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**
PLEASE CHECK BACK SOON
Download the files above while you wait.







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: 1647820
Sex: F
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: Electrolyte; Result Unstructured Data: Test Result:Unknown results; Test Name: CBC; Result Unstructured Data: Test Result:Unknown results; Test Name: Hormone; Result Unstructured Data: Test Result:Unknown results; Test Name: AMC; Result Unstructured Data: Test Result:Normal

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: I have a little bit of pain; My nose has like a little bit irritation and little bit asthma; My nose has like a little bit irritation and little bit asthma; This is a spontaneous report from a contactable consumer (patient reported for herself). A 51-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number: E or FJ168), dose 1 via an unspecified route of administration on 11Jan2021 (at the age of 51-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included autoimmune Auto immune condition, sjogren's syndrome from 2015 to an unknown date, fibromyalgia and covid-19 from Apr2020 to an unknown date. The patient was a respiratory therapist. Concomitant medication(s) included Ciclosporin (RESTASIS) taking for her eyes; Famotidine (PEPCID [FAMOTIDINE]); Albuterol [salbutamol] (ALBUTEROL [SALBUTAMOL]) and Estradiol (ESTROGEN), all taken for an unspecified indication, start and stop date were not reported. On an unspecified date in Jan2021, after the first dose of vaccination, the patient experienced a little bit of pain, her nose had like a little bit irritation and little bit asthma, which the patient thought it was a weather. The patient underwent lab tests and procedures on an unspecified date in 2021 included blood electrolytes: unknown results, full blood count: unknown results, Hormone test: unknown results, absolute monocyte count: normal. The patient outcome of the events was unknown at the time of this report. Follow-up attempts completed. No further information expected.

Other Meds: RESTASIS; PEPCID [FAMOTIDINE]; ALBUTEROL [SALBUTAMOL]; ESTROGEN

Current Illness:

ID: 1647821
Sex: F
Age:
State: CO

Vax Date: 01/30/2021
Onset Date: 01/31/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Allergic reaction to the vaccine; Have like a nerve down on my shoulder and down my arm and down my forearm; It is like a pain on my back down; Have like a nerve down on my shoulder and down my arm and down my forearm; It is like a pain on my back down; I broke out in hives. I had it on my left back, on my left arm; This is a spontaneous report from a contactable consumer. A 79-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Batch/Lot Number: EL9264), dose 1 via an unspecified route of administration on 30Jan2021 at noon (at the age 79-years-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history included blood cholesterol increased (High Cholesterol), gout and hypertension (High Blood Pressure) from an unknown date and unknown if on-going. Concomitant medications included allopurinol (ALLOPURINOL) taken for gout, losartan (LOSARTAN) and simvastatin (SIMVASTATIN) taken for an unspecified indication, start and stop date were not reported. Patient got a hold of somebody today and talked to her here at Pfizer (Further clarification was unknown, hence checked as initial report). She said she wanted patient to talk to the medical group and so patient call this number. Patient did not know, could find patient in computer because patient typed everything told her. Patient had a Pfizer vaccine on 30Jan first vaccine. Patient had it at noon, next day, broke out in hives. Patient had it on left back, on left arm. Patient had lot of hives. Patient called up a nurse at ER hospital and went to (Hospital name withheld). The doctor told, he said, patient have an allergic reaction to the vaccine. He said he gave prednisone but he said that would kill the vaccine. So he said what I want you to do is if you can wait till Monday and take it around noon and then you will have 48 hours for vaccine in you. Patient waited for Monday and he said if you get any-more hives make sure you take it then. Well, Patient got more hives. So patient had 5 days of 40 mg on each day, each morning patient took that for 5 days. Patient still have the hives. Patient was doing okay. Patient had like a nerve down on my shoulder and down arm and down forearm, that developed that patient never had before. It was like a pain on back down. So, patient just want to know Patient did not want to take second shot. Patient was afraid to take the second shot because patient was allergic to this one. Treatment include Prednisone. The outcome of the event urticaria was unknown while other events were unknown. Follow-up attempts completed. No further information expected.

Other Meds: ALLOPURINOL; LOSARTAN; SIMVASTATIN

Current Illness:

ID: 1647822
Sex: F
Age:
State: KY

Vax Date: 02/12/2021
Onset Date: 02/13/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Itchy red bump/rash around injection site; Itchy red bump/rash around injection site; This is a spontaneous report from a contactable consumer (patient). A 34-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL9269) via an unspecified route of administration in left arm on 12Feb2021 at 18:30 (at the age of 34-year-old) as single dose for COVID-19 immunization. Medical history of the patient included seasonal allergies. Concomitant medications/other medications in two weeks included ethinylestradiol, ferrous fumarate, norethisterone acetate [LO LOESTRIN FE], cetirizine hydrochloride [ZYRTEC], montelukast sodium [SINGULAIR], naproxen sodium [ALEVE] all taken for unspecified indications. Patient did not receive any other vaccine in four weeks of COVID-19 vaccine. Patient did not have COVID prior vaccination and was not tested for COVID post vaccination. Patient previously took Sulfa drug on an unspecified date and experienced allergy. Patient previously received first of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EJ9262) via an unspecified route of administration in right arm on 21Jan2021 at 18:15 as single dose for COVID-19 immunization. On 13Feb2021 at 22:00 patient experienced Itchy red bump/rash around injection site. No treatment was received in response to the event. Outcome of the event was not resolved. Follow-up attempts completed. No further information expected.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; LO LOESTRIN FE; SINGULAIR; ALEVE

Current Illness:

ID: 1647823
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Caller heard a doctor state he had a fever for 24 hours after the covid vaccine (doesn't specify which one); This is a spontaneous report from a contactable other HCP. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced caller heard a doctor state he had a fever for 24 hours after the covid vaccine (doesn't specify which one) on an unspecified date. She has two questions. She is getting the second vaccine today. When they were there getting the first one, the nurse said she had reaction from the second shot. She advised caller to take Tylenol before the second. Since then caller has read that you are not supposed to take Tylenol, Advil, or pain medication because it will decrease the effectiveness of the vaccine. She doesn't want to do that. She wanted to know what Pfizer's protocol or recommendation would be. Her neighbor said she had heard not to take it, but then read that the county said you can't take it before but you can take it after. How long is the effectiveness. She read something two days ago that said it is only good for 3 months. It didn't say Pfizer specifically. Caller clarified product as COVID19 Vaccine. The doctor that put caller on the list, because she is over 65 and it is hard to get the vaccine, said he had a fever and it was the best fever he ever had because it was helping him. Caller is a 65 y/o female. She received her first dose of the Pfizer Covid vaccine and reports she had a sore arm and swollen neck glands the following day. She says it lasted for several days and also experienced fatigue. She is getting her second dose of the vaccine 12Feb2021 and wants to know if it's ok to take a pain reliever before or after the vaccine is given. Additional AE information: caller reports a nurse at the vaccination site is telling recipients to take tylenol before the vaccine because she had a fever after the Pfizer vaccine. Caller's aunt was freezing after receiving the Moderna vaccine. Caller heard a doctor state he had a fever for 24 hours after the covid vaccine (doesn't specify which one). Caller wants to know if Pfizer is creating a booster to address the new variants of the Covid virus. Outcome of the event was unknown. Information about the Lot/batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647824
Sex: F
Age:
State: CA

Vax Date: 02/05/2021
Onset Date: 02/10/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Rash and itchy arms especially left arm which was vaccinated; Rash and itchy arms especially left arm which was vaccinated; This is a spontaneous report from a contactable consumer. A 71-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), dose 1 via an unspecified route of administration, administered in Arm Left on 05Feb2021 16:30 (at the age of 71-years-old) as a single dose for covid-19 immunization. Medical history included diabetes mellitus, blood cholesterol increased. Concomitant medication(s) in two weeks included metformin; atorvastatin (LIPITOR [ATORVASTATIN]). The patient was not pregnant at the time of vaccination. The patient did not have any allergies. The patient had no other vaccine within four weeks. 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 10Feb2021 16:00, the patient experienced rash and itchy arms especially left arm which was vaccinated (5th day after vaccination). Need to know if 2nd dose can be taken or not. Claritin taken on 12th and Benadryl taken on 14th as itching and rash are persistent. Applied hydrocortisone cream as well for itching on 14Feb2021. The patient recevied treatment for adverse events. Outcome of the event was not recovered, at the time of this report. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds: METFORMIN; LIPITOR [ATORVASTATIN]

Current Illness:

ID: 1647825
Sex: F
Age:
State: CA

Vax Date: 02/11/2021
Onset Date: 02/11/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: significant right armpit lymph node swelling; fatigue; headache; lymph node swelling is quite large, painful and concerning; This is a spontaneous report from a non-contactable other hcp (patient). A non-pregnant 46-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number: EN6201, Expiration date were not reported), via an unspecified route of administration administered in the right arm on 11Feb2021 00:15 (at the age of 46-years-old), as dose 2, single for COVID-19 immunisation. Medical history included Environmental allergies and topical product allergies in soaps and cosmetics but no medications. The patient had no concomitant medications. Patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number: EL8982, Expiration date were not reported), via an unspecified route of administration administered in the right arm on 21Jan2021 00:00 (at the age of 46-years-old), as dose 1, single for COVID-19 immunization and experienced injection site rash. Prior to vaccination, the patient was not diagnosed with COVID-19; and since the vaccination, has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. The patient experienced significant right armpit lymph node swelling, fatigue, headache, and lymph node swelling is quite large, painful and concerning on 11Feb2021 19:00. No treatment was received as a result of the events. The outcome of events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1647826
Sex: M
Age:
State: CA

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Pain radiating from lower back to backside of left leg (mostly thigh but also calf). Particularly when getting up after rest or sitting.; This is a spontaneous report from a non-contactable other healthcare professional (patient). A 40-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/lot number: EN6201; Expiration date was not reported), via an unspecified route of administration in the right arm on 11Feb2021 08:00 AM (at the age of 40-years-old) as dose 1, single for COVID-19 immunisation. Medical history included polycystic kidney disease from an unknown date and unknown if ongoing. The patient has no concomitant medications. No other vaccine was received by the patient in four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient has not been tested for COVID-19. The patient has no known allergies. The patient experienced pain radiating from lower back to backside of left leg (mostly thigh but also calf), particularly when getting up after rest or sitting on 12Feb2021 08:00 AM. Treatment with ibuprofen and paracetamol was taken for the event. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1647827
Sex: F
Age:
State: NY

Vax Date: 01/07/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: Electrolyte; Result Unstructured Data: Test Result:Unknown

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: I am still having like arm pain in my left arm; I get like tingling and now it is little weak; I get like tingling and now it is little weak; This is a spontaneous report from a contactable consumer (patient). A 52-years-old female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL0142, Expiration date: 21Mar2021), via an unspecified route of administration on 07Jan2021 (at the age of 52-years) as dose 2, single for covid-19 immunisation. The patient medical history included high blood pressure. The patient concomitant medications included Vitamins from an unknown date and unknown if ongoing. The patient previously first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EK5730, Expiration date: 20Mar2021), via an unspecified route of administration on 17Dec2020 (at the age of 52-years) as dose 1, single for covid-19 immunisation. On unspecified date, the patient experienced still having like arm pain in my left arm and get like tingling and now it was little weak. The patient received treatment for events with Advil, Tylenol. Patient stated that "After the second vaccine I noticed, but then like 2 days after the second one and then it just has not stopped, like sometimes it start tingling so bad that I have to open up my hand few times and almost like it went to the sleep, it just, I don't know it just hurts, yes few days after the vaccine. Recently yes, I have, yeah, they actually just checked it just to make sure my electrolyte is good, which was fine. It is just under control, I am taking medication for it." The outcome of the events was not recovered. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds: VITAMINS NOS

Current Illness:

ID: 1647828
Sex: F
Age:
State: NY

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210212; Test Name: Low grade fever; Result Unstructured Data: Test Result:99.4

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Low grade fever (99.4); Couldn't sleep after second dose/Woke up feeling just like I haven't slept; Got progressively achy in joints as day went on; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 26-years-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIOTEH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: el3247), via an unspecified route of administration, administered in Arm Left on 11Feb2021 15:30 (Age at vaccination: 26-years-old) as single dose for covid-19 immunization. Medical history included prior solid organ transplant from an unknown date and unknown if ongoing. Concomitant medication included ciclosporin (NEORAL) taken for an unspecified indication, start and stop date were not reported. Historical vaccine included first dose of BNT162B2 (BNT162B2, PFIZER-BIOTEH COVID-19 VACCINE, Solution for injection, Lot number el3247), via an unspecified route of administration, administered in Arm Left on 20Jan2021 12:00 PM (Age at vaccination: 26-years-old) as single dose for covid-19 immunization (Vaccination facility: Workplace clinic). The patient previously took azithromycin and experienced drug hypersensitivity. Patient did not receive other vaccine in four weeks. Patient had no covid prior vaccination. It was reported that on 12Feb2021, patient could not sleep after second dose. Woke up feeling just like she have not slept. Got progressively achy in joints as day went on. Low grade fever (99.4) at 7 pm day following second dose. It was unknown if patient received treatment for the events. Patient did not tested for covid post vaccination. The patient underwent lab tests and procedures which included body temperature: 99.4 on 12Feb2021. The outcome for the events was reported as recovering at the time of this report. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds: NEORAL

Current Illness:

ID: 1647829
Sex: F
Age:
State: TX

Vax Date: 02/11/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Nausea; Short of breath; weird sensation in head; racing heart; headache; slight tremor in head, arms and hands; extreme fatigue; This is a spontaneous report from a contactable consumer or other non-health care professional. A 64-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EN6201), via an unspecified route of admin-istration (at the age of 64-years), administered in arm left on 11Feb2021 at 12:00 as dose 1, single for COVID-19 immunization. Medical history included allergies to medications, food, or other products from an unknown date and unknown if ongoing. The patient concomitant medications were not re-ported. The patient did not take any other vaccine in four weeks. Patient does not have covid prior vaccination and had not been tested for covid post vaccination. On 11Feb2021 within 15 minutes after dose administration at 12:15, the patient experienced short of breath, weird sensation in head, racing heart, headache, slight tremor in head, arms and hands. Next day on 12Feb2021, experienced nausea. On an unknown date in Feb2021, experienced extreme fatigue. The treatment was not received for the all the events. The vaccination facility type was reported as school. The clinical outcome for all the events was reported as recovering. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647830
Sex: F
Age:
State:

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: eventually broke out into massive rash of armpits and torso; skin irritation itchiness; skin irritation itchiness; This is a spontaneous report from a non-contactable consumer (patient). A 50-years-old non-pregnant female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration, administered in right arm on 26Jan2021 at 12:00 hours as dose 1, single (at the age of 50-years-old) for COVID-19 immunisation. Medical history included hypothyroid from an unknown date and unknown if ongoing. Patient had no known allergies. Patient had no other vaccine in four weeks. Concomitant medication(s) included metronidazole benzoate (Flagyl) and doxycycline (both taken for an unspecified indication, start and stop date were not reported). Patient was not diagnosed with COVID-19, prior to vaccination and had not been tested for COVID-19 post vaccination. On 26Jan2021 at 15:00 hours, patient had skin irritation, itchiness which eventually broke out into massive rash of armpits and torso. Patient had doctor or other healthcare professional office/clinic visit for the events. Therapeutic measures were taken as a result of all the events and treatment included fluconizole oral and hydrocortisone topical. The outcome of all the events was not recovered. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds: FLAGYL [METRONIDAZOLE BENZOATE]; DOXYCYCLINE

Current Illness:

ID: 1647831
Sex: U
Age:
State:

Vax Date: 02/09/2021
Onset Date: 02/10/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: I have a swelling under my left arm; like about the size of half of an orange; it hurts; This is a spontaneous report from a contactable consumer (Patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EM9810, Expiry date was not reported), via an unspecified route of administration on 09Feb2021 in Arm left as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications was not reported. Previously patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot Number: EL0142 and Expiry date was not reported), via an unspecified route of administration on unspecified date as dose 1, single for COVID-19 immunization. On 10Feb2021, patient received the second dose of her/his vaccine (Covid-19 Vaccine by Pfizer) on Tuesday morning and he/she felt yesterday and this morning, he/she have a swelling under his/her left arm where it was given on the left arm like about the size of half of an orange and he/she know its listed swollen lymph node as possible side effects but he/she expected something like size of an almond not an orange, so he/she wondering if that was a problem and it hurts, so patient wondering if there was something that he/she can do about it and also stated that Well, patient assuming he/she can still go to work or probably patient should be getting ready do that So,he/she can take Ibuprofen. The outcome for the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647832
Sex: M
Age:
State: CT

Vax Date: 02/10/2021
Onset Date: 02/12/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Pain on my right side of the back. Pain during movement of my back.; Pain during deep breathings; This is a spontaneous report from a non-contactable consumer (patient, self-reported). A 46-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, in Arm Left, on 10Feb2021 at 10:30 AM (age at vaccination: 46 years), as a single dose for COVID-19 immunization at workplace clinic. The patient's medical history included Type 2 diabetes. Concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, in Arm Left, on 20Jan2021 at 09:30 AM (age at vaccination: 46 years), as a single dose for COVID-19 immunization at workplace clinic. The patient did not received any other vaccine in four weeks. The patient was not diagnosed with COVID prior vaccination. The patient was not tested for COVID post vaccination. On 12Feb2021 at 06:30 AM, the patient experienced pain on his right side of the back. Pain during movement of his back. Pain during deep breathings. The patient did not received any treatment for the events. Outcome of the events was not recovered. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected

Other Meds:

Current Illness:

ID: 1647833
Sex: F
Age:
State: NJ

Vax Date: 01/21/2021
Onset Date: 01/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: low grade temperature; Result Unstructured Data: Test Result:99.0

Allergies:

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

Symptoms: Headache; low grade temperature of 99.0 /fever; pain at the injection; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 54-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), dose 1 via an unspecified route of administration on 21Jan2021 (Batch/Lot Number: EL3302) as dose 1, single (age at vaccination 54-year-old) for covid-19 immunization. Medical history included ongoing diabetes mellitus. Concomitant medication(s) included dulaglutide (TRULICITY) taken for an unspecified indication, start and stop date were not reported. The patient experienced headache, low grade temperature of 99.0 /fever, pain at the injection on Jan2021. The first dose was given on 21Jan2021 and was the same lot as her second dose. When she got the first one, she had a low-grade temperature of 99.0 and a headache. The headache lasted 2-3 days and the fever lasted 2 days but she didn't have it during the day, only at night. There was also pain at the injection and this lasted about a week. Treatment: she had been taking Advil and Tylenol. She also spoke to one of the girls in her doctor's office and was told to speak to the place she got the vaccine, they would tell her what to do. It was also relayed if her fever got too high go to the ER. The patient underwent lab tests and procedures which included body temperature: 99.0 on an unknown date. Therapeutic measures were taken as a result of events includes Advil and Tylenol. The outcome for all events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: TRULICITY

Current Illness: Diabetes

ID: 1647834
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a Pfizer Sponsored Program COVAX US Support. A contactable male consumer or other non hcp reported. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, (Batch/Lot number was not reported)), dose 1 via an unspecified route of administration on an unspecified date as dose 1 single for COVID-19 immunisation. The patient's medical history concomitant medications were not reported. The patient experienced mild fever on an unspecified date. The outcome of the event was unknown. Information about lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647835
Sex: M
Age:
State: OR

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: some pain in his stomach; He was not feeling well; dizziness; This is a spontaneous report from a contactable consumer (patient). A male patient of an unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number: unknown) via unknown route of administration on an unknown date, dose 1, single for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that he was not feeling well and had some pain in his stomach and dizziness after the 1st dose. Patient wants to schedule for his 2nd dose. The outcome of the events was unknown. Information about lot/batch number has been requested. Follow-up (11May2021): Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647836
Sex: F
Age:
State: GA

Vax Date: 02/13/2021
Onset Date: 02/14/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Having a severe allergic reaction; lymph node swelling; sore throat; chills; lip was swollen and bumps all over; lip was swollen and bumps all over; rash; I feel sleepy; breaking out of the face; Swelling of the face and throat; Swelling of the face and throat; This is a spontaneous report from a contactable consumer reported for herself. A 71-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number and Expiration date was not reported), via an unspecified route of administration on 13Feb2021 as DOSE 1, SINGLE for covid-19 immunisation (at the age of 71-years-old). Medical history and concomitant medications included none. The patient experienced having a severe allergic reaction, lymph node swelling, sore throat, chills, lip was swollen and bumps all over, rash, feel sleepy, breaking out of the face, Swelling of the face and throat on 14Feb2021. Investigation assessment included none. Patient asked if it was advisable to go to the hospital and should take the second dose of the vaccine. Patient stated her weight as approximately 190 pounds. Patient took Covid-19 took the first dose or shot on Saturday and having a severe allergic reaction to it. Got the swollen lymph nodes and sore throat, face was breaking out, lip was swollen and bumps all over, everywhere. Start date of events was stated as 14Feb2021 (yesterday, Sunday; not clarified further). Patient stated the events were worsened (not appropriately clarified further, hence ongoing not checked of events). Patient did not receive treatment at the time of this report and that was why she was calling to let Pfizer know that she was experiencing side effect and stated to have care that was part of a Hospital and was thinking to go through them and see if they might be would in a situation like her they would give her something to count or acted on something, something that would just allow her to cope with the situation. Patient was trying to get some relief from the side effects. Consumer was informed that Pfizer medical information was the concerned department for all queries. Consumer denied taking the number and stated that she knew the side effects, had the literature and called Pfizer to know that she was experiencing these severe side effects and was going to the doctor. According to Pfizer literature that had on Covid, if she was experiencing side effects with the first shot, she should not get the second shot. Also, the literature said that if you are experiencing the side effects from the first dose of severe reaction, it says not to get the second shot. It says list of the Pfizer BioNTech COVID-19 vaccine and it says severe reactions like difficulty breathing, swelling of the face and neck, a fast heartbeat, a bad rash all over your body and patient was getting that rash. She was not dizzy and weak but felt sleepy, just didn't feel dizzy. Also, patient was getting the swelling of the face and throat and the rash and was feeling very sleepy. It also said that there was remote chance that Pfizer Covid-19 vaccine can cause a severe allergic reaction, the reaction can happen within 1 minutes to an hour but mine started to happen Sunday (14Feb2021). It also says what patient should do about side effects, it says if you have severe allergic reaction, call 911 and go to the nearest hospital. She was calling to let you Pfizer know that she was experiencing those reaction. Commented that as it was not clarified if consumer was experiencing difficulty breathing and fast heartbeat also, hence these were not captured as events. Clinical outcome of reported events was unknown. Information on lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1647837
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 02/14/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: she was in so much pain; unable to use her hand; This is a spontaneous report from a contactable consumer (patient), via Pfizer-sponsored program Pfizer First Connect. A 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN9581), via an unspecified route of administration, on an unspecified date at 13:30 (at the age of 68-year-old), as dose 2, single, in left arm for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's past drug included cortisone, taken for dog bite in left hand. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL1283), via an unspecified route of administration, on 23Jan2021 (at the age of 68-year-old), as single dose for COVID-19 immunization and experienced no symptoms. On 14Feb2021, after the second dose of vaccine, the patient was unable to use her hand "at all." Patient reported that it was improving but "just still hard to open that hand." Patient thought that the vaccine shot "may have hit a tendon and brought the pain back from the dog bite." On an unspecified date, after the second dose of vaccine, the patient was in so much pain. It was really bad. Patient reported that it was getting better. The clinical outcome of both the events was resolving. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647838
Sex: M
Age:
State: DC

Vax Date: 02/12/2021
Onset Date: 02/13/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210213; Test Name: Body temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Low fever of 100.2 F; This is a spontaneous report from a contactable consumer and other Health Professional. A 34-year-old male patient (consumer) received bnt162b2 (BNT162B2, Formulation: Solution for injection, Batch/Lot number was not reported), dose 2 via an unspecified route of administration, administered in Arm Left on 12Feb2021 07:15 (Age 34-year-old at the time of vaccination) as DOSE 2, SINGLE for covid-19 immunisation. The medical history included Factor XI bleeding disorder from an unknown date and unknown if ongoing, Left and Right hip replacements (Summer of 2003 and Summer of 2007). The patient had Non-hodgkin's lymphoma from 01Aug2001 and finished the treatment in the fall of 2003. Since then, the patient did not had cancer. Historical Vaccine included BNT162B2 dose1 given on 22Jan2021 at administration time 7:15 AM on Left arm (age 34-year-old at the time of vaccination, lot number unknown) for COVID-19 immunisation and developed Mild headache after first dose. The concomitant medication included dextroamphetamine [dexamfetamine] taken for an unspecified indication, start and stop date were not reported. Facility type vaccine was given at hospital. No other vaccine received in four weeks. The patient did not have covid prior vaccination and was not tested covid post vaccination. There were no Known allergies. The patient developed Low fever of 100.2 F the next morning on 13Feb2021 at 4:15 AM, after the second dose. Also, the patient mentioned, two days after the first dose, the patient developed a mild headache, but that could have been due to any number of other things. The patient underwent lab tests and procedures which included body temperature, which was found to be 100.2 Fahrenheit on 13Feb2021. The outcome of the event was reported as recovering. Follow-up attempts completed. No further information expected. Information on the lot/ batch number has been requested.

Other Meds: DEXTROAMPHETAMINE [DEXAMFETAMINE]

Current Illness:

ID: 1647839
Sex: M
Age:
State: KY

Vax Date: 02/13/2021
Onset Date: 02/14/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: flu like symptoms; chills; Fever; body pain; This is a spontaneous report from a contactable consumer or other non hcp. A 55-years-old male patient received second dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EL 9267) via an unspecified route of administration, administered in Arm Left on 13Feb2021 13:00(age at vaccination: 55 years) as DOSE 2, SINGLE for covid-19 immunisation. Patient didn't had covid prior to vaccination. Patient didn't receive other vaccines within 4weeks prior to vaccination, patient received other medication Lisinopril 10mg 1 tab daily within 2 weeks of vaccinations. Medical history included hypertension from an unknown date and unknown if ongoing. Concomitant medications included lisinopril (LISINOPRIL) taken for an unspecified indication, start and stop date were not reported. Patient had no allergies. Patient previously received first dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number EL9261) via unspecified route of administration in Arm left on 23Jan2021(age at vaccination: 55 Years) as DOSE 1, SINGLE for covid-19 immunisation. Patient was not tested for covid to post vaccination. On 14Feb2021 10:00 the patient experienced flu like symptoms, chills, fever, body pain. No therapeutic measures were taken for the events. The outcome of the events influenza like illness, chills, pyrexia, pain was recovering. Follow-up attempts completed. No further information expected.

Other Meds: LISINOPRIL

Current Illness:

ID: 1647840
Sex: F
Age:
State: NM

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Diarrhea; fatigue; sore arm; This is a spontaneous report from a contactable physician. A 3-decade-old female patient received bnt162b2 (BNT162B2, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date (age at the time of vaccination was not provided) as DOSE NUMBER UNKNOWN, SINGLE for an unspecified indication. The medical history included infected with COVID-19 prior to being vaccinated from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient in her 20's received the Pfizer Covid-19 vaccine on an unspecified date and had severe reaction on an unspecified date. The patient had been infected with COVID-19 prior to being vaccinated on an unspecified date. When she received the vaccine, the patient developed diarrhoea and fatigue that lasted about 3 days on an unspecified date. She also had a sore arm that lasted about a day on an unspecified date. The outcome of the events was reported as recovered on an unspecified date. Follow-up attempts completed. No further information expected. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1647841
Sex: F
Age:
State: PA

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: Slept almost the entire day; Headache; Joint pain in legs and neck; Joint pain in legs and neck; Joint pain in legs and neck; Loss of appetite; Chills and Shivers; Chills and Shivers; Sore left arm; Sore arm started at 5pm that day. It has improved, but it is a little itchy now.; This is a spontaneous report from a contactable consumer or other non hcp (patient). The initial case was missing the following minimum criteria: unspecified AE. Upon receipt of follow-up information on 15Feb2021, this case now contains all required information to be considered valid. A 73-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6021; Expiration Date: Jun2021) via intramuscular route of administration, administered in arm left on 12Feb2021 09:45 (at the age of 73-year-old) at dose 1, single for covid-19 immunisation. Medical history included Retroperitoneal Liposarcoma/Diagnosed 10 years ago with 4 surgeries last one being Aug 2020 and cancer (I am a cancer patient). Concomitant medications were not reported. The patient experienced Sore arm started at 5pm that day. It has improved, but it is a little itchy now on an unspecified date in 2021, sore left arm on 12Feb2021 17:00, chills and shivers on 12Feb2021 22:00, slept almost the entire day, headache, joint pain in legs and neck, loss of appetite on 13Feb2021. Reporter has experienced quite some side effects from the 1st dose of the vaccine and is asking if the side effects of the 2nd dose will be more severe as she's heard it to be like that. She is also asking for any contraindications of the vaccine as she is a cancer patient. Received covid vaccine on Friday. Calling in to report her side effects. Received call from consumer regarding the Pfizer COVID vaccine. She had her first dose last Friday. She would like to report symptoms from that. She did not wish to provide an address or email. There was no prescriber. She is with a Health Service and filled out a questionnaire, and the next day found out she was eligible. Sore arm started at 5pm that day. It has improved, but it is a little itchy now. She was not aware of the joint pain on 13Feb2021 because she was wiped out and was not totally aware. She was not eating and was sleeping all day that day. She is still feeling wiped out since yesterday, but it has improved. She has questions about second dose. She wanted to know if it will be worse with second dose. NO ER or physician's office required. Prior Vaccinations (within 4 weeks) was none. Adverse events following prior vaccinations was none. Outcome of the event Sore arm started at 5pm that day. It has improved, but it is a little itchy now was unknown and remaining other events was resolving. Follow-up (01Apr2021): Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647842
Sex: M
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable consumer via Pfizer sales Representative. (patient, reported for self). A 74-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: solution for injection; Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date) as dose 2, single for COVID-19 Immunisation. The patient medical history and patient's concomitant medications were not reported. The patient experienced chills, Headache on an unspecified date. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1647843
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:100.5; Comments: She has been running fever with 100.5 being the highest that it has gotten

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Well my arm at the injection site is about 5 times in size/ her arm is swollen 2-3 times the size since she received the vaccine on Sunday; My arm at the injection site is about 5 times in size; it's huge and hot to touch, it's red also; My arm at the injection site is about 5 times in size; it's huge and hot to touch, it's red also; the lymph nodes under arm are swollen; has been running fever with 100.5 being the highest that it has gotten.; redness; This is a spontaneous report received via Pfizer-sponsored Program Pfizer First Connect from a contactable nurse (the patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 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. Patient received 1st dose of Covid vaccine and was experiencing some side effects such as her arm was swollen 2-3 times the size since she received the vaccine on Sunday, the Lymph nodes under arm are swollen and she had been running fever with 100.5 being the highest that it has gotten. Nurse stated, I was trying to speak with someone regarding the vaccine, I received on Friday, I mean on Sunday. I know that it specified that you could have redness, swelling, fever and all of that stuff which I've had all of that and the swelling in the lymph node and stuff, well my arm at the injection site is about 5 times in size, when confirmed if nurse wanted to know if it was normal or not, nurse stated, yeah it was huge and it was hot to touch, and it's red also. The patient underwent lab tests and procedures which included fever (body temperature): 100.5 on an unspecified date. The outcome of all 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: 1647844
Sex: F
Age:
State: TX

Vax Date: 02/13/2021
Onset Date: 02/14/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: patch on my stomach/rectangular area on her stomach double the size of a stamp/woke up with a patch double the size of a stamp; This is a spontaneous report from a contactable consumer (patient herself). A 76-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Lot Number: EL9266; Expiration Date: 31May2021), via an unspecified route of administration, administered in Arm Left on 13Feb2021 between 8:45 and 9:00 as dose 1, single for COVID-19 immunisation. Patient medical history included Shellfish allergy, Nut allergy, Chocolate allergy (had the allergy for quite some time), High cholesterol and high blood pressure. Concomitant medications included Amlodipine 10mg and Hydrochlorothiazide 12.5 mg taken for high blood pressure, Rosuvastatin 10mg taken for High cholesterol, Colecalciferol (D3), Pyridoxine hydrochloride (B6) and multivitamin. The patient previously took Allegra as she suffers with hay fever. She didn't take Allegra the day she got the vaccine. She did not take any vaccinations within 4 weeks prior to COVID-19 vaccine. It was reported that, on 14Feb2021 between 7:30 and 8:00, the patient experienced patch on her stomach. She woke up with a patch double the size of a stamp. It is rectangular in shape. It is like a frame on her stomach on the right side. On the left side it is very faint and didn't completely come through. She reports that the area is not itchy and is not swollen. The patch has not worsened. It might of had a little improvement but she would say it has stayed the same. She has not visited the Emergency room or physician's office. The outcome of the event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: AMLODIPINE; HYDROCHLOROTHIAZIDE; ROSUVASTATIN; D3; B6

Current Illness:

ID: 1647845
Sex: M
Age:
State:

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: muscle pain; headaches; joint pain; chills; hands are swelling; knuckles are swelled up; breathing issues; This is a spontaneous report from a contactable consumer. This male consumer reported. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 27Jan2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that the patient had nothing but side effects since the patient got his first shot. The patient experienced muscle pain, headaches, joint pain, chills at times, hands are swelling, and knuckles are swelled up all on an unspecified date. The patient had breathing issues for a while one evening on an unspecified date. The patient called to ask what the patient should take for the side effects he had been experiencing since his first dose. The patient also asked whether he should take the second dose. Outcome of the events muscle pain, headaches, joint pain, chills at times, hands are swelling, and knuckles are swelled up were reported as Unknown at this time of the report. Outcome of the event breathing issues was reported as recovered on an unspecified date at this time of the report. Information about lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647846
Sex: M
Age:
State:

Vax Date: 02/04/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: This is a spontaneous report from a contactable consumer or other non hcp (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 04Feb2021 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took amoxicillin and experienced drug hypersensitivity. Patient stated he is allergic to Amoxicillin where he didn't have a rash reaction until 8 to 10 days later. On 12Feb2021, patient experienced swelling in his left armpit, the same side where he received the shot, little swelling in the right armpit. On an unspecified date in Feb2021, patient experienced little swelling of the arm. The outcome of the event little swelling of the arm was unknown, swelling in his left armpit, the same side where he received the shot was recovering, little swelling in the right armpit was recovered on an unspecified date in Feb2021. No follow up attempts are possible. Information about Lot and batch number could not be obtained.

Other Meds:

Current Illness:

ID: 1647847
Sex: F
Age:
State: IL

Vax Date: 01/28/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: rash on her under her arms, around ears and between her thighs, R arm injection site, rash on my left wrist and hand; rash on her under her arms, around ears and between her thighs, R arm injection site, rash on my left wrist and hand; darkness area; irritation; breaking out; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 78-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EL8982, Expiration date: unknown) via an unspecified route of administration, administered in right deltoid (right shoulder) on 28Jan2021 about quarter till nine in the morning (age at vaccination was 78 years) as dose 1, single for COVID-19 immunization. The patient's medical history included arthritis and ongoing hypertension from an unknown date. The patient had allergy to Penicillin (she hasn't had any Penicillin for years. She has had this allergy since she was a teenager). Concomitant medication included hydrochlorothiazide, lisinopril taken for hypertension from 2006 and ongoing. The patient hasn't had anything 14 days before or 14 days after. She didn't get the flu shot this year. It was over a year ago that she got her last flu shot. There was no history of all previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines were administered on same date of the Pfizer suspect. The facility where the most recent COVID-19 vaccine was administered was University hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had called because she had her first COVID19 vaccine on 28Jan2021. It said there was sucrose. She asked if that was the artificial sweetener. She could not use artificial sweeteners they tend to have an affect on her. On an unspecified date, the patient experienced a rash on her under her arms, around ears and between her thighs, R arm injection site, rash on her left wrist and hand, lasted a few days. She had to keep rubbing and putting ointment on it, there was a darkness area where the rash was and could still tell where the rash was. On an unspecified date, the patient experienced irritation and breaking out/breakout. It started a few days after. It went away, but she was still having some breaking out around her ears, under her arms and in between thighs. It went away when rubbed with alcohol. She had a rash on her hands and fingers that lasted for a few days. It was around the wrist. She still had some dark areas where the rash was. The patient asked if anyone had any of these reactions, she really wanted to know about any deaths. She had heard the second dose was stronger. The patient asked if there would there be harm if she does not receive the second dose. The adverse event did not require a visit to Emergency Room or Physician Office. There was a Product Complaint. The description of complaint was reported as she was calling because she had her first COVID19 vaccine. It said there was sucrose. She asked if that was the artificial sweetener. She had heard the second dose was stronger. She wanted to know if there would be harm if she didn't get the second vaccine. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: LISINOPRIL/HYDROCHLOROTHIAZIDE

Current Illness: Hypertension

ID: 1647848
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: She developed an allergic reaction with a rash; She developed an allergic reaction with a rash; This is a spontaneous report received from a non-contactable consumer or other non-health care professional (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: unknown), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Reporter called for information about if the treatment she was receiving for the management of an allergy could interact with the administration of the second dose of the Pfizer's COVID-19 vaccine on 03Mar2021. The consumer reports that she developed an allergic reaction with a rash on unknown date and she was received treatment for this condition. The outcome of the events was reported as unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1647849
Sex: M
Age:
State: NY

Vax Date: 02/05/2021
Onset Date: 02/10/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: lost his sense of taste; cannot feel anything in his mouth; lost his sense of taste and smell; runny nose; fever; headache; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 37-year-old male patient reported that they received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: EL9269), via unspecified route of administration in right arm on 05Feb2021 14:25 (at the age of 37 years) as a DOSE 1, SINGLE for COVID-19 immunization. Patient had no medical history and had not received concomitant medications (Other Products). Patient was not administered with any other additional Vaccines on Same Date of the Pfizer Suspect. The patient did not receive any other vaccines within four weeks prior to the vaccination. Patient reported that he had a very slight headache on 10Feb2021 that was no big deal. Patient stated that he received the Pfizer vaccine 10 days ago, on Friday before, then six days later on 11Feb2021 he had a fever which he knew was a side effect of the vaccine. The day before the fever was very brief, maybe two hours in the night. Then a couple of days later on 13Feb2021 he had a runny nose. It was a crazy runny nose, he had to breathe out of his mouth and was using lots of paper. On 14Feb2021 patient woke up and lost his sense of smell and on 15Feb2021 lost his sense of taste and he cannot feel anything in his mouth. He wanted to know if these are reported adverse events (AEs) associated with the vaccine. Then he noticed he could not smell anything. He put perfume up to his nose and could smell nothing. He thought maybe he lost his sense of smell due to the runny nose but the next day on 15Feb2021 he lost his sense of taste and he was concerned about that and was querying were these all are part of the side effects of the vaccine or something else and queried for was that the vaccine working on him. Patient reported that his wife cooks and puts in lots of flavors but he can smell or taste nothing, perfume nothing. He can't smell or taste cheese or ham. He doesn't taste or smell coffee. He can only tell hot or cold. He was scheduled to receive the second dose of the vaccine on 26Feb2021. Patient had not attended any physician or emergency room (ER) visit for the experienced events. Outcome of event headache was recovered on 10Feb2021, fever was recovered on 11Feb2021, runny nose recovered on 14Feb2021, lost his sense of taste and smell was not recovered, cannot feel anything in his mouth was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647850
Sex: F
Age:
State: NM

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: This is a spontaneous report from a contactable physician via a Pfizer sales representative. A 6-decade-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection; Batch/Lot Number: Unknown, Expiration date: Unknown) 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. On an unspecified date the patient had a sore arm for 1 day post vaccination. The clinical outcome of the event was unknown. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647851
Sex: F
Age:
State: OH

Vax Date: 01/30/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: Covid test; Result Unstructured Data: Test Result:unknown results; Test Name: strep test; Result Unstructured Data: Test Result:negative; Comments: No more information available

Allergies:

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

Symptoms: small fever; aching; high chest congestion; sore throat; getting sick; sore throat feels like there is ground up glass in there, and is red; This is a spontaneous report from a contactable consumer or other non HCP (Patient). A 76-year-old female patient received bnt162b2 (BNT162B2, formulation; solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 30Jan2021 10:30 (Batch/Lot Number: EN5318) as DOSE 1, SINGLE (at the age of 76-year-old) for COVID-19 immunisation. Medical history included mitral valve prolapse from 1980 to an unknown date, hypertension from an unknown date and unknown if ongoing (Caller says this was diagnosed 13 years ago). There were no concomitant medications. The patient did not receive any other product. The patient experienced small fever, aching, draining, high chest congestion and sore throat on 10Feb2021. It was reported that the patient started getting sick on 10Feb2021. Patient stated doesn't know if it was correlated to the vaccine, she has some symptoms and has been to the doctor twice, the worst thing was a terrible sore throat. Patient says that she has been taking a Z-Pak and was on day 5 of 6 days of that, but it doesn't seem to be helping. She says that they swabbed her throat for strep test, which was negative and had underwent a COVID test, waiting for results. Patient stated that her next dose was due 23Feb2021 for the vaccine and she has been terribly sick for 6 days. Patient wonders if 11-12 days afterwards would be too long for getting side effects of vaccine or if it was still within that time. The patient received Z-Pak sixth dose today (NDC 59762-2198-1, LOT ER7479, EXP 31Oct2024 manufactured by Greenstone) which was prescribed by the urgent care. The patient felt sore throat feels like there is ground up glass in there, and is red. The patient received gargle with salt, honey, lemon and used Chloraseptic spray. No details provided about Chloraseptic spray. It reported that patient wanted to know was sore throat a side effect of the Covid-19 vaccine. The patient took Z-pack but it was not helping. Therapeutic measures were taken as a result of sore throat and sore throat feels like there is ground up glass in there, and is red. The outcome of events small fever, aching and high chest congestion reported as unknown. The outcome of events sore throat feels like there is ground up glass in there, and is red, sore throat was not recovered and outcome of the other events was unknown. the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1647852
Sex: F
Age:
State:

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: experience itching at vaccine site; Patient complains of itching of skin; This is a spontaneous report from a non-contactable other health care professional. A 33-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL9266), via intramuscular route of administration in left arm on 12Feb2021 (at the age of 33 years old) as single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. During her 15-minute waiting period after the injection, the patient began to experienced itching at vaccine site on an unspecified date in Feb2021. She denied difficulty breathing, difficulty swallowing, wheezing, throat tightness, hoarseness, stridor, lightheadedness, dizziness, facial swelling, lip swelling and tongue swelling. The patient complains of itching of skin. The patient denies facial swelling, sore throat, frequent throat clearing, chest tightness, shortness of breath and wheezing. The outcome of events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1647853
Sex: F
Age:
State:

Vax Date:
Onset Date: 02/14/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Little bit of soreness at the site of injection; Constant runny nose; Sneezing; This is a spontaneous report from a contactable Nurse (patient).A 65-years-old female patient received first dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for covid-19 immunization.The patient medical history and concomitant medications were not reported. On 14Feb2021, the patient experienced constant runny nose and sneezing and on an unknown date patient experienced little bit of soreness at the site of injection, but that has gone now. She had no other symptoms, but her allergy medicine and Sudafed was not working when it normally would work for her with these symptoms. The outcome of the events runny nose and sneezing was unknown and little bit of soreness at the site of injection was recovered on an unknown date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647854
Sex: F
Age:
State: CA

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210107; Test Name: Pregnancy; Result Unstructured Data: Test Result:Positive

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: I tested (+) on my pregnancy test on 07Jan2021; Mild chills; This is a spontaneous report from a contactable nurse (Patient). A 30-years-old pregnant female patient received second dose of bnt162b2 (BNT162B2, PFIZER-BIOTECH COVI-19 VACCINE, Solution for injection, Batch/Lot Number: EJ1686), via intramuscular route of administration, administered in Deltoid Right on 06Jan2021 15:20 (Age at vaccination: 30-years-old) as single dose for covid-19 immunization. Medical history included colitis ulcerative from 01Jan2015 to an unknown date Currently taking Remicade IV infusions every 8 weeks. Concomitant medication included infliximab (REMICADE) taken for Ulcerative colitis from 04Feb2020 and ongoing. It was reported that patient received covid-19 vaccine both doses on 26Dec2020 and 06Jan2021 respectively. she tested positive on her pregnancy test on 07Jan2021. Currently, under a care of her high risk (obstetrician) OB. She is 9 weeks pregnant. she would like to make us aware of it, Since she know, these not a lot of data about pregnancies and vaccine. she is willing to be in a study or research for observation. It was also reported that patient experienced Very mild chills 11 hours after second dose. Patient did not receive any treatment for the event. Adverse event not resulted in Emergency room or Physician office visit. Patient did not receive any treatment for the event. The mother reported she became pregnant while taking bnt162b2. The mother was 9 Weeks pregnant at the onset of the event. The patient underwent lab tests and procedures which included pregnancy: positive on 07Jan2021. The outcome for the event Very mild chills was reported as resolved on 2021. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds: REMICADE

Current Illness:

ID: 1647855
Sex: F
Age:
State: MD

Vax Date: 02/05/2021
Onset Date: 02/07/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: having joint pain or inflammation of joints and tendons/ joint pain or pain around the joint, so it might be tendons or ligaments.; having joint pain or inflammation of joints and tendons/ joint pain or pain around the joint, so it might be tendons or ligaments.; having joint pain or inflammation of joints and tendons/ joint pain or pain around the joint, so it might be tendons or ligaments.; This is a spontaneous report from a contactable pharmacist (patient). A 66-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number: EM9810), via an unspecified route of administration, administered in Left arm on 05Feb2021 at 10:30 as dose 2, single (at the age of 66 years), for covid-19 immunization. There were no medical history and concomitant medications (Other Products: No, Patient History: No). The patient previously received fist dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number: EL0140), via an unspecified route of administration, on an unspecified date as dose 1, single for (at the age of 66 years), covid-19 immunization. The patient stated that, on 07Feb2021, she was having joint pain or inflammation of joints and tendons. She said her side effects were joint pain, though she was not sure if it was joint pain or pain around the joint, so it might be tendons or ligaments. She told that the side effects began, though she did not notice it right away, on Sunday night, on like the 7th. She reported that, it was not a lot of pain, more discomfort, but it was in her wrists, elbows, shoulders, and knees. She was not sure if it was her joints also because sometimes pain radiates into her arm. She told that the joint pain had gotten more noticeable yesterday and today, and she had done no treatment for it. She personally felt it was not serious, unless this was something that did not go away, and then that would be serious, depending on what was happening. She said that was the question, since she had never been diagnosed with arthritis and never had these before. No corrective treatment was received for the events. The outcome for the events was not recovered at the time of report. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647856
Sex: F
Age:
State: IL

Vax Date: 02/10/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: rash on her trunk and hair line; This is a spontaneous report from a contactable consumer or other non-hcp. A female patient of an unspecified age received bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration on 10Feb2021 as dose 1, single for COVID-19 immunisation. The patient medical history included allergic to penicillin from an unknown date and unknown if ongoing. Concomitant medications were not reported. The patient experienced rash on her trunk and hair line on an unspecified date. Therapeutic measures were taken with Prednisone and benadryl as a result of event. The outcome of the event was unknown. Information about lot/batch number has been requested. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647857
Sex: F
Age:
State:

Vax Date: 02/11/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: fatigue/exhaustion; headaches; she couldn't lift her arms, she couldn't do anything; short of breath; a little tired and has a rash on her arm; a little tired and has a rash on her arm; This is a spontaneous report from a contactable nurse. A 89-year-old female 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 on 11Feb2021 as dose 2, single for COVID-19 immunization. Historical vaccine included dose 1 of BNT162B2 via an unspecified route of administration on an unspecified date for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced fatigue/exhaustion, headaches on 16Feb2021, she couldn't lift her arms, she couldn't do anything, short of breath, a little tired and has a rash on her arm on an unspecified date in Feb2021. It was reported that, patient received the second dose on Thursday, 11Feb2021. She stated her mother "felt fine" that Thursday and she had: "fatigue , exhaustion and headaches", on the following Friday. She added patient "felt better" on the next day, Saturday and on the Sunday, she got up and had an "episode", which she described as: "she couldn't lift her arms, she couldn't do anything, she rested in bed all day, and she thought she felt short of breath". This morning, Monday, caller explained patient still felt "short of breath, a little tired and has a rash on her arm". Reporter enquired if the shortness of breath was reported as a side effect of the COVID-19 vaccine and what was suggested to do for the shortness of breath. The outcome of the events she couldn't lift her arms, she couldn't do anything, short of breath, a little tired and has a rash on her arm was unknown and fatigue/exhaustion, headaches was recovered on an unspecified date in Feb2021. Information about lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647858
Sex: F
Age:
State:

Vax Date: 02/09/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Little soreness in the arm after the 1st dose of the vaccine yesterday; This is a spontaneous report from a contactable consumer or other non-health care professional (patient) received from a Pfizer-sponsored program Pfizer First Connect. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 09Feb2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date in Feb2021, the patient experienced little soreness in the arm after the 1st dose of the vaccine yesterday. It was further reported that Caller is calling for her friend who had breast enhancement surgery and she had a reaction to the anesthesia. Is it safe for her friend to get the Pfizer COVID-19 vaccine? Caller mentioned that she had the first dose of the Pfizer BioNTech COVID-19 vaccine yesterday (09Feb2021) and had a little arm soreness from it. Caller declined to report the adverse events to DSU. The clinical outcome of the event little soreness in the arm after the 1st dose of the vaccine yesterday was reported as unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647859
Sex: F
Age:
State:

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: chills; neck and shoulder pain; neck and shoulder pain / intermittent joint pain in her left elbow, right shoulder, knee, and back; neck and shoulder pain / intermittent joint pain in her left elbow, right shoulder, knee, and back; fatigued; nausea; cold sweats; This is a spontaneous report from a contactable consumer (patient). A 76-year-old female patient received first 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 27Jan2021 (at the age of 76-years-old) as dose 1, single for covid-19 immunization. The patient medical history included she has pulmonary fibrosis at baseline. Concomitant medications were not reported. It was reported that, patient is 76 y/o female. She received her first dose of the Pfizer Covid vaccine on 27Jan2021. 3 hours after her shot, she started to experience intermittent chills that last about an hour then go away, neck and shoulder pain - was hard to turn her head due to the pain. Then intermittent joint pain in her left elbow, right shoulder, knee, and back. She felt fatigued and had an episode of nausea and cold sweats. She states she has pulmonary fibrosis at baseline. She is concerned that the side effects have been lasting for a while and wants to know if that's normal. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647860
Sex: F
Age:
State: CO

Vax Date: 01/23/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 2021; Test Name: fever; Result Unstructured Data: Test Result:less than 100; Comments: less than 100

Allergies:

Symptom List: Pain in extremity

Symptoms: Weird taste/metallic taste in mouth; Fever Less than 100; Chills/Bodyaches; Chills/Bodyaches; This is a spontaneous report received from a contactable consumer (Patient) via in response the Non HCP letter sent in cross referenced case. A 51-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection) via an unspecified route of administration at left arm (at the age of 51-year-old) on 23Jan2021 (Lot Number: EL9262) as single dose for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication included ibuprofen (ADVIL). No there are not any other products that were taken together with those Indicated above. Patient did not receive any other vaccine prior to this vaccination within 4weeks. Patient did not have any adverse events prior to the vaccination. There were no predisposing factors. The patient did not visit emergency room/ Physician office for the events. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection) via an unspecified route of administration at left arm (at the age of 50-year-old) on 02Jan2021 11:30 (Lot Number: EK9231) as single dose for COVID-19 immunisation and patient experienced 30 minutes after vaccine had a really weird taste in mouth for about 2 hours, throwingup/vomiting, fever more than 100, chills, bodyaches, mettalic taste in mouth. After second dose the patient experienced Same symptoms after 2 dose except vomiting i.e weird taste, fever less than 100 and chills/bodyaches on an unspecified date in 2021. The patient underwent lab tests and procedures which included body temperature: less than 100 on an unspecified date in 2021. Outcome of all events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: ADVIL [IBUPROFEN]

Current Illness:

ID: 1647861
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: fever; chills; hot flashes; headache; fatigue; This is a spontaneous report from a contactable consumer or other non hcp (reported for a patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), dose 2 via an unspecified route of administration on an unspecified date as DOSE 2, SINGLE for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Reportedly, event took place after use of product. After second dose of Covid vaccine, on an unspecified date, the patient experienced fever, chills, hot flashes, headache, and fatigue. Outcome of the events were resolved within 48 hours. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1647862
Sex: F
Age:
State: CO

Vax Date: 02/13/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported and expiry date: unknown), dose 1 via an unspecified route of administration, administered in Arm Left on 13Feb2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced has a spot the size of a lemon and is angry red on an unspecified date. Outcome of the event was not recovered. Follow-up (15Feb2021): This is a follow-up spontaneous report from a contactable consumer. Follow-up (12MAY2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647863
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: covid test; Result Unstructured Data: Test Result:negative

Allergies:

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

Symptoms: Fever; Body aches; Weakness; Diarrhea; She vomited once; Fatigue; low grade fever; This is a spontaneous report from a Pfizer-sponsored program. A Contactable consumer reported for a 83-years-old female patient (grandmother) that she received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. On an unknown date, the patient experienced fever (pyrexia) 48 hours ago, and currently the patient was having body aches (pain), weakness (asthenia), diarrhea (diarrhoea) since Saturday. She vomited once (vomiting), fatigue (fatigue), low grade fever (pyrexia) Sunday. On an unspecified date, the patient underwent lab tests and procedures which included sars-cov-2 test: negative. Therapeutic measures were taken as a result of fever (pyrexia), body aches (pain), weakness (asthenia), diarrhea (diarrhoea), she vomited once (vomiting), fatigue (fatigue) and low grade fever (pyrexia). She has been taking Tylenol every day, she has been afebrile since but she still has fatigue and some body aches The reporter wanted to know if the patient could still take the second dose tomorrow. The clinical outcome of the events was Unknown. Information on the Batch/Lot number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1647864
Sex: F
Age:
State:

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# not reported), via an unspecified route of administration, on Feb 9, 2021, single dose, for COVID-19 immunisation. Medical history included cholesterol (abnormal blood cholesterol) and asthma. Concomitant medication included Praluent (alirocumab) taken for abnormal blood cholesterol. On an unspecified date, patient experienced myalgia and influenza-like illness, (muscle aches and flu-like symptoms), which she also experienced with Praluent in the past. On Feb 9, 2021, patient experienced severe muscle spasms (like Charlie horses all over her body). This was an immediate, short-term reaction after receiving the COVID-19 vaccine. Her skin and throat turned bright red, and she had difficulty breathing. She needed her asthma pump but had 3 occurrences (one after the other) and required on-site observation for 1.5 hours. She no longer felt that afterwards. She was told to take Benadryl and a couple of puffs of her inhaler before her appointment for the 2nd dose on Mar 2, 2021, and she would be kept for observation. They made a note in her file and advised her primary care physician. At the time of this report, the outcome of events: unknown. Follow-up attempts completed. No further information expected.

Other Meds: Praluent

Current Illness: Abnormal blood cholesterol

ID: 1647865
Sex: F
Age:
State: MA

Vax Date: 02/11/2021
Onset Date: 02/14/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210118; Test Name: Q PCR; Test Result: Negative

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Rash on the lower left side of the lip; Lump felt below the chin close to the throat and also below the left ear.; Lump felt below the chin close to the throat and also below the left ear.; This is a spontaneous report from a contactable consumer (patient). A 25-year-old female non-pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: unknown) dose 1 via an unspecified route of administration in right arm on 11Feb2021, 06:45 PM (at the age of 25-year-old) as single dose for COVID-19 immunisation. Medical history and concomitant medications were none. No known allergies. No other vaccine in four weeks. No other medications in two weeks. No covid prior vaccination. On 14Feb2021 05:00 PM, the patient experienced rash on the lower left side of the lip. Lump felt below the chin close to the throat and also below the left ear. Events resulted in Doctor or other healthcare professional office/clinic visit. Received antiviral treatment for events. The patient underwent lab test post vaccination which included Q PCR, on 18Jan2021, result: Negative. The outcome of events was recovering. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647866
Sex: F
Age:
State: AZ

Vax Date: 02/13/2021
Onset Date: 02/13/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: injection site pain; tiredness; headache; muscle pain; chills; Joint pain; Fever; nausea; feeling unwell; This is a spontaneous report from a contactable consumer (patient). A 59-years-old, non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9262, Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 13Feb2021 (at the age of 59-years-old) as dose 2, single for covid-19 immunisation in other facility. The patient did not have covid prior vaccination. The patient was not tested for covid post vaccination. Medical history included known allergies shellfish. The patient's concomitant medications were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL1283, Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 23Jan2021 (at the age of 59-years-old) as dose 1, single for covid-19 immunisation in other facility. On 13Feb2021 at 22:30, the patient experienced injection site pain, tiredness, headache, muscle pain, chills, joint pain, fever, nausea and feeling unwell. No treatment was given for the events. The outcome of the events recovered on an unspecified date of 2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1647867
Sex: F
Age:
State: NC

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: mild flu like symptoms; A lot of inflammation, large, bright red area that is hot to the touch and has a large hard knot inthe center where injection was given in upper left arm; A lot of inflammation, large, bright red area that is hot to the touch and has a large hard knot inthe center where injection was given in upper left arm; lot of inflammation, large, bright red area that was hot to the touch and has a large hard knot in the center where injection was given in upper left arm; A lot of inflammation, large, bright red area that is hot to the touch and has a large hard knot inthe center where injection was given in upper left arm; hard knot in the center of her left upper arm at the injection site/ hard knot in the center where injection was given in upper left arm; Itching left upper arm; This is a spontaneous report from a contactable consumer (patient). A 74-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EM9810) via an unspecified route of administration, administered in upper left arm on 09Feb2021, at 10:30 (at the age of 74-years-old) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient had received pneumonia vaccine for immunisation about 5 years ago and had experienced localized inflammation on the arm where injection was administered, which lasted for couple of days. The concomitant medication(s) included romosozumab aqqg (EVENITY [ROMOSOZUMAB AQQG]) 2 weeks before administered of the Pfizer COVID-19 Vaccine, precursor to Prolia. It was reported that the patient experienced mild flu like symptoms and developed inflammation and a hard knot in the center of her left upper arm at the injection site. On night of 09Feb2021, the patient had onset of itching left upper arm. On morning of 10Feb2021, when patient woke up noticed onset of a lot of inflammation, large, bright red area that was hot to the touch and has a large hard knot in the center where injection was given in upper left arm, area was quite large and bright red, about 3 inches in diameter, hot to the touch, the center where she got the vaccine injection was a very large hard knot. Very large hard knot was still there, and was gradually see it spreading, it got a little larger and a little bit lighter. On 10Feb2021, unknown time the patient reported onset of mild flu like symptoms. The patient had been taking antihistamines and Aleve, used all the usual things. On 15Feb2021, the patient had a regular unrelated appointment with her Rheumatologist, who had started her on a course of Prednisone for her inflammation. Patient did not any AE(s) require a visit to emergency room and physician office. No hospitalization. The outcome of mild flu like symptoms was recovered on 11Feb2021 and rest all recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: EVENITY [ROMOSOZUMAB AQQG]; PROLIA

Current Illness:

ID: 1647868
Sex: F
Age:
State:

Vax Date: 02/08/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: having her go in for IV hydration; This is a spontaneous report from a non-contactable consumer (patient herself). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 08Feb2021 as dose 2, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unknown date in February2021, the patient was going in for iv hydration. Therapeutic measures were taken for the adverse event. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1647869
Sex: F
Age:
State: CT

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210212; Test Name: Fever; Result Unstructured Data: Test Result:99.9

Allergies:

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

Symptoms: Fever (99.9); fatigue; headache; muscle and joint aches; muscle and joint aches; chills; This is a spontaneous report from a contactable consumer (Patient). A 26-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EL 3247) via an unspecified route of administration in arm right on 12Feb2021 10:30 (age at vaccination 26-year-old, Patient non-pregnant at the time of vaccination) as DOSE 2, SINGLE for COVID-19 immunisation at workplace clinic. The patient's medical history was not reported. No other vaccines within 4 weeks PRIOR to the COVID-19 vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient had not been tested for COVID-19. The patient's concomitant medications were not reported. Patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EL3247), via an unspecified route of administration in arm right on 22Jan2021 10:45 AM (age at vaccination 26-year-old) on as DOSE 1, SINGLE for COVID-19 Immunization. The patient experienced Fever (99.9), fatigue, headache, muscle and joint aches and chills on 12Feb2021 22:30. The patient underwent lab tests and procedures which included body temperature (99.9) on 12Feb2021. The outcome of events were recovered on 13Feb2021. No follow-up attempts are needed. No further information was expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am