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: 1001443
Sex: F
Age: 60
State: NY

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Rash on chest and around injection site. Pounding headache lasted 2 days. Emesis all Friday night and Saturday and finally afebrile yesterday afternoon. lasting 3 days.

Other Meds:

Current Illness:

ID: 1001444
Sex: M
Age:
State: TX

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: Body temperature; Result Unstructured Data: Test Result:100.4; Test Date: 20210101; Test Name: CT scan; Test Result: Negative ; Test Date: 20210101; Test Name: Lab work; Test Result: Negative ; Test Date: 20210101; Test Name: X-Ray; Test Result: Negative

Allergies:

Symptoms: headache; sweating; neck was stiff; passed out for about 5-10 seconds; body ache; really bad chills; fever 100.4; unable to sleep; This is a spontaneous report from a contactable Consumer (patient). A 38-years-old male patient started to receive 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL0142, Expiry Date: 01Mar2021), via an unspecified route of administration at Left arm on 30Dec2020 18:17 at SINGLE DOSE for covid-19 immunisation. Patient's Medical History (including any illness at time of vaccination) was none. There were no concomitant medications. Prior Vaccinations (within 4 weeks) was reported as 'None' and AEs following prior vaccinations was reported as 'None'. AE(s) following prior vaccinations was reported as None. The patient experienced really bad chills, body aches, fever, unable to sleep on 31Dec2020 with outcome of recovered on 01Jan2021, passed out on bathroom floor for 5-10 seconds, sweating and neck was stiff on 01Jan2021 with outcome of recovered on 01Jan2021, headache on an unspecified data with outcome of unknown. Details were as follows: the patient received the Covi-19 vaccine 30Dec2021. He had a reaction to the vaccine. 24 hours after getting the vaccine he had really bad chills, body aches, fever 100.4. He didn't take any medication for a bit. He then took acetaminophen (TYLENOL). He had a headache, he was unable to sleep. The acetaminophen worked and he went to bed. At 5:00 am he started having a bad headache and took Ibuprofen. He woke up to go to the bathroom. He passed out for 5-10 seconds in the bathroom. His head was leaning in the wall by the door. He was sweating and was stiff all over. He went to the Emergency Room on 01Jan2021. They did an X-ray and a CT scan. They gave him 100ml of saline and some pills. They also did some lab work. Everything was negative. They assumed his body couldn't handle the vaccine. He was supposed to have received the second shot yesterday (20Jan2021). Employee Health said his Primary Care Physician would have to make the decision on him taking it or not. His doctor said he would have to do more research with Pfizer before he says if he can take it or not. Emergency Room visit required due to event passing out.

Other Meds:

Current Illness:

ID: 1001445
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

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

Allergies:

Symptoms: room seemed to be spinning; elevations in blood pressure; felt extremely dizzy; This is a spontaneous report from a contactable Pharmacist. A patient of unspecified age and gender 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 was a resident of a long-term care facility. The patient, within a few minutes of receiving first dose of vaccine (unspecified date), experienced elevations in blood pressure and felt extremely dizzy and described that the room seemed to be spinning. The outcome of the events elevations in blood pressure, felt extremely dizzy and room seemed to be spinning was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1001446
Sex: F
Age:
State: PA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; body aches; headache; fatigue; arm soreness; This is a spontaneous report from a contactable nurse, the patient. A 41-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EK9231), via an unspecified route of administration in the left arm on 20Jan2021 at 06:00 (at the age of 41-years-old) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient did not have any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient previously received the first dose of BNT162B2 (at the age of 41-years-old; Lot Number: EJ1685) on 30Dec2020 at 06:00 in the left arm for COVID-19 immunization. The patient did not receive any other vaccines within four weeks prior to the vaccination except the first dose of the vaccination. Since the vaccination, the patient had not been tested for COVID-19. On 20Jan2021 at 19:00, the patient experienced fever, body aches, headache, fatigue, and arm soreness. The patient was not treated for the events. The clinical outcomes of fever, body aches, headache, fatigue, and arm soreness, were not recovered.

Other Meds:

Current Illness:

ID: 1001447
Sex: F
Age: 75
State: IN

Vax Date: 01/22/2021
Onset Date: 01/26/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Physical exam performed in my office was consistent with left sided Bell's Palsy (and left-sided injection).

Allergies: Fluticasone Propionate-Salmeterol Sumatriptan Penicillin Simvastatin

Symptoms: The patient did okay on the day of the vaccine. She began to develop worsening immune response symptoms over the afternoon of the day after through the next 3-4 days. She woke up the morning listed with Bell's Palsy. I evaluated her one week after her vaccination.

Other Meds: Albuterol Alendronate 70mg q7d Amlodipine 5mg qd Aspirin 81mg EC daily Atenolol 25mg daily Atorvastatin 40mg daily Probiotic Breo Ellipta 100-25 one puff daily Cetirizine 10mg daily Vitamin D3 400 unit capsule daily Citalopram 40mg daily C

Current Illness: Patient had some minor viral illness 1-2 weeks prior to vaccination. She had a negative COVID test during this time period.

ID: 1001448
Sex: F
Age:
State:

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: tired; restless night of sleeping/poor sleep; This is a spontaneous report from a non-contactable consumer. An 81-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EL3247 and expiry date unknown) via unspecified route of administration on 22Jan2021 at single dose for Covid-19 immunization in a hospital. 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 vaccines within 4 weeks prior to the COVID vaccine. The patient experienced having a restless night of sleeping the night of having gotten the COVID-19 vaccine (22Jan2021). The patient was tired the next day (23Jan2021) but was unsure if it was related to poor sleep itself or as a side effect of the vaccine, otherwise she felt good and did not seek any medical attention. The patient has not been tested for COVID-19 since the vaccination. The patient did not receive treatment due to the events. The outcome of the events restless night of sleeping, tired was recovered. The reporter considered the event non-serious; did not results in death; not life threatening; did not caused/prolonged hospitalization, not disabling/incapacitating, no congenital anomaly/birth defect. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1001449
Sex: F
Age:
State: OR

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fuzzy; Unsteady; Weak/Not very energic/Fatigued; Lightheaded/Dizzy; Chest tight; My eyed began swimming with a sensatoin of shutters being opened and closed in front of me/could not see very well; Eyes very photosensitive; Chills; Headache; This is a spontaneous report from a contactable consumer (patient). This 68-year-old female patient received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3247), via an unknown route, on 14Jan2021 (at 08:30) at single dose on the left arm for COVID-19 immunization. Relevant medical history included orthostatic intolerance, myalgic encephalomyelitis and chronic fatigue syndrome (ME/CFS). Relevant concomitant medications included hydrocortisone (CORTEF), levothyroxine sodium (SYNTHROID), fludrocortisone acetate (FLUDROCORTISON) and pyridostigmine. No other vaccine was received in four weeks. On 14Jan2021, after vaccination, she began to feel unsteady, weak, lightheaded, chest tight, and dizzy. Her eyed began swimming with a sensation of shutters being opened and closed in front of her. She could not see very well, eyes were very photosensitive. Layed down and slept, rested in a dark room most of the day. She had also chills and headache. But nightfall she felt mostly recovered, although not very energetic. About one week later, on 20Jan2021, it all happened again, all at once. She also rested for the day and slowly recovered. But this time it hasn't all gone away. She is still weak, fuzzy, unsteady, fatigued, she had headache, and 'my eyes are not right' (as reported). Pre-vaccination and post-vaccination COVID tests were not performed. No treatments were given for the events. The outcome of the events 'unsteady', 'weak/not very energic/fatigued', 'Lightheaded/Dizzy', and 'chest tight' was not recovered while the outcome of the remaining events was unknown.

Other Meds: CORTEF [HYDROCORTISONE]; SYNTHROID; FLUDROCORTISON; PYRIDOSTIGMINE

Current Illness:

ID: 1001450
Sex: M
Age: 65
State: IN

Vax Date: 02/02/2021
Onset Date: 02/02/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies: NKA

Symptoms: Symptoms manifested approximately 12 hours after injection and lasted 30-36 hours. Started with rather severe chills, fever of 102 for next 24 hours, extreme fatigue, body aches, head ache, loss of appetite. NOTE that I was tested Covid positive on November 2, 2020. I was tested for Covid antibodies in December 2020.

Other Meds: Jardiance Zetia Amaryl Lisinopril Metformin CQ10 Vitamin D3 Aspirin (81mg) Mems Multivitamin Vitamin C Zinc

Current Illness: None

ID: 1001451
Sex: M
Age:
State: NY

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I took both doses of the pfizer vaccine and noticed that my thumb joints and my right wrist started to hurt. It hasn't resolved and it seems to not be getting any better

Other Meds:

Current Illness:

ID: 1001452
Sex: M
Age:
State: CT

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Soreness at injection site within 5 hours; This is a spontaneous report from a non-contactable consumer (patient). A 42-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3247), via an unspecified route of administration on 22Jan2021 12:00 at single dose in left arm for COVID-19 immunisation. Patient age at vaccination was 42 years. The vaccine was administered at workplace clinic. No other vaccine was given within 4 weeks prior to the COVID vaccine. The patient medical history was not reported. The patient has no allergies to medications, food, or other products. Concomitant medication included doxycycline. On 22Jan2021 at 05:00 PM, the patient experienced soreness at injection site within 5 hours, reported as non serious. Soreness was reducing within 24 hours. No treatment was received for the adverse event. The event had resolved on an unspecified date in Jan2021. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds: DOXYCYCLINE

Current Illness:

ID: 1001453
Sex: F
Age:
State: MI

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe itchiness from waist up - behind ears, head, back, neck, shoulders; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 78-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE;lot EL9261) on 21Jan2021 at 12:45 at single dose in Left arm for covid-19 immunisation. Medical history included chronic obstructive pulmonary disease (COPD), asthma, osteopenia/porosus and sulfa allergy. Patient was not pregnant. Concomitant medication included fluticasone propionate (FLONASE); nitrofurantoin (MACRODANTIN); alendronate sodium; budesonide/ formoterol fumarate (SYMBICORT); dupilumab (DUPIXENT) from12Jan2021. On 22Jan2021 the patient experienced severe itchiness from waist up - behind ears, head, back, neck, shoulders. Case is reported as non serious. No treatment administered for the adverse event. Outcome of the event was not recovered.

Other Meds: FLONASE; MACRODANTIN; ALENDRONATE SODIUM; SYMBICORT; DUPIXENT

Current Illness:

ID: 1001454
Sex: F
Age: 33
State: TX

Vax Date: 01/25/2021
Onset Date: 02/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: none

Allergies: none

Symptoms: The week after I received the Moderna COVID-19 shot 1st dose I had a big whelped circle at the injection site with warm to the touch feel and a lot of itching. Circle was about 4" in diameter. The date of the injection was 01/25/2021 and right at a week when this happened was 02/01/2021. To this day (02/04/2021) I still have a little itching and a circle still appears on my arm, it's not warm to the touch. Dr. at work place advised me to put CORTIZONE for the itch and keep it hydrated with eucrin cream.

Other Meds: vitamin D, Escitalopram oxalate, Labetalol, pepcid

Current Illness: none

ID: 1001455
Sex: F
Age:
State: VA

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Hit her pretty hard. Did not feel good; This is a spontaneous report from a contactable consumer received via a sales representative. A adult female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number unknown), at single dose on an unknown date for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient reported that the vaccine hit her pretty hard and she did not feel good on an unspecified date. The outcome was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1001456
Sex: F
Age:
State: NJ

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Body temperature; Result Unstructured Data: Test Result:Fever

Allergies:

Symptoms: really swollen and sore underneath her arm in her armpit; really swollen and sore underneath her arm in her armpit/Incredibly sore arm; Fever and chills; Red at injection site; Very tired; Bad headache; This is a spontaneous report from a contactable other health professional reported for herself. A 46-year-old female patient received the first dose of BNT162 (PFIZER-BIONTECH COVID-19 VACCINE, brand: Pfizer, lot number: EL9262,) via unspecified route of administration at age of 46 years old on 21Jan2021 10:15 AM at single dose and vaccine location at left arm, for COVID-19 immunization. Patient was not pregnant at the time of vaccination. Medical history included: prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications reported as there had other medications the patient received within 2 weeks of vaccination. The patient past drugs included: allergies to prochlorperazine (COMPAZINE) and amoxicillin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported really swollen and sore underneath her arm in her armpit. Patient presented fever and chills. Red at injection site. Incredibly sore arm. Patient was very tired and bad headache, the adverse events reported started on 21Jan2021. It was reported the non-serious, no results in death, no life threatening, no caused/prolonged hospitalization, no disabling/incapacitating, no congenital anomaly/birth defect. There was no treatment received for the adverse event. Outcome of events were not recovered.

Other Meds:

Current Illness:

ID: 1001457
Sex: F
Age:
State: MA

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Diarrhea; Chills; Slight headache; Very body tired; This is a spontaneous report from a contactable other HCP reported for herself that a 61-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: p9231), via an unspecified route of administration at the age of 61-years, on 22Jan2021 17:00 (05:00 PM) at single dose in left arm for COVID-19 immunization, in hospital. Medical history was not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient was not pregnant at the time of vaccination. Concomitant medications were not reported. The patient had slight headache on 23Jan2021 and was very body tired. On 24Jan2021 10:00 AM, she had diarrhea and chills. No treatment received for the adverse events. The events were considered as non-serious. Outcome of the events was recovering/resolving. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1001458
Sex: F
Age: 27
State:

Vax Date: 01/06/2021
Onset Date: 02/03/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Received 1st Pfizer dose on 12/18/20, received 2nd dose of Pfizer on 1/6/21. Tested positive for COVID 2/3/21, asymptomatic following high risk exposure on 1/29/21.

Other Meds:

Current Illness:

ID: 1001459
Sex: M
Age:
State: OH

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swelling of left index finger; This is a spontaneous report from a contactable (patient). An 85-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date unknown) via unspecified route of administration on 23Jan2021 16:00 at single dose for Covid-19 immunization in a facility. Medical history included recent finger injury. The patient was not diagnosed with COVID-19 prior to vaccination. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 23Jan2021 16:45, the patient experienced swelling of left index finger in area of recent injury. The patient has not been tested for COVID-19 since the vaccination. The patient did not receive treatment due to the event. The outcome of the event was unknown. The patient informed that this may not be related to the vaccine but thought it should be reported. The reporter considered the event non-serious; did not results in death; not life threatening; did not caused/prolonged hospitalization, not disabling/incapacitating, no congenital anomaly/birth defect. Follow-up activities are possible, information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 1001460
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe stomach pains; bad headache; dizzy; Didn't have any energy and strength; Cold sweats; Nauseous; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient not pregnant received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in the Left arm on 20Jan2021 at 02:45 PM as a single dose for COVID-19 immunisation, lot number: EL3247. Medical history included chronic lyme disease. Concomitant medications were not provided. Patient had no allergies to medications, food, or other products. Prior to vaccination the patient was not diagnosed with COVID-19. Patient did not receive other vaccine in four weeks prior to the COVID vaccine. On 23Jan2021 at 12:00 AM patient had severe stomach pains with a bad headache. Shortly after she got dizzy, did not have any energy and strength. She had cold sweats. Patient tried sips of water, but it made her nauseous. This all happened all at once and it hit patient hard in the middle of her work. No treatment received for the events. Since the vaccination patient had not been tested for COVID-19. Patient was recovering from the events.

Other Meds:

Current Illness:

ID: 1001462
Sex: M
Age: 45
State: CO

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies: NKDA

Symptoms: stomach pain, nausea pain, swelling, redness at injection site fever, chills legs, ankles and feet hurt when walking fatigue

Other Meds:

Current Illness: sinus infection

ID: 1001463
Sex: F
Age:
State: LA

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Roughly 90 minutes after my vaccination my left eye got itchy and swollen; Roughly 90 minutes after my vaccination my left eye got itchy and swollen. Both the eye itself and the area around the eye swelled; the eye was still a bit puffy and swollen; This is a spontaneous report from a contactable healthcare professional (patient herself). A 25-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL8983; expiry date: unknown) via an unspecified route of administration in the left arm, on 22Jan2021 at 17:00, at a single dose, for COVID-19 immunization. The patient has no relevant medical history. Concomitant medications included vitamin B complex (VITAMIN B), colecalciferol (VITAMIN D), and loratadine (CLARITIN) and unspecified birth control (BC) pills. The patient previously received codeine and experienced allergy. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the hospital. On 22Jan2021, roughly 90 minutes after vaccination (at 18:30) the patient's left eye got itchy and swollen. Both eyes and the area around the eye swelled. It went down upon icing and taking two over the counter Benadryl. However, the next morning, the eye was still a bit puffy and swollen. The events were considered non-serious. Outcome of the events was recovering. The patient has not been tested for COVID-19 since vaccination.

Other Meds: VITAMIN B; VITAMIN D; CLARITIN [LORATADINE]

Current Illness:

ID: 1001464
Sex: F
Age:
State: MI

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Raised, red rash over trunk, arms, scalp; This is a spontaneous report from a contactable other hcp. A 58-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EK923), at single dose into the left arm on 30Dec2020 at 03:45 PM for COVID-19 immunization. The patient medical history was not reported. Concomitant medication included diphenhydramine hydrochloride (BENADRYL) 25g and gabapentin 300mg. On 31Dec2020 at 06:00 PM the patient experienced raised, red rash over trunk, arms, scalp. The outcome of the event was recovered. It was reported that the patient received the second dose of BNT162B2 on 20Jan2021 at 07:45 AM in the Left arm.

Other Meds: BENADRYL; GABAPENTIN

Current Illness:

ID: 1001465
Sex: F
Age:
State: MI

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Body temperature; Result Unstructured Data: Test Result:fever

Allergies:

Symptoms: Fever; chills; nausea; body aches; headache; sore arm where injection was done; This is a spontaneous report from a contactable healthcare professional reporting for herself. A 32-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL3249), intramuscular on 21Jan2021 11:15 AM at single dose in right arm for COVID-19 immunisation. Patient age at vaccination was 32 years. The patient was vaccinated at workplace clinic. No other vaccine was given within 4 weeks prior to the COVID vaccine. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: 9231) intramuscular on 31Dec2020 06:30 PM, at single dose in left arm. The patient has no allergies to medications, food, or other products and had no relevant medical history. Concomitant medications included celecoxib (CELEXA), zonisamide (ZONEGRAN), loperamide hydrochloride (MEDIUM). On 21Jan2021 at 03:00 AM (as reported pending clarification) the patient experienced fever, chills, nausea, body aches, headache, sore arm where injection was done. The events were reported as non serious. No treatment was received for the events. The events were resolving. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, has not been tested for COVID-19.

Other Meds: CELEXA; ZONEGRAN; MEDIUM

Current Illness:

ID: 1001466
Sex: F
Age: 35
State: TX

Vax Date: 02/01/2021
Onset Date: 02/02/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: N/A

Allergies: NONE

Symptoms: CHILLS, LETHARGY, LOSS OF APPETITE, LOWER BACK PAIN, INJECTION SITE PAIN/SWELLING, SLIGHT DECREASE IN BREAST MILK PRODUCTION. I TESTED POSITIVE FOR COVID END OF OCTOBER AND REMAINED ASYMPTOMATIC. I HAD A WORSE REACTION TO THE FIRST DOSE OF VACCINE GIVEN 3 MONTHS LATER THAN ACTUAL COVID.

Other Meds: LEVOTHYROXINE 50MCG

Current Illness: NONE

ID: 1001467
Sex: M
Age: 34
State: MT

Vax Date: 12/23/2020
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: COVID-19 PCR TEST NA RES SWAB, 18-Jan-2021, Positive

Allergies: pollen and dust

Symptoms: I needed up get the Pfizer vaccine on Dec 23, 2020 since I worked in a Long Term Care Facility in a remote village and was scheduled to receive the next vaccine on Jan 6, 2021. However, I was released from my job on Jan 1, 2021. On Jan 4th, 2021, I was flown to another city. I spent some time there. Then, on Jan 16th, 2021, I landed in another city and checked in to a hotel. The next day, I was tested for the Corona Virus via nasal swab. The following day, they called me and said my test came back positive and said I had to quarantine for 10 days. I had minor pneumonia symptoms, but I felt they were not bad enough for me to go to the hospital. My symptoms were gone in about 5 days. I left being quarantine on Jan 30th, 2021.

Other Meds: Duloxetine 60 mg

Current Illness: alcohol use

ID: 1001468
Sex: F
Age:
State: CT

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Typical headaches; muscle aches; nausea; distorted sense of smell (rancid smell and altered smells) and sense of taste severely diminished at 24 hours after initial dose of vaccine.; distorted sense of smell (rancid smell and altered smells) and sense of taste severely diminished at 24 hours after initial dose of vaccine.; This is a spontaneous report from a contactable healthcare professional (patient). A 54-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), intramuscular in the right arm on 22Jan2021 12:15 at single dose for COVID-19 immunisation. Medical history included elevated blood pressure and allergy to raw walnuts and pecans. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was vaccinated at a hospital. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medications included biotin (BIOTIN), vitamin d nos (VITAMIN D NOS), vitamin c [ascorbic acid] (VITAMIN C [ASCORBIC ACID]), cyanocobalamin (VITAMIN B12 [CYANOCOBALAMIN]), fexofenadine, hydrochlorothiazide, lisinopril (LISINOPRIL/HCTZ), cetirizine. The patient previously took morphine and experienced drug hypersensitivity. On 23Jan2021 15:00, the patient experienced typical headaches, muscle aches, nausea, distorted sense of smell (rancid smell and altered smells) and sense of taste severely diminished at 24 hours after initial dose of vaccine. No treatment was received for the adverse events. Clinical outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds: BIOTIN; VITAMIN D NOS; VITAMIN C [ASCORBIC ACID]; VITAMIN B12 [CYANOCOBALAMIN]; FEXOFENADINE; LISINOPRIL/HCTZ; CETIRIZINE

Current Illness:

ID: 1001469
Sex: F
Age: 28
State: MA

Vax Date: 12/28/2020
Onset Date: 12/30/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies: none

Symptoms: -visible lymph node swelling in neck on same side of neck; 4-5 lymph nodes extremely swollen and tender; swelling slowly improved but happened again about 4 hours after 2nd dose of vaccine as well. lymph nodes currently still swollen/visible but no longer tender- went to see PCP for this 1 week after 1st vaccine, determined to be likely related to vaccine - after second dose had temp of 102.1, rigors, severe myalgias x 24 hours; did not seek medical care for this, just used tylenol w/ improvement of symptoms

Other Meds: Keppra 1g daily, Escitalopram 15mg

Current Illness: none

ID: 1001470
Sex: F
Age:
State: CA

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Allergic reaction; Itchiness on right side of head, forehead, and eye; Itchiness on right side of head, forehead, and eye; Cluster headaches; This is a spontaneous report from a contactable consumer (patient). This 43-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number EJ1686) via an unspecified route of administration in the left arm on 08Jan2021 at 11:00 at single dose for COVID-19 immunisation. The patient was not pregnant. Relevant medical history included migraines. Concomitant medications included magnesium, vitamin B12 and vitamins NOS (MULTIVITAMIN). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took neomycin sulfate/polymyxin b sulfate (NEOSPORIN) and experienced allergy. On 08Jan2021 at 20:00, the patient experienced allergic reaction, itchiness on right side of head, forehead, and eye and cluster headaches. The events resulted in Doctor or other healthcare professional office/clinic visit. Corrective treatments taken as a result of the events included diphenhydramine hydrochloride (BENADRYL), famotidine (PEPCID) and sumatriptan. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, she has not been tested for COVID-19. The patient recovered with sequel from the events on an unspecified date.

Other Meds: MAGNESIUM; VITAMIN B12 [CYANOCOBALAMIN]; MULTIVITAMIN [VITAMINS NOS]

Current Illness:

ID: 1001471
Sex: F
Age:
State: NY

Vax Date: 01/17/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: small bump at site with redness and mild itchiness; small bump at site with redness and mild itchiness; small bump at site with redness and mild itchiness; This is a spontaneous report from a contactable other health professional (patient). A 26-year-old female patient was administered the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), intramuscular (left arm) on 17Jan2021 16:30 at single dose for Covid-19 immunization. The patient was administered the first dose of BNT162B2 (lot number: EL0140) on 29Dec2020 at left arm for COVID-19 immunization. The patient's medical history was not reported. Concomitant medications included ethinylestradiol, ferrous fumarate, norethisterone acetate (JUNEL FE). The patient previously took Amoxicillin and experienced allergy. The patient was not diagnosed with COVID-19 prior to vaccination. The patient is not pregnant. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 23Jan2021 (also reported as "day 6 post vaccine"), the patient experienced small bump at site with redness and mild itchiness. There was no treatment received for the adverse event. The outcome of events was unknown. The outcome of events was unknown. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: JUNEL FE

Current Illness:

ID: 1001472
Sex: F
Age: 57
State: FL

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies: Sensitive to gluten

Symptoms: Around 4pm I felt a heavy fatigue come over me. By 6pm I had the chills, fever and nausea. This along with random pain throughout my body continued throughout the night an into the early morning. My arms at the site of the injection and around it was also painfully sore to the touch. The fatigue and overall flu like symptoms lasted throughout the following day and into the evening. I started to feel better around 7pm. The fatigue lasted into the next day.

Other Meds: B-12 and DHA Supplements

Current Illness: IBS - C

ID: 1001473
Sex: F
Age:
State: CA

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210122; Test Name: body temperature; Result Unstructured Data: Test Result:102 Fahrenheit

Allergies:

Symptoms: fever 102F; headache; chills; body aches, joint pain, injections site pain; joint pain; injections site pain; patient received the second dose of BNT162B2, which was 23 days after the first dose; This is a spontaneous report from a contactable pharmacist, the patient. A 52-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3247), via an unspecified route of administration in the left arm on 22Jan2021 at 07:45 (at the age of 52-years-old) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient did not have any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient previously received the first dose of BNT162B2 (Lot Number: EL1284) on 30Dec2020 at 16:00 (at the age of 52-years-old) in the left arm for COVID-19 immunization. The patient did not receive any other vaccines within four weeks prior to the vaccination (except the first dose). On 22Jan2021 at 07:45, the patient received the second dose of BNT162B2, which was 23 days after the first dose. On 22Jan2021 at 18:00, the patient experienced fever of 102 degrees Fahrenheit, headache, chills, body aches, joint pain, and injections site pain. Therapeutic measures were taken for the fever, headache, chills, body aches, joint pain, and injections site pain and included treatment with acetaminophen (TYLENOL) orally at 650 mg. The clinical outcomes of the fever, headache, chills, body aches, joint pain, and injections site pain were recovered in Jan2021.

Other Meds:

Current Illness:

ID: 1001474
Sex: M
Age:
State: FL

Vax Date: 01/19/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: Cholesterol; Result Unstructured Data: Test Result:high; Test Name: BP; Result Unstructured Data: Test Result:high

Allergies:

Symptoms: brainfuzz headache; Aches; woke up nauseous; wobbly Almost fell over twice. Had to steady self; This is a spontaneous report from a contactable consumer, the patient. A 78-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), via an unspecified route of administration in the left arm on 19Jan2021 at 11:15 (at the age of 78-years-old) as a single dose for COVID-19 immunization. Medical history included prostatitis, high blood pressure, and high cholesterol, all from unknown dates and unknown if ongoing. The patient previously had COVID-19 prior to the vaccination on an unknown date to an unknown date (not ongoing). The patient did not have any allergies to medications, food, or other products. Since the vaccination, the patient had not been tested for COVID-19. The patient was taking unspecified concomitant medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 23Jan2021 at 07:45, the patient experienced brainfuzz headache, aches, woke up nauseous, and wobbly (almost fell over twice and had to steady himself). The patient did not receive any treatment for the events. The clinical outcomes of brainfuzz headache, aches, nausea, and wobbly, were recovering. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1001475
Sex: M
Age:
State: WA

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Tiredness; Injection site pain; This is a spontaneous report from a contactable consumer. A 54-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EL3247), at single dose into the right arm on 22Jan2021 at 09:30AM for COVID-19 immunization. The patient medical history was not reported. On 11Jan2021 the patient had a negative nasal swab covid_test. The patient did not receive any concomitant medications. On 23Jan2021 at 08:00AM the patient experienced tiredness and injection site pain. No treatment was received. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1001476
Sex: F
Age:
State: SC

Vax Date: 01/14/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: experienced sudden onset of tinnitis mostly in my right ear, but both ears were affected. It sounded like I was hearing a lot of echoing/tinny sound in my ears every time someone was talking; This is a spontaneous report from a contactable pharmacist (patient). A 38-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 14Jan2021 at 5:00PM at single dose in left arm for COVID-19 immunisation at the age of 38-year-old. Lot number was EL3249. Medical history and concomitant medications were unknown. The patient was not pregnant at the time of vaccination. The patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 28Dec2020 at 1:00PM at single dose in left arm for COVID-19 immunisation (lot number was EL1284) at the age of 38-year-old. About 26 hours after 2nd dose of vaccine on 22Jan2021 at 7:00PM, the patient experienced sudden onset of tinnitis mostly in right ear, but both ears were affected. It sounded like the patient was hearing a lot of echoing/ tinny sound in ears every time someone was talking. It only lasted a few hours and hearing returned to normal, but the patient had never experienced anything like that before, and it was so close to the vaccine administration, that she had to wonder if there was a correlation. The patient was not treated for the event. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, she has not been tested for COVID-19. The patient recovered from the event. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1001477
Sex: F
Age: 74
State: OR

Vax Date: 01/29/2021
Onset Date: 01/30/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: None

Allergies: Sulfa, Latex

Symptoms: I had significant vertigo lasting 5 days. This is on the CDC list to ?call your physician?. I was not dizzy-by definition but vertiginous -trying to turn over in bed made my head feel like it was spinning. I think this is much more common than reported. As a physician in the community people frequently reach out to me for advice and I have been told several times about serious vertigo in elderly people with new onset after Covid immunization. I have no intention to delay or abort my second dose. My only current symptoms is fuzzy headedness that is sporadic. The elderly might need to be warned about this and advised accordingly-re not to drive etc. i am former physician and after TNTC immunizations in the past this was unique.

Other Meds: Rosuvastatin 20 mg, vitamin tablet, Vitamin D, ibuprofen 200 mg

Current Illness: None

ID: 1001478
Sex: F
Age:
State: PA

Vax Date: 01/15/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Running nose; Fatigue; Drip-age that causes sore throat (starting day 2-3 after vaccination and is current).; This is a spontaneous report from a contactable other healthcare professional (HCP) reporting for herself. A 36-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE on 15Jan2021 14:00 at single dose for covid-19 immunisation. Medical history included history of stroke and current depression, ongoing. No allergy to medications, food, or other products. Concomitant medication included topiramate (TOPAMAX) and acetylsalicylic acid (ASPIRIN) and Celebs (as reported), all within 2 weeks of vaccination. Patient was not pregnant and was not pregnant at the time of vaccination. On 15Jan2021 at 16:00 the patient experienced running nose and fatigue; she had "drip-age" that caused sore throat, starting day 2-3 after vaccination (Jan2021) and was current (as reported). No treatment given for the events. Fatigue last same day and 2 days after. Final outcome of running nose and fatigue was reported as unknown; outcome of the other event was not recovered. Information on the lot/batch number has been requested.

Other Meds: TOPAMAX; ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness: Depression

ID: 1001479
Sex: F
Age:
State: TN

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: The lymphnodes in my left armpit are swollen and tender; The lymphnodes in my left armpit are swollen and tender; This is a spontaneous report from a contactable consumer (patient). This 36-year-old female patient (not pregnant) received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3302), via an unknown route, on 21Jan2021 (at 07:30 AM) at single dose on the left arm, for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL1284) administered on 31Dec2020 (at 06:45 AM) on the left arm. The patient was vaccinated at hospital, age at vaccination was 36-year-old. No other vaccine was received in four weeks. Pre-vaccination and post-vaccination COVID tests were not performed. No known allergies. On 22Jan2021 (at 06:00 AM), the patient stated 'the lymphnodes in my left armpit are swollen and tender'. The events were assessed as non-serious. No treatments were given for the events. The patient had not recovered from the events.

Other Meds:

Current Illness:

ID: 1001480
Sex: M
Age: 78
State: IN

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: None

Allergies: none

Symptoms: Very severe aching and fatigue

Other Meds: Allopurinol 100 mg twice a day; irbesartin 150 mg 1 a day; amlodipine 2.5 mg once a day; metropolol 25 mg once a day; pravastatin 40 mg once a day; eliquis 5 mg twice a day; vitamin d 2000IU once a day, centrum silver multivitamin for men o

Current Illness: none

ID: 1001481
Sex: F
Age:
State: WA

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Piercing eye pain; Swollen/red left eye; Swollen/red left eye; Extreme photophobia; Body wide muscle pain; Fatigue; Increased dry mouth; GI upset; Nasal congestion; Wheezing; Shortness of breath; This is a spontaneous report from a contactable health care professional nurse, the patient. A 53-years-old non-pregnant female patient (nurse) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EL9262,), via an unspecified route of administration in left arm on 21Jan2021 at 16:45 as a single dose, for COVID-19 vaccination. The most recent COVID-19 vaccine was administered at a Workplace clinic. Medical history included rheumatoid arthritis dry eye, hypertension, anxiety and asthma. Concomitant medication included lisinopril (LISINOPRIL), paroxetine hydrochloride (PAXIL [PAROXETINE HYDROCHLORIDE]), iron (IRON), oxymetazoline hydrochloride (CLARITIN ALLERGIC), montelukast sodium (SINGULAIR). No other vaccines were given within 4 weeks. . Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Lot Number:PFR-20364-01; in the right arm on 29Dec2020, at 09:00. On 22Jan2021 at 05:00, the patient woke the day after at 5AM with piercing eye pain along with swollen/red left eye. extreme photophobia. body wide muscle pain. fatigue. increased dry mouth. GI upset. nasal congestion. Wheezing. Shortness of breath. No treatment was received given for the events. The clinical outcome of piercing eye pain along with swollen/red left eye. extreme photophobia. body wide muscle pain. fatigue. increased dry mouth. GI upset. nasal congestion. Wheezing. Shortness of breath was recovering. Prior to vaccination, was the patient diagnosed with COVID-19?:No Since the vaccination, has the patient been tested for COVID-19?:No Allergies to medications, food, or other products:no Vaccine Facility information available. Ethnicity information is available. Race information is available.

Other Meds: LISINOPRIL; PAXIL [PAROXETINE HYDROCHLORIDE]; IRON; CLARITIN ALLERGIC; SINGULAIR

Current Illness:

ID: 1001482
Sex: F
Age:
State: PA

Vax Date: 12/30/2020
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: A rash appeared two days after the 1st injection, mainly on stomach; This is a spontaneous report from a contactable nurse reporting for herself. A 28-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL0140), via an unspecified route of administration on 30Dec2020 07:00 AM at single dose in left arm for COVID-19 immunisation. Patient age at time of vaccination was 28 years. The patient was vaccinated at hospital. No other vaccine was given within 4 weeks prior to the COVID vaccine. Medical history included allergies to eggs, shellfish, peanuts. Concomitant medication included desogestrel, ethinylestradiol (APRI). On 01Jan2021 the patient experienced a rash appeared two days after the 1st injection, mainly on stomach. The event was reported as non serious and resulted in Doctor or other healthcare professional office/clinic visit. Treatment for the event included steroid cream. The event had not resolved. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, has not been tested for COVID-19.

Other Meds: APRI

Current Illness:

ID: 1001483
Sex: U
Age:
State: WA

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: [COVID-19 Vaccine] treatment under Emergency Use Authorization(EUA): 1 mL 25G x 1" *(REF 10161, LOTG200926) used for the Pfizer BioNTech Covid-19 Vaccine for IM injection. While drawing up the first dose of the COVID vaccine in a reconstituted vial, a Pharmacist noticed a green particulate in the syringe. Uncertain of the origin of the particulate, the subsequent dose was not used. Instead, a filter needle with a 1 mL BD Leur Lock syringe was used to draw up remaining doses, then the filter needle was replaced with a 25G x 1" needle. None of the COVID-19 vaccine was affected, and the particulate did not appear to have originated from the stopper of the vaccine vial, as the stopper was grey in color, not green like the particulate found in the syringe. All previously drawn-up doses were inspected and none of the syringes contained particulates.

Other Meds:

Current Illness:

ID: 1001484
Sex: M
Age: 66
State: KS

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies: cillians

Symptoms: Blood sugar dropped from 219 to 50 within 30 minutes after vaccination.

Other Meds: none

Current Illness: none

ID: 1001485
Sex: F
Age:
State: MA

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; severe chills; severe shivering/shakes; This is a spontaneous report from a contactable healthcare professional (patient). A 26-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: EL9261), intramuscularly in the left arm, on 21Jan2021 10:30 (at the age of 26-years-old) at a single dose for COVID-19 immunization. Medical history included latex allergy. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications, taken within two weeks of vaccination, included ethinylestradiol, etynodiol diacetate (KELNOR) taken as a contraceptive and fexofenadine hydrochloride (ALLEGRA). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: EL0142), intramuscularly in the left arm, on 31Dec2020 at 17:00 (at the age of 26-years-old) for COVID-19 immunization. The patient experienced headache, severe chills, and severe shivering/shakes on 21Jan2021 at 21:00. The events were reported as non-serious. The clinical course was reported as follows: Less than 12 hours after getting vaccinated, the patient experienced headache, severe chills, severe shivering/shakes that didn't stop. Being under blankets didn't help but using heating pad helped a lot. The shaking stopped the next morning, but patient still had a bit of chills and headache the next day. Therapeutic measures were taken as a result of the severe chills and severe shivering/shakes as aforementioned. The patient did not receive any treatment for headache as reported. The clinical outcome of headache and chill was recovering and of severe shivering/shakes was recovered on 22Jan2021. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds: KELNOR; ALLEGRA

Current Illness:

ID: 1001486
Sex: F
Age:
State: TN

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: FIrst dose was administered on 05Jan2021; Fever; Sore arm around injection site; swollen and sore lymph nodes: neck and arm of of injection; swollen and sore lymph nodes: neck and arm of of injection; Indigestion; This is a spontaneous report from a contactable 28-year-old female consumer reporting for herself A 28 years old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: El3300) on 22Jan2021 at 08:15 at single dose via an unspecified route of administration on right arm for COVID-19 immunization. Relevant medical history included Shellfish allergy and allergy to doxicicline. The patient received first dose of vaccine on 05Jan2021 at 03:00 PM on right arm, lot_number=Ej1685. On 22Jan2021 at 18:00 the patient experienced fever, sore arm around injection site, swollen and sore lymph nodes: neck and arm of injection Indigestion (as reported). At the time of the reporting the patient had not yet recovered from reported events.

Other Meds:

Current Illness:

ID: 1001487
Sex: F
Age:
State: ID

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; Arm pain; Fatigue; This is a spontaneous report from a non-contactable consumer. A non-pregnant 22-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration in the left arm on 21Jan2021, at 16:45 as single dose for covid-19 immunization. The patient's medical history was not reported. There were unspecified concomitant medications; this was reported as antibiotics within two weeks of vaccination. No other vaccines were received within four weeks prior to the COVID vaccine. On 22Jan2021, at 07:00, the patient experienced fever, arm pain and fatigue, which were non-serious. No treatment as received for the events. Prior to vaccination, the patient was not diagnosed with COVID-19, nor has the patient been tested for COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of experienced fever, arm pain and fatigue was not recovered.

Other Meds:

Current Illness:

Date Died: 01/31/2021

ID: 1001488
Sex: F
Age: 60
State: TX

Vax Date: 01/18/2021
Onset Date: 01/31/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Patient died several days after receiving the second dose of the vaccine. See additional information sent. An autopsy has been performed and results are pending.

Other Meds:

Current Illness: COVID infection November 2020

ID: 1001489
Sex: F
Age:
State: RI

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; neck pain; shoulder pain; This is a spontaneous report from a contactable healthcare professional. A 28-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 21Jan2021, at 10:30 as first single for covid-19 immunization. Medical history included tonsillectomy, appendicectomy and gastric bypass on unknown dates and unknown if ongoing. No allergies to medications, food, or other products were noted. The patient received unspecified bariatric multivitamin within two weeks of vaccination; the patient did not receive any other vaccines within four weeks prior to the vaccine. On 22Jan2021, at 09:00 patient experienced headache, neck pain and shoulder pain. The events were assessed as non-serious. No therapeutic measures were taken as results of 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. The outcome of headache, neck pain and shoulder pain was not recovered. The batch/lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up .

Other Meds:

Current Illness:

ID: 1001490
Sex: F
Age:
State: MA

Vax Date:
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fatigue; slight body aches; This is a spontaneous report from a contactable nurse (the patient) via Pfizer sales representative. A female patient of an unspecified age started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced fatigue and slight body aches on an unspecified date. The clinical outcome of the events fatigue and slight body aches was unknown. No follow-up attempts are possible; information about lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1001491
Sex: F
Age:
State:

Vax Date: 12/19/2020
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: numbness for an hour; burning sensation; joint pain; This is a spontaneous report from a non-contactable consumer reporting on behalf of the patient. A 49-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, unknown lot number and expiration), via an unspecified route of administration on 19Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced numbness for an hour, and subsequently burning sensation and joint pain which subsided with Tylenol use. The patient was recovering from the events burning sensation and joint pain, while unknown outcome for the remaining event. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1001492
Sex: F
Age: 31
State: AR

Vax Date: 01/28/2021
Onset Date: 01/31/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: CBC, CMP, UA, ultrasound, and abdominal CT scan with contrast. All on 2/2/21

Allergies: None

Symptoms: Moderate abdominal pain beginning on Sunday evening. The pain worsened throughout the day on Monday and became severe. It was accompanied by nausea and vomiting and made worse with food and water. I went to the ER on Tuesday (2/2/21) morning.

Other Meds: None

Current Illness: None

ID: 1001493
Sex: F
Age:
State: VA

Vax Date: 12/21/2020
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: small sore on vagina; This is a spontaneous report from a contactable nurse (patient). A 24-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EH9899), intramuscular on 21Dec2020, at 16:00 as first single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medication included ethinylestradiol, norgestimate (SPRINTEC). The patient experienced a small sore on vagina on an unspecified date, after the vaccination. The outcome of small sore on vagina was recovered on an unspecified date.

Other Meds: SPRINTEC

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm