VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

Total Manufacturer

Incidents per State

State Total
72,296
AK1,638
AL5,339
AR3,412
AS44
AZ13,316
CA58,147
CO11,002
CT7,824
DC1,626
DE1,670
FL36,235
FM3
GA13,429
GU82
HI2,195
IA4,332
ID2,473
IL19,261
IN22,568
KS4,284
KY6,945
LA4,714
MA13,886
MD11,901
ME2,997
MH8
MI17,865
MN11,345
MO8,919
MP30
MS2,676
MT2,147
NC15,401
ND1,273
NE2,732
NH2,859
NJ17,232
NM3,702
NV4,071
NY32,763
OH18,072
OK5,940
OR7,954
PA22,457
PR2,104
QM2
RI1,911
SC6,055
SD1,133
TN8,691
TX34,122
UT4,023
VA13,944
VI49
VT1,661
WA13,811
WI10,395
WV2,220
WY805
XB5
XL1
XV2

ID: 0957418
Sex: M
Age:
State:

Vax Date: 12/01/2020
Onset Date:
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Symptoms: exposed to covid; antibody test which also came back negative; This is a spontaneous report from a contactable physician. A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date were not reported), via an unspecified route of administration in Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that he was exposed to COVID, experienced no symptoms but had a rapid test that came back negative and the provider also did an antibody test which also came back negative. The patient asked if it was normal to have a negative IgG antibody test after being vaccinated with his first dose two weeks prior to reporting. Outcome of the events was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957419
Sex: M
Age:
State:

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

Vax Type:
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Symptom List:

Symptoms: having significant diarrhea intermittently; This is a spontaneous report from a non-contactable consumer. A male patient of unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced having significant diarrhea intermittently on an unspecified date and wanted to know if diarrhea is a common side effect of the vaccine. 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: 0957420
Sex: F
Age:
State: IA

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: Metallic taste (cold house key) 30-45 sec. middle of tongue, width 1-2 mm; Left lips went numb (upper and lower)/left tip of tongue numb; lower lip felt swollen again; left tip of tongue tingling; This is a spontaneous report from a contactable healthcare professional. A 41-year-old female patient received second dose (pending clarification) BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; lot number and expiration date: not reported), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. Medical history included known allergies. The patient is not pregnant. Concomitant medication included unspecified medications (the patient received medications within 2 weeks of vaccination). It was unknown if the patient was diagnosed with COVID-19 prior to vaccination and the patient had not been tested for COVID-19 since the vaccination. On 02Jan2021 10:30, the patient received first dose of COVID Pfizer vaccine. On 02Jan2021 11:00, the patient experienced "1st" tip of tongue numb, metallic taste, and lower left lip felt swollen. On an unspecified date, the patient experienced "2nd" (pending clarification) metallic taste (cold house key) 30-45 sec. middle of tongue, width 1-2 mm; left lips went numb (upper and lower); lower lip felt swollen again; and left tip of tongue numb and tingling, these tongue problems lasted for few days. The events resulted physician's clinic visit. The events were reported non-serious. Therapeutic measures were taken as a result of these events with injection 50 mg Benadryl left (L) thigh. The outcome of the events was recovered on an unspecified date. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0957421
Sex: F
Age:
State: IL

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/20/2021
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Vax Type:
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Symptoms: Muscle aches; fever; This is a spontaneous report from a contactable physician. A 50-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot numbers EL0140 and EK9231), first dose via an unspecified route of administration on the left arm on 19Dec2020 at 08:00 and then via an unspecified route of administration on the on second dose via an unspecified route of administration on the right arm at 08:30 at a single dose, all for Covid-19 vaccination. Patient medical history was not reported. The patient has known allergies. Concomitant medication included levothyroxine sodium (SYNTHROID). Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested. On 19Jan2021, The patient experienced muscle aches and fever. There was no treatment for the events. Outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: SYNTHROID

Current Illness:

ID: 0957422
Sex: F
Age:
State: CA

Vax Date: 12/21/2020
Onset Date: 12/26/2020
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Symptoms: currently lactating; currently lactating; Two swollen lymph nodes above left clavicle; This is a spontaneous report from a contactable other health professional. A 37-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular in the left arm, from 21Dec2020 08:45 at a SINGLE DOSE for covid-19 immunization. Medical history included currently lactating and penicillin allergy. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medication included fish oil, calcium and lecithin. The patient experienced two swollen lymph nodes above left clavicle on 26Dec2020. The patient underwent lab tests and procedures on 08Jan2021 which included nasal swab test with negative result. The outcome of event "two swollen lymph nodes above left clavicle" was not recovered whereas the outcome of other events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021027508 baby case

Other Meds: ; ;

Current Illness: Breast feeding

ID: 0957423
Sex: M
Age:
State:

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

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Symptoms: fever; Chills; Fatigue; had flu like symptoms; This is a spontaneous report from a non-contactable consumer (patient's wife). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were unknown), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On an unspecified date, the patient experienced fever, chills, fatigue and had flu like symptoms. Clinical outcome of the events was unknown. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0957424
Sex: U
Age:
State: CA

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

Vax Type:
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Symptoms: fatigue; flu like symptoms; This is a spontaneous report from a contactable nurse via Pfizer sales representative. A patient of unspecified age and gender 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 experienced fatigue and flu like symptoms on an unspecified date with outcome of unknown. The patient had to call in sick for days. That information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957425
Sex: M
Age:
State:

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

Vax Type:
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Symptoms: very little ache in the arm; This is a spontaneous report from a Pfizer-sponsored program from a contactable other healthcare professional (HCP). A male patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route single dose for COVID-19 immunization on unknown date. Medical history and concomitant medications were not reported. The patient experienced very little ache in the arm when he took the first dose. Action taken for BNT162B2 was not applicable. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957426
Sex: F
Age:
State:

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

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Symptoms: fever with temperature of 100.5; feel like I have the flu; freezing cold chills; nausea; not feeling well; swollen lymph nodes; poking under my arms. little bit to be irritated; more pain and discomfort under my arm/soreness on the arm; discomfort under my arm; This is a spontaneous report from a contactable consumer. A 53-year-old female patient received second dose of 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 was previously vaccination with first dose of BNT162B2 on unspecified date and experienced "soreness at reaction site, it was red and swollen. The patient got all but 1-2 regular small effects, fever with temperature of 100.5. The patient stated, "I feel like I have the flu, hit by a bus, freezing cold chills, nausea, not feeling well, swollen lymph nodes, poking under my arms, little bit to be irritated and on a scale of 1-10, it's a 4". The patient have more pain and discomfort under arm, soreness on the arm itself. On Saturday morning, the patient had all the other side effects. The patient has been taking 600-800mg of Tylenol for the events. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957427
Sex: F
Age:
State: CA

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Symptoms: sore left deltoid; mild muscle aches; mild neck/joint pain; mild neck/joint pain; tired; This is a spontaneous report from a contactable nurse. A 41-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: EL1283), via an unspecified route of administration in the left deltoid, on 09Jan2021 (at the age of 41-years-old) at a single dose for COVID-19 immunization. Medical history included hypertension (HTN) and COVID-19. The patient was not pregnant at the time of vaccination. The patient had no known allergies. Concomitant medications, taken within two weeks of vaccination, included amlodipine besilate (NORVASC), ascorbic acid (vitamin C; MANUFACTURER UNKNOWN), ergocalciferol (reported as: vitamin D; MANUFACTURER UNKNOWN), zinc (MANUFACTURER UNKNOWN), and magnesium (MANUFACTURER UNKNOWN). Other concomitant medications included unspecified daily multivitamins (MANUFACTURER UNKNOWN). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: EK5730), intramuscularly in left arm, on 19Dec2020 at 07:00 (at the age of 41-years-old) for COVID-19 immunization and experienced sore left deltoid (Day 1), body aches (Day 1), headache (HA) (Day 1, 2, & 3), all over body aches (Day 2), fatigue (Day 2, 3, & 4), chills (Day 2), myalgia/muscle ache (Day 3), all over joint pain (Day 3), lower/upper extremity (LUE) pain (Day 4), and muscle and bone pain (Day 4). The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient experienced sore left deltoid, mild muscle aches, mild neck/joint pain, and tired on 09Jan2021. The events were reported as non-serious. The events occurred on day 1 after vaccination and by day 2, the patient felt great with no side effects. Therapeutic measures were taken as a result of all of the events, which included paracetamol (TYLENOL) and ibuprofen (MOTRIN). The clinical outcome of sore left deltoid, mild muscle aches, mild neck/joint pain, and tired was recovered on 10Jan2021. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds: NORVASC; VITAMIN C [ASCORBIC ACID]; VITAMIN D [ERGOCALCIFEROL]; ;

Current Illness:

ID: 0957428
Sex: F
Age:
State: MO

Vax Date: 12/17/2020
Onset Date: 12/27/2020
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Symptoms: having symptoms, tested covid+(positive); having symptoms, tested covid+(positive); This is a spontaneous report from a contactable consumer (patient). This 57-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route, on 17Dec2020 at single dose for COVID-19 immunization. No relevant medical history and concomitant medications were provided. The patient started having symptoms on 23Dec2020 and she was tested for COVID 19 on 27Dec2020 and resulted positive. The outcome of the event was unknown. Information on the batch/lot number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021015240 Same patient/reporter, 2nd dose of drug, different AE

Other Meds:

Current Illness:

ID: 0957429
Sex: F
Age:
State: CO

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Symptoms: My hip feels sore and achy, but I only feel slight spasms when I put weight on it.; With the second dose I woke up the next morning feeling very fatigued; dry cough; dizziness/slight dizziness; an aching headache that felt heavy (4/10 pain)/slight headache (2/10 pain); muscle spasms in my hips, knees, shoulders, and jaw (7/10 pain).; muscle spasms in my hips, knees, shoulders, and jaw (7/10 pain).; This is a spontaneous report from a contactable healthcare professional (patient). This 26-year-old female patient (non-pregnant) received the second single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL1284) on 08Jan2021 at 16:45, in left arm, for COVID-19 immunization. Medical history included GERD, IBS, gastritis, asthma, anxiety/depression. The patient had known allergies to penicillin, cefalexin monohydrate (KEFLEX), lactose. The first dose of BNT162B2 vaccine (lot EH 9899) was given on 18Dec2020 at 16:00, in left arm and the patient experienced a sore throat for 3 hours, mild difficulty breathing, mild fever (99.1), fatigue and throbbing headache (6/10 pain). No other vaccine was given in 4 weeks. Concomitant medications included albuterol, pantoprazole, fluoxetine, cholestyramine. After the second dose of vaccine, the patient woke up on 09Jan2021 at 06:30 feeling very fatigued with a dry cough, dizziness, an aching headache that felt heavy (4/10 pain). Later in the day she started having muscle spasms in her hips, knees, shoulders and jaw (7/10 pain). These spasms felt like someone was stabbing her with an electric knife. Over the day the spasms settled into her right hip and knee. Paracetamol (TYLENOL) helped managing the pain and sleep helped the pain getting better. On 10Jan2021 the patient woke up with a slight headache (2/10 pain) and slight dizziness. Her hip felt sore and achy, but she only felt slight spasms when she put weight on it. The events were resolving at the time of report.

Other Meds: ALBUTEROL [SALBUTAMOL]; ; ; CHOLESTYRAMINE

Current Illness:

ID: 0957430
Sex: F
Age:
State: ID

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/20/2021
Hospital:

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Symptoms: Pregnant at the time of vaccination?: Yes;Pregnant at the time of vaccination?: Yes;Pregnant at the time of vaccination?: Yes; Dizziness;nausea;fever; This is a spontaneous report from a contactable nurse. This is the maternal report. A 38-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), intramuscular on 11Jan2021 14:30 at a single dose on right arm for COVID-19 immunization. Medical history included none. No allergies to medications, food, or other products. Concomitant medication included prenatal vitamins. The patient experienced dizziness, nausea, and fever on 12Jan2021 10:00. Treatment was not received for the events. The outcome of the events dizziness, nausea, and fever was recovering. The mother reported she became pregnant while taking bnt162b2 (Pregnant at the time of vaccination?: Yes). The events were assessed as non-serious. The mother was 24 Weeks (gestational period) pregnant at the onset of the event. The mother was due to deliver on 03May2021. Last menstrual date: 24Jul2020. Patient did not receive any other vaccines. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957431
Sex: F
Age:
State: CA

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Lab Data:

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Symptom List:

Symptoms: back ache; intense achy; rigors and chill; Could not sleep; second dose of BNT162B2 on 08Jan2021, first dose was given on 19Dec2020; This is a spontaneous report from a contactable physician (reported for herself). A 43-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: El3249), via an unspecified route of administration (left arm) on 08Jan2021 (10:00 AM) at single dose for Covid-19 immunization. The patient received the first dose of BNT162B2 on 19Dec2020 (10:00 AM). Medical history included Celiac disease and allergies to medications, food, or other products: Latex, salicylate, wheat (celiac). Concomitant medication included melatonin (MELATONIN). The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that at around 30 hours after second vaccine dose (09Jan2021, 05:00 PM), the patient experienced back ache. At 36 hours post vaccine she developed intense achy and rigors and chill that lasts about 6 hours. The patient could not sleep during that time (10pm-330am). The patient took Tylenol at 1:30am. The symptoms abruptly stopped and felt perfectly fine after. There was a treatment received for the adverse event. The outcome of events was recovered on an unspecified date. The patient has not been tested for COVID-19 since the vaccination. This case is non-serious.

Other Meds:

Current Illness:

ID: 0957432
Sex: F
Age:
State: IL

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
Manufacturer:
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Symptoms: body aches; fatigue; headache; This is a spontaneous report from a contactable nurse reporting for herself. A 35-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283), via an unspecified route of administration at left arm on 08Jan2021 14:30 at single dose for covid-19 immunization. The COVID-19 vaccine was administered at Hospital. Medical history included Seasonal allergies. Concomitant medications included omeprazole and Multivitamin. The patient historic vaccine included the first dose of BNT162B2 received on 18Dec2020 07:30 AM at Left arm for covid-19 immunization, 1st dose symptoms started about 4hrs after: Nausea, body aches, fatigue, severe headache-all lasting 3-4 days. The patient experienced on and off headaches, body aches, fatigue all starting around 18-20 hours post second injection on 09Jan2021 and lasting less than 48 hours. No treatment received for the events. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient was not been tested for COVID-19. The outcome of the events was recovered on an unknown date in Jan2021.

Other Meds:

Current Illness:

ID: 0957433
Sex: F
Age:
State: CA

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
Manufacturer:
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Symptoms: After 2nd dose myalgia body ache fever axillary lymph node swelling and pain dizziness nausea; After 2nd dose myalgia body ache fever axillary lymph node swelling and pain dizziness nausea; After 2nd dose myalgia body ache fever axillary lymph node swelling and pain dizziness nausea; After 2nd dose myalgia body ache fever axillary lymph node swelling and pain dizziness nausea; After 2nd dose myalgia body ache fever axillary lymph node swelling and pain dizziness nausea; After 2nd dose myalgia body ache fever axillary lymph node swelling and pain dizziness nausea; fatigue; This is a spontaneous report from a contactable nurse (patient). A 34-year-old female patient to received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0142 and expiration date not provided), via an unspecified route of administration (right arm) second dose on 08Jan2021 at single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medication included vitamin c [ascorbic acid]. The patient previously took Benzoyl peroxide and experienced allergies and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0142 and expiration date not provided) intramuscular (right arm) first dose on 18Dec2020 for Covid-19 immunization and experienced flu like symptoms for 48 hours plus bilateral cheek numbness for two weeks. On 08Jan2021, after the second dose the patient experienced myalgia body ache fever axillary lymph node swelling and pain dizziness nausea. This was day 4 post vaccine, still have severe dizziness and fatigue. On 04Jan2021, the patient underwent lab tests and procedure which includes Coronavir Pan 2019-NCOV, NAA with the result of Negative and Nasal Swab with the result of Negative. The patient did not receive any treatment for the events. The outcome of the events was not recovered. Facility where the most recent COVID-19 vaccine was administered in the Hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 Prior to vaccination.

Other Meds: VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 0957434
Sex: F
Age:
State: PA

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
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Symptoms: Tiredness; Headache; This is a spontaneous report from a contactable consumer. A 58-year-old non-pregnant female patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Jan2021 at 12:00 at single dose in left arm for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced tiredness and headache on 12Jan2021 at 16:00. The patient did not receive treatment for the events. It was unknown if the patient receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has been tested for COVID-19 with Nasal swab on an unspecified date since the vaccination, with unknown result. The outcome of the events was resolved in Jan2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957435
Sex: U
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List:

Symptoms: Lymph node swelling; This is a spontaneous report from a non-contactable consumer (patient) via a Pfizer sales representative. A patient of unspecified age and gender received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration, on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced lymph node swelling on an unspecified date. The clinical outcome of lymph node swelling was unknown. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0957436
Sex: F
Age:
State: MI

Vax Date: 01/10/2021
Onset Date: 01/10/2021
Rec V Date: 01/20/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Vax Site:

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Symptom List:

Symptoms: emesis; sweats; horrible headache; Extremely tired; chills; This is a spontaneous report from a contactable other health professional. A 54-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand: Pfizer, lot number: EL0142) via an unspecified route of administration at left arm on 10Jan2021 at a single dose (dose number: 2) for COVID-19 immunization. Medical history included allergies to cefaclor (CECLOR), azithromycin (ZITHROMAX Z-PACK, reported as z pack), pinapple, coconut. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications the patient received within 2 weeks of vaccination included warfarin sodium (JANTOVEN), sertiline, metformin (reported as metforman, to be clarified). Historical vaccination included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand: Pfizer, lot number: EK5730) intramuscularly at left arm on 20Dec2020 at 09:30 AM at a single dose (dose number: 1) for COVID-19 immunization and reported events included emesis within 40 minutes, upset stomach for 3 hours approx, sweating and headache, lasting about 4 hours. Facility where the most recent COVID-19 vaccine was administered was at hospital. The patient was not pregnant at the time of vaccination. After the 2nd shot, it was reported emesis within 40 minutes and lasting all day, extremely tired, horrible headache, sweats and chills. This lasted 36 hours. Start date of adverse event was reported as 10Jan2021 at 10:30 AM. No treatment received for the adverse events. The outcome of events was resolved in Jan2021. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Other Meds: JANTOVEN; ;

Current Illness:

ID: 0957437
Sex: M
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/20/2021
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Symptoms: Fever of up to 101.2 Fahrenheit; Chills; muscle soreness; This is a spontaneous report from a contactable other hcp (patient). A 60-years-old male patient received second dose of bnt162b2 (BNT162B2), via an unspecified route of administration on 12Jan2021 11:00 at SINGLE DOSE on Left arm for covid-19 immunisation. Medical history was none. The patient had no known allergies. Concomitant medication included ibuprofen (IBUPROFEN). The Historical Vaccine included product=COVID, brand=Pfizer, lot unknown=False, administration date=22Dec2020, administration time=10:30 AM, vaccine location=Left leg, dose number=1. The patient experienced fever of up to 101.2 fahrenheit, chills, muscle soreness on 12Jan2021 23:30. The patient underwent lab tests and procedures which included body temperature: 101.2 fahrenheit on 12Jan2021 23:30. No treatment was received. The event outcome was recovering. The events reported as non-serious. The patient was not diagnosed with COVID-19 Prior to vaccination. Since the vaccination, the patient had not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957438
Sex: M
Age:
State:

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Rec V Date: 01/20/2021
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Symptoms: Arm was sore after vaccine; This is a spontaneous report from a contactable consumer. This consumer reported for a 40-year-old male patient that received BNT162B2 (COVID vaccine), via an unspecified route of administration on unknown date at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Arm was sore after vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957439
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/20/2021
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Symptoms: injection site pain; headache; body aches; chills; joint pain; T 99.3; L axillary swollen lymph node; administration date=24Dec2020,dose number=1/administration date=11Jan2021, dose number=2; administration date=24Dec2020,dose number=1/administration date=11Jan2021, dose number=2; This is a spontaneous report from a contactable nurse reported for herself. The 48-year-old female patient (not pregnant) received second dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3248) , via an unspecified route of administration at left arm on 11Jan2021 16:15 at single dose for covid-19 immunisation. Medical history included none, had no allergies to medications, food, or other product. Concomitant medication included ethinylestradiol/norgestimate (ORTHO TRI-CYCLEN). Patient previously received first dose BNT162B2 ( lot number: EK5730) , via an unspecified route of administration at right arm on 24Dec2020 at 08:30Am at single dose for covid-19 immunisation. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 12Jan2021 04:00AM, 12hrs after 2nd dose injection she experienced injection site pain, headache, body aches, chills, joint pain, T 99.3, L(Left) axillary swollen lymph node; Symptom improvement with Tylenol and Ibuprofen. 48hrs later(14Jan2021)- all symptoms resolved except left axillary swollen lymph node. There is no covid prior vaccination. Patient had covid tested post vaccination, rapid antigen via nasal swab on 12Jan2021 with negative result. Treatment (Tylenol and Ibuprofen) were taken as a result of all events. Outcome of left axillary swollen lymph node was recovering, of injection site pain, headache, body aches, chills, joint pain, T 99.3 was recovered on 14Jan2021. Events were non-serious by reporter.

Other Meds: ORTHO TRI-CYCLEN

Current Illness:

ID: 0957440
Sex: F
Age:
State: VA

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/20/2021
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Symptoms: chills; Headache; muscle spasms; extreme weakness; body aches; fever; sinus congestion; This is a spontaneous report from a contactable consumer. A 53-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 09:45 at single dose for covid-19 immunisation. Medical history included hypertension (HTN), high cholesterol. Concomitant medication included lisinopril, levocetirizine dihydrochloride (EURO ZYSOL), ezetimibe (ZETIA) and stool softner. No other vaccines within 4 weeks prior to the COVID vaccine. No diagnosed with COVID-19 prior to vaccination. The patient experienced woke up with chills, headache, muscle spasms, extreme weakness, for 24 hours continued with body aches, fever, sinus congestion. Still have sinus congestion, all other symptoms ended in 24 hours from onset. Events onset date reported as 09Jan2021 01:00. No treatment received for the events. Outcome of events was recovered with sequelae. Since the vaccination the patient has not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds: ; EURO ZYSOL; ZETIA

Current Illness:

ID: 0957441
Sex: U
Age:
State: CA

Vax Date: 12/26/2020
Onset Date: 12/30/2020
Rec V Date: 01/20/2021
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Symptoms: tested + 9 days after dose #1; tested + 9 days after dose #1; exposed to Covid-19 four days after vaccination; This is a spontaneous report from a contactable patient. A patient of unknown age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on 26Dec2020 at single dose for COVID-19 immunisation. Medical history and concomitant medications were unknown. The patient was exposed to Covid-19 four days after vaccination and tested positive (+) nine days after dose 1 on 04Jan2021. The patient would like the advice for receiving the second dose. Outcome was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0957442
Sex: U
Age:
State:

Vax Date: 12/23/2020
Onset Date: 12/01/2020
Rec V Date: 01/20/2021
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Symptoms: Has been experiencing a dull headache since receiving the first dose; This is a spontaneous report from a contactable Other HCP. A patient (demographics unknown) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route, on 23Dec2020 for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. She has been experiencing a dull headache since receiving the first dose vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957443
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: ear infection; sinus infection; This is a spontaneous report from a contactable pharmacist (patient) received via the Pfizer Sales Representative. A female patient of unspecified age received pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) (PREVNAR 13), via an unspecified route of administration on an unspecified date at a single dose for immunization. Medical history included cochlear implants. Concomitant medications were not reported. The patient, who had cochlear implants, reported that she got an ear infection and then a sinus infection after her pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein). The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0957444
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: After he got his 2nd dose of the Covid-19 vaccine and his right axillary lymph nodes were swollen; This is a spontaneous report from a contactable pharmacist (patient). This pharmacist reported similar events for 2 patients. This is the second report out of 2 patients. This case is non-serious. The other case is serious, medically significant. A male patient of an unspecified age received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, 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. While reporting on another patient, the pharmacist also mentioned that after he got his 2nd dose of the Covid-19 vaccine and his right axillary lymph nodes were swollen. He said that it was not enough to report. He stated that a lot of people have reported it and it it was also reported during the clinical trials. The caller declined to complete a report on himself. The outcome of the event was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021018520 same reporter and drug/similar event/different patients

Other Meds:

Current Illness:

ID: 0957445
Sex: M
Age:
State: TX

Vax Date: 01/09/2021
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: arm pain; feeling a little more tired than normal; This is a spontaneous report from a non-contactable consumer (patient). A 4-decade-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 09Jan2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced arm pain and feeling a little more tired than normal on an unspecified date with outcome of not resolved at time reporting. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0957446
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: he felt feverish; had a headache; Fatigue; This is a spontaneous report from a contactable consumer. This consumer reported for a male patient that received the second 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 stated the reporter's husband has a family call weekly with his siblings. The reporter participated in the call on 10Jan2021. During that call, one of his sisters mentioned her son had a second COVID vaccination and had a mild reaction. Later in the conversation, it was clarified that it was the Pfizer vaccine. It was reported that the patient got the vaccine on 'Friday' (unspecified date); on the next day, he felt feverish, had a headache and fatigue and was better by Sunday. The events were resolving. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957447
Sex: F
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: sore throat; fever/low-grade fever; This is a spontaneous report from a contactable healthcare professional (patient) from a Pfizer-sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; batch/lot number and expiration date unknown), 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. The patient stated that she had the first vaccine last month (pending clarification) then experienced sore throat and fever. The patient mentioned, "I got the Pfizer vaccine on the sixth which is Wednesday (pending larification) and over the weekend before that, it was new year's eve we went camping, of course, we were outside but we had canopy because it was raining and there were people keep showing off but I never had any symptoms or I've never heard from anybody that they have symptoms but since I had a sore throat even before so like a week and a half now, but since I got the vaccine I had a low-grade fever." The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957448
Sex: F
Age:
State: GA

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: Swelling in the arm; This is a spontaneous report from a contactable nurse (patient) and a contactable consumer (patient's son). A 42-year-old female patient received pneumococcal 13-val conj vac (dipht crm197 protein) (reported as pneumonia vaccination), via an unspecified route of administration in 2012 at single dose for immunization. The patient medical history and concomitant medications were not reported. The patient stated she experienced swelling in the arm from a pneumonia vaccination, back in 2012, she had no lot number or expiry date of this vaccine. The outcome of the event was unknown. Pfizer is a marketing authorization holder of Pneumococcal 13-Val Conj Vac (Dipht CRM197 Protein) in the country of incidence or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of Pneumococcal 13-Val Conj Vac (Dipht CRM197 Protein) has submitted the same report to the regulatory authorities. No Follow-up attempts are needed, Information about lot/batch number cannot be obtained and no further information is expected.

Other Meds:

Current Illness:

ID: 0957449
Sex: F
Age:
State: MO

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/20/2021
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Symptoms: I'm exposed you know I do the testing at my office at school; Loss of taste; Loss of smell; Sneezing; This is a spontaneous report from a contactable nurse (patient). This 56-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot # not clarified, Expiry Date 30Apr2021) intramuscular at single dose in the deltoid on 08Jan2021 15:00 for Covid-19 immunisation. The patient medical history was not reported. Concomitant medications included unspecified several drugs. On 08Jan2021 22:00, the patient experienced loss of taste, loss of smell, sneezing with outcome of unknown. No treatment required. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 09Jan2021. Nurse stated: "I just wanted to know the Covid Vaccine would it have given me that symptoms I mean obviously I'm exposed you know I do the testing at my office at school." When probed for causality, Nurse stated, "No, I don't think it would be from the vaccine, probably you know just exposure." Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957450
Sex: U
Age:
State:

Vax Date: 01/09/2021
Onset Date: 01/01/2021
Rec V Date: 01/20/2021
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Symptoms: Fever; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date unknown), via an unspecified route of administration on 09Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) for COVID-19 immunization. The patient reported that got second dose of bnt162b2 yesterday (09Jan2021) and now the patient had fever in Jan2021, patient wanted to know if its okay to take paracetamol (TYLENOL) or fever reducer or no. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957451
Sex: F
Age:
State: AR

Vax Date: 01/07/2021
Onset Date: 01/08/2021
Rec V Date: 01/20/2021
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Symptoms: My arm is got really red but it's itchy; like skin allergy; I have a trouble hearing today as I am little congested; I have a trouble hearing today as I am little congested; My arm is got really red but it's itchy; like skin allergy; My arm is got really red but it's itchy; like skin allergy/ small red spot; This is a spontaneous report from a contactable Nurse. This 56-year-old female Nurse (patient) reported for herself that she received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL1284, Expiry Date: 30Apr2021) at single dose for COVID-19 immunization on 07Jan2021. Relevant history included blood pressure (abnormal). Relevant concomitant drug included Lisinopril 5 mg for blood pressure. The patient had the first BNT162B2 and she had no problems with this one. She had some side effects for this one, it's been 48 hours since she had the vaccine. On 08Jan2021, the patient had a very small red spot but its probably 6 inches long and probably 2 inches wide on 09Jan2021. Her arm was got really red, but it's itching almost like an skin allergy. Itching was much in the night. The patient want to know if it is okay to take Benadryl? The patient also had a trouble hearing on 09Jan2021 as she was little congested. The patient was taking Tylenol (not appropriately paraphrased and clarified). Outcome of events was unknown.

Other Meds:

Current Illness:

ID: 0957452
Sex: U
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/20/2021
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Symptoms: My eyes still very heavy and warm; My eyes still very heavy and warm; Dizzy; Started getting super super cold; Fever/101 fever; Heart was extremely fast; Blood pressure also went up; This is a spontaneous report from a contactable consumer (patient). This patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient got the vaccine yesterday and as soon as like not even about 12 minutes after patient had received the vaccine patient heart was extremely fast and blood pressure also went up. Patient stabilized like after 10 minutes 'signs were fine'. But then patient started getting super cold. Patient was extremely cold. The doctors monitored the patient at the hospital for a little bit but then they told the patient the best thing to do just go home rest and lay down which patient did .But the symptoms yesterday patient got a fever, it was 101 fever and then patient was fine so patient slept okay but this morning (09Jan2021) patient was not feeling better. Patient felt very dizzy. Patient did know the symptoms. But patient did not know if it is an allergic reaction to the vaccine. Patient eyes were still very heavy and warm and patient was again dizzy. Outcome of heart was extremely fast and blood pressure also went up was recovered on 08Jan2021, outcome of other events was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 0957453
Sex: F
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: Fever all the way up to 103.9.; Vomiting; My head hurt uncontrolled like it's excruciating pain in my head; Chills; Severe body aches; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received 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 had no relevant medical history. Concomitant medications were not reported. The patient reported she got the vaccine shot on Monday (unspecified date) and since Thursday night she had severe body aches. She have had the fever all the way up to 103.9. She have had fever for three days straight now (at reporting time). She had body aches, had been vomiting, head hurt uncontrolled like it's excruciating pain in head. She have chills. As treatment, the patient had taken Tylenol 500 mg, Ibuprofen is 200, NyQuil, Theraflu. The reporter stated, "I am a 'line person' (not clarified), I am a first responder." The patient wanted to know if for these symptoms it was recommended going to the doctor. Fever had not resolved, while outcome of other events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0957454
Sex: M
Age:
State: LA

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 01/20/2021
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Symptoms: I still have uncomfortable feeling in my arm/I was finally able to raise it above my head, my left arm, after two days but it was not comfortable to do it, it was painful; I have severe pain in my arm/it started hurting and then it continued to get worse and worse and it was severe; It was the worst pain I have ever had and I could not move my arm; It continued to get worse and that night I went to bed and I cannot sleep, it hurts so bad/I could not sleep on the right side or on a left side; This is a spontaneous report from a contactable consumer (patient). An 82-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date was not provided), via an unspecified route of administration (left arm) first dose on 30Dec2020 10:30 at single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated that I had the vaccine back a week and half ago on 30Dec2020 and was due to get the booster this month and wanted to report severe pain arm for two days. The patient stated that he had many vaccine (Unspecified Vaccine) over the years and have never had anything that hurts so bad after about six hours. The patient just wanted to know that was that normal. Consumer further stated, "I took the vaccine about 10:30 in the morning and about four hours later, it started getting sore but that thing was normal you know some vaccines (Unspecified Vaccine) do that but along with that it started hurting about four hours after the vaccine and it continued to get worse and that night I went to bed and I cannot sleep, it hurts so bad. The patient even have thoughts about getting up and go in to the emergency room. It was the worst pain I have ever had and I could not move my arm. I could not sleep on the right side or on a left side and all I did was take Tylenol as prescribed and that helped a little bit but not much but I did not go to the emergency room, I am not going to do that but I felt like it because it hurts so bad but I made it through the night and next day it continued to hurt really bad. I just keep taking Tylenol every four hours and that continued for two days and then finally I was able to raise my arm up above my head without little pain, it was discomfort, but it was not hurting so bad." The patient stated that the event started about two hours later it started, it started hurting and then it continued to get worse and worse and it was severe, that is the reason why I am calling that it was severe. I wanted a shot or morphine to relieve myself that how bad it was." (no clarified further). The patient stated that the vaccine was given in my left arm only about one inch below the top of my shoulder which I think that might have been the problem, I don't know if you can answer that or not but I have never received the vaccine or shot anywhere near that area, it is always three or four inches down in my muscle, on my arm either on left or right, this was given in my left arm but this was given almost in my joint I am wondering if that would cause pain." The patient stated it was given only one inch below the tip above shoulder may be that is causing so much pain." The patient just wanted to report the severe pain, that was for two whole days and then it was subsided and it lasted for four days and I still have uncomfortable feeling in my arm. I was finally able to raise it above my head, my left arm, after two days but it was not comfortable to do it, it was painful." The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0957455
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/20/2021
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Symptoms: Fever; My body is aching so bad; I can't walk; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 second dose on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Patient was having reaction to the vaccine, patient had fever, body was aching so bad, can't walk, going to the bathroom is so painful. Patient feel like need to go to the emergency room or don't know. The outcome of the events was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0957456
Sex: U
Age:
State:

Vax Date: 01/07/2021
Onset Date: 01/10/2021
Rec V Date: 01/20/2021
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Symptoms: My nasal passage got swollen and sore and puffy; My nasal passage got swollen and sore and puffy; upper lip little bit the same which seems to be a reaction from the vaccine; My nasal passage got swollen and sore and puffy and my upper lip little bit the same which seems to be a reaction from the vaccine; My nasal passage got swollen and sore and puffy and my upper lip little bit the same which seems to be a reaction from the vaccine; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration from 07Jan2021 to 07Jan2021 at a single dose for COVID-19 vaccination. It was reported by the patient that the nasal passage got swollen and sore and puffy and the upper lip little bit the same on unspecified dates. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0957457
Sex: F
Age:
State: VA

Vax Date: 01/09/2021
Onset Date: 01/01/2021
Rec V Date: 01/20/2021
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Symptoms: Mild headache; Weakness; Loose stools/diarrhea; it was hard for me to walk; stomach ache/stomach cramping; Fatigue; Some sweating in the middle of the night; some pain behind her eyes; Shoulder area is sore; This is a spontaneous report from a contactable consumer (patient herself). A 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EK4176), via an unspecified route of administration on 09Jan2021 11:00 in left arm at single dose for COVID-19 immunization. Patient take medications for mood and sleep with were very low doses. But she didn't have any medical problem. She took 10 mg of fluoxetine hydrochloride (PROZAC), 150 mg of bupropion hydrochloride (WELLBUTRIN) and 10 mg of doxepin for sleep. Yesterday after the vaccination towards the end of the day (09Jan2021 approximately 11 o' clock am), she developed a stomach ache about 5 pm and it went on throughout the night and she normally didn't have issues with her stomach. Maybe it was because she was hungry because she went ice skating with her son where they wore mask in the afternoon yesterday and she was feeling perfectly fine. But when she came home, she noticed her stomach started hurting at 5 pm and she wondered maybe it is because she was hungry. And after she ate it was still bothering her and then it got progressively worst in the middle of the night where it would wake her up periodically. But she was so fatigue that she was able to sleep still. But she noticed in the middle of the night that her stomach would wake her up because it was aching and cramping in the middle of the night. And then she also had some sweating in the middle of the night as well as some pain behind her eyes. And today (10Jan2021) she had some fatigue which she noticed was not usual, she had mild headache which she saw was a common side effect. And then in the morning (10Jan2021) some fatigue and weakness like when she walked to the bathroom it was hard for her to walk. And when she went to use the bathroom she had some loose stools which was not common for her unless at all she was sick or have eaten something that makes her stomach really sick which was very unusual for her. Her stomach was still hurting her, if she walked it will start getting cramped so she was sitting down. The only thing she toon this morning was 2 acetaminophen medicine tablets because she was having pain behind her eyes when she woke up. She was just going to say she had influenza type A and type B on several occasions. And these symptoms are similar to when she had type B influenza, which was not as difficult as type A. So this is, they seemed to be like a mild version of type B influenza which she had terrible stomach issues, diarrhea and fatigue and pain behind the eyes from type B influenza. She had not any sickness because she work from home and she had limited field contact. So, she hadn't had illness from past year now. Because she worked from home. She provided mental health counselling remotely. So, she didn't think it could be attributed from anything else. The left on arm which was up toward like shoulder area and it was sore but it was tolerable in Jan2021. Outcome of stomach ache/stomach cramping was not recovered, and outcome of other events were unknown.

Other Meds: PROZAC; WELLBUTRIN;

Current Illness:

ID: 0957458
Sex: U
Age:
State:

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 01/20/2021
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Symptoms: Spot on arm where I got the vaccine probably 4 days ago is continuing to increase in size and is red, swollen and hard; it's huge and it's purple and red and it feels like bee sting, it feels like an allergic reaction; purple and red; continuing to increase in size and it is red and swollen and hard now; Made me really, really sick like bedridden for 2 days; Spot on arm where I got the vaccine probably 4 days ago is continuing to increase in size and is red, swollen and hard; This is a spontaneous report from a contactable Other HCP (patient). An unknown age and gender patient received BNT162B2 (lot# unknown) on Jan2021 at single dose for COVID-19 immunization. Medical history and concomitant drug were not reported. Patient stated, "I just have a question, my Pfizer COVID Vaccine made me really, really sick like bedridden for 2 days which I am finding out is probably normal. But the spot on my arm where I got the vaccine, it was probably 4 days ago that I got it and it's continuing to increase in size and it is red and swollen and hard now. Like I am a Nurse Practitioner, this is not like a normal injection site reaction, it's huge and it's purple and red and it feels like bee sting, it feels like an allergic reaction, should I be concerned, do I need to go to the hospital?" Outcome of the event was unknown. Information on the lot/ batch number has been requested.; Sender's Comments: A causal association between BNT162B2 and the reported events cannot be excluded based on a compatible temporal relation between vaccination and onset of events. 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 RAs, Ethics Committees, and Investigators, as appropriate.

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Current Illness:

ID: 0957459
Sex: F
Age:
State: TN

Vax Date: 01/08/2021
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Rec V Date: 01/20/2021
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Symptoms: I have felt horrible; Every bone in my body ached except my eyebrows and eyelashes; I am so weak I have no energy; I can hardly walk; This is a spontaneous report from a contactable consumer (patient). An 82-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 at single dose for COVID-19 immunization. The patient medical history included autoimmune disease and "bad back", both from an unknown date and ongoing. The patient's concomitant medication included prednisone for autoimmune disease and tramadol 75 mg daily for back pain. On an unspecified date, the patient reported that: "I felt horrible, every bone in my body ached except my eyebrows and eyelashes, I am just wiped out when does this go away, I am so weak I have no energy, I can hardly walk". The patient underwent lab tests and procedures which included blood test: unknown result, on an unspecified date. The patient outcome of the events was unknown. The information on the batch number has been requested.

Other Meds: ;

Current Illness: Autoimmune disorder; Back disorder

ID: 0957460
Sex: U
Age:
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Rec V Date: 01/20/2021
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Symptoms: Have some swelling in my lymph node and one of my armpits and it is like going down the side of my body now; This is a spontaneous report from a contactable consumer (Patient). A patient of an unknown age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on unknown date (reported as the other day) as a single dose for COVID-19 immunization, lot number: EK9231. Medical history and concomitant medications were not provided. Patient stated that had some swelling in lymph node and one of armpits and it was like going down the side of patient's body at the time of the report. Patient wanted to know if this was a normal side effect or if was needed to see a doctor. Outcome of the event was unknown.

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Current Illness:

ID: 0957461
Sex: F
Age:
State: AR

Vax Date: 12/21/2020
Onset Date: 12/01/2020
Rec V Date: 01/20/2021
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Symptoms: Tested positive for Covid/had the (Covid) infection; Tested positive for Covid/had the (Covid) infection; Swollen lymph nodes under my right arm; This is a spontaneous report from a contactable nurse. This 42-year-old female nurse (patient) reported for herself that she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot#: nurse stated she thought she had a lot# it looked like EK5703), via unspecified route at right deltoid on 21Dec2020 at single dose for COVID-19 immunization. Medical history included blood pressure (patient had taken blood pressure medicine but hadn't taking currently because her blood pressure was being controlled). Concomitant medications included unspecified vitamins. Patient was tested positive for Covid on the 29Dec2020. She stated she didn't know about causality, she was saying no but she did have swollen lymph nodes under the right arm before getting sick (Dec2020), now she thought that might get from her vaccination but in her understanding she could get it from Covid so, she couldn't answer that, she tested positive, she didn't think it's from vaccination but her concern was because she had got the vaccination the first one then had the (Covid) infection and right now she should get the second one or not. Regarding treatment, patient stated she was taking methylprednisolone sodium succinate (SOLU-MEDROL) and salbutamol (ALBUTEROL) inhaler, taking over the counter Vitamin D3, Zinc and Vitamin C and acetylsalicylic acid (ASPIRIN). Patient reported she did go to the physician office/ emergency room. Outcome of events was unknown.; Sender's Comments: Based on the mechanism of action of BNT162B2 vaccine, it is unlikely the patient would have fully developed immunity for the vaccine to be effective, due to the number of days passed since the vaccine was given (8 days in this case). However, a causal relationship between events "Tested positive for Covid/had the (Covid) infection" (coded to Drug ineffective / COVID-19) and swollen lymph nodes and BNT162B2 vaccine cannot be completely 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.

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Current Illness:

ID: 0957462
Sex: F
Age:
State: RI

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Rec V Date: 01/20/2021
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Symptoms: my first one I had a lot of pain in my arm; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date at a single dose for covid-19 immunisation. Medical history was reported as none. The patient's concomitant medications were not reported. It was reported that when she received the first dose of BNT162B2, she had a lot of pain in her arm on an unspecified date. Outcome of event was unknown. Information on the lot/Batch number has been requested.

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Current Illness:

ID: 0957463
Sex: M
Age:
State: NH

Vax Date: 12/22/2020
Onset Date: 12/01/2020
Rec V Date: 01/20/2021
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Symptoms: simply had a sore arm at the injection site; This is a spontaneous report from a contactable physician reported for himself. A 59-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE brand: Pfizer, lot number: EL0140), via intramuscular at left arm on 22Dec2020, 10:00 AM at a single dose for COVID-19 immunisation. Facility of the most recent COVID-19 vaccine was administered in Nursing Home/Senior Living Facility. There were no allergies to medications, food, or other products reported, other medical history included: migraines, rosacea, overweight (not obese). Concomitant medication included (patient received within 2 weeks of vaccination) doxycycline, magnesium, vitamin d, sulfamethoxazole, trimethoprim (BACTRIM). Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. For the first 24 hours, patient simply had a sore arm at the injection site with the first vaccination. It was reported serious criteria as no, no results in death, no life threatening, not caused/prolonged hospitalization, no disabling/incapacitating, no congenital anomaly/birth defect. Prior to vaccination, the patient was not diagnosed with COVID-19, and since the vaccination, the patient had not been tested for COVID-19. Outcome of event was unknown. Patient received the second dose of BNT162B2 on 12Jan2021, 11:00 AM (refer to AER 2021028085).

Other Meds: ; ; VITAMIN D [COLECALCIFEROL]; BACTRIM

Current Illness:

ID: 0957464
Sex: F
Age:
State:

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Rec V Date: 01/20/2021
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Symptoms: congestion and runny nose; congestion and runny nose; This is a spontaneous report from a contactable consumer (reporting for herself). This consumer reported similar events for two patients (herself and her husband). This is the first of two reports. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration, on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced congestion and runny nose on an unspecified date. The clinical outcome of congestion and runny nose was unknown. The batch/lot number for the vaccine, BNT162B2, was not provided and has been requested during follow-up.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021042601 same drug/events/reporter, different patient

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Current Illness:

ID: 0957467
Sex: U
Age:
State: PA

Vax Date: 07/05/2011
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Rec V Date: 01/20/2021
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Symptoms: loss of vision in left eye; herpes zoster; Information has been received from a lawyer regarding a case in litigation referring to a patient (pt) of unknown age and gender. Information about concurrent condition, medical history and concomitant medication was not reported. On or about 05-JUL-2011 at the age of approximately 60 years old, the pt was vaccinated with zoster vaccine live (ZOSTAVAX) (strength, dose, lot#, expiration date and route unknown) for long-term prevention of shingles and zoster-related conditions. Subsequently, the pt was treated by a health care provider (reported as provider) for the following injuries resulting from zoster vaccine live (ZOSTAVAX) use: herpes zoster and loss of vision in left eye. The outcome of the events was not reported. Upon internal review, loss of vision in left eye was determined to be medically significant.

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Current Illness:

ID: 0957468
Sex: M
Age: 72
State: NJ

Vax Date: 10/12/2020
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Rec V Date: 01/20/2021
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Symptoms: pain in his neck; pain in his neck and shoulder on the right side; 3-4 days later a rash presented on the right side of his chest; This case was reported by a consumer and described the occurrence of neck pain in a 73-year-old male patient who received Herpes zoster (Shingrix) for prophylaxis. On 12th October 2020, the patient received the 1st dose of Shingrix. On an unknown date, less than a week after receiving Shingrix, the patient experienced neck pain, shoulder pain and rash. On an unknown date, the outcome of the neck pain, shoulder pain and rash were not recovered/not resolved. It was unknown if the reporter considered the neck pain, shoulder pain and rash to be related to Shingrix. Additional details were provided as follows: The patient received 1st dose of Shingrix in left arm. After receiving 1st dose of Shingrix, the patient experienced rash presented on the right side of his chest as well as pain in his neck and shoulder on the right side. The reporter did not consent to follow up.

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Current Illness:

ID: 0957469
Sex: F
Age:
State: NH

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/20/2021
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Symptoms: 8 week old infant received the PENTACEL but it was not mixed, the liquid part was given and not the powder with no adverse event; 8 week old infant received the PENTACEL but it was not mixed, the liquid part was given and not the powder with no adverse event; Initial information regarding this unsolicited valid non-serious case was received from a other health professional and transmitted to Sanofi on 12-Jan-2021. The case involved an 8 week old infant patient who received the DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] (DTap Lot Number: U6842BA, expiration Date: 05-Jul-2021, ACTHIB Lot Number: UJ336AA, expiration Date: 05-Jul-2021, Carton Lot Number: UJ336AAA, expiration Date :2021-07-05) via intramuscular route in the right thigh for prophylactic vaccination on 12-Jan-2021, but it was not mixed, the liquid part was given and not the powder (product administration error and product preparation issue). Relevant medical history, past medical treatment, vaccination details and family history were not provided. Concomitant medications included HEPATITIS B VACCINE; PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) and ROTAVIRUS VACCINE. It was a case of actual medication error due to product administration error and inappropriate reconstitution technique. At the time of reporting, no adverse event was reported. The reporter wanted to know the corrective measure to fix this and information about the patient next date to come. This suspected adverse reaction report was submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error was in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party had contributed to or was to be held liable for the occurrence of this medication error.

Other Meds: HEPATITIS B VACCINE; PREVNAR 13; ROTAVIRUS VACCINE

Current Illness:

Total 2021 VAERS Injuries: 599,999

Page last modified: 03 October 2021 5:28pm