and was supposed to go get her second dose on 19Mar2021. She reported that she had been trying to Google it, and she was supposed to have dental work the next day from the reporting to fill some cavities, she would like to know if Novocain might have an impact on the vaccine since she got her first dose 6 days ago and she did not want to take chance. The patient was not received any treatment for the event. Outcome of the event was not resolved. No follow-up attempts are needed. No further information is expected

Other Meds: TRELEGY; SINGULAIR; ALLEGRA; NASACORT; AZELASTINE

Current Illness:

ID: 1827592
Sex: F
Age:
State: IN

Vax Date: 01/15/2021
Onset Date:
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: sleeping for 2 days; Bad side effect; Not eaten anything or had anything to drink; Little weak; Felt extremely tired; This is a spontaneous report from a contactable consumer (Patient). A 77-year-old female patient received first dose of bnt162b2 (BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 15Jan2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date in 2021, after the first dose of vaccination, she was mostly in bed, sleeping for 2 days. She felt extremely tired but was ok after resting. The patient reported that she had "bad side effect'"with Pfizer's COVID-19 vaccine. She was "a little weak" the next 2 days. She had not eaten anything or had anything to drink. The patient suspected that the adverse events she experienced for the 2 doses were similar. However, she did not feel the weakness since she was sleeping excessively. She said her AEs are so severe that she has to report it. Because the COVID-19 virus is evolving to be a more dangerous virus, considering the adverse event, she wanted to know if she still should get the Pfizer vaccine if there may come a time that additional doses are needed to be covered for the new strains of the virus. She also wanted to know if she could switch to another kind of COVID-19 vaccine (like Moderna) after completing the Pfizer COVID-19 vaccine vaccination series. She also wanted to know if the third booster had to be Pfizer's vaccine or it could be another vaccine. The patient reported that there was no product quality complaint present. She is following up to receive the answer to her questions. She had already received two Pfizer vaccine doses. She heard on the news they are studying a third shot of Pfizer's vaccine and was wondering if she could receive a third booster shot with it once it is studied. If she gets a third dose or booster, would she be able to switch to another vaccine. The clinical outcome of events was reported as inknown. Follow-up (01Mar2021): This is a follow-up spontaneous report from a contactable consumer. Gender of the patient, events and narrative updated. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827593
Sex: M
Age:
State: CT

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Feeling tired on the second day (27Feb2021) after vaccination of the 2nd dose.; A little bit muscle aches around the injection site and on the back; This is a spontaneous report from a contactable consumer or other non hcp. A 35-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in Arm Left on 26Feb2021 14:30 (at the age of 35-years-old) as dose 2, single for covid-19 immunisation. The medical history and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the vaccination. The patient did not receive any other medication within 2 weeks of vaccination. The patient did not received treatment for the adverse event. The patient received first dose of BNT162B2 on 05Feb2021 at 2:15 PM (lot number: EL3247, Location: left arm) for covid-19 immunization. On 27Feb2021 at 10:00 the patient experienced feeling tired on the second day (27feb2021) after vaccination of the 2nd dose and a little bit muscle aches around the injection site and on the back. The outcome of both the events was resolving. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1827594
Sex: M
Age:
State: TN

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: Gum infection; This is a spontaneous report from a Sponsored Program from a contactable consumer (patient's wife). A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced gum infection. Reporter stated that her husband and herself were scheduled for their 2nd dose of the Pfizer Covid vaccine this week however her husband had a gum infection for which he requires penicillin. She would like to know if there was any interaction between penicillin and the Covid vaccine. It was unclear if this started before or after he received the 1st dose of the Pfizer Covid vaccine however caller did state that the 2nd dose was scheduled for this week. The outcome of the event unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827595
Sex: F
Age:
State: PA

Vax Date: 02/24/2021
Onset Date: 02/25/2021
Rec V Date: 10/29/2021
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: she notices mild symptoms of withdrawal described as electrical impulses in finger tips and visual flashes (mild strobe like effect).; visual flashes (mild strobe like effect); This is a spontaneous report from a contactable consumer (patient) and physician. A 36-year-old non pregnant female patient received BNT162B2 (BNT162B2, solution for injection, Lot Number: EN6202), via an unspecified route of administration, administered in the left arm on 24Feb2021 (at the age of 36 years old) as DOSE 2, SINGLE for COVID-19 immunization. Patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 vaccine administered was hospital. Medical history included Crohn's (has had ileostomy), allergies to medications, food, or other products: sulfa, feraheme & gadolinium contrast, PCOS (polycystic ovarian syndrome), depression, anxiety. Concomitant medication(s) included Humira, Methotrexate, Folic acid, Pepcid, Lo lo estrin, Depakote, Trazadone, venlafaxine & medical marijuana (cannabis). Patient previously received BNT162B2 (BNT162B2, solution for injection, Lot Number: EL8982), via an unspecified route of administration, administered in the left arm on 01Feb2021 as DOSE 1, SINGLE for COVID-19 immunization. No other vaccines were given within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 25Feb2021 08:00 the patient experienced she notices mild symptoms of withdrawal described as electrical impulses in fingertips and visual flashes (mild strobe like effect), visual flashes (mild strobe like effect). No treatment was received for events. Reporter stated that events was similar to what she's experienced when she's been a couple of hours late with a dose. The clinical outcome of the events was reported as recovering. No Follow-up attempts are needed. No further information expected.

Other Meds: HUMIRA; METHOTREXATE SODIUM; FOLIC ACID; PEPCID AC; LO LOESTRIN FE; DEPAKOTE; TRAZODONE; VENLAFAXINE HYDROCHLORIDE; CANNABIS

Current Illness:

ID: 1827596
Sex: F
Age:
State: CT

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 10/29/2021
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: jaw tightness; right jaw tenderness; little tired; right jaw stiffness; This is a spontaneous report from a contactable consumer or non-health care professional (patient) via medical information team and from a sponsored program Support. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number was not reported), via an unspecified route of administration, administered in right arm on an unspecified date in Feb2021 10:30 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date in Feb2021, after the first dose of the vaccine, the patient felt a little tired. The following day patient woke up and patient had some jaw tightness and jaw tenderness which occurred the morning after patient got vaccinated. Her right jaw was the one that felt tender when patient opened the mouth, patient could feel that it got affected. Patient also stated that felt like it was just hard to open her mouth and that lasted for about 12 hours and it was resolved or maybe 8 hours and that was resolved by Thursday night (unspecified date). Patient also had jaw stiffness on the side of the where the patient received vaccine. Patient wanted to know if what patient had experienced would increase patient's possibility of having Bell's palsy. Outcome of the events jaw tightness and right jaw tenderness was recovered on an unspecified date in Feb2021 and outcome of rest of other events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827597
Sex: F
Age:
State: VA

Vax Date: 02/27/2021
Onset Date:
Rec V Date: 10/29/2021
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: I am only having soreness of arms.; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female (patient) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, lot/batch number: not reported) via an unspecified route of administration on 27Feb2021 (at the age of 69 years) as dose 1, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient had her first shot and she was due to see her primary care doctor on 10Mar2021 where she would get a Cortisone shot in her knee. She was wondering if that would cause any reaction with the COVID-19 vaccine. The second shot of vaccine would be on 20Mar2021. On an unknown date, the patient was only having soreness of arms. The outcome of event was unknown. No follow-up attempts are possible; Information about Lot/Batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827598
Sex: M
Age:
State: CA

Vax Date: 02/22/2021
Onset Date: 02/28/2021
Rec V Date: 10/29/2021
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: rash around the injection site; blood blister where the injection site was; his arm started itching where he got his shot; This is a spontaneous report from a contactable consumer. This consumer reported for a male patient (Husband) that: A 74-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), dose 2 via an unspecified route of administration, administered in left arm on 22Feb2021 (at the age of 74-years-old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included lymphoma (product injected into an arm that previously had lymphoma). The patient's concomitant medications were not reported. Patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, in right arm on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation with no adverse effect. Patient went a week ago to get his last COVID-19 shot(22Feb2021) and caller states that she didn't notice it before but last night (28Feb2021), his arm started itching where he got his shot, and the caller looked at it and her husband had a rash around where the shot was administered, and he had like a blood blister where the shot was administered (rash around the injection site and also he had a blood blister where the injection site was). Caller states that she put some coconut oil on it so that he would not scratch it anymore, and it was warm to the touch. Caller states that the coconut oil helped to stop the itching, but caller is concerned because her husband had lymphoma in that arm, and the VA did not ask which arm her husband wanted the shot in, they just gave it to him in his left arm. But caller states that her husband got his first dose of the product in the right arm. Caller is wondering if the vaccine will take if it was administered in the arm that her husband had lymphoma and he didn't have a lot of muscle mass in his left arm. Patient received treatment for event vaccination site pruritus. The clinical outcome of the event vaccination site pruritus was recovered on 2021 while other was unknown. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827599
Sex: M
Age:
State: PA

Vax Date: 02/14/2021
Onset Date:
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Trigeminal neuropathy; Headache.; This is a spontaneous report from a contactable consumer or other non hcp (patient himself) via a sponsored program. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: Unknown) via an unspecified route of administration in left arm on 14Feb2021 as dose 1, single for COVID-19 immunization. The patient medical history includes covid was in hospital for a month and trigeminal neuropathy from unknown start and stop dates. The concomitant medications were not reported. The patient experienced trigeminal neuropathy, constant headache on an unspecified date in 2021. He reported that he thinks the first dose triggered his condition, trigeminal neuropathy and the vaccine was administered on his left arm where his condition is most prominent. With this, he wants to know if it is still safe for him to receive the second dose. The clinical outcome of all events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827600
Sex: M
Age:
State: FL

Vax Date: 01/30/2021
Onset Date:
Rec V Date: 10/29/2021
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: after he had the second injection he has not had to use anything, it seems like it's gone; This is a spontaneous report from a contactable consumer (Patient). A 77-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: RN5318, Expiry date was not reported), via an unspecified route of administration on 30Jan2021 (at the age of 77-years-old) as dose 2, single for COVID-19 immunization. The Patient Medical history included arthritis from an unknown date and unknown if ongoing he had arthritis which was self-diagnosed it his hands for quite a while and he had been using copper infused gloves and sometimes if the pain was very bad, he would put cannabis cream on them to ease the pain, blood pressure abnormal from an unknown date and unknown if ongoing. The patient concomitant medications not reported. Previously patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/Lot Number: EL3246 and Expiry date was not reported), via an unspecified route of administration on 09Jan2021 (at the age of 77-years-old) as dose 1, single for COVID-19 immunization. The patient not received other products. Caller is calling about the Pfizer vaccine, the COVID vaccine. He had 2 injections on the 09Jan2021 and second on 30Jan2021. He did not have a adverse reaction, he had a positive reaction. He had arthritis which was self-diagnosed it his hands for quite a while, and he had been using copper infused gloves and sometimes if the pain was very bad, he would put cannabis cream on them to ease the pain. But after he had the second injection, on unspecified date, he has not had to use anything, it seems like it's gone, and he was wondering if there had been any other reactions like that where a condition seems to have improved. He says as long as there won't be 17 calls ahead of him. He says if it is, it is fine, he will drop it. He asks is it possible to have someone call him back. If he can be transferred to someone now otherwise. He had trouble on the web site sending something, he wanted to call but he doesn't want to make this his life's work. But after he had the second injection, he has not had to use anything, it seems like it's gone, and he was wondering if there had been any other reactions like that where a condition seems to have improved. Primary Care: The phone number is in his phone, and he is not able to get it right now. He thinks she is at. He thinks that is it. Patient details: he will be 78 soon. He used to be 6'3 he may be a little less than that now, they say you lose an inch every now and then, but he has good posture so maybe not. The only medication he takes if for blood pressure daily shouldn't have anything to do with that. He says he would rather have someone call him back since call handler does not know whether he would have to hold in a queue or not. The outcome for the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1827601
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: The patient felt like she's been raped; This is a spontaneous report from a non-contactable consumer (patient) received via the Medical Information Team. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient reported that she felt like she's been raped on an unspecified date, after being vaccinated. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827602
Sex: M
Age:
State: MO

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: At about, the one-hour mark had a metallic taste in my mouth for a few minutes; 1st shot, just soreness to the injection site for like 5 hours; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Right on 27Jan2021 (Batch/Lot Number: EN5318) (at the age of 66 years) as dose 1, single for covid-19 immunisation. Medical history included heart, digestive, knee injuries, post-traumatic stress disorder, all from an unknown date and unknown if ongoing. There were no known allergies. There were other medications in two weeks. There was no other vaccine in two weeks. There was no COVID prior vaccination. The patient was not tested post vaccination. After 1st shot, patient experienced just soreness to the injection site for like 5 hours. At about, the one-hour mark (as reported) had a metallic taste in the mouth for a few minutes. The outcome of events was recovered. No follow-up attempts are Possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1827603
Sex: F
Age:
State: OH

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: Bitter metal taste; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient). An 84-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Historically the patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. On an unspecified date, the patient experienced bitter metal taste. It was reported that, the patient experienced bitter metal taste after the second covid vaccine shot. She enquired will this go away and was there any way to get rid of it and said she was 84 years old, and no one seemed to be able to answer this question for her, not doctors or health department. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1827604
Sex: M
Age:
State: NC

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 10/29/2021
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: Altered mental status; This is a spontaneous report from a contactable pharmacist. A 74-year-old male patient received bnt162b2 (BNT162B2 Formulation; solution for injection), dose 1 intramuscularly, administered in Arm Left on 25Feb2021 (Batch/Lot Number: EN6203) as DOSE 1, SINGLE (at the age of 74-year-old) for covid-19 immunisation. Medical history included hypertension, hyperlipidemia, diabetes and Known allergies Adhesive tape: silicones from an unknown date and unknown if ongoing. The patient did not have COVID prior vaccination. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was unknown if other medications in two weeks received or not. The patient experienced altered mental status on 25Feb2021. The patient not tested for COVID post vaccination. It was unknown if any treatment received for event or not. The outcome of event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1827605
Sex: M
Age:
State: IL

Vax Date: 03/02/2021
Onset Date: 03/02/2021
Rec V Date: 10/29/2021
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: Injection site pain/soreness starting at ~12:00 PM Central Time; This is a spontaneous report from a contactable consumer (patient). A 30-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EJ1685) via an unspecified route of administration, administered in Arm Right on 02Mar2021 at 08:30 (at the age of 30-year-old) as dose 1, single for COVID-19 immunisation. Medical history included asthma, Penicillin allergy. Concomitant medications included albuterol [salbutamol] (ALBUTEROL [SALBUTAMOL]); fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA); fluticasone all taken for an unspecified indication. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination reported as Albuterol, Breo, Fluticasone, Allergy Shots. On 02Mar2021 the patient experienced injection site pain/soreness starting at 12:00 pm central time. Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient was not tested for COVID-19. Patient did not receive treatment for the event. Outcome of the event was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds: ALBUTEROL [SALBUTAMOL]; BREO ELLIPTA; FLUTICASONE

Current Illness:

ID: 1827606
Sex: U
Age:
State: PA

Vax Date: 02/24/2021
Onset Date: 02/01/2021
Rec V Date: 10/29/2021
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: Runny nose; lots of cold; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 24Feb2021 (lot number and expiry date: unknown) as dose number unknown, single, for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. On unspecified date in Feb2021, the patient experienced runny nose and lots of cold. Outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827607
Sex: M
Age:
State:

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 10/29/2021
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: terrible time sleeping; swelling at injection site; Redness at injection site; pain at the injection; This is a spontaneous report from a contactable consumer (patient). A 67-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: not reported), via an unspecified route of administration on 01Mar2021 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 01Mar2021, the patient experienced pain also had redness, swelling at the injection site and he had terrible time sleeping due to the pain on an unspecified date. He wanted to know what medication he can take for pain in the arm that is safe to take with the vaccine. He did not use or taken anything to treat this event, but he wanted to know if there is anything he can take or use like salt to soak the area or Aspirin or Tylenol or something with no side effects. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1827608
Sex: M
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: swelling in left elbow; This is a spontaneous report from a contactable consumer or other non HCP (Patient). A 81-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration, administered in Arm Left on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history included diabetes and Guillain-Barre syndrome (GBS), under control. The patient's concomitant medications were not reported. The Caller was an 81-year male consumer, asking "was his symptom a reaction to the vaccine" and "did his shot take effect and do he get the second shot" Caller reports that he has swelling in left elbow on an unspecified date, and it looks like a golf ball and asks if this was a side effect of the vaccine. He reports that he received his first dose of the Pfizer covid 19 vaccine on Sunday morning about 10:00 am. The caller got the shot in the left arm. On mid-day Monday (on an unspecified date), he started noticing "left elbow had very slight swelling, / slight swelling in his left elbow he didn't think anything about it" but "this morning, right now, there was a swelling on his left elbow the size of a golf ball, a big round knot, really soft like it was full of fluid, but no pain". The caller states he thinks it was because of the shot because he has been very careful to not do anything after receiving the vaccine. The caller wants to know that knot on his elbow an adverse event to the covid shot, have we seen this before. Caller reports a history of diabetes and Guillain-Barre syndrome (GBS), under control. He also reports having spoken to his doctor who said it was nothing. He now asks what Pfizer thinks. He was very disappointed that Pfizer can't provide him direction on what he should do. Serious: No. The outcome of the event was unknown. No follow up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827609
Sex: F
Age:
State: NJ

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 10/29/2021
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: Throat and voice are much worse than yesterday; throat and voice are much worse than yesterday; Got sick after; Feeling sick; This is a spontaneous report from a contactable consumer (patient). A 51-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Batch/Lot Number: EN6203) via an unspecified route of administration, administered in arm left on 28Feb2021 (at the age of 51-years-old) as dose 1, single for covid-19 immunization. Patient medical history included blood pressure high (diagnosed about ten years ago) from 2011 to an unknown date. There were no concomitant medications. On 01Mar2021, the patient reported that her throat and voice was worse, got sick after the vaccine and on an unspecified date in 2021, patient was feeling sick. Patient was asking if it is normal to get sick after the vaccine. Patient treated feeling sick with tylenol and Theraflu. The outcome of events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1827610
Sex: F
Age:
State: CA

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: She said her HCP told her she could do a different one for her second; feeling that she was very ill; lethargic/ feeling lethargic and could not get out of bed; lightheaded; nauseated; This is a spontaneous report from a contactable consumer (patient) or other non-healthcare professional from a Pfizer sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: Unknown), dose 1 via an unspecified route of administration on 03Feb2021 as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 03Feb2021within 4-5h after the vaccination, the patient felt patient that she was very ill, lethargic and could not get out of bed, lightheaded, nauseated and she would not have survived without Benadryl. Patient second dose on 28Feb2021 and did not go to appointment due to being very sick. Caller stated she felt like she was going to die. Caller mentioned she took Benadryl and it pulled her out of it. The patient's doctor has advised her not to take the second Pfizer Vaccine, that she should take Johnson and Johnson vs Pfizer. She said her HCP told her she could do a different one for her second. Patient wanted to know what to Do she was very scared of the receiving the Second dose. Therapeutic measures were taken as a result of feeling that she was very ill, lethargic/ feeling lethargic and could not get out of bed, lightheaded, nauseated. The clinical outcome of the events was unknown. No Follow-up attempts are possible. Information on lot/batch number cannot obtained.

Other Meds:

Current Illness:

ID: 1827611
Sex: F
Age:
State: CA

Vax Date: 02/28/2021
Onset Date: 02/28/2021
Rec V Date: 10/29/2021
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: Sore injection site; Sore neck; sore pelvic lymph nodes; This is a spontaneous report from a contactable consumer or other non hcp. A 65-years-old female non-pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EN6203, expiry date: unknown) via an unspecified route of administration in arm left on 28Feb2021 at 09:30 (age at vaccination: 65-years-old) as dose 2, single for covid-19 immunization. The patient medical history included penicillin allergy from unknown date. The patient medical history and concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 and patient has not been tested positive for COVID-19 since the vaccination. Patient historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL9264, expiry date: unknown) via an unspecified route of administration in Arm Left on 7Feb2021 at 09:30 (age at vaccination: 65-years-old) as dose 1, single for covid-19 immunization. On 28Feb2021 at 10:00, the patient experienced sore injection site, sore neck (back of neck) and sore pelvic lymph nodes. Case was assessed as non-serious. Patient did not get any treatment for the adverse event. The outcome of events was recovered on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1827612
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: felt a little tired; This a spontaneous report from a contactable consumer (patient). A female patient of unspecified age (Age: 81; Unit: unknown) received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on an unspecified date, as DOSE 1, SINGLE for COVID-19 immunization. The patient medical history included COVID-19 (recovered from a mild/moderate case of Covid 3 weeks ago). Concomitant medications were not reported. The patient reported that she just received her first dose of the vaccine and states she had no symptoms just felt a little tired on an unspecified date. She was wondering if she already had Covid will she overdose from the second dose of the vaccine and will the side effects be more severe. Her brother who was a doctor told her the side effects could be very bad and asked what was the rate of false negatives when receiving a mammogram after the vaccine. Outcome of the event was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827613
Sex: F
Age:
State: NJ

Vax Date: 02/17/2021
Onset Date: 02/01/2021
Rec V Date: 10/29/2021
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: She has been getting very tired/tiredness/Getting very tired in the afternoon; She can't stay awake. She nods out; This is a spontaneous report from a contactable consumer (Daughter) reported for patient (Mother). A 87-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: unknown, Expiration date: unknown), via an unspecified route of administration, administered at an unspecified anatomical location on 17Feb2021 (age at vaccination was 87 years) as dose 1, single for COVID-19 immunization. The patient's medical history included ongoing glaucoma. Concomitant medication included brimonidine tartrate, brinzolamide (SIMBRINZA) taken for glaucoma, start and stop date were not reported. On Feb2021 the patient experienced "She has been getting very tired/tiredness/Getting very tired in the afternoon" and she can't stay awake. she nods out. Patient has been getting very tired in the afternoons for past 9-10 days after COVID Vaccine. Is not sure if her eye drops for severe glaucoma and COVID Vaccine are aggravating one another. She reported that before the vaccination, her mom had more energy than a 30 year old; she was up at 6:30 in the morning, was cooking, baking, and driving. She was due to get the second shot and asked if they can expect her to be more tired after that one. Reporter stated she herself is allergic to a lot of medications and she wanted to know if there is any information on if anyone has had a severe allergic reaction to the vaccine yet. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: SIMBRINZA

Current Illness: Glaucoma

ID: 1827614
Sex: M
Age:
State: AZ

Vax Date: 02/02/2021
Onset Date: 02/04/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: strong headache; This is a spontaneous report from a non-contactable consumer (patient). A 66-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Lot number: EL3302; Expiration date: May2021) via unspecified route of administration in the left arm on 02Feb2021 (at the age of 66-years-old) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient had no additional vaccines administered on same date of the Pfizer suspect. Patient had not prior vaccinations within 4 weeks. The reporter stated that their company was asking for reporting of any possibility of reaction after vaccination. On 04Feb2021, about 48 hours after the first dose, the patient experienced strong headache which was resolved in 48 hours. The adverse event did not result in an emergency room or physician office visit. The outcome of the event was recovered on 06Feb2021. It was reported that the patient was very irritated that he has been on hold for 93 minutes. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1827615
Sex: M
Age:
State: CA

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 10/29/2021
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: site pain on left arm; This is a spontaneous report from a contactable consumer (patient). A 69-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EN5318, Expiration date: Unknown), via an unspecified route of administration, administered in arm left on 03Feb2021 (age at vaccination was 69 years) as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. On 03Feb2021, the patient experienced site pain on left arm. The patient stated that the site pain started 1.5 hours after the first shot and had resolved about a day and a half later. The patient stated that if he was not getting much pain, he not getting much benefit from the Covid vaccine. Outcome of the event was recovered on an unspecified date in Feb2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1827616
Sex: F
Age:
State: FL

Vax Date: 02/02/2021
Onset Date:
Rec V Date: 10/29/2021
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: Test Name: Blood Sugar; Result Unstructured Data: Test Result:Low

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Dizziness; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number: EL9265), dose 1 via an unspecified route of administration on 02Feb2021 (at the age of 71years) as dose 1, single for Covid-19 immunization. Medical history included type 1 diabetes mellitus. Concomitant medications were not reported ("Yes, I take a lot of medication, well there is awful lot of them"). The patient experienced dizziness on an unspecified date. The patient underwent lab tests and procedures which included blood glucose decreased: low on an unspecified date. The patient reported that the first time she got the shot she had little bit of dizziness several hours afterwards and it went away, and she also have diabetes (later clarified as medical history); the patient 'attributed' dizziness to a low blood sugar or whatever, blood sugar going down, so she really was not concerned about that. The outcome of event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained. No further information expected.

Other Meds:

Current Illness:

ID: 1827617
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: a little bit of soreness in the area of injection; This is a spontaneous report from a non-contactable consumer (patient) received via a sales representative. A 27-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose number unknown, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced a little bit of soreness in the area of injection on an unspecified date. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827618
Sex: F
Age:
State: CA

Vax Date: 02/02/2021
Onset Date: 02/02/2021
Rec V Date: 10/29/2021
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 Name: Blood work; Result Unstructured Data: Test Result:normal

Allergies:

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

Symptoms: after the first dose she was real tired and slept for the first day; after the first dose she was real tired and slept for the first day; This is a spontaneous report from a contactable consumer (patient) and physician. A 77-year-old female patient received bnt162b2 (BNT162B2, solution for injection, Lot Number: EN5318; Expiration Date: May2021), dose 1 via an unspecified route of administration, administered in the left arm on 02Feb2021 (at the age of 77 years old) as dose 1, single for COVID-19 immunisation at primary care office. No investigation assessment was reported. Medical history included (COPD) chronic obstructive pulmonary disease (diagnosed about 6-8 years ago), emphysema (diagnosed about 6-8 years ago), atrial fibrillation (A fib) (diagnosed 10 years ago, probably longer than that), lost her spleen in car accident when she was 26 years old; this causes her immune system to be compromised. There were no concomitant medications. The patient previously took flu and experienced feels like, her arm was painful even hurts to comb her hair, everything hurts. On 02Feb2021, the patient experienced after the first dose she was really tired and slept for the first day. The patient underwent lab tests and procedures which included blood test resulted normal. Reporter stated that the first time the side effects happened within 2.5 hours after the first shot. She felt really out of it, really tired, slept for 4 hours and got up and felt very weak, very tired and that lasted during the night. The patient got up the next day and felt the same way and decided to stay up because she hated the way she felt when she went to bed. The patient mentioned that between 5 and 6 she felt like herself and bam that was it. The patient says she goes in and out of it, feels great then boom she goes right back into it. She woke up and felt fantastic and within a half hour she was back in bed. The reporter was unable to verify if the events are improved, worsened, or persisting, stating they are the same. When it does improve, she feels like herself and when it goes back to the symptoms, it doesn't feel like it's any worse or any better. The clinical outcome of the events was reported as unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1827619
Sex: F
Age:
State: TX

Vax Date: 01/31/2021
Onset Date: 02/25/2021
Rec V Date: 10/29/2021
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: Dizzy; Not feeling well; This is a spontaneous report from a contactable consumer(Patient) via Pfizer-sponsored program. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRna VACCINE, solution for injection, Lot number was unknown), dose 1 via an unspecified route of administration on 31Jan2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On 25Feb2021, the patient felt dizzy and was not feeling well. She was supposed to have her second dose today (26Feb2021) she wanted to reschedule her second dose as she started feeling dizzy yesterday (25Feb2021). At the time of this report, the outcome of dizzy was not recovered and unknown for rest of the event. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021235315 similar report from same reporter

Other Meds:

Current Illness:

ID: 1827620
Sex: F
Age:
State: OH

Vax Date: 02/27/2021
Onset Date:
Rec V Date: 10/29/2021
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: Burning and then pain gave me the shot somewhere other than my muscles; pain on the injection site; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot/batch number was not reported) via an unspecified route, administered in left arm on 27Feb2021 as dose 2, single for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot/batch number was not reported) via an unspecified route, administered in right arm on an unspecified date as dose 1, single for covid-19 immunization. She got her first Covid shot 3 weeks ago on her right arm. She had no pain in her arm, no symptoms on her body. Then she went to yesterday to get her second Covid shot. First of all, well her first shot was done by a pharmacist. Her second shot she did not realize it until she gave her the shot, she took alcohol pad and wiped her left arm, her shoulder and then she took an envelope and wiped around to dry the alcohol. Since when was a tech allowed to give because she did not think anything other in beginning however her left arm where she gave her shot yesterday since then it was burning and then pain, burning and then pain. She had no other symptoms, no other physical symptoms. Now she was wondering the girl gave her the shot somewhere other than her muscles because it was just unbelievable that she had burning and pain in another arm and nothing was 3 weeks ago and no other symptoms. First of all is Pfizer allowing technicians in a pharmacy to give a shot. The patient had the second dose on the day of reporting and her arm experienced burning sensations followed by pain on the injection site. She also asked if a pharmacist technician is allowed to administer the vaccine. The outcome of events was unknown. No follow-up attempts were possible. Information on Lot/batch number could not be obtained.

Other Meds:

Current Illness:

ID: 1827621
Sex: F
Age:
State: OR

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: chills; headache; tired; This is a spontaneous report from a contactable consumer (patient) via the Pfizer-sponsored program. A female patient of an unspecified age received bnt162b2 (BNT162B2), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced chills, headache, tired. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827622
Sex: F
Age:
State: NY

Vax Date: 02/17/2021
Onset Date:
Rec V Date: 10/29/2021
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: weak; tingling from hip to toes; wanted to sleep and sleep; legs were hurting; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Solution for injection), via an unspecified route of administration, on 17Feb2021 (lot number not reported), as dose 1, single, for COVID-19 immunisation. Relevant medical history and concomitant medications were not reported. On an unspecified date, after the first dose, the patient felt weak, experienced tingling from hip to toes, wanted to sleep and sleep and her legs were hurting but no swelling. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827623
Sex: F
Age:
State: CA

Vax Date: 02/23/2021
Onset Date: 02/01/2021
Rec V Date: 10/29/2021
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: fatigue; long hour sleep; sore arms; headache; swelling at injection site; inflammation; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a female patient of unspecified age received second dose of BNT162B2 (Pfizer Covid-19 Vaccine), via an unspecified route of administration on 23Feb2021 as single dose for COVID-19 immunisation. The patient previously received the first dose on an unspecified date. Medical history and concomitant medications were not reported. The patient was experiencing adverse events after the second dose of the vaccine given on 23Feb2021. On Feb2021, adverse events experienced by the patient were fatigue, long hour sleep, sore arms, headache, swelling at injection site, and inflammation. She was asking if these are normal. Outcome of events was unknown. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827624
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: Chills; body aches; exhaustion; ha (headache); This is a spontaneous report from a contactable consumer (patient). A 40-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) was administered on an unknown date for Covid-19 immunisation and had no adverse event. On an unspecified date, after the second dose, the patient experienced chills, body aches, exhaustion, and ha (headache) that lasted for 24 hours. Outcome of the events was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1827625
Sex: F
Age:
State: GA

Vax Date: 02/25/2021
Onset Date: 02/27/2021
Rec V Date: 10/29/2021
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: Excruciating left hip pain; This is a spontaneous report from a contactable Nurse (patient). A 44-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9263, Expiry date: Unknown) via an unspecified route of administration, administered in Arm Right on 25Feb2021 at 16:00 (age at vaccination: 44years-old) as dose 1, single for COVID-19 immunization. The patient had no medical history and concomitant medications were not reported. Patient was not pregnant at the time of vaccination. Patient did not receive any other vaccines within 4 weeks prior and received other unspecified medications 2 weeks prior to the COVID vaccine. Patient had no known allergies. The patient was not tested positive for covid-19 prior to vaccination and had not been tested post vaccination. On 27Feb2021 at 03:00 AM patient experienced excruciating left hip pain. The adverse events resulted in doctor or other healthcare professional office/clinic visit. The outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1827626
Sex: M
Age:
State: TN

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: he had a little soreness in that arm; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program Support. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in arm on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced he had a little soreness in that arm on an unspecified date. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827627
Sex: M
Age:
State: VA

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: is now sick.; This is a spontaneous report from a contactable consumer (patient) via the Pfizer sponsored program. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (lot number and expiry date: unknown) as dose number unknown, single, for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient reported that he received the vaccine on unspecified date and is now sick. Outcome of the event was unknown. No follow-up attempts are possible; information about batch/ lot number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1827628
Sex: F
Age:
State: FL

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 10/29/2021
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: sick in stomach; sick in stomach; arm hurts; slept for 12 hours; This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL9262; Expiration Date: 21May2100), dose 2 via an unspecified route of administration, administered in Deltoid Left on 12Feb2021 14:30 (at the age of 74years) as dose 2, single for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 on 22Jan2021 in which the patient experienced for a couple minutes she can't think, arm hurts, pain in head/ head it just felt like a bowling ball, it's still heavy, and slept for 12hours (she doesn't usually sleep that much). The patient experienced sick in stomach on 12Feb2021, arm hurts, and had to sleep (slept for 12 hours, she doesn't usually sleep that much on 12Feb2021. The outcome of events was recovered on an unspecified date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1827629
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: Her arm around where they gave her the shot, its like reddish and purple and there is a lump on it. Its also itching a lot; Her arm around where they gave her the shot, its like reddish and purple and there is a lump on it. Its also itching a lot; Her arm around where they gave her the shot, its like reddish and purple and there is a lump on it. Its also itching a lot; This is a spontaneous report from a contactable consumer (patient son). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation:Solution for injection; Batch/Lot number, Expiry date, NDC number was not reported), via an unspecified route, administered in Arm on an unspecified date as Dose 1,Single for covid-19 immunization. The patient medical history and concomitant medications were not reported. Reporter calling about his mom, he was just calling for her because she doesn't speak very good English, so he was interpreting. She got the vaccine and had few questions. She got her first dose at the hospital. They gave her this paper to call if she had questions. The patient arm around where they gave her the shot, its like reddish and purple and there is a lump on it. Its also itching a lot on an unspecified date, she has been putting cold towels on it and putting no pressure on it. She wants to know what she can do further, Is the red, purple, and itching normal. She wants to know if she can put a band aid or cream like Neosporin on it. The clinical outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827630
Sex: F
Age:
State: NY

Vax Date: 02/26/2021
Onset Date:
Rec V Date: 10/29/2021
Hospital:

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

Lab Data: Test Name: cholesterol; Result Unstructured Data: Test Result:High; Test Name: BMI; Result Unstructured Data: Test Result:High

Allergies:

Symptom List: Pain in extremity

Symptoms: she has high cholesterol; she also has a high BMI; This is a spontaneous report from a contactable consumer. A 60-year-old female patient received bnt162b2 (Formulation: Solution for injection; Batch/Lot number was not reported), dose 1 via an un-specified route of administration on 26Feb2021 as dose 1, single for covid-19 immunisation (at the age of 60-year-old). The patient medical history and concomitant medications were not reported. The patient took her first dose on 26Feb2021. She is concerned about having to change her facility for her next dose of vaccine because as she mentioned, she has high cholesterol, she also has a high BMI and she is 60 years old. Her next dose will be given on 19Mar2021. The patient underwent lab tests and procedures which included blood cholesterol: high on an unspecified date, body mass index: high on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827631
Sex: F
Age:
State: NJ

Vax Date: 03/09/2021
Onset Date: 03/01/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: problem with her shoulder; she couldn't lift her arm over her head; needle was probably injected too high on her arm; problem with her shoulder; she couldn't lift her arm over her head; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Batch/Lot Number: EN6206) via an unspecified route of administration, administered in right arm on 09Mar2021 10:30 (age at vaccination 77 years) as DOSE 1, SINGLE for COVID-19 immunisation. Medical history included mastectomy therefore she could not get the vaccine in her left arm. Concomitant medication was not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient reported that a few days afterward she started to have a problem with her shoulder; she could not lift her arm over her head on an unspecified date in Mar2021. She called the COVID hotline in and they advised the needle was probably injected too high on her arm. The patient called her physician, and she did go in to see the nurse practitioner who started her on physical therapy and gave her a prescription for Naproxen. The patient had to do ten sessions to get her shoulder back to where it was supposed to be. She thought that was a little better on the day of report. The patient scheduled for the second dose and she was scared to get it because she did not want to have another problem on an unspecified date in Mar2021. The patient was scheduled to receive the second dose on 29Mar2021 at 11:00. She was asking for recommendations about what to do in that situation. The patient was received Naproxen 500 mg and physical therapy for treatment of events. Outcome of event problem with her shoulder; she could not lift her arm over her head was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1827632
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/22/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data: Test Date: 202012; Test Name: blood test; Result Unstructured Data: Test Result:Positive; Test Date: 20200616; Test Name: PCR; Result Unstructured Data: Test Result:Negative; Test Date: 20200920; Test Name: PCR; Result Unstructured Data: Test Result:Negative; Test Date: 20201126; Test Name: PCR; Result Unstructured Data: Test Result:Negative; Test Date: 20210123; Test Name: PCR; Result Unstructured Data: Test Result:Negative

Allergies:

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

Symptoms: Tiredness; Lump in left armpit, noticed 30-32 hours after vaccination; Soar arm,; acute pain in left arm and extend to neck; (Very strong pain in left arm started 3 or 4 hours after the shot and lasted 48 hours; Area of shot swelled; This is a spontaneous report from a contactable consumer (patient). A 52-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3247), via intramuscular route, administered in Arm Left on 22Mar2021 10:15 (at the age of 52-year-old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included Retina's detachment both eyes with surgeries (2 surgeries 2004 and 2013), cataract (2013- 2015), appendicitis (Surgery in 1986), silent reflux, white blood cell count (Regular checks on an annual basis with haematologist). Family history included Prostate Cancer, cholesterol increased, Fibrosis (Lung fibrosis) (father) and Arthritis Rheumatoid, atherosclerosis, Glaucoma (Mother). Patient did not have any illness at time of vaccination. Concomitant medication(s) included pantoprazole sodium taken for gastrooesophageal reflux disease, start and stop date were not reported; monascus purpureus (RED RICE) taken for blood cholesterol, start and stop date were not reported. Patient was not pregnant at the time of vaccination. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL3247) via intramuscular route, administered in Arm Left on 01Mar2021 09:30 (at the age of 52-year-old) as DOSE 1, SINGLE for covid-19 immunisation and experienced Sore arm, menstruation five days after shot. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination included Pantoprazole; Red rice for cholesterol. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 22Mar2021 13:00, the patient experienced tiredness, lump in left armpit noticed 30-32 hours after vaccination; sore arm, acute pain in left arm and extended to neck. Very strong pain in left arm started 3 or 4 hours after the shot and lasted 48 hours. Area of shot swelled. The patient underwent lab tests and procedures which included blood test: positive on Dec2020, polymerase chain reaction: negative on 16Jun2020, negative on 20Sep2020, negative on 26Nov2020, negative on 23Jan2021. Patient did not receive treatment for adverse events. The outcome of all events was recovering. Follow-up attempts are completed. No further information is expected; Sender's Comments: Linked Report(s) : -PFIZER INC-2021244974 similar report from same reporter

Other Meds: PANTOPRAZOLE SODIUM; RED RICE

Current Illness: Appendicitis (Surgery in 1986)

ID: 1827633
Sex: F
Age:
State: CA

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: second dose of vaccine on 01Apr2021, ER 2613 has given her what feels like lump under left arm still there on 05Apr2021; This is a spontaneous report from a contactable consumer (patient). A 58-year-old non pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: ER2613), via an unspecified route of administration, administered in right arm on 01Apr2021 (at age of 58-year-old) as dose 2, single for covid-19 immunization. The patient was not pregnant at time of vaccination. Medical history included iodine allergy, egg allergy. The patient did not receive any other vaccine in four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. Concomitant medications included vitamin A (VITAMIN A [RETINOL]) taken for an unspecified indication, start and stop date were not reported, vitamin c [ascorbic acid] taken for an unspecified indication, start and stop date were not reported, vitamin D3 taken for an unspecified indication, start and stop date were not reported (within 2 weeks of vaccination). Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6203), via an unspecified route of administration, administered in right arm on 03Mar2021 at 15:00 (at age of 58-year-old) as dose 1, single for covid-19 immunization and experienced kaleidoscope vision in right eye lasting about an hour a mild headache for 24 hours. The patient did not usually get headache. On an unspecified date in Apr2021, the patient reported that second dose of vaccine on 01Apr2021, ER 2613 has given her what feels like lump under left arm still there on 05Apr2021. The patient did not received treatment for the event. The outcome of event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: VITAMIN A [RETINOL]; VITAMIN C [ASCORBIC ACID]; VITAMIN D3

Current Illness:

ID: 1827634
Sex: F
Age:
State:

Vax Date: 04/06/2021
Onset Date: 04/01/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: really sick; fever; crying; screaming; This is a spontaneous report from a contactable consumer (reporting for her mother). A female patient of an unspecified age received BNT162b2 (Pfizer BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration on 06Apr2021 as dose 2, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Historical vaccine included patient received BNT162b2 (Pfizer BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunisation. On Apr2021, patient had fever, was crying and screaming. On 07Apr2021, patient was really sick. Reporter stated that everything was wrong with the patient and wanted to know what to do. The outcome of all the events was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827635
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/29/2021
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: Fever; achy; Allergic reaction; face swelling; Hives; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient medical history included UTI from an unknown date. Concomitant medications were not reported. The patient previously received Cipro for UTI and she never had a problem with Cipro previously. The patient experienced fever, achy, allergic reaction, face swelling, hives on an unspecified date. The caller had the first Pfizer Covid-19 vaccine. She had the Pfizer covid shot and had been normal. She felt a little fever and was achy, but nothing major. About a week out, all of a sudden she got an allergic reaction. They weren't sure, but she had taken Cipro for a UTI. She never had a problem with Cipro previously. However, she had face swelling and hives. She had to stop taking the Cipro. She received a shot of steroids because the Benadryl was not working. The Benadryl was not working for an allergic reaction that occurred. The outcome of the events was unknown. No follow-up attempts are Possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1827636
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/24/2021
Rec V Date: 10/29/2021
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: 20210407; Test Name: Ultrasound; Result Unstructured Data: Test Result:Nodules 4mm on right side and a 2mm and a 3mm; Comments: They found a nodules 4 mm on right side and a 2 mm and a 3 mm on the left side and they will doing biopsy on the right side

Allergies:

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

Symptoms: They found a nodules 4 mm on right side and a 2 mm and a 3 mm on the left side; Getting ear pressure in right ear; Ear ache on right side of my ear and kind of went down to my throat when you get hoarse, when you get sore throat, trouble right side of my neck around thyroid area; swollen; Ear ache on right side of my ear and kind of went down to my throat when you get hoarse, when you get sore throat, trouble right side of my neck around thyroid area; swollen; This is a spontaneous report from a contactable consumer. This 59-year-old female patient reported for herself. A 59-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: EP7534), dose 1 via an unspecified route of administration, administered in Arm Right on an unspecified date as a single dose for covid-19 immunization. Medical history included blood glucose- an elevated A1C last year, cardiac disorder -Husband has heart issues. Concomitant medication(s) included telmisartan; glipizide ER; empagliflozin (JARDIANCE); rabeprazole; estradiol; mirabegron (MYRBETRIQ). On 24Mar2021, about 3, 4 days later she noticed that getting like an ear pressure, ear ache on the right side of her ear and kind of went down to throat like a when you a get hoarse, when you get a sore throat and had trouble in neck around the thyroid area on the right side of the neck was swollen and lasted for about 3 days. She went to ENT yesterday, by Tuesday it had already gone down but she went yesterday, Wednesday to my ENT to be on the safe side, have it checked out to make sure it was nothing serious. She guess it went down, the swelling and haven't done a blood work yet. On 07Apr2021, they found a nodules 4 mm on right side and a 2 mm and a 3 mm on the left side and they will doing biopsy on the right side. On the neck it just feels very slight. It's kind of very hard to tell if it went completely down or it just the thyroid. She was not sure. There was no soreness to it like it was before. She will be taking the 2nd dose on the April 11th. The patient did not receive any treatment. Outcome of the event thyroid mass was recovering and rest all events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: TELMISARTAN; JARDIANCE; RABEPRAZOLE; ESTRADIOL; MYRBETRIQ

Current Illness:

ID: 1827637
Sex: F
Age:
State: CT

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 10/29/2021
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: Test Date: 20210408; Test Name: Body temperature; Result Unstructured Data: Test Result:101; Comments: fever of 101

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: sore/achy; she had fever of 101; Body chills; lymph node reaction everywhere; sore arm; burning immediately at site; This is a spontaneous report from a contactable consumer (patient). A 49-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0150) via an unspecified route of administration in the left arm on 07Apr2021 at 17:15 (at the age of 49-years-old) as dose 2, single for COVID-19 immunisation. Medical history included paroxysmal atrial fibrillation (reported as Paroxmal afib), supraventricular tachycardia (SVT), graves' disease and hashimoto's disease. Concomitant medications taken within two weeks prior to vaccination included levothyroxine sodium (TIROSINT), via unspecified route of administration from unknown date to unknown date at unknown dose and frequency for an unspecified indication; hydrochlorothiazide (HCTZ) (reported as hgtz), via unspecified route of administration from unknown date to unknown date at unknown dose and frequency for an unspecified indication; atenolol (ATENOL), via unspecified route of administration from unknown date to unknown date at unknown dose and frequency for an unspecified indication; vitamin d nos (VITAMIN D), via unspecified route of administration from unknown date to unknown date at unknown dose and frequency for an unspecified indication and potassium (MANUFACTURER UNKNOWN), via unspecified route of administration from unknown date to unknown date at unknown dose and frequency for an unspecified indication. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: En6199) via an unspecified route of administration in the left arm on 17Mar2021 at 17:15 (at the age of 48-years-old) as a dose 1, single for COVID-19 immunisation and had got a raised red bump for a day. The patient was not a pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 07Apr2021 at 17:15, when given the second shot of injection the patient had a burning immediately at site. On 08Apr2021 (next day), the patient woke up sore arm and but sore by 15:30 she had fever of 101, Body chills, achy and lymph node reaction everywhere. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No therapeutic measures were taken as a result of the events. The patient underwent lab tests which included body temperature with 101 (units unspecified) on 08Apr2021 fever of 101. The clinical outcome of the events were recovering. No follow-up attempts are needed. No further information is expected.

Other Meds: TIROSINT; HCTZ; ATENOL; VITAMIN D NOS; POTASSIUM

Current Illness:

ID: 1827638
Sex: F
Age:
State: CA

Vax Date: 04/06/2021
Onset Date: 04/01/2021
Rec V Date: 10/29/2021
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: Entire shoulder swollen; Underarm glands swollen all the way down to breast area, collarbone gland swelling; All areas affected are hot; All areas affected are itchy. All on left arm. Still swollen after 48 hrs; This is a spontaneous report from a contactable consumer, the patient. A 44-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: ER8737) via an unspecified route of administration in the left arm on 06Apr2021 at 13:00 (at the age of 44-year-old) as a single dose for COVID-19 immunization. Medical history included hypertension and allergies to food. Concomitant medications included losartan and zolpidem. The patient previously took sulfa and experienced sulfonamide allergy and Keflex and experienced drug allergy to Keflex. Historical vaccine included first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: EN6208) via an unspecified route of administration in the left arm on 16Mar2021 at 13:00 (at the age of 44-year-old) as a single dose for COVID-19 immunisation and experienced large hive/welt the size of a fist over the vaccine site in her left arm for two plus weeks. It was hot and itchy. She had large lump underneath. It left a mark which may be permanent. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On an unknown date in Apr2021 after the second vaccine, the patient experienced entire shoulder swollen, underarm glands swollen all the way down to breast area and collarbone gland swelling. All areas affected were hot and itchy. All on left arm. It was still swollen after 48 hours. The events resulted in doctor or other healthcare professional office/clinic visit. No therapeutic measures were taken as a result of the events. The clinical outcome of the events after the second vaccine, entire shoulder was swollen, underarm glands swollen all the way down to breast area, collarbone gland swelling, all areas affected were hot and itchy, all on left arm and it was still swollen after 48 hours was not resolved at the time of report. No follow-up attempts are needed. No further information is expected.

Other Meds: LOSARTAN; ZOLPIDEM

Current Illness: Hypertension

ID: 1827639
Sex: M
Age:
State:

Vax Date: 03/26/2021
Onset Date: 04/01/2021
Rec V Date: 10/29/2021
Hospital:

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

Lab Data: Test Date: 20210407; Test Name: COVID test; Test Result: Negative

Allergies:

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

Symptoms: severe lower abdominal pain; little bit of a cough; a little rash on the arm he received injection; stomach pain; really severe nausea; really bad chills; Migraine; body aches; weird vivid dreams; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: ER8730, expiration date was not reported), via an unspecified route of administration on 26Mar2021 as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that the patient stated he was calling about the COVID 19 vaccine first dose that he had got on 26Mar2021. He stated he did not have side effects until 2 nights ago and had really severe nausea, really bad chills, migraine, body aches, and weird vivid dreams on an unspecified date of Apr2021. He stated last night it was slightly better and on 07Apr2021 had severe lower abdominal pain, little bit of a cough, and a little rash on the arm he received injection. He stated he is slightly better this morning but still has stomach pain on an unspecified date of Apr2021. He stated he was reading an article online and some people experience symptoms 10 days later but nothing was mentioned about 12 days later. He stated he went to get a COVID test yesterday which was negative. He asked does these side effects ring a bell and experiencing them in this time frame. The patient underwent lab tests and procedures which included COVID test (sars-cov-2 antibody test): negative on 07Apr2021. The outcome of the event stomach pain was not recovered and outcome was unknown for other events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am