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: 1062093
Sex: M
Age:
State: FL

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Pulled his band aid there was a little blood; This is a spontaneous report from a contactable consumer (wife of patient). An 80-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date unspecified), via an unspecified route of administration on 27Jan2021 at single dose (left arm) for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Her husband had his first dose today but at a different location and when he pulled his band aid there was a little blood. This was his first dose and it was given in his left upper arm. Outcome of event was unknown. Information about Lot/ Batch has been requested.

Other Meds:

Current Illness:

ID: 1062094
Sex: F
Age:
State: NJ

Vax Date: 01/23/2021
Onset Date: 01/24/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Diffuse red macular rash over arms legs trunk and chest. Neck also. Face and hands and feet spared; Extremely itchy; This is a spontaneous report from a contactable other health professional. A 45-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot and expiry not reported), via an unspecified route of administration on 23Jan2021 at 10:30 at a single dose on left arm for COVID-19 immunisation. The patient's medical history was not reported. Concomitant medication included modafinil. On 24Jan2021 at 12:00, the patient experienced diffuse red macular rash over arms legs trunk and chest. Neck also. Face and hands and feet spared. Started next day. So far lasting for 4 days. Extremely itchy. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds: MODAFINIL

Current Illness:

ID: 1062095
Sex: F
Age:
State: NM

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: After the first vaccine I had arm, shoulder and neck pain on my right side along with a lasting headache for a week or so; After the first vaccine I had arm, shoulder and neck pain on my right side along with a lasting headache for a week or so; After the first vaccine I had arm, shoulder and neck pain on my right side along with a lasting headache for a week or so; After the first vaccine I had arm, shoulder and neck pain on my right side along with a lasting headache for a week or so; This is a spontaneous report from a contactable other healthcare professional (HCP). A 40-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date: unknown) via an unspecified route of administration in the right arm, on 06Jan2021 at a single dose, for Covid-19 immunization. Patient had no relevant medical history and no known allergies. Concomitant medication included escitalopram oxalate (LEXAPRO). 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. Facility type where vaccine was administered was reported as other . On an unspecified date in Jan2021, after the first vaccine the patient had arm, shoulder and neck pain on my right side along with a lasting headache for a week or so. The patient did not receive treatment for the events. Outcome of the events was recovering. The patient has not been tested for COVID-19 since vaccination. Information about batch/lot number has been requested.

Other Meds: LEXAPRO

Current Illness:

ID: 1062096
Sex: F
Age:
State: MA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: soreness at injection site; lethargy after the vaccine; headache; This is a spontaneous report from a contactable consumer. A 37-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 26Jan2021 at 13:30 at a single dose on the left arm for COVID-19 immunization. Medical history was reported as none. Concomitant medication included loratadine (CLARITIN). 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. On 26Jan2021 at 16:00, the patient experienced soreness at injection site, lethargy after the vaccine, and headache. The patient received ibuprofen as treatment for the events. Since the vaccination, the patient has not been tested for COVID-19. The patient was not pregnant at the time of vaccination. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds: CLARITIN [LORATADINE]

Current Illness:

ID: 1062097
Sex: F
Age:
State: NM

Vax Date: 01/26/2021
Onset Date:
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm pain; fever; chills; headache; muscle aches; nausea; This is a spontaneous report from a contactable other HCP. A 40-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration in right arm on 26Jan2021 at a single dose for COVID-19 immunization. There were no relevant medical history was not reported. there were no known allergies.Concomitant medication included escitalopram oxalate (LEXAPRO). The patient previously received the first dose ofbnt162b2 on 06Jan2021 in right arm and experienced arm, shoulder and neck pain on my right side along with a lasting headache for a week or so. After the 2nd vaccine, the patient experienced arm pain, fever, chills, headache, muscle aches and nausea on an unspecified date. there outcome of the events was recovering. There was no treatment for the events. The patient was not tested for COVID-19 prior and after the vaccination. Information on the lot/batch number has been requested.

Other Meds: LEXAPRO

Current Illness:

ID: 1062098
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Arm is swollen; Pain; This is a spontaneous report from a contactable consumer (patient's wife). A male patient of an unspecified age received bnt162b2 (BNT162B2 reported as COVID SHOT; unknown lot number and expiration date) at unknown age of vaccination via an unspecified route of administration in the arm on an unspecified date at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The wife reported that her husband who had a COVID shot Friday in his arm. The patient's arm was swollen and he was having pain. She inquired what can he do for that. The outcome of the event was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1062099
Sex: F
Age:
State: OH

Vax Date: 01/25/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: the lumpy, red area is not itchy, but it is tingling, and stings sometimes.; stings; lumpy, red area on the opposite shoulder from where she received the COVID-19 Vaccine/lumpy, red raised up bumps area on her left shoulder; lumpy, red area on the opposite shoulder from where she received the COVID-19 Vaccine/lumpy, red raised up bumps area on her left shoulder; This is a spontaneous report from a contactable consumer (patient). A 68-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date unknown), via an unspecified route of administration on the right upper arm on 25Jan2021 at 11:30 at a single dose for COVID-19 immunization. Medical history was reported as none. Concomitant medications included Influenza vaccine in Dec2020 and Balance of Nature Fruits as supplement since Jan2021 - she started taking Whole Foods brand Balance of Nature Fruits pills and has been taking them off and on for the last couple weeks. On 27Jan2021, the patient had a lumpy, red area on the opposite shoulder from where she received the COVID-19 vaccine. She said she discovered the lumpy, red raised up bumps area on her left shoulder that morning. She said the lumpy, red area is on the back of her left shoulder, neck and hairline area. She said her husband said the lumpy, red area is a couple square inches in size. She said the lumpy, red area is not itchy, but it is tingling, and stings sometimes. She also asked if what she is experiencing is a side effect of the vaccine. The patient declined any treatment for the events saying she didn't know what to do. The event "lumpy, red area on the opposite shoulder from where she received the COVID-19 Vaccine/lumpy, red raised up bumps area on her left shoulder" had not resolved while the outcome of the rest of the events was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1062100
Sex: F
Age:
State:

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Pt developed left lower lip paresthesia that radiated to L side of face.; Pt developed left lower lip paresthesia that radiated to L side of face.; This is a spontaneous report from a non-contactable pharmacist. A 75-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9262), intramuscular on 26Jan2021 at 10:00 at a single dose for covid-19 immunisation. Medical history included transient ischaemic attack (TIA), stroke and chronic kidney disease (CKD) from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient previously took gabapentin for facial nerve pain. The patient developed left lower lip paresthesia that radiated to the left (L) side of face on 26Jan2021. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1062101
Sex: F
Age:
State: TX

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sinus pain congestion; Sinus pain congestion; coughing; tiredness; headaches; chills; muscle pain; feeling unwell; back pain; achy all over; very dizzy; nausea; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EN5318 and expiry date: unknown), via an unspecified route of administration on the left arm, on 26Jan2021 18:45 at a single dose for COVID-19 immunization. Medical history included High BP, diverticulosis, vertigo and blood clot in artery (healing), allergy to red licorice, hayfever dogs and cats. Patient was not pregnant at the time of vaccination. Concomitant medication included doxycycline, aspirin [acetylsalicylic acid], Multi vit, fiber gummy, and BP meds. There was no other vaccine in four weeks. The patient previously took hydrocodone and prednisone, and experienced allergies. The patient experienced sinus pain and congestion, coughing, tiredness, headaches, chills, muscle pain, achy all over, nausea, felling unwell, very dizzy and back pain on 26Jan2021 19:30. No treatment was received for the events. Outcome was unknown. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination.

Other Meds: DOXYCYCLINE; ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 1062102
Sex: F
Age:
State: TN

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210123; Test Name: fever; Result Unstructured Data: Test Result:99.7 Fahrenheit

Allergies:

Symptoms: injection site is painful; chills; fever with temperature of 99.7 F; headache; tiredness; loss of appetite; joint pain; feeling unwell; received the first dose of Pfizer Covid 19 vaccine on 05Jan2021 and the second dose on 22Jan2021; This is a spontaneous report from a non-contactable consumer (patient). A 46-year-old non-pregnant female patient received her second dose of bnt162b2 (BNT162B2 reported as PFIZER COVID 19 VACCINE) at the vaccination age of 46-year-old via an unspecified route of administration in the left arm on 22Jan2021 13:15 (lot number: EL3302; expiration date: unknown) at a single dose for covid-19 immunization. Medical history included mental disease, seasonal allergy in spring and allergies to sulfa antibiotics. The patient was not diagnosed with Covid-19 prior to vaccination. Concomitant medication included aripiprazole (ABILIFY). The patient received her first dose of bnt162b2 (BNT162B2 reported as PFIZER COVID 19 VACCINE) at the vaccination age of 46-year-old via an unspecified route of administration in the right arm on 05Jan2021 13: 45 (lot number: EJ1685) at a single dose for covid-19 immunization. The patient received the first dose of Pfizer Covid 19 vaccine on 05Jan2021 and the second dose on 22Jan2021. On 23Jan2021 02:00 AM, she had chills, fever with temperature of 99.7 F, headache, tiredness, loss of appetite, joint pain and feeling unwell for 2 days post vaccination. She also mentioned that the injection site was painful on 25Jan2021 for 4 days post vaccination. The patient did not received treatment for the adverse events. The patient has not been covid tested post vaccination. The outcome of the events was unknown.

Other Meds: ABILIFY

Current Illness:

ID: 1062103
Sex: F
Age:
State: AR

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

Lab Data:

Allergies:

Symptoms: light headed; nervous; really tired; made me really sleepy; i had a few skipped heart beats while laying down; weird/ didn't feel normal; get restless; This is a spontaneous report from a contactable other healthcare professional (patient). A 31-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL9261) via an unspecified route of administration on the left arm on 20Jan2021 13:45 at a single dose for COVID-19 immunization. Medical history included having one thyroid and had a benign tumor removed from behind heart when she was young and birth control. Concomitant medication included benzalkonium chloride, sodium chloride (ALIVE) and desogestrel, ethinylestradiol (ISIBLOOM) for birth control. After taking the shot she got light headed as she was walking to her car on 20Jan2021 15:00. Didn't think nothing of it since she was nervous about taking the shot. Then once she got home, she got really tired. She only had one thyroid so the shot made me really sleepy and she had a few skipped heart beats while laying down. After she slept, she felt fine but weird then after being up for a few hours she would get restless again. She got light headed again the next day going to the grocery store then back restless. She didn't feel normal until this Tuesday, she was not feeling weird and she was not as tired as she had been since she took the shot. She had tried to get seen from her doctor but she was booked up. No treatment was received for the events. The facility where the vaccine was administered was in a Nursing Home/Senior Living Facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not pregnant. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. No known allergies. Outcome of the events was recovering.

Other Meds: ALIVE; ISIBLOOM

Current Illness:

ID: 1062104
Sex: M
Age:
State: MO

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

Lab Data:

Allergies:

Symptoms: dizzy; sinus infection; This is a spontaneous report from a contactable consumer (patient). A 48-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) lot number and expiry date unknown, via unspecified route of administration on unspecified date at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had the first round of the vaccine and was dizzy on unspecified date. The patient informed that it was not like vertigo but similar. The patient informed that he did not know if it has something to do with what was going on or if it was a sinus infection. The patient informed that he went to bed dizzy. The patient informed that he was dizzy right now but not all the time. The outcome of the events was unknown. Follow-up activities are possible, information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 1062105
Sex: M
Age:
State: FL

Vax Date: 01/27/2021
Onset Date: 01/01/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; not eating; This is a spontaneous report from a contactable consumer (patient's wife). An 81-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not provided), via an unspecified route of administration on 27Jan2021 at a single dose for COVID-19 immunization. Medical history included headache on 26Jan2021. There were no concomitant medications. The reporter stated that her husband (patient) received the first dose of the vaccine about two and one-half to three weeks ago and he had some aches and pain but it was not that bad. She reported that a day or two after the first dose he was achy and didn't feel like himself. Then on 26Jan2021, he got a major headache; he would sleep and wake up and sleep again trying to get rid of the headache. She gave him paracetamol (TYLENOL) 650 mg one by mouth and it didn't help. He got the second dose on 27Jan2021 between 07:00 and 09:00AM she was unsure of the arm. He came home and is sleeping now and had a headache on 27Jan2021. She was asking what can she give him for the headache. She also stated that he also was not eating on an unspecified date in Jan2021. She wanted more information on what to do for him. The events did not require a visit to the physician or ER. The outcome of the event headache was not recovered while the outcome of the event not eating was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1062106
Sex: F
Age:
State: CA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Lymph nodes hurting/burning pain on chest and breast area/ Her Lymph nodes are tender on the Left Side, it goes down the breast arm; This is a spontaneous report from a contactable consumer reporting for herself. A 92-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number unknown), via an unspecified route of administration (arm right) on 26Jan2021 at SINGLE DOSE for COVID-19 immunization, at 92 years old. Medical history lung cancer 12 years before from 2009, breast cancer on an unspecified date, and a lump already on the breast from the surgery and she usually get pain there from an unspecified date. She is a cancer survivor. She had surgery for breast cancer on same side, that's where the pain was. She also had a stroke and speech is slurry from an unspecified date. The patient asked to bear with her as she had a stroke in the past and her speech is slurry. She lost the COVID card, she did not even know they gave a card, until somebody told her that they had their card. She lives in a Senior citizen facility, and she does not remember any card. They just gave her information sheets. It was reported that the patient had the vaccine and she was having a lot of pain on the left side, however she got the vaccine on the right side. She had surgery for breast cancer on same side, that's where the pain was, however the vaccine was on the other arm. Patient stated that she thinks it was the lymph nodes, she does not know what to do about it, since she is a Cancer survivor. The patient requested the call handler to talk slow, she is 92 years old. She cannot call the doctor because he is retired and so she does not have a doctor. The patient expressed that its especially in the Lymph nodes, she read the papers that she got, she thought this is common. Her First Dose was on 26Jan2021, probably around 9:30AM or 10AM. The Lymph nodes began hurting on 26Jan2021, it was a burning pain on chest and breast area. She took a Vicodin and it went away and did not bother her for the rest of the day, but it was bothering her this morning and it woke her up. She has a lump already on the breast from the surgery and she usually get pain there, but this is not the same pain today. As of reporting time, it was different, it was a stronger pain, it goes down the breast arm. Her Lymph nodes are tender on the Left Side which is the same side she had surgery on in the past. She got the vaccine on the right arm. Outcome of the event was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1062107
Sex: F
Age:
State: CA

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

Lab Data: Test Date: 20210119; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: axillary lymphadenopathy x 2 weeks right side (same side as first injection).; nausea; vomiting; transitory trigeminal neuralgia - right sided; This is a spontaneous report from a contactable physician (patient). A 38-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284), intramuscular at the right arm on 30Dec2020 14:30 at single dose for COVID-19 immunization. The patient has no medical history. The patient has no known allergies. The patient was not pregnant at the time of vaccination. Concomitant medication included influenza vaccine (FLU) on 10Dec2020 at the left arm. The patient experienced axillary lymphadenopathy for 2 weeks right side (same side as first injection), nausea, vomiting, and transitory trigeminal neuralgia - right sided; all on 01Jan2021. The patient did not receive any treatment for the events. The patient underwent lab tests and procedures which included nasal swab (COVID PCR): negative on 19Jan2021. The patient recovered from the event axillary lymphadenopathy on 15Jan2021 and recovered on an unspecified date for the rest of the events.

Other Meds:

Current Illness:

ID: 1062108
Sex: M
Age:
State: MS

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Diarrhea; his arm was a little sore; This is a spontaneous report from a contactable consumer (patient's wife). An 82-year-old male patient received his first dose of bnt162b2 (BNT162B2 reported as PFIZER BIONTECH COVID-19 VACCINE; lot number: EL3247; expiration date: unknown) at the vaccination age of 82-year-old intramuscularly in the left arm on 25Jan2021 14:00 at a single dose for COVID-19 vaccination (COVID-19 immunization). The patient's medical history and concomitant medications were none. The patient did not received other vaccine within 4 weeks prior to vaccination. The wife reported that her husband got the first dose of the Covid-19 Vaccine on 25Jan2021 about 14:00 and did not have any reaction except his arm was a little sore on 25Jan2021 18:00. It is sore if he rubs the area, but has gotten better She said that last night, he developed diarrhea at about 22:30 26Jan2021. She inquired if this is a coincidence, he got the diarrhea or is it a side effect from the shot. She added that the diarrhea started about 36 hours after he got the first dose. He had the diarrhea at 22:30 26Jan2021, he had it again at 02:00 27Jan2021, and again at 07:00 27Jan2021 and he has not had it since. She said that her husband was saying he thinks it was getting better. She mentioned that after he received the vaccine, they waited for 15 minutes to make sure there was no reaction. She added that the vaccination facility type was health department drive through vaccination. The adverse events did not require emergency room or physician office visit. The outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 1062109
Sex: F
Age:
State: MI

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Name: Weight; Result Unstructured Data: Test Result:236-238

Allergies:

Symptoms: weight was 236-238 and bounces back and forth; Started getting real dizzy that comes and goes/ if she moves too fast that the dizziness comes and goes; Right arm is sore and not tender; This is a spontaneous report from a contactable consumer (patient). An 81-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number: EL3249 expiration date: May2021, via an unspecified route of administration on 26Jan2021 at a single dose in the right arm for COVID-19 immunization. Medical history included heart problem from Nov2019 and ongoing and angina pectoris. Concomitant medication included a lot of pills for her heart problem. She was on blood thinners, sugar pills, and uric acid because of the diuretics. The patient stated that she got her shot yesterday (26Jan2021) a little after 1. Later this morning (27Jan2021), that she started getting real dizzy that comes and goes. She was reading the list and dizziness was one of more serious side effects. She wanted to know what to do about it, it was one of things. She has another shot coming up on 16Jan (as reported). The patient further mentioned that her right arm was sore and not tender on 27Jan2021. If she moves too fast that the dizziness comes and goes. Her weight was 236-238 and bounces back and forth because she was on diuretics. The outcome of the events dizziness was not recovered, right arm was sore was recovering while for weight was 236-238 and bounces back and forth was unknown.

Other Meds:

Current Illness: Heart disorder (Verbatim: heart problem)

ID: 1062110
Sex: F
Age:
State: FL

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: With the first dose she felt the little warmth or gush of the medication going in; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246), via an unspecified route of administration at the upper left arm on 06Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. With the first dose she felt the little warmth or gush of the medication going in on 06Jan2021, not pain but she could feel it going in but with this second shot there was nothing and no blood. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1062111
Sex: F
Age:
State: NY

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Her hand is a purple color; Her skin feels like a BP cuff is on it; entire left arm is swollen and red; entire left arm is swollen and red; Her entire left arm, which is the arm that received the vaccine is swollen and red. It feels like the circulation is being cut off; This is a spontaneous report from a contactable consumer (patient). A 40-year-old female patient received the 1st dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, Lot number: EL8982 and Expiration date: 31May2021), via an unspecified route of administration at the left arm on 21Jan2021 at a single dose for covid-19 immunization. The patient's has no medical history. There were no concomitant medications. On 22Jan2021, her entire left arm, which is the arm that received the vaccine is swollen and red. It feels like the circulation is being cut off. It hasn't been seeming to get better. The first time she noticed it was the morning after the vaccine. Her entire arm was swollen. She thought it would dissipate. At times it has kind of gotten better, but then the swelling keeps coming right back. Like right now her arm was uncomfortable in her coat. On an unspecified date, her hand was purple color. Her skin feels like a BP cuff was on it. She has not had treatment for it. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1062112
Sex: F
Age:
State: MO

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210127; Test Name: temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit

Allergies:

Symptoms: soreness at the injection site; Headache; elevated temperature (100.2 F); This is a spontaneous report from a contactable consumer (patient). A 28-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection lot no. and expiry date not reported), via an unspecified route of administration in left arm on 26Jan2021 08:30 at a single dose for covid-19 immunization. Medical history was reported as none. There was no other vaccine administered to the patient in four weeks. No known allergies. Patient was not pregnant at time of vaccination. The patient's concomitant medications were not reported. On 27Jan2021 at 07:00, patient experienced soreness at the injection site, headache and elevated temperature (100.2 F). Outcome of the events was unknown. Patient was given the vaccine in a workplace clinic. The patient has not tested with Covid since vaccination. Information about Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1062113
Sex: F
Age:
State: IL

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: This is a spontaneous report from a contactable consumer. A 58-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL8982), via an unspecified route of administration by injection once to left arm, upper part, on 26Jan2021 at a single dose for COVID-19 immunization. The patient has no medical history. There were no concomitant medications. The patient experienced tingling on right side by cheek bone on 27Jan2021 and she did not have it yesterday, and the shot was on the left side, later clarified as the left arm. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1062114
Sex: F
Age:
State: OH

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210109; Test Name: Temperature; Result Unstructured Data: Test Result:101 Fahrenheit; Test Date: 20210107; Test Name: O2%; Result Unstructured Data: Test Result:99-98 %; Comments: repositioning

Allergies:

Symptoms: HSV 1 eruption and subli; withdrawal bleeding 3 days late and heavier and longer than usual; migraine; Left index finger petechiae; had an insect bite; lymphadenopathy on the left deltopectoral (1x1 cm tender freely mobile) and on the left supraclavicular (2x1 cm tender freely mobile); temperature was 101 F; Acne flare-up; no withdrawal bleeding and she was on oral contraceptive pill (OCP)/withdrawal bleeding 3 days late; woke up at 2:00 AM and 2:35 AM because of the tenderness rolling over and she had to take central analgesia to be able to sleep; puffy face; tenderness at the site of injection; Constipation; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0142), via an unspecified route of administration on the left arm, on 06Jan2021 15:45, at single dose, for covid-19 immunization. The patient has no medical history; unknown if there were any allergies. Concomitant medications included oral contraceptive pill (OCP) and multivitamins. The patient had no Covid prior to vaccination. She did not receive any other vaccines within 4 weeks prior to the Covid vaccine. She took pre-vaccination analgesia. The vaccine was given at the hospital. On 06Jan2021 (day 0) she experienced tenderness at the site of injection. She also experienced constipation on 06Jan2021. However, she couldn't "comment" about temperature since she was taking NSAIDs. She woke up at 2:00 AM and 2:35 AM on 07Jan2021 (day 1) because of the tenderness rolling over and she had to take central analgesia to be able to sleep. On 07Jan2021 she experienced tenderness at the site of injection and; puffy face but it wasn't angioedema. Her O2% was "99-98% repositioning" on 07Jan2021. She still had constipation and still couldn't comment about temperature since she was taking NSAIDs. On 08Jan2021 (day 2) she had an acne flare-up; and no withdrawal bleeding and she was on oral contraceptive pill (OCP). For the constipation she started on OTC fiber gum. On 09Jan2021 (day 4) she experienced lymphadenopathy on the left deltopectoral (1x1 cm tender freely mobile) and on the left supraclavicular (2x1 cm tender freely mobile) which hadn't resolved. She still was experiencing constipation. Her temperature was 101 F on 09Jan2021. On 10Jan2021 (day 5) she had withdrawal bleeding 3 days late and heavier and longer than usual, migraine, constipation, and left index finger petechiae because on "23/11" she had an insect bite on 10Jan2021. On 11Jan2021 (day 6) her lymphadenopathy on the left posterior cervical (1x1 cm tender freely mobile) hasn't resolved; she still had migraine and was now back to regular bowel habit. On 15Jan2021 (day 10) she had HSV 1 "eruption and subli". She received treatment (also reported as symptomatic treatment) for all these adverse events. At the time of the report, she recovered from constipation on 11Jan2021 with lasting effects; while she also recovered from all the other remaining adverse events on Jan2021 with lasting effects. She has not been Covid-tested post-vaccination.

Other Meds:

Current Illness:

ID: 1062115
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: achy / aches and pain; didn't feel like himself; This is a spontaneous report from a contactable consumer (patient's wife). An 81-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date were not provided) solution for injection, via an unspecified route of administration on an unspecified date at a single dose for Covid-19 immunization. Medical history was reported as none. There were no concomitant medications. The reporter stated that her husband (patient) received the first dose of the vaccine about two and one-half to three weeks ago and he had some aches and pain but it was not that bad. She was unsure of the exact day or time and does not know which arm. She reported that a day or two after the first dose he was achy and didn't feel like himself. He didn't say much about it. Then yesterday 26Jan2021 he got a major headache after the second dose; he would sleep and wake up and sleep again trying to get rid of the headache. She gave him Tylenol 650mg one by mouth and it didn't help. Outcome of the events was unknown. Information about batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1062116
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Feels terrible now; Sinus headache; This is a spontaneous report from a Pfizer-sponsored program. A non-contactable consumer (patient's husband) reported that a female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) at a single dose, with route of administration and therapy date unspecified, for COVID-19 vaccination. The patient's medical history and concomitant medications were not reported. On an unspecified date, after the first dose of vaccination, the patient had felt "terrible now"; and had sinus headache. The outcome of the events, 'felt terrible' and 'sinus headache', was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1062117
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/20/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: swollen lymph nodes around collarbone and neck; This is a spontaneous report from a non-contactable consumer (patient). A 29-years-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EL3246 and expiration date unknown), via an unspecified route of administration on the left arm on 14Jan2021 at a single dose for COVID-19 immunization. Medical history was not reported. Concomitant medications included fexofenadine hydrochloride (ALLEGRA), probiotics (PROBIOTICS) and multivitamin. The patient had no other vaccine in four weeks and was not diagnosed with COVID-19 prior to the vaccination. The patient experienced swollen lymph nodes around collarbone and neck on 20Jan2021. No treatment was administered for the event. The patient underwent lab tests and procedures which included nasal swab: negative on 04Jan2021. The event had not resolved. The event required a physician office visit. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds: ALLEGRA; PROBIOTICS

Current Illness:

ID: 1062118
Sex: F
Age:
State: TN

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Nausea; Dizzy; left arm soreness; This is a spontaneous report received from a contactable consumer (patient). A 53-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3249, expiry date: May2021), intramuscular on the left arm, on 08Jan2021 16:29, at single dose, for Prevention/COVID-19 immunization, at a public health department. There were no medical history and concomitant medications. The patient did not receive other vaccinations within 4 weeks. On 09Jan2021 at 08:00, the patient experienced left arm soreness. On 27Jan2021 at 07:00, the patient felt dizzy. Shortly after, at 07:15, the nausea started. The patient wanted to know if these could be side effects and would it still be okay to get the scheduled second dose on 29Jan2021. The patient also asked if she can get the second dose if she has a fever on the day she is supposed to get the second dose. The events did not require emergency room or physician's office visits. The patient was recovering from the events. The reporter assessed the events as non-serious.

Other Meds:

Current Illness:

ID: 1062119
Sex: F
Age:
State: IN

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: For 24 hours I had muscle spasms down the middle of my back and in my neck; severe malaise; This is a spontaneous report from a contactable nurse (patient). A 22-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL1824; expiry date: unknown) via an unspecified route of administration in the right arm, on 20Jan2021 at 10:00, at a single dose, for Covid-19 immunization. Other medical history included depression, anxiety, and hypothyroidism. The patient had no known allergies. Concomitant medications included sertraline, prednicarbate (TOPIMAX), levothyroxine, and ethinylestradiol, norelgestromin (XULANE). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EI1284) in the right arm, on 26Dec2020 at 06:15 AM, for Covid-19 immunization. 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 21Jan2021, at 12:00 AM, for 24 hours, the patient had muscle spasms down the middle of her back and in her neck, and severe malaise. The patient did not receive therapy for the events. Outcome of the events was recovered.

Other Meds: SERTRALINE; TOPIMAX [PREDNICARBATE]; LEVOTHYROXINE; XULANE

Current Illness:

ID: 1062120
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: 4 inch area of erythema around the injection site; 4 inch area of erythema around the injection site/There was no induration or hives, nothing other than pain due to injection; This is a spontaneous report from a contactable physician. A patient of unspecified age and gender received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient got the first shot and over 4 days developed a 4-inch area of erythema around the injection site. There was no induration or hives, nothing other than pain due to injection. The outcome of the events was unknown. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1062121
Sex: M
Age:
State: DE

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

Lab Data:

Allergies:

Symptoms: body aches; Low grade fever; swelling of upper lip/recurrent swelling of the upper lip; This is a spontaneous report from a contactable physician. A 54-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date not provided), via an unspecified route of administration on Jan2021 at SINGLE DOSE for COVID-19 immunisation. Patient's medical history included benign prostatic hyperplasia from an unknown date and unknown if ongoing. Concomitant medication included morniflumate (FLOMAX [MORNIFLUMATE]) for benign prostatic hyperplasia. It was also reported that patient was not on an ACE inhibitor. The physician reported that the patient received the second dose of the Pfizer COVID 19 vaccine two weeks ago today (unspecified date). Eleven to thirteen hours later, the patient had the typical symptoms including body aches and low grade fever. Patient also experienced swelling of the upper lip. All of these effects resolved within 24 hours and the patient had recovered completely. Then 14 days later, the patient had recurrent swelling of the upper lip again. It was stated that the events were not serious. Outcome of the events 'body aches' and 'low grade fever' was recovered; outcome of the event 'swelling of upper lip/recurrent swelling of the upper lip' was not recovered. Information on the lot/ batch number has been requested.

Other Meds: FLOMAX [MORNIFLUMATE]

Current Illness:

ID: 1062122
Sex: F
Age:
State: NC

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: itching at her head, face and shoulders and the back; This is a spontaneous report from a contactable consumer (patient). An 81-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE lot#: EL9261), via an unspecified route of administration on the right arm on 26Jan2021 10:30 at SINGLE DOSE as COVID-19 immunization at the hospital. Medical history heart attack, ongoing bone disorder (reported as bone), ongoing blood pressure abnormal (reported as blood pressure), ongoing pain in leg, ongoing blood cholesterol abnormal (reported as cholesterol), ongoing allergy, and ongoing blood clots in leg. The patient was also allergic to sulfa. Ongoing concomitant medications included hydrochlorothiazide, triamterene (MAXZIDE) since 2011 (taking for 10 years) and for blood pressure, cetirizine hydrochloride (ZYRTEC) from unknown date (taking for long time) for allergy, losartan (LOSARTAN) since 2016 (taking for 5 years) for cholesterol, potassium (POTASSIUM) from unknown date (taking for long time) for pain in leg, metoprolol tartrate (LOPRESSOR) since 2011 (taking for 3 years) for blood pressure, omeprazole (PROTONIX) since 2011 (taking for 3 years) for blood clots in leg, fish oil (FISH OIL) from unknown date and indication, acetylsalicylic acid (ASPIRIN) since 2001 (taking for 20 years) for heart attack, colecalciferol (D3) since 2016 (taking for 5 year) for calcium supplementation reported as (calcium and body build up), and calcium (CALCIUM) from unknown date for bones. The patient first dose of the Pfizer COVID 19 vaccine on 26Jan2021 at 10:30AM in the right arm. She noticed about 9PM last night, she started itching at her head, face, shoulders and back. The itching only lasted for a little over an hour (26Jan2021 10:00 PM). She took some diphenhydramine (BENADRYL) and it helped, gave her some relief. She was fully recovered today 27Jan2021. She was scheduled for the next dose 16Feb2021.

Other Meds: MAXZIDE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; LOSARTAN; POTASSIUM; LOPRESSOR; PROTONIX [OMEPRAZOLE]; FISH OIL; ASPIRIN [ACETYLSALICYLIC ACID]; D3; CALCIUM

Current Illness: Allergy; Blood cholesterol abnormal; Blood pressure abnormal; Bone disorder; Pain in leg; Thrombosis

ID: 1062123
Sex: M
Age:
State: TX

Vax Date: 01/16/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:little over 100 degrees; Comments: Yesterday he had a fever a little over 100 degrees

Allergies:

Symptoms: Fever; Chills; extreme weakness; so weak he couldn't stand up out of a chair; extreme weakness; so weak he couldn't stand up out of a chair; felt really bad; This is a spontaneous report from a contactable consumer (patient himself). A 79-year-old male patient received BNT162B2 (Pfizer-BIONTECH COVID-19 Vaccine; EL3247), via an unspecified route of administration in the left arm near the shoulder on 16Jan2021 at about 2-3:00 PM as a single dose for COVID-19 immunization (also reported as to protect himself; hopefully). The patient's medical history was not reported. There were no concomitant medications. The patient did not receive any other vaccines on the same day as BNT162B2 or even four weeks prior and had no problems with vaccines in the past. The patient experienced fever, chills, extreme weakness; so weak he couldn't stand up out of a chair, and felt really bad on 26Jan2021. He had a fever a little over 100 degrees, extreme weakness. He was so week he couldn't stand up out of a chair. He also had chills and just felt really bad. The patient thinks he was over it, he hoped. The events did not require any visit to the Emergency Room or Physician's office. Outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1062124
Sex: F
Age:
State: FL

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Name: Height; Result Unstructured Data: Test Result:5'; Comments: who stated she has been shrinking

Allergies:

Symptoms: she has been shrinking; the COVID-19 Vaccine injection site was a little itchy, red, and hot when she first noticed the adverse reaction on 15Jan2021; the COVID-19 Vaccine injection site was a little itchy, red, and hot when she first noticed the adverse reaction on 15Jan2021; the COVID-19 Vaccine injection site was a little itchy, red, and hot when she first noticed the adverse reaction on 15Jan2021; This is a spontaneous report from a contactable consumer, the patient. A 78-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number 61R84), via an unspecified route of administration on 14Jan2021 at 12:00 (at the age of 78-years-old) as a single dose in the left arm for COVID-19 immunization. Medical history included macular degeneration from an unknown date (for which patient received macular degeneration shot in her eye on 11Jan2021. The shot was the medication "Elyce"), high blood pressure and thyroid condition (both for which patient takes unspecified medications) and bad back for which patient received epidural (unspecified medication) on 13Jan2021. Concomitant medications Elyce (as reported) for macular degeneration, epidural (unspecified medication) for back pain, and unspecified mediations for high blood pressure and thyroid condition. The patient did not receive any other vaccines within four weeks prior to the vaccination and had no additional vaccines administered on the same date of the vaccination. On 15Jan2021 the patient experienced vaccine injection site was a little itchy, red, and hot when she first noticed the adverse reaction on the second day, 15Jan2021. She said the COVID-19 Vaccine injection site stayed warm and itchy for 3 days. She said she noticed the red spot was still at the COVID-19 Vaccine injection site this morning, and asked does she need to worry about the red spot. She clarified the redness at the vaccine injection site is a half circle, and the vaccine injection site is not burning or itching. The patient did not receive any treatments for the vaccine injection site was a little itchy, red, and hot> The patient stated she "has been shrinking" from an unknown date. The patient also reported she has a history of a bad back and she had an epidural the day before getting her first COVID-19 Vaccine dose. She clarified she had the epidural on 13Jan2021. The patient stated she does not have the epidural medication name, dose, NDC, Lot and Expiration Date, since the epidural was given at the orthopedist's office. She said she received a notice from her orthopedist, who administered the epidural on 13Jan2021, stating that Pfizer recommended not to have an epidural when having the COVID-19 Vaccine because the epidural may not be as effective. She said she is not going to go back for her second epidural with the orthopedist, but plans to have her second COVID-19 Vaccine dose. She clarified that the letter from her orthopedist stated she can schedule her next epidural a week after receiving the COVID-19 Vaccine. The patient stated she was more concerned about getting her second dose of the COVID-19 Vaccine than getting a second epidural with her orthopedist. The patient reported she still had a half dollar sized red mark at the COVID-19 Vaccine injection site. The clinical outcomes of the vaccine injection site was a little itchy, red, and hot were recovering. The outcome of the event she has been shrinking was unknown.

Other Meds:

Current Illness:

ID: 1062125
Sex: M
Age:
State: OH

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: had trouble with his stomach in the bowels while sleeping; arm sore; This is a spontaneous report from a contactable consumer. An 85-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) first dose, lot number and expiration date unknown, via an unspecified route of administration on 23Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated that his arm was sore the first night (23Jan2021) and did not take anything for it. On Monday night (25Jan2021), he had trouble with stomach in bowels while sleeping. He wanted to know if this was an occurrence from the vaccine or if it was a random occurrence. In all things that he read, diarrhea like symptoms were not mentioned. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1062126
Sex: F
Age:
State:

Vax Date: 12/19/2020
Onset Date:
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sore arm; mild headache; nausea; This is a spontaneous report from a contactable healthcare professional (patient). A 34-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), via an unspecified route of administration at the right arm on 19Dec2020 08:45 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. The patient experienced sore arm, mild headache, and nausea after the first dose on an unspecified date with outcome of not recovered. The patient did not receive any treatment for the events. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1062127
Sex: F
Age:
State:

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Name: Weight; Result Unstructured Data: Test Result:157-158lbs

Allergies:

Symptoms: arm pain/soreness; This is a spontaneous report from a contactable nurse (patient). A 49-year-old female patient received the 1st dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, Lot number: EK9231), intramuscular at the left upper arm on 05Jan2021 10:20 at a single dose for COVID-19 immunization. The patient had no medical history. There were no concomitant medications. On 05Jan2021, the patient experienced arm pain/soreness she took some Tylenol, not that she needed too much. She recovered from the arm pain/soreness within a day or two days. It was not a big deal. The patient weight was 157-158lbs on an unspecified date. The outcome of the event was recovered on Jan2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1062128
Sex: F
Age:
State:

Vax Date: 12/28/2020
Onset Date: 12/29/2020
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Name: culture; Result Unstructured Data: Test Result:no bacterial growth; Test Name: Covid-19 rapid swab; Result Unstructured Data: Test Result:negative; Test Name: urinalysis; Result Unstructured Data: Test Result:urine had leukocytes and blood present

Allergies:

Symptoms: mild discomfort to my urethra; UTI symptoms; Burning upon urination; pain upon urination; urgency; frequency; This is a spontaneous report from a non-contactable healthcare professional (patient). A 30-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number: EL0140) solution for injection, via an unspecified route of administration in left arm on 28Dec2020 15:45 at a single dose for Covid-19 immunization. Medical history included Hashimoto's Thyroiditis. Patient was not pregnant. The patient's concomitant medications included levothyroxine, unspecified daily multivitamin, and collagen. The patient previously took trimethoprim/sulfamethoxazole (BACTRIM) and had allergies. The patient experienced UTI symptoms, burning upon urination, pain upon urination, urgency, and frequency on 29Dec2020, and mild discomfort to her urethra on an unspecified date. The patient visited her physician. Patient received antibiotic - Keflex. The patient underwent lab tests which included culture: no bacterial growth on an unknown date, Covid-19 rapid swab: negative on an unknown date, and urine analysis: urine had leukocytes and blood present on an unknown date. Outcome of the event mild discomfort to my urethra was unknown while the rest was recovered. No follow-up attempts are possible. No further information is expected. Information about lot/batch number has been obtained.

Other Meds: LEVOTHYROXINE; COLLAGEN

Current Illness:

ID: 1062129
Sex: M
Age:
State: FL

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm was sore; This is a spontaneous report from a contactable consumer. An 88-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient got his on 14Jan2021, and his arm was sore in Jan2021 but he did not have any redness, itchiness, or warmth. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1062130
Sex: F
Age:
State: PA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fever; chills; headache; overall fatigue; pain and tenderness at injection site as well as in the armpit underneath the injection site; pain and tenderness at injection site as well as in the armpit underneath the injection site; patient with autoimmune thyroiditis (not yet clear if Hashimoto's or Graves) received PfizerBiontech Covid-19 Vaccine; patient with autoimmune thyroiditis (not yet clear if Hashimoto's or Graves) received PfizerBiontech Covid-19 Vaccine; This is a spontaneous report from a contactable healthcare professional (patient). A 26-year-old non-pregnant female patient received her second dose of bnt162b2 (BNT162B2 reported as PFIZERBIONTECH COVID-19 VACCINE; unknown lot number and expiration date) at vaccination age of 26-year-old intramuscularly in the left arm on 26Jan2021 12:15 at a single dose for covid-19 immunization. Medical history included autoimmune thyroiditis (not yet clear if Hashimoto's or Graves), appendicectomy and pyelonephritis. The patient was not diagnosed with Covid-19 prior to vaccination. Concomitant medication included methimazole, atenolol, valaciclovir hydrochloride (VALACYCLOVIR HCL), ethinylestradiol, norgestimate (NORGESTIMATE & ETHINYL ESTRADIOL) and magnesium. The patient did not receive other vaccine in four weeks. The patient previously took azithromycin but drug allergy. The patient received the first dose of of bnt162b2 (BNT162B2 reported as PFIZERBIONTECH COVID-19 VACCINE; unknown lot number and expiration date) at vaccination age of 26-year-old intramuscularly in the left arm on 05Jan2021 02:15 PM at a single dose for covid-19 immunization but had pain and tenderness at the injection site. It was reported that the patient with autoimmune thyroiditis (not yet clear if Hashimoto's or Graves) received PfizerBiontech Covid-19 Vaccine in a hospital on 26Jan2021 12:15. On 27Jan2021 12:00 AM, the patient had fever, chills, headache, overall fatigue, pain and tenderness at injection site as well as in the armpit underneath the injection site. The events required treatment which included acetaminophen. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds: METHIMAZOLE; ATENOLOL; VALACYCLOVIR HCL; NORGESTIMATE & ETHINYL ESTRADIOL; MAGNESIUM

Current Illness:

ID: 1062131
Sex: M
Age:
State: SC

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210127; Test Name: Fever; Result Unstructured Data: Test Result:low grade fever

Allergies:

Symptoms: Fever; Chills; Body Ache; Pain in face; Pain in back; pain in hip; Headache for 2 days; Vivid nightmares; Sweats; This is a spontaneous report from a contactable consumer (patient). A 52-year-old male patient received the first dose of BNT162B2 (BNT162B2, Solution for injection, lot number: EL3249, expiry date: not reported), via an unspecified route of administration, on 25Jan2021 03:00 PM at a single dose on the left arm for COVID-19 immunization. The vaccine was administered at a hospital. Medical history was none. The patient was not diagnosed with covid prior to vaccination. He had no known allergies. Concomitant medications were not reported. On 26Jan2021 01:15 AM, the patient experienced fever, chills, sweats, body ache, pain in face, pain in back, pain in hip, headache for 2 days, vivid nightmares. 2 days later (at the time of report, 27Jan2021), the patient still had low grade fever, sweating, body ache and headache. No treatment was received for the reported adverse events. Outcome of the events was reported to be recovering. The patient was not tested for covid post vaccination.

Other Meds:

Current Illness:

ID: 1062132
Sex: M
Age:
State: FL

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Rash all over his body; rash which is red patchy tiny blistery things; rash which is red patchy tiny blistery things; pain of the rash and blisters; Itching; Shoulder pain; This is a spontaneous report from a contactable consumer (patient). A 64-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number: EH9899) solution for injection, via an unspecified route of administration on 21Jan2021 at a single dose for Covid-19 immunization. Medical history was reported as none. There were no concomitant medications. The patient experienced shoulder pain on 22Jan2021; itching started on 23Jan2021; rash all over his body which has worsened, rash which was red patchy tiny blistery things on 24Jan2021. Patient further reported that he had a rash over his entire body. It started as an itch on his legs which developed into more itching which turned into a rash which was red patchy tiny blistery things. Now it was on his arms, back, belly, neck, and legs. He had shoulder pain and it was hurting the day after he got the vaccine on Friday 22Jan2021. Rash started on Sunday 24Jan2021, it was like a chicken pox type rash. It was like red dots that become sensitive and look slightly blistered. Shoulder pain: this was nothing compared to the pain of the rash and blisters (24Jan2021). He had taken off the bandage and was sore. He was not even sure if he was still sore or not because he was only paying attention to everything else. It was overwhelming. Treatment: He called his doctors and they said that he should use Calamine lotion as a temporary soother for itch and rashes. They also told him to take Benadryl and his doctor prescribed Prednisone. Outcome of the event shoulder pain was unknown while the other events was not recovered. No follow-up activities are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1062133
Sex: M
Age:
State: TN

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Felt as though truck kept turning over, but it was all in his head; Felt as though truck kept turning over, but it was all in his head; Was hot and everything; This is a spontaneous report from a contactable consumer (patient). A 78-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: PK12ER/EL9261; Expiration date was not reported) on 26Jan2021 (11:30) at a single dose on the right arm, with route of administration unspecified, for COVID-19 immunization/to not get COVID at the public health department. The patient had no relevant medical history and concomitant medications. The patient had no history of problems with vaccines in the past. On 27Jan2021, the patient had felt as though a truck kept turning over, but it was all in his head; and was "hot and everything". The outcome of the events, 'felt as though a truck kept turning over, but it was all in his head' and '"hot and everything"', was recovering.

Other Meds:

Current Illness:

ID: 1062134
Sex: F
Age:
State:

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210126; Test Name: temperature; Result Unstructured Data: Test Result:101 degrees; Comments: running a temperature of 101 degrees

Allergies:

Symptoms: sick; temperature of 101 degrees; headache/frontal type of headache; This is a spontaneous report from a contactable nurse (patient). A 50-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EL3249 and expiration date unknown), intramuscular on 26Jan2021 at 10:20 at a single dose for COVID-19 immunization. There were no medical history and no concomitant medications. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), batch/lot number: EK9231, intramuscular injection in left upper arm on 05Jan2021 as COVID-19 immunization and only had arm pain/soreness. As a nurse, the patient has given tons of vaccines. On 26Jan2021, she was given her second dose of COVID-19 vaccine around 10:20 a.m. She didn't hurt right away, it started later on. By 6pm, she got home, so sick and had a temperature of 101 degrees. She didn't go to work as she has been running a temperature and she has taken Tylenol. She knows the vaccine works the same, but everybody acts different. The patient also asked if a high temperature of 101 degrees a common side effect and if it is a normal reaction and how long it typically last. The patient states she has never been so sick like this in her life. The patient never gets sick and wanted to know if this is a common thing. She hasn't called her primary doctor. She took Tylenol Extra Strength, 6 or 7pm, also in the middle of the night and then again at 9am the following morning. Her fever has gone down a little bit, but the headache was so bad. It's like a frontal type of headache and it hurts so bad. The headache also began around 6pm yesterday and has converted into fever. The patient wanted to know if it is common to have this type of reaction. The patient is getting so tired and declined to continue with the report, stating she just wants to lay down. The event temperature of 101 degrees was resolving while the outcome of the rest of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1062135
Sex: F
Age:
State: NM

Vax Date: 01/19/2021
Onset Date: 01/01/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swelling and soreness at the injection site; soreness at injection site; red, and a little swollen at the injection site; felt itchy at the injection site; This is a spontaneous report from a contactable consumer (patient). A 53-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3249 and expiry date: unknown), intramuscular on the right arm near shoulder on 19Jan2021 09:00 at a single dose for COVID-19 immunization. There were no medical history and concomitant medications. There were no other vaccine received within 4 weeks prior to COVID vaccination. After she got a tetanus shot (probably needs another since it had been ten years) her arm/ muscle was sore. Patient had typical swelling and soreness at the injection site on Jan2021that went away within a couple of days and then did not have any symptoms. Then today all of a sudden it felt sore, red, and a little swollen at the injection site again. It has been more than a week since the symptoms initially resolved and now they have reemerged. It felt itchy at the injection site, it had a raised red area that was itchy on Jan2021. She did go running this morning and has been running several times, she went running the day after she got the vaccine. Events did not require emergency room nor a visit to the physician's office, and no treatment was given. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1062136
Sex: F
Age:
State:

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: runny eyes, very itchy, discharge, and was like pink eye; runny eyes, very itchy, discharge, and was like pink eye; runny eyes, very itchy, discharge, and was like pink eye; This is a spontaneous report from a non-contactable consumer (patient herself). A 74-year-old female patient received the first dose of BNT162B2 (Pfizer-BIONTECH COVID-19 Vaccine; Lot number: EL9261), via an unspecified route of administration in the left arm on 25Jan2021 as a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient did not have COVID prior to vaccination, did not receive any other vaccine in four weeks, and was not pregnant. The patient experienced runny eyes, very itchy, discharge, and was like pink eye on 25Jan2021. It was reported that the events started about six hours after vaccine shot and lasted 48 hours. The patient had not tested positive for COVID-19 post vaccination. The patient did not receive any treatment for the events. Outcome of the events was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1062137
Sex: F
Age:
State: CA

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data: Test Date: 20210112; Test Name: heart beat; Result Unstructured Data: Test Result:fast heart beat; Comments: fast heart beat/she felt her heart started rushing more, she had rapid heart beat

Allergies:

Symptoms: legs cramps; stomachaches; has a history of heart palpitations/she felt her heart started rushing more, she had rapid heartbeat; sore arm; This is a spontaneous report received from a contactable consumer (patient). A 56-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283, expiry date: unknown), via an unspecified route of administration on the left arm, on 09Jan2021, at single dose, for COVID Prevention/COVID-19 immunization. Medical history included heart palpitations. Concomitant medication included unspecified medication for heart palpitations. The patient did not receive any other vaccines on the same day as BNT162B2. On 09Jan2021 (the same day as the patient received the vaccine), she developed sore arm which went on about for three days. The patient reported she put rubbing alcohol on it and that helped. On 12Jan2021 (day three after the vaccine), the patient experienced leg cramps and stomachache which went on about for 24 hours. The patient reported that she has a history of heart palpitations, but when she got the vaccine, on 12Jan2021 (day three after the vaccine), she felt her heart started rushing more, she had rapid heartbeat, but then she got it under control. She reported she has some pills for that, so she took an extra dose of her pills and that helped out with the palpitation. The patient recovered from the event sore arm on 12Jan2021; from leg cramps and stomachaches on 13Jan2021; and from "has a history of heart palpitations/she felt her heart started rushing more, she had rapid heartbeat" on an unspecified date.

Other Meds:

Current Illness:

ID: 1062138
Sex: F
Age:
State:

Vax Date: 01/09/2021
Onset Date: 01/01/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: intense body aches; fever; joint pain; several episodes of tachycardia; This is a spontaneous report from a contactable other healthcare professional (patient). A 34-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL1283), via an unspecified route of administration on 09Jan2021 10:00 at a single dose on right arm for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 on 19Dec2020 at 08:45 AM on right arm (lot number: EH9899) for COVID-19 immunization and experienced sore arm, mild headache/nausea. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 09Jan2021 20:00, the patient experienced intense body aches, fever, joint pain; and approximately 1 week after through more than 2 weeks after (Jan2021) had several episodes of tachycardia. No treatment was received for the adverse events. The patient has not recovered from the events. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. The events were reported as non-serious.

Other Meds:

Current Illness:

ID: 1062139
Sex: F
Age:
State: PA

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Body ache; Headache; Tiredness; Sore arm; Insomnia; Chills in eve; This is a spontaneous report from a non-contactable healthcare professional (patient). A 59-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL1283; Expiration date was not reported) on 22Jan2021 (12:45) at a single dose, with route of administration unspecified, for COVID-19 immunization at the hospital. The patient's medical history was not reported. Concomitant medications included bupropion hydrochloride (WELLBUTRIN), calcium, magnesium, vitamin d nos (CAL MAG), calcium carbonate;colecalciferol;phytomenadione (VIT D+K) and fish oil (OMEGA 3). The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK5730; Expiration date was not reported) on 30Dec2020 (when the patient was 59 years old) for COVID-19 immunization. The patient was not pregnant at the time of vaccination. On 22Jan2021, the patient had sore arm; insomnia; and chills in the evening ("eve"). On 23Jan2021, the patient had body ache, headache and tiredness. The patient did not receive any treatment for the events. The outcome of the events, 'sore arm', 'insomnia', 'chills', 'body ache', 'headache' and 'tiredness', was recovered in Jan2021. The patient was not diagnosed with COVID-19 prior to vaccination, and had not been tested since the vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds: WELLBUTRIN; CAL MAG; Vit D+K; Omega 3

Current Illness:

ID: 1062140
Sex: F
Age:
State: MO

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm started to get sore; This is a spontaneous report received from a contactable consumer (patient). A 37-year-old female patient receive the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN5318, expiry date: unknown), via an unspecified route of administration on the left arm, on 26Jan2021 12:00, at single dose, for covid-19 immunization, at the workplace clinic. There were no medical history and concomitant medications. The patient has no known allergies and was not pregnant at the time of vaccination. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. The patient did not receive other vaccines in four weeks. On 26Jan2021 at 17:00, the patient's arm started to get sore and continued to get more sore throughout the evening. It was much better when she woke up in the morning of 27Jan2021, and the pain was fully resolved by 17:00 on 27Jan2021. No treatment was given for the event. The patient recovered from the event on 27Jan2021 at 17:00.

Other Meds:

Current Illness:

ID: 1062141
Sex: M
Age:
State:

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Soreness around the injection site for approximately 30 hours.; This is a spontaneous report from a non-contactable consumer. A 40-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number; EN5318), via an unspecified route of administration in right arm on 26Jan2021 09:30 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced soreness around the injection site for approximately 30 hours on 26Jan2021 10:15 with outcome of recovered. There was no treatment for the event. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1062142
Sex: F
Age:
State: NY

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe joint pain; chills; muscle weakness, causing minimal ability to walk (bed bound); muscle weakness, causing minimal ability to walk (bed bound); This is a spontaneous report from a contactable nurse (patient). A 22-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration on the left arm on 26Jan2021 at a single dose for COVID-19 immunization. Medical history included type 1 diabetes mellitus and attention deficit hyperactivity disorder (ADHD). Concomitant medication included dextroamphetamine (dexamfetamine) and ethinylestradiol, norgestimate (TRI ESTARYLLA). The patient took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231) on 07Jan2021 on the right arm On 27Jan2021 10:00, the patient experienced severe joint pain and muscle weakness, causing minimal ability to walk (bed bound) and chills. No treatment was given for the events. The patient was recovering from the events.

Other Meds: DEXTROAMPHETAMINE [DEXAMFETAMINE]; TRI ESTARYLLA

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm