VAERS 2021 Database www.vaers.hhs.gov

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

Total Manufacturer
46,870MODERNA
532GLAXOSMITHKLINE BIOLOGICALS
353PFIZER\BIONTECH
231MERCK & CO. INC.
221UNKNOWN MANUFACTURER
62SEQIRUS, INC.
25DYNAVAX TECHNOLOGIES CORPORATION
13EMERGENT BIOSOLUTIONS
12SANOFI PASTEUR
9NOVARTIS VACCINES AND DIAGNOSTICS
5PFIZER\WYETH
5PAXVAX
2TEVA PHARMACEUTICALS
2PROTEIN SCIENCES CORPORATION
1BERNA BIOTECH, LTD.
1INTERCELL AG
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL1,906
1,575
289
IMM209286
252
236
229
s029456178
171
UT7065MA166
155
149
145
S034636133
107
U62828AA103
100
98
P10025327596
U6737AA85
UJ446AA79
78
78
59
57
4BH3254
4F47253
52
27656352
50
PP9L548
49TM346
42
40
38
MENVEO38
4F47237
R1B252M36
34
C5763AA30
93362229
25
300057A24
UNK24
22
CW311621
18
17
15
UH894AB15
3Y7NL12
R1B743M12
EJ168611
el128410
10
10
10
9
ARBA141A9
UNK9
8
UNK8
8
1F4EB8
Unknown7
7
No batch number6
5
5
UJ090AA5
5
5
4
4
4
UNK4
JEV18K95E4
UNK3
A115A3
Z127A3
3
3333324181073
2
2
2
TAR352
1
1
1
1
1
A739081
1
1
1
1
1
037K20A68,542
EL128447,700
133

Incidents per State

State Total
15,185
CA14,096
NY7,507
TX7,196
FL6,939
IN5,527
PA4,560
IL4,179
OH4,054
AZ3,856
MI3,771
NJ3,411
MA3,278
VA3,208
NC3,114
WA3,034
GA2,864
MD2,652
MN2,534
CO2,532
WI2,457
MO2,029
OR1,943
TN1,715
CT1,693
KY1,603
OK1,226
AL1,201
KS1,162
IA1,157
SC1,106
NM1,065
UT973
AR951
LA945
NE829
NV797
ME795
MT789
NH756
ID674
AK661
WV661
PR650
MS585
HI536
RI510
VT441
SD361
ND356
DE350
DC239
WY209
GU32
AS16
VI13
MP9
MH3
FM2
QM1
XB1

ID: 1010495
Sex: F
Age:
State: FL

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

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:Unknown

Allergies:

Symptoms: arm pain; itching; It's become difficult to move her arm and has worsened since the injection/ I had a hard time lift my arm in changing clothes; It's become difficult to move her arm and has worsened since the injection/ I had a hard time lift my arm in changing clothes; I feel in my arm, around that shot you know I had the injection, start itchy start feel itchy; my arm feel pink, it's swell up and it's scratch; my arm feel pink, it's swell up and it's scratch; This is a spontaneous report from a contactable consumer (patient herself). A 77-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246, expiry date not reported), via an unspecified route of administration on 09Jan2021 at single dose for COVID-19 immunisation. Medical history included bone disorder (reported as bad bone problem). Concomitant medication included denosumab (PROLIA) for bone disorder. The patient received her first injection on 09Jan2021 and had been experiencing arm pain which was mild to moderate but about a week later she developed itching in the same arm. It's become difficult to move her arm and had worsened since the injection. She wanted to know if this type of experience had been reported and if she should receive the second vaccination scheduled for the 30th. The patient stated that she had a hard time lift my arm in changing clothes and she can't her shoulder. After one week later about almost 1 week later she felt in her arm, around that shot she had the injection, started itchy started to feel itchy and she was afraid maybe infection, dead skin, maybe infection or something. She showed it to her friend, saying "Look my arm feel pink, it's swell up and it's scratch, it's itchy." Clinical outcome of event "difficulty to move her arm and had worsened since the injection" was not recovered while for the other events was unknown.

Other Meds: PROLIA

Current Illness:

ID: 1010496
Sex: M
Age:
State: MD

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: vertigo starting the evening of vaccination; This is a spontaneous report from a contactable consumer (patient). A 35-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL1283, expiry date not reported), via an unspecified route of administration on 15Jan2021 13:00 at single dose for COVID-19 immunization. Medical history included vertigo from an unknown date and unknown if ongoing. There were no concomitant medications. The patient experienced vertigo starting the evening of vaccination on 15Jan2021 and continues to persist 6 days later with decreasing intensity. The patient further reported they had vertigo that seems to resolve a couple hours after taking the vaccine and has persisted with positional changes. It was further reported that it was diminishing for the past couple of days but they were pretty intense about vertigo in particular. When they were in a laying down position like the whole room is spinning. It was horrible. The day after vaccine like they were spinning for hours at night and with positional changes from laying down to getting out of bed. When they initially lay down they got like a vertigo. The patient was recovering from the event.

Other Meds:

Current Illness:

ID: 1010497
Sex: F
Age:
State: WA

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

Lab Data:

Allergies:

Symptoms: bleeding out of her left ear; The injection site feels like bruising; This is a spontaneous report from a contactable consumer (reporting for mother in law). A 90-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EL1284, expiry date unknown), via an unspecified route of administration on an unspecified date in Jan2021 at a single dose for COVID-19 immunization. Medical history included patient was diabetic. The patient's concomitant medications included that patient was on blood thinner (unspecified). Reporter's mother-law (patient) received the Pfizer Covid vaccine yesterday (also reported as today), Jan2021. About 5 hours after receipt of the vaccine, patient was bleeding out of her left ear. It's been an ooze, like a capillary bleed. It's intermittent but it has not stopped. This was her first dose. She can hear OK and the ear was not painful. Her respiratory system seemed to doing fine. The injection site felt like bruising (Jan2021). The site looked fine, no bruising around the band aid and no swelling. She has never bled from her ear. There have not been any medication changes and no known damage to the ear. Patient asked if bleeding in the left ear been associated with the Covid vaccine. No treatment was received for the event bleeding out of her left ear. The outcome of the events bleeding out of her left ear and injection site felt like bruising was unknown.

Other Meds:

Current Illness:

ID: 1010498
Sex: F
Age:
State: MI

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Very sore upper arm and shoulder; Very sore upper arm and shoulder/pain through shoulder and neck throughout the night; pain through shoulder and neck throughout the night; difficulty sleeping; This is a spontaneous report from a contactable consumer. A 37-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in the left arm, on 15Jan2021 14:00 at SINGLE DOSE for COVID-19 immunization. The patient's medical history was not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Concomitant medication included birth control (not specified). On 15Jan2021 16:00, the patient experienced a very sore upper arm and shoulder, pain through shoulder and neck throughout the night, caused difficulty sleeping; ibuprofen helped, lasted 1 day. Therapeutic measures were taken as a result of events. Outcome of events was reported as recovered. Follow-up attempts are completed. The following information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 1010499
Sex: M
Age:
State: OR

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Body temperature; Result Unstructured Data: Test Result:100-101; Comments: Fever of about 100-101; Test Date: 20210121; Test Name: Body temperature; Result Unstructured Data: Test Result:101.3; Test Date: 20210121; Test Name: Body temperature; Result Unstructured Data: Test Result:100.9

Allergies:

Symptoms: Fever of about 100-101/fever of 101.3/He still has the fever and he just took it and it's now 100.9; slight headache; chills during the night but not now; a stuff neck; This is a spontaneous report from the Medical Team. A contactable consumer (patient) reported that a 73-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number: EL1283, intramuscular ("in the muscle") in the right arm, on 20Jan2021 14:30 at a SINGLE DOSE for covid-19 immunization. The patient's relevant medical history was not reported. There were no concomitant medications. Patient received first dose of BNT162B2 (lot number: EJ1685) on 30Dec2020 for covid-19 immunization. The patient experienced 'Fever of about 100-101, chills during the night but not now and a stuff neck'. The patient later reported that he got some chills that evening when he got the second dose of vaccine (20Jan2021). Woke up this morning (21Jan2021) with a fever of 101.3 and slight headache. Patient wanted to know if he could take Tylenol, Ibuprofen, or Aspirin, if it's okay. He wanted to clarify that chills started later that evening (second dose vaccination) but it was not bothering him now. He still has the fever and he just took it and it's now 100.9. Patient was recovering from the events "a stuff neck" and "chills during the night but not now". Whereas he had not recovered from " Fever of about 100-101/fever of 101.3/He still has the fever and he just took it and it's now 100.9" and headache. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds:

Current Illness:

ID: 1010500
Sex: F
Age:
State: IN

Vax Date: 01/10/2021
Onset Date: 01/10/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: temperature; Result Unstructured Data: Test Result:37.8 Centigrade; Comments: low grade temp (37.8 C)

Allergies:

Symptoms: swollen left arm pit which is also slightly tender to touch; swollen left arm pit which is also slightly tender to touch; sore arm; low grade temperature (37.8 C); fatigue; chills; Second dose administered on 10Jan2021; first dose was administered on 29Dec2020; This is a spontaneous report from a contactable nurse (patient). A 33-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9Z61), intramuscular (left arm) on 10Jan2021 15:00 at single dose for Covid-19 immunization. The patient received the first dose of BNT162B2 (lot number: EL1284) intramuscular (left arm) on 29Dec2020 (02:00 PM) for Covid-19 immunization. The patient's medical history included Covid-19; no known allergies. Concomitant medication included citalopram hydrobromide (CELEXA) taken PO (oral) daily before, during and after vaccination period. The patient is not pregnant. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no issues on day zero; on day 1 (11Jan2021) she had sore arm, low grade temperature (37.8 C), fatigue, and chills. All have resolved by 6am on day 2 (12Jan2021). On day 3 (13Jan2021), she noticed swollen left arm pit which is also slightly tender to touch but not bothersome. No other lymph areas are noticeably swollen or tender at this time. There was no treatment received for the adverse event. The outcome of events sore arm, low grade temperature, fatigue, and chills was recovered on 12Jan2021; the outcome of events swollen left arm pit which is also slightly tender to touch was recovering. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: CELEXA [CITALOPRAM HYDROBROMIDE]

Current Illness:

ID: 1010501
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: felt a little tender where the shot was; This is a spontaneous report from a contactable consumer (patient). This consumer reported for two patients (herself and her husband). This is the first of two reports. An 88-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on 09Jan2021 at single dose for Covid-19 immunization. Medical history included ongoing cancer cell on eyelid. The patient's concomitant medications were not reported. The patient reported that she received the first dose of Pfizer vaccine on 09Jan2021. The patient reported that she has not had any reaction at all, maybe felt a little tender where the shot was, also reported as felt nothing except maybe a little soreness on the arm in Jan2021. She added that she is due to get her next shot on 30Jan2021 and is also due to have a surgery; she added eye surgery as she have a cancer cell eyelid and she was supposed to have cancer surgery on the 1st, and wanted to know if there would be a complication if she had the vaccine two days before that surgery. She also wanted to know if they will be getting the vaccination on 30Jan2021 and what to do if the facility run out of the vaccine when they are due for the second shot. The outcome of event is unknown. Information about lot/batch has been requested.; Sender's Comments: Linked Report(s) : same reporter, suspect product, and event, different patient

Other Meds:

Current Illness: Malignant neoplasm of eyelid (due to have a surgery)

ID: 1010502
Sex: F
Age:
State: WA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: After second dose pain at injection site; chills; diarrhea; GI upset; unwell feeling; This is a spontaneous report from a contactable Other Health Professional reported for herself. A 27-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number unknown), via an unspecified route of administration left arm, on 20Jan2021 at SINGLE DOSE for covid-19 immunisation. Medical history reported as none. No reported allergies to medications, food or other products. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Facility where the most recent COVID-19 vaccine was administered as at the hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient is not pregnant at vaccination time. The patient's concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 30Dec2020 on the left arm. The patient experienced after second dose, pain at injection site, chills, diarrhea, GI upset, and unwell feeling on 20Jan2021 21:00. No treatment was given for the events. Outcome of the events was unknown. The reporter assessed the events as non-serious. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010503
Sex: F
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: her throat feels scratchy; allergic reaction; itchy dermatitis baby hives on the inside of her left elbow; itchy dermatitis baby hives on the inside of her left elbow; felt a strange sensation throughout her body; This is a spontaneous report from a non-contactable nurse (patient herself). A 32-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration (left deltoid), on 20Jan2021, at single dose, for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated that she received the first dose of the COVID vaccine yesterday, 20Jan2021. She experienced an allergic reaction two hours after receiving the vaccine and also experienced itchy dermatitis baby hives on the inside of her left elbow all on 20Jan2021. The vaccine was administered in the left deltoid muscle. Furthermore, when she walked away from the vaccination site, she felt a strange sensation throughout her body on 20Jan2021, but she was able to drive herself home. Her throat feels scratchy today 21Jan2021. With all this, she was concerned about receiving the second dose. She wanted to know if her symptoms have been reported and; if she should receive the second dose of the vaccine. The outcome of the events was unknown. No follow-up attempts are possible; information about the batch/lot number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1010504
Sex: F
Age:
State: WA

Vax Date: 01/13/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: 3 day after my vaccine I got a hard bump on the back of my ear; right lymph nodes is swollen from the inside; This is a spontaneous report from a contactable Healthcare Professional, the patient. A 26-year-old female patient started to receive the first dose BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via intramuscular route in the right arm on 13Jan2021 12:15 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. The patient did not have any allergies to medications, food, or other products. On 15Jan2021 12:00 AM, after receiving her vaccine she got a hard bump on the back of her ear and her right lymph nodes was swollen from the inside. No treatment was received for the events. Since the vaccination the patient had not been tested for COVID-19. The clinical outcome of the event hard bump and lymph node swollen was not recovered. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1010505
Sex: F
Age:
State: NY

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Name: Blood pressure; Result Unstructured Data: Test Result:90/60; Test Date: 20210115; Test Name: Blood pressure; Result Unstructured Data: Test Result:127/90; Test Name: Heart rate; Result Unstructured Data: Test Result:53-60; Test Date: 20210115; Test Name: Heart rate; Result Unstructured Data: Test Result:100bpm

Allergies:

Symptoms: Heart rate went from normal (53-60) to 100 bpm; Felt flushing feeling; blood pressure went up to 127/90 (usually 90/60); Had difficulty swallowing; Fingers started tingling; Chills (lasted 15-20 minutes); This is a spontaneous report from a contactable consumer. A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 15Jan2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient was not pregnant. Patient was not diagnosed with COVID-19 prior to vaccination. It was unknown if the patient has been tested for COVID-19 since the vaccination. On 15Jan2021, after 2 minutes of the vaccine, patient heart rate went from normal (53-60) to 100 bpm; the patient felt flushing feeling and blood pressure went up to 127/90 (usually 90/60); patient had difficulty swallowing and fingers started tingling, followed by chills (lasted 15-20 minutes, as reported). The patient was ok 90 minutes after the shot. No treatment given. The final outcome of all the events was recovered in Jan2021.Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1010506
Sex: M
Age:
State: HI

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: He feels lousy himself; This is a spontaneous report from a contactable consumer, reporting for himself. A male patient of an unspecified age received his second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on 20Jan2021 as a single dose for COVID-19 vaccination. Medical history and concomitant medications were not reported. The patient received his first dose of BNT162B2 on an unspecified date for covid-19 vaccination. On an unspecified date in Jan2021, the patient stated that he feels lousy. The clinical outcome of he feels lousy was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1010507
Sex: U
Age:
State: PA

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

Lab Data:

Allergies:

Symptoms: received the entire vial contents (0.45 mL), without dilution/overdose; received the entire vial contents (0.45 mL), without dilution/overdose; This case has been considered invalid since the reporters has no first-hand knowledge of the patients and events. This is a spontaneous report from contactable two Nurse, two Pharmacist and two Physician. These Nurse, Pharmacist and Physician reported similar events for 8 patients. This report is for 7th of 8 patient. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not provided), via an unspecified route of administration on an unspecified date at single dose (the entire vial contents 0.45 mL) for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that eight healthcare workers in a (facility name) received the entire vial contents (0.45 mL), without dilution, for their first dose of the Pfizer-BioNTech vaccine. Four of the eight workers were hospitalized as a precaution after experiencing flu-like symptoms from the overdose. Information on the Lot/batch number has been requested. Follow-up (22Jan2021): This is a follow-up spontaneous report received from a contactable Pharmacist in response to the mail trail sent regarding the confirmation of below mentioned query. This Pharmacist reported for a patient that: Query: (name) from Drug Safety Office phoned yesterday & today. She asked that (name) phone or be in touch with her because (name) wrote the article in the newsletter. (name) is interested in whether (name) had first hand knowledge of the patients mentioned in the article. If so, (name) has questions to ask about them & their reactions. Response: We are a national reporting program. We do not have any patient data. Just what you already saw. We cannot supply additional information. Reporter is confirming there is no first-hand knowledge of events. Information on the Lot/batch number has already been requested.; Sender's Comments: Linked Report(s) : Same reporter/drug; different patient/event

Other Meds:

Current Illness:

ID: 1010508
Sex: F
Age:
State: TX

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Numbness of my tongue and lips; This is a spontaneous report from a contactable nurse (patient). A 38-year-old non-pregnant female patient started to receive bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE; lot number: EL8982; expiration date: unknown), via an unspecified route of administration left arm on 21Jan2021 17:00 at a single dose for covid-19 immunization. Medical history included migraine. The patient was not diagnosed with COVID prior vaccination. The patient has no known allergies. Concomitant medication included allopurinol (ELAVIL), paracetamol (TYLENOL), vitamin c [ascorbic acid] (VITAMIN C) zinc and prenatal vitamins. The patient has not had other vaccine in four weeks. The patient received her vaccine in a hospital. On 22Jan2021 01:00 AM, the patient experienced numbness of her tongue and lips. No treatment was received for the adverse events. The patient has not been COVID tested post vaccination. The outcome of the event was not recovered.

Other Meds: ELAVIL [ALLOPURINOL]; TYLENOL; VITAMIN C [ASCORBIC ACID]; ZINC

Current Illness:

ID: 1010509
Sex: M
Age:
State: SD

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Injection site quite sore; body aches; This is a spontaneous report from a contactable consumer (patient). A 57-year-old male patient received bnt162b2 (BNT162B2), lot number Ez9261, via an unspecified route of administration Left arm from 21Jan2021 09:00 to 21Jan2021 09:00 at SINGLE DOSE (first dose) for COVID-19 immunisation. Medical history included COVID-19 prior vaccination. The patient's concomitant medications were not reported. The patient experienced injection site quite sore and body aches on 22Jan2021 03:00. The outcome of the events was not recovered. The patient was not tested for COVID-19 post vaccination. No treatment was received for the events.

Other Meds:

Current Illness:

ID: 1010510
Sex: M
Age:
State: IN

Vax Date: 01/12/2021
Onset Date: 01/17/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210117; Test Name: pain scale; Result Unstructured Data: Test Result:4-7

Allergies:

Symptoms: Non-pulsatile headaches in the bilateral temporal areas. The pain can range from 4-7/10 on the pain scale; This is a spontaneous report from a contactable other health professional (patient). A 46-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in the left arm on 12Jan2021 at SINGLE DOSE for COVID-19 immunization. Medical history included undifferentiated connective tissue disease and penicillin allergies. Patient received the first dose of BNT162B2 (lot number: EJ2685) in the left arm on 22Dec2020, 11:00 for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Concomitant medications included metoprolol and valaciclovir hydrochloride (VALTREX). On 17Jan2021, around four to five days after second vaccination, patient started developing non-pulsatile headaches in the bilateral temporal areas. The pain can range from 4-7/10 on the pain scale and has caused him to miss work. The outcome of event was unknown. Patient took pain medication for headache as a result of events but "OTC did not work". No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: METOPROLOL; VALTREX

Current Illness:

ID: 1010511
Sex: F
Age:
State: MD

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Itchy throat; left side of face burning; left side of face burning/tingling sensation; burning/tingling sensation left side of lip; burning/tingling sensation and left side of lip; This is a spontaneous report from a contactable other healthcare professional. A 28-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration second dose (lot number: EL3302) on 21Jan2021 17:00 at single dose on right arm for COVID-19 immunization. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number: E11284, on 29Dec2020 13:30 on right arm. Medical history included asthma and seasonal allergies. The patient did not test for COVID post vaccination. The patient is not pregnant. The patient experienced itchy throat, left side of face burning/tingling sensation and left side of lip on 21Jan2021 17:45. The patient took Benadryl as treatment for the events. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1010512
Sex: M
Age:
State: NC

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: blood work; Result Unstructured Data: Test Result:Unknown; Comments: they said he had no COVID; Test Name: Height; Result Unstructured Data: Test Result:5ft 6 inches; Test Date: 20210122; Test Name: temperature; Result Unstructured Data: Test Result:100; Test Name: weight; Result Unstructured Data: Test Result:160 lbs; Comments: Probably 160 pounds; Test Date: 20210121; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown; Comments: they said he had no COVID

Allergies:

Symptoms: tightness on the chest; chest was hurting and felt like it has been compressed; congested; body aches/ his body is still aching/ body was aching/ achy; headaches; fever/ he has a temperature at 100; tired; felt weak; feeling kind of hot and achy; This is a spontaneous report from a contactable consumer (patient). A 46-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Solution for injection (lot number: EL9261, expiry date unknown) via an unspecified route of administration on 20Jan2021 at a single dose on the left arm for COVID-19 immunization. The patient had no medical history and no known allergies. There were no concomitant medications. The patient did not receive medications within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to BNT162B2. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient had not been tested for COVID-19. The patient received the first dose of BNT162B2 (lot number: EL1284, expiry date unknown) on 29Dec2020, 11:00AM at a single dose on the left arm for COVID-19 immunization. The patient reported he is probably 160 pounds, 5ft 6 inches; he received the second dose of the COVID-19 vaccine on 20Jan2021, while being due for it on 19Jan2021. He explained having body aches, headaches, fever, tired, and felt weak the following morning (21Jan2021, 04:30 AM) and therefore went to the ER. He had blood works and an X-ray done on 21Jan2021 (results unknown) and they said he had no COVID. Today, 22Jan2021, he has a temperature at 100, his body is still aching, the headaches are there along with a tightness on the chest that concerns him. He also described it as his chest was hurting and felt like it has been compressed. Patient asked what to do. He then mentioned that the nearby urgent care had refused to take him because the vaccine is still 'under investigation' and the ER is far away. Patient also reported that he was feeling kind of hot and achy, body was aching on 21Jan2021.Today, 22Jan2021, he was still the same. He got a fever, was congested, and his body is aching. Patient did not received treatment for the events. Outcome of the events 'body aches/ his body is still aching/ body was aching/ achy,' headaches, 'fever/ he has a temperature at 100,' tired, felt weak, 'feeling kind of hot and achy,' and congested was not recovered. Outcome of the other events was unknown. The events body aches/ his body is still aching/ body was aching/ achy,' headaches, 'fever/ he has a temperature at 100,' tired, and felt weak required Emergency room visit and were reported as medically significant.

Other Meds:

Current Illness:

ID: 1010513
Sex: F
Age:
State: MA

Vax Date: 01/16/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital: Y

Lab Data: Test Date: 20210120; Test Name: COVID-19 PCR test (nasal swab); Test Result: Negative

Allergies:

Symptoms: Acute appendicitis; This is a spontaneous report from a contactable physician reporting for herself. A 31-year-old female patient received the 2nd dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech, lot# EK4176), intramuscular in the left arm, on 16Jan2021 at 18:30, at single dose, for COVID-19 immunisation. Medical history included iron deficiency anaemia, migraine and drug allergy to amoxicillin. The patient was not diagnosed with COVID-19 prior to vaccination. Concomitant medications included multivitamin and ferrous sulfate (unknown manufacturer). Previously the patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech, lot# EH9899), on 26Dec2020 at 04:15 PM, intramuscular in left arm for COVID-19 immunisation. The patient experienced acute appendicitis on 20Jan2021 at 09:00 with outcome of recovering. The patient went to the emergency room and was hospitalized due to the event in Jan2021 for 1 day. Therapeutic measures were taken as a result of the event and included laparoscopic appendectomy. The patient underwent lab tests and procedures which included COVID-19 PCR test (nasal swab): negative on 20Jan2021.; Sender's Comments: Given the nature of the medical condition and the overall clinical picture, the event appendicitis is most likely an intercurrent medical condition and is assessed as unrelated to bnt162b2. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds: FERROUS SULFATE

Current Illness:

ID: 1010514
Sex: F
Age:
State: VT

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: high fever of 101.8; body aches; headache; rigors/chills; shaking; increased pain at injection site; one instance of vomiting; This is a spontaneous report from a contactable other health professional (patient). A 30-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number: El3302, via an unspecified route of administration on 20Jan2021 02:00 at a SINGLE DOSE for covid-19 immunization. Medical history included allergies to penicillin and cephalosporin. Patient received her first dose of BNT162B2 on 30Dec2020 at (12:00) (lot number: ELO140), (in the right arm) for COVID-19 immunization. Patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. The patient's concomitant medications were not reported. The patient developed a high fever of 101.8 (unit not provided), chills, body aches, headache, rigors, shaking, increased pain at injection site, and one instance of vomiting starting approximately 6 hours after her second dose (for clarification) of the vaccine (20Jan2021, 20:00). the outcome of event was reported as 'recovering'. the patient did not receive any treatment due to the events. The events were considered as non-serious by the reporter. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds:

Current Illness:

ID: 1010515
Sex: M
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Back problems; This is a spontaneous report from a contactable consumer (patient's wife). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 20Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's wife and the patient both had their shot two days ago (20Jan2021) and patient had back problems and the doctor wanted him to get a cortisone shot. The reporter was asking if it can interfere with the COVID shot. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010516
Sex: F
Age:
State:

Vax Date:
Onset Date: 01/14/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Weak; Fatigued; Fever; Muscle Aches; Couldn't Taste; Pounding Headache; This is a spontaneous report from a non-contactable consumer (reporting for a friend). A 42-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: Unknown), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine includes 1st dose of bnt162b2 on an unspecified date for COVID-19 immunization. The reporter's friend (who is a doctor) could not leave bed for one whole day after the 2nd shot and felt weak, fatigued, fever, muscle aches, could not taste and pounding headache on 14Jan2021. The patient did not receive treatment for the events. Prior to vaccination the patient has no COVID. The outcome of the events was recovered on Jan2021. No follow-up attempts are possible. Information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1010517
Sex: F
Age:
State: NM

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Medical history included systemic lupus; Medical history included systemic lupus; Fever; Vomiting; Diarrhea; Abdominal pain; Joint/muscle pain; Joint/muscle pain; Nausea; Fatigue; Severe headache; Sore arm; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number: EL3249, via an unspecified route of administration in the right arm on 15Jan2021 13:00 at SINGLE DOSE (first dose) for COVID-19 immunization. Medical history included systemic lupus, "hypothyroid", Leiden Factor V. Patient's known allergies: penicillin, erythromycin and tetracycline. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Concomitant medications included hydroxychloroquine, clopidogrel bisulfate (PLAVIX), acetylsalicylic acid (ASPIRIN), fluoxetine hydrochloride (PROZAC), bupropion hydrochloride (WELLBUTRIN). The patient previously took erythromycin and experienced drug hypersensitivity, tetracycline and experienced drug hypersensitivity. On 15Jan2021 16:00, the patient experienced fever, vomiting, diarrhea, abdominal pain, joint/muscle pain, nausea, fatigue, severe headache and sore arm. Outcome of events was fever, vomiting, diarrhea, abdominal pain, joint/muscle pain, nausea, fatigue, severe headache and sore arm not recovered. Outcome of the other events was unknown. Patient did not receive any treatment for the events. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: HYDROXYCHLOROQUINE; PLAVIX; ASPIRIN [ACETYLSALICYLIC ACID]; PROZAC; WELLBUTRIN

Current Illness:

ID: 1010518
Sex: F
Age:
State:

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; Nausea; extreme Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 43-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3249), via an unspecified route of administration at the left arm on 21Jan2021 14:30 at a single dose for covid-19 immunization. The patient medical history includes chronic kidney disease. The patient was not pregnant from the time of administration. The patient was taking numerous unspecified medications. The patient previously took amoxicillin sodium;clavulanate potassium (AUGMENTIN) and experienced allergy. On 21Jan2021 at 04:30 PM the patient experienced headache, nausea and extreme diarrhea. The events were assessed as non-serious, did not result in death, not life threatening, did not cause/prolonged hospitalization, not disabling/incapacitating, did not cause congenital anomaly/birth defect. Treatment was not received for the adverse events. The vaccine was administered in doctor's office/urgent care. The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient has not been tested for COVID-19. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1010519
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: haven't felt like herself; dizziness/lightheadedness; stomach started to turn/nausea; no ambition; stomach pain; This is a spontaneous report from a contactable consumer (patient). An 87-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: not reported), via an unspecified route of administration on an unspecified date in Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient stated that she haven't felt like herself. She woke up in the morning and felt good but by 2pm, she experienced dizziness/lightheadedness, stomach started to turn/nausea, no ambition and stomach pain. She took a pain pill and sat down for a couple of hours and then the stomach pain resolved. She wanted to know if these were all normal and if she should get the second dose given the side effects that she experienced. The outcome of the event stomach pain was recovered on an unspecified date while unknown for the other events. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1010520
Sex: F
Age:
State: IL

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: both of her legs seized. The muscles so tight that I was unable to walk (like a spasm); The muscles so tight that I was unable to walk/ just a muscular contraction that left me unable to walk properly (the left side seem to be the tightest side of by body); like a spasm; bilateral jaw pain; slight numbness on by left face; face still has a bit of muscle sensitivity (tingling sensation) near the mouth and jaw; redness on my left cheek; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on the left arm on 21Jan2021 09:15 at a single dose for COVID-19 immunization. Medical history included shellfish allergy. Concomitant medications included received within 2 weeks of vaccination but were not reported. The patient previously took codeine and experienced allergy. On 21Jan2021 11:30, both of her legs seized. The muscles so tight that she was unable to walk (like a spasm). There was no twitch just a muscular contraction that left her unable to walk properly (the left side seem to be the tightest side of by body). The patient also had bilateral jaw pain (not sure if it was because she was in so much pain in the legs that she was clenching my teeth). She also had slight numbness on by left face and by the evening she had redness on her left cheek but it went away. Her face still had a bit of muscle sensitivity (tingling sensation) near the mouth and jaw. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not pregnant. Since the vaccination, the patient has not been tested for COVID-19. Prior to vaccination, the patient was not diagnosed with COVID-19. Events were reported as non-serious. Outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1010521
Sex: F
Age:
State: MI

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: terrible case of diarrhea; arm is sore; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3749), intramuscular on 20Jan2021 15:30 at a single dose on left arm for COVID-19 immunization. Medical history included ongoing COPD, diagnosed probably 7 years ago. There were no concomitant medications. The patient's arm began to get sore the day after receiving the vaccine, 21Jan2021. She had a CAT scan earlier last week, but this was prior to the vaccine. She had the terrible case of diarrhea this morning, 22Jan2021, but she hasn't had diarrhea since then. She got up this morning. She was feeling fine, she drank 2 cups of coffee. She was pouring herself a cup of orange juice, and she had a terrible case of diarrhea. The outcome of the event diarrhea was unknown, arm is sore was recovering. Vaccination Facility Type was Physician's office. Adverse events did not require a visit to Emergency Room nor Physician Office. No prior vaccinations (within 4 weeks). No adverse events following prior vaccinations.

Other Meds:

Current Illness: COPD (Verbatim: COPD, Caller was diagnosed with COPD probably 7 years ago)

ID: 1010522
Sex: F
Age:
State: MA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sweating while sleeping overnight; pain/soreness in arm; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL9261) in the hospital, via an unspecified route of administration on 20Jan2021 at a single dose on the left arm for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. It was reported that the patient experienced pain/soreness in arm that has remained for 2 days and experienced sweating while sleeping overnight which is not typical for her sleep patterns. The events were reported to have occurred on 20Jan2021. The outcome of the events was recovering. The patient did not receive any treatment for the events. The events were reported as non-serious. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1010523
Sex: F
Age:
State: IN

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: injection site left arm turned "kinda pinky/red and a little puffy; her arm turned "kinda pinky/red and puffy."; injection site left arm/tender to the touch; injection site left arm/little heat/warm; This is a spontaneous report from a contactable consumer (patient). An 83-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3248, expiry date: unknown), via an unspecified route of administration in the left arm on 19Jan2021 14:20 at a single dose for covid-19 immunisation. Medical history included ongoing obesity from 2018 (onset was around time her husband died in 2018. She thinks she started getting more sedentary and picking up weight about then). The patient's concomitant medications were not reported. The patient had no history of previous immunization with the Pfizer vaccine and no additional vaccines administered on same date of the bnt162b2. The patient previously had smallpox vaccine for immunization when she was a child and that of which really worked, but it was not just a neat little thing and she still has the scar on her upper arm; and varicella zoster vaccine rge (cho) (SHINGRIX) on unspecified date in 2019 for immunization. She had quite a reaction to this first dose of SHINGRIX vaccine but cannot remember what the symptoms she had were; she was down for a few days with that. She told her family doctor about the reaction, and that she received the vaccine at (pharmacy name); the family doctor said she should not get the second dose of the SHINGRIX. On 20Jan2021, the patient experienced her injection site left arm turned "kinda pinky/red and a little puffy, with a little heat/warm and tender to the touch." Outcome of the all the events was unknown.

Other Meds:

Current Illness: Obesity (around time her husband died in 2018/started getting more sedentary and picking up weight)

ID: 1010524
Sex: M
Age:
State: CO

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: this shot was much too high, barely in the deltoid.; immediate pain; This is a spontaneous report from a contactable physician (patient). A 72-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EL3247), via an unspecified route of administration at left arm on 21Jan2021 at 19:00 (reported as 07:00 PM) at SINGLE DOSE for COVID-19 immunisation. The patient was administered COVID-19 vaccine at the hospital. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID prior to vaccination. Medical history included Allergies: Penicillin. The patient's concomitant medications were not reported. The patient reported "Received first covid vaccine 21Jan. Nurse's technique was poor and I had immediate pain. I'm a physician, I know where the deltoid is and this shot was much too high, barely in the deltoid. I'm concerned about vaccine failure. Should we check antibody levels?" The event started on 21Jan2021 at 19:00 (reported as 07:00 PM). The reporter considered the events as non-serious. The patient did not receive treatment for the events. It was also reported that since the vaccination, the patient has not been tested for COVID-19. The patient had not yet recovered from the event immediate pain.

Other Meds:

Current Illness:

ID: 1010525
Sex: F
Age:
State: AZ

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

Lab Data: Test Name: cholesterol; Result Unstructured Data: Test Result:high; Test Name: blood pressure; Result Unstructured Data: Test Result:high; Test Date: 20210121; Test Name: COVID-19 rapid POC test; Test Result: Positive

Allergies:

Symptoms: due to get the 2nd dose, but she tested positive for COVID yesterday; due to get the 2nd dose, but she tested positive for COVID yesterday; Dizzy; starting to get foggy; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EH9899 or EH9897), via an unspecified route of administration at the left arm on 04Jan2021 at single dose for COVID-19 immunization. Medical history included ongoing diabetic, blood pressure high, high cholesterol and sore arms from previous vaccines (unspecified).She had energy for a whole week after getting the vaccine, that she has not had for a long time, she even cleaned out her whole garage; has been waiting to do that for 3 years; had to make herself stop to rest. There were no concomitant medications. The patient got her first dose on 04Jan2021 and was due to get the 2nd dose this coming 25Jan2021, but she tested positive for COVID on 21Jan2021. She has been sick for a week which started with an irritating cough on 14Jan2021. She went to the ER because she was dizzy as could be on Jan2021. She does not remember which day; she was starting to get foggy on Jan2021. She was not admitted. She did a drive through rapid test on 21Jan2021 and it was positive. Lot numbers: Handwriting on her card was bad and she cannot tell if the last digit of the Lot number is a 9 or 7. The vaccine was administered in an open tent clinic outside in a parking lot outside a hospital and not in a military facility. The outcome of the event was unknown. Information on Lot/Batch has been requested.

Other Meds:

Current Illness: Diabetic

ID: 1010526
Sex: M
Age:
State: VA

Vax Date: 01/08/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: PCR; Test Result: Negative ; Test Date: 20210111; Test Name: Nasal swab; Test Result: Negative

Allergies:

Symptoms: Stuffed nose, developed after 7 days; Nose became painful to touch; Light chills; light headache; lack of strength; This is a spontaneous report from a contactable other hcp (patient himself). A 57-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection, lot no. EL1284, expiry date not reported), via an unspecified route of administration on 08Jan2021 12:00 at a single dose on right arm for covid-19 immunization. Medical history included hay fever. Prior to vaccination patient was not diagnosed with Covid-19. Concomitant medication included melatonin taken within 2 weeks of vaccination on unspecified date for unspecified indication. On 15Jan2021 (also reported as 17Jan2021-pending clarification), it was reported that patient had stuffed nose, developed after 7 days of vaccination. Nose became painful to touch. Light chills, light headache and lack of strength. Patient received treatment of TYLENOL and decongestant. Since the vaccination the patient has been tested for Covid-19. On 11Jan2021, patient had PCR and nasal swab, and both were negative. The facility where the most recent Covid-19 vaccine administered was in a hospital. The outcome of events was recovering.

Other Meds: MELATONIN

Current Illness:

ID: 1010527
Sex: F
Age:
State: FL

Vax Date: 01/16/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:101; Test Date: 20210121; Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: Chills; Fever of 101; Swollen glands or lymph nodes at the base of her skull; lymph node venapathy; Aches; This is a spontaneous report from a contactable nurse (patient). An 81-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration in right deltoid, on 16Jan2021 (also reported as 15Jan2021), at a single dose, for COVID-19 immunization. The patient's medical history included therapy for her back. There were no concomitant medications. After the patient got her first vaccine on 16Jan2021 (also reported as 15Jan2021) which was almost a week now, she was experiencing side effects. In Jan2021, the patient had chills, fever of 101, swollen lymph nodes, and aches. The patient had swollen glands or lymph nodes at the base of her skull, the lymph node venapathy (unspecified; as reported). The patient underwent a COVID-19 test yesterday (21Jan2021) to be sure (unknown results). The patient asked that if this is from the vaccine, how long could she expect to have these side effects. The patient was scheduled for it for the second dose in February. As treatment for the events, the patient was taking ibuprofen (MOTRIN), had taken paracetamol (TYLENOL EXTRA STRENGTH) at 1000 mg every 6 hours, and ibuprofen (ADVIL) at 400 mg. The patient had not recovered from the events. The patient considered that the events had a causality with the suspect product. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1010528
Sex: F
Age:
State: NY

Vax Date: 12/31/2020
Onset Date: 12/31/2020
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 2020; Test Name: pregnancy test; Test Result: Negative ; Test Date: 202101; Test Name: pregnancy test; Test Result: Positive ; Comments: she had a negative pregnancy test before getting the first vaccine dose, but then had a positive pregnancy test a few days after the first dose.

Allergies:

Symptoms: unfortunately she had a miscarriage about 5-6 days before her second dose; positive pregnancy test a few days after the first dose.; positive pregnancy test a few days after the first dose.; This is a spontaneous report from a contactable consumer. A 32-year-old female patient (3 weeks pregnant at time of vaccination) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on left arm on 31Dec2020 at single dose for covid-19 immunisation. The patient medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included iron and minerals nos, vitamins nos (PRENATAL VITAMINS). The patient had a negative pregnancy test in 2020 before getting the first vaccine dose, but then had a positive pregnancy test in Jan2021 a few days after the first dose, but unfortunately she had a miscarriage in Jan2021, about 5-6 days before her second dose. She has an appointment scheduled with OBGYN for the miscarriage. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the miscarriage was recovering.; Sender's Comments: Based on the temporal relationship, the association between the event miscarriage with BNT162b2 can not be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds: IRON; PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]

Current Illness:

ID: 1010529
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: I can't get feeling myself; feeling sick; having dizziness, lightheadedness; pain in the stomach; tired; head is going around; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age (Age: 87; Unit: Unspecified) received first single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, batch/lot number and exp date not reported), 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. Patient stated that she had the covid vaccine first dose on a Monday and after the shot she had been feeling sick (onset date not reported). She further stated "I can't get feeling myself, having dizziness, lightheadedness, pain in the stomach, feeling sick, tired, head is going around." She wanted to know if that was due to the vaccine. The events were considered as non-serious by the reporter. Patient wanted to know if she should take the second dose. The outcome of the events was unknown. Information about lot number and expiry date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1010530
Sex: F
Age:
State: MI

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Covid test Nasal Swab; Test Result: Negative ; Comments: nasal swab

Allergies:

Symptoms: Sore throat; headache; severe pain at injection site; body aches; congestion/runny nose; congestion/runny nose; fever; This is a spontaneous report from a contactable consumer (patient). A 29-year-old female patient receive the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL3248) in the hospital, via an unspecified route of administration on 19Jan2021 at 15:15 on the left arm at a single dose for COVID-19 immunization. Medical history included migraine with aura from an unknown date and unknown if ongoing. Concomitant medication included unspecified prenatal vitamins. The patient had no known allergies. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that the patient experienced sore throat, headache, severe pain at injection site, body aches, congestion/runny nose and fever all on 19Jan2021 at 17:30. The patient did not receive treatment for the events. The outcome of the events was recovering. The events were reported as non-serious. The patient underwent a post vaccination COVID test via nasal swab on 21Jan2021 with a negative result.

Other Meds:

Current Illness:

ID: 1010531
Sex: F
Age:
State: IL

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: dizzy; This is a spontaneous report from a contactable consumer. A 70-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on 21Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient woke up on 22Jan2021 and was feeling dizzy. She was asking if that was normal. Outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010532
Sex: F
Age:
State: CA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sudden onset of chest tightening around my rib cage; pain was about a 4. It did not travel to other parts of my body; This is a spontaneous report from a contactable other healthcare professional (patient). A 70-year-old female patient received bnt162b2 (BNT162B2), Lot number=EL1283, via an unspecified route of administration Left arm from 20Jan2021 09:46 to 20Jan2021 09:46 at SINGLE DOSE (first dose) for covid-19 immunisation. Medical history included colon cancer (S/P colon cancer), Sulfa allergies which caused sores in mouth, and latex fibers allergy which caused eye swelling and sneezing. Concomitant medication included trazodone 50mg, levothyroxine 75ug. The patient received the vaccine at 9:46 am. One half-hour after receiving it, the patient experienced sudden onset of chest tightening around her rib cage. She was able to breathe normally at rest. The pain was about a 4. It did not travel to other parts of her body and she had no other symptoms. It may have worsened gradually and then, ultimately subsided at 1.5 hours after the pain onset. She haven't had any other symptoms since. The outcome of the events was recovered. The patient is not pregnant at the time of vaccination. No treatment was given for the events.

Other Meds: TRAZODONE; LEVOTHYROXINE

Current Illness:

ID: 1010533
Sex: F
Age:
State: IL

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Got the first dose of the vaccine yesterday. About an hour after is when her arm starting getting sore; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received bnt162b2 (BNT162B2), lot number not reported, via an unspecified route of administration from 21Jan2021 to 21Jan2021 as SINGLE DOSE (first dose) for COVID-19 immunisation. Medical history included none. There were no concomitant medications. The patient is a 70/yo female who is very concerned that she 'took half of a Tylenol Migraine' yesterday morning before receiving her first dose of Pfizer-Biontech Covid19 vaccine. She stated she came home, started reading on the internet, and is worried now that the dose won't be efficacious. She also reports a sore arm and wants to know 'if that's a good sign' of immune response. She also stated that her doctors 'don't know, and told me to call you'. Got the first dose of the vaccine yesterday. About an hour after is when her arm starting getting sore. It got progressively more sore throughout the day. This morning it has improved but is still sore when she raises her arm. Treatment: Took Tylenol. This was before she read this article. The nurse was the one who told her to take Tylenol. She goes for her second dose on 11Feb2021. The patient got the first dose of the COVID Vaccine yesterday. Before she went to get her shot she was getting a migraine so she took half of a Tylenol Migraine. She read that if you take Tylenol before getting the vaccine that it can effect the efficacy, the patient was asking if this was true. The outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 1010534
Sex: F
Age:
State: MO

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: getting intermittent sharp zapping pains on my left side of my external Obliques; woke up with my left armpit hurting and lymph nodes swollen on my left breast; woke up with my left armpit hurting and lymph nodes swollen on my left breast; feel achy; had chills; This is a spontaneous report from a contactable nurse (patient). A 37-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EJ1686) via an unspecified route of administration on the left arm on 19Jan2021 18:00 at a single dose for COVID-19 immunization. Medical history included celiac, anxiety depression, ADHD, cold sores sometimes, secondary infertility, seasonal allergies, sulfa allergy. Concomitant medication included lisdexamfetamine mesilate (VYVANSE), sertraline hydrochloride (ZOLOFT), metformin, ibuprofen, pyridoxine hydrochloride (B6) and folic acid. Previously the patient experienced allergies: hydrocodone, naproxen. The patient received first dose of BNT162B2 on 28Dec2020 for COVID-19 immunization (lot number: EL1284, left arm). After her 2nd vaccine (20Jan2021) she felt achy and had chills, no fever that was expected. Then the second day after her vaccine on 21Jan2021 12:00 AM, she woke up with her left armpit hurting and lymph nodes swollen on her left breast. Then on my third day (22Jan2021) she woke up and still had the left armpit pain and swelling and now she was getting intermittent sharp zapping pains on her left side of her external Obliques. She could not find anything online about the armpit pain and swelling and the Obliques pain. She was a nurse also and just wanted reassurance her that this was normal she was gonna get better. No treatment was received for the events. The events resulted to a doctor or other healthcare professional office/clinic visit. The facility where the vaccine was administered was in a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient has not been tested for COVID-19. Prior to vaccination, the patient was not diagnosed with COVID-19. Events were reported as non-serious. Patient was not pregnant. Outcome of the events was not recovered.

Other Meds: VYVANSE; ZOLOFT; METFORMIN; IBUPROFEN; B6; FOLIC ACID

Current Illness:

ID: 1010535
Sex: M
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: feeling really weak; feeling so run down; real bad headache; aches and pains; Nausea; Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EK9231) via an unspecified route of administration on the right arm on 12Jan2021 at a single dose for COVID-19 immunization. Medical history included rheumatoid arthritis and asthma both were ongoing. There were no concomitant medications. The patient reported 10 minutes after receiving the COVID-19 Vaccine on 12Jan2021 he developed a real bad headache. He said his headache was followed by aches and pains, nausea, and some diarrhea. Clarified by Saturday, 16Jan2021, his symptoms had mostly cleared up. He was feeling really weak on 13Jan2021. His doctor checked him over on his 13Jan2021 appointment. He said his doctor told him there had been a lot of reports of side effects from the COVID-19 Vaccine. He said his doctor wanted him to just keep an eye on if any symptoms got worse. He said from 13Jan2021 his headaches were starting to go away, and were less frequent. He said from 13Jan2021 he was still feeling pretty achy, and had occasional diarrhea. He said by 16Jan2021 his headache, ache, pain, nausea, and diarrhea had resolved. He said he was still feeling really weak. He said he was feeling really run down on 13Jan2021, so went to his doctor again on 19Jan2021, and was given a B12 shot. He was told to stay home from work on 20Jan2021. Reported he went back to work on 21Jan2021, and 22Jan2021. He said he was told by his boss that he needed to report his side effects from the COVID-19 Vaccine. Reported he was scheduled to receive his second COVID-19 Vaccine shot on 02Feb2021. He asked if he should go for his second vaccine dose or should he wait. Reported he did not have any blood work performed when he went to the doctor on 13Jan2021 and 19Jan2021. The facility where the vaccine was administered was in a Public Health Department. There was no history of all previous immunization with the Pfizer vaccine considered as suspect. There were no additional vaccines administered on same date of Pfizer suspect. The events resulted to a physician Office visit. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No relevant tests done. The patient recovered from the events headache, aches and pain, nausea, and diarrhea on 16Jan2021; feeling really weak in Jan2021 and outcome of the other event was recovering.

Other Meds:

Current Illness: Asthma; Rheumatoid arthritis

ID: 1010536
Sex: M
Age:
State: NC

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

Lab Data: Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:103 Fahrenheit; Test Date: 202101; Test Name: liver enzymes; Result Unstructured Data: Test Result:elevated; Test Date: 202101; Test Name: hepatitis serology; Result Unstructured Data: Test Result:negative

Allergies:

Symptoms: myalgia; joint pain; 103 F fever for 6 days; elevated liver enzymes; This is a spontaneous report from a contactable physician. A male patient of an unspecified age received his second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient took the 2nd dose of the vaccine on 12Jan2021 and had myalgia, joint pain, and 103 F fever for 6 days (Jan2021). The patient also had an elevated liver enzymes (Jan2021) and a negative hepatitis serology result. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1010537
Sex: M
Age:
State: PA

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20200120; Test Name: Body temperature; Result Unstructured Data: Test Result:100 Fahrenheit

Allergies:

Symptoms: Significant chills; Spiked a fever (100 F at peak); Night sweats; Joint/muscle aches; Joint/muscle aches; This is a spontaneous report from a contactable healthcare professional (patient). A 38-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL1283; Expiration date was not reported), intramuscularly on the left arm on 19Jan2021 (18:00) at a single dose for COVID-19 immunization at the public health clinic. Medical history included diabetes type II, asthma, high cholesterol and sulfa allergy. Concomitant medications included metformin, montelukast, finasteride, atorvastatin, cetirizine and fluticasone propionate (FLUTICASON). The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK5730; Expiration date was not reported), intramuscularly on the left arm on 28Dec2020 (when the patient was 38 years old) for COVID-19 immunization. On 20Jan2021 (06:00), the patient had joint/muscle aches. On 20Jan2021 (19:30), the patient had significant chills for "about 15 minutes"; had spiked a fever (100 F at peak); and had night sweats. The patient had not receive any treatment for the reported events. The outcome of the events was recovered in Jan2021 for 'joint aches', 'significant chills' and 'night sweats'; was recovered on 21Jan2021 for 'spiked a fever'; and was recovering for 'muscle aches'. The patient was not diagnosed with COVID-19 prior to vaccination, and had not been tested since the vaccination.

Other Meds: METFORMIN; MONTELUKAST; FINASTERIDE; ATORVASTATIN; CETIRIZINE; FLUTICASON

Current Illness:

ID: 1010538
Sex: F
Age:
State: PA

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

Lab Data:

Allergies:

Symptoms: Chills; This is a spontaneous report from a non-contactable consumer. An adult female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EJ1685), via an unspecified route of administration, on 11Jan2021, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (Lot Number: EJ1685) on 21Dec2020 for COVID-19 immunization. The most recent COVID-19 vaccine was administered in a hospital facility. On an unspecified date, the patient experienced chills. Therapeutic measures were taken as a result of the event which included ibuprofen (ADVIL). The event was considered non-serious. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1010539
Sex: F
Age:
State: MN

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: shaking chills lasting 10 hours; severe frontal headache; nausea; intermittent dizziness; muscle pain; joint pain; fatigue; This is a spontaneous report from a contactable nurse (patient herself). A 64-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3302), intramuscular (left arm), on 20Jan2021 09:00, at single dose, for covid-19 immunization. Medical history included allergies: penicillin, sulfa, environmental. Concomitant medications included levothyroxine; cetirizine hydrochloride (ZYRTEC ALLERGY); calcium; and colecalciferol (VIT D3). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EJ1685), on 30Dec2020 16:00, intramuscular (left arm), for covid-19 immunization at 64-years-old. The patient experienced, "10-11 hr" post injection, on 20Jan2021 20:00 started shaking chills lasting 10 hours. The patient also experienced on 20Jan2021 20:00 severe frontal headache with nausea and intermittent dizziness, muscle pain, joint pain, and fatigue - which all resolved after about 24 hr after onset. No treatment was received for these adverse events. The patient recovered from all the events on 21Jan2021. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have COVID prior to vaccination and have not been COVID tested post vaccination.

Other Meds: LEVOTHYROXINE; ZYRTEC ALLERGY; CALCIUM; VIT D3

Current Illness:

ID: 1010540
Sex: F
Age:
State: MI

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210120; Test Name: Temperature; Result Unstructured Data: Test Result:102

Allergies:

Symptoms: Temperature of 102; body aches; chills; headache; This is a spontaneous report from a contactable nurse (patient herself). A 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Jan2021 at a SINGLE DOSE for covid-19 immunization. The patient's medical history was not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. the patient was not pregnant. Concomitant medication included celecoxib (CELEXA) and vitamin D. The patient previously took stadol and experienced allergies. Patient previously received the first dose of bnt162b2 (lot number: EJI1686) on 29Dec2020 via intramuscular in the right arm for covid-19 immunization and experienced Right sided supraclavicular lymph node enlargement and pain. On 20Jan2021 01:00, 24 hours after the vaccine administration, the patient had a temperature of 102 body aches, chills and headache. The outcome of events was reported as "recovering". The patient did not receive any treatment for the events. the events were considered as non-serious. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: CELEXA [CELECOXIB]; VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 1010541
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: have a situation on my arm. it is swollen, hot, and the size of 2 o3 half dollars put together; have a situation on my arm. it is swollen, hot, and the size of 2 o3 half dollars put together; headache; tiredness; muscle pain; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 13Jan2021 at a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that the patient had a situation on her arm, it was swollen, hot and the size of 2 "o3 half dollars" put together on 14Jan2021. It was also reported that the patient experienced headache, tiredness and muscle pain on 14Jan2021. Outcome of events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010542
Sex: F
Age:
State:

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Name: Blood; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: Stomach hurt/stomach pain; feels like throwing up/Nausea/feels nauseous/sick to her stomach; some pain after inoculation in her arm at the site; dizzy; This is a spontaneous report received from a contactable consumer. A 71-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982, expiry date: 31May2021), intramuscular in the left arm, on 21Jan2021 13:00, at 0.3 mL, single, for COVID-19 immunization. Medical history included "kashi disease" which the reporter further explained as a rare disease that affects shape of red blood cells and has to do with spleen; and brittle bones (pending clarification). Concomitant medications included an unspecified infusion which the patient has to go to every other week (also reported as every two weeks) for "kashi disease" and unspecified medications for brittle bones (pending clarification). The patient did not have any other recent vaccinations. On 21Jan2021, the patient had some pain after inoculation in her arm at the site, was a bit dizzy and had stomach issues which started at night. The patient started feeling "stomach hurt"/stomach pain or sick to her stomach on 21Jan2021 at around 23:00 (reported as "11:00PM-12:00PM"), experienced nausea/felt nauseous, stomach pain, and felt like throwing up. The patient still has that in the morning of 22Jan2021. It was reported that they were not treating the stomach pain with anything. The patient's dizziness went away. The reporter wanted to know if the patient would get the same side effects after the second shot. It was also reported that they check the patient's blood once a month doing labs, results were unknown. The outcome of dizziness was resolved on an unspecified date; "stomach hurt/stomach pain" and nausea were not recovered; and vaccination site pain was unknown.

Other Meds:

Current Illness:

ID: 1010543
Sex: M
Age:
State: OH

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: right knee was swollen like there is "water on his knee"; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on 21Jan2021 11:00 at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that he received the COVID-19 vaccine yesterday at 11AM (21Jan2021). This morning (22Jan2021), he woke up and his right knee was swollen like there is "water on his knee". He doesn't know any other problems that may have caused it aside from the vaccine. He was wondering if this is a side effect of the vaccine. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010544
Sex: F
Age:
State: NC

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

Lab Data: Test Name: ultrasound; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: large inflamed swollen lymph nodes under her arm / extremely swollen large lymph node under the right arm; large inflamed swollen lymph nodes under her arm / extremely swollen large lymph node under the right arm; fatigue; This is a spontaneous report from a contactable consumer reporting for a female patient (daughter). A 25-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date were unknown) via an unspecified route of administration in the right arm on an unspecified date at SINGLE DOSE for covid-19 immunization. Medical history was reported as none. There were no concomitant medications. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unspecified date via unspecified route of administration in the right arm at single dose for covid-19 immunization. She received both shots (first and second dose) in the same arm. The reporter stated that patient (daughter) took her second shot (Covid-19 Vaccine by Pfizer) on unspecified date (reported as "this past Tuesday") and the next morning she woke up with a large inflamed swollen lymph nodes under her arm; upper arm but certainly it's in her armpit side. Reporter wanted to know how long the lymph nodes will just take swollen. The event was further described as extremely swollen large lymph node under the right arm. This happened on unspecified date, reported as the night patient received the vaccine (also reported as occurred the next morning). She did have additional side effects such as fatigue but no fever, no diarrhea, no upset stomach. Fatigue to the point she couldn't go to work on the day after receiving the vaccine. The fatigue passed but not the swollen lymph nodes. Patient went to see the doctor and said it could be a possible side effect of the vaccine or something else. Ultrasound was performed on unspecified date with unknown results. No treatment was received for the event (not at this time) but patient has been to physician. The outcome of the event "large inflamed swollen lymph nodes under her arm / extremely swollen large lymph node under the right arm" was not recovered. Outcome of the event fatigue was recovered on unspecified date. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm