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

ID: 1254705
Sex: F
Age:
State: VA

Vax Date: 03/23/2021
Onset Date: 03/23/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: hearing is also coming and going periodically in both ears; I also felt like I was going to pass out about 5 minutes after the shot; Tinnitus in both ears started within about a half hour; I also have some facial numbness/tightness; I also have some facial numbness/tightness; intermittent ear pain; My joints in my feet and the bottom of my feet hurt.; ear fullness; very sensitive to sound; This is a spontaneous report from a contactable consumer. A 50-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in right arm on 23Mar2021 at 10:15 (Batch/Lot Number: ER8727) as single dose for COVID-19 immunisation. Medical history included Lyme disease from an unknown date. The patient has no known allergies. The patient is not pregnant. Concomitant medications included colecalciferol (VITAMIN D); probiotics; fish oil all taken for an unspecified indication, start and stop date were not reported. On 23Mar2021 at 10:30 AM, the patient reported of tinnitus in both ears started within about a half hour of receiving first dose. The patient also felt like she was going to pass out about 5 minutes after the shot. The patient also has some facial numbness/tightness that started the same day as her shot (after the shot). The tinnitus, intermittent ear pain, ear fullness was reported as still continuing. The patient reported that her hearing is also coming and going periodically in both ears. The patient was also very sensitive to sound now. The patient's joints in her feet and the bottom of her feet hurt. Therapeutic measures were taken as a result of the events. Treatment of antihistamine and nasal spray was recommended. The patient do not have covid prior to vaccination and was not tested for covid post vaccination. The patient has not recovered from the events.

Other Meds: VITAMIN D [COLECALCIFEROL]; PROBIOTICS; FISH OIL

Current Illness:

ID: 1254706
Sex: M
Age:
State: TX

Vax Date: 03/17/2021
Onset Date: 03/17/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: slightly faint; Instantly was dizzy; Instantly had tingling in my hands and feet; Turned into cramping in forearms, shins, and calves; mild arm pain; mild headache; This is a spontaneous report from a contactable consumer (patient). A 36-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in Arm Left on 17Mar2021 15:00 (3:00 PM) (Batch/Lot Number: eng206) as SINGLE DOSE for covid-19 immunisation. There was no medical history included. There was no covid prior vaccination, not covid tested post vaccination. The patient had no known allergies. No other vaccine in four weeks and no other medications in two weeks. The patient's concomitant medications were not reported. The patient reported that: "Instantly was dizzy and slightly faint upon injection. Instantly had tingling in my hands and feet which still has not gone away (still about 50% as bad 3 weeks later). Turned into cramping in forearms, shins, and calves. Only other symptoms were mild arm pain and mild headache, no fever, no chills." The events occurred on 17Mar2021 at 15:00 (03:00 PM). The outcome of the events was recovering. The events resulted in Doctor or other healthcare professional office/clinic visit. The treatment was unknown.

Other Meds:

Current Illness:

ID: 1254707
Sex: F
Age:
State: WV

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: headache all night; swelling with bubbling around the wrist; This is a spontaneous report from Pfizer Sponsored program. A contactable consumer (patient) reported a female patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route single dose for COVID-19 immunization on 31Mar2021. Medical history and concomitant medication were not reported. On 31Mar2021, the patient developed a swelling with bubbling around the wrist. she stated that she was prone to hives. The swelling only lasted about 5 minutes. She had a headache all night. Outcome of the event headache was unknown; outcome of the other event was resolved on 31Mar2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1254708
Sex: F
Age:
State: FL

Vax Date: 01/26/2021
Onset Date: 01/31/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: pronounced nose bleed; This is a spontaneous report received from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1, via an unspecified route of administration on 26Jan2021 (Lot number: UNKNOWN) as a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On 31Jan2021, the patient experienced pronounced nose bleed. The clinical course was reported as follows: The patient reported that she received her first dose of the Pfizer-Biontech Covid19 vaccine on 26Jan2021. Then, 5 days later, she had a "very pronounced nose bleed" which landed her in the ER, with the bleed having to be packed. She has since had cauterization done by two different ENTs to stop the residual bleeding. Her HCP said they did not believe the vaccine caused the nose bleed, and have given her the go-ahead to receive the second dose. The clinical outcome of pronounced nose bleed was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254709
Sex: F
Age:
State: NY

Vax Date: 04/01/2021
Onset Date: 04/03/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: she had a rash that looks like measles all over and she was still itchy since she started; It's a bright red rash all over her body my arm, her legs and her waist; and want to scratch the bumps and then they turn red and it has not gone away; Itchy Measle like rash all over body; This is a spontaneous report from a contactable consumer(patient). A 59-year-old female patient received first dose BNT162B2 (Pfizer BioNTech Covid 19 vaccine), via an unspecified route of administration at Arm Right on 01-APR-2021 09:30 at the 59 years old at single dose for COVID-19 immunization. The medical history included Asthma, Anxiety, food allergies(Penn, Kiwi fruit). The concomitant medications were alprazolam(XANAX) for Anxiety, salbutamol(PROVENTIL) for Asthma. For 2 days, the pateint felt ok and then started becoming itchy, ever since she become itchy, on 03APR2021 21:00 she had a rash that looks like measles all over and she was still itchy since she started. It never went away. It's a bright red rash all over her body her arm, her legs and her waist. It felt itchy, and want to scratch the bumps and then they turn red and it has not gone away. When told the role of the department and asked for permission to probe questions, consumer stated, "Her internal medicine doctor told her to call Pfizer and tell them an ask what to do about the rash and she need future vaccination?" The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There was no treatment received for all the adverse events. Prior to vaccination, the patient was not diagnosed with COVID-19.Since the vaccination, the patient has not been tested for COVID-19. About the lot number, the patient stated "It looks like EW0151. It looks like that or it EW6. Is it supposed to be 3 letters or 2 letter in front of that? It looks like EW0151 or it is EW6151. She can't see if it was a zero or six". The outcome of the events was not recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: XANAX; PROVENTIL [SALBUTAMOL]

Current Illness:

ID: 1254710
Sex: F
Age:
State:

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: headache; small rash around the vaccination area.; This is a spontaneous report from Pfizer-sponsored program. A contactable consumer reported for self. A female patient of an unknown age received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose via an unknown route on an unknown date in Mar2021 for Covid-19 immunization. Medical history and concomitant drug were not provided. Patient experienced a headache and small rash around the vaccination area. Outcome of the events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254711
Sex: F
Age:
State: NY

Vax Date: 03/27/2021
Onset Date: 04/17/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: diagnosed with COVID; diagnosed with COVID; This is a spontaneous report from a contactable consumer or other non hcp. A 62 year old female patient received the first dose of bnt162b2 (BNT162B2, Solution for injection) via an unspecified route of administration on 27Mar2021as SINGLE DOSE and was scheduled for her second dose on 17Apr2021 for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On or about 17Apr2021, the patient underwent lab tests and procedures and diagnosed with covid positive which was considered serious as medically significant with an unknown outcome. Further patient asked if she can still take the second dose after more than 21 days. It was reported that patients husband also had COVID and was supposed to get vaccinated but had to cancel his appointment because of his diagnosis. The action taken in response to the event for bnt162b2 was not applicable. Follow up needed, further information was requested. information about lot/batch number needed.

Other Meds:

Current Illness:

ID: 1254712
Sex: M
Age:
State: NY

Vax Date: 03/23/2021
Onset Date: 03/27/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: pain all over his body/pain in my joints and all over my body; pain all over his body/pain in my joints and all over my body; This is a spontaneous report received from a contactable consumer (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 23Mar2021 (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine included 1st dose of BNT162B2 for COVID-19 immunisation. About 4 days later (27Mar2021) of receiving 2nd dose of BNT162B2, patient got the pain in joints and all over body. Outcome of the events was unknown. No follow-up attempts are possible. Information on lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254713
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: allergic reactions; she developed herpes breakouts again but this time it appeared outside her mouth/around her mouth; she felt the endometriosis pain again.; She said her whole lower half is inflammed and bloated; She said her whole lower half is inflammed and bloated; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. Medical history included second degree endometriosis, the pain of her endometriosis started when she was 16 years old and it was treated until she was 23, she had 3 exploratory surgeries, and the endometrial area was cauterized years ago. The patient was previously vaccinated with the first dose of BNT162B2 at the age of 67-year-old for Covid-19 immunization and developed herpes breakout inside of her mouth and the upper part of her mouth turned into a blister. With the second dose of the vaccine, she developed herpes breakouts again but this time it appeared outside her mouth, it was around her mouth on an unspecified date. She felt the endometriosis pain again and her whole lower half was inflamed and bloated on an unspecified date. She was reading an article about mast cells which are part of the reaction in allergies involvement in the reaction of the Pfizer COVID-19 vaccine. She said the mast cells in a reproductive disorder increases the activation release of mediators. The patient was convinced that she was experiencing allergic reactions. She was surprised that she had these reactions since she said that she was in great shape and she was not overweight. She wanted to know if Pfizer has more information about how long the adverse events that she was experiencing would occur. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1254714
Sex: F
Age:
State: NY

Vax Date: 03/13/2021
Onset Date: 04/03/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: runny nose on one side of her nostril.; sneezed; This is a spontaneous report from a Pfizer sponsored program Pfizer First Connect from a contactable female consumer (patient) reported for herself. A female patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 13MAR2021 at single dose for COVID-19 Immunization. Medical history and concomitant medications were not reported. Patient got her first dose last March 13. She is scheduled to return today which is April 3 for her second dose. However, at 3 AM today upon waking up, she sneezed and started to have a runny nose on one side of her nostril. She is not sure if this is an allergy and she wanted to know if it was okay to get the shot. Provided PMI's number and hours of operation in case call gets disconnected since the caller has a medical inquiry. Cold Transferred to DSU and Created Manual AE Form. Customer and/or medical inquiry forwarded or referred to MI. Reported as non-serious. Patient stated she just had really, it was just a simple question. She had the first Pfizer shot on March 13th and she had no problem with it and she was scheduled today to get her second one and she woke up like in the middle of the night like she sneezed and like she just had this runny nose and she had no other symptoms. She felt fine and she just want to know if it was okay to get the shot. Outcome of event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1254715
Sex: F
Age:
State:

Vax Date: 04/03/2021
Onset Date: 04/05/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: she began experiencing watery vomiting and diarrhea; she began experiencing watery vomiting and diarrhea; She also has chills; was having a hot flash; felt like she was going to faint/pass out; This is a spontaneous report from a contactable consumer. A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 03Apr2021 (Batch/Lot number was not reported) as a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 05Apr2021, the patient she was at work and felt like she was having a hot flash, then felt like she was going to faint/pass out. The following day (06Apr2021) she began experiencing watery vomiting and diarrhea. She also had chills. The patient wanted to know if this is normal and was also asking if she experienced these side effects because she weighs 110 lbs. The outcome of the events was unknown. No follow-up attempts are possible, information about the batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254716
Sex: F
Age:
State: MI

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: feel my heart pound really fast/her heart felt like it was pounding out of her chest; feeling of severe doom or dread; felt very bizarre/felt like she was going to lose her breath/felt like she was going to hyperventilate; began to become very tachycardic; This is a spontaneous report from a contactable nurse (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: EW0130, expiry date not reported), via an unspecified route of administration on 01Apr2021 as a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient received the first dose of the Pfizer COVID-19 vaccine on 01Apr2021 and she would like to know if she should proceed with getting the second dose based on the nature of her reaction to the first dose. The patient stated, she received the vaccine and then 90 minutes later she began to feel her heart pound really fast and it started to feel like it was pounding out of her chest, accompanied by feeling of severe doom or dread. It felt very bizarre, felt like patient was going to die. She felt like she was going to lose her breath but she didn't. Her throat did not close up. She did not have a rash, and was not itchy anywhere. Patient took some Benadryl right away and it subsided. It lasted about a total 5 minutes, it felt like a very long 5 minutes. The anxiety was the worst she had every experienced. She had never experienced anything like that before. She would like some guidance regarding her second dose. She would like to know any information regarding the efficacy after one dose of the Pfizer COVID-19 vaccine. She also said she began to become very tachycardic on 01Apr2021 and felt extreme anxiety and it was the worst anxiety that came over her. She felt like she was going to die and might call it that and she did not really have trouble breathing but felt like she was going to hyperventilate. Therapeutic measures were taken as a result of the events "feel my heart pound really fast/her heart felt like it was pounding out of her chest" and "felt very bizarre/felt like she was going to lose her breath/felt like she was going to hyperventilate". The patient recovered on an unspecified date in Apr2021 from the events "feel my heart pound really fast/her heart felt like it was pounding out of her chest" and "felt very bizarre/felt like she was going to lose her breath/felt like she was going to hyperventilate". The outcome of the other events reported was unknown.; Sender's Comments: Considering the plausible drug-event temporal association, a contributory role of the suspect product bnt162b2 to the reported events cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1254717
Sex: M
Age:
State:

Vax Date: 03/23/2021
Onset Date: 03/23/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Tingling all over his body; body tingles; May have lost weight; Wheezing sound whenever he breathes; Feeling numb; Feeling weak; no energy; Hands are shaking; Electrolytes were out of whack; electrolytes were too low; Phosphorus level was too low; Throwing up; vomiting; Vertigo; head was spinning; looked like the building was going up and down; vision was spinning; Fell three times; Face pale yellowish; Feel like going to pass out; Nausea; Felt there is pinching on left side of his chest; Heavy sweating (sweating all over his body); Head felt heavier; head was heavy in the front side of his head, not in the back; Feeling hot; 99.9 degrees body temperature; pre fever; Head felt a lttle dizzy; no control to his body like he was going to faint; Arm soreness; sore arm; Headache; it is only a little bit of pain; frontal headache; head is hurting; This is a spontaneous report from a contactable consumer (patient). A 36-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number was unclear and reported as either ER8727 or ED8727), via an unspecified route of administration, on 23Mar2021, at a single dose, for COVID-19 immunization. The patient's medical history included asthma. The patient's concomitant medication included an unspecified inhaler. The patient was healthy. He has asthma, but other than that he has no health issues. He has never been hospitalized. The patient was calling to share his side effects after receiving the vaccine. He took the vaccine because it has been recommended. Most importantly, he took it for his elderly parents. He does not want to hurt them. He wants to help the community. The pharmacist told him he needed to call and report, so he googled Pfizer's phone number. On Tuesday (23Mar2021), the patient received his first dose of the COVID-19 vaccine. At first, he felt nothing. The patient's head felt a little dizzy (clarifies that it is a heavy feeling) and had a little bit of arm soreness at night (resolved about a day and a half later), but he could not complain. When the patient had the first dose, he experienced headache and sore arm the night on 23Mar2021. After the first dose, his head felt nothing like the day he went to the emergency room. He would say it was maybe 10% of the day he went to the emergency room. The next day (24Mar2021) in the morning, the patient experienced heavy sweating (sweating all over his body), feeling hot, headache, 99.9 degrees (also reported as 9.8) body temperature, and more pain on the arm. On the morning of 24Mar2021, the patient's head felt heavier. He heard people get chills, he did not get chills. He checked his temperature and it was 99.9 degrees. The patient considers that a pre fever, anything over 100 degrees is a fever to him. Sweating all over his body has gotten better. But it comes back from time to time, along with tingling all over his body (unspecified date). His body tingles, he sweats a little bit and then it goes away. His body tingling and sweating go back to back. Time passed by two days and nothing. On the sixth day (29Mar2021), the patient's mother had a doctor's appointment. After the patient got home from taking his mother to the doctor, he started sweating all over his body (started sweating again). His head was heavy (head is a bit heavy again), but not painful. It is heavy in the front side of his head, not in the back. It (head) is only a little bit of pain. He feels like his brain is going to come out of the front of his head. He started throwing up as soon as he got home. He got vertigo. He was running through the house, trying to make it to the bathroom and he fell three times (before he went to the emergency room). His head was spinning, and he could not open his eyes. The patient clarified that he could open up his eyes, but he did not want too. It looked like the building was going up and down. On 29Mar2021, the patient's face was pale yellowish, feel like going to pass out, time to time nausea and vomiting, vertigo, vision was spinning, tingling sensation, no control to his body like he was going to faint, vomited a total of 3 times, felt there is pinching on left side of his chest (the left side of his chest was pinching in the emergency room), and frontal headache. He felt like everything around him was spinning. The patient took meclizine for vertigo and medication for vomiting. The patient's father has vertigo, so his father gave him some meclizine for his vertigo. The patient also took ondansetron (ZOFRAN). The patient's family called the hotline and took him to the emergency room (ER). He has not fell again. He vomited three times, and then another in the ambulance, for a total of four times. When he got to the hospital, they started treating him. When he went to the emergency room, he did not open his eyes, and was talking with his eyes closed. All of his symptoms happened at the same time, when he came home from his mother's doctor appointment. The doctor at the emergency room told him that his electrolytes were out of whack, and that his phosphorus level was too low. They gave him some sodium sulfate right away. The doctor recommended that he stay overnight. The patient did not want to stay overnight because his parents are elderly, and he takes care of them. The doctor told him since he was not willing to stay, to go home and drink a lot of water. Per laboratory works done on 29Mar2021, the patient's phosphorous and electrolytes were too low, so they gave him saline and sodium phosphate for management. Also, the patient had abdominal and heart X-ray and computerized tomography (CT) scan done and everything came normal. Also, both X-rays came back clear. The patient had no diarrhea. Heaviness of head started feeling better after his emergency room visit on 29Mar2021. Around 02Apr2021 or 03Apr2021 is whenever it started feeling better. It comes back, and he gets scared. On 30Mar2021, the patient was almost improving and was advised to drink lots of fluids. Every now and then patient was feeling weak and head is hurting, hands are shaking on 30Mar2021. Every single day, he feels dizzy, weak and tingles all over his body. When the patient went to the emergency room, the doctor could not tell him what caused his symptoms. The doctor told him that it could possibly be because of the vaccine. He has never felt like this in his life. He has never fell in his life. He felt hopeless and was crying. He was worried about his elderly parents, and who would take care of them. The patient's second dose of the COVID-19 vaccine is due 13Apr2021. He is debating on whether to take it or not. He cannot afford to take it if it is going to make him feel worse. He has read that the second dose of the COVID-19 vaccine makes people feel worse. He is scared. He is asking if he should get the second dose of the COVID-19 vaccine. Within one week (unspecified date), he may have lost weight. The patient has to use his inhaler more now as he has a wheezing sound whenever he breathes. He has been using his inhaler more often, whenever he starts wheezing. He always feels like his whole body is tingling. He has no energy. He has only visited this doctor once. His long-term primary care physician is not practicing anymore, he thinks that he may have lost his license. It is hard for him to get an appointment with his primary care doctor since the pandemic. The patient is going to try to see his doctor through tele health. The emergency room doctor recommended that he follow up with a neurologist. The patient was advised to go to a neurologist. The patient reported these symptoms as side effects and asked how long the symptoms last. At the time of reporting, the patient currently still has that nausea and vomiting feeling, but it is better; and he feels heavy (pertaining to vertigo). If he starts to get vertigo again, he knows he will throw up. He can feel whenever the vertigo is coming, he begins to feel like the floor is moving. He can be standing still quietly, and the floor will start moving. The pharmacist told him to call Pfizer and share what happened to him. Since he took the first dose of the Pfizer COVID-1

Other Meds:

Current Illness:

ID: 1254718
Sex: F
Age:
State:

Vax Date: 03/27/2021
Onset Date: 03/27/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: I've already had Covid; I've already had Covid; The facility just called and said she needs another shot because the dose she received was mixed with sterile water due to running out of the "saline"; The facility just called and said she needs another shot because the dose she received was mixed with sterile water due to running out of the "saline"; This is a spontaneous report from a contactable consumer. A 51-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: ER8732), dose 2 via an unspecified route of administration on 27Mar2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient said I have already had covid on an unspecified date. The facility just called and said she needs another shot because the dose she received was mixed with sterile water due to running out of the saline (off label use and product use issue) on 27Mar2021. Caller states the vaccination site claims that someone from Pfizer told them that day that sterile water could be used as a diluent. When asked who at the site told her that she said she doesn't know. The patient underwent lab tests and procedures which included sars-cov-2 test: unknown results. The outcome of the events off label use and product use issue recovered and others was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1254719
Sex: M
Age:
State: NJ

Vax Date: 03/17/2021
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Caused me to test positive for COVID-19 10 days after receiving vaccine; Caused me to test positive for COVID-19 10 days after receiving vaccine; This is a spontaneous report from a contactable consumer (patient). A 54-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EP7534), via an unspecified route of administration in left arm on 17Mar2021 as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. Patient caused to test positive for COVID-19 after receiving vaccine (drug ineffective).The patient underwent lab tests and procedures which included investigation: COVID-19 test positive on unspecified date .The outcome of the events was recovered with Sequel.

Other Meds:

Current Illness:

ID: 1254720
Sex: M
Age:
State: FL

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Temporary hearing loss; ringing of the ears; Extreme cold sweats; Blurred vision; This is a spontaneous report from a non-contactable consumer for a 25-years-old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in right arm on 07Apr2021 14:00 (Batch/Lot Number: EP7533) as SINGLE DOSE for covid-19 immunisation. Medical history included Covid-19 (Covid prior vaccination: Yes). Concomitant medications included sulfamethoxazole, trimethoprim. The patient previously took a tetanus booster on left arm. The patient had a Covid prior vaccination and not Covid tested post vaccination. On 07Apr2021 at 14:00, the patient experienced temporary hearing loss, ringing of the ears, extreme cold sweats, and blurred vision. The patient did not receive treatment for the events. The outcome of events was recovered on 07Apr2021. No follow up attempts are possible. No further information is expected.

Other Meds: SULFAMETHOXAZOLE+TRIMETHOPRIM

Current Illness:

ID: 1254721
Sex: M
Age:
State:

Vax Date: 06/30/2005
Onset Date: 03/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Feeling a bit under the weather; This is a spontaneous report received from specialty pharmacy from a contactable consumer(patient). A 24-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via unknown route on Mar2021 (Batch/Lot number was not reported) at single for covid-19 immunisation; treprostinil sodium (REMODULIN, concentration of 5 mg/ml), iv drip from 30Jun2005 (Lot Number: 2101734; Expiration Date: 30Nov2021) to an unspecified date, at 0.150 ug/kg, continuing, for pulmonary arterial hypertension. Medical history included ongoing pulmonary arterial hypertension. Concomitant medication(s) included warfarin sodium, ambrisentan and tadalafil, all taken for an unspecified indication, start and stop date were not reported. It was reported that the patient felt a bit under the weather as he had his COVID shot recently. Action taken with IV Remodulin was not reported for the event of malaise. At the time of reporting, the outcome of malaise was unknown. The reporter did not provide causality for the event of malaise. No follow up attempts are needed. No further information expected.

Other Meds: WARFARIN SODIUM; AMBRISENTAN; TADALAFIL

Current Illness: Pulmonary arterial hypertension

ID: 1254722
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: My arm did become sore; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received first dose and second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), via an unspecified route of administration, administered in left arm on an unspecified date at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient experienced really weird side effects after first dose of vaccination, patient arm become sore. The second shot was really bad, got a huge red blotch on her arm It was a big welt that look like a cloud, It became swollen and hot and 2 weeks later, patient arm is still really hurting but not red, hot or swollen". The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254723
Sex: F
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Experiencing pain in hands/wrists; Experiencing pain in hands/wrists; This is a spontaneous report received from a Pfizer-sponsored program, from a contactable other healthcare professional and consumer (patient). A thirty-eight-year-old female patient received BNT162b2 (BNT162B2), dose 1 via an unspecified route of administration on 31, Mar2021 (Batch/Lot number was not reported) as single dose for COVID-19 Immunizations. Medical history included depression, rheumatoid arthritis from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient experienced pain in hands/wrists and trouble opening bottles due to the missed doses of tofacitinib citrate (XELJANZ) on an unspecified date in 2021 with outcome of unknown. Follow-up (19Apr2021): New information included report type updated as spontaneous. This follow-up is being submitted to notify that the batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1254724
Sex: M
Age:
State: NJ

Vax Date: 03/02/2021
Onset Date: 03/02/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Diagnosed with Bell's Palsy on right side of my face; administration date 02Mar2021/ number 2; administration date 09Mar2021/dose number 1; administration date 02Mar2021/ number 2; administration date 09Mar2021/dose number 1; This is a spontaneous report from a contactable consumer (patient). A 32-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route of administration at 32-years, at single dose in right arm on 02Mar2021 (as source reported; pending clarification) at 13:00 (Lot number: unknown) for COVID-19 immunisation. Medical history included high blood pressure and high cholesterol. Concomitant medications included atenolol, amlodipine and atorvastatin, all taken for an unspecified indication, start and stop date were not reported. The previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) also via an unknown route of administration at 32-years, at single dose in right arm on 09Mar2021 at 08:30 for COVID-19 immunisation. The patient did not receive other vaccines within 4 weeks prior to the COVID vaccine. The patient was diagnosed with Bell's Palsy on right side of his face on 06Apr2021 06:00. The adverse event resulted in "Doctor or other healthcare professional office/clinic visit". And the patient received treatment with prednisone and valacyclovir for it. The patient was not diagnosed with COVID-19 prior to vaccination. He had Covid test (IDNOW COVID-19 rapid diagnostic test (nucleic acid amplification test NAAT)) post vaccination with type of Nasal Swab on 30Mar2021 with a result of negative. Event outcome was recovering. Information on the lot/batch number has been requested.

Other Meds: ATENOLOL; AMLODIPINE; ATORVASTATIN

Current Illness:

ID: 1254725
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: sore throat; This is a spontaneous report from a Pfizer sponsored COVAX Support reported by a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162b2 (Pfizer-BioNTech COVID-19 Vaccine), via an unspecified route of administration on an unspecified date as single dose for Covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient was due for her 2nd dose of Covid vaccine next Saturday but she would like to reschedule as she has a sore throat. Event outcome was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254726
Sex: F
Age:
State: FL

Vax Date: 02/27/2021
Onset Date: 03/04/2021
Rec V Date: 04/25/2021
Hospital: Y

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: and 09Mar diagnosed with pneumonia, caller was released from hospital on 24Mar; COVID 04Mar, and 09Mar diagnosed with pneumonia, caller was released from hospital on 24Mar; This is a spontaneous report from a contactable consumer (patient). A female patient of unknown age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection),via an unspecified route of administration on 27Feb2021 as single dose for COVID-19 immunisation. The patient medical history was none. The concomitant medications were not reported. Patient received first dose 27Feb2021. Diagnosed with COVID 04Mar2021, and 09Mar2021 diagnosed with pneumonia, she was released from hospital on 24Mar2021. Caller would like to know if she can get the second dose of vaccine. The patient outcome for the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts were completed. No further information was expected.

Other Meds:

Current Illness:

ID: 1254727
Sex: M
Age:
State: NY

Vax Date: 04/06/2021
Onset Date: 04/06/2021
Rec V Date: 04/25/2021
Hospital: Y

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

Lab Data:

Allergies:

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

Symptoms: fear of death/doom; I went into a full Anaphylaxis shock; This is a spontaneous report from a contactable consumer (patient). A 32-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot Number: EW0150) via an unspecified route of administration, administered in Arm Left, at the age of 32-year-old, on 06Apr2021 09:45, as SINGLE DOSE for covid-19 immunisation. Medical history included allergy to shrimp. The patient was not diagnosed with COVID nor was he tested post vaccine. The patient's concomitant medications were not reported. On 06Apr2021 at 10:00 am, 15 mins after the vaccine, a large hive appeared on his forehead and then 1.5 hours later the patient went into a full Anaphylaxis shock with difficulty breathing, throat closing up, fear of death/doom, tingling sensation in whole body, heart pounding rapidly, chest pain, dizziness. The patient went to the emergency room/ urgent care and was hospitalized for 1 day. Therapeutic measures taken in response to the events included administration of Steroids, antihistamines, and pain killers. Outcome was recovering at the time of the report.

Other Meds:

Current Illness:

ID: 1254728
Sex: F
Age:
State: NJ

Vax Date: 03/15/2021
Onset Date: 03/16/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: She had a rash only on the parts of her that were exposed to the sun; She had a bruise on the corner of her face by her left eye. She said her primary care doctor said she had some kind of internal bleeding. She said it was like an old lady bruise & was a deep purple; She had a bruise on the corner of her face by her left eye. She said her primary care doctor said she had some kind of internal bleeding. She said it was like an old lady bruise & was a deep purple; This is a spontaneous report from a contactable consumer reporting for self. A 54-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 15Mar2021 (Batch/Lot Number: EN6205) as single dose for covid-19 immunisation. Medical history included rash. There were no concomitant medications. The patient reported she had her first COVID-19 Vaccine dose, and was due to get the second COVID-19 Vaccine (today, 07Apr2021, at 4:20PM). She said she went to her (primary care) doctor, and wanted to check with Pfizer because she had a weird reaction after she had her first COVID-19 Vaccine. She said she had a bruise on the corner of her face by her (left) eye. She said her (primary care) doctor said she had some kind of internal bleeding. The caller said it was like an old lady bruise, and was a deep purple color. She clarified she noticed the bruise when she woke up at a little before 7:00AM on 16Mar2021. She said the bruise lasted for 5 days, and kind of dissipated on its own, and then the bruise was gone. She said she had her COVID-19 Vaccine shot in her left arm (on 15Mar2021), and then woke up in the morning (on 16Mar2021), and the bruise (on the left side of her face) was there. She said she went to her eye doctor to check to see if there was any bleeding in her left eye, and there was no bleeding. She said her (primary care) doctor had blood work done (on 23Mar2021), and checked to see if she had any internal bleeding. She said her blood work seemed OK. She said she knows her doctor can't answer any questions about the COVID-19 Vaccine, so that was why she contacted Pfizer. She said she also had her blood checked for the COVID-19 Virus antibodies (on 31Mar2021). She said she does have the COVID-19 Virus antibodies. She said she knew the COVID-19 Virus antibody testing was new. She said she didn't know what was considered to be a high versus low COVID-19 Virus antibody level, and that her COVID-19 Virus antibody level was a 6.12. She said she had her COVID-19 Virus antibody test 16 days after her first COVID-19 Vaccine. She said she made sure her COVID-19 Virus antibody test was done at least 2 weeks after getting her first COVID-19 Vaccine. Reported she also had a rash on either 04Apr2021 or 05Apr2021. She said in the past, she had a rash happen the first time she went in the sun, and she wasn't sure if her rash was related to sun exposure, or her first COVID-19 Vaccine dose. She clarified she was pretty sure her rash was from sun exposure. She said since she had been out of the sun, her rash was starting to go away. She clarified she had a rash only on the parts of her that were exposed to the sun. She said she seemed to get a rash after her first exposure to the sun. She said she had read up on having a rash to sun exposure, and the rash was like an immune reaction to the UVA rays. She said the rash was not itchy, and was only bumps. No further details provided. Reported she was one of those small percent of people who gets a really weird reaction to things, so her doctor wasn't surprised when she had the bruise after getting the first COVID-19 Vaccine. She said she was very small at 105 lbs., and always takes a children-size portion of things. No further details provided. Reported half of her wanted to get the second COVID-19 Vaccine dose, and the other half of her was afraid she would have some sort of weird reaction. She said since she was already protected with the COVID-19 Virus antibodies, did she need to get the second COVID-19 Vaccine. Caller asked how long do the COVID-19 Virus antibodies last, saying she heard their might be a COVID-19 Vaccine booster shot in the future. Caller stated she had so many questions she wanted to ask. Caller was advised she would be transferred to Pfizer Medical Information for further assistance. Outcome of event rash was recovering, of other was recovered in Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1254729
Sex: F
Age:
State:

Vax Date: 03/25/2021
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: headache; aches; injection site soreness; This is a spontaneous report from Pfizer-sponsored program from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on 25Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included knee pain and nausea. Concomitant medication(s) included paracetamol (TYLENOL) taken for knee pain. Patient was told to take Tylenol. She had issue with her knee. She wanted to know if she can take any other pain reliever. She has had knee issue prior to getting vaccinated. She had been having nausea as well. She had experienced headache, aches, and injection site soreness on unspecified date. But it has gone away. The event outcome for events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: TYLENOL

Current Illness:

ID: 1254730
Sex: F
Age:
State: NY

Vax Date: 04/06/2021
Onset Date: 04/06/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Fatigue; vomiting; This is a spontaneous report from a contactable consumer. A 26-year-old female patient (non pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 06Apr2021 at the age of 26-year-old (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced fatigue and vomiting on 06Apr2021 21:00 with outcome of recovered on an unspecified date in Apr2021. No treatment was received for the adverse events. No COVID 19 diagnosed prior vaccination, since the vaccination the patient hadn't been tested for COVID-19. No follow-up attempts are possible, information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254731
Sex: F
Age:
State: MD

Vax Date: 04/05/2021
Onset Date: 04/05/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Bell's Palsy; something felt weird; asthma; facial numbness and tingling; facial numbness and tingling; This is a spontaneous report from a contactable consumer (patient). A 51-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration administered in arm left on 05Apr2021 (Batch/Lot Number: ER8727) at age of 51 years old as single dose for covid-19 immunisation. There was no medical history. There was no history of all previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations within 4 weeks. No events following prior vaccinations. There were no concomitant medications. The patient had her 1st dose of Pfizer Covid-19 vaccine on Monday morning (05Apr2021). The patient experienced facial numbness and tingling on 05Apr2021. After the injection she sat and waited for 15 minutes. When she got in the car, she felt her face tingling. It had been a couple days of having the sensation in her face. She called her physician and it was labeled as Bell's Palsy. Her physician suggested she phone and report her experience. She had her appointment at 11:30. She was back in her car around 13:00. She noticed as she was driving, that something felt weird. She didn't know if it was numbness or tingling. She added it was not painful and she was not distorted. She thought it's numb. Her physician advised she take Motrin. Her physician shared an article about a trial that some people may experience this after, it included 4-5 people. Her symptoms shifted. First in her cheeks, then over the course of yesterday and today, she feels it's on the side of her face. The forehead had gone away, but it's on the right side of her face. She added the symptoms were improving and clarified they were persisting. She had asthma and wanted to minimize the severity of Covid if she would ever get it. She had loved ones around and added that you never know. She wanted to protect herself. She wanted to get out and see her family and friends. Some of them have already been fully vaccinated. She was concerned when it started. It wasn't affecting her breathing, but she called her physician and asked if she needed to come in. Her physician suggested to just monitor it. The events did not require visit to emergency room or physician office. The outcome of events facial numbness and tingling was not recovered. The outcome of other events was unknown.

Other Meds:

Current Illness:

ID: 1254732
Sex: F
Age:
State: MO

Vax Date: 04/05/2021
Onset Date: 04/05/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: I felt a little woosy; This is a spontaneous report from a contactable other health care professional (patient). A 62-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), dose 1st via an unspecified route of administration, administered in Arm Right on 05Apr2021 13:00 as single dose for covid-19 immunisation. Medical history included Severe back problems. Patient had allergies to Chocolate. Concomitant medication was not reported. On 05Apr2021 01:15, patient felt a little woosy. She was not pregnant at the time of vaccination, did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient received other medications within 2 weeks of vaccination. She was not received treatment for the adverse event. Patient was not diagnosed with COVID-19 Prior to vaccination, since the vaccination, not been tested for COVID-19. The outcome of the event was recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254733
Sex: M
Age:
State: MD

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: he had been sweating profusely for almost 3 weeks; This is a spontaneous report from a contactable consumer (patient). This unknown age male patient received 1st dose of COVID-19 Vaccine BNT162B2 (Batch/lot number: Not Provided) at single dose for COVID-19 immunization. Medical history and concomitant drug were not reported. Reported he had his first COVID-19 Vaccine and had a weird reaction. He said he had been sweating profusely for almost 3 weeks. He said everyone kept telling him that his sweating doesn't make sense, and his sweating should only have lasted a few days. Outcome of the event was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254734
Sex: F
Age:
State: FL

Vax Date: 03/15/2021
Onset Date: 03/15/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Painful lump in left armpit; administration date26Feb2021, administration date 15Mar2021; administration date 26Feb2021, administration date 15Mar2021; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient (not pregnant) received bnt162b2 (COVID-19 vaccine), dose 2 via an unspecified route of administration, administered in Arm Left on 15Mar2021 09:45 AM (Batch/Lot number was not reported) at single dose for covid-19 immunisation. The patient' medical history was not reported, no allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications within 2 weeks of vaccination included: Metformin, alprazolam (XANAX) and multivitamin. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received the first dose of bnt162b2 administered in Arm Left on 26Feb2021 09:00 AM for covid-19 immunization and experienced black nasal discharge. The patient experienced painful lump in left armpit since vaccines. It's been almost a month. Adverse event started from 15Mar2021 09:45 AM. No treatment was received for the event. Since the vaccination, the patient had not been tested for COVID-19. The outcome of the event was not recovered. The report was non-serious. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: METFORMIN; XANAX

Current Illness:

ID: 1254735
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/05/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: This is spontaneous report received from contactable consumer. A female patient of an unspecified age received the second dose of BNT162B2 (COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced chills, throwing up, can't move, everything hurts on 05Apr2021. The reporter was calling for her sister and she has got every symptom yesterday (05Apr2021) after getting the second shot. The patient had chills, throwing up, can't move, everything hurts, and just every single thing from the list. The reporter was asking is this normal having all these at the same time. The reporter was thinking if her sister had the vaccine and has such a reaction can she get an antibody infusion. The patient had a list of symptoms and checked them off and she has all of them. The reporter is wondering if her sister is a candidate if she got the vaccine and not like it's a live vaccine, she knew that, but would antibody therapy be good for her and she doesn't know what to do she felt helpless. Caller stated she knew these are side effects. The outcome of the events was unknown. No Follow-up attempts are needed. No further information is expected. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254736
Sex: F
Age:
State: IL

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Rash; Itchy; Body aches; Fatigue; Lethargy; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 36 years-old-female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) first dose (lot number: EL3248, expiration date: not provided), via an unspecified route of administration, in arm right, on 15Jan2021(at the age of 36-years-old) as a single dose for COVID-19 immunisation at workplace clinic. The patient also took second dose of BNT162B2 (Lot number: EM9810 and expiration date: Not provided), in arm right on 05Feb2021(at the age of 36-years-old) for COVID-19 immunisation. Medical history included depression from 07Jan2016 to unspecified date, Gluteus Medius Tedinopathy from 20Aug2020 to unspecified date, Platelet rich plasma injection from 22Dec2020 to unspecified date. Concomitant medication included Zoloft/Sertaline (50mg started on Apr2018). On 06Feb2021, the patient had body aches, fatigue, lethargy, and general malaise. She woke up on 07Feb2021 and felt fine. In the afternoon of 08Feb2021, she noticed itching and raised red bumps on her arms, which spread across her chest and legs by the evening. She woke up on 09Feb2021 and noticed the rash had spread across her entire body. She visited the urgent care clinic on the morning of 09Feb2021 and the nurse practitioner believed this was a delayed reaction to the vaccine and prescribed a topical steroid cream. The morning of 10Feb2021, she woke up with moderate swelling in her face that subsided within about an hour. The rash persisted with continued itching. Allergy medication did not help with the redness nor itchiness. The topical steroid was minimally helpful as well. Ibuprofen did help with some of the itching and allowed her to sleep. On 11Feb2021, she spoke to a nurse practitioner and allergist from contactable consumer, where she received the vaccine. They stated that her reaction sounded like a robust immune response that was likely linked to the vaccine, particularly as this has never happened to her before. The rash peaked around on 10Feb2021 and slowly improved until it was mostly resolved by 14Feb2021. The outcome for the events were recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: Zoloft

Current Illness:

ID: 1254737
Sex: F
Age:
State: WI

Vax Date: 03/11/2021
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: A spike in her BP; This is a spontaneous report from a contactable pharmacist. A 52-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; solution for injection) intramuscularly in the left arm on 11Mar2021 (at the age of 51-years-old) as a single dose for COVID-19 immunisation. Medical history included hypertension from an unspecified date and unspecified if ongoing (not taking meds for this prior to this event) and strawberries - anaphylaxis from an unspecified date and unspecified if ongoing. It was unknown whether the patient was diagnosed with COVID-19 prior to vaccination. It was unknown if the patient was pregnant. Concomitant medications ("other medications in two weeks") included acetaminophen taken for an unspecified indication from an unspecified date and unspecified if ongoing, as needed. It was unknown whether the patient received any other vaccine within four weeks of the COVID-19 vaccine. The patient experienced a spike in her BP (blood pressure) on an unspecified date ("with her first dose"). The clinical outcome of the event a spike in her BP was unknown. Since the vaccine, it was unknown whether the patient was tested for COVID-19. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected; Sender's Comments: Based on the information currently available, a possible contributory role of the suspect vaccine BNT162B2 in triggering the onset of "a spike in her BP" cannot be excluded. The event was confounded by underlying hypertension. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds: ACETAMINOPHEN

Current Illness:

ID: 1254738
Sex: F
Age:
State: FL

Vax Date: 04/03/2021
Onset Date: 04/03/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: ordinary flu like symptoms; nose is stuffy; ears hurt; throat is sore; running a little temperature of 99.6F; hurts everywhere; allergic response; small rash; 2 hives developed; slurred speech; no balance; tongue thickening; trouble swallowing; breathing was slowing down; hard to keep her eyes open; reaction time was slowing down; This is a spontaneous report from a contactable consumer. This 73-year-old female consumer (patient) reported that she received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Right on 03Apr2021 09:25 AM (Lot Number: ER8732) as SINGLE DOSE for covid-19 immunisation. Medical history included ongoing arthritis right hand (she has to be managed with pain medications since 2005); ongoing severe chronic debilitating arthritis in her whole body particularly in her spine; ongoing allergic to some antibiotics and Tylenol (She had a major anaphylactic reaction to Tylenol about 20 years ago); a torn rotator cuff and will have surgery to repair that when she's feeling better; allergies gotten better over the years (She can react to anything, dust, pollen, chemicals, food, medicine). Concomitant medication(s) included thyroid (ARMOUR THYROID) since she was 32 years old. Historical vaccine included flu vaccine for immunization in Jan2021 that gave her flu like symptoms, she was in bed for a week. Patient received her first dose of the Covid 19 vaccine on 03Apr2021. She had an allergic response within a few hours after receiving the Covid 19 vaccine on 03Apr2021. Within an hour of receiving the Covid 19 vaccine she had a small rash, the rash got considerably worse in that next hour. She developed 2 hives. She thought it was a mild response. She does have allergies and has had reactions to things before. She then developed slurred speech, had no balance, tongue was thickening and she had trouble swallowing. She received her Covid 19 vaccine at 9:25AM and after she started having the reaction she took her first line of defense medication, Alka Seltzer Gold and it didn't work. She took one Benadryl at 11:55AM and a second Benadryl at 12:20PM, about 25 minutes in between the 2 Benadryl doses. Alka Seltzer Gold expired Jun2020 btak4x4 is the only number she sees on the package. She wants to add that her breathing was slowing down, it was hard to keep her eyes open and her reaction time was slowing down. Her breathing slowing down was really frightening to her and she thought she might have to go to the Urgent Care. She does have an epi pen. She's asked her doctor for another epi pen but her doctor's medical assistant keeps putting getting her an epi pen off. Her epi pen is out of date, the epi pen expired in 2019. She was going to use the epi pen if she needed too but she didn't have to use it. She reports that her initial reaction (above) all resolved within 11 hours on 03Apr2021 from the time she received the Covid 19 vaccine. Now she has ordinary flu like symptoms. Her nose is stuffy. Her ears hurt and her throat is sore. She is running a little temperature of 99.6F and she hurts everywhere. The flu like symptoms started around 36 hours after she received the Covid 19 vaccine. Maybe 8:00PM or 9:00PM Sunday evening 04Apr2021. She is still having these symptoms (outcome as not recovered). The urgent care was closed on Saturday, 03Apr2021. On Monday she was feeling better anyway and knew she had a regular check up with her doctor this week. She will see her primary care doctor this Thursday, 08Apr2021. Emergency Room/ Physician Office was not required for events. No follow-up attempts are needed. No further information is expected.

Other Meds: ARMOUR THYROID

Current Illness: Allergy to antibiotic; Arthritis (in her whole body particularly in her spine); Hand arthritis (managed with pain medications since 2005)

ID: 1254739
Sex: F
Age:
State: NJ

Vax Date: 03/17/2021
Onset Date: 03/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: ringing in her ears; flu like symptoms; achy; severe headache; not feeling well; This is a spontaneous report from a contactable consumer reporter for herself that a 75-years-old female patient received bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration on 17Mar2021 (Batch/Lot number was unknown) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient started having severe headaches 2.5 days following first Pfizer shot, Doctor sent her to hospital for CT Scan which was normal. Headaches dissipated right before receiving second Pfizer shot on 17Mar2021 and 2.5 days (unknown date in Mar2021) later severe headaches started again along with ear ringing, flu like symptoms, achy, not feeling well and no temperature. The outcome of the events were unknown. No further follow up required for this activites.

Other Meds:

Current Illness:

ID: 1254740
Sex: M
Age:
State: CT

Vax Date: 04/03/2021
Onset Date: 04/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Sore arm at injection site; This is a spontaneous report from two contactable consumer (one of them is parent). A 23-year-old male patient received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number was not reported), via an unspecified route of administration at age of 23-year-old at arm on 03Apr2021 12:30 PM at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. The patient hadn't allergies to medications, food, or other products. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Facility where the most recent COVID-19 vaccine was administered in Pharmacy or Drug Store. The patient experienced sore arm at injection site in Apr2021. No treatment received for event. The outcome of event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254741
Sex: F
Age:
State: HI

Vax Date: 03/13/2021
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: scratchy throat; This is a Spontaneous report from Pfizer program. A contactable female consumer (patient) of unspecified age reported that she received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 13Mar2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The medical history and concomitant medications were not reported. The patient experienced scratchy throat in 2021 with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254742
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: can not walk at all; Swelling; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received second dose BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot number unknown), 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 unknown date, the patient experienced cannot walk at all and swelling. The outcome of the events were unknown. No Follow-up attempts are needed. No further information is expected

Other Meds:

Current Illness:

ID: 1254743
Sex: F
Age:
State: TX

Vax Date: 03/06/2021
Onset Date: 04/07/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This week i should take my 2nd dose but i was scheduled for surgery on 09Apr2021, so they let me do covid test then the results is positive; This week i should take my 2nd dose but i was scheduled for surgery on 09Apr2021, so they let me do covid test then the results is positive; This is a spontaneous report from a contactable Other-health care professional. A 33-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Right on 06Mar2021 13:15 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. Patient not administered other vaccine in four weeks. This week patient should take her 2nd dose but she was scheduled for surgery on 09Apr2021, so patient underwent lab test on 07Apr2021 14:00, covid test type post vaccination=Nasal Swab, covid test name post vaccination Rapid test, covid test date 07Apr2021, covid test result=Positive. Patient received treatment with Tylenol. Patient not had Covid prior vaccination; Patient was tested Covid post vaccination. The outcome of the events was not recovered. Information on the lot/batch number has been requested.; Sender's Comments: Based on the known safety profile and a strong temporal association, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported COVID-19.

Other Meds:

Current Illness:

ID: 1254744
Sex: F
Age:
State: GA

Vax Date: 03/17/2021
Onset Date: 03/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: she feels weak; Blood Sugar Drops at Lunch; feeling bad; hear wheezing in the stethoscope; Shortness of breath; kind of fatigued; This is a spontaneous report received from a contactable consumer reporting for his wife (patient). This 64 year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number EP7534), single dose, dose 1 via an unknown route of administration in the left arm on 17Mar2021 at 08:30 (at the age of 64 years-old) for COVID-19 vaccination. Medical history included aortic aneurysm from 2012 to 2012, thyroid problems and headache. There was no family history. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. There were no events following prior vaccinations. Concomitant medications were not reported. In Mar2021, a week after vaccine administration, the patient was kind of fatigued. She went to the doctor in Mar2021 because she was feeling bad and they said they could hear wheezing in the stethoscope when they listened to her lungs. She was sent her for x-ray and they are waiting on the results. He said that this can also be symptoms of something going on with her thyroid and he has been trying to get her to go to the doctor. He stated she goes up and down the stairs at work and hasn't had problems but has noticed she feels weak and he has noticed she is getting more fatigued everyday. On 24Mar2021, the patient had no energy and her blood sugar has been dropping sometimes at lunch and has never had problems with it before. it is not all the time but when she comes home for lunch after she eats, it drops low. It happens sometimes at lunch, never at breakfast nor supper. In Mar2021, the patient experienced shortness of breath for the last couple of weeks, especially with the stairs. The patient went to the physician's office on 07Apr2021. Laboratory tests included blood work due to the patient's thyroid problems, blood sugar decreased and chest x-ray all on 07Apr2021. The clinical outcome of weak, shortness of breath, feeling bad, wheezing, fatigued and blood sugar dropped was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1254745
Sex: M
Age:
State: LA

Vax Date: 03/16/2021
Onset Date: 03/17/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: extreme arm pain; shoulder pain; arm and shoulder pain/it was not really a soreness, it was an injury; This is a spontaneous report from a contactable consumer (patient). This 58-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in left shoulder or arm on 16Mar2021 15:00 (Lot Number: EN6200; Expiration Date: 30Jun2021) at single dose for COVID-19 immunization. Medical history included sports injuries. Patient said he has had sports injuries, when he used to play tennis, but nothing on his left side. The patient's concomitant medication was none. Patient said they have not had any other recent vaccinations or started any new medications. He said there was a new med he thought he started before getting the first vaccine, it said March 30th, so it had to be in February that he started this, this was date for second dose, so he didn't think that there was anything close to second vaccine dose. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at age of 58-year-old, administration on 23Feb2021 4:00 PM in left shoulder or arm (Lot number: EN6200, Expiration date: 30Jun2021) for COVID-19 Immunization. Patient has had vaccines all his life with no problems. He has had extreme arm pain mostly to his shoulder into his arm after he took the second shot dose roughly three weeks ago. He said that his arm and shoulder pain began 17Mar2021, and had lasted to today. He said it was not really a soreness, it was an injury. He said it had gotten a little worse the last couple of days. He said he stopped taking Aleve since you are not supposed to take that long because of bleeding problems. He was taking 4 a day for a week then stopped taking it. He said he was taking two in the morning and two at night, strength unknown. He said his pain was almost getting better, but it seemed worse since he stopped taking the Aleve. He said the pain affect what he normally did like tennis and yard work, it woke him in the middle of the night with pain, he was right handed. He said he also tried Bengay and things that didn't seem to work. The outcome of the events was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1254746
Sex: M
Age:
State: TX

Vax Date: 01/18/2021
Onset Date: 03/22/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Loss of hearing in left ear; tinnitus/echoing; numbness around area of left ear; This is a spontaneous report from a contactable health care professional (patient). A 46-year-old male patient received the second dose BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: El3248), via an unspecified route of administration, administered in the left arm on 18Jan2021 as a single dose for COVID-19 immunization. Medical history included Hashimoto's disease, high cholesterol and is prediabetic all from an unknown date and unknown if ongoing. The patient has no known allergies. The patient did not have COVID prior to vaccintion and has not been tested for COVID post vaccination. Concomitant medications included empagliflozin (JARDIANCE); levothyroxine (manufacturer unknown); metoprolol (manufacturer unknown); rosuvastatin (manufacturer unknown) and fish oil (OMEGA 3 [FISH OIL]), all taken for an unspecified indication, start and stop date were not reported. The patient previously received the first dose of bnt162b2 (lot number: Es1685) on 28Dec2020 at 12:00 PM via intramuscular route on the right arm for COVID-19 immunization. The patient experienced loss of hearing in left ear, tinnitus/echoing and numbness around area of left ear all on 22Mar2021 at 12:00. The ENT prescribed prednisone 10mg as treatment for the events. The outcome of the events was not recovered.; Sender's Comments: Based on the information currently available, a causal association between the reported events and BNT162B2 cannot be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and investigators, as appropriate.

Other Meds: JARDIANCE; LEVOTHYROXINE; METOPROLOL; ROSUVASTATIN; OMEGA 3 [FISH OIL]

Current Illness:

ID: 1254747
Sex: F
Age:
State:

Vax Date: 03/28/2021
Onset Date: 03/28/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: muscle pain; generalized pain in left side of body mainly; doesn't allow her to walk or move; second dose on March 28th, 14 days after first dose; second dose on March 28th, 14 days after first dose; This is a spontaneous report from a non-contactable consumer (patient) reported for herself. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration in left arm on 28Mar2021 at single dose for COVID-19 immunisation. She previously received the first dose on 14Mar2021 for COVID-19 immunisation and experienced injection site pain. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient called in requesting information about the symptoms she experienced post second dose administration of Pfizer's COVID-19 vaccine. She received the first dose on 14Mar2021 and second dose on 28Mar2021, 14 days after first dose. She only had injection site pain after vaccine first dose. After second dose she had muscle pain and generalized pain in left side of body mainly, described as deep pain that doesn't allow her to walk or move. She hasn't been able to communicate with physician. Events outcome was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254748
Sex: F
Age:
State: CA

Vax Date: 03/26/2021
Onset Date: 03/26/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: developed hives; This is a spontaneous report from a contactable consumer (patient's mother). This consumer reported same event for two patients.This is the second of two reports. A 64-year-old female patient received first dose of BNT162B2via an unspecified route of administration in her arm (unknown know if right or left) on 26Mar2021 11:00 AM (Batch/Lot number and expiriaton date were not reported) as single dose for covid-19 immunisation. The patient medical history (including any illness at time of vaccination), family medical history relevant to event were none. The patient's concomitant medications were not reported. Patient did not receive any prior vaccine within 4 weeks. In the middle of the night on 26Mar2021, patient experienced hives. Both she and her mother got BNT162B2 and both got hive. She had been taking Benadryl and the hives are ongoing. They had worsened for her. The outcome of event was not recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained; Sender's Comments: Linked Report(s) : same reporter/event/drug, different patient

Other Meds:

Current Illness:

ID: 1254749
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: sick; lethargic; This is a spontaneous report from a contactable consumer via a company representative This is the first report for one of two female patients. A female patient received Pfizer COVID-19 Vaccine BNT162B2 on an unspecific date at single dose for covid-19 immunization. Medical history and concomitant drug were not reported. Patient experienced sick and feeling lethargic. Outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021384159 Same reporter/drug/event, different patient.

Other Meds:

Current Illness:

ID: 1254750
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: sick; lethargic; This is a spontaneous report from a contactable consumer via a company representative. This is the second report for one of two female patients. A female patient received Pfizer COVID-19 Vaccine BNT162B2 on an unspecific date at single dose for covid-19 immunization. Medical history and concomitant drug were not reported. Patient experienced sick and feeling lethargic. She did get to a doctor. No Emergency Room visit. Outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : -PFIZER INC-2021384123 Same reporter/drug/event, different patient.

Other Meds:

Current Illness:

ID: 1254751
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Burning pain in back; This is a spontaneous report from a contactable consumer. A patient of an unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), first dose via an unspecified route of administration on unknown date as a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date, the patient experienced Burning pain in back. The outcome of the event was Unknown. No follow-up attempts are needed; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254752
Sex: F
Age:
State: IN

Vax Date: 03/19/2021
Onset Date: 03/19/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Her platelets are 200, which is very low; Bell's palsy; Shot on the top of my shoulder; excruciating pain/shoulder pain/given high on the top of her shoulder. It hurt; sore arm; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose at the age of 61-years old via an unspecified route of administration on 19Mar2021 10:10 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included systemic lupus erythematosus from 1985 and ongoing, arthritis and osteoarthritis from an unknown date and unknown if ongoing (She has osteoarthrosis throughout her body and her feet). Family history included stroke (husband died at the age of 59, he was having stroke upon stroke). The patient's concomitant medications were not reported. It was reported that when she received the shot, it was given high on the top of her shoulder and it hurt. She could not move her arm for 3 days. The pain was excruciating. On the 4th day, her arm was sore, but she could move it. She had no fevers, she didn't get sick, but she just couldn't move her arm. The shot was given at at 10:10 am, and by noon she could barely move her arm. Her left side of the mouth doesn't want to work properly. Her Bells Palsy started on 05Apr2021. She was in her car and driving to the store, when all of a sudden her left eye was watering. She got home and she didn't see anything wrong with her eye, except it was watering. She could tell a difference between the left and right side of face when she touched it. Something was wrong with her right side. Her eye was not opening all the way, it's been dropping, and her lip was down. She can't smile, and when she drinks water it's comes out. The patient clarified that it was her left side that is drooping. She went to the emergency room due to Bell's palsy. She could not move her arm within 2 hours of getting the shot. The patient mentioned her whole body aches from the Lupus and arthritis, but the shoulder pain was different after the vaccine. The shot itself hurt, and she thinks the one who administered the vaccine might have hit something. There's not a day that doesn't go by that she is not in pain. Her platelets are 200, which is very low. The patient underwent lab tests and procedures which included activated partial thromboplastin time: unknown result, blood glucose: unknown result, computerised tomogram: unknown result, full blood count: unknown result, glomerular filtration rate: unknown result; all on 06Apr2021, magnetic resonance imaging: showed a darkened area in her brain that looks like its connected with Bells Palsy on an unspecified date, basic metabolic panel: unknown result on 06Apr2021, platelet count: her platelets are 200, which is very low on an unspecified date, prothrombin time: unknown result, troponin i: unknown result (High sensitive ); both on 06Apr2021. The patient did not recover from Bell's palsy, recovered from vaccination site pain on 23Mar2021, from sore arm on 19Mar2021 and the outcome of the remaining event was unknown. Information about Lot/batch number is requested.

Other Meds:

Current Illness: Lupus erythematosus

ID: 1254753
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: they were extremely tired; felt their skin was itchy/tingly; felt their skin was itchy/tingly; They felt that they were having cold like symptoms; This is a spontaneous report from contactable consumer. An adult female patient received BNT162B2 second dose on unspecified date at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Pregnant at the time of vaccination was No. Prior to vaccination, was the patient was not diagnosed with COVID-19. The patient previously receive first dose of BNT162B2 on unspecified date for Covid-19 Immunisation. After the second dose was received, the patient mentioned that they were extremely tired and felt their skin was itchy/tingly in Mar2021. They felt that they were having cold like symptoms in Mar2021. The patient did not have any fever and the event only last a day or two. No treatment received for the adverse event. The outcome of the events was recovered. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1254754
Sex: F
Age:
State: KY

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 04/25/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: It is not comfortable. It goes under arm all the way under her boob and down her side. It is not comfortable and cannot rest; It is not comfortable and cannot rest; Pain and Soreness in left shoulder; Muscle under right arm real sore like lymph nodes are sore/cannot lift her arm; Muscle under right arm real sore like lymph nodes are sore/cannot lift her arm; Muscle under right arm real sore like lymph nodes are sore/cannot lift her arm; Right arm swollen/arm was swelling/right arm is swollen underneath and on top; her arm was swelling and really hurting; has not been able to sleep in about 2 days because of this; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 55-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot Number: EW0150) intramuscularly in left arm on 01Apr2021 10:00 at single dose for COVID-19 immunisation. Medical history included diagnosed allergies, compromised immune status, respiratory illness, genetic /chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity: diabetes diagnosed 3-4 years ago, blood pressure abnormal, and hiatal hernia. She has to take Prilosec for a hiatal hernia but has been taking it for years. Concomitant medications included omeprazole magnesium (PRILOSEC) for hiatal hernia, and blood pressure medication and diabetes medication. She previously received the first dose of BNT162B2 on 04Mar2021 (Lot EN6202) in right arm in the muscle for COVID-19 immunisation. She took the second one on Thursday and it was not bothering her until Friday night until Saturday morning. On 03Apr2021 05:00, it woke her up and it felt like it went in the muscle under her arm. It was real sore like lymph nodes are sore and she cannot lift her arm. She got the second shot on Thursday morning and that is what caused it. Sometime toward daybreak on Saturday morning is when she first felt that her arm was swelling and really hurting on 03Apr2021 05:00. Her right arm is swollen underneath and on top. On 04Apr2021 08:00, pain in left shoulder is like when old people say they have pleurisy in the back. She has not been able to sleep in about 2 days (Apr2021) because of this. No ER or physician's office required. She felt like going but did not took Ibuprofen. She thought it was going to be great because she did not have any symptoms, but this has whooped her. It is not comfortable. It goes under arm all the way under her boob and down her side. It is not comfortable and cannot rest. She read over the paperwork and saw that there were Lymph nodes and she wanted to know if there was anything she can do for it. She is just taking blood pressure medication and diabetes medication and has been on them for several years. Event outcome of not comfortable and cannot rest, insomnia was unknown, while for others was not recovered.

Other Meds: PRILOSEC [OMEPRAZOLE MAGNESIUM]

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am