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
92,076
AK1,880
AL6,345
AR4,151
AS46
AZ14,991
CA66,887
CO12,550
CT8,943
DC1,795
DE2,009
FL42,724
FM4
GA17,031
GU124
HI2,580
IA4,919
ID2,892
IL22,128
IN24,197
KS5,047
KY9,111
LA5,500
MA15,718
MD13,434
ME3,351
MH8
MI20,971
MN13,585
MO10,747
MP30
MS3,198
MT2,477
NC18,051
ND1,501
NE3,109
NH3,218
NJ20,216
NM4,218
NV4,728
NY37,667
OH20,793
OK6,692
OR9,244
PA25,607
PR2,588
QM2
RI2,163
SC7,261
SD1,282
TN10,445
TX39,890
UT4,618
VA15,980
VI67
VT1,830
WA16,071
WI12,042
WV2,571
WY926
XB5
XL1
XV2

ID: 1290788
Sex: F
Age:
State: SC

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

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: tiny bit of dizziness, felt like everything was going dark; This is a spontaneous report from a contactable Consumer. A 78-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL0140; Expiration Date: 31Mar2021) via intramuscular route administered in left deltoid on 14Jan2021 12:41 as single dose (0.3mL) for COVID-19 immunization. Medical history included atrial fibrillation and blood pressure high. She was on medication for this condition. The patient's concomitant medications were not reported. No prior vaccinations within 4 weeks. The patient experienced tiny bit of dizziness, felt like everything was going dark on 14Jan2021. Caller stated that she received the second COVID-19 vaccine. She was scheduled to receive her second vaccine and she doesn't know whether or not to do it. Caller explains she had the shot, and her facility had her wait 15 minutes. She didn't think much about it. She went to the bathroom to kill some time. It was about 1 minute until it was time to leave, and she was getting her husband gathered up so by the time they got to the door, she could probably leave. Very quickly she had this tiny bit of dizziness and it felt like everything was going dark. She states this episode was very quick and didn't last long at all. After that, she was totally fine. She doesn't know whether to have her second vaccine or not. No relevant tests done. The outcome of the event was recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Atrial fibrillation (Diagnosed at about 32 years of age); Blood pressure high (She was diagnosed maybe 15 years ago, but she might be years off. She doesn't really know. Her blood pressure is controlled.)

ID: 1290789
Sex: F
Age:
State: OH

Vax Date: 01/19/2021
Onset Date: 01/26/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Red lump 0.5 inches on anteromedial edge of axilla, Painful to touch and raise right arm; Red lump 0.5 inches on anteromedial edge of axilla, Painful to touch and raise right arm; Firm palpitation; This is a spontaneous report from a non-contactable other Health Professional (patient). A 30-year-old non pregnant female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: EK5730) via intramuscularly, administered in left arm on 19Jan2021 (at the age of 30-year-old) as single dose for covid-19 immunization. Medical history and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since vaccination, patient had not tested for COVID-19. The patient received first dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: unknown) on an unspecified date as a single dose for Covid-19 immunization. On 26Jan2021, the patient experienced red lump 0.5 inches on anteromedial edge of axilla, painful to touch and raise right arm and Firm palpitation. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1290790
Sex: F
Age:
State: TX

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: body rash/Rash was noted by caller on her right and left arms, back of her legs, entire abdomen and back/full body rash; This is a spontaneous report from a contactable consumer(patient) via medical information team. A 33-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: Unknown) via an unspecified route of administration on 25Jan2021 as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On unspecified date on Jan2021 at 14:00 about 48hrs after vaccination, the patient got body rash, her right and left arms, back of her legs, entire abdomen and back was full of body rash. The outcome of the event was unknown. Information about lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1290791
Sex: F
Age:
State: SC

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

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: back pain; legs, calves, feet extreme pain; cramping; extreme fatigue for 6 days and nights better 7th day; headache; This is a spontaneous report from a contactable consumer or other non-health care professional. A 75-years-old non-pregnant female patient received first dose of BNT162B2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EL3246; Expiration Date: unknown), via an unspecified route of administration, administered in Arm Left on 20Jan2021 10:15 as single dose for COVID-19 immunization. Medical history included chronic obstructive pulmonary disease, cardiac failure, atrial fibrillation, renal failure, rheumatoid arthritis, gastroesophageal reflux disease, irritable bowel syndrome, hypertension from an unknown date. Concomitant medications included apixaban (ELIQUIS), metoprolol, pravastatin sodium, indapamide for an unspecified indication. The patient previously took morphine and experienced drug hypersensitivity. Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. It was reported that patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. On Jan2021 at 7:00PM, the patient experienced back pain, legs, calves, feet extreme pain, cramping, extreme fatigue for 6 days and nights better 7th day, headache. The clinical outcome of the events was recovering. No follow-up attempts are possible, no information is required.

Other Meds: ELIQUIS; METOPROLOL; PRAVACHOL; INDAPAMIDE

Current Illness:

ID: 1290792
Sex: F
Age:
State: TX

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: Nausea; 20 hrs after second shot severe shaking chills; fever 103F; chest burning; severe headache; severe weakness; This is a spontaneous report from a contactable consumer (patient). A 63-year-old (non-pregnant) female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EL9262, Expiry date: unknown) via unspecified route of administration on right arm on 26Jan2021 as single dose for COVID-19 immunization. The patient medical history includes chronic lymphocytic leukemia, hypertension, type 2 diabetes, metastatic thyroid cancer, pulmonary metastases and allergic to Keflex and clindamycin. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL1263) in right arm on 07Jan2021 15:00 as single dose for COVID-19 immunization. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient was not tested for COVID. On 27Jan2021 at 03:00, 20 hours after second shot, the patient experienced severe shaking chills, fever 103F, chest burning, severe headache, severe weakness and nausea. The patient did not receive any treatment for the events. The outcome of events was recovering.

Other Meds:

Current Illness:

ID: 1290793
Sex: F
Age:
State: WA

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: rash on the upper part of my arm/Small rash circles, not red raised skincolor circles like a bunch of pea sizes circles or smaller; This is a spontaneous report from a contactable consumer (Patient). A 38-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL3247) via an unspecified route of administration on 26Jan2021 at 10:15 (at the age of 37-year-old), as single dose in right arm for COVID-19 immunisation at Doctor's office/urgent care. The patient's medical history included allergic to eggs, seasonal allergies and cats. Patient was not pregnant at the time of vaccination. Concomitant medication included multivitamin. The patient did not receive any other vaccines within four weeks prior to the COVID vaccination. On 27Jan2021 at 06:15, the patient woke up with a rash on the upper part of her arm. Small rash circles, not red raised skin colour, circles like a bunch of pea sizes circles or smaller. They did not itch, but they seemed to be closer to the injection site with less on the outer arm area. Patient continued to monitor. There was no treatment received for the adverse event. The patient had no COVID prior vaccination and was not tested COVID post vaccination. The clinical outcome of the event was not recovered. Follow-Up (15-Apr-2021): Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1290794
Sex: M
Age:
State: MA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Headache; This is a spontaneous report from a contactable consumer (reporting himself). A 53 -year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247), via an unspecified route of administration in left arm on 26Jan2021 at 12:00 as a single dose for COVID-19 immunization. Patient did not receive other vaccine in four weeks. The patient's concomitant medication included losartan, armodafinil, baby asprin, multivitamin. The patient was not diagnosed with COVID prior vaccination. On 26Jan2021 at 12:30, the patient experienced headache. The patient did not received treatment for the event. The outcome of the event was not recovered. Follow-up attempts are completed. No further information was expected.

Other Meds: LOSARTAN; BABY ASPIRIN

Current Illness:

ID: 1290795
Sex: F
Age:
State: TX

Vax Date: 01/22/2021
Onset Date: 01/24/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: temperature went up to 99; Feeling dragged out; This is a spontaneous report from a contactable consumer. A 72-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE,Lot number: not reported), dose 1 intramuscular, administered in Arm Left on 22Jan2021 at single dose for covid-19 immunisation. Medical history included ongoing atrial fibrillation diagnosed about 5 years ago. None Prior Vaccinations within 4 weeks. AE(s) following prior vaccinations: Sore arm with flu shot that she got in Sep2020, she does not know the name or have lot number to provide. Concomitant medication(s) included apixaban, 5mg tablet twice a day by mouth (ELIQUIS) metoprolol, 25mg tablet, half tablet once a day by mouth (METOPROLOL) and flecainide, 50mg, one tablet every twelve hours by mouth taken for atrial fibrillation. The patient experienced feeling dragged out on 24Jan2021, temperature went up to 99. The patient underwent lab tests and procedures which included body temperature: around 97 or 98 on, body temperature: up to 99 on 26Jan2021 little bit of temperature hike/usually temperature was around 97 or 98 and her temperature went up to 99. Additional Context included She was calling about the Pfizer first dose of covid shot. She was asking when you get a reaction from the shot, is it immediate or it does it take a while to have a reaction. She clarifies it is the Pfizer sars-cov2 vaccine. Her second dose was scheduled for 12Feb2021. She clarifies that she was not know if she has a sinus infection or a reaction to the shot since the symptoms are similar. She was felt dragged out for a couple of days, today she was feeling a little bit better but not 100%. She got the first dose on Friday afternoon and she did not have any problems right after receiving it. She had to wait there for 15 minutes after receiving the shot. Reports she started feeling dragged out Sunday night but it was not that bad and it started getting bad Monday afternoon, Yesterday was bad, and today she was a tiny bit better, but still feels dragged out. She had a little bit of temperature hike but nothing major, her usually temperature was around 97 or 98 and her temperature went up to 99 yesterday. The outcome of the event(Feeling abnormal) was recovering and event (Body temperature abnormal) was recovered on 27Jan2021. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds: ELIQUIS; METOPROLOL; FLECAINIDE

Current Illness: Atrial fibrillation (diagnosed about 5 years ago)

ID: 1290796
Sex: F
Age:
State: CA

Vax Date: 01/24/2021
Onset Date: 01/24/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: temperature of 99.8; lower back pain; severe headache; This is a spontaneous report from a contactable consumer (patient's husband). A 45-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, lot number: unknown) (Age at Time of Vaccination was 45 years) via unspecified route of administration on 24Jan2021 around 9-9:15 a.m. in the left arm as a single dose for COVID-19 immunization. There were no additional vaccines administered on same date of the Pfizer Suspect. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient's medical history and Concomitant medication was not reported. It was reported that on Sunday, the caller and his wife received the vaccine. He does not have any symptoms. However, his wife had a severe headache and feels like the veins in her head are getting inflamed. Caller wants to know was this kind of a normal side effect or does she need to go to the hospital. Caller stated that his wife also had a temperature of 9.8 degrees (later clarified as 99.8 degrees). Caller tried to call the doctor, but no one answered. Caller confirmed that his wife received her first vaccine Sunday, 24Jan2021. That same night, she had a headache. She took pills for the headache and the headache went away. Monday, 25Jan2021, she had a light headache. Yesterday afternoon (26Jan2021), she had a really bad headache. The pain was getting bigger, she felt more pain in her head. It was confirmed that his wife's temperature was checked yesterday morning and it was 99.8 degrees. Today, she just took it and her temperature has gone up to 100 degrees. It was stated that his wife was also noticing some pain in her lower back. This pain started on Monday and it was not as strong as the pain in her head, but she was starting to feel more discomfort. The patient did not visit emergency Room/Physician Office. The outcome of the events was not recovered/not resolved. Information about lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1290797
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Fatigue after 2nd dose for 1 day; This is a spontaneous report from contactable physician via Pfizer sales representative. This Physician (Patient) reported that an unspecified age and gender received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unknown date the patient experienced fatigue after 2nd dose for 1 day. The reporter stated that event took place after use of product. The clinical outcome of the event was recovered on an unknown date. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290798
Sex: M
Age:
State: NV

Vax Date: 01/26/2021
Onset Date: 01/28/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: have cold symptoms; Cough; Fever; Stuffiness/Congestion; This is a spontaneous report from a contactable consumer (Patient). A 40-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in left arm on 26Jan2021 at 15:00 (at the age of 40-years) as single dose for COVID-19 immunisation. Medical history included diabetes and hypertension. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included jardiance, atorvastatin, unspecified vitamins and some unspecified prebiotics. On 28Jan2021, the patient had cold symptoms, cough, stuffiness/congestion and fever. The patient did not receive treatment for the events. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was not recovered. The batch/lot number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds: JARDIANCE; ATORVASTATIN

Current Illness:

ID: 1290799
Sex: M
Age:
State: NC

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Continue to have a sore throat; a cold with massive amounts of mucous since injection.; tiredness; joint pain; arm pain; This is a spontaneous report from a contactable consumer (patient). A 66-years-old male patient received bnt162b2 (BNT162B2, solution for injection, Lot Number: EL3248), dose 1 via an unspecified route of administration at left arm on 27Jan2021 07:15 as single dose for covid-19 immunisation. Medical history included from an unknown date and unknown if ongoing. Concomitant medication(s) included Lisinopril 20 mg, Atorvastatin calcium 10 mg, Sildenafil 100 mg taken for an unspecified indication. Patient did not suffer any Allergies to medications, food, or other products. Prior to vaccination patient was not diagnosed with COVID-19. Even after vaccination, patient has not tested for COVID-19. On 27Jan2021 10:00 am, the patient experienced continue to have a sore throat and a cold with massive amounts of mucous since injection. Has subsided a bit, but it continues today. Also had usual side effects (joint pain, arm pain, tiredness, etc). The outcome of the event was not recovered. Follow-up attempts have been completed and no further information is expected.

Other Meds: LISINOPRIL; ATORVASTIN; SILDENAFIL

Current Illness:

ID: 1290800
Sex: F
Age:
State: NY

Vax Date: 01/27/2021
Onset Date: 01/28/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: felling of SOB with normal sat; dizziness; nausea; abd pian; elevated HR; headaches; body aches; sore throat; This is a spontaneous report from a contactable consumer. This 41-year-old female (Non pregnant) consumer (patient) reported that she received second dose of BNT162B2 (Pfizer-BIONTECH COVID-19 VACCINE, solution for injection, LOT: EL3302 Expiry date: unknown), via an Intramuscular route of administration in right arm on 27Jan2021 at 13:00, at a single dose for covid 19 immunization. Patient historical vaccine included she received first dose of BNT162B2 (Pfizer-BIONTECH COVID-19 VACCINE, solution for injection, LOT: EL0140, Expiry date: unknown), via an Intramuscular route of administration in right arm on 06Jan2021 at 12:00, at a single dose for covid 19 immunization. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient was not tested for COVID-19 since the post vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient's concomitant medications included Clonazepam, fiber, but vitamin D3 and medical history included that 'Botox' done on 20Jan21 for hemifacial spasms on right side of my face. Patient had no allergies. On 28Jan2021 05:00 after received the second dose the patient was feeling dizziness, nausea, abdominal pain, elevated HR, felling of SOB with normal sat, headaches and body aches, on 3rd day better but now with a sore throat, headaches and every some often heart rate going fast. Patient didn't take treatment for the events. The outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: CLONAZEPAM

Current Illness:

ID: 1290801
Sex: F
Age:
State: CA

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: dizzy; sensation of brief increased heart rate; Flu sx; nausea; This is a spontaneous report from a contactable nurse (patient herself). A 44-year-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL8982, Expiry Date: unknown) via intramuscular in the left arm on 25Jan2021 at 13:15 (at the age of 44-year-old) as a single dose for COVID-19 immunization. The patient medical history included asthma. The patient had no allergies to medications, food, or other products. Concomitant medication (within 2 weeks) included ascorbic acid (VIT C), ergocalciferol (VIT D), biotin, loratadine, calcium, silybum marianum (MILK THISTLE), paracetamol (TYLENOL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Past drug included Claritin (patient was premeditated 1 hour before the shot). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot number: EL1284, Expiry Date: unknown) via intramuscular in the left arm on 04Jan2021 at 13:30 as a single dose for Covid-19 immunization. After receiving her second dose of BNT162B2 on 25Jan2021 at 13:15, within five minutes the patient experienced dizzy with sensation of brief increased heart rate, MD on site was notified. The patient was provided with water and snacks and went home after 30 minutes observation as the symptoms resolved and on an unspecified date in Jan2021 (day2-3), the patient had Flu sx (flu symptoms), Dizzy spell on and off existed till day 5 and nausea was still ongoing. Patient did not received treatment for the events. The outcome for the events sensation of brief increased heart rate was recovered, Flu sx (flu symptoms) and dizzy was recovered with sequel (reported as recovered with lasting effects) on an unspecified date in Jan2021 and nausea was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: VIT C; VIT D; BIOTIN; LORATADINE; CALCIUM; MILK THISTLE; TYLENOL

Current Illness:

ID: 1290802
Sex: F
Age:
State:

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: feeling tired.; This is a spontaneous report from a Pfizer-sponsored program. A non-contactable female consumer (patient, self-reported). A female unspecified age received the first dose of dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date: unknown), via an unspecified route of administration, on 27Jan2021, as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unknown date, the patient did take a nap due to feeling tired, she had never called before. The patient stated that she was fine after the vaccination. 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: 1290803
Sex: F
Age:
State: MS

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: diarrhea; This is a spontaneous report from contactable consumer (patient) from a Pfizer-sponsored program. A female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number- UNKNOWN) via an unspecified route of administration on 26Jan2021 as single dose for COVID-19 immunization. The patients medical history and concomitant medications were not reported. On 27Jan2021, patient experienced diarrhea all day. The outcome of event was unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1290804
Sex: M
Age:
State: NM

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: body pain; This is a spontaneous report from a contactable consumer, the patient. A male patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date were not reported) via unspecified route on 27Jan2021 at single dose for covid-19 immunization. The patient took vaccine earlier morning. Medical history was not reported. The patients concomitant medications an OTC aspirin 81mg for blood thinner. The patient experienced body pain. Patient took tramadol 50mg, and naproxen 500mg for his body pain. The outcome of the event was unknown. Follow-up attempts have been completed and no further information is expected.

Other Meds: ASPIRIN

Current Illness:

ID: 1290805
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Headache; chills; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer reported for an 83-year-old female patient (Reporters mother) received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 20Jan2021, as SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. In Jan2021, after 2 or 3 days, the patient experienced headache and chills (non-serious events). The outcome of both the event was reported as unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1290806
Sex: F
Age:
State: CA

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: soar muscle at injection site; fatigue; This is a spontaneous report from a contactable other hcp. A 48-years-old female patient reported for herself that she received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number unknown) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated that she contacted initially for questions regarding the vaccine safety while on Dupixent shots for asthma and allergies, not to report side effects. She did not respond to first letter because that was not apply to her. patient clarified to 2nd letter, that she received both vaccines with no side effects at this time other than sore muscle at injection site and fatigue following 2nd vaccine which subside after a day or two. The outcome of events was reported as recovered. It was notified that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1290807
Sex: F
Age:
State: PA

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

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

Lab Data:

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: Arm pain; nausea; dizziness; aches; fever; This is a spontaneous report from a contactable nurse. A 45-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration, administered in right arm on 20Jan2021 17:30 (at the age of 45-year-old, Non-pregnant) (Lot Number: EL3247) as single dose for covid-19 immunisation. Medical history included migraine, essential tremor, fibromyalgia, arthritis and allergic to Sulfa. Patient has not covid-19. Concomitant medications included methylphenidate hydrochloride (CONCERTA), Propranolol, Tizanidine and Trazodone all for unknown indication. The patient experienced arm pain, nausea, dizziness, aches and fever on 21Jan2021 13:00. Since the vaccination, the patient not been tested for COVID-19. No treatment for events.Outcome of the events was recovered on an unknown date in 2021. Follow-up attempts are completed. No further information is expected.

Other Meds: CONCERTA; PROPRANOLOL; TIZANIDINE; TRAZODONE

Current Illness:

ID: 1290808
Sex: F
Age:
State: TX

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

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

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: achiness in her body; This is a spontaneous report from contactable other health professional (patient) Pfizer via Sales Representative. A female patient of an unspecified age received BNT162B2 (Pfizer COVID 19 vaccine, Solution for injection), dose 2 via an unspecified route of administration on an unspecified date as SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took first dose of BNT162B2 for covid-19 immunisation. The patient had some achiness in her body after the second dose of the vaccine. Adds outside of that achiness, she felt fine. The patient recently received the second dose of the vaccine but was unsure of the exact date, time or the site. Outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1290809
Sex: F
Age:
State: PA

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

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: pain and tenderness at the injection site; This is a spontaneous report from a contactable other HCP (patient). A 26-years-old female patient received BNT162B2 (BNT162B2), dose 1 intramuscular, administered in Arm Left on 05Jan2021 14:15 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included autoimmune thyroiditis, appendicectomy, pyelonephritis from an unknown date and unknown if ongoing. Concomitant medication included methimazole, atenolol, valaciclovir hydrochloride, ethinylestradiol, norgestimate (NORGESTIMATE & ETHINYL ESTRADIOL) and magnesium taken for an unspecified indication. The patient previously took azithromycin and experienced drug hypersensitivity. The patient experienced pain and tenderness at the injection site on an unspecified date. The action taken in response to the event for bnt162b2 was not applicable. The outcome of event was unknown. Information about lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds: METHIMAZOLE; ATENOLOL; VALACYCLOVIR [VALACICLOVIR HYDROCHLORIDE]; NORGESTIMATE & ETHINYL ESTRADIOL; MAGNESIUM

Current Illness:

ID: 1290810
Sex: F
Age:
State: VA

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

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

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: Severe headache; low grade fever; severe nausea; severe nausea and abdominal pain; severe to moderate body aches; severe to moderate body aches and bone achiness; extreme fatigue; soreness at injection site; mild dizziness; feeling as if I were to have a recurrence of Shingles; severe to moderate flushing; redness on face, neck, and trunk with feeling hot all over; redness on face, neck, and trunk with feeling hot all over; increased aurora migraines; SaO2 levels which dropped from my usual 98-99% to 92-94% with slight elevation in HR; SaO2 levels which dropped from my usual 98-99% to 92-94% with slight elevation in HR; This is a spontaneous report from a contactable health care professional (other HCP; patient herself). A 47-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EL3302; Expiration date was not reported), via unspecified route of administration in the right arm on 20Jan2021 14:15 (at the age of 47-years-old) at a single dose for covid-19 immunization at a nursing home/ Senior Living Facility. Medical history included early menopause on HRT at this time, aurora migraines with or without headache (migraine with aura), chronic anxiety and depression; all of which from an unknown date and unknown if ongoing. Medical history also included allergies with milk and color dyes. Concomitant medications included medroxyprogesterone, clonazepam, quetiapine, and estradiol (ESTRA); all were taken for an unspecified indication and start and stop dates were not reported. The patient previously took Cefalexin monohydrate (KEFLEX) and experienced drug allergy. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 21Jan2021, the patient experienced severe headache, low grade fever, severe nausea and abdominal pain, severe to moderate body aches and bone achiness, extreme fatigue, soreness at injection site, mild dizziness, feeling as if she were to have a recurrence of Shingles, severe to moderate flushing and redness on face, neck, and trunk with feeling hot all over, increased aurora migraines (flushing, headache and mild fatigue were reported to be within 24 hours and onset of severe symptoms were reported to have begun the following day approximately 20 hours post second injection). The patient's oxygen saturation levels also dropped from her usual 98-99% to 92-94% and had slight elevation in heart rate on 21Jan2021. The patient's blood pressure was not checked. All severe to moderate symptoms were reported to have lasted for seven days post vaccination until 26Jan2021 and events fatigue and headache lasted for next two weeks. The patient was reported to have start feeling better around 02Feb2021. There were no issues with any other vaccines in her life. The patient never had mRNA vaccine before these two (first dose was reported to be uneventful). The events were reported as non-serious. No treatment or medical intervention was received for the events. The patient underwent lab tests and procedures which included sars-cov-2 test (Nasal swab): inconclusive on 06Jan2021 and negative on 08Jan2021; and oxygen saturation: 92-94% on 21Jan2021. The outcome of the events severe nausea and abdominal pain, severe to moderate body aches and bone achiness and severe to moderate flushing and redness on face, neck, and trunk with feeling hot all over was recovered on 26Jan2021 (with the reported duration of 7 days); outcome of events: extreme fatigue and severe headache was also recovered on an unspecified date (which was reported to have lasted for the next 2 weeks); and outcome of events low grade fever, soreness at injection site, mild dizziness, feeling as if I were to have a recurrence of Shingles, increased aurora migraines and SaO2 levels which dropped from my usual 98-99% to 92-94% was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: MEDROXYPROGESTERONE; CLONAZEPAM; QUETIAPINE; ESTRA

Current Illness:

ID: 1290811
Sex: M
Age:
State: AZ

Vax Date: 12/26/2020
Onset Date: 12/27/2020
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: shingles; This is a spontaneous report from a contactable other hcp (patient himself). A 42-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: E49899, expiration date not reported), intramuscularly, administered on the left arm on 26Dec2020 09:45 (at the age of 42-years-old) at a single dose for COVID-19 immunisation. Patient's medical history and concomitant medications were not reported. The patient previously took aspirin and experienced allergy with aspirin. Prior to vaccination, the patient was not diagnosed with COVID-19; and since the vaccination, has not been tested for COVID-19. The patient experienced fever of 99.4 degrees, fatigue, muscle pain in left hip with radiating burning pain along posterior aspect of leg running from hip to calf , burning pain running across top of foot, blistering on left arch of foot, second, and forth toe; which was later diagnosed as shingles on 27Dec2020 19:30. The patient underwent lab tests and procedures which included body temperature: 99.4 degrees fahrenheit (fever) on 27Dec2020. Patient consulted a physician and treatment was received as a result of the event reported (reported as culture taken to confirm shingles). Events were assessed as non-serious by the reporter. The outcome of the event was recovered with sequalae. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1290812
Sex: F
Age:
State: FL

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

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Headache; Tiredness; Muscle pain; Chills; Joint pain; Swelling; Nausea; Feeling unwell; This is a spontaneous report from a contactable consumer (Patient). A 66-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE: Solution for injection), dose 1 via an unspecified route of administration on 20Jan2021 (Batch/Lot Number: EL8982) as single dose for an unspecified indication. Medical history included multiple sclerosis (Verbatim: MS), hypertension (Medical condition: Consumer stated, "High pressure") and covid-19 from an unknown date and unknown if ongoing (I had COVID in the last days of October around 21sth, 30 or 31st October). Concomitant medications included losartan taken for an unspecified indication. The patient experienced headache, tiredness, muscle pain, chills, joint pain, swelling, nausea, feeling unwell on an unspecified date. Patient had vaccination, Pfizer's dose, 20Jan2021 and should have my second dose of the vaccine on 09Feb2021 but had COVID in the last days of October around 21sth, 30 or 31st October and was diagnosed with MS (Later clarified as Medical history). Patient had very bad reaction the second day, I have the vaccination on Wednesday, didn't have any reaction in the moment or one hour or two hour but Thursday since the morning felt really bad with all the side effects that are listed in the paper that they gave me, I had everything, I had headache, tiredness, muscle pain, chills, joint pain, swelling and nausea, felling unwell." The action taken in response to the event for bnt162b2 was not applicable. The outcome of events was unknown. Information about Lot/batch no has been requested. Follow-up (05Feb2021): Follow-up attempts are completed. No further information is expected.

Other Meds: LOSARTAN

Current Illness:

ID: 1290813
Sex: M
Age:
State: WI

Vax Date: 01/24/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: sore arm, from the injection, for only 1-2 days"; left arm discomfort; shoulder pain; This is a spontaneous report from a contactable consumer or other non hcp. A 58-years-old male patient received bnt162b2 (PFIZER; Solution for injection; Lot number: EL3248) dose 1 via an unspecified route of administration, administered in left arm on 24Jan2021 as single dose for COVID-19 immunization. The patient's medical history included Chronic lymphocytic leukemia patient since Jul2015 and disrupt GI. Concomitant medications included ibrutinib taken for chronic lymphocytic leukaemia, meloxicam for arthralgia, flecainide taken for arrhythmia, aciclovir taken for antiviral treatment, guaifenesin, sulfamethoxazole, trimethoprim. The patient had a sore arm, from the injection, for only 1-2 days and was also taking meloxicam daily at the time. He then developed some "GI problems, due to the possible side effects of the meloxicam, and PCP told him to stop taking this medication. The patient stated that on day 8 the soreness reappeared and became worse each day, then on day 10 took a meloxicam and the arm pain was better. The patient stated that he can no longer take the meloxicam and he still had moderately sore. Upon follow up received on 05Feb2021, His oncologist recommended him to get it. 12 days after he got the vaccine his side effect came back. He got it in his left arm. He had left arm discomfort for a couple of days. The discomfort disappeared. He was also taking Meloxicam 7.5mg because he needs his hip replaced. It started to disrupt his GI, so he discontinued it. After he discontinued the Meloxicam, the arm soreness came back. He believes the Meloxicam was masking the shoulder soreness. He discontinued the Meloxicam, and 12 days later after the vaccine, his shoulder pain came back. He thinks once the anti-inflammation medication wore off it came back. His symptoms came back. He was just wondering how long people have been symptomatic after the injection. His next vaccine on 17Feb2021, and his arm was still sore from the first. He felt like this should have been more transient, and in a quicker time frame. The outcome of the events was reported as an unknown. Follow up received on 05Feb2021: New significant information was received. Follow-up attempts are completed. No further information is expected.

Other Meds: IBRUTINIB; MELOXICAM; FLECAINIDE; ACICLOVIR; BACTRIM BALSAMICO

Current Illness: Chronic lymphocytic leukaemia; Gastritis

ID: 1290814
Sex: M
Age:
State: NJ

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Redness at injection site.; Slight itch; This is a spontaneous report from a contactable consumer (patient himself). A 69-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot Number: EM9809; Expiration Date: Unknown) via an unspecified route of administration in Arm Left on 04Feb2021 12:30 as single dose for COVID-19 immunization. The patient medical history included Cardiac and penicillin allergy. The concomitant medication included atorvastatin. The patient experienced redness at injection site and slight itch on 05Feb2021. The patient had not received any other treatments for adverse events. The patient was not tested positive since the vaccination. The outcome of events was recovering.

Other Meds: ATORVASTATIN

Current Illness:

ID: 1290815
Sex: F
Age:
State:

Vax Date: 01/12/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Came down with shingles; This is a spontaneous report from a Pfizer-sponsored program . A contactable consumer or other non hcp (patient herself) reported that a female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number, and expiration date not reported), via an unspecified route of administration on 12Jan2021 at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient was supposed to get her 2nd dose on 02Feb2021 but came down with shingles on an unspecified date so her HCP advised her to not get the 2nd dose. She wants to know when she should get the 2nd dose. The outcome of the event reported was unknown. No follow-up attempts are possible; information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290816
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Diagnosed with shingles recently.; This is a spontaneous report from contactable consumer (patient) received via a Pfizer-sponsored program. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot number and Expiration Date: not reported), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced shingles (recently diagnosed, as reported) on an unspecified date. It was reported that "Had first pfizer covid shot. Due for 08Feb". Outcome of the event was unknown. No follow-up attempts are possible; information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290817
Sex: F
Age:
State:

Vax Date: 01/28/2021
Onset Date: 02/06/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: shingles on her body described as having rashes on her body; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 28Jan2021 (Lot Number: EL3246) as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient was previously vaccinated with 2 doses of Shingrix on an unspecified date. On 06Feb2021 she had shingles on her body which she described as having rashes on her body. She went to the hospital, they said it was shingles. So, now she was asking whether there was a relationship with the vaccine and shingles. She was scheduled to have the second dose on 18Feb2021. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1290818
Sex: F
Age:
State: NJ

Vax Date: 01/28/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: hip started hurting; shingles; The initial case was missing the following minimum criteria: no adverse effect. Upon receipt of follow-up information on 08Feb2021, this case now contains all required information to be considered valid. This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program A 72-year-old female patient received bnt162b2 (BNT162B2), first dose via an unspecified route of administration on 28Jan2021 (Batch/Lot Number: EL9269) as single dose (at the age of 72-years-old) for COVID-19 immunisation; and ibuprofen (MOTRIN [IBUPROFEN]), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at 1800 mg, daily as anti-inflammatory. Medical history included hypertension. Concomitant medication included amlodipine taken for hypertension, start and stop date were not reported. The patient had her first Pfizer vaccination on 28Jan2021 and was scheduled for her next one in 18Feb2021. Days later she started noticing that she had no other symptom, she stated that "nothing happened to me, I didn't feel bad, my arm didn't hurt, I had no problems with the vaccine." A couple of days later, her hip started hurting and then just Wednesday (Feb2021) she went to her doctor and he said it was shingles and was given valacyclovir. No investigation assessment was done. The outcome of the events was unknown.

Other Meds: AMLODIPINE; MOTRIN [IBUPROFEN]

Current Illness:

ID: 1290819
Sex: F
Age:
State: MI

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

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

Lab Data:

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: pressure in her head; Tension headache; neck ache; muscle ache; Back ache; I guess my headache is due to the muscles being inflamed from the vaccine, this is on my scalp, my neck and then my shoulder; This is a spontaneous report from a contactable physician reporting for herself. This 50 years old female patient received the first single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL1283) on 21Jan2021, for COVID-19 immunization. Medical history and concomitant medications were none. On 21Jan2021, within a minute of having vaccine, the patient had pressure in her head and got a headache. It was since 17 days and she had still not fully recovered. The headache had subsided but she had neck ache, muscle ache and back ache. She guessed her headache was due to the muscles being inflamed from the vaccine, this was on her scalp, her neck and then her shoulder. She went to her primary care doctor and he said she had tension headache and this all happened on the same side of the vaccine. The events required treatment with Aleve, Motrin and Tylenol. She had still to get the second shot and was wondering if she should wait until fully recovered. The patient had not yet recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1290820
Sex: F
Age:
State: NM

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: Swelling; This is a spontaneous report from a contactable consumer(patient). A 75-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: not reported) via unspecified route of administration on arm left at a single dose on 26Jan2021 15:00 for COVID-19 immunization. Medical history was not reported. Patient had no known allergies. Patient received lisinopril(LISINOPRIL) as concomitant medications within 2 weeks of vaccination. 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. The patient tested for Covid-19 post vaccination. On 27Jan2021 patient experienced swelling that still hasn't gone down. No other adverse effects at all. Not painful. On 28Feb2021 patient had nasal swab resulted negative. Patient didn't received treatment for the event. The outcome of event was not recovered. No follow up attempts are possible. Information about Lot/batch number cannot be obtained.

Other Meds: LISINOPRIL

Current Illness:

ID: 1290821
Sex: F
Age:
State:

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: I have shingles that started the day after the shot. The shingles are on the left side of my neck, along the jawline, and behind the left ear.; This is a spontaneous report from a non-contactable consumer. A 54-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 26Feb2021 17:30 (Batch/Lot Number: EN6198) as SINGLE DOSE for covid-19 immunisation. Medical history included hypothyroidism. Concomitant medication(s) included rosuvastatin (ROSUVASTATIN); levothyroxine sodium (LEVOTHYROXIN); loratadine (LORATADINE). The patient previously took clindamycin, and amoxicillin and experienced known allergies. On 27Feb2021, it was reported "I have shingles that started the day after the shot. The shingles are on the left side of my neck, along the jawline, and behind the left ear." Therapeutic measures were taken as a result of the event: given an antiviral medicine. The patient did not have COVID prior vaccination, the patient was not COVID tested post vaccination. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: ROSUVASTATIN; LEVOTHYROXIN; LORATADINE

Current Illness:

ID: 1290822
Sex: M
Age:
State: TX

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Testes felt very tender; especially on the right side of my body; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male consumer received bnt162b2 (PFIZER-BIONTECH COVID-19 m-RNA VACCINE, Formulation: Solution for injection, Lot Number: MRN:70697732, Expiration date: unknown), dose 1 via an unspecified route of administration in left arm on 25Feb2021 at 12:30, as single dose for COVID-19 immunisation. The patient medical history included asthma. The patient did not had any known allergies. Concomitant medications included pseudoephedrine hydrochloride (SUDAFED) and ibuprofen (ADVIL). The patient did not receive other vaccine in four weeks. The patient did not had COVID prior to vaccine. Post vaccination, the patient did not had COVID test. On 25Feb2021 at 14:00, the patient experienced testes felt very tender, especially on the right side of his body. Therapeutic measures were not taken as a result of event. The outcome of the event was recovered. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds: SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]; ADVIL [IBUPROFEN]

Current Illness:

ID: 1290823
Sex: F
Age:
State: NC

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

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

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: shingles; This is a spontaneous report from a contactable consumer (patient) via Pfizer-sponsored program. A female patient of an unspecified age BNT162B2 (Pfizer Covid-19 Vaccine), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient mentioned that she was due for the second dose the next Tuesday at the time of reporting. She currently has shingles (onset date not specified) and would like to know if that would interfere with her second dose. 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: 1290824
Sex: F
Age:
State: DE

Vax Date: 03/23/2021
Onset Date: 03/23/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: Sever chills; Fever off and on for 30 hours\Temperature 99.8 - 103.2 for 6 hours; Heart rate increased; This is a spontaneous report received from a contactable consumer (Patient). A 75-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE: Solution for injection), dose 2 intramuscular, administered in Arm Left on 23Mar2021 13:00 (Batch/Lot Number: EN6207) as single dose for covid-19 immunisation. Medical history included herpes zoster from an unknown date and unknown if ongoing (Had a similar reaction to shingles vaccine). Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE: Solution for injection), dose 1, administered in Arm right on 02Mar2021 18:15 (Batch/Lot Number: EN6198) as single dose for covid-19 immunisation. Concomitant medication included metoprolol succinate 25 mg and diltiazem hydrochloride 120 mg (DILTIAZEM CD). On 23Mar2021 05:30, the patient experienced sever chills, Fever off and on for 30 hours\Temperature 99.8 - 103.2 for 6 hours and heart rate increased. The patient underwent lab tests and procedures which included body temperature: 99.8 - 103.2 on 23Mar2021 (Temperature 99.8 - 103.2 for 6 hours), heart rate increased: 100-120 on 23Mar2021 (Heart rate increased to between 100 -120 / bpm for 6 hours). The action taken in response to the events for bnt162b2 was not applicable. The outcome of events was recovered. Follow-Up(03May2021): Follow-up attempts are completed. No further information is expected. Amendment: This follow-up report is being submitted to amend previously reported information which included: Deleted the event "Temperature 99.8 - 103.2 for 6 hours LLT: Body temperature" and subsumed to existing LLT: Fever.

Other Meds: METOPROLOL SUCCINATE; DILTIAZEM CD

Current Illness:

ID: 1290825
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: slight sore arm; This is a spontaneous report from a contactable consumer (patient). This 70-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EN6206) via an unspecified route of administration in the right arm in Mar2021 as a single dose for COVID-19 immunisation. Medical history included lung cancer several years ago, surgery, multiple sclerosis, mild chronic obstructive pulmonary disease (COPD), arthritis, and irritable bowel syndrome, all from unknown dates and unknown if ongoing. Concomitant medications included phenazepam and nitrazepam, both from unknown dates for unknown indications. The patient reported she received her first dose on a Wednesday, three weeks earlier as of 05Apr2021, and only had one side effect, a slight sore arm. The patient received her second dose on 31Mar2021 at 08:30 for COVID-19 immunisation. The patient inquired if she should get a booster when it comes out. The clinical outcome of slight sore arm was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds: PHENAZEPAM; NITRAZEPAM

Current Illness:

ID: 1290826
Sex: F
Age:
State:

Vax Date: 03/29/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
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Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: dominant hand and wrist is still slightly swollen; dominant hand and wrist is still slightly swollen; her dominant hand and wrist is still slightly swollen and still hurts to use it.; her dominant hand and wrist is still slightly swollen and still hurts to use it.; slight pain under her arm in her lymph node; This is a spontaneous report received from a non-contactable consumer (patient). A 67-year-old female patient received dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration on 29Mar2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unspecified date the patient had slight pain under her arm in her lymph node but that went away pretty quickly. It had been 8 days and her dominant hand and wrist were still slightly swollen and still hurt to use. The outcome of slight pain under her arm in her lymph node was recovered. The outcome of dominant hand and wrist were still slightly swollen and still hurt to use was unknown. No follow-up attempts are possible; information about lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1290827
Sex: M
Age:
State: MA

Vax Date: 03/29/2021
Onset Date: 04/05/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: some fatigue; throat is very sore and very dry; throat is very sore and very dry; it is difficult to swallow; his throat does still feel "a bit swollen."; This is a spontaneous report received from a contactable consumer (patient) via a Pfizer Sponsored Program. This male patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number unknown) via an unspecified route of administration on 29Mar2021 as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient reported receiving his first dose of BNT162B2 on 29Mar2021 and that his second dose had been schedule for 12Apr2021 which was 14 days and inquired if this was okay as he knew the recommended interval was 21 days. He reported that after his first dose, he did not experience any side effects initially, just "some fatigue." However, he stated that this morning (as of 05Apr2021) his throat was very sore and very dry and reported that it was difficult to swallow. He stated that it had been a couple of hours and he felt a bit better but reports that his throat still felt "a bit swollen." The patient inquired if the side effects he was experiencing with his throat were common with the vaccine of if he could just be getting a cold. He stated that he did read that "there is an issue with lymph nodes" and thinks that the throat is a common area where lymph nodes are. The clinical outcomes of fatigue, throat is very sore and very dry, it is difficult to swallow, and throat does still feel a little bit swollen were unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1290828
Sex: M
Age:
State:

Vax Date: 03/24/2021
Onset Date:
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: heel pain; This is a spontaneous report from a contactable consumer (patient). This 71-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number unknown) via an unspecified route of administration on 24Mar2021 as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient reported he had an appointment tomorrow (as of 05Apr2021) with a podiatrist for heel pain that his podiatrist said he could give him a shot for; the patient assumed it would be a cortisone injection. The patient inquired if he could take the steroid injection. The patient stated his second dose was due 14Apr2021 and that he would probably wait for the injection until after he'd received his second dose. The clinical outcome of heel pain was unknown. No follow-up attempts are needed. No further information is expected

Other Meds:

Current Illness:

ID: 1290829
Sex: U
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
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Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: pain; This is a spontaneous report from a non-contactable consumer (patient). This patient of unspecified age and gender received a dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number unknown) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient called regarding pain experienced on an unspecified date. The clinical outcome of pain was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290830
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: received the first dose on January 14 and due to a cardiovascular condition her Physician recommended to wait until her cardiovascular condition was monitored; cardiovascular condition; received the first dose on January 14 and due to a cardiovascular condition her Physician recommended to wait until her cardiovascular condition was monitored; This is a spontaneous report from a non-contactable consumer (patient). A female patient of unspecified age received dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration on 14Jan2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient wanted information about dose 2 of BNT162B2 because she received the first dose on 14Jan2021 and due to a cardiovascular condition her physician recommended to wait until her cardiovascular condition was monitored. The outcomes of received first dose on 14Jan2021 and cardiovascular condition were unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290831
Sex: M
Age:
State: IL

Vax Date: 03/27/2021
Onset Date: 04/03/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: tired; coughing; This is a spontaneous report from a contactable consumer (patient's wife). This consumer reported similar events for two patients. This is the second of two reports. A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date were unknown), via an unspecified route of administration on 27Mar2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced coughing two days prior to reporting (03Apr2021) and was very tired on an unspecified date. It was reported that patient did not have any fever and was taking Tylenol for the events. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021372956 Same reporter/drug, different patient/event.

Other Meds:

Current Illness:

ID: 1290832
Sex: F
Age:
State: WI

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 05/05/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: her lower back started hurting; It makes her feel like throwing up; She got chills and aches 14 hours later; She got chills and aches 14 hours later; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program. This female patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number unknown) via an unspecified route of administration on an unspecified date in 2021 as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient reported she got her first dose on Wednesday (as of 05Apr2021). She got chills and aches 14 hours later. She reported that on "this Saturday" (as of 05Apr2021) her lower back started hurting, also reporting it made her feel like throwing up. The outcomes of she got chills and aches 14 hours later, her lower back started hurting and it made her feel like throwing up were unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1290833
Sex: F
Age:
State: MD

Vax Date: 03/22/2021
Onset Date: 04/17/2021
Rec V Date: 05/05/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: She had a severe headache/Excruciating head pain; rash which turned into Shingles; rash which turned into Shingles; This is a spontaneous report from a contactable consumer (patient). A 65 years old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscularly at the age of 64 years old, administered in arm left on 22Mar2021 15:30 (Lot Number: ER8730) at single dose for covid-19 immunisation. Medical history included sjogren's syndrome from 2011 and ongoing which caused dry eyes. The patient's concomitant medications were not reported. The patient experienced she had a severe headache/excruciating head pain on 17Apr2021, rash which turned into shingles on 17Apr2021. The patient stated she got the first dose of the vaccine on 22Mar2021 and was due for her second dose 19Apr2021. However, on 17Apr2021 (reported as the day before yesterday) she had a severe headache, rash which turned into shingles. She stated she has an autoimmune disorder, Sjogren's which causes dry eyes. She asked if the Pfizer Covid vaccine could activate shingles for someone with this specific autoimmune disorder. The events resulted in emergency room. The outcome of the events was not recovered.

Other Meds:

Current Illness: Sjogren's (Verbatim: Sjogren's which causes dry eyes)

ID: 1290834
Sex: F
Age:
State:

Vax Date: 04/12/2021
Onset Date: 04/01/2021
Rec V Date: 05/05/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Lab Data:

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: Experienced chills with really cold feet and headache. Today her chills was gone but still feels like she has a mild fever and head still hurts; Experienced chills with really cold feet and headache. Today her chills was gone but still feels like she has a mild fever and head still hurts; Experienced chills with really cold feet and headache. Today her chills was gone but still feels like she has a mild fever and head still hurts; Experienced chills with really cold feet and headache. Today her chills was gone but still feels like she has a mild fever and head still hurts; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 42-year-old on 12Apr2021 at single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. patient has gotten her first shot of the Pfizer Covid 19 vaccine last 12Apr2021 and on 17Apr2021, she experienced chills with really cold feet and headache. Today her chills was gone but still feels like she has a mild fever and head still hurts. Asking if this is normal and as to how many days it usually lasts. Outcome of headache and fever was not recovered, outcome of chill was recovered and outcome of cold feet was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290835
Sex: F
Age:
State: VA

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: She was having pain in her sternum randomly, it was happening multiple times per day; pain radiating across her chest; took her breath away/ was not breathing right; she got severe chills; her throat was hurting, it hurt to swallow,; her throat was hurting, it hurt to swallow,; she was just feeling bad/ she felt so bad; strep throat with a sinus infection; strep throat with a sinus infection; bronchial spasm; not feeling well; everything started hurting, her jaw; tiredness/ extreme fatigue/ exhausted; low grade temp/ fever/ fever of 101.5; coughing/ dry cough/ couldn't talk without coughing; she got nauseous/ nausea; body aches; Headache/ head hurt; This is a spontaneous report from a contactable consumer (patient). A 50-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 29Jan2021 (lot number: EL1284, expiry date: Apr2021) at single dose for COVID-19 immunisation. The relevant medical history included IBS (Irritable bowel syndrome) with constipation from unspecified date and flu from unspecified date (5 years prior to the report). Concomitant medications included ibuprofen (MOTRIN), naproxen sodium (ALEVE), albuterol, azithromycin, prednisone and oxymetazoline hydrochloride (AFRIN SINUS). The patient previously received the first dose of BNT162B2 on 08Jan2021 (Lot number: EL1284) at the age of 50 years old for COVID-19 immunisation. The patient received her second Pfizer Covid 19 Vaccine. She had experienced tiredness, low grade temp and coughing for eight weeks at the time of the report. She had side effects from the COVID vaccine. She could go through a report but the thing she didn't think any one knew but she had a reaction 45 minutes after the second one and she was still having symptoms post 8 weeks out. She had read where it could happen post 6 weeks out but she was perfectly fine before getting it so she could not figure out what was going on. She called her work and they told her she needed a note to come back to work and she was frustrated going through a whole process and going to the doctor and no one knew anything. She needed to know what she needed to do at this point. She would like to know had this happened to anyone else, she did not think they know, the vaccine was just like the virus no one knew, and she was curious, but she thought it was just like, no one knew what was going to happen if you got it. The second dose date was 29Jan2021. She got the shot then she told the nurse she was going for a walk, and the nurse told her to hydrate well so she got a bottle water, 20 ounce and drank it on the ride home. Then on the way home, she clarified it was about 30 minutes after because she was almost home, she got nauseous. She came home, she just went straight to bed, she had body aches, headache, fever, nausea extreme fatigue, she confirmed that was the same day as the shot. Then that went on until, she had to go to Monday, so it began on that Friday at 7:30 in the morning, on Sunday she was feeling better but she was not herself. Monday morning she went to work, she wasn't having fever or nausea so she went to work, she felt pretty okay for a little bit. When asked if the symptoms were ongoing, she said it was really sporadic, which was frustrating. She said that would put her in to first week of Feb, she was not sure of the exact timeline but she was feeling pretty good. Then she was telling her dad she was having symptoms. She was having pain in her sternum randomly, it was happening multiple times per day, it had happened twice where the pain was radiating across her chest like someone was lifting her chest out of her body, it took her breath away. She was supposed to have a colonoscopy on 19Mar2021 and she was trying to decide if she should go in for that, she had no fever no other symptoms. She had to have a colonsopscopy because she had IBS with constipation and they wanted her to have a colonoscopy before they would give her medicine for that, they were going to give her Lunesta. No further information provided. She clarified the IBS was an issue for her prior to receiving the vaccine. She went in for that and she was fine that was Monday 22Feb2021 then at 9:30 that night she was laying in bed and she got severe chills, fever of 101.5, she had to take 1 Motrin and then another 2 Aleve, she thought she didn't remember for sure if that was what she took but she had to take 2 doses of medicine to get it down. No further information provided. Then the next morning she was fine. So this was still ongoing, off and on, she had had to miss work then on 31Mar2021, she was going to work everyday that previous week but the next week she was tired. She was coming home on Wednesday 31Mar2021 she was coming home from class that night because she was in school too and she was tired, her throat was hurting, it hurt to swallow, her head hurt and then, everyone was different but her temperature was 99.5, normally her temp is 97.5. She knew there was debate over whether that was a fever or not a fever not but it was not her normal. She had been taking her temperature for so long because of COVID and going to work they take temperature every day. So she was just feeling bad, she felt so bad, so she didn't go to work that day, she went to the urgent care and when she went back at the urgent care she told them she felt like, she told them she had no body aches, it was just from the neck up, like she had strep throat with a sinus infection combined and since she had gotten the COVID vaccine and the flu shot they did not think it was that but she decided to test her for strep and flu, they did not think it was covid becuase she works at a hospital she did not think she had it either but since she was presenting with symptoms they tested for that too and all that was negative so she thought maybe it's viral, they do have a lot going around and it is the season for allergies with pollen or it maybe a viral sinus infection, that was on Thursday, she slet Friday Saturday and still Sunday and the whole time she was still having like a 99.5 fever by the end of the day so Sunday she was supposed to go back to work. The 31Mar2021 she started feeling really bad and she went to the urgent care 01Apr2021 and had those tests done that were negative and she was home Thursday and the weekend she was not back to herself she was tired but she was not having symptoms COVID but like with her sinuses allowed to use Afrin for 3 days 3 times per day and then stop so she did that then developed a dry cough and by the end of week Sunday she couldn't talk without coughing every time she opened her mouth and air touched her throat she would cough. She didn't know date of that it was not this past Sunday, but the Sunday before she went back to urgent care and they did a chest x-ray and retested for covid, they gave her an Albuterol treatment, they told her there was nothing in her chest and wrote script for a Zpack if she needed it. No further information provided. Then Monday of last week she called her allergist and went to see the allergist and she told her she was not breathing right there was something in there like a bronchial spasm was what she called it and she said everything looked angry, like her ears and her throat. She was not sure why. Her allergist gave her a Z pack, nothing against urgent care but she wanted to get the prescription from her doctor. This had been going on so long so last Wednesday she got the z-pack she left work early at 2 PM and slept for Wednesday through Friday, she did not shower at all she was just exhausted and she was just not feeling well. The cough did get better with a prescription cough drop that she could use 3 times per day for 10 days and her cough was a lot better not totally gone but nothing like it was that Wednesday night. Saturday she was better enough and took a shower and got up and did not feel horrible, she was still tired still, but then Sunday, yesterday, she had a low grade fever at night and was tired and had pain. She said they gave her Prednisone at the urgent care too when she got the chest Xray and

Other Meds: MOTRIN [IBUPROFEN]; ALEVE; ALBUTEROL [SALBUTAMOL]; AZITHROMYCIN; PREDNISONE; AFRIN SINUS

Current Illness:

ID: 1290836
Sex: M
Age:
State:

Vax Date: 04/15/2021
Onset Date: 04/01/2021
Rec V Date: 05/05/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: headache; feel fatigued/super worn out; pretty lethargic/Lethargic as all get out; kind of almost flu-like feeling; arm pain/soreness like "someone punching me in the arm."/arm hurt; Not feeling too good; This is a spontaneous report from a contactable consumer (patient). A contactable 32-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 32-year-old, on 15Apr2021 at single dose for COVID-19 immunization. Medical history included COVID (Patient had COVID probably within the first few months of COVID being a thing, so that was a while ago). Concomitant medication was not reported. patient received his first Pfizer Covid vaccine dose on 15Apr2021. The following day (16Apr2021) he experienced arm pain/soreness like "someone punching me in the arm." On 18Apr2021 he states he started to feel fatigued, "super worn out", and a headache (19Apr2021). Patient asked if it was normal to experience. He is not feeling too good and doesn't know if that is from the Pfizer Covid-19 Vaccine. Caller's wife got the Moderna shot and caller got the Pfizer Covid-19 Vaccine shot on 15Apr2021. It seemed like his arm hurt on Friday. Saturday it seemed like he was alright. Sunday (18Apr2021) he felt pretty lethargic and kind of almost flu-like feeling, today (19Apr2021) just severe headache and just lethargic as all get out, walking to refrigerator is kind of a task. He was wondering, he heard of like the day after, but if it is a normal thing to have these events a few days after the Pfizer Covid-19 Vaccine. He does not feel like he needs to be rushed to the hospital. Outcome of arm pain was recovered on 17Apr2021 and outcome of other events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1290837
Sex: M
Age:
State: FL

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

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Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: He feels like something is stuck in his eyes; eyes were itching; He has a lot of sickness; Left arm warm and pain after second shot; Left arm warm and pain after second shot/ arm was sore; This is a spontaneous report from a contactable consumer (patient). A 63-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: LL3302) via an unspecified route of administration at left arm on 05Feb2021 at 12:00 (63-year-old at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history included diabetes from 2009 or 2010 and ongoing; high blood pressure from 2009 or 2010 and ongoing; ongoing cirrhosis of the liver (As a little boy at 8 years old he got a cut on his right hand. His Mother took him to the Emergency Department and they gave him blood. All that time he didn't know, until he discovered it at age 32-34. He found out from his primary doctor he had Hepatitis C. His doctor asked if he shot up drugs. He said he did a little pot. He cut the main artery in his wrist); ongoing heart problems (He always felt problems with his heart. It started in 2014 when he went to the Emergency Room for pain in his chest. They checked his heart and found his blood didn't flow to the right. It flowed to the left. The Cardiologist told him sometimes his heart beats and sometime it doesn't. He had 2 veins with blockage, they couldn't do anything and put him on medication for that); prostate cancer From Dec2019 (He had Cancer twice. He was first diagnosed of Prostate Cancer and received Radiation therapy. He had an exam and the Cancer was back. He had surgery for the Prostate Cancer 18Feb2020); COVID-19 (in the past. His wife had COVID-19 and he had COVID with the same symptoms. He lost his taste for 9 days at the end of Dec2020. He got sick after his wife had COVID-19. His wife got better after having COVID-19. He had no appetite, it was pretty bad). Concomitant medications included a lot of medication (Details were not provided). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: BL3302) via an unspecified route of administration at left arm on 14Jan2021 at 16:30 (62-year-old at time of vaccination), at 0.3ml, single, for COVID-19 immunization and experienced left arm hurt. There were no prior vaccinations within 4 weeks. There were no additional vaccines administered on same date of the Pfizer suspect. History of all previous immunization with the Pfizer vaccine considered as suspect was none. Patient weighs between 158-159 pounds. Patient experienced left arm warm and pain after second shot was from 05Feb2021 to 06Feb2021. Patient states he received the second dose on 05Feb2021 and within 30 minutes he started to feel the shot, it was working up in his head, felt like something was working. It was warm and sore. Patient states a couple hours later he was taking Tylenol because his arm was sore. He applied the muscle rub/muscle wrap the next day and it was better. Patient states the day before reporting he began using eyedrops more than usual and using 5 drops because he feels like something is stuck in his eyes. States it's almost like COVID is in his eyes. In the past month he has been using eye drops more often. He had been using them before the vaccine. His eyes were itching and he would use the drops to flush them out. Patient would like to know if feeling like something is in the eye is something related to the vaccine or a symptom of COVID-19. He has a lot of sickness. Adverse events did not require a visit to emergency room or physician office. The outcome of Left arm warm and pain after second shot was recovered on 06Feb2021; outcome of other events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness: Blood pressure high (from 2009 or 2010); Cirrhosis of liver (As a little boy at 8 years old he got a cut on his right hand. His Mother took him to the Emergency Department and they gave him blood. All that time he didn't know, until he discovered it at age 32-34. He found out from his primary doctor he had Hepatitis C. His doctor asked if he shot up drugs. He said he did a little pot. He cut the main artery in his wrist.); Diabetes (from 2009 or 2010); Heart disorder (He always felt problems with his heart. It started in 2014 when he went to the Emergency Room for pain in his chest. They checked his heart and found his blood didn't flow to the right. It flowed to the left. The Cardiologist told him sometimes his heart beats and sometime it doesn't. He had 2 veins with blockage, they couldn't do anything and put him on medication for that.)

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am