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**
PLEASE CHECK BACK SOON
Download the files above while you wait.






Manufacturers

Total Manufacturer

Incidents per State

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

ID: 1530634
Sex: M
Age:
State: LA

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Extreme Rapid Heartbeat; dizziness; Felt sick to my stomach; chill; Had fever the second day 101; headache; tired; have pins and needle feeling all over; Slight confusion; Ice cold feet and hands but was burning; This is a spontaneous report from a contactable consumer. A 55-years-old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 12Feb2021 17:00 (at the age of 55-year-old) (Batch/Lot Number: EN6201) as dose 1, single for covid-19 immunization. The patient other medical history was reported none. Concomitant medications included valaciclovir hydrochloride (VALTREX); ascorbic acid (VITAMIN C ACID); zinc; nitric oxide (NITRIC OXIDE) taken for an unspecified indication, start and stop date were not reported. The patient previously took dexamethasone and experienced drug hypersensitivity. On 12Feb2021 17:00, the patient experienced extreme Rapid Heartbeat and dizziness immediately after injection. Had to empty my bowel right away. Hands and feet were freezing but my body was hot. Slight confusion. Felt sick to my stomach. Almost went to emergency room but decided to go home. Increase heart rate and chill lasted for a day. Ice cold feet and hands but was burning up. Heart rate slowed after a full 24 hours or so. Increased HR came back off and on for a day or two. Had fever the second day 101 and headache. Tired. Broke on the third day. Now on the third day, have pins and needle feeling all over mild. Cold hands and feet and extremely tired. The patient did not received treatment for AEs. The patient had other vaccine in four weeks. Other medications in two weeks are Valtrex, Vitamin C, Zinc, Nitric Oxide. The patient does not have covid prior vaccination. Covid tested post vaccination was reported as no. The outcome of event was reported as recovering. Follow-up attempts completed. No further information expected.

Other Meds: VALTREX; VITAMIN C ACID; ZINC; NITRIC OXIDE

Current Illness:

ID: 1530635
Sex: F
Age:
State: IL

Vax Date: 01/30/2021
Onset Date: 01/30/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: chills; rash on my neck and upper chest area. The rash got worse with a hot shower; pain at the injection site; got very bad body aches everywhere; This is a spontaneous report from a contactable nurse (patient). A 55-year-old female patient (not pregnant) received the second dose of BNT162B2 via intramuscular on the right arm on 30Jan2021 at 09:00 AM (Lot Number: EL9265) at the age of 55-year-old as single dose for COVID-19 immunization. Medical history included: allergies to medications, food, or other products: pine nuts, sunflower seeds. The patient did not received 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 had been tested for COVID-19. Concomitant medications included atorvastatin, fish oil (OMEGA 3), zinc, ergocalciferol (VIT D) and vitamin c [ascorbic acid] (VITAMIN C). The patient previously received the first dose of BNT162B2 via intramuscular on the left arm on 09Jan2021 at 09:00 AM (lot number: EL3248) at the age of 55-year-old as single dose for COVID-19 immunization and experienced pain at the injection site. On 30Jan2021 at 10: 00 PM, the patient experienced pain at the injection site, the night of the 2nd, the patient got very bad body aches everywhere. On 31Jan2021, the next day, the patient experienced chills and rash on neck and upper chest area, the rash got worse with a hot shower. The outcome of events was recovered. Took Advil was taken as treatment for events. No follow-up attempts are possible. No further information is expected.

Other Meds: ATORVASTATIN; OMEGA 3; ZINC; VIT D; VITAMIN C

Current Illness:

ID: 1530636
Sex: F
Age:
State:

Vax Date: 02/15/2021
Onset Date: 02/15/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: flushing on her cheeks; This is a spontaneous report from a contactable female Consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; Batch/Lot number: Not reported) via an unspecified route of administration, administered on 15Feb2021 as a single dose for covid-19 immunisation. The patient medical history included ongoing migraine, ongoing fibromyalgia. The patient concomitant medications were not reported. It was reported that she received the vaccine yesterday (15Feb2021) morning and experienced flushing on her cheeks after within an hour. It was persisting today (16feb2021). She was wondering if it was a common side effect of the vaccine as she had not seen it in the fact sheet. She also mentioned that she takes medication for migraines and fibromyalgia and was asking if it could have interactions with the vaccine that may have caused this. The patient was not recovered from the events. Information on lot/ batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Fibromyalgia; Migraine

ID: 1530637
Sex: F
Age:
State: FL

Vax Date: 01/22/2021
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Caller extremely confused and flustered; I am depressed; This is a spontaneous report from a non-contactable consumer (patient) via medical information team. A female patient of an unspecified age (reported as 78 without units) received bnt162b2 (Solution for injection) via an unspecified route of administration on 22Jan2021 as dose 1, single for COVID-19 immunisation. Medical history included arthritis. The patient's concomitant medications were not reported. On an unknown date in 2021, it was reported that the patient was extremely confused and flustered while giving all kinds of dates and states. The patient stated, she took the first one 4 weeks ago. The patient provided Identification number on the white card she was provided at the vaccination site. The patient received the first shot of the Pfizer COVID vaccine on 22Jan2021. The patient was scheduled on 19Feb2021 at 3:12PM. The patient stated they texted her with the gate she was supposed to go in and then asked for her phone number, they told her it was the wrong number, and it was on the card as the right number. The prompt said sorry we could not help. The patient was concerned that her appointment was cancelled. The patient stated that she was not angry but depressed on an unknown date in 2021 and was going to go take something. On top of everything else, the patient had arthritis and she got it when she moved down. She blamed her husband. Outcome of the events were unknown. No follow-up attempts are Possible. Information on lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1530638
Sex: F
Age:
State: CA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: L arm soreness; neck/shoulder ache; neck/shoulder ache; fatigue; Pregnant at the time of vaccination? Yes; This is a spontaneous report from a contactable other Health care professional (patient). A 34-year-old pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3249), via an unspecified route of administration in left arm on 20Jan2021 at 10:15 (at the age of 34-year-old) as dose 1, single for COVID-19 immunisation in public health clinic. Medical history included fetal distress from an unknown date and unknown if ongoing (Hx of emergency c-section with 1st pregnancy due to fetal distress). Concomitant medications included PRENATAL VITAMINS [ASCORBIC ACID; BETACAROTENE; CALCIUM SULFATE; COLECALCIFEROL; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; NICOTINAMIDE; PYRIDOXINE HYDROCHLORIDE; RETINOL ACETATE; RIBOFLAVIN; THIAMINE MONONITRATE; TOCOPHERYL ACETATE; ZINC OXIDE] taken for an unspecified indication, start and stop date were not reported; calcium gummies taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient did not have COVID prior vaccination and not COVID tested post vaccination The patient was pregnant on 20Jan2021 at the time of vaccination. On 20Jan2021 at 15:00, the patient experienced L arm soreness, neck/shoulder ache, fatigue on. The mother reported she became pregnant while taking bnt162b2. The patient was 9 Weeks pregnant at the onset of the event. The patient was due to deliver on 18Sep2021 and last menstrual date on 12Dec2020. The patient did not receive any treatment for the events. The outcome was events was reported as resolved on an unknown date.

Other Meds: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; CALCIUM

Current Illness:

ID: 1530639
Sex: M
Age:
State: CT

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Weakness; dizziness; This is a spontaneous report from a Contactable Consumer. A 84-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL9263), via an unspecified route of administration, administered in Left arm on 28Jan2021 16:00 (at the age of 84-years-old) as DOSE 1, SINGLE for covid-19 immunization. The patient's medical history and concomitant medications were not reported. Patient had no known allergies. Patient had not received other vaccines within 4 weeks. Patient had not received other medications in two weeks. Prior to vaccination, patient was not diagnosed with COVID-19. The patient was not tested for COVID-19. On 28Jan2021, the patient experienced weakness, dizziness. No treatment received for the events. The clinical outcome of events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1530640
Sex: F
Age:
State: TX

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: I had a little bit of tachycardia you know like heart rate little bit like 100 & 102 for about like 3 hours; This is a spontaneous report from a contactable consumer reported for herself. A 45-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE Solution for injection Batch/Lot Number: EL9269) via an unspecified route of administration on 12Feb2021 as dose number unknown, single at the age of 45-years-old for COVID-19 immunization.Medical history included headache and migraine. Concomitant medications included galcanezumab gnlm (EMGALITY [GALCANEZUMAB GNLM]) monthly taken for headache and migraine.On 12Feb2021, she experienced tachycardia 10 to 15 minutes ago, that lasted for 3 to 4 hours and wanted to know if she should get the second dose of vaccine and if there was any listed drug interactions listed when taking the vaccine. Patient reported that she had a little bit of tachycardia you know like heart rate little bit like 100 & 102 for about like 3 hours and asked if this is that normal. No treatment was received for event. The patient did take a drug Emgality, which was monoclonal antibodies injections that prevent taking once in month you know for prevention of headache or migraine. Reporter asked is there any interaction between this and vaccine because she have to take it like be safe. The patient underwent lab tests which included Complete Blood Count resulted as regular checkup labs nothing on an unspecified date and heart rate resulted as 100 & 102 on 12Feb2021. The patient recovered from event on unspecified date in 2021. No Follow-up attempts are possible. Information about lot/batch cannot be obtained.

Other Meds: EMGALITY [GALCANEZUMAB GNLM]

Current Illness:

ID: 1530641
Sex: F
Age:
State: VA

Vax Date: 02/07/2021
Onset Date: 02/07/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: pressure type headache; bad foggy brain; moderate tightness in the patient's left chest that moved to the center of her chest and began moving upward before was subsided and moved back to her left chest; pain; symptoms began so quickly after the vaccine shot that she was not sure if it was an allergic reaction or side effects; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot number and Expiration Date: not reported), via an unspecified route of administration, administered in left arm on 07Feb2021 at 08:15 (at the age of 67 years old) as dose 1, single for COVID-19 immunisation in workplace clinic. Medical history included type 2 diabetes, asthma, known allergies to penicillin and known allergies to many "mycin" antibiotics - all from an unknown date. The patient was not pregnant at the time of vaccination and did not have COVID-19 prior to vaccination. Concomitant medications included glipizide and fluticasone propionate, salmeterol (WIXELA INHUB) - both taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccine in four weeks. On 07Feb2021 at 08:15, reported as within 2 minutes of receiving the vaccine, the patient got a horrible pressure type headache with bad foggy brain. This was followed by moderate tightness in the patient's left chest that moved to the center of her chest and began moving upward before was subsided and moved back to her left chest. The headache, fog and pain subsided a bit after about 20 minutes and the patient was able to drive. However all of the symptoms have continued to a lesser degree into the third day. The patient further reported that the symptoms began so quickly after the vaccine shot that she was not sure if it was an allergic reaction or side effects. No treatment was given in response of the events. The patient was not tested for COVID-19 after vaccination. Outcome of all events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: GLIPIZIDE; WIXELA INHUB

Current Illness:

ID: 1530642
Sex: M
Age:
State: NJ

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: He felt very weak and dizzy; He felt very weak and dizzy; I couldn't get out of the bed, I was struggling; Drowsiness; felt like a drunk; First dose administered 08Feb2021, second dose administered 17Feb2021; This is a spontaneous report from a contactable consumer (patient). A 76-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9266, Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 17Feb2021 as dose 2, single for covid-19 immunisation in pop up clinic. No prior vaccinations were given within 4 weeks and no other vaccinations was given within four weeks prior to the first administration date of the suspect vaccine. Medical history included allergy to penicillin. The patient's concomitant medications were not reported. The patient previously took indocin [indometacin] and experienced hypersensitivity. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9264, Expiration date: Unknown), via an unspecified route of administration, administered in left arm on 08Feb2021 as dose 1, single for covid-19 immunisation. The patient was administered with first dose on 08feb2021, second dose administered on 17feb2021 and experienced he felt very weak and dizzy, he couldn't get out of the bed, he was struggling, felt like a drunk and drowsiness on 18Feb2021. The events did not result in emergency room or physician office. Patient received the second dose of the Pfizer-BioNtech Covid-19 vaccine on 17feb2021, next morning he felt very weak and dizzy, this symptom disappeared 15 hours later, patient stated he felt like a drunk. He would like to know if this could be related to the vaccine. The outcome of the event felt like a drunk was unknown and recovered for other events on 18Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530643
Sex: M
Age:
State: OH

Vax Date: 01/29/2021
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: She said after her father got his first COVID-19 Vaccine shot, in a couple days, he felt drained and had no energy; her father had 2-3 spells with his stomach in that he threw up; Tiredness; her father to not feel well; This is a spontaneous report from a contactable consumer (patient's daughter). A 94-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration Date: unknown), via an unspecified route of administration, administered in right arm on 29Jan2021 (at the age of 93-years-old) as dose 1, single for covid-19 immunisation, Lidocaine hcl (LIDOCAINE HCL), via an unspecified route of administration from 2021 (Batch/Lot number was not reported) to an unspecified date, at Patch with 4% Lidocaine for right shoulder and right arm trouble. Medical history included skin cancer on his one ear from an unknown date and unknown if ongoing. Patient's daughter reported that, her father got his first covid-19 vaccine shot, in a couple days, he felt drained and had no energy, he had 2-3 spells with his stomach, in that he threw up, tiredness and weakness on an unspecified date in 2021. She said she had checked her father's vital signs, and his heart rate, oxygen level, and temperature were ok. She said her father had no fever. The reporter stated that she was not sure if either the patches, or the COVID-19 Vaccine may be causing her father to not feel well. Reported on 18Feb2021 that her father said he felt a little better, but on 19Feb2021 her father said he felt tired and weak again. She also reported that, before her father received his first covid-19 vaccine dose, he had trouble with his right shoulder and right arm. She said her father's doctor gave her father some patches for his right shoulder and right arm around the same time her father got his first covid-19 vaccine shot. She said her father was supposed to get his second covid-19 vaccine dose on 19Feb2021 but was told by the pharmacist he had up to 6 weeks to receive the second covid-19 vaccine dose. She said her father had always gotten around good, and her father doesn't drink or smoke. Reported her father usually has blood work every couple of months, and her father's doctor follows her father closely. The event did not require emergency room or physician office visit. Patient did not receive any prior vaccinations within 4 weeks. The outcome of events he had 2-3 spells with his stomach her father to not feel well were unknown and other events were not resolved. No follow-up attempts are needed; information about lot/batch number cannot been obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1530644
Sex: F
Age:
State: NV

Vax Date: 02/16/2021
Onset Date: 02/18/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: feeling general weakness which is new; dizziness worse than normal; Loose bowels; This is a spontaneous report from a contactable other hcp (Nurse). A 87-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6201, Expiration date: unknown), dose 1 via intramuscular, administered in Arm Right on 16Feb2021 14:00 as (Age at vaccination 87 years-old) dose 1, single for covid-19 immunisation. Medical history included atrial fibrillation episode, peripheral neuropathy, hyperlipidaemia-diet controlled vertigo, hypothyroid, bilateral mastectomy prophylactic, osteoarthritis and skin tape (known allergies: skin tape). Concomitant medication(s) included asa, gabapentin; levothyroxine and diazepam, all taken for unspecified indication start and stop date were not reported. The patient previously took bactrim (Bactrim Known allergies) and lovenox (Known allergies: Lovenox). On 18Feb2021 08:00 the patient experienced feeling general weakness which is new, dizziness worse than normal and loose bowels. Patient did not received any treatment for events. Facility type vaccine was administered at hospital. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has been not tested for COVID-19. The clinical outcome of all events were unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: ASA; GABAPENTIN; LEVOTHYROXINE; DIAZEPAM

Current Illness:

ID: 1530645
Sex: F
Age:
State: CO

Vax Date: 02/11/2021
Onset Date: 02/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Very dizzy; Heartbeat was beating fast; Muscles were weak; This is a spontaneous report from contactable female consumer (patient) via Pfizer-sponsored program COVAX US Support. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration Date was not reported), via an unspecified route of administration on 11Feb2021 as dose 1, single for covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient reported that she had the Pfizer Covid vaccine shot on Thursday 11Feb late afternoon. On her way to home she felt very dizzy, and her heartbeat was beating fast, and her muscles were weak on unspecified date in Feb2021. How can she reschedule her second shot so her husband can drive her to the facility. The patient underwent lab tests and procedures which included heart rate: heartbeat was beating fast. The outcome of events was unknown. Information about batch/lot number has been requested. Follow-up (12MAY2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1530646
Sex: M
Age:
State: MI

Vax Date: 02/18/2021
Onset Date: 02/19/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Headache, Fever,Joint pain, irregular heart beat; Headache; Fever; Joint pain; This is a spontaneous report from a contactable consumer or other non hcp. A 76-year-old male patient received second dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: en6200), dose 2 via an unspecified route of administration, administered in Arm Left on 18Feb2021 at 13:30 (age at vaccination was 67 years old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included hypertension from an unknown date and unknown if ongoing. Concomitant medications included atenolol (ATENOLOL) taken for an unspecified indication, start and stop date were not reported; pravastatin (PRAVASTATIN) taken for an unspecified indication, start and stop date were not reported. Patient didn't receive other vaccines within 4 weeks prior to vaccination. Patient previously received first dose bnt162b2 (COMIRNATY, Solution for injection, Batch/Lot Number: el9264,) via intramuscular in Left arm, on 28JAN2021 13:30 (age at vaccination was 67 years old) as DOSE 1, SINGLE for covid-19 immunisation. patient had no allergies patient didn't had covid prior to vaccination and patient was not tested for covid to post vaccination. The patient experienced headache, fever, joint pain, irregular heartbeat on 19Feb2021 at 04:00. The outcome of the events heart rate irregular, headache, pyrexia, arthralgia was recovered on unspecified date. Follow-up attempts completed. No further information expected. FUP#1 (13May2021): Follow-up activities closed: Follow-up attempts completed.

Other Meds: ATENOLOL; PRAVASTATIN

Current Illness:

ID: 1530647
Sex: F
Age:
State: HI

Vax Date: 02/18/2021
Onset Date: 02/20/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Extreme weakness, especially of legs; ache in lower abdomen; vomiting and inability to hold even water down; diminution of vision; fever of 100.3; I slept almost full time from 9:00am until 6:30am the following day, with very brief waking periods.; This is a spontaneous report from a non-contactable consumer or other non-healthcare professional. An 80-years-old female patient (non-pregnant) received the second dose bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection) via an unspecified route of administration, administered in Arm Left on 18Feb2021 16:30 (Lot Number: EN6201, Expiry date was not reported) (at the age of 80-years-old) as a single dose for COVID-19 immunization at the hospital. Medical history included mild allergy to dairy and some fruits. Other medical history was reported as none. The patient previously received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection), dose 1 via an unspecified route of administration, administered in Arm Left on 20Jan2021 16:30 Lot Number: F(E?) L3248, Expiry date was not reported) for COVID-19 immunization. The patient did not receive any other vaccine in 4 weeks of COVID vaccine. The patient did not have other medications in two weeks. The patient did not have COVID prior vaccination and COVID was not tested post vaccination. On 20Feb2021, 07:00 the patient experienced extreme weakness, especially of legs, ache in lower abdomen, vomiting and inability to hold even water down, diminution of vision, fever of 100.3, the patient slept almost full time from 9:00am until 6:30am the following day, with very brief waking periods. Laboratory tests on an unspecified date included body temperature: 100.3 (fever 100.3). There was no treatment received for the events. The clinical outcome of the events was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530648
Sex: F
Age:
State: FL

Vax Date: 02/09/2021
Onset Date: 02/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: It left her weak and tired; It left her weak and tired; Diarrhea; She was exhausted all day and all night, most exhausted she has ever been.; This is a spontaneous report from a contactable consumer or other non hcp (patient). An 83-year-old female patient received second dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: E19269), via an unspecified route of administration on 09Feb2021 (at the age of 83-year-old) at dose 2, single for covid-19 immunisation. Medical history was reported as none. Concomitant medications were not reported. Patient previously received first dose of BNT162B2 via an unspecified route of administration on 09Jan2021 (at the age of 83-year-old) at dose 1, single for covid-19 immunisation (She says they have the first dose written too but she had no side effects with the first dose. She can't make that lot number out either on the vaccine card it might be FL or EL3247). On an unspecified date in Feb2021 the patient experienced it left her weak and tired, diarrhea, she was exhausted all day and all night, most exhausted she has ever been. Reporter says she is 83, she will be 84 at the end of the month. She says she had the second shot yesterday and it left her weak and tired, she stayed in bed all day and she had diarrhea. Her second dose was yesterday 09Feb2021 and after she was exhausted all day and all night, most exhausted she has ever been. Product details: She says the lot number looks like E19269 or it could be FL but to her it looks on the vaccine card like E19269. It just says the date she got it which was 09Feb2021 and the first dose was 09Jan2021. Now that she has gotten 2 shots can they say if she can be out and about among people now or does she still need to stay isolated. She would like an answer to that because she had a chiropractor with no social distancing. He had 15-20 people all together in one room and actually he had her between 2 people in a massage chair and that chiropractor treated a patient and didn't wash his hands and he helped her but that night she had nightmares so she stopped going to him. She says with the diarrhea she was lucky to get home in time it was 20 minutes later, almost instant and she is fine today. She confirms everything is good today, she says when you sleep all day you have to be okay the next day. She would like to know if she can socialize now. She doesn't use a physician so there is no one to follow up with she is not sick, she is a healthy person, other than a chiropractor and he would not know. Events were reported as non-serious. Outcome of all the events was unknown. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1530649
Sex: F
Age:
State:

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: rapid heart beat; Chest tightness; massive pressure in rectum; Weakness; Headache; heart rate lingered; asthma; This is a spontaneous report from a contactable consumer (patient). A 55-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL9269, expiry date: not provided), via an unspecified route of administration on 9Feb2021 (Age at vaccination: 55 years) as DOSE 1, SINGLE for COVID-19 immunisation. The patient medical history included ongoing hemorrhoids. The patient Concomitant medications were not reported. On 9Feb2021, the patient experienced rapid heart beat. On an unspecified date, the patient experienced Chest tightness, massive pressure in rectum, Weakness and headache. It was reported that she received the Covid-19 vaccine on 09Feb2021. After receiving the vaccine she experienced a rapid heart beat. Her heart beat is usually 78. Her heart was fluctuating at 99-100 beats. She has asthma, predetermined. She didn't use her inhaler because she didn't know what it would do. She had chest tightness. She called because she read that severe reactions of the vaccine are increased heart rate. She is asking should she not get the second dose because of the increased heart rate? In the past she has had hemorrhoids. Since getting the vaccine she has had massive pressure in her rectum. She also experienced weakness and a headache. Is increased heart rate a severe reaction to the vaccine? She is unsure about getting the second dose. Her heart rate lingered. It was still there the next day but had decreased before it was back to normal. The lab test included test: Heart rate irregular, result: usually 78,fluctuating at 99-100 beats,increased (lingered,next day but had decreased before it was back to normal) on an unknown date. The outcome of rapid heart beat was recovered on 12Feb2021, while outcome of other events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Hemorrhoids (In the past she has had hemorrhoids.)

ID: 1530650
Sex: U
Age:
State: AZ

Vax Date:
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Also stated another neighbor had the injection previously and was "very" bruised in the injection site "looks like I was beat up"; This is a spontaneous report from a contactable Consumer. This consumer reported for a patient (neighbor). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number and expiry date were not reported) via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The re-porter stated that another neighbor had the injection previously and was "very" bruised in the injection site "looks like I was beat up" on an unspecified date. The outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1530651
Sex: M
Age:
State: FL

Vax Date: 02/01/2021
Onset Date: 02/17/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: anorexia; tachycardia; chills; sweats; temperature 100.8; slight nausea; fatigue; weakness; This is a spontaneous report from a contactable physician (patient himself). A 76-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number and Expiry date was not reported) via an unspecified route of administration in arm left on 01Feb2021 at 09:00 (at the age of 76-years-old) as dose 2, single for COVID-19 immunisation at Other. Medical history included hypertension, chronic kidney disease, coronary artery, malignant melanoma and drug hypersensitivity to penicillin and Cephalosporins. Concomitant medication(s) included lisinopril (LISINOPRIL), atorvastatin (ATORVASTATIN) and ergocalciferol (VIT D). 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. The patient previously received cephalosporin nos and experienced drug hypersensitivity and bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number and Expiry date was not reported via an unspecified route of administration in arm left on 11Jan2021 at 09:00 (at the age of 76-years-old) as dose 1, single for COVID-19 immunisation at Other. On 17Feb2021, the reporter stated that the patient experienced temperature 100.8, chills, sweats, anorexia, tachycardia (102), slight nausea, fatigue, weakness. Fever stopped after 48-60hours. weakness persists to day5. covid rapid antigen test, covid PCR, and Flu negative. Much improved by day 4. No known contact with sick individuals. Always wore a mask, social distancing. Since the vaccination, the patient tested for COVID-19 on 18Feb2021. The reporter stated the events result in Doctor or other healthcare professional office/clinic visit. No treatment was given for the events. The patient underwent lab tests and procedures which included body temperature: 100.8, influenza virus test: negative on 17Feb2021 and sars-cov-1 test: negative (Nasal Swab), sars-cov-2 test: negative on 18Feb2021 (Rapid antigen test and PCR). The outcome of the event temperature 100.8 was recovered on an unspecified date in Feb2021 and other events was recovering. Follow-up attempts completed. No further information expected.

Other Meds: LISINOPRIL; ATORVASTATIN; VIT D

Current Illness:

ID: 1530652
Sex: F
Age:
State: VA

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Tachycardia; heart started racing and pounding; felt like heart was going to burst; This is a spontaneous report from a contactable physician. A 73-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: not reported, Expiration date: Unknown) via an unspecified route of administration on 15Jan2021 (73-year-old at vaccination) in arm (unknown which arm) as a Dose 1, single for Covid-19 immunization. The patient's medical history included ongoing anxiety. There were no concomitant medications. On 19Jan2021, the reporter received a message from her about her reaction to the vaccine that frightened the patient. On 15Jan2021, ten minutes after the shot, her heart started racing and pounding. She thought it was going to burst. It went on 5 minutes. Then it paused for 30 seconds, but then continued for 10-15 minutes more. A nurse monitored her vital signs during that time. The patient didn't have any other symptoms of anaphylaxis. She had no coughing, wheezing, shortness of breath, red itchy eyes, throat swelling, or anything. The reported stated that, the patient developed severe tachycardia for about 5 minutes, stopped for about 30 seconds and then started again. The reporter had talked to 2 infectious disease doctors about this. She also sent the patient to see an allergist, but that didn't really get her any further along than before. The patient was reluctant to take the next one but wanted to get vaccinated at the same time. The reporter did a literature search, and any literature with tachycardia in it with the Covid vaccine was only about anaphylaxis. The doctor was not sure that this was anaphylaxis. She felt like it wasn't. She was looking for any knowledge about tachycardia with the Covid vaccine. She did submit a VAERS report. The patient went to a local hospital system where they are vaccinating people older, and people associated with the school system. There was complete control of her symptoms. They are just trying to figure out what to do about the second dose. She was inquiring to see if she should receive the second dose or not. The patient had underlying anxiety, which had been a lifelong problem. The patient said that she had been anxious before, but this was completely different. She felt like her heart was going to burst. She talked to other doctors that wonder if it was a vasovagal reaction. The reporter doesn't think was an anxiety attack either. The doctor though this occurred and then she became anxious. The patient got the vaccine because she was about the right age, and because her husband had multiple significant health issues. She mostly got it to protect her husband. No investigational assessment was reported. The outcome of the events was recovered on 15Jan2021. A causal relationship between BNT162B2 and Heart started racing and pounding was assessed as being related by the primary source reporter. Method of assessment was Global introspection. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness: Anxiety

ID: 1530653
Sex: F
Age:
State: OH

Vax Date: 02/08/2021
Onset Date: 02/08/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Not in good shape; Hardly has any strength; Tingling; Weakness; Arms and legs numb; Shortness of breath; This is a spontaneous report from a contactable consumer (the patient). A 66-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 08Feb2021 11:00 (at the age of 66-years-old) as a single dose for COVID-19 immunisation (reported as preventative). The patient has no medical history. There were no concomitant medications. The patient did not received any additional vaccines on same date of Pfizer suspect. The patient did not receive prior vaccinations within 4 weeks. On 08Feb2021, the patient experienced weakness, arms and legs numb, shortness of breath. On an unspecified date, the patient was not in good shape, hardly has any strength and tingling. It was reported that she had first COVID-19 Vaccine on Monday (08Feb2021). Ever since then felt so weak, she has almost fallen a couple times. Finally took a shower on the day of reporting because she wasn't up to it before. For a couple of days her arms and legs were numb, which was weird. She was short of breath when she gets up to go to the bathroom. Hardly has any strength. The patient stated that she hasn't been in shape to contact Pfizer. Has been in bad shape and that was the first dose. The patient stated that she did not know if she needs the second dose or what to do about that. She further stated that weakness was within hours of the COVID-19 Vaccine. Almost fell a couple of times and was a little better. Tingling and numbness was getting better, but not 100%. Wanted to see her family again who was high risk. The patient thought about going to the Emergency room (ER) but stated that as long as she was able to get up and go to the bathroom she will not go to the ER. The patient has not felt like going to a regular doctor and was not in good shape because she was afraid that her doctor would advise her to go the ER. She did not want to go to the ER. The patient clarified she did not fall, but almost. The outcome of events arms and legs numb and weakness, tingling was recovering whereas the outcome of all other events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1530654
Sex: F
Age:
State:

Vax Date: 02/05/2021
Onset Date: 02/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: sore throat; sore ears; little cough at night when laying down; feeling down; it was going in her chest; feeling unwell; This is a spontaneous report from a contactable consumer reported for herself received via medical information team. A 67-year-old female patient received bnt162b2 (BNT162B2, formulation: Solution for injection, Batch/Lot Number: EL3247), dose 1 via an unspecified route of administration, injected in her left arm on 05Feb2021 (at the age of 67-year-old) as single for covid-19 vaccination. Medical history included diabetes mellitus from an unknown date and unknown if ongoing, Caller said was diagnosed about 5 years ago. The patient stated that Height: Caller said she was 5 feet 2 inches tall and shrinking, which she clarified was before vaccine. The patient said concomitant medications, they have not had any other recent vaccinations or started any new medications. On 21Feb2021, the patient experienced sore throat, sore ears, little cough at night when laying down and feeling down. On an unspecified date in Feb2021, the patient experienced it was going in her chest and feeling unwell. Consumer called about the Pfizer COVID-19 vaccine who said she had her first COVID-19 vaccine dose back on 05Feb2021 and then was supposed to have her second one, she was not sure if that was supposed to be today or Friday of this week. She said since Sunday she has been feeling down, she has a sore throat and ears, and a little cough at night when she was laying down. She said she doesn't know if she caught something or if it was just allergies or something. She said she was unsure if she should take second dose or not right now, and she also doesn't know when they will have it again at the hospital. Caller said, not provided on handwritten vaccine card. She said that the first dose was given to her around 12:15-12:30 PM. Caller said that her sore throat and ears and cough have stayed about the same. She says it started with just the sore throat, now it was going in her chest. Caller wanted to know if it would be okay to get the second dose of the covid vaccine this week because she's had a sore throat, sore ears and a little cough at night. Can she receive second vaccine, no fever but feeling unwell as described. If she have to put off the vaccine was that okay, What about past 6 weeks, does she have to restart the vaccine series. Outcome of the events sore throat, sore ears and little cough at night when laying down were not recovered and unknown for other events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530655
Sex: F
Age:
State:

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Heart racing/palpitations; slight lightheadedness.; This is a spontaneous report from a non-contactable consumer (patient). A 60-year-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6201) dose 1 via an unspecified route of administration in Arm Right on 23Feb2021 11:15 (at the age of 60 years old) as single for COVID-19 immunisation at public health clinic/veterans administration facility. Medical history included allergy to only MRI contrast. Concomitant medication included ascorbic acid, ergocalciferol, nicotinamide, retinol, riboflavin, thiamine hydrochloride (VITAMINS [ASCORBICACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]) taken for an unspecified indication, start and stop date were not reported and hormones. Patient did not received other vaccine within four weeks of COVID vaccine. Patient did not have COVID prior to vaccination. The patient experienced heart racing/palpitations, slight lightheadedness on 23Feb2021 12:15. Reported as, heart racing/palpitations, slight lightheadedness. This happened within seconds of receiving vaccine. Stopped after 15 minutes. No Treatment was given for adverse event. Patient did not tested for COVID post vaccination. Outcome of the events were recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]

Current Illness:

ID: 1530656
Sex: F
Age:
State: NY

Vax Date: 02/08/2021
Onset Date: 02/10/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: increasingly weak; tired; sleepy; nauseous; not hungry; This is a spontaneous report from a contactable consumer (patient). A 74-years-old non-pregnant female patient received BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: EL9269, Expiration date was not reported), via an unspecified route of administration, administered in left arm on 08Feb2021 at 11:00 hours, as dose 1, single (at the age of 74-years-old) for covid-19 immunisation. Medical history included myalgic encephalomyelitis (ME), Chronic fatigue syndrome (CFS) and penicillin allergy (all from an unknown date and unknown if ongoing). Patient had no other vaccine in four weeks. Patient was not diagnosed with COVID-19, prior to vaccination. Since vaccination, patient had not been tested for COVID-19. Concomitant medication(s) and other medications in two weeks included atorvastatin, liothyronine (NP Thyroid), multivitamin and calcium (all taken for an unspecified indication, start and stop date were not reported). Historical vaccine included patient took tetanus vaccine and had allergy to tetanus vaccine. Patient was ok for first few days. On 10Feb2021 at 09:00 hours, patient was increasingly weak, tired, sleepy, nauseous and not hungry. Patient had no treatment for all the events. The outcome of all the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: ATORVASTATIN; NP THYROID; CALCIUM

Current Illness:

ID: 1530657
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: rapid heart beat; muscle weakness like when you exercise a lot; ears ringing; felt weak; tachycardic; This is a spontaneous report from a contactable other healthcare professional (patient). A female patient (age: 55, Unit: Unknown) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date, as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced rapid heartbeat, muscle weakness like when you exercise a lot and ears ringing. She stated that almost three weeks after the vaccine she still had weakness and her heart rate goes up. It was reported 19 days post-dose 1, she felt weak and 20 days post-dose 1 she was feeling better - no longer weak/tachycardic. The outcome of events felt weak and tachycardic were resolved and unknown for rest of the events. Information about lot and batch number was requested. One follow-up attempt are completed; information about batch/lot cannot be obtained.

Other Meds:

Current Illness:

ID: 1530658
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: received both doses of the Covid vaccine. Patient was currently 38 weeks pregnant and was going to deliver on Monday 22Feb2021; Patient had both doses with only a sore injection site; This is a spontaneous report from a contactable consumer, the patient. A pregnant female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: not provided) via an unspecified route of administration, on an unspecified date Dose 1,Single for COVID-19 immunization and received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: not provided) via an unspecified route of administration, on an unspecified date Dose 1,Single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient recently received both doses of the Covid vaccine. Patient was currently 38 weeks pregnant and was going to deliver on Monday Feb2021. Patient was hoping she could help with blood testing for antibodies from baby id that would help. Patient had both doses with only a sore injection site. No other complications. Outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1530659
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: too weak; This is a spontaneous report from a Contactable consumer. This consumer reported for a 79 year old male patient (Father) that he received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number, Expiry Date: Unknown), via an unspecified route of administration on an unspecified date as dose 2, single for covid-19 immunization. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number, Expiry Date: Unknown), via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunization. Medical history included arrhythmia, heart failure, CKD, T2DM, high cholesterol. He had the Covid infection in Nov2020 which put him in the hospital for a week and wiped him out (bed-ridden) for at least a month after he returned from the hospital in Nov2020. Patient had his 2nd Covid vaccine on Friday (unspecified date) and on Saturday (unspecified date) he was on the bedroom floor, he was too weak to get back into bed after crawling to the bathroom. Reporter's sister would give the reporter an update later that day on his status. Reporter notified that he felt much better just after reporter's initial report, on 22Feb (Monday). The outcome for the all the event was recovering. No follow-up attempts are possible, information about lot (or) batch no. cannot be obtained

Other Meds: METFORMIN; LANTUS

Current Illness: COVID-19 (hospital for a week and wiped him (rest detail captured in narrative))

ID: 1530660
Sex: F
Age:
State: LA

Vax Date: 02/20/2021
Onset Date: 02/20/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Rapid heart beat; Joint pain; Muscle pain; Fatigue; Swelling in the area of shot; This is a spontaneous report from a contactable consumer (patient). A 74-years-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Left on 20Feb2021 00:30 (Batch/Lot Number: EL9267, Expiry date: unknown, Age at the vaccination: 74-year-old) as dose 2, single for covid-19 immunization. Medical history included asthma and known allergies: sulfur drugs, papaya, mango. Concomitant medications included metformin, procaterol hydrochloride (PRO-AIR), ergocalciferol (VIT D), montelukast and losartan; all drugs taken for an unspecified indication, start and stop date were not reported. Historical vaccine included patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Right on 27Jan2021 12:30 AM (Batch/Lot Number: EL8982, Expiry date: unknown, Age at the vaccination: 74-year-old) as dose 1, single for covid-19 immunization and experienced after the first shot the patient had rapid heartbeat for four days. After the first shot, the patient had rapid heartbeat for four days. Covid prior vaccination and covid tested post vaccination was mentioned as no. On 20Feb2021 14:30, the patient experienced rapid heartbeat, joint pain, muscle pain, fatigue, swelling in the area of the shot. The patient underwent lab tests and procedures included heartbeat with rapid results on 20Feb2021. The patient was not received any treatment with respect to events. The outcome of events was recovering. 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: METFORMIN; PRO-AIR; VIT D; MONTELUKAST; LOSARTAN

Current Illness:

ID: 1530661
Sex: F
Age:
State:

Vax Date: 02/10/2021
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: pain through my entire body. The pain was going through my skull, bones on my face, chin, thighs, neck, shoulder and lower back; Thought maybe vaccine kicked up her fibromyalgia; I feel so sick now; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (BNT162B2, Batch/Lot number was not reported) via an unspecified route of administration on 10Feb2021 as dose 1, single for covid-19 immunisation. The patient medical history was not reported. There were no concomitant medications. She had a severe allergic reaction after a previous dose of this vaccine and to any ingredient of this vaccine. The patient experienced pain, thought maybe vaccine kicked up her fibromyalgia on an unspecified date. She stated "I got my first vaccine shot on 10Feb2021. 3-4 days after I developed pain through my entire body. The pain was going through my skull, bones on my face, chin, thighs, neck, shoulder and lower back. It's hurting so much that I feel nauseas. I was okay until I had the vaccine. I feel so sick now. The pain has not gone away. At first she thought maybe the Pfizer COVID-19 Vaccine kicked up her fibromyalgia but this happened maybe 4 days after the Pfizer COVID-19 Vaccine injection. She was nauseous from pain. Her second dose of Pfizer COVID-19 Vaccine is this Wednesday, 03Mar2021 and she does not know if she should get it relative to these events; asked for dosing recommendations relative to events." Caller wants to know if she was eligible to receive the second dose. After I told her two doses are required for full protection she mentioned her friend died from COVID after receiving the two doses of the vaccine. She already had done bloodwork, urine test and was prescribed with prednisone. She wanted to know if she could take prednisone. The outcome of the events was unknown. Follow-up attempts not completed; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1530662
Sex: F
Age:
State: VA

Vax Date: 02/20/2021
Onset Date: 02/23/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: elevated heart rate; Heart rate high; sweats at night; This is a spontaneous report from a contactable Nurse reported for herself. A 76-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE Solution for injection Batch/Lot number was not reported) via an unspecified route of administration on 20Feb2021 (at the age of 76-years-old) as single dose for COVID-19 immunisation. Medical history included palpitations from an unknown date and unknown if ongoing. Concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 on 20Jan2021 for COVID-19 immunisation. Patient queried asking if her elevated heart rate was a side effect from the vaccine and how long it was expected to last and had anyone died from the vaccine and have you received any calls from people who had experienced this. It was reported that she had both doses of the Pfizer vaccine, her second dose of the vaccine was on 20Feb and on 23Feb she went to the ER and was admitted for 5 hours. On 23Feb2021, she had been experiencing an elevated heart rate around 120bpm, heart rate high, sweats at night. She had spoken to her doctor and was advised to increase her dose of metoprolol. She wants to file a report, she was a registered nurse, retired. The caller had the Pfizer COVID vaccine, she had the first dose 20Jan2021, then she did not have any problems. The caller believed that the second dose was more potent, and on 20Feb, 3 days after she received the vaccine, she noticed her heart rate was going up to around 150. The problem was she did not have any symptoms. The caller took her vital signs while watching TV, her husband is a doctor. The caller had no symptoms then she had sweats at night and couldn't take it anymore, so she went to the Emergency Room. The caller was worked up and they did all the tests, which came back negative. The Emergency Room did an EKG two times, they drew troponins two times, they hydrated her with Lactated Ringers solutions, she consumed about 1,500 ccs, pulse was high, it came down to 120, not real down. Then the Emergency Room decided to let her go, she stayed there for 5 hours. The caller called her primary doctor. The caller already takes metoprolol for blood pressure and sometimes she would also have tachycardia would have palpitations so she would have to take extra then. The caller always takes it for her blood pressure and she always had symptoms if her heart rate was high and has to add more metoprolol then. She was still monitoring her heart rate, her primary care provider gave her something to go by if the heart rate goes up to 120, she was to take another 50mg, she could adjust it. Description of complaint: The caller already took metoprolol for blood pressure and sometimes she would also have tachycardia would have palpitations so she would have to take extra then, always takes it for her blood pressure and she always had symptoms if her heart rate was high and had to add more metoprolol then. Product strength and count size dispensed: metoprolol. Caller declined safety report, no additional information or details captured at this time. The patient underwent lab tests and procedures which included EKG resulted as unknown results on 23Feb2021, heart rate resulted as 120 bpm and around 150 on 23Feb2021, pulse resulted as high, it came down to 120 on an unspecified date, test resulted as negative on 23Feb2021, troponin resulted as unknown results on 23Feb2021 they drew troponins two times, they hydrated her with Lactated Ringers solutions, she consumed about 1,500 ccs. The clinical outcome of the events was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1530663
Sex: F
Age:
State: NC

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: heart was beating fast; hard time breathing; This is a spontaneous report from a contactable consumer (patient) via Pfizer-sponsored program COVAX US Support. A 70-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6201), via an unspecified route of administered on 09Feb2021 at 14:00 (at the age of 70-year-old), as dose 1, single in left arm for COVID-19 immunisation at hospital. The patient's medical history was none, and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had no additional vaccines administered on same date of the Pfizer vaccine. On 09Feb2021, while waiting after the first dose of vaccine, the patient's heart was beating fast and experienced a hard time breathing. It slowed and was back to normal before she left. Patient was concerned about getting the second dose on 02Mar2021. The patient underwent lab test and procedure which included heart rate: beating fast, on 09Feb2021. The clinical outcome of both the events was resolved on 09Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530664
Sex: F
Age:
State: TN

Vax Date: 03/02/2021
Onset Date: 03/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: heart was racing, fast heart beat; sore arm and joints; sore arm and joints; Chills; it was still a little faint; This is the spontaneous report from a contactable Consumer. A 66-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot Number: EN6205 and Expiry Date: Jun2021), via an unspecified route of administration, administration at Arm Left on 02Mar2021 around 09:30 in morning (vaccinated at the age of 66 years) as DOSE 1, SINGLE for covid-19 immunisation. The patient was not pregnant at the time of vaccination. The patient medical history included hypertension, high cholesterol, Non-Hodgkin's lymphoma (she was a cancer survivor, she had her last treatment 16 years ago). She was not allergic to vaccines. Historical vaccine included Influenza vaccine in October and a pneumonia shot. She says she also had the shot for the virus where the sores come on you, she had that shot for where red bumps come all over you, or blisters, she forgets when she had that one or what it is called, they have a vaccine for it now. The Concomitant medications were not reported. Patient stated that it was injected in her left arm. She says that her arm and joints are sore still, a little sore, she had some chills too and at night she woke up and her heart was racing, fast heartbeat. She know sometimes when she was dreaming, she woke up and her heart was beating a little fast. When she woke up this morning, it was beating more faintly still a little fast not hard, like boom boom boom." Caller said she was able to breathe deeply and her heart rate slowed down, then she went back to sleep. Consumer who says she thought she would be pleased with getting the vaccine, then last night she woke up with a fast heartbeat. She says she didn't have other reactions like the difficulty breathing, swelling, rash, or dizziness, she just woke up in the middle of the night with a fast heartbeat that gradually quieted down. She says she would like to know if this could be one of the side effects, or what's going on with that. She says that she had the regular reaction of sore arm and joints as well, it was just it seemed her heartbeat was a little fast, and when she got up and took her blood pressure medicine (no further details provided about this medication) it was still a little faint. She says she was usually not allergic to vaccines, she couldn't understand, sometimes when dreams wake her up, she will feel her heart beating but she didn't have a nightmare or anything. She says she just woke up to a rapid heartbeat that quieted down after she breathed hard, so it quieted down, and she went to sleep. Patient said she was wondering if this was common, she didn't have any other serious side effects. Outcome the events heart was racing, fast heartbeat, sore arm and joints and sore arm and joints was unknown, and it was still a little faint was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530665
Sex: F
Age:
State: TN

Vax Date: 03/02/2021
Onset Date: 03/03/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Rapid heart rate. Beats per minute as high as 108-110 at highest point. Noticed redness on both arms below elbows. Primarily on arm where had injection. Tried to take blood pressure with home bl; Blood pressure higher than normal with diastolic above 100; redness on both arms below elbows. Primarily on arm where had injection; redness on both arms below elbows. Primarily on arm where had injection; This is a spontaneous report from a contactable Consumer (patient reported for herself). A 65-year-old non-regnant female patient received bnt162b2 (BNT162B2, formulation: Solution for injection, Lot Number: EN6205), dose 1 via an unspecified route of administration, administered in Arm Left on 02Mar2021 12:30 (at the age of 65-year-old) as dose 1, single for covid-19 immunization. The patient Other medical history included PVCs (Premature ventricular contractions), high blood pressure, high cholesterol and migraines. The patient had no covid prior vaccination. The patient received unspecified concomitant medications. The patient previously took and had Known allergies to wheat, amoxicillin-pot Clavulanate, sulfamethoxazole-trimethoprim, Benzonatate and Nitrofurantoin Macro. The patient received no other vaccine in four weeks. The patient received unknown medications in two weeks of vaccination. The patient had not been covid tested post vaccination. On 03Mar2021 at 12:00 AM, the patient experienced Rapid heart rate. Beats per minute as high as 108-110 at highest point, noticed redness on both arms below elbows, primarily on arm where had injection. Tried to take blood pressure with home blood pressure cuff and blood pressure higher than normal with diastolic above 100. The patient Went to emergency room and symptoms had lessened by the time she arrived. The patient received no treatment for the events. The outcome of the events was resolving at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1530666
Sex: F
Age:
State: IL

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: receive the COVID vaccine while pregnant/COVID dose 2 04Jan2021/Date of outcome of pragnancy: 01Feb2021; Flu like symptoms; fever; This is a spontaneous report from a contactable nurse (patient). This nurse reported in response to HCP follow-up letter sent in cross reference case that included: A 34-year-old pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EJ1685; Expiration Date: Mar2021), intramuscular, administered in Deltoid Right on 04Jan2021 (at the age of 34-year-old) as dose 2, single for COVID-19 immunization. Medical history included, Fallopian tube rupture/removal (Ectopic pregnancy in Oct2019 W/R fallopian tube rupture/removal) from Oct2019 to an unknown date (Previous maternal pregnancy complications). There were no concomitant medications and did not taken other drugs during pregnancy like prescription, over-the-counter). Patient was pregnant at the time of vaccination. The patient previously received first dose of BNT162B2 (Lot Number: EH9899; Expiry Date: Mar2021), intramuscular, administered in R deltoid on 17Dec2020 (at the age of 34-year-old) for Covid-19 Immunization and received the COVID vaccine while pregnant. Facility where vaccination was administered at Hospital. Vaccine was not administered at military Facility. The patient received the covid vaccine while pregnant/covid dose 2 04Jan2021/date of outcome of pregnancy: 01Feb2021 on an unspecified date, flu like symptoms on Jan2021 (12 hrs after 2nd dose that lasted 24 hrs from start fever), fever on Jan2021. The mother reported she became pregnant while taking bnt162b2. The patient was 8 Months pregnant (3rd Trimester) at the onset of the event. The patient delivered the pregnancy on 01Feb2021 via vaginal delivery. The baby was delivered full-term. The baby weighed 2721.5 grams. APGAR Score 1 was 8 (8/9), APGAR Score 2 was not provided, APGAR Score 3 was not provided. The fetal outcome is normal. Normal vaginal birth 39 weeks. Illness/AE: Pregnant, Onset Date: 15May2020. Patient did not drink alcohol, not use illicit drugs during this pregnancy. Patient did not have previous pregnancy and not had children. Patient did not have any problems before delivery and not had any problems during delivery including delivery complications, fetal distress, amniotic fluid abnormal, abnormal placenta. Did not had any problems after delivery and mode of delivery was natural birth checked epidural and induction at 39 weeks. Outcome of Infant was normal new born and sex was Female and Length at Birth: 19 in. Father did not take any other drug (e.g., over-the-counter, medical prescription), did not smoke and not use illicit drugs during the mother's pregnancy, drink alcohol during the mother's pregnancy (2x per week). Patient first day of last menstrual period was 01May2020 and estimated date of conception was 15May2020. Patient was not admitted to hospital. Patient received Tylenol/(Acetaminophen), Oral 650 mg every 6 hrs, administered on 05Jan2021 (After vaccine approx. 12 hours). The patient underwent lab tests and procedures which included Blood tests: unknown results, Fever: 99.8 on Jan2021, Urine Culture: unknown results, Ultra Sounds: unknown results. Therapeutic measures were taken as a result of flu like symptoms, fever. The outcome of events was unknown and recovered for flu like symptoms on an unspecified date in Jan2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1530667
Sex: F
Age:
State: IL

Vax Date:
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: feeling like a muscle injury; decline in range of motion; This is a spontaneous report from a contactable consumer or other non Health care professional (patient, self-reporting) via Pfizer Spontaneous Program. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), via an unspecified route of administration in arm on an unspecified date as single dose and second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported) via an unspecified route of administration in arm on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced feeling like a muscle injury and decline in range of motion on an unspecified date. She reported that had her first and second dose of the COVID-19 vaccine, reporter stated that injections were both in the same arm, complaints of feeling like a muscle injury and decline in range of motion. The outcome of the events was unknown. No follow up attempts are possible. Information about lot/ batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1530668
Sex: F
Age:
State:

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: her skin is very tight/ the skin stretches so much.; My cheeks were very feverish; I was chill; I got a little bit of rash on my cheeks and my face; my ankles had swelled up so much; got worse/it continues to swell up again as the day progresses; very or extremely dizzy; walking wobbly/I couldn't walk in a straight line; her legs got really swollen; lymphedema in the legs; very weak; This is a spontaneous report from a contactable consumer or other non hcp reporting for herself. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EM9809; Expiration date was not reported), via an unspecified route of administration on 01Mar2021 at about 13:00 or 15:00 hr as dose 1, single for covid-19 immunisation. The patient' medical history included lymphoedema (history details in legs) from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. On 01Mar2021 at 18:00 hr, patient experienced very or extremely dizzy and was walking wobbly or couldn't walk in a straight line if she wanted to and felt like she was drunk or drinking that's what she does that but that was it looked like and very weak. Patient experienced lymphedema in the legs, started the evening of her vaccination (01Mar2021) and got worse the next day (02Mar2021). Prior to vaccination she had managed (in control) of her condition and she had lymph massages. However, after the vaccine her legs got really swollen to the point that her skin was very tight. Patient said she hadn't gotten this reaction in a year. However, the issue at hand was, she knew that she had lymphedema (history details) in legs and knew that the swelling was developing, the next morning (02Mar2021) when she woke up, her cheeks were very feverish. Patient was chill and got a little bit of rash on cheeks and face, but legs were continuing to swell and by the end of the day by mid-day, it was hard for her to walk that ankles had swelled up so much. The swelling went down on the morning of this report (04Mar2021), but it continued to swell up again as the day progressed. Patient wanted to know if these adverse events are associated with the vaccine. Patient was scheduled for a second vaccine and was not sure if she should take it because of the lymphedema and the side effects, was really feeling dizzy. Patient asked what the signs of a severe allergic reaction are. When paraphrased about her concerns, patient stated no. Firstly, it was both legs and secondly it was difficult to walk, was able to walk, the skin stretches so much. Patient did not want to put it that she couldn't walk but it was not normal walking like your skin was stretched so much, so it was in both legs. The rash did go away during the course of the day, it was very slight red, and it went away. Consumer was informed about the Pfizer Medical Information and filing a safety report. Further probing could not be done as consumer didn't want to share further information. Hence, limited information available over the call. Clinical outcome of rash was recovered on unspecified date in Mar2021, of legs got really swollen was not recovered while outcome of the other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530669
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: her heart rate dropped to 40-45 beats per minute.; This is a spontaneous report from a contactable female consumer or other non hcp from a Pfizer-sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch Number/Lot Number: Not reported) via an unspecified route of administration on an unspecified date as Dose 2, Single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch Number/Lot Number: Not reported) via an unspecified route of administration on an unspecified date as Dose 1, Single for COVID-19 immunization. The patient experienced her heart rate dropped to 40-45 beats per minute on an unspecified date. Patient had a weird side effect after the Covid vaccine with dose 2. The patient underwent lab tests and procedures which included heart rate: 40-45 on an unspecified date dropped to 40-45 beats per minute. The outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1530670
Sex: F
Age:
State: MO

Vax Date: 01/01/2021
Onset Date: 01/11/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Dizziness; Tachycardia; Nausea; Diarrhoea; This is a spontaneous report from a contactable patient. A 36-year-old female received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: unknown) via an unspecified route of administration on an unspecified date in Jan2021 as single dose for COVID-19 immunization at hospital. Medical history was not reported. Patient had no known allergies. Concomitant medications were not reported. Patient did not receive any other vaccine in four weeks of Covid-19 vaccine. Patient did not have covid prior vaccination and was not tested for Covid post vaccination. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number EK5730) intramuscular in left deltoid on an unspecified date at 08:45am as single dose for COVID-19 immunization and experienced nausea and diarrhoea. On 11Jan2021 at 12:30 after second dose of vaccination, patient experienced dizziness and tachycardia [24th-48th hours after the vaccine]. On an unspecified date in 2021, after second dose patient experienced nausea and diarrhoea again. Patient underwent lab tests which included Heart rate monitored as 155 vesting (range 60-100). Adverse event did not result in a visit to Emergency room and Physician room. No culture was performed and there were no predisposing factors. Treatment received in response to the events was unknown. Outcome of the event was recovered on an unspecified date of Jan2021. Outcome of nausea and diarrhea was recovered on an unspecified date of 2021. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : PFIZER INC-2020508576 same patient, vaccine first dose events

Other Meds:

Current Illness:

ID: 1530671
Sex: F
Age:
State: CA

Vax Date: 02/24/2021
Onset Date: 02/28/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Fast heartbeat; This is a spontaneous report from a contactable consumer (Patient herself). A 72-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6265), via an unspecified route of administration, administered in Arm Left on 24Feb2021 12:45 (at the age of 72-years-old) as dose number unknown, single for covid-19 immunization at Pharmacy or Drug Store. The patient's medical history included hypertension. Concomitant medication included losartan and acetylsalicylic acid (ASPIRIN) (low dose aspirin) both for unknown indication and start stop date not reported. The patient had no other vaccine in four weeks. The patient had no covid prior vaccination. The patient was not tested for covid post vaccination. The patient previously took amoxicillin;clavulanic acid (AUGMENTINE) and alendronate and experienced known allergies. On 28Feb2021, the patient experienced fast heartbeat. The patient did not received treatment for event. The outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: LOSARTAN; ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 1530672
Sex: F
Age:
State: MI

Vax Date: 03/04/2021
Onset Date: 03/06/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Rapid heart beat/my heart seemed to be beating faster when I woke up; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 75-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE solution for injection,Batch/Lot Number: EL9Z6F) dose1, via an unspecified route of administration on 04Mar2021 (age at vaccination was 75 years) as single dose for covid-19 immunization. Medical history included diabetes mellitus from an unknown. Concomitant medication included insulin glargine (LANTUS) taken for an unspecified indication, start and stop date were not reported. On06Mar2021, the patient experienced rapid heartbeat/my heart seemed to be beating faster when woke up then it went back to normal. She wants to know if this is something she should be concerned about. Caller states she weights 220 lbs. The patient underwent lab tests and procedures which included heart rate: rapid on 06Mar2021 this morning heart seemed to be beating faster, weight: 54.43 kg on an unspecified date. the outcome of the events was recovered on 06Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: LANTUS

Current Illness:

ID: 1530673
Sex: F
Age:
State: IL

Vax Date: 03/01/2021
Onset Date: 03/02/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Rapid heartbeat and face flushed the next day; face flushed; This is a spontaneous report from a non-contactable consumer (patient). A 77-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: unknown), via an unspecified route of administration on 01Mar2021 at 15:00 as dose 1, single for covid-19 immunisation. Medical history included hypertension from an unspecified date. The patient had no known allergies. Concomitant medications included amoxicillin (AMOXICILLIN) taken for an unspecified indication, start and stop date were not reported; metronidazole (METRONIDAZOLE) taken for an unspecified indication, start and stop date were not reported received in two weeks of vaccination. The patient did not receive other vaccine in four weeks of vaccination. The patient was not diagnosed with COVID-19 prior vaccination. The patient has not been tested for COVID-19 post vaccination. On 02Mar2021 at 10:00, the patient experienced rapid heartbeat and face flushed the next day and face flushed. Adverse events resulted in Doctor or other healthcare professional office/clinic visit. Treatment for adverse events was Unknown. The patient underwent lab tests and procedures which included heartbeat (heart rate): Rapid heartbeat on 02Mar2021. The outcome of events was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds: AMOXICILLIN; METRONIDAZOLE

Current Illness:

ID: 1530674
Sex: F
Age:
State: TX

Vax Date: 03/03/2021
Onset Date: 03/04/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: tachycardia; heartbeat was fast; This is a spontaneous report from a contactable consumer (patient). An 81-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection) via an unspecified route of administration on 03Mar2021 (Batch/Lot number: not reported) as first dose, single for COVID-19 immunization. Medical history included atrial fibrillation. The patient's concomitant medications were not reported. On 04Mar2021, the patient experienced an episode of tachycardia and heartbeat was fast. Patient wanted to know if this can be related to vaccine. She further asked that after the side effects she experienced, did she need to get the second dose. Laboratory tests on an unspecified date included heart rate: fast. The clinical outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1530675
Sex: F
Age:
State: TN

Vax Date: 02/22/2021
Onset Date: 02/22/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: I started to cry; for 1 week I had depression; general sadness for 1 week; back aches; nausea; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 72-years-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EL9266), via an unspecified route of administration on 22Feb2021 11:45 (at the age of 72-year-old) as dose 1, single for covid-19 immunisation. Medical history included lung neoplasm malignant from an unknown date and unknown if ongoing Remission 9 years, known allergies- Highly sensitive to many drugs. No concomitant medications were taken. 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. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other medications within 2 weeks of vaccination. On 22Feb2021, twenty minutes after vaccination, patient started to cry, for 1 week patient had depression, general sadness for 1 week, back aches, nausea. No treatment was taken as a result of events. The outcome of the events were recovered on an unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1530676
Sex: F
Age:
State: MA

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Tachycardia 140's occurred for both vaccine; This is a spontaneous report from a contactable Other HCP (patient). A 41-years-old female patient received second dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EK9231; Expiration Date: 30Apr2021) via intramuscular in Deltoid Left on 20Jan2021 09:10 (age at vaccination was 41 Years old) as SINGLE for covid-19 immunization. On 20Jan2021 at 8:10 (one hour prior to 2nd vaccine), the patient administered with unspecified antipyretic (unknown dose). The patient medical history was unknown whereas, relevant tests was reported as none. The patient's concomitant medications were not reported. Patient previously received first dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EK5730 Expiration: 31Mar2021) via intramuscular in deltoid on 28Dec2020 11:00 (age at vaccination was 41 Years old) as SINGLE for covid-19 immunization and experienced GI issues, sore arm, chills, shivering, high fevers, tachycardia, head aches, nasal/sinus congestion, fatigue, dehydration, dizziness, sore throat. The patient experienced tachycardia 140's occurred for both vaccines on an unspecified date in 2021 and was resulted in physician office visit for the event. The outcome of the event tachycardia was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1530677
Sex: F
Age:
State: PA

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: very fast heart rate; vice-like tightness across lower back; Weak /greater weakness; not walking straight forward; growing tightness of my lower back from side to side with significant pain; arm pain; severe headache; This is a spontaneous report from a contactable consumer (patient). An elderly non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EN9581) via an unspecified route of administration in Arm Right on 17Feb2021 08:30 as dose 1, single for COVID-19 immunisation at hospital. Medical history included known allergies. Concomitant medication taken in two weeks included montelukast sodium (SINGULAIR), hydrochlorothiazide (HYDROCHLOROTHIAZIDE), acetylsalicylic acid (ASPRIN), and VITAMINS all taken for an unspecified indication, start and stop date were not reported. Patient did not received other vaccine within four weeks of COVID vaccine. Patient did have COVID prior to vaccination. The patient experienced very fast heart rate, vice-like tightness across lower back, weak /greater weakness, not walking straight forward, arm pain, severe headache, growing tightness of my lower back from side to side with significant pain on 17Feb2021 08:45. Event reported as, within a half hour, very fast heart rate, vice-like tightness across lower back, weak and not walking straight forward. By evening, arm pain, severe headache, greater weakness, and growing tightness of my lower back from side to side with significant pain. All effects continued to increase for three and a half days until patient was taken to the emergency room. weeks later patient was a bit weak and have occasional minor pain. Treatment was received with many tests and then IV pain medication. Patient did not tested for COVID post vaccination. The patient underwent lab tests and procedures which included heart rate: very fast, laboratory test: unknown results on an unspecified date. Outcome of all the events were recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: SINGULAIR; HYDROCHLOROTHIAZIDE; ASPRIN

Current Illness:

ID: 1530678
Sex: F
Age:
State: CA

Vax Date: 03/16/2021
Onset Date: 03/16/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Muscle pain in arm; Received vaccine while pregnant; This is a spontaneous report from a contactable consumer(Patient). A 41-years-old pregnant female patient received first dose of bnt162b2 (BNT162B2, PFIZER-BOTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6208), via an unspecified route of administration, administered in Arm Left on 16Mar2021 14:00 (Age at vaccination: 40-years-old) as single dose and second dose via an unspecified route of administration, administered in Arm Left on 06Apr2021 13:00 (Batch/Lot Number: ER8737) as single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medication included ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL VITAMINS) taken for an unspecified indication, start and stop date were not reported. last menstrual date was 25Sep2020. Gestational period was 25 weeks. expected delivery date was 06Jul2021. Patient was not diagnosed with covid-19 prior to vaccination. Patient did not receive any other vaccine in four weeks. It was reported that on 16Mar2021 14:00 received vaccine while pregnant. Upon date 07Apr2021 it was reported that on 06Apr2021 received second dose while pregnant. Muscle pain in arm. Patient did not receive treatment for the events. Patient did not tested for covid post vaccination. The outcome for the event muscle pain in arm was reported as resolving at the time of this report. Follow up information has been requested.

Other Meds: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS

Current Illness:

ID: 1530679
Sex: F
Age:
State: CO

Vax Date: 03/10/2021
Onset Date: 03/11/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: severe tachycardia; severe muscle tremor; fatigue; what seems to be a skip in my heart beat.; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 66-year-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EN6198), via an unspecified route of administration, administered in arm left on 10Mar2021 09:30 AM (at the age of 66-year-old) as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient had no known allergies. Patient did not receive any other vaccine in four weeks. Patient did not receive any other medications in two weeks. Patient was not diagnosed with COVID prior vaccination. Patient was not COVID tested post vaccination. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EN6200), via an unspecified route of administration, administered in arm left on 17Feb2021 09:30 AM (at the age of 66-year-old) as dose 1, single for COVID-19 immunization. On 11Mar2021, the patient experienced severe tachycardia, severe muscle tremor, fatigue, what seems to be a skip in my heartbeat. Adverse event: 16 hours post 2nd injection experienced severe tachycardia and severe muscle tremor on and off for several hours during the night. There is no history of this occurring. I am experiencing fatigue and what seems to be a skip in my heartbeat. The patient did not receive treatment for the events. Outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1530680
Sex: F
Age:
State: NM

Vax Date: 03/17/2021
Onset Date: 03/01/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: experienced fast heart beat; little lightheadedness; This is a spontaneous report from a contactable consumer (patient) reported for herself. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE Solution for injection Batch/Lot number was not reported) via an unspecified route of administration on 17Mar2021 11:30 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 17Mar2021, the patient experienced fast heartbeat started around 12:50 after the vaccine and stated that she is feeling better now just a little lightheadedness on unspecified date in Mar2021 but other than that she is good and wanted to know what she should do. The patient underwent lab tests and procedures which included heartbeat resulted as experienced fast on 17Mar2021. The clinical outcome of the events was resolving. No follow-up attempts are Possible. Information on Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1530681
Sex: F
Age:
State: NJ

Vax Date: 03/15/2021
Onset Date: 03/15/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: Experienced fast heart beat within 40 mins after receiving first shot.; This is a spontaneous report from Non-contactable other HCP. A 44-year-old non-pregnant female patient first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: ep7534), via an unspecified route of administration on arm left on 15Mar2021 10:30 AM (Age at Vaccination: 44 years) as DOSE 1, SINGLE for COVID-19 immunisation. The patient medical history included pre-diabetic and had no known allergies. If other vaccine in four weeks and other medications in two weeks was reported as no. If covid prior vaccination and If covid tested post vaccination was reported as no. The patient Concomitant medications were not reported. On 15Mar2021 11:00 AM, the patient experienced fast heart beat within 40 mins after receiving first shot. The treatment received as a result of events was reported as no. The outcome of the event was recovered on an unknown date in Mar2021

Other Meds:

Current Illness:

ID: 1530682
Sex: F
Age:
State: AZ

Vax Date: 03/16/2021
Onset Date: 03/16/2021
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: fast heartbeat; Dizziness; Weakness; heart started palpitating; This is a spontaneous report from a contactable consumer (patient). A 63-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: ER2613, Expiration date: Unknown) via an unspecified route of administration, administered in left arm on 16Mar2021 13:30 (at the age of 63-years-old) as dose 1, single for COVID-19 immunization. History of all previous immunization with the Pfizer vaccine considered as suspect was none. No prior vaccinations were given within 4 weeks. Medical history included schizophrenia, blood cholesterol increased, gastrooesophageal reflux disease, calcium deficiency, breast cancer, bone loss, osteopenia, mastectomy. Family medical history was none. Concomitant medications included paliperidone (INVEGA [PALIPERIDONE]) taken for schizophrenia, from unknown start date to 05Mar201; atorvastatin taken for blood cholesterol increased from an unspecified start date and ongoing; famotidine taken for an unspecified indication from 05Mar2021 and ongoing; calcium taken for calcium deficiency from an unspecified start date and ongoing; anastrozole (ARIMIDEX) taken for bone loss, osteopenia, calcium deficiency, start and stop date were not reported. On 16Mar2021 at 15:30, the patient experienced fast heartbeat, dizziness, weakness and heart started palpitating. Patient stated right after the shot her heart started palpitating, fast heartbeat, happened all 16Mar2021 at 15:30 lasted till 5 am of 17Mar2021. Patient stated the fast heartbeat started the same time as heart palpitation, dizziness, and weakness and lasted all the way until about 5 am of 17Mar2021. The events did not result in emergency room or physician office. The patient stated the side effects are almost all gone. The patient underwent lab tests and procedures which included heart rate: fast on 16Mar2021. No treatment was given for the events. The outcome of the events was recovered on 17Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: INVEGA [PALIPERIDONE]; ATORVASTATIN; FAMOTIDINE; CALCIUM; ARIMIDEX

Current Illness:

ID: 1530683
Sex: M
Age:
State:

Vax Date: 03/07/2021
Onset Date:
Rec V Date: 08/06/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List:

Symptoms: fast heartbeat; Boredom; Fatigue; This is a spontaneous report from a contactable consumer (patient). A 83-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration Date: unknown), via an unspecified route of administration on 07Mar2021 as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 07Mar2021, the patient experienced following symptoms fast heartbeat, boredom and fatigue. The patient underwent lab tests and procedures which included heart rate: fast on an unknown date. Outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 599,999

Page last modified: 03 October 2021 5:28pm