VAERS 2021 Database www.vaers.hhs.gov

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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: 1823735
Sex: M
Age:
State:

Vax Date: 02/23/2021
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data: Test Name: temp; Result Unstructured Data: Test Result:97.6 up to 99.5; Comments: his temperature goes up and down from his normal temp of 97.6 up to 99.5

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: his temperature goes up and down from his normal temp of 97.6 up to 99.5; This is a spontaneous report from a contactable consumer (patient). A 75-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown) via an unspecified route of administration on 23Feb2021 as dose 1, single for COVID-19 immunization. Medical history of the patient included Guillain-Barre syndrome in 1975 and was completely paralyzed, hospitalized, flu. Concomitant medications were not reported. Patient read an article which suggested the vaccine can trigger an auto-immune response if you have a history of Guillain-Barre syndrome. Reportedly, patient had history of Guillain-Barre syndrome. He didn't get it from the vaccine. He just got it from the flu. Patient was hospitalized for 6 months and put on a ventilator for 2 months. It was shown one dose is 70% effective. Patient would just get one dose. Patient have asked doctor's and pharmacist if eligible to receive the second. They referred patient to call Pfizer." Patient asked if he was eligible to receive the vaccine. On an unspecified date after first dose of vaccination, patient had noticed that his temperature goes up and down from his normal temp of 97.6 up to 99.5 but stated that his immune response could be triggering temperature. Patient asked if there was any contraindication to using Norco, Lortab or Mobic when getting the covid vaccine. Patient had his first Pfizer shot 3 days ago [date unspecified] and he has done a lot of research but can't find anything other than don't take Tylenol or medicine like that because it can affect the efficacy. He asked if there was any more information and how much does it affect the immune response? Patient only takes those medicines as needed and will likely not take it to prevent any kind of decreased effectiveness. Patient asked "when does the vaccine start protecting me? How does the vaccine work? Is antibody testing helpful to determine immunity?" 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: 1823736
Sex: F
Age:
State: MA

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 10/28/2021
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: feel sleepy; headache; Three hours after administrating the 1st dose on my left arm, the whole arm suffered a big pain; some numbness on the left hand; could not move the arm at all because of the pain; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 m-RNA VACCINE, solution for injection, Batch/Lot number: EL3247), via an unspecified route of administration, administered in left arm on 24Feb2021 at 10:00 as a single dose for covid-19 immunization. The patient's medical history included DCIS on left breast. The patient's concomitant medications were not reported. The patient had no known allergies. The patient did not receive any other medications in four weeks. The patient had no COVID prior to vaccination and was not COVID tested post vaccination. On 24Feb2021 at 13:00, three hours after administrating the 1st dose on left arm, the whole arm suffered a big pain and there was even some numbness on the left hand. The patient could not move the arm at all because of the pain. Six hours after administrating, on 24Feb2021 at 16:00 hours, the patient started to feel sleepy and have headache. The patient did not receive any treatment for the adverse events. The outcome for the events was recovered on an unspecified date in 2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1823737
Sex: F
Age:
State: PA

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 10/28/2021
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: Also experienced a headache; Soreness in left arm; This is a spontaneous report from a contactable consumer (patient). A 55-year-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL3247), via an unspecified route of administration, administered in Arm Left on 25Feb2021 11:15 (at the age of 55-year-old) as single dose for COVID-19 immunization. Medical history included COVID-19 (Prior to vaccination, the patient was diagnosed with COVID-19). The patient did not have allergies to medications, food or other products. There were no concomitant medications. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine and did not receive any other medications within 2 weeks of vaccination. On 25Feb2021, the patient experienced soreness in left arm following injection that increased throughout the day but was much improved by morning of 26Feb2021. Also experienced a headache the morning after, on 26Feb2021 which resolved after taking Advil. The patient had not been tested for COVID-19 since the vaccination. The outcome of the event soreness in left arm was recovered on 26Feb2021; headache was recovered in Feb2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823738
Sex: F
Age:
State: NH

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 10/28/2021
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: felt a little dizzy about 1 hour 1/2 after dosage; I had an upset stomach with multiple bowel movements; I had an upset stomach with multiple bowel movements; This is a spontaneous report from a contactable consumer (patient). A 52-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL3247), via an unspecified route of administration in right arm on 23Feb2021 at 15:30 (at the age of 52 years old) as dose 1, single for covid-19 immunisation. Medical history included self-known allergic to dust/animal hair allergy. Concomitant medications in two weeks included acetylsalicylic acid (ASPIRIN (E.C.)); pseudoephedrine hydrochloride (NASAL DECONGESTANT [PSEUDOEPHEDRINE HYDROCHLORIDE]); alprazolam (XANAX), vitamins. The 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. Since the vaccination, the patient hasn't been tested for COVID-19. On 23Feb2021 at 17:00 patient experienced felt a little dizzy about 1-hour 1/2 after dosage. She had an upset stomach with multiple bowel movements afterwards. Next day she felt fine. The patient did not receive any treatments for the events. Reporter considered events as non-serious. The outcome of events was recovered on an unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds: ASPIRIN (E.C.); NASAL DECONGESTANT [PSEUDOEPHEDRINE HYDROCHLORIDE]; XANAX

Current Illness:

ID: 1823739
Sex: F
Age:
State: IL

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 10/28/2021
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: scratchy and sore throat; scratchy and sore throat; her ribs are sore; her muscles are aching (muscle near the injection site).; chills; her head feels like she is in the clouds; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 70-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6202) via an unspecified route of administration on 26Feb2021 (at the age of 70 years old) as dose 1, single for COVID-19 immunisation. Medical history included allergic to whole strawberries. No concomitant medications were reported. Patient got the first dose of the Pfizer BioNTech COVID-19 vaccine today (26Feb2021) and she developed adverse events. Her adverse events are scratchy and sore throat, and she feels like she has the flu, her ribs are sore, her muscles are aching (muscle near the injection site), her head feels like she was in the clouds and also chills, she began feeling all of this about 45 minutes after the shot. She wanted to know if it was a typical reaction with the Pfizer COVID-19 vaccine. Patient also stated instead of the standard 15 minutes they had her wait 30 minutes. She didn't feel sick or anything at all, her throat didn't start bothering her. She was telling her daughter about how she got the vaccine and everything was flawless, she had no aches and pains then she had to tell her she was going to have to go because her throat, she thought she was talking too much she told her daughter maybe her throat was dry. She told her daughter she was going to have to stop talking and it has gone since then. The outcome of the events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823740
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: pain at injection site on the day of injection; This is a spontaneous report from a contactable consumer (patient). A male patient of unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: Unknown), via an unspecified route on unspecified date as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced pain at injection site on the day of injection on unspecified date. Both he and his wife experienced pain at injection site on the day of injection. On the second day after the vaccine, she started suffering from joint pain, muscle pain and inflammation (swelling in hands and wrist) and has been ongoing since and had not noticeably resolved. States her pain seems to subside during day but comes back at night. Also reports that the pain seems to travel throughout her body from one shoulder to the next shoulder. She had consulted her hcp who has prescribed anti inflammatory which helps the pain. The outcome of the event was unknown. Information about lot/batch number has been requested Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823741
Sex: F
Age:
State: OH

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 10/28/2021
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: stomach cramps; stomach "noises"/noises in her stomach; diarrhea; This is a spontaneous report from a contactable consumer or other non hcp (patient) and physician. A 67-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: EN6198; Expiration Date: 30Jun2021) via an unspecified route of administration, administered in arm right on 22Feb2021 (at the age of 67-year-old) at dose 1, single for covid-19 immunisation. Medical history and concomitant medications were not reported. Patient is 67 y/o. Received her first dose of the Pfizer Covid vaccine on Monday 22Feb2021. On 23Feb2021 around 8 pm she experienced stomach "noises" and diarrhea. On 24Feb2021 she said she was ok with no diarrhea. On 25Feb2021 around 11:30 pm she had stomach cramps and diarrhea, and on 26Feb2021 she has experienced just stomach cramping. She wants to know how long will the diarrhea last. Additional Context: Reporter stated that she has questions about reactions to the vaccine, states she had the vaccine on Monday 22Feb2021, and initially had no reaction, states Tuesday she thought she felt ok, states she took her dog to the park, Tuesday night around 8PM she started having diarrhea and noises in her stomach, on Wednesday she was fine, mostly solid stools, states yesterday 25Feb2021 she had one small bowel movement and last night around 11:30PM she had diarrhea again. Should the side effects be lasting this long. Reporter encouraged to reach out to health care provider for any medical advice. Outcome of the event diarrhea was not resolved and remaining other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823742
Sex: F
Age:
State:

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 10/28/2021
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: Really dizzy; Really nauseous; Felt like weakness in her arms and legs; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 27-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot/batch number: EN6202 and expiry date was not reported), via an unspecified route of administration in arm left, on 26Feb2021 at 08:00 (at the age of 27-year-old), as a dose 1, single for COVID-19 immunization. The patient's medical history includes allergy to morphine probably around 2018, when she had her son. The patient stated that she had no reactions to vaccinations. It was reported that on an unspecified date in Jul2020 the patient had COVID and due to having COVID the patient developed really bad allergies that sometimes make it hard for her to breathe, but nothing else that she was aware of. The patient concomitant medication includes mepyramine maleate, pamabrom, paracetamol (Pamprin) (Start: Unknown Stop: Unknown) for cramps. Reportedly within four weeks prior to the first administration date of the suspect vaccine the patient did not receive any other vaccine. On 26Feb2021, probably around 5 hours after being administered the vaccine, around 13:00, the patient felt fine almost all morning but then she felt really dizzy, really nauseous and felt like weakness in her arms and legs and she could still hold things and stuff. She wanted to make sure that these are normal reactions to the vaccine, or if they are serious events, and if she should follow-up with doctor or medical attention. The clinical outcome of all the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: PAMPRIN

Current Illness:

ID: 1823743
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: slight sore throat; This is a spontaneous report from a contactable consumer (patient). A female patient of an un-specified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient reported a slight sore throat as she was speaking. Patient was scheduled to receive the second dose of the vaccine but doesn't know the time and date. The outcome of the event unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823744
Sex: M
Age:
State: KY

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 10/28/2021
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: sore arm after both injections.; This is a spontaneous report from a contactable consumer or other non hcp via Pfizer-sponsored program. A male patient of an unspecified age (Age: 60; Unit: Unknown) received first dose of BNT162B2 (PFIZER BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: Not reported) via an unspecified route of administration on 25Jan2021 as single dose and first dose via an unspecified route of administration on 04Jan2021 (Batch/Lot number was not reported) as single dose for COVID-19 immunization. The patient's medical history was not reported. The patient's concomitant medications included paracetamol (TYLENOL). It was reported that caller was calling on behalf of her husband who works in healthcare and has received both doses of the Covid vaccine. Caller had question on behalf of her husband. Caller stated that her husband took Tylenol prior to receiving both doses of the vaccine with the intention of pre-medicating and wanted to know if that was okay. Caller then clarified husband only took Tylenol before first dose. Caller stated that he was unaware of the guideline to not take Tylenol prior to receiving the vaccine and did not take Tylenol after receiving the vaccine. Caller stated that her husband experienced a sore arm after both injections on Jan2021. Caller was asking if her husband needs to take a booster due to him medicating with Tylenol prior to receiving either dose. Caller stated, it was her fault on telling him to do that. They used to tell her to do that with their kids. Caller asked if Tylenol would lessen the effectivity of the vaccine and if need to take any other shot of the vaccine again. Precautionary AE. Seriousness of the event was non serious. The outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number cannot been obtained.

Other Meds: TYLENOL

Current Illness:

ID: 1823745
Sex: M
Age:
State: NY

Vax Date: 02/16/2021
Onset Date:
Rec V Date: 10/28/2021
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: hearing sounds in his ear that sound "like water falling"; This is a spontaneous report from a contactable consumer or other non hcp. A 78-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration on 16Feb2021 (at the age of: 78-years-old) as dose 2, single for COVID-19 immunization. Medical history included earaches (needing eardrops for wax build-up), COVID-19 from Mar2020 to an unknown date, pneumonia. It was reported that that the patient had COVID back in 2020 and COVID pneumonia he had cleared his self of that but when it came time for him to go to take his semi annual physical, he saw his doctor and he complained of having ear aches and she recommend some ear drops and he put it in and it worked a little bit. There were no concomitant medications. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EK4176), via an unspecified route of administration on 27Jan2021 (at the age of 78-years-old) as dose 1, single for covid-19 immunization. On an unspecified date, the patient experienced hearing sounds in his ear that sound "like water falling". It was reported that the patient got the second dose and everything was going okay then last week he got in the bed and all of a sudden he started feeling little tingling in his ears. He wondered this could be something that the organization had received as a complaint of ear effects or if he might have a cold in his ear or water in his ear but he hears tingling right now. He just thought it may have been coming from the radiator then it was just in his head and still ongoing. It has stayed about the same, sometimes it will be a little lower and he will think it is going away then it comes back. It sounds like water falling. He does not report any headache, fever, chills, or anything. His medical history includes problems with earaches, needing eardrops for wax build-up, and he also had Covid19 back in Mar2020. He stated may be the antibodies are acting up and causing problems. He did have a problem with his ears. No further information provided. But lately last week he does not know whether he has a cold, they have had a lot of cold weather or if he had water in it or if it is a problem with the side effect. He had not had any other side effect, no swelling or nothing so he wanted to see if they had heard any other complaints or reports about this. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823746
Sex: M
Age:
State: MA

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: Described as a "minor thing" and pointed at arm; This is a spontaneous report from a contactable consumer or other non hcp. A male patient of an unspecified age received 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 UNKNOWN, SINGLE for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient described as a minor thing and pointed at arm on an unspecified date. The event outcome was reported as recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1823747
Sex: F
Age:
State: VA

Vax Date: 02/05/2021
Onset Date: 02/26/2021
Rec V Date: 10/28/2021
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: typical soreness; flu like symptoms; weak; tired; he administered the Pfizer-BioNTech COVID-19 Vaccine second dose to 3 Patients but he has drawn more than the required volume (0.5mL instead of 0.3mL).; This is a spontaneous report from a contactable pharmacist. This Pharmacist reported similar events for 3 patients. This report is for 1st of 3 patients. A 30-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL3302; Expiration Date: 28May2021), via an unspecified route of administration on 26Feb2021 as DOSE 2, 0.5 ML SINGLE, on 05Feb2021 (Batch/Lot Number: EL3302; Expiration Date: 28Mar2021) as DOSE 1, SINGLE for covid-19 immunisation. No prior vaccination within 4 weeks. The patient medical history was not reported. There were no concomitant medications. On 26Feb2021 the patient experienced he administered the pfizer-biontech covid-19 vaccine second dose to 3 patients but he has drawn more than the required volume (0.5ml instead of 0.3ml), weak, tired, on an unspecified date typical soreness, flu like symptoms. On an unknown date in 2021 the outcome of other events were recovered. The outcome of he administered the pfizer-biontech covid-19 vaccine second dose to 3 patients but he has drawn more than the required volume (0.5ml instead of 0.3ml) was unknown. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021223835 Same reporter/drug/event, different patient.;US-PFIZER INC-2021223836 Same reporter/drug/event, different patient.

Other Meds:

Current Illness:

ID: 1823748
Sex: F
Age:
State: CT

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 10/28/2021
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: Chills; Headaches; Very tiredness; Body aches; This is a spontaneous report from a contactable consumer (patient). A 25-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection), via an unspecified route of administration, administered in left arm on 25Feb2021 (Lot Number: EL3247, at the age of 25-year-old) as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient had previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection), via an unspecified route of administration on 05Feb2021 (Lot Number was not reported, at the age of 25-year-old) as dose 1, single for COVID-19 immunization. The patient was not pregnant at the time of vaccination. On 25Feb2021 at 22:00 (after about 10 hours following vaccination), the patient had experienced chills, headaches, very tiredness and body aches. The patient did not receive any treatment for the events. The patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. The outcome of the events tiredness and body aches was recovered on the morning of 27Feb2021, and the other events was recovered on an unspecified date. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823749
Sex: M
Age:
State: SC

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 10/28/2021
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: This is a spontaneous report from a contactable other-HCP (patient). A 55-year-old male patient received the 2nd dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, batch/lot# EN6202), at the age 55, via an unspecified route of administration, in left arm, on Feb 25, 2021, single dose, for COVID-19 immunization. The patient's medical history not reported. Historical vaccine included received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, solution for injection, batch/lot# EL9262), at the age 55, via an unspecified route of administration, in left arm, on Jan 27, 2021, at 08:30, single dose, for COVID-19 immunization. The patient has no known allergies. The patient did not received any other vaccines within 4 weeks. Reportedly, patient took other medications in two weeks of vaccination. Prior to the vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not tested for COVID-19. On Feb 26, 2021, patient developed tender and swollen lymph nodes in left arm pit, fatigue and slight dizziness. The patient did not received any treatment for the events. The outcome of events: recovering. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1823750
Sex: F
Age:
State: NC

Vax Date: 01/22/2021
Onset Date: 01/30/2021
Rec V Date: 10/28/2021
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: 8 days after vaccine, woke up and injection site was bright red and the size of a dime. Area was incredibly itchy and there was about a 5 inch rash around the injection site; 8 days after vaccine, woke up and injection site was bright red and the size of a dime. Area was incredibly itchy and there was about a 5 inch rash around the injection site; 8 days after vaccine, woke up and injection site was bright red and the size of a dime. Area was incredibly itchy and there was about a 5 inch rash around the injection site; This is a spontaneous report from a contactable other healthcare professional (Patient). A 33-Year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH m-RNA COVID-19 VACCINE, formulation: Solution for injection, Lot number and expiry date was not reported), via Intramuscular route into left arm on 22Jan2021 at 02:15 pm as dose 1, single (Age at vaccination: 33-year-old) for Covid-19 immunization. Medical history included: Poly cystic ovarian syndrome. The patient had no Known allergies. The patient had not received any other vaccine within 4 weeks. The patient was not pregnant at the time of vaccination. The patient neither had covid prior vaccination and nor tested for covid post vaccination. Concomitant medications in two weeks included: semaglutide (OZEMPIC), spironolactone, ergocalciferol (VIT D) and birth control medicine (unspecified). On 30Jan2021 at 08:00 AM (8 days after vaccine), the patient woke up and injection site was bright red and the size of a dime. Area was incredibly itchy and there was about a 5-inch rash around the injection site. The patient did not receive any treatment for adverse events. Outcome of events was recovered on an unspecified date. Follow-up attempts completed. No further information expected.

Other Meds: OZEMPIC; SPIRONOLACTONE; VIT D

Current Illness:

ID: 1823751
Sex: M
Age:
State: FL

Vax Date: 02/23/2021
Onset Date: 02/26/2021
Rec V Date: 10/28/2021
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: vertigo-type dizziness; slight headache; vertigo-type dizziness; This is a spontaneous report from a contactable consumer (patient). A 77-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EN6200, and Expiration date: Unknown), via an unspecified route of administration, administered in upper left arm on 23Feb2021 09:00 (at the age of 77-year-old) as dose 2, single for COVID-19 immunization. The patient medical history included vertigo. Concomitant medications included losartan (LOSARTAN), alprazolam (ALPRAZOLAM), and simvastatin (SIMVASTATIN). The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EL9262, and Expiration date: Unknown), via an unspecified route of administration, administered in upper left arm on 02Feb2021 (at the age of 77-year-old) as dose 1, single for COVID-19 immunization. No investigation assessment. It was reported that, the patient received vaccine on Tuesday morning at 9 o'clock. The patient had normal adverse events from the second shot of the vaccine, first 2 days he had common symptoms which are of little significance, typical symptoms, nothing usual, all within the parameters, on which he got on the following day (24Feb2021, Wednesday) and the symptoms were "basically gone" (like the symptoms had passed, and the patient felt really good) by Thursday (25Feb2021). On Friday (26Feb2021), also he felt great. However, on the same day (on 26Feb2021), he started to develop vertigo-type dizziness with slight headache. The patient reported that "I have vertigo". So, he did his typical vertigo exercises which seemed to have a little impact whatsoever and seem to had a different reaction then he normally do when he get vertigo. The patient classified his headache as mild and his vertigo-type dizziness as severe since it interferes with him when he had to go to the bathroom late at night. The headache was mild, the patient called the doctor's office and spoke to the Nurse practitioner, and she prescribed Meclizine 12.5 mg, one tablet twice daily for the vertigo-type dizziness. So, the patient had taken one a day of those. He said that he did not feel other adverse events like fever or trouble breathing. The patient reported the vertigo-type dizziness was still happening until the day of reporting (28Feb2021). The patient had also been in touch with a pharmacist and the pharmacist reported that he had multiple calls about reports of vertigo-type dizziness with a slight headache. The patient said that his adverse event did not occur immediately after the vaccine was administered but it occurred days after getting the shot. Pharmacist told him that the vertigo-type dizziness that were reported to the pharmacist had a duration of 5-10 days. The patient was sure if the other people have a history of vertigo. The patient was convinced that there was a correlation with his adverse event with the Pfizer COVID-19 vaccine because he had heard multiple reports about this happening with other people. He believed it was an emerging adverse event associated with the vaccine. The patient just wanted to inquire "is that something that you are aware of and have heard about especially when you thought all the side effects were gone and all of a sudden this issue. And it's a typical vertigo". The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: LOSARTAN; ALPRAZOLAM; SIMVASTATIN

Current Illness:

ID: 1823752
Sex: M
Age:
State:

Vax Date: 02/26/2021
Onset Date: 02/01/2021
Rec V Date: 10/28/2021
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: he hadn't informed the vaccination provider about being on Xarelto; had soreness on the injection site/he had soreness on the injection site that lasted for a day after getting the vaccine; This is a spontaneous report from a contactable consumer (patient). A 64-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Batch/Lot Number: not reported) via an unspecified route of administration on 26Feb2021 as DOSE 1, SINGLE for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication included rivaroxaban (XARELTO). The patient explained when reading the fact sheet after vaccination, he got concerned when he realized he had not informed the vaccination provider about being on Xarelto on an unspecified date. The patient added the vaccination provider did not ask him about allergies or his medical conditions. He asked why you should you tell the vaccination provider about all of your medical conditions, including if you have a bleeding disorder or on a blood thinner. He also asked if the combination of the two, the Xarelto and the COVID-19 vaccine can cause him to have side effects; and if so, which ones should he look at for. The patient had no bruising or bleeding after vaccination. He also reported that he had soreness on the injection site that lasted for a day after getting the vaccine. The sore was already little and not painful on an unspecified date in Feb2021. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. The lot number for BNT162B2, was not provided and will be requested during follow up.

Other Meds: XARELTO

Current Illness:

ID: 1823753
Sex: F
Age:
State: CT

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 10/28/2021
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: Approx. 12 hours after 2nd dose of vaccine, woke up with chills that lasted-3 hours.; Rest of the day only symptoms were fatigue and aches; Rest of the day only symptoms were fatigue and aches; This is a spontaneous report from a contactable consumer. A 23-year-old female patient received second dose of BNT162B2 (Pfizer COVID 19 Formulation: Solution for Injection Batch/Lot Number: EL3247 Expiration Date: Unknown) via an unspecified route of administration, administered in Arm Left on 25Feb2021 11:00 (at the age of 23-year-old) as single dose for COVID-19 immunization. Patient previously received first dose of Pfizer COVID 19 vaccine (lot number: EL3247) on 04Feb2021 11:00 administered in left arm. The patients medical history and concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and received Birth Control medication within 2 weeks of vaccination. Prior to vaccination, patient was not diagnosed with COVID-19 and Since the vaccination patient has not been tested for COVID-19. On 26Feb2021 12:00 Approx. 12 hours after 2nd dose of vaccine, patient woke up with chills that lasted for approximately 3 hours. No temperature was taken. Rest of the day only symptoms were fatigue and aches. Outcome of all the event chills was recovered on 26Feb2021 15:00 and rest all events was recovered on an unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823754
Sex: F
Age:
State:

Vax Date: 02/19/2021
Onset Date: 03/01/2021
Rec V Date: 10/28/2021
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: sore arm; she's feeling nauseous (slightly queasy, come and go); This is a spontaneous report from a contactable consumer (patient). A female patient of an unknown age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot number and expiry date: unknown) via unspecified route of administration on 19Feb2021 as DOSE 2, SINGLE for COVID-19. The patient's medical history and concomitant medications were not reported. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot number and expiry date: unknown) via unspecified route of administration on an unspecified date as DOSE 1, SINGLE for COVID-19. It was reported that the patient clarified she had her second shot on 19Feb2021 and this morning (01Mar2021) she was feeling slightly nauseated. She suspects it was not connected. Caller asks the call handler as a nurse in her professional opinion, could it be related to the vaccine this long after. The caller states the only reaction she had to the vaccine was a sore arm. 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: 1823755
Sex: F
Age:
State: IL

Vax Date: 02/21/2021
Onset Date: 02/21/2021
Rec V Date: 10/28/2021
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: tendonitis; received BNT162B2 first dose on 03Jan2021 and second dose on 21Feb2021; This is a spontaneous report from a contactable consumer (Patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Lot number: EN6202) via an unspecified route of administration on 21Feb2021 as dose 2, single for COVID-19 immunization. Medical history included allergy from an unspecified date and unknown if ongoing. Concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Lot number: EL3249) via an unspecified route of administration on 03Jan2021 as dose 1, single for COVID-19 immunization and steroid shots (Lot number: unknown) via an unspecified route of administration on an unspecified date as dose number unknown, single for flare ups. It was reported that on an unspecified date patient experienced tendonitis. Patient wanted to know when she can have the steroid for her tendonitis in her hands. She also added that she is going to have steroids put into the hands, the lady also told her she cant have her allergy shots. She would get the steroid shots before the covid vaccine, when she would have flare ups, she gets it a couple times a year. She also has been getting the Allergy shots for about 30 years now she has not had an allergy shot in 5 weeks. Reporter also stated when getting the shot she was told that she should not get a mammogram and would have to wait for a month. The Mammogram was initially scheduled on 25Feb2021, and she rescheduled and couldn't get in till 19May2021.Reporter wanted to know when she schedules this appointment after having had the covid vaccine. RA was not present. Outcome of the event tendonitis was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823756
Sex: F
Age:
State: NJ

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 10/28/2021
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: Slight Soreness at Site of Injection; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 73-years-old female patient (patient was not pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN6203, Expiration date: unknown) via an unspecified route of administration, administered in left arm on 24Feb2021 at 10:30 am (age at vaccination was 73 years) as dose 1, single for COVID-19 immunization. The patient's medical history included 2 bowel obstruction surgeries and COVID-19 from an unknown date. Concomitant medications and other medications the patient received within 2 weeks of vaccination included multivitamins [vitamins NOS], ascorbic acid (VIT C), ergocalciferol, retinol (VITAMIN A & D [ERGOCALCIFEROL; RETINOL]) and zinc all taken for an unspecified indication. The patient previously took eritrovis [erythromycin] and experienced allergies to it. The facility where the most recent COVID-19 vaccine was administered was Public Health Clinic. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 24Feb2021 at 17:00 pm, the patient experienced slight soreness at site of injection. No treatment was received for the adverse event. 2 weeks from dose 1 date there were no side effects to report. The patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EP7534, Expiration date: unknown) via an unspecified route of administration, administered in left arm on 17Mar2021 at 10:15 am (age at vaccination was 73 years) as dose 2, single for COVID-19 immunization. The outcome of the event was resolved on an unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds: MULTIVITAMINS [VITAMINS NOS]; VIT C; VITAMIN A & D [ERGOCALCIFEROL;RETINOL]; ZINC

Current Illness:

ID: 1823757
Sex: F
Age:
State: TX

Vax Date: 02/23/2021
Onset Date:
Rec V Date: 10/28/2021
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: arm was sore; Headache; Lightheadedness; Fatigue; This is a spontaneous report from a contactable consumer (patient herself). A 70-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EN6202; Expiration date: unknown) via an unspecified route of administration on 23Feb2021 (at the age of 70-years-old) as DOSE 2, SINGLE for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient had previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, 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 immunization. It was reported that patient received her second shot of the Pfizer BioNTech COVID-19 vaccine last week and on the way to the vaccination appointment, she reported she took one Tylenol. She stated it was then about a half hour later that she received her vaccine and would like to know if this affected her vaccine in any way. Caller did report after her second shot on an unspecified date her arm was sore "for maybe an hour" and then went away. She received 2nd dose of vaccine. Was stuck in traffic and got a headache so she popped an Tylenol not thinking about vaccine. So when she got shot, arm was little sore in the beginning like when she was walking back to her car and then it went away. She didn't have any symptoms other than lightheadedness and little fatigue. She was so scared that she knocked out the second shot with that one Tylenol. She was thinking as - What did I do? Did I ruin the second shot by taking that Tylenol? I get that some time, I feel protected. Therapeutic measures were taken as a result of headache as patient took Tylenol. The outcome of arm was sore was resolved on an unspecified date while it was unknown for all other events. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021580889 same patient/drug, different dose/event.

Other Meds:

Current Illness:

ID: 1823758
Sex: M
Age:
State: MO

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 10/28/2021
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: He is now not able to move the arm; Lightheaded episodes; Severe shakes; This is a spontaneous report from a contactable consumer. This consumer reported for a male patient (Husband) of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration, administered in unspecified Arm on 01Mar2021 as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine include dose 1 bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. On an unspecified date of 2021 it was reported that patient was not able to move the arm he got the injection in without being in severe pain, having lightheaded episodes where patient has to sit down and severe shakes. The case was assessed as non serious. The outcome of the events were unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1823759
Sex: F
Age:
State: CA

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 10/28/2021
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: injection site pain; arm pain; headache; fatigue; her glands on the left side of throat are swollen; This is a spontaneous report from a contactable consumer. This 54-year-old female consumer (Patient) reported that: A 54-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID -19 VACCINE, solution for injection, Lot Number: not reported, Expiry date: unknown) via an unspecified route of administration, on 12Feb2021 (54-years-old at the time of vaccination) as dose 1, single for COVID-19 immunization. Medical history included tonsil issues from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. On an unspecified date in Feb2021, the patient experienced injection site pain, arm pain, headache, fatigue and her glands on the left side of throat are swollen. Patient stated that received first dose of Pfizer Covid vaccine 12Feb2021. It was reported that the patient experienced injection site pain, arm pain, headache, and fatigue within the first 24 hours of receiving the vaccine. On an unspecified date on 2021, a week later, she started to experience left neck sided lymph node gland swelling which has continued for 2 weeks. She has an appointment with her ENT MD soon to discuss further. She is due to receive her second dose this Friday 05Mar2021. She wants to know if there is any information on this side effect. After 1st dose, her glands on the left side of throat are swollen and she is wondering if she should take 2nd dose. The outcome of the events were unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1823760
Sex: F
Age:
State: TN

Vax Date: 01/26/2021
Onset Date:
Rec V Date: 10/28/2021
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: dizziness; arm pain; This is a spontaneous report from a contactable consumer (patient). An 84-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: FL9261), via an unspecified route of administration, administered in Arm Right on 26Jan2021 (at the age of 84-year-old) as single dose for COVID-19 immunization. Medical history included flu (The patient went to (place) for winter. Last year when they both got home, they were really sick. Both patient and her husband, had to go to the Emergency room. Were sick for 3-4 weeks. Believes they had the COVID virus. Can't say for sure if it was COVID but was told they both had the Flu. Patient mentioned this to the doctor and some say she and her husband might have had the COVID virus. Confirmed this was a year ago, prior to receiving the COVID vaccines). Concomitant medication included heart pills and a blood pressure pill (unspecified). She takes two pills a day. The patient did not receive additional vaccines on same date of Pfizer suspect. The patient did not receive prior vaccinations within 4 weeks and had no AEs follow prior vaccinations. The patient had no family medical history. The patient received first dose of the Pfizer Covid vaccine on 26Jan2021. She experienced dizziness after the first dose and arm pain. The patient had no relevant tests. Outcome of the events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823761
Sex: F
Age:
State: NY

Vax Date: 02/12/2021
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: all over sore/like all over my body; my lower back pain; my leg, my thigh pain; muscle pain; my arm pain; This is a spontaneous report from a contactable consumer (Patient). A 74-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EM9809), dose 1 intramuscular, administered in Arm Right on 12Feb2021 17:00 (age at vaccination 74-year-old) as dose 1, single for covid-19 immunization. The patients medical history and concomitant medications were none. On an unspecified date, the patient experienced all over sore, her arm, her lower back, her leg, her thigh pain, like all over her body and muscle pain and ache in back. The patient was tried exercising and it does not go away. This was patient first dose and she was getting her second dose on Friday (unspecified date). The patient assessed the events as non-serious. No adverse event following prior vaccinations. The outcome of the events was not recovered. No follow up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823762
Sex: F
Age:
State: NY

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 10/28/2021
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: lymph nodes were swollen/she has swollen lymph nodes under her arm and in her groin; This is a spontaneous report from a contactable consumer. A 53-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE: Solution for injection; Batch/Lot Number: EM9809; Expiration Date: Jun2021), dose 1 via an unspecified route of administration, administered in Arm Right on 11Feb2021 18:30 as dose 1, single for covid-19 immunisation (at the age of 53-year-old). Medical history included was none. The patient's concomitant medications were not reported. Caller states that she called earlier and spoke to someone about her Pfizer BioNTech COVID-19 vaccination and a side effect that she is experiencing. Caller states that she received her first dose and the very next day noticed her lymph nodes were swollen. Caller states that she did read that swollen lymph nodes is one of the side effects. She is due to receive her second dose on Thursday and states that it has gotten better but still a little swollen. Caller would like to know if she should expect this to get any worse. The caller said that right after her vaccination, she noticed swollen lymph nodes. She said that it is a listed side effect on the paperwork that she received. It is contraindicated for her to get the second dose with still having swollen lymph nodes. The caller said that she has swollen lymph nodes under her arm and in her groin the day after the vaccination. She said that she noticed more swollen lymph nodes on the left side of her body. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823763
Sex: F
Age:
State: FL

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: loss of appetite/no appetite; sleepiness/sleeping all day long; really tired; dizzy; drowsy; lack of attention; mouth is very dry; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EM1200, Expiry date: Unknown), via an unspecified route of administration on arm right on 25Feb2021 11:00 (age at vaccination: 75 years) as DOSE 2, SINGLE for COVID-19 immunization. The patient medical history included asthma, glaucoma, heart, Blood disorder, angina, high blood pressure, hiatal hernia, cholesterol, asthma attack. History of all previous immunization with the Pfizer vaccine considered as suspect included first Covid vaccine on 23Jan2021 (lot EL9269) and experienced no adverse events following prior vaccinations. Additional Administered Vaccines If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect was reported as no. The patient Concomitant medications included fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA) taken for Asthma from an unknown date in 2000 to ongoing, bimatoprost (LUMIGAN) taken for glaucoma from an unknown date to ongoing, Carvedilol taken for cardiac disorder from an unknown date to ongoing, clopidogrel bisulfate (PLAVIX) taken because of her heart, so her blood won't be too thick (blood disorder) from an unknown date in 2006 to ongoing, aspirin [acetylsalicylic acid] taken for Heart from an unknown date in 2006 to ongoing, ranolazine (RANEXA) taken for Heart from an unknown date in 2020 to ongoing, Amlodipine taken for angina and high blood pressure from an unknown date in 2019 to ongoing, Omeprazole taken for hiatal hernia from an unknown date to ongoing, ongoing Montelukast taken for asthma from an unknown date to ongoing, Atorvastatin taken for cholesterol from an unknown date to ongoing, Ipratropium Bromide taken for asthma attack from an unknown date to ongoing. On 25Feb2021, the patient experienced sleeping all day long, sleepiness lack of attention, loss of appetite (no appetite), really tired, dizzy, mouth is very dry. It was reported that She had her second vaccine on 25Feb2021. She's been sleeping all day long, she can't even read a paper or watch tv. She has no appetite, she is dizzy, and she's really, really tired. She's drinking lots of water like they told her to but it's not helping. She states she was told to drink lots of water. It was explained to her that it is normal. She's talking about right now, there were 22 calls before her and she was asleep on the phone. she stays longer but somehow she fell asleep the minute she sat down and she was snoring. She read the paper from the vaccine and they told her it was normal but it has been going on for a bit. She's trying to remember if it started on Thursday she came home, laid down, didn't feel like eating but she ate, she's drinking lots of water but her mouth is very dry. She's old and doesn't want to die. She doesn't want to go to hospital, there is to much Covid there. Antipyretic Use was reported as not applicable. The outcome of events was not resolved. No follow-up attempts are possible; No further information is expected.

Other Meds: BREO ELLIPTA; LUMIGAN; CARVEDILOL; PLAVIX; ASPIRIN [ACETYLSALICYLIC ACID]; RANEXA; AMLODIPINE; OMEPRAZOLE; MONTELUKAST; ATORVASTATIN; IPRATROPIUM BROMIDE

Current Illness: Angina pectoris; Asthma; Blood disorder; Blood pressure high; Cholesterol; Glaucoma; Heart disorder; Hiatal hernia

ID: 1823764
Sex: F
Age:
State: CT

Vax Date: 03/23/2021
Onset Date: 03/01/2021
Rec V Date: 10/28/2021
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: Injection site pain; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 30-year-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EP6955), via an unspecified route of administration, administered in Arm Right on 23Mar2021 11:45 (at the age of 30-year-old) as dose 2, single and received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL3247) via an unspecified route of administration, administered in left arm on 01Mar2021 10:30 (at the age of 30-year-old) as dose 1, single for COVID-19 immunization at Workplace clinic. The patient medical history was not reported. Patient had no allergies. Concomitant medication(s) within 2 weeks included ethinylestradiol, norgestimate (NORGESTIMATE AND ETHINYL ESTRADIOL). The patient was not pregnant at time of vaccination. The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19 and since the vaccination, the patient had not been tested for COVID-19. On 01Mar2021 13:00 The patient experienced injection site pain. The patient had injection site pain approximately 2-3 hours after vaccine. Patient did not received any treatment for the event. The outcome of the event was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds: NORGESTIMATE AND ETHINYL ESTRADIOL

Current Illness:

ID: 1823765
Sex: F
Age:
State: MA

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 10/28/2021
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: feeling achy; This is a spontaneous report received from a contactable consumer reporting for a patient. An 80-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: unknown), via an unspecified route of administration on 26Feb2021 14:00 at the age of 80-years-old as dose 1, single for covid-19 immunisation. The patient was not pregnant at the time of vaccination. The patient's medical history and concomitant medications were not reported. It was unknown if the patient received any other vaccines within 4 weeks prior to the COVID vaccine. It was unknown if the patient was diagnosed with COVID-19 prior to vaccination. It was unknown if the patient has been tested for COVID-19 since the vaccination. On 27Feb2021, the patient experienced feeling achy, a day after receiving her first Pfizer Covid19 vaccine shot. It was unknown if the patient received treatment for adverse event. Adverse event resulted in none of the above. The outcome of event was recovered on an unspecified date in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1823766
Sex: F
Age:
State: MA

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: She had mild side effects to the first vaccine; This is a spontaneous case received from a contactable consumer (patient) via a Pfizer sponsored program. A female patient of age 90 (units unspecified) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was not reported), via an unspecified route of administration, administered on an unspecified date as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was not reported) via an unspecified route of administration, administered on an unspecified date for Covid-19 immunization. On an unspecified date, the patient reported that she had mild side effects to the first vaccine. 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: 1823767
Sex: F
Age:
State: CA

Vax Date: 02/07/2021
Onset Date: 02/01/2021
Rec V Date: 10/28/2021
Hospital:

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

Lab Data: Test Name: height; Result Unstructured Data: Test Result:Unknown result; Comments: Height: She stated she may have shrunk about a 0.5 inch.

Allergies:

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

Symptoms: missed her second dose; still feels terrible; Diarrhea; Flu like symptoms; This is a spontaneous report received from a from a contactable consumer received via Pfizer-sponsored program Support. This consumer (patient) reported for herself that a 87-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot Number: EL3249), via an unspecified route of administration, administered at arm left on 07Feb2021 (age at vaccination was 87 year) as dose 1, single for covid-19 immunisation. The patient medical history include allergic to various medication, penicillin allergy, drug allergy to azithromycin and any of the mycin. The concomitant medications were not reported. The caller stated that, she reported that she missed her appointment for her second dose, she has been sick for about 3 days and did not think it was good for her to have the appointment to get her second dose. On an unspecified date, the patient experienced still feels terrible and missed her second dose; on unspecified date in Feb2021, flu like symptoms; on 28Feb2021, diarrhea. The caller said that she had flu like symptoms. Her appointment was at like 09:30, but someone called her and told her there was another appointment available at around 16:00. Caller does not know if she should go get the second shot or if it is contraindicated. She said that she had diarrhea. She said that she still feels terrible. She has some sort of flu like stuff and last night had diarrhea. Stated that this is an old problem with her. She said that she is supposed to have the second shot, but it has been like 3 weeks and a day. She said that her symptoms did not happen immediately, they happened like 3 weeks later, states it is just her body. Height: She stated she may have shrunk about a 0.5 inch. She said that she has not felt good for the last 3 days. She said that she had diarrhea last night and felt terrible during the day. For 3 days she did not feel well like she had the flu or something. She went for her walk day before yesterday, and she walks about a half a mile usually 5 times a week. Caller said that she has a lot of low back pain and has to move because of the pain. She has to keep moving or she will be in bed all the time. She stated that she had the back pain long before she had the Covid-19 vaccine and stated that it was from an injury. States the back pain has nothing to do with the vaccine. Caller said that she feels like she is on the verge of diarrhea and was afraid she would not be able to get out of the bathroom. She has been to the bathroom a few times. When she had bouts of diarrhea before it is constant out of bed and in the bathroom back and forth. This is her body's way of getting rid of whatever bug she could have. States this is seemingly so connected to her coming back to get the second dose, which she confirms she has not received the second dose yet. She said that she does not vomit easily, she usually gets diarrhea instead. Caller said that her left arm is still a little sore. She thinks she asked for it on the left side since she is right-handed. Said that she has a list of other medications that she is allergic to. No further details provided. Caller said her first thought is that she might be allergic to the Covid vaccine. The clinical outcome of events was not recovered. Investigation Assessment: No No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823768
Sex: M
Age:
State:

Vax Date: 02/28/2021
Onset Date:
Rec V Date: 10/28/2021
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: injection site being a little sore; This is a spontaneous report from a contactable consumer (patient). A 73-years-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6198, Expiration date: 30Jun2021), via an unspecified route on 28Feb2021 (at the age of 73-years) as dose 2, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN5318, Expiration date: May2021), via an unspecified route on unspecified date as dose 1, single for covid-19 immunisation. The patient experienced injection site being a little sore on unspecified date. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823769
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: Sore arm; Fatigue; This is a spontaneous report from a Pfizer sponsored program . A contactable 63-years-old male consumer (patient) reported to received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: 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 immunisation. It was reported that first dose about 3 weeks ago, second dose due to 03Mar2021. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced sore arm, fatigue. Patient requested information regarding antibodies testing or T-cells tests to assess for immunity/effectiveness after vaccination. Patient asked if he use antipyretics before or after vaccination with the Pfizer-BioNTech COVID-19 vaccine. The outcomes of events were 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: 1823770
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: sore arm; wondering if you have discomfort in the injection site after the first dose, and no; This is a spontaneous report from a contactable physician (patient). A 54-years-old female patient received 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 DOSE 1, SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously took Shingrix and experienced sore arm. The patient received both doses of Pfizer's COVID vaccine 22 days apart. The reporter stated that she had a mild response to the first vaccine with a sore arm, but had no fever nor headache and for her second dose, she had no symptoms whatsoever. Caller asked what statistics do you have in having less adverse reactions of the second dose compared to the first dose, How likely is it that a vaccine recipient would have injection site soreness after dose 1, but no symptoms/no reaction after dose 2. Would there be any concern that the second dose had been mishandled and this was ineffective. 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: 1823771
Sex: F
Age:
State: SD

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 10/28/2021
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: she uses a walker all the time now; She said that her legs were floppy; she lost the use of her legs; This is a spontaneous report from a contactable consumer (patient). A 86-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EL3248), via an unspecified route of administration, administered in arm right on 11Feb2021 (at the age of 86-years) as dose 2, single for covid-19 immunization. Patient had no relevant medical history. The patient concomitant medications were not reported. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, batch number: EL0140) at the age of 86-years, dose 1, on 28Dec2020 in right arm for covid-19 immunization. The patient got first vaccine 28Dec2020 and then got the second vaccine on 11Feb2021 on a Thursday, states the next day 12Feb2021, the patient had no use of legs, they were flopping all over. The patient wants to know why this happened, the patient was wondering why did her legs go bopping around, states it improved a couple of days later but the patient uses a walker all the time now. The outcome of had no use of her legs was recovering and outcome of other events was unknown. No follow up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823772
Sex: F
Age:
State: CA

Vax Date: 02/13/2021
Onset Date: 02/01/2021
Rec V Date: 10/28/2021
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: she has an inflammatory/rheumatologic disease and she had a flare just this week/relapsing polychondritis flare; sore right arm; Arm discomfort; This is a spontaneous report from a contactable consumer(patient). A 59-year-old female had received bnt162b2 (Pfizer-biontech covid-19 vaccine, Solution for injection, Batch/lot number: EM9809) via an unspecified route of administration into arm right on 13Feb2021 08:30 (age at vaccination 58 Years) as DOSE 1, SINGLE for covid-19 immunization. The patient medical history was Relapsing polychondritis, (she was diagnosed with about 7 years ago. she has an inflammatory/rheumatologic disease). Concomitant medications:None. The patient was reported that she was diagnosed with polychondritis about 7 years ago and clarified about 1 in 1,000,000 people are diagnosed with the disease . It was reported that patient did not take any vaccine within 4 weeks prior to vaccination. On Feb2021the patient had experienced she had a sore right arm for several days after receiving her first dose of the COVID-19 Vaccine, arm discomfort and an inflammatory/rheumatologic disease and she had a flare just this week/relapsing polychondritis flare because of that, she decided that she is no longer going to get the 2nd dose this weekend(06Mar2021). She wants to know the efficacy rate of the vaccine with just 1 dose. Therapeutic measures were taken for the AE inflammatory/rheumatologic disease and she had a flare just this week/relapsing polychondritis flare and treatment was given with Colchicine 0.6mg 1 to 2 times daily and was taking Ibuprofen 400mg daily.She said her doctor was considering putting her on other medication because the Colchicine 0.6mg doesn't work as good as it used to. The clinical outcome of the events inflammatory/rheumatologic disease and she had a flare just this week/relapsing polychondritis flare was not recovered and sore right arm, arm discomfort was recovered on Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1823773
Sex: M
Age:
State: AZ

Vax Date: 02/24/2021
Onset Date: 02/01/2021
Rec V Date: 10/28/2021
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: heart palpitations; chills; nauseous; dizzy; previous steroids shot was given on 20Feb2021; previous steroids shot was given on 20Feb2021; This is a spontaneous report from a contactable nurse. A 82-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, lot number: EP7534, Expiry date: unknown) (age at the time of vaccination was 82 years), administered in Arm Left on 24Feb2021 at 12:57 as dose 2, single for COVID-19 immunization. The patient's medical history included neck problem received 6 or 7 cortisone injections, for a nerve rubbing a bone, heart palpitations. Historical vaccine included shingles vaccine had a slight reaction to the shingles vaccine that took last summer. The patient's concomitant medication was not reported. The patient did not take any other vaccine in four weeks prior COVID -19 vaccine. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: EL3249), administered in Arm Left on 20Jan2021 at 12:40 as dose 1, single for COVID-19 immunization. The patient had sore arm/numb arm while taking first dose. The patient was really happy, but had some side effects. On 20Feb2021, the patient received steroids shot given in between vaccine doses. The patient had chills after getting second dose of the vaccine. The patient was fairly dizzy and kind of nauseous the first night. The patient know that chills were part of the Covid-19 vaccine, but wants to know how long would expect to have the chills before it goes away. Where patient first came home he was very excited and also had heart palpitations. The patient had heart palpitations before vaccine also. Got through the night alright. The patient was concerned about it. Once patient get under covers he was ok. Thought the chills would gradually go away would be less each day. The outcome of the events was unknown. No follow-up attempts were possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1823774
Sex: M
Age:
State: NJ

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 10/28/2021
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: Diarrhea; This is a spontaneous report from a contactable consumer. This 35-year-old Male consumer (Patient) reported that who received bnt162b2 (BNT162B2) solution for injection, dose 1 (Batch/Lot Number: EN6203) via an unspecified route of administration, administered in arm left on 28Feb2021 09:30 (at the age of 35-years-old) as dose 1 single for covid-19 immunisation. Medical history included from an unknown date and unknown if ongoing other_medical_history: No. Concomitant medication(s) included amoxicillin (AMOXICILLIN) taken for an unspecified indication, start and stop date were not reported. Prior to the vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. Patient did not have known allergies. No treatment was received for the adverse events. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 01Mar2021 09:00 the patient experienced diarrhoea. Outcome of the event was recovered on an unspecified date. Follow-up (12MAY2021): Follow-up attempts completed. No further information expected.

Other Meds: AMOXICILLIN

Current Illness:

ID: 1823775
Sex: M
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: sore arm/muscle; sore arm/muscle; This is a spontaneous report from a contactable consumer (patient). A male patient (Age 73; units: Unspecified) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution of injection, 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 and the concomitant medications were not reported. On an unspecified date the patient experienced sore arm/muscle. The reporter reported that 3 and 1/2 weeks ago the patient took the first shot, everything went good and it felt like it was kicking in and it went well. The patient didn't have any allergy or reactions. The patient had a sore arm/muscle for a little while and then felt good. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823776
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
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: This is a spontaneous report from a contactable consumer (patient). A 71-year-old female received the second dose of BNT162B2 (Comirnaty, solution for injection, batch/lot# not reported, expiration date: unknown), via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunization. The patient's medical history and concomitant medications not reported. The patient previously received the first dose of BNT162B2 (Comirnaty, solution for injection, batch/lot# not reported, expiration date: unknown), via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunization and had a headache. On an unspecified date, patient had fatigue; with outcome of unknown. No follow-up attempts possible. Information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1823777
Sex: F
Age:
State: OK

Vax Date: 02/22/2021
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: On the day of both shots, arms were sore. And there was a considerable increase of energy and alertness felt.; This is a spontaneous report from a contactable nurse. This 30-year-old female nurse (patient) reported. A 30-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: UNKNOWN), dose 2 via an unspecified route of administration, administered in Arm Left on 22Feb2021 (at the age of 30-years-old) as a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. Patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: UNKNOWN), dose 1 via intramuscular, administered in Arm right on 27Jan2021 10:30 (at the age of 30-years-old) as a single dose for covid-19 immunization. The patient did not have any allergies. The patient had no other vaccine within four weeks and no other medications received within 2 weeks 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 experienced on the day of both shots, arms were sore. and there was a considerable increase of energy and alertness felt on an unspecified date. The patient did not receive any treatment. Outcome of the event was recovered. Information about lot/ batch number has been requested Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1823778
Sex: M
Age:
State: AZ

Vax Date: 02/15/2021
Onset Date:
Rec V Date: 10/28/2021
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: he wasn't feeling really well; chills; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Lot Number: not reported), via an unspecified route of administration on 15Feb2021 as dose number unknown, single for covid-19 immunization. Medical history included the patient has a pacemaker. The patient concomitant medications were not reported. The patient reported that he got the shot first shot 15Feb2021. He confirms the Pfizer COVID 19 vaccine. He felt good for quite a while then he started getting chills. He may have had some chills before but he was supposed to go up this morning to the drug store and have them run a test to see if had the COVID or if he does not have it. He asked would that test tell him if had the COVID or if this was a reaction from the shot. He has not had fever, he was not sure if he had chills before the vaccine or after but about week after had the vaccine, maybe a little less, he was not feeling really well, he just does not feel up to par. It just so happens he has a pacemaker and he was going to see his doctor for a check up on Thursday of this week and he told them he was not feeling well and they said okay they told him they were going to have him go into the pharmacy this morning and have them run a test to see if he has the COVID virus. He said his main concern was he was going in week from next Monday for the second shot. He asked was there any chance that they will tell him not to get the second shot because he would be due to have the other shot so if he gets that he wanted to know if he would have the same reactions or little bit less. The outcome of events 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: 1823779
Sex: F
Age:
State: MD

Vax Date: 02/21/2021
Onset Date: 02/22/2021
Rec V Date: 10/28/2021
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: Swollen arm; skin hot to touch; mimics effects of bee sting; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient (non-pregnant) received second dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9266), dose 2 via an unspecified route of administration, administered in Arm Left on 21Feb2021 16:00 (at the age of 37-year-old) as dose 2, single for COVID-19 immunization. The patient was not pregnant at the time of vaccination. The patient medical history was not reported. Concomitant medications included atorvastatin, metformin. Previously patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL8982), dose 1 via an unspecified route of administration, administered in Arm Left on 31Jan2021 (37-year-old) 16:00 as dose 1, single for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not have covid prior vaccination and no covid tested post vaccination. The patient had no known allergies. On 22Feb2021 09:00 the patient experienced swollen arm, skin hot to touch, mimics effects of bee sting. The patient did not receive any treatment for events. AE resulted in Doctor or other healthcare professional office/clinic visit. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: ATORVASTATIN; METFORMIN.

Current Illness:

ID: 1823780
Sex: F
Age:
State: MA

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 10/28/2021
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: muscle pain in my arm; This is a spontaneous report from a contactable consumer (patient) or other non-healthcare professional. A 24-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was unknown), dose 1 via an unspecified route of administration, administered in Arm Left on 20Jan2021 12:00 (at the age of 24-year-old) as dose 1, single for COVID-19 immunization. Medical history reported as no. The patient concomitant medications were not reported. Patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines in 4 weeks prior to the COVID vaccine. Patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had not been tested for COVID-19. On an unspecified date in 2021 the patient experienced muscle pain in arm. The clinical outcome of event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1823781
Sex: F
Age:
State: WI

Vax Date: 01/28/2021
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: she lost her taste and smell and it stayed gone up until that first shot and then everything began to come back; she lost her taste and smell and it stayed gone up until that first shot and then everything began to come back; she lost her taste and smell; she lost her taste and smell; This is a spontaneous report from a contactable consumer (patient) and physician. A 68-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/lot number: EL9262, Expiry Date: Not Reported), via an unspecified route of administration on 28Jan2021 (at the age of 68-year-old) as dose 1, single for COVID-19 immunisation. There was no medical history, no concomitant medications, and no investigation assessment. The patient had taken a COVID test many times. It was last year she had gone to the store; she wore her mask, but her niece did not. She told her doctor she lost her taste and smell and it stayed gone up until that first shot and then everything began to come back, and she was happy. Everyone was saying how do you feel some, she knows some of her friends and family had problems, but she got her taste and smell back. She clarifies she has not been tested for COVID since it the taste and smell came back, she will see at her doctors appointment next month, what was going on. Outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1823782
Sex: F
Age:
State: CA

Vax Date: 01/31/2021
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Arm still sore, but that also happened after first shot; This is a spontaneous report from a contactable consumer (patient). An elderly non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection) via an unspecified route of administration, administered in left arm on 31Jan2021 15:30 (Lot Number: EI9262) as dose 1, single for COVID-19 immunisation. Patient was not pregnant at the time of vaccination. Medical history included unspecified known allergies to Penicillin and Demerol. Concomitant medications included ascorbic acid, biotin, folic acid, iodine, pantothenic acid, pyridoxine hydrochloride, retinol, vitamin B12 NOS, vitamin D NOS, vitamin E NOS, zinc (CENTRUM MULTIGUMMIES); calcium and Vitamin C [ascorbic acid] form unknown date and unknown if ongoing. No other vaccine administered in four weeks. On an unspecified date, the patient stated arm still sore, but that also happened after first shot. Patient had no COVID prior vaccination and not tested for COVID post vaccination. Outcome of the event was unknown at the time of reporting. No follow up attempts are needed. No further information is expected.

Other Meds: CENTRUM MULTIGUMMIES; CALCIUM; VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 1823783
Sex: F
Age:
State: AZ

Vax Date: 02/16/2021
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:everything was good

Allergies:

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

Symptoms: achiness; getting sick; Could not even sleep because of the achiness; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received second dose, bnt162b2 (BNT162B2; PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection; Batch/Lot number: not reported), via an unspecified route of administration on 16Feb2021 (at the ag of 73 years-old) as dose 2, single for COVID-19 immunisation. Medical history included Diabetes and cholesterol from an unknown date and unknown if ongoing. Concomitant medication(s) included janumet for an unspecified indication, start and stop date were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection) on 16Jan2021 as single dose for covid19 immunisation. The patient experienced achiness, getting sick, could not even sleep because of the achiness on an unspecified date. Patient stated that she was kind of just wondering, she already got her second shot, and she got it last Tuesday and this week, it was not until now that she was feeling, thinks she was not sure, if that was side effect from the shot. Like towards the evening, she felt achy, it's like she was got sick, but then she wake up in the morning okay. Would she still be getting side effects from second shot, well, last night, after the second one. But the first one, she started getting sick the next day. The patient underwent lab tests and procedures which included blood work: everything was good on an unspecified date. Tylenol were taken as a result of achiness. The outcome of events was unknown. No follow-up attempts are needed. Information about lot/ batch number cannot be obtained.

Other Meds: JANUMET [METFORMIN HYDROCHLORIDE;SITAGLIPTIN]

Current Illness:

ID: 1823784
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: experienced pain in his arm; tired; This is a spontaneous report from a contactable consumer or other non health care professional. This female (daughter) consumer reported for a 60-year-old male patient (father). A 60-year-old male patient (father) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: EN6202, expiration date 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 and concomitant medications were not reported. It was reported that reporter father has experienced pain in his arm this morning and feeling tired. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am