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
199,106MODERNA
36,710JANSSEN
5,381PFIZER\BIONTECH
2,555GLAXOSMITHKLINE BIOLOGICALS
1,469UNKNOWN MANUFACTURER
897MERCK & CO. INC.
627SEQIRUS, INC.
112DYNAVAX TECHNOLOGIES CORPORATION
91SANOFI PASTEUR
75NOVARTIS VACCINES AND DIAGNOSTICS
40EMERGENT BIOSOLUTIONS
14PAXVAX
12TEVA PHARMACEUTICALS
12PROTEIN SCIENCES CORPORATION
9PFIZER\WYETH
4BERNA BIOTECH, LTD.
4SMITHKLINE BEECHAM
3INTERCELL AG
1MEDIMMUNE VACCINES, INC.
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL7,949
7,473
2,547
1,506
1,187
1,051
1,049
s0294561,043
866
IMM209861
816
UT7065MA766
657
579
U62828AA563
557
538
U6737AA516
515
S034636506
4F472471
458
P100253275449
444
276563436
429
418
4BH32414
MENVEO404
PP9L5362
UJ446AA337
319
306
290
271
49TM3270
R1B252M253
4F472179
933622147
C5763AA144
CW3116134
3Y7NL126
UNK114
113
ARBA141A105
104
103
96
300057A90
79
1F4EB73
R1B743M62
56
UJ090AA55
51
UH894AB46
45
UNK44
UNK42
42
EJ168638
Unknown36
35
34
32
32
26
el128424
24
A115A22
22
EN620222
21
UNK20
20
19
Z127A19
19
17
JEV18K95E15
12
111798PI12
10
A739088
No batch number8
3333324181078
6
6
TAR356
5
5
U6935AA5
UNK5
4
unknown4
3
2
55RB72
2
2
2
2
2
U7124AA2
JEV18A68E2
2
ABYB05BA1
1
1
1
1
AMVA436A1
1
1
TJ3521
A130A; VIS give1
1
U7140BB1
1
1
SP UP016AA1
1
1808P08802/ESV01
037K20A300,947
EL1284288,578
57,766
1,432

Incidents per State

State Total
82,750
CA62,821
FL38,209
TX36,512
NY34,921
PA23,646
IN23,622
IL20,597
MI19,590
OH19,426
NJ18,413
NC16,769
GA15,932
WA15,351
VA15,234
MA14,876
AZ14,206
MN12,940
MD12,656
CO11,908
WI11,425
MO10,240
TN9,685
OR8,768
KY8,437
CT8,300
SC6,700
OK6,293
AL5,692
LA5,025
IA4,825
KS4,821
UT4,637
NV4,374
NM3,967
AR3,807
ME3,161
NH3,096
NE2,918
MS2,859
ID2,785
WV2,469
HI2,459
PR2,417
MT2,414
RI2,076
DE1,868
AK1,830
VT1,734
DC1,715
ND1,388
SD1,269
WY866
GU118
VI69
AS47
MP29
MH8
XB6
FM4
QM3
XV2
XL1

ID: 1645547
Sex: M
Age:
State: MI

Vax Date: 06/23/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: Blood pressure; Result Unstructured Data: Test Result:high; Test Name: heart beat; Result Unstructured Data: Test Result:High

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: High heartbeat; Blood pressure high; Hives all over the body; Rash; Shortness of breath; Losing his eye sight; Losing my eye sight; Cold; Chills; Sweat; This is a spontaneous report from a Pfizer-sponsored program. A contactable male consumer reported for himself that. A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 23Jun2021 as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced high heartbeat, blood pressure high, hives all over the body, rash, shortness of breath, losing his eyesight; losing my eyesight, cold, chills, and sweat on an unspecified date. Transferring agent stated, "they have a consumer on the line who received his first dose, he should be receiving his second dose today, but he says that he has all of the adverse event symptoms as well as losing his eyesight." Later it was reported that patient had cold, got chills, rashes, and hives all over the body, have sweat, like losing his eyesight." Consumer stated, "he got everything high heartbeat, high blood pressure whatever, hives, rashes, losing my eyesight, shortness of breath, everything like 'still persists'." It was reported that patient administration of the first dose on the 23Jun2021 and he was going to administration of second shot, but he doesn't know if he should because he got everything. Patient wants to know what he should do, should he call his doctor. Consumer was informed about the role of Pfizer Drug Safety and also informed that Pfizer Medical Information is the dedicated department to answer the question and offered the number. Consumer stated, "he was talking with them, they told a bunch of stuff he tried to tell, and they get through to your number." Consumer was informed that transferring agent transferred the consumer to Pfizer Drug Safety to file a safety report and for the question that consumer have regarding the side effects, Pfizer Medical Information is the right department to answer the question, consumer stated, "he trying to figure out what he should do, should he call his doctor, or should he do like (incomplete sentence)" Consumer was again informed about the role of Pfizer Drug Safety and that Pfizer Medical Information is the right department to answer those questions. In response consumer stated, "Well they just tell bunch of stuff about getting his next shot, or should he call his doctor, he was asking you what he should do. They didn't help, they got me to you. He got all the numbers on the papers here, he just called you to figure out what he should do." Consumer was provided with the number of Pfizer Medical Information # and was requested to select option 3, timings as and 8 am to 8 pm Monday to Fridays as per (EST). Consumer stated, he was going to hang up and call somebody else. and hung up the call abruptly. Further probing could not be done as the consumer hung up the call abruptly. Hence limited information available over the call. The patient underwent lab tests and procedures which included blood pressure measurement: high, heart rate: high on unspecified date. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 1645548
Sex: F
Age:
State:

Vax Date: 04/29/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: My thing was like if you feel cold, if you have a cold; My thing was like if you feel cold, if you have a cold; I feel my shoulder stiff or something; This is a spontaneous report from a contactable consumer or other non HCP (patient). This is the second case out of the 2 cases. A female patient of an unspecified age received bnt162b2 (BNT162B2, formulation; solution for injection), dose 2 via an unspecified route of administration on 29Apr2021 (Batch/Lot Number: EW0169) as DOSE 2, SINGLE for covid-19 immunisation. The patient medical history and concomitant medication was not reported. Historical vaccine included BNT162B2 first dose (Batch/Lot number; EW0162) for Covid-19 immunization. The patient stated "It was not like a serious. I din't have fever, nothing but just mine was okay, it was minor, I felt my shoulder stiff or something, maybe it was nothing to do with this". The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645549
Sex: F
Age:
State:

Vax Date: 07/22/2021
Onset Date: 07/23/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: all over aches, pain in the injection arm, pain in her other arm and nausea/ queasy today.; all over aches, pain in the injection arm, pain in her other arm and nausea/ queasy today.; all over aches, pain in the injection arm, pain in her other arm and nausea/ queasy today.; all over aches, pain in the injection arm, pain in her other arm and nausea/ queasy today.; headache; so tried; unable to sleep; This is a spontaneous report from a contactable consumer (reported for herself). A female patient of an unspecified age received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection), dose 2 via an unspecified route of administration on 22Jul2021 (Batch/Lot number was not reported) as DOSE 2, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. Patient received first dose of BNT162B2 on unspecified date for COVID-19 immunisation. It was reported that received her 2nd dose yesterday (22Jul2021), patient experienced all over aches, pain in the injection arm, pain in her other arm and nausea/ queasy on 23Jul2021. It was reported that from night patient had been aching and she was wondering if she can Tylenol or Ibuprofen. because she got headache and ache. Reporter stated that she went back in her room, she needs to write a number down. she woke up and so tried, unable to sleep. The outcome of all the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1645550
Sex: U
Age:
State:

Vax Date: 07/01/2021
Onset Date: 07/01/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: It's been, kind a like, somebody sitting on my chest.; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for covid-19 immunisation. No medical history and concomitant medications were not reported. On an unspecified date, the patient reported it was been, kind a like, somebody sitting on my chest. The patient reported he had got the vaccine yesterday (Jul2021) and today (Jul2021), it was been, kind a like, somebody sitting on his chest. Patient said, he was just wondering, if he should just go back to where, he got the shot from. He enquired if this was a sign of some kind of a serious allergic reaction to it or was normal. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1645551
Sex: U
Age:
State:

Vax Date: 03/20/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: Developed a small spot, rash on my arm near the site of the injection; red rash size of a quarter on my arm where I got the injection; Developed a small spot, rash on my arm near the site of the injection; red rash size of a quarter on my arm where I got the injection; Developed a small spot, rash on my arm near the site of the injection; red rash size of a quarter on my arm where I got the injection; I have spots over different places in my entire upper torso, generally upper arms and my chest and my back, my stomach; This is a spontaneous report from a contactable consumer or other non hcp. A patient of unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection Lot Number: EN6204) via an unspecified route of administration, administered in Arm on 20Mar2021 as single dose for COVID-19 immunisation. The patient medical history and the patient's concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection Batch/Lot number: was not reported) via an unspecified route of administration on 27Feb2021 as single dose for COVID-19 immunisation. On unknown date in Mar2021, The patient had developed a small spot, rash on my arm near the site of the injection; red rash size of a quarter on my arm where I got the injection. It was surely after getting his/her second shot, he/she did not know exactly when it was, precisely 3 days or four days or a week. It had actually continued to grow 'not in' the armpits, that spot is not growing very much but now he/she had spots over different places in his/her entire upper torso, generally upper arms and chest and back, stomach, not that much but he/she had gotten them, so it seems like it was growing. His/her clinic dermatologist could not schedule anything for 2 months. The seriousness of events was non-serious. The outcome of events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1645552
Sex: F
Age:
State: WI

Vax Date: 07/11/2021
Onset Date: 07/11/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: Cough started the same day of vaccination, productive, 2 weeks; This is a spontaneous report from a contactable consumer, the patient. A 38-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 11Jul2021 at 11:00 (at the age of 38-years-old) as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient had no allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any vaccination within four weeks prior to the vaccination. On 11Jul2021, the patient had cough started the same day of vaccination, which was productive, 2 weeks. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The patient did not receive any treatment for the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event cough started the same day of vaccination, productive, 2 weeks was not recovered at the time of this report. The batch/lot number for BNT162b2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1645553
Sex: M
Age:
State: SC

Vax Date: 07/06/2021
Onset Date: 07/01/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: injected in the wrong area; He says in the joint he can feel it in there; under his arm pit down kind of close to his rib cage.; Shoulder Injury Related to Vaccine Administration; inflammation in the shoulder joint; history of shoulder pain because of arthritis, but it wasn't bothering him until after he got the vaccine; bad shoulder and arm pain; bad shoulder and arm pain; This is a spontaneous report from a contactable consumer. This 69-year-old Male consumer (patient, reported for self). A 69-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EW0161, Expiration date: Unknown), via an unspecified route of administration, administered in Arm Left on 06Jul2021 as (At the age of 69-years) dose 1, single for COVID-19 immunisation. Medical history included arthritis (shoulder pain because of arthritis) from an unknown date and unknown if ongoing. There were no concomitant medications reported by the reporter (Other Products: No). It was reported that on 06Jul2021 around between 1:00PM to 1:30PM parient received the first dose. Reporter stated that it was after this vaccination, that the pain began a couple days after that he had bad shoulder and arm pain. He says this started a couple days after that and it has not gone away or gotten any better. Reporter stated his pain is in the shoulder and arms closer to his elbow, and under his arm pit down kind of close to his rib cage. He says in the joint he can feel it in there. It was reported that he has a history of shoulder pain because of arthritis, but it wasn't bothering him until after he got the vaccine. Upon Follow-up it was reported that reporter was 70 years old but noted that he was 69 when he got the Pfizer- BioNTech COVID-19 Vaccine. The reporter state that bad shoulder and arm pain has not gone away and not gotten better. His main concern was having Shoulder Injury Related to Vaccine Administration (SIRVA) an injury and inflammation in the shoulder joint due to the vaccine being injected in the wrong area. Reporter hung up before survey could be offered. No investigation assessment. Reporter stated he was currently taking medication for pain, Hydrocodone, which came in an orange pill bottle. He says the Hydrocodone dose is 7.5-325mg, and it comes from (Place name withheld) Home RX in (redacted). Hydrocodone LOT/EXP: Unknown, product dispensed in pharmacy bottle. Hydrocodone NDC: 65162-0115-11. He says he takes this once every 6 hours. The outcome of event bad shoulder and arm pain had not recovered, outcome of other events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645554
Sex: F
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: fatigue; This is a spontaneous report from a contactable consumer (Patient). A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number: Unknown), via unspecified route of administration, on an unknown date, as dose 1, single for COVID-19 Immunization. Medical history and concomitant medications were not reported. On an unknown date, the patient experienced fatigue after first dose for three weeks. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1645555
Sex: M
Age:
State: FL

Vax Date:
Onset Date: 07/20/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: They diagnosed that it was a spasm; severe back and nerve pain; severe back and nerve pain; This is a spontaneous report from a contactable consumer. A 45-year-old male received BNT162b2 (BNT162B2, Formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date (age at the time of vaccination was 45 years) as single dose for COVID-19 immunisation. The patient's medical history included bipolar 1 on an unspecified date. The patient's concomitant medications were not reported. The reporter was calling for her son. On 20Jul2021, the patient was in the ER (emergency room) two days ago with severe back and nerve pain and she clarified as lower back nerve pain. They diagnosed that it was a spasm and gave him a muscle relaxer and a few pain meds. the patient got the second Pfizer vaccine just a couple of weeks ago. The patient's body metabolizes things differently because he has bipolar 1. The outcome of the events back pain and neuralgia were recovering, muscle spasms was unknown.

Other Meds:

Current Illness:

ID: 1645556
Sex: F
Age:
State:

Vax Date: 06/10/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Tingling in her arm, hands and legs; they thought it was maybe like a hit nerve when they gave me injection but since then it has all traveled down to my hands and legs; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported for herself. A female patient of an unspecified age received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, Solution for injection), dose 1 via an unspecified route of administration on 10Jun2021 (Batch/Lot Number: EW0180) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient received the Pfizer COVID-19 Vaccine on 10Jun2021 and after receiving it she experiencing tingling in the arm. The symptoms did not go away when in the patient had to be referred to a neurologist and she still have the symptoms the tingling in her arm, hands and legs and also she is asking if there are any others who experienced the side effect. When paraphrased the concern, consumer stated, yes, thought it was maybe like a hit nerve when they gave me injection but since then it had all traveled down to my hands and legs and it had not just isolated to one arm it spread. When probed if it was the first vaccine, Consumer stated that the patient just had the first vaccine because as far as know it was the adverse reaction and so the patient was concerned with taking the second dose. The patient was still trying to remain a little bit anonymous until got more information to whether was this a normal reaction. Have you guys heard this before and typically how long does it take to go away, ight now, the patient was just trying to fish for some information because concern was whether to have the second vaccination especially with this not going away. Patient was informed about the Medical Information Department for the concern and was provided with the contact for Pfizer Medical Information as Option 3 and was informed that the department was open from Monday to Friday, from 8am to 8pm. Patient stated, If you do not mid transferring her, that would be great. The patient was unwilling to complete the report and requested for transfer. Call was disconnected and transfer was unsuccessful. Hence, limited information was available. The outcome of event was unknown.

Other Meds:

Current Illness:

ID: 1645557
Sex: M
Age:
State: NY

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: After received second injection arm felt sore for a couple days; This is a spontaneous report from a contactable consumer (patient) or other non hcp via a Pfizer-sponsored program. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported, Expiry date: unknown), dose 2 via an unspecified route of administration on an unspecified date as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient received first dose of BNT162B2 (PFIZ-ER-BIONTECH COVID-19 VACCINE, Lot number: not reported) on unspecified date for covid-19 immunisation. The reporter believed that the first dose was given correctly but not the second dose. After received second injection arm felt sore for a couple days on an unspecified date. Reporter was asking if there was a test he can receive (at name withheld) whether he had full protection from receiving both shots. Questionable concern about receiving the first shot. Stated there was a mix-up at the vaccination site, questions whether he actually received first dose due to faulty equipment. Asked vaccination provider, did not seem to provide an appropriate answer. Stated there was no indication that he received an injection. No indication of receiving an injection, no sensation, no indication received injection and no reaction. After received second injection arm felt sore for a couple days. Really doubts he received the first. Asking if there was a test to determine whether her had full protection. Stated he called the county where he resides, stated they have no control over. Reporter received both doses of the Pfizer Covid-19 Vaccine and wants to know if there was a blood test that he can take to confirm that he had the full benefit of the vaccine. The clinical outcome of event was unknown. Information on the lot/batch number has been requested. F/U #2 17Aug2021: Follow-up activities closed. Batch/lot number not available.

Other Meds:

Current Illness:

ID: 1645558
Sex: F
Age:
State:

Vax Date: 05/21/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: nerve issues; cold feels in neck, arms and back.; This is a spontaneous report from a contactable consumer or other non-healthcare professional. A 56-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, on 21May2021 as dose 2, single for covid-19 immunisation. The patient's medical history was not reported. The concomitant medications were not reported. Historical vaccine includes first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization and experienced fatigue. On an unspecified date on 2021, 5 weeks after vaccination, the patient experienced cold feels in neck, arms and back. The patient Describes it as nerve issues. The patient stated "Mint fall" on her arms, neck and back which she never had before while she was walking her dog and was still going through it. The patient wanted to know if this was coincidental. HCP indicated could persist up to six weeks. The outcome of the events were unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645559
Sex: F
Age:
State: CA

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: sore arm two or three days; This is a spontaneous report from a contactable consumer (parent). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number and Expiration date were not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced sore arm two or three days on an unspecified date. The outcome of the event was recovered. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1645560
Sex: M
Age:
State: TX

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: Soreness on my shoulder where they gave me the shot; I felt liquid down my arm when he pulled it out. Then he was still squeezing liquid out.; I felt liquid down my arm when he pulled it out. Then he was still squeezing liquid out.; I felt liquid down my arm when he pulled it out. Then he was still squeezing liquid out.; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 63-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection) via an unspecified route of administration, administered in arm on unspecified date in Feb2021 (at the age of 63-years-old) as single dose for COVID-19 immunization. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) administered on an unspecified date in Jan2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date in Feb2021, the second vaccine a young man gave him the shot and he stuck it in faster than he had ever seen. He felt liquid down his arm when he pulled it out. Then he was still squeezing liquid out (at the time of report). Patient asked if there was a test to see if he received the full dose. Upon follow-up on 23Jul2021, the patient stated that he felt as if the vaccination provider had put in the needle very quickly and felt as if some of the vaccine had dripped out when removing the needle, perhaps didn't receive a full second vaccination and also reported that gave him the shot it was a real quick, when he pulled it out felt some liquid hit his arm, his shoulder, saw some stuff coming out the needle, not confident that he got the full dose on that second shot. On unknown date, patient experienced soreness on his shoulder where they gave the shot. Patient could not provide the date of administration and LOT# as the vaccination card is not with the consumer. Consumer stated regarding concomitant medication as no and he had taken is some over the counter Advil and Tylenol at different points. Patient inquired that whether he need another shot or is it enough which he got already. Outcome of the events were unknown. Information on lot/batch number has been requested. Follow-up (23Jul2021): New information received from contactable consumer (patient) via Pfizer-sponsored program includes: patient weight and height, age at time of onset of reaction, event (Soreness on my shoulder where they gave me the shot) added and clinical information updated.

Other Meds:

Current Illness:

ID: 1645561
Sex: M
Age:
State: NY

Vax Date: 07/21/2021
Onset Date: 07/22/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: Fever; Swollen lymph Nodes; Swollen arm; Painful Arm; Muscle aches; Weakness; This is a spontaneous report from a contactable consumer, the patient. A 42-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FA7485) via an unspecified route of administration in left arm on 21Jul2021 at 09:45 (at the age of 42-years-old) as a single dose for COVID-19 immunisation. The patient had no medical history. Prior to the vaccination, it was unknown whether the patient diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medication within two weeks of vaccination. The patient had no known allergies to food, medication or other products. On 22Jul2021, the patient experienced fever, swollen lymph nodes, swollen arm, painful arm, muscle aches and weakness. The events did not result in a visit to the doctors or other healthcare professional office/clinic visit and emergency room/department or urgent care. No therapeutic measures were taken as a result of adverse events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events, fever, swollen lymph nodes, swollen arm, painful arm, muscle aches and weakness were recovering at the time of this report.

Other Meds:

Current Illness:

ID: 1645562
Sex: M
Age:
State: NY

Vax Date: 06/24/2021
Onset Date: 06/27/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: Random headaches; Loss of energy; Stomach pains; This is a spontaneous report from a contactable consumer, the patient. A 33-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ew0181) via an unspecified route of administration in the left arm on 24Jun2021 at 11:30 (at the age of 33-years-old), as a single dose for COVID-19 immunisation. The patient had no medical history. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient did not take any concomitant medications. On 27Jun2021 at 00:30, the patient experienced random headaches, loss of energy and stomach pains. The events did not result in doctor or other healthcare professional office or clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as the result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events random headaches, loss of energy and stomach pains were unknown at the time of reporting.

Other Meds:

Current Illness:

ID: 1645563
Sex: M
Age:
State: GA

Vax Date: 07/22/2021
Onset Date: 07/23/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: Right foot pain and swelling; Right foot pain and swelling; This is a spontaneous report from a contactable consumer, the patient. A 39-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 22Jul2021 at 14:00 (at the age of 39-years-old), as a single dose for COVID-19 immunisation. Concomitant medications were not reported. The patient previously received sulfur (MANUFACTURER UNKNOWN) for unspecified indication on unknown date and experienced drug allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 23Jul2021 at 10:00, the patient experienced right foot pain and swelling. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event right foot pain and swelling was not recovered at the time of this report. The batch/lot numbers for BNT162b2 were not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1645564
Sex: M
Age:
State: MI

Vax Date: 07/21/2021
Onset Date: 07/21/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Facial muscle spasm; This is a spontaneous report from a contactable consumer, the patient. A 17-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0180) via an unspecified route of administration in the left arm on 21Jul2021 at 14:15 (at the age of 17-year-old) as a single dose and the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Fa6780) via an unspecified route of administration in the left arm on an unspecified date in 2021 as a single dose for COVID-19 immunisation. Medical history included asthma, seasonal allergy and COVID-19. Prior to the vaccination, the patient was diagnosed with COVID-19. Concomitant medications included levocetirizine dihydrochloride (XYZALL) and multivitamins (MANUFACTURER UNKNOWN) for unknown indications, started from unknown dates and unknown if ongoing. The patient was allergic to shellfish, ragweed and mold. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 21Jul2021 at 21:00, the patient experienced facial muscle spasm. It was unknown whether any therapeutic measures were taken as a result of the event facial muscle spasm. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event facial muscle spasm was unknown at the time of this report.

Other Meds: XYZALL

Current Illness:

ID: 1645565
Sex: F
Age:
State: NC

Vax Date: 07/23/2021
Onset Date: 07/23/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: really tired; Chills 7 hours after vaccine; achy including at hips; achy including at joints; This is a spontaneous report from a contactable consumer, the patient. A forty-eight-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: FA6780) via an unspecified route of administration in the left arm on 23Jul2021 at 15:00 (at the age of forty-eight-year-old) as a single dose for COVID-19 immunisation. The medical history included COVID-19, allergy to penicillin and sulfas. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The concomitant medications included bupropion hydrochloride (WELLBUTRIN) and cetirizine hydrochloride (ZYRTEC), all from unknown dates and for unknown indications. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: 6W0181) via an unspecified route of administration in the left arm on 02Jul2021 at 12:00 (at the age of 47-year-old) as a single dose for COVID-19 immunisation. On 23Jul2021 at 22:00, 7 hours after vaccination, the patient experienced chills, achy including at hips and joints. On 24Jul2021, next full day, patient was achy and was really tired. The adverse events did not result in doctor or other health care professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures were taken as a result of the reported events which included treatment with Tylenol and Advil OTC(over the counter). Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events chills, achy at hips and joints and really tired was not recovered at the time of this report.

Other Meds: WELLBUTRIN; ZYRTEC (CETIRIZINE HYDROCHLORIDE)

Current Illness:

ID: 1645566
Sex: F
Age:
State: NC

Vax Date: 07/24/2021
Onset Date: 07/24/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data:

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: Dizziness; Feeling flush; "Feeling as if i were having a panic attack"; This is a spontaneous report from a contactable consumer, the patient. A 54-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FA7484) via an unspecified route of administration in the left arm on 24Jul2021 at 15:45 (at the age of 54-years-old) as a single dose for COVID-19 immunisation. Medical history included panic disorder. The patient had no allergies to medications, food and other products. Concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 24Jul2021 at 22:30, the patient experienced dizziness, feeling as if she were having a panic attack and feeling flush. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The patient did not receive any treatment for the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events dizziness, "feeling as if having a panic attack" and feeling flush were unknown at the time of this report.

Other Meds:

Current Illness:

ID: 1645567
Sex: F
Age:
State: AL

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: Vasculitis; Result Unstructured Data: Test Result:Unknown result

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: developed a rash similar to hives; developed a rash similar to hives; This is a spontaneous report from a contactable physician. A 17-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number and expiration date were 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 medication were not reported. The patient developed a rash similar to hives in appearance is now being tested for vasculitis. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1645568
Sex: F
Age:
State: MA

Vax Date: 04/28/2021
Onset Date: 07/12/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: 2 menstrual periods in a space of less than 1 month:1st day pf period: June 20 Last day of period: June 271st day of period: July 12 Last day of period: ongoing; This is a spontaneous report from a contactable consumer, the patient. A 38-year-old female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW182) via an unspecified route of administration in the right arm on 28Apr2021(at the age of 37-years-old) as a single dose for COVID-19 immunisation. The patient had no other medical history and had no known allergies to medications, food, or other products. Concomitant medications taken within two weeks of vaccination included paracetamol (ACETAMINOPHEN) and docusate sodium (STOOL SOFTENER). The patient previously took first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0170) via an unspecified route of administration in the right arm on an unknown date (age at vaccination unknown) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 12Jul2021 at 12:00, the patient experienced a shortened menstrual cycle. It was reported that the patient experienced two menstrual periods in a space of less than one month: first day pf period: 20Jun2021 Last day of period: 27Jun2021; first day of period: 12Jul2021 Last day of period: ongoing at the time of report. No therapeutic measures were taken as a result of the events. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The clinical outcome of the event two menstrual periods in a space of less than one month: first day pf period: 20Jun2021 Last day of period: 27Jun2021; first day of period: 12Jul2021 Last day of period: ongoing at the time of report was not resolved at the time of this report. No follow-up attempts are possible. No further information is expected.

Other Meds: ACETAMINOPHEN; STOOL SOFTENER

Current Illness:

ID: 1645569
Sex: F
Age:
State: AR

Vax Date: 03/18/2021
Onset Date: 03/20/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210702; Test Name: NACR; Test Result: Negative ; Comments: Nasal Swab

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: Burping; Intestinal gas; Ongoing burping and intestinal gas -since first dose but worse after 2nd; This is a spontaneous report from a contactable consumer, the patient. A 56-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6198) via an unspecified route of administration in the left arm on 18Mar2021 (at the age of 56-years-old) as a single dose for COVID-19 immunisation. The patient also received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on an unknown date in 2021 as a single dose for COVID-19 immunisation. Medical history included ongoing sinus disorder for decades. Patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The patient received other medications within two weeks of COVID- 19 vaccine, names were unspecified. On 20Mar2021, the patient experienced ongoing burping and intestinal gas - since first dose but worse after second. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had been tested for COVID-19. On 02Jul2021, the patient underwent NACR (SARS COV-2 test; Nasal swab), and the result was Negative. The clinical outcome of the events ongoing burping and intestinal gas was unknown at the time of this report.

Other Meds:

Current Illness: Sinus disorder (Ongoing sinus issues for decades)

ID: 1645570
Sex: M
Age:
State: NE

Vax Date: 07/23/2021
Onset Date: 07/24/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Bloody nose twice; This is a spontaneous report from a contactable consumer, the patient. A 15-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 23Jul2021 at 13:15 (at the age of 15-years-old) as a single dose for COVID-19 immunisation. Medical history included bicuspid aortic valve. The patient was allergic to penicillin. The patient did not receive any other medications within 2 weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 24Jul2021 at 00:00, the patient experienced bloody nose once and again on the same day at 03:00. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No therapeutic measures were taken as a result of the event. The clinical outcome of the event bloody nose twice was resolving at the time of this report. The lot number for BNT162b2 was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1645571
Sex: F
Age:
State: VA

Vax Date: 04/05/2021
Onset Date: 07/04/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Date: 202107; Test Name: Ultrasound; Result Unstructured Data: Test Result:UNKNOWN; Test Date: 202107; Test Name: Preventative Mammogram; Result Unstructured Data: Test Result:UNKNOWN

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Possible enlargement of the lymphatic node (1) due to COVID-19 vaccination. No other abnormalities; This is a spontaneous report from a contactable consumer, the patient. A 41-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 05Apr2021 (at the age of 40-year-old) as a single dose for COVID-19 immunisation. Medical history included thyroid carcinoma (post thyroid carcinoma/remission since 2016). The patient did not have any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included levothyroxine (MANUFACTURER UNKNOWN) 137 mcg for unknown indication received within 2 weeks of vaccination. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. On 04Jul2021, the patient had a preventative mammogram, called back for additional ultrasound on the left breast and experienced possible enlargement of the lymphatic node (1) due to COVID-19 vaccination. The patient did not have other abnormalities. The event resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had not been tested for COVID-19. No therapeutic measures were taken as a result of the reported event. The clinical outcome of the event possible enlargement of the lymphatic node was unknown at the time of this report. The batch/lot numbers for, BNT162b2, were not provided and will be requested during follow up.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1645572
Sex: F
Age:
State: NC

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Date: 20210302; Test Name: Body temperature; Result Unstructured Data: Test Result:102; Comments: at 15:00

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: Fever of 102; Aches; Chills; General weakness; Very tired; Dose 1: 17Feb2021; Dose 2: 01Mar2021 at 11:00; Pain in L arm seemed to spread up the left side of neck in the tendon; Neck stiffness; Pain in L arm seemed to spread up the left side of my neck in the tendon; Tingling and numbness in left hand outer 3 fingers off and on all day for weeks; Tingling and numbness in left hand outer 3 fingers off and on all day for weeks, the tingling led to numbness after a few weeks of outer two fingers and the left side of foot below the ankle.; Feel sick; This is a spontaneous report from a contactable healthcare professional, the patient. A 67-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6206) via an unspecified route of administration in the left arm on 01Mar2021 at 11:00 (at the age of 67-year-old) as a single dose for COVID-19 immunisation. The patient had no medical history. The patient had no known allergies reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6200) via an unspecified route of administration in the left arm on 17Feb2021 (at the age of 67-year-old) as a single dose for COVID-19 immunisation. On 02Mar2021 at 15:00, a day after the second vaccination, the patient experienced a fever of 102 (unspecified units). The fever had lasted for two days with aches and chills. The patient was out of work for 3 to 4 days with general weakness due to fever and was very tired for 2 to 3 weeks. On an unknown date in Mar2021, following the fever, in the first few days, the patient experienced pain in the left (L) arm which seemed to spread up the left side of the neck in the tendon (neck stiffness). On an unknown date in 2021, the patient experienced tingling and numbness in the left hand outer three fingers off and on all day for weeks. The patient reported that the tingling led to numbness after a few weeks of the outer two fingers and the left side of the foot below the ankle became numb. The patient sought help from a physical therapist but it was so painful that the patient felt sick the following day. In Jun2021, the patient began to notice returning of feeling to the left hand. The numbness had gone but the outer part of the left foot still had an area that felt different, as it would tingle from time to time. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were taken as a result of the events pain in L arm seemed to spread up the left side of neck in the tendon and neck stiffness which included treatment with massage therapy and for event tingling and numbness in left hand outer 3 fingers off and on all day for weeks, the tingling led to numbness after a few weeks of outer two fingers and the left side of foot below the ankle which included unspecified treatment from a physical therapist. The clinical outcome of the event fever of 102 (unspecified units), aches, and chills were recovered on 04Mar2021, after the duration of 2 days. The clinical outcome of the events general weakness and very tired were recovered on an unknown date in Mar2021. The clinical outcome of the events pain in L arm seemed to spread up the left side of neck in the tendon, neck stiffness, tingling and numbness in left hand outer 3 fingers off and on all day for weeks, the tingling led to numbness after a few weeks of outer two fingers and the left side of foot below the ankle, feel sick were recovered on an unknown date in 2021.

Other Meds:

Current Illness:

ID: 1645573
Sex: F
Age:
State: MO

Vax Date: 07/19/2021
Onset Date: 07/23/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: It still has fever in the injection site; I broke out in hives and it still has fever in the injection site; This is a spontaneous report from a contactable consumer, the patient. A 44-year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EWO182) via an unspecified route of administration in the left arm on 19Jul2021 at 10:15 (at the age of 44-years-old) as a single dose for COVID-19 immunisation. Medical history included heart problems but still waiting on her test results. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included acetylsalicylic acid (BAYER CHILDREN'S ASPIRIN) from on an unknown date for unknown indication and unknown if ongoing. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: TR8765) via an unspecified route of administration in the left arm on 28Jun2021 at 10:15 (at the age of 44-years-old) as a single dose for COVID-19 immunisation. The patient also took codeine (MANUFACTURER UNKNOWN) for unknown indication on an unknown date and experienced drug allergy. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 23Jul2021 at 09:00, the patient experienced broke out in hives and still it had fever in the injection site 4 days after. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were taken as a result of reported events which included treatment with over-the-counter allergy medication. The clinical outcome of events broke out in hives and still had fever in the injection site was recovering at the time of this report.

Other Meds: BAYER CHILDREN'S ASPIRIN

Current Illness:

ID: 1645574
Sex: F
Age:
State: CO

Vax Date: 07/20/2021
Onset Date: 07/22/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Menstrual bleeding began two weeks ahead of schedule. Have been regular 28 day period for 20 years with no spotting; This is a spontaneous report from a contactable nurse, the patient. A 35-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0181) via an unspecified route of administration in the arm right on 20Jul2021 at 15:30 (at the age of 35-year-old) as a single dose for COVID-19 immunisation. Medical history included hypertension (HTN), cold sores, endometriosis and infertility. The patient was allergic to penicillin. Concomitant medication included labatelol (MANUFACTURER UNKNOWN) and famcyclovir (MANUFACTURER UNKNOWN), all from an unknown date for an unknown indication. Prior to vaccination, the patient was not diagnosed with COVID-19.Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 22Jul2021 at 08:00, the patient experienced menstrual bleeding began two weeks ahead of schedule. Have been regular 28 day period for 20 years with no spotting. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. The clinical outcome of the event irregular menstrual cycle was unknown.

Other Meds:

Current Illness:

ID: 1645575
Sex: M
Age:
State:

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 20210710; Test Name: Nasal swab; Test Result: Negative

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Persistent, constant ringing in both ears since the second shot.; Some dizziness; Loss of balance; Headaches; This is a spontaneous report from a contactable consumer, the patient. A 54-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 27Jan2021 (at the age of 54-years-old) as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient had no known allergies. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 06Jan2021 (at the age of 54-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 27Jan2021, since the second shot, the patient experienced persistent constant ringing in both ears, dizziness, loss of balance and headaches. The events resulted in doctor or other healthcare professional office/clinic visit, and the doctor diagnosed it as tinnitus. The patient had mentioned that there was some data on these symptoms after Pfizer second shot and the doctor said there was not enough data. Therapeutic measures were taken as a result of the events and included treatment with prescription medication and over the counter medications. On 10Jul2021, the patient underwent COVID-19 test (nasal swab) and the result was negative. The clinical outcome of the events persistent constant ringing in both ears, dizziness, loss of balance and headaches were not resolved at the time of this report. The lot number for BNT162b2 was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1645576
Sex: F
Age:
State: PA

Vax Date: 07/02/2021
Onset Date: 07/03/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Swollen and very painful lymph nodes in injected arm/ Occasional lymph node pain; Swollen and very painful lymph nodes in injected arm; This is a spontaneous report from a contactable consumer, the patient. A 66-year-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0181) via an unspecified route of administration in the left arm on 02Jul2021 at 17:15 (at the age of 66-years-old) as a single dose for COVID-19 immunisation. Medical history included allergy related asthma and COVID-19 (Prior to the vaccination, the patient was diagnosed with COVID-19). The patient had known allergies to penicillin, dairy and latex. Concomitant medications included centrum vitamins, linum usitatissimum seed oil (FLAX SEED OIL) and loratadine (CLARITIN ALLERGY) from on an unknown date for unspecified indication and unknown if ongoing. The patient took ibuprofen (MANUFACTURER UNKNOWN) for unknown indication on an unknown date and experienced drug allergy. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 03Jul2021 at 17:00, the patient experienced swollen and very painful lymph nodes in injected arm for 4 days. Lessened, but continuous pain for 1 week. Occasional lymph node pain for 3 weeks to date. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. No therapeutic measures were taken as a result of the reported events. The clinical outcome of event swollen and very painful lymph node was not recovered at the time of this report.

Other Meds: FLAX SEED OIL; CLARITIN [LORATADINE]

Current Illness:

ID: 1645577
Sex: M
Age:
State: NY

Vax Date: 07/23/2021
Onset Date: 07/23/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 2021; Test Name: BMI; Result Unstructured Data: Test Result:> 99 percentile

Allergies:

Symptom List: Injection site pain

Symptoms: He had a sore arm; Things smelled different but did not lose sense of smell; Intermittent nosebleeds; Headache; It was just one patient who got an entire vial of vaccine/ it was full vial of .45mL of undiluted vaccine that was administered for the 6x overdose.; It was just one patient who got an entire vial of vaccine/ it was full vial of .45mL of undiluted vaccine that was administered for the 6x overdose.; This is a spontaneous report from a contactable consumer or other non-Health Care Professional. A 17-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and Expiry date: Unknown, age at vaccination 17 years), via an unspecified route of administration on 23Jul2021 as DOSE 1, 0.45 ML SINGLE for covid-19 immunization. The patient's medical history includes severe obesity from Jun2021 and ongoing Severe obesity due to excess calories and BMI > 99 percentile for age in pediatric patient. Concomitant medications include METFORMIN for severe obesity from Mar2021 and ongoing. Caller reported it was just one patient who got an entire vial of vaccine on an unspecified date 2021. The patient got first dose of Pfizer vaccine (unspecified vaccine) on 23Jul2021, but they got all six doses from the 3 ml instead of just one. Reporter sent them to the emergency room because, don't know how they are going to react to all the six doses one time, but wanted to know if Pfizer had any additional information report, if it happened before. Upon follow-up on 03Aug2021, Nurse confirmed it was full vial of .45mL of undiluted vaccine that was administered for the 6x overdose on 23Jul2021. Patient went to ER for monitoring. The ER sent him home and on an unspecified date his mother reported he had a sore arm, things smelled different but did not lose sense of smell, intermittent nosebleeds, and headache on an unspecified date. The update was provided on 27Jul2021, but the symptoms happened before the mother called, so the nurse was not sure of the exact onset for each. Clinical outcome of all symptoms was recovered or resolved on unspecified date in 2021 and the outcome of other events was unknown. Information about lot/batch number has been requested. Follow-up (23Jul2021): New information received from a contactable other hcp (Nurse) included: patient's gender (male), relevant medical history, event onset date, concomitant medications. Follow up(03Aug2021): This is a follow up-spontaneous report from a contactable Nurse in response to HCP letter sent via follow-up letter which included that: Additional events coded along with outcome (he had a sore arm; things smelled different but did not lose sense of smell, intermittent nosebleeds, and headache); verbatim of overdose updated (it was just one patient who got an entire vial of vaccine/ it was full vial of .45mL of undiluted vaccine that was administered for the 6x overdose) and coded as Product preparation issue and other relevant information. Information about lot/batch number will be requested during follow up.

Other Meds: METFORMIN

Current Illness: Obesity (Severe obesity due to excess calories and BMI > 99 percentile for age in pediatric patient)

ID: 1645578
Sex: U
Age:
State:

Vax Date: 07/21/2021
Onset Date: 07/22/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: Fever; Runny nose; Fatigue; Tenderness/ soreness at injection site; Tenderness/ soreness at injection site and left side of breast; Swollen lymph nodes; Redness near injection site; Pain at armpit area; Left arm warmer, where injection site is on, than the right arm; This is a spontaneous report from a non-contactable consumer, the patient. A 35-year-old patient of unknown gender received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 21Jul2021 at 10:30 (at the age of 35-years-old), as a single dose for COVID-19 immunisation. Medical history included rheumatoid arthritis. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications included salbutamol (ALBUTEROL), allergy pills (MANUFACTURER UNKNOWN) and nasal spray for allergies; all from unknown dates for unknown indications. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 30Jun2021 at 17:30 (at the age of 35-years-old), as a single dose for COVID-19 immunisation. The patient previously took amoxicillin (MANUFATURER UNKNOWN) on unknown date for an unspecified indication and experienced drug allergy. On 22Jul2021 at 03:30, the patient experienced fever, runny nose, fatigue, tenderness/ soreness at injection site and left side of breast, swollen lymph nodes, pain at armpit area, redness near injection site that was still visible after 36 hours and left arm warmer, where injection site is on, than the right arm. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events fever, runny nose, fatigue, tenderness/ soreness at injection site and left side of breast, swollen lymph nodes, pain at armpit area, redness near injection site that was still visible after 36 hours and left arm warmer, where injection site is on, than the right arm were unknown at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: ALBUTEROL [SALBUTAMOL]

Current Illness:

ID: 1645579
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: trouble breathing; This is a spontaneous report from a contactable consumer (reported for self). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), dose 2 via an unspecified route of administration on an unspecified date as dose 2, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunisation. On an unspecified date, the patient experienced trouble breathing. The outcome of the event was unknow. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1645580
Sex: M
Age:
State: DC

Vax Date: 03/08/2021
Onset Date: 03/14/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Ears swollen inside-no infection anywhere; Loss of taste and smell; Loss of taste and smell; This is a spontaneous report from a contactable consumer, the patient. A 66-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6199) via an unspecified route of administration in the right arm on 08Mar2021 at 12:00 (at the age of 66-year-old) as a single dose for COVID-19 immunisation. Medical history included asthma, thyroid, and type 2 diabetes mellitus (controlled) from an unknown date. The patient had an allergy to dust and dog and cat dander. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any vaccines within four weeks prior to the COVID-19 vaccine. Concomitant medications included unspecified thyroid medication and metformin (MANUFACTURER UNKNOWN) for unknown indications from unknown dates and unknown if ongoing. On 14Mar2021 at 12:00, the patient had a loss of smell and taste. The ears were swollen inside and there was no infection anywhere. Other than the events reported, the patient actually felt okay and could exercise and live as normal. The patient could only smell or taste the dust. The events resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were taken as a result of the events which included treatment with montelukast sodium (SINGULAIR). The clinical outcome of the events loss of taste and smell and ears swollen inside-no infection anywhere were not recovered at the time of this report.

Other Meds: METFORMIN

Current Illness:

ID: 1645581
Sex: F
Age:
State: AR

Vax Date: 07/22/2021
Onset Date: 07/22/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210722; Test Name: Fever; Result Unstructured Data: Test Result:over 102.1

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Then about 10:30 pm I started vomiting. And continued vomiting all night long/Around 9:30 am finally quit vomiting; The nausea was awful/feel very nauseous.; The nausea was awful; The second shot was way worse; Running a fever/My fever was over 102.1; Aching/My whole body ached; Head hurting/my head felt like it was going to explode; This is a spontaneous report from a contactable consumer (patient herself). A 54-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: 59267-1000-01), via an unspecified route of administration, administered in left arm on 22Jul2021 10:00 (age at vaccination: 54 years) as DOSE 2, SINGLE for covid-19 immunisation. The patient's medical history included food allergy to hazelnuts and almonds. There were no concomitant medications. The patient previously took sulfamethoxazole and experienced drug hypersensitivity, bnt162b2 for covid-19 immunisation on 01Jul2021 00:00 in the left arm and experienced headache, neck pain and malaise. The second dose of vaccine was administered in the pharmacy. There were no other medications the patient received within 2 weeks of vaccination. On 22Jul2021 21:30, the patient experienced was awful/felt very nauseous, the second shot was way worse, running a fever/ fever was over 102.1 ((because that was taken after vomiting, brushing my teeth, and drinking cold water), aching/her whole body ached, head hurting/ head felt like it was going to explode, then on the same date about 22:30, she started vomiting and continued vomiting all night long/around 9:30 am finally quit vomiting but continued to feel nauseous. On 22Jul2021, the patient underwent lab tests and procedures which included body temperature was over 102.1. The patient did not receive treatment for the adverse events. The patient was not diagnosed with covid-19 prior to vaccination nor was tested for covi-19 since the vaccination. The outcome of vomiting was recovered on 23Jul2021 09:30 and all the other events were not recovered. The device date was 23Jul2021. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645582
Sex: M
Age:
State:

Vax Date: 07/15/2021
Onset Date: 07/18/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: Insomnia for 3 nights; This is a spontaneous report from a contactable consumer, the patient. A 34-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FA 6780) via an unspecified route of administration in the left arm on 15Jul2021 (at the age of 34-years-old) as a single dose for COVID-19 immunisation. The patients' medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER 8727) via an unspecified route of administration on 18Jun2021 (at the age of 34-years-old) as a single dose for COVID-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccination. On 18Jul2021, the patient experienced insomnia for 3 nights. The event did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event insomnia for 3 nights resolving at the time of this report.

Other Meds:

Current Illness:

ID: 1645583
Sex: F
Age:
State:

Vax Date: 07/10/2021
Onset Date: 07/11/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 2021; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result: Unknown; Comments: Nasal Swab.

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: Persistent headache; This is a spontaneous report from a non-contactable consumer (patient). A 43-year-old (also the age at time of vaccination) non-pregnant at the time of vaccination female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 10Jul2021 16:00 (Batch/Lot Number: EW0198) as DOSE 2, SINGLE for COVID-19 immunization. The patient had COVID-19 on unknown date prior to vaccination. There were no concomitant medications. The patient had the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on 10Jun2021 (Lot number: EW0186) at 09:45 AM at the age of 43-years-old as COVID-19 immunization. Then, the 2nd dose on 10Jul2021 16:00. On 11Jul2021 08:00 (also reported as two weeks after second injects), the patient experienced persistent headache. The event resulted to emergency room/department or urgent care and was treated with unspecified intravenous (IV) medication. The patient had nasal swab in 2021 with unknown results. Outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1645584
Sex: F
Age:
State: CA

Vax Date: 07/23/2021
Onset Date: 07/23/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: She was given her first Pfizer COVID-19 vaccination and within 20 minutes she experienced a tight and swollen throat.; She was given her first Pfizer COVID-19 vaccination and within 20 minutes she experienced a tight and swollen throat; This is a spontaneous report from a contactable consumer. A 58-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: unknown, expiry date: unknown) via unspecified route of administration on 23Jul2021 (age at vaccination: 58-years) as dose 1, single for covid-19 immunisation. Patients medical history included anaphylaxis reactions from an unspecified date and un-known if ongoing (has a history of anaphylaxis reactions). Concomitant medications were not reported. On 23Jul2021, within 20 minutes of vaccination, she experienced a tight and swollen throat. She stated the symptoms were mild and that she had experienced anaphylaxis many times in the past and carries an EpiPen. She was observed in the clinic for worsening and she declined steroids. She never used her EpiPen and was sent home. The clinic advised her not to get the second vaccine. No treatment was given for the adverse events. The outcome of the events was not recovered. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1645585
Sex: F
Age:
State: NC

Vax Date: 07/24/2021
Onset Date: 07/24/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: super sleepy; worst headache; eyes are watering; just feel like absolute trash; I feel exactly how I felt if not worse than when I actually got Covid-19 months ago.; This is a spontaneous report from a contactable consumer, the patient. A 19-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 24Jul2021 at 16:00 (at the age of 19-years-old), as a single dose for COVID-19 immunisation. Medical history included asthma, anxiety, depression, transgender, allergies and COVID-19. Prior to the vaccination, the patient was diagnosed with COVID-19. Concomitant medications included testosterone (MANUFACTURER UNKNOWN), fluoxetine hydrochloride (PROZAC) and cetirizine hydrochloride (ZYRTEC); all for unspecified indication from unknown date and unknown if ongoing. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 24Jul2021 at 01:00, the patient just felt like absolute trash, was super sleepy, had the worst headache, eyes were watering and felt exactly how she felt if not worse than when patient actually got COVID-19 months ago. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event just felt like absolute trash, was super sleepy, had the worst headache, eyes were watering and felt exactly how she felt if not worse than when patient actually got COVID-19 months ago was not recovered at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: TESTOSTERONE; PROZAC; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1645586
Sex: M
Age:
State:

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: Rash on arm where shot was at and the chest; Rash on arm where shot was at and the chest; This is a spontaneous report from a contactable consumer or other non HCP (patient). A male patient of an unspecified age received bnt162b2 (BNT162B2, formulation; Solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient had rash on arm where shot was at and the chest. The outcome of events was unknown. The lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645587
Sex: F
Age:
State: FL

Vax Date: 07/02/2021
Onset Date: 07/09/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Right lower eyelid twitching; Sore deltoid muscle; This is a spontaneous report from a contactable healthcare professional, the patient. A 52-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8735) via intramuscular route of administration in the left arm on 02Jul2021 at 11:00 (at the age of 52-year-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies to sulfa and penicillin. The patient did not receive any concomitant medications. prior to the vaccination, it was unknown if the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0176) via intramuscular route of administration in the left arm on 11Jun2021 at 11:00 (at the age of 52-year-old) as a single dose for COVID-19 immunisation. On 09Jun2021 the patient experienced sore deltoid muscle and right lower eyelid twitching. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. No therapeutic measures were taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19.The clinical outcome of the events sore deltoid muscle and right lower eyelid twitching was not resolved at the time of this report.

Other Meds:

Current Illness:

ID: 1645588
Sex: F
Age:
State: AR

Vax Date: 07/23/2021
Onset Date: 07/24/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: Headache (waning); Tiredness; Arm muscle pain; Clammy; hot and cold flashes; This is a spontaneous report from a non-contactable consumer, the patient. A 31-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 23Jul2021 at 16:45 (at the age of 31-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient did not have any allergies to medications, food, or other products. The patient did not receive any concomitant medication within two weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 24Jul2021 at 00:00 the patient experienced headache (waning), tiredness, arm muscle pain, clammy, hot and cold flashes. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. No therapeutic measures were taken as a result of the reported events. The clinical outcome of the events headache (waning) was recovering and the clinical outcome of the events tiredness, arm muscle pain, clammy and hot and cold flashes was unknown at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1645589
Sex: U
Age:
State: FL

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: Covid test; Test Result: Positive; Comments: patients who have been vaccinated (unsure of which Covid-19 vaccine or vaccines) and that many of them test positive afterwards.

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: patients who have been vaccinated (unsure of which Covid-19 vaccine or vaccines) and that many of them test positive afterwards,; patients who have been vaccinated (unsure of which Covid-19 vaccine or vaccines) and that many of them test positive afterwards, many of them are positive with the variants of Covid-19; The initial case was missing the following minimum criteria: ICH unspecified no. of patients. Upon receipt of follow-up information on 13Aug2021, this case now contains all required information to be considered valid. This is a spontaneous report from a contactable consumer (Patient). A 57-year-old patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot Number: Unknown) via intramuscular, in the left arm (left shoulder) on Mar2021 at 12:00 (at the age of 57-years-old) as dose 2, single and dose 1 bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot Number: Unknown) via intramuscular, in the left arm (left shoulder) on Feb2021 at 11:00 (at the age of 57-years-old) as dose 1, single for covid-19 immunisation. Vaccination facility type was military base. The patient medical history and concomitant medications were none. The patient did not receive any vaccines within four weeks prior to the vaccination. Caller stated that patients who have been vaccinated (unsure of which covid-19 vaccine or vaccines) and that many of them test positive afterwards, (drug ineffective and sars-cov-2 test positive). Although fully vaccinated patient became severally infected with Delta Covid variant, within 6 months of vaccinations. Patient had no reactions to the vaccine when given. Seriousness criteria reported persistent, significant disability, incapacity, important medical event. The patient did not receive any treatment for the event. Adverse event required visit to emergency room. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on an unspecified date. Outcome of the events was recovering. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up. Sender's Comments: Linked Report(s): US-PFIZER INC-202100942252 Same reporter, drug and different patient, event.

Other Meds:

Current Illness:

ID: 1645590
Sex: F
Age:
State:

Vax Date: 05/01/2021
Onset Date: 05/01/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: Atrial fibrillation; feeling weak; Dizzy; Nauseous; chronic fatigue; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 01May2021 (Batch/Lot number was not reported; at the age of 61-years) as DOSE 1, SINGLE for COVID-19 immunisation. The patient's medical history was not reported. Concomitant medications included gabapentin (NEURONTIN); famotidine (PEPCID [FAMOTIDINE]). On 01May2021, it was reported that the patient had horrible symptoms with the Pfizer Covid-19 Vaccine. Patient stayed there out of the place because they thought she was drunk, but she slept all weekend long basically and later found out that she went into atrial fibrillation because of that. On the same day, patient also was feeling weak and dizzy; was nauseous and had like chronic fatigue. The patient was advised not to take the second dose. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds: NEURONTIN; PEPCID [FAMOTIDINE]

Current Illness:

ID: 1645591
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Shingles; This is a spontaneous report from a contactable consumer. A patient of unknown age and gender received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNOWN) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Prior to vaccination, it was unknown whether the patient was diagnosed with COVID-19. It was unknown if the patient received any other vaccines within 4 weeks prior to the COVID vaccine. On an unknown date, the patient experienced shingles. Since the vaccination, it was unknown whether the patient had been tested for COVID-19. It was unknown whether any therapeutic measures were taken as a result of the event. The clinical outcome of the event shingles was unknown at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1645592
Sex: M
Age:
State: IN

Vax Date: 07/09/2021
Onset Date: 07/10/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: pain in arm; This is a spontaneous report from a contactable consumer, the patient. A 33-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 09Jul2021 at 15:30 (at the age of 33-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies. The patient did not receive any medication within 2 weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 17Jun2021 at 17:00 (at the age of 33-years-old) as a single dose for COVID-19 immunisation. On 10Jul2021 at 00:00, the patient experienced pain in arm and it was ongoing 14 plus days after the vaccine. The event did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. The clinical outcome of the event pain in arm was not resolved at the time of this report. The lot number for BNT162b2 was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1645593
Sex: F
Age:
State: NH

Vax Date: 06/21/2021
Onset Date: 06/22/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 202106; Test Name: bi-weekly at client; Test Result: Negative

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: she had a fever; sore arm; tired; swollen tonsils with red/white spots; Within a couple days she had swollen tonsils with red/white spots; This is a spontaneous report from a contactable consumer. A 20-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number: EW0196) dose 2 via an unspecified route of administration on 21Jun2021 (at the age of 20-year-old) as single dose for COVID-19 immunisation at pharmacy or drug store. Medical history was none. No known allergies. Concomitant medications were unspecified. Historical Vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number: EW0180) dose 1 an unspecified route of administration on 30May2021 (at the age of 20-year-old) as single dose for COVID-19 immunisation and she was fine after 1st vaccine. 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. On 22Jun2021, after the second dose she had a fever, sore arm, and tired. Within a couple days she had swollen tonsils with red/white spots. She has been on antibiotics for month, which has helped with spots, but still has swollen tonsils. She still feels more tired than usual but not as bad as day after the 2nd vaccine. She is going to an ENT on 30Jul2021. The adverse event resulted in Doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had been tested for COVID-19. The patient underwent lab tests which included post vaccination bi-weekly at client in Jun2021: Negative. The outcome of events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645594
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: MRI; Result Unstructured Data: Test Result:lipoma; Test Name: ultrasound; Result Unstructured Data: Test Result:lipoma

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Had a very bad reaction and I have a lifetime deformity on my arm; Got a golf ball size bump; I am stuck with this bumps on my arm, its awful; Had a very bad reaction and I have a lifetime deformity on my arm; Got a golf ball size bump; I am stuck with this bumps on my arm, its awful; I have allergies; Allergic to the something that is in the shot, in the vaccine; Lipoma; Got a big bump it looks like a golf ball sticking out where the injection site was; This is a spontaneous report from a contactable consumer. This consumer (patient) received pneumococcal 13-val conj vac (dipht crm197 protein) (Prevnar 13, Solution for injection in pre-filled syringe) via unspecified route of administration on an unspecified date as dose number unknown, single for Immunization. Medical history and concomitant medications were not reported. Consumer stated, "I got this shot (Prevnar 13), I had a very bad reaction and I have a lifetime deformity on my arm and I already have talked to someone at your place maybe last year (further clarification unknown). So, I do not recommend this to anybody, and I have got a golf ball size bump. Regarding Lot# of Prevnar 13: Consumer stated, "I don't know what you mean a LOT number, I don't have this, I don't know where the LOT number would be. The doctors, they just give you the shot they don't tell you the numbers or anything. I am not the nurse or the physician, I am just the patient who received the Prevnar 13 three years ago and I got, my doctor said that I have a very bad rare, very rare reaction. I have allergies, he said that you probably were allergic to the something that is in the shot, in the vaccine and then he sent me for ultrasound, MRI and they both said, it is a lipoma and I have got a big bump it looks like a golf ball sticking out where the injection site was and I tell you doctor said no more vaccines for you, it's too risky. So, I didn't take Covid vaccine, I take no flu vaccine, I have to live with this now, I tell you I am very angry that this happened, I am very angry that the side effect with the vaccines is terrible and I am so upset with myself that I probably, like you know when you are at the doctor's office for your annual check-up and they say you are over 65 you want the, we can do it and then he want to mail and then a year later you get the 'Prevnar 26' (not clarified further, hence captured as-Unspecified Medication) and all this. So, you trust the doctor and they you say I am here now and will talk to it and it was the worst experience that I ever have." Consumer further stated, I am angry, but you know it may have saved my life in one respect because of this Prevnar 13 reaction that I got, I will never get another injection, another vaccine and I am seeing with the Covid vaccine and all the reactions like people dying (further clarification unknown). So, in a way it may have saved my life because I am not taking the Covid vaccine (not clarified further). Outcome of the events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1645595
Sex: M
Age:
State: NY

Vax Date: 05/02/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: Fatigue; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 53-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0172) on 02May2021 (at the age of 53-year-old) at dose 2, single and received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: ER8729) on 11Apr2021 (at the age of 53-year-old) at dose 1, single, both the doses via an unspecified route of administration, administered in arm left for covid-19 immunisation. Medical history included sleep apnoea syndrome (uses an air mask at night and has for a long time). Reporter stated that he takes medication, no further details provided, stated he has sleep apnea, uses an air mask every night, been using it for a long time now. Concomitant medications were not reported. On an unspecified in 2021 the patient experienced fatigue. Reporter stated that he got the 2nd dose of the Pfizer Biontech Covid vaccine on 02May2021 then he came down with an awful fatigue he's never experienced before. He said he's been experiencing fatigue ever since the 2nd dose. Reporter asked how come his fatigue is lasting very long. He mentioned that for the 1st shot, he experienced a little bit of fatigue and for the 2nd shot, he's had it ever since. Question: Reporter commented that MI has no answer as to why his symptom is taking too long. Reporter stated that he is reporting side effects from Pfizer vaccine, states he got second shot around beginning of May, states about 3 weeks or a month later came down with awful fatigue, states has had bad fatigue ever since, states he usually walks everywhere and never had any trouble and now he has to rest a couple of times on the bench. Wants to know if this is a side effect of the vaccine. Event Details: unknown exact start date of event, gotten a little bit better but it is still persisting. Outcome of the event was unknown. Information on Lot/Batch number was available. Additional information has been requested. Follow-Up (05Aug2021): Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1645596
Sex: F
Age:
State: MI

Vax Date: 03/29/2021
Onset Date: 03/30/2021
Rec V Date: 08/28/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: I have Constant Ringing in my ears. It never goes away; This is a spontaneous report from a contactable consumer, the patient. A 61-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8727) via an unspecified route of administration in the left arm on 29Mar2021 at 13:00 (at the age of 61-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medication was not reported. The patient had no known allergies to food, medication or other products. On 30Mar2021 at 13:00, the patient experienced constant ringing in ears and it never gone away. The events did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Patient did not receive any treatment for the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event constant ringing in ears were not resolved at the time of this report.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am