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: 0980616
Sex: F
Age:
State: LA

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:103.8

Allergies:

Symptoms: chills; body aches; fever up to 103.8; headache; weakness; malaise; This is a spontaneous report from a contactable nurse. A 26-year-old female patient received her second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3246) on her left arm, via an unspecified route of administration on 13Jan2021 12:30 at a single dose for COVID-19 immunization. Medical history included Asthma and GERD. Concomitant medication included baclofen, buspirone hydrochloride (BUSPAR), paracetamol (TYLENOL). The patient previously took protonix, reglan and ambien; experienced allergies with all. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on 12Dec2020 (first dose). The patient experienced chills, body aches, fever up to 103.8, headache, weakness and malaise; all on 13Jan2021 23:00. No treatment has been received for the events. The outcome of the events was not recovered.

Other Meds: BACLOFEN; BUSPAR; TYLENOL

Current Illness:

ID: 0980617
Sex: F
Age:
State: TN

Vax Date: 01/08/2021
Onset Date: 01/10/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: Urine Culture; Result Unstructured Data: Test Result:Negative; Comments: Started UTI medication, but urine culture came back negative

Allergies:

Symptoms: Dizziness; history included compromised immune status; history included compromised immune status; getting really tired/fatigue; Gets real sweaty; chills; almost passed out at doctor's office; Nausea; Felt cold; Blood in urine; Feeling unwell; Feeling bad; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EJ1686), intramuscular in the left upper arm on 08Jan2021 at 15:45 at 0.3 mL, single for COVID-19 immunization. Medical history included Leighten Plantar Alopecia (hair follicle is an enemy), skin infection (infection in body most of the time, at least on skin), diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities, obesity, autoimmune disorder (diagnosed 8 months ago). She has lost some height, prior to taking the vaccine and she said it was related to age. There were no concomitant medications. The patient experienced feeling unwell on 10Jan2021; blood in urine on 10Jan2021 at 17:00; nausea at 10:00, chills at 11:00, almost passed out at doctor's office at 10:00, felt cold - all on 11Jan2021; getting really tired/fatigue on 14Jan2021 at 09:30; gets really sweaty on 13Jan2021 at 10:00; and dizziness on unknown date. The patient had the first shot on Friday (08Jan2021). On Sunday (10Jan2021), she started feeling bad. She was feeling good about getting it and had no reaction. She has an autoimmune disorder that made her a little afraid to take, but with all the indications, they said it would be much better for her to take it than to get the COVID virus. Sunday (10Jan2021), she does not feel good. So, she started having blood in urine. She thought she had a UTI and had not had one in 20 years. It felt like that is what she had and with the blood in urine. She just took Tylenol and waited until Monday morning because she does not like sitting in doctor's office. They gave her a cup to give sample and said she didn't need to see provider. They will have it checked and in the meantime call in a prescription. It kept getting worse and worse. She was about to passed out in the doctor's office on 11Jan2021, she got nauseous and almost threw up. She got in the car with her husband and he was trying to get her home. She got chills and got so cold and could not warm her body up. Her husband gave her Phenergan and it kind of knocked her out for a while to ease her nausea. She was thinking of going later today (14Jan2021), when she gets enough energy, to get a COVID test. She does not know if it will give false positive or not. She had chills and now she gets sweaty since 13Jan2021. She took her temperature and she did not have one. She just now got up. It is 10:00. She got up this morning (14Jan2021) and was really tired. She was not sweating this morning. Tiredness is kind of new, and when she talked to the nurse, she sort of felt like maybe it was a reaction to the COVID vaccine, but then she talked to her daughter and she said the symptoms she was having are usually symptoms that occur with second dose of the vaccine. It is not uncommon for people to have symptoms she was having. She wanted to know if she should have a COVID test. If she has had just one shot, would the test give a false positive coming from the COVID. They were asking if patient should take the second dose, and should she continue her UTI medication. Doctor's visit to give urine sample on 11Jan2021 (results: negative for UTI). She did not see a doctor though. They sent sample and prescribed a sulfa based medication for a UTI. She did start feeling a little better and stopped having blood in her urine. She plans to continue it because she does not like to stop taking an antibiotic. She did not have any clue that it was not a UTI until the nurse from her provider's office called to tell her results of urine sample was negative. Outcome of event getting really tired/fatigue was not recovered; events almost passed out at doctor's office, blood in urine, chills, and gets really sweaty was recovering; and unknown for other events.

Other Meds:

Current Illness:

ID: 0980618
Sex: F
Age:
State: MO

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Nausea; Vomiting; Muscle pain; Fatigue; Chills; This is a spontaneous report from a contactable healthcare professional (patient). A 46-year-old female patient (non-pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EJ1686), intramuscular in left arm, on 11Jan2021 at 14:15, at a single dose, for COVID-19 immunization. The patient's medical history included hypertension, Hashimoto's, and allergies to sulfa. The patient had unspecified concomitant medications. The patient previously took the first dose of BNT162B2 (Lot Number: EK5730) on 19Dec2020 at 08:00 AM (intramuscular in left arm) for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior vaccination. No other vaccine was administered in four weeks. The vaccine was administered in a hospital facility. On 12Jan2021 at 10:30 PM, the patient experienced nausea, vomiting, muscle pain, fatigue, and chills. No treatment was administered for the events. The patient had not been tested for COVID-19 post-vaccination. The patient was recovering from the events.

Other Meds:

Current Illness:

ID: 0980619
Sex: F
Age:
State: IN

Vax Date: 12/31/2020
Onset Date: 01/02/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: tenderness on the left arm where she received the vaccine dose.; severe pain in right shoulder joint and right hip joint/It was so severe she could hardly get out of bed; Headache; This is a spontaneous report from a contactable nurse (patient). A 71-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EJ1686, expiration date unspecified), via an unspecified route of administration on 31Dec2020 11:00 at single dose (left arm) for COVID-19 immunization. Medical history included arm soreness from flu shot 2-3 months ago. There were no concomitant medications. It was reported that she received her 1st dose of the vaccine on her left arm on 31Dec2020 as she works with elderly at nursing home and she was of age. Two days after her shot, on 02Jan2021, she experienced little headache which lasted all day but was gone by the following day. On 12Jan2021, 2 days ago, when she woke up and got of bed with severe pain in right shoulder joint and right hip joint which lasted for maybe 10 minutes. It was so severe she could hardly get out of bed. Currently, she had no joint pain. The right shoulder and right hip pain were so odd she thought, but it has also improved since. It's been 2 weeks and she never had this happen before. This lasted a little while, but thought it was from the cold weather since it's been 2 weeks since having the vaccine. She still has a bit of tenderness on the left arm where she received the vaccine dose on an unspecified date. She mentioned this to her supervisor and was encouraged to call and she wants to know if this could be a side effect. The patient had no vaccines the same day or 4 weeks prior. She had the flu shot before in past and the area would be sore for a few days, but now with this Covid vaccine this arm was still tender. Also, she had gotten the shingles shot the same day as the flu shot but that was about 2-3 months ago, at least 2 months ago. The patient had no additional vaccines administered on same date of the Covid vaccine. The patient had no prior vaccinations within 4 weeks prior to the first administration. Outcome of event headache was recovered on 03Jan2021; severe pain in right shoulder joint and right hip joint/it was so severe she could hardly get out of bed was recovered in Jan2021; and outcome of tenderness on the left arm where she received the vaccine dose was not recovered.

Other Meds:

Current Illness:

ID: 0980620
Sex: M
Age:
State:

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

Lab Data: Test Date: 20210108; Test Name: fever; Result Unstructured Data: Test Result:in excess of 102 Fahrenheit; Test Date: 20210111; Test Name: Rapid COVID-19 Test; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: soreness in left arm; feeling kind of achy; was wanting to run a fever/Very high fever in excess of 102 degrees Fahrenheit; This is a spontaneous report from a contactable consumer (patient). A 63-year-old male patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EJ1686) via an unspecified route of administration on 04Jan2021 at a single dose on the left arm for vaccination. Medical history included ongoing hypothyroidism. Concomitant medication include levothyroxine (manufacturer unknown) from an unspecified date probably 2-3 years ago and ongoing for hypothyroidism. The patient reported that the first dose was administered of the Pfizer COVID-19 Vaccine on 04Jan2021. He had onset of soreness in left arm that day, 14Jan2021 which he recovered completely from by 05Jan2021. He stated that starting maybe 05Jan2021 or 06Jan2021, he had onset of feeling kind of achy and like he was wanting to run a fever. Starting 08Jan2021, he started running a very high fever in excess of 102 degrees Fahrenheit which has been ongoing and persistent since then. He has been taking Tylenol every 6 hours to try to control the high fever but the high fever is just not going away. He was wondering if there is anything he can do because his primary care physician (PCP) can't really help him at the clinic; He was wondering if Pfizer is familiar with this reaction and if there are any recommendations regarding them. He has taken Tylenol to help, but it is not making it go away. He wanted to know if steroids could be used to counteract this side effect. He added that he is supposed to get the second dose 25Jan2021 but he does not plan to get the second dose, at this point he does not want to do that. He was administered the vaccine because his mother lives in an assisted living facility where the vaccine was offered to residents; and because he acts as a sitter at the facility it was offered to him. On 11Jan2021 he went to Urgent Care for these events, and was given a Rapid COVID-19 Test which had negative result. The outcome of the event soreness in left arm was recovered on 05Jan2021, the outcome of the event was wanting to run a fever/very high fever in excess of 102 degrees fahrenheit was not recovered and the outcome of the event feeling kind of achy was unknown.

Other Meds: LEVOTHYROXINE

Current Illness: Hypothyroidism

ID: 0980621
Sex: F
Age:
State: AZ

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210114; Test Name: heart rate; Result Unstructured Data: Test Result:150; Comments: Rapid heart rate noted in the 150's

Allergies:

Symptoms: Rapid heart rate; Feeling shaky and anxious; Feeling shaky and anxious; This is a spontaneous report from a contactable nurse (patient). A 24-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number:EL0142, expiration date unknown) , via an unspecified route of administration in the left arm on 14Jan2021 at 09:15 AM at a single dose for COVID-19 immunization. Medical history included COVID-19 on unknown date prior to vaccination, patient had no known allergies. Patient is not pregnant. Concomitant medications included over the counter (OTC) vitamins. The patient had not received other vaccines in four weeks. On 14Jan2021, the patient experienced rapid heart rate noted in the 150s approximately five minutes after receiving first dose lasting only a few minutes and was feeling shaky and anxious. There was no treatment received for the adverse events. The patient was not tested for COVID post vaccination. The outcome of the event rapid heart rate was recovered on 14Jan2021 while the rest of events was unknown.

Other Meds:

Current Illness:

ID: 0980622
Sex: M
Age:
State: KY

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Name: Temperature; Result Unstructured Data: Test Result:101; Comments: 101 Temperature

Allergies:

Symptoms: 101 Temperature; Headache; Chills; Fatigue; This is a spontaneous report from a contactable healthcare professional. A 50-year-old male patient received his first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on his right arm, via an unspecified route of administration on 13Jan2021 09:15 at a single dose for COVID-19 immunization. Medical history included covid-19. Concomitant medication included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL). The patient experienced 101 Temperature, Headache, Chills, Fatigue; all on 13Jan2021. The patient did not receive any treatment for the events. The outcome of the events was recovering. No follow-up attempts are possible, information about lot/batch cannot be obtained. No further information is expected.

Other Meds: ADDERALL

Current Illness:

ID: 0980623
Sex: F
Age:
State: MI

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; headache; body aches; This is a spontaneous report from a contactable other health professional. A 49-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number: EL1283, intramuscular in the right arm, on 12Jan2021 17:00 at a SINGLE DOSE for covid-19 immunization. Prior vaccination, the patient had COVID-19 on an unspecified date. Concomitant medications included venlafaxine hydrochloride (EFFEXOR), rosuvastatin calcium (CRESTOR), colecalciferol (VITAMIN D), ibuprofen, paracetamol (TYLENOL). Patient was not pregnant during vaccination. The patient previously took Tetracycline and Wellbutrin; she experienced allergy to both on unspecified dates. On 13Jan2021 17:00, the patient experienced chills, headache and body aches. outcome of events was recovered. The patient did not receive any treatment due to events. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds: EFFEXOR; CRESTOR; VITAMIN D [COLECALCIFEROL]; IBUPROFEN; TYLENOL

Current Illness:

ID: 0980624
Sex: M
Age:
State:

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

Lab Data: Test Date: 20210111; Test Name: body temperature; Result Unstructured Data: Test Result:102

Allergies:

Symptoms: High fever (102); chills; lymphadenopathy; headache; This is a spontaneous report from a non-contactable physician. A 36-year-old male patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK4176 and expiry date: unknown), via an unspecified route of administration on 11Jan2021 07:00 at a single dose for COVID-19 immunization. The 1st dose was received on 21Dec2020 07:00. The patient's medical history and concomitant medications were not reported. The patient experienced high fever (102), chills, lymphadenopathy, headache on 11Jan2021. Outcome of the events was unknown. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0980625
Sex: F
Age:
State: AR

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: Fever; Result Unstructured Data: Test Result:102

Allergies:

Symptoms: Fever 102; chills; headache; back pain; lymphadenopathy in cervical, axilla, and groin; This is a spontaneous report from a contactable other healthcare professional (hcp, reported for herself). A 34-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date not reported), via an unspecified route of administration on 12Jan2021 15:30 at a single dose in the left arm for COVID-19 immunization. Medical history included allergies to penicillin. The patient was not pregnant at the time of the report. The patient had no covid prior to vaccination. The patient's concomitant medications were not reported. The patient had no other vaccine in four weeks. The patient had first dose of COVID-19 vaccine bnt162b2 on 23Dec2020 08:30 AM in the left arm (at the age of 34 years old). On 13Jan2021 12:00 PM, patient experienced fever 102, chills, headache, back pain, and lymphadenopathy in cervical, axilla, and groin. No treatments received in response to the events reported. The patient was not COVID tested post vaccination. The outcome of the events fever 102, chills, headache, back pain, and lymphadenopathy in cervical, axilla, and groin was recovering. Information on batch/lot number was requested.

Other Meds:

Current Illness:

ID: 0980626
Sex: M
Age:
State: MI

Vax Date: 12/23/2020
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: For the first dose, individual stated the only had a sore shoulder (at point of injection) and foggy head for the few hours; For the first dose, individual stated the only had a sore shoulder (at point of injection) and foggy head for the few hours; This is a spontaneous report from a contactable consumer (non-healthcare professional reporting for a patient). A 35-year-old male received first single dose BNT162B2 (Solution for injection, Lot number: EJ1685, exp date not reported), via an unspecified route of administration (anatomical location: shoulder [not further specified]) on 23Dec2020 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. For the first dose, patient only had a sore shoulder (at point of injection) and foggy head for the few hours on an unspecified date. No treatment was provided for the adverse events. It was unknown if patient had Covid prior vaccination. It was unknown if patient was Covid tested post vaccination. The patient recovered from the events on an unspecified date.

Other Meds:

Current Illness:

ID: 0980627
Sex: M
Age:
State: IL

Vax Date: 12/23/2020
Onset Date: 12/30/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20201231; Test Name: Nasal Swab; Test Result: Positive

Allergies:

Symptoms: I developed COVID positive test; I developed COVID positive test; Had mild to moderate illness; This is a spontaneous report from a contactable physician reporting for himself. A 45-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) intramuscular, on 23Dec2020, single dose for COVID-19 immunization. Relevant medical history and concomitant medication was reported as none. The patient had no other vaccine in four weeks and no other medications in two weeks. The patient was not diagnosed with COVID before vaccination. On 30Dec2020 at 4:15 PM, after the first vaccine dose, within a week the patient developed COVID positive test. The patient had mild to moderate illness on an unspecified date. Therapeutic measure taken in response to the events included administration of Tylenol. The patient underwent covid test via nasal swab on 31Dec2020 and showed positive result. Outcome of the events was not recovered. Information for Lot/Batch number has been requested; Sender's Comments: The PFIZER-BIONTECH COVID-19 VACCINE provides protection after 7 days from the second dose.

Other Meds:

Current Illness:

ID: 0980628
Sex: F
Age:
State: MI

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: pain, redness, and swelling at injection site; pain, redness, and swelling at injection site; pain, redness, and swelling at injection site; has a bruise and a palpable lump about the size of an almond at the injection site; has a bruise and a palpable lump about the size of an almond at the injection site; This is a spontaneous report from a contactable other healthcare professional (reported for herself). A 24-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number; Ek9231), via an unspecified route of administration (left arm) on 04Jan2021 (15:00) at single dose for Covid-19 immunization. The patient's medical history included "known allergies: Whey". Concomitant medications included colecalciferol (VITAMIN D), curcuma longa rhizome (TURMERIC), bifidobacterium bifidum, bifidobacterium lactis, bifidobacterium longum, lactobacillus acidophilus, lactobacillus rhamnosus (PROBIOTIC), and Multivitamin (unspecified). The patient was not diagnosed with COVID-19 prior to vaccination. The patient is not pregnant. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient reported that initially on 05Jan2021, she had pain, redness, and swelling at injection site. She also experienced a bruise and a palpable lump about the size of an almond at the injection site. There was no treatment received for the adverse event. The outcome of events was not recovered. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: VITAMIN D [COLECALCIFEROL]; TURMERIC [CURCUMA LONGA RHIZOME]; PROBIOTIC [BIFIDOBACTERIUM BIFIDUM;BIFIDOBACTERIUM LACTIS;BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACIDO

Current Illness:

ID: 0980629
Sex: F
Age:
State: OR

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

Lab Data:

Allergies:

Symptoms: Fever; chills; muscle aches; pain at injection site; headache; chest pain; This is a spontaneous report from a contactable nurse (patient). A 35-year-old female patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EK9231), via an unspecified route of administration in right arm on 12Jan2021 at single dose for covid-19 immunisation. Medical history included sulfa allergy, canteloupe allergy. The patient's concomitant medications were not reported. No any other medications the patient received within 2 weeks of vaccination. The patient previously received 1st dose of BNT162B2 (lot# EJ1685) via intramuscular in right arm on 22Dec2020 13:00 for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced fever, chills, muscle aches, pain at injection site, headache, chest pain on 12Jan2021 17:00. The patient was not pregnant. No treatment received for the events. The outcome of events was recovered on an unspecified date of Jan2021. This case was reported as non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 0980630
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: a coin-sized redness that is flat and not raised; She wasn't sure if it was subcutaneous or what but the injection was way too lateral and low; This is a spontaneous report from a contactable physician (patient). A 44-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number and expiration date not reported) via an unspecified route of administration on 12Jan2021 at a single dose for COVID-19 immunization. The patient had no medical history. There were no concomitant medications. The second dose was low laterally and 48 hours later the caller started seeing a coin-sized redness that was flat and not raised on 14Jan2021. The second vaccine was given way too low and lateral and she has developed a coin shaped redness at the injection site as if the vaccine was given subcutaneously instead of intramuscularly. She mentions were arm is a little fat, too. Patient wanted to know does she need antibody testing or a repeat dose? Does the COVID vaccine even work if they are given subcutaneous? She wasn't sure if it was subcutaneous or what but the injection was way too lateral and low. It was 8 fingerbreadths away from the top of her arm. Event was reported as non-serious. Outcome of the event was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980631
Sex: F
Age:
State: AZ

Vax Date: 01/11/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Exanthema on fingers and back; This is a spontaneous report from a contactable Other Health Professional reported for herself. The 46-year-old female patient that received second dose of bnt162b2 ( COVID 19, Pfizer Biotech, lot number: EL9231), via Intramuscular on 11Jan2021 09:30 AM on Left arm at a single dose for covid-19 immunisation. The patient is not pregnant at the time of vaccination. Medical history included Migraine w aura. No allergies to medications, food, or other products. Concomitant medications the patient received within 2 weeks of vaccination included cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) Zyrtec, vitamin D and vitamin C. The patient previously took first dose of bnt162b2 (COVID 19, BioNTech/Pfizer, lot number: EL5730) via Intramuscular on 21Dec2020 01:00 PM on Left arm at single dose for covid-19 immunisation. The patient experienced Exanthema on fingers and back from 14Jan2021 06:00 AM. The outcome of the event was recovering. The event was assessed non-serious. Facility where the most recent COVID-19 vaccine was administered was hospital. The patient was not receive any other vaccines within 4 weeks prior to the COVID vaccine. No treatment was received for the adverse event. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, has the patient has not been tested for COVID-19.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; VITAMIN D [VITAMIN D NOS]; VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 0980632
Sex: M
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: Muscle pain; swelling of upper arm; body aches; headache; chills; slight fever; This is a spontaneous report from a contactable consumer reported for himself. A26-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration in right arm on 12Jan2021 16:00 at single dose for COVID-19 immunisation. The patient received the vaccine at workplace clinic. Medical history included Penicillin allergy. The patient's concomitant medications were 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 had not been tested for COVID-19. The patient experienced muscle pain and swelling of upper arm, body aches, headache, chills, slight fever on 12Jan2021 23:30. No treatment was received for the events. The events did not result in Emergency Room visit or physician office visit. The outcome of events was recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980633
Sex: F
Age:
State: TX

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Swollen lymph node to right axillary; Swollen lymph node to right axillary. Pain radiates to right breast, down right arm and around to the back and right scapula area/ tender to touch; Pain radiates to right breast; Pain radiates to right breast, down right arm; Pain radiates to right breast, down right arm and around to the back; Pain radiates to right breast, down right arm and around to the back and right scapula area; Pain caused inability to do daily activities; This is a spontaneous report from a contactable nurse (patient). A 29-years-old female patient ( received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at right arm on 12Jan2021 07:30 at single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medication included ethinylestradiol, norethisterone acetate (MICROGESTIN). The patient had allergies to sulfamethoxazole, trimethoprim (BACTRIM), amoxicillin. The historical vaccine included the first dose of BNT162B2 at right arm on 21Dec2020 07:30 for covid-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced swollen lymph node to right axillary, pain radiates to right breast, down right arm and around to the back and right scapula area, pain caused inability to do daily activities and area was tender to touch from 13Jan2021 02:00. No treatment received for the adverse events. The events outcome was not recovered. No COVID prior vaccination, since the vaccination the patient hadn't been tested for COVID-19. It was not reported as serious. Information on the batch number has been requested.

Other Meds: MICROGESTIN

Current Illness:

ID: 0980634
Sex: F
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Name: bloodwork; Result Unstructured Data: Test Result:unknown results; Test Name: height; Result Unstructured Data: Test Result:4'11" or 5'; Test Name: Hemoglobin A1C; Result Unstructured Data: Test Result:pre-diabetic

Allergies:

Symptoms: experience nausea; This is Spontaneous report from a contactable consumer (patient). A 67-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL3246), via an unspecified route of administration on left upper arm on 13Jan2021 09:30 at single dose COVID-19 vaccination. Medical history included high blood pressure and prediabetic. Patient reported that she has high blood pressure that she is on medication for. She said she takes Metformin twice a day, clarifying she is pre-diabetic according to her Hemoglobin A1C. Patient was on top of her bloodwork, saying she has her bloodwork done regularly. Reported patient's height was 4'11" or 5'. Concomitant medications included Metfiormin as patient is pre-diabetic. Reported she has had the flu and Shingles vaccines in the past, and never had any prior reactions to vaccines. No prior vaccinations (within 4 weeks). The patient had her first dose of the Pfizer COVID-19 Vaccine yesterday morning, 13Jan2021, at 9:30. She said she had some nausea last night. She said she woke up in the middle of the night with nausea. She said she woke up this morning and had nausea again, but ate something and got better. She said the nausea is like morning sickness, clarifying if she eats something the nausea goes away, but once her stomach is empty, the nausea comes back. She said she has not had a fever. She asked how long should she expect her nausea to last. The event did not require a visit to Emergency Room or Physician. The outcome of the event was not recovered.

Other Meds: METFORMIN

Current Illness:

ID: 0980635
Sex: F
Age:
State: AK

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: tired; sweaty; nauseous light headed when standing; rush of hotness through entire body; severe nausea/nauseous light headed when standing; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received the first dose of BNT162B2 (Lot number: 3302), via an unspecified route of administration in right arm on 13Jan2021 13:00 at single dose for covid-19 immunization. Medical history was none. Concomitant medication included escitalopram, vitamin d. At the time of shot, maybe 3 mins after, rush of hotness through entire body and severe nausea. Passed after about 4 mins then occurred a second time lasting for about 5 mins. Rested about 45 mins before feeling well enough to drive. All better after about 2 hours. Next day (14Jan2021), tired, sweaty, nauseous light headed when standing. No treatment received. No pregnant at the time of vaccination. The outcome of the events was unknown.

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

Current Illness:

ID: 0980636
Sex: M
Age:
State: GA

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

Lab Data:

Allergies:

Symptoms: mild dyspepsia; loose stools; Moderate deltoid soreness at injection site; chills; myalgias; hyperalgesia; headache; fatigue; grogginess; This is a spontaneous report from a contactable physician reported for himself. A 33-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0142), via an unspecified route of administration on 07Jan2021 08:45 at single dose in left arm for covid-19 immunization. The patient medical history was not reported. The patient had no known allergies to medications, food, or other products. Concomitant medications within 2 weeks of vaccination included triamcinolone 1% cream and diphenhydramine 2% cream. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EJ1685), via an unspecified route of administration on 17Dec2020 05:00 PM at single dose in left arm for covid-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19, since the vaccination, the patient had not been tested for COVID-19. On 07Jan2021 12:00, the patient experienced moderate deltoid soreness at injection site within 2-3 hours; chills, myalgias, hyperalgesia, headache, fatigue, grogginess from 12-36 hours post injection (on 07Jan2021); mild dyspepsia and loose stools 24-36 hours post-injection (on 08Jan2021). The patient did not received treatment for the events. The outcome of the events was recovered in Jan2021.

Other Meds: TRIAMCINOLONE; DIPHENHYDRAMINE

Current Illness:

ID: 0980637
Sex: F
Age:
State: CA

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe rigors; severe arthralgias; myalgias; skin paraesthesia; severe cold sweats; profound weakness; This is a spontaneous report from a contactable Other Health Professional. A 48-year-old female patient (not pregnant) received 2nd dose of bnt162b2 ((PFIZER-BIONTECH COVID-19 VACCINE, lot: EJ1686), via intramuscular on 12Jan2021 13:30 at single dose on left arm for covid-19 immunisation. Medical history included mild asthma. There were no concomitant medications. Historical vaccine included 1st dose of bnt162b2 (lot: EJ1685) on 23Dec2020 left arm at single dose for COVID-19 Immunization (age at vaccination was 48 years old). Approximately 11 hrs after 2nd vaccine, patient developed severe rigors, severe arthralgias and myalgias as well as skin parasthesia, severe cold sweats and profound weakness. Symptoms improved with APAP (acetaminophen) plus ibuprofen alternating q3 hrs x24 hrs. Outcome of the events was resolving. This case was reported as non-serious.

Other Meds:

Current Illness:

ID: 0980638
Sex: F
Age:
State: VA

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

Lab Data:

Allergies:

Symptoms: arm pain; light headedness; abdominal pain; swollen, tender lymph node left axillary area; swollen, tender lymph node left axillary area; This is a spontaneous report from a contactable nurse (patient). A 60-year-old non-pregnant female patient received her second dose of bnt162b2 (BNT162B2 reported as PFIZER COVID 19 VACCINE; lot number: EK4176; expiration date: unknown), via an unspecified route of administration left arm on 08Jan2021 08:30 at a single dose for covid-19 immunization. The patient medical history was not reported. The patient has no known allergies. There were no concomitant medications. The patient received her first dose of bnt162b2 (BNT162B2 reported as PFIZER COVID 19 VACCINE; lot number: EK5730; expiration date: unknown), via an unspecified route of administration left arm on 18Dec2020 10:30 at a single dose for covid-19 immunization. The patient experienced arm pain, light headedness, abdominal pain and swollen, tender lymph node left axillary area on 08Jan2021 04:00 PM. The patient received treatment for the adverse events includes acetaminophen (TYLENOL) and ibuprofen (MOTRIN). The outcome of the events was recovered on in Jan2021.

Other Meds:

Current Illness:

ID: 0980639
Sex: M
Age:
State: MO

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: Body Temperature; Result Unstructured Data: Test Result:99.9 Fahrenheit

Allergies:

Symptoms: chills; body aches/aching all over; headaches; tired; not resting well last night/didn't rest well last night; a temperature of 99.9F/ fever; where he got the shot was achy; feels like he has a bad case of the flu; tremoring; muscles are achy; This is a spontaneous report from a contactable healthcare professional (patient). A 67-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3302 and expiry date: unknown), via an unspecified route of administration on 13Jan2021 at a single dose for COVID-19 immunization. Medical history included ongoing high cholesterol since 90s and was taking medication to keep it down, and ongoing neuropathy in the feet back in the 90s. Patient seemed to be okay after the vaccination until he didn't rest well last night on 13Jan2021. The morning of 14Jan2021, he had chills and was aching all over. He has a headache, and he was pretty tired on 14Jan2021. His temperature was 99.9. and wanted to make sure he was okay. They gave him the sheet of side effects but was wondering how long it was going to last. He also had fever and chills on Jan2021. He has been just resting all day long which was all he felt like doing. Patient felt he has a bad case of the flu. When his chills started, he noticed he was tremoring and shaking and his muscles are achy on Jan2021. He usually waits until his temperature is over 100 to take something and noticed where he got the shot was achy on Jan2021. During the night he went to aching more. He was not too excited about getting up and doing anything now. He was tired on 14Jan2021, because he didn't rest well last night and slept in late today. He finally got around, and ate cereal and stuff. He has just been sitting. He would still get the second vaccine, which was not exciting. Outcome of the events aching all over, headaches, and tired are not recovered while for the remaining events was unknown.

Other Meds:

Current Illness: High cholesterol; Peripheral neuropathy

ID: 0980640
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Watery drainage from her right eye; Nose feels full; congestion; Phlegm; Fever blister on her tongue (sore blister on the right side of her tongue); sores on her tongue; Feels a little weird; Dizzy or dizziness like vertigo (funny feeling like vertigo); Headache; Slept hard - she never sleeps that much; Drinking a lot of water; Fever; feverish; This is a spontaneous report from a contactable nurse (patient). An 81-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL1284, Expiration Date: 30Apr2021), via an unspecified route of administration, on 11Jan2021 at 09:00, at a single dose, for COVID-19 immunization. The patient's medical history included colitis and diverticulitis (chronic; diagnosed years ago); and allergies. The patient's concomitant medications included chlordiazepoxide/ clidinium bromide (LIBRAX) for colitis, omeprazole (PROTONIX), levocabastine hydrochloride (ZYRTEC) for allergies, and cyanocobalamin (VITAMIN B12) for colitis. The patient previously took the first dose of BNT162B2 (Lot Number: EH9899, Expiration Date: 31Mar2021) on 21Dec2020 for COVID-19 immunization and experienced a little sore on site; and varicella zoster vaccine (SHINGLES VACCINE) for immunization and it hurt and she got blisters at the injection side. The patient just got her second shot on Monday (11Jan2021) at 9 in morning. After a couple of hours (11 AM), the patient feels a little weird, dizzy or dizziness like vertigo (funny feeling like vertigo), and headache. That night, the patient took ibuprofen (MOTRIN) and paracetamol (TLENOL) and she just slept hard - she never sleeps that much, she is drinking a lot of water. The patient also had a fever that night and received treatment for this. On Tuesday (12Jan2021), the patient was okay but, in the evening, she started feeling feverish and has a fever blister on her tongue (sore blister on the right side of her tongue). The patient never had a fever blister before. Last night (13Jan2021), the patient was a little feverish, still has the sores on her tongue and she was having watery drainage from her right eye and her nose feels full; congestion and phlegm. The patient wanted to know if she should go to work tomorrow but was encouraged to reach out to a health care professional for medical advice. The patient asked health employee and they told her to call the company. Got the vaccine from work at a center. The patient recovered from "Dizzy or dizziness like vertigo (funny feeling like vertigo)" in Jan2021. The outcome of "Feels a little weird", "Headache", "Slept hard - she never sleeps that much", and "Drinking a lot of water" was unknown. The patient had not recovered from the remaining events.

Other Meds: LIBRAX [CHLORDIAZEPOXIDE;CLIDINIUM BROMIDE]; PROTONIX [OMEPRAZOLE]; ZYRTEC [LEVOCABASTINE HYDROCHLORIDE]; VITAMIN B12 [CYANOCOBALAMIN]

Current Illness:

ID: 0980641
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Face, neck, arms turned bright red; Face extremely swollen; Nausea; This is a spontaneous report from a contactable healthcare professional. A 56-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0142), intramuscular (left arm) on 12Jan2021 10:00 at a single dose for COVID-19 immunization. The patient medical history was not reported. Concomitant medication included lamotrigine. The patient experienced Face, neck, arms turned bright red, Face extremely swollen, Nausea; all on 12Jan2021 10:45 AM. The outcome of the events was recovering.

Other Meds: LAMOTRIGINE

Current Illness:

ID: 0980642
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fatigue; A visibly swollen lymph node in her neck; This is a spontaneous report from a contactable healthcare professional (the patient). A 23-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: KK9231, expiration date not reported), via an unspecified route of administration (reported left arm), on 13Jan2021 at 09:45 at a single dose for COVID-19 immunization. Medical history included psoriasis from an unknown date. Concomitant medications were not reported. The patient previously received the first dose of BNT162B2 on 23Dec2020 on her left arm (lot number: EJ1685). After receiving the second dose of the vaccine on 13Jan2021 at 20:15, the patient experienced fatigue and a visibly swollen lymph node in her neck. The patient was recovering from the events. There was no treatment given for the events.

Other Meds:

Current Illness:

ID: 0980643
Sex: F
Age:
State: CA

Vax Date: 12/20/2020
Onset Date: 12/01/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20201224; Test Name: TSH; Result Unstructured Data: Test Result:high/ slightly elevated; Test Date: 20201226; Test Name: TSH; Result Unstructured Data: Test Result:higher than before; Test Date: 20201224; Test Name: heart rate; Result Unstructured Data: Test Result:130s - it was sinus tachycardia; Test Date: 20201224; Test Name: heart rate; Result Unstructured Data: Test Result:100-150; Test Date: 20201224; Test Name: labs; Result Unstructured Data: Test Result:looked good/were normal; Test Date: 20201226; Test Name: labs; Result Unstructured Data: Test Result:everything was normal; Test Date: 20201224; Test Name: T4; Result Unstructured Data: Test Result:normal

Allergies:

Symptoms: Chills; heart started beating really bad/heart beating fast for 45 mins/ tachycardia/ heart rate was 100-150/ heart started beating fast; palpitations; heart rate was in 130s - it was sinus tachycardia; TSH was high/ slightly elevated/ TSH was higher than before; Sore arm; This is a spontaneous report from a contactable nurse (patient). A 38-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date unknown), via an unspecified route of administration, on 20Dec2020, at single dose, for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the first dose of the vaccine last 20Dec2020. On her first shot, she did good the first couple of days but had a sore arm in Dec2020. However, on 24Dec2020 while at work, her heart started beating really bad/heart beating fast and she had tachycardia/palpitations for 45 mins. She then mentioned she was a nurse and that the doctor hooked her up to a monitor and her heart rate was in 130s - it was sinus tachycardia on 24Dec2020. She informed that she had filed a report with the CDC. She went to the emergency room and her heart rate was 100-150 on 24Dec2020. She got fluids and her labs looked good, labs were normal on 24Dec2020. The only thing on 24Dec2020 was her TSH was high/ slightly elevated but her T4 was normal. Then she took it easy the next day. On Saturday, 26Dec2020 she began experiencing chills and took Tylenol and; her heart started beating fast again. She went to the emergency room and they repeated the labs, and everything was normal on 26Dec2020. Her TSH was higher than before on 26Dec2020. She went to see her doctor and the doctor thought that it was from her drinking a lot of caffeine before the vaccine and then her body building up antibodies days later. She was going off on tangent and unable to clarify details. She wanted to know if there was any data between the vaccine and the thyroid. Her doctor "feels like safe" and she had sinus tachycardia. She was asking if there were any reports on elevated TSH and tachycardia as a vaccine side effect. She further informed that she was trying to decide whether to take her second shot or not. She wanted to know if it was safe to take her second shot. Her doctor said it would be fine, but she wanted to know what Pfizer has to say. The outcome of the events was unknown. Information about the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980644
Sex: F
Age:
State: FL

Vax Date: 01/05/2021
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: her arm was a little sore; This is a spontaneous report from a non-contactable consumer (reporter's husband). 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 05Jan2021 at a single dose for COVID-19 immunization. The patient's medical history was not reported. The patient's concomitant medications were not reported. The patient had her first dose too and her arm was a little sore but it felt better after her aerobics class and she was totally fine. The patient was recovering from the event. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980645
Sex: F
Age:
State: KY

Vax Date: 01/04/2021
Onset Date: 01/07/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: pulses; Result Unstructured Data: Test Result:good

Allergies:

Symptoms: deltoid was still sore, but felt cold/entire arm and hand feels cold, worse when the area is rubbed; Deltoid still sore/soreness in the forearm; This is a spontaneous report from a contactable other healthcare professional (patient). A 47-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: ES1686), via an unspecified route of administration in the left arm on 04Jan2021 14:45 at a single dose for COVID-19 immunization. There were no medical history. The patient was not pregnant at the time of vaccination. The patient had no known allergies to medications, food, or other products. Concomitant medications included colecalciferol (VITAMIN D), probiotics, and elderberry [sambucus nigra]. 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 and had not been tested for COVID-19 since the vaccination. The patient's deltoid was still sore, but felt cold on day 3 (07Jan2021). By day 7 (11Jan2021), the entire arm and hand feels cold, worse when the area is rubbed. By day 8 (12Jan2021), the patient had soreness in the forearm and still unchanged at day 11. No weakness was noted. The patient had good pulses on Jan2021 and no visible change to the skin. No treatment was received for the adverse events. Outcome of the events was not recovered.

Other Meds: VITAMIN D [COLECALCIFEROL]; PROBIOTICS; ELDERBERRY [SAMBUCUS NIGRA]

Current Illness:

ID: 0980646
Sex: M
Age:
State: FL

Vax Date: 01/10/2021
Onset Date: 01/11/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: rash on the belly; This is a spontaneous report from a contactable consumer. An 80-year-old male patient (reporter's boss) received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EK9231) in the Hospital (a family member that works there and the worker's were allowed to pick one of their family members to give the vaccine to) via an unspecified route of administration on 10Jan2021 at 11:30 AM at a single dose on the left upper arm for COVID-19 immunization. The patient had no medical history. Concomitant medication included simvastatin (manufacturer unknown), dutasteride (manufacturer unknown) and montelukast (manufacturer unknown) all from an unknown date and unknown if ongoing. The reporter stated that her boss received the first dose on 10Jan2021 and developed a rash on the belly. She wanted to know if he could take the second dose as scheduled or if he needs to wait. He was scheduled in 3 weeks. He has a rash all over his belly and the doctor said it was like a reaction to the vaccine. She does not know if he has to go the ER or what. His primary care physician (PCP) ordered him Benadryl pills and ointment. The reporter confirmed that the patient was ordered both oral and ointment. The outcome of the event was not recovered.

Other Meds: SIMVASTATIN; DUTASTERIDE; MONTELUKAST

Current Illness:

ID: 0980647
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Lightheaded; Sore arm; This is a spontaneous report from a non-contactable consumer reported that a patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), 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. The patient experienced lightheaded for an hour or so after and really sore arm about 12 hours later; both on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980648
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Sore arm; Tired than usual; This is a spontaneous report from a non-contactable consumer (patient). A patient of unspecified age and gender received 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. It was reported that the patient experienced sore arm on day 1 and was a little more tired than usual on day 2, both on unspecified dates. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980649
Sex: U
Age:
State:

Vax Date: 12/31/2020
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: soreness; stinging; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 31Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the dose on 31Dec2020, and experienced little soreness that lasted for 2 days and stinging that lasted for 2 hours. No other problems reported. The events resolved on an unspecified date. Information about the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980650
Sex: U
Age:
State:

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

Lab Data: Test Name: temp; Result Unstructured Data: Test Result:increased

Allergies:

Symptoms: Arm pain; fatigue; slept nearly nonstop starting the night of injection; odd cheek canker; GI issues; increased temp; headache; body ache; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), 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. The patient reported, "Arm pain was worse than any previous immunizations I have had. Massive fatigue (slept nearly nonstop starting the night of injection), odd cheek canker, GI issues, increased temp, headache, body ache. Day 3 now, seem to be better!" on an unspecified date. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980651
Sex: F
Age:
State: OR

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

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

Allergies:

Symptoms: colds; This is a spontaneous report from a contactable healthcare professional via a Pfizer sponsored program Pfizer First Connect and Medical information team. An adult female (reported as in her late 30s) patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), 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. On unspecified date, it was reported that the patient has colds but tested negative for COVID and was asking if she can get the vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980652
Sex: F
Age:
State: CT

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

Lab Data: Test Date: 20201122; Test Name: covid; Test Result: Positive

Allergies:

Symptoms: slept all day; very sore arm; woke up trembling with chills; terrible chills; headache/bad headache; fatigue; diarrhea; This is a spontaneous report from a contactable consumer (patient). A 79-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 the left arm, on 12Jan2021 at a single dose for COVID-19 immunization. Medical history included major reaction to eating conch, and tested positive for COVID on 22Nov2020 There were no concomitant medications. Patient read that was not a good thing to do, to get the vaccine after only 2 months instead of 3 from diagnoses. When she had COVID she had major headache, chills, and diarrhea. After the vaccine she had had the same thing, terrible chills, bad headache and diarrhea on Jan2021. The side effects say that this was normal but she wants to know should she have waited the 90 days before getting the vaccine. Patient still had the headache and chills but she took an Imodium and the diarrhea was better. Patient had also fatigue in Jan2021,and slept all day yesterday (13Jan2021). She has had a very sore arm and at 2am she woke up trembling with chills on Jan2021. Outcome of the event chills and headache was not recovered, for diarrhea was recovering and for the remaining events was unknown. Patient had a major reaction to eating conch and wanted to make sure there was no shellfish involve in the vaccine. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0980653
Sex: F
Age:
State: MI

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: dizziness; This is a spontaneous report from a contactable consumer. An 87-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL3249, expiration date not reported) via an unspecified route of administration on 13Jan2021 15:00 at a single dose for COVID-19 immunization. Medical history included pernicious anemia from 2019 and ongoing (gets B12 shots). There were no concomitant medications. The reporter's mother had the Pfizer COVID vaccine at 3 o'clock in the afternoon of 13Jan2021. At 1 o'clock on 14Jan2021, she started experiencing dizziness. The caller's sister is with the patient as this time. The past 4 hours the patient has experienced dizziness. As she tried to get up, it gets worse. Outcome of the event was not recovered.

Other Meds:

Current Illness: Pernicious anemia (gets B12 shots)

ID: 0980654
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: running a fever; This is a spontaneous report from a contactable consumer (patient's mother). A female patient of an unspecified age (age: 19, units: unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date unknown), via an unspecified route of administration, on 09Jan2021, at single dose, for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's mother stated that the patient got the second dose of the Covid-19 vaccine on Saturday, 09Jan2021. The patient has been running a fever since possibly Saturday night 09Jan2021, but definitely since Sunday morning. The fever was mostly in the morning and at night around 7-8 pm. Fever in the morning lasts until 10 -11 am. The mother added that today was the first day the fever has lasted all day, and the patient had the fever at 3PM. The mother wanted to know if this was a typical response to the vaccine (i.e. the duration of the fever). The mother was concerned about the duration of the fever and she has given the patient ibuprofen and Tylenol. The mother asked for herself if she can use antipyretics before or after vaccination with the Pfizer-BioNTech COVID-19 vaccine. The mother was responded per the interim guidelines, "Antipyretic or analgesic medications (e.g., acetaminophen, non-steroidal anti-inflammatory drugs) may be taken for the treatment of post-vaccination local or systemic symptoms, if medically appropriate. However, routine prophylactic administration of these medications for the purpose of preventing post-vaccination symptoms is not currently recommended, as information on the impact of such use on Pfizer-BioNTech COVID-19 vaccine-induced antibody responses is not available at this time." The mother was told to discuss this with her healthcare provider. The outcome of the event was not recovered. Information about the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980655
Sex: F
Age:
State: TX

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Arm sore at injection site; Hot to touch at injection site; Knot at injection site; Slight fatigue; Joint pain worse than normal; Occasional headache; This is a spontaneous report from a contactable nurse (patient). A 42-year-old female patient (non-pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL3248), via an unspecified route of administration in left arm, on 12Jan2021 at 10:30, at a single dose, for COVID-19 immunization. The patient's medical history included rheumatoid arthritis, eczema, depression, anxiety, slipped disc in back, overweight, and allergies to sulfa and latex. The patient had unspecified concomitant medications. The patient previously took the first dose of BNT162B2 (Lot Number: EJ1685) on 21Dec2020 (10:00 AM), for COVID-19 immunization (left arm). The patient was not diagnosed with COVID-19 prior vaccination. No other vaccine was administered in four weeks. The vaccine was administered in a hospital facility. On 13Jan2021 at 4 AM, the patient experienced arm sore, hot to touch, and knot at injection site; slight fatigue; joint pain was worse than normal; and occasional headache. No treatment was administered for the events. The patient has not been tested for COVID-19 post-vaccination. The patient had not recovered from the events.

Other Meds:

Current Illness:

ID: 0980656
Sex: F
Age:
State: MI

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

Lab Data: Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:99; Comments: 99-100 during the day; Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:100; Comments: 99-100 during the day; Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:101; Comments: 101-102 for 6 nights now; Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:102; Comments: 101-102 for 6 nights now

Allergies:

Symptoms: Fever/Temperature running 99-100 during the day and running 101-102 for 6 nights now; Sore arm the first day; This is a spontaneous report received from a contactable nurse (who is also the patient). A 51-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0142, expiry date: unknown), via an unspecified route of administration in the left arm, on 08Jan2021 11:00, at single dose, for covid-19 immunization, in the hospital. Medical history included asthma, Raynaud's phenomenon, eczema, environmental allergies, and COVID-19 (prior to vaccination). The patient is not pregnant. Concomitant medication included ergocalciferol (VIT D), calcium, ascorbic acid (VIT C), thiamine and zinc. The patient did not receive other vaccines in four weeks. The patient experienced sore arm the first day, on 09Jan2021. Fever started about 30 hours after injection, on 09Jan2021 at 17:00. Her temperature was running 99-100 during the day and running 101-102 for 6 nights now. The patient did not receive treatment for the events. The patient was not tested for COVID-19 post vaccination. The outcome of the events was not recovered.

Other Meds: VIT D; CALCIUM; VIT C; THIAMINE; ZINC

Current Illness:

ID: 0980657
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: allergic reaction; This is a spontaneous report from a non-contactable other healthcare professional (patient). A 38-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date were not reported), 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. The patient reported that after receiving the first dose of the vaccine, she experienced an allergic reaction on an unspecified date. She wanted to know if she should still receive the second dose despite this. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980658
Sex: M
Age:
State: SC

Vax Date: 10/20/2020
Onset Date: 10/20/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Had an allergic reaction with Prevnar 13; The back of his legs started aching/his whole middle extremities were doing the same thing/it went down his arms and came back up; This is a spontaneous report from a contactable consumer. A 72-years-old male patient received second dose of pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) (PREVNAR 13, Solution for injection in pre-filled syringe, lot number and expiry date not reported), via an unspecified route of administration on 20Oct2020 at a single dose for immunization. The patient's medical history was not reported. There were no concomitant medications. Patient previously had the Pneumonia shot as immunization on an unknown date (first dose) (tradename unspecified, reported as Pfizer pneumonia vaccine). On 20Oct2020, patient had an allergic reaction with pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) and was asking if he was safe to have the COVID 19 vaccine and will not have any allergic reaction as he had with pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein). Patient was asking for the ingredients of the vaccine. Received call from patient regarding the Pfizer COVID vaccine and Pneumonia shot. He had the second pneumonia shot Pfizer product on 20Oct2020, and never had a reaction before to a shot in his life. He left the doctor's office and walked outside. The back of his legs started aching (20Oct2020). By the time he got in the car, his whole middle extremities were doing the same thing. So, he parked his car and went back inside, then it went down his arms and came back up. It was pretty quick. They took his blood pressure and it was fine. He had no temperature, no rash, no nausea, no palpitations or anything like that. He just hurt like nothing he had before. It hurt more to sit down than stand up. They kept him an hour and he walked around and was fine. He went home and was fine. He did not have anything more happen. He was 72 years old and in good health. He doesn't take medications. He was reading that you should not get the Pfizer shot if you had an allergic reaction to a dose of the COVID or any ingredient in this vaccine. He talked to his doctor yesterday or again today (14Jan2021) and he suggested he call Pfizer to see what his options are and if should he get it. He did not wish to complete report and requested he be transferred to have his question answered. No further details provided. The outcome of the events allergic reaction and "the back of his legs started aching/his whole middle extremities were doing the same thing/it went down his arms and came back up" was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0980659
Sex: F
Age:
State: CA

Vax Date: 12/22/2020
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Welt on her left groin; Maybe infected lymph node; Skin breakdown; Bruise; Could not walk on right foot; Ligament in back of right ankle felt injured; This is a spontaneous report from a contactable healthcare professional (patient). A 48-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EH9899), intramuscular in left arm, on 22Dec2020 at 10:30, at a single dose, for COVID-19 immunization. The patient had no medical history and concomitant medications. The patient had no known allergies. The patient was not diagnosed with COVID-19 prior vaccination. No other vaccine was administered in four weeks. The vaccine was administered in a hospital. On 05Jan2021 at 04:45 PM (2 weeks after the first dose), the patient developed a welt on her left groin - maybe infected lymph node, and skin breakdown which later turned into a bruise that improved slowly with cleanse and bacitracin/ neomycin sulfate/ polymyxin B sulfate (NEOSPORIN). Though applied with bacitracin/ neomycin sulfate/ polymyxin B sulfate, the patient was still with visible bruising one week later. A few days later (Jan2021), the patient could not walk on right foot and ligament in back of right ankle felt injured. The patient was administered with the second dose of BNT162B2 (Lot Number: EL3302) on 12Jan2021 in left arm. The patient had not been tested for COVID-19 post-vaccination. The patient was recovering from "Skin breakdown". The patient had not recovered from the remaining events.

Other Meds:

Current Illness:

ID: 0980660
Sex: F
Age:
State: CA

Vax Date: 12/21/2020
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210101; Test Name: Nasal Swab; Test Result: Positive

Allergies:

Symptoms: nasal swab covid test result positive; nasal swab covid test result positive; This is a spontaneous report from a contactable Other HCP (for herself) reported that a 38-year-old female (not pregnant) received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot Number: EJ1685 and Expiration Date unknown) intramuscularly on 21Dec2020 01:45 PM at single dose (Left arm) for COVID-19 immunisation. The patient's medical history was known allergies: Penicillin, clindamycin, doxycycline. The concomitant medications was not reported. No other vaccine in four weeks. Patient experienced nasal swab covid test type post vaccination on 01Jan2021 was positive. The outcome was unknown with no treatment.; Sender's Comments: Based on the information available, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported nasal swab covid test positive based on the known safety profile. However the short duration of 10 days since the vaccine first dose is given it is unlikely patient would have fully developed immunity.

Other Meds:

Current Illness:

ID: 0980661
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: urinary tract infection; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age 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 at a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient received the first dose of the Covid-19 vaccine and her second dose is scheduled on 26Jan2021. She has currently a urinary tract infection and she may receive an antibiotic (Nitrofurantoin) she would like to know if this would affect the vaccine. Patient also asked if it is okay if she does not take the second dose of the vaccine 21 days after the first dose, but a couple of weeks later. The outcome of the event was unknown. The event was assessed as non-serious. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980662
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Had a hot flash or flushing sensation; Had a hot flash or flushing sensation; Tingles and a decreased sensation around her lips/numbness and a tingling to her lips and nose; Numbness and a tingling to her lips and nose; This is a spontaneous report from a contactable nurse. A 34-year-old female patient received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3246), intramuscular (left arm) from 14Jan2021 16:30 to 14Jan2021 16:30 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported by the patient that 10 minutes after the injection, she had a hot flash or flushing sensation, as well as numbness and a tingling to her lips and nose. She explained having "tingles and a decreased sensation around her lips", which she also referred to as a "diminished sensation" during the interaction. She says that she has done no treatment for this. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0980663
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Both arms hurt; Fatigue; Headache that moves; Ear aches; Noises are louder; Mind goes blank while recalling information in a conversation; Feverish feeling but no fever; Heaviness of the body like moving in honey; Achiness; This is a spontaneous report from a contactable other healthcare professional (patient). A 40-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL3248, expiration date not reported) via an unspecified route of administration on the right arm on 12Jan2021 18:45 at a single dose for COVID-19 immunization. Medical history included PCOS, Raynauds, PTSD; and known allergies: Sulpha, sulfites, pseudafed, penicillin, cephalosporins, bromfed, IV contrast, pineapple. Concomitant medication in two weeks included levocetirizine dihydrochloride (XYZAL), omeprazole, escitalopram oxalate (LEXAPRO), lamotrigine (LAMICTAL) and levothyroxine sodium (LEVOTHYROXIN). On 12Jan2021 08:45 PM, the patient experienced both arms hurt, fatigue, achiness, headache that moves, ear aches, noises are louder, mind goes blank while recalling information in a conversation, feverish feeling but no fever, heaviness of the body like moving in honey. Therapeutic measures were taken as a result of the events which included Ibuprofen (ADVIL) and acetaminophen (TYLENOL). 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. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. Outcome of the events was not recovered.

Other Meds: XYZAL; OMEPRAZOLE; LEXAPRO; LAMICTAL; LEVOTHYROXIN

Current Illness:

ID: 0980664
Sex: M
Age:
State: MI

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: chills; This is a spontaneous report from a contactable consumer. A 68-year-old male patient received bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: EL3249), via an unspecified route of administration in the left arm on 13Jan2021 10:00 at a single dose for COVID-19 immunisation. Medical history included Hypothyroidism controlled with meds. Concomitant medication included levothyroxine. On 14Jan2021 0130 (reported about 14 hours after injection), the patient experienced chills. The chills occurred about 2 in the morning and lasted only a short while. The patient had not tested for COVID post vaccination. The patient did not receive treatment for the event. The outcome of the event was recovered in Jan2021.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 0980665
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: muscle soreness; She had some arm soreness at the injection site/injection area hurt; This is a follow-up spontaneous report from Pfizer-sponsored program, from a contactable physician. A 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot and expiry not reported), intramuscular on 30Dec2020 at a single dose for COVID-19 vaccination. Medical history included pains in her arm (so any injection would hurt). There were no concomitant medications. Physician had muscle soreness after getting the 1st dose of the COVID 19 vaccine last 30Dec2020. Took ibuprofen (ADVIL) for pain management and wondering if this will affect the antibody response. Requesting for data regarding people that took pain medications during the clinical trials and asking for antibodies titer after taking pain medications. She will have the 2nd dose on 20Jan2021 and wants to know the options. On 14Jan2021, it was reported that right after the patient took the vaccine, she took some ADVIL because the injection area hurt. She is now seeing she was not supposed to take ADVIL, acetaminophen (TYLENOL), ibuprofen. She also wanted to know during the clinical trials, did they notice a decrease in antibodies after taking ADVIL or TYLENOL. Confirms she took ADVIL right after the injection. She already had pains in her arm so any injection would hurt. She was explaining she is now seeing on Medical (Social site name), a study in mice shows with COVID infections, NSAIDS were given, clarified as meloxicam, and it reduces the neutralizing antibody response. Now, all over Medical (Social site name), physicians are saying you shouldn't take ibuprofen, Naproxen, or Tylenol after receiving a dose. Wanted to know what was seen in the clinical trial data. Mice are mice. It's now all over Medical (Social site name). She has her second dose coming on Wednesday. She also wants to know what is she going to tell her patients? They are not going to want to know what happened in mice, they are going to want to know what happened in Phase 3 of Clinical trials. She had some arm soreness at the injection site. She confirms the arm soreness was gone in less than 48 hours, but she took ADVIL every 8 hours. Once the soreness was gone, she didn't take it. But now she is freaking out, wondering if she didn't get an antibody response? She received the standard dose, which she believes is 3mL of the solution, but she isn't sure. Therapeutic measures were taken as a result of muscle soreness and 'she had some arm soreness at the injection site'. The outcome of the event muscle soreness was unknown, while of 'She had some arm soreness at the injection site/injection area hurt' was recovered on Jan2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm