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: 1792668
Sex: F
Age:
State:

Vax Date: 03/18/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: choking sensation in neck; jaw felt like it was getting huge; couldn't stand; couldn't walk; This is a spontaneous report from a contactable consumer (patient) received via the Medical Information Team. An 86-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, on 18Mar2021 (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date in Mar2021, the patient experienced choking sensation in neck. It was really bad, her daughter gave her many glasses of water and that seemed to help. Her jaw felt like it was getting huge and she couldn't stand or walk for a few days. Her doctor told her to take paracetamol (TYLENOL) and diphenhydramine (BENADRYL) before and after she gets the vaccine. The patient asked if she should get the second vaccine. It was scheduled on 08Apr2021. The outcome of events choking sensation in neck, jaw felt like it was getting huge, couldn't stand, and couldn't walk was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792669
Sex: F
Age:
State: NY

Vax Date: 03/18/2021
Onset Date: 03/27/2021
Rec V Date: 10/16/2021
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: She started not feeling well/she is sick; congestion; cold like symptoms; lost her sense of taste; sore throat; This is a spontaneous report from a contactable consumer. A 36-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EP6955), via an unspecified route of administration on arm left on 18Mar2021 at 10:10 (at the age of 36-years-old) as dose 1, single for COVID-19 immunization at clinic. The patient's medical history included Autoimmune compromised since Sep2011 and ongoing, Immune compromised since Sep2020 and Splenectomy in Dec2012. Concomitant medications was none. Historical vaccine included meningococcal and flu vaccines on 17Feb2021. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no AEs following prior vaccinations. On 27Mar2021, the patient experienced sore throat, on 02Apr2021, the patient lost her sense of taste, on an unknown date the patient started not feeling well/she was sick, congestion and cold like symptoms. That morning when eating she noticed she had lost her sense of taste. She started not feeling well last weekend-experiencing sore throat and congestion, but due to the weather was unsure if it was due to allergies or covid. She was getting tested for Covid tomorrow, but wanted to know since she already received the first dose could she potentially get a false positive? If she does test positive what should she do? She was scheduled to receive next dose on 08Apr2021. She said that unfortunately she thought she was sick and lost her sense of taste today and was being tested for Covid tomorrow. She had her first Pfizer Covid-19 dose 18Mar2021 and was asking could that affect the result of the test. She has auto-immune disease and immune compromised. She had a little sore throat last weekend on Saturday that went away, and then earlier this week she was congested, but she thought it was allergies. Has not run a fever or had any other symptoms. Until today, when eating breakfast and she couldn't taste it. She was drinking sparkling water during the call and couldn't taste it. She hasn't lost her sense of smell. She was immune compromised and doesn't have a spleen. She was auto immune compromised. She said that she really wasn't doing well health wise. She had an Emergency Room visit 3 weeks ago and urgent care visit 2 weeks ago. She saw a Gastrointestinal specialist and is scheduled for an endoscopy with colonoscopy at the hospital. She also has gall stones and has a consult for that issue. She has had a lot happen recently. The consumer stated she got her 1st dose last 18Mar2021 and experienced loss of sense of taste, cold like symptoms, sore throat and congestion. She mentioned she will have her 2nd dose on 08Apr2021. She has Idiopathic thrombocytopenic purpura, and her hematologist told her that people with this could experience adverse reactions similar to having the Covid virus and it could trigger an auto immune reaction. The adverse event did not resulted in emergency room or physician office visit. The outcome of event was not recovered for lost her sense of taste and unknown for started not feeling well/she is sick, congestion and cold like symptoms and recovered from sore throat on an unspecified date in 2021. Follow-up (02Apr2021): This is a follow-up spontaneous report from . New information included: The consumer stated she got her 1st dose last 18Mar2021 and experienced loss of sense of taste, cold like symptoms, sore throat and congestion. She mentioned she will have her 2nd dose on 08Apr2021 and asked if it was fine to test whether she was covid-19 positive or not, will there be an effect since she already got her 1st dose and could that provide false positive. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Autoimmune disorder NOS (Verbatim: Autoimmune compromised); Immune disorder (NOS) (Verbatim: Immune compromised)

ID: 1792670
Sex: F
Age:
State: WI

Vax Date: 04/01/2021
Onset Date: 04/02/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210402; Test Name: Fever; Result Unstructured Data: Test Result:101; Comments: 101 (units not specified)

Allergies:

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

Symptoms: body ache; Teeth and Gums Hurt; Teeth and Gums Hurt; Nausea; Bad Muscle Aches; Headache/headache before the second vaccine but now it is worse; face hurts; fever; chills; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 66-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration in right arm, on 01Apr2021 at 15:30 (lot number: EW0150 and expiry date was not reported, age at vaccination: 66-year-old), as a single dose for COVID-19 immunization. The patient's medical history was COVID in Dec2021. The concomitant medications were not reported. It was reported that 40 years ago the patient got a shot of penicillin in her butt and lost her blood pressure so now she wears a bracelet. The historical vaccine included first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration in arm right, on 11Mar2021 (lot number: EN6207 and expiry date was not reported), as a single dose for COVID-19 immunization. On 02Apr2021, the patient had headache/headache before the second vaccine but now it is worse, face hurts, fever, chills, body ache, teeth and gums hurt, nausea and bad muscle aches. It was reported that on 02Apr2021 (yesterday) after receiving the second dose of the Pfizer COVID-19 vaccine patient head and face hurts. It was reported that the patient woke up in the middle of the night at 03:30 A.M. with bad muscle aches, nausea, headache, fever over 101, and chills. Reportedly the patient had a headache on/off before getting the vaccine. It was reported that she had the headache before the second vaccine but now its worse. The patient stated that she was told that unless she had a fever, she could take the vaccine. The patient mention that it was funny because she had fever the next day with chills and body ache. The patient head and face hurts even after taking Tylenol and ibuprofen. Reportedly her headache was still there, and patient headache was worsened. The patient stated that that her teeth, gums, and face hurt as well. The patient reported she does not know if it was a delayed reaction or if she could've gotten COVID again. The patient queried is it normal to have all these symptoms after receiving the vaccine. The patient contacted the doctor and they just said to use a nasal rinse and contact them if she does not feel better in 7-10 days. The patient clarifies that her face still hurts but her teeth and gum pain was completely gone. The patient stated that when she bit it hurt, it was like they hit each other. Reportedly the patient currently did not have fever and chills, the medicine brought it down, but she was sure if it is completely gone. The patient also took ice and heat as corrective treatment. Reportedly the patient took Tylenol, Ibuprofen (lot/batch number: OCE2790A, Expiry date: Dec2021) and acetaminophen (ASPIRIN) (lot/batch: P139389 and expiry date: May2022) post vaccination to treat symptoms and the Tylenol did not seem to help much and Ibuprofen did not help either. The patient queried if it was safe to take aspirin, ibuprofen and Tylenol post vaccination to treat symptoms. The patient also wanted to know if it's safe for a COVID positive patient to receive the Pfizer COVID-19 vaccine. The outcome of the event headache/headache before the second vaccine but now it is worse, face hurts was not recovered. Outcome of the event bad muscle aches was resolving. Outcome of the event nausea, teeth and gums hurt was recovered on 02Apr2021. Outcome of the event body ache, fever and chills was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792671
Sex: F
Age:
State: OH

Vax Date: 03/12/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: but day 10 the bump came back and it was not quite as big a bump, but it hurt with a red lump underneath it; swelling; redness and large welt; redness and large welt; neck tightness; itching and achy; she moved her arm it was achy; back of neck and shoulder were sore; back of neck and shoulder were sore; back of neck and shoulder were sore; HCP was worried it may be worse than the first allergic reaction; she slept for hours and hours; injection site pain/injection site hurt; Injection site redness; injection site was itchy; Injection site swelling; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program. A 62-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6206 and Expiration date: unknown) via an unspecified route of administration, administered in left arm on 12Mar2021 02:00 (at the age of 62-years-old) as dose 1, single for covid-19 immunization. The patient medical history included breast cancer from Sep2001 and unknown if ongoing. Patient stated she has had reactions to some antibiotics, and the only other thing is that she does not get the flu vaccine so she cannot compare them. Patient stated that the only thing else she had reaction to, which was maybe normal, was that there was a breast cancer chemo drug that she had a reaction to that they still gave to her at a lower rate. It was reported that the reaction happened during treatment, and she found out she had a lot of different reactions to medications, like Darvocet and pain things, and antibiotics that bothered her. Reporter stated for the Taxol she does not know if that was a reaction, it was not full blown to where she could not use it, they just gave it to her at a slower rate. No further details provided about antibiotics or pain medications. Concomitant medications included dextropropoxyphene napsilate, paracetamol (DARVOCET) NDC/LOT/EXP: Unknown; taxol NDC/LOT/EXP: Unknown. Reporter stated that she and her daughter (34 years old) both received the Pfizer covid vaccine, first dose, on 12Mar2021, and experienced injection site pain, swelling, redness and large welt. Patient said they do not have it now but they both had them after the vaccine. Patient also experienced arm soreness, neck tightness, itching and achy. Patient stated that they had a reaction and went to pharmacist for second shot both for her daughter and her, they both had a reaction the first time around, but was turned away because the HCP was worried it may be worse than the first allergic reaction. Patient reported that the pharmacist gave them a number to call to discuss this with Pfizer so they could get advised because they feel it could be an allergic reaction, and they were wanting to make sure they could be given second shot. Patient stated that the pharmacy basically turned them away, and they did not get their second shot today. Patient reported that their first shot was three weeks ago, 12Mar2021 around 02:00PM. Patient stated that when her reaction began it hurt obviously right away, then it got red with like a welt, after she got home for sure. She stated that it took about hour to get home from there, then later in evening and overnight it got more of a welt. Patient stated that she did not receive any treatment, she just took a shower and let water run on it and that was it. It got really sore and kind of stayed that way for 2-3 days, the redness grew and got bigger, and welt got bigger. She stated that the welt was not as big as the red area and analogy they have been using is the red area was around the size of a hamburger bun, just the redness. She said that the welt underneath was hard, raised, firm to the touch, and sore to the touch. Patient stated that they had a few other side effects and this only happened to her, and it went away after 4 days or so, but day 10 the bump came back and it was not quite as big a bump, but it hurt with a red lump underneath it, and when she moved her arm it was achy. She stated that all that she felt like was it was also in her neck a little bit and the back of neck and shoulder were sore and honestly her arm was still a little achy after 3 weeks. She clarifies that the injection site for both of them was where all lumps and redness were. Patient stated that one other thing was that her injection site was itchy, but this was not true for her daughter and hers was red like that, it was not horrific, but it was definitely itchy, she scratched it and was like what was going on, and after she scratched it, it was all red again, which lasted two days then went away again, maybe a little longer than that, 3 days. Patient daughter stated that her elbow was really sore for 5-6 days, and she was very tired, which was a thing that was a common side effect and slept for hours and hours. she also stated that the main thing that was out of the norm was the red bump, swelling or welt, and redness. Patient stated that her daughter's reaction lasted longer, the redness and lump, they lasted 5-6 days, and hers went away. Patient stated that hers came back but her daughters did not. Patient wanted to know the efficacy of the first dose, the time frame for the second dose, would it be less effective if taken later then, 21 days, what were the chances of them getting an allergic reaction and also would like to know if they should get the second shot. Outcome of the event injection site itching was recovered and the rest events were unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: DARVOCET; TAXOL

Current Illness:

ID: 1792672
Sex: F
Age:
State: PA

Vax Date: 03/18/2021
Onset Date: 03/23/2021
Rec V Date: 10/16/2021
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: He described it as a very horrendous itching hives/ hives on a scale of 1-10 for itching factor were a 15; she had hives on her entire body from her neck down, not her face or head.; horrific allergic reaction; the color of her skin, like her entire body was covered in this irritation, her skin had this blotchiness to it; the color of her skin, like her entire body was covered in this irritation, her skin had this blotchiness to it; This is a spontaneous report from a contactable consumer. This consumer reported for his wife: A 51-years-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, administered in arm right on 18Mar2021 (age at vaccination 51 years) as dose 1, single for covid-19 immunisation. The patient's medical history included environmental allergies, basal cell cancer, blood pressure. dermatologist takes chunks off of her a couple times a year for basal cell cancer, he's not sure if it's called that. His wife's father has the same thing. Concomitant medication included losartan 50mg daily for blood pressure. She's been taking this for a while maybe 3 months. NDC number of Covid 19 Vaccine was unknown. reason for no lot number: of Covid 19 Vaccine was patients husband reports the facility that administered the Covid 19 vaccine did not provide a card with the first injection. They are to receive their vaccination card with the second Covid 19 vaccine. patient was taking Covid 19 Vaccine for protection and to travel. There was no vaccine Administered at Military Facility. There was no history of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available). There was no vaccines administered on same date with the Pfizer vaccine considered as suspect. Adverse event require a visit to emergency Room, Physician Office. There was no prior Vaccinations (within 4 weeks). Regarding adverse event following prior vaccinations patient's husband reports he can't say she's never had reactions to any vaccines. He reports maybe a red arm with a flu vaccine. The patient's husband reports he and his wife got their first Covid 19 Vaccine together. His was great, but his wife had a horrific allergic reaction 5 days after the vaccine. She received her first Covid 19 vaccine on 18Mar2021 and on 23Mar2021, she had hives on her entire body from her neck down, not her face or head. It looked like she had acid thrown on her, on her genitals, and even the bottoms of her feet. The hives on a scale of 1-10 for itching factor were a 15. It was just horrendous. The hives would come and peak and then subside then literally her skin would completely clear up. Then around 5 hours later the hives would come back. She would go through this 2-3 times a day. Her whole body would be covered with hives. His wife went to a (Name) like an urgent care and they gave her a steroid shot and it didn't help. She went to the emergency department and the emergency department said there was nothing else they can do if she had already received a steroid shot. She's seen her dermatologist, her ear nose and throat doctor, and her allergist. She does have environmental allergies and she takes a shot for things like mold, grass, cat dander, things like that. She has no pharmaceutical allergies or food allergies. She takes an allergy shot every 2 weeks or so. These hives have gone on and off and no one can give he or his wife any answers. His wife essentially got the steroid injection from (Name) and a 5 day steroid prescription. She started on that and her dermatologist gave her a stronger antihistamine. He's not sure if it's prescription strength. He doesn't know the name. He stated he wishes his wife were here to answer these questions because she would know. He reports that she started having the allergic reaction on Tuesday, 23Mar2021 and on 25Mar2021, the hives subsided that morning and the hives haven't come back. He says his wife is still itching like a 2 on a scale of 1 to 10 with 10 being the most itchy. There is nothing visible on her skin now. He reports he and his wife don't know what to do. They are supposed to get their second Covid 19 vaccines next week and his wife is not going to get her second Covid 19 vaccine. He hasn't been able to talk to any one who might have an answer. Maybe this has happened to other folks. They don't know what to do with the Covid 19 vaccine. Would she be better taking the Johnson and Johnson Covid 19 vaccine. He reports they are both 51 and retired and they want to go to travel in July. They don't want to travel without getting completely vaccinated. He thinks his wife may be covered about 80% with just one Covid 19 vaccine. He and his wife know the implications of not getting vaccinated and they're doing it for personal reasons. Only her dermatologist seemed to take an interest in his wife's reaction to the Covid 19 vaccine. The dermatologist thought maybe the hives could be related to the Covid 19 vaccine but the hives could be coincidental. The dermatologist felt that the hives likely came from the Covid 19 vaccine. When asked to clarify what the patients husband meant when he said it was like someone threw acid on her, he reports the color of her skin, like her entire body, was covered in this irritation, her skin had this blotchiness to it, like someone threw something on her that irritated her skin. He reports there was nothing on her arm from the injection itself. He reports about a week ago she still had an itching sensation where she wanted to scratch her skin. She could feel the hives coming on before they even started to appear and then she would see the hives. She walked around with mittens on her hands and she was taking ice baths. He reports she may have some minor itching sensation now but he doesn't believe she has any symptoms any more. She takes allergy injections. He's not even sure she had an allergy injection around the time she received the Covid 19 vaccine but she might have because she gets the allergy injections every week or 2 weeks. He states she had an allergy injection on 12Mar2021. They are self administered injections. The allergy injections (treatment) are made up for her. He reports vial A is dust extract and vial B is pollen extract. They are weekly injections. He thinks she was at the maximum dose which is 0.50. He thinks it says mg but it's handwritten and he can't read the handwriting. His daughter was an registered nurse in one of the local emergency departments and they went to his daughter's emergency department and the doctor looked at her and said there was nothing he could do. The outcome of events was reported as not recovered from Itching, recovered from hives on 25Mar2021 and unknown for other events. Follow-up attempts completed. No further information expected.

Other Meds: LOSARTAN

Current Illness: Allergy

ID: 1792673
Sex: M
Age:
State:

Vax Date: 02/25/2021
Onset Date:
Rec V Date: 10/16/2021
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: muscle and joint pain that has been ongoing ever since; muscle and joint pain that has been ongoing ever since; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received BNT162B2 (PFIZER-BIOTECH COVID-19 VACCINE, solution for injection) via an unspecified route of administration on 25Feb2021 as dose 2, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received BNT162B2 on an unspecified date as dose 1, single for COVID-19 immunisation. On an unspecified date a week later, the patient experienced muscle and joint pain that has been ongoing ever since, stating that "it has been a month of pain" (as reported). The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792674
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: sore arm; low grade fever; chills; body aches; This is a spontaneous report from a contactable consumer (patient). A 39-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number and expiration date: not reported), via an unspecified route of administration, on an unspecified date, as DOSE 2, SINGLE for covid-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), as DOSE 1, SINGLE for covid-19 immunization. The patient experienced sore arm, low grade fever, chills and body aches on an unspecified date. The outcome of the events was unknown at time of report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792675
Sex: F
Age:
State: NM

Vax Date: 03/30/2021
Onset Date:
Rec V Date: 10/16/2021
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: Right arm injection site discomfort; Low grade fever; Lethargy; This is a spontaneous report from a contactable consumer via a Pfizer sales representative. A 50-year-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in arm right at the age 50 years old on 30Mar2021 (Batch/Lot number was not reported) as dose number unknown, single for covid-19 immunisation. Medical history and concomitant medications were not reported. On an unspecified date, the patient experienced right arm injection site discomfort, low grade fever and lethargy the next day. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792676
Sex: M
Age:
State:

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
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: weakness; myalgia; fatigue; joint/lower back pain; joint/lower back pain; This is a spontaneous report from a non-contactable consumer (patient) received via a sales representative. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not reported), via an unspecified route of administration on 31Mar2021 as dose 2, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced weakness, myalgia, fatigue and joint/lower back pain on 31Mar2021. Outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792677
Sex: U
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: chills; fever; fatigue; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (BNT162B2), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 2, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced chills, fever, and fatigue. The outcome of the events was recovered after 24hours. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792678
Sex: M
Age:
State: CT

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: at his workplace, one of the technicians tested positive; my allergies seem to be in my head; headache; My arm was a little sore too.; my eyes very red; eye watering and nasal congestion; eye watering and nasal congestion; This is a spontaneous report from a contactable consumer (patient). A 49-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot Number: not reported), via an unspecified route of administration on an unspecified date (at the age of 49 years) as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported, after 4 days of first dose he had eyes watering and nasal congestion on 01Apr2021. It was like he was having allergies. At his workplace, one of the technicians tested positive, he felt like allergies seem to be in his head and between his eyes and he had a headache. His arm was a little sore too. He was feeling tiredness (not clear, hence not captured as event) his eyes very red, like allergy symptoms like that. The clinical outcome of the events lacrimation increased and nasal congestion was not recovered; unknown for the rest of the events. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792679
Sex: F
Age:
State: NY

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
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: neck very tender only right side; itchy hives on neck same side as injection /neck got itchy; itchy hives on neck same side as injection /neck got itchy; sore jaw on the right side(shot was on the left); enlarged lymph node /Swollen lymph node behind her ear, right where the jaw kind of connects; This is a follow-up spontaneous report from a contactable consumer or other non hcp. A 49-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID -19 VACCINE, formulation: solution for injection, via an unspecified route of administration, administered in Left Arm on 31Mar2021 13:15 PM (Batch/Lot Number: EP7534, expiry date: unknown) as dose 1, single for COVID-19 immunization ( age at vaccination:49-Year-old) from Public Health Clinic. Medical history included blood pressure abnormal (she has been on medication for this condition for the last 4 months), hepatic steatosis /liver disease (she was diagnosed 4 to 5 months ago by ultra scan), asthma (she has had this condition for a couple years), vitamin d abnormal( she reports a history of low vitamin D /She has been low for about 12 years ago. She says she lives in the northeast so she has a very short summer. She has been low for about 12 years ago, and she had to be on the super D pill. She thinks she was on it twice and then after that she just started taking vitamin D regularly. When she got tested, her doctor said her level was excellent), alcohol problem and ex-tobacco user. Concomitant medication(s) included losartan potassium (LOSARTAN POTASSIUM) 25 mg tablet once day taken for blood pressure abnormal, vitamin d [vitamin d nos] (VITAMIN D [VITAMIN D NOS]) 25 mcg (1,000 IU) two pills, once a day taken for vitamin d abnormal; cyanocobalamin (VITAMIN B12 [CYANOCOBALAMIN]) 3,000 mcg once a day sublingual (lozenge under tongue) taken for hepatic steatosis for probably 2 months, and vitamin d3 (VITAMIN D3). All medications were taken for an unspecified indication, start and stop date were not reported. Allergic history are unknown. No Family Medical History Relevant to AE. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. No additional Vaccines Administered on Same Date of the Pfizer Suspect. She said she gets the flu shot every year with no problems. No AE(s) following prior vaccinations. The patient had received other medications within 2 weeks prior to the vaccination includes Losartan Potassium, B12, D3. The patient was not diagnosed with covid-19 before vaccination, and not tested post vaccination. On 31Mar2021 14:00 PM the patient experienced itchy hives on neck same side as injection /neck got itchy, enlarged lymph node /Swollen lymph node behind her ear, right where the jaw kind of connects, and sore jaw on the right side(shot was on the left). On 03Apr2021 the patient experienced neck very tender only right side. The events are not resulted visiting emergency room/physician office. Therapeutic measures were taken as a result of itchy hives on neck same side as injection /neck got itchy includes Benadryl(lot number: unknown, expiry date: unknown). Patient had not received treatment for other events. The outcome of event itchy hives on neck same side as injection /neck got itchy was recovered on 31Mar2021. The outcome of the enlarged lymph node /Swollen lymph node behind her ear, right where the jaw kind of connects was recovering. The outcome of the other events was not recovered. No follow-up attempts are possible. No further information is expected. \

Other Meds: LOSARTAN POTASSIUM; VITAMIN D [VITAMIN D NOS]; VITAMIN B12 [CYANOCOBALAMIN]; VITAMIN D3

Current Illness:

ID: 1792680
Sex: F
Age:
State: HI

Vax Date: 03/24/2021
Onset Date: 03/29/2021
Rec V Date: 10/16/2021
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: Shooting pain from shoulder to fingers on both arms/Shooting pain from shoulder to fingers on both arms; Extreme pain 12/10.; Arms got hotter than rest of body; Hives; This is a spontaneous report from a contactable other health professional(patient). A 32-year-old non-pregnant female patient received first dose of BNT162B2(PFIZER BIONTECH COVID19 vaccine, Solution for injection, Batch/Lot Number: ER8732) via an unspecified route of administration, administered in Arm Left on 24Mar2021 10:00 (At the age of 32-year-old) as single dose for COVID-19 immunisation. Medical history included food allergy, hypersensitivity to drywall, mok orange, allergy to arthropod bite, iodine allergy,allergy to animal, allergy to arthropod sting, seasonal allergy from an unknown date. Concomitant medications included clarithromycin (MACROBID) taken for an unspecified indication, start and stop date were not reported.The patient didn ot received any other vaccines within 4 weeks prior to the COVID vaccine.Prior to vaccination patient was not diagnosed with COVID-19 and Since the vaccination, the patient had not been tested for COVID-19. On 03Apr2021 03:00 the patient experienced shooting pain from shoulder to fingers on both arms/shooting pain from shoulder to fingers on both arms, extreme pain 12/10, arms got hotter than rest of body and hives on 29Mar2021 20:00. The outcome of the events was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds: MACROBID

Current Illness:

ID: 1792681
Sex: F
Age:
State: CA

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 10/16/2021
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: hives all over the body; lip swelled up as well as the right eye; lip swelled up as well as the right eye; This is a spontaneous report from a contactable healthcare professional (patient) received via COVAES. A 20-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in right arm, on 14Jan2021 at 11:30 AM (Batch/Lot Number: EK5730) (at the age of 20 years old) as dose 2, single for COVID-19 immunisation in a workplace clinic. The patient has no relevant medical history. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. The patient has no known drug allergies. The patient was not pregnant at the time of vaccination. Concomitant medication included ibuprofen 600mg tablet, taken as needed for unspecified indication. The patient was previously administered the first dose of BNT162B2, via an unspecified route of administration, administered in right arm, on 23Dec2020 at 11:45 AM (Batch/Lot Number was not reported) (at the age of 20 years old) as dose 1, single for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 14Jan2021 at 19:30, 8 hours after the second dose of vaccination, the patient experienced hives all over the body and lip swelled up as well as the right eye. This has been happening since the second vaccine on 14Jan2021 until today, 03Apr2021. These episodes of hives and swelling happened at least 3 times a week. The healthcare professional reported the events as non-serious. The patient received no treatment for the events. The outcome of all events was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds: IBUPROFEN

Current Illness:

ID: 1792682
Sex: F
Age:
State: CT

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 202102; Test Name: Body Temperature; Result Unstructured Data: Test Result:102

Allergies:

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

Symptoms: back spasms; FEVER 102 for several hours; This is a spontaneous report from a contactable consumer. A non-pregnant adult female patient of unknown age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Unknown) via an unspecified route of administration on an unknown date in Feb2021 as a single dose for COVID-19 immunisation. It was unknown if patient had any medical history. It was unknown if patient had allergies to food, medications, or other products. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunisation and experienced back spasms. It was unknown if prior to vaccination the patient was diagnosed with COVID-19. It was unknown if since the vaccination the patient had been tested for COVID-19. It was unknown whether the patient received any other vaccines within four weeks prior to the vaccination. It was unknown whether the patient received other medications within 2 weeks of vaccination. On an unknown date in Feb2021, the patient experienced back spasms and fever of 102 for several hours with the second shot. On an unknown date, the patient underwent tests which include body temperature and the result was 102 (units unspecified). It was unknown whether the patient received treatment for the events. The adverse event did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of the event fever 102 and back spasms was recovered on an unknown 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: 1792683
Sex: F
Age:
State:

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: rash on arm; mucous in her throat; Teeth chattering; This is a spontaneous report from a non-contactable consumer (parent). A 16-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number, expiration date was not reported) via an unspecified route of administration, on Mar2021 (at the age of 16-year-old), at dose 1, single for covid-19 immunization. Medical history included allergies to tree nuts; had anaphylactic reactions to tree nuts. The patient's concomitant medications were not reported. The patient experienced rash on arm, mucous in her throat, and teeth chattering on Mar2021. Therapeutic measures were taken included Benadryl and she was fine. The outcome of the event was recovered on Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792684
Sex: M
Age:
State: NV

Vax Date: 02/18/2021
Onset Date: 02/01/2021
Rec V Date: 10/16/2021
Hospital:

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

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

Allergies:

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

Symptoms: Sore arm; Shoulder pain a little bit; This is a spontaneous report from a contactable consumer (patient). A 72-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EN6200), via an unspecified route of administration, in left arm on 18Feb2021 (at the age of 72-years-old) as dose 2, single for COVID-19 immunization. The patient's medical history was not reported. There were no concomitant medications. Historical vaccine included flu shots, shingles vaccine, pneumonia vaccine and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL9262), via an unspecified route of administration, in left arm on 28Jan2021 as dose 1, single for COVID-19 immunization after which the patient experienced painful arm, shoulder pain, vaccination site pain and incorrect product administration duration. The patient experienced sore arm on 18Feb2021 and shoulder pain a little bit in Feb2021. The patient underwent lab tests and procedures which included sars-cov-2 test: negative. The outcome of event sore arm was 18Feb2021 and event shoulder pain a little bit was recovered in Feb2021. No follow-up attempts needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792685
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: malaise; fever; sweats; This is a spontaneous report from a contactable pharmacist (patient). A patient of unspecified age and gender received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) was administered on 10Mar2021 for covid-19 immunisation and experienced soreness in arm. The patient's concomitant medications were not reported. After second dose of Covid vaccine, patient developed malaise, fever, and sweats on an unspecified date. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792686
Sex: U
Age:
State:

Vax Date: 02/14/2021
Onset Date:
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Swelling of the feet and lower legs; 4lbs water weight gain overnight; intermittent swelling; This is a spontaneous report from a non-contactable physician (patient) via sales representative. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 14Feb2021 (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced swelling of the feet and lower legs, 4lbs water weight gain overnight, and intermittent swelling. Events were treated with aspirin. The outcome of the events was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792687
Sex: F
Age:
State: CT

Vax Date: 03/30/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
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: Fairly sore arm near injection site; Slight fever; Tired; Achy; This is a spontaneous report from a contactable consumer (patient). A 44-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EP6955, Expiration date: Not reported), via an unspecified route of administration in right arm on 30Mar2021 at 14:45 (at the age of 44-years-old) as dose 2, single for COVID-19 immunization in a workplace clinic. There were no patient's relevant medical history reported. No known allergies to medications, food, or other products. Concomitant medications/other medications received within 2 weeks of vaccination included fexofenadine hydrochloride (ALLEGRA); cyanocobalamin (VITAMIN B12); esomeprazole sodium (NEXIUM); probiotics and glucosamine. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL3247, Expiration date: Not reported), via an unspecified route of administration in right arm on 09Mar2021 at 14:30 (at the age of 44-years-old) as dose 1, single for COVID-19 immunization and experienced right arm soreness near the injection site. The patient was not pregnant at the time of vaccination and didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient had not been tested for COVID-19. The patient experienced fairly sore arm near injection site, slight fever, tired and achy on 31Mar2021 at 09:00. No treatment was received by the patient for these adverse events. These events were considered as non-serious and the outcome of these events was reported as recovering at the time of report. No follow-up attempts are needed. No further information is expected.

Other Meds: ALLEGRA; VITAMIN B12 [CYANOCOBALAMIN]; NEXIUM [ESOMEPRAZOLE SODIUM]; PROBIOTICS; GLUCOSAMINE

Current Illness:

ID: 1792688
Sex: F
Age:
State: NY

Vax Date: 03/25/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210329; Test Name: COVID-19 nasal swab test (rapid); Test Result: Negative

Allergies:

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

Symptoms: Itchy nostrils; Left arm hurt a little; Left arm was a little itchy; It is also pink; Allergy related; This is a spontaneous report from a contactable consumer (patient). A non-pregnant 80-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number was not reported), via an unspecified route of administration in left arm, on 25Mar2021 at 02:00 PM (14:00), as dose 2, single, for COVID-19 immunization. The patient's medical history included mild emphysema, eye (map dot fingerprint dystrophy; cornea not smooth), irritable bowel syndrome (sometimes), eye pressure, allergies to many foods (chocolate, nuts, tomatoes, etc.), stomach, and allergy. The patient's concomitant medications included loratadine (CLARITIN) for allergy and aluminium magnesium silicate (GELUSIL) for stomach. The patient previously received the first dose of BNT162B2 (Lot Number: EM9810) on 04Mar2021 at 03:00 PM for COVID-19 immunization and experienced tongue burns (tongue started to bother her and is still bothering her); and cyanocobalamin (B-12) and gold and experienced allergies to both. The most recent vaccine was administered in a hospital facility. In Mar2021 at 02:30 PM (also reported as on 04Mar2021 and on the seventh day after the second vaccine was administered; clarified as after the second vaccine), the patient had itchy nostrils almost immediately and her left arm hurt a little and was a little itchy. The patient looked at it and it is also pink. This was possible right after the shot, but this is a week (as reported). The doctors say it's nothing but to the patient it's been going on for quite a while. The patient thinks that most of this is allergy related (Mar2021). The adverse events resulted in doctor or other healthcare professional office or clinic visit. No treatment was administered for the adverse events. The patient underwent COVID-19 nasal swab test (rapid) on 29Mar2021 that was negative. The patient had not recovered from the events. No follow-up attempts are possible; information about lot or batch number cannot be obtained. No further information is expected.

Other Meds: CLARITIN [LORATADINE]; GELUSIL [ALUMINIUM MAGNESIUM SILICATE]

Current Illness:

ID: 1792689
Sex: F
Age:
State: MO

Vax Date: 02/05/2021
Onset Date:
Rec V Date: 10/16/2021
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: swollen, red lymph node; 2 months after 2nd vaccine swollen, red lymph node came back in same armpit has been inflamed one week to date; swollen, red lymph node; This is a spontaneous report from a contactable consumer (Patient). A 52-year-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 05Feb2021 as dose 2, single for covid-19 immunisation from hospital. Medical history high blood pressure, hypothyroidism, depression, allergies to several antibiotics. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and Patient received prescription medications within 2 weeks of vaccination. The patient was not diagnosed with covid prior to vaccination and patient was not tested for COVID-19 post vaccination. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 15Jan2021 as dose 1, single for covid-19 immunisation and had Large swollen lymph node in armpit of shot went away after 2 weeks. In 2 months after 2nd vaccine patient experienced swollen, red lymph node came back in same armpit has been inflamed one week to date. The patient did not receive any treatment in response to the events. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected

Other Meds:

Current Illness:

ID: 1792690
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: itching; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced itching on an unspecified date. Outcome of event was resolved on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021366674 Same reporter/drug/event for different patients.

Other Meds:

Current Illness:

ID: 1792691
Sex: M
Age:
State: MA

Vax Date: 03/26/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: fatigue/tired; arm pain; chills; fever; malaise; body aches in joints; not feeling well; aches and pains in the joints and knees; difficult to walk; This is a spontaneous report from a contactable consumer (patient) reporting for self. A 65-year-old male patient received BNT162B2 (BNT162B2, Solution for injection, PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EP6955) via an unspecified route of administration administered in left arm on 26Mar2021 05:00 as DOSE 2, SINGLE for covid-19 immunization. Medical history reported as patient had an autoimmune disease 7-8 years ago. It went away in 1-2 years, arthritis, polymyalgia rheumatica, gets prednisone shots in knees, that helps with inflammation because PMR would turn the body on it's joints. surgeries in knee Lifetime abuse on both knees, inflammatory disease of joints and all were managed from an unknown date and unknown if ongoing. Patient had done athletics, multiple sport injuries, surgeries, and osteoarthritis in both his knees. On the first shot it made his knees react badly too, like getting inflammation all over the body and patient theory was that if have a weakness in a joint, it was going to it and exacerbating it. Patient walked with a limp. The patient's concomitant medications were not reported. Historical vaccines included BNT162B2 (BNT162B2, Solution for injection, PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 05Mar021 as DOSE 1, SINGLE for COVID-19 immunization and experienced achy creaky uncomfortable knees, sore arm and fatigue. The patient experienced fatigue/tired, huge arm pain, chills, fever, malaise, body aches in joints, not feeling well, aches and pains in the joints and knees, difficult to walk walking with a limp all on an unspecified date in Mar2021; 18 hours later after receiving the vaccine. These continued for saturday and sunday. By monday, those other symptoms started to dissipate except his joints and knee's continued to ache and it was difficult to walk. The outcome of the events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792692
Sex: F
Age:
State: OR

Vax Date: 03/18/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: Headache; injection site pain; has pain in her arm that has kind of moved toward her armpit and it is a struggle there in the underarm area; has pain in her arm that has kind of moved toward her armpit up to her elbow; has pain in her arm that has kind of moved toward her armpit and spread to her left breast; This is a spontaneous report from a contactable consumer (patient). A 33-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in left arm on 18Mar2021 10:00 (Lot Number: EP7534; Expiration Date: 31Jul2021) (at the age of 33-years-old) as dose 1, single for covid-19 immunisation. Medical history included polycystic ovaries (PCOS autoimmune disease) diagnosed when she was a teenager at age 16 years. There were no concomitant medications. There were no prior vaccinations within 4 weeks of COVID-19 vaccine. Adverse event following prior vaccinations included maybe she gets injection site soreness or a 24-hour cold but not every time, once in a blue moon, patient stated it's like the flu shot and patient does not have name, dose of the vaccinations. Patient stated she wanted to report a symptom she was having. She got the 1st shot on 18Mar2021 and she did have a 24-hour headache that went away. The headache started within 2 hours after the shot on 18Mar2021 and was gone by the end of the day 19Mar2021. She had injection site pain from the get-go on 18Mar2021 and would say she noticed it first closer to maybe her left breast, that she was wearing a sports bra and thought it may be too tight. She had pain in her arm that has kind of moved toward her armpit and it was a struggle there in the underarm area in Mar2021. It was her armpit up to her elbow and spread to her left breast in Mar2021. Patient stated that was maybe 3 days after and the arm injection site was still hurting, that she didn't feel underarm until 3 days later. The pain was up to her elbow and she noticed that about a week later, that it traveled into her armpit and out to the side of her arm to her elbow about a week later. This was all on the left side which was where she got the shot. The events did not require emergency room and physician office visit. During supplemental form patient stated she read an article that said all the symptoms should clear within 6 weeks and if it persists to see somebody and she was holding out, but she was a little nervous as the symptoms are the same as breast cancer. She stated then again it pretty much followed the shot and she was just hoping it was a side effect from the shot. Patient just wanted to report this, and she read an article back in January and was wondering if there have been other reports of swollen lymph nodes. The outcome of the event headache was recovered in 19Mar2021 and outcome of all other events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792693
Sex: M
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 10/16/2021
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: headaches; flu like symptoms; joint soreness; This is a spontaneous report from a contactable consumer. A 38 years old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE,Solution for injection,Batch/Lot number was not reported,Expiry date was not reported), dose 2 via an unspecified route of administration on 31Mar2021 as DOSE 2,SINGLE for covid-19 immunisation.The patient medical history and concomitant medications were not reported. Previously patient took first dose of bnt162b2 via an unspecified route of administration on an unknown date for covid-19 immunization. The patient experienced headaches, flu like symptoms, joint soreness.The reporter wants to know can he take Tylenol as a treatment for the adverse event. The clinical outcome of the event was unknown. No follow up attempts are possible, information about lot or batch number cannot been obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021360708 same reporter/drug/AE with different patient

Other Meds:

Current Illness:

ID: 1792694
Sex: M
Age:
State: PA

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 10/16/2021
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: body aches; feeling pretty miserable; Fever; worn out; This is a spontaneous report from a contactable consumer. A 80-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number and expiration date was not reported), via an unspecified route of administration in right arm on 30Mar2021 11:30 (at the age of 80-years-old) at dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number and expiration date was not reported), via an unspecified route of administration in arm right on 09Mar2021 11:30 (at the age of 80-years-old) at dose 1, single for covid-19 immunization. The patient experienced body aches, felt pretty miserable, fever and worn out on 30Mar2021. Patient was taking Tylenol for the events. The outcome of the event fever was recovered, outcome of the event worn out was unknown outcome of rest of the events was not recovered. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021366575 same reporter/drug/similar events, different patient.

Other Meds:

Current Illness:

ID: 1792695
Sex: F
Age:
State: FL

Vax Date: 03/29/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: must have had a fever because she was sweating it out; night sweats; massive headache; lymph nodes started to get swollen/lymph nodes were still swollen; in her left arm, her lymph nodes in her armpits are like a ball and they are painful; very tired; didn't sleep well; then at night, got more painful; she put her arm down by her side and she said it felt uncomfortable; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received BNT162B2 (PFIZER-BINTECH COVID-19 VACCINE; Lot Number: EP7534, Expiration date: Not reported), via an unspecified route of administration in left arm on 29Mar2021 at 07:00 (at the age of 42-years-old) as dose 1, single for COVID-19 immunization in a military facility. Medical history included COVID-19 and headache in Oct2020. No family history was reported. There were no concomitant medications/other products reported. No prior vaccinations within 4 weeks of COVID vaccine. On 30Mar2021 at 02:00, the patient woke up with massive headache and it was getting worse. She took paracetamol (TYLENOL) and her headache was fine. On 30Mar2021, the patient's lymph nodes started to get swollen/lymph nodes were still swollen; the patient was little worried because in her left arm, her lymph nodes in her armpits were like a ball and they were painful; felt very tired and didn't sleep well because she had headache. The patient had swelling and took another dose of Tylenol before bed. It was reported that there was a slight improvement with her lymph nodes. On 31Mar2021, the patient might have a fever because she was sweating it out when she woke up, she was all sweaty by having night sweats. At the night in Mar2021, the patient got more painful, and put her arm down by her side and she said it felt uncomfortable. She is wondering if she's at the point where she needs to see the doctor. The patient doesn't require visit to emergency room (ER) or physician's office visit. It was reported that there was no investigation assessment and no relevant tests. The outcome of massive headache and fever was recovered on 31Mar2021 and the events lymph nodes in her armpits in her left arm were like a ball and they were painful, lymph nodes started to get swollen/lymph nodes were still swollen and tiredness was recovering while the outcome of other events was unknown at the time of report. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792696
Sex: F
Age:
State: PA

Vax Date: 03/08/2021
Onset Date: 03/09/2021
Rec V Date: 10/16/2021
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: First COVID-19 vaccine: tired; did not feel good; First COVID-19 vaccine: felt so sick, felt like she was going throw up; First COVID-19 vaccine: little diarrhea; First COVID-19 vaccine: allergies were triggered; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: ER7833), via an unspecified route of administration on 08Mar2021 08:40 (at the age of 56-years-old) as dose 1, single for COVID-19 immunization. Medical history included compromised immune system, seasonal allergy, allergic reactions to things like smells, bites or stings, super hypersensitive. The patient's concomitant medications were not reported. The patient felt so sick, felt like she was going throw up on 10Mar2021, allergies were triggered on 09Mar2021, little diarrhea on 10Mar2021, tired on 11Mar2021 and did not feel good on 10Mar2021. The outcome of all events was recovered on 18Mar2021 or 19Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Immune system disorder (Verbatim: Compromised immune system)

ID: 1792697
Sex: F
Age:
State: NC

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210202; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Nausea

Symptoms: I noticed tingling down my arm and into my 4th and 5th fingers; I noticed aching in my wrists, more on the left than the right; This is a spontaneous report from a contactable Nurse (patient). A 39-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EJ1685 and expiration date: not reported), via an unspecified route of administration, in Left Arm, on 22Dec2020 (at the age of 39-year-old) as DOSE 1, SINGLE for covid-19 immunization. Medical history included hypothyroidism. The patient had no known allergies. Concomitant medications included vortioxetine hydrobromide (TRINTELLIX), lamotrigine and levothyroxine sodium (SYNTHROID). The patient was not pregnant at time of vaccination. The patient didn't receive any other vaccines within 4 weeks prior to the COVID -19 vaccine. The Patient had not been diagnosed with COVID-19 prior to vaccination and had been tested since the vaccination. On 22Dec2020, the patient experienced tingling down on arm and into 4th and 5th fingers and noticed aching in wrists, more on the left than the right. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 02Feb2021. It was reported that adverse events resulted in Doctor or other healthcare professional office/clinic visit. Therapeutic measures (unspecified) were taken as a result of events. The outcome of the event Tingling feet/hands was recovered in 22Dec2020 and Wrist pain was recovered on an unspecified date. No follow up attempts are possible. No further information is expected.

Other Meds: TRINTELLIX; LAMOTRIGINE; SYNTHROID

Current Illness:

ID: 1792698
Sex: F
Age:
State: PA

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 10/16/2021
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: Second COVID-19 vaccine: Rash on right hand; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number: ER7833, expiration date was not reported) via an unspecified route of administration, in left arm, on 29Mar2021 09:30 (at the age of 56-year-old) at dose 2, single for covid-19 immunization. Medical history included ongoing compromised immune system, hypersensitive and has allergic reactions to things like smells, bites, or stings and her seasonal allergies are horrible. There were no concomitant medications. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number: EN6203, expiration date was not reported) via an unspecified route of administration, on 08Mar2021 08:40 (at the age of 56-year-old) at dose 1, single for covid-19 immunization and felt so sick, felt like she was going throw up, allergies were triggered, little diarrhea and tired. The patient did not receive any other vaccines within 4 weeks prior to the covid-19 vaccine. No additional vaccines administered on same date of vaccination. On 29Mar2021, three or four hours after second covid-19 vaccine, the patient had rash on right hand (weird strawberry looking); she clarified that she received the vaccine in her left arm and the rash is on her right hand. The event resulted in physician office visit. There were no investigation assessments. Therapeutic measures were taken included: Doxycycline Hyclate, antibiotics. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Immune system disorder

ID: 1792699
Sex: F
Age:
State: FL

Vax Date: 03/23/2021
Onset Date: 03/26/2021
Rec V Date: 10/16/2021
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: Arm pain; Sleepiness; Sweating and low pressure sensation; Sweating and low pressure sensation; Nausea; Shortness of breath; A never-felt pain in veins and arteries by several parts of the body: left arm, right ankle, anterior skull, left armpit, heart, several points in the lungs.; This is a spontaneous report from a contactable consumer (patient). A 62-years-old non pregnant female patient received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 Vaccine, Solution for injection; Lot Number: EP6955), via an unspecified route of administration, administered in left arm on 23Mar2021 at 16:15 (at the age of 62-years-old) as dose 1, single for COVID-19 immunization. Medical history included mononucleosis from 2011 to an unknown date and hemorrhagic dengue from 2014 to an unknown date. Concomitant medications were not reported. Patient did not have any allergies to medications, food, or other products. The patient had not received any other vaccine within 4 weeks and other medications in two weeks. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. On 26Mar2021, after first vaccination, the patient experienced arm pain, sleepiness, sweating and low pressure sensation, nausea, shortness of breath and a never-felt pain in veins and arteries by several parts of the body: left arm, right ankle, anterior skull, left armpit, heart, several points in the lungs. Patient did not receive any treatment for the events. Outcome of all events were not recovered at the time of report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792700
Sex: F
Age:
State: CA

Vax Date: 03/14/2021
Onset Date: 03/14/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Felt nauseated; Headache; Pain visible swelling in right hand; Swelling in right hand; Joint swelling in left knee; Pain in left knee; This is a spontaneous report from a contactable consumer (patient). A 45-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 14Mar2021 16:00 (at the age of 45-year-old) (Lot Number: EN6208) as dose 1, single for COVID-19 immunization, The patient was not pregnant at the time of vaccination. Medical history included Bechet's disease, Ehlers Danlos syndrome, chronic migraine, celiac disease, and asthma. Concomitant medication(s) included apermilast (OTEZLA), meloxicam (MANUFACTURER UNKNOWN), montelukast (MANUFACTURER UNKNOWN), cetirizine hydrochloride (ZYRTEC) and levothyroxine sodium (SYNTHROID), all taken for an unspecified indication, start and stop dates were not reported. The patient previously received pneumococcal vaccine polysacch (PNEUMOVAX VACCIN) on an unknown date for an unknown indication and experienced serious adverse reactions including prolonged high fever and erythema nodosum. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 14Mar2021 at 19:00, the patient experienced visible joint swelling and pain in the left knee with no injury. The patient reported that symptoms had lessened since 14Mar2021. On 15Mar2021, the patient woke up at 03:00 due to pain and visible swelling in the right hand. The left knee and right hand had continued swelling periodically during that time, usually in the late afternoon-evening. On 17Mar2021, for three days following the first dose, the patient felt nauseated and had a headache that felt different from usual migraines. The adverse events resulted in a visit to the doctor or other healthcare professional office/clinic visit. The patient did not receive any treatment for the events. The clinical outcome of felt nauseated, headache, joint swelling in left knee, pain in left knee, pain visible swelling in right hand, and swelling in right hand was resolving at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: OTEZLA; MELOXICAM; MONTELUKAST; SYNTHROID; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1792701
Sex: F
Age:
State: NJ

Vax Date: 03/24/2021
Onset Date: 03/24/2021
Rec V Date: 10/16/2021
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: Tired; Muscle ache; Redness marks on the skin near the vaccine area; This is a spontaneous report from a contactable consumer, the patient. A 33-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 24Mar2021 at 12:00 (at the age of 33-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not take concomitant medications within 2 weeks of vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 24Mar2021, the patient experienced tired, muscle ache, redness marks on the skin near the vaccine area. The events did not result in doctor or other healthcare professional office/clinic, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events tired, muscle ache, redness marks on the skin near the vaccine area was recovered on an unknown date in 2021. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792702
Sex: U
Age:
State:

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 10/16/2021
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: I am experiencing a lot of pain in my hip like muscle. I am experiencing a lot of pain in my hip like muscle. This is a spontaneous report from a contactable consumer. This consumer (patient) of unknown gender reported for self that he/she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown) via an unspecified route of administration on 30Mar2021 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unknown date the patient experienced a lot of pain in his/her hip like muscle. The patient was wondering if I could take Tylenol or Aspirin or something maybe that it help relieve it. The event outcome was unknown. No follow-up attempts were possible; Information about lot/batch number could not be obtained.

Other Meds:

Current Illness:

ID: 1792703
Sex: F
Age:
State:

Vax Date: 03/30/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
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: Swollen lymph node in under arm on side of vaccination; This is a spontaneous report from a non-contactable consumer, the patient. A 29-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8732) via an unspecified route of administration in the left arm on 30Mar2021 (at the age of 29-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 09Mar2021 (at the age of 29-years-old) as a single dose for COVID-19 immunisation. On 31Mar2021, the patient experienced swollen lymph node in under arm on side of vaccination. No therapeutic measures were taken as a result of the reported event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event Swollen lymph node in under arm on side of vaccination was unknown at the time of this report. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792704
Sex: F
Age:
State:

Vax Date: 03/31/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: Sore throat; This is a spontaneous report from a non-contactable healthcare professional, the patient. A 19-year-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8727) via an unspecified route of administration in the left arm on 31Mar2021 at 08:30 (at the age of 19-year-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the vaccination. The patient did not receive any other medications within two weeks of vaccination. On 01Apr2021 at 07:00, the patient experienced sore throat. The event did not result in doctor or other healthcare professional office/clinic, emergency room/department or urgent care. No therapeutic measures were taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event sore throat was recovering at the time of report. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792705
Sex: M
Age:
State: NY

Vax Date: 03/25/2021
Onset Date: 03/26/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Name: x-ray of his chest; Result Unstructured Data: Test Result:Unknown result

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: nose is running; back of throat is itching; coughing a lot; eyes are burning; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered on the left arm on 25Mar2021 08:00 (Lot Number: NE6208) (at the age of 59 years old) as dose 1, single for COVID-19 immunisation. The vaccine was administered in a Hospital facility. The patient's medical history included ongoing high blood pressure (diagnosed 10 or 12 years ago) and surgery (had surgery ten years ago). The patient takes his normal medications every day. On 26Mar2021, the patient experienced nose is running, back of throat is itching, coughing a lot, and eyes are burning. The patient stated that his "nose is running" has dried up now, but in a little bit, it'll start running again soon. The patient underwent lab tests and procedures which included an x-ray of his chest: unknown result on an unspecified date. The patient started taking dextromethorphan hydrobromide;doxylamine succinate;ephedrine sulfate;ethanol;paracetamol (NYQUIL), paracetamol (TYLENOL), guaifenesin (ROBITUSSIN), eucalyptus globulus oil;menthol (HALLS), and hot tea but the events keep on persisting. The patient has not recovered from the events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Blood pressure high (diagnosed 10 or 12 years ago)

ID: 1792706
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: This is a spontaneous report from a contactable consumer or other non-healthcare professional. A patient, of unspecified age and gender, received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# and expiry date not reported), via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. On an unspecified date, patient had a rash. Patient stated, "I have a rash and it's now 5 weeks. My dermatologist has got me on a program of steroids (unspecified steroids). I am wondering if there is any advice that you have or someone to give me that is the right program to be on?" Patient also stated, "It is from the COVID-19 vaccine. It happened after my first shot. I went to my dermatologist and my general practitioner and they said well it's a rash; go take the second shot because that is more important and we can resolve the rash. Well that was 5 weeks ago, now I want to know how get these things clean down." The outcome of the event: unknown. No follow-up attempts possible. Information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792707
Sex: M
Age:
State: PA

Vax Date: 03/17/2021
Onset Date:
Rec V Date: 10/16/2021
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: left shoulder bothered/ feeling of bother in the morning had been going on for over a week and was getting a little bit worse; got a pulsating feeling where the vaccine was given; got a pulsating feeling where the vaccine was given; muscle in left arm got a little sore; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EN6207), via an unspecified route of administration, administered in the left arm (reported as left upper shoulder) on 17Mar2021 (between 13:30 and 13:45, as reported) as dose 1, single for COVID-19 immunisation. The patient has no medical history and concomitant medications. The patient did not receive any other vaccines within four weeks of vaccination. The patient reported that he received the vaccine on 17Mar2021 and the first week he was fine but in the previous weekend he was not. In the morning (on an unspecified date in 2021), his left shoulder bothered. The patient reported that he received the vaccine in his left shoulder and he sometimes slept on his left shoulder. In the morning, it bothered the caller and this bother did go away later on. This feeling of bother in the morning had been going on for over a week and was getting a little bit worse. On an unspecified date in 2021, the patient also got a pulsating feeling where vaccine given. He was working in the yard for about an hour and a half, after he got a pulsating feeling where the vaccine was given. The patient stated that it didn't bother him for a long time, it was just annoying and kept occurring every day. He called the county where he was located after receiving the vaccine and was told by a nurse to massage it and take paracetamol (TYLENOL) if symptoms continued. The patient took paracetamol and stated it did go away on its own. In the morning when caller awakened (on an unspecified date in 2021), it bothered him, not a lot but it was annoying. The patient wanted to know how long the symptoms is going to go on, and what to do to get rid of them. He was told when he goes back to receive his second dose vaccine to make sure it was given in his other arm. The patient also reported that some days the left shoulder bothered a little bit more than other days. This depended on how much pressure, the patient was lying in bed in the morning (on an unspecified date) and leaned down on elbow and the muscle in left arm got a little sore. The patient stated that it was not real, real, painful but it was there. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792709
Sex: M
Age:
State:

Vax Date: 03/17/2021
Onset Date: 03/28/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Name: Weight; Result Unstructured Data: Test Result:200, actually it is 199 I was rounding it up.; Comments: 200, actually it is 199 I was rounding it up. Give me the benefit of doubt, 199

Allergies:

Symptom List: Pain in extremity

Symptoms: Have pain at the site; Slight headache; Muscle pain; Chills; Have severe itching all over my body; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 68-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: EN6205, Expiry date was not reported) via intramuscular route of administration, administered in Arm Left on 17Mar2021 (at the age of 68 years old) as DOSE 2, SINGLE for covid-19 immunisation. Also, the patient has received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: GL9266, Expiry date was not reported) via intramuscular route of administration, administered on 24Feb2021 as DOSE 1, SINGLE for covid-19 immunisation which leads to pain at the site. The patient medical history included cholesterol and acid reflux from an unknown date and unknown if ongoing. The reporter stated that, I do not know what I wanted to tell you about myself as far as medical conditions. I do not have anything that should affect this, I normally every year get the flu shot for instance, I have Pneumonia shot, I have Shingles shot, so I get all my inoculations as far as others. Concomitant medication(s) included atorvastatin (ATORVASTATIN) taken for blood cholesterol abnormal from an unspecified start date and ongoing; omeprazole (OMEPRAZOLE) taken for gastroesophageal reflux disease, start and stop date were not reported, saccharomyces boulardii (FLORASTOR SACCHAROMYCES BOULARDII) taken for an unspecified indication, start and stop date were not reported; vitamin d3 (VITAMIN D3) taken for an unspecified indication, start and stop date were not reported. On 28Mar2021 the patient experienced have severe itching all over my body. On an unspecified date the reporter stated that, he has pain at the site from both shots (COVID Shot), the second was worse than the first, he did have the second time slight headache and muscle pain for about a day. He also has chills but that was only for an hour. The patient underwent lab tests and procedures which included blood test with results as normal on unspecified date, electrocardiogram with results as normal on unspecified date, weight 200, actually it is 199 I was rounding it up on unspecified date. The outcome for the event, have severe itching all over my body was not recovered and the outcome for the events have pain at the site, slight headache, muscle pain, chills was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: ATORVASTATIN; OMEPRAZOLE; FLORASTOR [SACCHAROMYCES BOULARDII]; VITAMIN D3

Current Illness:

ID: 1792710
Sex: F
Age:
State: NJ

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210330; Test Name: Body temperature; Result Unstructured Data: Test Result:102 Fahrenheit

Allergies:

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

Symptoms: Chills; Fever (102 Fahrenheit); Headache; Body aches; This is a spontaneous report from a contactable consumer (patient). A 23-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EP6955), via an unspecified route of administration in the left arm on 30Mar2021 at 09:00 (at the age of 23-year-old), dose 2, single for COVID-19 immunisation. Medical history included migraines. Concomitant medication included propranolol. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247) administered via an unspecified route of administration in the left arm on 09Mar2021 at 09:00 (at the age of 23-year-old), dose 1, single for COVID-19 immunisation. On 30Mar20221, the patient experienced chills, fever (102 Fahrenheit), headache, body aches. No treatment was received for the event. The outcome of the event chills was recovered on an unspecified date and outcome of other events was recovered on 01Apr2021. No follow-up attempts are possible; No further information is expected.

Other Meds: PROPRANOLOL

Current Illness:

ID: 1792711
Sex: M
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 10/16/2021
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: Extreme fatigue; Minor redness at injection site; This is a spontaneous report from a non-contactable pharmacist. A 35-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 31Mar2021 as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On an unknown date in 2021, the patient experienced Patient reported extreme fatigue starting around 20 hours post vaccination. No other side effects to vaccine besides minor redness at injection site. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.Since the vaccination, the patient had not been tested for COVID-19. No therapeutic measures were taken as a result of the reported events The clinical outcome of the event extreme fatigue and minor redness at injection site was resolved on an unknown 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: 1792712
Sex: F
Age:
State: VA

Vax Date: 02/01/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: Like an influenza thing you know like a cold with sneezes; Each time she is sneezing there is a burning sensation in the palate and the throat; Like an influenza thing you know like a cold with sneezes; Like an influenza thing you know like a cold with sneezes; Each time she is sneezing there is a burning sensation in the palate and the throat; This is a spontaneous report from a contactable consumer (husband of patient) reported for the patient (wife). A 63-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EN6198, and Expiration date: 30Jun2021), via an unspecified route of administration, administered in left arm on unspecified date in Feb2021 as dose 2, single for COVID-19 immunization. The patient medical history included cholesterol and thyroid imbalance. The concomitant medications included levothyroxine (LEVOTHYROXINE) taken for thyroid imbalance, atorvastatin calcium (LIPITOR [ATORVASTATIN CALCIUM]) taken for cholesterol, and vitamin d2 (VITAMIN D2) taken for an unspecified indication. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: Unknown, and Expiration date: Unknown), via an unspecified route of administration, administered in left arm on unspecified date on unspecified date as dose 1, single for COVID-19 immunization. No investigation assessment was done. The reporter reported that, it started about 10 days back and the patient had already got the both the shots of the Pfizer vaccine Covid-19. On an unspecified date in Mar2021 (around 19Mar2021 or 20Mar2021), it was like an ongoing "like an influenza thing you know like a cold with sneezes" and no temperature registration. Everything was normal temperature wise but definitely like an onset of allergy attack which happens in spring, but it was not actually allergy, but it was more like an ongoing cold when you have sneezes and throat irritation was there and each time, she was sneezing she was registering a burning sensation in the where the tonsils were, that area and in the base of the palate. So, it was like a burning sensation of the palate as well as the throat both (Each time she is sneezing there is a burning sensation in the palate and the throat). The reporter stated, it had been almost 4 weeks. The second dose was administered on the 3rd week of Feb2021. So, this was the end of Mar2021, and it had been 10 days now. The patient was taking treatment as over the counter supplement like Emergen-C, Sucrets for throat relieve, the itching and Vicks VapoRub as well just one time. The Vicks VapoRub balm which you apply outside of your skin. Emergen-C, it was an over the counter antioxidant supplement comes in powder form and you mix it up with water and drink it. It was basically 1000 mg of vitamin C, and these Socrates and Epicor were two lozenges you take for your throat relief, the itching. The reporter added something like that had not really happened prior to the vaccine. There was no temperature. The outcome of events was not resolved, at the time of report. No follow-up attempts are possible. No further information is expected.

Other Meds: LEVOTHYROXINE; LIPITOR [ATORVASTATIN CALCIUM]; VITAMIN D2

Current Illness:

ID: 1792713
Sex: F
Age:
State: PA

Vax Date: 02/25/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: itchy; This is a spontaneous report from a contactable consumer (patient). An 80-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot number: EM9809), via an unspecified route of administration, administered in left arm (reported as left upper arm), on 25Feb2021 at 11:30 (age at vaccination was 80-year-old) as dose 1, single for COVID-19 immunization. The patient's medical history included allergies to sulfa and penicillin. The patient's concomitant medications were reported as none. The patient previously took nitrofurantoin (MACROBID) and experienced allergy. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. On Mar2021, the patient experienced itchy. It was further reported that four or five days later after the vaccine, patient had itchy (no rash), just itchy. The patient's dermatologist prescribed triamcinolone acetonide cream 0.1% in the tube for 3-4 times a day as needed and was reported that it helped a little bit (it worked), but then it didn't work. It was reported that itchy had sort of tapered off, wasn't gone but had tapered off. The outcome of the event was recovering. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792714
Sex: F
Age:
State:

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210331; Test Name: body temperature; Result Unstructured Data: Test Result:100.8 degrees; Comments: 08:57; fever; Test Date: 2021; Test Name: body temperature; Result Unstructured Data: Test Result:100 degrees; Comments: under

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: legs were aching; fever was 100.8 degrees; could not sleep; could not lift her leg; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot Number: EN6205; Expiration Date: Jun2021 at 10:20), via an unspecified route of administration, administered in left arm on 31Mar2021 (age at vaccination was 77-year-old) as dose 2, single for COVID-19 immunization. The patient's medical history included allergies, compromised immune status, respiratory illness, genetic /chromosomal abnormalities, endocrine abnormalities, diabetes and obesity. There was no concomitant medications. The patient previously took aspirin [acetylsalicylic acid]. The patient's historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot Number: EL9254; Expiration Date: May2021), via an unspecified route of administration, administered in left arm on 09Mar2021 (age at vaccination was 77-year-old) as dose 1, single for COVID-19 immunization. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. On 31Mar2021, the patient experienced fever was 100.8 degrees at 08:57, legs were aching at 10:21, could not sleep and could not lift her leg. It was further reported that the patient woke up and her legs were aching. It was reported that it felt like someone was stabbing her with a butcher knife in her legs and she could not sleep. It got worse and better and at the report date it was a little better. The patient's fever was 100.8 degrees and at time of report it was under 100 degrees. She can lift her leg a little now since she could not before. The patient would like to know if she can take an aspirin or paracetamol (TYLENOL), 24 hours after having the second vaccine. The patient underwent lab tests and procedures which included body temperature of 100.8 degrees (fever) on 31Mar2021 at 08:57 and under 100 degrees on an unspecified date of 2021. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792715
Sex: F
Age:
State: OH

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

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

Lab Data: Test Name: sugar; Result Unstructured Data: Test Result:Drop

Allergies:

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

Symptoms: I am also having the side effects; this hurts me really bad; The tissue inside around the bones and in joints it just 'baffled'; I have so much pain I can't move my foot; I have pain in my hip bone; I have pain in my back; I can't hear well; Headache; Ankles swollen; It makes my sugar drop; This is a spontaneous report from a contactable consumer (patient). A 72-year-old female patient received bnt162b2 (COMIRNATY, solution for injection, Batch/Lot Number: EN6204), via an unspecified route of administration on an unspecified date (at the age of 72-years) as dose 1, single for covid-19 immunization. Patient had relevant medical history. The patient did not had concomitant medications. The patient also had the side effects from the first shot (Covid Vaccine by Pfizer), this hurts her really bad, the tissue inside around the bones and in joints it just baffled and the patient had so much pain. The patient did not move her foot, had pain in her hip bone and pain in her back. The patient did not hear well and had headache and her ankles was swollen. The patient had the shot for long time and it makes her sugar drop that was common or not. The pain started after a week. The patient should go ahead or not for the second dose that was main thing that the patient want to know. The patient was informed about the Pfizer Medical Information and provided with the (number withheld) and requested to dial the option 3 and informed about timings as 8 AM to 8 PM from Monday to Friday and for Saturday and Sunday timings are 9 AM to 3 PM as per EST. The patient stated, 15Mar2021 and scheduled for second dose on 05Apr2021. Other medications: the patient stated, she took a lot of medications, about 20, she did not know and they need to know where the patient took the vaccine at the place. The patient went lab test: Blood glucose abnormal: drop. The outcome of the events was unknown. QR Comment: Reason of delay: Daily spike of incoming calls due to COVID19 vaccine. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792716
Sex: F
Age:
State: PA

Vax Date: 03/18/2021
Onset Date: 03/26/2021
Rec V Date: 10/16/2021
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: a high fever; Persistent dry cough; shortness of breath; This is a spontaneous report from a non-contactable other healthcare professional (nurse). A 61-years-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EP7534), via an unspecified route of administration, administered in left arm on 18Mar2021 (at the age of 61-years) as dose 1, single for covid-19 immunization at a Pharmacy or Drug Store. The patient medical history included asthma since 4yo, under control; high cholesterol. The patient had known allergies to drug Penicillin, Floxin, Singulaire. The patient's concomitant medications included budesonide, formoterol fumarate (SYMBICORT); hctz (HCTZ); simvastatin (SIMVASTATIN) taken for unspecified indication, start/stop date not reported. The patient was not pregnant at the time of vaccination. The patient had not received any other vaccine within 4 weeks. The patient had been diagnosed with COVID-19 prior to vaccination on an unspecified date in Mar2021. One week following vaccination on 26Mar2021, the patient had persistent dry cough, shortness of breath. On 28Mar2021, the patient had high fever for 24 hours. The patient did not receive any treatment for the events. The patient had not been tested for COVID-19 since the vaccination. The outcome of the event high fever was recovered while the other events was recovering. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: SYMBICORT; HCTZ; SIMVASTATIN

Current Illness:

ID: 1792717
Sex: F
Age:
State:

Vax Date: 03/27/2021
Onset Date: 03/28/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: sinus congestion; chest congestion; mild cough; laryngitis; loss of voice; nasal congestion; nasal congestion and drainage; mild sore throat; tired; headache; muscle aches; chills; This is a spontaneous report from a contactable consumer (patient). A 42-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot number: ER8727), via an unspecified route of administration, administered in left arm on 27Mar2021 (age at vaccination was 42-year-old) as dose 2, single for COVID-19 immunization. The patient's medical history included seasonal allergies and allergy to penicillin and latex. Concomitant medications included biotin, cetirizine hydrochloride (ZYRTEC) and multivitamins; all from an unspecified date and unknown indication. The patient previously took amoxicillin and doxycycline and experienced allergy. The patient's historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot number: EN6205), via an unspecified route of administration, administered in left arm on 06Mar2021 (age at vaccination was 42-year-old) as dose 1, single for COVID-19 immunization. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. Prior to vaccination, the patient has not been diagnosed with COVID-19 and since the vaccination, the patient has not been tested for COVID-19. The patient experienced tired, headache, muscle aches and chills on 28Mar2021; nasal congestion and drainage, and mild sore throat on 30Mar2021; laryngitis and loss of voice on 31Mar2021; and sinus congestion, chest congestion and mild cough on 01Apr2021. It was further reported that the patient experienced the following: tired, headache, muscle aches and chills on day 1 post vaccine; no symptoms on day 2 post vaccine; onset of nasal congestion and drainage, mild sore throat, headache and chills on day 3 post vaccine; nasal congestion, headache, onset of laryngitis, loss of voice on day 4 post vaccine; and nasal and sinus congestion, chest congestion, mild cough, full loss of voice and headache on day 5 post vaccine (day of report). No therapeutic measures were taken as a result of the events. The outcome of event tired and muscle aches was recovered on 28Mar2021; nasal congestion and drainage (rhinorrhea), mild sore throat and chills was recovered on 30Mar2021; laryngitis was recovered on 31Mar2021; while other reported events was not recovered. No follow-up attempts are possible. No further information is excepted.

Other Meds: BIOTIN; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1792718
Sex: F
Age:
State: NC

Vax Date: 03/17/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210329; Test Name: Abdominal X-ray; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210329; Test Name: Blood Work; Result Unstructured Data: Test Result:Unknown result

Allergies:

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

Symptoms: edema on thighs made it difficult for the patient to walk; edema in stomach which persisted and moved around to other parts of the body; edema in stomach which persisted and moved around to other parts of the body; left arm soreness; edema in hip/ edema on thighs made it difficult for the patient to walk; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in left arm, on 17Mar2021 at 02:30 PM (Batch/Lot Number: EN6205) (at the age of 77 years old) as dose 2, single for COVID-19 immunisation. Medical history included pulmonary arterial hypertension on Jul2020. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was previously administered the first dose of BNT162B2, intramuscularly, administered in left arm, on 21Feb2021 (Lot Number: EN6200) (at the age of 76 years old) as dose 1, single for COVID-19 immunisation. On an unspecified date in Mar2021, the patient experienced edema in stomach which persisted and moved around to other parts of the body, left arm soreness, and edema in hip. On 01Apr2021, the patient's edema on thighs made it difficult for the patient to walk. Clinical course of the events was as follows: The patient reported that she had edema in her stomach. She clarified the edema started a day or two after she had her second COVID-19 Vaccine shot on 17Mar2021, and the edema had persisted since that time. The patient said the edema had moved around since it started, from her stomach to her hip. She said last night (31Mar2021) she had elevated her feet and legs when she went to sleep, and when she woke up this morning, the liquid (edema) was located on the inside of her thighs. The patient said the edema on the inside of her thighs made it difficult for her to walk this morning. She said she was now lying on the sofa with her legs elevated, trying to see if the liquid (edema) would keep moving from the inside of her thighs. The patient went to a doctor, and the doctor had her scheduled for a sonogram of her tummy (abdomen) on 05Apr2021. The patient also had left arm soreness for about a week which completely resolved. Treatment: Declined any. The doctor won't do anything for her until all the test results are in. The patient underwent lab tests and procedures on 29Mar2021 which included unknown results of abdominal x-ray and blood work. The outcome of events edema in stomach which persisted and moved around to other parts of the body and edema in hip/edema on thighs made it difficult for the patient to walk was not recovered; the event left arm soreness was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am