VAERS 2021 Database www.vaers.hhs.gov

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

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

COVID19 Lot Number

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

Incidents per State

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

ID: 1661329
Sex: F
Age:
State: NJ

Vax Date: 02/11/2021
Onset Date: 02/16/2021
Rec V Date: 09/01/2021
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: inner elbow was sore; feels numb; I have terrible muscle pain in my upper left arm where I received the injection which radiates up my neck and shoulder blade; I have terrible muscle pain in my upper left arm where I received the injection which radiates up my neck and shoulder blade; I have terrible muscle pain in my upper left arm where I received the injection which radiates up my neck and shoulder blade; I have terrible muscle pain in my upper left arm where I received the injection which radiates up my neck and shoulder blade; This is a spontaneous report from a contactable other healthcare professional, (patient). A 53-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6201), dose 1 via an unspecified route of administration, administered in Arm Left on 11Feb2021 14:45 (at the age of 53-years-old) as a single dose for covid-19 immunization. Medical history included autoimmune thyroiditis: Hashimoto thyroid, hypertension. The patient did not have any allergies. The patient had no other vaccine within four weeks and other medications was received within 2 weeks of vaccination (not sepcified). 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 16Feb2021, the patient experienced inner elbow was sore for a day. Since, I have terrible muscle pain in my upper left arm where I received the injection which radiates up my neck and shoulder blade. Sometimes it feels numb and radiates down my arm to my fingers. The patient did not receive any treatment. Outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661330
Sex: F
Age:
State: AZ

Vax Date: 02/06/2021
Onset Date: 02/07/2021
Rec V Date: 09/01/2021
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: swelled up and itching/when she got up on Monday, the area on her arm at the injection side was raised like it was swollen a little bit more; swelled up and itching; pain and stuff; breaking out with bumps around the injection site/then noticed a few little pink bumps just small ones; This is a spontaneous report from a contactable consumer. This 79-year-old female consumer (patient) reported that. A 79-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration, administered in Arm Left on 06Feb2021 12:25 as (At the age of 79-years) dose 1, single for covid-19 immunisation; paracetamol (TYLENOL), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at for an unspecified indication; calamine, zinc oxide (CALADRYL [CALAMINE;ZINC OXIDE]), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at for swelling, pruritus. The patient medical history was not reported. Concomitant medication(s) included diazepam 2mg (caller states this is a high dose of the Diazepam) taken for an unspecified indication from 1975 and ongoing; butalbital, caffeine, paracetamol (BUTALBITAL, ACETAMINOPHEN & CAFFEINE) taken for an unspecified indication from an unspecified start date and ongoing. The patient experienced pain and stuff, breaking out with bumps around the injection site/then noticed a few little pink bumps just small ones, and swelled up and itching on 07Feb2021, patient experienced swelled up and itching/when she got up on monday, the area on her arm at the injection side was raised like it was swollen a little bit more on 08Feb2021. It was reported that Patient got the Pfizer injection COVID19 Vaccine last Saturday, 06Feb2021. On Sunday she had pain and stuff. On Sunday night she started breaking out with bumps around the injection site. It is swelled up and itching. She was asking Is that normal. She just wants to know why it still swollen and itches. It doesn't have that in the pamphlet. She has read it. She has been using Caladryl and that helps a little, but the itching comes back. She is not scratching it. Today it is swollen. It is pink. Later reporter reports that This was her first dose. She has called several times, but it says more than 7 people ahead of you. She sat for 30 to 45 minutes and had things to do. She will have to call USMI back, because she has to go take her cat to the vet. If someone is going to get something different it will be her. She is the biggest, odd ball her doctor has seen in his entire life. What the doctor could give to anyone else he couldn't give it to her. Her mom was the same way, but caller is worse than her mom was. Caller can't take medication, not even pain medication. She can't even take Tylenol. She suffers through any pain. Description of Product Complaint: Caller reporting adverse event with COVID19 Vaccine. On Sunday night she started breaking out with bumps around the injection site. It is swelled up and itching. She has been using Caladryl and that helps a little, but the itching comes back. She is not scratching it. Caller can't take medication, not even pain medication. She can't even take Tylenol. She suffers through any pain. Caller declined to proceed with report. Upon Follow-up Caller states she got the Pfizer Covid shot and went in to have it last Saturday 06Feb2021 and her arm started itching where she had the vaccine injected in her left arm. Caller states she was fine after being administered the Covid vaccine and then she got up in the mid-afternoon on Sunday and her arm started itching; states she then noticed a few little pink bumps just small ones on Sunday; states when she got up on Monday, the area on her arm at the injection side was raised like it was swollen a little bit more, but it did not itch continuously, and it had started out itching all the time. Caller states she did not scratch because she knows better than to do that but the area near the injection site looked like it had pink bumps around the injection site where they put the vaccine in; states that area near the injection site is swollen now and itches off and on but for a couple of days, it itched all the time. Caller states she is just wondering if this is one of the side effects of the Covid Vaccine or if she may be allergic to something in the medication of the Covid Vaccine. Caller states she used Calodril that is like calomine lotion and the Calodril helped a little bit, and she uses it for a short period of time, and it helped the itching; states when she starts itching again she just uses the Calodril again. Caller states she does not have the lot, expiry date or UPC or NDC number for the Calodril as it is not handy and not with her at this time at all, but she thinks the expiry date is Sep2021. Caller states this is her initial report, and she was told to call the number for USMI and was hoping she would not have to hold for very long, but she forgot to look and see the option to select for #3 for USMI. Caller states she happens to be over age 75 and is actually 79 years old. Caller states the itching is ongoing and less at this time she thinks because it comes and goes; states the raised area that looks swollen near the injection site is still ongoing and she can feel the bumps, and this is ongoing, and she feels about the same. Caller states the indication for the Covid vaccine is that she does not want to get the coronavirus because she is 79 years old and the chances of her surviving the coronavirus are really small; states she has other medical problems, so she does not need to get coronavirus. Caller states she did not get the itching, swelling and bumps near the injection side until she got the Pfizer Covid shot; states she has other medical problems and is on medications for it but does not know whether this is relevant; states the medications she takes are prescribed by her HCP and she has taken them for a long time, and they have never given her a side effect and she has been taking them for years. Caller states she used to have to spell this and she was never able to pronounce it and it used to be called valium but is now called butalbital-acetaminophen and caffeine; states she has taken it for a long time and the dosage is 50mg/355mg/40mg and it is in a white bottle; caller states she has to get the tape off of the bottle, aware not to remove the label; states the label has her name, Rx number and states Revised 416 cib703098, lot 20249986A expiry date Sep2022 and does not locate the NDC number; states she is currently taking it and has taken it for a long time. Caller states she is scheduled for her 2nd dose of Covid vaccine on 27Feb2021 at 12:25pm. Description of complaint: Caller states she got the Pfizer Covid shot and went in to have it last Saturday 06Feb2021 and her arm started itching where she had the vaccine injected in her left arm. Caller states she used Calodril that is like calomine lotion and the Calodril helped a little bit, and she uses it for a short period of time, and it helped the itching; states when she starts itching again, she just uses the Calodril again. Caller states she does not have the lot, expiry date or UPC or NDC number for the Calodril as it is not handy and not with her at this time at all, but she thinks the expiry date is Sep2021. Caller states she used to have to spell this and she was never able to pronounce it and it used to be called valium but is now called butalbital-acetaminophen and caffeine; states she has taken it for a long time and the dosage is 50mg/355mg/40mg and it is in a white bottle; caller states she has to get the tape off of the bottle, aware not to remove the label; states the label has her name, Rx number and states Revised 416 cib703098, lot 20249986A expiry date Sep2022 and does not locate the NDC number; states she is currently taking it and has taken it for a long time. The outcome of event breaking out with bumps around the injection site/then not

Other Meds: DIAZEPAM; BUTALBITAL, ACETAMINOPHEN & CAFFEINE

Current Illness:

ID: 1661331
Sex: M
Age:
State:

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: fatigue; malaise; I then noticed a set of flu-like symptoms; pain at injection site; muscle pain; joint pain; fever; chills; increased thirst; increased appetite; insomnia; This is a spontaneous report from a non-contactable consumer. This male consumer (patient) reported that: A 31-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EN5318), via an unspecified route of administration on 19Feb2021 at 11:45 as single dose for covid-19 immunisation. Medical history included known peanuts allergy. Patient not diagnosed with covid-19 prior to vaccination. Concomitant medication(s) included colecalciferol (D3) and cyanocobalamin (B12 [CYANOCOBALAMIN]) taken for an unspecified indication, start and stop date were not reported. The patient previously took bactrim and experienced drug allergy. Patient's historical vaccine included first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EN5318), via an unspecified route of administration on 29Jan2021 at 11:45 as single dose for covid-19 immunisation. Patient reported shortly after the injection was administered on 19Feb2021 at 13:00, I experienced fatigue and malaise. I then noticed a set of flu-like symptoms that persisted for around two days. These included pain at injection site, muscle pain, joint pain, fatigue, fever, chills, increased thirst, increased appetite, insomnia. All have resolved except the pain at the injection site. Since vaccination patient not tested for covid-19. No therapeutic measures were taken as a result of the events. The outcome of the event pain at the injection site was recovering and all other events were recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: D3; B12 [CYANOCOBALAMIN]

Current Illness:

ID: 1661332
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/01/2021
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: her arm got red 5 days after the vaccine; This is a spontaneous report from a Pfizer-sponsored program via Medical Information team. A contactable reporter (patient) reported for herself that a female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection), dose 1 via an unspecified route of administration in arm on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included allergic to shellfish, peanuts. The patient's concomitant medications were not reported. The patient's arm got red 5 days after the vaccine on an unspecified date. The outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1661333
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/01/2021
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: pressure on her chest; headache/ bad headache; cold symptoms; sinus pain; This is a spontaneous report from a non-contactable consumer (patient) via a medical information team. A female patient of an unspecified age received first dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unknown date in 2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date in the patient experienced pressure on her chest, bad headache, cold symptoms and sinus pain. All of it went away yesterday. However, she is still experiencing the headache. Patient was due to get the second dose. Her daughter got tested for COVID-19 since possibly exposed to the virus. Therefore, the patient may have been exposed too. The outcome of the event headache was not recovered, and rest 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: 1661334
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/01/2021
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: her face feels a little warm and flush; headache; injection site pain in my left arm; This is a spontaneous report from a non-contactable consumer (parent). A 32-year-old female patient(daughter) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number was not reported, expiration date was not reported), via an unspecified route of administration, administered in left arm on an unspecified date as dose number unknown, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that, reporter 32 y/o daughter had the Pfizer covid vaccine today, her face feels a little warm and flush, she doesn't look red, she's had reaction, no temperature, doesn't look flushed. reporter gave her Tylenol and advil, she took one of each. Daughter states that, she have a headache at this point, a little flush, injection site pain in my left arm. Her arm feels a little better. Her head is still in pain. Is it normal, can she take an antihistamine or what you would recommend. Can she take a Benadryl. Therapeutic measures were taken as a result of her face feels a little warm and flush, headache, injection site pain in my left arm. The outcome for event injection site pain in my left arm was recovering, outcome for event headache was not recovered and outcome for event her face feels a little warm and flush was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1661335
Sex: F
Age:
State: FL

Vax Date: 02/12/2021
Onset Date: 02/21/2021
Rec V Date: 09/01/2021
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: Swelling; hot to touch; itchy at injection site; This is a spontaneous report from a contactable consumer (patient). A 79-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9269), via an unspecified route of administration in right arm on 12Feb2021 at 10:00 (at the age of 79-year-old) as dose 1, single for COVID-19 immunisation at doctor's office/urgent care. Medical history included allergy to sulfa from an unknown date and unknown if ongoing. Concomitant medications included metoprolol, omeprazole, lovastatin, hydrochlorothiazide, triamterene (TRIAMTERENE/HYDROCHLOROTHIAZIDE) all from unknown dates to unknown dates for unknown indications. The patient previously took keflex [cefalexin], clindamycin, flonase [fluticasone propionate] and experienced drug hypersensitivity. Historical vaccine included dpt vaccine administrated in left arm on 01Feb2021. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient experienced swelling, hot to touch, itchy at injection site, starting on 21Feb2021 at 10:00, and continuing. The patient did not receive any treatment for the events. The outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds: METOPROLOL; OMEPRAZOLE; LOVASTATIN; TRIAMTERENE/HYDROCHLOROTHIAZIDE

Current Illness:

ID: 1661336
Sex: M
Age:
State: NH

Vax Date: 02/10/2021
Onset Date: 02/11/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data: Test Date: 20210212; Test Name: COVID test/Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Injection site soreness; Rash all over upper body since injection; Very itchy; This is a spontaneous report from a contactable consumer (patient). A 58-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9262), via an unspecified route of administration, administered in Arm Left on 10Feb2021 13:15 (at the age of 58-year-old) as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient did not receive any other vaccines in 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had been tested for COVID-19. Patient had no known allergies. Patient reported that injection site soreness 1 week. Rash all over upper body since injection. 12 days now. Very itchy (11Feb2021 12:00 AM). Patient visited doctor or other healthcare professional office/clinic. There was no treatment for the events. The patient underwent lab tests and procedures which included COVID test/Nasal Swab: negative on 12Feb2021. The clinical outcome of events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1661337
Sex: F
Age:
State: MN

Vax Date: 02/18/2021
Onset Date: 02/20/2021
Rec V Date: 09/01/2021
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: red rash on lower inner sides of feet, and toes; Psoriasis patch on eyeline; This is a spontaneous report from a contactable consumer (Patient). An elderly non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6201), Solution for injection, via an unspecified route of administration, administered in Arm Right on 18Feb2021 13:00 as single dose for covid-19 immunisation. Medical history included osteoarthritis, blepharitis, angle closure glaucoma, colitis, psoriasis and latex sensitivity allergy. There were no concomitant medications. Patient did not receive any other vaccine with four weeks of Pfizer vaccine. He did not receive any other medication in two weeks. Patient was not diagnosed with COVID-19 prior to receiving Pfizer vaccine. He was not tested for COVID-19 since vaccination. Patient historic vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL3302) via an unspecified route of administration, administered in Arm Right on 28Jan2021 at 10:15 AM for COVID-19 immunisation. On 20Feb2021 23:00, the patient experienced red rash on lower inner sides of feet, and toes and psoriasis patch on eyeline. It was reported that patient had red rash on lower inner sides of feet, and toes. 1-1/2" band from heel to mid foot, also bottom of feet Psoriasis (?) patch or ?? raised bumps centered on lower back starting 2" below waistline on 3" long , 1-/2" wide and psoriasis patch on eyeline. The outcome of event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661338
Sex: M
Age:
State: GA

Vax Date: 02/20/2021
Onset Date: 02/21/2021
Rec V Date: 09/01/2021
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: Mild headache; Mild itching; Swelling at injection site; This is a spontaneous report from a contactable consumer or non-health care professional (patient). A 66-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, administered in Left arm on 20Feb2021 05:15 PM (at the age of 66-year-old) as dose 2, single for covid-19 immunization at Doctor's office/urgent care. Medical history included HBD (High blood pressure), pre-diabetes and high cholesterol from an unknown date and unknown if ongoing. Concomitant medications included other medications taken within two weeks included Amlodipine besilate, Olmesartan medoxomil (AMLODIPINE AND OLMESARTAN MEDOXOMIL), Metformin taken as 500 mg and Famotidine all were taken for an unspecified indication, start and stop date were not reported. Patient had no known allergies. Patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Historical vaccine included the 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 Left arm on 30Jan2021 (at the age of 66-year-old) as single for COVID-19 immunization. Patient neither diagnosed with COVID-19 prior to vaccination nor tested since the vaccination. On 21Feb2021 09:00 AM, the patient experienced mild headache, mild itching and swelling at injection site. AE was not resulted in physician visit or ER. No treatment was received for the events. Outcome of the events were recovered on an unspecified date in 2021. Information about Lot Number/Batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds: AMLODIPINE AND OLMESARTAN MEDOXOMIL; METFORMIN; FAMOTIDINE

Current Illness:

ID: 1661339
Sex: F
Age:
State: GA

Vax Date: 01/30/2021
Onset Date: 01/31/2021
Rec V Date: 09/01/2021
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: pain; itching; swelling at injection site; headache; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female non-pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number and expiration date was not reported) via an unspecified route of administration in left arm on 30Jan2021 17:45 as dose 1, single for COVID-19 immunization (at the age of 68-year-old, non-pregnant). Medical history included diabetes mellitus, high cholesterol and no known allergies. Concomitant medication(s) (in two weeks) included metformin. Patient did not receive any other vaccine in four weeks. Patient had no covid prior vaccination and was not covid tested post vaccination. The patient experienced pain, itching, swelling at injection site and headache on 31Jan2021. Patient did not receive treatment for the events. The outcome of the events was recovered. Information on Lot/Batch number has been requested Follow-up attempts completed. No further information expected.

Other Meds: METFORMIN

Current Illness:

ID: 1661340
Sex: F
Age:
State: OR

Vax Date: 02/19/2021
Onset Date: 02/21/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data: Test Name: Pain; Result Unstructured Data: Test Result:7/10

Allergies:

Symptom List: Rash, Urticaria

Symptoms: several canker sores and blisters on lip 24 hrs after vaccine; Eyes are puffy - hurt to touch; Small Red dots in mouth Woke up with painful sores/blisters in mouth; Itchy eyes; Small Red dots in mouth Woke up with painful sores/blisters in mouth; several canker sores and blisters on lip 24 hrs after vaccine; This is a spontaneous report from a contactable other healthcare professional. A 27 year old non pregnant female patient received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in Arm Right on 19Feb2021 18:30 (Batch/Lot number was not reported) as DOSE NUMBER, UNKNOWN, SINGLE for covid-19 immunisation. Medical history included asthma from an unknown date and unknown if ongoing , allergy to chemicals from an unknown date and unknown if ongoing , allergy to plants and hair dye, sesame seeds from an unknown date and unknown if ongoing. Concomitant medication(s) included vitamin d [vitamin d nos] (VITAMIN D [VITAMIN D NOS]) taken for an unspecified indication, start and stop date were not reported. The patient experienced several canker sores and blisters on lip 24 hrs after vaccine leading to aphthous ulcer on 21Feb2021 with outcome of not recovered , eyes are puffy, hurt to touch leading to periorbital swelling on 21Feb2021 with outcome of not recovered, small red dots in mouth woke up with painful sores or blisters in mouth on 21Feb2021 with outcome of not recovered, itchy eyes on 21Feb2021 with outcome of not recovered. pain 7/10 grading. Therapeutic measures were taken as a result of these events with Ibuprofen and Benadryl Information of lot and batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds: VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 1661341
Sex: F
Age:
State: NY

Vax Date: 02/21/2021
Onset Date: 02/22/2021
Rec V Date: 09/01/2021
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: Vomiting; Aches; slight fever; tired; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 47-year-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EL9269), via an unspecified route of administration, administered in arm left on 21Feb2021 at 16:30 (04:30 PM) (at the age of 47-year-old) as dose 2, single for COVID-19 immunization. The patient medical history included birth control, COVID-19 (COVID prior vaccination: Yes). The patient had no known allergies. The patient concomitant medications included ethinylestradiol, ferrous fumarate, norethisterone acetate (LARIN FE) taken for birth control, start and stop date were not reported. The patient did not receive any other vaccine within four weeks. The patient was diagnosed with COVID-19 prior vaccination. Patient had not COVID tested post vaccination. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EL9264), via an unspecified route of administration, administered in arm left on 31Jan2021 at 16:00 (04:00 PM) (at the age of 47-year-old) as dose 1, single for COVID-19 immunization. On 22Feb2021 at 11:30 AM, the patient experienced vomiting, aches, slight fever, tired. The patient did not receive treatment for the events. Outcome of the events was not recovered. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds: LARIN FE

Current Illness:

ID: 1661342
Sex: F
Age:
State: AL

Vax Date: 02/10/2021
Onset Date: 02/11/2021
Rec V Date: 09/01/2021
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: Test Name: x-ray; Result Unstructured Data: Test Result:Unknown Results

Allergies:

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

Symptoms: Nauseated; sick to her stomach; achy; arm sore when she moves it; Swollen arm; light chills; legs achy; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 66-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM9809), dose 1 via an unspecified route of administration, administered in Arm Right on 10Feb2021 12:53 (at age of 66-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included pernicious anaemia from 1992 and ongoing (Verbatim: Pernicious anemia), ongoing renal failure (Verbatim: kidney failure stage four/from 5 years), ongoing cardiac disorder (Verbatim: microvascular heart disease/from 8 years), ongoing ischaemia (Verbatim: Ischemia/from 8 years), ongoing diastolic dysfunction (Verbatim: Diastolic dysfunction/from 7 or 8 years), ongoing bundle branch block left (Verbatim: Left bundle branch block/from 9 years), ongoing cardiomyopathy (Verbatim: cardiomyopathy/from 6 or 7 years), ongoing cardiac failure congestive (Verbatim: Congestive heart failure/from 5 years), ongoing neuromyopathy (Verbatim: Neuromuscular disorder NOS/3 years ago; mentions she was falling and stumbling and they did a muscle biopsy to confirm she has a neuromuscular disease but they don't know which one), ongoing eye disorder (Verbatim: microvasular disease eye/diagnosed a year ago and the doctor mentioned she also has this in her brain, Liver damage (Verbatim: Liver damage/Caller mention she had COPD, and because of a weaken immune system she ended up with fungus in her lungs; by x-ray 21 something growing in her lungs. The medicine they gave was Ketoconazole and Sporanox. These products caused hepatitis due to medicine damage to the liver. She has no product or information to provide NDC, lot or expiration date for these products.), ongoing COPD (Verbatim: COPD), heart (Heart disorder), stomach from getting upset, potassium level, keep vitamin d up, keep vitamin E up, relax at night, regulate stomach, severe nerve damage in her legs, memory, keep hair from falling out, thyroid, levocarnitine deficiency, fluid retention. Family medical history was none. No patient's medical history (including any illness at time of vaccination). No prior vaccinations (within 4 weeks). No additional vaccines administered on same date of the Pfizer Suspect. History of all previous immunization with the Pfizer vaccine considered as suspect was none. Concomitant medications included acetylsalicylic acid (ASPIRIN (E.C.) taken for cardiac disorder from an unspecified start date and ongoing; amitriptyline hydrochloride (AMITRIPTYLINE HCL) taken for nerve injury from an unspecified start date and ongoing; riboflavin (B2 ASMEDIC) taken for vitamin b complex deficiency from an unspecified start date and ongoing; biotin taken for hair disorder from an unspecified start date and ongoing; cyanocobalamin (B 12 ROTEXMEDICA) taken for pernicious anaemia from an unspecified start date and ongoing; levocarnitine (CARNITOR) taken for protein deficiency, start and stop date were not reported; ubidecarenone (CO Q 10 [UBIDECARENONE]) taken for cardiac disorder from an unspecified start date and ongoing; furosemide taken for fluid retention from an unspecified start date and ongoing; ginkgo biloba taken for memory impairment from an unspecified start date and ongoing; isosorbide mononitrate taken for cardiac disorder from an unspecified start date and ongoing; magnesium taken for abdominal discomfort from an unspecified start date and ongoing; glyceryl trinitrate (NITRO DUR) taken for cardiac disorder from an unspecified start date and ongoing; glyceryl trinitrate (NITRO) taken for cardiac disorder from an unspecified start date and ongoing; (PROBIOTIC ORAL CAPSULES) taken for abdominal discomfort, start and stop date were not reported; potassium taken for blood potassium from an unspecified start date and ongoing; pravastatin sodium taken for blood cholesterol from an unspecified start date and ongoing; ranolazine (RANEXA) taken for cardiac disorder from an unspecified start date and ongoing; levothyroxine sodium (SYNTHROID) taken for thyroid disorder from an unspecified start date and ongoing; ergocalciferol (VITAMIN D2) taken for hypovitaminosis from an unspecified start date and ongoing; colecalciferol (VITAMIN D3) taken for hypovitaminosis from an unspecified start date and ongoing; tocopherol (VIT E) taken for vitamin e increased, cardiac disorder from an unspecified start date and ongoing; alprazolam (XANAX) taken for feeling of relaxation from an unspecified start date and ongoing. On 11Feb2021, the patient experienced nauseated, sick to her stomach, achy, arm sore when she moves it, swollen arm, light chills, legs achy. Patient called to report side effects from the first dose of the Pfizer COVID 19 vaccine 10Feb2021 at 12:53PM in the right arm. When she got up this morning she was nauseated; sick to her stomach; achy; arm sore when she moves it; arm swollen; light chills that are about gone but no fever and achy legs. She was planning to receive the second dose of the vaccine on 03Mar2021. Mentions she has been through a lot worse and she was sure she will be able to lay around a little today and get over this. She was determined to get the second dose of the vaccine. Any adverse event did not require a visit to physician or ER. The patient underwent lab tests and procedures which included x-ray: unknown results. No investigation assessment. Outcome of event nauseated was recovering, sick to her stomach, achy, arm sore when she moves it, swollen arm was not recovered, and light chills was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: ASPIRIN (E.C.); AMITRIPTYLINE HCL; B2 ASMEDIC; BIOTIN; B 12 ROTEXMEDICA; CARNITOR; CO Q 10 [UBIDECARENONE]; FUROSEMIDE; GINGKO BILOBA; ISOSORBIDE MONONITRATE; MAGNESIUM; NITRO DUR; NITRO [GLYCERYL TRINITRATE]; POTASSIUM; PRAVASTATIN SODIUM;

Current Illness: Cardiomyopathy (Verbatim: cardiomyopathy/from 6 or 7 years); Congestive heart failure (Verbatim: Congestive heart failure/from 5 years); COPD (Verbatim: COPD); Diastolic dysfunction (Verbatim: Diastolic dysfunction/from 7 or 8 years); Eye disorder (Verbatim: microvasular disease eye/diagnosed a year ago); Heart disease, unspecified (Verbatim: microvascular heart disease/from 8 years); Ischemia (Verbatim: Ischemia/from 8 years); Kidney failure (Verbatim: kidney failure stage four/from 5 years); Left bundle branch block (Verbatim: Left bundle branch block/from 9 years); Neuromuscular disorder NOS (Verbatim: Neuromuscular disorder NOS/3 years ago.); Pernicious anemia (Verbatim: Pernicious anemia)

ID: 1661343
Sex: F
Age:
State: CA

Vax Date: 01/20/2021
Onset Date: 02/09/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Abdominal pain; diarrhea; body aches; lethargic; chills; This is a spontaneous report from a contactable consumer (patient). A 76-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot Number: EL9263), dose 1 via an unspecified route of administration, administered in arm left on 20Jan2021 at 13:00 (at the age of 76-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Patient had known sulfa and penicillin allergies and other medical history hypertension (HTN) from an unknown date and unknown if ongoing. Patient was received other medications (unknown) in two weeks. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. The patient experienced abdominal pain, diarrhea, body aches, lethargic and chills on 09Feb2021 at 19:00. It was reported that it was unknown if the patient received any treatment for the events. The outcome of events was recovering. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661344
Sex: F
Age:
State: NV

Vax Date: 02/20/2021
Onset Date:
Rec V Date: 09/01/2021
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: Headache; dizziness; taste of metal in mouth; heaviness in chest/tightness in chest; sore arm; This is a spontaneous report from a contactable consumer. This 67-Year-Old female consumer (patient) reported that: A 67-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EN6200), via an unspecified route of administration, administered in Arm Left on 20Feb2021 (at the age of 67-year-old) as single dose for covid-19 immunisation. Patient was not pregnant at the time of vaccination. Medical history included stable tiny right apical nodule and allergy to sulfa drugs and Penicillin. Patient not diagnosed with covid-19 prior to vaccination. Patient was not received any other vaccine four weeks prior vaccination. Patient received unspecified medication two weeks prior vaccination. The patient experienced Headache, dizziness, taste of metal in mouth, sore arm, tightness in chest and heaviness in chest on 07Feb2021. Since vaccination patient not tested for covid-19. No therapeutic measures were taken as a result of the events. The outcome of the events was reported as not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661345
Sex: F
Age:
State: NY

Vax Date: 02/20/2021
Onset Date: 02/20/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: a slight headache; fever; This is a spontaneous report from a Pfizer-sponsored program Support from a contactable consumer. A female patient of an unspecified age received bnt162b2 (Formulation: Solution for injection; Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 20Feb2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The caller had her first shot of COVID-19 vaccine yesterday (20Feb2021). She reported that she experienced a slight headache and then fever as well. She was also asking whether she could take Advil. The outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661346
Sex: M
Age:
State: FL

Vax Date: 02/10/2021
Onset Date: 02/10/2021
Rec V Date: 09/01/2021
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: Vertigo; Its swollen base of my left ear down to my jaw, mandible particular and when I open my mouth I can feel like pain; Its swollen base of my left ear down to my jaw, mandible particular and when I open my mouth I can feel like pain; Chills; Nauseated; This is a spontaneous report from a contactable physician (Patient). A 74-years-old male patient received first dose of bnt162b2 (BNT162B2, PFIZER-BOTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9262; Expiration Date: 31May2021), via an unspecified route of administration, administered in Arm Right on 10Feb2021 (Age at vaccination: 74-years-old) as dose 1 single for covid-19 immunization. Medical history included Chronic Otitis Media from an unknown date and unknown if ongoing. Concomitant medication included hctz (HCTZ), lisinopril (LISINOPRIL) both taken for an unspecified indication from an unspecified start date and ongoing. It was reported that patient had his first Pfizer vaccine dosage yesterday although he did not have any immediate allergic reactions within the first 15min, after 15 minutes he started getting chills, he had vertigo and he was nauseated so he laid down rest of the day. This morning his symptoms were pretty much same and its swollen base of his left ear down to his jaw, mandible particular and when he open his mouth he can feel like pain. he suffer from Chronic Otitis Media. It was reported maxilla, mandible, his ear to there, its swollen, if he open his mouth wide, it hurts little bit on that side. Stated hard to say all he know was approximately 30 min after the injection, it was terrible the jaw swelling does not bother me that much than he stand up he feel vertigo. Patient did no received treatment for the events. The outcome for the events was reported as not resolved at the time of this report. Follow-up attempts completed. No further information expected.

Other Meds: HCTZ; LISINOPRIL

Current Illness:

ID: 1661347
Sex: F
Age:
State: AK

Vax Date:
Onset Date:
Rec V Date: 09/01/2021
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: severe allergic reaction; This is a spontaneous report from a contactable consumer. A 49-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 1 SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced severe allergic reaction after the first dose on an unspecified date with outcome of unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021193923 same patient, different drug/AE

Other Meds:

Current Illness:

ID: 1661348
Sex: M
Age:
State: MS

Vax Date: 02/08/2021
Onset Date: 02/23/2021
Rec V Date: 09/01/2021
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: Severe night time nose bleed 2 weeks after first Pfizer COVID vaccination; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 59-year-old male patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, administered in arm left on 08Feb2021 09:45 (at the age of 59-year-old) at dose 1, single for covid-19 immunisation. Medical history included diabetic, high blood pressure, obese (other medical history). Patient Known allergies were none. Patient did not have other vaccine in four weeks. Patient did not have covid prior vaccination. Patient was not tested for covid post vaccination. Concomitant medications included lisinopril (LISINOPRIL) 5 mg; metformin (METFORMIN) 500; pantoprazole (PANTOPRAZOLE) 40 mg (Other medications in two weeks). On 23Feb2021 01:00 the patient experienced severe night time nose bleed 2 weeks after first pfizer covid vaccination. Adverse event led to Doctor or other healthcare professional office/clinic visit. It was unknown whether the patient received treatment for the adverse event. Outcome of the event was unknown. Information about Lot/batch number has been requested. Follow-up (06Apr2021): Follow-up attempts are completed. No further information is expected.

Other Meds: LISINOPRIL; METFORMIN; PANTOPRAZOLE

Current Illness:

ID: 1661349
Sex: F
Age:
State: CA

Vax Date: 01/08/2021
Onset Date: 01/16/2021
Rec V Date: 09/01/2021
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: 202102; Test Name: covid test; Test Result: Negative ; Test Date: 202102; Test Name: Nasal Swab; Test Result: Negative

Allergies:

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

Symptoms: mild headache for 3 days after Dose 2; Initial fatigue; diaphoresis; bilateral axillary pain; This is a spontaneous report from a contactable physician. A 37-years-old female patient received bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number: EL1283, Expiry date: Unknown) via intramuscular route of administration on 08Jan2021 12:00 in left arm as dose 2, single for COVID-19 immunisation. The patient medical history was not reported. There were no other vaccines within 4 weeks. No COVID prior vaccination. There were no known allergies. Covid tested post vaccination. On 18Dec2020 12:00 PM, the patient administered first dose of bnt162b2 intramuscularly in left arm (lot number: EK5730) for COVID-19 immunisation. The patient's concomitant medications were not reported. On 16Jan2021, the patient experienced initial fatigue, mild headache for 3 days after dose 2, as commonly described. Starting about 7-10 days after dose 2, diaphoresis, fatigue, bilateral axillary pain continued for 10 days, and recurring now in late Feb2021. The adverse events resulted in doctor or other healthcare professional office/clinic visit. Patient took antipyretics as treatment. The patient underwent lab tests and procedures on an unknown date in Feb2021 which included sars-cov-2 antibody test: negative, viral test: negative. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661350
Sex: F
Age:
State: FL

Vax Date: 02/10/2021
Onset Date: 02/01/2021
Rec V Date: 09/01/2021
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: started experiencing headaches that got worse; nausea; chills; cramps in my legs; She felt so sick; She could not move both her legs; Both her legs were aching; I had a slight fever; This is a spontaneous report from a contactable consumer or other non-HCP (patient herself) via Medical Information Team. A 73-year-old female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration on 10Feb2021 (also reported as 13Feb2021 07:00) as dose 1, single (at the age of 73-years-old) for COVID-19 immunization. Patient medical history included COVID-19 from an unspecified date in 2020. She was infected with the Covid-19 virus last year (2020) and got better after a month and a half. The concomitant medications were not reported. Patient asked if she did not get the second dose, will the first one be any good. She received her first Pfizer Covid-19 vaccine on last Wednesday (10Feb2021). However, she stated it was 13Feb2021 around 07:00. She experienced some bad side effects. She went to work and about 2 or 3 in the afternoon started experiencing headaches that got worse, nausea, and chills, that Wednesday night she felt so sick and both her legs were aching, she could not move both her legs on 10Feb2021. The cramps in her legs subsided the next day (11Feb2021) after taking some Flexiril. She had a slight fever on an unspecified date in Feb2021. She asked should she take the second vaccination. The outcome of the event cramps in her legs was resolved on 11Feb2021, while that of the other events was unknown. Information for lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1661351
Sex: F
Age:
State: IL

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 09/01/2021
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: body ache; Chills; fever; This is a spontaneous report from a contactable other hcp. A 40-year-old female non pregnant patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via intramuscular route, administered in right arm on 22Feb2021 10:30 (age at vaccination 40-year-old, Batch/Lot Number: EN5318) as single dose for COVID-19 immunisation. The patient had no medical history. The patient concomitant medications were not reported. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via intramuscular route administered in right arm on 01Feb2021 09:00 AM (Batch/Lot Number: EL3248) as single dose for COVID-19 immunisation. The patient experienced body ache, chills and, fever on 23Feb2021 12:00. Patient not received treatment. The No other vaccine in four weeks. Patient had no known drug allergies. No COVID prior vaccination and no COVID tested post vaccination. The outcome of events was recovered on unknown date in 2021. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1661352
Sex: F
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 09/01/2021
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: have colds; respiratory issue; This is a spontaneous report from a Pfizer-sponsored program Support. A contactable female consumer reported similar events for 2 patients (Herself and Husband). This is 1st of 2 reports. This female consumer reported for herself that: A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number and Expiration Date was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that she have colds and her 2nd dose due tomorrow. Patient was not sure if it was the right place but her husband and she have the COVID-19 Vaccine three weeks ago. We are due to have it again tomorrow but we have had enough of respiratory issue for the last week and her doctor said she thought it would be best if we postpone taking the second dose for at least two weeks and she was trying to let them know that we can't come tomorrow for the appointment to get our second injection and how will that affect us as far as being protected if we wait another 2 weeks. Patient need to cancel the appointment for our second injection that would be done in the (facility address). The outcome of the events was unknown. Follow-up attempts completed. No further information expected.; Sender's Comments: Linked Report(s) : -PFIZER INC-2021199395 Different patient, same drug and event

Other Meds:

Current Illness:

ID: 1661353
Sex: M
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 09/01/2021
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: have colds; respiratory issue for the last week; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer reported similar events for 2 patients (Herself and Husband). This is 2nd of 2 reports. This consumer reported for a male patient (husband) that: A male patient of unspecified age had received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: unknown), via an unspecified route of administration on unknown date as a single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, patient had colds and their 2nd dose is due tomorrow and have had enough of respiratory issue. Consumer stated, "I am not sure if it is the right place but my husband and I have the COVID-19 Vaccine three weeks ago. We are due to have it again tomorrow but we have had enough of respiratory issue for the last week and my doctor said she thought it would be best if we postpone taking the second dose for at least two weeks and I am trying to let them know that we can't come tomorrow for the appointment to get our second injection and how will that affect us as far as being protected if we wait another 2 weeks". "I am trying to cancel the appointment, how I can I cancel this appointment. At the time of reporting, the outcome of the events were unknown. Follow-up attempts completed. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021199393 Different patient, same drug and event

Other Meds:

Current Illness:

ID: 1661354
Sex: F
Age:
State: IL

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 09/01/2021
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: Broke out into a light pink colored rash on upper torso of body; This is a spontaneous report from a contactable consumer or other non-hcp (Patient). A 62-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection; Lot Number: EN6200) via an unspecified route of administration (age at vaccination 62-year) in Left Arm on 18Feb2021 at 03:15 PM as dose 1, single for COVID-19 immunization. Medical history included known allergies to Doxycycline, Aleve, Augmentin, Benadryl cream, Steristrips; break out into rash with above products. Concomitant medications included levothyroxine; cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]); Bone health supplement; all taken for an unspecified indication, start and stop date were not reported. The patient previously took Doxycycline, Aleve, Augmentin, Benadryl cream experienced allergy. Reported facility type vaccine was Public Health Clinic/Veterans Administration facility. No Covid prior vaccination was reported. The patient not tested Covid post vaccination. The patient received no other vaccine in four weeks. On 18Feb2021 at 09:00 PM the patient experienced broke out into a light pink colored rash on upper torso of body. The patient received no treatment for the adverse event. The clinical outcome of the event was recovered by morning of Saturday, on 20Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds: LEVOTHYROXINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1661355
Sex: F
Age:
State: CA

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data: Test Date: 20210221; Test Name: Body temperature; Result Unstructured Data: Test Result:100.0 degree Fahrenheit

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: fever; sore arm; This is a spontaneous report from a non-contactable other healthcare professional (nurse). A female patient of (Age: 74; Unit Unknown) received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), dose 1 via an unspecified route of administration on 19Feb2021 (Batch/Lot number and Expiry date was not reported) as DOSE 1, SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. On 19Feb2021, the patient experienced sore arm and on 21Feb2021, the patient had fever. Laboratory tests on 21Feb2021 included body temperature was 100.0 degree Fahrenheit (Fever). The patient took Tylenol. The clinical outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number could not be requested. No further information is expected.

Other Meds:

Current Illness:

ID: 1661356
Sex: F
Age:
State: FL

Vax Date: 02/06/2021
Onset Date:
Rec V Date: 09/01/2021
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: Ache at the site of application; joint pain; barely walk; hip pain; back pain; can't even get out of bed and can't even turn when she lay down; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 72-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection, Batch/Lot Number: Not reported), via an unspecified route of administration on 06Feb2021 as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection, Batch/Lot Number: Not reported) 21 days before the second dose for covid-19 immunisation. On an unspecified date, a few days after the second one, she had ache at the site of application but then she felt a little better. After that Friday she got very bad joint pain, she took a pain med, Aleve, and felt better. She still has joint pain and can barely walk. She also had back pain for which she applied Salonpas, and hip pain, stated she can't even get out of bed and can't even turn when she lay down. The patient inquired if was this because of the vaccine. She was wondering if she will have this pain her whole life. Therapeutic measures were taken as a result of joint pain (arthralgia) and back pain. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661357
Sex: F
Age:
State: AL

Vax Date: 01/27/2021
Onset Date: 02/01/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data: Test Date: 20210201; Test Name: urine analysis; Result Unstructured Data: Test Result:some blood in my urine

Allergies:

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

Symptoms: light headache; but I still see my pee is real yellow; saw some blood in my urine; This is a spontaneous report from a contactable consumer (patient). A 76-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection) first dose via an unspecified route of administration on 27Jan2021 (Batch/Lot number was not reported) as single dose and second dose via an unspecified route of administration on 17Feb2021 (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. Medical history included yeast infection and ongoing glaucoma (in my right eye so need to put on glasses to see the names of the prescriptions - preexisting condition). Concomitant medication included fluconazole (tablet, strength: 15 mg) taken for yeast infection and cefdinir (capsule, strength:300 mg). The patient stated, "I wanted to get the vaccine. People tell me not to take the vaccine but I did what I felt I needed to do for me and I am happy about it. I have not had no side effects beside a light headache and I feel good on an unspecified date. On 01Feb2021, I went for my annual check up and they saw some blood in my urine so that's when they gave me the first antibiotic (name not provided) and I took all of them but I still see my pee is real yellow. I decided to call my doctor the other day after my second Pfizer vaccine dose on last Wednesday, 17Feb2021, and they called in these antibiotics that I just picked up: fluconazole and cefdinir (note: When looking up antibiotic names, she stated "I have glaucoma in my right eye so need to put on glasses to see the names of the prescriptions - preexisting condition). They think it's a yeast infection. I have called my doctor to see if it was ok to start taking these but decided to call you as well. I will wait for them to call me back. The patient underwent lab tests and procedures which included urine analysis: some blood in my urine on 01Feb2021.Therapeutic measures were taken as a result of but I still see my pee is real yellow and saw some blood in my urine. The outcome of the event "but I still see my pee is real yellow" was not recovered and other events was unknown. Follow-up attempts completed. No further information expected; Information about lot/Batch number cannot be obtained.

Other Meds: FLUCONAZOLE; CEFDINIR

Current Illness: Glaucoma (right eye so need to put on glasses to see the names of the prescriptions preexisting condition)

ID: 1661358
Sex: F
Age:
State: NJ

Vax Date: 02/21/2021
Onset Date: 02/21/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: About two hours later from injection, my right sinus became inflamed; skin became itchy and red. Started with my left arm and then spread to my chest and neck; skin became itchy and red. Started with my left arm and then spread to my chest and neck; This is a spontaneous report from a contactable consumer. This 32-year-old non pregnant female consumer(patient) reported for herself. A 32-year-old non pregnant female patient received bnt162b2 (PFIZER BIONTECH COVID-19 MRNA VACCINE Solution for injection Lot Number: E19266) via an unspecified route of administration in arm left on 21Feb2021 14:30 as dose 1, single (age at vaccination: 32 years) for COVID-19 immunisation. Medical history included known allergies: walnuts, cats, environmental, all from an unknown date and unknown if ongoing. Concomitant medications were not reported. No other vaccine in four weeks. No covid prior vaccination and did not tested covid post vaccination. On 21Feb2021 2:30PM, the patient experienced after first dose- skin became itchy and red. Started with my left arm and then spread to my chest and neck. About two hours later from injection, my right sinus became inflamed and stayed like that. Seems to be resolving slowly. Treatment received was benedryl. The clinical outcome of the events was resolving. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661359
Sex: F
Age:
State: CA

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 09/01/2021
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: This is a spontaneous report from a contactable consumer or other non-HCP. A female consumer (patient) reported for herself. A 73-year-old (non-pregnant) female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, batch/lot# EN6200, expiration date not reported), age at the vaccination age of 73, via an unspecified route of administration, left arm, on Feb 18, 2021, 10:45, single dose, for COVID-19 immunisation. The patient has no known allergies. Concomitant medication not reported. The patient had a horrible rash all over body, privates and head on Feb 18, 2021. Prior to the vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not tested for COVID-19. The outcome of the event: not recovered. Follow-up (Jun 17, 2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661360
Sex: F
Age:
State: AZ

Vax Date: 02/21/2021
Onset Date: 02/21/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: she had itching both ears and throat; she broke out in a rash, first on her left knee, then on her left leg, then on her right knee, now it's also on her back; This is a spontaneous report from a contactable consumer (patient herself). A 64-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection and lot number: EL9267) via an unspecified route of administration in left arm on 21Feb2021 14:30 as single dose for COVID-19 immunisation. Medical history included crps (Complex regional pain syndrome), svt- super ventricular and allergies to wheat. Concomitant medications included naproxen sodium (ALEVE). Patient previously took codeine and experienced with Allergies. On 21Feb2021 patient stated that she broke out in a rash, first on her left knee, then on her left leg, then on her right knee, now it's also on her back and a little on chest and arms. This morning on 23Feb2021 she had itching both ears and throat. Therapeutic measures were taken as a result of events and the patient took the treatment. The outcome of events was not recovered. Information about lot/ batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds: ALEVE

Current Illness:

ID: 1661361
Sex: F
Age:
State: CO

Vax Date: 02/21/2021
Onset Date: 02/22/2021
Rec V Date: 09/01/2021
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: I then had a high fever; body aches; I got intense arm pain; a headache; This is a spontaneous report from a contactable consumer or other non health care professional. A 38-years-old non-pregnant female patient received bnt162b2 (solution for injection, Age at Vaccination: 38-years), dose 1 via an unspecified route of administration, administered in Arm Left on 21Feb2021 12:15 (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunization at Doctors office/urgent care. Medical history included covid-19 from an unknown date in January month and unknown if ongoing. The patients concomitant medications were not reported. There were no allergies. No other vaccine in four weeks. It was unknown that covid tested post vaccination. The patient experienced intense arm pain and headache on 22Feb2021 at 12:00. The headache continued the following day. The patient had a high fever and body aches on 23Feb2021. No treatment was required for adverse events (AE). The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1661362
Sex: M
Age:
State:

Vax Date: 02/22/2021
Onset Date:
Rec V Date: 09/01/2021
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: FEVER; Result Unstructured Data: Test Result:mild 99 degree fever; Test Name: pain scale; Result Unstructured Data: Test Result:9 out of 10

Allergies:

Symptom List: Tremor

Symptoms: muscle pain; unable to sleep; tendonitis; fever; shoulder pain; This is a spontaneous report from a contactable consumer (patient). A 72-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number was not reported, expiration date was not reported), via an unspecified route of administration on 22Feb2021 as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient historical vaccine included first dose of BNT162B2 for COVID-19 immunization received on 22Jan2021. It was reported that, Patient is male, aged 72, received first Pfizer vaccine on 22Jan2021 and his second Pfizer vaccine on 22Feb2021. He developed very bad muscle pain in the arm muscle where he was injected. He says at night it reaches a 9 out of 10 on the pain scale. He is unable to sleep. He went to the doctor and he said it may be tendonitis. He also experienced a mild 99 degree fever and a little shoulder pain. Patient was asking are these common side effects of the vaccine and Dr prescribed Medrol dose pack for patient, is this okay to take right after receiving second vaccine. The patient underwent lab tests and procedures which included FEVER (body temperature): mild 99 degree fever on an unspecified date, pain scale (pain assessment): 9 out of 10 on an unspecified date. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1661363
Sex: F
Age:
State: GA

Vax Date: 02/18/2021
Onset Date: 02/19/2021
Rec V Date: 09/01/2021
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: Swelling; Itching; This is a spontaneous report from a contactable consumer or other non hcp. A 40-years-old non-pregnant female patient received second dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: el9264) dose 2 via an unspecified route of administration, administered in Arm Left on 18Feb2021 08:45(age at vaccination:40 Years) as DOSE 2, SINGLE for covid-19 immunisation. Patient didn't receive other vaccines within 4 weeks prior to vaccination, Patient had received other medications Nifedipine, Xolair, Symbicort, Flonase, Vitamin D within 2weeks of vaccination. Medical history included asthma from an unknown date and unknown if ongoing, hypertension from an unknown date and unknown if ongoing, food allergy (sea food) from an unknown date and unknown if ongoing, food allergy (shellfish) from an unknown date and unknown if ongoing, food allergy (peanuts, tree nuts) from an unknown date and unknown if ongoing, anaphylactic shock from an unknown date and unknown if ongoing. Concomitant medications included nifedipine (NIFEDIPINE) taken for an unspecified indication, start and stop date were not reported; omalizumab (XOLAIR) taken for an unspecified indication, start and stop date were not reported; budesonide, formoterol fumarate (SYMBICORT) taken for an unspecified indication, start and stop date were not reported; fluticasone propionate (FLONASE ALLERGY RELIEF) taken for an unspecified indication, start and stop date were not reported; cholecalciferol (VITAMINE D) taken for an unspecified indication, start and stop date were not reported. Patient didn't had covid prior to vaccination. Patient previously received first dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: el3248) via unspecified route of administration in Arm right on 28Jan2021 14:30(age at vaccination:40 years) as DOSE 1, SINGLE for covid-19 immunisation. No Therapeutic measures were taken for the events. Patient was not tested for covid to post vaccination. On 19Feb2021 the patient experienced swelling, itching. The outcome of the events swelling pruritus was recovering. Follow-up attempts completed. No further information expected.

Other Meds: NIFEDIPINE; XOLAIR; SYMBICORT; FLONASE ALLERGY RELIEF; VITAMINE D

Current Illness:

ID: 1661364
Sex: F
Age:
State: CA

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 09/01/2021
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: my tongue was dry; tongue swelling slightly; This is a spontaneous report from a contactable consumer. A 43-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6200) dose 1 administered in Arm Right via an unspecified route, on 18Feb2021 14:00 (Age at vaccination: 43 years old) as DOSE 1,SINGLE for covid-19 immunisation. Medical history included urticaria, fungal infection and scoliosis.The patient experienced drug hypersensitivity previously from aspirin/salicins, monistat varieties, tobramycin/dexamethasone.The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.The patient did not receive any other medications in two weeks prior to the COVID vaccine. The patient experienced tongue was dry and tongue swelling slightly on 18Feb2021 14:15. Patient was given two Benadryl thirty minutes after the vaccination.Within 2 hrs, patient felt her tongue was not swelling or dry.The outcome of the events are recovered on 18Feb2021. Follow-up (13May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661365
Sex: F
Age:
State: CA

Vax Date: 02/16/2021
Onset Date: 02/16/2021
Rec V Date: 09/01/2021
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: asthma; vaccine was not administered in the deltoid, it was given like in the tricep; This is a spontaneous report from a contactable physician. This physician reported for 2 patients. This is 2nd of 2 reports. A female patient of an unspecified age received bnt162b2 (BNT162B2), via an unspecified route of administration on 16Feb2021 (Batch/Lot number was not reported) as DOSE NUMBER, UNKNOWN, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced vaccine was not administered in the deltoid, it was given like in the triceps leading to product administered at inappropriate site on 16Feb2021 and asthma on an unspecified date with outcome of unknown. Follow-up (17Feb2021): This is a follow-up spontaneous report from a contactable physician. This physician reported for a patient that: Describes the administration site on himself as "from the shoulder 7 inches down and then from the elbow it's another 7 inches. Also would like to know what should be done if this is considered to be an incorrect injection site. Information on the lot/batch number has been requested. Follow-up (12May2021): Follow-up attempts completed. No further information expected.; Sender's Comments: Linked Report(s) :-PFIZER INC-2021170851 same reporter/drug/AE with different patient

Other Meds:

Current Illness:

ID: 1661366
Sex: F
Age:
State: TX

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Chest felt odd; then rapid heartbeat began about 25 min after injection; Headache; This is a spontaneous report from a contactable consumer (patient). A 72-years-old non pregnant female patient received first dose of bnt162b2 (BNT162B2, Solution for injection, Lot Number: EL9269) via an unspecified route of administration, administered in left arm on 05Feb2021 13:45 (at the age of 72 years-old) as dose 1, single for COVID-19 immunization (Hospital). Patient medical history included ongoing hypothyroidism and insulin resistance, along with supraventricular tachycardia, and obesity unknown if both ongoing. Concomitant medications included levothyroxine sodium (UNITHROID), chlorthalidone (CHLORTHALIDONE), finasteride (FINASTERIDE), and colecalciferol (VIT D3) and zinc all taken for an unspecified indication. The patient previously took codeine, morphine, statins and experienced drug hypersensitivity. On 05Feb2021, after 15 minutes of drug administration, the patient's chest felt odd, followed by rapid heartbeat began about 25 minutes after injection and headache. The patient did not have COVID tested post vaccination and did not have COVID prior vaccination. Patient took no other vaccine within four weeks of drug administration. Patient did not receive any treatment. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: UNITHROID; CHLORTHALIDONE; FINASTERIDE; VIT D3; ZINC

Current Illness: Hypothyroidism; Insulin resistance

ID: 1661367
Sex: F
Age:
State: NJ

Vax Date: 02/08/2021
Onset Date: 02/12/2021
Rec V Date: 09/01/2021
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: red rash on the chest area (under breast); This is a spontaneous report from a contactable consumer or other non hcp (patient herself). A 76-years-old female patient received bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration on 08Feb2021 13:00 as dose 1, single in Left arm for COVID-19 immunisation. The patient medical history was not reported. The patient was not pregnant. There were no known allergies. No other vaccine in four weeks. No COVID prior vaccination. Patient was not tested for COVID post vaccination. There were no concomitant medications. On 12Feb2021, the patient experienced red rash on the chest area (under breast). Therapeutic measures were not taken as a result of adverse event. The outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661368
Sex: F
Age:
State: CA

Vax Date: 02/16/2021
Onset Date: 02/01/2021
Rec V Date: 09/01/2021
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: Severe Headache; significant arm pain again -decrease ROM to less 90'; significant arm pain again -decrease ROM to less 90'; Body aches; significant joint pains-especially in hands and wrists; This is a spontaneous report from a contactable other-HCP (Nurse, patient herself). A 55-year-old female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EN 6201) intramuscularly in right arm on 16Feb2021 11:45 as dose 2, single (at the age of 55-years-old) for COVID-19 immunization. Patient was not pregnant at the time of vaccination. Vaccination facility type was reported as Hospital. Patient did not receive any other vaccine in four weeks. Patient medical history were reported as liver injury from 1986 to 1986, blood transfusion for lacerated liver repair, seasonal allergy, allergy to cats and dogs (animal), various Trees and various Nuts. Patient known allergies included allergies to Synalgos, Zyrtec. The concomitant medications were reported as estrogens conjugated, progesterone, mesterolone (RESTORE) taken for an unspecified indication, start and stop date for all medications were not reported. Historical vaccine included BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EL3246) intramuscularly in left arm on 26Jan2021 as dose 1, single for COVID-19 immunization. Patient experienced significant arm pain, with decrease ROM to less 90, chills, brain fog, felt agitated and unsettled, headache as moderate with the first dose which lasted 3 days. Patient experienced significant arm pain again, decreased ROM to less than 90, severe headache, body aches and significant joint pains especially in hands and wrists on an unspecified date in Feb2021 which lasted for 3 days. The patient did not receive any treatment for the adverse events. The outcome of the events was resolved on an unspecified date in Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds: ESTROGENS CONJUGATED; PROGESTERONE; RESTORE

Current Illness:

ID: 1661369
Sex: F
Age:
State: IN

Vax Date: 02/23/2021
Onset Date: 02/24/2021
Rec V Date: 09/01/2021
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: fever; Result Unstructured Data: Test Result:100.1

Allergies:

Symptom List: Pain in extremity

Symptoms: Severe arm pain; numbness and tingling in left arm; tingling in left arm; night chill/sweats; night chill/sweats; fever 100.1; headache; feeling unwell; This is a spontaneous report from a contactable other hcp (Nurse) (patient). A 35-year-old (non-pregnant) female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6201) via an unspecified route of administration, administered in arm left on 23Feb2021 16:30 (at the age of 35-year-old) at dose 1, single for covid-19 immunisation. Medical history was reported as none. Concomitant medications were not reported. Other medications in two weeks: Sprinters. Patient had no known allergies. Patient did not have other vaccine in four weeks. Patient did not have covid prior vaccination. Patient was not tested for covid post vaccination. On 24Feb2021 16:00 the patient experienced severe arm pain, numbness and tingling in left arm, night chill/sweats, fever 100.1, headache, feeling unwell. The patient underwent lab tests and procedures which included fever: 100.1 on an unspecified date. Patient did not receive treatment for the adverse events. Outcome of the events was not resolved. Follow-up (25May2021): Follow-up attempts completed. No further information expected

Other Meds:

Current Illness:

ID: 1661370
Sex: F
Age:
State: CT

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Nausea all the day; Tiredness; chills evening; severe heartburn; High Blood Pressure; vertigo when got out of Bed; Joint pain in shoulder; This is a spontaneous report from a contactable consumer or other non hcp. A 69-year-old female non pregnant patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in left arm on 19Feb2021 17:00 (age at vaccination 69-year-old, Batch/Lot number was not reported) as single dose for COVID-19 immunisation. Medical history included hepatitis C (recovered), cholelithiasis from an unknown date and unknown if ongoing. Concomitant medications included colecalciferol, menaquinone-7 (VITAMIN D3 K2) and ubidecarenone (COQ 10) taken for an unspecified indication, start and stop date were not reported. Patient had no known allergies. It was reported that facility type vaccine was hospital and no other vaccine in four weeks. No COVID prior vaccination and no COVID tested post vaccination. On 19Feb2021, the patient experienced joint pain in shoulder above the injection (adverse event Day1). Next morning she had vertigo when got out of bed on 20Feb2021. On 21Feb2021 (Day 3) she had high blood pressure. On 22Feb2021 (Day 4), she had vertigo in morning /high blood pressure and severe heartburn in evening. On 23Feb2021 (Day 5), she had nausea all day and tiredness and chills evening. It was reported that on day 6, she had tiredness and some chills. Patient not received treatment. The outcome of all events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: VITAMIN D3 K2; COQ 10

Current Illness:

ID: 1661371
Sex: F
Age:
State: CT

Vax Date: 02/22/2021
Onset Date: 02/22/2021
Rec V Date: 09/01/2021
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: Cold sore on my upper lip; Injection site soreness; Migraine; Headache; This is a spontaneous report from a contactable consumer (patient herself). A 52-years-old non-pregnant female patient received first dose of BNT162B2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number and expiration date was not reported) via an unspecified route of administration, administered in Arm Left on 22Feb2021 11:30 (at age of 52-years-old) as DOSE 1, SINGLE for COVID-19 immunization. The patient was not pregnant at the time of vaccination. No medical history and concomitant medications were reported. Patient had not known allergies. Other medical history was no. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine nor received any other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. On 22Feb2021 21:30 the patient experienced injection site soreness, migraine and headache while patient experienced cold sore on my upper lip on 23Feb2021. Patient did not receive any treatment for AEs. Since the vaccination, patient has not been tested for COVID-19. The outcome of all events was recovering. Information about lot batch requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661372
Sex: F
Age:
State: MI

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 09/01/2021
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: Itching; Swelling of injection site; Sore throat; This is a spontaneous report from a contactable other hcp (patient). A 35-years-old female (non pregnant) patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL3248 and Expiration Date was not reported), via an unspecified route of administration administered in Arm Left on 18Jan2021 as dose 2, single for COVID-19 immunization. Medical history included , food allergy from an unknown date and unknown if ongoing Verbatim known allergies: Almonds , arthropod sting from an unknown date and unknown if ongoing Verbatim known allergies: bee stings , glucose tolerance impaired from an unknown date and unknown if ongoing other medical history : Pre-diabetes. The patient's concomitant medications were not reported. Patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL0140 and Expiration Date was not reported), via an unspecified route of administration administered in Arm Left on 26Dec2020 as dose 1, single for COVID-19 immunization. Patient did not receive any other vaccine in four weeks. The patient was not diagnosed with COVID-19 prior to vaccination. Post vaccination the patient was not tested for COVID 19. On 18Jan2021, the patient experienced itching, swelling of injection site and sore throat. Patient received treatment of Ibuprofen for adverse events.The outcome of the events was recovered in 2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661373
Sex: F
Age:
State: NC

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 09/01/2021
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: Red itchy sore blotch on upper left arm (although not exactly at vaccination site); Red itchy sore blotch on upper left arm (although not exactly at vaccination site); Red itchy sore blotch on upper left arm (although not exactly at vaccination site); This is a spontaneous report from a contactable consumer (patient). A 67-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EN6203), dose 2 via an unspecified route of administration, administered in Arm Left on 22Feb2021 11:45 as dose 2, single for COVID-19 immunization. The patient medical history was not reported. Concomitant medication(s) included venlafaxine, glucosamine and multivitamin taken for an unspecified indication, start and stop date were not reported (Other medications in two weeks). The patient was not pregnant at the time of vaccination. The patient previously received first dose of BNT162B2 (Lot number: EL8982), via an unspecified route of administration, administered in Right arm on 01Feb2021 11:45 AM for COVID-19 immunization. The patient did not receive any other vaccines in 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had not been tested for COVID-19. Patient did not know about known allergies. Facility where COVID-19 vaccine was administered at Doctor office/urgent care. On 23Feb2021 22:00, patient experienced red itchy sore blotch on upper left arm (although not exactly at vaccination site). There was no treatment for the events. The clinical outcome of events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: VENLAFAXINE; GLUCOSAMINE

Current Illness:

ID: 1661374
Sex: F
Age:
State: NY

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: tightness in face; saliva glands ached; prickly sensation; slight "asthma-like" breathing; hot flash lasting 20 min; dizziness; nausea upon standing; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 53-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection) via an unspecified route of administration, administered in Arm Left on 24Feb2021 at 09:30 am (Batch/Lot Number: EN6203) as dose 1, single for covid-19 immunization (at the age of 53-years-old). Medical history included diabetes, HBP (high blood pressure) and heart murmur from an unknown date and unknown if ongoing. Patient had known allergies to BHT/BHA preservatives. Concomitant medication(s) included metformin; amlodipine and furosemide all were taken for an unspecified indication, start and stop date were not reported. Patient had not received any other vaccine in four weeks. Patient had no if covid prior vaccination. Patient had not tested for covid post vaccination. Facility type vaccine was reported as other. It was reported that after receiving the dose of vaccine on 24Feb2021 at 10:00 pm the patient experienced tightness in face, saliva glands ached, prickly sensation, slight "asthma-like" breathing, hot flash lasting 20 min, dizziness and nausea upon standing. Patient had not received any treatment. Patient was recovering from the events at the time of report. Follow-up attempts completed. No further information expected.

Other Meds: METFORMIN; AMLODIPINE; FUROSEMIDE

Current Illness:

ID: 1661375
Sex: F
Age:
State: FL

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data: Test Date: 20210223; Test Name: Body temperature; Result Unstructured Data: Test Result:100; Test Name: MRI; Result Unstructured Data: Test Result:Unknown result

Allergies:

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

Symptoms: Lymph nodes under arm hurt; Fever; Chills; Muscle aches and pain; Truly feeling lousy; Headache; Itchy but no hives; nausea; Weak; This is a spontaneous report from a contactable consumer (patient herself). A 68-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267), via an unspecified route of administration, administered in right arm on 23Feb2021 10:00 (age at vaccination: 68 years) as DOSE 2, Single for covid-19 immunisation. The patient's medical history included ongoing just diagnosed with ductal carcinoma in situ breast cancer (recently had mri with contrast). The patient's concomitant medications were not reported. The patient did not have no known allergies. The patient's historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unknown date as DOSE 1, single. The patient did not have any other vaccine in four weeks. On 23Feb2021 22:15, the patient experienced lymph nodes under arm hurt, fever, chills, muscle aches and pain, truly feeling lousy, headache, itchy but no hives, nausea and weak. The patient received Tylenol as treatment for the adverse events. On 23Feb2021, the patient's body temperature was 100 and on an unknown date, magnetic resonance imaging with unknown result. The patient did not have covid prior vaccination nor was tested since vaccination. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1661376
Sex: F
Age:
State: TX

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 09/01/2021
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: Headache; severe joint pain; flush face; snow chills; injection site pain; This is a spontaneous report from a contactable consumer. This 49-Year-old female consumer (Patient) reported that: A 49-years-female patient (non-pregnant) received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: not provided), via an unspecified route of administration, administered on left arm (age at the vaccination was 49 years) on 22Feb2021 02:45 PM at single dose for COVID-19 immunisation. Patient previously had first dose of bnt162b2. Patient medical history included Hypothyroidism, migraines and knee/foot surgeries. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No known allergies. Patient concomitant medications included Tylenol, Excedrine and ibuprofen, prescriptions. On 23Feb2021 10:00Am, patient had experienced headache, severe joint pain, flush face, snow chills and injection site pain (Vaccination site pain).. No treatment was received in response to the adverse events. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient was not tested for COVID-19. On an unspecified date in 2021, the outcome of the events were recovered. Follow-up attempts completed. No further information expected.

Other Meds: TYLENOL; EXCEDRIN; IBUPROFEN

Current Illness:

ID: 1661377
Sex: M
Age:
State: MI

Vax Date: 01/25/2021
Onset Date: 02/03/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data: Test Name: Qualitative PCR; Result Unstructured Data: Test Result:Positive

Allergies:

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

Symptoms: I lost most of my sense of taste for two days; This is a spontaneous report from a contactable consumer (patient). A 67-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via unknown route of administration at left arm on 25Jan2021 at 07:00 PM (lot number: EL3247) (age at vaccination 67-year-old) as dose 1, single for COVID-19 immunisation. The patient had allergy to toradol. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient did not take any other medications within two weeks prior to the vaccination. Prior to vaccination, the patient was diagnosed with COVID-19 (early November). The patient medical history and concomitant medications were not reported. Since the vaccination, has the patient was not tested for COVID-19. The patient had lost most of the sense of taste for two days on 03Feb2021. The patient had not received any treatment for the event. The outcome of the event was recovered on an unspecified date. Follow-up attempts completed. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021226820 same drug and AE, different patient;US-PFIZER INC-2021226818 same drug and AE, different patient;US-PFIZER INC-2021226817 same drug and AE, different patient;US-PFIZER INC-2021226819 same drug and AE, different patient

Other Meds:

Current Illness:

ID: 1661378
Sex: U
Age:
State: IN

Vax Date: 02/18/2021
Onset Date: 02/22/2021
Rec V Date: 09/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Headache; Injection site pain; tiredness; chills; joint pain; Nausea; feeling unwell; This is a spontaneous report from a contactable consumer(patient) reported that. A 66-years-old patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 18Feb2021 09:00 (Batch/Lot Number: Pfizer Eng201) as DOSE 1 SINGLE for covid-19 immunization(Age at vaccination 66 years). The patient Medical history included compression fracture L1 vertebrae from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. There were no allergies reported. The patient did not receive any other vaccine within 4 weeks prior to covid-19 vaccination. On 22Feb2021, the patient experienced headache, injection site pain, tiredness, chills, joint pain, Nausea and feeling unwell. No treatment was reported. The event outcome was not recovered. 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