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: 1018427
Sex: M
Age:
State:

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Injection site soreness; tiredness; headache; muscle soreness; chills; joint soreness; This is a spontaneous report from a non contactable consumer (patient). A 44-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number:EL9261), via an unspecified route of administration on 22Jan2021 10:30 at single dose in left arm for COVID-19 immunisation. The patient was vaccinated at Military Base. Patient age at time of vaccination was 44 years. No other vaccine was given within 4 weeks prior to the COVID vaccine. Medical history included chronic sinusitis. The patient has no known allergies. Concomitant medications included atorvastatin, ibuprofen (ADVIL), guaifenesin (MUCUS RELIEF), ascorbic acid, cyanocobalamin, ergocalciferol, nicotinamide, pyridoxine hydrochloride, retinol, riboflavin, thiamine mononitrate (ONE-A DAY). On 23Jan2021 20:00 the patient experienced injection site soreness, tiredness, headache, muscle soreness, chills, joint soreness. No treatment was received for the events. The events were resolving. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds: Atorvastatin; Advil [Ibuprofen]; Mucus Relief; One-A-Day [Ascorbic Acid; Cyanocobalamin; Ergocalciferol; Nicotinamide; Pyridoxine Hydrochloride; Retinol

Current Illness:

ID: 1018429
Sex: F
Age:
State: VA

Vax Date: 01/21/2021
Onset Date: 01/01/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: chills; headache; feeling sore in her arm; tiredness; she was also breastfeeding; she was also breastfeeding; itching/itching was worse on her chest and back/allergy like a reddish thing, an itching thing was on her body, on her chest area, her breast area; was breastfeeding; it was full of milk that also hurts very bad; allergy like a reddish thing, an itching thing was on her body, on her chest area, her breast area; on her back as well; allergy like a reddish thing, an itching thing was on her body, on her chest area, her breast area; on her back as well; feeling unwell; This is a spontaneous report from a contactable consumer (patient). This consumer reported information for both mother and baby. This is the maternal report. A 44-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via unspecified route of administration on 21Jan2021 (lot number and expiry date unknown) at single dose for Covid-19 immunization. The patient stated "just to protect myself". Medical history included blood pressure high, lost weight because she was breastfeeding now (ongoing). Concomitant medication included labetalol from unspecified date for blood pressure high, and blood pressure medicine. Historical vaccine included first dose of BNT162B2 on 31Dec2020 for Covid-19 immunization and experienced allergy. The patient informed that she already reported to a pharmacist. The female patient received the second dose of the COVID vaccine on Thursday (21Jan2021). The patient informed that she was fine the same day she received the vaccine and had some itching (21Jan2021), but the next day (22Jan2021) she had a headache and was feeling sore in her arm. The patient experienced a little bit sore in her arm, bad sore on her arm; after she had the first one maybe after a day, but it was not that bad. The patient informed that she received the covid vaccine on Thursday (21Jan2021) and has been feeling unwell ever since (Jan2021). The first day it was okay, she meant a little bit sore in her arm, her sore arm. On Friday (22Jan2021), she started like having tiredness, headache, and sore like bad sore on her arm. Then now she has seen, she said it was okay then she knew because there was a side effect so she tried to take rest and drink water. What happened was, now (Jan2021) on her body it looked like some kind of allergy like a reddish thing, an itching thing was on her body, on her chest area, her breast area and she was a breastfeeding mom and on her back as well. The patient informed that after 3rd day (Jan2021) it got like especially on her breast area and her chest area got like itchy. Today (24Jan2021), the headache came back, and she was experiencing chills and her itching was worse on her chest and back. The patient informed that she was also breastfeeding. The patient wanted to know what she was supposed to do. The patient informed that she has headache, the headache was back today, now when she woke up, she has headache. The patient was asking for guidance if she was breastfeeding and has received the second dose of the COVID vaccine. The patient informed that she was to feed her son, because she didn't feed him yesterday, so it was full of milk that also hurts very bad. The patient was scared, because it was itchy area on her breast, so she was scared to breastfeed her son. The patient informed that it was like back and forth, but now this morning (Jan2021) the patient has headache, yesterday (Jan2021) she was okay. The patient informed that about her treatment, she didn't take even a painkiller; she just only took her blood pressure medicine. The outcome of the event headache was not recovered, while itching/itching was worse on her chest and back/allergy like a reddish thing, an itching thing was on her body, on her chest area, her breast area, feeling sore in her arm, feeling unwell, tiredness, allergy like a reddish thing, an itching thing was on her body, on her chest area, her breast area; on her back as well, chills, was breastfeeding; it was full of milk that also hurts very bad was unknown. Follow-up activities are possible, information on the batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021092765 baby case

Other Meds: Labetalol

Current Illness: Breast feeding

ID: 1018430
Sex: F
Age:
State: VA

Vax Date: 01/17/2021
Onset Date: 01/17/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Joint swelling hands; nausea; diarrhea; body aches; first dose: 31Dec2020/second dose: 17Jan2021; This is a spontaneous report from a contactable nurse (patient). This 52-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular on 17Jan2021 08:30 at single dose on the right arm for COVID-19 immunization. The patient's medical history was none. No other medications received in two weeks. The patient previously took first dose of bnt162b2 (lot number=EL1284), via intramuscular on 31Dec2020 09:30 at single dose on the right arm for COVID-19 immunization, took erythromycin and experienced allergies. No other vaccine received in four weeks. Facility type vaccine was hospital. Patient was not pregnant. The patient experienced joint swelling hands, nausea, diarrhea, body aches on 20Jan2021 01:00. No COVID prior vaccination. No COVID tested post vaccination. No treatment received. Outcome of the events joint swelling hands, nausea, diarrhea, body aches was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018432
Sex: F
Age:
State: MD

Vax Date: 01/11/2021
Onset Date: 01/19/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Nasal Swab; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab covid test name post vaccination=Pixel by LabCorp covid test date=21Jan2021 covid test result=Negative

Allergies:

Symptoms: On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine; On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine; On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine; On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine; On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine; On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine; This is a spontaneous report from a contactable nurse (patient). A 65-years-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration on 11Jan2021 14:00 at SINGLE DOSE on Right arm for covid-19 immunisation. Medical history was none. No-covid-prior-vaccination. No Known- allergies. Concomitant medication included atenolol (TENORMIN), clonazepam (KLONOPIN), sertraline hydrochloride (ZOLOFT), atorvastatin calcium (LIPITOR [ATORVASTATIN CALCIUM]). No-other-vaccine-in-four weeks. Since 19Jan2021, On the 8th day after vaccine, I had 24 hours of stomach ache, chills, fatigue, headache, backache, hip ache, and then stomach ache for a few days, and then totally fine. AE-resulted-in: [Doctor or other healthcare professional office/clinic visit]. No treatment received. Covid-test-post-vaccination: included Nasal Swab, Pixel by Labcorp, covid test date on21Jan2021 was Negative. The event recovered in Jan2021. Information about lot/batch number has been requested.

Other Meds: TENORMIN; KLONOPIN; ZOLOFT; LIPITOR [ATORVASTATIN CALCIUM]

Current Illness:

ID: 1018434
Sex: F
Age:
State: FL

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Body temperature; Result Unstructured Data: Test Result:Low grade fever

Allergies:

Symptoms: feeling very dizzy; Very sick feeling; low grade fever; Vertigo; My head does not feel like it's attached to my body; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 21Jan2021 12:30 at single dose in left arm for COVID-19 immunisation. Patient age at vaccination was 73 years. No other vaccine was given within 4 weeks prior to the COVID vaccine. Medical history included heart stent. The patient has no known allergies. Concomitant medications included lisinopril, clopidogrel besylate (CLOPIDOGREL), metoprolol, rosuvastatin. On 21Jan2021 16:00 the patient started feeling very dizzy, vertigo, she stated: 'It's two days now I still feel it, very sick feeling, had a low grade fever, my head does not feel like it's attached to my body'. No treatment was given for the events. The events had not resolved. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, has not been tested for COVID-19. Information about Batch/Lot number has been requested.

Other Meds: LISINOPRIL; CLOPIDOGREL [CLOPIDOGREL BESYLATE]; METOPROLOL; ROSUVASTATIN

Current Illness:

ID: 1018435
Sex: F
Age:
State: CA

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: vomiting; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration from 05Jan2021 at a 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 COVID-19 Vaccine on 05Jan2021 and she experienced vomiting the next day 06Jan2021, multiple times during the day. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018436
Sex: F
Age:
State: FL

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: The heat from the elbow (not clarified further), besides the knees and the ankle and the toes.; pain in knees, ankles and feet and lower leg with the cramping and tingling, mostly tingling and burning like a radiating pain; discomfort with burning , tingling and radiating sensations in both knees , lower legs and feet during the night , those sensations have returned 10 days after vaccine; discomfort with burning , tingling and radiating sensations in both knees , lower legs and feet during the night , those sensations have returned 10 days after vaccine; I experienced discomfort with burning , tingling and radiating sensations in both knees , lower legs and feet during the night , those sensations have returned 10 days after vaccine; Also occasionally pain in hips, elbows and other joints/Pricking pain in my left hip/mild burning radiating from around the joints; cramping in my left footmy knees, my ankles and my feet, the lower leg felt cramp; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female patient received first dose bnt162b2 (BNT162B2, lot number: EL1283), via an unspecified route of administration, at arm left, on 12Jan2021 15:00 at single dose for COVID-19 immunisation. Medical history included blood cholesterol increased, chronic productive cough, known allergies to sulfa, sinus disorder. Is pregnant: No. Concomitant medication included mometasone furoate (FLONASE) for sinus, ascorbic acid (VITAMIN C). No other vaccine in four weeks. No covid prior vaccination, no covid tested post vaccination. 4 days after receiving vaccine, on 16Jan2021 12:00 AM the patient experienced discomfort with burning, tingling and radiating sensations in both knees , lower legs and feet during the night , those sensations have returned 10 days after vaccine and have continued for more than 30 hours now , Also occasionally pain in hips, elbows and other joints. As of 23Jan2021, it was reported the patient experienced burning, tingling sensations around ankles, knees and lower leg. Yesterday started feeling same thing, the feet, toes, around ankles, up legs and around knees. Sometime it feels like it's a mild burning radiating from around the joints and in the lower leg too. It is mainly her feet up to above the knees, burning, tingling, radiating. Sometimes have occasional pain little bit in some of the other joints, this is a little bit more than joint pain. Consumer stated, that she received the first dose of this Pfizer Vaccine on 12Jan2021. And about four days after during the night she was feeling some kind of burning, tingling sensations around ankles and knees and lower leg. It went away it lasted maybe about 4 hours, but then yesterday which is on the 22nd started in early afternoon started feeling the same thing, the feet and the toes, around ankles, up the legs and around the knees. Sometime it feels like it's a mild burning radiating from you know around the joints and in the lower leg too. It is mainly feet up to above the knees, burning, tingling, radiating. And sometimes I have occasional pain in just a little bit in some of the other joints you know that's been going on after the vaccine occasionally. The heat from the elbow (not clarified further), besides the knees and the ankle and the toes. The patient called this number because that is the number that was on the page to say if there was anything to report and then you know she was wondering if this is, she saw that some of the side effects could be joint pain but this is a little bit more than joint pain. So, she was wondering if there is anything. She mean she was going to see doctor on Monday, this has been going on for more than 30 hours now, but she was wondering if there is any advice in this. Pricking pain in her left hip started on 12Jan2021, Little bit of cramping in left foot started on 12Jan2021, Knees, ankles and feet, the lower leg felt cramp, like a radiating pain started on 16Jan2021. Consumer stated, initially, when she just got the vaccine, she felt a little prick in her left hip, like a little pain but it did not stay, pricking pain in her left hip. A little bit of cramping in her left foot, but it went away. So she did not think anything of it. 4 days later, on the 16Jan2021 (later confirmed), during the night her knees, her ankles and feet, the lower leg felt cramp, like a radiating pain. It was not very severe, like a mild pain in the knees and the lower legs and feet, a type of tingling but it went away. Pain was like a radiating, sort of burning but it was mild burn. Date when started experiencing pain is on the same day, 12Jan2021. Lab work was no. Treatment was no, because it was transient but afterwards what concerned her is on Friday which is the 22nd, she started experiencing a pain in knees, ankles and feet and lower leg with the cramping and tingling, mostly tingling and burning like a radiating pain. The whole, above her knees, down the lower leg, ankles, feet and toes and it continued up till last night and so more than for 30 hours that is what concerned her. That is why she called last night. The outcome of the event feeling hot , pain in extremity, muscle spasm was unknown, of the other events was not recovered.

Other Meds: FLONASE [MOMETASONE FUROATE]; VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 1018438
Sex: F
Age:
State: MD

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: vomiting; Diarrhea; Nausea; This is a spontaneous report from a contactable other healthcare professional (patient). A 31-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number and expiration date not reported) via an unspecified route of administration on the right arm on 23Jan2021 16:00 at a single dose for COVID-19 immunization. The patient had no medical history. Concomitant medications included sea moss gel and elderberry syrup received within 2 weeks of vaccination. On 23Jan2021 07:00 PM, the patient experienced vomiting, diarrhea and nausea. No treatment was received for the events. There were no other vaccines administered on same date of Pfizer suspect. 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. Patient was not pregnant. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. No known allergies. Outcome of the events was recovering. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1018439
Sex: M
Age:
State: FL

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Hiccups started approximately 6 hours after receiving the vaccine; This is a spontaneous report from a contactable consumer (patient). A 76-year-old male received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection lot no. EL1283, expiry date not reported, via an unspecified route of administration on right arm on 21Jan2021 12:00 at a single dose for covid-19 immunization. Patient has no COVID prior vaccination and has not tested post vaccination. Patient has no known allergies. The patient's medical history and concomitant medications were not reported. It was reported that Hiccups started approximately 6 hours after receiving the vaccine on 21Jan2021 at 18:30. No treatment was given. Outcome of the event was unknown. The vaccine was given in Public Health Clinic/Veterans Administration facility. Mo other vaccines were given in four weeks.

Other Meds:

Current Illness:

ID: 1018440
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: hiccups; This is a spontaneous report from a contactable nurse (patient's wife). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL1283), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history was reported as none. The patient's concomitant medications were not reported. The patient experienced hiccups on an unspecified date. When asked for the treatment, nurse stated, that they have been doing all the usual hiccup kind of stuff, Tums, Gas-X, and sipping on ice. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1018442
Sex: F
Age:
State: WI

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210123; Test Name: heart rate; Result Unstructured Data: Test Result:125 bpm; Comments: Elevated heart rate at rest (125 bpm)

Allergies:

Symptoms: Elevated heart rate at rest (125bpm) 24 hours after 2nd dose.; This is a spontaneous report from a non-contactable consumer (patient). A 24-year-old female patient (pregnant: unknown) received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot/batch number and expiration date not provided), via an unspecified route of administration on 22Jan2021 13:45 at single dose in right arm for COVID-19 immunization. The patient's medical history was none, no known allergies. The patient's concomitant medications were not reported. The patient previously took the first dose of bnt162b2 on 07Jan2021 11:45 in right arm for COVID-19 immunization. Facility type vaccine at Hospital. No other vaccine in four weeks. No other medications in two weeks. On 23Jan2021 13:00, the patient experienced elevated heart rate at rest (125bpm) 24 hours after 2nd dose. No treatment received for the event. No COVID prior vaccination and no COVID tested post vaccination. The 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: 1018443
Sex: F
Age:
State: CA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Within minute of injection began to have numbness at back of throat and tongue; Within minute of injection began to have numbness at back of throat and tongue; This is a spontaneous report from a contactable nurse (patient). A 37-year-old non-pregnant female patient received her second dose of bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE; lot number: EL1287; expiration date: unknown), via an unspecified route of administration left arm on 20Jan2021 14:45 at a single dose for covid-19 immunization. The patient medical history was not reported. The patient has no known allergies before vaccination. The patient was not diagnosed with COVID prior vaccination. Concomitant medication included duloxetine hydrochloride (CYMBALTA) and cetirizine hydrochloride (ZYRTEC). The patient did not have other vaccine in four weeks. The patient received her first dose of bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE; lot number: EH9899) at the age of 37-year-old via an unspecified route of administration left arm on 28Dec2021 11:00 AM at a single dose for covid-19 immunization. The patient received her vaccine Public Health Clinic/Veterans Administration facility. The patient reported that within minute (20Jan2021 02:45 PM) of injection, began to have numbness at back of throat and tongue. No swelling or difficulty breathing was experienced by the patient. The patient received treatment for the adverse events which included diphenhydramine 50mg IM. The patient did not have COVID tested post vaccination. The adverse event required a doctor or other healthcare professional office/clinic visit. The outcome of the events was recovered in Jan2021.

Other Meds: CYMBALTA; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1018444
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Arm was not that sore, a little bit/Arm was not that sore, a little bit; This is a spontaneous report from a contactable consumer(patient). A female patient of unspecified age started to receive second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9261), via an unspecified route of administration at arm in Jan2021 at single dose for covid-19 immunisation. Medical history and concomitant medication were not reported. Patient previously took the first dose of bnt162b2 at single dose for covid-19 immunisation (The 1st dose was Pfizer EL, then it has a 0 with a line through it. And then 14 and then another 0 with a line through it). Reporter asked if the vaccine make antibodies. if she needed an antibody test since she has only had mild soreness as a side effect. Her companion had the vaccine with another person and had no side effects either. they had it at a medical school so hopefully they had people who knew what they were doing. She was hoping the doses were good. she got the second dose of the Covid 19 vaccine last week on Wednesday. She has had no side effects other than a little bit of a sore arm (Jan2021). She has heard the second dose of the vaccine causes more side effects than the first and that was supposed to show that the vaccine is taking effect. She asked if it was correct. She is not questioning if the vaccine was given correctly or not. She asked if there was anything that states how many people had no side effects. She had the second vaccine Pfizer, last Wednesday. And she had heard that it gives one some fever and may be chills or small things that shows that one are taken it and what worries them was they had no symptoms at all. Even her arm was not that sore, a little bit. But she just wondered if there had people that had no symptoms does that mean it did not take. she was worried because they do not have any symptoms. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1018446
Sex: F
Age:
State: NC

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe swollen lymph node left axilla/ Injection site left arm; This is a spontaneous report from a contactable nurse (patient). A 45-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: El9262), via an unspecified route of administration on 22Jan2021 13:00 at a single dose on left arm for COVID-19 immunization. Medical history included Hypothyroidism, depression, vit D def., penicillin allergy and COVID-19. Concomitant medication included liothyronine sodium (CYTOMEL), levothyroxine sodium (SYNTHROID), celecoxib (CELEXA [CELECOXIB]), omega-3-acid ethyl ester (LOVAZA), aspirin [acetylsalicylic acid] (ASPIRIN [ACETYLSALICYLIC ACID]), and an unspecified vitamin. The patient experienced Severe swollen lymph node left axilla/ Injection site left arm on 22Jan2021 18:00. No treatment received for the event. The outcome of the event was recovering. The patient was not pregnant. No other vaccine in four weeks. Not COVID tested post vaccination.

Other Meds: CYTOMEL; SYNTHROID; CELEXA [CELECOXIB]; LOVAZA; ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 1018447
Sex: F
Age:
State: TX

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: soreness and redness where given the injection; soreness and redness where given the injection; Fever; Headache; Chills; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9262, expiry date not reported), via an unspecified route of administration at the left arm on 20Jan2021 17:30 at single dose for COVID-19 immunization. Medical history included high blood pressure, high cholesterol, thyroid disorder and COVID-19. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. The patient had no allergies to medications, food, or other products. Concomitant medications (unspecified) in two weeks were given. On 21Jan2021 15:00, the patient experienced soreness and redness where given the injection, fever, headache, and chills. No treatment was received for the adverse events. Clinical outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1018449
Sex: F
Age:
State: DE

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; muscle cramps; rash; This is a spontaneous report from a contactable other hcp (patient). This 42-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot # unknown), via an unspecified route of administration at single dose in the left arm on 13Jan2021 for covid-19 immunisation. The patient medical history was not reported. Concomitant medication included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL), venlafaxine hydrochloride (EFFEXOR). The patient previously took Keflex [cefalexin] and experienced drug allergy. On 13Jan2021, the patient experienced headache, muscle cramps, rash, all with outcome of recovering. No treatment required. The vaccine was administered at Hospital Facility. The patient had not been tested for COVID-19 post the vaccination. The patient was not pregnant at the time of vaccination. Information on the lot/batch number has been requested.

Other Meds: Adderall; Effexor

Current Illness:

ID: 1018450
Sex: F
Age:
State: FL

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe sinus like headaches come on in evening with severe neck pain.; hard to sleep; severe sinus like headaches come on in evening with severe neck pain.; This is a spontaneous report from a contactable consumer. An 80-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Jan2021 10:30 at single dose (Lot # EL8982, EXP-20May2021) for covid-19 immunisation Medical history included Osteoporosis of spine, left thyroid removed, acid reflux. Known allergies: penicillin, latex. No other vaccine in four weeks. No COVID prior vaccination. Concomitant medication included levothyroxine sodium (SYNTHROID), lisinopril, colecalciferol (VIT D3), omeprazole. The patient experienced after 2nd day severe sinus like headaches come on in evening with severe neck pain. Have had this for 4 nights, hard to sleep. Events start date: 20Jan2021 08:00 PM. Treatment included Advil (cold and sinus) every day to help. It did help, but did not like to take this type of medicine that often. No COVID tested post vaccination. Outcome of events was not recovered.

Other Meds: SYNTHROID; LISINOPRIL; VIT D3; OMEPRAZOLE

Current Illness:

ID: 1018452
Sex: F
Age:
State: ND

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Raised rash on face; Raised rash on face and injection site; flushed feeling face; chills; Body aches; brain fog/ overall not up to feeling like myself; This is a spontaneous report from a contactable nurse reported for herself. A 40-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 right arm on 22Jan2021 15:00 at a SINGLE DOSE for covid-19 immunisation. Medical history included rheumatoid arthritis from an unknown date and unknown if ongoing and cerebrovascular accident from an unknown date and unknown if ongoing. The patient previously took morphine and experienced drug hypersensitivity. On 23Jan2021 10:30, the patient experienced raised rash on face and injection site, flushed feeling face, chills, overall not up to feeling like myself, body aches and brain fog. No treatment was received for the events. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018453
Sex: F
Age:
State: AZ

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; neck pain; numbness into extremities; extreme pain in left arm; Extreme muscle pain in neck caused me to go to ER; Significant bilateral shoulder pain; Weakness; This is a spontaneous report from a contactable consumer (patient). This 36-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date unknown), via an unspecified route of administration on 20Jan2021 16:45 at a single dose on the left arm for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient is not pregnant at the time of report and at the time of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. Patient has not been tested for COVID-19 since the vaccination. Patient has no known allergies. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received the first dose on 31Dec2020 on the left arm. On 20Jan2021 21:00, the patient's extreme muscle pain in neck caused her to go to the ER and tramadol and Norflex were administered. The patient had significant bilateral shoulder pain and weakness. The head and muscle pain in neck persisted. Events resulted in emergency room/department or urgent care. Treatment received were tramadol and Norflex. On 20Jan2021 22:00, the patient experienced headache, neck pain, numbness into extremities, and extreme pain in left arm. The events resulted in emergency room/department or urgent care. Tramadol was received as treatment but it worsened the symptoms. The tramadol was administered on the left arm at the hospital. Outcome of the events "extreme muscle pain in neck", "significant bilateral shoulder pain", and "weakness" was unknown and of the other events was not recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018455
Sex: F
Age:
State: CA

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; heart racing; Vomiting; This is a spontaneous report from a contactable healthcare professional (patient). A 26-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number and expiry date: not known), via an unspecified route of administration in the left arm on 23Jan2021 15:15 at single dose for COVID-19 immunization. The patient's medical history was not reported. There were no concomitant medications. No known allergies. The patient is not pregnant. No other vaccine in four weeks and no other medications in two weeks. The patient had no COVID prior vaccination and not tested with COVID test post vaccination. The patient experienced chills, heart racing, and vomiting, 4 hours after vaccination on 23Jan2021 19:15. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018456
Sex: F
Age:
State: HI

Vax Date: 01/13/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210122; Test Name: Heartbeat; Result Unstructured Data: Test Result:racing

Allergies:

Symptoms: Heaviness in chest; Racing heartbeat; Fatigue; This is a spontaneous report from a contactable other hcp (patient). The 41-years-old female patient (not pregnant) received bnt162b2 (BNT162B2), via an unspecified route of administration on 13Jan2021 10:15 in Left arm at single dose for covid-19 immunisation. Medical history included none. No other vaccine in four weeks, no other medications in two weeks, increased protein. No covid prior vaccination. No covid tested post vaccination. No Known allergies. The patient's concomitant medications were not reported. The patient experienced Heaviness in chest, racing heartbeat, fatigue on 22Jan2021. No treatment received. The outcome of the events was not recovered. No follow-up attempts are possible, information on batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1018458
Sex: F
Age:
State: MN

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; chills; runny nose; ear ache; body aches; swollen glands; This is a spontaneous report from a contactable Other HCP (patient). This 27-Year-old female Other HCP patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number El3248/expiration date: unknown), via unknown route of administration, on 22Jan2021 01:45 PM (at the age of 27 years old) as a single dose on left arm for COVID-19 immunisation at a hospital. Relevant medical history included Depression, insomnia. The patient had no known allergies. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number Ek9231/expiration date: unknown), via unknown route of administration, on 04Jan2021 01:00 PM (at the age of 27 years old) as a single dose on left arm for COVID-19 immunisation. The patient was not pregnant at time of vaccination. Relevant concomitant medications were not provided. 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. It was reported that on 23Jan2021 01:00 AM, the patient experienced fever, chills, runny nose, ear ache, body aches, swollen glands. The outcome of the events fever, chills, runny nose, ear ache, body aches, swollen glands was not recovered. No treatment was received for the events. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1018459
Sex: F
Age:
State: CA

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210115; Test Name: pain; Result Unstructured Data: Test Result:10/10; Test Date: 20210122; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Burning pain internally for over a week; weakness on the left arm; This is a spontaneous report from a contactable Nurse (patient). A 44-years-old female patient received second dose of bnt162b2 (BNT162B2), intramuscular on 15Jan2021 08:00 at SINGLE DOSE for covid-19 immunisation. Medical history and concomitant medications was none. Historical vaccine at 44 year old included product=COVID 19, brand=Pfizer, lot unknown=False, administration date=25Dec2020, administration time=08:45 AM, vaccine location=Left arm, dose number=1} for covid-19 immunisation. No Known allergies. No covid prior vaccination. No other vaccine in four weeks. The patient experienced burning pain internally for over a week, weakness on the left arm on 15Jan2021 09:00 with outcome of not recovered. Still on pain 10/10 throbbing pain Tylenol, ibuprofen, ice packs, heating pad have not reduced the pain. The patient underwent lab tests and procedures which included pain: 10/10 on 15Jan2021, Covid test post vaccination: covid test type post vaccination=Nasal Swab: negative on 22Jan2021. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1018460
Sex: F
Age:
State:

Vax Date: 01/22/2021
Onset Date: 01/24/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Left chest pain; Difficulty breathing; This is a spontaneous report from a contactable other healthcare professional (patient). A 31-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), intramuscular (right arm) on 22Jan2021 (15:30 )at single dose for Covid-19 immunization. There was no medical history. Concomitant medications included Flu shot (reported as other vaccine in 4 weeks) 1 dose on 08Jan2021.The patient was not diagnosed with COVID-19 prior to vaccination. The patient is not pregnant at the time of vaccination. On 24Jan2021 (12:00 PM), the patient experienced left chest pain and difficulty breathing. There was no treatment received for the adverse events. The patient has not been tested for COVID-19 since the vaccination. The outcome of events was unknown. Information about lot/batch no has been requested.

Other Meds:

Current Illness:

ID: 1018462
Sex: M
Age:
State: PA

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: lower lip became swollen; throat began feeling irritated/scratchy; lips started tingling, then itching; lips started tingling, then itching; This is a spontaneous report from a contactable Nurse (also the patient). A 63-year-old male patient (also the age at vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EK4176, expiry date: Not available/provided by the reporter at the time of report), via an unspecified route of administration in left arm from 21Jan2021 10:00 AM at single dose for covid-19 immunization. The patient is vaccinated in a hospital. Medical history included bilateral iliac aneurysms on an unspecified and inferior wall MI in 2004. No other vaccine was administered in four weeks. The patient had no known allergies. No covid prior vaccination and not covid tested post vaccination. Concomitant medication included (reported as other medications in two weeks): aspirin [acetylsalicylic acid] (ASPIRIN [ACETYLSALICYLIC ACID]), simvastatin, metoprolol succinate (TOPROL), alfuzosin, colecalciferol (D3), zinc gluconate (ZINC (GLUCONATE). It was reported that at home, approximately 45 minutes after shot (reported start time: 10:45 AM), lips started tingling, then itching. Around 10 minutes later (10:55 AM; 55 minutes), throat began feeling irritated/scratchy. Approximately 10 minutes (11:05 AM; 65 minutes) later lower lip became swollen. The patient took half a Benadryl. Never had any difficulty breathing or swallowing. The presentation never got any worse. Tingling of lips lasted most of day, but milder than initial reaction - other symptoms gone in approximately an hour after taking the Benadryl (reported also as: No treatment was received for the events; pending clarification). The outcome of the event lips started tingling was recovered on 21Jan2021; and for all other events was recovered on an unspecified date.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; SIMVASTATIN; TOPROL; ALFUZOSIN; D3; ZINC (GLUCONATE)

Current Illness:

ID: 1018463
Sex: F
Age:
State: MD

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Injection site pain; Tiredness; Headache; Chills; Nausea; vomiting; Feeling unwell; Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 24-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL9262, expiration date unspecified), via an unspecified route of administration on 23Jan2021 13:45 at single dose (left arm) for COVID-19 immunization. The patient had no medical history. The patient was not pregnant and had no known allergies. The patient's concomitant medications were not reported. On 23Jan2021 22:00, the patient experienced injection site pain, tiredness, headache, chills, nausea, vomiting, feeling unwell and diarrhea. There was no therapy for the events. The patient had no other vaccine in four weeks and no other medications in two weeks. The patient did not have Covid prior vaccination and was not Covid tested post vaccination. Outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1018465
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: sore arm; This is a spontaneous report from a non-contactable consumer. A male patient of an unspecified age started received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot and expiration date unknown), 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. The patient experienced sore arm on an unspecified date with outcome of unknown. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1018466
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:101 degrees; Comments: fever of 101 degrees

Allergies:

Symptoms: fever; small rash below the injection site; chills; achy shoulders; throat feels raw; nasal congestion; feels like sinus; This is a spontaneous report from a Pfizer-sponsored Program, from a contactable consumer. An 88-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received her first dose of the Pfizer COVID-19 vaccine on 14Jan2021 and 6 days later (unspecified date in Jan2021), she started having a fever of 101 degrees which has been occurring only at night and resolving with aspirin, small rash below the injection site, has chills, achy shoulders, throat feels raw and nasal congestion "feels like sinus." She does not have a cough and is not short of breath. She was calling to find out if these are common side effects this long after receiving the vaccine or if it could potentially be a cold. She stated that her son, who lives with her, wants her to go to the Emergency Room right now. She does not feel that bad and is going to call her primary care doctor tomorrow when their office is open. She wants to know if she is still having these symptoms at the time of her second dose, which is scheduled for 04Feb2021, should she still take the dose. The patient underwent lab tests and procedures which included body temperature: 101 degrees (fever) on an unspecified date. Therapeutic measures were taken as a result of fever. The outcome of the event fever was recovering, while of the other events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018467
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: the patient has been waking up with a stiff neck which was worse at night; This is a spontaneous report from a medical team. A contactable consumer (patient himself) reported that a male patient of an unspecified age (Age:70; Unit: Unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at SINGLE DOSE (first dose) for covid-19 immunization. The patient's medical history and concomitant medications were not reported. Over the past two days (unspecified dates), the patient has been waking up with a stiff neck which was worse at night. The outcome of event was unknown. Follow-up attempts are completed. The following information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 1018469
Sex: M
Age:
State: NJ

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: local pain at the vaccine location; Tiredness/fatigue; This is a spontaneous report from a contactable consumer (patient). A 66-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE solution for injection, lot/batch number: EL9262) , via an unspecified route of administration on the right arm on 20Jan2021 17:15 at SINGLE DOSE for COVID-19 immunization. Medical history included blood pressure abnormal (reported as BP). Concomitant medication included amlodipine (AMLODIPINE) for unknown indication and unspecified BP medication. On 21Jan2021 06:00, the patient experienced local pain at the vaccine location and tiredness/fatigue and recovered in Jan2021. The patient did not receive treatment for the event. The patient was not diagnosed with COVID-19 prior and not tested since vaccination.

Other Meds: AMLODIPINE

Current Illness:

ID: 1018470
Sex: F
Age:
State: AZ

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I had a light presentation of hives. The locations of the hives were in the crease of my right arm (elbow area), torso (tummy area), top of foot and ankles.; This is a spontaneous report from a contactable consumer (patient). A 63-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE solution for injection, lot/batch number: ELI283), via an unspecified route of administration on the left arm on 23Jan2021 11:45 at SINGLE DOSE for COVID-19 immunization. It was reported that the patient was allergic to Amoxicillin. The patient was not pregnant (including at the time of vaccination). Medical history and concomitant medications were not reported. On 23Jan2021 22:00, the patient had a light presentation of hives. The locations of the hives were in the crease of the right arm (elbow area), torso (tummy area), top of foot and ankles. The patient did not receive treatment for the event. The patient was not diagnosed with COVID-19 prior and not tested since vaccination. Outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 1018472
Sex: F
Age:
State: WA

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Head and nasal congestion; Head and nasal congestion; ear ache; body aches; fatigue; sore arm; This is a spontaneous report from a contactable nurse (patient). A 41-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL1283), via an unspecified route of administration on 22Jan2021,16:30 at SINGLE DOSE (first dose, left arm) for COVID-19 immunization. Medical history included allergies: Latex from an unspecified date. Patient did not have COVID-19 prior vaccination. Patient is not pregnant. No other vaccine in four weeks. The patient's concomitant medications were not reported. The patient experienced head and nasal congestion, ear ache, body aches, fatigue and, sore arm all on 23Jan2021 01:00. No treatment was given. Patient was not tested for COVID-19 post vaccination. Outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1018473
Sex: F
Age:
State: MN

Vax Date: 12/24/2020
Onset Date: 12/26/2020
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: left eye keeps twitching; No immediate vision changes until later in the day when left eye gets tired; This is a spontaneous report from a contactable nurse (patient) reported that a 30-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular on the right arm on 24Dec2020 07:45 at a single dose for Covid-19 immunization. The vaccine was administered at the hospital. The patient's medical history and concomitant medications were not reported. Patient is not pregnant. On 26Dec2020 (also reported as 'approximately 2 days after the first vaccination'), the patient's left eye keeps twitching. No pain. May intensify and becomes obvious. No immediate vision changes until later in the day when left eye gets tired. No treatment received for the reported events. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018474
Sex: F
Age:
State: OR

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: vomited; chills; headache; had some itching, ongoing soreness and lump at site; had some itching, ongoing soreness and lump at site; had some itching, ongoing soreness and lump at site; nauseous; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received the first dose of bnt162b2 (Pfizer-Biontech COVID-19 Vaccine, Lot number: EL9262), via an unspecified route of administration in the left arm on 22Jan2021 19:00 at a single dose for COVID-19 immunization. She takes thyroid daily (as reported) as it was removed when she was 20. The patient was not pregnant at the time of vaccination. The patient had no COVID prior to vaccination. The patient had not been tested for COVID post vaccination. The patient has not received any vaccine in 4 weeks. Concomitant medication included teriparatide (FORTEO) daily injection, diphenhydramine hydrochloride (BENADRYL). The patient previously took codeine and experienced allergies: codeine. The patient reported that no one knew if she should inject with teriparatide. On 22Jan2021, she received teriparatide at 4pm and bnt162b2 at 7pm. She took a diphenhydramine and had some itching, ongoing soreness and lump at site. She took teriparatide at 3:30pm at about 7pm she was nauseous and vomited. She had chills but felt better afterwards. She went to bed and have headache, not sure if she should discontinue teriparatide or discontinue before next shot. According to the reporter, the events started on 23Jan2021 19:00; vomited started on 23Jan2021 21:00. The outcome of the event was recovering.

Other Meds: FORTEO; BENADRYL

Current Illness:

ID: 1018476
Sex: F
Age:
State: FL

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Very bad arm pain on injection arm; tiredness; mild headache; chills; feeling unwell; This is a spontaneous report from a contactable consumer (patient herself). A 67-year-old female patient received bnt162b2 (BNT162B2 also reported as COVID 19 vaccine, lot/batch number and expiry date were not reported), via an unspecified route of administration in arm on 16Jan2021 10:30 at SINGLE DOSE for Covid-19 immunisation. Medical history included allergy to latex, iodine, motrin. No other vaccine in four weeks. There were no concomitant medications. On 16Jan2021 15:00, the patient experienced very bad arm pain on injection arm, tiredness, mild headache, chills, feeling unwell overall for 4 solid days. No treatment was given. The outcome of events was recovered on 20Jan2021. Information about lot and batch number was requested.

Other Meds:

Current Illness:

ID: 1018477
Sex: F
Age:
State: NJ

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Body aches; Injection arm began to hurt; Body tremble; Armpit very painful; Arm pit swelling; This is a spontaneous report from a contactable healthcare professional (patient). A 53-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK9231; Expiration date was not reported) on 23Jan2021 (11:45) at a single dose on the right arm, with route of administration unspecified, for COVID-19 immunization at the hospital. Medical history included early diabetes and high blood pressure. Concomitant medications included valsartan, sitagliptin (JANUVIA) and rosuvastatin. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL0140; Expiration date was not reported) on 02Jan2021 (when the patient was 53 years old) for COVID-19 immunization. The patient was not pregnant at the time of vaccination. On 23Jan2021 (19:00), the patient had chills; body aches; injection arm had begun to hurt; body tremble; armpit was very painful; and armpit was swelling. The patient had no fever. The patient had taken paracetamol (TYLENOL) as treatment for the reported events. The outcome of the events, 'chills', 'body aches', 'injection arm had begun to hurt', 'body tremble', 'armpit was very painful' and 'armpit was swelling', was recovering. The patient was not diagnosed with COVID-19 prior to vaccination, and was not tested post-vaccination.

Other Meds: VALSARTAN; JANUVIA [SITAGLIPTIN]; ROSUVASTATIN

Current Illness:

ID: 1018479
Sex: F
Age:
State: FL

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fever; persistent cough; This is a spontaneous report from a contactable consumer (patient herself). A 66-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration in the left arm on 22Jan2021 15:00 at a single dose for COVID-19 immunization. The patient's medical history was not reported. The patient had no known allergies and was not pregnant. She had not been diagnosed with COVID prior to vaccination. Concomitant medications included metformin 500 mg and hydrochlorothiazide 12.5 mg. The patient experienced fever a persistent cough and fever on 22Jan2021 19:00. No treatment was received for the events. The outcome of the events was recovering. The patient was not tested for COVID post vaccination. Information on the lot/batch number has been requested.

Other Meds: METFORMIN; HYDROCHLOROTHIAZIDE

Current Illness:

ID: 1018480
Sex: F
Age:
State: LA

Vax Date: 01/22/2021
Onset Date: 01/24/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fatigue; headache; weakness; nausea; tingling on right side of body; This is a spontaneous report from a contactable other health professional (patient). A 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration (right arm) on 22Jan2021 17:30 at single dose for Covid-19 immunization. The patient's medical history was not reported. Concomitant medication included lisinopril from an unspecified date for an unspecified indication. The patient previously took Codeine and Compazine and experienced allergy. 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. On 24Jan2021 (13:00), the patient experienced fatigue, headache, weakness, nausea, and tingling on right side of body. There was no treatment received for the adverse event. The outcome of events was recovering. The patient has not been tested for COVID-19 since the vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds: Lisinopril

Current Illness:

ID: 1018482
Sex: F
Age:
State: NC

Vax Date: 01/20/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: right ear began to hurt; eustachian tube inflammation; slight vertigo; metallic taste in mouth; phlegm drainage in throat; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration (left arm) on 20Jan2021 (15:00) at single dose for Covid-19 immunization. Medical history included penicillin allergy (Known allergies: penicillin, ciprofloxin, levofloxacin, hylan G-F, lexapro, bacitracin). Concomitant medication included potassium chloride. The patient previously took Ciprofloxin, Levofloxacin, Hylan G-F, Lexapro, and Bacitracin and experienced allergy. 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. On 22Jan2021 (10:00), the patient began to experience slight vertigo accompanied by metallic taste in mouth and phlegm drainage in throat (reported as "phlym"). When she laid down in bed at right side mainly her vertigo got worse. Late Saturday afternoon (23Jan2021), her right ear began to hurt. She went to urgent care at 7:30 pm. The doctor prescribed vertigo exercises, Flonase nasal spray for possible eustachian tube inflammation and ibuprophin. On Sunday (24Jan2021: today), the patient was still experiencing pretty severe vertigo; not much improved. The adverse events resulted in doctor or other healthcare professional office/clinic visit. The patient had vertigo exercises, ibuprophin, and Flonase spray as treatment. The outcome of events was not recovered. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: POTASSIUM CHLORIDE

Current Illness:

ID: 1018483
Sex: F
Age:
State: WA

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Name: heart beat; Result Unstructured Data: Test Result:90; Test Name: Rh; Result Unstructured Data: Test Result:Neg A blood type

Allergies:

Symptoms: headache; heart-pounding, racing heart beat,; dizziness; feelings of passing out; This is a spontaneous report from a contactable consumer. A 66-year-old non-pregnant female received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL9262), via an unspecified route of administration in the left arm on 23Jan2021 10:00, at 0.3ml, single for covid-19 immunization.The patient medical history was not reported. Patient is an Rh Neg A blood type and did not have Covid, as she's been isolated for a year. Concomitant medication included gabapentin, paroxetine hydrochloride and atorvastatin. On 23Ja2021, after half an hour (10:30) of receiving 1st dose of the vaccine, patient experienced heart pounding, racing heart beat, dizziness, feelings of passing out. These symptoms lasted up to 3 hours. Patient sat her my car outside of the an emergency parking lot for 3 hours because she couldn't drive home during these symptoms. Patient was on the verge of going into emergency care. For the remainder of the day, patient's sitting heart beat was at 90. The next day, 24Jan201, she felt better but have on and off slight headache. She did not plan on taking the 2nd dose. The outcome of the events was recovering. The patient has not tested positive for Covid-19 post vaccination.

Other Meds: GABAPENTIN; PAROXETINE HYDROCHLORIDE; ATORVASTATIN

Current Illness:

ID: 1018485
Sex: F
Age:
State: WA

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chill; fever; body aches; migraine; dizziness; soreness at injection site; headache; lymph node swollen on left arm pit area; This is a spontaneous report from a contactable other healthcare professional(patient). A 47-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: El3302), intramuscularly into the left arm on 23Jan2021 11:45 at a single dose for covid-19 immunisation. Medical history was reported as none. Patient was not pregnant. Concomitant medication included escitalopram oxalate (LEXAPRO), riboflavin (RIBOFLAVIN), multivitamins and antihistamine (unspecified). The patient was previously administered with the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: El0140), intramuscularly into the left arm on 02Jan2021 12:30 at a single dose for covid-19 immunization. On 23Jan2021 20:30, patient experienced chill, fever, body aches, migraine and dizziness. On 23Jan2021, patient experienced soreness at injection site, headache and lymph node swollen on the left armpit area. The patient did not receive treatment for the events reported. Outcome of events were recovering.

Other Meds: LEXAPRO; RIBOFLAVIN

Current Illness:

ID: 1018487
Sex: F
Age:
State: FL

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Pain through back across both arms and neck.; A headache that feels like my heads going to explode.; swell up like a balloon; Nauseated; Chills; fever; Pain on both my legs cannot walk; Pain through back across both arms and neck. Cannot lift my arms; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date not reported), via an unspecified route of administration on the right arm on 20Jan2021 16:00 at single dose for covid-19 immunization. Medical history included atrial fibrillation from an unknown date and unknown if ongoing , hypersensitivity (Known allergies: Yes) from an unknown date and unknown if ongoing, covid-19 (if covid prior vaccination: Yes) from an unknown date and unknown if ongoing. Concomitant medications included unspecified medications. The patient experienced pain through back across both arms and neck, the patient cannot lift their arms. The patient also experienced pain on both their legs cannot walk, a headache that feels like their heads going to explode, nauseated all the time, swell up like a balloon, chills and fever. It was reported that the events occurred on 21Jan2021. Therapeutic measures were taken as a result of pain through back across both arms and neck. The patient did not recover from the events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018488
Sex: F
Age:
State: AZ

Vax Date: 01/20/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Hives and red rash on legs; Hives and red rash on legs; This is a spontaneous report from a contactable consumer. An 85-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3249, expiration date not reported), via an unspecified route of administration (right arm), on 20Jan2021 12:15 at a single dose for COVID-19 immunisation. Medical history included prinzmetal angina, hypothyroidism, and penicillin and sulfa allergies, all from an unknown date. Concomitant medication included diltiazem, estradiol, pantoprazole, and atorvastatin calcium (ATORVAS). On 22Jan2021, the patient had a reaction to her first dose of vaccination, and she was wondering if that would be a problem when she takes the second dose. The reaction she had was some hives and some red rash on her leg and it happened about 48 hours after she got the shot. The patient took Claritin pill and some Anti-Itch SavOn as treatment. Her second dose of vaccine was scheduled 15Feb2021. The patient was recovering from the events.

Other Meds: DILTIAZEM; ESTRADIOL; PANTOPRAZOLE; ATORVAS

Current Illness:

ID: 1018489
Sex: F
Age:
State: NY

Vax Date: 01/22/2021
Onset Date:
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: stress; This is a spontaneous report from a contactable other healthcare professional (HCP) (patient) via a Pfizer-sponsored program. A 62-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 22Jan2021 at a single dose as vaccine. Medical history and concomitant medications were not reported. The patient experienced stress on an unspecified date. It was noted that she was unable to keep her 2nd dose appointment and she's having surgery before her second dose. She had the vaccine last Friday, 22Jan2021. Her 2nd dose would be on 12Feb2021 and she wanted to change it to 2/8 because she's scheduled for surgery on 11Feb2021. Could her appointment be changed? She has been trying to change the appointment for the past 4 hours. She called one number and they said it was not the correct number and they gave me another number. She told the person before what she wanted and needed to do and didn't listen either. The patient said thank you, had been very helpful and alleviated her stress right now. Now, she could relax. The outcome of the event was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1018491
Sex: F
Age:
State: PA

Vax Date: 12/28/2020
Onset Date:
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; Body aches; Nausea; Vomiting; Headache; This is a spontaneous report from a contactable nurse (patient). A 38-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not provided), via an unspecified route of administration first dose on 28Dec2020 at single dose for covid-19 immunisation. The patient's medical history Covid-19 from Apr2020. The patient's concomitant medications were not reported. On an unspecified date, the patient would like to know if she should receive the second dose of the Pfizer COVID-19 vaccine after having an adverse reaction with her first dose of the COVID-19 vaccine. The patient experienced "fever, body aches, nausea, vomiting, headache, all that stuff and it lasted about 5 or 6 days. The patient had to miss work for a couple of days. The patient did not have any anaphylactic type reactions though. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1018492
Sex: M
Age:
State: FL

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210123; Test Name: Temperature; Result Unstructured Data: Test Result:100.5 degrees

Allergies:

Symptoms: Chills and uncontrollable shivering; Kept me awake; Slept most of the next day; Temperature rose to 100.5 degrees/fever; Very lethargic; No appetite; No bowel movements; Soreness at the injection site; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL9263; Expiration date was not reported) on 22Jan2021 (14:45) at a single dose on the left arm, with route of administration unspecified, for COVID-19 immunization at the public health clinic/veterans administration facility. Medical history included large B-cell lymphoma (recovered); chemotherapy from an unspecified date to Jul2020; and had a bad case of pneumonia from Oct2020 to an unspecified date. Concomitant medications included meloxicam, latanoprost and paracetamol (TYLENOL). On 23Jan2021 (01:00), the patient was very lethargic; had no appetite; and no bowel movements. On 23Jan2021 (23:45), the patient had soreness at the injection site; chills and uncontrollable shivering; was kept awake, and had slept most of the next day; and had fever/temperature rose to 100.5 degrees. The patient had received treatment for all the reported events. The outcome of the events, 'lethargic', 'no appetite', 'no bowel movements', 'soreness at the injection site', 'chills and uncontrollable shivering', 'kept awake and slept most of the next day' and 'fever', was recovered in Jan2021. The patient was not diagnosed with COVID-19 prior to vaccination, and was not tested post-vaccination.

Other Meds: MELOXICAM; LATANOPROST; TYLENOL

Current Illness:

ID: 1018494
Sex: M
Age:
State: CA

Vax Date: 12/16/2020
Onset Date: 12/24/2020
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210102; Test Name: PCR; Test Result: Negative ; Test Date: 20210102; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: severe vertigo and nystagmus; severe vertigo and nystagmus; labyrinthitis; vestibular neuritis; This is a spontaneous report from a contactable physician (reporting for himself). A 37-year-old male patient received bnt162b2 (BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date: unknown), via intramuscular route on his right arm on 16Dec2020 15:00 at single dose for covid-19 immunisation. The patient's medical history was not reported. The patient had no known allergies and had no COVID prior vaccination. There were no concomitant medications. On 24Dec2020 at 19:00 (reported as 8 days after vaccine), the patient experienced severe vertigo and nystagmus. Presumed diagnosis vestibular neuritis or labyrinthitis. It has now been one month since onset of symptoms. Much improved but still some persistent vertigo. The reporter was thinking that the events were unlikely to be due to COVID-19 vaccine but given uncertainty of etiology, he thought he should report it. The events resulted in doctor or other healthcare professional office/clinic visit. The patient underwent lab tests and procedures which included nasal swab and polymerase chain reaction (PCR): negative on 02Jan2021. The patient had no prior vaccination. Therapeutic measures were taken as a result of onset of severe vertigo, nystagmus, "vestibular neuritis" and "labyrinthitis" which included prednisone. The outcome of the event vertigo was not recovered while recovering for the event nystagmus, "vestibular neuritis" and "labyrinthitis". Information on the lot/batch number has been requested.; Sender's Comments: The reported events vertigo, nystagmus, vestibular neuritis, and labyrinthitis are likely intercurrent and are unrelated to suspect drug BNT162B2.

Other Meds:

Current Illness:

ID: 1018495
Sex: F
Age:
State: CO

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210112; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Fever; body aches; chills; This is a spontaneous report from a non-contactable healthcare professional. A 36-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982), intramuscular, left arm, on 22Jan2021 12:30 at a single dose for COVID-19 immunization. Medical history was not reported. No known allergies. Concomitant medications included multivitamins. The patient received the first dose of BNT162B2 (lot number: EK9231) on 31Dec2020, 3:30 intramuscular, right arm for COVID-19 immunization. The patient had no COVID prior to vaccination. COVID test post vaccination via nasal swab on 12Jan2021 was negative. On 23Jan2021, at 02:00, the patient experienced fever, body aches and chills. The patient did not receive any treatment for the adverse events. The patient has recovered from the events in Jan2021. No follow-up attempts are possible. No further information is expected.

Other Meds: Multivitamins [Vitamins NOS]

Current Illness:

ID: 1018497
Sex: F
Age:
State: SC

Vax Date: 01/05/2021
Onset Date: 01/22/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data: Test Date: 20210122; Test Name: Nasal Swab, PCR; Test Result: Positive

Allergies:

Symptoms: Acquired covid 19, exposed 18Jan2021. Symptoms began 22Jan2021. Positive PCR through DHEC; Acquired covid 19, exposed 18Jan2021. Symptoms began 22Jan2021. Positive PCR through DHEC; This is a spontaneous report from a contactable other healthcare professional (patient). A 42-year-old female patient (not pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK5730), via an unspecified route of administration on 05Jan2021 at 09:15 am in the Left arm at single dose for COVID-19 immunization in hospital. Medical history was not reported. Prior to vaccination, it was unknown if patient was diagnosed with COVID-19. The patient's concomitant medications included fludrocortisone acetate, loratadine, escitalopram oxalate (LEXAPRO). Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient acquired COVID 19 on 22Jan2021, exposed 18Jan2021. Symptoms began 22Jan2021. Positive PCR through DHEC. Since the vaccination, patient had been tested for COVID-19 PCR on 22Jan2021: Nasal Swab, result was Positive. No treatment was received for the events. The outcome of the events was not recovered.; Sender's Comments: The positive COVID-19 test occurred 17 days after the injection of suspect vaccine BNT162B2. The lack of efficacy of suspect BNT162B2 to the COVID-19 infection cannot be totally excluded. While the steroid fludrocortisone acetate and the target disease may predispose the patient to the virus infection.

Other Meds: FLUDROCORTISONE ACETATE; LORATADINE; LEXAPRO

Current Illness:

ID: 1018498
Sex: M
Age:
State: WA

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/10/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sore arm; lack of energy; Headaches on occasion.; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient received bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: El1283), via an unspecified route of administration in the left arm on 18Jan2021 14:00 at a single dose for covid-19 immunization. The patient has no medical history and concomitant medications. On 19Jan2021 06:00, the patient reported sore arm, noticeable lack of energy and headaches on occasion. The patient does not have covid prior vaccination and had not tested positive post vaccination. The patient did not receive treatment for the events. The outcome of the events was not recovered.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm