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: 0990396
Sex: M
Age:
State: AZ

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

Lab Data: Test Date: 202012; Test Name: Body temperature; Result Unstructured Data: Test Result:104 Fahrenheit; Comments: High grade fever up to 104F after booster dose on first 24 hours with headache.; Test Date: 20210104; Test Name: Covid-19; Test Result: Positive ; Comments: Tested positive symptomatic COVID- 19

Allergies:

Symptoms: Tested positive symptomatic COVID-19 on 04Jan2021.; Tested positive symptomatic COVID-19 on 04Jan2021.; High grade fever up to 104F after booster dose on first 24 hours with headache; High grade fever up to 104F after booster dose on first 24 hours with headache; This is a spontaneous report from a contactable physician (patient). A 42-year-old male patient received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot unknown: EK5730), intramuscularly on left arm on 23Dec2020 at 08:45 AM at single dose for COVID-19 immunization. Medical history included hyperuricaemia and hypertriglyceridaemia. Concomitant medication included fenofibrate and febuxostat. The patient was tested positive symptomatic COVID- 19 on 04Jan2021. Symptoms started 01Jan2021: recovered at home. High grade fever up to 104F after booster dose on first 24 hours in Dec2020 with headache. The patient received other vaccine same date (reported as) on 13Jan2021 as second dose on IM left. The patient did not receive any treatment from events. The outcome of events was recovered on unknown date.; Sender's Comments: The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) on 23Dec2020, and COVID-19 test positive on 04Jan2021. No complete effect of the suspect vaccine could be reasonably achieved from first dose to protect from the targeted infection.

Other Meds: FENOFIBRATE; FEBUXOSTAT

Current Illness:

ID: 0990397
Sex: F
Age:
State: CA

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

Lab Data: Test Date: 20210113; Test Name: T; Result Unstructured Data: Test Result:101.3 Fahrenheit; Comments: 13:30; Test Date: 20210113; Test Name: T; Result Unstructured Data: Test Result:98.3 Fahrenheit; Comments: 18:30; Test Date: 20210114; Test Name: HR; Result Unstructured Data: Test Result:64; Comments: 18:00; Test Date: 20210114; Test Name: spO2; Test Result: 85 %; Comments: 15:45; Test Date: 20210114; Test Name: spO2; Test Result: 99 %; Comments: 18:00

Allergies:

Symptoms: Struggle to balance; lightheaded/ Lightheadedness/ dizzy; cold hands; Wake up w/ T 101.3F; hot flashes; Dizziness with too much exertion; Chills; SOB with normal work activities/ out of breath; Mild nausea; mild HA; sore arm; Felt more tired than usual/Fatigue/fatigued; This is Spontaneous report from a contactable Other Health Professional (HCP) (patient). A 31-year-old female patient (pregnant: No) received the second dose of BNT162B2 (COVID-19 MRNA VACCINE BIONTECH, lot number: EK9231), via Intramuscular on left arm on 12Jan2021 at 7:15 AM at single dose for COVID-19 immunization. The relevant medical history included anterior uveitis (HLA-B27), known allergies: Kiwi, kiwiberry, Meloxicam, pineapples, certain lactose products (milk, cream). Concomitant medications included colecalciferol, menaquinone (D3 +K2), borago officinalis oil, fish oil, hippophae rhamnoides oil, linum usitatissimum oil (OMEGA 3,6,7,9), ascorbic acid, biotin, boron citrate, calcium pantothenate, calcium phosphate, choline bitartrate, chromium picolinate, colecalciferol, cyanocobalamin, dl-alpha tocopheryl acetate, folic acid, inositol nicotinate, potassium iodide, pyridoxine hydrochloride, retinol palmitate (VITAFUSION WOMEN'S), ascorbic acid, fish oil, selenium, tocopheryl acetate, xantofyl, zeaxanthin, zinc (EYE CARE), vitamin d3 and Nature's Bounty Hair, Skin, and Nails Gummies. The patient previously received first dose of BNT162B2 at the age of 31 years old on 22Dec2020 (lot number=EK5730, at 04:30 PM, via Intramuscular on left arm) for COVID-19 immunization. On 12Jan2021 at 16:30: the patient woke up, felt more tired than usual. 19:00: Arrived at work, fatigue, sore arm. 20:00: Sore arm, fatigue, mild HA (headache). Drank coffee and fatigue and HA improved. 21:00: Mild nausea started. Still able to eat. 22:00: Chills. SOB with normal work activities. 23:00: Coworkers kept asking her why she was always out of breath. Chills worsen. Dizziness with too much exertion. I take 650mg Tylenol. On 13Jan2021 at 05:30 Almost normal. 13:30: Wake up w/ T 101.3F, chills, hot flashes. 14:30: Take 1000mg Tylenol after eating. 18:30: T 98.3F. Fatigued and sleep. On 14Jan2021 at 04:30 feel completely normal. 15:45: Lightheadedness, cold hands, and HA. spO2 85%. spO2 improves with deep breaths. Pattern repeats several times. 16:30: Take 1000mg Tylenol. Struggle to balance. 18:00: At Urgent Care spO2 is 99%, HR 64. Her hands are no longer cold. 22:00: Still dizzy. Sleep. On 15Jan2021 at 02:30: Still lightheaded & fatigued, but no balance issues. 06:30: Sleep. 15:00: Mild fatigue. Events resulted in Emergency room/department or urgent care. No other vaccine in four weeks. No COVID prior vaccination. No COVID tested post vaccination. Therapeutic measures were taken as a result of the events. The outcome of the events was recovered on an unspecified date in Jan2021.

Other Meds: D3 +K2; OMEGA 3,6,7,9; VITAFUSION WOMEN'S; EYE CARE [ASCORBIC ACID;FISH OIL;SELENIUM;TOCOPHERYL ACETATE;XANTOFYL;ZEAXANTHIN;ZINC]; VITAMIN D3

Current Illness:

ID: 0990398
Sex: M
Age:
State: PA

Vax Date: 12/23/2020
Onset Date: 12/30/2020
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Name: CT Scan; Result Unstructured Data: Test Result:Unknown result; Test Date: 20201230; Test Name: COVID-19; Result Unstructured Data: Test Result:COVID-19; Comments: 1 week later I came down with COVID-19.; Test Date: 20210103; Test Name: Nasal Swab: COVID-19; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: came down with COVID-19; came down with COVID-19/Nasal Swab: positive; This is a spontaneous report from a contactable nurse (patient). A 32-year-old male patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, lot number: EL0140), via an unspecified route of administration on 23Dec2020 at a single dose in right arm for COVID-19 immunization. Medical history included asthma, atrial fibrillation, allergy to wasp. Concomitant medication included flecainide, metoprolol, budesonide, formoterol fumarate (SYMBICORT), albuterol (SALBUTAMOL). The patient previously took CECLOR and acetylsalicylic acid (ASPIRIN), both experienced allergy. There was no other vaccine in four weeks. The patient came down with COVID-19 1 week later on 30Dec2020. The patient had no exposures and no one else around the patient was sick. Adverse event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. There was a treatment for adverse event: multiple doctor visits, urgent care visit, computerised tomogram (CT) scan: unknown result. There was no COVID prior vaccination. There is a COVID tested post vaccination: Nasal Swab on 03Jan2021: result positive. The outcome of events was not recovered.; Sender's Comments: Based on the information provided, the positive COVID-19 nasal swab test cannot be excluded for the ineffective protection of vaccine BNT162B2.

Other Meds: FLECAINIDE; METOPROLOL; SYMBICORT; ALBUTEROL [SALBUTAMOL]

Current Illness:

ID: 0990399
Sex: F
Age:
State: CA

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

Lab Data: Test Name: Blood works; Result Unstructured Data: Test Result:Unknown result

Allergies:

Symptoms: diminished sensation on the lateral aspect of left leg from knee below and whole left foot/felt numbness on left leg; This is a spontaneous report from a contactable Other healthcare professional (patient). A 44-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0142), via an unspecified route of administration on 14Jan2021 10:30 at single dose in Left arm for COVID-19 immunization. Medical history included hypertension, covid prior to vaccination. Concomitant drug included unspecified products which the patient received in two weeks. There were no other vaccines received in four weeks. The patient previously took cefalexin monohydrate (KEFLEX) and experienced allergies. The patient did not have COVID tested post vaccination. Approximately 10 hours after the patient got the vaccine on 14Jan2021 21:00, she felt numbness on her left leg. It got worse this afternoon so she left work to go to urgent care. She had diminished sensation on the lateral aspect of her left leg from knee below and her whole left foot on 14Jan2021 21:00. The reported adverse events resulted in Emergency room/department or urgent care. Therapeutic measures were taken as a result of events 'diminished sensation on the lateral aspect of left leg from knee below and whole left foot', 'felt numbness on left leg'. The patient underwent lab tests which included blood works with unknown result on an unspecified date. The outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 0990400
Sex: F
Age:
State: OK

Vax Date: 01/10/2021
Onset Date: 01/15/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: exhaustion; Chills; feeling feverish; aching left arm at injection site; This is a spontaneous report from a contactable other health professional (HCP). A 61-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283), intramuscular on 10Jan2021 at 15:30 on her left arm at a single dose for COVID-19 immunization. Medical history included breast cancer from an unknown date and unknown if ongoing and known penicillin (PCN) allergy. There were no concomitant medications. The patient previously took erythromycin and clindamycin and experienced allergies. The patient received the first dose of BNT162B2 (lot number: EH9899), intramuscularly on left arm on 20Dec2020 at 03:30 PM. The patient experienced chills, feeling feverish, aching left arm at injection site and exhaustion on 15Jan2021 at 16:45. On 16Jan2021, consumer stated, "I recently had the COVID vaccine and it was last Sunday. Is that possible to have a reaction 5 days out?" There was no treatment received for the events. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0990401
Sex: F
Age:
State: GA

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

Lab Data:

Allergies:

Symptoms: Allergic reaction; This is a spontaneous report from a contactable consumer (patient's spouse). A 42-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; batch/lot number and expiration date unknown), via an unspecified route of administration in the left arm on 14Jan2021 15:00 at a single dose in a hospital for COVID-19 immunization. Medical history included allergy to sulfur and latex. There were no concomitant medications. The patient previously took dexamethasone (DECADRON) and experienced allergy. The patient had Covid vaccine at the hospital yesterday (14Jan2021) about 3pm and around 315-320, she had an allergic reaction. The patient was given epinephrine and stuff like that but ended up having to call an ambulance and took to another hospital. There, they had to put her in ICU and on a ventilator. The patient's spouse asked what might have been in the product that she would have been allergic to. The patient was transferred to hospital. She is a respiratory therapist. The patient was treated with epinephrine, albuterol and she was put on a bi-pap but she couldn't breathe and was told by the doctors that her body can't take it so they intubated her about 7:30 pm, she was put on a ventilator. The patient had an emergency visit. The patient had no prior vaccination (within 4 weeks). The outcome of the event was not recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990402
Sex: M
Age:
State: WV

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: site soreness; nasal stuffiness; difficulty breathing; throat began closing up; This is a spontaneous report from a contactable consumer (patient). A 78-year-old male patient (also reported as age at vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL8982), via an unspecified route of administration on 14Jan2021 at 12:00 at a single dose on the left arm for COVID-19 immunization. Medical history included two recent right shoulder surgeries. Concomitant medication included oxaprozin. The patient previously took oxycontin and experienced allergies and an unspecified allergy shot last 06Jan2021 on the left & right arm. The patient was not diagnosed with COVID-19 prior to vaccination. On 15Jan2021 at 01:30, the patient was having difficulty breathing and throat began closing up. Patient's wife was going to call 911 but after about an hour, incident appeared to be getting better. On the next day (16Jan2021), the patient felt better with minor site soreness and nasal stuffiness. The patient did not receive any treatment for the events. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovering.

Other Meds: OXAPROZIN

Current Illness:

ID: 0990403
Sex: F
Age:
State: OR

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

Lab Data:

Allergies:

Symptoms: Severe arm pain; unable to move arm without excruciating pain; This is a spontaneous report from a contactable nurse (patient). A 49-year-old female patient received their second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK9231, expiry date not reported), via an unspecified route of administration on the left arm on 15Jan2021 15:00 at single dose for COVID-19 immunization. Medical history included was not reported. Concomitant medication included ibuprofen, vitamin D NOS, magnesium and fish oil. The patient received their first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date not reported) on the right arm on 25Dec2020 for COVID-19 immunization. The patient experienced severe arm pain; unable to move arm without excruciating pain on 15Jan2021 15:00. The outcome of the event was unknown.

Other Meds: IBUPROFEN; VITAMIN D NOS; MAGNESIUM; FISH OIL

Current Illness:

ID: 0990404
Sex: F
Age:
State: PA

Vax Date: 12/28/2020
Onset Date: 01/07/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Date: 20210107; Test Name: Covid; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: Soreness on the arm/ soreness at the site; felt a little achy/ achiness like you have on flu; I am COVID positive/ woke up with every COVID symptoms/ got real sick with positive COVID; I am COVID positive/ woke up with every COVID symptoms/ got real sick with positive COVID; This is a spontaneous report from a contactable nurse (patient herself). A 57-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ELO140, reporter stated "could be ELO or ERO"), via an unspecified route of administration on 28Dec2020 at a single dose for COVID-19 immunization. Medical history included bronchitis from Oct2020 and ongoing and occasional cough. Concomitant medications were not reported. The patient reported that "I am a nurse I work with COVID patients. I got my vaccination on 28Dec2020. After the vaccination I had soreness on the arm and I felt a little achy. I felt like that with the flu shot (no further clarification) for couple of few days maybe. Then my whole family developed COVID and I am COVID positive. On 06Jan2021, I woke up with every COVID symptoms. I tested positive on the 7th. So, I have been in isolation for 10 days from work. The reason I called you guys is that I am getting 10 different answers. I am due to get my vaccination on 18th. I still have some symptoms and I did not know I am hearing where symptoms go away. I am concerned, my shot is not going to work. If I have mild symptoms can I get it? I am getting tensive for answers, she gave a little bit of information. Do you want me to tell you all my symptoms the time I contracted the COVID? What I told you about the shot was from 28th. Yes, the vaccination on the 28th was soreness at the site like achiness like you have on flu. I had bronchitis (Intent: History) back in at the month of Oct. I have an occasional cough. So, I do not even count that because that is being going on but then I got real sick with positive COVID on the 6th. I am concerned about getting my second shot. That is the reason of my call. The symptoms from the 28th is just what I told you. I have COVID so I am on a lot of medication right now. I am taking medications for the COVID. I am on budesonide (SYMBICORT) inhaler, albuterol (VENTOLIN) inhaler, I am taking acetaminophen (TYLENOL), guaifenesin (MUCINEX). As of Thursday I am taking ranitidine (ZANTAC) and some Steroids, pepper too and cough medicine as needed. When asked about causality, the patient stated "No because my whole family got COVID. Like my daughter, in-laws. It just went through our whole family. I do not think anything is related to the vaccine." Nurse added, "I do not really know what to do about this. If I feel better, I am just wondering if I should go ahead and get it because she told me there is no studies beyond that day. That was my main reason for the call." She was referring to the 'TCP'. "When I am going to get it if I am having mild symptoms because I do not want to lose my immunity. I am kind of troubling with myself what to do." The outcome of the event "I am COVID positive/ woke up with every COVID symptoms/ got real sick with positive COVID" was not recovered and of the remaining events was unknown. Information on the lot/ batch number has been requested.; Sender's Comments: Based on the information available, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported event positive for corona virus infection based on the known safety profile. However the short duration of 10 days since the vaccine first dose is given it is unlikely patient would have fully developed immunity. It worth to note that the patient's whole family developed COVID.

Other Meds:

Current Illness: Bronchitis

ID: 0990405
Sex: M
Age:
State: VA

Vax Date: 12/28/2020
Onset Date: 01/10/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: coags (to rule out ITP); Result Unstructured Data: Test Result:Normal; Test Date: 20210111; Test Name: CBC; Result Unstructured Data: Test Result:Normal; Test Date: 20210111; Test Name: Flu A/B test; Result Unstructured Data: Test Result:Normal; Test Date: 20210111; Test Name: CMP; Result Unstructured Data: Test Result:Normal; Test Date: 20210111; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: Myalgias; Neck stiffness; Diffuse pruritic rash over my whole body; Mild headaches/Headaches worsened to about 4/10; This is a spontaneous report from a contactable physician (patient himself). A 41-year-old male patient received his first dose of bnt162b2 (BNT162B2 also reported as COVID 19, brand Pfizer/BioNTech, lot EH9899), via an unspecified route of administration in the right arm on 28Dec2020 11:45 at SINGLE DOSE for Covid-19 immunisation. Medical history included OSA (obstructive sleep apnea) and PFO (patent foramen ovale). He had no known drug allergy. No other vaccine in four weeks. Concomitant medication included aspirin [acetylsalicylic acid]. On 10Jan2021, he began having mild headaches. On 11Jan2021 the headaches worsened to about 4/10 associated with myalgias, neck stiffness and a diffuse pruritic rash over his whole body. To return to work he had to go get tested so he went to the ER, got Flu A/B test, Covid antigen, then PCR test, a CBC, CMP, and coags (to rule out ITP). All tests were normal, Nasal Swab was negative. Treatment given was Normal saline bolus and ketorolac 30mg IV. The outcome of events was recovered.; Sender's Comments: ~~~

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 0990406
Sex: M
Age:
State: VA

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: hives; itching; itchy feeling tongue; This is a spontaneous report from a contactable nurse. A 45-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: LEK5230), intramuscular at the right arm on 18Dec2020 08:00 at a single dose for COVID-19 immunization at a hospital. Medical history included allergies with latex, sulfa., and penicillin (PCN). Concomitant medications were unspecified. The patient previously took erythromycin (ERY) and experienced allergies. The patient experienced hives, itching and itchy feeling tongue on 18Dec2020 09:30. Patient took 50 mg of diphenhydramine (BENADRYL), 20 mg famotidine (PEPCID) and 10 mg of cetirizine (ZYRTEC). The patient has not been tested prior and post vaccination. The patient was recovering from the events.

Other Meds:

Current Illness:

ID: 0990407
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Sore arm; This is a spontaneous report from a contactable consumer (patiet). A 73-years-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL3248) in the Public Health Clinic/Veterans Administration facility, via an unspecified route of administration on 16Jan2021 09:15 AM at a single dose on the left arm for COVID-19 immunization. The patient's medical history was not reported. The patient has not had COVID-19 prior to vaccination. The patient did not have any other vaccine in four weeks. Concomitant medication included losartan (manufacturer unknown), levothyroxine (manufacturer unknown), hctz (manufacturer unknown), montelukast (manufacturer unknown, also reported as 'monounsatu'). The patient experienced sore arm on 16Jan2021 at 09:45 AM. The patient did not receive any treatment for the event. The outcome of the event was recovering. The patient has not been tested for COVID-19 post vaccination.

Other Meds: LOSARTAN; LEVOTHYROXINE; HCTZ; MONTELUKAST

Current Illness:

ID: 0990408
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: left arm where the injection was, was swollen and itchy and painful most of the night; left arm where the injection was, was swollen and itchy and painful most of the night; left arm where the injection was, was swollen and itchy and painful most of the night; This is a spontaneous report from a contactable consumer (patient). A 72-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on left arm on 15Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received her first dose of Pfizer-Biontech Covid19 vaccine yesterday (15Jan2021). She was reporting symptoms that started yesterday evening at 21:00. On her left arm where the injection was, was swollen, itchy and painful most of the night and hurts even when she's not moving it. She wanted to know if this is normal, how long does it last and what she can do to treat it. She doesn't know if she can put icepack on it or take a shower. She asked if she can use antipyretics before or after vaccination with the Pfizer-BioNTech COVID-19 vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990409
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: Restriction in normal breezing when sleeping, feels like a lump in my lower throat; Restriction in normal breezing when sleeping, feels like a lump in my lower throat; This is a spontaneous report from a contactable other healthcare professional (patient herself). A 77-year-old female patient (not pregnant) received her second dose of bnt162b2 (BNT162B2 also reported as Covid19 Brand: Pfizer, lot EK4176), intramuscular in left arm on 15Jan2021 15:45 at SINGLE DOSE for Covid-19 vaccination. Medical history included Irritable Bowel Syndrome, Sinal Stenosis, Atrial Fibrillation, Lactose intolerant and Gluten intolerant. She received her first dose of bnt162b2 on 23Dec2020 (lot number: EL128), given via IM in left arm. Concomitant medications included paracetamol (TYLENOL), atropine sulfate, diphenoxylate hydrochloride (DIPHENOXYLATE/ATROPINE) and metoprolol tartrate. The patient experienced restriction in normal breezing when sleeping and felt like a lump in her lower throat on 15Jan2021 22:00. No treatment given. The outcome of events was not recovered.

Other Meds: TYLENOL; DIPHENOXYLATE/ATROPINE; METOPROLOL TARTRATE

Current Illness:

ID: 0990410
Sex: F
Age:
State: IL

Vax Date: 01/11/2021
Onset Date: 01/13/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; shivering; sweats; glandular pain in neck; Sore throat; Fatigue; This is a spontaneous report from a contactable other healthcare professional(patient). A 56-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL1283) intramuscularly into the left arm on 11Jan2021 08:00 at a single dose for covid-19 immunisation. The patient's medical history was not reported. Patient was not pregnant. Concomitant medication included bupropion (BUPROPION). The patient previously took her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: Ek5730) intramuscularly into the left arm on 21Dec2020 at a single dose for covid-19 immunization and morphine (MORPHINE) and experienced drug allergy. On 13Jan2021, patient experienced headache, shivering, sweats, glandular pain in neck, sore throat and fatigue. Patient did not receive treatment for the reported events. Outcome of events recovered on an unspecified date in Jan2021.

Other Meds: BUPROPION

Current Illness:

ID: 0990411
Sex: F
Age:
State: MO

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

Lab Data: Test Date: 20210115; Test Name: Body Temp; Result Unstructured Data: Test Result:100.0 F; Test Date: 20210116; Test Name: Body Temp; Result Unstructured Data: Test Result:101.4 F

Allergies:

Symptoms: piercing headache at temples; diarrhea; Nausea; severe chills; severe arthralgia; severe myalgia; fever (100.0 F, 101.4 F); This is a spontaneous report from a contactable other healthcare professional (patient). A 22-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on 15Jan2021 at a single dose on right arm for COVID-19 immunization. Medical history included depression. Concomitant medication included ibuprofen, vortioxetine hydrobromide (TRINTELLIX), buspirone, ondansetron (ZOFRAN MELT), ethinylestradiol, levonorgestrel (LUTERA). The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), via an unspecified route of administration on 26Dec2020 at a single dose on left arm for COVID-19 immunization. The patient experienced nausea, severe chills, severe arthralgia, severe myalgia, fever (100.0 F) on 15Jan2021 19:30, approx. 12/hrs post 2nd dose. Then on 16Jan2021, patient experienced all the above, and piercing headache at temples, fever (101.4 F), diarrhea, approx. 24/hrs post 2nd dose. No treatment received for the adverse events. The outcome of the events was not recovered. The patient is not pregnant. Facility type vaccine was Workplace clinic. No other vaccine in four weeks. Not diagnosed with covid prior vaccination. Not covid tested post vaccination.

Other Meds: IBUPROFEN; TRINTELLIX; BUSPIRONE; ZOFRAN MELT; LUTERA

Current Illness:

ID: 0990412
Sex: M
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Little queasy; Swelling arm; Pain in arm; Little headache; The initial case was missing the following minimum criteria: No adverse effect. Upon receipt of follow-up information on (16Jan2021), this case now contains all required information to be considered valid. This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: EK5730), via an unspecified route of administration on an unspecified date in Jan2021 for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient reported that he was better during administration (Thursday) and by Friday (Jan2021), the patient had a little pain in his arm and little headache. Morning of 16Jan2021, the patient felt a little queasy. The patient reported that he felt a little bit different on Friday. The swelling in his arm was not a problem that's gone down and little pain not much. The patient would like to know the extent of effects the shot could take. The outcome of the event swelling arm was unknown; all other events was unknown.

Other Meds:

Current Illness:

ID: 0990413
Sex: F
Age:
State:

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

Lab Data: Test Name: Covid-19; Test Result: Positive

Allergies:

Symptoms: tested positive for Covid-19; tested positive for Covid-19; This is a spontaneous report from a contactable pharmacist. This pharmacist reported similar events for two patients. This is the second of the two reports. A 65-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 31Dec2020 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. This patient was vaccinated and has tested positive for Covid-19 on an unspecified date, not sure when she tested positive for the Covid-19. She was asymptomatic. It was also reported that she got sick on 03Jan2021. The second dose is due 21Jan2021, is it ok for her to receive it? How long can she wait if she does not get the vaccine at 21 days? The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on the information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the first vaccine dose and the event onset.,Linked Report(s) : US-PFIZER INC-2021051642 same reporter/product, similar events and different patient

Other Meds:

Current Illness:

ID: 0990414
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: fever; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date not reported), 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. Patient was receiving his second dose on the day same as his surgery (unspecified). Patient was going to postpone his second shot because he had fever after receiving the first shot on an unknown date. The patient wanted to know the maximal interval between doses. The events were reported as non-serious. The outcome of the event fever was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0990415
Sex: M
Age:
State: NV

Vax Date: 01/14/2021
Onset Date: 01/16/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Name: Lab test; Result Unstructured Data: Test Result:Unknown; Comments: make sure I have no issues with Pradaxa; Test Name: Lab test; Result Unstructured Data: Test Result:Unknown; Comments: I had lab test because I have acid

Allergies:

Symptoms: My knee joints and elbow joints feel very stiff and feel as if they were swollen but they're not/My joints do not look physically swollen up but they feel; My knee joints and elbow joints feel very stiff and feel as if they were swollen but they're not/My joints do not look physically swollen up but they feel; I'm having trouble walking; got up every 15 minutes after that with frequent urination/ I got up 5 or 6 times and even could not get bathroom fasten up and couple of occasion is very unusual for me; This is a spontaneous report from a contactable consumer (patient). An 81-year-old male patient received BNT162B2 (lot number: EL3249), via an unspecified route of administration on 14Jan2021 at single dose in the arm for COVID-19 immunization. Medical history included atrial fibrillation, diabetes and a heart attack 30 years ago. Concomitant medication included dabigatran etexilate mesilate (PRADAXA) for A-fib, empagliflozin (JARDIANCE) for Diabetes, metformin hydrochloride (METFORMIN ER) for Diabetes. It was reported that the patient had no after effects the day he had the shot. In the morning of 16Jan2021, he got some things going on but he was not sure if it is connected with Pfizer or not. Usually he wakes up and go to the bathroom once in middle of a night. Last night he got up 5 or 6 times because he had to go and couple of times, he did not even get to the bathroom on time so he really had to urinate. Stated this is very unusual for him. And when he woke up this morning, her joints do not look physically swollen up but they feel, stated "how do I describe it, they feel very (incomplete sentence)". His knee joints and elbow joints felt very stiff and felt as if they were swollen but they're not. Stated that he's having trouble walking. Stated that it may be totally unrelated. The patient stated, "The only thing I had was, every year they make me go to a lab and make sure I have no issues with Pradaxa because it is a blood thinner. I have that lab. Work done couple of weeks ago. I have not gotten the answers yet". Also stated that he had lab test because he has acid. The outcome of the events was unknown.

Other Meds: PRADAXA; JARDIANCE; METFORMIN ER

Current Illness:

ID: 0990416
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: upset stomach; I literally cried all day. I cried even at work for a whole 24 hours, crying for no reason/When I woke up I was crying; like I was depressed; This is a spontaneous report from a contactable healthcare professional (patient). A 53-years-old female patient received the first dose of BNT162B2 (Pfizer-BIONTECH Covid-19 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 reported the side effects she experienced from the first shot. She stated that it wasn't real severe. The first day she was fine, upset stomach. On the second day, she literally cried all day. She cried even at work for a whole 24 hours, cried for no reason, like she was depressed. She didn't think anything about it. She mentioned it during the second shot and they told her to report it. She was fine after that, it was just for that whole day, when she woke up she was crying. Outcome of the events crying and depressed mood was recovered, while for the event abdominal discomfort was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990417
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: arm pain; redness; itchiness; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age (Age: 70, Unit: Unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on 14Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced arm pain, redness and itchiness on Jan2021. The patient wanted to know if she can still receive second vaccine. She asked if these are common side effects and the efficacy after one dose. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990418
Sex: F
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Name: Lab test; Result Unstructured Data: Test Result:Unknown Result

Allergies:

Symptoms: it hurts a little bit if she touches it; arm got red and it was little bump and then it spread and got itchy, and it was a little swollen/It is a big red mark, probably the size of a lemon; arm got red and it was little bump and then it spread and got itchy, and it was a little swollen; arm got red and it was little bump and then it spread and got itchy, and it was a little swollen; felt like she was going to come down with something, she didn't feel right; This is a spontaneous report from a contactable consumer (patient) reported that a 72-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 13Jan2021 at a single dose as the patient don't want to have COVID. Medical history included arrhythmia, mitral valve prolapse, acid reflux, high cholesterol, and heart murmur; all from an unknown date. Concomitant medications included verapamil, rosuvastatin, pantoprazole, estradiol (ESTRACE), and acetylsalicylic acid; all were taken from an unspecified date for an unspecified indication. The patient had the first dose of the vaccine 3 days ago (13Jan2021) and stated that her arm got red and it was little bump and then it spread and got itchy, and it was a little swollen on 14Jan2021. She also felt like she was going to come down with something, she didn't feel right. It is not swollen today (16Jan2021) but it hurts a little bit if she touches it. It is a big red mark, probably the size of a lemon. The patient took Tylenol, Zyrtec, and put ice on it all last night (15Jan2021), and it became little itchy and this morning (16Jan2021) it's little itchy, still red but the bump is gone. The patient was asked if she still experiencing the events and she stated that the bump was gone, but now it's like red and a little itchy, the red got bigger, it was also like she was coming down with something but so far today she feel okay. The patient underwent lab test with an unknown results on an unspecified date. The outcome of the event 'it hurts a little bit if she touches it' was unknown; event 'it was a little swollen' was recovered and not recovered for the rest of the events. Information on the batch number/lot number has been requested.

Other Meds: VERAPAMIL; ROSUVASTATIN; PANTOPRAZOLE; ESTRACE; ACETYLSALICYLIC ACID

Current Illness:

ID: 0990419
Sex: F
Age:
State: NY

Vax Date: 01/04/2021
Onset Date: 01/16/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: tender, visible left supraclavicular lymphadenopathy; This is a spontaneous report from a contactable physician. A 33-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number EK9231, intramuscular on 04Jan2021 15:00 to at a single dose on left arm for COVID-19 immunization. The patient medical history was not reported. The patient was not pregnant. The patient ha no known allergies, no prior vaccination and did not have a covid test post vaccination. Concomitant medication included sertraline, lamotrigine, melatonin and biotin. The patient experienced tender, visible left supraclavicular lymphadenopathy on 16Jan2021 12:00AM. The patient did not receive treatment for the event. The outcome of the event was unknown.

Other Meds: SERTRALINE; LAMOTRIGINE; MELATONIN; BIOTIN

Current Illness:

ID: 0990420
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Asthmas/having asthma attacks; bronchitis; This is a spontaneous report from a contactable consumer (patient) via Medical Information team and Pfizer sponsored program, Pfizer First Connect. A 69-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in arm on 13Jan2021 at single dose for COVID-19 immunization. The patient's medical history included asthma. Concomitant medication includes a bunch of medications for asthma. The patient had her first dose of COVID vaccine on 13Jan2021. The patient said that she does have asthma anyway and her asthma goes into bronchitis in 2021 very quickly. So she was just put on Prednisone. She is wondering if she can start Prednisone and an antibiotic for her asthma. The patient already had asthma but she is starting Prednisone and an antibiotic. And antibiotic is not something that she normally takes. The patient stated, "I took the Pfizer vaccine on Wednesday, the first dose and I am having a bad asthma attack (in Jan2021) and I don't know what my doctor put me on, wanted me to take Prednisone and an antibiotic (Unspecified Medication). The patient ask, "Can I take those after taking the vaccine?" The patient was asked about treatment for the event and stated, "Not until 2 days but right now I am having one. I just want to know if I can take Prednisone and antibiotic to get rid of this. Just my regular asthma medications that I am taking. My Albuterol inhaler, my Nebulizer and that's it." The outcome of the events was unknown. Information about Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 0990421
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: I had anaphylaxis yesterday; Throat is still swollen; This is a spontaneous report from a contactable consumer (patient). A 65-years-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL3249), via an unspecified route of administration on 15Jan2021 at single dose for COVID-19 immunisation. Medical history included diabetes mellitus. Concomitant medication included metformin (unknown manufacturer), levothyroxine sodium (LEVOXYL), fluoxetine (unknown manufacturer), empagliflozin (JARDIANCE), rosuvastatin (unknown manufacturer). The patient experienced anaphylaxis and throat was still swollen on 15Jan2021 about 30 minutes after when she received the shot, with outcome of recovering. The patient was transferred to emergency and was treated for the event.

Other Meds: METFORMIN; LEVOXYL; FLUOXETINE; JARDIANCE; ROSUVASTATIN

Current Illness:

ID: 0990422
Sex: F
Age:
State: TX

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Mild swelling of face and lips; Mild swelling of face and lips; This is a spontaneous report from a contactable physician. A 21-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3249, expiry date: unknown), intramuscular in the right arm, on 15Jan2021 11:00 at a single dose for covid-19 immunization. Medical history was reported as none. The patient's concomitant medications were not reported. The patient is not pregnant. The patient was not diagnosed with covid-19 prior to vaccination and was not tested for covid-19 post vaccination. The patient had no known allergies. On 16Jan2021, the patient experienced mild swelling of face and lips. Both the events resulted in emergency room visit. Therapeutic measures were taken as a result of mild swelling of face and lips which included steroid shot, told to take ZYRTEC and PEPCID. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0990423
Sex: F
Age:
State: PA

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

Lab Data:

Allergies:

Symptoms: ended up getting coronavirus; ended up getting coronavirus; This is a spontaneous report from the Pfizer marketing program. Information received from a contactable consumer reporting for the mother. A female patient of an unspecified age received the first dose of bnt162b2 (BNT162B2) vaccine , via an unspecified route of administration on an unspecified date at single dose for Covid-19 immunisation . The patient medical history and concomitant medications were not reported. It was reported that the patient took the first dose of the vaccine but ended up getting Coronavirus a week after her first dose. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990424
Sex: F
Age:
State: CA

Vax Date: 12/24/2020
Onset Date: 01/13/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: COVID-19 virus test; Test Result: Positive

Allergies:

Symptoms: COVID-19 virus test positive; COVID-19 virus test positive; This is a spontaneous report from a Pfizer-sponsored program "Pfizer RXPathways" from a contactable other health professional. A female patient of an unspecified age received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on 24Dec2020, at single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced COVID-19 virus test positive on 13Jan2021 with outcome of unknown. The patient underwent lab tests and procedures which included COVID-19 virus test: positive on 13Jan2021. The information on the lot/batch number has been requested.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 cannot be excluded for reported events.

Other Meds:

Current Illness:

ID: 0990425
Sex: F
Age:
State: FL

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe headache; confusion; unable to get clear thoughts communicated; This is a spontaneous report from a contactable other healthcare professional. An 83-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number and expiration date not reported) intramuscular on the left arm on 15Jan2021 10:45 at a single dose for COVID-19 immunization. The patient had no medical history. The patient's concomitant medications were not reported. On 16Jan2021 08:00 AM, the patient experienced severe headache, confusion, unable to get clear thoughts communicated. No treatment was received. Patient was not pregnant. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There were no other medications the patient received within 2 weeks of vaccination. 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 not recovered. Information on Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 0990426
Sex: F
Age:
State: CA

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: rigors; muscle aches; head ache; pain in my inner ears; photophobia; feeling of exhaustion; too weak to walk further than the bathroom; This is a spontaneous report from a contactable other hcp. A 75-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686), via an unspecified route of administration on 09Jan2021 13:45 at a SINGLE DOSE for covid-19 immunisation. Medical history included hypertension and atrial fibrillation from an unknown date and unknown if ongoing. Concomitant medication included benazepril (BENAZEPRIL), diltiazem (DILTIAZEM), rivaroxaban (XARELTO) and estrogen/methyl te. The patient previously had the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899) on 21Dec2020. The patient stated, "I woke from sleep about 12 hours later (10Jan2021) with rigors, muscle aches, head ache and pain in my inner ears as well as photophobia and feeling of exhaustion. The rigors had resolved by 8am but other symptoms persisted. I was too weak to walk further than the bathroom. I was able to consume only warm liquids, although I had no nausea, vomiting or diarrhea. Note that since onset post infectious irritable bowel symptoms in February after visiting a city, weeks before the pandemic was recognized, I have had very abnormal but not absent sense of taste and smell, making me wonder whether I was infected in February without the usual symptoms." The patient recovered from rigors on 10Jan2021, outcome of the event weakness was unknown while other events were not recovered.

Other Meds: BENAZEPRIL; DILTIAZEM; XARELTO

Current Illness:

ID: 0990427
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: swelling of the hands and tongue; swelling of the hands and tongue; some injection site redness; This is a spontaneous report from a contactable consumer. A 69 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 12Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the first dose of vaccine on 12Jan2021 and developed swelling of the hands and tongue as well as some injection site redness on unspecified dates. Pharmacist gave her Benadryl and symptoms resolved. Her doctor has advised her not to receive the second vaccine. She had previous history of having an allergic reaction to the tetanus shot and was unable to receive the shingles shot. The patient recovered from the events on unspecified date. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990428
Sex: F
Age:
State:

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

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

Allergies:

Symptoms: Soreness in the arm; Conjunctivitis; Episcleritis; This is a spontaneous report from a contactable physician (dentist, dental surgeon/patient's husband). A 57-year-old female patient received the bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EL1284), via an unspecified route of administration on 30Dec2020 at 57-years-old at a single dose for COVID-19 immunization. Medical history included blood pressure increased, and blood cholesterol increased; both from an unknown date and unknown if ongoing. Concomitant medications included atenolol (MANUFACTURER UNKNOWN) taken for blood pressure from an unspecified date to an unspecified date, "normal hormones" from an unspecified date to an unspecified date, "statin for cholesterol" from an unspecified date to an unspecified date. On 10Jan2021, the patient experienced conjunctivitis (non-serious). In Jan2021, the patient experienced episcleritis (non-serious). On an unspecified date, the patient experienced soreness in the arm (non-serious). The clinical course was reported as follows: The physician (patient's husband) stated that he and his wife received the Pfizer COVID-19 vaccine on 30Dec2020; and both had "a little bit of soreness in the arm, nothing spectacular." The patient developed a pink eye and was diagnosed with conjunctivitis 12 days (also reported as "approximately 10Jan or so") later after getting the vaccine (as reported). The doctor prescribed some topical cortical steroid eye drop. The eye was still swollen, and not totally resolved; "continually got worse." The patient consulted an ophthalmologist who gave the patient some prednisone ophthalmic (also reported as cortisone) and over the counter lubricant for the eyes. The patient was still symptomatic. The patient was diagnosed with episcleritis. The ophthalmologist classified the episcleritis as an autoimmune disease. Regarding the causality between the vaccine and the events, the patient's husband stated that his wife did not think it was related, and that the events could be totally idiopathic and there could be no correlation. The patient underwent lab tests and procedures which included COVID test: negative on an unspecified date. Therapeutic measures were taken as a result of conjunctivitis and episcleritis. The clinical outcome of the events was unknown.

Other Meds: ATENOLOL

Current Illness:

ID: 0990429
Sex: F
Age:
State: CO

Vax Date: 01/07/2021
Onset Date: 01/08/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:103 to 103 Fahrenheit; Comments: Starting about 10 hours post vaccine, fever between 103 to 103 F.

Allergies:

Symptoms: fever between 103 to 103 F; Severe body aches; fatigue; generalized weakness; This is a spontaneous report from a contactable physician (patient). A 52-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231 and expiration date not provided), via an unspecified route of administration in the left arm on 07Jan2021 17:30 at a single dose for COVID-19 immunization. Medical history included Meniere's disease, and allergies to Latex. The patient previously took cefalexin (KEFLEX) and codeine and experienced allergies. The patient also took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899) on 17Dec2020 17:30 in the left arm for COVID-19 immunization. The patient is not pregnant. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included unspecified medications. On 08Jan2021 03:00, about 10 hours post vaccine, the patient experienced fever between 103 to 103 f, severe body aches, fatigue, and generalized weakness which lasted until about 60 hours post vaccination. The patient has not undergone COVID testing post vaccination. The outcome of the events was recovered on 10Jan2021 15:30.; Sender's Comments: Based on a compatible temporal association, a causal relationship between reported events and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 0990430
Sex: F
Age:
State: KY

Vax Date: 01/13/2021
Onset Date: 01/15/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: two inches of redness and swelling at the injection site that is tender to touch; two inches of redness and swelling at the injection site that is tender to touch; two inches of redness and swelling at the injection site that is tender to touch; This is a spontaneous report from a contactable nurse (patient). A 27-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: not reported), via an unspecified route of administration on 13Jan2021 at 16:45 at a single dose on the left arm for COVID-19 immunization. The patient's medical history was reported as none. The patient has no known allergies. Concomitant medication included topiramate (TOPAMAX). The patient was not diagnosed with COVID-19 prior to vaccination. On 15Jan2021, the patient had two inches of redness and swelling at the injection site that is tender to touch. The patient did not receive any treatment for the reported 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 unknown. Information on the lot/batch number has been requested.

Other Meds: TOPAMAX

Current Illness:

ID: 0990431
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: very red circle around injection site; This is a spontaneous report from a contactable consumer (patient). A 65-year-old non-pregnant female patient received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot/batch number and expiry date were unknown), via an unspecified route of administration in the left arm on 05Jan2021 16:00 at a single dose for COVID-19 immunization. The patient was vaccinated in a hospital facility. Medical history included anxiety. The patient has no known allergies. The patient had no covid prior vaccination. The patient was not tested for covid post vaccination. The patient is not pregnant at the time of vaccination. Concomitant medications included escitalopram oxalate (LEXAPRO), curcumin, vitamin b12, vitamin c (also known as ascorbic acid), vitamin d, and biotin. The patient did not receive other vaccine in four weeks. On 16Jan2021 at 12:00 (also reported as day 12; possibly discrepant), the patient experienced very red circle around injection site. The patient did not receive treatment for the reported adverse event. The outcome of the event was not recovered. Information on the lot/batch number has been requested.

Other Meds: LEXAPRO; CURCUMIN; VITAMIN B12 [VITAMIN B12 NOS]; VITAMIN C [ASCORBIC ACID]; VITAMIN D [VITAMIN D NOS]; BIOTIN

Current Illness:

ID: 0990432
Sex: F
Age:
State: ID

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Injection site pain; Headache; Body aches; Joint pain; This is a spontaneous report from a contactable consumer, reporting for herself. A 46-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: Ek9213), via an unspecified route of administration at the left arm on 15Jan2021 14:00 at single dose for COVID-19 immunization. Vaccination was done in a health clinic. Medical history included diabetes, psoriasis, asthma and Covid (prior vaccination), all from an unknown date and unknown if ongoing. The patient was not pregnant. The patient had no known allergies. The patient's concomitant medications were not reported. On 16Jan2021 07:00, the patient experienced injection site pain, headache, body aches and joint pain. No treatment was received. There was no other vaccine in four weeks. The patient has not had covid tested post vaccination. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 0990433
Sex: F
Age:
State: PA

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

Lab Data: Test Name: Covid-19; Result Unstructured Data: Test Result:Positive; Comments: developed positive

Allergies:

Symptoms: COVID-19 confirmed by positive COVID-19 test; COVID-19 confirmed by positive COVID-19 test; This is a spontaneous report from a Pfizer-sponsored program from a contactable nurse reporting for herself. A female patient of an unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient received the vaccine and 2 days later developed positive COVID-19 test and go bed. The patient wanted to know how many days she needs to wait until she receives the 2nd vaccine. The outcome of the event was unknown. Information on lot number/batch number was requested.; Sender's Comments: The patient developed positive COVID-19 test two days after vaccination of BNT162B2. No complete protection can be achieved to prevent from the targeted infection/disease due to the very short time lag. The company considers that the COVID-19 is more likely pre-existing condition prior to vaccine use, and unrelated to BNT162B2.

Other Meds:

Current Illness:

ID: 0990434
Sex: F
Age:
State: TX

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

Lab Data: Test Name: COVID-19 virus test; Test Result: Positive

Allergies:

Symptoms: COVID-19 virus test positive; COVID-19 virus test positive; This is a spontaneous report from a Pfizer-sponsored program contactable consumer reporting for herself. A 53-year-old female patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on an unspecified date, at single dose, for COVID-19 immunisation. Medical history included blood pressure. Concomitant medication included losartan (unknown manufacturer) for blood pressure. The patient experienced COVID-19 virus test positive on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included COVID-19 virus test: positive (unknown date). The information on the lot/batch number has been requested.

Other Meds: LOSARTAN

Current Illness:

ID: 0990435
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Arm soreness; Aches; Exhaustion; Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 50-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration in left arm on 15Jan2021 11:30 at single dose for COVID-19 immunization. Medical history included drug allergy to Quinolones, asthma and thyroid cancer from an unknown date and unknown if ongoing. Concomitant medication included omeprazole, levothyroxine sodium (SYNTHROID), topiramate (TOPAMAX) and sertraline hydrochloride (ZOLOFT). The facility where the most recent COVID-19 vaccine was administered was in the Public Health Clinic/Veterans Administration facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 15Jan2021 02:00 PM, the patient experienced arm soreness, aches, exhaustion, diarrhea. No treatment was received for the events. The outcome of the events was recovering. The events were considered non serious as it did not result in death, was not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and were not a congenital anomaly/birth defect.

Other Meds: OMEPRAZOLE; SYNTHROID; TOPAMAX; ZOLOFT

Current Illness:

ID: 0990436
Sex: F
Age:
State: MI

Vax Date: 12/18/2020
Onset Date: 12/19/2020
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Pain at injection; headache; fatigue; nausea; chills; brain fog; diarrhea; joint pain; This is a spontaneous report from a contactable other healthcare professional (hcp). A 42-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date were not reported), intramuscular on 18Dec2020 16:00 at a single dose in the left arm for COVID-19 immunization. The patient's medical history included depression, anxiety, and known allergies to IVP dye. The patient was not pregnant at the time of the vaccination. The patient had no COVID prior to vaccination. Concomitant medications (reported as other medications in two weeks) included bupropion hydrochloride (WELLBUTRIN), sertraline hydrochloride (ZOLOFT) and unspecified multivitamin. The patient had no other vaccine in four weeks. The patient previously took cefalexin (KEFLEX) but had known allergies. On 19Dec2020 08:00 AM, the patient experienced pain at injection, headache, fatigue, nausea, chills, brain fog, diarrhea, and joint pain. No treatment received in response to the events. The patient was not tested for COVID post vaccination. The outcome of the events pain at injection, headache, fatigue, nausea, chills, brain fog, diarrhea, and joint pain was recovered on an unknown date. Information on the Lot/Batch Number has been requested.

Other Meds: WELLBUTRIN; ZOLOFT

Current Illness:

ID: 0990437
Sex: M
Age:
State: TN

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Numbness and tingling in left leg; Numbness and tingling in left leg; burning sensation all over leg; unable to walk; This is a spontaneous report from a contactable consumer (patient). A 43-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3302 and expiration date not provided), via an unspecified route of administration (right arm) second dose on 09Jan2021 17:15 at single dose for covid-19 immunisation. The patient medical history was not reported. There were no concomitant medications. Historical vaccine includes BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0140) via an unspecified route of administration (left arm) first dose on 21Dec2020. On 09Jan2021 22:30, the patient experienced Numbness and tingling in left leg, burning sensation all over leg, unable to walk. The patient did not received treatment for the events. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0990438
Sex: F
Age:
State: TX

Vax Date: 12/29/2020
Onset Date: 01/01/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Date: 20210101; Test Name: Fever; Result Unstructured Data: Test Result:103.5

Allergies:

Symptoms: Fever of 103.5; severe body aches; Migraine; Fatigue; Insomnia; This is a spontaneous report from a contactable other health professional (patient). A 36-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK5730), via an unspecified route of administration on 29Dec2020 at 15:00 at a single dose on the right arm for COVID-19 immunization. The patient's medical history included GERD and allergy to latex. The patient was also 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 has concomitant medications but were not specified. On 01Jan2021 at 02:00, the patient experienced fever of 103.5, severe body aches, migraine, fatigue, and insomnia. The patient did not receive any treatment for the reported 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.

Other Meds:

Current Illness:

ID: 0990439
Sex: U
Age:
State: MI

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

Lab Data: Test Date: 20210115; Test Name: body temperature; Result Unstructured Data: Test Result:low fever; Comments: 19:00

Allergies:

Symptoms: Pain at injection; muscle aches; chills; fatigue; joint pain; low fever; nausea; loss of appetite; second dose of the Pfizer Covid-19 Vaccine on 15Jan2021, but the first dose was received on18Dec2020; This is a spontaneous report from a contactable healthcare professional (patient). A 42-year-old patient of an unspecified gender received the second dose of bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE; unknown lot number and expiration date), intramuscular left arm on 15Jan2021 09:00 at a single dose for covid-19 immunization. Medical history included depression, anxiety and known allergies to IVP dye. The patient was not diagnosed with Covid prior to vaccination. Concomitant medication included bupropion hydrochloride (WELLBUTRIN), sertraline hydrochloride (ZOLOFT) and vitamins NOS (MULTIVITAMINS reported as MULTI VITAMIN). The patient did not receive other vaccines in the last 4 weeks. The patient previously took cefalexin monohydrate (KEFLEX) but had allergies. The patient received the first dose of bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE; unknown lot number and expiration date), intramuscular left arm on 18Dec2020 16:00 at a single dose for covid-19 immunization but had pain at injection, chills, fatigue, nausea, joint pain, headache, brain fog and diarrhea. The patient received the second dose of the Pfizer Covid-19 Vaccine in a pharmacy or drug store on 15Jan2021, but the first dose was received on18Dec2020. The patient experienced pain at injection, chills, fatigue, muscle aches, joint pain, low fever, nausea and loss of appetite on 15Jan2021 19:00 which did not received treatment. The patient has not been covid tested post vaccination. The outcome of the event pain at injection, chills, fatigue, muscle aches, joint pain, low fever, nausea, loss of appetite were recovering while the outcome of the other event was unknown. The following information on the batch/lot number has been requested.

Other Meds: WELLBUTRIN; ZOLOFT; MULTIVITAMINS [VITAMINS NOS]

Current Illness:

ID: 0990440
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: feeling like I was 500 lbs; I felt like an impending sense of doom; swollen lymph nodes in my neck; stiff neck; severe shivering; I needed assistance to walk safely to avoid falling; Intense pain in my left arm; dryness in my throat/severely dry throat; This is a spontaneous report from a contactable healthcare professional (patient). A 36-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) , via an unspecified route of administration in right arm on 23Dec2020 17:15 at single dose for COVID-19 immunization. Medical history included acid reflux from an unknown date and unknown if ongoing. There were no concomitant medications. The patient was not pregnant. The facility where the most recent COVID-19 vaccine was administered was in the hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient received the first Pfizer vaccine on 23Dec2020 at approximately 5:15 PM. The patient felt fine until about 11 PM at night, the patient stated, "when I began experiencing intense pain in my left arm and dryness in my throat" on 23Dec2020. I took a Benadryl and went to bed. At approximately 1 AM (24Dec2020) I woke up feeling like I was 500 lbs (I am about 175 lbs). I also had swollen lymph nodes in my neck, a stiff neck, a severely dry throat, and severe shivering. I attempted to navigate to the bathroom and felt like I needed assistance to walk safely to avoid falling. I felt like an impending sense of doom, and called my mom who is a nurse. She told me to contact the Pfizer #, but nobody was answering the phone at that time. I then started looking up on the internet if anyone else had experience what I was feeling after the vaccine and if the feeling passed, as I was not sure if I should go to the ER. I ended up falling asleep." The outcome of the events was recovering. The patient took Benadryl for events "intense pain in my left arm and dryness in my throat" as treatment. No treatment was given to the patient from the remaining events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0990441
Sex: F
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe upper stomach pains and stomach pains all over and cramps; all over body pain; headache; nausea; ankles swelling more the right one; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not provided), via an unspecified route of administration in the right arm on 13Jan2021 13:00 at a single dose for COVID-19 immunization. Medical history included Coronary artery disease (CAD), 2nd degree AV heart block, acid reflux, gastritis, high blood presure, fibromyalgia, gammaglobulinemia, allergies to sulfa, eggs, milk, fish, shrimp, and nuts. The patient is not pregnant. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included valsartan (DIOVAN), esomeprazole sodium (NEXIUM), acetylsalicylic acid (BABY ASPIRIN), alprazolam, atorvastatin (LIPITOR). The patient previously took codeine, morphine, clopidogrel (PLAVIX), isosorbide mononitrate (IMDUR) and experienced allergies. On 13Jan2021 15:00, approximately 1 hour after the shot, the patient experienced severe upper stomach pains and stomach pains all over and cramps. A few hours later, she got all over body pain, headache, nausea, and her ankles were swelling more the right one. These events are all still going on 3 days later. Treatment was not provided in response to the events. The patient has not undergone COVID testing post vaccination. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds: DIOVAN; NEXIUM [ESOMEPRAZOLE SODIUM]; BABY ASPIRIN; ALPRAZOLAM; LIPITOR [ATORVASTATIN]

Current Illness:

ID: 0990442
Sex: F
Age:
State: FL

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fatigue; joint discomfort; mild fever; mild headache; This is a spontaneous report from a contactable nurse (patient). A 68-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number: EL1283, via an unspecified route of administration in left arm on 15Jan2021 at 08:30 AM at single dose for COVID-19 immunization. Medical history included CAD (coronary artery disease), mild COPD (chronic obstructive pulmonary disease) and GERD (gastroesophageal reflux disease). Patient had Covid prior vaccination. Patient was not pregnant. Patient has no known allergies. No other vaccines in four weeks. Concomitant medications included rosuvastatin calcium (CRESTOR), carvedilol (COREG) and vitamins (unspecified). On 16Jan2021 at 01:00 PM, the patient experienced fatigue, joint discomfort, mild fever, and mild headache. Patient did not receive treatment for the events. Patient was not tested for Covid post vaccination. The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: CRESTOR; COREG

Current Illness:

ID: 0990443
Sex: F
Age:
State: OR

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: temp; Result Unstructured Data: Test Result:103; Comments: 09:00; Test Date: 20210116; Test Name: temp; Result Unstructured Data: Test Result:99.9

Allergies:

Symptoms: temp 103/temp 99.9; severe headache; severe fatigue; muscle soreness; yellow nasal secretions; yellow and bloody sputum; yellow and bloody sputum; This is a spontaneous report from a contactable nurse. A 59-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL1284, expiry date unknown), intramuscular (right arm) on 12Jan2021 15:45, at single dose, for covid-19 immunization. The patient had no medical history and had no known allergies. There were no concomitant medications. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EH9899), on 21Dec2020 14:00 for covid-19 immunization, vaccine location left arm, at 59 years old. After 18 hours of obtaining shot, on 13Jan2021 09:00 the patient experienced temp 103, severe headache, severe fatigue, muscle soreness, yellow nasal secretions, yellow and bloody sputum. Now on day 4 after shot, 16Jan2021, the patient still had temp 99.9, headache, fatigue, nasal secretions and, sputum secretions less. No treatment was received for the adverse events reported. The patient was recovering from the events. The patient had no other vaccine in four weeks, had no other medications in two weeks, had no Covid prior vaccination, and had not been Covid-tested post-vaccination.

Other Meds:

Current Illness:

ID: 0990444
Sex: F
Age:
State: FL

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 02/01/2021
Hospital:

Lab Data:

Allergies:

Symptoms: left auxiliary Lymphadenopathy and lymphadenitis; left auxiliary Lymphadenopathy and lymphadenitis; eyelid swelling; left eye swelling; left eye swelling and tenderness; This is a spontaneous report from a contactable physician (patient). A 40-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on the left arm, on 14Jan2021 07:30 at a single dose for COVID-19 immunization. Medical history included seizure, COVID prior to vaccination and penicillin allergy. Patient was not pregnant at the time of vaccination. Concomitant medication included levetiracetam (KEPPRA) and lacosamide (VIMPAT). No additional vaccines administered within 4 weeks before the vaccination. The patient previously took LAMICTAL and experienced allergy. The patient experienced Left auxiliary lympadenopathy and lymphadenitis, eyelid swelling, and left eye swelling and tenderness on 15Jan2021 15:00. Patient took BENADRYL as treatment for the events and was recovering. Patient had not been tested since the vaccination. Information on the lot/batch number has been requested.

Other Meds: KEPPRA; VIMPAT

Current Illness:

ID: 0990445
Sex: F
Age:
State:

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

Lab Data: Test Name: COVID; Result Unstructured Data: Test Result:Unknown results; Comments: tested for COVID multiple times

Allergies:

Symptoms: Fatigue; Shortness of breath; Chest pain; Cough; This is a spontaneous report from a contactable consumer. A 22-year-old female patient (daughter) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 23Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The reporter stated that her daughter had a reaction to the COVID vaccine. The patient received the first dose of the vaccine on 23Dec2020. The adverse reaction has lasted the past three weeks to include fatigue, shortness of breath, chest pain, and cough on unspecified date. The patient is now on inhalers and she was not on inhalers before. The reporter stated that her daughter has been tested for COVID multiple times. Outcome of the events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm