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: 1010545
Sex: F
Age:
State: VA

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:97.3; Comments: daily average; Test Name: fever; Result Unstructured Data: Test Result:99.8; Comments: For 24 hours following injection

Allergies:

Symptoms: Swollen axillary lymph on left arm; low grade fever (daily average: 97.3. For 24 hours following injection was 99.8); Significant lethargy; "railroad spike" headaches that correlate with the right parietal and right occipital lasting approx 30 hours; This is a spontaneous report from a contactable healthcare professional (patient). A 45-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EK4176), via an unspecified route of administration in the left arm on 20Jan2021 at 07:00 at a single dose in the hospital for covid-19 immunization. Medical history included hyperlipidaemia, depressive disorder, chronic anxiety disorder, hypertensive, allergies to PCN (anaphylactic) and sulfa (allergic). The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medication included atorvastatin (LIPITOR [ATORVASTATIN]), escitalopram oxalate (LEXAPRO), losartan, and Mg/Ca supplement. The patient experienced swollen axillary lymph on left arm, "railroad spike" headaches that correlate with the right parietal and right occipital lasting approx 30 hours, low grade fever (daily average: 97.3. For 24 hours following injection was 99.8), and significant lethargy on an unspecified date. The patient did not receive treatment for the events. Outcome of the event headache was recovered and for other events was reported as recovering.

Other Meds: LIPITOR [ATORVASTATIN]; LEXAPRO; LOSARTAN

Current Illness:

ID: 1010546
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: feeling like I had the flu without the high fever; had a very bad headache; soreness in the arm where I received the shot; This is a spontaneous report from a contactable consumer reported for self. This 65-year-old female patient (not pregnant at the time of vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot#: EL8982) at single dose in right arm on 20Jan2021 at 10:30 AM for COVID-19 immunization. Medical history included hypothyroidism. Allergies to medications, food, or other products were unknown. Concomitant medications included duloxetine; levothyroxine; montelukast; trazodone. 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 had not been tested for COVID-19. Patient felt fine the day she received the vaccine, with only soreness in the arm where she received the shot. The next day at 11:00 AM, she started feeling like she had the flu without the high fever. The worse symptom was that she had a very bad headache. These symptoms were continuing 48 hours after the vaccine was administered. She was generally very healthy, had a very active life, and didn't get headaches. She was rarely sick. She just didn't seem to be feeling any better. Seriousness was no: not results in death, not life threatening, not caused/prolonged hospitalization, not disabling/incapacitating, not congenital anomaly/birth defect. There was no treatment received for the adverse events. The adverse events was not resolved.

Other Meds: DULOXETINE; LEVOTHYROXINE; MONTELUKAST; TRAZODONE

Current Illness:

ID: 1010547
Sex: U
Age:
State:

Vax Date: 01/07/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: Antibody testing; Result Unstructured Data: Test Result:This showed I have antibodies for both IgG and IgM; Comments: This showed I have antibodies for both IgG and IgM; Test Date: 202101; Test Name: Covid-19; Test Result: Positive

Allergies:

Symptoms: covid test came back positive; covid test came back positive; This is a spontaneous report from a contactable other hcp (patient). The patient received bnt162b2 (BNT162B2), via an unspecified route of administration on 17Dec2020 (first dose) and 07Jan2021 (second dose) at SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported "I am a healthcare professional and I have had both doses of the vaccine (17Dec and 07Jan). I was scheduled for surgery this past Wednesday but it was cancelled as my covid test came back positive. I have no symptoms. I was advised to get antibody testing. This showed I have antibodies for both IgG and IgM. I was still told I cannot have the surgery. " The outcome of the events was unknown. No follow-up attempts are possible, information on batch number cannot be obtained.; Sender's Comments: Based on the information currently available, a lack of efficacy with the suspected vaccine BNT162B2 in this patient cannot be completely excluded. Further information like confirmative virus genome /nucleic acid detection is needed for meaningful medical assessment.

Other Meds:

Current Illness:

ID: 1010548
Sex: M
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: sciatica with pain radiating from lower back to glute and then down to the left foot; This is a spontaneous report from a contactable healthcare professional (patient). A 36-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL3247), intramuscular in the left arm on 19Jan2021 at 13:15 at a single dose in the Nursing Home/Senior Living Facility for COVID-19 immunization. Medical history included stroke, hodgkin's lymphoma, cerebral vasculitis, seizures, chronic venous insufficiency, and had COVID prior to vaccination. Concomitant medication included levetiracetam (KEPPRA), apixaban (ELIQUIS), and levothyroxine sodium (SYNTHROID). The patient experienced sciatica with pain radiating from lower back to glute and then down to the left foot on 19Jan2021. Leg feels like it is going to give out. The patient did not receive treatment for the event. The patient was not tested for COVID post vaccination. The patient was recovering from the event.

Other Meds: KEPPRA; ELIQUIS; SYNTHROID

Current Illness:

ID: 1010549
Sex: M
Age:
State: MO

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

Lab Data:

Allergies:

Symptoms: headache; chills; muscle ache; Fatigue; pain at injection site; This is a spontaneous report from a contactable consumer. A 31-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# unknown), via an unspecified route of administration left arm single dose on 21Jan2021 10:00 for covid-19 immunisation. No other vaccine was received in four weeks. Medical history included renal cancer (currently no evidence of disease), migraine with aura, irritable bowel syndrome, attention deficit hyperactivity disorder, cyclothymic disorder. The patient's concomitant medications included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL), Hemp-derived CBD/CBG, magnesium, polycarbophil calcium (FIBER). The patient had allergy to clindamycin and azithromycin. The patient experienced headache on 21Jan2021 13:00, chills on 21Jan2021 13:00, muscle ache on 21Jan2021 13:00, fatigue on 21Jan2021 13:00, pain at injection site on 21Jan2021 13:00. No treatment administered. The events outcome was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained

Other Meds: ADDERALL; MAGNESIUM; FIBER

Current Illness:

ID: 1010550
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: minor discomfort on the injection site; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program. A female patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, unknown lot number and expiration), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history included ongoing discomfort on her lower back/back pain (prior to getting the shot). Concomitant medications included levothyroxine sodium (SYNTHROID), rosuvastatin calcium (CRESTOR), ibuprofen (ADVIL) for discomfort on her lower back and naproxen for discomfort on her lower back. The patient reported that she received her first dose of COVID-19 vaccine on Sunday. The patient experienced minor discomfort on the injection site on 17Jan2021, she barely noticed it. She had no other side effects. She does experience back pain, but this was prior to getting the shot and the pain is still the same as it always has been. She took two Advil on 22Jan2021 and asked if it will have an impact on the efficacy of her vaccination. She usually takes Advil or naproxen, as needed, for discomfort on her lower back (not associated to the COVID-19 vaccine). Prior to the shot he didn't take anything, no Advil or ibuprofen. The patient recovered from the event on 18Jan2021. Information on the lot/batch number has been requested.

Other Meds: SYNTHROID; CRESTOR; ADVIL [IBUPROFEN]; NAPROXEN

Current Illness: Low back pain (prior to getting the shot)

ID: 1010551
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: feeling itchy; itch could possibly be from dry skin; This is a spontaneous report from a contactable consumer. A 75-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# unknown, via an unspecified route of administration single dose on 17Jan2021 for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced feeling itchy on Jan2021, itch could possibly be from dry skin on Jan2021. The outcome was unknown. Information on Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010552
Sex: F
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/14/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; nausea; fatigue; site injection pain, red and swollen; site injection pain, red and swollen; site injection pain, red and swollen; This is a spontaneous report from a contactable healthcare professional (patient). A 25-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231 and expiry date unknown), intramuscular on the left arm on 12Jan2021 15:30 at a single dose for COVID-19 immunization. Medical history included polycystic ovarian syndrome. Concomitant medications included metformin, vitamin D [vitamin D NOS], and unspecified birth control. Patient is not pregnant at the time of vaccination. Patient has no allergies to medications, food, or other products. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not diagnosed with COVID-19 prior to vaccination. Patient has not been tested for COVID-19 since the vaccination. On 14Jan2021, the patient experienced headache, nausea, fatigue, injection site pain, red and swollen. Outcome of the events was recovered with sequelae. The events were reported as non-serious. No treatment was received for the adverse events.

Other Meds: METFORMIN; VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 1010553
Sex: F
Age:
State: CA

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

Lab Data: Test Name: Temperature; Result Unstructured Data: Test Result:99.8; Comments: Caller reports Temperature of 99.8, "not feverish".

Allergies:

Symptoms: Allergies and nasal drip in back of throat and sneezing; Allergies and nasal drip in back of throat and sneezing; Allergies and nasal drip in back of throat and sneezing; Eyes watering; This is a spontaneous report from a contactable consumer (patient). A 58-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EJ1686), via an unspecified route of administration on 20Jan2021 at 08:40 at 0.3 mL, single on arm left for covid-19 immunisation. Medical history included high blood pressure diagnosed for a while. Historical vaccine included flu shot for immunization and experienced allergies. Concomitant medication included hydrochlorothiazide/lisinopril and ascorbic acid/ betacarotene/ biotin/ calcium/ chromium/ colecalciferol/ copper/ folic acid/ iodine/ iron/ lycopene/ magnesium/ manganese/ nicotinamide/ pantothenic acid/ phosphorus/ phytomenadione/ potassium/ pyridoxine hydrochloride/ retinol/ riboflavin/ selenium/ vitamin b1 nos/ vitamin b12 nos/ vitamin e nos/ xantofyl/ zinc (CENTRUM SILVER). Patient had the first Pfizer vaccine on Wednesday, 20Jan2021 at about 8:40AM, yesterday (22Jan2021) she started with allergies and nasal drip in back of throat, eyes watering and sneezing around 10 AM. Stated that this was normal for her to have these allergies this time of the year. Caller reports Temperature of 99.8, "not feverish", no nausea. Caller wanted to know if she was contagious because of the vaccine, if it was possible the vaccine triggered her allergies. States she was just wanting to know if she was able to go to work tomorrow. Caller said "the first time i got the flu shot, it triggered my allergies real bad". Patient was treated symptoms with diphenhydramine hydrochloride (BENADRYL) and stated it got better with the diphenhydramine hydrochloride. Outcome of the events was resolving.

Other Meds: LISINOPRIL AND HYDROCHLOROTHIAZIDE; CENTRUM SILVER [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM;CHROMIUM;COLECALCIFEROL;COPPER;FOLIC ACID;

Current Illness:

ID: 1010554
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: his wife experiencing some pain in her 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 and expiration date not reported), 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 experienced some pain in arm on an unspecified date. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010555
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: fatigue; chills; headache; a rash from her face to her waist; fever; pain at injection site; This is a spontaneous report from a contactable nurse reporting for herself. A 53-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231, expiry date: not reported), via an unspecified route of administration on 20Jan2021 at a single dose on the right arm for COVID-19 immunization. Medical history included gluten sensitivity; she develops a rash when she eats gluten. Concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number was either EJ7685 or EJ1685, expiry date: not reported), via an unspecified route of administration on 30Dec2020 at a single dose on right deltoid for COVID-19 immunization and experienced pain at injection site; patient was 53-year-old at the time of vaccination. The patient received the second dose of the COVID vaccine on 20Jan2021. On 21Jan2021, she experienced fatigue, fever, chills, headache, which have resolved. However, on 21Jan2021 later in the evening she broke out in a rash. She reported that she is gluten sensitive. She asked if there is any gluten involved in the 2nd dose and if they do grow anything for the serum that might be gluten contained. The patient also experienced pain at injection site with second dose on 21Jan2021. She experienced fever, chills, headache and fatigue. She has a rash from her face to her waist. She has a gluten sensitivity and develops a rash when she eats gluten. She didn't see it on the information sheet. She is wondering if any aspect of the vaccine was grown containing grain. She will be seeing her doctor on Monday. She has a fever where she takes her temperature on the skin that is elevated with the rash. She does not have a fever on the areas that she does not have a rash. She noticed the rash late on 21Jan2021. She had a long sleeve on during the day. She still has chills at night. The patient reported the events as non-serious. Outcome of the event fatigue was recovered on 22Jan2021, of headache was recovered on an unspecified date, in Jan2021 of chills and pain at injection site was recovering, while outcome of other events was unknown.

Other Meds:

Current Illness:

ID: 1010556
Sex: F
Age:
State: NY

Vax Date: 01/06/2021
Onset Date: 01/13/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: numbness to her knees/feeling soft bilaterally and symmetrically/ wearing tights; weakness in her legs; This is a spontaneous report from a contactable physician (patient's daughter). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 06Jan2021 at single dose for covid-19 immunization. Medical history included hernia, and herniated disc in her cervical spine, but she was fine prior. The patient's concomitant medications were not reported. On 13Jan2021, her mom started to experience numbness to her knees and it was described as "feeling soft bilaterally and symmetrically"; the feeling was described as "wearing tights", the patient also had a little weakness in her legs. On 16Jan2021, the symptoms were at its worst and on 18Jan2021, her mom started to feel better. Her mom was taking Motrin and Ibuprofen. She didn't have any other symptoms. It was symmetrical and bilateral on both legs. The Physician wanted to know if this has been seen in any other patients and was it safe to get the second vaccine. The outcome of the events was recovering. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1010557
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Lymph Nodes in armpits; COVID-19 vaccine was administered on the same date as the other vaccine; This is a spontaneous report from a contactable consumer (patient himself). A 74-year-old male patient receive the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot/batch number and expiration date were unknown), via an unspecified route of administration on the right arm on 17Jan2021 at 07:45 at a single dose for COVID-19 immunization. The first dose of another vaccine (unspecified trade name; reported product: "Phizer," lot number and expiration date were unknown) was also administered on the same date on 17Jan2021, via an unspecified route of administration on the left arm at unknown dosage and frequency for an unspecified indication. The facility where the most recent COVID-19 vaccine was administered was at the hospital. The patient's medical history was not reported. Concomitant medication included morniflumate (FLOMAX). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 17Jan2021 at 07:45, the patient experienced lymph nodes in armpits, which was considered as non-serious. COVID-19 vaccine was administered on the same date as the other vaccine on 17Jan2021. The patient did not receive any treatment for the adverse event "lymph nodes in armpits." The patient was not recovered from the event lymph nodes in armpits. Information on the lot/batch number has been requested.

Other Meds: FLOMAX [MORNIFLUMATE]

Current Illness:

ID: 1010558
Sex: F
Age:
State: AL

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

Lab Data: Test Date: 20210122; Test Name: temperature; Result Unstructured Data: Test Result:101 degree; Test Date: 20210122; Test Name: temperature; Result Unstructured Data: Test Result:100 degree; Test Date: 202102; Test Name: temperature; Result Unstructured Data: Test Result:99.9 degrees

Allergies:

Symptoms: Fever; Fatigue; This is a spontaneous report from a contactable consumer (patient's spouse). A 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date were unknown), via an unspecified route of administration on 21Jan2021 at a single dose for COVID-19 immunization. Medical history included covid-19 in 2020 wherein the reporter and the patient had it last year. The patient's concomitant medications were not reported. The patient experienced fever with outcome of recovering. She already took TYLENOL to treat her fever. It was queried if the patient can use antipyretics before or after vaccination with the Pfizer-BioNTech COVID-19 vaccine. The patient was a nurse, she got the Pfizer vaccine yesterday on 21Jan2021, that at 3am this morning (22Jan2021), she had a 101 degree temperature, a 100 degree temperature at 8AM and a while ago it was 99.9 degrees at around 9:30 this morning. The reporter wanted to known if these were expected and what they should do. The reporter mentioned that his wife's case was not so bad, states that he himself was in the unit for some weeks. The patient also had fatigue 22Jan2021 with outcome of not recovered. Information about Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 1010559
Sex: F
Age:
State: CA

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

Lab Data: Test Date: 20210113; Test Name: Covsars2 swab/Nasal Swab; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: Severe headache; Fevers; nausea; body aches; severe prolonged fatigue; swollen underarms; This is a spontaneous report from a contactable nurse (patient). A 45-year-old female patient received the second dose of BNT162B2 (lot number: EL1283 and expiry date was unknown), via an unspecified route of administration in the left arm on 10Jan2021 08:30 at single dose for Covid-19 immunization. The patient is not pregnant. Medical history included asthma. There were no concomitant medications. The patient previously received the first dose of BNT162B2 (lot no. and expiry date were unknown) in the left arm on 21Dec2020 12:00 PM for Covid-19 immunization. The most recent COVID-19 vaccine was administered at the hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine nor any other medications received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. On 10Jan2021 at 08:30 AM, the patient experienced severe headache for 12 days, nausea, body aches, severe prolonged fatigue, swollen underarms, fever for 7 days. The adverse events resulted in doctor or other healthcare professional office/clinic visit. Treatment for the events included fluids and analgesics round the clock. The patient underwent laboratory test which included Covsars2 swab/nasal swab on 13Jan2021 and the result was negative. The events recovered with sequelae.

Other Meds:

Current Illness:

ID: 1010560
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: felt warm; lower lip was slightly itchy; pinpoint itch mostly in her scalp left ear; cluster fine rash in her bilateral forearm near the wrist; on and off pinpoint itch in different parts of her body; medical history of Chronic Hep B, borderline DM, HTN, high cholesterol; medical history of Chronic Hep B, borderline DM, HTN, high cholesterol; This is a spontaneous report from a contactable nurse (patient). A 51-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL8982), via intramuscular route of administration on 22Jan2021 at 08:15 at a single dose in the left arm for COVID-19 immunization. The patient's medical history included Chronic Hep B, borderline DM, HTN, high cholesterol. Concomitant medications included losartan, amlodipine, atorvastatin, metformin, fish oil, and docusate sodium (COLACE). The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK5730) on 04Jan2021 at 08:30 am (age: 51 years), intramuscular, in the left arm for COVID-19 immunization; flu vaccine in 2010 and experienced allergies; and Penicillin G and experienced allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. On 22Jan2021 at 08:35, the patient felt warm. At the same time, her lower lip was slightly itchy. She also had pinpoint itch mostly in her scalp left ear and cluster fine rash in her bilateral forearm near the wrist, and four hours on and off pinpoint itch in different parts of her body. The patient was given Zyrtec as treatment for the events. Since the vaccination, the patient has not been tested for COVID-19. The patient was not pregnant at the time of vaccination. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: LOSARTAN; AMLODIPINE; ATORVASTATIN; METFORMIN; FISH OIL; COLACE

Current Illness:

ID: 1010561
Sex: F
Age:
State:

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

Lab Data: Test Name: Covid Virus; Test Result: Positive

Allergies:

Symptoms: Caller stated that she tested positive for the Covid Virus after she received her first dose of the vaccine; Caller stated that she tested positive for the Covid Virus after she received her first dose of the vaccine; This is a spontaneous report from a contactable consumer reporting for the mother. A female patient of an unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Caller, calling on behalf of mother, wanted to know if she should receive her second vaccine today while positive for the Covid Virus. Caller stated that she tested positive for the Covid Virus after she received her first dose of the vaccine. The outcome of the events was unknown. Information on lot number/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010562
Sex: F
Age:
State:

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

Lab Data: Test Date: 20210122; Test Name: COVID-19 Rapid test; Test Result: Positive

Allergies:

Symptoms: a person who has received the covid vaccine but tested positive to the infection; a person who has received the covid vaccine but tested positive to the infection; This is a spontaneous report from a contactable pharmacist. This pharmacist reported that an 85-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number unknown) intramuscular at single dose on 21Jan2021 for COVID-19 immunisation. The patient received the first dose on unknown date. Relevant history and concomitants drugs were not reported. Per reporter, the patient was not seeing anything crazy on her chart. The patient got the second dose of the COVID vaccine on 21Jan2021. On 22Jan2021, she had been tested positive for COVID-19 (COVID-19 Rapid test). The patient had cough and low grade fever since unknown date. Relevant test was none. Outcome of event was unknown. The nurse practitioner wanted to do a monoclonal antibody infusion and the pharmacist was wondering if they could do that? When probed for causality, the pharmacist responded: "I guess not I'm not going to comment on that, I don't know. I don't have the patient's actual file." Information on the Lot/Batch number has been requested.; Sender's Comments: Based on the information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the second vaccine dose and the event onset.

Other Meds:

Current Illness:

ID: 1010563
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: nervous; back started to itch/There was irritation; back felt itchy; back felt itchy and pinkish red/back was red; Arm soreness; This is a spontaneous report from a contactable consumer (patient) via a Medical information team. A 30-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration on 20Jan2021 at single dose for COVID-19 immunization. Medical history included steel rods in back from 2006 and ongoing. The patient's concomitant medications were not reported. The patient was vaccinated and felt fine. She experienced arm soreness on 20Jan2021 originally. Then today, it was so bizarre, about an hour and a half ago, her back started to itch on 22Jan2021. There was irritation. She checked in the mirror, and her back was red on 22Jan2021. She was wondering if this was a reaction from the vaccine. She was getting nervous. A medical student gave her the vaccine. She didn't have a prescribing doctor. Twenty minutes after getting the vaccine, she noticed the arm soreness. It was worse yesterday, but today she thinks it is the same or maybe a little better. The irritation on her back seems a little better since she first noticed it. The outcome of the events back felt itchy and pinkish red and irritation was recovering. The outcome of the event arm soreness was not recovered. The outcome of the event nervous was unknown.

Other Meds:

Current Illness: Back surgery

ID: 1010564
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: she felt pain in the arm and body; she felt pain in the arm and body; inflammation in the injections site; fever; This is a spontaneous report from a contactable consumer (patient herself). A 47-year-old female patient received her first dose of bnt162b2 (BNT162B2 also reported as PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date were not reported), via an unspecified route of administration on 21Jan2021 at single dose for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On 21Jan2021, she felt pain in the arm and body, inflammation in the injections site and fever and had taken 6 Tylenol tablets as treatment, but the fever has not been fully controlled. The outcome of event fever was not recovered; for other events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010565
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: extreme weakness; increase in my spasticity; This is a spontaneous report from a contactable healthcare professional (patient herself). A 62-year-old female patient (non-pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 20Jan2021 16:15 at single dose for covid-19 immunization. Medical history included MS (multiple sclerosis); kidney disease. Prior to vaccination, the patient was diagnosed with COVID-19. Concomitant medication included glatiramer acetate (COPAXONE) from 19Jan2021, escitalopram oxalate (LEXAPRO) and antihistamine, magnesium. The patient previously took sulfamethoxazole, trimethoprim (BACTRIM) and experienced allergies. The patient received other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced extreme weakness and an increase in her spasticity related to MS on 20Jan2021 12:00. Since the vaccination, the patient had not been tested for COVID-19. The events were reported non-serious. Outcome of events were recovering. No treatment was received for the events. Information on the lot/batch number has been requested.

Other Meds: COPAXONE; LEXAPRO; MAGNESIUM

Current Illness:

ID: 1010566
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: pain down left arm to wrist and hand (still there); pain down left arm to wrist and hand (still there); unable to open & close left hand until next morning; Headache; occasional chills; fever; fatigue; Mild facial swelling; This is a spontaneous report from a contactable consumer (patient) reported that a 68-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL9263; expiry date: unknown) via an unspecified route of administration in the left arm, on 21Jan2021 at 14:00, at a single dose, for COVID-19 immunization. Medical history included allergies to Sulfa. The patient did not have other chronic health conditions. Concomitant medications included turmeric [curcuma longa rhizome], and ashwagandha. The patient previously took doxycycline and experienced allergies. On 21Jan2021, the patient had mild facial swelling 20 minutes after inoculation, at 14:30 the patient had pain down left arm to wrist and hand (still there), unable to open and close left hand until next morning, headache, occasional chills, fever and fatigue. The patient did not receive treatment for the events. The events were considered non-serious. The patient was recovering from the events.

Other Meds: TURMERIC [CURCUMA LONGA RHIZOME]; ASHWAGANDHA

Current Illness:

ID: 1010567
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Injection site it was sore; This is a spontaneous report from a Pfizer-sponsored program, via a contactable consumer (patient). A 70-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCIN) on 11Jan2021 at single dose for covid-19 immunization. Medical history and concomitant medication were not reported. patient received the first dose of the Pfizer-BioNtech Covid-19 vaccine on 11Jan2021, he was scheduled to receive the Moderna vaccine however the Pfizer vaccine was available and he received it (he was originally scheduled for Moderna and Moderna is 28 days where Pfizer is 21 days and he's having a hard time moving his 2nd appointment). He's scheduled to receive the second dose of the vaccine on 08Feb2021, which is 28 days after the first dose instead of the 21 days recommended. He would like to know if there's a problem with waiting because he doesn't want to lose the effectiveness of the vaccine. He wanted to know what happens if he can't get it on the 21st day. He also stated that he had no side effects, no pain, the only thing was when he pushed around the injection site it was sore, like when one got a normal shot. Outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010568
Sex: M
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Caller is a consumer who received his first Pfizer-Biontech Covid19 vaccine, yesterday, and is reporting a sore throat that "just feels raw"; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; batch/lot number and expiration date unknown), via an unspecified route of administration on 21Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received his first Pfizer-Biontech Covid19 vaccine, yesterday (21Jan2021), and is reporting a sore throat that "just feels raw". He wanted to know if this is normal. He also stated that the weather was poor yesterday and might have contributed to his symptom. The patient got the shot about 24hrs ago; the patient stated, "sore throat - raining and kind of nasty sore - just raw". The outcome of the event was unknown. Information on the LOT/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1010569
Sex: F
Age:
State: PA

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210116; Test Name: COVID test; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: Feeling tired; Discovered she was Covid 19 positive; Discovered she was Covid 19 positive; This is a follow-up spontaneous report from a Pfizer-sponsored program Pfizer. A contactable consumer reported that a 52-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 15Jan2021 at single dose for covid-19 immunisation. Medical history included Allergies from an unknown date and unknown if ongoing, bad back aches from an unknown date and unknown if ongoing. Concomitant medication included ibuprofen (ADVIL [IBUPROFEN]), mometasone furoate (FLONASE [MOMETASONE FUROATE]). On 16Jan2021, she had her first dose of COVID vaccine, and two hours later she had a positive COVID test done. She is wondering when she can get the second dose, her doctor said she had to wait 3 months for the second, dose, she is questioning that, and wants to know, should she be retested for COVID, since she thinks it may be a false positive, since she has no symptoms of COVID. She states she didn't really have any symptoms other than feeling tired. The outcome of event fatigue was unknown, while the outcome of the other events was not resolved. Information about lot/batch number has been requested.

Other Meds: ADVIL [IBUPROFEN]; FLONASE [MOMETASONE FUROATE]

Current Illness:

ID: 1010570
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: Numbness and tingling in the face; Numbness and tingling in the face; This is a spontaneous report from a contactable consumer reported for herself. A 24-years-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9261), via an unspecified route of administration on right arm on 20Jan2021 12:00 at SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. Concomitant medications include multivitamins [vitamins nos]. The patient experienced numbness and tingling in the face on 20Jan2021 12: 30 pm. Started after injection, in the lips, spreading to the mouth, chin, and lower face. Within two or three hours, it spread to the ears and upper face, lasting the entire evening. No treatment received for the events. Outcome of the events was recovered. The patient was not pregnant at the time of vaccination.

Other Meds: MULTIVITAMINS [VITAMINS NOS]

Current Illness:

ID: 1010571
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: Sore arm; Swollen injection site and halo formation; This is a spontaneous report from a non-contactable consumer reported for herself. A 30-year-old female patient (not pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3247), via an unspecified route of administration on 20Jan2021 11:15 on right arm at single dose for COVID-19 immunization. Facility where the most recent COVID-19 vaccine was administered at workplace clinic. Medical history and concomitant medications were not reported. The patient experienced sore arm within 20 minutes from vaccination on 20Jan2021 11:30, swollen injection site and halo formation at 18h on 20Jan2021. Soreness subsided after 72h. No treatment was received for the events. The outcome of the events were resolving. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1010572
Sex: F
Age:
State: NV

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

Lab Data: Test Date: 20210121; Test Name: blood pressure; Result Unstructured Data: Test Result:Her blood pressure was also up; Test Name: height; Result Unstructured Data: Test Result:5'9"; Test Date: 20210121; Test Name: heart rate; Result Unstructured Data: Test Result:fast heart rate, 125bpm; Test Date: 20210121; Test Name: heart rate; Result Unstructured Data: Test Result:down to 110; Test Date: 20210121; Test Name: heart rate; Result Unstructured Data: Test Result:heart rate came down, it was running in the 90s

Allergies:

Symptoms: she has probably shrunk in height; 5am on 21Jan2021, for the whole day i had a fast heart rate, 125bpm; blurry eyes; dizziness; Her blood pressure was also up; In the morning of the 20Jan2021 I was weak; This is a spontaneous report from a Pfizer-sponsored program, received from a contactable consumer (patient). A 73-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number: EL1283, expiry date: 30Apr2021) solution for injection, via an unspecified route of administration on 19Jan2021 10:02 at a single dose for Covid-19 immunization. Medical history included ongoing Seasonal Allergies (probably started in the last 4-5 years; reoccurs every year from about Oct through Mar), ongoing high blood pressure since like 2006 or 2004, ongoing Iliac artery stent placed started couple of years ago, anxiety from 2010 and ongoing (her cardiologist put her on Xanax around 2010-ongoing). Concomitant medication included ongoing alprazolam (XANAX) since 2010 for anxiety. She gets the flu shot every year and has never had a problem with the flu shot. She got her last flu shot in Oct2020, no adverse events with that or other flu shots historically. On the second dose of Pneumococcal vaccine, it swelled her arm up from the injection site all the way down to her wrist; she went to the urgent care for that. They gave her some medicine and eventually the adverse event went away. She experienced some side effects following that injection. The patient reported that in the morning of the 20Jan2021, she was weak and just kind of rested. She did not have any other side effects until 21Jan2021. At 5am on 21Jan2021, for the whole day she had a fast heart rate, 125bpm, she woke up with her heart rate up, fast heartbeat, then down to 110 and then just toggled a little bit, she had blurry eyes so she could not really focus her eyes, weakness and dizziness. These events continued all throughout 21Jan2021 but her heart rate came down, it was running in the 90s and she was weak all day. Her blood pressure was also up on 21Jan2021. She thinks the blurry eyes, with her eyes being squirrely was related to her heart rate being up and blood pressure being up. She feels like she recovered completely from these events by this morning 22Jan2021. She feels good, strong and her eyes are clear today, felt better than yesterday but not 100%. She has probably shrunk in height, her last known height was 5' 9. She called to ask if she should or should not get the second dose as scheduled for 12Feb2021 in response to the side effects. Outcome of the event 'she has probably shrunk in height' was unknown while the rest of the events was recovered on 22Jan2021. No follow-up activities are needed. No further information is expected.

Other Meds: XANAX

Current Illness: Anxiety (her Cardiologist put her on Xanax around 2010-ongoing); Blood pressure high (Since like 2006 or 2004.); Seasonal allergy (Probably started in the last 4-5 years; reoccurs every year from about Oct through Mar.); Stent placement (started couple of years ago)

ID: 1010573
Sex: F
Age:
State:

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

Lab Data: Test Name: test; Result Unstructured Data: Test Result:normal

Allergies:

Symptoms: she noticed a little nipple drainage after receiving both doses; This is a spontaneous report from a contactable nurse (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date unspecified), via an unspecified route of administration on an unspecified date at single dose (first dose); and then via an unspecified route of administration on an unspecified date at single dose (second dose) for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that she noticed a little nipple drainage on an unspecified date after receiving both doses of Covid-19 vaccine. The patient wanted to know if this was a side effect of the vaccine. The patient underwent a lab test and procedure which included an unspecified test which was normal on an unspecified date. Outcome of event was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1010574
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: gallbladder attack; 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, Solution for injection; lot number and expiry date: not known), via an unspecified route of administration on 20Jan2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. She got the first dose of the vaccine on Wednesday (20Jan2021) and she got a gallbladder attack afterwards (unspecified date in Jan2021). She wanted to report this and also wanted to know if there had been reports about this before. She said that she was not given an appointment for the second dose and wanted to know if Pfizer could help her with that. The outcome of the event was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1010575
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Sinus headache; Can feel the sinuses draining; This is a spontaneous report from a contactable consumer. A 60-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date not reported), via an unspecified route of administration on 22Jan2021 at a single dose for COVID-19 immunization. Medical history included sinus issues from the past couple of days from an unknown date. Concomitant medications were not reported. It was reported that the patient woke up with a sinus headache, but as the day went on, it's gotten worse and she can feel the sinuses draining. She reported she got the 1st dose of the COVID-19 vaccine at the morning of the report. Outcome of the events was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1010576
Sex: F
Age:
State: WA

Vax Date: 01/15/2021
Onset Date: 01/18/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Tingling in the hands; This is a spontaneous report from a contactable other healthcare professional (patient). A 51-year-old female patient (not pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: ED1283), intramuscularly on 15Jan2021 in the Right arm at single dose for COVID-19 immunization in hospital. Medical history included Celiac Disease, Dystonia, Hypothyroid, GERD (Gastrooesophageal reflux disease), Anemia, Ovarian cancer, Migraines, gastroparesis and known allergies with Penicillin. Prior to vaccination, patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took and had known allergies with prochlorperazine maleate (COMPAZINE), nicergoline, metoclopramide, dihydroergotamine, doxycycline, prochlorperazine, sulfamethoxazole and trimethoprim (SULFAMETHOXAZOLE-TRIMETHOPRIM). The patient experienced tingling in the hands on 18Jan2021. Since the vaccination, patient had not been tested for COVID-19. No treatment was received for the event. The outcome of the event was not recovered. The report was reported as non-serious, with seriousness criteria-Results in death: No; Life threatening: No; Caused/prolonged hospitalization: No; Disabling/Incapacitating: No; Congenital anomaly/birth defect: No.

Other Meds:

Current Illness:

ID: 1010577
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: nausea; vomiting; diarrhea; sweating; This is a spontaneous report from a contactable pharmacist reported a 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route single dose for COVID-19 immunization in Jan2021 at 33-year-old. Medical history and concomitant medication were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient experienced nausea, vomiting, diarrhea, and sweating; all in Jan2021 and was reported as non-serious. Action taken for BNT162B2 was not applicable. Outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010578
Sex: F
Age:
State:

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

Lab Data: Test Name: COVID-tested; Result Unstructured Data: Test Result:unkown results; Comments: post vaccination

Allergies:

Symptoms: significant pain in the arm; headache; Mild lightheadedness; nausea; This is a spontaneous report from a non-contactable healthcare professional. A 32-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration, on an unspecified date, at single dose, for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient, on an unspecified date, experienced significant pain in the arm starting approximately 4 hours after injection lasting into the next day; a headache a few hours within injection; mild lightheadedness and; nausea. No treatment was received for these adverse events and the patient recovered from these events on an unspecified date. The adverse events were assessed as non-serious. 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. The patient has been COVID-tested post vaccination on an unspecified date with unknown results. No follow-up attempts are possible; information about the lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1010579
Sex: F
Age:
State: MD

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210105; Test Name: body temperature; Result Unstructured Data: Test Result:100.5 Fahrenheit; Comments: highest; Test Date: 20210119; Test Name: COVID test: PCR; Test Result: Negative

Allergies:

Symptoms: fever highest of 100.5 F; body aches; headache; This is a spontaneous report from a contactable nurse. An adult female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular on 04Jan2021 14:45 at single dose for COVID-19 immunization. The patient was not pregnant at time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have COVID prior vaccination. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced fever highest of 100.5 f, body aches, headache all on 05Jan2021 with outcome of recovered in Jan2021. The patient underwent lab tests and procedures which included body temperature: 100.5 fahrenheit highest on 05Jan2021, COVID test: PCR: negative on 19Jan2021. Therapeutic measures naproxen was taken as a result of events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010580
Sex: F
Age:
State: ID

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210108; Test Name: Nasal Swab; Result Unstructured Data: Test Result:unknown results; Test Date: 20210115; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210108; Test Name: rapid test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210115; Test Name: rapid test; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: fever//Next day: Severe Headache and Fever/Day after: Fever; extremely bad headache/Day of: Severe Headache and sore arm; sore arm/Day of: Severe Headache and sore arm; This is a spontaneous report from a contactable other health professional (patient). A 25-year-old female patient received the first dose of BNT162B2 (lot no. and expiry date were not reported), intramuscular in the left arm on 07Jan2021 11:45 at single dose for Covid-19 immunization. Medical history included COVID-19, Sjrogrens diagnosed last year in 2020, diabetes and breast cancer. Prior to vaccination, the patient was diagnosed with COVID-19. The patient is not pregnant. The patient had no known allergies. Concomitant medication included levothyroxine. The patient did ot receive any other vaccines within 4 weeks prior to the COVID vaccine. The COVID-19 vaccine was administered in Nursing Home/Senior Living Facility. On 07Jan2021 at 13:30, the patient had a day of extremely bad headache/severe headache and sore arm. Then the next day on 08Jan2021, the patient had severe headache and fever. Then day after the patient had fever. The events were considered as non-serious. No treatment was received for the events. Since the vaccination, the patient has been tested for COVID-19. Covid test post vaccination included nasal swab and rapid test; both were taken on 08Jan2021 and 15Jan2021 with unknown results. The patient recovered from the events on unspecified date. Information on the lot/batch number has been requested.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1010581
Sex: M
Age:
State:

Vax Date: 12/26/2020
Onset Date: 01/06/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Tingley feet; light headed; This is a spontaneous report from a contactable Other Health Professional reported for himself. This 44-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at right arm on 26Dec2020 09:30 at single dose for COVID-19 immunization. Medical history included asthma. Patient not diagnosed with COVID-19 prior to vaccination. The patient's concomitant medications were not reported. No other vaccines within 4 weeks prior to the COVID. The patient experienced tingley feet and light headed for days after getting the vaccine on 06Jan2021. No treatment received for the adverse event. Events outcome was recovering and reported as non-serious. Patient has not been tested for COVID-19 since the vaccination. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1010582
Sex: F
Age:
State: FL

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

Lab Data: Test Date: 20210122; Test Name: Body temperature; Result Unstructured Data: Test Result:102; Comments: fever; Test Date: 20210122; Test Name: Heart rate; Result Unstructured Data: Test Result:140; Test Date: 20210122; Test Name: Heart rate; Result Unstructured Data: Test Result:53; Test Date: 20210122; Test Name: Heart rate; Result Unstructured Data: Test Result:123; Test Date: 20210122; Test Name: Heart rate; Result Unstructured Data: Test Result:maintaining high

Allergies:

Symptoms: Shivering uncontrollably; Fever; Heart rate was erratic; dysautonomia; High heart rate; patient received bnt162b2 with concomitant medication prednisone; patient received bnt162b2 with concomitant medication prednisone; Stomach ache; This is a spontaneous report from a contactable consumer (patient). A 50-year-old female patient (non-pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 21Jan2021 11:00 am at single dose at left arm for COVID-19 immunisation. Medical history included penicillin allergy, nonspecific myositis, small fiber neuropathy, stroke, neurogenic orthostatic hypotension, hypermobile EDS, osteoarthritis, osteoporosis, Raynauds, esophageal dysmotility from an unknown date. Concomitant medications within 2 weeks of vaccination included fexofenadine hydrochloride (ALLEGRA), gabapentin, prednisone (PREDNISON), tramadol. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. On same day after vaccination on 21Jan2021, patient had bad stomach ache. Woke up next day shivering uncontrollably, fever of 102 on 22Jan2021 07:45 am. Also heart rate was erratic (patient had dysautonomia) - 140 then dropped to 53 then back up to 123 all in same minute. This happened repeatedly and maintaining high heart rate. Patient didn't receive treatment for events. The adverse events resulted in emergency room/department or urgent care. Outcome of above events was not recovered. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient had not been tested for COVID-19. The report was considered as non-serious. Information on the lot/batch number has been requested.

Other Meds: ALLEGRA; GABAPENTIN; PREDNISON; TRAMADOL

Current Illness:

ID: 1010583
Sex: M
Age:
State: NM

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

Lab Data:

Allergies:

Symptoms: The typical sore arm; puffy around my eyes/little puffy under his eyes; sensation around his eyes/felt a sensation on the side of his eyes; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received his first dose of bnt162b2 (BNT162B2 reported PFIZER-BIONTECH COVID-19 VACCINE; unknown lot number and expiration date), via an unspecified route of administration on Jan2021 at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient inquired if his symptoms after the first dose of the vaccine are normal, was this a reaction to the vaccine and if he should get the second dose. He mentioned that he got the first dose of the covid vaccine earlier this week (Jan2021) and he had "the typical sore arm" but went on to report that about 3 hours afterward, he felt a sensation on the side of his eyes and below them so he asked his wife, "am I puffy around my eyes". He had no severe reaction or anything like that. He had no shortness of breath or rapid heartbeat or anything. He did not have any of those issues at all. Like any other shot, he had a sore arm. Then about 3 hours after he got it, he noticed a sensation around his eyes that last for about 20 minutes. He thought it had something to do with vaccine. His wife said he looked a little puffy under his eyes. He knows there is a "glad" under the eye area. He reported that he looked at the common side effects but didn't see his reaction so he doesn't know if he should be concerned. In the instructions for the vaccine it said there could be an issue with skin mucosa, but he had no swelling of the lips, throat, face, or anything. He wants the second dose. Obviously if someone had a severe reaction, they would not get the second shot. He inquired if he should be concerned about or not, if this is a side effect. The outcome of the events was unknown. The following information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1010584
Sex: F
Age:
State: NM

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

Lab Data: Test Date: 20210121; Test Name: fever; Result Unstructured Data: Test Result:100.1 Fahrenheit; Comments: about 10:00AM or 11:00AM; Test Date: 20210121; Test Name: fever; Result Unstructured Data: Test Result:100.8 Fahrenheit; Comments: in the afternoon at 02:00PM; Test Date: 20210121; Test Name: fever; Result Unstructured Data: Test Result:99.8 Fahrenheit; Comments: after taking medication, before bed

Allergies:

Symptoms: high fever/100.1 degrees Fahrenheit/100.8 degrees Fahrenheit/99.8 degrees Fahrenheit; arm swelling; arm was very sore; headache; This is a spontaneous report from a contactable consumer (patient). A 60-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3249) via an unspecified route of administration in left arm on 20Jan2021 15:15 at single dose for COVID-19 vaccination. Medical history included ongoing coeliac disease diagnosed four years ago in 2017, allergic to dairy and corn, COVID in Nov2020. There were no concomitant medications, no other recent vaccinations and had started no new medications. The patient had a reaction with a high fever, a headache, and her arm was very sore after vaccination, that were similar to how she felt when she had COVID in Nov2020. The patient's arm was swollen and sore that evening on 20Jan2021. Her first fever was yesterday morning on 21Jan2021, probably at about 10:00AM or 11:00AM, and at that time it was 100.1 degrees Fahrenheit then later in the afternoon at 02:00PM it was 100.8 degrees Fahrenheit. She took Tylenol, applied cold moist cloth, drank lots of liquid for treatment, and she did sleep. Tylenol was clarified to be generic pain reliever, Acetaminophen 500mg. Acetaminophen 500mg, EXP Apr2021, LOT P114992, UPC: 1191717759. Her temperature improved after taking this medication, and it was 99.8 degrees Fahrenheit before bed. She hadn't taken any Acetaminophen this morning on 22Jan2021, but she took two tablets the first time yesterday on 21Jan2021 and then one tablet right before bed. She didn't go to the doctor for this. The outcome of events was unknown.

Other Meds:

Current Illness: Celiac disease (diagnosed four years ago.)

ID: 1010585
Sex: F
Age:
State: MN

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body aches; headache; fatigue; This is a spontaneous report from a contactable other healthcare professional (patient). A 27-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) intramuscular at the left arm on from 04Jan2021 13:15 (lot number Ek9231 and expiry date unknown) at single dose for Covid-19 immunization in a hospital. Medical history included depression and insomnia. The patient has no COVID prior vaccination. Concomitant medication included bupropion hydrochloride (WELLBUTRIN), melatonin, escitalopram oxalate (LEXAPRO), drospirenone, ethinylestradiol betadex clathrate (YAZ), amitriptyline; all from unspecified date for unspecified indication. The patient did not receive other vaccine in four weeks. On 05Jan2021 12:00 AM, the patient experienced body aches, headache, and fatigue. The patient was not COVID tested post vaccination. The patient did not receive treatment due to the events. The outcome of the events body aches, headache, and fatigue was recovered in Jan2021.

Other Meds: WELLBUTRIN; MELATONIN; LEXAPRO; YAZ; AMITRIPTYLINE

Current Illness:

ID: 1010586
Sex: F
Age:
State: IL

Vax Date: 01/20/2021
Onset Date: 01/22/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; chills; This is a spontaneous report from a contactable Other HCP (patient). A 49-year-old female patient (not pregnant) received second dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot Number and Expiration Date unknown) via Intramuscular on 20Jan2021 08:00 AM (vaccine location: Left arm) at single dose for COVID-19 immunisation. Previous vaccine included first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot Number Left arm and Expiration Date unknown) via Intramuscular on 30Dec2020 08:00 AM (vaccine location: Left arm) at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications was not reported. Patient experienced Headache and chills on 22Jan2021 06:00 AM, without treatment received. The outcome of events was unknown. Information on the batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1010587
Sex: F
Age:
State: WI

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

Lab Data: Test Date: 20210121; Test Name: 2019 Novel Coronavirus RNA Testing by PCR (Nasal Swab); Test Result: Negative ; Comments: post vaccination; Test Date: 20210118; Test Name: Influenza/COVID-19 Nucleic Acid Amplification Test (Nasal Swab); Test Result: Negative ; Comments: post vaccination

Allergies:

Symptoms: Severe chills; Severe lower extremity pain; Headache; Body ache; Shooting joint pain; Nausea; Vomiting; Diarrhea; Fever; Sore throat; Swollen glands; Sweating; This is a spontaneous report from a contactable other health professional (patient). A 38-year-old female (not pregnant) patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number El1283), intramuscular at left arm on 12Jan2021 22:45 at single dose for COVID-19 immunization at a hospital. Medical history included asthma and attention deficit hyperactivity disorder (ADD). Concomitant medication within 2 weeks prior to the COVID vaccine included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took sumatriptan succinate (IMITREX) and experienced drug allergy (known allergies: Imitrex). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number El1284), intramuscular at left arm on 22Dec2020 15:30 for COVID-19 immunization at a hospital. The patient had no COVID prior to vaccination, and had been tested for COVID since the vaccination. The patient underwent lab tests and procedures post vaccination which included 2019 Novel Coronavirus RNA Testing by PCR (Nasal Swab) on 21Jan2021: negative, and Influenza/COVID-19 Nucleic Acid Amplification Test (Nasal Swab) on 18Jan2021: negative. It was reported that, started from 12Jan2021 23:30, the patient experienced severe chills, headache, body ache, shooting joint pain, nausea, vomiting, diarrhea, fever, sore throat, swollen glands, severe lower extremity pain, and sweating. All the events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care visit. No treatment was received for the above events. The outcome of all the events was not recovered.

Other Meds: ADDERALL

Current Illness:

ID: 1010588
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Lost her sense of taste; This is a spontaneous report from a contactable consumer via medical information team. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date not reported), via an unspecified route of administration on 21Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient received the COVID shot on 21Jan2021 and on 22Jan2021 she noticed that she lost her sense of taste starting a few hours ago. She has no other symptoms aside from that. She said she feels fine. She asked if it is normal to lose the sense of taste after receiving the COVID-19 vaccine. The outcome of the event was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1010589
Sex: F
Age:
State:

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: couldn't move her arm; soreness in the muscle; This is a spontaneous report from a non-contactable consumer. A 90-year-old female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 18Jan2021 at first single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient previously received flu shot for immunization and her arm was sore. The reporter's mother said she couldn't move her arm for a day after receiving the first dose of the Pfizer Covid vaccine on Monday (18Jan2021). She had soreness in the muscle. By the 3rd day after receiving the vaccine, she was feeling fine. Outcome of the events was recovered 21Jan2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1010590
Sex: F
Age:
State: TX

Vax Date: 01/05/2021
Onset Date: 01/13/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: Nasal Swab; Test Result: Positive

Allergies:

Symptoms: tested positive for covid; tested positive for covid/Nasal Swab: positive; This is a spontaneous report from a contactable nurse. An 84-year-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine), via an unspecified route of administration on 05Jan2021 at a single dose for COVID-19 immunization. Medical history included Alzheimer's disease, cough (she has had a cough forever), cellulitis, constipation, dementia, depression, appendicectomy, and right hip replacement surgery. The patient's concomitant medications were not reported. The patient experienced tested positive for COVID on 13Jan2021. The patient underwent lab tests and procedures which included Nasal Swab: positive on 13Jan2021. The reporter was calling for information about administration of the COVID vaccine at an interval greater than the 21 days and recommendations for a patient who tested positive after the first dose of the vaccine. The patient got the first dose of the COVID vaccine on 05Jan2021, She tested positive for COVID on 13Jan2021 and then next time she will be seen and tested will be 15Feb2021. Due to this it seems like they can't give her the vaccine this following Monday because she tested Positive and the Next time, the clinic gets vaccines is on 15Feb2021, Caller asks is that too long of a time frame for the second Dose. Or would they have to start over on 15Feb2021 with another first dose. The First Dose was on 05Jan2021. The Positive Covid Test was on 13Jan2021, it was done by a Nasal Swab. Patient won't be due for another COVID test for 14 days after, she is due for her next COVID test on 27Jan2021. If she is Negative on the 27Jan2021, then she will get her next COVID Vaccine on 15Feb2021. This is non-serious report. The outcome of events was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: The patient received the first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine), on 05Jan2021, and COVID-19 test, including Nasal Swab, positive on 13Jan2021. No effect of the suspect vaccine could be reasonably achieved to protect from the targeted infection/disease due to the very short time lag. Instead, the positive COVID 19 test likely represents a pre-existing infection prior to vaccine use. Further information is needed for full medical assessment.

Other Meds:

Current Illness:

ID: 1010591
Sex: M
Age:
State: OH

Vax Date: 01/04/2021
Onset Date: 01/11/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: COVID; Test Result: Positive

Allergies:

Symptoms: tested positive for COVID-19; tested positive for COVID-19; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program . The male patient received first dose of bnt162b2 (BNT162B2), via an unspecified route of administration on 04Jan2021 at SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. He received the Pfizer BioNTech COVID-19 vaccine on 04Jan2021 and tested positive for COVID-19 on 11Jan2021. He said he is already back to work and is scheduled for the second dose on 25Jan2021. He asked if he should go forward with the scheduled dose or should he wait 6 more weeks for the second dose. The outcome of the events was unknown. No follow-up attempts are possible, information on batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1010592
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: feeling slightly weak; feeling unwell; felt as if she is getting the flu or in the beginning stages of the flu; tired; This is a spontaneous report from a contactable consumer (patient). An 85-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot#: EL3247), via an unspecified route of administration on 21Jan2021 20:00 at single dose for COVID-19 immunization. The patient's medical history included uses a walker on a regular basis for spinal stenosis. Concomitant medications were not reported. Patient received first dose of Pfizer COVID vaccine on 21Jan2021 around 8pm, at the vaccination site she was tired and was given a chocolate chip cookie and felt better. On 22Jan2021 morning she was feeling slightly weak nothing violent she is just feeling unwell. She generally feels weak, but said this is hard to explain. She felt as if she is getting the flu or in the beginning stages of the flu. Patient does not have a fever. Generally doesn't get reactions to the flu shot or pneumonia shot, that is very minor. The outcome of tired was recovering, of other events was unknown. Patient would like to know if her symptoms are to be expected after receiving the first dose of the vaccine and how long will her symptoms last, what to do about her symptoms.

Other Meds:

Current Illness:

ID: 1010593
Sex: F
Age:
State: TX

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

Lab Data: Test Date: 20210120; Test Name: heart palpitations; Result Unstructured Data: Test Result:159/110

Allergies:

Symptoms: body aches; heart palpitations that speeded up to 159/110; heart palpitations that speeded up to 159/110; chills; This is a spontaneous report from a contactable consumer (patient). This 53-year-old female patient received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration at left shoulder/deltoid left on 20Jan2021 at single dose for covid-19 immunisation. Medical history included ongoing hypertensive diagnosed four years ago. Concomitant medications the medication that she took for her blood pressure. The patient took first dose Covid 19 vaccine two days ago. She started feeling chills on 20Jan2021 and body aches on 21Jan2021. The patient stated two days ago that she had heart palpitations that speeded up to 159/110 all day on 20Jan2021. She was a hypertensive person and her blood pressure will go up. She was told there would be risks. She wanted to know if she should take the second dose on 10Feb. Wanted to know if something will happen to her if she took it. The chills lasted only two hours. The body aches stopped at 5PM. She had heart palpitations with activity and only lasted for 24 hours. The patient had none while laying down. No treatment was received. Outcome of the event chills was recovered on 20Jan2021, of the events body aches and heart palpitations that speeded up to 159/110 was recovered on 21Jan2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Hypertensive (diagnosed four years ago.)

ID: 1010594
Sex: F
Age:
State: MO

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 02/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: symptoms of COVID/ believes it could be COVID; symptoms of COVID/ believes it could be COVID; terrible diarrhea; constant headache; Gas; Bloating; Her arm was sore for 24 hours; This is a spontaneous report from a contactable consumer (patient). A 55-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, lot number: EL8982, unknown expiration), via injection once to right arm on 14Jan2021 at a single dose as she is eligible with first tier for vaccination. Medical history and concomitant medications reported as none. The patient reported that she received the first dose of COVID vaccine on 14Jan2021 (Thursday). The next day (15Jan2021), her arm was sore for 24 hours after the shot, and she didn't have any side effects over the weekend. On 19Jan2021, Tuesday, she started having constant headache, and was experiencing problems with gas and bloating, it is very rare for her to have this issue, and it was building the last of couple days, she was uncomfortable and was taking over the counter medication for relief. She was keeping the headaches at bay with generic ibuprofen (lot: S200378, expiry: Mar2023), but if she missed a dose or is feeling better and doesn't take, it is coming back, it is consistent. Gas and bloating are primarily after eating, on Wednesday, after 24 hours it was ridiculous. She got some generic Extra Strength Gas Relief one tablet after eating (lot: 75257, expiry: Jun2022), and it was giving her some relief until early this morning. Tuesday, Wednesday, and Thursday, the gas and bloating was worse. Last night, her entire chest, she wanted to burp so bad, but couldn't because it really hurt, and it took a while for the next tablet to kick in and give relief, she was like where is this coming from, she didn't know it could build up so much. On 22Jan2021, she had a terrible diarrhea. Diarrhea was painful and intense, she took generic Pepto Bismol 1-2 tablets, and she took 4, The first time she woke up at 04:30 AM and at 7 another wave hit her, so she took another two tablets. Right now, she is feeling okay, but the gas is building up, her chest is filling, she is uncomfortable. The patient asked if these are reported side effects. She works in a dental office, and the doctor is knowledgeable and sensitive to COVID, and even though those symptoms are not listed as side effects on the information sheet, the doctor said they are symptoms of COVID, and even though those symptoms are not listed as side effects on the information sheet, the doctor said they are symptoms of COVID, are these side effects or may she have COVID, though she doesn't know who she could have gotten COVID from. Out of protection for patients at dental clinic, the HCP at clinic wants her to get the COVID test as he believes it could be COVID and not side effect of the vaccine. She doesn't want to quarantine for nothing if it is just side effects of the vaccine. She will be getting rapid diagnostic for COVID and not the antibody test. She thinks she should get tested, but there is no testing appointment available until tomorrow, and she does not want to self-quarantine needlessly, she will live through it, she is happy to get the test, but she doesn't want to lose 2 weeks of pay if others are reporting the same side effects. She was happy to get the vaccine. The patient recovered from the event arm sore on 16Jan2021; not yet recovered from events constant headache, gas, and bloating; while unknown outcome for the remaining events.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm