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: 0973421
Sex: M
Age:
State:

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Bone aches; Minor HA; Diarrhea; Violent vomiting; A jaundice color of skin; This is a spontaneous report from a non-contactable pharmacist. A 55-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL3246), intramuscular on 12Jan2021 at a single dose for COVID-19 immunization in a hospital. The patient's medical history and concomitant medications were not reported. On 12Jan2021, the evening after the vaccine was administered, the patient experienced chills, bone aches, and minor HA that then worsened to explosive diarrhea and violent vomiting with a jaundice color of skin. The events resulted in a doctor or other healthcare professional office/clinic visit. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0973422
Sex: F
Age:
State: LA

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: menstrual cycle started 4 days early with heavier than usual flow; Myalgias; Chills; Tmax 100.7; This is a spontaneous report from a contactable physician reported for herself. A 41-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL0142), intramuscular in the right arm on 08Jan2021, 15:00 at a single dose for covid-19 immunisation. The patient's medical history was not reported. The patient did not have Covid prior to vaccination. Patient did not have other vaccine in four weeks. Concomitant medications included multivitamin. The patient previously took amoxicillin and experienced hypersensitivity (reported as known allergies to amoxicillin). The patient received the first dose of bnt162b2 (lot:EK5730), intramuscularly in the right arm on 18Dec2020 at 11:00AM at a single dose for covid-19 immunization. The patient experienced myalgias, chills, tmax 100.7 on 09Jan2021 09:00. It was also reported that patient's menstrual cycle started 4 days early with heavier than usual flow on 09Jan2021 11:00. Patient did not received treatment for the events. The outcome of the event myalgia, chills and pyrexia, was recovered on 09Jan2021, 21:00 and recovered on an unknown date for the event menstrual cycle abnormal. Patient was not tested positive for Covid-19 post vaccination.

Other Meds: MULTIVITAMIN [VITAMINS NOS]

Current Illness:

ID: 0973423
Sex: F
Age:
State: VA

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Swollen and tender left neck lymph node; Swollen and tender left neck lymph node; Headache; Tiredness; This is a spontaneous report from a contactable other health professional (HCP). A 35-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK4176), intramuscular on left arm, on 12Jan2021 at 09:15, at a single dose for COVID-19 immunization. Medical history included anxiety and migraine from an unknown date and unknown if ongoing. Concomitant medication included escitalopram. The patient received the first dose of BNT162B2 (lot number: EH9899), intramuscularly on left arm at 23Dec2020, 03:30 PM. The patient experienced swollen and tender left neck lymph node, headache and tiredness; all on 12Jan2021 at 17:30. There was no treatment given for the events. The outcome of the events was not recovered.

Other Meds: Escitalopram

Current Illness:

ID: 0973424
Sex: F
Age:
State: NC

Vax Date: 12/28/2020
Onset Date: 01/03/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210103; Test Name: Rapid Covid testing; Test Result: Positive

Allergies:

Symptoms: Sore arm; a little tired; second dose was due 25Jan2021; Tested positive for COVID-19 on 03Jan2021/congestion and cough; Tested positive for COVID-19 on 03Jan2021/congestion and cough; This is a spontaneous report from a contactable nurse via a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs). This 39-year-old female nurse (patient) reported that she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EK9231), via intramuscular at left deltoid on 28Dec2020 11am at single dose for COVID-19 immunization. Medical history included non-smoker with no other illness. Concomitant medication was none. The patient had not been treated with immunomodulating or immunosuppressing medications or received any other vaccines around the time of COVID-19 vaccination. Patient reported after receiving her first dose of the COVID-19 vaccine on 28Dec2020, she had sore arm and a little tired, other than that felt fine. She stated second dose was due 25Jan2021. She was tested positive for COVID-19 (Rapid Covid testing) on 03Jan2021. She already decided going to wait the 90-day-period to get the second dose of the vaccine. Since she was quarantined she wanted to what she should do. She stated her having testing positive for Covid did not have anything to do with the vaccine. She still had some lingering symptoms, congestion and cough. Nothing had worsened, but just wouldn't go away. She did not receive any other vaccines the same day or 4 weeks prior. No history of problems with vaccines in past. She had not had antibodies checked yet. It was reported no AE required a visit to emergency room/physician office. The patient was not hospitalized. The patient received no additional therapies for COVID-19. Patient's outcome with COVID-19 was recovering, and the rest of events was unknown.; Sender's Comments: The Company cannot completely exclude the possible causality between the reported tested positive for COVID-19 (Rapid Covid testing), which is considered ineffective of BNT162B2, and the administration of BNT162B2.

Other Meds:

Current Illness:

ID: 0973425
Sex: F
Age:
State: FL

Vax Date: 12/18/2020
Onset Date: 12/19/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: mild swelling and tenderness of corresponding vaccine site arm in armpit lymph nodes; mild swelling and tenderness of corresponding vaccine site arm in armpit lymph nodes; This is a spontaneous report from a contactable pharmacist. A 44-year-old female patient received bnt162b2 (BNT162B2), the first dose (lot number: EH9899, expiry date: not reported), intramuscularly, on 18Dec2020 04:00 PM, at a single dose, on the left arm; and the second dose (lot number: EL1284, expiry date: not reported), intramuscularly, on 07Jan2021 11: 00 AM, at a single dose, on the right arm, both for COVID-19 immunization. The vaccine was administered in a hospital. The patient was not pregnant. Medical history included COVID. It was reported that patient was diagnosed with COVID prior to vaccination and was not tested for COVID post vaccination. The patient had no known allergies. Concomitant medications included ethinylestradiol, levonorgestrel (JOLESSA), cyanocobalamin (VITAMIN B12 [CYANOCOBALAMIN]), ergocalciferol (VIT D); these are the other medications she received in two weeks. The patient did not receive any other vaccine within four weeks. The patient experienced mild swelling and tenderness of corresponding vaccine site arm in armpit lymph nodes the evening following both covid 19 vaccine doses 1 and 2. This lasted 48-72 hours and then resolved. The first dose was received on 18Dec2020 with reaction occurred on 19Dec2020. The second dose was received on 07Jan2021 with reaction occurred on 08Jan2021 06:00 PM (also reported as "09Jan2021"). The patient did not receive any treatment for the reported adverse events. Outcome of the events was recovered on an unspecified date.

Other Meds: JOLESSA; VITAMIN B12 [CYANOCOBALAMIN]; VIT D

Current Illness:

ID: 0973426
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Tiredness/Exhaustion; Chills; Low grade fever; Muscle aches; Weakness; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK9231; expiry date: unknown) via an unspecified route of administration, on an unspecified date in Jan2021 at 15:30, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient received first dose of the Pfizer BioNTech Covid-19 vaccine on Monday at 3:30 P.M. He woke up yesterday morning with exhaustion, tiredness, chills, low grade fever, muscle aches, and just weakness that hasn't stopped since yesterday morning. All these lasted for 48 hours. Patient then asked how long he will experience these. Outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0973427
Sex: M
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: numbing on right side of face/numbness in my right arm; hard time swallowing; dizziness; fogginess; disorientation; hard of hearing; right ear felt very clogged; This is a spontaneous report from a contactable healthcare professional. A male patient of an unspecified age (reported as 43 with unspecified units) received his first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE and also reported as covid vaccine; unknown lot number and expiration date), via an unspecified route of administration on 11Jan2021 at a single dose for covid-19 immunization. The patient's concomitant medications and medical history were not reported. The patient reported that he received the covid vaccine on Monday late afternoon on 11Jan2021. He reported side effects of numbing on right side of face, hard time swallowing and numbness in his right arm on Jan2021. On Jan2021, he had initial symptoms of dizziness, fogginess and disorientation and then went to bed and woke up with additional symptoms (what he mentioned earlier). The patient added that his right ear felt very clogged and was hard of hearing at the time, but now it has resolved (that was the last thing that went away). The patient inquired if he should get the second dose. He mentioned that all the symptoms cleared up and he inquired as to what are the recommendation. The outcome of the events was recovered on Jan2021. The following information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0973428
Sex: F
Age:
State: TX

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: red and blotchy spots to the arm of injection site; This is a spontaneous report from a contactable consumer. An 83-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EL1283), via an unspecified route of administration on 13Jan2021 13:00 at SINGLE DOSE at arm right for COVID-19 immunization. Medical history included Chronic Lymphomatic Leukemia (CLL), and Heart attack in 2016. The patient's concomitant medications were not reported. The patient had the vaccine 4 hours ago and her whole arm down to the fingers is blotchy red as well as where the injection was given, it's her whole arm, just blotchy red dots. She received the First Dose at 1PM Eastern Time and probably about 2 and a half hours later is when the blotchiness appeared. The patient was experiencing red and blotchy spots to the arm of injection site. Redness and blotchy coloration appear to be under the skin down to her hand and wrist. She asks if this is a normal side effect. She has had no positive test for Covid Before the Vaccine. She has had No Antibody Tests. She has had No issues with vaccines in the past. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 0973429
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: arm swelled up and she had a lump; arm swelled up and she had a lump; This is a spontaneous report from a contactable Pharmacist. A female patient (age: 70s) received first dose of bnt162b2 (BNT162B2), via an unspecified route of administration on an unspecified date at SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced arm swelled up and she had a lump on an unspecified date with outcome of unknown. Information about Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973430
Sex: M
Age:
State: NM

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
Hospital:

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

Allergies:

Symptoms: Approximately 3 minutes post injection the patient began hyperventilating 2/2 SOB; Approximately 3 minutes post injection the patient began hyperventilating 2/2 SOB; This is a spontaneous report from a contactable pharmacist. A 38-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: EL3302), intramuscular on the left arm on 13Jan2021 10:15 at a single dose for COVID-19 immunization. The patient had the vaccine in a hospital. The patient had no other vaccine in four weeks. The patient's medical history and concomitant medications were not reported. The patient was not tested for COVID post vaccination. The patient took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: EL1284, expiry: unknown) on 23Dec2020 at 10:15, intramuscularly on the left arm for COVID-19 immunization. Approximately 3 minutes post injection (13Jan2021 "10:15"), the patient began hyperventilating "2/2" SOB. RR notified. Patient was placed on 4L O2. The event hyperventilation was not treated. The patient fully recovered on Jan2021.

Other Meds:

Current Illness:

ID: 0973431
Sex: F
Age:
State: CT

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: had numbness/to her bottom jaw bone/switched between her cheek and jaw and then her nose; face started tingling/from her lower eyelid/switched between her cheek and jaw and then her nose; face started tingling and had numbness/from her lower eyelid; face started tingling and had numbness/affects her lips/and mouth sometimes; face started tingling and had numbness/affects her lips/and mouth sometimes; It is just very annoying/It is irritating; This is a spontaneous report from a contactable nurse (patient). A 34-year-old female patient received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: EL3284), via an unspecified route of administration in the left arm on 11Jan2021 12:00 at a single dose for COVID-19 immunization. Medical history included ongoing anxiety since she was 13 years old. The patient's concomitant medications were not reported. The patient received the vaccine on Monday at 12 o'clock. She got it for work. She doesn't have a prescribing doctor. She developed the side effect Tuesday at 2 am. The left side of her face started tingling and had numbness, which is the same side she received the vaccine on. She doesn't have weakness. It is not resolving. It is from her lower eyelid to her bottom jaw bone. When asked if it was improving persisting or worsening, she said it depends. Sometimes it gets worse and affects her lips, and sometimes it is on and off. It won't be completely gone. It switched between her cheek and jaw and then her nose and mouth sometimes. If she bends over, it tingles worse. It is just very annoying. It felt like if she had Novocain on the top and bottom of her mouth. It is irritating. She got it because she doesn't want COVID and she works as a nurse. She does have really bad anxiety. She has nothing else medical. She is just really nervous. It is not going away. She is freaking out. She would like more information. The outcome of the event "It is just very annoying/It is irritating" was unknown, while for the other events was not recovered.

Other Meds:

Current Illness: Anxiety (since 13 years old).

ID: 0973432
Sex: F
Age:
State: GA

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: the rash was getting worse and she had "little bumps"; itching on her back; This is a spontaneous report from a contactable nurse. This nurse reported for self that the female patient of unknown age who received first dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Dec2021 at single dose for covid-19 immunisation. Medical history included allergies: persimmon. Concomitant medications were unknown. Prior to receiving the vaccine she had rashes on her arms which she thinks was a reaction from eating persimmons. She thinks the rash was from organic persimmon fruit since she was eating one a day. She stayed at the facility for an hour after receiving the vaccine and then went home. She states that after receiving the first dose of the vaccine she went home and took a shower and noticed that the rash was getting worse and she had 'little bumps'. On the third day the rash started getting better and now it is completely gone. She realizes that it is hard to tell if the COVID-19 vaccine caused any adverse effects because she already had the skin rash prior to receiving the first dose, however. she is due for the second dose of the vaccine and wants to know if she could safely proceed with getting the second dose. She was taking a shower and she noticed itching on her back and she was scratching and saw bumps. Reports the rashes were a little bit more, and it was not too much itching, and on the third day she took Benadryl. Reports it is all gone now. She was thinking to talk to her doctor and thought it must be from the persimmon fruit since she had the rashes prior to the vaccine. She is asking if she should get the second dose. The outcome of the events was recovered. Information about Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 0973433
Sex: F
Age:
State: TX

Vax Date: 12/22/2020
Onset Date: 12/31/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20201231; Test Name: COVID-19; Test Result: Positive

Allergies:

Symptoms: Tested positive for Covid 19 after receiving the vaccine/illness; Tested positive for Covid 19 after receiving the vaccine/illness; This is a spontaneous report from a contactable consumer (patient) from the Pfizer-sponsored program, Pfizer First Connect. A 61-years-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number: EL0140, expiration date: 31Mar2021), via an unspecified route of administration on the upper left arm on 22Dec2020 at a single dose for COVID-19 immunization. There was no medical history and no concomitant medications. The patient received her first dose of the COVID-19 vaccine on 22Dec2020. On 31Dec2020, the patient tested positive for COVID-19. The patient was scheduled to receive her second dose and wanted to know if it is okay to get it, clarified that she was supposed to receive her second shot on 12Jan2021 (the day before the report). The doctor gave her a script that showed that she clinically recovered from illness and okay to get the second vaccine (dose). No treatment was administered for the event. The event "tested positive for COVID-19 after receiving the vaccine/illness" resolved on 13Jan2021.

Other Meds:

Current Illness:

ID: 0973434
Sex: F
Age:
State: CA

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: First day-headache; second day feeling unwell; 3rd day tenderness; lymphadenopathy, right underarm.; swollen lump nose; swollen lump nose; This is a spontaneous report from a contactable nurse. A 49-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0140), intramuscular in right arm on 07Jan2021 10:30 at a single dose for COVID-19 immunization. Medical history included valley fever treatment for 4 months. No known allergies. Concomitant medication included fluconazole. On 07Jan2021 18:00, the patient experienced first day-headache, second day feeling unwell, and third day tenderness/ swollen lump nose, lymphadenopathy, right underarm. Patient did not have COVID prior vaccination. The patient was not tested for COVID post vaccination. Treatment received for the events included TYLENOL tabs. The outcome of the events was not recovered.

Other Meds: Fluconazole

Current Illness:

ID: 0973435
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Developed "a hive" within 24 hours; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), 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. Patient received the first dose of the COVID 19 vaccine and developed "a hive" within 24 hours. Is it safe for them to get a second dose? He has no other information on the patient. The outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973436
Sex: F
Age:
State: LA

Vax Date: 01/09/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: she felt like her heart was cold; This is a spontaneous report from a contactable consumer (patient) via Medical information team. A 72-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: CL0142), via an unspecified route of administration in left arm on 09Jan2021 at single dose for COVID-19 immunization. Medical history included stage 3 kidney disease and high blood pressure from an unknown date and unknown if ongoing. The patient was asking, "Does the vaccine stay cold in your body? Since the vaccine has to be kept at such a cold temperature in storage when it is injected does it have to stay cold. Is it ok to take the medicine that the doctor has given me along with the vaccine, should I stop or hold some of my medicine?" Is it normal to have a "cold feeling in her heart after getting the vaccine?" The patient stated that she felt like her heart was cold on 12Jan2021 so "I put my hand there to keep it warm". She stated, "Is this normal after getting the vaccine? The patient received her first vaccine dose on Saturday and yesterday she felt like her heart was cold. The patient saw her primary care in Dec2020 for her annual check up and they recommended that she get the vaccine. She is only on her normal medications. She called her doctor to ask if any of her medications could have reacted with the vaccine, but they said to take her medication like usual. The patient stated, "this feeling lasted about an hour." The outcome of the event was recovered on 12Jan2021. No treatment was given to the patient for the event.

Other Meds:

Current Illness:

ID: 0973437
Sex: M
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: my arm is hurting; cause his neck to hurt. It is hurting.; might have slept wrong; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age (reported as 66 [units unspecified]) received his first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; unknown lot number and expiration date), 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 he got the first dose of the vaccine yesterday and his arm was hurting and wondering if it could cause his neck to hurt. It is hurting. He might have slept wrong. The outcome of the events was unknown. The following information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0973438
Sex: M
Age:
State:

Vax Date: 01/12/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:99 Fahrenheit; Comments: Low grade fever

Allergies:

Symptoms: he started to have a low grade fever (99F); This is a spontaneous report from a contactable other hcp (patient) reported that a male patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Jan2021 at a single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. On Jan2021, the patient stated that he started to have a low grade fever (99F) that has lasted about 25 hours. He wanted to know if this is an expected side effect and how long to expect it. The outcome of the event was unknown. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0973439
Sex: M
Age:
State: CT

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

Lab Data: Test Date: 20210112; Test Name: MRI; Result Unstructured Data: Test Result:bulging disk

Allergies:

Symptoms: crawling up the stairs on my hands and knees and getting out of bed in agony; bulging disk; severe lower back pain; This is a spontaneous report from a contactable physician (patient). A 62-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The physician (who is also the patient), was asking about the Pfizer COVID19 vaccine for any reports of back pain or back problems/issues. The patient stated: "I got the Pfizer COVID-19 vaccine and got the second dose on Friday (08Jan2021). Over the weekend in Jan2021, I had pretty severe lower back pain that has continued. I had an MRI yesterday morning (12Jan2021) and it showed a bulging disk. I have had issues on and off over the years but nothing like this, ie: I am crawling up the stairs on my hands and knees and getting out of bed in agony. What's interesting is, I called a friend of mine and she had a similar reaction. She has a horrific neck issue and a history of minor lower back issues. She also got the second dose of the Pfizer COVID19 vaccine on Friday and over the weekend she was crawling on her hands and knees as well. That raises a red flag for me. I am trying to determine best treatment options for my back issue, either an epidural steroid or surgery or continue on this 'conservative stuff' (undefined) that's not working. I am meeting with my neurosurgeon tomorrow. Once I mentioned this connection to another person I know, he said he had someone complain of unbelievably severe back pain that lasted a few days." The physician (who is also the patient), also asked about the Pfizer COVID19 vaccine regarding any data on use with steroids and impact on mounting an immune response? If a systemic or local steroid is given, after the vaccine, will it inhibit the body's ability to mount immune response? The patient also asked about concomitant corticosteroids and if "Inhaled (except in Phase 1), topical, or localized injections of corticosteroids (e.g., intraarticular or intrabursal administration) were permitted. What were the percentage of patients on corticosteroids that were included in trials and any assessment off outcomes specifically for this group?" The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973440
Sex: M
Age:
State: FL

Vax Date: 01/12/2021
Onset Date:
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sore arm; This is a spontaneous report from a contactable consumer. A 66-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on 12Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient received the first dose of the Pfizer covid 19 vaccine on 12Jan2021. He wants to verify the Pfizer dose is 3 weeks apart and who can he contact to change his appointment. All of the websites are shut down because there are no appointments available. His second dose is scheduled for 29 days out. Wanted to know if that is okay. Mentioned that he had a sore arm on an unspecified date. Clarified that in the beginning that they were scheduling for Moderna vaccine. They did not have Moderna so they gave him the Pfizer Covid 19 vaccine. He was told that his second one should be in 21 days. The Moderna would have been 28 days. Later clarified that his second dose is scheduled for 30 days later. His is scheduled for 11Feb2021. He cannot get in to schedule anything. No one he asked has the correct answer. Patient does not want to take the vaccine and not have the right scheduling. The outcome of the event sore arm was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0973441
Sex: U
Age:
State: MA

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Pending resutls

Allergies:

Symptoms: right side of my face was red with a rash; my eyes are very itchy; headache; felt Nausea; my right arm was itchy where i got the shot and sore/noticed from my shoulder to my elbow had rash, swollen and was very itchy; my right arm was itchy where i got the shot and sore; noticed from my shoulder to my elbow had rash, swollen and was very itchy; noticed from my shoulder to my elbow had rash, swollen and was very itchy; i am having allergic reaction; This is a spontaneous report from a contactable healthcare professional (patient). A 45-year-old patient of an unspecified gender started to receive bnt162b2 (BNT162B2 reported as PFIZER COVID VACCINE; unknown lot number and expiration date), intramuscular right arm on 12Jan2021 11:15 at a single dose for covid-19 immunization. Medical history included allergies to latex and cillin family, and seasonal allergy. Concomitant medication included hydroxyzine pamoate (HYDROXYZINE PAMOATE), calcium carbonate, colecalciferol (VITAMIN D 2000), ketotifen fumarate (ZADITOR) for seasonal allergy, azelastine (AZELASTINE) and clarithromycin (CLARITIN). The patient did not receive other vaccines in four weeks and was not diagnosed with Covid prior to vaccination. The patient previously took but had allergies to amoxicillin, oxycodone hydrochloride; oxycodone terephthalate; paracetamol (PERCOCET), fusidate sodium (FUCIDIN) and morphine. The patient received the first dose of bnt162b2 (BNT162B2 reported as PFIZER COVID VACCINE; unknown lot number and expiration date), via unspecified route of administration on an unspecified date at a single dose for covid-19 immunization. The patient reported that she the shot at her job 12Jan2021 11:15am, sat down for 15 minutes and she got up fine. She mentioned that around 04:00 pm, she had headache and felt nausea. Her right arm was itchy where she got the shot and sore, so she took off her sweater to check her right arm where she got vaccine and noticed from her shoulder to her elbow had rash, swollen and was very itchy. She took a Benadryl and put ice on her right arm. She waited an hour after she took the Benadryl. She noticed the rash was not itchy or as red as it was before but was still swollen. These adverse events started at 12Jan2021 15:45. She mentioned that she went to bed woke up at 5:30 am the next day (13Jan2021) and the right side of her face was red with a rash. She mentioned that when she checked her right arm, the rash was still there and was red again. She took her allergy medication and waited an hour and the rash still on her face and arm but not as red. It was mentioned that once her allergy medication wore off, the rash was red on her right arm and face, and her eyes are very itch. She took allergy medication again and waited 1 hour, the rash was not so itchy. She mentioned that she was having allergic reaction. The patient reported that she was COVID tested post vaccination (nasal swab) on 13Jan2021with pending results. The outcome of the events was not recovered. The following information on the batch/lot number has been requested.

Other Meds: HYDROXYZINE PAMOATE; VITAMIN D 2000; ZADITOR [KETOTIFEN FUMARATE]; AZELASTINE; CLARITIN [CLARITHROMYCIN]

Current Illness:

ID: 0973442
Sex: F
Age:
State:

Vax Date: 12/16/2020
Onset Date: 12/25/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20201231; Test Name: Covid; Test Result: Positive ; Comments: tested positive

Allergies:

Symptoms: The patient developed symptoms on 25Dec2020, tested positive on 31Dec2020; She was supposed to receive second vaccine on 06Jan2021, but put it off; The patient developed symptoms on 25Dec2020, tested positive on 31Dec2020; This is a spontaneous report from a other HCP. A female patient (Age: 45, Unit: Unknown) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration on 16Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient developed symptoms on 25Dec2020, tested positive on 31Dec2020. She was supposed to receive second vaccine on 06Jan2021, but put it off because she was told by Pfizer she had to wait 90 days. She was calling for guidance because her hospital was telling her she was eligible to receive the vaccine. She already filed a report with safety when she initially developed symptoms that included loss of smell, taste and headaches. The outcome of the event was unknown. Information about lot/batch number has been requested.; Sender's Comments: Based on the information currently available, a lack of efficacy with BNT162B2 in this patient cannot be completely excluded.

Other Meds:

Current Illness:

ID: 0973443
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: worse than the swine flu; This is a spontaneous report from a contactable consumer. A female patient of unspecified age received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date: 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. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) for COVID-19 immunization. The patient received the second dose of the vaccine and the side effects was reported as 'worse than the swine flu.' The nurse reported that the side effects lasted 24 hours. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973444
Sex: F
Age:
State: TN

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: Fever; Result Unstructured Data: Test Result:102; Test Date: 20210113; Test Name: Fever; Result Unstructured Data: Test Result:100; Comments: still running 100 at 5:42 pm.

Allergies:

Symptoms: horrible headache; felt really bad; 102 fever; achy; fatigued; This is a spontaneous report from a contactable other health professional reporting for herself. A 60-year-old female patient received the first dose of bnt162b2 (BNT162B2, lot number and expiry date were not reported), via an unspecified route of administration, on 12Jan2021 11:15 AM, at a single dose on the left arm for COVID-19 immunization. The vaccine was administered at a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not pregnant at time of vaccination. Medical history included known allergies to penicillin and COVID. The patient had COVID prior to vaccination. Concomitant medications included lisinopril and escitalopram; these are the other medications the patient received in two weeks. The patient previously took betadine and experienced allergies. On 13Jan2021 02:30 AM (as reported), the patient experienced a horrible headache, felt really bad, 102 fever, achy, and fatigued. The patient woke up at about 2:30 am and had a horrible headache. Got out of bed at 4:30 and felt really bad. She had 102 fever. She was still running 100 at 5:42 pm. She was achy, still have a headache and am very fatigued at the time of report. She asked if she can take something for the fever and headache. The patient was not tested for COVID post vaccination. The patient did not receive any treatment for the reported adverse events. Outcome of the events was not recovered. Information on the Lot/Batch number has been requested.

Other Meds: Escitalopram; lisinopril

Current Illness:

ID: 0973445
Sex: F
Age:
State: TN

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20200601; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: my face became numb from the nose down; This is a spontaneous report from a contactable consumer (patient). A 32-year-old female patient received first single dose of BNT162B2 (Solution for injection, lot number: EL3246, exp date not reported), via an unspecified route of administration (vaccine location: right arm) on 11Jan2021 12:30 for COVID-19 immunization. Facility type vaccine: Hospital. The patient had allergies: any sulfa medication. The patient was not pregnant. The patient did not have covid prior vaccination. There were no other vaccine/s in four weeks. Other medications in two weeks include: ethinylestradiol, ferrous fumarate, norethisterone acetate (Blisovi 24 FE), citalopram and lamotrigine. On 11Jan2021 12:45, also reported as 'after 20 minutes of receiving the vaccine,' the patient's face became numb from the nose down. Within three hours, the right side of her face had feeling again. Then, another three hours later she began to have feeling in her nose. She went to bed, and the next morning she had complete feeling in the face. No treatment was received for the event. On 01Jun2020, nasal swab: negative. The patient recovered from the event on 12Jan2021.

Other Meds: Blisovi 24 Fe; Citalopram; Lamotrigine.

Current Illness:

ID: 0973446
Sex: F
Age:
State: NJ

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: exhausted/ tired; Fever; Chills/she had off and on chills; headache; This is a spontaneous report from a non-contactable nurse. A 29-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, from 11Jan2021 10:00 at a single dose, for covid-19 immunization. The patient has no other relevant medical history (reported as none). There were no concomitant medications used. The patient received her first dose of BNT162B2 on an unspecified date for covid-19 immunization. It was reported that she had an immune response to her 2nd COVID-19 vaccine received on 11Jan2021. She has had a fever, chills and headache during the night (11Jan2021). During the day on 12Jan2021, she had off and on chills and was exhausted. Today, (13Jan2020) patient reported she was feeling better, but still tired. Patient did not received treatment due to events. outcome of events fever, chills and headache was recovering. Outcome of event exhausted/tired was not recovered. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0973447
Sex: F
Age:
State: FL

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: has not been herself; bad diarrhea; chills; could not eat; feeling "very, very sick; general weakness; This is a spontaneous report from a contactable consumer. An 89-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration from 11Jan2021 to 11Jan2021 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 has not been herself and having bad diarrhea, chills, and general weakness. It was also reported that the patient could not eat and was feeling very, very sick. The outcome of the events was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973448
Sex: F
Age:
State: FL

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: persistent headache; even touching her head hurts/hurts to the touch; with this shot her arm really hurt when getting it/pain in the arm the shot was given/uncomfortable pain/in their arm after receiving the injection; insist on giving the next dose in 4 weeks; insist on giving the next dose in 4 weeks; This is a spontaneous report from a contactable consumer (patient). This consumer reported similar events for two patients. This is the first of two reports. A 71-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EL1283) via an unspecified route of administration in the left upper arm on 06Jan2021 09:40 at a single dose as COVID vaccine. The patient had no medical history. Concomitant medications noted as on other medications but nothing new. She previously got the shingle shot for immunization then her arm hurt a few days. She had no other reaction to vaccines in the past. She received no vaccine on the day of or in the prior 4 weeks. Last Wednesday on 06Jan2021, the patient took the vaccine and has had a headache since; even touching her head hurts. She had a persistent headache that started the day after the vaccine and has continued since. The next day on 07Jan2021 was when the headache started. She took regular Motrin (lot OFE3249A, expiry: May2022) and Tylenol extra strength (lot: LMA051, expiry: Jul2019, perhaps not working anymore) sometimes but they didn't really seem to help. She felt the best when she was standing up or laying down, and she would rather be laying down. She asked "Is this a normal side effect, am I dying? I am not a headache kind of person, I take a Motrin, it goes away and I do not have one for months. It actually hurts to the touch." Should she be worried? She did call the clinic about the headache and was told if it got serious to go to the emergency room, she didn't think it was that serious. It was just persistent. She could leave with the pain if it kept her from getting COVID but the fact it was persistent worried her. It was also reported that on 06Jan2021 with this shot her arm really hurt when getting it and that day but that was all (pain in the arm the shot was given), the next night there was no pain. Her and her husband both oooo'd and ahhhh'd with the pain in the arm but that was it (a very uncomfortable pain they experienced in their arm after receiving the injection). She asked how long a side effect lasts after the vaccine? She also stated that on Jan2021, they insist on giving the next dose in 4 weeks. Asked if the vaccine was given a week later would the efficacy be lower? The outcome of persistent headache was not recovered; of vaccination site pain was recovered on 07Jan2021; and of the other events was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021036651 same reporter and drug, different patient and AE

Other Meds:

Current Illness:

ID: 0973449
Sex: F
Age:
State: NJ

Vax Date: 12/24/2020
Onset Date: 01/07/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: Covid PCR testing; Test Result: Negative ; Test Date: 20210107; Test Name: Covid PCR testing; Test Result: Positive ; Test Date: 20210101; Test Name: rapid covid testing; Test Result: Negative ; Test Name: weight; Result Unstructured Data: Test Result:lost a lot of weight, but still plump

Allergies:

Symptoms: lost a lot of weight, but still plump; tightness in chest; Upper chest tightness with post nasal drip, like the flu; got Covid virus/ Covid PCR testing: positive; got Covid virus/ Covid PCR testing: positive; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect from a contactable consumer (patient). A 63-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/lot number: EJ1685) via an unspecified route of administration on left arm on 24Dec2020 11:00 at single dose for COVID-19 immunisation. Medical history included ongoing asthma, ongoing allergies. She was asthmatic and believed that the virus would have affected her differently if she didn't get the vaccine. If she was to catch the virus and didn't have the vaccine she may not have come out of it. The patient's concomitant medications were not reported. The patient denied getting any other vaccines that day or 4 weeks prior. No problems with vaccines in past. Received the COVID vaccine at her workplace. The patient got COVID virus on 07Jan2021. It was also reported that the patient lost a lot of weight, but still plump, coughing, tightness in chest, upper chest tightness with post nasal drip, like the flu, body aches, all on an unspecified date. Emergency room visit needed for the events (body aches, runny nose). The patient underwent lab tests and procedures which included Covid PCR testing: negative on 04Jan2021, positive on 07Jan2021, rapid COVID testing: negative on 01Jan2021. The outcome of the event (got COVID virus) was not recovered, of other remain events was unknown. Clinical course: The patient received the first dose of BNT162B2 on 24Dec2020, and a couple weeks later she got the COVID virus (07Jan2021). Mentioned she lost a lot of weight, but still plump. Probably be in the hospital now. Still had some coughing, tightness in chest, but it's not as bad. Upper chest tightness with post nasal drip, like the flu, runny nose in throat that goes down into the lungs and when it goes down she coughs and hacks to get rid of it. Went to the doctor office on the 01Jan2021 and did a rapid test and it was negative. Then on 04Jan2021 she did another PCR Covid test and it was negative. On 07Jan2021 she had symptoms and was insistent on getting another test since having body aches, runny nose. Got the re-test and it came back positive when she went to the emergency room. Got the PCR test. The patient thought that the way they were testing is how it's spreading. Did the testing on the 04Jan2021 and they used a swab bigger than a cue tip, it was huge and couldn't get far up enough instead of the tiny ones. On the 07Jan2021 at her job, emergency room, they had the tiny ones and was able to go further up and that's when she tested positive. Mentioned using salbutamol (ALBUTEROL) nebulizer, over the counter cough syrup, prescription azelastine hydrochloride;fluticasone propionate (DYMISTA) nasal spray, and pseudoephedrine hydrochloride (SUDAFED). When has the dry cough she uses the ALBUTEROL nebulizer with the machine and vials at home and that slows down the coughing a lot and the other stuff with the lungs. Not taking any steroids. Using SUDAFED to stop the runny nose from post nasal drip from going into lungs.

Other Meds:

Current Illness: Allergy; Asthmatic

ID: 0973450
Sex: M
Age:
State: FL

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: he has a hearing and memory problem; he has a hearing and memory problem; Very bad headache; Fatigue; Dizziness; This is a spontaneous report from a contactable consumer. A 95-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, 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 medical history and concomitant medications were not reported. On an unspecified date, the patient has a hearing and memory problem. He later clarified the main thing is he wanted to know if he can continue with getting the second COVID vaccination. He wanted to continue but wanted to know if these symptoms will prevent him from continuing with getting the COVID vaccination. He confirmed he has no problems around the injection site. However, this is the second day and in Jan2021, he had dizziness. On 11Jan2021, last night he had a very bad headache and fatigue. This morning he is feeling better, but he still has slight dizziness. He is still three weeks away from getting the next vaccine. He wanted to know if he would be able to still take it. He wanted to be immune and to know if there would be any reason why he cannot take the second dose of the vaccine. He then mentioned these symptoms that he is speaking of are general symptoms and he assumed other people have reported them along with him because it is listed on the information sheet. Outcome of the events of dizziness, fatigue and headache was recovering, other events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0973451
Sex: F
Age:
State: PA

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

Lab Data:

Allergies:

Symptoms: hives from head to toe/Her Hives are on her ears, lips, neck, going all the way down to her toes/Hives are worse; first dose on 21Dec2021, second dose on 08Jan2021; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received the second dose of BNT162b2 (Lot: EL3246), via an unspecified route of administration in right arm on 08Jan2021 08:45 at single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medication included meloxicam. The patient previously received the first dose of BNT162b2 (Lot: EK5730), at the age of 58-year-old, via an unspecified route of administration in right arm on 21Dec2020 at single dose for covid-19 immunization. She is not allergic to anything at all. She got the 2nd shot on Friday (08Jan2021) 8:45 and then on Sunday (10Jan2021) she had hives from head to toe. She has not tried anything new, no food, products, or detergents. She has no hives at the injection site. Her Hives are on her ears, lips, neck, going all the way down to her toes. At 4 o'clock on 10Jan2021 if when the hives began and by 6 the hives had exploded. Her Hives are worse now. She has had No Positive tests for Covid prior to the vaccine. She has had no antibody test prior to the vaccine. She has had No issues with vaccines in the past. She is using Benadryl to treat her Hives, however it puts her to sleep in 30 minutes and so she cant do that at work. The patient received the first dose on 21Dec2021, second dose on 08Jan2021. The outcome of the event hives was not recovered.

Other Meds: Meloxicam

Current Illness:

ID: 0973452
Sex: F
Age:
State: OK

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swollen lymph node under her arm; Pain; This is a spontaneous report from a contactable consumer (patient). A 23-years-old female patient received second dose of bnt162b2 (COVID-19 Vaccine, lot# EL1283), via an unspecified route of administration on 08Jan2021 at single dose on right arm for covid-19 immunisation. Medical history was none. There were no concomitant medications. The patient previously received first dose of COVID-19 Vaccine for COVID-19 immunisation on 18Dec2020. On 09Jan2021, she noticed she had a swollen lymph node under her arm that hadn't gone away. It had gotten more swollen and had spread. The pain had gotten more intense. The pain started as an ache then it was sharp and was now painful to touch. Both conditions were reported as worsen. The event outcome was not recovered.

Other Meds:

Current Illness:

ID: 0973453
Sex: M
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Fever; Diarrhea; This is a spontaneous report from a contactable nurse (patient). A 34-year-old male patient received the second dose of BNT162b2 (Lot/batch number and Expiration date were not provided), via an unspecified route of administration on 11Jan2021 at single dose for covid-19 immunization. There were no medical history and concomitant medications. The patient experienced fever, chills, and diarrhea on 12Jan2021. 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: 0973454
Sex: M
Age:
State: VA

Vax Date: 01/10/2021
Onset Date: 01/10/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Name: height; Result Unstructured Data: Test Result:5'7"; Test Name: height; Result Unstructured Data: Test Result:5'6" or 5'5"

Allergies:

Symptoms: tiredness; Chills; Fever; generalized aches; could hardly sleep through the night; This is a spontaneous report from a contactable Physician (patient). A 64-year-old male patient reported received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK4176 and expiry date: Mar2021) via an unspecified route of administration on 10Jan2021 08:45 at a single dose for COVID-19 immunization. Medical history bypass surgery (10.5 years ago, in June it will be 11 years ago) and hard of hearing. Patient said he used to be 5'7" but right now he is 5'6" or 5'5". He says that change in his height happened before he got the vaccine, that is effects of being short. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN) and simvastatin. It was reported that the patient had been healthy all his life, he doesn't have any medical conditions which could have contributed to side effects. He does not think they would have contributed but he takes Simvastatin and Baby Aspirin. The patient got the vaccination, the first one (BNT162B2 for COVID-19 immunization, on unspecified date) he did not have anything happen, no side effects or nothing. It was as if he didn't receive any vaccine. The second dose he received it at 8:45 AM on Sunday (10Jan2021) and Sunday night he began experiencing tiredness and then chills, fever, generalized aches and could hardly sleep through the night. It was reported as the worst night in his life and then, fortunately during the day on Monday, gradually, the intensity and severity of the symptoms began to subside but he was not able to do any of his normal functions. Then last night Monday night (11Jan2021) he slept well and today on Tuesday (12Jan2021) he was okay, this morning everything was fine. On Tuesday night he took Acetaminophen for pain, he clarified that was Sunday night after he had gotten the vaccine he took Acetaminophen and he still had the problems then Monday night he thought it would be the same so he put the medicine next to the bed on the night stand but he did not need to take it. He slept and woke up this morning and his back to work. Now it is like nothing has happened. He has recovered completely from all effects. The outcome of the event could hardly sleep through the night was recovered on 11Jan2021 and all the other events recovered on 12Jan2021.

Other Meds: BABY ASPIRIN; SIMVASTATIN

Current Illness:

ID: 0973455
Sex: F
Age:
State: IL

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: nuchal rigidity; migraine; photosensitivity; auditory sensitivity; arthralgia; lethargy chills/ rigors; nasal stuffiness; chest congestion; wet cough; This is a spontaneous report from a contactable physician. A 40-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number:EL1283), intramuscular on 08Jan2021 17:00 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. The patient had the first dose last 18Dec2020 (lot number=EJ1685). The patient experienced nuchal rigidity, migraine, photosensitivity, auditory sensitivity, arthralgia, lethargy chills, rigors, nasal stuffiness, chest congestion, wet cough on 09Jan2021 05:00. The outcome of the event nuchal rigidity was not recovered while other events were recovered with sequelae.

Other Meds:

Current Illness:

ID: 0973456
Sex: F
Age:
State: PA

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Enlarged lymph nodes on the left side of her neck and under the left armpit; Flu like symptoms; The lymph nodes are also a little painful.; This is a spontaneous report from a contactable consumer (patient). A 29-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0142), via an unspecified route of administration on 06Jan2021 at single dose by injection in the left arm for covid-19 immunization. The patient had no medical history. There were no concomitant medications. The patient experienced flu like symptoms on 10Jan2021, enlarged lymph nodes on the left side of her neck and under the left armpit on 11Jan2021, the lymph nodes are also a little painful in Jan2021, this is on the same side that she received the vaccine, on the left. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0973457
Sex: F
Age:
State: VA

Vax Date: 12/18/2020
Onset Date: 12/01/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sinus infection; stuffy head; I do have tinnitus, and noticed that both injections made that worse; This is a spontaneous report from a contactable nurse (patient). A 63-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date not reported), intramuscular on the left arm, on 18Dec2020 at 11:30 at a single dose for Covid-19 immunization. Medical history included at one time a severe allergic reaction to pecans have since eaten small amts without problems and tinnitus. The patient has no Covid prior to vaccination. The patient is not pregnant. The patient's concomitant medications were not reported. No other vaccines in four weeks and no other medication in two weeks. In Dec2020, the patient stated that she does have tinnitus, and noticed that both injections made that worse, it is not yet subsiding since last injection the only other signs and symptoms (s/s) she had from the 1st injection, second day after, about 2 hrs of feeling like she had a sinus infection, stuffy head, wanted to go to bed and rest. The patient was treated with naproxen sodium (ALEVE), paracetamol (TYLENOL), and diphenhydramine hydrochloride (BENADRYL) for the events. The patient was not Covid tested post vaccination. The outcome of the event of tinnitus was not recovered, while other events were unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973458
Sex: F
Age:
State: NY

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: cold symptoms; This is a spontaneous report from a contactable consumer patient. This 55-year old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL3248) shot at single dose on 11Jan2021 via an unknown route at left arm Covid-19 vaccination. Medical history and concomitant drug were reported as "none". Patient stated that she got a shot yesterday (11Jan2021) and had cold symptoms today (12Jan2021), and further stated that the cold symptoms come and go. No investigation assessment performed. No treatment performed. Outcome of the event was resolving.

Other Meds:

Current Illness:

ID: 0973459
Sex: F
Age:
State: FL

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

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result: fine.

Allergies:

Symptoms: arm got sore instantly; I have no feeling in fingertips; chills; shakes; fever; hot cold; itchy out of control; no appetite is forcing food; is drinking a lot, can't get enough liquid in me; This is a spontaneous report from a contactable consumer (patient herself). A 65-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# el1283), 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. Caller reported that she was supposed to get the shot, got to her vaccination provider was told she was getting the Pfizer shot. She reported that she was on antibiotics and had blood work done the week before, was told that was fine. She reported that she took the shot and stated her arm got sore instantly. She went to leave she was asked how she was and reported, she had no feeling in fingertips and reported that they said that was ok. Caller reported that Monday night she started having chills, shakes and fever, hot cold, now since yesterday and all day today she was itchy out of control. Caller stated she was not going back for the second shot. Caller went on to report she had no appetite was forcing food and was drinking a lot, can't get enough liquid in her. Outcome of events were unknown.

Other Meds:

Current Illness:

ID: 0973460
Sex: F
Age:
State: TX

Vax Date: 12/24/2020
Onset Date: 12/24/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20201224; Test Name: blood pressure; Result Unstructured Data: Test Result: high.

Allergies:

Symptoms: Dizziness within 15 minutes of receiving vaccine; headache; high blood pressure; This is a spontaneous report from a contactable other health care professional. A 29-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EK5730), intramuscular on 24Dec2020 08:00 at SINGLE DOSE at right arm for COVID-19 immunization. Medical history included allergic to nuts and peaches. There were no concomitant medications. On 24Dec2020 08:15, the patient experienced Dizziness within 15 minutes of receiving vaccine; couple of hours after patient reported headache and high blood pressure x2 days. After 2 days both headache and high blood pressure subsided. The patient received treatment for the event headache (Tylenol). It was reported that the patient had a physician office visit. The outcome of the event dizziness was recovered on an unspecified date, while the events headache and hypertension was recovered on 26Dec2020.

Other Meds:

Current Illness:

ID: 0973461
Sex: F
Age:
State: NJ

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: upper respiratory infection; Fatigue; Headache; Ringing of the ears/Ringing in ears; Nausea; This is a spontaneous report from a contactable nurse (patient). A 50-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0142, expiry date: unknown), via an unspecified route of administration on 04Jan2021 10:25 at single dose (left upper arm) for COVID-19 immunization. Medical history included asthma (diagnosed at 8 years old), covid from 2020 (she had Covid last year twice). There were no concomitant medications. The patient experienced nausea, headache, and ringing of the ears/ringing in ears on 04Jan2021; and fatigue on 05Jan2021. This went on for 2.5 days. By day 3 post vaccine (06Jan2021) got upper respiratory infection. Stated she is pre disposed because she is asthmatic. She states she took Zofran to treat the nausea, 8 mg, and that she took 1000mg Tylenol for the headache. States she received the vaccine at her employer, (healthcare center name). States the symptoms resolved after about 3 days, exact dates unknown. She wanted to know if the second vaccination is the exact same as the first. She wanted to know if Pfizer manufactures the Shingrix vaccine. Therapeutic measures were taken as a result of nausea, headache. The outcome of the event upper respiratory infection was unknown, while for other events was recovered on an unspecified date in Jan2021.

Other Meds:

Current Illness:

ID: 0973462
Sex: F
Age:
State: CA

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: Fever; Result Unstructured Data: Test Result:101.4

Allergies:

Symptoms: Chills; Body aches; Fever of 101.4; Headache; This is a spontaneous report from a contactable nurse (patient). A 43-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL7249; Expiration date was not reported), intramuscularly on the left arm, on 12Jan2021 (17:30) at a single dose for COVID-19 immunization at the hospital. Medical history included migraine headache and arthritis of knees. Concomitant medication included topiramate (TOPAMAX). The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL1284; Expiration date was not reported) on the left arm on 22Dec2020 for COVID-19 immunization (when the patient was 43 years old). The patient was not pregnant at the time of reporting. On 13Jan2021 (12:00 AM), the patient had chills; body aches; fever of 101.4 (unit was not reported); and headache. It was unknown if the patient had received treatment for the reported events. The outcome of the events, 'chills', 'body aches', 'fever', and 'headache', was not recovered. The patient was not diagnosed with COVID-19 prior to vaccination, and had not been tested post-vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds: Topamax

Current Illness:

ID: 0973463
Sex: M
Age:
State: CA

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:low grade fever

Allergies:

Symptoms: low grade fever; This is a spontaneous report from a Pfizer-sponsored program via a contactable nurse (patient wife). A male patient (husband) of an unspecified age received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number not reported), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient received his first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date for covid-19 immunization. It was reported that her husband had a low grade fever after 24 hours of receiving his second dose covid vaccine. The outcome of the event was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0973464
Sex: F
Age:
State: WI

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body aches; migraine; numbness in left hand; This is a spontaneous report from a contactable nurse (patient). A 22-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686, expiry date not reported), via an unspecified route of administration in the left arm on 12Jan2021 15:45 at single dose for COVID-19 immunisation. Medical history included iron deficiency anaemia. Concomitant medication included bupropion hydrochloride (WELLBUTRIN). The patient previously took amoxicillin; clavulanic acid (AUGMENTIN) and experienced allergies. The patient previously took first dose of bnt162b2 (lot number: EK5730, expiry date not reported) in the left arm on 23Dec2020 10:00 at single dose for COVID-19 immunisation. On 12Jan2021 16:30, the patient experienced body aches, migraine and numbness in left hand. No treatment was received for the adverse events. Clinical outcome of the events was not recovered.

Other Meds: Wellbutrin

Current Illness:

ID: 0973465
Sex: F
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm soreness; very achy; Drowsiness; bad headache; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686), via an unspecified route of administration on 11Jan2021 at single dose (1.8 cc but unsure ((heard that but could be wrong) recommended dose)) as works with COVID positive patients. Medical history was none. No concomitant medications. Caller just wanted to know if she could take Tylenol for mild symptoms after having the COVID 19 vaccine. She received the vaccine yesterday. She was wondering if it would make the symptoms a little less. She didn't have a prescribing doctor. The side effects started last night. On 11Jan2021, she was expecting arm soreness, but this was worse. She developed it about 6 hours after the shot. This was the sorest her arm has ever been from any injection, and she had had a lot of them. Her arm was almost too sore to move. This morning, it was much better. It was really bad last night. She was also very achy, and experienced drowsiness, also has a very bad headache on 11Jan2021. The CDC website stated before the vaccine patients should not take Tylenol because it can tamper with the immune system response. It said it was alright to take after, but she just wanted to call to make sure. Investigation Assessment was no. The outcome of the event very achy was not recovered, of the events was recovering.

Other Meds:

Current Illness:

ID: 0973466
Sex: F
Age:
State: ME

Vax Date: 12/20/2020
Onset Date: 12/21/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Tiredness/exhausted; injection site pain in her right arm; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, unspecified lot number, reported as EH9899 or TH9899), intramuscularly at site of right arm at 10:00 on 20Dec2020 at single dose for COVID-19 immunization. Medical history included ongoing hypothyroidism for the last 15 years. The patient's concomitant medications included ascorbic acid, biotin, calcium, chromium, colecalciferol, copper, folic acid, iodine, iron, magnesium, malpighia glabra fruit, manganese, molybdenum, nicotinamide, pantothenic acid, phytomenadione, pyridoxine hydrochloride, retinol, riboflavin, selenium, vitamin b1 nos, vitamin b12 nos, vitamin e nos, zinc (MULTIVITAMIN ACTIVE WOMAN, lot number: 300045; Expiration date: May2022) from Jan2021. The patient previously took cetirizine hydrochloride (ZYRTEC) daily for allergies forever. Clinical course: Patient received the first dose of the BNT162B2 on 20Dec2020, and was tired afterwards, she didn't feel tired continually. She began to feel tired on 21Dec2020, she was just exhausted, she was so tired and she just slept, she couldn't get out of her own way. On 22Dec2020, she was fine, but on 23Dec2020, she began to feel tired and exhausted again. By 24Dec2020, her symptoms were over. She also experienced injection site pain in her right arm that started on 21Dec2020 and resolved by the evening of the same day. No treatment received for this event. Vaccination Facility Type was in hospital. No vaccine administered at Military Facility. No emergency room visit needed. It was unknown that physician office visit needed. No prior vaccinations within 4 weeks. Adverse event(s) following prior vaccinations was N/A. Family medical history relevant to adverse event(s) was not provided. Relevant tests were none. The outcome of event 'tiredness/exhausted' was recovered on 24Jan2021; of event 'injection site pain in her right arm' was recovered on 21Dec2020. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness: Hypothyroidism (for the last 15 years.)

ID: 0973467
Sex: F
Age:
State: CA

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Cough; has a metallic taste in her mouth; This is a spontaneous report from a contactable consumer (patient) reported that a 76-year-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, lot number and Expiration Date unknown) via an unspecified route of administration on 04Jan2021 at single dose for covid-19 immunisation. The patient's medical history and concomitant medications was not reported. Patient was getting a cough and has a metallic taste in her mouth in Jan2021. Wanted to know if it was from the vaccine or Covid. The outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973468
Sex: U
Age:
State: TN

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Welts and rashes; Welts and rashes; This is a spontaneous report from a contactable nurse. This nurse reported similar events for two patients. This is the 2nd of the two reports. A patient of unspecified age and gender received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date: unknown), via an unspecified route of administration on 11Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date for COVID-19 immunization. The nurse reported that the patient received the second dose of the vaccine on Monday (11Jan2021) and broke out in welts and rashes in Jan2021. The patient was given steroids at home and did not report respiratory distress. The outcome of the events was unknown Information on the batch/lot number has been requested. ; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021030825 Same reporter/drug/event; different patient

Other Meds:

Current Illness:

ID: 0973469
Sex: M
Age:
State: CA

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

Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:Low grade

Allergies:

Symptoms: low grade fever; he did not feel well; This is a spontaneous report from a Pfizer-sponsored program. A contactable nurse reported that a male patient of an unspecified age received second dose of bnt162b2, via an unspecified route of administration on an unspecified date at single dose for covid-19 vaccine. The patient's medical history and concomitant medications were not reported. The patient experienced low-grade fever, he did not feel well on an unspecified date. Caller was reporting on herself, her husband, and her doctor. This was the report for the caller's doctor. Her doctor told her that he had a low grade fever after his second dose and he did not feel well. The patient underwent lab tests and procedures which included body temperature: low grade on an unspecified date. The outcome of events unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973471
Sex: F
Age:
State: GA

Vax Date: 12/22/2020
Onset Date:
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: This is a spontaneous report from a contactable nurse (patient) and a contactable consumer (patient's son). A 50-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: ER5730, Expiry Date: Mar2021), via an unspecified route of administration on 22Dec2020 at a single dose on Left Deltoid for COVID-19 immunization. Medical history included asthma and sickle cell disease. There were no concomitant medications. She has had issues with vaccines in the past but not to this extent. Prior she experienced swelling in the arm from a pneumonia vaccination for immunization, back in 2012, she has no Lot or Expiry of this previous vaccine. She adds that she did feel dizzy after the first vaccine dose but that subsided. She has had no positive tests for COVID, and no antibody tests. The outcome of the event was recovered on an unspecified date.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm