VAERS 2021 Database www.vaers.hhs.gov

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

Total Manufacturer

Incidents per State

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

ID: 1373315
Sex: F
Age:
State: AL

Vax Date: 02/09/2021
Onset Date: 02/11/2021
Rec V Date: 06/04/2021
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Symptoms: tested positive for Covid; she did not have any taste for two weeks; This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EM9809; Expiration Date: Jun2021), via an unspecified route of administration, administered in left arm on 09Feb2021 (at the age of 74 years) as 1st single dose for COVID-19 immunization. Medical history included pulmonary fibrosis from 2015 and it was ongoing. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 11Feb2021, after vaccination the patient tested positive for COVID and she did not have any taste for two weeks in Feb2021 (date unspecified). The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 11Feb2021. The patient received antibody infusion as treatment for event on 12Feb2021 and she thought it was the monoclonal. The patient was scheduled to receive the second dose on 02Mar2021 and enquired if it was safe to take it or does she need to it put off until she has been COVID free for 3 months. On 28Feb2021, the patient recovered from events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Pulmonary Fibrosis (Verbatim: Pulmonary Fibrosis)

ID: 1373316
Sex: F
Age:
State: NC

Vax Date: 01/21/2021
Onset Date: 01/25/2021
Rec V Date: 06/04/2021
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Symptoms: stomach cramps; daily bouts of diarrhea; This is a spontaneous report from a contactable consumer (patient). This is one of two reports from same patient. A 65-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9261 and expiration date was not reported), via an unspecified route of administration, administered in Left arm on 21Jan2021 13:00 as single dose for covid-19 immunization. The patient received second dose of BNT162B2 (solution for injection: Lot number: EM9809), via an unspecified route of administration on 02Feb2021 at 01:15 pm on the left arm as a single dose for COVID-19 immunization. The patient medical history included osteoporosis, arthritis and allergies to crabmeat and wool. Concomitant medication included meloxicam 7.5 mg. The patient did not receive any vaccines 4 weeks prior to covid vaccination. The patient stated that, on 25Jan2021 (reported as 3 to 4 days after the first dose), she had 36 hours of stomach cramps, followed by ongoing daily bouts of diarrhoea. The patient stated that changes in diet did not help. The patient started to plan to call her doctor (today). The patient was not treated for the events. The outcome of the events was not resolved. No follow-up attempts are possible. No further information is expected.

Other Meds: MELOXICAM

Current Illness:

ID: 1373317
Sex: F
Age:
State:

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 06/04/2021
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Symptoms: sore throat; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age (Age:50; unit-unknown) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 28Feb2021 as unknown single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 01Mar2021, the patient experienced sore throat. Patient stated she received the pfizer covid 19 vaccine on Sunday, 28Feb2021. She reported a sore throat on Monday that has progressed. She wanted to know if she gets tested for covid, will the test come back postiive for the vaccine. The outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number could not be requested. No further information is expected.

Other Meds:

Current Illness:

ID: 1373318
Sex: M
Age:
State: TX

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 06/04/2021
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Symptoms: Vomiting; no energy; This is a spontaneous report from a contactable consumer (patient). A 64-years-old male patient received bnt162b2 (BNT162B2, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 26Feb2021 11:00 as SINGLE DOSE for covid-19 immunisation. Medical history included cancer from an unknown date and unknown if ongoing and Patient had no known allergies. There were no concomitant medications. Patient had no other vaccine in four weeks and no other medications in two weeks. Patient had no covid prior vaccination and no covid tested post vaccination. On 27Feb2021 12:00 AM, the patient experienced vomiting and no energy. The outcome of the events was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373319
Sex: F
Age:
State: OK

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 06/04/2021
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Symptoms: mental exhaustion; Recurring cluster headaches; migraines; confusion; This is a spontaneous report from a contactable consumer (patient). A 30-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection, #lot: EN6202), via an unspecified route of administration, administered in Arm Right on 25Feb2021 14:45 (at the age of 30-years-old) as single dose for covid-19 immunisation. The patient's medical history included obesity and tree nuts. Patient was vaccinated at a hospital. Patient did not receive other vaccine in four weeks of vaccination. Patient was not diagnosed with COVID, prior vaccination. Patient has not been tested for COVID, post vaccination. The patient's concomitant medications included ibuprofen (MIDOL) and mepyramine maleate, pamabrom, paracetamol (PAMPRIN). On 25Feb2021 at 18:15, the patient experienced mental exhaustion, recurring cluster headaches, migraines and confusion. The outcome of the events was not recovered. The patient did not receive any treatment for the adverse events experienced by the patient. No follow-up attempts are possible. No further information is expected.

Other Meds: MIDOL [IBUPROFEN]; PAMPRIN

Current Illness:

ID: 1373320
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: weakness; She got a little temperature; Woozy; symptoms of " a really bad flu"; can't get out of bed; This is a spontaneous report from a contactable other healthcare professional (patient) via medical information team. A female patient of an unspecified age (Age: 83; unit: Unknown) received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection) via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced weakness, she got a little temperature, woozy, symptoms of a really bad flu. Husband of patient reported that his wife received the second dose of the Covid vaccine yesterday in which she is experiencing some weakness and a temperature. Patient got on the phone at this time to provide demographics and the rest of her symptoms she has been experiencing. Outbound disclaimer was provided during this time. Patient stated that she was experiencing symptoms of a really bad flu, no nausea and a headache. Patient states that she can't get out of bed. Patient states that her and her husband are elderly, and they have been seeing specialists and don't have a primary care physician. Reporter stated its Pfizer COVID-19 vaccination that they had yesterday. His wife is having a sort of, he doesn't know how you call it, she got a little temperature, she is feeling woozy today, the day after. He was wondering what you expect will be the end result, when did you think it might clear up. In response to further probing, reporter stated that not actually he wants to find out what is the prediction for of her condition. So, let him go and talk to them okay. The outcome of all events was unknown. No follow-up attempts are Possible. Information on Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373321
Sex: F
Age:
State: WI

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 06/04/2021
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Symptoms: bump on her tongue and it looks like she has a "U" on tip of her tongue; 6-8 hours later her tongue began swelling and her nose and back of throat felt funny.; nose and throat felt funny; nose and throat felt funny; tongue became like misshapen, it has an extra point on it, that is like a blister or something, but it is not really a blister, but it is definitely not normal; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 69-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, (Batch/Lot number was not reported) via an unspecified route of administration in Arm Left on 24Feb2021 as 1st dose, single dose for COVID-19 immunization. The patient medical history was not reported. Patient has lots of medicine allergies years ago she took Advair discus inhaler. Patient had no other vaccines on the day of COVID vaccine. Concomitant medications included cetirizine hydrochloride (ZYRTEC) (MANUFACTURER UNKNOWN), via an unspecified route of administration on an unspecified date at unknown dose and frequency for unknown indication and diphenhydramine hydrochloride (BENADRYL), via an unspecified route of administration on an unspecified date at unknown dose and frequency for unknown indication. Patient states she had an adverse event when she got her first dose of the product last Wednesday (24Feb2021). She is a little nervous about getting her second dose on 18Mar2021. On 24Feb2021 about 6-8 hours after first shot her tongue got swollen/began swelling, nose and throat felt funny. She took Benadryl and same symptoms occurred next day. She states that her tongue became like misshapen, it has an extra point on it like a blister or something but it is not really a blister but it is definitely not normal. She has a bump on her tongue and it looks like she has a "U" on tip of her tongue. She states that her niece is a Nurse Practitioner and she talked to her niece about it. She took Zyrtec D in the morning and her niece told her to also take regular Zyrtec at night. She has been doing that for a few days and it is about 80-85 % better. She states that the little blister thing is gone, but her tongue is still misshapen. The swelling went right away after her Benadryl and Zyrtec D, and no more swelling issues, but her tongue is still misshapen and tender. She would like to report her side effects but also wants to know if she needs to do anything special for the second dose, like should she get an Epi Pen. She also reports that in the past she had a reaction to the Advair Discus inhaler and experienced "tongue swelling". ER gave Benadryl shot and symptoms calmed down. She then got virus and had tongue thing for 8 months. She was given Benadryl and prednisone, saw an allergist, and stated no one knew what to do. It ended up worked itself out. She would like to know if there are any similar ingredients with that or if it plays a part in the vaccine. The clinical outcome of the events were unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds: ZYRTEC; BENADRYL

Current Illness:

ID: 1373322
Sex: F
Age:
State: MO

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 06/04/2021
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Symptoms: Stiffness (going to the elbow) in the left arm; Sleepy for 3 days; This is a spontaneous report from a contactable consumer or other non-HCP. This is one of two cases from same reporter. A 57-year-old non-pregnant female patient (at the age of 57-years) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), via an unspecified route of administration, administered in Left Arm on 09Feb2021 02:15 PM as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient did not receive other vaccines 4 week prior to Pfizer vaccine. The patient had not diagnosed with COVID prior vaccination. And post vaccination, patient had not tested with covid. On 09Feb2021 04:00 PM, the patient experienced stiffness (going to the elbow) and sleepy for 3 days. No treatment was received for the events. The outcome of events was resolved approximately on unknown date in 2021. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1373323
Sex: F
Age:
State: TX

Vax Date: 02/25/2021
Onset Date: 03/01/2021
Rec V Date: 06/04/2021
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Symptoms: sore throat; cough; This is a spontaneous report from a contactable Consumer. A 49-years-old female patient received first dose of bnt162b2 (BNT162B2, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, administered in Arm Left on 25Feb2021 as SINGLE DOSE for covid-19 immunisation. Medical history included mild covid-19. The patient's concomitant medications were not reported. On 01Mar2021 05:00, the patient experienced sore throat and cough. Patient reported to someone before speaking to you. She told me her name but patient forgot. They took all of the information from patient, she asked patient for the card that they gave her, but patient don't have it, it is in the car and her husband has it. Patient got the Pfizer shot on Thursday 25Feb2021. As of yesterday at 5am, she have had a sore throat, went away after couple of hours, have cough, no fever, no nausea, only have a cough. Patient asked whether these adverse effects from the vaccine because she usually baby sit her grandbaby, because she was not sure if it is a side effect or a cold. Maybe she caught it again, she had covid before, it wasn't like this, it was very mild. Upon follow-up on (02Mar2021), Patient reports that she took the Pfizer Inc, BioNTech COVID shot on Thursday, and now she had a really bad cough. Caller reports that she had no fever, no body aches, no nausea, so she was wondering if the cough could be a side effect of the vaccine. Coughing started yesterday early morning about 5am 01Mar2021. Patient had no other vaccines on the same day as her COVID vaccine. The outcome of sore throat was recovered and the outcome of cough was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373324
Sex: F
Age:
State: NY

Vax Date:
Onset Date: 03/02/2021
Rec V Date: 06/04/2021
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Symptoms: urge to have a BM; left side of head had a funny sensation; Chills; hot flashes in my upper body; feels strange and voice has changed; feels strange and voice has changed; suddenly had to have a bowel movement; This is a spontaneous report from a contactable consumer or other non-HCP. A 76-years-old female patient (at the age of: 76-years) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6203; Expiration Date: 30Jun2021), via an unspecified route of administration, administered in Left Arm on an unspecified date as 1st dose, single for covid-19 immunization. The patient Medical history was not reported. Concomitant medication included losartan potassium 50 mg once a day, ergocalciferol (VIT D) and calcium taken for an unspecified indication, start and stop date were not reported. No vaccination within four weeks prior to the first administration date of the suspect vaccine and No Family medical history relevant to ae and relevant tests. The patient experienced chills, hot flashes in my upper body, feels strange and voice has changed, and suddenly had to have a bowel movement on 02Mar2021, urge to have a bm and left side of head had a funny sensation on an unspecified date. she got the first dose of the Pfizer Covid vaccine this morning around 08:00 AM, then the person who gave her the shot asked her what medication she takes and she told them, they did not say anything to her about it. States she took her medication for blood pressure around 09:30 AM at her regular time to take the medication, wants to know if it is okay Takes Losartan Potassium 50mg one time a day, states she took it with Vitamin D and Calcium. And States her voice is changed, she feels strange, states around 10:20 wanted to take bowel movement suddenly, could be a regular thing, states she feels some sort of hot flash sensations not bad, here and there and then feel chills. The patient underwent lab tests and procedures which included weight fluctuates between 144 and 145 on unspecified date. The outcome of the events feels strange, and voice has changed was not resolved and other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: LOSARTAN POTASSIUM; VIT D; CALCIUM

Current Illness:

ID: 1373325
Sex: F
Age:
State: NJ

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: soreness on her arm/ sore arm; felt very cold; weird sensation which she can't fully explain. It was like electrical impulses all over her body started appearing and like her blood is running inside all over her body; heart rate went a little fast, recorded at 110-112; could not sleep; This is a spontaneous report from a contactable Nurse. A 60-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection), via an unspecified route of administration on 01Mar2021 (Batch/Lot Number: EN6205; Expiration Date: Jun2021) as 1st dose, single dose for covid-19 immunisation. Medical history included covid-19 from 27Nov2020 to an unknown date and aggressive fever. The patient's concomitant medications were not reported. The patient previously took albuterol, tylenol and mucinex for covid-19. The patient reported that she was fine after 1st dose of the Pfizer vaccine but experienced some soreness on her arm and took tylenol. When she got home, she felt very cold but did not have a fever and had a normal temperature. As she was laying down, she felt a weird sensation which she can't fully explain. It was like electrical impulses all over her body started appearing and like her blood is running inside all over her body. Her heart rate went a little fast, recorded at 110-112 while her normal is 100-110. She could not sleep because of this. She woke up today and mentioned that her symptoms are lessening, not as intense as they were last night, and there is a little improvement. She took Tylenol for her symptoms and did not go to work. She received the vaccine amidst having a previous COVID Diagnosis last thanksgiving, 27Nov2020 and stated that she may still have antibodies from her infection and that the vaccine might be interacting with it. She knew that the Pfizer vaccine was not tested in people with previous COVID Diagnosis and just followed the CDC's recommendation to get vaccinated after 90 days after the infection and inquired for information, Pfizer may have on these topics and if she should receive the 2nd dose on 22Mar2021. She had covid around thanksgiving being about 3 months ago, so she waited the 90 days to get the vaccine. She reported that since she was a covid patient, she was thinking is it because she had antibodies. She was checked 2 weeks in Feb2021 and she was positive for antibodies and wanted to know the relationship between antibodies and the vaccine. Therapeutic measures were taken as a result of soreness on her arm/ sore arm. The patient underwent lab tests and procedures which included heart rate: 110-112, heart rate went a little fast, recorded at 110-112 while her normal is 100-110, sars-cov-2 antibody test: positive on Feb2021. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373326
Sex: F
Age:
State: AZ

Vax Date: 02/16/2021
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: Tingling started around her mouth, went up her face, and in her head/tingling lips; Left ear is bothering her; Headache; Felt a rush go through her; This is a spontaneous report from a contactable consumer (patient) received via medical information team. A 68-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot/Batch number: unknown), via an unspecified route of administration on 16Feb2021 as a single dose for COVID-19 immunization. The patient's medical history included intractable itching. The patient had a reaction to an epidural injection when she had a surgery 25 years ago. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced tingling started around her mouth, went up her face, and in her head/tingling lips, left ear is bothering her, headache, felt a rush go through her. As soon as she had the needle in her arm she felt a rush throughout her arm. She's also experiencing tingling in her mouth, around her lips, head and face. Before putting on her mask her lips start tingling in the outside only. Doesn't know if that should be expected or not. Everyone else she talked to has not had this experience. Tingling is periodic and not constant. Today, her lips are tingling and her left ear is bothering her. She would like to know if this has been reported before and if she should receive the second dose of the vaccine. The clinical outcome of the tingling started around her mouth, went up her face, and in her head/tingling lips, left ear is bothering her, headache, felt a rush go through her were unknown. No follow-up attempts are Possible. Information on Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373327
Sex: M
Age:
State: NY

Vax Date: 01/29/2021
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: test positive after 1st dose; little, slight muscle aches; pain at the injection site; This is a spontaneous report from a Non contactable Consumer. This Consumer reported for a male patient (husband) that: A 72-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), 1st dose Solution for injection, Lot number EL9264-A) via an unspecified route of administration, on 29Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient experienced SARS-CoV-1 test positive, muscle pain, vaccination site pain. The patient went into quarantine. Quarantine ended on 19Feb2021. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 07Feb2021 and on 22Feb2021 sars-cov-2 test: negative. on an unspecified date with outcome of the events was unknown. The reporter stated that their quarantine is way over, and they have no symptoms or anything like that, and they were told to wait to get the second dose after a couple weeks, and it has been more than couple weeks that have gone by. They were told that they may have antibodies, and that they should wait 3 months until after they contracted COVID to get the second dose, which they would like to know if this is correct. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373328
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: We noticed changes in her speech and cognition and legs, after the first shot; We noticed changes in her speech and cognition and legs, after the first shot; We noticed changes in her speech and cognition and legs, after the first shot; The initial case was missing the following minimum criteria: No adverse event. Upon receipt of follow-up information on (04Mar2021), this case now contains all required information to be considered valid. This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient's medical history included multiple sclerosis for about 26 years, diabetes, covid-19 from an unknown date in Nov2020 to an unknown date, tracheostomy and has been in a nursing home. The patient's concomitant medications were not reported. The patient has had Multiple Sclerosis for about 26 years. Recently she has been in a nursing home. She had Covid end of Nov2020. Once she recovered, they urged her to get her vaccinated for Covid. Noticed changes in her speech and cognition and legs, after the first shot, but did not put two and two together, until after the second shot. In under 24 hours of receiving the second shot, 28Jan2021 at approximately 3pm, she could barely hold her head up and she could only move her lips, making a mumbling sound at best. She suffered optical injury, and as the hours passed unable to talk, unconscious, unable to move her body, etc. She had to receive a tracheostomy and food peg and is in a long-term acute hospital. She has since become more alert (awake versus sleeping and not responding), tracks people with her eyes, fairly consistently. As of 27Feb201, she is tracking better but not following commands and the biggest thing is she can turn her head a little, left to right. Today I saw her swallow, twice (she still has a tracheostomy). The teach can only come out if she can follow commands, this do some therapy with the respiratory therapist. The patient received the Pfizer gene therapy shot. Her primary care physician was the attending physician at the time was urged to give permission for her to receive the first shot. Following poor conditions at this facility and having found a 5-star facility/home near, the patient was moved before the second shot. The patient was currently at an acute care facility. We are hoping she won't need to have the tracheostomy much longer, so that she can return to another faciltity, a home which close to my residence. The acute care facility where she was at now. With no disrespect intended, but rather frustration, the regular or primary physician there who I've only spoken to (not their neurologist, because I have yet to speak to him), is useless- beyond her basic care or progress thinking in care. The reporter want to provide any treatment or care that could potentially reverse the garbage that was injected into her. She has had Multiple Sclerosis for decades, is diabetic, and she had Covid end of November. She should not have received this synthetic toxic serum. In other countries, they are advising people with MS not to receive this shot. There are some doctors I'm now learning about, one a MS specialist/neurologist, that has advised his MS patients NOT to get this shot, stating there are better shots or a real vaccine expected in summer. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373329
Sex: M
Age:
State: CA

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

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Symptoms: fever; chills; This is a spontaneous report from a contactable consumer (patient). A 29-year- old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration administered on arm left on an unspecified date (Batch/Lot number was not reported) as 1st dose, single for COVID-19 immunization. Medical history and concomitant medications were not reported. One week after receiving the vaccine, the patient later experience fever and chills. It was reported that the chills that began at night and lasted until early afternoon (as reported). No treatment was received for the events. The patient was not diagnosed with COVID-19 prior to vaccination and not tested for COVID-19 since the vaccination. The patient recovered from the events on unknown date. Patient thought it was not related to the vaccine. No follow-up attempts are possible, information about lot/batch number cannot be obtained; Sender's Comments: Based on the information available and reported non-relatedness, contributory role of the suspect BNT162B2 can be excluded for pyrexia and chills. Since they could be concurrent condition.

Other Meds:

Current Illness:

ID: 1373330
Sex: M
Age:
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Rec V Date: 06/04/2021
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Symptoms: Had pain before getting the vaccine but it's now getting worst; This is a spontaneous report from a contactable consumer or other non hcp. A 71-years-old elderly male patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: unknown) via an unspecified route of administration on an unspecified date at Single dose for COVID-19 immunization. The patient's Medical history included arthritis. She reported that her husband has stopped taking medications since 4 days now. They stopped taking a couple of mediations such as blood thinners, muscle relaxant and etc. The patient's concomitant medications were not reported. The patient was taking muscle relaxant to help with his pain related to arthritis. He also had pain before getting the vaccine but it's now getting worst because he hasn't taken his medication for a while. The outcome for the events was Unknown. Caller states that the pain her husband is experienced is not related to the vaccine. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373331
Sex: F
Age:
State: FL

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 06/04/2021
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Symptoms: Felt like she had flu/mild flu like symptoms; congested; fatigue; BP shot sky high/after the vaccine her BP had gone to 190/105/BP is borderline high/sporadic or borderline high BP; face felt funny it was like tingling; Trouble Swallowing; felt like throat muscles closing; Dry mouth; This is a spontaneous report received from a contactable consumer (Patient). A 67-year-old female patient received first dose of BNT162B2(COVID-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Right on 23Feb2021 15:00 (Batch/Lot Number: EN6200) as 1st dose, single for covid-19 immunisation. Medical history included Type 1 diabetes, but she got it as an adult. They initially thought it was Type 2 but it was not gradually over time she Lost her Beta Cells, she tested for antibodies and its Type 1 Diabetes Lada. She was totally dependent on Insulin. LADA stands for Latent Autoimmune Diabetes of Adults. She also had Serious Allergy problems, she had had allergies since she was a child, they were respiratory and environmental, she was allergic to yeast she gets in trouble if she eats it, she was allergic to Mold, she had 2 autoimmune diseases. The type 1 diabetes was triggered by a night she spent in a Hotel, something in there bothered her in which she had a severe allergic reaction, she diagnosed as Type 2 diabetes at this point, before her A1C was good, but then weeks later to that event her Blood sugar was out of control. For the past 5 years she had been changing medications and foods and finally became insulin dependent that was precipitated by the allergies in the hotel, it was a bad exposure, even her eyes were puffy. She did not need a Epipen or anything and it was not at that level, but allergies can do serious damage, this event triggered her Pancreas. She was also allergic to Dust, Tobacco in other words secondhand smoking, feathers, animal dander like dogs and cats, she is not allergic to pollen or has hay fever or anything. She also had Hyper-tension, High Cholesterol that was also controlled with medication, Hashimotos Thyroiditis, she clarifies that all is being treated for, all her number levels are good for all of it. Patient concomitant medication included insulin for type 1 diabetic. Patient has had No other vaccines on the same day or in the 4 weeks prior to the COVID vaccine. She had never really had other vaccine as an adult. She did not have to go to the emergency room, but she does think she will call her doctor. She had no relevant family history. After vaccination, she was advised to wait 30 minutes after receiving her first dose. In about 10 minutes of receiving the vaccine, on 23Feb2021, she had a really weird headache, the symptoms that were concerning to her was trouble swallowing, she wanted water, her face felt funny it was like tingling, it was a weird thing, and they took her Blood Pressure (BP), her BP shot sky high. She does have high BP and she takes medications and its well-controlled with Medications but after the vaccine her BP had gone to 190/105. They kept the cuff on her, brought her water. After drinking the water, she could swallow, she doesn't know if this was because her mouth got dry. They kept checking her BP, it took about 24 hours for her BP to go back to normal. She added that on 24Feb2021, she felt like she had the flu for 3 days after the vaccine, it was mild flu like symptoms, she had no body aches but just felt fatigue and was really congested. She felt these symptoms start. The patient underwent lab tests and procedures which included blood pressure measurement. She had no testing since the vaccine. But had just been testing her own BP at home. She had all of her BP result in the BP Machine, and she doesn't know how to access them, she has not kept a physical log, but she recalls from memory that her BP was 120/75 2 days after getting the vaccine and that was the lowest, she had had. Her highest was 150/95 within 24 hrs. of receiving the vaccine. Last night it was 140/90. This morning it was 128/80. The events Headache, face felt funny it was like tingling, Trouble Swallowing, Dry mouth, were recovered on 23Feb2021, flu, fatigue, fatigue, congested were recovered on 26FEB2021 and high blood pressure was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: INSULIN

Current Illness: Type 1 diabetes mellitus (Got it as an adult.)

ID: 1373332
Sex: F
Age:
State: NC

Vax Date: 03/02/2021
Onset Date: 03/02/2021
Rec V Date: 06/04/2021
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Symptoms: my lips and the sides of my tongue felt tingly and somewhat numb...no swelling; my lips and the sides of my tongue felt tingly and somewhat numb...no swelling; my lips and the sides of my tongue felt tingly and somewhat numb...no swelling; metallic taste in mouth; This is a spontaneous report received from a contactable consumer (Patient). A 68-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN8203) via an unspecified route of administration, administered in left arm, on 02Mar2021 at 01:45 PM (at the age of 68-years-old), as a single dose for COVID-19 immunization. The patient medical history included thyroid disease, and had known allergies which included Gluten, hydrocodone, penicillin, sulfa, clindamycin, ACE inhibitors, Batrim, Azithromycin. The patient did not receive any other vaccine within four weeks of vaccination. Patient did not have COVID-19 prior vaccination. Concomitant medications included Synthroid, Cytomel, HCTZ, Olmesartan, Vit D. On 02Mar2021 at 02:00 PM (within the first 15 minutes of 30 minute required post vaccine wait time), patient lips and the sides of tongue felt tingly and somewhat numb but no swelling. She also noticed a metallic taste in mouth around the same time. The strange taste quickly resolved with drinking warm coffee and lips/mouth slight tingling and numbness issue stayed the same beyond wait time. Total time around 45-minutes to an hour. Patient did not receive any treatment for events. The patient was not tested for Covid post vaccination. The outcome of all the events was reported as recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: SYNTHROID; CYTOMEL; HCTZ; OLMESARTAN; VIT D

Current Illness:

ID: 1373333
Sex: M
Age:
State: IL

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: uncomfortable; my upper Right lip began to swell, slowly; This is a spontaneous report from a contactable consumer. A 63-years-old male patient received second dose BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection; Lot Number: EN6203), via an unspecified route of administration, administered in Left arm on 04Mar2021 16:45 as 2nd dose, single dose; and previously took 1st dose of BNT162B2 for COVID-19 immunization. No covid prior vaccination and no known allergies. The patient medical history and concomitant medications were not reported. No vaccines within 4weeks. On 04Mar2021 17:00, 18 minutes after vaccination, patient upper Right lip began to swell, slowly. 30 minutes later when home it was very noticeable and uncomfortable. patient reported it was only point of concern. 6 hours later after 2 Tylenols, the swelling has decreased, Somewhat. No covid tested post vaccination. Patient reported no treatment was received. Patient was not recovered from events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373334
Sex: F
Age:
State: FL

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Vomiting; Nausea; Diarrhea; Headache; Chills; Fever; This is a spontaneous report from a contactable consumer (patient). A 42 years old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route, administered in Left arm on 04Mar2021 at 13:45 (at an age of 42 years during vaccination) as 1st dose, single dose for covid-19 immunisation. Medical history included known latex allergy. The patient had received other medications in two weeks prior to vaccination. The patient was not tested for covid prior to vaccination. Facility type vaccine was reported as Other. The patient had no other vaccine in four weeks to Covid-19 vaccination. On 04Mar2021 at 14:30, the patient experienced vomiting, nausea, diarrhea, headache, chills, fever. The patient was not tested for covid post to vaccination. The patient had not received any treatment medication for the resulted events. The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1373335
Sex: F
Age:
State: PA

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: dizziness; headache; Itching from head to toe including throat; Itching from head to toe including throat; This is a spontaneous report received from a non-contactable consumer (Patient). A 36-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 04Mar2021 14:00 (Batch/Lot Number: EN6199) as unknown, single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had no known allergies, but he had other unspecified medical history. The patient was not diagnosed with COVID-19 Prior to vaccination. The patient had not been tested for COVID-19 Since the vaccination. On 04Mar2021 14:00, the patient experienced dizziness, headache, itching from head to toe including throat. Patient received several rounds of Benadryl max dose to treat adverse events. No follow up attempts are possible. No further information is expected.

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Current Illness:

ID: 1373336
Sex: F
Age:
State: NC

Vax Date: 02/21/2021
Onset Date: 02/22/2021
Rec V Date: 06/04/2021
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Symptoms: my lips swelled up severely; Facial swelling; I had giant itchy welts on legs and back and scalp; hives on back; This is a spontaneous report from a contactable other healthcare professional reported for herself. A 66-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER COVID-19 VACCINE, Batch number: Unknown), via an unspecified route in the right arm on 21Feb2021 at 09:00, as a single dose for covid-19 immunization (age at Vaccination was 66years). Medical history included chronic, osteopathic hives for more than 15 years ago. No known allergies reported. Concomitant medications taken in two weeks included Vitamin c (VITAMIN C [ASCORBIC ACID], curcuma longa (TURMERIC [CURCUMA LONGA], boswellia serrata (BOSWELLIA), ergocalciferol (VIT D) and cyanocobalamin (B12 [CYANOCOBALAMIN] (sublingual). Patient has not taken any other vaccine in four weeks. Since the vaccination, the patient had not been tested positive for COVID-19. On 22Feb2021 at 01:00, the next day, patient experienced hives on back, within 36 hours her lips swelled up severely, facial swelling and she had giant itchy welts on legs, back and scalp. Therapeutic treatment received as a result of the events included Benedryl, self-administered. Events assessed as non-serious by reporter. Reported that facial swelling subsided in about 6 hours, itchy welts come and go but are still present (11 days after the shot). Outcome of facial swelling was resolved and for all other events was resolving. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: VITAMIN C [ASCORBIC ACID]; VIT D; B12 [CYANOCOBALAMIN]; TURMERIC [CURCUMA LONGA]; BOSWELLIA

Current Illness:

ID: 1373337
Sex: M
Age:
State: MI

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 06/04/2021
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Symptoms: Body aches/ achiness; Lethargy; Fever; This is a spontaneous report from a contactable other HCP. A 60-year-old male patient reported for himself that he received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number was not reported) via an unspecified route of administration on 12Jan2021 08:30 in left arm as a second dose, single for COVID-19 immunization at public health clinic facility. The patient medical history and concomitant medications were not reported. The patient historical vaccine included first dose of BNT162B2 (COVID Pfizer vaccine) on an unspecified date for COVID-19 immunization. The patient did not receive any other vaccine within four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had not been tested for COVID-19. The patient experienced body aches, achiness, lethargy and fever on 12Jan2021 at 11:00. The patient did not receive any treatment. The outcome of all events was recovered in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 1373338
Sex: F
Age:
State: OH

Vax Date: 02/24/2021
Onset Date: 02/25/2021
Rec V Date: 06/04/2021
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Symptoms: Trigeminal Neuralgia; This is a spontaneous report from a contactable consumer (patient). A 43-year-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EL9267), via an unspecified route of administration in Arm Left on 24Feb2021 at 09:30(at the age of 43 years old) as 2nd dose, single dose for covid-19 immunisation at Health Clinic. Medical history was none. Known allergies was none. Other vaccine received in four weeks included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EM9810) via an unspecified route of administration in Arm Left on 03Feb2021 as first dose, single dose for covid-19 immunisation. Concomitant medication included lisdexamfetamine mesilate (VYVANSE) taken for an unspecified indication. The patient was not tested covid prior to vaccination. On 25Feb2021 at 20:00 the patient experienced trigeminal neuralgia. Adverse event resulted in doctor or other healthcare professional office/clinic visit. Reporter reported as, "Doctor suspects a diagnosis of Trigeminal Neuralgia. Referred to a neurologist for confirmation and treatment plan". Therapeutic measures were taken as a result of trigeminal neuralgia. Treatment received as, medication to help with inflammation and pain. The patient was not tested for covid post vaccination. Outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: VYVANSE

Current Illness:

ID: 1373339
Sex: F
Age:
State: ME

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Large lump at injection site; Large redness area almost half the top of arm; This is a spontaneous report from a contactable nurse (patient) or other Health Care Professional. A 69-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN6203 and Expiry date: Unknown), via an unspecified route of administration in Arm Left, on 04Mar2021 at 12:00 PM (at the age of 69-years-old) as UNKNOWN, SINGLE for Covid-19 immunization. The patient medical history was not reported. The patient known allergies were not reported. The patient concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the vaccination. The patient did not receive other medications within 2 weeks of vaccination. Patient was not diagnosed with COVID, prior vaccination. Patient has not been tested for COVID, post vaccination. On 04Mar2021 at 16:00, the patient had experienced large lump at injection site, large redness area almost half the top of arm. The patient did not receive treatment for events. The outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373340
Sex: F
Age:
State: AZ

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: nausea; my heart started beating hard and fast; my heart started beating hard and fast; headache; This is a spontaneous report from a contactable consumer or other non hcp. A 65-years-old non pregnant female patient received bnt162b2 (Pfizer-BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot Number: EN6205), via an unspecified route of administration, administered on left arm on 04Mar2021 (at 65-years age) 10:45 as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history was none. The patient did not receive any other vaccines within 4 weeks. Prior to vaccination, patient was not diagnosed with COVID-19. Concomitant medications included Multivitamin, fexofenadine hydrochloride (ALLEGRA); curcuma longa (TURMERIC [CURCUMA LONGA]); vitamin b complex (B COMPLEX [VITAMIN B COMPLEX]) taken for an unspecified indication. The patient previously took celebrex and experienced drug hypersensitivity. On 04Mar2021 10:45, it was reported that within a minute or two of injection my heart started beating hard and fast. A headache in the forehead began simultaneously with some nausea. she removed mask, rolled down the window for fresh air. The feeling had lessened by end of 15 minutes. The headache and racing heart returned several times during the day, with last one around 5:30 pm. Patient checked BP around 2 pm and it was 130/75. Didn't have any problems overnight. It was now 7:12 am Friday and she was fine so far. The patient not sure whether she should take the second shot. The patient underwent lab tests and procedures which included blood pressure measurement was 130/75 on 04Mar2021. No treatment received for the events. The outcome of events was recovered on an 05Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: ALLEGRA; TURMERIC [CURCUMA LONGA]; B COMPLEX [VITAMIN B COMPLEX]; MULTIVITAMIN [VITAMINS NOS]

Current Illness:

ID: 1373341
Sex: F
Age:
State: TX

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 06/04/2021
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Symptoms: Pain in arm and armpit; Pain in arm and armpit; Sore neck and jaw; Sore neck and jaw; Tongue very sensitive and still sensitive; Now I have a knot in my armpit that is very tender; Now I have a knot in my armpit that is very tender; Headache; tired; irritable; My back hurt for days; This is a spontaneous report from a contactable consumer (patient). A 48-years-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9266), via an unspecified route of administration, administered in arm right on 18Feb2021 at 16:30 (at an age of 48-years-old) as 2nd dose, single dose for COVID-19 immunisation. The patient medical history and concomitant medication was not reported. She had known allergies and had other medical history. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN5318) via an unspecified route of administration, administered in arm right on 28Jan2021 at 16:15 as 1st dose, single dose for COVID-19 immunisation. She did not take other vaccine in four weeks. She had taken other medications in two weeks. Patient not had COVID prior vaccination and not had COVID tested post vaccination. On 18Feb2021 at 18:00, the patient experienced pain in arm and armpit, pain in arm and armpit, sore neck and jaw, sore neck and jaw, tongue very sensitive and still sensitive, now she had a knot in her armpit that is very tender that won't go away, headache, tired, irritable, her back hurt for days. The patient did not receive any treatment for the events. The clinical outcome of the pain in arm and armpit, pain in arm and armpit, sore neck and jaw, sore neck and jaw, tongue very sensitive and still sensitive, now she had a knot in her armpit that is very tender that won't go away, headache, tired, irritable, her back hurt for days were resolving. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373342
Sex: F
Age:
State: WV

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Arm started hurting; Arm started burning instantly; Arm sore; Trouble raising it up; Pain in neck; Pain in shoulder; This is a spontaneous report from a contactable consumer (patient). A 65-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: EN6199), via an unspecified route of administration, administered in left arm on 04Mar2021 14:45 (at the age of 65-years-old) as single dose for COVID-19 immunization. The patient's medical history included diabetic, thyroid, high cholesterol, high blood pressure. The patient previously took demerol and experienced known allergies. The patient's concomitant medication included metoprolol. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 04Mar2021 after the vaccination, the patient experienced arm started hurting/burning instantly. radiated to entire arm. arm sore, pain in neck and pain in shoulder. It was reported arm started hurting/burning instantly. Radiated to entire arm. arm sore. Trouble raising it up. Later pain in neck and shoulder. Been almost 18hours since injection. Still in pain. The patient underwent lab tests and procedures which included on an unspecified date blood cholesterol: high and blood pressure measurement: high. Since the vaccination, the patient has not been tested for COVID-19. The patient did not receive any treatment for the adverse event. The outcome of events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: METOPROLOL

Current Illness:

ID: 1373343
Sex: F
Age:
State:

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: weird taste; Lightheaded; A funny taste in my mouth; This is a spontaneous report from a contactable consumer (patient). A 47-years-old non pregnant female patient received first dose of bnt162b2 (BNT162B2, solution for injection, Batch/Lot number: not reported) administered in left arm via an unknown route of administration, on 04Mar2021 at 12:30pm as single dose for covid-19 immunization. Medical history included multiple sclerosis, complex regional pain syndrome, fibromyalgia, hypertension, hypothyroidism, hypokalaemic syndrome, intervertebral disc degeneration, vitamin d deficiency, hypersensitivity. On 04Mar2021 at 13:30pm, the patient was lightheaded for about 4 hours, a funny taste in mouth started about 30 minutes after the vaccine and lasted a few hours but food still has a weird taste the next day. No treatment was received for the events. The outcome of the events was recovered with sequelae. It was reported that patient received no other vaccine in four weeks. In two weeks, patient received other unspecified vaccine first dose on left arm on o4Mar2021. The patient was not diagnosed with covid prior vaccination and not tested for covid post vaccination. The patient had known allergies. No follow up attempts were possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373344
Sex: F
Age:
State: NJ

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Face tingling and numbness; Face tingling and numbness; swelling around mouth; swelling anad itchiness of throat; swelling anad itchiness of throat; This is a spontaneous report from a contactable consumer (Patient, self-reported). A 36-years-old (non pregnant) female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EN6205), via an unspecified route of administration, administered in Left arm on 04Mar2021 14:45 (At 36-years-old) as a single dose for COVID-19 immunisation. Medical history included asthma from an unspecified date and unknown if ongoing, known allergies: Penicillin. Concomitant medications taken in two weeks included budesonide, formoterol fumarate (SYMBICORT) (MANYFACTURER UNKNOWN) 160/4.5 from an unspecified date and unknown if ongoing. No other vaccine in four weeks. Patient did not received any vaccine on same date. Patient was not diagnosed with COVID-19 prior vaccination. Patient has not been tested for COVID-19, post vaccination. On 04Mar2021 15:45, patient experienced Face tingling and numbness, swelling around mouth, swelling and itchiness of throat, very minor and occurred after the 15 minute wait time - about 20 minutes after vaccination, symptoms disappeared approx. 10 minutes after appearing. Patient did not received treatment for adverse events. Events were non-serious. Outcome of the reported events had recovered on 04Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: SYMBICORT

Current Illness:

ID: 1373345
Sex: F
Age:
State: GA

Vax Date: 03/04/2021
Onset Date: 03/05/2021
Rec V Date: 06/04/2021
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Symptoms: metallic taste; salivating black; tongue is stained black; This is a spontaneous report from a contactable consumer (patient herself). A 47-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) intramuscular on the left upper arm on 04Mar2021 at 14:00 (at the age of 47-year old) (Batch/Lot number EL9264) at single dose for Covid-19 immunization. Relevant medical history included allergy to doxycycline described as vomiting from in 1990s or 1990. Concomitant medications were not reported. Starting about 07:45 on 05Mar2021 when she woke up she had a metallic taste in her mouth; she began salivating black, spitting up black saliva which turned her tongue black, tongue was stained black in stripes. She still had the metallic taste in the back of her throat; but was not actively spitting up black saliva any longer. The outcome of metallic taste was recovering, the outcome of other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373346
Sex: F
Age:
State: PA

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Rec V Date: 06/04/2021
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Symptoms: Bad body aches from lower back down legs; Unwell feeling all night; feverish; chills; bad taste in mouth; restless; Stomach turning; A red very warm blotch on my arm around the injection site; Anxiety; Feelings disappeared then came back not as harsh around 30 hours after; This is a spontaneous report from a contactable consumer (patient) or other non hcp. A 44-years-old non-pregnant female patient received bnt162b2 (BNT162B2, Solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot Number: EN8581) as unknown, single for covid-19 immunisation. Medical history included CVC (Central venous catheter). Concomitant medications included Metoprolol succinate 25 mg, Omeprazole 40 mg, Cetirizine hydrochloride. Patient had known allergies. Patient did not receive any other vaccine within 4 weeks. Patient neither diagnosed with COVID-19 prior to vaccination nor been tested for COVID-19 post vaccination. On an unknown date, the patient experienced bad body aches from lower back down legs 12 hours later, unwell feeling all night, feverish, chills and bad taste in mouth, restless, stomach turning. Her feelings disappeared then came back not as harsh around 30 hours after. Patient went to work feeling ok thought she was back to normal but when she showered, she noticed a red very warm blotch on her arm around the injection site which slightly disappeared after 12 hours and had anxiety. The patient was recovering from the event red very warm blotch on her arm around the injection site. The outcome of all other events was reported as unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: METOPROLOL SUCCINATE; OMEPRAZOLE; ZYRTEC

Current Illness:

ID: 1373347
Sex: F
Age:
State:

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Muscle pain at injection site; This is a spontaneous report from a non-contactable consumer (patient). A 25-year-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EL3248) via an unspecified route of administration on 04Mar2021 09:45 am (at the age of 25-year-old) as unknown, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient had no known allergy. COVID prior vaccination was none. Since the vaccination, patient had not been tested for COVID-19. COVID tested post vaccination was none. On 04Mar2021, the patient experienced muscle pain at the injection site. The patient did not receive any treatment for the event. The outcome of the event was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373348
Sex: M
Age:
State:

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Rec V Date: 06/04/2021
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Symptoms: arm was barely sore; This is a spontaneous report from a contactable consumer (patient). A 63-year-old male consumer received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported) via an unspecified route of administration on an unspecified date as first dose, single for COVID-19 immunization. The Patient medical history included knee pain for which he periodically gets a steroid injection, and he will eventually have surgery. He has a doctor appointment coming up and wonders if he can get the steroid injection in his knee. He has been referred all over the place looking for answers and no one can tell him. He was referred to Pfizer. The patient concomitant medications were not reported. The patient reported that his arm was barely sore after first Pfizer covid vaccine injection and after the second dose, his arm was sore for 24 hours and he got a little headache. The patient stated that he was on oral steroids and got the flu vaccine and he got sick as a dog. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373349
Sex: M
Age:
State: AZ

Vax Date: 02/19/2021
Onset Date: 02/21/2021
Rec V Date: 06/04/2021
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Symptoms: Rash/Hives occurring two days after vaccination; Rash/Hives occurring two days after vaccination; This is a spontaneous report from a contactable other hcp. A 35-years-old male patient received second dose of bnt162b2 (BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot number was not reported) intramuscular, administered in arm right on 19Feb2021as second dose, single for COVID-19 immunization. It was reported that the patient had no allergies. The patient medical history and concomitant was not reported. The patient did not receive any other vaccine in four weeks. Prior to vaccination patient was not diagnosed with COVID was unknown. Post vaccination patient did not test for COVID. Patient previously took first dose of bnt162b2 (BNT162B2, solution for injection, Batch/Lot Number was not reported) via an unspecified route of administration, administered on unknown date as first dose, single for COVID-19 immunization. It was reported that on 21Feb2021 the patient experienced Rash/Hives occurring two days after vaccination. Treated with 5 days of prednisone and hydroxyzine without relief. Therapeutic measures were taken as a result of rash/hives occurring two days after vaccination. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1373350
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/05/2021
Rec V Date: 06/04/2021
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Symptoms: L arm tingling; malaise; shortness of breath; tired/fatigue; This is a spontaneous report from a non-contactable other healthcare professional. A 66-years-old female patient the first dose of received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6203), via an unspecified route of administration on an unspecified date as a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced tired/fatigue on 05Mar2021, l arm tingling, malaise and shortness of breath on an unspecified date. During her 15-minute waiting period after the injection, the patient began to experience L arm tingling. Patient complains of malaise/fatigue (feels tired today.) And shortness of breath (chronic, not with exertion, tires easily. Not changed from baseline.) Treatment included: water, snacks and reassurance/observation for about 40 minutes Follow up response to treatment: excellent. Patient discharge: Stable to go home and follow up with PCP. Therapeutic measures were taken as a result of tired/fatigue, malaise and shortness of breath. The outcome of the events was unknown. No follow-up attempts are Possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373351
Sex: F
Age:
State: KS

Vax Date: 02/10/2021
Onset Date: 03/01/2021
Rec V Date: 06/04/2021
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Symptoms: sinusitis; soreness in the shoulder on the side she received the injection; This is a spontaneous report from a contactable nurse (patient). This female patient of unspecified age received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) via unspecified route of administration on 10Feb2021 at single dose for Covid-19 immunization. Relevant medical history included sinus infection on an unknown date ("before") treated with antibiotics ("generally the antibiotics help"). Concomitant medications were not reported. On an unknown date the patient experienced soreness in the shoulder on the side she received the injection. a couple of days ago, she reports soreness on the left side of her face, her eye was hurting and had a slightly sore throat. She noticed swelling in her eye, face, had a headache and pain. Clarified her eye was aching. Her left cheek and side of face was swollen. She visited the doctor who said it was sinusitis and gave her antibiotic: amoxicillin/clavulanic acid (AUGMENTIN) every 12hours for 10 days since 04Mar2021. The second dose of vaccine was planned on 08Mar2021. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1373352
Sex: F
Age:
State: FL

Vax Date: 02/18/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: I feel a very slight sore throat; slight cough; Slight diarrhea; mild headache; body temperature 97.2; This is a spontaneous report from a contactable consumer, the patient. A 74-years-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9267), via an unspecified route of administration, administered in left arm on 18Feb2021 (at the age of 74-years-old) as a single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medications included nebivolol hydrochloride (BYSTOLIC) 10 mg; losartan 25mg; rosuvastatin 10mg. The patient was not pregnant at the time of vaccination. The patient had no other vaccine within four weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 04Mar2021, the patient reported 'I feel a very slight sore throat, slight cough, mild headache, slight diarrhea, body temperature 97.2, was this a normal reaction 2 weeks after first covid vaccine'. The patient did not receive any treatment. The outcome of the events was unknown. No follow-up attempts are possible; No further information is expected.

Other Meds: BYSTOLIC; LOSARTAN; ROSUVASTATIN

Current Illness:

ID: 1373353
Sex: F
Age:
State: CA

Vax Date: 03/03/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Extreme diarrhea; vomiting; sore throat; dizziness; headache; chills; tiredness; low grade fever; body aches; This is a spontaneous report from a contactable consumer (Patient). A 71-year-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection: Lot number: EN6199) via an unspecified route of administration on 03Mar2021 at 11:45 am, in the left arm (at the age 71-year-old) as a single dose for COVID-19 immunisation. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection: Lot number: EN5318) on 10Feb2021 at 11:45 am in the left arm (at the age 71-year-old) as a single dose for COVID-19 immunisation. Patient's medical history included Irritable bowel syndrome, allergy to Amoxicillin. Patient's concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient's 2 weeks prior medication included Bupropion, Atenolol, butalbital, red yeast rice. Prior to vaccination, patient was not diagnosed with COVID-19. COVID prior vaccination was none. Since the vaccination, patient had not been tested for COVID-19. COVID tested post vaccination was none. On 04Mar2021 at 1:00 am, the patient experienced extreme diarrhea, vomiting, sore throat, dizziness, headache, chills, tiredness, low grade fever, body aches. The patient did not take any treatment medication for the events. The outcome of events was not recovered. No follow-up attempts are possible; No further information is expected.

Other Meds: BUPROPION; RED YEAST RICE; ATENOLOL; BUTALBITAL

Current Illness:

ID: 1373354
Sex: M
Age:
State: IN

Vax Date:
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: eye fatigue after 1st dose; This is a spontaneous report from a contactable consumer reported for herself that. A 68 age and unit: unknown male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unspecified date as SINGLE DOSE for covid-19 immunization. The patient medical history was not reported. The patient is sensitive to medication like Flu shot. Patient concomitant medications were not reported. He experienced eye fatigue after first dose eyes started feeling fatigued 2 weeks later and continued until getting 2nd dose. He is very sensitive to medications for example flu shot usually makes me feel yucky for about a week. Patient asking how long symptoms are expected to last. Outcome of the event eye fatigue was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 1373355
Sex: M
Age:
State: WI

Vax Date: 03/04/2021
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: Nothing major; slight redness at injection site and a sore arm for 24 hours; Sore arm; This is a spontaneous report from a contactable consumer (patient). A 61-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EN6195), via an unspecified route of administration on 04Mar2021 12:30 as unknown, single for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient has not had other vaccine in four weeks. The patient has no history of COVID prior vaccination. The patient was not COVID tested post vaccination. The patient experienced nothing major; slight redness at injection site and a sore arm for 24 hours on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1373356
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: lightheadedness; headache; vision changes; increased respirations; This is a spontaneous report from a non-contactable healthcare professional. A 51-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot number: EN6205, Expiration date was not reported), intramuscularly on an unspecified date (at the age of 51-years-old) as 1st dose, single dose for COVID-19 immunisation. Medical history included asthma (often triggered by stress and does have albuterol inhaler on hand) from an unknown date. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced lightheadedness, headache, vision changes and increased respirations. It was reported that during the 15-minute waiting period after the injection, the patient began to experience lightheadedness, headache, vision changes and increased respirations. The patient denied rash, hives, difficulty swallowing, wheezing, throat tightness and hoarseness. The patient has a history of asthma often triggered by stress and does have albuterol inhaler on hand but has not used today. The patient denied frequent use of albuterol inhaler. Treatment included was water and TYLENOL 1000mg. The followup response to treatment was good. The patient's symptoms all resolved prior to discharge. The patient's O2 remained 99-100%, denied difficulties breathing and respirations decreased while she was in the bay. The patient was discharged, stable to go home and for follow up with PCP. The outcome of the events was recovered. No follow-up attempts are possible. No further information expected.

Other Meds:

Current Illness:

ID: 1373357
Sex: M
Age:
State:

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Onset Date:
Rec V Date: 06/04/2021
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Symptoms: blood splotches/ some splotches of what looked like blood on the towel; This is a spontaneous report from a contactable consumer reporting for himself. A 71-years-old male patient received the second dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine via intramuscular route on an unspecified date, at 71 years of age, (Batch/Lot number was not reported) for COVID-19 immunization. The patient's medical history was not reported. Concomitant medication included acetaminophen twice a day, one in the morning and one in the evening, taken for an unspecified indication, since an unknown date. The patient reported that the nurse put the little Band-Aid where she gave the shot. About 2 hours (or maybe a little more) after his second dose, he came home and took a hot shower and the band-aid fell off and when he was drying himself he noticed some blood splotches/some splotches of what looked like blood on the towel and he didn't see any bleeding from that spot. He thinks it was from the spot where the injection was given. It didn't continue to bleed. The event was assessed as non-serious. The event outcome was unknown at the time of the report. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: ACETAMINOPHEN

Current Illness:

ID: 1373358
Sex: M
Age:
State: CA

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Sore arm; This is a spontaneous report from a contactable consumer (patient). A 40-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot number: EN6205, Expiration Date: not reported), via an unspecified route of administration on 04Mar2021 at 09:15 (at the age of 40 years old) as first dose, single for COVID-19 immunisation in a Pharmacy or Drug Store.Medical history included high blood pressure from an unknown date. The patient's concomitant medications were not reported. The patient did not receive any other vaccines in 4 weeks, has no known allergies and prior to vaccine the patient was not diagnosed with COVID-19. On 04Mar2021 at 14:00 (reported as 02:00PM), the patient experienced sore arm. No treatment was received for the adverse event and since vaccination, the patient has not been tested for COVID-19. Outcome of the event was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 1373359
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/04/2021
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Symptoms: numbness in right forearm; headache; This is a spontaneous report from a non-contactable healthcare professional. A 53-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot number: EN6205, Expiration date was not reported), via an unspecified route of administration on an unspecified date as 1st dose, single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced numbness in right forearm and headache. It was reported that during the 15-minute waiting period after the injection, the patient began to experience numbness in right forearm and headache. He denied difficulty breathing, difficulty swallowing, itching and lightheadedness. Treatment included was Tylenol 1000 mg and water. The follow up response to treatment was good and symptoms were completely resolved. The patient reported that he would take Ibuprofen in the evening if he experiences some numbness in the right forearm or fingers. He denied symptoms of headache and numbness; resolved prior to discharge. The reporter walked with the patient to exit the facility. The patient was discharged, stable to go home and for follow up with PCP. The outcome of the events was recovered. No follow-up attempts are possible. No further information expected.

Other Meds:

Current Illness:

ID: 1373360
Sex: M
Age:
State:

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: floaters in both eyes; This is a spontaneous report from a contactable consumer (patient). A 67-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number and expiration date were not reported), via an unspecified route of administration on 04Mar2021 (at the age of 67-years-old) as first dose, single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 04Mar2021, 10 mins after the first dose, the patient experienced floaters in both eyes. The outcome of the event was not recovered; floaters in right eye resolved however the patient continued to have significant floaters in left eye. The patient was querying if this was a known side effect. No follow up attempts are possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 1373361
Sex: F
Age:
State: HI

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Dizziness; headache; congestion (which existed but got worse),; coughing (which existed but got worse); congestion (which existed but got worse); This is a spontaneous report from a contactable consumer (patient). A 50-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EN6199; expiration date was not reported), via an unspecified route, administered in the left arm on 04Mar2021 09:00 (at the age of 50-years-old) as first dose, single dose for COVID-19 immunisation at a Public Health Department. Medical history included hypothyroidism, hypertension, joint pain, reflux and insomnia, all from an unknown date and unknown if ongoing; and congestion and coughing, both are ongoing. Concomitant medications included meloxicam and amlodipine-olmesartan; both taken for an unspecified indication, start and stop dates were not reported. The patient was not pregnant at the time of vaccination. No other vaccine was given to the patient in four weeks. The patient had no COVID prior vaccination and was not tested for COVID post vaccination. The patient has no known allergies. On 04Mar2021 09:00 AM, the patient experienced dizziness, headache, congestion (which existed but got worse) and coughing (which existed but got worse). No treatment was taken as a result of the events. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: MELOXICAM; AMLODIPINE;OLMESARTAN

Current Illness: Congestion nasal; Coughing

ID: 1373362
Sex: F
Age:
State: NJ

Vax Date: 03/03/2021
Onset Date: 03/05/2021
Rec V Date: 06/04/2021
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Symptoms: Slightly dizziness; running nose; This is a spontaneous report from a contactable consumer or other non hcp (patient herself). A 64-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EN6205, expiration date not reported), via an unspecified route of administration, administered on the left arm on 03Mar2021 16:15 (at the age of 64-years-old), as first dose, single dose for COVID-19 immunisation. Medical history included high blood pressure (hypertension). The patient previously took meloxicam (manufacturer unknown) and experienced drug hypersensitivity. The patient received other unspecified medications within 2 weeks of vaccination. The patient was not pregnant at the time of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19; and since the vaccination, has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced slightly dizziness and running nose on 05Mar2021 07:00. Events did not result to physician office visit and emergency room visit. No treatment was given as a result of the events. The outcome of all events reported was unknown. No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 1373363
Sex: F
Age:
State: IA

Vax Date: 03/03/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: chronic persistent coughing; strong headache; chills; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot number: EL9266, Expiration Date: not reported), via an unspecified route of administration, administered in right arm on 03Mar2021 at 13:45 (reported as 01:45 PM) (at the age of 62 years old) as first dose, single for COVID-19 immunisation in a Health Clinic. Medical history included lobectomy on 31Aug2020 and COVID-19 from an unknown date. Patient was not pregnant at the time of vaccination and has no known allergies. Concomitant medication included bupropion hydrochloride (WELLBUTRIN) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines in 4 weeks. On 04Mar2021 at 14:00 (reported as 02:00PM), the patient experienced chronic persistent coughing, strong headache, and chills. No treatment was received for the adverse event. Since vaccination, the patient has not been tested for COVID-19. Outcome of all of the events was recovering No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds: WELLBUTRIN

Current Illness:

ID: 1373364
Sex: M
Age:
State: NC

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/04/2021
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Symptoms: Fever; Chills; body aches; nausea; feeling unwell; This is a spontaneous report from a contactable consumer or other non hcp (patient himself). A 49-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EN6203, expiration date not reported), via an unspecified route of administration, administered on the left arm on 04Mar2021 12:45 (at the age of 49-years-old), as first dose, single dose for COVID-19 immunization. Medical history included anxiety. Concomitant medication included buspirone (manufacturer unknown) taken for an unspecified indication, start and stop date were not reported. Patient has no reported allergies. Prior to vaccination, the patient was not diagnosed with COVID-19; and since the vaccination, has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced fever, chills, body aches, nausea, and feeling unwell on 04Mar2021 15:00. Events did not result to physician office visit and emergency room visit. No treatment was given as a result of the events. The outcome of all events reported was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: BUSPIRONE

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 03 October 2021 5:28pm