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: 1004261
Sex: M
Age:
State: NM

Vax Date: 01/11/2021
Onset Date: 01/13/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm pain; fatigue; beginning 1/13 a constant high pitch whine in whole head; probably tinnitus; This is a spontaneous report from a contactable consumer (patient). A 49-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3246; expiry date: unknown) via an unspecified route of administration in the left arm, on 11Jan2021 at 07:30, at a single dose, for COVID-19 immunization. Medical history included seasonal allergies and mild jackfruit allergy. Concomitant medications included testosterone, finasteride, and unspecified vitamins. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK5730; expiry date: unknown) on 21Dec2020, at 07:30 AM, in the left arm, for COVID-19 immunization and experienced arm pain and fatigue. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. On an unspecified date, the patient had arm pain and fatigue from second dose but milder. On 13Jan2021, at 07:00 AM, the patient experienced a constant high pitch whine in whole head, probably tinnitus. The patient has not sought medical attention yet. The events were considered non-serious. Outcome of the events "beginning 1/13 a constant high pitch whine in whole head" and tinnitus was not recovered, while outcome of the other events was unknown. The patient has not been tested for COVID-19 since vaccination.

Other Meds: FINASTERIDE; TESTOSTERONE

Current Illness:

ID: 1004262
Sex: F
Age:
State: WI

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

Lab Data:

Allergies:

Symptoms: Immediate itching at site which spread to generalized body; Immediate itching at site which spread to generalized body; Red rash and warmth to entire upper arm; Red rash and warmth to entire upper arm; This is a spontaneous report from a contactable nurse (patient). A 44-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL1284), via an unspecified route of administration on 02Jan2021 07:00 AM at single dose on left arm for COVID-19 immunization. COVID-19 vaccine was administered in the hospital. Patient is not pregnant. Medical history included hypothyroid. No other vaccines within 4 weeks prior to COVID vaccine. Concomitant medications (received within 2 weeks of vaccination) included thyroid (ARMOUR THYROID), prednisone, famotidine (PEPCID) and fexofenadine hydrochloride (ALLEGRA). The patient previously took influenza vaccine, azithromycin and monistat, and experienced allergies to all. Patient was not diagnosed with COVID-19 prior vaccination. The patient experienced immediate itching at site which spread to generalized body. Patient also experienced red rash and warmth to entire upper arm. All events occurred on 02Jan2021 07:15 AM. No treatment was given for the events. Events were assessed as non-serious. Outcome of the events was recovered in Jan2021. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: ARMOUR THYROID; PREDNISONE; PEPCID; ALLEGRA

Current Illness:

ID: 1004263
Sex: F
Age:
State: NV

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

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

Allergies:

Symptoms: she was not good with needles, so it was certainly good that it went quicker and less painful than she expected; This is a spontaneous report from a contactable consumer reporting for herself. An 18-year-old female patient received bnt162b2 (BNT162B2, lot number: EL1283, expiration date: not reported), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The vaccine was administered at a school or student health clinic. The patient was not pregnant at the time of vaccination. She did not receive any other vaccines within 4 weeks prior to the COVID vaccine. She was not diagnosed with COVID-19 prior to vaccination. Medical history and concomitant medication were not reported. The patient was just nervous for a good amount of the time. When she got the vaccine she was overthinking and her left hand began to throb. She was not in pain but just a sinking feeling. She stated that she was not good with needles, so it was certainly good that it went quicker and less painful than she expected. She added that her nurse treated her so well and was so patient with her and she appreciated it so much. Since the vaccination, the patient has been tested for COVID-19: Nasal Swab with result of negative on an unspecified date. No treatment was received for the event. Outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1004264
Sex: F
Age:
State: CT

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

Lab Data:

Allergies:

Symptoms: very weak; couldn't stand or walk; couldn't stand or walk; fever; could barely speak; lethargic; fell into a deep sleep; This is a spontaneous report from a contactable consumer (patient). A 95-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL9261) via an unspecified route of administration on the left arm on 19Jan2021 17:30 at a single dose for COVID-19 immunization. Medical history included AFIB, chronic anemia, hip surgery in Aug2020 (recovering) and diagnosed with COVID-19 (prior to vaccination). Concomitant medication included levothyroxine sodium (L-THYROXINE), omeprazole (PRILOSEC), calcium carbonate, magnesium carbonate, magnesium trisilicate (TUMS); sodium chloride; ferrous sulfate; folic acid; vitamin D3; guaifenesin (MUCINEX) and clarithromycin (CLARITINE) reported as 'Claratinde'. Approximately 22 hours after injection, on 20Jan2021 03:30 PM patient became very weak, couldn't stand or walk, had a fever, could barely speak, lethargic and fell into a deep sleep. No treatment was received for the events. Events were reported as non-serious. Patient was not pregnant. The facility where the vaccine was administered was in a clinic. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient has not been tested for COVID-19. Prior to vaccination, the patient was not diagnosed with COVID-19. Outcome of the events was unknown.

Other Meds: L-THYROXINE; PRILOSEC; TUMS; SODIUM CHLORIDE; FERROUS SULFATE; FOLIC ACID; VITAMIN D3; MUCINEX; CLARITINE

Current Illness:

ID: 1004265
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: trouble breathing; fatigue; muscle and body aches; muscle and body aches; trouble standing up; This is a spontaneous report from a contactable consumer (patient). An 80-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EK 4176), via an unspecified route of administration on 18Jan2021 11:30 AM at single dose on left arm for COVID-19 immunization. Vaccine facility type is hospital, Medical history included dialysis patient, "dibeties" and High blood pressure. No known allergies and no COVID prior vaccination. No other vaccines in four weeks. Concomitant medications included unspecified medications (reported as "other medications in two weeks: yes"). The patient experienced trouble breathing, muscle and body aches, trouble standing up and fatigue which occurred within 1 hour after taking shot on 18Jan2021 12:15 PM. No treatment was given for the events. Outcome of the events was recovered in Jan2021. Patient was not tested for COVID post vaccination.

Other Meds:

Current Illness:

ID: 1004266
Sex: F
Age:
State: TX

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

Lab Data: Test Date: 202010; Test Name: Covid; Result Unstructured Data: Test Result:positive

Allergies:

Symptoms: hard large lump that hurts at the injection site /Left arm has a knot in it from injection site; hard large lump that hurts at the injection site; chest pain; shortness of breath; This is a spontaneous report from contactable consumer (patient). A 26-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration into the upper left arm on 05Jan2021 at single dose as a precaution because she works in nursing home (COVID-19 immunisation). Medical history included Covid positive back in Oct2020. Concomitant medication included biotin and one a day women's vitamin. Family members have medical issues. Dad has heart tumors, seizure, sleep apnea and osteoporosis. Mom has asthma, diabetes, has had cancer, neuropathy and macular degeneration. The patient received first dose of the covid vaccine on 05Jan2021 and had some symptoms after the vaccine. On unspecified date in Jan2021, the patient hard large lump that hurts at the injection site, chest pain and shortness of breath; similar to when she had Covid positive back in October. She still has a lump at the injection side which has gotten smaller in size but still hurts to touch. Left arm has a knot in it from injection site; does not reuired ER or visit to physician's office. It feels like a bump with something in her arm. She doubts that is the case. She wanted to see if that was normal and when it might go away, especially since she should be getting second dose on 26Jan2021. She is a speech therapist. There is no prescriber. They came and gave to everyone all at once. It was really big at first. It felt like someone punched her. It was a big giant lump, but it is getting better. The injection was given in the upper left arm and it felt like it went into the muscle. The outcome of the event vaccination site mass was recovering, and the outcome of the remaining events was unknown.

Other Meds: BIOTIN

Current Illness:

ID: 1004267
Sex: F
Age:
State: GA

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

Lab Data:

Allergies:

Symptoms: feeling nauseous from the first dose of vaccine; shoulder hurting; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EK9231), via an unspecified route of administration on 20Jan2021 at 12:30 on the left arm at a single dose for COVID-19 immunization. The patient had no medical history. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient reported that she was feeling nauseous from the first dose of the vaccine. She called to find out how long she will be nauseous because this is the second day. The patient stated that she started feeling nauseous about 15 minutes after. The only other symptom is her shoulder hurting since an unspecified date in Jan2021. The patient added that she still feels nauseous. The outcome of the event feeling nauseous from the first dose of vaccine was not recovered while the outcome of the event shoulder hurting was unknown. The case was reported as non-serious.

Other Meds:

Current Illness:

ID: 1004268
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: headache; nausea; This is a spontaneous report from a contactable consumer via Medical information team. A 48-year-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient took her 1st dose of the COVID vaccine and experienced side effects such as 9 days of strong headache and 4 days of nausea. The consumer wants to know if her mother should get her 2nd dose or not. The outcome of the events was recovered on unspecified dates. Information on lot number/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004269
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: a lot of the volume of the vaccine came out of the arm after the needle was drawn out; a lot of the volume of the vaccine came out of the arm after the needle was drawn out; a lot of the volume of the vaccine came out of the arm after the needle was drawn out; a lot of the volume of the vaccine came out of the arm after the needle was drawn out; This is a spontaneous report received from a contactable pharmacist. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration in the arm, on an unspecified date, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The pharmacist reported that the patient received the first dose of the vaccine on an unspecified date and mentioned that a lot of the volume of the vaccine came out of the arm after the needle was drawn out. The patient wanted to get revaccinated and the pharmacist wanted to confirm if this is recommended as she has not seen anything on the website. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004270
Sex: M
Age:
State: FL

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

Lab Data: Test Name: Blood pressure; Result Unstructured Data: Test Result:120s to 130s on the top, mid 50-60 on the bottom; Test Name: Blood pressure; Result Unstructured Data: Test Result:132/56; Test Name: Blood pressure; Result Unstructured Data: Test Result:150s

Allergies:

Symptoms: Increased blood pressure; This is a spontaneous report from a contactable consumer (patient). An 87-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL1288 and expiry date: unknown), via an unspecified route of administration on the left shoulder, on 14Jan2021 at a single dose for covid-19 immunisation. Medical history included ongoing acid reflux, atrial fibrillation, and cholesterol. Concomitant medication included omeprazole, apixaban (ELIQUIS), and atorvastatin. Patient previously took pneumonia vaccine. On Jan2021, patient noticed an increased blood pressure (usually his BP is around 120, now has consistently been around 150). Prior to the shot, he has not been on blood pressure medication. His blood pressure usually runs high 120s to 130s on the top, and mid 50-60 on the bottom. His blood pressure prior to the vaccine that day was 132/56. Then a couple of days after the first shot, the top number of his blood pressure was in the high 150s, but the same on the bottom. Patient was wondering if he has a problem, or is this a side effect. He went in as a senior. He didn't have a prescribing doctor. The blood pressure difference started a couple of days after his first shot. He was scheduled for his second shot 4Feb2021. He has had no other side effects or anything. There was no swelling, no fever, no chills and he felt good. Just his blood pressure has been an issue. Outcome of the event was not recovered.

Other Meds: OMEPRAZOLE; ELIQUIS; ATORVASTATIN

Current Illness: Acid reflux (esophageal)

ID: 1004271
Sex: M
Age:
State: AZ

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

Lab Data:

Allergies:

Symptoms: Injection site pain; Moderate to severe myalgia; Arthralgia; Uncontrollable rigors began 12 h post vaccination lasting for 2.5 h; Mild odynophagia; xerostomia; This is a spontaneous report from a non-contactable physician (patient). A 72-year-old male patient received the second dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL0142), via an unspecified route of administration on 19Jan2021 at 09:30 on the right arm at a single dose for COVID-19 immunization. Medical history included allergies to mussles from an unknown date and unknown if ongoing. The patient did not have COVID-19 prior to vaccination. Concomitant medication included atenolol (manufacturer unknown), amlodipine (manufacturer unknown), asa (acetylsalicylic acid, manufacturer unknown), tamsulosin hydrochloride (TAMSULO) and hctz (hydrochlorothiazide, manufacturer unknown). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EH9899) on 29Dec2020 at 10:30 AM on the left arm for COVID-19 immunization. The patient reported that the events began 8 hours post vaccination and peaked 12 hours post vaccination. The patient experienced moderate to severe myalgia, arthralgia, injection site pain, uncontrollable rigors began 12 hours post vaccination lasting for 2.5 hours which was finally relieved by 500mg Tylenol/25mg Benadryl (Tylenol PM ES). The patient also experienced mild odynophagia and xerostomia. All the events were reported to have occurred on 19Jan2021 at 15:00. All symptoms has basically resolved by 60 hours post vaccinations. The events were reported to have recovered on an unspecified date in Jan2021. The patient has not been tested for COVID-19 post vaccination. No follow up attempts are possible. No further information is expected.

Other Meds: ATENOLOL; AMLODIPINE; ASA; TAMSULO; HCTZ

Current Illness:

ID: 1004272
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: experienced a bad headache; had arm pain in the vaccinated arm (left), only when lifting my arm; This is a spontaneous report received from a contactable consumer (patient). A 41-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247, expiry date: unknown), via an unspecified route of administration in the left arm, on 19Jan2021 13:00, at single dose, for COVID-19 immunization, at workplace clinic. There were no medical history and no allergies to medication, food, or other products. The patient was not diagnosed with COVID-19 prior to vaccination and was not tested for COVID-19 since vaccination. The patient was not pregnant at the time of vaccination. Concomitant medication included vitamin c, colecalciferol (VITAMIN D), vitamin b and ibuprofen (ADVIL). The patient did not receive other vaccines within 4 weeks prior to BNT162B2 vaccine. On 20Jan2021 at 08:00, the patient had a bad headache and had arm pain in the vaccinated arm (left), only when lifting her arm. The headache went away during the evening without treatment. The patient did not take any pain relief medication. No treatment was given for the events. The patient recovered from headache on the evening of 20Jan2021 and recovered from "had arm pain in the vaccinated arm (left), only when lifting my arm" on an unspecified date. The events were assessed as non-serious. No follow-up attempts are possible. No further information is expected.

Other Meds: VITAMIN C; VITAMIN D; VITAMIN B; ADVIL

Current Illness:

ID: 1004273
Sex: M
Age:
State: KS

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

Lab Data:

Allergies:

Symptoms: Headache; Chills; Fever; Sore Throat; Body aches; This is a spontaneous report from a contactable Nurse. A 49-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number and expiration date unknown) intramuscularly on 20Jan2021 (at the age of 49-years-old) as a single dose for COVID-19 vaccination. The patient's medical history was not reported. Historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE on 30Dec2020. Prior to vaccination, the patient had not been diagnosed with COVID-19. The patient was administered the vaccine in a Nursing Home/Senior Living Facility. The patient's concomitant medications were not reported. On 20Jan2021 at 11:00 the patient experienced headache, chills, fever, sore throat, and body aches. Treatment was not received for the events. The clinical outcome of headache, chills, fever, sore throat, and body aches was reported as not recovered. It was also reported that since the vaccination the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1004274
Sex: M
Age:
State: FL

Vax Date: 01/15/2021
Onset Date: 01/17/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Rash on right side of chest, sensitive to touch and liquid filled; Rash on right side of chest, sensitive to touch and liquid filled; This is a spontaneous report from a contactable consumer. A 75-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date not reported), via an unspecified route of administration on 15Jan2021 at a single dose for COVID-19 immunization. Medical history included arthritis, apnea, and post-traumatic stress disorder (PTSD), all from unknown dates. Concomitant medications were not reported. The patient experienced rash on right side of chest, sensitive to touch and liquid filled on 17Jan2021 13:00 (reported started 2 days after vaccination). It was subsiding as of 3 days after initial appearance. The events were recovering at the time of report. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1004275
Sex: M
Age:
State: CA

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

Lab Data: Test Date: 20210120; Test Name: BP; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210120; Test Name: Internal temp (taken under tongue); Result Unstructured Data: Test Result:about 95 degrees (very low)

Allergies:

Symptoms: Lightheaded/dizziness; Feeling warm; Uncomfortable tingling sensations that started in my fingers and moved up my arms; Uncomfortable tingling sensations that started in my fingers and moved up my arms; Feeling quite unwell; Strong flu symptoms; Felt very hot/cold; Intense aching; Muscle soreness all over; Inflamed lymph nodes (esp in neck); Some nausea; Internal temp (taken under tongue) was also very low, about 95 degrees; This is a spontaneous report from a contactable consumer (patient). A 37-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3302; Expiration date was not reported) on 20Jan2021 (14:30) at a single dose on the left arm, with route of administration unspecified, for COVID-19 immunization. The patient's medical history was not reported. Concomitant medications included naproxen sodium (ALEVE) and cannabidiol (CBD OIL). On 20Jan2021 (14:45), after the vaccination, the patient became lightheaded/dizziness; had started feeling warm; and had uncomfortable tingling sensations that started in the fingers and moved up to the arms. On 20Jan2021, about an hour or two after the vaccination, the patient had begun feeling quite unwell; had strong flu symptoms; was feeling very hot/cold; had intense aching; muscle soreness all over; inflamed lymph nodes (especially in the neck); some nausea; and internal temperature (taken under the tongue) was very low at about 95 degrees. The patient had received treatment for the reported events; blood pressure was taken; and he was given water. The adverse events had required doctor or other healthcare professional office/clinic visit. The outcome of the events, 'lightheaded/dizziness', 'feeling warm', 'uncomfortable tingling sensations that started in the fingers and moved up to the arms', 'feeling quite unwell', 'strong flu symptoms', 'feeling very hot/cold', 'intense aching', 'muscle soreness all over', 'inflamed lymph nodes (especially in the neck)', 'nausea' and 'internal temperature (taken under the tongue) was very low at about 95 degrees', was recovering. The patient was not diagnosed with COVID-19 prior to vaccination, and had not been tested since the vaccination.

Other Meds: ALEVE; CBD OIL

Current Illness:

ID: 1004276
Sex: M
Age:
State: GA

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

Lab Data: Test Date: 20210120; Test Name: COVID-19 rapid test; Test Result: Positive

Allergies:

Symptoms: patient received first dose on 14Jan2021 and tested positive for COVID-19 on 20Jan2021; patient received first dose on 14Jan2021 and tested positive for COVID-19 on 20Jan2021; Sore Arm; This is a spontaneous report from a contactable consumer (patient). A 74-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3246), intramuscular on 14Jan2021 at a single dose on left arm for COVID-19 immunization. Medical history included heart disease (unspecified). The patient is taking a lot of medication (unspecified). The patient had no prior vaccinations within 4 weeks. He tested positive yesterday, 20Jan2021, for COVID-19. His question was if he should get the second shot. The patient stated he had a sore arm on 14Jan2021, but really had no adverse reactions. The patient underwent COVID-19 rapid test: positive on 20Jan2021. The patient recovered from sore arm on 15Jan2021. Outcome of event "tested positive for COVID-19" was unknown.

Other Meds:

Current Illness:

ID: 1004277
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: splotches/ hives on my cheeks; splotches/ hives on my cheeks; face was swollen around my nose; sick; lightheaded; lethargic; This is a spontaneous report from a contactable consumer (patient) via a Medical information team. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that the patient experienced side effects following her first dose of PFIZER-BIONTECH COVID-19 VACCINE. She wants to know how well she will be protected if she refuses the second dose? She stated it protected "up to 25%" in what she read. She also asked "if she could still spread COVID? Why would the CDC recommend social distancing and mask wearing if the vaccine works so well?" The patient experienced not severe splotches/hives on my cheeks and was just starting to subside. The patient stated, "I could see that my face was swollen, and my face was swollen around my nose (Wednesday). Then saturday I was so sick all day lightheaded and lethargic so I'm inclined not to receive the second dose since experiencing these effects". The outcome of the events was unknown. Information about lot number and expiry date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1004278
Sex: M
Age:
State: NC

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

Lab Data: Test Name: Height; Result Unstructured Data: Test Result:5'10'' or 5'11''

Allergies:

Symptoms: not feeling that great; his arm hurts where he was given the shot/left arm sore; two nosebleeds; headache; sneezed; medical history included: real bad arthritis and adrenal insufficiency; medical history included: real bad arthritis and adrenal insufficiency; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received the dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK9231), via intramuscular route of administration on 19Jan2021 at 14:30 in the arm left at a single dose to prevent covid. The patient's medical history included high blood pressure from Feb2019, cancer (three times, for clarification), real bad arthritis and adrenal insufficiency. Also, the patient had lost a kidney, two adrenal glands, and part of his prostate. Concomitant medications included hydrocortisone (strength: 10 mg) for adrenal insufficiency, amlodipine (strength: 5 mg) for high blood pressure, colchicine (strength: 0.6 mg), irbesartan (strength: 150 mg), and fludrocortisone (strength: 0.1 mg) for adrenal insufficiency. The patient previously took a flu shot in Oct (as reported) and experienced sore arm. Patient goes to the doctor to get the flu shot each year. On 20Jan2021, the patient had two nosebleeds and headache. He has never had a nose bleed and could not remember the last time he had a nose bleed. The first nose bleed was worse and was concerning. He sneezed and that is what started the second nose bleed. The first nose bleed was worse than the second one. He asked if nosebleed was one of the side effects of the vaccine. It was not listed as side effect on the website when he looked it up. He also stated that his arm hurts where he was given the shot/left arm sore and was not feeling that great on an unspecified date. His height was 5'10'' or 5'11'' on an unspecified date. The outcome of the events two nosebleeds and headache was recovered on 21Jan2021; events not feeling that great and his arm hurts where he was given the shot/left arm sore was recovering; while unknown for the other events.

Other Meds: HYDROCORTISONE; AMLODIPINE; COLCHICINE; IRBESARTAN; FLUDROCORTISONE

Current Illness:

ID: 1004279
Sex: F
Age:
State: MN

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: discomfort in her chest vs the burning/ chest discomfort; discomfort in her chest vs the burning/while the chest discomfort had subsided the burning was back; burning in her lungs; coldness/ all over body coldness; fatigue; chills; This is a spontaneous report from a contactable consumer (patient herself, a medical assistant) via Medical Information team. A 49-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EK9231, expiration date: 30Apr2021), via an unspecified route of administration on the right deltoid on 13Jan2021 at 12:30 at a single dose for COVID-19 immunization. The vaccination facility was the clinic. Vaccine was not administered at a military facility. Relevant medical history included sleeping (problem). Concomitant medications included ongoing trazodone as a sleeping pill and an unspecified multivitamin. The patient had no previous immunizations with a Pfizer vaccine as this was the first dose. She had no prior vaccinations within 4 weeks. The patient was having concerns about the side effects was experiencing after her first dose. The patient received the first dose on 13Jan2021 and afterwards she felt fatigue on 13Jan2021; coldness on 14Jan2021 at 07:30; and chills on an unspecified date in Jan2021. On Tuesday, on 19Jan2021, she started having "burning in her lungs" then the day prior reporting, on 20Jan2021 was a vigorous day at work and she had discomfort in her chest versus (vs) the burning." She stated that at the time of the report (21Jan2021), she was working at home and while the chest discomfort had subsided, the burning was back. The patient was asking if this was normal or expected and she didn't call her doctor; she was asking what should she do. The patient further reported that she did have some common side effects and the some of them were the normal ones such as: fatigue, chills, and feeling cold for a few days. The patient further reported that all over body coldness occurred at 7:30 AM on 14Jan2021; she noticed it shortly after she woke up. She actually noticed it after drinking coffee and then it was like the coldness kicked in. It would get worse as she drank things. It did not matter if it was hot or cold things. It was like the hot things intensified the cold feeling. At the time of the report she was having more concerning symptoms. On Tuesday (19Jan2021), she started to have burning in her lungs and the day prior reporting (20Jan2021) at work, she had chest discomfort. It was a little busy day at work running around on the floor. The chest discomfort was nothing significant, but it was a discomfort, especially on the left side. She confirmed she did not have that discomfort at the time of the report. However, she was having the burning again. She was having concerns and wanted to speak to someone about this. She went on to explain she noticed the fatigue during the night on the day she got the vaccine. It resolved around 16Jan2021. She added she had all over body coldness. She confirmed this was the same as the chills and feeling cold. This feeling comes and goes. She added, it was also winter so it was really hard to tell what it was from. The first two days, she had this chills, cold feeling for two days straight. However, at the time of the report it was better. The chest discomfort started the day prior reporting; however, she was doing a lot of activity and she did not have it today. At the time of the report, she was sitting all day working from home. However, the burning was back. The adverse events did not require any visit to an emergency room or a physician office. She stated she thought about calling the doctor's office, but she had not called them yet. She knew they probably won't be able to help or tell her anything. The patient had no investigation assessment and no relevant test. The patient recovered from the event "fatigue" on 16Jan2021; she was recovering from the events "coldness/ all over body coldness and chills," she was not recovered from the event "burning in her lungs," while the outcome of the events "discomfort in her chest vs the burning/ chest discomfort /while the chest discomfort had subsided the burning was back" was unknown.

Other Meds: TRAZODONE

Current Illness:

ID: 1004280
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: loud noise in ear, that comes and goes; This is a spontaneous report from a non-contactable consumer (patient). This female patient of an unspecified age (age: 55, unit: unknown) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date unknown), via an unspecified route of administration on 20Jan2021 17:00 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced loud noise in ear, that comes and goes on 21Jan2021 10:00 with outcome of unknown. The reporter wanted to know if this has been reported before and wanting guidance. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1004281
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: chills; nausea; It goes from mild then goes to a point where she feels really tired; This is a spontaneous report from a non-contactable nurse. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date: unknown), via an unspecified route of administration, on 13Jan2021, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date in Jan2021, after receiving the first dose of the vaccine, the patient experienced chills and nausea. The event nausea does not go away. It was mild then it goes to a point where she felt really tired. The patient wanted to know if it is normal for her nausea to last for 7 days. Outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1004282
Sex: M
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: Chills; headache; fever; body aches; This is a spontaneous report from a contactable other Healthcare professional reporting for himself. A 33-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL1283), via an unspecified route of administration on 20Jan2021 10:00 at SINGLE DOSE (left arm) for covid-19 immunisation. The patient medical history and concomitant medications were not reported. No other vaccines were taken in four weeks. Patient did not have COVID-19 prior vaccination and patient was not tested for COVID-19 post vaccination. The patient previously look the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE (Lot number: Ek5730) on 28Dec2020, 10:00 AM, left arm for covid-19 immunisation. The patient experienced chills, headache, fever, body aches on 20Jan2021 22:00. Treatment was not given. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1004283
Sex: M
Age:
State: MA

Vax Date: 01/16/2021
Onset Date: 01/17/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Extreme fatigue; Heavy and achy legs; Heavy and achy legs; Headache; No appetite; Nausea; Lethargic; Injection site pain; This is a spontaneous report received from a contactable consumer (patient). A 49-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284), via an unspecified route of administration in the left arm, on 16Jan2021 17:15, at single dose, for COVID-19 immunization, at the hospital. There were no medical history and no known allergies. The patient did not have COVID-19 prior to vaccination. Concomitant medication included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL). The patient did not receive other vaccines in four weeks. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231, expiry date unknown), via an unspecified route of administration in the left arm, on 28Dec2020 16:45, for COVID-19 immunization. The patient did not test for COVID-19 post vaccination. On 17Jan2021 at 08:00, the patient experienced extreme fatigue, heavy and achy legs, headache, no appetite, nausea, lethargic and injection site pain. No treatment was provided for the events. The outcome of the events was resolved on an unspecified date.

Other Meds: ADDERALL

Current Illness:

ID: 1004284
Sex: F
Age:
State: KS

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

Lab Data: Test Date: 20210121; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Headache; Body aches; This is a spontaneous report from a contactable nurse. A 38-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number and expiration date not reported) intramuscular on 20Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received vaccine (unspecified Pfizer vaccine) on 30Dec2020 within 4 weeks prior to the COVID vaccine. On 20Jan2021 the patient experienced headache and body aches. No treatment was received for the events. Post vaccination, the patient has been tested for COVID-19 (Nasal swab) on 21Jan2021, test result was negative. Patient was not pregnant. The facility where the vaccine was administered was in a Nursing Home/Senior Living Facility. Prior to vaccination, the patient was not diagnosed with COVID-19. Outcome of the events was recovering. Information on lot number/batch number was requested.

Other Meds:

Current Illness:

ID: 1004285
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: chills; body aches; Miss dosed, I reportedly received 0.3 mL of the UNDILUTED vaccine.; Miss dosed, I reportedly received 0.3 mL of the UNDILUTED vaccine.; myalgias; fatigue; headache; fevers/feverish; This is a spontaneous report from two contactable healthcare professionals (one is the patient). A 27-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL8982, expiry date: 31May2021), via an unspecified route of administration on 20Jan2021 07:30 AM at 0.3 mL, single (0.3 mL of the undiluted vaccine) on the right arm for COVID-19 immunization (reported as "frontline worker"). Patient is not pregnant. There were no medical history. Patient did not have COVID prior vaccination. Patient has no known allergies. Concomitant medication included ethinylestradiol, ferrous fumarate, norethisterone acetate (LO LOESTRIN FE). Vaccine facility type is hospital. No other vaccine in 4 weeks. The patient reported "Miss dosed, I reportedly received 0.3 mL of the UNDILUTED vaccine", she given an undiluted dose of 0.3 on 20Jan2021. The patient had been experiencing some expected symptoms such as fevers, chills, myalgias, fatigue, headache. No treatment was received for the events. It was further reported that one of the nurses gave an undiluted dose of Pfizer 0.3 to an employee (patient). He has filled out the VAERS. The patient was fine. She has experienced normal post vaccination symptoms. She has had chills, body aches on 21Jan2021 and was feverish in Jan2021. They asked "what to do from here? Does she need the second dose?" Patient was told to take Advil, hydrate and rest. The reporter also asked "Have their been any other issues like this? Has this happened before?". Patient did not have a prescribing doctor. It was just an employee vaccination. The nurse who administered it, thought it was already diluted. It was a fresh vial just opened and undiluted, but she thought it was just the last dose in a vial. So she drew up 0.3. It was a miscommunication. Patient got the vaccine at 7:30 am yesterday (20Jan2021). They found this out later because the inventory did not add up. There was an extra vial, but less people were vaccinated. The nurse thought it was diluted already. They called the patient late in the afternoon yesterday around 5:30 or 6 o'clock. She said she was fine. Then, this morning she relayed to her supervisor that she was experiencing normal vaccination side effects. He was looking for more information before he called her again today to check on her. The patient is was a Physician assistant, so she was aware of what to do. She was told yesterday to take NSAID or Ibuprofen. The reporter does not know the seriousness of the events until he gets more information. He does feel like the side effects she was having were normal. Compared to what others have reported. Patient is a front line health care worker. She did work in the ICU during the beginning of the pandemic. She has no listed allergies. She was fully vaccinated because she was a healthcare worker. She has her HepB and MMR vaccines. Outcome of the events chills, body aches and feverish was not recovered (reported as ongoing), for "Miss dosed, I reportedly received 0.3 mL of the UNDILUTED vaccine" was unknown while for other events was recovering. Patient was not tested for COVID post vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021064350 Pfizer

Other Meds: LO LOESTRIN FE

Current Illness:

ID: 1004286
Sex: F
Age:
State: RI

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

Lab Data: Test Date: 20210118; Test Name: Blood Pressure; Result Unstructured Data: Test Result:much higher; Comments: blood pressure was much higher than normal; Test Date: 20210113; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210116; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: feeling tired but also edgy; edgy/ nervous; anxious; unable to focus; headaches; blood pressure was much higher than normal; This is a spontaneous report from a contactable nurse (patient). A 61-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL1284) via an unspecified route of administration on the left arm on 11Jan2021 10:30 at a single dose for COVID-19 immunization. Medical history included hypothyroidism and back pain. Concomitant medication included levothyroxine sodium (SYNTHROID), ibuprofen and ergocalciferol (VIT D). The patient previously received 1st dose of BNT162B2 on 20Dec2020 for COVID-19 immunization (left arm, lot number: EH9899). After receiving second dose on 11Jan2021 the patient was feeling tired but also edgy, nervous, anxious, unable to focus, some headaches. Discovered 18Jan2021 that blood pressure was much higher than normal and associated with the way I was feeling. Had to go to primary care to have medication prescribed. The events resulted to a doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of the events. Patient was not pregnant. No known allergies. The facility where the vaccine was administered was in a workplace clinic. 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. Post vaccination, the patient has been tested for COVID-19 (Nasal swab), on 13Jan2021 and 16Jan2021 both test results were negative. Outcome of the events was not recovered.

Other Meds: SYNTHROID; IBUPROFEN; VIT D

Current Illness:

ID: 1004287
Sex: F
Age:
State: TN

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

Lab Data:

Allergies:

Symptoms: having a rash all over her body; This is a spontaneous report from a contactable physician (patient). A 37-year-old female patient received the second dose of bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Lot number: Unknown), via an unspecified route of administration on 19Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient is not pregnant at the time of vaccination. Historical vaccine includes first dose of bnt162b2 on an unspecified date for COVID-19 immunization. The patient experienced having a rash all over her body on 20Jan2021. The outcome of the event was unknown. Information on lot and batch number has been requested.

Other Meds:

Current Illness:

ID: 1004288
Sex: M
Age:
State: FL

Vax Date: 01/19/2021
Onset Date: 01/21/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fatigued and tired; weak; This is a spontaneous report from a contactable consumer (patient's wife). A 63-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982), via an unspecified route of administration (arm) on 19Jan2021 at single dose for Covid-19 immunization (also reported as Covid protection). The patient has no medical history. The patient's concomitant medications were not reported. The reporter confirmed that the patient does take other medications, but they never make him tired or weak. The reporter also confirmed that the patient did not receive any other vaccines on the same day as the COVID vaccine. It was reported that the patient took the Covid 19 vaccine on Tuesday (19Jan2021). The patient was fatigued and tired on 21Jan2021. It was further reported that the patient was tired and weak on 21Jan2021. The reporter added that that she knows tiredness and weakness are known side effects of the product, but she wanted to know how long after they get the vaccine those side effects last, and to what degree do they occur. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 1004289
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: her arm where she had the vaccine is still sore and tingling; her arm where she had the vaccine is still sore and tingling; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration into the arm on Jan2021 at a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that the patient's arm where she had the vaccine was still sore and tingling on an unspecified date. Outcome of events was unknown. Information about Lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 1004290
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: his shoulder hurt when he received the vaccine because of the needle; This is a spontaneous report from a non-contactable consumer (patient himself) via Medical Information team. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EL3302, expiration date was unknown), via an unspecified route of administration on 20Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that his shoulder hurt when he received the vaccine because of the needle on 20Jan2021, but no other symptoms. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1004291
Sex: F
Age:
State: OK

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

Lab Data:

Allergies:

Symptoms: Left side Swollen Lymph nodes was reported as worsned.; Left Forearm hurting and swelling; forearm hurts super bad; the lymph nodes were really tender, she would push it and it would hurt; lymph nodes on her arms got swollen to softball size/ Left side Swollen Lymph nodes/ the lymph nodes getting bigger; This is a spontaneous report from a contactable consumer reporting for herself. A 26-years-old female patient received the second 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 19Jan2021 at a SINGLE DOSE for covid-19 immunisation. Medical history was reported as none. Concomitant medication included etonogestrel (NEXPLANON) for contraceptive implant. The patient received the first dose of BNT162B2 on 29Dec2020. The patient reported a side effect from receiving the vaccine, lymph nodes on her arms got swollen to "softball size" since 19Jan2021 when she received the second dose of the vaccine and wants to know if this was normal. She understands that the arm was going to hurt, but she was noticing that her forearm hurts super bad and it a bit swollen, just on the side of the forearm its swollen, but under that arm her lymph nodes are swollen, she can barely pick up the arm and it just hurts on 20Jan2021. She noticed yesterday (19Jan2021), the lymph nodes were really tender, she would push it and it would hurt. Then when she got home from work, she lifted the arm to look at it, and she could see the swollen lymph nodes, the longer she kept the arm up, she could see the lymph nodes getting bigger. She wants to know how long this will last. She was talking to her mom and she was freaking out saying that people are dying from covid and the swollen lymph nodes, and that's why she has called today. She also stated that her left side swollen lymph nodes was worsened on an unspecified date. The outcome of the event swollen lymph nodes was not recovered, left forearm hurting and swelling and forearm hurts super bad was recovering while other events were unknown. Information on the Lot/Batch number has been requested.

Other Meds: NEXPLANON

Current Illness:

ID: 1004292
Sex: F
Age:
State: SC

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

Lab Data:

Allergies:

Symptoms: cough; injection site pain; headache; muscle pains; joint pain; fever, but not a high fever; nausea; feeling freezing cold; chills; ache; cold; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3246), via an unspecified route of administration at left arm on 19Jan2021 08:15 at a single dose for COVID-19 immunization. She was sick (COVID symptoms) all Dec2020 when she was with her sister who had COVID-19. She does not know for sure that she had COVID 19 because she was never tested. She recovered from that illness about two weeks before getting the Pfizer COVID 19 vaccine first dose. The cough was all gone before she had the Pfizer COVID 19 vaccine. No prior vaccinations (within 4 weeks). There were no concomitant medications. The patient had the vaccine on 19Jan2021, two days ago and had not had a problem. She left there and went to the gym for 1 hour afterwards. Then yesterday morning she woke up and has been sick ever since with a cough and chills. She never tested positive for COVID but she was with her sister who had it during Dec2020. She had a cough similar to the one she had in Dec2020 when she was quarantined for COVID symptoms. She was not expecting anything, but it says you can have side effects if you have had COVID-19 so she was calling in about that. On 20Jan2021 she woke up at 02:00 in the morning with a cough; injection site pain which was not sore before; headache; muscle pains, chills; joint pain; fever, but not a high fever; feeling freezing cold; and nausea. She reported 'cold, chills, fever, ache'. She felt a little bit better today on 21Jan2021. She was scheduled to receive the second dose on 15Feb2021 at 08:15. The patient would like to know whether her history of COVID symptoms from Dec2020 may have aggravated her post-vaccination symptoms. The patient would like to know whether there have been other reports of similar post-vaccination as hers. The outcome of the events cough, injection site pain, headache, fever and feeling freezing cold was recovering; event muscle pain, joint pain and nausea was not recovered; event chills was recovered on 21Jan2021; and unknown for the other events.

Other Meds:

Current Illness:

ID: 1004293
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: 24 hours later I came down with diarrhea; This is a spontaneous report from a non-contactable consumer reporting for herself. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on 20Jan2021 11:00 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated, "I had the vaccine yesterday morning at 11 o'clock, and 24 hours later I came down with diarrhea (21Jan2021). How long will it last? Okay... other than contacting the doctor, do you have Diet recommendations? I haven't eaten anything." The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1004294
Sex: U
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: Severe forehead and scalp itching 1h after vaccination; This is a spontaneous report from a contactable pharmacist. A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had severe forehead and scalp itching, 1 hour after vaccination. The pharmacist gave the patient Benadryl and it cleared up. The pharmacist followed up with the patient and the patient was not having any more issues. He just wanted to know if the patient should get the second dose after the event. The outcome of the event was recovered on unspecified date.Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004295
Sex: F
Age:
State: WI

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

Lab Data:

Allergies:

Symptoms: Hives; itching; shortness of breath; chest tightness; severe hip and low back pain; severe hip and low back pain; headache; concomitant medications included mercaptopurine; concomitant medications included mercaptopurine; This is a spontaneous report from a contactable nurse (patient). A 28-year-old female patient (not pregnant) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283), intramuscular at right arm on 19Jan2021 at 15:00 at single dose for COVID-19 immunization. The patient medical history included Crohn's disease from an unknown date and unknown if ongoing. The patient's concomitant medications included mercaptopurine, mirtazapine (REMERON), sertraline hydrochloride (ZOLOFT), cetirizine hydrochloride (ZYRTEC). The patient previously took ADDERALL, HUMIRA and REMICADE and experienced allergies. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284), intramuscular at right arm on 30Dec2020 at 15:45 at single dose for COVID-19 immunization. On 20Jan2021 at 06:00, the patient experienced hives, itching, shortness of breath, chest tightness, severe hip and low back pain and headache. Therapeutic measures were taken as a result of the events and included treatment with diphenhydramine, EPI PEN, TORADOL, acetaminophen, DECADRON, DILAUDID. The patient outcome of the events was resolved with sequel.

Other Meds: MERCAPTOPURINE; REMERON; ZOLOFT; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness: Crohn's disease

ID: 1004296
Sex: F
Age:
State: LA

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

Lab Data:

Allergies:

Symptoms: swelling of tongue and mouth; swelling of tongue and mouth; Trouble swallowing normally; dizzy; seeing stars; This is a spontaneous report from a contactable consumer (the patient). A 70-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number EL8982), via an unspecified route of administration in the left arm on 21Jan2021 (at the age of 70-years-old) as a single dose for COVID-19 immunization. Medical history included allergies when growing up: food allergies, allergic to pollens, allergic to iodine. The patient took allergy shots for years. The patient did not have trouble very often anymore. The patient stated she was healthy. The patient did not have COVID prior to vaccination. The patient was not pregnant at the time of vaccination. Concomitant medication included: clarithromycin (CLARITIN). The patient had not received any other vaccine within 4 weeks prior to the vaccine. On 21Jan2021, the patient experienced a little swelling of tongue and mouth, trouble swallowing normally, and dizzy and seeing stars. For treatment of these events, the patient took diphenhydramine hydrochloride (BENADRYL). The clinical outcome a little swelling of tongue and mouth, trouble swallowing normally, and dizzy and seeing stars was recovered on an unspecified date in Jan2021. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds: CLARITIN [CLARITHROMYCIN]

Current Illness:

ID: 1004297
Sex: M
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: Severe headache; nausea; dry mouth; chills without fever; This is a spontaneous report from a contactable pharmacist. A 50-year-old male patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL3246), intramuscular on 19Jan2021 on the right arm at a single dose for COVID-19 immunization. The patient had no relevant medical history and no known allergies. The patient's concomitant medications were not reported. It was unknown if the patient had COVID-19 prior to vaccination. It was unknown if the patient had other vaccines within 4 weeks prior to the COVID vaccine. The patient has not been tested for COVID-19 post vaccination. It was reported that the patient experienced severe headache, nausea, dry mouth and chills without fever all on 20Jan2021. Treatment for the events was acetaminophen and diphenhydramine. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1004298
Sex: F
Age:
State:

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

Lab Data: Test Name: BP; Result Unstructured Data: Test Result:fine; Test Name: Pulse ox; Result Unstructured Data: Test Result:fine; Test Name: Weight; Result Unstructured Data: Test Result:99 lbs

Allergies:

Symptoms: headache; nauseated; achy; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age (reported as 73 [unit unspecified]) received her first dose of bnt162b2 (BNT162B2 reported as Pfizer-Biontech Covid-19 Vaccine; unknown lot number and expiration date), via an unspecified route of administration on 16Jan2021 at a single dose for covid-19 immunization. Medical history included SARS-Cov-2 from 09Dec2020 to an unknown date and IBS (irritable bowel syndrome). The patient's concomitant medications were not reported. The patient reported that she had the injection which was basically painless. The patient reported that she had headache, nauseated and achy on an unspecified date in Jan2021. The patient underwent lab tests and procedures which included blood pressure was fine, oxygen saturation (pulse ox) was fine, and weight was 99 lbs., all on an unspecified date. The outcome of the events was unknown. The following information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1004299
Sex: M
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Throwing up; This is a spontaneous report from a contactable consumer (patient's wife). A 91-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL3247), via an unspecified route of administration in left arm, on 21Jan2021 at 10:00, 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 the COVID-19 vaccine along with his wife this morning, at 10 AM. They were both monitored for 15 minutes post-vaccination (waited 15 minutes). Shortly after being home on 21Jan2021 (10 minutes after getting home), the patient started throwing up and seemed to be alright now. The patient's wife asked if she should be concerned and if this experience was reported as a side effect after vaccination; if the patient's vomiting is from the shot or not. The patient recovered from the event on 21Jan2021.

Other Meds:

Current Illness:

ID: 1004300
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Vertigo; Ataxia; This is a spontaneous report from a contactable other healthcare professional (patient herself). A 64-year-old female patient (not pregnant) received her first dose of bnt162b2 (BNT162B2 also reported as product COVID 19 vaccine brand Pfizer, lot EL3302), intramuscularly in the left arm on 20Jan2021 10:15 at SINGLE DOSE for Covid-19 vaccination. The patient's medical history was not reported. No known allergies. No Covid prior to vaccination. Concomitant medications included levothyroxine sodium (SYNTHROID), naproxen sodium (NAPROSYN), sertraline hydrochloride (ZOLOFT) and esomeprazole sodium (NEXIUM). The patient experienced vertigo and ataxia on 21Jan2021 08:30. No treatment was given. The outcome of events was recovering.

Other Meds: SYNTHROID; NAPROSYN [NAPROXEN SODIUM]; ZOLOFT; NEXIUM [ESOMEPRAZOLE SODIUM]

Current Illness:

ID: 1004301
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: bad headache; This is a spontaneous report from a contactable consumer (patient). A 22-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3248), via an unspecified route of administration at right arm on 20Jan2021 at a single dose for COVID-19 immunization The patient's medical history and concomitant medications were not reported. The patient is not pregnant at the time of vaccination. The patient had no other vaccine in four weeks. The patient was having a bad headache on unspecified date. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1004302
Sex: F
Age:
State: MN

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

Lab Data: Test Date: 20210120; Test Name: platelet count; Result Unstructured Data: Test Result:8,000; Comments: ITP with baseline platelet count of 60,000; Test Date: 20210120; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: admitted to hospital with platelet count of 8,000; petechiae; This is a spontaneous report from a contactable physician. A 60-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EL0140) via Intramuscular on 18Jan2021 into left arm at a single dose for covid-19 immunization. Medical history included hypothyroidism and neomycin allergies. The patient did not get covid prior vaccination. Concomitant medications included calcium, levothyroxine sodium (SYNTHROID), trazodone, tocopherol (VIT E) and no other vaccine in four weeks. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EL9261) via Intramuscular on 28Dec2020 into left arm at a single dose for covid-19 immunization. 24 hours after injection she developed petechiae and was admitted to hospital with platelet count of 8,000 on 20Jan2021 22:00, the patient has ITP with baseline platelet count of 60,000. All events lead to hospitalization for 5 days (PENDING CLARIFICATION) and received IgG and oral Dexamethas as treatment. On 20Jan2021, the patient did Sars Co V 2 RNA test via Nasal Swab and result negative. The outcome of the events was recovering.; Sender's Comments: Based on a close chronological association, a causal relationship between events petechiae and thrombocytopenia and BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) cannot be excluded. The case will be reevaluated should additional information become available. 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: CALCIUM; SYNTHROID; TRAZODONE; VIT E [TOCOPHEROL]

Current Illness:

ID: 1004303
Sex: M
Age:
State: NY

Vax Date: 01/17/2021
Onset Date: 01/18/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data: Test Date: 20210118; Test Name: temperature; Result Unstructured Data: Test Result:low grade

Allergies:

Symptoms: chills; body aches; low grade temperature; left axilla has become very swollen and painful; left axilla has become very swollen and painful; fluid accumulation in the subcutaneous tissue; This is a spontaneous report from a contactable physician (patient). A 43-year-old male patient received his second dose of bnt162b2 (BNT162B2 reported as Pfizer COVID 19; lot number: EL3247; expiration date: unknown), via an unspecified route of administration left arm on 17Jan2021 09:30 at a single dose for covid-19 immunization. Medical history included known penicillin allergies. The patient was not diagnosed with COVID prior vaccination. The patient's concomitant medications were none. The patient previously took sulfamethoxazole-trimethoprim (BACTRIM) but had allergies. The patient historically vaccine included first dose of bnt162b2 (BNT162B2 reported as Pfizer COVID 19; lot number: EL0140; expiration date: unknown) at the age of 43-year-old via an unspecified route of administration right arm on 29Dec2020 10:00 AM at a single dose for covid-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and any other medications the patient received within 2 weeks of vaccination. The patient received the vaccine in a hospital but 36 hours after the vaccine (18Jan2021), the patient developed chills, body aches and low-grade temperature. Then 48 hours later, her left axilla has become very swollen and painful. The pain has subsided but remains mild and swelling persists. The area seems to show fluid accumulation in the subcutaneous tissue but no erythema or e/o [evidence of (pending confirmation)] abscess infection noted. It's now been present for 4 days. The patient received treatment which included NSAIDs. The patient had not been COVID tested post vaccination. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1004304
Sex: F
Age:
State: KS

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

Lab Data: Test Date: 20210121; Test Name: Nasal Swab; Test Result: Negative ; Comments: covid test name post vaccination=Abbott POC

Allergies:

Symptoms: Headache; Chills; Fatigue; This is a spontaneous report from a contactable nurse. A 43-year-old female patient received the second dose of bnt162b2 (BNT162B2, lot number and expiry date were not reported), intramuscular, on 20Jan2021, at a single dose for COVID-19 immunization. The vaccine was administered at a nursing home/senior living facility. The patient was not pregnant at the time of vaccination. Medical history included COVID-19. The patient had covid prior to vaccination. Concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (BNT162B2, lot number and expiry date were not reported), on 30Dec2020 for COVID-19 immunization. The patient experienced headache, chills, fatigue on 21Jan2021. The patient was tested for COVID-19 post vaccination: Nasal Swab (covid test name post vaccination=Abbott POC) on 21Jan2021 with result of negative. No treatment was received for the reported events. Outcome of the events was recovering. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1004305
Sex: M
Age:
State: MT

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

Lab Data:

Allergies:

Symptoms: Very sore right arm; large lump in right armpit; This is a spontaneous report from a contactable other healthcare professional (HCP reported for self). A 47-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot EL3246, expiry date not reported), via an unspecified route of administration on 19Jan2021 at a single dose in the right arm for COVID-19 immunization. The patient had no medical history. The patient had no known allergies. The patient had no COVID prior to vaccination. Concomitant medications included vitamins nos (DAILY VITAMINS), and atorvastatin; both reported as other medications in two weeks. The patient received the first dose of BNT162B2 (brand: Pfizer, Lot: EK 9231, expiry date not reported), on 29Dec2020 at 08:00 PM in the left arm. The patient had no other vaccine in four weeks. On 21Jan2021 11:00 AM, the patient had very sore right arm after shot; and large lump in right armpit formed about 20 hours after 2nd dose (20Jan2021). The events were reported as non-serious and resulted in doctor or other healthcare professional office/clinic visit. It was unknown if treatments were received in related to the reported events. The patient was not tested for COVID post vaccination. The outcome of the events very sore right arm and large lump in right armpit was not recovered.

Other Meds: DAILY VITAMINS; ATORVASTATIN

Current Illness:

ID: 1004306
Sex: F
Age:
State: KS

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

Lab Data: Test Date: 20210121; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative; Comments: covid test name post vaccination=Abbott POC

Allergies:

Symptoms: Headache; Body aches; Swelling at site; This is a spontaneous report from a contactable nurse. A 59-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date: unknown) via an unspecified route of administration, on 20Jan2021, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 30Dec2020 for COVID-19 immunization. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the Nursing Home/Senior Living Facility. On 20Jan2021, the patient experienced headache, body aches and swelling at site. The patient did not receive treatment for the events. Outcome of the events was recovering. The patient underwent nasal swab on 21Jan2021 and showed a negative COVID test result. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1004307
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: vomiting after 48 hours of the second COVID-19 vaccination dose; This is a spontaneous report from a contactable consumer (parent of patient). This 35-year-old male patient received his second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unspecified date as single dose for COVID-19 immunisation. No medical history or concomitant medication was reported. The patient previously took COVID-19 vaccination dose 1. The patient experienced vomiting after 48 hours of the second COVID-19 vaccination dose on unspecified date. Outcome of event vomiting was unknown. Information on the Lot/Batch number has been requested

Other Meds:

Current Illness:

ID: 1004308
Sex: F
Age:
State: IL

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 02/05/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Joint pain for two weeks so far since second dose/started by aching then becomes extremely sore and then goes away in one day; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: EL1283, expiry: unknown), via an unspecified route of administration in the left arm on 08Jan2021 08:30 at a single dose for COVID-19 immunization on a hospital. Medical history included ADHD. The patient has no known allergies and no Covid prior to vaccination. The patient's concomitant medications were not reported. The patient had no other vaccine in four weeks. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: EK5730, expiry: unknown) on 18Dec2020 at 13:00 in the right arm for COVID-19 immunization. The patient experienced joint pain for two weeks so far since second dose (08Jan2021 09:30). It started in the left shoulder of the arm she received it in. That same day, it started in her knee on the left side, then went to both knees, moved to her right shoulder then left shoulder then to her right elbow for one day. Now it's her left shoulder again for one day. It started by aching then becomes extremely sore and then goes away in one day. The event was not treated. The patient was not tested for Covid post vaccination. The outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 1004309
Sex: F
Age:
State: KS

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

Lab Data:

Allergies:

Symptoms: Congestion; This is a spontaneous report from a nurse. An 88-year-old female patient received the second dose of bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Lot number: Unknown), intramuscular on 20Jan2021 at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. Historical vaccine includes first dose of bnt162b2 on 30Dec2020 at the age of 88 years for COVID-19 immunization. The patient experienced congestion (pending clarification) on 21Jan2021 13:00. Treatment was not received for the adverse event. The vaccine was administered in a Nursing Home/Senior Living Facility. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient has not been tested for COVID-19. The outcome of the event was recovering. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1004310
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: bilateral feet were numb and hands felt weak; bilateral feet were numb and hands felt weak; fatigued; This is a spontaneous report from a contactable Nurse (the patient). A 67-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EJ1685, expiration date unknown), intramuscularly in the left arm, on 28Dec2020 as a single dose for COVID-19 vaccination. Medical history was not reported. The patient's concomitant medications were not reported. The patient was not pregnant at the time of vaccination. It was unknown if the patient received any other vaccines within four weeks prior to the vaccination. On 28Dec2020 the patient experienced fatigue. On 29Dec2020 the patient states that her feet were numb bilaterally and her hands felt weak. The patient did not seek any medical attention and no treatment of the events was reported. The clinical outcome of fatigue, numbness of feet and weakness of hands was recovered (reported as "resolved entirely on its own") on an unspecified date.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm