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: 1004211
Sex: F
Age: 76
State: TN

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

Lab Data: Test Date: 20210102; Test Name: Blood sugar; Test Result: Inconclusive ; Result Unstructured Data: 150

Allergies:

Symptoms: Afib; Feeling uncomfortable; Blood sugar was around 150, which is higher than her normal levels; A spontaneous report was received from a consumer who is 76-year-old, female patient, who received Moderna's COVID-19 Vaccine (mRNA-1273) and experienced atrial fibrillation, feeling uncomfortable, and increased blood sugar. The patient's medical history included diabetes and atrial fibrillation. Concomitant medications were not reported. On 02 Jan 2021, the patient received their first two planned doses of mRNA-1273 (Batch number: 025LZ0A) intramuscularly in her right arm for the prophylaxis of COVID-19 infection. On 02 Jan 2021, the patient experienced heart beating very fast and feeling uncomfortable; it lasted for a few hours. She stated it was atrial fibrillation, she had a diagnosis of this, and it only lasted a few hours. The patient also stated that her blood glucose was 150, which was higher than normal. Treatment for the events was not provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of events, increased blood sugar, was considered not resolved. The outcome of the events, atrial fibrillation and feeling uncomfortable, was considered resolved.; Reporter's Comments: This case concerns a 76 year-old female patient with a significant medical history of atrial fibrillation and diabetes, who experienced a serious unexpected event of Atrial fibrillation and non-serious unexpected events of Discomfort and Blood glucose increased. The events occurred one day (same day) after first dose of mRNA-1273, lot # 025LZ0A. Treatment was not reported. Based on the current available information and temporal association between the use of the product and onset of the event a causal relationship cannot be excluded. However, patient's medical history of atrial fibrillation and diabetes were considered strong confounders.

Other Meds:

Current Illness: Atrial fibrillation; Diabetes

ID: 1004212
Sex: M
Age:
State: TX

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210115; Test Name: Blood pessure; Result Unstructured Data: Test Result:high; Test Date: 20210115; Test Name: knee examination; Result Unstructured Data: Test Result:the doctor said it was alright

Allergies:

Symptoms: Blood pressure was high; tired from the night before; Itchy; slight headache; little lightheaded; Heart racing; panic attack; Hot flashes; Sweating; Chills; achy/body aches; This is a spontaneous report from a Pfizer sponsored program Pfizer First Connect. A contactable consumer reported for himself, a 62-year-old male patient who received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3249), via an unspecified route of administration (reported as by injection) to left arm on 14Jan2021 at 3pm at single dose to prevent COVID/COVID-19 immunization. Medical history included anxiety. Concomitant medications included antidepressants. The patient received his first dose of Pfizer COVID vaccine last 14Jan2021 at 3pm, and everything went well. When he left the place, he had a slight headache. He had to stay there for 15-20 minutes to make sure he had no reaction. He just got a little lightheaded, he didn't think much, and it didn't get worse. The patient took 2 paracetamol (TYLENOL) and forgot about it. It went away for a while. He took the shot at 3 pm and he took paracetamol at 4 pm. Later that night, about 10 pm, everything kicked in. He was sick again at 10:30 pm, or so, the headache was gone for several hours. He was ok between 4 pm and 10 pm. Then about 10 to 10:30 pm, when he went to go to sleep, his heart started racing, like he was having a panic attack, then he started getting hot flashes, sweating, chills, and aching, and this went all night from like 10 pm to 11 to the next morning. He had a doctor's appointment to get his knee examined for an upcoming knee surgery. The patient clarified that he didn't go to the doctor because of the symptoms, he went for his knee. He asked the doctor, before getting examined, and the doctor said he got off easy, as the doctor himself was sick for 3 days. The patient asked the doctor if he could take something to calm down, as his blood pressure was high on 15Jan2021 at 8 am. They had taken his blood pressure to examine his knee, and the doctor said it was alright. He was prescribed with alprazolam (XANAX), and the doctor said it would be fine. The next day, he was tired from the night before. He had no symptoms the next day. After he took alprazolam, he slept fine, he felt better. The hot flashes, heart racing, body aches, and chills were gone, and he read everything as far as symptoms. The heart racing went away about 11 the next morning because he took alprazolam. The patient stated that he forgot to add one more, he had all the symptoms described as side effects, but he also had itching. He had very mild itching and was given cetirizine hydrochloride (ZYRTEC, lot number: OHE2723, expiry date: Feb2022, UPC: 4122053077), it was like 80% gone. Every now and again he has a little itch, but it was bothering him all night that first night. Currently, the patient felt pretty good. He has no symptoms other than the slight itch. He further stated that his second dose is on 04Feb2021. Out of all symptoms, the thing that freaked him out the most was the heart racing, he asked if he could take diphenhydramine hydrochloride (BENADRYL) before the shot. He has been on antidepressants for a while, he has a lot of anxiety, but the day he went in, he felt good, and didn't take alprazolam. He also asked if this have triggered all that heart racing stuff. He was seeking for information if there was anything to do to prepare him better, he knew you have to sit there for 15-20 minutes to see if there was a reaction. The outcome of the event headache and lightheadedness was recovered on 14Jan2021, unknown for blood pressure high and tiredness, recovering for itchy, and recovered on 15Jan2021 at 11 am for all other events.

Other Meds:

Current Illness:

ID: 1004213
Sex: F
Age:
State: UT

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: felt like she was running a fever; didn't feel well; when she stood up to use the bathroom...she was standing and felt dizzy, like she was going to black out; she was standing and felt dizzy, like she was going to black out; heart was racing; pale; sweating/drenched her clothes in sweat; felt so weak she could not get back to my bed; breathing was rapid; stomach pain; diarrhea; patient received the first dose of bnt162b2 on 21Dec2020. She received the second dose on 14Jan2020; This is a spontaneous report from a contactable nurse. A 40-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EL0142), via an unspecified route of administration in the left arm, on 14Jan2021 15:15 at SINGLE DOSE for COVID-19 immunization. The patient's medical history was not reported. There were no concomitant medications. 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 hasn't been tested for COVID-19. The patient received the first dose of bnt162b2 on 21Dec2020. She received the second dose on 14Jan2020. Then, it was about 12 hours later (15Jan2021 at 04:00), when she stood up to use the bathroom. She felt like she was running a fever and didn't feel well: she was standing and felt dizzy, like she was going to black out, her heart was racing, and she had to lie down. She was pale and sweating; and felt so weak she could not get back to bed. Patient's husband had to help her. These feelings lasted for about 25 minutes. Patient drenched her clothes in sweat and her breathing was rapid. Then she got stomach pain and diarrhea. The outcome of events was recovered on Jan2021. The patient did not receive any treatment for the events. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds:

Current Illness:

ID: 1004214
Sex: F
Age:
State: MI

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: temperature; Result Unstructured Data: Test Result:99.5 to 101

Allergies:

Symptoms: had been running a temperature of 99.5 to 101; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female non-pregnant patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EL 3249 and expiry date unknown) via unspecified route of administration at the left arm on 11Jan2021 at single dose for Covid-19 immunization. The patient medical history was not reported. The patient has no covid prior vaccination. Concomitant medication included losartan and vitamin; both from unspecified date for unspecified indication. The patient previously took vancomycin and Keftab; both experienced allergies. The patient had no other vaccine in four weeks. The patient had been running a temperature of 99.5 to 101 since Monday 11Jan2021 during the night (also reported as 11Jan2021 12:00 AM). The patient was not covid tested post vaccination. The patient did not receive treatment due to the event. The outcome of the event had been running a temperature of 99.5 to 101 was not recovered.

Other Meds: LOSARTAN

Current Illness:

ID: 1004215
Sex: F
Age:
State: MI

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: skin on her face feels burnt and sore to touch; skin on her face feels burnt and sore to touch; Bad headache; medical history: lupus anticoagulant positive; medical history: lupus anticoagulant positive; This is a spontaneous report from a contactable nurse (patient). A 50-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3248), via intramuscular route of administration on 19Jan2021 at 12:00 at a single dose in the arm left for COVID-19 immunization. The patient's medical history included high blood pressure, hypothyroidism, depression, lupus anticoagulant positive, and anemia. Concomitant medications included venlafaxine hydrochloride (EFFEXOR), verapamil, apixaban (ELIQUIS), montelukast sodium (SINGULAIR), levothyroxine sodium (SYNTHROID) , ergocalciferol (VIT D), cetirizine hydrochloride (ZYRTEC), hydrocodone bitartrate, paracetamol (NORCO). The patient previously took sulfamethoxazole, trimethoprim (BACTRIM) and acetylsalicylic acid (ASPIRIN) and experienced allergies. The patient also previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0140 ) on 29Dec2020 at 08:00 pm, via intramuscular route in the left arm for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior to vaccination. On 19Jan2021 at 19:00, the patient stated that her skin on her face feels burnt and sore to touch without any redness or signs of injury and had a bad headache. The patient did not receive any treatment for the reported events skin on her face feels burnt and sore to touch and bad headache. Since the vaccination, the patient has not been tested for COVID-19. The patient was not pregnant at the time of vaccination. The patient has not recovered from the events.

Other Meds: EFFEXOR; VERAPAMIL; ELIQUIS; SINGULAIR; SYNTHROID; VIT D; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; NORCO

Current Illness:

ID: 1004216
Sex: F
Age:
State: FL

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm hurt; This is a spontaneous report from a contactable consumer, the patient. This 72-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine) (Lot number: EH9899, Expiration date: 31Mar2021), first dose, via an unspecified route of administration in the left arm on 28Dec2020 at 09:30 (at 72-years-old) as a single dose for COVID-19 vaccination. Medical history included gastrooesophageal reflux disease from an unknown date and unknown if ongoing, chronic obstructive pulmonary disease from an unknown date and unknown if ongoing, glaucoma from an unknown date and unknown if ongoing and hypersensitivity from an unknown date and unknown if ongoing. Concomitant medication included famotidine (FAMOTIDINE), tiotropium bromide (SPIRIVA), latanoprost (LATANOPROST), timolol (TIMOLOL) and loratadine (LORATADINE). The patient did not receive any other vaccines within four weeks prior to the vaccination. On 28Dec2020, the patient experienced arm hurt. The event did not require a visit to physician or ER. The outcome of the event arm hurt was resolved on 29Dec2020.

Other Meds: FAMOTIDINE; SPIRIVA; LATANOPROST; TIMOLOL; LORATADINE

Current Illness:

ID: 1004217
Sex: M
Age:
State: NH

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Muscle pain remote from injection site; Headache; Painful lymphadenopathy (left axilla); Administration date=19Jan2021, dose number=2/ Administration date=21Dec2020, dose number=1; This is a spontaneous report from a contactable other health professional (patient). A 58-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3249), intramuscular on 19Jan2021 at a single dose on left arm for COVID-19 immunization. The patient medical history was not reported. Patient has no known allergies. Concomitant medication included atorvastatin and lisinopril. The patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), intramuscular on 21Dec2020 at a single dose on left arm for COVID-19 immunization. The patient experienced chills, muscle pain remote from injection site, headache, and painful lymphadenopathy (left axilla) on 20Jan2021. No treatment received for events. The outcome of the events was recovering. Facility type vaccine was Hospital. No other vaccine in four weeks. Not diagnosed with COVID prior vaccination. Not COVID tested post vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds: ATORVASTATIN; LISINOPRIL

Current Illness:

ID: 1004218
Sex: F
Age:
State: OK

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills/rigors; wheezing; shortness of breath; cough; myalgias; local vaccination site swelling as well as tenderness and colorimetric changes (looked like a POPeye arm with yellow/green tingling hanging down in a large tear drop); local vaccination site swelling as well as tenderness and colorimetric changes (looked like a POPeye arm with yellow/green tingling hanging down in a large tear drop); local vaccination site swelling as well as tenderness and colorimetric changes (looked like a POPeye arm with yellow/green tingling hanging down in a large tear drop); local vaccination site swelling as well as tenderness and colorimetric changes (looked like a POPeye arm with yellow/green tingling hanging down in a large tear drop); This is a spontaneous report from a contactable physician (patient). A 66-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3283), via an unspecified route of administration on 20Jan2021 at a single dose on Right deltoid for COVID-19 immunization. Medical history included Chronic lymphocytic leukemia with 65% of cells lymph's, low WBC count (13500) otherwise; DM2, A1C usually close to 6.1; HTN. Unspecified concomitant medication taken. The patient previously took nickel and experienced allergies. The patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9331), intramuscular on 31Dec2020 12:15 PM at a single dose on left arm for COVID-19 immunization. The patient experienced chills, rigors, wheezing, shortness of breath, local vaccination site swelling as well as tenderness and colorimetric changes (looked like a POPeye arm with yellow/green tingling hanging down in a large tear drop), cough, myalgias on 20Jan2021 23:30. Therapeutic measures were taken as a result of the events which included Benadryl, Aleve, Nebulizer treatment, change in local temperature to help stop rigors. The outcome of the events was recovering. No other vaccine in four weeks. The patient was not pregnant. Not diagnosed with COVID prior vaccination. Not COVID tested post vaccination.

Other Meds:

Current Illness:

ID: 1004219
Sex: F
Age:
State: MI

Vax Date: 01/07/2021
Onset Date:
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe joint pain; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date were not reported), via an unspecified route of administration on 07Jan2021 at a single dose for COVID-19 immunization. There were no medical history and concomitant medications. The patient reported having severe joint pain and she was questioning if she should get the second dose of the vaccine. The second dose is scheduled for 28Jan2021. Outcome of the event was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 1004220
Sex: F
Age:
State: MI

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; tiredness; nose bleeding; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3248, expiration date was unknown), via an unspecified route of administration in the left arm on 20Jan2021 01:30 at a single dose for COVID-19 immunization. Medical history included chronic migraine from an unknown date and unknown if ongoing. Concomitant medication included citalopram and trazodone. The patient was not pregnant. The patient had no other vaccine in four weeks prior vaccination. She had no covid prior vaccination nor was she tested post vaccination. The patient experienced headache, tiredness, she had a nose bleed and added that most of the time, if she had a headache, her nose will bleed. The events occurred on an unspecified date in Jan2021 at 03:00 AM with outcome of recovered in Jan2021. No treatment received for the events.

Other Meds: CITALOPRAM; TRAZODONE

Current Illness:

ID: 1004221
Sex: F
Age:
State: RI

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Minor sore arm at injection site; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration (left arm) on 20Jan2021 11:45 at single dose for Covid-19 immunization. The patient's medical history included "known allergies: phenothiazine drugs". There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received TDAP vaccine and experienced sore arm at injection site. The patient was not diagnosed with COVID-19 prior to vaccination. The patient is not pregnant. On 21Jan2021, the patient experienced minor sore arm at injection site reported as "not nearly as bad as TDAP vaccine". There was no treatment received for the adverse event. The outcome of event is recovering. The patient has not been tested for COVID-19 since the vaccination.

Other Meds:

Current Illness:

ID: 1004222
Sex: M
Age:
State: TX

Vax Date: 01/14/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: mild diarrhea post shot; This is a spontaneous report from a contactable consumer (patient). A 21-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL3302) via an unspecified route of administration on the left arm on 14Jan2021 13:00 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 20Jan2021 05:00 AM, the patient experienced mild diarrhea post shot. No treatment was received for the event. Event resulted to a doctor or other healthcare professional office/clinic visit. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The facility where the vaccine was administered was in a hospital in a Military Base. Post vaccination, the patient has not been tested for COVID-19. Outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1004223
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: wrist got really itchy; I had rash on bicep over a week/I also broke out in a rash on my biceps of the same arm; slight rash and some kind of sprinkling; it is a slightly itchy; She also had a headache the night off and felt flushed; She also had a headache the night off and felt flushed; This is a spontaneous report from a contactable healthcare professional (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took tamiflu for flu and had allergy. The patient said that the after getting the vaccine her wrist was inoculated and itchy. Her wrist got really itchy that was the only side effect from the vaccine for the first hour. The patient had rash on bicep over a week. She broke out in a rash on her biceps of the same arm. It was slight rash and some kind of sprinkling but it lasted for over a week and it was slightly itchy. She also had a headache the night off and felt flushed. She wanted to know if she can receive the second dose. The outcome of the event itchy rash was recovered on unspecified date and unknown for the other events. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004224
Sex: F
Age:
State: MD

Vax Date:
Onset Date: 01/12/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: very cold; nausea; weak; light headed; tingly sensation in my limbs (like little needles); This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received the first dose of bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Lot number: EL3247), via an unspecified route of administration at the right arm on 19Jan2021 08:00 AM (as reported) at a single dose for covid-19 immunization. Medical history included sarcoid and premature heart disease. The patient was not pregnant at the time of vaccination. Concomitant medication included atorvastatin, rabeprazole, acetylsalicylic acid (ASPRIN) and chlorthalidone. On 12Jan2021 10:30 pm, the patient experienced very cold, nausea, weak, light-headed, tingly sensation in my limbs (like little needles). The events were assessed as non-serious, did not result in death, not life threatening, did not cause/prolonged hospitalization, not disabling/incapacitating, did not cause congenital anomaly/birth defect. Treatment was not received for the adverse events. The vaccine was administered in a hospital. The patient has not received 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 recovering.

Other Meds: ATORVASTATIN; RABEPRAZOLE; ASPRIN; CHLORTHALIDONE

Current Illness:

ID: 1004225
Sex: M
Age:
State: MO

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Site pain; joint pain in knees, back, and neck; This is a spontaneous report from a contactable consumer (patient). A 70-year-old male patient received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ek9231), via an unspecified route of administration in the right arm on 20Jan2021 15:15 at a single dose for covid-19 immunization. Medical history included rheumatoid arthritis (RA) and Sjogren's syndrome; both from an unknown date. Concomitant medication included methotrexate, hydroxychloroquine, levothyroxine sodium (SYNTHROID), and folic acid. The patient previously took Codine and experienced allergy. The patient experienced site pain; and joint pain in knees, back, and neck on 21Jan2021 03:00. Outcome of the events was recovering. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The events were assessed as non-serious. No treatment was received for the adverse events. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient has not been tested for COVID-19.

Other Meds: METHOTREXATE; HYDROXYCHLOROQUINE; SYNTHROID; FOLIC ACID

Current Illness:

ID: 1004226
Sex: F
Age:
State: MO

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210120; Test Name: Heartbeat; Result Unstructured Data: Test Result:rapid

Allergies:

Symptoms: rapid heart beat; severe anxiety; This is a spontaneous report from a contactable healthcare professional (patient). A 44-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on the left arm on 20Jan2021 09:15 at single dose for COVID-19 immunization. Medical history included allergies: artificial orange in food and anxiety. Concomitant medication included ethinylestradiol, norgestimate (SPRINTEC) for birth control. The patient previously took first dose of BNT162B2 for covid-19 immunization on an unspecified date; and ammonia and experienced allergies. The patient was not pregnant at the time of vaccination. On 20Jan2021 14:00, the patient experienced rapid heartbeat and severe anxiety. The patient didn't go to the hospital and just worked through it herself as she has anxiety anyway. This lasted for about 4 hours. The patient did not receive treatment for the events. Prior to vaccination the patient was not diagnosed with COVID-19 and since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was recovered on 20Jan2021.

Other Meds: SPRINTEC

Current Illness:

ID: 1004227
Sex: F
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: muscle aches and pain; muscle aches and pain; dizziness; This is a spontaneous report from a contactable consumer (patient herself) via medical information team. A female patient of an unspecified age received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not reported), via an unspecified route of administration on 20Jan2021, 10:30 at a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On 20Jan2021 at 21:00, the patient experienced muscle aches and pain, and dizziness. The patient wanted to know if these were common side effects and if she can use TYLENOL after her first vaccination with the PFIZER-BIONTECH COVID-19 VACCINE. The patient has not recovered from the events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004228
Sex: F
Age:
State: WI

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sore throat; had chills; hot with a slight fever; hot with a slight fever; dizzy; tired/slept all day; congestion; severe headache; severe cough; achy/was in such pain all over; This is a spontaneous report from a contactable healthcare professional (patient). A 61-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL3249, expiration date unspecified), intramuscular on 18Jan2021 12:00 at single dose (left arm) for COVID-19 immunization. Medical history included slight hypertension and allergies to penicillin. The patient was not pregnant at the time of vaccination. Concomitant medication included losartan. The patient took first dose of bnt162b2 on 28Dec2020, at 10:00 (lot EL1284) at left arm for COVID-19 immunization. When the patient went to bed that night about 10 hours after the shot, I was just achy on 18Jan2021, at 22:30. When she got up at 02:30, she was in such pain all over and had chills and was hot with a slight fever, was dizzy, and tired on 19Jan2021. When she woke up later and had to call off, she had all of that (worsening), plus congestion and severe headache on 19Jan2021. The patient slept all day, but developed a severe cough by that night and she took nighttime cold medication to sleep and when she woke up on Wednesday, she took the daytime ones. The patient reported that she still have achiness, was tired, and a sore throat and some cough on Thursday, 21Jan2021. The patient received therapy for the event severe cough; and patient did not received treatment for the rest of events. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. Outcome of events was recovering.

Other Meds: LOSARTAN

Current Illness:

ID: 1004229
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: shingles; This is a spontaneous report from a contactable other health professional (HCP). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot and expiry not reported), via an unspecified route of administration on 02Jan2021 at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced shingles after receiving the first dose the following week (unspecified date) and was wondering if she should get the second dose. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004230
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Bruise on the injection site/bruise around the area of the vaccine; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3248; Expiration date was not reported) in Jan2021 at a single dose, with route of administration unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. In Jan2021, after the first dose of vaccination, the patient had bruise on the injection site/bruise around the area of the vaccine. The outcome of the event, bruise on the injection site/bruise around the area of the vaccine, was not recovered.

Other Meds:

Current Illness:

ID: 1004231
Sex: F
Age:
State: DC

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Swelling of armpit lymph nodes; This is a spontaneous report from a contactable other health care professional. A 27-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EL3247), via an unspecified route of administration from 18Jan2021 11:15 at SINGLE DOSE at left arm for covid-19 immunisation. Medical history included Prior to vaccination, the patient was diagnosed with COVID-19. The patient was not pregnant at the time of vaccination. The patient did not receive any vaccine within 4 weeks prior to the vaccine. There were no concomitant medications. On 18Jan2021 23:00, the patient experienced Swelling of armpit lymph nodes that started 12 ish hours later and is still here a full 60 hours later. It was unknown if the patient receive treatment for the event. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1004232
Sex: M
Age:
State: CA

Vax Date: 01/06/2021
Onset Date: 01/16/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: left supraclavicular lymphadenopathy; This is a spontaneous report from a contactable other health professional (patient). A 54-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: FK5730), via an unspecified route of administration (left arm) on 06Jan2021 03:30 at single dose for Covid-19 immunization. The patient has no medical history. The patient's concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced left supraclavicular lymphadenopathy over a centimeter in diameter noticed it 10 days after injection on 16Jan2021 (16:00). There was no treatment received for the adverse event. The outcome of event was not recovered. The patient has not been tested for COVID-19 since the vaccination. This case is non-serious.

Other Meds:

Current Illness:

ID: 1004233
Sex: F
Age:
State: KY

Vax Date: 12/21/2020
Onset Date: 12/28/2020
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20201228; Test Name: nuetraphils; Result Unstructured Data: Test Result:increased; Test Date: 20210102; Test Name: PCR for COVID-19; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20201228; Test Name: white count; Result Unstructured Data: Test Result:increased

Allergies:

Symptoms: Swollen cervical lymph node on right side with lump in throat; Swollen cervical lymph node on right side with lump in throat; temperature; fatigue; fatigue; increased white count and nuetraphils; increased white count and nuetraphils; This is a spontaneous report from contactable nurse (patient). A 38-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number requested), via an unspecified route of administration on 21Dec2020 at 16:00 on the right arm at a single dose for COVID-19 immunization. Medical history included fatigue and allergies to sulfa both from an unknown date and unknown if ongoing. Prior to vaccination, the patient has not been diagnosed with COVID-19. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced swollen cervical lymph node on right side with lump in throat, temperature and fatigue with increased white count and neutrophils (reported as nuetraphils) on 28Dec2020. The events resulted in a doctor or other healthcare professional office/clinic visit. The patient was still being treated with antibiotics and had unspecified labs. The outcome of the events was not recovered. Since the vaccination, the patient had a nasal swab PCR test for COVID-19 on 02Jan2021 with a negative result. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004234
Sex: M
Age:
State: NC

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Brain fog; anxiety; (minor) sudden brief sharp headache; soreness at injection site; This is a spontaneous report from a contactable consumer reporting for self. A 81-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), Lot# EL9261,via an unspecified route of administration on 19Jan2021 15:30 (at the age of 81-years old), Dose 1, as a single dose, left arm for COVID-19 immunization. Medical history included high cholesterol and hypothyroidism. The patient had not been diagnosed with COVID-19 prior to vaccination. Concomitant medication included levothyroxine, guaifenesin (ROBITUSSIN), and rosuvastatin calcium (CRESTOR). The patient did not receive any other vaccinations in the 4 weeks prior to the COVID-19 vaccination. On 19Jan2021 at 15:45, the patient experienced brain fog and anxiety, which lasted approximately 20 minutes. Also (minor) sudden brief sharp headache and soreness at injection site. There was no hospitalization for the events. The patient received treatment for the events, reported as "Calming talk, deep breathing, rest." The events were reported as non-serious. The patient recovered from the events brain fog, anxiety on 19Jan2021 at 16:05 and recovered from sudden brief sharp headache and soreness at injection site on unspecified date(s). The patient had not been tested for COVID-19 since the immunization.

Other Meds: LEVOTHYROXINE; ROBITUSSIN [GUAIFENESIN]; CRESTOR

Current Illness:

ID: 1004235
Sex: M
Age:
State: PA

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210119; Test Name: temp; Result Unstructured Data: Test Result:101.3; Test Date: 20210121; Test Name: temp; Result Unstructured Data: Test Result:96.1

Allergies:

Symptoms: weakness; chills; nausea; temp was 101.3/fever; swollen lymph nodes; This is a spontaneous report from a contactable consumer (patient). A 57-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK9231), via an unspecified route of administration on left arm on 18Jan2021 19:45 at a single dose for COVID-19 immunization. The patient had no medical history. The patient had no known allergies. The patient received other vaccines within 4 weeks prior to the COVID vaccine including Whooping cough vaccine (Pertussis vaccine) on 11Dec2020 (dose number 1, left arm). On 19Jan2021 19:30, the patient had weakness, chills, nausea and his temperature (temp) was 101.3. He came home Wednesday from work at the 44th hour and had all symptoms "accept" (as reported) for swollen lymph nodes. Patient's fever broke 6 hours later at 22:00 (as reported) Wednesday night (on 20Jan2021, also reported as 50 hours after the injection), he slept all night comfortably, woke up with no issues and temp was 96.1 (21Jan2021). At the time of the report the patient felt fine. There was no treatment received for the adverse events. 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 event fever was recovered on 20Jan2021 and other events recovered in Jan2021.

Other Meds:

Current Illness:

ID: 1004236
Sex: F
Age:
State: MA

Vax Date: 12/18/2020
Onset Date: 12/19/2020
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210118; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: headache; tiredness; get palpitations; chest pain; arm weakness when standing too long; Anxiety; This is a spontaneous report from a contactable other HCP (patient). A 45-year-old female patient (not pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number reported as 5730, pending clarification), via an unspecified route of administration on 18Dec2020 at single dose in left arm for COVID-19 immunisation. Patient age at vaccination was 45 years. The patient was vaccinated at hospital. No other vaccine was given within 4 weeks prior to the COVID vaccine. Medical history included asthma and known allergies to epinephrine, latex, sulfa. Concomitant medications included amoxicillin (AMOXICILLIN), ibuprofen (MOTRIN). On 19Dec2020 at 01:00 PM the patient had headache and tiredness ever since get palpitations, chest pain, arm weakness when standing too long or when first get up. Heart doctor thinks it's due to vaccine or anxiety but never had this before shot. The events resulted in doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Treatment for the events included anti anxiety medication, metoprolol. The events had not resolved. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination the patient was tested for COVID-19 (nasal swab) on 18Jan2021 which resulted negative. Information about lot/batch number has been requested.

Other Meds: AMOXICILLIN; MOTRIN [IBUPROFEN]

Current Illness:

ID: 1004237
Sex: F
Age:
State:

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: metal taste in her mouth; She also felt like she was burning up inside; She was sweating and her body felt extremely warm inside; This is a spontaneous report from a contactable other healthcare professional (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number and expiration date not reported) via an unspecified route of administration on 21Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the COVID vaccine morning on 21Jan2021, and 15 to 30 minutes later, she had a metal taste in her mouth and was still having the metal taste in her mouth. She also felt like she was burning up inside out. She was sweating and her body felt extremely warm inside. Events were reported as non-serious. Outcome of the event metal taste in her mouth was not recovered, while unknown for the other events. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1004238
Sex: M
Age:
State: MD

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Some irritation in my nose/on the inside of his left nostril; Runny nose; Little pain in the arm; Some minor pain at the COVID-19 Vaccine injection site; Headache; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 20Jan2021 (09:00) at a single dose, with route of administration unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 20Jan2021, in the evening, the patient had a little pain in the arm; some minor pain at the COVID-19 vaccine injection site; and headache. The patient had received paracetamol (TYLENOL) as treatment for the headache. On 21Jan2021, the patient had some irritation in the nose/on the inside of his left nostril; and runny nose. The outcome of the events, 'little pain in the arm', 'minor pain at the vaccine injection site', 'headache', 'some irritation in the nose/inside of left nostril' and 'runny nose', was unknown. Information about lot/batch number is requested.

Other Meds:

Current Illness:

ID: 1004239
Sex: F
Age:
State: FL

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: test; Result Unstructured Data: Test Result:she does not have covid; Comments: She thought she had covid and took a test but she does not have covid

Allergies:

Symptoms: not feeling well/general malaise/feeling sick; feeling really bad; a bad headache; feeling sick and nauseated/nausea; worried it will not go away; frustrated; This is a spontaneous report received from a contactable consumer (patient). A 76-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ELI283, expiry date unknown), via an unspecified route of administration in the right arm, on 11Jan2021, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient reported she had her first vaccine on 11Jan2021. On 19Jan2021, the patient was feeling really bad, had a bad headache, general malaise and was feeling sick and nauseated. She was not feeling well and has not been feeling well the last 3 days. She thought the side effect would be right after getting the vaccine however hers started on 19Jan2021 (2 days ago). She stated she had an awful headache which she still has and had nausea. She wanted to know if it was normal to have happened this far away from receiving the vaccine, this amount of time from the vaccine. The patient reported that she is not quite as bad now, but she still feels it. The patient was worried it will not go away (Jan2021). The patient became frustrated and stated that she was just trying to find out if what she was feeling was normal. The patient also thought she had COVID and took a test in Jan2021 but she did not have COVID (negative). The outcome of the events "not feeling well/general malaise/feeling sick", "feeling really bad", "a bad headache" and "feeling sick and nauseated/nausea" was recovering; and the outcome of "worried it will not go away" and "frustrated" was unknown.

Other Meds:

Current Illness:

ID: 1004240
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: first injection of the Pfizer BioNTech COVID-19 vaccine 2 weeks ago and the only side effect she experienced was some mild pain at the site of injection; I was told we had no side effects at all thank goodness just the sore arm; This is a spontaneous report from a contactable consumer. A 70-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously had a flu and shingles shot. The patient asked the side effects after the second shot compared to the first in older people. She wanted to known if they need to be monitored more after the second shot. The consumer reported receiving her first injection of the Pfizer BioNTech COVID-19 vaccine 2 weeks ago and the only side effect she experienced was some mild pain at the site of injection that lasted only a day. The consumer reports the pain was similar to what she experienced in the past after a flu shot and a shingles shot. The consumer reported when she was told by people where she received her injection that people react more to the second shot compared to the first, and younger people react more to the injections that older people for side effects like headache and fever. The consumer also stated, "Here is the question, my mother who is going to be 97 and I, who is going to be 70 received the first Pfizer Shot a couple (Covid-19 Vaccine) of weeks ago, we are due for the second shot for next Thursday actually and I was told we had no side effects at all thank goodness just the sore arm. Now I was told for the second shot that you usually do get some kind of side effects, so my question is my mother and I taking a shot at the same time, I live along with her and should I have somebody with me just what are the odds we are going to have side effects from the second shot, I guess that's my question." The outcome of the event mild pain at the site of injection was recovered while other event was unknown. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 1004241
Sex: F
Age:
State:

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: bad headache that felt like migraine; bad headache that felt like migraine; thought it might be a sinus headache; pain on the right side of the back of her neck that radiated behind her right eye; pain on the right side of the back of her neck that radiated behind her right eye; dizziness; sweating; swollen lymph nodes in her throat; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: not reported), via an unspecified route of administration on 15Jan2021 at 07:00 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 15Jan2021, the patient experienced dizziness, sweating, and swollen lymph nodes in her throat. On 18Jan2021, the patient started to get a really bad headache that felt like migraine and thought it might be a sinus headache. On the same day, the patient also had pain on the right side of the back of her neck that radiated behind her right eye. The patient would like to know if she could take anything for her headache. The outcome of the event bad headache that felt like migraine was not recovered while the other events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004242
Sex: F
Age:
State: IL

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210118; Test Name: Blood Pressure; Result Unstructured Data: Test Result:keeps going up and down

Allergies:

Symptoms: Blood pressure keeps going up and down for couple hours; This is a spontaneous report from a contactable nurse (patient herself). A 49-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: expiry date: unknown) via an unspecified route of administration in the right arm, on 18Jan2021 at 13:15, at a single dose, for COVID-19 immunization. Relevant medical history included blood pressure abnormal. Concomitant medications included spironolactone. The patient previously received 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 Nursing Home/Senior Living Facility. On 18Jan2021, at 13:15, the patient's blood pressure keeps going up and down for couple hours. The patient did not receive treatment for the event. Outcome of the event was recovered with sequel. The patient has not been tested for COVID-19 since vaccination. Information on batch/lot number has been requested.

Other Meds: SPIRONOLACTONE

Current Illness:

ID: 1004243
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: fever; chills; nausea; headache; myalgias; This is a spontaneous report from a non-contactable healthcare professional. A 25-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on unspecified date at single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient was not pregnant at the time of vaccination. There were no other vaccine received within 4 weeks prior to COVID vaccination. The patient experienced fever, chills, nausea, headache and myalgias. No treatment was received. Outcome of the events was unknown. The event was reported non-serious. It was unknown if patient was diagnosed with COVID-19 prior to vaccination and has not been tested since the vaccination. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1004244
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 01/06/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Experienced dizziness the first week after vaccination; Axillary lymph node swelling to arm of injection; Axillary lymph node swelling to arm of injection; hands and feet tingling/numbness/Feels as if hands and feet are falling asleep often; hands and feet tingling/numbness/Feels as if hands and feet are falling asleep often; This is a spontaneous report received from a contactable nurse (who is also the patient). A 25-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration, on 30Dec2020 14:00, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to BNT162B2 vaccine. The patient was not diagnosed with COVID-19 prior to vaccination and was not tested for COVID-19 since the vaccination. On 06Jan2021 at 14:00, first week after the vaccination, the patient experienced dizziness, axillary lymph node swelling to arm of injection 1 week until now after vaccination, and hands and feet tingling/numbness at random times of the day and feels as if hands and feet are falling asleep often. The events resulted to "doctor or other healthcare professional office/clinic visit". No treatment for the events was given. The outcome of the events was not recovered. The events were assessed as non-serious. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004245
Sex: F
Age:
State: NY

Vax Date: 01/07/2021
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Left arm has red itchy mark about the size of a silver dollar where shot was; Left arm has red itchy mark about the size of a silver dollar where shot was; This is a spontaneous report from a contactable consumer, the patient. This 34-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine) (Lot number: EL0142), dose number 1, via an unspecified route of administration in the left arm on 07Jan2021 at 11:30 (at the age of 34-years-old) as a single dose for COVID-19 vaccination. Medical history included asthma from an unknown date and unknown if ongoing, depression from an unknown date and unknown if ongoing, sulfa allergy from an unknown date and unknown if ongoing and penicillin allergy from an unknown date and unknown if ongoing. Concomitant medication included sertraline hydrochloride (ZOLOFT), unspecified birth control and salbutamol sulfate (ALBUTEROL [SALBUTAMOL SULFATE]). Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient was not pregnant at the time of vaccination. On 21Jan2021 at 10:00, the patient experienced her left arm has a red, itchy mark about the size of a silver dollar where the shot was. No therapeutic measures were taken as a result of the events. The clinical outcomes of her left arm has a red, itchy mark about the size of a silver dollar where the shot was not resolved. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds: ZOLOFT; ALBUTEROL [SALBUTAMOL SULFATE]

Current Illness:

ID: 1004246
Sex: F
Age:
State: MO

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: Temperature; Result Unstructured Data: Test Result:100.2; Comments: She took her temperature and it was 100.2 degrees Fahrenheit.

Allergies:

Symptoms: She has a fever of 100.2F and loss of appetite/No appetite; She has a fever of 100.2F and loss of appetite.; Feeling unwell; Injection site pain; Tiredness; Headache; Chills; This is a spontaneous report from a contactable nurse reporting for herself. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on 20Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient and her husband received the COVID vaccine yesterday early in the morning at a hospital. She was fine until the middle of the night and early this morning. On Jan2021, she had 6 of the 12 side effects, which she described as injection site pain, tiredness, headache, chills, feeling unwell and no appetite. She had a headache and felt her forehead and it felt warm, so she took her temperature and it was 100.2 degrees Fahrenheit. She has a fever of 100.2F. The patient underwent lab tests and procedures which included body temperature: 100.2 on Jan2021. The outcome of the events was unknown. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1004247
Sex: M
Age:
State:

Vax Date:
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: nosebleed; This is a spontaneous report from a non-contactable consumer reporting for their husband via the medical information team. An 87-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration, on an unspecified date (Tuesday afternoon) at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. A consumer reported that their husband received the first dose of vaccine on Tuesday afternoon of unspecified date. He developed a nosebleed on 21Jan2021 at 0230. 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: 1004248
Sex: M
Age:
State: GA

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210119; Test Name: blood sugar; Test Result: 130 mg/dl; Comments: numbers have been higher than normal

Allergies:

Symptoms: blood sugar crowding to the 130 mg/dL upper limit/numbers have been higher than normal; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect. A contactable consumer (patient) reported that an 81-year-old male patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number requested), via an unspecified route of administration on 19Jan2021 at a single dose for COVID-19 immunization. Medical history included being diagnosed as pre-diabetic from an unknown date. The patient's concomitant medications were not reported. The patient reported that he noticed in the last 2 days his blood sugar crowding to the 130 mg/dL upper limit on 19Jan2021. He stated that after getting vaccine, numbers have been higher than normal. The patient wants to know if that's from vaccine or something else. The outcome of the event was unknown. Information on the batch number/lot number has been requested

Other Meds:

Current Illness:

ID: 1004249
Sex: F
Age:
State: GA

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: bad allergic reaction; itching and welts, like hives; itching and welts, like hives; didn't get any sleep last night; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3302 and expiration date not provided), via an unspecified route of administration in the left arm on 18Jan2021 18:00 at a single dose for COVID-19 immunization. The patient has no medical history. Concomitant medication included other medications that she has never had a reaction to. The patient stated that she got her first dose of COVID vaccine on 18Jan2021 evening. On 19Jan2021, she had a bad allergic reaction, itching and welts, like hives or whatever that started on her arms that progressed to the rest of her body especially the buttocks, everywhere. She did not get any sleep on 19Jan2021 and was itching. She called the doctor's office to see if they could help her and they said they couldn't and told her she needed to contact the health department "or something." They aren't familiar with the vaccine and does not want to do anything that would put them in a legal situation. She stated she has an appointment on 08Feb for her next dose and she doesn't know if she can go through this again. She asked what can she do about this reaction. She started to get itching and "stuff" that was not bad until last night (unspecified date). She stated that it was like she had hives all over and itching out of control. She did not get any sleep and is still itching out of control. She wanted to know if she goes back to hospital if they will be able to do anything for her. It was her first shot and is scheduled for her second one on 08Feb2021. She was wondering will she have to go through all of this again. She had noticed hives on her arms on 19Jan2021 morning but mostly now are on her buttocks and thighs. She stated that she had thought it was an allergic reaction to a fabric softener that she changed to. No treatment was given in response to the events. She has stated that she takes other medications that she has never had a reaction to. She does not think that they were related to this. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1004250
Sex: F
Age:
State: FL

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: little soreness; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EH9899), via an unspecified route of administration on 20Jan2021 at single dose for COVID-19 immunization. Patient is taking medications as blood like thinner and for osteoporosis. She has allergies previously to grass and dust mites. She always has a wet nose when having allergies and does a nose drop and cleaner. Her nose was always on the runny side, she cannot live without a tissue. She uses a nasal spray and the cleaner. Concomitant medication included levothyroxine sodium (SYNTHROID), lisinopril, amlodipine, simvastatin, acetylsalicylic acid (BABY ASPIRIN) as blood thinner and paracetamol (TYLENOL ARTHRITIS) for osteoporosis. On an unspecified date in Jan2021 she had little soreness and had no other symptoms. The patient was asking if she should stop taking the BABY ASPIRIN and TYLENOL ARTHRITIS now that she got the vaccine. She read some place one should not take any aspirin. The case was reported as non-serious. The outcome of the event was unknown.

Other Meds: SYNTHROID; LISINOPRIL; AMLODIPINE; SIMVASTATIN; TYLENOL ARTHRITIS; BABY ASPIRIN

Current Illness:

ID: 1004251
Sex: F
Age:
State: MN

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body and muscle aches; muscle ache; Neck pain; Pounding headache; This is a spontaneous report from a contactable health care professional (patient). A 38-year-old female patient received the second dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL3302), via an unspecified route of administration on 20Jan2021 at 08:30 on the left arm at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other medications within two weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine) for COVID-19 immunization. The patient has not been tested for COVID-19 since the vaccination. The patient experienced body and muscle aches, neck pain and pounding headache on 20Jan2021 at 08:30. The patient did not receive treatment for the events. The outcome of the events was unknown. The events were reported as non-serious.

Other Meds:

Current Illness:

ID: 1004252
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I had the sensations of facial tingling; eye swelling; lip swelling; This is a spontaneous report from a contactable Nurse. A 69-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3247), via an unspecified route of administration on the right arm on 20Jan2021 08:15 at a SINGLE DOSE for covid-19 immunisation. Medical history included drug hypersensitivity from an unknown date and unknown if ongoing known allergies: Sulfa and allergy to animal (cats) from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. On 20Jan2021 08:45 AM, the patient stated, "I had no symptoms during the 15 minute observation after the vaccine. After leaving the site, about 30 minutes after the shot I had the sensations of facial tingling, eye swelling and lip swelling (nothing visible on a photograph). My pulse remained stable and I had no throat symptoms or trouble breathing. This all resolved spontaneously within an hour after the shot. I am allergic to cats and sulfa but have never had anaphylaxis. I plan to stay in observation for a little longer after the 2nd shot. Any other recommendations?" No treatment was received for the events. The outcome of the events was recovered on 20Jan2021.

Other Meds:

Current Illness:

ID: 1004253
Sex: M
Age:
State: TX

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sore arm; This is a spontaneous report from a contactable consumer. A 54-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EL9262), via an unspecified route of administration on 20Jan2021 19:00 at SINGLE DOSE at right arm for covid-19 immunisation. Medical history included Prior to vaccination, the patient was diagnosed with COVID-19. Concomitant medication included tamsulosin hydrochloride (FLOMAX), atorvastatin (LIPITOR), duloxetine hydrochloride (CYMBALTA), varicella zoster vaccine rge (cho) (SHINGRIX). On 21Jan2021 02:00, the patient experienced sore arm, normal effect with most shots. The patient did not receive treatment for the adverse event. The outcome of the event was recovering.

Other Meds: FLOMAX; LIPITOR; CYMBALTA

Current Illness:

ID: 1004254
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Name: body temperature; Result Unstructured Data: Test Result:101.9; Test Date: 20210120; Test Name: body temperature; Result Unstructured Data: Test Result:101.6

Allergies:

Symptoms: Fever recorded was 101.6/fever recorded was 101.9; body aches; feel chill/fet chill; This is a spontaneous report from a contactable other hcp (patient). A 47-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247; expiration date not provided), via an unspecified route of administration (anatomical location: left arm) on 20Jan2021 at 09:20 am at SINGLE DOSE for covid-19 immunisation. Patient's medical history was reported as none. The patient's concomitant medications were not reported. Patient was not pregnant at the time of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has not been tested for COVID-19 since the vaccination. The patient has no allergies to medications, food, or other products. Patient reported that she got the vaccine at 9:20 am on Tuesday (20Jan2021). Patient started to feel chill at 08:30 pm. Fever recorded was 101.6 at 11 pm. Patient took paracetamol (TYLENOL extra strength). Felt chill again and fever recorded was 101.9. Took again 1 extra strength paracetamol. Felt chill and fever at 11 am. It was reported that patient also experienced body aches on 20Jan2021 at 08:30 pm. The patient underwent lab tests and procedures which included body temperature with result of 101.9 and body temperature with result of 101.6 on 20Jan2021. The events were assessed as non-serious. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1004255
Sex: F
Age:
State: CA

Vax Date: 01/16/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: body aches/ body and legs aches; body and legs aches; joint pain; fatigues; chills; This is a spontaneous report from a contactable consumer (patient herself) via Medical Information team. A 72-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EL8982, expiration date was unknown), via an unspecified route of administration on the right arm on 16Jan2021 at 18:15 at a single dose for COVID-19 immunization. The vaccination facility was a public health department. The vaccine was not administered at the Military facility. The patient had no additional vaccines administered on the same date of the Pfizer vaccine. Relevant medical history included gastroesophageal reflux disease (GERD) from an unknown date and unknown if ongoing. The patient had no family medical history. Concomitant medication included cimetidine for GERD, which she had been taking for years and years. The patient had no other vaccinations within four weeks prior to the first vaccination. The patient woke up on Tuesday, 19Jan2021, feeling off; she experienced body aches, joint pain, and fatigues. The symptoms (Sxs) were still ongoing. The patient had question regarding the side effects and duration: if these had been reported and was it normal to still feel the side effects and how long would it last for. The patient was also asking if these were indicative of something more serious. The patient added that her healthcare provider (hcp) told her to take 2 paracetamol (TYLENOL) every 6 hours; however, the Tylenol only lasted for 5 hours. The patient further asked that if she continued to have side effects, at what point should she be do something and wanting recommendations on management. The patient was also asking if the side effects would happen with the second shot. The patient further reported that she felt pretty good on Sunday and Monday (17Jan2021 and 18Jan2021), maybe just a little off, and stated that on Tuesday (19Jan2021), she woke up and started with the classic side effects body aches, joint pain, fatigue, and chills that had continued. She stated she was taking Tylenol 2 extra strength; it worked for about 5 hours and then the effects came back. The patient wanted to know if this was normal to last this long and had this been reported by others. She stated she had contacted her doctor and her doctor did not know. The adverse events did not require any visit to an emergency room or a physician office. Therapeutic measures were taken as a result of body aches/ body and legs aches, joint pain, fatigues, and chills. There were no relevant tests. The patient was not recovered from the events "body aches/ body and legs aches, joint pain, fatigues, and chills."

Other Meds: CIMETIDINE

Current Illness:

ID: 1004256
Sex: F
Age:
State: WV

Vax Date: 01/15/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: lower left side back pain; received the first dose of the Pfizer COVID 19 vaccine on 15Jan2021 at 12:53PM in the left arm/ she noticed a sore arm right afterward; rash; This is a spontaneous report from a contactable consumer reporting for herself. A 62-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982, expiry date: not reported), via an unspecified route of administration, on 15Jan2021 12:53PM at a single dose on the left arm for COVID-19 immunization. The vaccine was administered at a hospital. It was not administered at a military facility. The patient did not receive other vaccines within 4 weeks prior to receiving the Pfizer vaccine. Medical history included allergies/allergy from childhood 4 years old, back problem from 2001, back surgery in 2015, vaginal dryness, high cholesterol, depression, acid reflux, surgery in 2015, physical therapy, and allergy to mold, dogs, roaches. She has multiple allergies from childhood including allergy to mold, dogs, and roaches. She also mentioned she has had back problems since her first surgery in 2015. All of these predate treatment with Pfizer COVID 19 vaccine and Lipitor. She got to where she couldn't stand up straight, but she went to physical therapy. She had surgery in 2015. She had a problem in 2018 and they gave her shots and that helped. Family history was none. Concomitant medications included estradiol (ESTRING) (for three years) for vaginal dryness, fish oil (taking for three to four years) for high cholesterol, paroxetine hydrochloride (PAXIL) (taking for 20 years) for depression, cyamopsis tetragonoloba gum (BENEFIBER FIBER SUPPLEMENT) (using for a year), vitamin d3 (VITAMIN D3) (using for five years; she used to be on calcium but it can cause heart problems so her doctor told to take Vitamin D), dexlansoprazole (DEXILANT) (taking for five years) for acid reflux, (ALLEGRA) (taking for 5 years ) for allergy, (QNASL) (using for 3 years), allergy shots (used forever) for allergy and stool softener (taking for 5 years) to "keep things moving"; all were from unspecified dates and ongoing. The patient previously took atorvastatin (LIPITOR) for high cholesterol from 2017 to 2017 and experienced back pain from 2017 to 2017 (recovered). She also previously took calcium. The patient experienced "received the first dose of the Pfizer COVID 19 vaccine on 15Jan2021 at 12:53PM in the left arm/ she noticed a sore arm right afterward" on 15Jan2021, lower left side back pain on 20Jan2021, and rash on an unspecified date in Jan2021. The patient called to report a problem with her lower back after receiving the 1st dose of the vaccine. "I've had surgery and a couple of shots, the CAT scan kind. I have been fine for a while, just had a sore arm and yesterday I noticed a problem with my lower back and thought it may have been because I painted, but it is still bothering me. I remembered when I went on Lipitor I started having problems with my back about 3 weeks in, same deal. The doctor took me off and I went back on a month later and I started having problems again. Because I don't know if it was the vaccine, I am wondering if I should get the second dose." She clarified she received the first dose of the Pfizer COVID 19 vaccine on 15Jan2021 at 12:53PM in the left arm. She noticed a sore arm right afterward which lasted at least 48 hours. Then on 20Jan2021, she noticed lower left side back pain. Mentions she thinks it is at the L4 or L5 and this is the same place she had a shot there in 2018 for back pain and previously had surgery on that location in 2015. With regard to Lipitor, she is unsure of the exact year, but states it was probably back in 2017. After taking Lipitor she noticed her back pain coming back. Her doctor took her off of Lipitor for a month and it got better. Then he put her back on Lipitor and she had the same back pain problem. She stated that she is unsure if she will take the second dose and asked with regard to her back pain should she take the second dose. Outcome of "received the first dose of the Pfizer COVID 19 vaccine on 15Jan2021 at 12:53PM in the left arm/ she noticed a sore arm right afterward" was recovered on 18Jan2021, outcome of lower left side back pain was not recovered, while outcome of rash was unknown.

Other Meds: FISH OIL; PAXIL [PAROXETINE HYDROCHLORIDE]; ESTRING; BENEFIBER FIBER SUPPLEMENT; VITAMIN D3; DEXILANT; ALLEGRA; QNASL

Current Illness:

ID: 1004257
Sex: F
Age:
State: IN

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Covid test nasal swab; Result Unstructured Data: Test Result:Unknown results; Test Date: 202101; Test Name: PCR test; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: clavical lymph node swelling on injection side; This is a spontaneous report from a contactable other healthcare professional (patient). A 60-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EJ1686 and expiry date unknown) via unspecified route of administration at the right arm on 18Jan2021 08:45 at single dose for Covid-19 immunization in a hospital. Medical history was none. The patient was not diagnosed with COVID-19 prior to vaccination. The patient's concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 on unspecified date for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 19Jan2021 12:00, the patient experienced clavical lymph node swelling on injection side. The event resulted in doctor or other healthcare professional office/clinic visit. The patient underwent lab tests and procedures which included Covid test nasal swab: unknown results on 21Jan2021, PCR test: unknown results post vaccination (Jan2021). The patient did not receive treatment due to the event. The event was clavical lymph node swelling on injection side recovering. The event was reported non-serious; results in death, life threatening, caused/prolonged hospitalization, disabling/incapacitating, congenital anomaly/birth defect; all no.

Other Meds:

Current Illness:

ID: 1004258
Sex: F
Age:
State: CO

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210116; Test Name: body temperature; Result Unstructured Data: Test Result:low grade fever

Allergies:

Symptoms: Low grade fever; fatigue for 4-5 days post injection; This is a spontaneous report from a contactable nurse (patient). A 70-year-old female received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on the left arm, on 16Jan2021 08:00 at single dose for covid-19 immunisation. Medical history included Hashimoto's thyroiditis, celiac and allergy to wheat. Patient was not pregnant at the time of vaccination. Concomitant medication included levothyroxine, estradiol (ESTRACE) and colecalciferol (VIT D3). The patient experienced low grade fever and fatigue for 4-5 days post injection on 16Jan2021 at 16:30. Patient recovered from the events on Jan2021 and had not received any treatment. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. The events were reported as non-serious. Information on the lot/batch number has been requested.

Other Meds: LEVOTHYROXINE; ESTRACE; VIT D3

Current Illness:

ID: 1004259
Sex: F
Age:
State: MO

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: felt overall crummy; muscle aches; headache; fatigue; cold; This is a spontaneous report from a non-contactable consumer. A 32-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot EJ1686, expiry date not reported), via an unspecified route of administration on 19Jan2021 at a single dose in the right arm for covid-19 immunization. The patient's medical history was not reported. The patient was not pregnant at the time of the vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included citalopram at 20 mg, daily; melatonin at 5 mg, as needed; and ibuprofen at 400 mg, as needed. The patient received the first dose of BNT162B2 (brand Pfizer, lot number EL1284, expiry date not reported, age at vaccination as 32 years old) on 28Dec2020 at the right arm. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The recent COVID-19 vaccine was administered in the hospital. Morning after vax, 20Jan2021, patient felt overall crummy, muscle aches, headache, fatigue, cold (cold is unusual for patient). The events improved throughout the day. Next morning, woke up with similar headache, but improved with daily activity and otherwise felt normal. The events were reported as not serious (did not result in death, not life-threatening, did not cause/prolonged hospitalization, not disabling/incapacitating and not a congenital anomaly/birth defect). No treatments received in response to the events reported. Since the vaccination, the patient has not been tested for COVID-19. The events felt overall crummy, muscle aches, headache, fatigue, and cold were recovered in Jan2021.

Other Meds: CITALOPRAM; MELATONIN; IBUPROFEN

Current Illness:

ID: 1004260
Sex: F
Age:
State: FL

Vax Date: 01/11/2021
Onset Date: 01/20/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210120; Test Name: Saliva; Result Unstructured Data: Test Result:unknown result

Allergies:

Symptoms: Gland swelling in neck and clavicle, same side as injection site, 8 days post vaccination.; This is a spontaneous report from a contactable 38-year-old female consumer reporting for herself. A 38-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL1284), via an unspecified route of administration (left arm) on 11Jan2021 20:15 at SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. Patient is not pregnant at vaccination time. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medication included fluoxetine hydrochloride (PROZAC), albuterol [salbutamol], fluticasone propionate, salmeterol (WIXELA INHUB) from unspecified dates for unspecified indications. Patient is also using unspecified birth control product. The patient was administered on workplace clinic. The patient experienced gland swelling in neck and clavicle, same side as injection site, 8 days post vaccination on 20Jan2021 06:00. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient been tested for COVID-19. Test Name: Saliva on 20Jan2021 with unknown result. No treatment was given. Outcome of the event was not recovered. Event was reported as non-serious.

Other Meds: PROZAC; ALBUTEROL [SALBUTAMOL]; WIXELA INHUB

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm