VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

Total Manufacturer
46,870MODERNA
532GLAXOSMITHKLINE BIOLOGICALS
353PFIZER\BIONTECH
231MERCK & CO. INC.
221UNKNOWN MANUFACTURER
62SEQIRUS, INC.
25DYNAVAX TECHNOLOGIES CORPORATION
13EMERGENT BIOSOLUTIONS
12SANOFI PASTEUR
9NOVARTIS VACCINES AND DIAGNOSTICS
5PFIZER\WYETH
5PAXVAX
2TEVA PHARMACEUTICALS
2PROTEIN SCIENCES CORPORATION
1BERNA BIOTECH, LTD.
1INTERCELL AG
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL1,906
1,575
289
IMM209286
252
236
229
s029456178
171
UT7065MA166
155
149
145
S034636133
107
U62828AA103
100
98
P10025327596
U6737AA85
UJ446AA79
78
78
59
57
4BH3254
4F47253
52
27656352
50
PP9L548
49TM346
42
40
38
MENVEO38
4F47237
R1B252M36
34
C5763AA30
93362229
25
300057A24
UNK24
22
CW311621
18
17
15
UH894AB15
3Y7NL12
R1B743M12
EJ168611
el128410
10
10
10
9
ARBA141A9
UNK9
8
UNK8
8
1F4EB8
Unknown7
7
No batch number6
5
5
UJ090AA5
5
5
4
4
4
UNK4
JEV18K95E4
UNK3
A115A3
Z127A3
3
3333324181073
2
2
2
TAR352
1
1
1
1
1
A739081
1
1
1
1
1
037K20A68,542
EL128447,700
133

Incidents per State

State Total
15,185
CA14,096
NY7,507
TX7,196
FL6,939
IN5,527
PA4,560
IL4,179
OH4,054
AZ3,856
MI3,771
NJ3,411
MA3,278
VA3,208
NC3,114
WA3,034
GA2,864
MD2,652
MN2,534
CO2,532
WI2,457
MO2,029
OR1,943
TN1,715
CT1,693
KY1,603
OK1,226
AL1,201
KS1,162
IA1,157
SC1,106
NM1,065
UT973
AR951
LA945
NE829
NV797
ME795
MT789
NH756
ID674
AK661
WV661
PR650
MS585
HI536
RI510
VT441
SD361
ND356
DE350
DC239
WY209
GU32
AS16
VI13
MP9
MH3
FM2
QM1
XB1

ID: 0936594
Sex: F
Age: 41
State:

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

Lab Data:

Allergies: History of allergic reactions to other vaccinations. Many other food and drug allergies.

Symptoms: Patient is mildly tachycardic, flushed, complaining of shortness of breath and sensation that her throat is closing. Patient has some inspiratory stridor. She was moved to a room and given intramuscular epinephrine, diphenhydramine, famotidine, and methylprednisolone.

Other Meds:

Current Illness:

ID: 0936595
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Muscle cramp at the site injection/Intractable neck cramp the last 8 days post shot; Muscle cramp at the site injection; This is a spontaneous report from a non-contactable pharmacist. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on Dec2020 (ten days before 04Jan2021) at single dose for covid-19 immunization. Vaccine location was arm. The patient medical history and concomitant medications were not reported. The patient experienced muscle cramps and intractable neck cramp the last 8 days post shot in Jan2021. The shot was given ten days ago and after 08 days of time intent Muscle cramp at the site injection would be proximal to the shot injection site of the basically trapezius muscle and external emasculate muscle. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0936596
Sex: F
Age:
State: AZ

Vax Date: 12/30/2020
Onset Date: 01/03/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Name: no fever; Result Unstructured Data: Test Result:no fever

Allergies:

Symptoms: I felt some fatigue just little tired; I have allergies too and I battle with allergies all the time; Feeling a little under the weather; runny nose; Feeling a little under the weather; runny nose; This is a spontaneous report from a contactable consumer (patient). A 53-year-old female patient received BNT162B2 (Pfizer/BioNTech Covid-19 vaccine, lot/ batch number EL1284) on 30Dec2020 at a single dose for Covid-19 immunization. The patient had no medical history and had no concomitant medications. The patient got her vaccine on 30Dec2020 in the morning and she had not experienced any type of severe side effects from the Covid vaccine and only felt some fatigue just little tired. But she started feeling a little under the weather and runny nose on 03Jan2021. The patient also reported that she had allergies too and battled with allergies all the time (clarification required). The patient had no treatment received for the events. The patient had no fever. The events little under the weather and runny nose resolved on 03Jan2021 and outcome of other events was unknown. The patient would like to ask whether the events were related to the vaccine as it was happening a few days later.

Other Meds:

Current Illness:

ID: 0936597
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: sore site; This is a spontaneous report from a non-contactable consumer via a Pfizer-sponsored program Corporate (Pfizer) Social Media Platform. A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration on an unspecified date (at an unknown age) at an unspecified dose for COVID-19 vaccination. The patient's medical history was not reported. The patient's concomitant medications were not reported. The patient experienced a "sore site" after vaccination No treatment information was reported. The clinical outcome of vaccination site pain was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 0936598
Sex: F
Age: 29
State:

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

Lab Data:

Allergies:

Symptoms: Pt presents with tachycardia after receiving first COVID vaccine at 1710 today. She initially believed she was anxious but when it was time to drive home, she figured it might be more than just a little anxiety. Hypertensive, remained tachycardic into the 130's and RRT EKG revealed PVCs. Received IV Benadryl with resolution of symptoms over 1-2 hours in the ED.

Other Meds:

Current Illness:

ID: 0936599
Sex: F
Age:
State:

Vax Date: 12/17/2020
Onset Date: 12/19/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: small swollen lymph node under her chin; This is a spontaneous report from a contactable consumer (patient). A 35-year-old female patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EJ1685), via an unspecified route of administration in upper right arm on 17Dec2020 15:00 at single dose for vaccination. Medical history and concomitant medications were none. The patient who was administered the first dose of Pfizer COVID-19 Vaccine on 17Dec2020. She developed a small swollen lymph node under her chin on 19Dec2020 which was ongoing. She called to ask if the small swollen lymph node would be considered a serious adverse event; and if she should or should not still receive the second dose of Pfizer COVID-19 Vaccine as scheduled for today. The outcome of event was not recovered.

Other Meds:

Current Illness:

ID: 0936600
Sex: F
Age:
State: VA

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

Lab Data:

Allergies:

Symptoms: Hot flash, lasted whole day; Itching all over whole body/Itching in hands and feet all the time; This is a spontaneous report from a contactable Nurse (patient). A 51-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EK5730), via an unspecified route of administration on 18Dec2020 at single dose for covid-19 immunization. Vaccine location was arm. None medical history. The patient's concomitant medications were not reported. Patient stated she had the COVID vaccine on Dec18th, her first one and she was fine, no issues and she would say the following Wednesday (23Dec2020), she started getting like a hot flash, it lasted whole day and then her feet started itching. And now, she have got itching all over her whole body and especially in her hands and her feet all the time. She went to her family doctor. She have not had this issue before and she don't have any known allergies. And she went to family doctor and he prescribed some antihistamines and of course they are still bothering patient. Besides itching, she was not having any other complication. Patient went to family doctor last week and he put her on a prescription of antihistamine trying to help. It is not helping, Benadryl helped her. When probed for the name of the product, patient stated she think the name of it is Lyrica. The events were persisting. She had better times but then it was other times when it is worse. When asked the causality, the patient stated she think so. She has never had a reaction like this and it has been going on everyday ever since. The only thing that worries is she was due to get her second one on the 8th which is this Friday and she have heard people rumors saying that when get second vaccine, whatever symptoms she was having are even worse. Patient don't know is it true. And of course everyone is saying like, normally they say - any reactions you get like the first 24-48 hours but her didn't happen until almost halfway till first week.

Other Meds:

Current Illness:

ID: 0936601
Sex: F
Age:
State: FL

Vax Date: 12/24/2020
Onset Date: 01/03/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Rash; Minor swelling; Itching; Pain at the injection site; This is a spontaneous report from a contactable consumer (patient). A 32-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EK9231), via an unspecified route of administration from 24Dec2020 at single dose for covid-19 immunization. None medical history nor concomitant medications. It was reported that yesterday (03Jan2021) there was a rash with very minor swelling, itching, pain at the injection site. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 0936602
Sex: F
Age: 47
State: VA

Vax Date: 01/01/2021
Onset Date: 01/05/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: penicillin, lactose

Symptoms: CHILLS, FEELING UNWELL, FEVER, HEADACHE, INJECTION SITE PAIN, INJECTION SITE REDNESS, INJECTION SITE SWELLING, JOINT PAIN, MUSCLE PAIN, NAUSEA, VOMITING, DIARRHEA, SWOLLEN LYMPH NODES AND TIREDNESS. HAVE RECOVED FROM MOST OF THESE SYMPTOMS BUT THE SWOLLEN LYMPH NODES AS OF 1/12/20.

Other Meds: None

Current Illness: None

ID: 0936603
Sex: M
Age:
State: TN

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

Lab Data:

Allergies:

Symptoms: Has soreness today with triceps injection; It was given subcutaneously in his triceps, when it should be given intramuscularly in the deltoid; He received 2nd dose of Covid vaccine today and received it subcutaneously on his triceps which he thinks is an incorrect site of administration; This is a spontaneous report from a contactable physician (patient). A male patient of unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), subcutaneously in the triceps on 07Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The physician called about the COVID-19 vaccine and stated that he was given his second dose that morning after the three weeks, and he was pretty sure it was given subcutaneously in his triceps, when it should be given intramuscularly in the deltoid. He says that he would like to inquire about recommendations for his next step, since it was given not per recommendations, and see if there is anything in Pfizer's recommendations such as check for antibodies in a couple weeks or to get another injection. He says that this injection was done a lot lower than his first dose, and he was reading Pfizer vaccine recommendations to be the deltoid, and he is guessing they gave it to him in the triceps subcutaneously. He says after the first shot, he had mild arm soreness with no other symptoms, he so far has soreness that day with triceps injection. He would like to know what recommendations are to do next, or if there is a higher risk of side effects since it was given into soft tissue, if there is any information or studies with data about subcutaneous administration of this vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936604
Sex: F
Age:
State: OK

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: very bad headache; feels terrible/feeling bad; she was sick; This is a spontaneous report from a contactable consumer. A 70-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL4238, Expiration date: 30Apr2021), via an unspecified route of administration at site of right arm at 14:00 on 06Jan2021 at single dose for COVID-19 immunization. Medical history included ongoing high cholesterol for several years. Concomitant medication included rosuvastatin calcium (CRESTOR) for cholesterol (had taken it for several years). The patient had a bad headache and feels terrible at 6 am on 07Jan2021, she wanted to know if she could take something for the headache. She got up at 6 am and feeling bad on 07Jan2021, she left for work and came home, and she was sick. Her feeling terrible started sometime during the night. She was feeling fine on 06Jan2021. These events were identified as non-serious by reporter. Vaccination Facility Type was in public health department. Vaccine was not administered at military facility. No history of all previous immunization with the Pfizer vaccine considered as suspect. Additional Vaccines Administered on Same Date of the Pfizer Suspect: none. No adverse events required a visit to emergency room. No prior vaccinations within 4 weeks. No adverse events following prior vaccinations. The outcome of events 'headache' was not recovered; of rest events was unknown.

Other Meds: CRESTOR

Current Illness:

ID: 0936605
Sex: M
Age: 55
State:

Vax Date: 01/07/2021
Onset Date: 01/08/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: Extreme Chills, Muscle Aches, Tiredness, Joint pain throughout the body. Rest and Motrin used. Length: 48hrs

Other Meds: Metformin, Zoloft

Current Illness: None

ID: 0936606
Sex: M
Age:
State: OK

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe diarrhea, followed by severe muscle cramps; Severe diarrhea, followed by severe muscle cramps; This is a spontaneous report from a contactable nurse reported for himself. A 64-year-old male patient received first dose of bnt162b2 (BNT162B2, lot number EL1283), intramuscular in right arm on 05Jan2021 11:00 at single dose for COVID-19 immunization. Medical history included ankylosing spondylitis, ulcerative colitis, prediabetes, previous hypertension, hypothyroidism, partial heart block and known allergies: Sulfa. Concomitant medication included mesalazine (LIALDA), indometacin (INDOMETHACIN), levothyroxine sodium (SYNTHROID), esomeprazole magnesium (NEXIUM), zolpidem tartrate (AMBIEN), metformin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have COVID tested post vaccination and did not have COVID prior vaccination. The patient experienced severe diarrhea, followed by severe muscle cramps on 05Jan2021 16:00 with outcome of recovered in Jan2021. The events were reported as non-serious.

Other Meds: LIALDA; INDOMETHACIN [INDOMETACIN]; SYNTHROID; NEXIUM [ESOMEPRAZOLE MAGNESIUM]; AMBIEN;

Current Illness:

ID: 0936607
Sex: M
Age:
State: OK

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Injection site is very sore; arm swelling; fatigue; This is a spontaneous report from a contactable Physician (patient). A 34-year-old male patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EK9321), via an unspecified route of administration on 06Jan2021 at 08:00 at single dose in left arm for covid-19 immunization. There were no medical history or concomitant medications. The patient experienced injection site was very sore, arm swelling, and fatigue on 06Jan2021 at 08:00. The patient did not receive treatment for the events. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination, and the patient had not been tested for COVID-19 since vaccination. The outcome of the events was resolving.

Other Meds:

Current Illness:

ID: 0936608
Sex: F
Age: 55
State: WA

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

Lab Data: Visual inspection, vital signs

Allergies: Penicillin, cephalosporins

Symptoms: Developed cellulitis at injection site. It should be noted that injection was to be given intramuscularly but the RN who administered it gave to the back of the arm which was likely subcutaneous rather than intramuscular.

Other Meds: NP thyroid 90mg

Current Illness: None

ID: 0936609
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: The day after vaccine administration, pt was still experiencing vertigo, spinning and headache.; The day after vaccine administration, pt was still experiencing vertigo, spinning and headache.; This is a spontaneous report from a non-contactable other healthcare professional (hcp). A 27-year-old female patient receive first dose of bnt162b2 (Pfizer BioNTech COVID vaccine, lot number: EL0140), intramuscularly on 30Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. There is unknown if any other vaccine received in four weeks. The patient experienced the day after vaccine administration, patient was still experiencing vertigo, spinning and headache, all on 31Dec2020 the day after vaccine administration. The outcome of events was unknown. This is a non-serious report. It's unknown if patient was diagnosed with COVID-19 or tested for COVID-19 since the vaccination. The adverse did not result in 'doctor or other HCP visit or emergency room or urgent care, hospitalization or prolongation, life threatening illness, disability or death or congential anomaly'. No follow-up attempts are possible. Information about Lot/Batch cannot be obtained.

Other Meds:

Current Illness:

ID: 0936610
Sex: F
Age:
State: AZ

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: 5 minutes post vaccine experienced tingling lips and dry mouth; 5 minutes post vaccine experienced tingling lips and dry mouth; 6 hours followed by lip numbness still occurring (23 hours post vaccine so far); This is a spontaneous report from a contactable nurse (patient). A 37-year-old female patient (non-pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: ELO142), via an unspecified route of administration on 06Jan2021 16:45 at single dose at right arm for covid-19 immunization. The patient's medical history and concomitant medications were not reported. No known allergies to medications, food, or other products. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine, patient didn't receive other medication within 2 weeks of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient has not been tested for COVID-19. The patient experienced 5 minutes post vaccine experienced tingling lips and dry mouth x 6 hours followed by lip numbness still occurring (23 hours post vaccine so far) with outcome of recovered with lasting effects in Jan2021. Patient received Benadryl 37.5mg x 1 dose for events. The adverse events resulted in neither doctor or other healthcare professional office/clinic visit, nor emergency room/department or urgent care. The report is considered non-serious.

Other Meds:

Current Illness:

ID: 0936611
Sex: F
Age: 33
State: CO

Vax Date: 01/07/2021
Onset Date: 01/08/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: n/a

Allergies: none

Symptoms: Severe Nausea, Headache, Fatigue, Body aches. kidney stones and sore throat.

Other Meds: none

Current Illness: none

ID: 0936612
Sex: F
Age:
State: CA

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 20210106; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: anaphylaxis; throat tightening; throat tightening/tingling; throat tightening/tingling/soreness; dry wheezy cough a little dizziness; dizziness; tachycardia; Itching; chills; numb R foot; Low grade temp; h/a today; This is a spontaneous report from a contactable Nurse (patient). A 51-years-old female patient (no pregnant) started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number el3248), via an unspecified route of administration on 06Jan2021 11:00 at the first single dose at left arm for covid-19 immunisation. Medical history included supraventricular tachycardia, adrenal insufficiency, hypothyroidism, attention deficit hyperactivity disorder, hypermobility syndrome, developmental hip. Concomitant medication included hydrocortisone, trazodone, levothyroxine sodium (LEVOTHROID), bupropion hydrochloride (WELLBUTRIN). The patient previously took erythromycin, morphine and experienced drug hypersensitivity. The patient experienced anaphylaxis, throat tightening/tingling/soreness, dry wheezy cough a little dizziness and tachycardia. Itching, numb R foot, Low grade temp and chills and headache on 06Jan2021 11:15. Seriousness criteria reported as life threatening. Taken to ER had IV benadryl, solumedrol, pepcid for anaphylaxis. Placed on O2 and given albuterol nebulizer. Had IV fluid bolus. Now on benadryl and 5 days of prednisone. The patient felt completely fine prior to vaccine. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 06Jan2021. The outcome of events was recovering. No other vaccine in four weeks; No covid prior vaccination.; Sender's Comments: A possible causal association between administration of BNT162B2 and the onset of anaphylaxis presented as throat tightening/tingling/soreness, dry wheezy cough a little dizziness and tachycardia. Itching, numb R foot, Low grade temp and chills and headache cannot be excluded, considering the plausible temporal relationship and the known adverse event profile of the suspect product. The underlying predisposing condition of drug allergies may put the patient at high risk of anaphylactic reactions. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds: ; ; LEVOTHROID; WELLBUTRIN

Current Illness:

ID: 0936613
Sex: F
Age:
State: NV

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

Lab Data:

Allergies:

Symptoms: Hives all over her body; Shortness of breath; This is a spontaneous report from a contactable nurse reported for patient (coworker). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 30Dec2020 at occupational health department at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient had a worse reaction than reporter did. The patient's worse reaction included hives all over her body and shortness of breath. Caller cannot believe the patient was still working like this. The outcome of events was unknown. Caller declined to provide any further information for this report. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936614
Sex: M
Age: 32
State: IN

Vax Date: 01/05/2021
Onset Date: 01/11/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body itchiness

Other Meds: Allupurinol

Current Illness:

ID: 0936615
Sex: M
Age:
State: TN

Vax Date: 12/21/2020
Onset Date: 12/27/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 20201230; Test Name: Labs; Result Unstructured Data: Test Result:negative and normal; Test Date: 20201230; Test Name: MRI; Result Unstructured Data: Test Result:negative and normal; Test Date: 20210102; Test Name: Covid antibody; Result Unstructured Data: Test Result:Positiive; Test Date: 20210102; Test Name: Covid test; Result Unstructured Data: Test Result:negative; Test Date: 20201230; Test Name: Xray; Result Unstructured Data: Test Result:negative and normal

Allergies:

Symptoms: Shortness of breath on exertion; weakness; fatigue; chills; tingling sensation of extremities that continues on; This is a spontaneous report from a contactable healthcare professional, the patient. A 50-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EK9231) solution for injection intramuscular on 21Dec2020 (at the age of 50-years-old) as a single dose for COVID-19 vaccination. Medical history included neuropathy. Concomitant medication included gabapentin. Past drug history included known allergies: TOPAMAX. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. On 27Dec2020, the patient experienced fatigue, chills, tingling sensation of extremities that continues on. Treatment for the events fatigue, chills, tingling sensation of extremities included ibuprofen (MOTRIN) and acetaminophen (TYLENOL) taken with minimal or short temporary relief. On 30Dec2020, the patient experienced shortness of breath on exertion and weakness and tried to go to Urgent care clinic for Covid test but no available test so the doctor prescribed ZITHROMAX in case it was Covid. On 30Dec2020, MRI, XRAY, LABS were taken and all came back negative and normal except having all these symptoms. On 02Jan2021, Covid test done and result was negative, tested for antibody and it was positive. The outcome of the event fatigue was unknown. The outcome of the events chills and tingling sensation of extremities was recovered in Jan2021. The outcome of the events shortness of breath on exertion and weakness was not recovered. The events fatigue, chills, tingling sensation of extremities that continues on, shortness of breath on exertion and weakness required a physician office visit.

Other Meds:

Current Illness:

ID: 0936616
Sex: F
Age:
State: WA

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: injection site was really red. It was the size of a 50 cent piece if not bigger; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# 037K20A, expiration date: Jul2021), via an unspecified route of administration in left arm on 05Jan2021 at single dose for Covid-19 immunisation. Medical history was none. Concomitant medication included escitalopram oxalate (LEXAPRO), warfarin and another medication. The patient worked in health care. She received the Covid-19 injection. The injection site was really red on 06Jan2021. It was the size of a 50 cent piece if not bigger. She wasn't sure if she should be worried. The outcome of event was not recovered.

Other Meds:

Current Illness:

ID: 0936617
Sex: F
Age:
State:

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

Lab Data: Test Name: feverish (yet afebrile); Result Unstructured Data: Test Result:feverish (yet afebrile)

Allergies:

Symptoms: Rigors; Feverish (yet afebrile); Myalgias; Fatigue; This is a spontaneous report from a non-contactable consumer (patient herself). This 30-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route, on unknown date at single dose; and the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 04Jan2021 at single dose, for COVID-19 immunisation. Vaccine location was right arm. The patient did not have a relevant medical history. No known allergies. No relevant concomitant medications were provided. No other vaccine was received in four weeks. On unknown date, the patient developed rigors, feverish (yet afebrile), myalgias, and fatigue. Pre-vaccination and post-vaccination COVID tests were not performed. The patient was not treated for the events. She recovered from the events on unknown date. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0936618
Sex: F
Age: 36
State: AZ

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

Lab Data:

Allergies: None

Symptoms: Soreness at injection site started at 1600 Body aches, headache, and low grade fever woke me up around 0100

Other Meds: Magnesium, fish oil, vitamin b12, maca powder, CoQ10, biotin

Current Illness: None

ID: 0936619
Sex: U
Age:
State: MT

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

Lab Data:

Allergies:

Symptoms: Patient with Covid between their first and second doses of the Covid vaccine; Patient with Covid between their first and second doses of the Covid vaccine; This is a spontaneous report from a Pfizer-sponsored program from a contactable Pharmacist reported similar events for 2 patients. This is the 2nd of 2 reports. A patient of an unspecified age and gender received the first dose of BNT162B2 (Pfizer/BioNTech Covid-19 vaccine) on an unspecified date for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient got Covid between first and second doses of the Covid vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The association between the event lack of effect (got COVID between first and second doses) with BNT162b2 can not be fully excluded.,Linked Report(s) : US-PFIZER INC-2021011515 same reporter/drug/AE, different patient

Other Meds:

Current Illness:

ID: 0936620
Sex: U
Age:
State:

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

Lab Data: Test Name: Ultrasound; Result Unstructured Data: Test Result:extremely swollen lymph nodes

Allergies:

Symptoms: some axillary tenderness; some localized site tenderness; swollen lymph nodes; This is a spontaneous report from two contactable Other HCPs. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Dec2020 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced some localized site tenderness, some axillary tenderness in the days after the vaccine and then symptoms went away. The past couple of days she was experiencing extremely swollen lymph nodes and an ultrasound confirmed this. No other symptoms at this time. The outcome of events some axillary tenderness and some localized site tenderness was recovered; of event swollen lymph nodes was unknown. Information on lot number/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936621
Sex: U
Age:
State: MT

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

Lab Data:

Allergies:

Symptoms: patient with covid between their first and second doses of the covid vaccine; patient with covid between their first and second doses of the covid vaccine; This is a spontaneous report from a Pfizer sponsored program IBCC (Inbound Call Center for HCPs). A contactable pharmacist reported similar events for two patients. This is the first case out of 2 cases. A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231, expiration date: Apr2021, NDC#59267-1000-1), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient with Covid between the first and second doses of the Covid vaccine on an unspecified date. The reporting pharmacist wanted to know if the patients with covid between their first and second doses of the covid vaccine what their risk would be, Reportedly 2 different patient. The outcome of the events was unknown.; Sender's Comments: The association between the event lack of effect (COVID between first and second dose) with BNT162b2 can not be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-2021011471 same reporter/drug/event, different patient..

Other Meds:

Current Illness:

ID: 0936622
Sex: F
Age: 20
State: HI

Vax Date: 01/04/2021
Onset Date: 01/10/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: None taken yet because I don't know what to do about it.

Allergies: n/a

Symptoms: Moderna COVID-19 Vaccine EUA. Large bump (1/2 inch raised from the rest of my arm) on injection site appeared roughly a week after vaccine. Roughly 2.5 inches in diameter and firm to the touch. Mildly itchy and red with a few small bumps.

Other Meds: Trazodone Hydrochloride, Alprazolam, Tylenol

Current Illness: n/a

ID: 0936623
Sex: M
Age:
State: NJ

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Off-label use; Severe headache; Chills; This is a spontaneous report from a contactable consumer (patient himself). This 39-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL1284 with Expiration Date Mar2021), via an unknown route, on 19Dec2020 at single dose; and the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL1284 with Expiration date Apr2021), via an unknown route, on 05Jan2021 at 18:30; both doses for COVID-19 immunisation. Vaccine location was right arm. The patient did not have a relevant medical history. No additional drugs were reported. The patient was vaccinated at hospital, age at vaccination was 39-year-old. Then last night, on 06Jan2021 around 23:00PM-23:30 she started to have chills that lasted throughout the night. He stated he felt 95% better. Just minor lingering effects there with the chills, nothing too bad. On 07Jan2021, he woke up with a severe headache. It took a fewhours to subside. Therapeutic measures taken as result of the events included ibuprofen (strength: 200 mg) which pretty much resolved. It had resolved 95%, ibuprofen helped. It took several hours for it to subside. The patient took 4 tablets of ibuprofen. The patient was recovering from the events headache and chills.

Other Meds:

Current Illness:

ID: 0936624
Sex: F
Age:
State: DC

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/12/2021
Hospital:

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

Allergies:

Symptoms: Nausea; Feeling unwell; 1st dose Pfizer covid vaccine administered on 17Dec2020/second shot of the Pfizer Covid vaccine yesterday (04Jan2021); back pain/back pain was pretty severe and was worse than it would normally be; severe headache that turned into a migraine; severe headache that turned into a migraine; This is a spontaneous report from a contactable consumer. A 30-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL1284, Expiry Date: Apr2021) intramuscular at left deltoid on 04Jan2021 16:00 at single dose for covid-19 immunisation. 1st dose Pfizer covid vaccine was administered on 17Dec2020 (Lot number: EH9899). She was covid positive the day after receiving her first dose of the Pfizer covid vaccine. Her primary care informed her to get the booster despite testing positive for the virus. She was told since she was asymptomatic that she could get the vaccine. Medical history included back pain, covid from 3 weeks ago (Dec2020). There were no concomitant medications. The patient experienced back pain and severe headache that turned into a migraine on 04Jan2021, nausea and feeling unwell on 05Jan2021. She got the second shot of the Pfizer Covid vaccine yesterday (04Jan2021) around 16:00. Overnight she had back pain, severe headache that turned into a migraine. Now she had developed nausea and was generally feeling unwell. She had covid 3 weeks ago and she was instructed to get the vaccine. She has a history of back pain but states it was obviously triggered. Reports that last night her back pain was pretty severe and was worse than it would normally be. Nausea and feeling unwell was reported as worsened. Back pain was slightly improved. Headache that turned into migraine improved with medication. The outcome of events back pain and severe headache that turned into a migraine was recovering; of events nausea and feeling unwell was not recovered.

Other Meds:

Current Illness:

ID: 0936625
Sex: U
Age:
State: CA

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

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

Allergies:

Symptoms: tested positive and also received the vaccine from COVID-19; tested positive and also received the vaccine from COVID-19; This is a spontaneous report from a Pfizer sponsored program. This contactable physician reported similar events for the physician herself and a patient. This is the second report, the patient report of 2 reports. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The physician reported there was another person in her clinic that tested positive and also received the COVID vaccine on an unspecified date with outcome of unknown. The information on the batch number has been requested.; Sender's Comments: Based on the information currently available, a lack of efficacy with the suspected vaccine BNT162B2 in this patient cannot be completely excluded. Further information like confirmative virus genome /nucleic acid detection needed for meaningful medical assessment.,Linked Report(s) : US-PFIZER INC-2021000799 Same reporter, same drug, different patients

Other Meds:

Current Illness:

ID: 0936626
Sex: M
Age: 33
State: NV

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: Mild to moderate muscular pain around injection site. Pain present upon any kind of movement (7/10), even when resting if arm was not in a fully relaxed and supported position, and upon palpation. Mild swelling present, but no visible bruising, redness, rash, or bleeding. General body weakness and slight body aches. Mild fever (typical temperature mid-97, highest temperature that day of 99.3). Lethargy all day. Treatment consisted of increased fluid/electrolyte intake and rest. No medications taken. Approximately 22-23 hours after the first symptoms occurred, they went away. After waking up the next day, none of the symptoms were present with the exception of very mild pain (1-2/10) around the injection site on palpation only. No other symptoms present.

Other Meds: None

Current Illness: None

ID: 0936627
Sex: F
Age:
State:

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 20201221; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasopharyngeal

Allergies:

Symptoms: Myalgia; This is a spontaneous report from a non-contactable physician (the patient). A 29-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, first dose on 16Dec2020 (lot EK5730) and second dose on 06Jan2021 at 18:00 (lot EL3246), both in left arm at single dose for covid-19 immunisation. The vaccine was administered at Hospital Facility. The patient did not receive other vaccine in four weeks. The patient medical history and concomitant medications were not reported. The patient experienced myalgia on 07Jan2021 08:00. The patient underwent lab tests and procedures which included Nasopharyngeal Nasal Swab/sars-cov-2 test: negative on 21Dec2020. No treatment was given for the event. The event was non-serious with outcome of recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0936628
Sex: F
Age:
State: CA

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

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:increased

Allergies:

Symptoms: dizziness/light headedness; increased blood pressure; anxiety; a rash that developed down to the elbow; cramping; bladder pressure; received the menstrual period earlier than expected; This is a spontaneous report from a contactable other healthcare professional (patient) via Pfizer sales representative. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unspecified date at single dose for COVID-19 immunization. Medical history included kidney stones. Concomitant medications were not reported. Patient experience dizziness, light headedness after receiving the vaccine. Additionally, the patient had increased blood pressure and anxiety, as well as a rash that developed down to the elbow. The rash resolved the following day. The day after receiving the vaccine, the patient reported cramping, bladder pressure and received the menstrual period earlier than expected. Events took place after use of product. The outcome of events cramping and bladder pressure is not recovered. The outcome of event rash was recovered. The outcome of other events was unknown. Information on the lot number has been requested.

Other Meds:

Current Illness:

ID: 0936629
Sex: F
Age:
State: AZ

Vax Date: 01/05/2021
Onset Date: 01/01/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 202012; Test Name: tested for COVID; Test Result: Negative ; Test Date: 202101; Test Name: tested for COVID; Result Unstructured Data: Test Result:unknown results

Allergies:

Symptoms: notice a rash on her left hand; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EH9899), via unspecified route of administration on left arm on 05Jan2021 at single dose for Covid. The relevant medical history and concomitant medications were reported as none. The patient stated that she just got the first shot of COVID vaccine and noticed a rash on her left hand. She stated that it was the same arm that she got the shot. She wanted to know if there was anything that she needed to do. She stated that she got it through the state as a healthcare worker. She stated that she noticed the rash 20 minutes prior to the report. The patient had no treatment for the event. The patient was tested for COVID the week prior the report in Dec2020 and it was negative. She was going in at the time of the report to get another COVID test. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 0936630
Sex: F
Age: 58
State:

Vax Date: 01/04/2021
Onset Date: 01/07/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: 4 cm area of redness, slightly warm to the touch

Other Meds: Ca/Mg/Zn with Vit D Acetaminophen 325mg x2 tabs

Current Illness: None

ID: 0936631
Sex: F
Age:
State: CA

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: consumed alcohol yesterday and was woozy afterwards; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231) via unspecified route of administration on 05Jan2021 at single dose for COVID-19 immunization. Medical history included consume alcohol. Concomitant medications were not reported. Patient took the vaccine at work yesterday (05Jan2021), she works in the healthcare industry, and wants to know if after getting the vaccine can a person consume alcohol. The patient remarked that she did consume alcohol yesterday and was woozy afterwards. She read somewhere that a person should not consume alcohol for 2 months as the vaccine will not work as well. She wanted to know if this was true. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0936632
Sex: M
Age:
State: TX

Vax Date: 12/15/2020
Onset Date: 12/01/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: injection site pain; This is a spontaneous report from a contactable consumer (patient). A 21-year-old male patient received BNT162B2 (batch/lot number: EH9899) first dose on 15Dec2020 13:00 Intramuscular Deltoid Left at single dose for COVID-19 prophylaxis. Medical history and concomitant medications were none. Prior Vaccinations (within 4 weeks) None. AE(s) following prior vaccinations None. Family Medical History Relevant to AE(s) None. He said that he had no side effects with the first dose except for injection site pain. Vaccination Facility Type was Hospital. Vaccine not Administered at Facility. No events require a visit to: Emergency Room or Physician Office. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0936633
Sex: F
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: Diarrhea continue for a couple days, resolved for a couple days, and then returned for a couple more days before resolving; Dehydrated from the diarrhea; Stomach cramps; Headache; Migraine; This is a spontaneous report from a contactable other HCP (patient) via Pfizer sales representative. This other HCP reported information for two patients. This is the first of the two reports. A female patient of unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unknown date at single dose via unknown route of administration for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient reported diarrhea that began about 1 hour after receiving the vaccine. Diarrhea continued for a couple days, resolved for a couple days, and then returned for a couple more days before resolving. The patient was dehydrated from the diarrhea and also had stomach cramps the days that she had the diarrhea. Patient also reported headache/migraine since she received the vaccine. The outcome of the event Diarrhea was recovering. The outcome of other events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936634
Sex: F
Age: 68
State: FL

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

Lab Data: None

Allergies: sulfa

Symptoms: None

Other Meds: Nifedipine 30 ml 1x Bupropion 100ml 1X

Current Illness: High BP, Depression

ID: 0936635
Sex: U
Age:
State:

Vax Date: 09/30/2020
Onset Date: 09/30/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sore arm; The patient got the flu and pneumococcal 13-valent conjugate vaccines at the same appointment; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received pneumococcal 13-valent conjugate vaccine (diphtheria crm197 protein) (PREVNAR 13), via an unspecified route of administration on 30Sep2020 at single dose for immunization; and influenza vaccine (FLU), via an unspecified route of administration on 30Sep2020 at an unspecified dose for immunization. The patient's medical history and concomitant medications were not reported. The patient got the flu and pneumococcal 13-valent conjugate vaccines at the same appointment. The patient had a very sore arm for 48 hours. While it was sore, the patient was able to fully use it. The shots were administered on 30Sep. The outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 0936636
Sex: F
Age:
State: CA

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:101.4; Comments: fever went up to 101.4; Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:99.6; Comments: fever down 99.6

Allergies:

Symptoms: first dose on 21Dec2020/ second dose on 04Jan2021; first dose on 21Dec2020/ second dose on 04Jan2021; her fever went up to 101.4/ her fever is down to 99.6; still does not feel good/ felt sick/ felt terrible; wanted throw up; shaking chills; extreme weakness; This is a spontaneous report from a contactable consumer (patient). An 82-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK5730), via unspecified route of administration on 21Dec2020 at single dose, and second dose (lot number: EL3246), via unspecified route of administration on 04Jan2021 at single dose for COVID-19 immunisation. The relevant medical history and concomitant medications were not reported. The patient stated that she got it in the evening and had a fever and felt sick like she wanted throw up. She stated that her fever went up to 101.4, that she felt terrible, had shaking chills and extreme weakness. She tried to drink a lot of liquids thinking that would help. Stated that it was a really bad experience. She clarified that all of these side effects were with the second dose. She had no side effects with the first dose. She reported all of this previously. She stated that she called in fever down 99.6 and did not feel good. She stated that the Tylenol brought fever down a little bit. She was still not able to go to work. The outcome of the event "her fever went up to 101.4/ her fever is down to 99.6" was recovering, the event "still does not feel good/ felt sick/ felt terrible" was not recovered, while other events were unknown.

Other Meds:

Current Illness:

ID: 0936637
Sex: M
Age: 47
State: WV

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: Sulfa

Symptoms: The morning after the injection when I woke up my entire body was sore to even walk. That lasted 1 day. Since then I have experienced chills, lightheadedness, confusion and an overall feeling of exhaustion.

Other Meds: Daily Multi Vitamin

Current Illness:

ID: 0936638
Sex: F
Age:
State: GA

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

Lab Data:

Allergies:

Symptoms: headache; This is spontaneous report from a contactable nurse (patient, an oncology nurse navigator) via a company representative. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route of administration on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. Patient received Pfizer COVID-19 vaccine and got a headache. Patient is a female and. The nurse was excited to share that they received the vaccine. Event took place after use of product. 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: 0936639
Sex: F
Age:
State: KS

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 20210105; Test Name: Body temperature; Result Unstructured Data: Test Result:101 Fahrenheit

Allergies:

Symptoms: experiencing fever of 101 degrees F; muscle aches; chills; This is a spontaneous report from a Pfizer-sponsored program, received via a contactable consumer. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date unknown), dose number 1, via an unspecified route of administration on 05Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient was experiencing fever of 101 degrees F, muscle aches, and chills on 05Jan2021. The outcome of the events was unknown. Information about Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0936640
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: chills; Headache; body aches; This is a Spontaneous report from a contactable physician (patient) via a Pfizer Sponsored Program Corporate (Pfizer) Social Media Platforms. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported "Hang in there immune response kicked my butt at about 12 hr point (chills, headache, body aches)". The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0936641
Sex: M
Age: 31
State: CA

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

Lab Data:

Allergies: Children's Motrin, pistachio

Symptoms: Sore arm

Other Meds:

Current Illness:

ID: 0936642
Sex: U
Age:
State:

Vax Date: 12/21/2020
Onset Date: 12/25/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: did develop COVID that week probably symptoms in general by 25Dec/probably infected whenever got the vaccine; did develop COVID that week probably symptoms in general by 25Dec/probably infected whenever got the vaccine/I don't feel very well right now; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1685), via an unspecified route of administration on 21Dec2020 at single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received 1st vaccine on 21Dec2020. The patient did develop COVID that week probably symptoms in general by 25Dec2020. She was probably infected whenever she got the vaccine and the patient was scheduled to have second vaccine on 11Jan2021 which was next Monday and the patient was still sick, should the patient delayed that. The patient also did not feel very well on an unknown date ("right now"). The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0936644
Sex: F
Age:
State: OR

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

Lab Data:

Allergies:

Symptoms: Difficult time sleeping last night; Woke up with all joints achy; Aching all up my spine; sort of weird headache; body aching; This is a spontaneous report from a contactable nurse (patient). A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231) via unspecified route of administration on 03Jan2021 at single dose for COVID-19 immunization. Medical history included depression, had hip surgery last year (from 2020) and anxiety. Concomitant medication included escitalopram oxalate (LEXAPRO) for anxiety and depression. esomeprazole magnesium (NEXIUM [ESOMEPRAZOLE MAGNESIUM]), on regular basis naproxen sodium (ALEVE) and paracetamol (TYLENOL) because of her hip. Patient was calling because she was vaccinated yesterday, 03Jan2021. Patient was a nurse and she got the COVID Vaccine yesterday. she wanted to go into the symptom checker or whatever because she was having, she woke, she wasn't (incomplete sentence). she had a difficult time sleeping last night. She woke up like with all her joints start just achy and she did not have a great time. she wanted to report her symptoms. patient have other things. No really big co-morbidities, like, she had depression. she had some body issues like she had a "torn labor" and stuff like that but that needs to be repaired but not like blood pressure, diabetes, none of those things. she had hip surgery last year. she took two Aleve in the morning and two 500 Tylenol. And she took one more Aleve in the evening and two more Tylenol. As of causality, patient stated she believe so. It's much more intense than it was, than she was feeling yesterday. she definitely could feel it after she had the vaccination. she got like this aching all up her spine and sort of the weird headache for about (incomplete sentence). it was for the rest of the day about an hour after she got the vaccination. She was a little too un-tuned with her body aching. Consumer stated, "Is there, I mean, more I was calling to register with that CDC thing or whatever to report, you know just what's happening. I figured it was probably, kind of part of the research study or whatever for symptoms and tracking and all that. Is that what I am doing as well too by doing this or is that something separate?" When probed if reported through CDC questionnaire, consumer stated, "No, I went onto the website and it said that on CDC website the worst thing and it said that you needed a code or something a key code to get into the program and I don't. Is this where the reporting is going or how do I register with the (app Name) or whatever? Is that what I did by telling you what's going on?" When informed about the role of Pfizer Drug Safety, consumer stated, "I did not understand that safety report or I figured that we were like also assisting in some kind of research trial type thing too. Are they going to call me or no? Is this the last time I'm hearing from anyone?" No investigation assessment. No Lab Work. No Treatment. Outcome of the events was unknown.

Other Meds: LEXAPRO; NEXIUM [ESOMEPRAZOLE MAGNESIUM]; ALEVE; TYLENOL

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm