VAERS 2021 Database www.vaers.hhs.gov

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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: 0929470
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: developed Covid infection after being vaccinated with COVID-19 vaccine; developed Covid infection after being vaccinated with COVID-19 vaccine; This is a spontaneous report from a contactable physician (patient) received via a Pfizer sales representative. A female patient of an unspecified age received BNT162B2 via an unspecified route of administration on an unspecified date at a single dose as COVID-19 vaccine. Medical history included exposed several days prior to patients with Covid (exposed prior to receiving the vaccine to individuals who had an active Covid infection). Concomitant medications were not reported. It was reported that on an unspecified date, the female physician developed Covid infection after being vaccinated with COVID-19 vaccine (also reported as she received the COVID-19 vaccine and developed active Covid a few days later). The events took place after use of product. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: There is not a reasonable possibility that reported "Covid infection" is related to BNT162B2 per current available information. The patient exposed to individuals who had an active Covid infection prior to receive the vaccine.

Other Meds:

Current Illness:

ID: 0929471
Sex: F
Age:
State: NY

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: pain in her whole arm; numbness in right cheek/numbness in arm/hand; Swollen lymph nodes; This is a spontaneous report from a contactable consumer. A 61-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 30Dec2020 12:12 at SINGLE DOSE at right arm for covid-19 immunisation. Medical history included SVT this was recognized at least 20 years ago, around the age of 30, she started to deal with high blood pressure, allergic to penicillin. The patient's concomitant medications were not reported. The patient previously took codeine, levothyroxine: allergic to codeine, levothyroxine. The patient also previously took Tylenol with Codeine and that was horrible and she can't ever take it again, when she was around the age of 40 years old. The patient received the COVID vaccination around Wednesday 30Dec2020 at 12:12 p.m. She was perfectly fine until late Thursday afternoon 31Dec2020, around 3:30-4:00 pm. She started to have swollen lymph nodes. It was only a little bad at first and then she started getting more and more swelling. She spoke with her facility's RN who suggested she use some cold and warm packs/compresses and also take some Tylenol to deal with it. She has had the swelling for this many days now. It's not bad swelling but she her lymph nodes are still so swollen. She thought it was a regular reaction, but now it's been too long. Her lymph nodes are not swollen humongous. There is no redness. Her lymph nodes are not hard, just swollen. The swelling was a little bit better on Friday and Saturday but yesterday, it started bothering her again. She has had pain in her whole arm on an unspecified date. On 03Jan2020, her face also started to feel funny. She clarifies by "feeling funny", she meant she started to experience numbness in her right cheek, only her cheek, like when one gets a vaccination when they go to a doctor's office/dentist office and it starts working and one can feel it getting numb. She also experienced numbness in her arm. She clarifies when she puts pressure on her arm (like putting her arm on the desk), she feels numb in her hand. She verifies the numbness in both her cheek and arm started occurring on 03Jan2020 around 7-8pm. She is fine today and then she'll start to feel the numbness again in her cheek and arm. She clarifies the numbness comes and goes. It comes in the morning and then goes away and then the numbness starts again. She started to feel numb in her face and cheek, like when one gets a Novocain at the dentist office and it starts working- it's like the same feeling. The outcome of the events Swollen lymph nodes and numbness in right cheek/numbness in arm/hand was not recovered, while unknown for the other event. Information on the lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0929472
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: the consumer experienced inflamed lymph nodes in the axilla area of the arm that was injected (left arm).; This is a spontaneous report from a non-contactable consumer (patient) via Pfizer Sales Representative. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: not provided), via an unspecified route of administration on the left arm on unknown date at SINGLE DOSE for COVID-19 immunization. It was reported that the patient was a cancer survivor. The patient's concomitant medications were not reported. On an unknown date shortly after receiving the vaccine, the patient experienced inflamed lymph nodes in the axilla area of the arm that was injected (left arm). Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0929473
Sex: F
Age:
State: MN

Vax Date: 12/03/2020
Onset Date: 12/04/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Initially, soreness at the injection site. Over the next 4 days (today is day 4), pain in left shoulder, back, and up the back of head/neck is getting progressively worse - now excruciating.; Initially, soreness at the injection site. Over the next 4 days (today is day 4), pain in left shoulder, back, and up the back of head/neck is getting progressively worse - now excruciating.; Initially, soreness at the injection site. Over the next 4 days (today is day 4), pain in left shoulder, back, and up the back of head/neck is getting progressively worse - now excruciating.; Initially, soreness at the injection site. Over the next 4 days (today is day 4), pain in left shoulder, back, and up the back of head/neck is getting progressively worse - now excruciating.; Initially, soreness at the injection site. Over the next 4 days (today is day 4), pain in left shoulder, back, and up the back of head/neck is getting progressively worse - now excruciating.; This is a spontaneous report from a contactable nurse (patient herself). A 48-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EH9899; expiry date: unknown) intramuscular (left arm), on 03Dec2020 at 16:00, at a single dose, for COVID-19 immunization. Medical history included hypertension (HTN). The patient has no known allergies. Concomitant medications were not reported. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in a Public Health Clinic/Veterans Administration facility. On 04Dec2020, at 05:00 a.m., the patient initially experienced soreness at the injection site. Over the next 4 days (today is day 4), patient experienced pain in left shoulder, back, and up the back of head/neck which was getting progressively worse - now excruciating. Ibuprofen managed the pain for the first two days, but the soreness/pain was no longer managed with NSAID's and other comfort measures. Patient was hoping that these are normal and was hoping they will get better. Outcome of the events was not recovered. The patient has not been tested for COVID-19 since vaccination.

Other Meds:

Current Illness:

ID: 0929474
Sex: F
Age:
State: CA

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Joint and muscle pain; Joint and muscle pain; This is a spontaneous report from a contactable physician. A 46-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1685), intramuscular on the left arm on 28Dec2020 08:45 at single dose for COVID-19 immunisation. The patient had no medical history. Concomitant medication included ethinylestradiol, norethisterone acetate (LOESTRIN) and naproxen sodium (ALEVE). The patient experienced joint and muscle pain on 28Dec2020 20:00. The patient received no treatment. The outcome of the events was recovered on an unspecified date.

Other Meds: LOESTRIN; ALEVE

Current Illness:

ID: 0929475
Sex: F
Age:
State: NJ

Vax Date: 12/21/2020
Onset Date: 12/29/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20201229; Test Name: Nasal Swab; Test Result: Positive ; Comments: NAA nasal swab; Test Date: 20201229; Test Name: Other (Rapid covid test); Test Result: Positive

Allergies:

Symptoms: received a covid positive diagnosis; received a covid positive diagnosis; This is a spontaneous report from a contactable nurse (patient). A 35-year-old non-pregnant female patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular in the left arm on 21Dec2020 09:45 at a single dose for COVID-19 immunization at the hospital. The patient has no medical history. The patient has no known allergies. The patient's concomitant medications were not reported. The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine and did not received other medications within 2 weeks of vaccination. The patient received a COVID positive diagnosis on 29Dec2020, 8 days later. The events led to a doctor or other healthcare professional office/clinic visit. The patient underwent COVID tests post vaccination on 29Dec2020 - Nasal Swab (NAA nasal swab) and Rapid COVID test, both showed positive test results. The patient was not diagnosed with COVID-19 prior to vaccination. Outcome of the events was recovering. No treatment was given for the events. The events were assessed as non-serious. Information on the lot/batch number has been requested.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors; however, a contributory role of the suspect product BNT162B2 to the reported drug ineffective and COVID-19 cannot be ruled out.

Other Meds:

Current Illness:

ID: 0929476
Sex: F
Age:
State: VA

Vax Date: 12/21/2020
Onset Date: 12/21/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: felt a strange feeling in the right-side of the neck that ended around the base of the head/Since then, it just doesn't feel right; felt a strange feeling in the right-side of the neck that ended around the base of the head/Since then, it just doesn't feel right; nausea; Since then, it just doesn't feel right; since the vaccine have stiffness when turning my neck; a few headaches; This is a spontaneous report from a contactable nurse (patient) A 41-years-old female patient started to the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot number: EJ1685, intramuscularly on 21-DEC-2020 09:30 (at the age of 41-years-old) as a single dose in the right arm for COVID-19 immunization. Medical history was none. The patient did not have allergies to medications, food, or other products. Concomitant medication included multivitamin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The most recent COVID-19 vaccine was administered in the hospital. The patient was not pregnant at the time of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Soon after receiving the vaccine in my right arm, she felt a strange feeling in the right-side of the neck that ended around the base of the head and nausea on 21Dec2020. Since then, it just doesn't feel right and still have the nausea and since the vaccine have stiffness when turning my neck on 21Dec2020. "I can't really describe it much more than it feels strange and hasn't gotten better". The patient had a few headaches on 21Dec2020 but am unsure if that's related to the vaccine as they didn't occur immediately after receiving it. The events felt a strange feeling in the right-side of the neck that ended around the base of the head, nausea, Since then, it just doesn't feel right, since the vaccine have stiffness when turning my neck and a few headaches did not result in death, was not life-threatening, did not cause/prolonged hospitalization, was not disabling/incapacitating and did not cause congenital anomaly/birth defect. No treatment was received for the events. Outcome of the events felt a strange feeling in the right-side of the neck that ended around the base of the head, nausea, Since then, it just doesn't feel right, since the vaccine have stiffness when turning my neck and a few headaches was recovering. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 0929477
Sex: F
Age:
State: CO

Vax Date: 12/31/2020
Onset Date: 12/31/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; Chills; This is a spontaneous report from a non-contactable healthcare professional (patient). A 26-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686), intramuscular on 31Dec2020 08:45 in arm (reported as left and right) at single dose for COVID-19 immunization. The patient medical history was not reported. Concomitant medication included ethinylestradiol, norgestimate (NORGESTIMATE AND ETHINYL ESTRADIOL). It was reported that on 31Dec2020, the patient had chills and headache that started around 11:00 pm on the day the patient received the vaccine. The patient took 400mg of ibuprofen the next morning and had no recurrent symptoms. The facility where the most recent COVID-19 vaccine was administered was in the hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovered on unspecified date. The event was considered non serious as it did not results in death, was not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and had no congenital anomaly/birth defect.

Other Meds: NORGESTIMATE AND ETHINYL ESTRADIOL

Current Illness:

ID: 0929478
Sex: F
Age:
State: TX

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20201229; Test Name: Body temperature; Result Unstructured Data: Test Result:low grade fever

Allergies:

Symptoms: muscle aches, joint aches, sore throat, low grade fever; muscle aches, joint aches, sore throat, low grade fever; muscle aches, joint aches, sore throat, low grade fever; muscle aches, joint aches, sore throat, low grade fever; This is a spontaneous report from a contactable other hcp. A 46-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number and expiry date unknown, via an unspecified route of administration on 29Dec2020 10:00 at a SINGLE DOSE for covid-19 immunisation. Medical history included anxiety and food allergy from cashews from an unknown date and unknown if ongoing. Concomitant medication included paroxetine (PAROXETINE), cetirizine (CETIRIZINE), iron (IRON), vitamin d3 (VITAMIN D3) and magnesium (MAGNESIUM). The patient experienced muscle aches, joint aches, sore throat and low grade fever (non-serious) on 29Dec2020 18:00. The patient underwent lab tests and procedures which included body temperature: low grade fever on 29Dec2020. The outcome of event was recovered with sequelae. Information about lot/batch number has been requested.

Other Meds: ; ; ; VITAMIN D3;

Current Illness:

ID: 0929479
Sex: M
Age:
State: NH

Vax Date: 12/29/2020
Onset Date: 12/30/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: left eyelid severely swollen; eye lid or perhaps eyeball under lid sore to touch; This is a spontaneous report from a contactable consumer (patient). A 42-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot #: unknown), via an unspecified route of administration on 29Dec2020 13:00 in left arm at single dose for COVID-19 immunization. Medical history included seasonal allergy and asthma from an unknown date and unknown if ongoing. Concomitant medication included zinc, vitamin C [ascorbic acid], vitamin B3 and Elipta for asthma. The patient had historical vaccine Tetanus and experienced allergies. On 30Dec2020, the patient woke up the next morning with left eyelid severely swollen then took anithistamine Allegra, it got better as the eye lid or perhaps eyeball under lid sore to touch for next 24 hours but getting progressively better. The facility where the most recent COVID-19 vaccine was administered in a nursing home or senior living facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovered on unspecified date. The event was considered non serious as it did not results in death, was not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and had no congenital anomaly/birth defect. Information on the lot/batch number has been requested.

Other Meds: ; VITAMIN C [ASCORBIC ACID]; VITAMIN B3

Current Illness:

ID: 0929480
Sex: F
Age:
State: TN

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20040110; Test Name: Fever; Result Unstructured Data: Test Result:101.4; Comments: fever of 101.4; Test Name: COVID-19 posoiive; Result Unstructured Data: Test Result:positive; Comments: Prior to vaccination

Allergies:

Symptoms: fever of 101.4 and myalgias; fever of 101.4 and myalgias; This is a spontaneous report from a contactable nurse. This 24-Year-old female nurse reported for herself that: A 24-year-old female patient received the 1st dose of bnt162b2 (BNT162B2) intramuscular at single dose at left arm on 22Dec2020 for Covid-19 immunisation, administered at hospital. Medical history included anxiety, depression, attention deficit hyperactivity disorder (ADHD), had experienced Covid prior vaccination. She was not pregnant at time of vaccination. The patient's concomitant medications were not reported. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced fever of 101.4 and myalgias on 22Dec2020. The patient underwent lab tests and procedures which included body temperature: 101.4 on 10Jan2004 fever of 101.4. No treatment received. Since the vaccination, the patient has not been tested for COVID-19. The outcome of event was recovered. Information on Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929481
Sex: F
Age:
State: SC

Vax Date: 12/15/2020
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20201228; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Injection site soreness, fatigue/chills (day). Bad diarrhea at night.; Injection site soreness, fatigue/chills (day). Bad diarrhea at night.; Injection site soreness, fatigue/chills (day). Bad diarrhea at night.; Injection site soreness, fatigue/chills (day). Bad diarrhea at night.; This is a spontaneous report from a contactable other hcp reporting for herself. This 28-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) the first dose on 15Dec2020 14:00 (Lot # EK5730) in the left arm and the second dose on 04Jan2021 12:45 (Lot # EL1284) in the right arm, both via an unspecified route of administration at single dose for Covid-19 immunisation. Medical history included asthma and allergies to Penicillin and Oxycodone. Concomitant medication included omalizumab (XOLAIR), salbutamol sulfate (PROAIR [SALBUTAMOL SULFATE]), fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA). On 04Jan2021 23:00, the patient experienced injection site soreness, fatigue/chills (day). Bad diarrhea at night. No treatment was performed. The outcome of the events was recovered. The patient underwent lab tests and procedures which included Nasal Swab, Covid test on 28Dec2020 was negative. The vaccine was administered at Hospital Facility. 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.

Other Meds: XOLAIR; PROAIR [SALBUTAMOL SULFATE]; BREO ELLIPTA

Current Illness:

ID: 0929482
Sex: F
Age:
State: CO

Vax Date: 12/31/2020
Onset Date: 01/01/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swollen hives and welts around mouth area; Muscle pain at injection site; extreme fatigue; This is a spontaneous report from a contactable other healthcare professional (HCP) (patient). A 22-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) intramuscular from on 31Dec2020 16:30 (04:30 PM) at a single dose on the left arm as Covid vaccine. The patient had no medical history. It is unknown if the patient had known allergies to medications, food, or other products. Concomitant medication included birth control (other medications within 2 weeks of vaccination). The patient was not pregnant at the time of vaccination. The patient was vaccinated in a hospital (facility where the most recent COVID-19 vaccine was administered). She did not receive other vaccines within four weeks prior to the COVID vaccine. The patient experienced muscle pain at injection site, extreme fatigue x 2 days, swollen hives and welts around mouth area x 3 days and still persistent, all on 01Jan2021 12:00. The events did not result in death, not life threatening, did not caused/prolonged hospitalization, not disabling/incapacitating, did not cause congenital anomaly/birth defect. No treatment was received for the events. She was not diagnosed with COVID-19 prior to vaccination and did not have Covid tested post vaccination (had not been tested for COVID-19 since the vaccination). The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929483
Sex: F
Age:
State: CA

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Current symptoms are ear ringing and tingling all over.; 5 minutes after injection I had ear ringing that has persisted. Additionally, I was woken with extreme nausea after ~56 hours and was ill for 24 hours. Current symptoms are ear ringing and tingling a; 5 minutes after injection I had ear ringing that has persisted. Additionally, I was woken with extreme nausea after ~56 hours and was ill for 24 hours. Current symptoms are ear ringing and tingling a; This is a spontaneous report from a contactable other healthcare professional. A 61-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: unknown ), via an unspecified route of administration (left arm) on 29Dec2020 15:30 at SINGLE DOSE for COVID-19 immunization. Medical history included migraine and allergies to penicillin from an unknown date. No other vaccine was taken in four weeks. The patient was not diagnosed with COVID-19 prior vaccination. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medication included rizatriptan benzoate (MAXALT) from an unspecified date. On 29Dec2020 15:35, 5 minutes after injection, the patient had ear ringing that has persisted. Additionally, she was woken with extreme nausea after 56 hours, on 31Dec2020 23:30 (also reported as 29Dec2020 03:45), and was ill for 24 hours. Current symptoms were ear ringing and tingling all over. Treatment was not given. Event outcome was not recovered. The reporter considered the events as non-serious. Information on the lot/batch number has been requested.

Other Meds: MAXALT

Current Illness:

ID: 0929484
Sex: U
Age:
State:

Vax Date: 12/29/2020
Onset Date: 12/31/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Name: hurt; Result Unstructured Data: Test Result:4

Allergies:

Symptoms: Injection site beside the little red it's 6 to 8 inch; It's just hurt like too much 4 out of 10/ a lot of pain just 6-8 inch from the injection site; No strength, zero to go do anything/weak; did not eat all day; dizzy; ill; Could not sleep/ being up all night long; fatigued/ tired; headache; Muscle pain; chills; I was cold; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender started to receive first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: EL1284), via an unspecified route of administration on 29Dec2020 14:00 at a single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient previously took flu shot and was goofy for the next 2 days. The patient reported that he/she had all the symptoms, side effects of the vaccine. The patient just got his/her first injection on 29Dec2020, 2 o clock in the PM. The first and the second day he was so much okay. The patient doesn't see any swollen lymph node or fever, but the rest all the things he/she stated to have. The patient stated that he/she is pretty ill, could not sleep, cold, fatigued, and had a big "done" (not clarified) headache where low mount of Tylenol could quite that down. It's just on and on and on. The injection site beside the little red it's 6 to 8 inch. It's just hurt like too much 4 out of 10 and it should not be. The patient has no strength, zero to go do anything. The patient did not eat all day. The patient reported that he/she does not have those severe symptoms of difficulty breathing, swelling of the face, and fast heart rate or thing like that, but he/she has been dizzy and very weak. It was further reported that yesterday (31Dec2020), the patient got very sick with the headache which will not go away. The patient had muscle pain, chills, and was so cold. The patient was not sure if he/she had fever last night, but he/she could not get up from his/her bed. Right now, the patient has a lot of pain just 6-8 inch from the injection site, and he/she just wanted to report all of this to the company. He had to call in sick this morning, because he was so tired being up all night long. The patient's second dose is due on the 19Jan2021. The patient wanted to know if he/she should delay the second vaccine. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0929485
Sex: M
Age:
State: NY

Vax Date: 12/28/2020
Onset Date:
Rec V Date: 01/08/2021
Hospital:

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

Allergies:

Symptoms: tested positive after taking the first dose of the vaccine; exposed to a family member with the virus/tested positive after taking the first dose of the vaccine; tested positive after taking the first dose of the vaccine; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect. A contactable nurse reported for a 60-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 28Dec2020 at single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient who tested and was positive for the virus after being exposed to a family member with the virus after taking the first dose of the vaccine. Patient was asymptomatic. The Nurse asking if we have any recommendations for the 2nd dose. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The association between the events lack of effect (suspected COVID-19, tested and was positive) with BNT162b2 can not be completely excluded.

Other Meds:

Current Illness:

ID: 0929486
Sex: M
Age:
State: MA

Vax Date: 12/24/2020
Onset Date: 01/01/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: contracted covid after getting the vaccine; contracted covid after getting the vaccine; This is a spontaneous report from a Pfizer-sponsored program. A contactable physician reported similar events for 4 patients. This is 1st of 4 reports. A 46-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: Unknown, does not have lot number to provide) via an unspecified route of administration on 24Dec2020 at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient contracted COVID after getting the vaccine on 01Jan2021. The outcome of the events was unknown. Information on the Lot/Batch number has been requested; Sender's Comments: The association between the event lack of effect (contracted COVID) with BNT162b2 can not be completely excluded.,Linked Report(s) : US-PFIZER INC-2021003894 same reporter/drug/event, different patient;US-PFIZER INC-2021003893 same reporter/drug/event, different patient;US-PFIZER INC-2021003895 same reporter/drug/event, different patient

Other Meds:

Current Illness:

ID: 0929487
Sex: U
Age:
State: MA

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

Lab Data:

Allergies:

Symptoms: Contracted covid after getting the vaccine; Contracted covid after getting the vaccine; This is a spontaneous report from a Pfizer Sponsored Program. A contactable physician reported similar events for 4 patients. This is 2nd of 4 reports. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date not provided), 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 experienced contracted covid after getting the vaccine on an unspecified date. The report was non-serious per the reporter. The outcome of the events was unknown. Information on Lot/Batch number has been requested.; Sender's Comments: The association between the event lack of effect (contracted COVID) with BNT162b2 can not be completely excluded.,Linked Report(s) : US-PFIZER INC-2021003873 same reporter/drug/event, different patient

Other Meds:

Current Illness:

ID: 0929488
Sex: U
Age:
State: MA

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

Lab Data:

Allergies:

Symptoms: contracted covid after getting the vaccine; contracted covid after getting the vaccine; This is a spontaneous report from a Pfizer-sponsored program. A contactable Physician reported similar events for 4 patients. This is 3rd of 4 reports. A patient of an unknown age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: Unknown) via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient contracted COVID after getting the vaccine. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021003873 same reporter/drug/event, different patient

Other Meds:

Current Illness:

ID: 0929489
Sex: U
Age:
State: MA

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

Lab Data: Test Name: covid; Result Unstructured Data: Test Result:contracted Covid after getting the vaccine

Allergies:

Symptoms: contracted covid after getting the vaccine; contracted covid after getting the vaccine; This is a spontaneous report from a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs). A contactable physician reported similar events for 4 patients. This is 4th of 4 reports. A patient of unspecified age and gender received bnt162b2 (lot/batch number and expiration date not provided), via an unspecified route of administration, on an unspecified date, at single dose, for Covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient contracted COVID after getting the vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The association between the event lack of effect (contracted COVID) with BNT162b2 can not be fully excluded.,Linked Report(s) : US-PFIZER INC-2021003873 same reporter/drug/event, different patient

Other Meds:

Current Illness:

ID: 0929490
Sex: F
Age:
State: MA

Vax Date: 12/17/2020
Onset Date:
Rec V Date: 01/08/2021
Hospital:

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

Allergies:

Symptoms: Arm/muscle pain; Arm/muscle pain; Exhaustion lasting two days; This is a spontaneous report from a non-contactable nurse (patient herself). A 25-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date were unknown) intramuscular (arm right), on 17Dec2020 at 06:00, at a single dose, for COVID-19 immunization. Relevant medical history included depression, anxiety, exercise endured asthma, migraines, and allergies to estrogen supplements. Concomitant medications included sertraline hydrochloride (ZOLOFT), galcanezumab (EMGALITY), clarithromycin (CLARITIN), and norethindrone. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the hospital. On an unspecified date, the patient experienced exhaustion lasting two days, and arm/muscle pain. The patient did not receive treatment for the events. Outcome of the events was unknown. The patient showed a negative post vaccination nasal swab result. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: CLARITIN [CLARITHROMYCIN]; EMGALITY [GALCANEZUMAB]; NORETHINDRONE [NORETHISTERONE]; ZOLOFT

Current Illness:

ID: 0929491
Sex: M
Age:
State: NY

Vax Date: 12/29/2020
Onset Date: 12/30/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Name: CT scan; Test Result: Negative ; Comments: negative for appendicitis

Allergies:

Symptoms: severe abdominal pain, waking him from sleep. Pain was periumbilical and supra- public region/Pain has recurred twice (24 and 48 hours post vaccination) waking from sleep each successive night; severe abdominal pain, waking him from sleep. Pain was periumbilical and supra- public region/Pain has recurred twice (24 and 48 hours post vaccination) waking from sleep each successive night; Recurrent events were also associated with a left sided headache, dull and throbbing in nature; This is a spontaneous report from a contactable other healthcare professional. A 68-year-old male patient received bnt162b2n(PFIZER-BIONTECH COVID-19 VACCINE, lot: EL0140), intramuscular in the right arm on 29Dec2020 19:00 at a single dose for COVID-19 immunization. The patient's medical history included dyslipidaemia and hypothyroidism from an unknown date and unknown if ongoing. the patient has no known allergies. Concomitant medications included acetylsalicylic acid (ASPIRIN 81), levothyroxine sodium (SYNTHROID), and atorvastatin calcium (LIPITOR). On 30Dec2020 (5-6 hours post injection), the patient developed severe abdominal pain, waking him from sleep. Pain was periumbilical and supra- public region. Relieved with analgesia (over the counter analgesia). CT scan the following days negative for appendicitis. Pain has recurred twice (24 and 48 hours post vaccination) waking from sleep each successive night and relieved with analgesia. Recurrent events were also associated with a left sided headache, dull and throbbing in nature, the initial event was not associated with a headache. The outcome of the event was recovering. The vaccine was administered in a hospital. 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 has not been tested for COVID-19 since the vaccination.

Other Meds: ASPIRIN 81; SYNTHROID; LIPITOR

Current Illness:

ID: 0929492
Sex: F
Age:
State: NJ

Vax Date: 12/29/2020
Onset Date: 12/30/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20201230; Test Name: COVID test; Test Result: Negative

Allergies:

Symptoms: Headache; Body aches; This is a spontaneous report from a contactable nurse (patient). A 55-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EH9899), intramuscular (hope it was IM, but did not know for sure because she was not watching) at right arm deltoid on 29Dec2020 08:40 at single dose for COVID-19 immunization, at the hospital where she works. The vaccine was not administered at military facility. The patient's second dose was scheduled to be 19Jan2021. The patient's medical history included potassium low, hypertension, pericarditis, asthma, herniated disc in back, pain, gastrointestinal infection (GI), Vitamin D low, wheezing, exposed to someone who was positive with COVID at a wedding on 28Dec2020, "diuretic", "cardiac/heart" and "Cholesterol". Concomitant medication included ranolazine (RANEXA) for heart, isosorbide for cardiac, potassium chloride for potassium Low, furosemide for diuretic, atorvastatin (LIPITOR) for cholesterol, acetylsalicylic acid (ASPIRIN) for cardiac, montelukast sodium (SINGULAIR) for asthma, pregabalin (LYRICA) for herniated disc in back take for pain, nebivolol hydrochloride (BYSTOLIC) for blood pressure, pantoprazole sodium sesquihydrate (PROTONIX) for GI, celecoxib (CELEBREX) for pain, spironolactone for diuretic, vitamin D for Vitamin D low, nitroglycerin for angina, salbutamol (ALBUTEROL) for wheezing, and oxycodone for pain; all ongoing. History of all previous immunizations with the Pfizer vaccine considered as suspect was reported as none. No additional vaccines administered on same date of the Pfizer Suspect. No prior vaccinations within 4 weeks. The patient reported events on the Pfizer COVID Vaccine. She reported after getting the vaccine she had body ache and headaches. On 30Dec2020 16:00, the patient experienced headache and body aches. The event headache was reported as serious medically significant. She received the COVID vaccine on 29Dec2020 and had significant body aches, but she still had a headache that had not gone away since she got the vaccine. The patient explained the body aches were mild to non-existent/resolved, later confirmed as still ongoing, but better. Her main issue was the headaches that had not gone away. The events headache and body aches started around 16:00. She worked nightshift and she woke up with it. The events did not require a visit to the emergency room or physician office. The day after she received the COVID Vaccine she was tested for COVID. She found out she was exposed the day before she received the COVID vaccine, 28Dec2020 to someone who was positive with COVID at a wedding. She later found out her COVID test on 30Dec2020 was negative. The reporter assessed both events headache and body aches as related to the suspect vaccine. She believed the body ache and headache were related to the COVID Vaccine itself. She added, she felt it's related because these events are not part of her typical health problems. She added they're not going away even with medications (oxycodone, Celebrex, and ibuprofen). Oxycodone was located in an orange pharmacy filled bottle and she was unable to provide a lot/exp/NDC. Celebrex was located in an orange pharmacy filled bottle and unable to provide a lot/exp/NDC. She saw a use by date of 10Mar2021. Ibuprofen (Lot number: OCE2824A and expiration date: Dec2021). The outcome of the event headache was not recovered, for the event body aches was recovering.; Sender's Comments: There is a reasonable possibility that the event headache was related to BNT162b2 based on known drug safety profile and close temporal relationship. 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: RANEXA; ; ; ; LIPITOR [ATORVASTATIN]; ASPIRIN [ACETYLSALICYLIC ACID]; SINGULAIR; LYRICA; BYSTOLIC; PROTONIX [PANTOPRAZOLE SODIUM SESQUIHYDRATE]; CELEBREX; ; VITAMIN D [VITAMIN D NOS]; NITROGLYCERIN; ALBUTEROL [SALBUTAMOL];

Current Illness:

ID: 0929493
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: arm pain (unspecified) following the injection; shoulder and neck stiffness; Pain was bilateral shoulders earlier; Neck is till sore, midline to posterior; This is a spontaneous report from a non-contactable nurse (patient herself that works at the surgical center of the hospital). A 54-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EX9231, expiry date: Apr2021), via an unspecified route of administration on 03Jan2021 at a single dose as Covid-19 vaccine. The patient's medical history and concomitant medications were not reported. Patient received flu vaccine on 29Oct2020. On 03Jan2021, the nurse reported some arm pain (unspecified) following the injection and shoulder and neck stiffness after going to sleep that night. The nurse reported that her arm pain resolved the next day. On 03Jan2021, pain was bilateral shoulders earlier, now subsiding. Neck was till sore, midline to posterior. The event arm pain (unspecified) following the injection was recovered on 04Jan2021. The patient was recovering from shoulder and neck stiffness and "pain was bilateral shoulders earlier". The outcome of the event neck was till sore, midline to posterior was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0929494
Sex: M
Age:
State: CA

Vax Date: 12/20/2020
Onset Date: 12/21/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20201228; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: covid 19 test result came up positive; covid 19 test result came up positive; severe left arm pain; This is a spontaneous report from a contactable unspecified Healthcare professional reporting for himself. This 52-year-old male patient received on 20Dec2020 02:30 PM first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EK5730) at single dose intramuscular in the left arm for COVID-19 immunization. No allergies to medications, food, or other products. Medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID 19. Concomitant medications (all started on an unknown date and received within 2 weeks of vaccination) included buspirone hydrochloride (BUSPIRON), atorvastatin (manufacturer unknown) and acetylsalicylic acid (BABY ASPIRIN). On 21Dec2020, 10 hours after getting vaccine the patient had body aches, cold and severe left arm pain. 4 days after getting vaccine again the patient had cold, body aches and sore throat for couple of days. On 28Dec2020, covid 19 test (nasal swab) result came up positive. The patient went to Emergency room. Outcome was recovered on an unknown date. It was unknown if a treatment was performed.; Sender's Comments: The association between the event lack of effect (COVID 19 nasal swab test result came up positive) with BNT162b2 can not be fully excluded.

Other Meds: BUSPIRON [BUSPIRONE HYDROCHLORIDE]; ; BABY ASPIRIN

Current Illness:

ID: 0929495
Sex: F
Age:
State: MN

Vax Date: 12/21/2020
Onset Date: 12/21/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Getting sick; I am so upset; typical body aches; headaches; cough; nasal congestion; Pain injection site; This is a spontaneous report from a nurse (patient herself). A 57-year-old female patient received her first dose of bnt162b2 (BNT162B2 also reported as Pfizer Covid-19 Vaccine, lot E"JI"1685 but not clarified), via an unspecified route of administration on 21Dec2020 at single dose, for Covid-19 immunisation. The patient's medical history was not reported. Concomitant medication included levothyroxine. The patient got her first Covid Vaccine on 21Dec202 and got the minimal pain at the injection site which was no big deal but about 10 days later (31Dec2020), she started getting sick. She was getting sick with Covid type symptoms, so she was off of the work and get swabbed yesterday and waiting her result to come out. She had typical body aches, headaches, cough and nasal congestion everything was along with that. She does not think these were side effects of the vaccination but just "quite" (not clarified) wondering how you she felt. She was so upset. She took Ibuprofen and Alcazar. The outcome of events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: There is a reasonable possibility that the events vaccination site pain and headache were related to BNT162b2 based on known drug safety profile. Based on the temporal relationship, the association between the other reported events 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.

Other Meds:

Current Illness:

ID: 0929496
Sex: F
Age:
State: PA

Vax Date: 12/22/2020
Onset Date: 12/31/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Intermittent internal vibration/Buzzingsensation in right lower leg (outer calfarea mainly, sometimes radiating upto knee); This is a spontaneous report from a contactable nurse (patient). A 57-year-old female patient received single dose of BNT162B2 (Pfizer- BioNTech Covid-19 Vaccine, Solution for injection, Lot number: EL0140, exp date not reported), intramuscular (vaccine location: left arm) on 22Dec2020 20:00 for COVID-19 immunization. Facility type vaccine: Hospital. Medical history included rheumatoid arthritis and cancer wherein patient received radiation and chemo (patient was a cancer survivor 10 years post radiation and chemo). The patient was not pregnant. The patient had no known allergies. Concomitant medication (other medications in two weeks) included etanercept (ENBREL) and atorvastatin (LIPITOR). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced intermittent internal vibration/buzzing sensation in right lower leg (outer calf area mainly, sometimes radiating up to knee) beginning 31Dec2020 16:00 (4:00 pm), 01Jan2021, 02Jan2021, and 03Jan2021. Patient was also started feeling this sensation in left foot on 02Jan2021. Further stated that if feels like a massager was on her leg/foot. No treatment was provided for the events. The reporter considered the events as non-serious. The patient did not have Covid prior vaccination. The patient was not Covid tested post vaccination. The outcome of the events was not recovered.

Other Meds: ENBREL; LIPITOR [ATORVASTATIN]

Current Illness:

ID: 0929497
Sex: M
Age:
State: FL

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20210101; Test Name: CT scan; Result Unstructured Data: Test Result:Normal; Test Date: 20210101; Test Name: EKG normal; Result Unstructured Data: Test Result:Normal; Test Date: 20210101; Test Name: X-ray; Result Unstructured Data: Test Result:Normal

Allergies:

Symptoms: sharp pains on left side of chest/ when taking a deep breath there is a little soreness right below the ribcage; received shot and felt soreness/like with a tetanus shot; This is a spontaneous report from a contactable consumer (patient himself). A 50-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration at site of left arm at 09:00 on 29Dec2020 at single dose for COVID-19 immunization. Medical history included colitis (in remission right now). There were no concomitant medications. The patient received shot and felt soreness on 29Dec2020, had sharp pains on left side of chest on 30Dec2020, and when taking a deep breath there is a little soreness right below the ribcage. Clinical course: patient got the vaccine on 29Dec2020 and felt soreness, like with a tetanus shot. On the 30th2020 he was kind of sore and then by midday all of a sudden felt the sharp pain in his chest, and once in a while when taking a deep breath there is a little soreness right below the ribcage. He went to the emergency room on 01Jan2021 and they first did the EKG, then the X-ray and they both were normal. To rule out pulmonary embolism they did CT scan and that was all fine. He also just wanted to rule out heart or lung problems since he is pretty healthy. He did not receive any other vaccines the same day and none 4 weeks prior. Vaccination facility type in hospital. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 0929498
Sex: F
Age:
State: PA

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: flushed; small amount of tingling to left hand; face warm; This is a spontaneous report from contactable consumer (patient). A 47-year-old female patient first dose received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot number: EKS730, intramuscular Left arm from 18Dec2020 16:00 to 18Dec2020 16:00 as single dose for COVID-19 immunisation. Medical history included osteoarthritis. Concomitant medication included paracetamol (TYLENOL), ibuprofen (ADVIL). On 18Dec2020 16:30, immediately after injection, the patient experienced small amount of tingling to left hand, face warm, and flushed, which resolved within 30 minutes without intervention. The outcome of the events was recovered. No treatment was received for the events.

Other Meds: TYLENOL; ADVIL [IBUPROFEN]

Current Illness:

ID: 0929500
Sex: F
Age:
State: MD

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Diarrhea; This is a spontaneous report from a non-contactable healthcare professional (patient). A 62-year-old female patient the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: not provided), via an unspecified route of administration on the left arm on 30Dec2020 08:15 at SINGLE DOSE for COVID-19 immunization at the hospital. Medical history included asthma, psoriasis, arthritis, overactive bladder, and obesity. The patient also had allergies with penicillin and many non-steroidal anti-inflammatory drugs (NSAIDS). Concomitant medications included etodolac (LODINE), zinc (ZINC), mirabegron (MYRBETRIQ), colecalciferol (VIT D3), ascorbic acid (VIT C), and famotidine (PEPCID). It was reported that the patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. On 30Dec2020 18:00, the patient experienced diarrhea. The patient received bismuth subsalicylate (PEPTO-BISMOL) and loperamide as treatment. The patient was recovering from the event. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds: LODINE; ; MYRBETRIQ; VIT D3; VIT C; PEPCID [FAMOTIDINE]

Current Illness:

ID: 0929501
Sex: F
Age:
State: NY

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: rash on body; The patient reported she became pregnant while taking bnt162b2/Gestation Period at Exposure was 20 weeks; The patient reported she became pregnant while taking bnt162b2/Gestation Period at Exposure was 20 weeks; The patient reported she became pregnant while taking bnt162b2/Gestation Period at Exposure was 20 weeks; This is a spontaneous report from a contactable other healthcare professional (patient). A 26-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK9231), via an unspecified route of administration in the left arm on 04Jan2021 14:30 at a single dose for COVID-19 immunization. The patient's medical history included allergies to sulfa drug. Concomitant medication included minerals nos, vitamins nos (PRENATAL VITAMINS). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took cipro [ciprofloxacin] and experienced allergy to cipro. The patient was not diagnosed with COVID-19 prior to vaccination and had not been tested for COVID-19 since the vaccination. The patient's husband noticed a rash on the patient's body when the patient was getting into pajamas for bed. She took a shower and paracetamol (TYLENOL) and went to bed. She woke up in the morning and rash was gone. The mother reported she became pregnant while taking bnt162b2. Last menstrual period date was 13Aug2020. The mother was 20 weeks pregnant at the onset of the event. The mother was due to deliver on 20May2021. Outcome of the rash was recovered. The events were considered non-serious by the reporter.

Other Meds: PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]

Current Illness:

ID: 0929502
Sex: F
Age:
State:

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Excessive abdominal gas with pain; This is a spontaneous report from a non-contactable nurse (patient). A 56-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot number not reported, via an unspecified route of administration on Arm Left from 04Jan2021 14:45 to 04Jan2021 14:45 as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 04Jan2021 18:00, the patient experienced excessive abdominal gas with pain with outcome of recovering. No treatment was received for the event. Since the vaccination, has the patient has not been tested for COVID-19. No follow-up attempts are possible; Information about batch/lot number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0929503
Sex: F
Age:
State: NY

Vax Date: 12/30/2020
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Painful Lymphadenopathy on day 6 post vaccination, not present prior to day 5, localized to axilla on the same side as vaccination; This is a spontaneous report from a contactable nurse (patient). A 33-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL0140; expiry date: unknown) via an unspecified route of administration (left arm), on 30Dec2020 at 07:15 a.m., at a single dose, for COVID-19 immunization. The patient's medical history was not reported. Concomitant medication included an unspecified birth control. The patient previously took amoxicillin and experienced allergies. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the hospital. On 04Jan2021, at 07:00 a.m., the patient experienced painful lymphadenopathy on day 6 post vaccination, not present prior to day 5, localized to axilla on the same side as vaccination. The patient did not receive treatment for the event. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0929504
Sex: F
Age:
State: GA

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Nausea; malaise; injection site pain; injection site swelling; This is a spontaneous report from a contactable physician (patient herself). A 43-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK5730; expiry date: unknown) via an unspecified route of administration (arm right), on 04Jan2021 at 15:00, at a single dose, for COVID-19 immunization. Relevant medical history included migraines, seasonal allergies, and history of breast cancer in remission. The patient has no known allergies. Concomitant medication included (FLONASE) fluticasone propionate. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. On 04Jan2021, at 16:45, the patient experienced nausea, malaise, injection site pain, and injection site swelling. The patient did not receive treatment for the events. Outcome of the events was not recovered. The patient has not been tested for COVID-19 since vaccination.

Other Meds: FLONASE [FLUTICASONE PROPIONATE]

Current Illness:

ID: 0929505
Sex: F
Age:
State: CA

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Extreme pain in vaccine area for 72 hours post shot/ dull ache; Could not perform daily activities; This is a spontaneous report from a contactable other healthcare professional. A 31-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EH9899;expiry date: unknown) via an unspecified route of administration (arm left), on 29Dec2020 at 15:30, at a single dose, for COVID-19 immunization. The patient has no relevant medical history and has no known allergies. Concomitant medication included an unspecified birth control. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the hospital. On 29Dec2020, at 18:00, the patient experienced extreme pain in vaccine area for 72 hours post shot. The patient could not perform daily activities. Post 72 hours extreme pain subsided and became a dull ache for 2 days. The patient received pain medication as treatment for extreme pain. Outcome of the events "extreme pain in vaccine area for 72 hours post shot/ dull ache" was recovering, while for the other event was unknown.

Other Meds:

Current Illness:

ID: 0929506
Sex: F
Age:
State:

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: dizziness; tongue and lip tingling; welt on bottom lip; chest tightness; SOB with activity for 2-4 hours; itching; burning; diarrhea; redness traveling up arm into chest; This is a spontaneous report from a contactable nurse reporting for herself. A 47-years-old non-pregnant female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscular in the right arm on 29Dec2020 03:30 at single dose for COVID-19 immunization. Medical history included breast cancer, allergy to peanuts, dogs, cats, the outdoors. Concomitant medication included tamoxifen (unknown manufacturer). On 29Dec2020 04:00 the patient experienced dizziness, tongue and lip tingling, welt on bottom lip, chest tightness, SOB with activity for 2-4 hours, itching immediately after injection (as reported), then burning, then redness traveling up arm into chest, and immediate onset of diarrhea. The outcome of the events was recovered. The patient received famotidine (PEPCID) and Cetirizine as treatment for the event. No other vaccine was administered in four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination the patient had not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929507
Sex: M
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Salt water taste in mouth, lasted strongly 5 min immediately after injection. Got less strong as time went on for approx 45 min after injection; Dry mouth with lasted an addition 30 min; This is a spontaneous report from a contactable consumer (patient himself). This 19-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EK5730), via an unknown route, on 05Jan2011 at 13:30 at single dose for COVID-19 immunisation. Vaccine location was arm left. Relevant medical history included asthma. No relevant concomitant medications were provided. The patient was vaccinated at hospital, age at vaccination was 19-year-old. No known allergies. No other vaccine was received in four weeks. Post-vaccination COVID test was not performed. The patient had salt water taste in mouth, lasted strongly 5 minutes immediately after injection. Got less strong as time went on for approx 45 minutes after injection. This was followed with dry mouth with lasted an addition 30 minutes. The onset date of the events 05Jan2021 at 13:45 (as reported). The patient was not treated for the events. The patient recovered from the events on 05Jan2021.

Other Meds:

Current Illness:

ID: 0929508
Sex: F
Age:
State:

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: heartbeat; Result Unstructured Data: Test Result:rapid heartbeat that lasted more than 20 mins

Allergies:

Symptoms: A rapid heartbeat that lasted more than 20 mins.; This is a spontaneous report from a non-contactable other healthcare professional. A 33-year-old female patient started to receive first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL0142; expiry date: unknown) via an unspecified route of administration, on 04Jan2021, at a single dose, for COVID -19 immunization. The patient's medical history and concomitant medications were not reported. The patient has no known allergies. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. On 04Jan2021, the patient experienced a rapid heartbeat that lasted more than 20 minutes (mins). The patient did not receive treatment for the event. The patient recovered from the event on the same day. The patient has not been tested for COVID-19 since vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0929509
Sex: F
Age:
State:

Vax Date: 12/21/2020
Onset Date: 12/22/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Name: pulse ox; Test Result: 92 %; Comments: her oxygen saturation dropped for 48 hours

Allergies:

Symptoms: headache/had a headache for 24 hours; both arms being shaky; short of breath/shortness of breath wigged her out/shortness of breath; sore in both arms/Both of her arms were sore; Her sats dropped to 92% on a pulse ox/oxygen saturation dropped; shortness of breath wigged her out; This is a spontaneous report from a contactable nurse reporting for herself. A 37-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on 21Dec2020 at single dose for COVID-19 immunisation. The medical history included she had COVID back on 11Oct2020. The concomitant medications were not reported. The patient received the first dose of COVID-19 vaccine on 21Dec2020 and 2nd dose is due on Friday. She reported being sore in both arms and short of breath, stats 92% on pulse ox. The day after the vaccine, on 22Dec2020 she had the same symptoms as when she had COVID. Both of her arms were sore. She was short of breath. Her sats (saturation) dropped to 92% on a pulse ox (oximetry). The shortness of breath wigged her out. She stated she experienced shortness of breath and her oxygen saturation dropped for 48 hours. She was healthy before this with no preexisting conditions. She didn't know if she should get the second vaccine. She read most people are getting a bigger response from the second vaccine. She stated she also had a headache on an unspecified date. She had a headache for 24 hours and she experienced both arms being shaky on an unspecified date. The patient stated her symptoms were similar to when she had COVID and that she did not wait 90 days before getting the first dose of the COVID vaccine since she had COVID. She was scheduled to receive her second dose of COVID vaccine on 08Jan2021. She wanted to know if she was going to end up with a bigger reaction. The patient would like to know if she should receive the second dose since she had a reaction to the first dose. The events were reported as non-serious. The event outcome was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0929510
Sex: M
Age:
State: CA

Vax Date: 12/31/2020
Onset Date: 01/02/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 2020; Test Name: COVID 19 test; Test Result: Negative ; Comments: Had the COVID 19 test 3 months ago and it was negative.

Allergies:

Symptoms: headache/ his head was really pounding; nausea; chills; he had no appetite; This is a spontaneous report from a contactable consumer (patient). A 41-years-old male patient received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/lot number: EL1284, Expiry Date: Apr2021), via an unspecified route of administration in the right arm on 31Dec2020 at 14:00 at single dose for COVID-19 immunization as front line health care worker. There were no medical history and no concomitant medications. The patient received the Pfizer COVID 19 vaccine first dose 31Dec2020 at 14:00 in the right arm and then experienced a headache, nausea, and chills on 02Jan2021. He took two days off from work and now felt better, had no more symptoms. He noticed the symptoms on Saturday 02Jan2021, then Sunday he was able to go to work then he took off on Monday because the symptoms got worse. He had no appetite on 02Jan2021. Today he felt great. He was supposed to get the second dose 21Jan2021. He did take Ibuprofen with strength 600 mg oral once on 02Jan2021, because his head was really pounding and then he went to sleep and it was better the next day. He had no history of all previous immunization with the Pfizer vaccine considered as suspect. There were no additional vaccines administered on same date of the Pfizer suspect. There were no prior vaccinations -within 4 weeks. There was no family medical history. He had the COVID 19 test 3 months ago in 2020 and it was negative. The outcome of the events was recovered on 04Jan2021.

Other Meds:

Current Illness:

ID: 0929511
Sex: F
Age:
State:

Vax Date: 12/24/2020
Onset Date: 12/24/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Name: Chest x-ray; Result Unstructured Data: Test Result:negative

Allergies:

Symptoms: Swollen lymph node with no relief.; experiencing left shoulder, left muscle, cannot lift, push, pull and pain has not decreased; experiencing left shoulder, left muscle, cannot lift, push, pull and pain has not decreased; experiencing left shoulder, left muscle, cannot lift, push, pull and pain has not decreased; This is a spontaneous report from a contactable other hcp. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 24Dec2020 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The reporter stated states she previously reported adverse event. Received first dose of vaccine 24Dec2020 experiencing left shoulder, left muscle, cannot lift, push, pull and pain has not decreased. Swollen lymph node with no relief. Chest x-ray was negative. Muscle relaxer made her feel like a "pile of goo". Therapeutic measures were taken as a result of experiencing left shoulder, left muscle, cannot lift, push, pull and pain has not decreased (arthralgia), experiencing left shoulder, left muscle, cannot lift, push, pull and pain has not decreased (myalgia). The outcome of the events was not resolved. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929512
Sex: F
Age:
State: TN

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

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

Allergies:

Symptoms: experiencing in upper body chills; This is a spontaneous report from a contactable Pharmacist reporting for a patient. A 6-decade-old (early 50s) female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on unknown date at single dose for COVID-19 immunisation. The medical history and concomitant medications were not reported. The Pharmacist reported two patients with delayed onset symptoms, he was not entirely sure if they were related to the vaccine. The Pharmacist wanted to know if there is any data on delayed onset side effects. 10 days after vaccine, the patient in early 50s and was experiencing in upper body chills on an unspecified date and negative for COVID on unknown date. The event outcome was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929513
Sex: F
Age:
State:

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: itchiness that the administration of the Pfizer's COVID-19 vaccine left her in the administration site; stiffness that the administration of the Pfizer's COVID-19 vaccine left her in the administration site; stiffness that the administration of the Pfizer's COVID-19 vaccine left her in the administration site; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 04Jan2021 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient asked if she should use Benadryl for the itchiness and stiffness that the administration of the Pfizer's COVID-19 vaccine left her in the administration site in Jan2021. She was administered with the first dose of the vaccine yesterday 04Jan2021 and she was experiencing these symptoms after that. She was going to contact her Physician for that information. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0929514
Sex: F
Age:
State:

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: muscle aches and pain; sinus infection; fatigue; pain at the injection site; This is a spontaneous report from a Pfizer-sponsored program. From a contactable nurse (patient). A female patient of unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 04Jan2021 at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient received 1st dose of vaccine yesterday (04Jan2021). She needed to see her PCP for a sinus infection. She usually received a "Z-pack, a steroid injection and a Rocephin injection." She also stated some fatigue, muscle aches and pain at the injection site, but the fatigue and aches could be her sinus infection. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929515
Sex: F
Age:
State: MO

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 01/08/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Urinary tract infection; Injection site soreness/ Injection site pain; Achy; Headache; Sore on the injection arm; Her arm was stiff feeling; This is a spontaneous report from a Pfizer sponsored program Pfizer First Connect. A contactable consumer (patient) reported that a 63-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number EL0140), intramuscular on 18Dec2020 15:00 at single dose for COVID-19 immunization. Medical history was none. There were no concomitant medications. The transferring agent stated that she has a caller on the line that received the first dose of the Covid-19 vaccine on 18Dec2020. She is supposed to get the second dose tomorrow 06Jan2021. She developed a urinary tract infection over new years and was put on antibiotics. She wanted to know if she could get the second dose while on antibiotics. The transferring agent stated that the caller reported that she started feeling achy and had a headache, but did not think it was related to the shot. She stated that she had injection site pain and was sore on the injection arm. She had the shot late in the afternoon around 15:00 on 18Dec2020. She said that she was sore later on that evening at the injection site and her arm was stiff feeling the next day, but it was resolved by the day after. She said that the headache came and went. She treated it with Tylenol. She said that she did not feel real good most of the day on Saturday 19Dec2020, but by Sunday she was back to normal again. The outcome of the event Urinary tract infection was unknown while the outcome of the other events was resolved on 20Dec2020.

Other Meds:

Current Illness:

ID: 0929516
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: lethargic; unable to get out of bed; This is a spontaneous report from a contactable nurse. A patient in late 50's or 60's of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on unknown date at single dose for COVID-19 immunisation. The medical history and concomitant medications were not reported. It was reported one of the report's doctors in late 50's or 60's was lethargic and was unable to get out of bed for 2 days on an unspecified date after getting the vaccine. The event outcome was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929517
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: He has acute gout attack; some pains in the toes; left foot full blown gout attack happened; This is a spontaneous report from a contactable physician (patient). A 45-years-old male patient received his first dose of 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 patient reported potential side effect of the vaccine. He had acute gout attack. On the 1st week he had experienced some pains in the toes - left foot full blown gout attack happened. He wanted to know what to do if he will continue on getting the 2nd dose since he did not want to experience another episodes of flare ups. He asked if it had aluminum adjuvant on the vaccine. The events were reported as non-serious. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0929518
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: tingling; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received her first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient was apprx 54 year old activities coordinator at a long term care facility. She had first dose of vaccine and had tingling. She was wondering how long the tingling will last and will it ever go away? She was also asking what did the expiration date mean. The event outcome was not resolved. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0929519
Sex: M
Age:
State: TX

Vax Date: 01/04/2021
Onset Date: 01/04/2021
Rec V Date: 01/08/2021
Hospital:

Lab Data: Test Date: 20210105; Test Name: blood sugar; Result Unstructured Data: Test Result:101; Test Name: TSH; Result Unstructured Data: Test Result:low; Test Name: TSH; Result Unstructured Data: Test Result:normal; Test Name: temperature; Result Unstructured Data: Test Result:usually 98 or 97 Fahrenheit; Test Date: 20210104; Test Name: temperature; Result Unstructured Data: Test Result:99.5 Fahrenheit

Allergies:

Symptoms: Caller took his temperature under his tongue and the reading was 99.5?F last night/his temperature is usually 98 or 97?F/ he maintains his temperature around 96 or 97; some injection site pain; some body pains/ a lot of body pain; he could not sleep much states it was intermittent/He woke up every hour; his vision is not really good; He was experiencing an uncomfortable feeling in his body; This is a spontaneous report from a contactable consumer (patient). A 74-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number: EK5730, Expiration date: Mar2021, at single dose on 17Dec2020, and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EK9231, expiration date Apr2021, Intramuscular at single dose in left shoulder on 04Jan2021 for prevention of covid. Medical history included ongoing Diabetes which was controlled with medication, blood pressure abnormal, microalbumin level that was high in urine, TSH was low. Concomitant medications included metformin for two or three years for Diabetes, lisinopril for blood pressure and kidney albumin control (he was found to have a microalbumin level that was high in urine and it was prescribed by his doctor several months ago. It was a kidney albumin control), and ongoing levothyroxine since TSH was low (now his TSH was normal and he was taking it per his doctor). The patient received his second dose of Covid vaccine yesterday (04Jan2021). He took his temperature under his tongue and the reading was 99.5?F last night. His temperature was usually 98 or 97?F. He took two Tylenol tablets last night and he did not go to work today. He also had some injection site pain. He had some body pains. He did not have these side effects with the first dose and understood this vaccine was more than the flu vaccine but he was concerned with the side effects. He received the second dose yesterday at 9:30 am. He did not have any problems with the first dose, absolutely nothing. Since last night he could not sleep much states it was intermittent, a lot of body pain, his temperature under the tongue is 99.5 degrees F and most of the time he checks his temperature with a frontal scan and he maintains his temperature around 96 or 97. He was calling to ask if the vaccine can cause covid infection. He did not have any problems yesterday at all prior to the vaccine being administered. When querying outcome of his body pain he stated it was mild. He took 2 caplets of Tylenol yesterday in the middle of the evening. He woke up every hour. He was experiencing an uncomfortable feeling in his body. His temperature was taken about 5 or 10 minutes ago and was 99.3 (states there may be a difference between under the tongue and frontal scan reading). He had to get his temperature checked behind the ear at his workplace since he was coming in from the cold outside. His blood sugar this morning (05Jan2021) was 101. His vision was not really good. Sometimes with the flu vaccine he got the same effect he was getting now but he did not worry about it with the flu vaccine. He received the flu vaccine a long time ago. The outcome of all events was unknown.

Other Meds: ; ;

Current Illness: Diabetes (Patient Medical comments: Verbatim: Diabetes)

ID: 0929520
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: she had some mild redness; swelling in the whole arm; This is a spontaneous report from a contactable Nurse (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. She already received the first dose and she had some mild redness and swelling in the whole arm. The outcome of the events was unknown. Information on lot/Batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm