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: 1381233
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: body ache; This is a spontaneous report from a contactable consumer or non-Health Care Professional. A patient of unspecified age and gender received bnt162b2 PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and Expiry date: Unknown), dose 1 via an unspecified route of administration on 01May2021 as 1ST DOSE, SINGLE DOSE for covid-19 immunization. The patient medical history was not reported.The patient's concomitant medications were not reported. Patient took Second dose of bnt162b2 (COMIRNATY, Solution for injection, Batch/Lot number was not reported on 22May2021 for covid-19 immunization. The reporter stated, the patient first shot was on 01May2021 and patient did not have any symptoms, mean just body ache but that was all. The first shot did not gave me any problem. The outcome of event body ache was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1381234
Sex: F
Age:
State: NY

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

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: second dose-soreness to unknown arm at injection site; metallic taste/salty taste; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EN6207) via an unspecified route of administration as 2nd dose, single dose for COVID-19 immunization. Medical history included hypothyroidism (Stated that she has had it since she was a child) Concomitant medications included oral liothyronine (5 mcg by mouth every day), levothyroxine (200 mcg by mouth every day) for hypothyroidism. Patient started levothyroxine when she was 8 years old. Patient previously received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- unknown) via an unspecified route of administration on an unspecified date as 1st dose, single dose for COVID-19 immunization. Patient stated that she took the Pfizer vaccine first and second dose and had no symptoms prior to it. Stated that after approximately two weeks that she had a metallic, salty taste a lot of times not all of times. Stated that when she was not eating that the taste was on the tip of her tongue. Is not sure if it is from the vaccine but she was reporting it due to the timing. Is getting feedback. Clarified that it was for Pfizer Covid vaccine. Stated that she had soreness to her unknown arm at injection site. Later clarified it as Pfizer BioNTech. Wanted to see if they can help her in any way. Stated that she hopes that this helps someone in some way. Patient stated that the second dose was given closer to four weeks than three weeks after. On 05Apr2021, patient experienced second dose - soreness to the injection site lasted the first day and was gone. Stated that the second dose was given closer to four weeks instead of three weeks because she could not go on that date. Stated that the metallic taste started on 17Apr2021 or 18Apr2021. Does not have the NDC or expiration date for the second dose. Provided a lot number of EN6207. Stated that it was an unknown dose injection into the arm. Stated that it was for the prevention of Covid. The outcome of the event second dose- soreness to unknown arm at injection site was recovered on 05Apr2021 and outcome of the other event was not recovered.

Other Meds: LIOTHYRONINE; LEVOTHYROXINE

Current Illness: Hypothyroidism (Verbatim: Hypothyroidism Stated that she has had it since she was a child.)

ID: 1381235
Sex: F
Age:
State: FL

Vax Date: 01/12/2021
Onset Date: 01/19/2021
Rec V Date: 06/08/2021
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: Anaphylactic reaction; itching/generalized pruritus/ some prickly the itching; shortness a breath; hives; skin rash; body flushed; Iv infection; This is a spontaneous report from a contactable other healthcare professional (patient). A 74-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot Number: EL1284), via an unspecified route of administration, in Arm Left on 12Jan2021 at 17:00 as 0.3ml, single for covid-19 immunization. Medical history included asthma. The patient concomitant medications were not reported. On 19Jan2021, the patient had anaphylactic reaction. The anaphylactic reaction started within minute lasted upto 6 hours with shortness a breadth and was on prednisolone for six days (40mg). The sign and symptoms of the anaphylactic reaction included: vital sign was normal; itching began with in minute and IV infection and body flushed; began to get treated with antihistamines for her hives and precaution. The patient had hives and its thing (unbelievable); then difficulty breathing without wheeze. She had generalized itching and some prickly; the itching was at times like if her body was of hive (generalized pruritus with skin rash). The patient received treatment with Benadryl 6 mg above and pro air - prednisone for 6 days and then with a prescribed. No 2nd dose. The patient did not require any medical intervention; all prescribed her allergy for fused me to go to hospital too much condition. The outcome of the events was recovered on an unspecified date in 2021. No follow-up attempts are needed. 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 reported events Anaphylaxis, rash, urticaria, dyspnea and pruritis and flushing cannot be excluded. But also consider medical history of asthma 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: 1381236
Sex: M
Age:
State: FL

Vax Date: 04/24/2021
Onset Date: 04/29/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Feet skin dry and my head dry also; Rash on my chest, back, arms, legs and hands; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program. A 55-year-old male patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EW0171) via an unspecified route of administration in left arm on 24Apr2021 at 09:00 AM as 2nd dose, single for COVID-19 immunization. Patient previously received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EP7533) via an unspecified route of administration in left arm on 04Apr2021 at 08:00 AM as 1st dose, single for COVID-19 immunization. Medical history included blood cholesterol and COVID 19. Concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was diagnosed with COVID-19. On 29Apr2021 at 04:00 PM, patient experienced small red rashes only back after a week my hole chest, my back, legs, my arms get a really bad rash and my hands are very dry and my feet also and my head dry also. Can you contact me and let me know what can I do please. I been like this 30 days. Patient treated with Medroll 16 mg 2 a day. Since the vaccination, patient had not been tested for COVID-19. The outcome of the events was not recovered. Information on Lot/Batch number was available. Additional information has been requested

Other Meds:

Current Illness:

ID: 1381237
Sex: M
Age:
State: NY

Vax Date: 04/21/2021
Onset Date: 04/30/2021
Rec V Date: 06/08/2021
Hospital: Y

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: BPPV; burning sensation; partial loss of hearing; fullness and burning sensation in ears; tinnitus; brain fog; pressure in the back of my head; severe vomiting; shortness of breath; Pyrexia; Mental status changes; This is spontaneous report from contactable consumer (patient). A 50-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 21Apr2021 14:30 (Batch/Lot Number: EWO161), at the age of 50 years, as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Previously the patient received first dose of bnt162b2 on 30Mar2021, at the age of 50 years, Time: 03:45 PM, Lot no. EW8730, anatomical location: Left arm. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 30Apr2021 19:30 the patient experienced Benign Paroxysmal Positional Vertigo (BPPV) (hospitalization, life threatening). On 30Apr2021 19:30 the patient experienced fullness and burning sensation in ears, tinnitus, brain fog, pressure in the back of head, severe vomiting, shortness of breath, pyrexia, mental status changes. On 12May2021 the patient experienced partial loss of hearing. On 28May2021 the patient experienced burning sensation. Clinical course: Nine days after taking a second dose of the Pfizer vaccine it started with multiple episodes of vertigo for 2 days, followed by severe vomiting, non-stop vertigo, shortness of breath. Taken into Emergency Room (ER) by ambulance on 02May2021, multiple tests performed (CT scan, blood, EKG) diagnosed with BPPV. Discharged the same night. The symptoms escalated into fullness and burning sensation in ears, partial loss of hearing, tinnitus, brain fog, pressure in the back of my head. Went to primary care physician on 05Jun2021, again multiple tests (blood, urine, EKG). Referred to ENT. Visited ENT on 12May2021, audiology test confirmed partial hearing loss. On 28May2021 the patient was still suffering with burning sensation and fullness in the right ear, as well as loss of hearing (high frequencies) and tinnitus. Periodic episodes of brain fog and severe vertigo. The patient underwent lab tests and procedures which included blood test: diagnosed with BPPV on 02May2021, blood test: unknown results on 06May2021, CT scan: diagnosed with BPPV on 02May2021, electrocardiogram: diagnosed with BPPV on 02May2021, electrocardiogram: unknown results on 06May2021, audiology test: partial hearing loss on 12May2021, urine output: unknown results on 06May2021. The patient received treatments due to the events: Diazepam, Meclizine, Potassium Chloride, Metoclop. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1381238
Sex: F
Age:
State: FL

Vax Date: 05/26/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
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: she is having sinuses; it happened at night time as soon as night comes, my nose are close; because there is no way I can't take sleep like that; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: ER8737) via an unspecified route of administration, administered in arm left on 26May2021 (at the age of 56 years) as 1st single dose for COVID-19 immunisation. Medical history included hyperactive sinus from 2007 about roundabout for a while. Patient stated no family medical history of sinuses. The patient's concomitant medications were not reported. On an unspecified date in May2021, last night the patient had sinused and she took Sudafed. Patient enquired if it was okay that she had Sudafed in the dose of Pfizer Vaccine will this interfere wanted to know more information about this situation. Patient wanted to know if this was gone a affect her vaccine in any way that she took Sudafed other day, because she was going to watch tonight and see what happens tonight, If she can take another one or not. Patient informed it happened at night time as soon as night comes, her nose are close. Patient know it's not from the vaccine, that's just something that happens. Patient just wanted to make sure it was okay with taking Sudafed because she read about taking any Ibuprofen or any Tylenol prior to take a shot. Patient was not able to take sleep like that, so that's why, she just wanted to make sure that's okay. Patient clarified she did not have any sinus at the time of vaccination, just that night and this was something that happened all the time, not all the time whenever feels up, it just happens every now or then it just happened that night. Patient informed that the second dose will be on 16Jun2021. As therapeutic measure patient took Sudafed pill orally night only as per needed. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected

Other Meds:

Current Illness:

ID: 1381239
Sex: M
Age:
State: NV

Vax Date: 04/29/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
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: My left leg, it started when I fell asleep during the night, it started to feel numb; Side of my ankle on the left side, my left leg ankle outside is numb and its numb over down to my foot; I got up and shook it of with my foot and so, everyday it is goes worse and worse; This is a spontaneous report from a contactable consumer (patient). A 64-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: ZW0173), dose 2 via an unspecified route of administration, administered in Arm Left on 29Apr2021 09:30 (at the age of 64-year-old) as 2nd dose, single dose for COVID-19 immunization. Medical history included diabetes. Concomitant medication included Naproxen taken for pain, a muscle relaxer; and dapagliflozin propanediol monohydrate, metformin hydrochloride (XIGDUO) taken for diabetes. The patient previously received first dose of BNT162B2 (Lot number: ER8729) in Arm Left on 06Apr2021 (1:30 in afternoon) for COVID-19 immunization. Patient did not receive any other vaccines within 4 weeks prior to the vaccination. The patient stated, "I would say around the 10th of this month, I was waking up with my left leg, it started when I fell asleep during the night, it started to feel numb, I got up and shook it with my foot and so, everyday it is goes worse and worse but I can't, side of my ankle on the left side, my left leg ankle outside is numb and its numb over down to my foot and I can't move my foot back so it's like my foot is numb and it stays that way and it has not gone away" on an unspecified date in May2021. When probed for time of vaccination again, the patient stated that "No, it's not but I remember on 29th, it was at, the first shot was on 1:30 in afternoon, you know the second shot was on 9:30, it was early, right after the open". No treatment received for the events. There was no investigation assessment and lab test. The outcome of event numbness in feet was not recovered and was unknown for other events.

Other Meds: NAPROXEN; XIGDUO

Current Illness:

ID: 1381240
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: trouble in the shoulder where they put the shot in; my back, my shoulder where they gave me the shot, it is like constantly pain like it is just like come and goes where in middle of the night I wake up; I have a bruise. Its been 4 week but I still have a bruise on my shoulder, my shoulder is hurting it. Its like my neck down my elbow; It is a rash or something itchy and its appear on me; It is a rash or something itchy and its appear on me; my back, my shoulder where they gave me the shot, it is like constantly pain like it is just like come and goes where in middle of the night I wake up; This is a spontaneous report from a contactable consumer, the patient. A patient of an unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Batch/Lot number, number, UPC number and Expiry Date: Unknown), via an unspecified route of administration on an unspecified date as 1st dose, single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. About month ago, patient took the first Pfizer shot (further clarification was unknown hence captured as unspecified vaccine) and patient never had COVID yet. Patient was having so much trouble in the shoulder, where they put the shot in. Patient must back up or something because it's like all sudden his track or patient should always dumb the elbow just like. Patient didn't even think that the shot might be the problem but the back and shoulder where they gave the shot was constantly in pain (like it came and went). In middle of the night, patient woke up and it was just like drubbing, like a pinch nerve which patient thought that might be back was out. Patient went to chiropractor and realized about having a bruise. It had been 4 weeks, but patient still had a bruise on the shoulder where the needle was put in. Patient realized the shoulder was hurting. It's like neck down my elbow. Outcome of the event bruise was not recovered while of other events was unknown. Follow-up attempts are needed. Further information is expected.

Other Meds:

Current Illness:

ID: 1381241
Sex: F
Age:
State: WA

Vax Date: 04/29/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: my chest to all the way up to my neck was brilliant, brilliant red and felt like really hard sandpaper; my chest to all the way up to my neck was brilliant, brilliant red and felt like really hard sandpaper; around my neck 2 long red lines, It looked like someone is trying to strangle me; my whole body got covered in little red spots, and then slowly it started to peel off and the peeling was even on top of my hand; when as far as the top of my neck where the chin starts because I thought oh my god it has got my face too but it stopped their but everything else is got it; I am still peeling, my rear end is still peeling skin off, It's like big sheets coming off, It's like big sheets coming off/skin is still 'fluffing' off; It scares the hell out of me; This is a spontaneous report from a contactable consumer (Patient). A 77-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for Injection; Lot number: EW0753; Expiration date: unknown), via an unspecified route of administration on 29Apr2021 (at the age of 77-year-old) as 2nd dose, single dose in left arm for COVID-19 immunisation. The patient's medical history included surgeries. Concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for Injection; Lot Number: EW0173), as single dose for COVID-19 immunisation. On unspecified date in May2021, a few days later after second dose, the patient's chest to all the way up to neck was brilliant, brilliant red and felt like really hard sandpaper, and around neck 2 long red lines, it looked like someone was trying to strangle. The patient went to the dermatologist, they did not know what it was, and they sent the sample out. In the meantime, the patient's whole body got covered in little red spots, and then slowly it started to peel off and the peeling was even on top of the hand, the patient still peeling, her rear end was still peeling skin off, It was like big sheets coming off, It scared the hell out of her, she did not know what was going on. Patient just told that no one else was having that kind of reaction that she had. It really scared her when it reached this far on the top of her neck where the chin starts because she thought oh my god it has got on the face too, but it stopped their and everything else got it. The first symptom was on her chest and that became brilliant red and looked like she was on fire and that was just as hard as a sandpaper. That was the first thing and slowly other things started, that brilliant red start and her body all started coming out with red spots. It did not itch and slowly it started to 'fluffing' off and the skin was still 'fluffing' off. Patient had the second vaccine almost a month ago. On the top of her hand there was peeling. It scared her to death because this thing has not been happened it was 6 months and she do not know why she got it and really do not know. She just wanted to report because she went to her own doctor and then to dermatologist. The clinical outcome of the events was unknown. Follow up needed, further information has been requested.

Other Meds:

Current Illness:

ID: 1381242
Sex: F
Age:
State: AL

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

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: serious side effects like breathing problems and rashes; serious side effects like breathing problems and rashes; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), 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. On an unspecified date, after first dose patient experianced serious side effects like breathing problems and rashes. She was due to take her second dose after a week. She wanted to talk to someone about the side effects that she had. The outcome for the events was Unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1381243
Sex: F
Age:
State: MA

Vax Date: 05/24/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
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: I got a really really bad severe case of vertigo; Nausea; Dizziness; Headache; Fatigue; My backache that problem have like tripled it got much much worse since I got the shot you know like the muscle ache you know my arm hurt really bad; My backache that problem have like tripled it got much much worse since I got the shot you know like the muscle ache you know my arm hurt really bad; My backache that problem have like tripled it got much much worse since I got the shot you know like the muscle ache you know my arm hurt really bad; I didn't feel good; I couldn't eat, couldn't walk, couldn't get myself once a dinner; I couldn't eat, couldn't walk, couldn't get myself once a dinner; Abdominal discomfort; I couldn't eat, couldn't walk, couldn't get myself once a dinner; This is a spontaneous report received from a contactable consumer (the patient). A 59-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot number: EW0187, Expiration date: not reported) via an unspecified route of administration in left arm on 24May2021 (Monday) (at the age of 59 years) as 1ST DOSE, SINGLE DOSE for COVID-19 immunisation. The patient medical history included Asthma, Head trauma, Had car accidents, Allergies from on unknown date and unknown if ongoing. Concomitant medications included budesonide, formoterol fumarate (SYMBICORT) taken for Asthma and loratadine (CLARIDIN) taken for Allergies on daily, start and stop date were not reported. On 27May2021, Patient stated that got a really really bad severe case of vertigo yesterday which was like what 72 hours after the shot, I got it on monday and it happened yesterday so I woke up with it like actually like really bad nausea and severe vertigo and I still have it and you know I can't get to a doctor to get it or therapist to get it treated because they don't have any availability but I tried to doing head movement myself but I haven't really had any relief. Consumer stated, when I got vertigo it can take weeks for it to go away. Unless I can get treatment from a therapist who specializes and then she was not available then I can suffer for weeks so three weeks from now you know If we gonna get severe dizziness and vertigo that's gonna really distrust people from gonna go and get the second one. I went for my shot at noon time on Monday and then on Thursday, 27May I woke up with really upset stomach which is typical in vertigo. So, I got severe vertigo exactly 3 days later so a little bit less than 24, 48 a little bit less than whatever it is 72 hours later. Consumer stated, Yeah but you know what else I got within 5 minutes of getting the shot I started getting the horrible headache and then It just got progressively worse. I mean my asthma so you know I have like a lousy immune system (further not clarified) so I think I'm more prone to having side effects but I didn't realize it was gonna be that bad also so on the 24 within 5 minutes of getting it. I've started getting wild headache and then horrible headache and I took Motrin for like 24 hours(treatment) and it didn't even help the headache not one single bit. It was so like my head was like in a vice like someone was squeezing it in a vice that's how severe it was like to disabling. On May2021, I couldn't eat, couldn't walk, couldn't get myself once a dinner or anything. It was terrible that's how bad it was so and then you know the nausea started immediately so a mild upset stomach on May2021 for about 48 hours and then the third day it was much much more worse because of the vertigo so it was severe headache all over. It was horrible, it felt like someone was hitting the head with sludge hammer and the dizziness started immediately on 24May2021, the headache started immediately on 24May2021 and the extreme fatigue on 24May2021 that haven't gone away since I got it. So I don't know what you need to write down but that's it. Those are side effect. and then I take on a daily basis for my bad back I mean I have really really bad back on 24May2021, so I've actually my backache seems to when I took Motrin(treatment) obviously but my backache that problem have like tripled it got much much worse since I got the shot you know like the muscle ache you know my arm hurt really bad for 48 hours the minute it stopped, but my bad back has been horrible since I got the shot because its been much much worse and like I said I haven't done anything to exacerbate so. Then the vertigo started 3 days, little bit less than 3 days later I woke up with it horrible vertigo pretty severe. It was slightly better today, well it was earlier but the more I move around so since I got the shot 4 days ago the more I move around the more I do whether its like doing laundry getting lunch or whatever like the dizziness will just come back like full force. If I try to sit and rest and don't leave and only watch TV it stabilizes a little bit but yeah the dizziness I've talked to a lot of people and they've all had the side effect not just from the shot I got but from the other shots as well. So, Its crazy. Consumer stated that I don't know, I will try to go back in the couple of weeks. So, whatever date that is, 14 may be. On 14Jun2021 I'm gonna try to go back. These are the 14 or 15 but they just told to come back in 3 weeks afterwards so that's what I'm gonna do. Medical Condition was reported as so I have you know thin fever but I don't have any other issue the only thing I have is asthma you know all my doctor saying Oh you have asthma so you should really get it so like an idiot If I had known I was gonna have this horrible you know side effect the first time I never would have getting it first place so you know that all these people would these horrible side effects are saying screw it we are not gonna get back for second shot you know who wants to suffer like this again its been an entire week and I'm not any better than I was on Monday So, you know the headache is better the upset stomach is better but the dizziness I can deal with the headache and the upset stomach but the vertigo, if you have ever experienced it. It is pure hell because you know you can't lay down and sleep you can't and I live alone so that's really scary you know what I'm saying. I can't get anything to eat. I can't go out. I can't drive when I get vertigo but I do have a history of it. I think the last time I had it might've been like February or March maybe when I get treated for it you know but I haven't done anything at all to set it off. I haven't been doing any heavy lifting or heavy cleaning or bending or whatever which sometimes sets it off. So, I'm just you know been resting since Monday. I haven't done anything or left the house. The outcome of the events she got a really really bad severe case of vertigo, nausea was not recovered and other events were reported as unknown. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds: SYMBICORT; CLARIDIN

Current Illness:

ID: 1381244
Sex: F
Age:
State: TN

Vax Date: 05/04/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
Hospital:

Vax Type:
Manufacturer:
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Lot:
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Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: redness in left arm; swelling in left arm; itching in left arm; numbness from shoulder down to 2 fingers but mainly had the numbness in her upper arm; hives around both wrists and joints and knees; This is a spontaneous report received from a contactable consumer (patient husband) via a Pfizer sponsored Programme. A 38-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: ER8731, Expiration date: Unknown) via an intramuscular route, administered in left shoulder (left arm) on 04May2021 at 8:15 (at the age of 38-year-old) at a single dose for covid-19 immunization at public health department. Patient medical history included seasonal allergies, illness at time of vaccination was overweight. Patient had reactions to flu shots in the past, not hives but her immune system gets ramped up; just like the normal side effects being a little bit more for her and had like a natural allergic reaction and she had a reaction to cat hair. Concomitant medications were not reported. Patient had no history of previous immunization with the Pfizer vaccine. The patient did not receive additional vaccines on same date of the Pfizer Suspect. The patient did not receive prior vaccinations within 4 weeks. On 04May2021, after got shot the patient experienced redness, swelling, itching in the left arm. She also experienced numbness from her shoulder all the way down to two of her fingers, but mainly had the numbness in her upper arm. These symptoms were what she initially got and then it evolved over the 12-24 hours after receiving the shot, patient was developed with hives around both wrists and joints and knees. Patient received Benadryl as a treatment for the events. The events did not result in emergency or physician room. She did not have any problems of breathing or anything like that. Patient was consulted by doctor and stated no reason to have blood work or tests or anything. She had the numbness for about 24 hours and the hives resolved after about 48 hours. The outcome of events numbness from her shoulder all the way down to two of her fingers, but mainly had the numbness in her upper arm, hives around both wrists and joints and knees was recovered on an unspecified date in May2021, and the rest of the events was unknown. Reporter wants to know how patient will be authorized to get the second shot. Follow-up attempts are needed. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1381245
Sex: F
Age:
State: IL

Vax Date: 04/19/2021
Onset Date: 04/19/2021
Rec V Date: 06/08/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

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

Symptoms: Pain to left breast into right leg then left leg and shot back up into her heart area, then would shoot into her head; Shoulders and back achy and tense; Shoulders and back achy and tense; Stiffness; Arm swollen and red from site of injection to elbow for a week; Arm itching; Arm heated; This is a spontaneous report from a contactable consumer (patient. Self-reported). A 71-Years-old female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0162, NDC 59267-1000-1, and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 19Apr2021 at 12:00 PM, as a single dose, 0.3 mL, for COVID-19 immunization at hospital. The patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: ER8732, NDC 59267-1000-1, and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 29Mar2021 at 12:00, as a single dose, 0.3 mL, for COVID-19 immunization at hospital. The patient stated both hands started itching at some point the evening of 29Mar2021, beginning around midnight, between midnight and 5 am on 30Mar2021 and described as kind of itch that was internally itching and couldn't scratch, it was inside of her itching. It fully resolved by the time she woke up on 30Mar2021. The patient taking Pfizer COVID vaccine because she didn't want to live like she lived for a year and wanted to be healthy and normal for grandchildren. The patient's medical history included history of breast cancer (from Sep2006) and she completed 6 rounds of chemo and 37 days of radiation and finished in Aug2007 and right mastectomy on 13Oct2006 (also had chemo and radiation) and she had 3 surgeries in 3 weeks and had 27 lymph nodes removed. The patient stated she had heart damage from chemo and radiation, she had congestive heart failure which was reaction to Herceptin which started in Dec2006. She only had half of it and didn't take it for a year. She didn't die from breast cancer, but that's her history. She was one of the first patients to have a cardiologist going through chemo because it was a new drug then, been with the cardiologist for 15 years. Caller states she previously had echos done monthly between chemo that was every 3 weeks to check the ejection fraction. Ejection fraction at some point started showing she was in trouble and he called the oncologists and said the Herceptin was done. They stopped it and she was told she had congestive heart failure, heart damage, but it was reversed now, and she still had that tagged on her. Caller adds it's a mandate now for men and women who were on Herceptin to have an echo or doppler done. The patient did not receive any vaccine prior vaccinations (within 4 weeks). The patient did not have any adverse event prior vaccinations. Concomitant medications included carvedilol (COREG) for heart at slower pace and had been on it 14 years, and Lisinopril had been taking 14 years for kept blood pressure low due to chemo and radiation. The patient reported that on 19Apr2021 at 12:10, she experienced arm swollen and red from site of injection to elbow for a week and lasted a week until the following Monday. The patient clarified swelling lasted a week, but not the itching which only lasted that first day on 19Apr2021. The patient also had arm itching and arm heated on 19Apr2021 at 12:10. She had shoulders and back achy and tense which occurred from noon until 22:00 on 20Apr2021. The patient added that the pain she felt was like a cartoon, didn't know how to explain it, was weird very odd and forceful, and stated it hurt. She stated she was worried about her heart. The patient had pain like a bullet went through her and entered her left chest wall and like a ricochet reaction on 20Apr2021 at 18:00. She stated first it hit her left side, then go down into her upper thigh, go to her right leg, her left leg, her right leg; Pain to left breast into right leg then left leg and shot back up into her heart area, then would shoot into her head which started around 18:00 on 20Apr2021. It would do a round and would stop and do it again maybe 10, 20, 30 minutes later then do it again. It would do the whole body. She went to bed and when she woke up it was gone on 21Apr2021. The patient also had stiffness. The patient stated she had family members that won't do this, they thought it was conspiracy and that's what she had to deal with. She didn't think it was and thought COVID was very real. The patient stated that this was in the past, but she wanted to report her reaction to her second COVID shot. She also stated it was very odd and hadn't talked to anyone who has had this and thought she would tell Pfizer. The patient stated the symptoms started almost 24 hours to the minute, actually while driving and it started in shoulders and back kind of like achy and tense like you've been driving for a long time. She got to her destination, and it seemed like every time she would get out and walk for a while, she felt better and got to her destination. It was like a bullet went through her and entered her left chest wall and like a ricochet reaction. First it hit her left side go down into her upper thigh, go to her right leg, her left leg, her right leg. The patient clarified that the stiffness in her body started 24 hours after, but the ricochet started about another 6 hours after that, after she arrived at her destination. The patient described symptoms in shoulder and back as really tense and sudden. She had a mastectomy and only had one breast on the left side like it shot through and was painful, put her on the floor. She had a high pain tolerance and went to left breast into right leg then left leg and shot back up into her heart area, then would shoot into her head. The patient stated when she had surgeries, she didn't take drugs, Tylenol knocks her out. She was not a user of pain meds. She clarified she was not saying it literally knocks her out, Tylenol was like a big pain med for her and stated Tylenol for some people was what they do daily, but it puts her to sleep. She also stated that all of her life when queried about dates of use when this occurred, and she did not have any specific product available for documentation of lot number or anything related to this. The patient stated Aleve gave her for hives and this occurred when it first came out, but she was not sure when that was and confirmed she did not have the bottle of Aleve available. The patient reported there were certain things she couldn't take. She wanted to add that when she went to bed that night, she told husband if she dies tonight make sure to do an autopsy. Husband said he needed to take her to the hospital, and she stated she really thought it was just from the COVID shot and she didn't think the hospital could do anything. She just wanted to bed and woke up and she was fine, she did not go to the hospital. The events did not require a visit to emergency room or physician office. No treatment was reported for events except for bed. The patient had a doppler echo which was scheduled on 21Jun2021 and which was a yearly echo done for heart function. The patient stated she hope this helped and might be someone else has had this, she was not the only nut case. She was concerned about the talk of possible booster and was a little leary about booster after that one experience, that was a concern. She didn't want to make a bad choice and not did it; this was her real concern. The patient confirmed she would like to know if there was any more information about other reports of this or about the booster. Outcome of the events arm swollen and red from site of injection to elbow for a week and arm heated was resolved on Apr2021. Outcome of the event arm itching was resolved on 19Apr2021, shoulders and back achy and tense, and stiffness was resolved on 20Apr2021, and pain to left breast into right leg then left leg and shot back up into her heart area, then would shoot into her head was resolved on 21Apr2021. Information on Lot/Batch number was available. Additional information has been request

Other Meds: COREG; LISINOPRIL

Current Illness:

ID: 1381246
Sex: M
Age:
State: MD

Vax Date: 05/25/2021
Onset Date:
Rec V Date: 06/08/2021
Hospital:

Vax Type:
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Allergies:

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

Symptoms: I woke up my whole bed and my clothes were sweaty, my bed was sweaty; This is a spontaneous report from a contactable consumer (patient). A 71-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection,Lot Number: EW0179 and Expiry date: Unknown), via an unspecified route of administration on an unspecified date as single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated that he just had the shot on the 25May2021 and the last night, the first night after he got the shot on the "26th" (further not clarified) he did the same thing. The patient stated that when he was sleeping and he was awake and had sweating so much in his bed and had protective pad underneath his sheet and it was soaked wet. He woke up his whole bed and his clothes were sweaty, his bed was sweaty and second night the same thing happened. The outcome of event was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 1381247
Sex: F
Age:
State: NH

Vax Date:
Onset Date: 05/22/2021
Rec V Date: 06/08/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Allergies:

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

Symptoms: patient started it thing really bad and it will not stop; This is a spontaneous report received from a contactable consumer (patient) reported that 19-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), first dose (lot number: Ew0151) and second dose (lot number: Er8731) both via an unspecified route of administration in right arm on unknown date in 2021 (at the age of 19 years) as a single dose for COVID-19 immunisation. The patient medical history was not reported. Patient was not pregnant at time of vaccination. Concomitant medications included fluoxetine. Patient has taken birth control medications in two weeks and has not taken any other medications in four weeks. Patient previously took lactose and had allergies. It was reported that on 22May2021, the patient started it thing really bad and it will not stop and this event resulted in Doctor or other healthcare professional office/clinic visit. Prior to vaccination the patient was not diagnosed with COVID-19 and since the vaccination the patient has not been tested for COVID-19, has not received any other vaccines within 4 weeks prior to the COVID vaccine. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: FLUOXETINE

Current Illness:

ID: 1381248
Sex: F
Age:
State: WA

Vax Date: 03/26/2021
Onset Date: 04/28/2021
Rec V Date: 06/08/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

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

Symptoms: Rash on aqueduct of both eyes/Both eyes have a rough rash under them/rash lower down to where aqueduct and passing eye entering cheek area; allergic reaction that is not going away; lowered her immune system; she might be shrinking; This is a spontaneous report from a contactable consumer (patient). A 64-years-old female patient received second dose of BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: EP6955, Expiration date was not reported), via intramuscular route of administration, administered in left arm on 26Mar2021 as 2ND DOSE, SINGLE DOSE (at the age of 64-years-old) for COVID-19 immunization. Medical history included compromised immune status, obesity, respiratory illness and allergies to pollen (from an unknown date and unknown if ongoing). Patient had ongoing genetic/chromosomal abnormalities, ongoing endocrine abnormalities (including diabetes) and ongoing asthma (born with it). Patient did not have any asthma attack. Concomitant medications included ibuprofen (occasionally) and vitamins not otherwise specified (NOS) taken for an unspecified indication (start and stop date were not reported). Patient previously received first dose of BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: EN6204, NDC number and Expiration date: unknown), via intramuscular route of administration in left arm on 05Mar2021 at 15:00 hours, as 1ST DOSE, SINGLE DOSE for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had an allergic reaction that was not going away. Patient reported that this started after the vaccine. Patient thought Pfizer COVID vaccine had lowered her immune system. When patient got up in the morning, she had a rash in aqueduct of both eyes (lower down to where aqueduct passing eye entering cheek area) which could be felt on touching. It started a month ago on 28Apr2021 after second dose. Both eyes had a rough rash under them. Patient noticed it when she washed her face in the morning (did not have an exact time). Patient was not using any harsh products and face wash was same as before and the moisturizer was just extra virgin olive oil because she did not want to use any chemicals. She waited patiently for it to subside but it was not going away. Patient stated she might be shrinking and said it occurred after she received the vaccine. She was going to have a checkup on 08Jun2021, and blood work done. Outcome of the event rash in aqueduct of both eyes was not recovered while of other events was unknown.

Other Meds: IBUPROFEN; VITAMINS NOS

Current Illness: Asthma; Cytogenetic abnormality; Diabetes (endocrine abnormalities (including diabetes))

ID: 1381249
Sex: M
Age:
State: GA

Vax Date: 05/25/2021
Onset Date: 05/26/2021
Rec V Date: 06/08/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

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

Symptoms: He broke out in a rash that is itching; This is a spontaneous report from a contactable consumer (patient's wife). A 62-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot Number unspecified, expiration date unspecified), dose 2 via an unspecified route of administration, administered in arm left on 25May2021 as 2nd dose, single for covid-19 immunization. Medical history included Blood pressure and AFib. Concomitant medication included losartan (50 mg) taken for blood pressure and tenecteplase (ELAXIM). On 26May2021, the patient broke out in a rash that was itching and reported as worsened. patient Just had normal meal, he never had been allergic to anything. The outcome of the event was not recovered. Information about lot/batch number has been requested.

Other Meds: LOSARTAN; ELAXIM

Current Illness:

ID: 1381250
Sex: U
Age:
State: PA

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

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

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: A sore arm; This is a spontaneous report received from a Pfizer sponsored program from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection, Batch/lot number and expiry date were not provided), unspecified dose 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. On an unspecified date, the patient experienced sore arm for a couple of days and the key was to be well hydrated beforehand. The outcome of event was unknown. Information about Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1381251
Sex: U
Age:
State:

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

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

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: allergic reaction/I had broke out after my second shot, 'its a rash'/it's been spread over my body, its there and it itch real bad; allergic reaction/I had broke out after my second shot, 'its a rash'/it's been spread over my body, its there and it itch real bad; allergic reaction/I had broke out after my second shot, 'its a rash'/it's been spread over my body, its there and it itch real bad; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received second dose of BNT162B2 (FIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot number was not reported, NDC number, UPC number and Expiry Date were unknown), 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. Historical vaccine included first dose of BNT162B2 (FIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, on an unspecified date, as a single dose for COVID-19 immunization. Patient reported that patient experienced, allergic reaction; Had broke out after second shot, it's been spread over body, it itch real bad; Spreading over body, had a rash and it's spread on body on an unspecified date. Patient stated that, was trying to see what have to do to get the rash out of my body, from the shot?". Also stated that what need to do after shot would give me cream or something." Patient added, that is going to the ER. Seriousness of the events was not reported. The outcome of the events was unknown. Information about Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1381252
Sex: F
Age:
State: OH

Vax Date: 05/19/2021
Onset Date: 05/20/2021
Rec V Date: 06/08/2021
Hospital:

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

Allergies:

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

Symptoms: Severe itching; redness; welts; This is a spontaneous report from a contactable consumer or other non hcp. A 46-years-old female patient received first dose of bnt162b2 (BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection) via an unspecified route of administration, administered in Arm Right on 19May2021 19:00 (at the age of 46-years-old) (Batch/Lot Number: EW0168, Expiration date: unknown) as 1ST DOSE, SINGLE DOSE for covid-19 immunisation. Medical history included none from an unknown date. The patient known allergies was none. Concomitant medication included minocycline taken for an unspecified indication, start and stop date were not reported. on 20May2021 19:00 the patient experienced severe itching, redness, welts. Started taking antihistamine on 21May2021. The problem still persist after taking the antihistamine for a week. Went to the Urgent Care on 29May2021. The Nurse Practitioner prescribed methylprednisolone tablets and cream. she have taken Day 1 dose of the methylprednisolone and still no relief. she regret getting the vaccine. Outcome of events was not recovered. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had not COVID prior vaccination and not tested covid post vaccination No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: MINOCYCLINE

Current Illness:

ID: 1381253
Sex: F
Age:
State: MA

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

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

Allergies:

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

Symptoms: First dose: gas; sore arm; This is a spontaneous report received from a contactable Nurse (patient). This 70-year-old (same age at vaccination) female patient received first dose of bnt162b2 (BNT162B2, Solution for injection, lot: EM9809) via an unspecified route of administration on 22Feb2021 at 11:30 AM in left arm as single dose to prevent Covid 19 virus. Medical history reported was parkinsons disease, chronic lymphocytic leukemia, sleep apnea, chronic fatigue, hypothyroidism, all ongoing. She has not had any changes to her medications. She has taken the same medications for years. Concomitant medication reported was immunoglobulin g human (IGG) ongoing Infusion, every 4 weeks. Patient does have a slight allergy to Miralax. She vomited when she took it. She had the Miralax in 2012 when she broke her hip, she was at a rehab hospital. The hospital didn't have any prunes, so they gave her Miralax twice. She reported she has no immunity because of her cancer, and she was hoping she can still receive the Covid 19 vaccine booster if needed. She received her IgG infusion on the days after she received her first and second Covid 19 vaccine. She's been getting IgG for 15 years. The patient experienced gas after first dose of vaccine on an unspecified date.it was reported She did fine with the first Covid 19 vaccine other than some gas. She reported she was a very young and very active. She mentioned to have maybe a sore arm on an unspecified date. The patient underwent investigations on an unspecified date included, blood work, Electromyographic Nerve Test with unspecified result and units and COVID-19 antibody test with negative result. Outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds: IGG

Current Illness: Chronic fatigue; Chronic lymphocytic leukemia; Hypothyroidism; Parkinson's disease; Sleep apnea

ID: 1381254
Sex: F
Age:
State: CA

Vax Date: 03/30/2021
Onset Date: 03/01/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: Low grade fever that finally broke 5/29/2021; Been very fatigued; This is a spontaneous report from a contactable consumer (patient herself). A 43-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: Er8732) via an unspecified route of administration, administered in left arm on 30Mar2021 12:00 as single dose for COVID-19 immunization. Medical history included asthma, mild depression, aneurysm, food allergy (milk, eggs ragweed newly discovered), penicillin allergy. Patient was not pregnant at time of vaccination. No covid prior vaccination. Concomitant medications included montelukast, zingiber officinale (GINGER), diphenhydramine hydrochloride (BENADRYL) and trisleep. The patient had previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: En6203) administered in left arm as single dose for COVID-19 immunization for which the patient had experienced events of anemia and monocytosis. It was reported that in Mar2021 the patient experienced low grade fever that finally broke 5/29/2021, been very fatigued. The patient had not tested positive prior to vaccination, later on since the vaccination, the patient underwent lab tests and procedures which included Nasal Swab test which was negative on an unspecified date. Adverse events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Therapeutic measures were taken as a result of low-grade fever and fatigued as iron pills were taken by patient. The outcome of events was unknown Follow-up attempts are needed. further information is expected.

Other Meds: MONTELUKAST; GINGER [ZINGIBER OFFICINALE]; BENADRYL

Current Illness:

ID: 1381255
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 05/28/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Weakness/she was too weak to get up; Feels like there is a bruise behind her eyes; Achy muscles; Does not feel well: all she wants to do is sleep.; Temperature after second vaccine, most recent is 102 degrees; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCIN, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date and second dose bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCIN, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date in May2021 (reported as yesterday) both as a single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, patient does not feel well: all she wants to do is sleep, feels like there was a bruise behind her eyes, achy muscles, weakness. On 28May2021, at 3 am, her temperature was 100.1 degrees, at 10 am, her temperature was 101 degrees, and a later (reported as half hour ago), her temperature was 102 degrees (after second dose). Patient stated she had the same symptoms after the first vaccine, but then they went away. Patient ate broth and crackers. Patient took an Extra Strength Tylenol (Expiration, May2024), one 500 mg pill and a couple of hours prior, she took two Ibuprofen (lot number, expiration date unknown, stated bottle was in the other room and she was too weak to get up) for her achy muscles. Stated neither medication has been effective in improving her symptoms. Patient stated that she had every symptom, that was mentioned in important safety information guide. Patient was recommended go to a local Urgent Care if her symptoms become more concerned. Outcome for the event Fever was not recovered and for rest of the events was unknown. Follow up needed; Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1381256
Sex: U
Age:
State:

Vax Date: 05/28/2021
Onset Date: 05/29/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Headache; Woozy feeling; feeling like you have been drinking the alcohol; Feeling of unwell; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number and Expiration date: not reported) via an unspecified route of administration on 28May2021 at 3:00 as UNKNOWN, SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported that I just had Pfizer vaccine yesterday (28May2021) at 3 and I pretty much felt okay yesterday (28May2021) but today (29May2021) I was feeling very strange and I knew all of this is side effects. The one I had maybe like was a little bit of headache. I thought I should hydrate more and I did try to do that but the weirdest feeling was like a woozy feeling like it just came and went. It was kind of a feeling like you have been drinking the alcohol and all. That's a weird feeling I was getting that concerned me. I was really concerned about that. And I know that the symptoms are the feeling of unwell. So, it feels really strange to me. When the patient was asked for medical help, the patient reported that I mean, it's not severe enough. I was just resting in my bed right now. I did not drive anywhere because I thought it would not be a good idea. I just thought it was a good idea to tell you what was going on. I know we were supposed to contact the pharmacy, but the pharmacy was closed right now where I had the vaccine. I do not know, I just thought I would tell someone what is going on because I was concerned. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1381257
Sex: F
Age:
State: MA

Vax Date: 05/25/2021
Onset Date: 05/26/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Diarrhea; Left cheek was all red, my arms were red and the bottom of my legs, now usually the bottom of my leg that happens because I have lymphedema in my leg but the bottom of my leg are swollen; Left cheek was all red, my arms were red and the bottom of my legs, now usually the bottom of my leg that happens because I have lymphedema in my leg but the bottom of my leg are swollen; now usually the bottom of my leg that happens because I have lymphedema in my leg but the bottom of my leg are swollen; Hand aren't cold; During the night I had the chills, I was burning; During the night I had the chills, I was burning; Could only sleep for an hour, so wake up an hour or so and wake up; Rash and that was very itchy; Rash and that was very itchy; Very tired and mushy mush; Felt very lethargic; Very tired and mushy mush; Felt very lethargic; Arm hurt and it hurt up to my neck; Arm bothered me and it went in to my neck; Arm hurt and it hurt up to my neck; Arm bothered me and it went in to my neck; This is a spontaneous report received from a contactable consumer (Patient). A 73-year-old female patient received first dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 25May2021 at noon time (Batch/Lot Number: EW0183) as 1st dose, single dose for covid-19 immunization.Medical history included hypertension, ongoing diabetes mellitus and atrial fibrillation. Concomitant medications included metformin (METFORMIN) 500 mg, 2x/day taken for diabetes mellitus, metoprolol succinate (TOPROL XL) 100 mg, 2 Tablets in Morning and 2 Tablets at night, diltiazem (DILTIAZEM) 180 mg, 2x/day, furosemide (FUROSEMID) 40 mg, 1x/day, losartan (LOSARTAN) 50 mg, 1x/day, 1 tablet a day, atorvastatin calcium (LIPITROL [ATORVASTATIN CALCIUM]) 20 mg, 1x/day, ergocalciferol (VIT D) 1000, 2x/day, blood thinner :dabigatran etexilate mesilate (PRADAXA) 150 mg, 2x/day and nitrofurantoin (NITROFURANTOIN) 100 mg, 1x/day for 10 days. On 25may2021, the patient received the Pfizer shot and was fine all day on tuesday and on 26May2021 (Wednesday) patient was like very tired and mushy mush, her arm hurt and it hurt up to my neck, so she took it easy all day Wednesday and got up Thursday fine. On 27May2021 and 28May2021, the patient was perfectly fine and then when she went to bed last, well other than that she had that rash going on and actually she should say that she had the rash and that was very itchy and that was thursday and fridays and the cream that she had taken by doctor had given her a while back she used that and that subsided the itching. The patient got up friday fine and last night on 28May2021, during the night patient had the chills, she was burning. The patient do have and do had a rash but it's a rash that had gotten before and used the medicine that that doctor had given her and it had taken it, it had cleared it away, so she know on the directions here it says about a rash. And so when she got up this morning on 29May2021, she have some diarrhea and when got up this morning actually she got up during the night and was like maybe it's my diabetes. So patient had some orange juice in water and went back to bed but she could only sleep for an hour, so wake up an hour or so and wake up. When patient got up this morning i.e on 29May2021, the left cheek was all red, my arms were red and the bottom of my legs, now usually the bottom of my leg that happens because patient have lymphedema in her leg but the bottom of her leg are swollen. So now as the morning has gone on things are subsiding her hand aren't cold anymore and she was feeling better. The patient reported, that was Clotrim/ Beta CRE Diprop and that's topically applied twice a day but she have only done it once a day on the last 2 days, Thursday and Friday (further clarification unknown) and also she told that on 28May2021 was her last day on 10 days of antibiotic, that's Nitrofurantoin and that's a 100 mg and that was one a day, no twice a day for 10 days and yesterday was the 10th day.The outcome of events insomnia, diarrhea , burning sensation , chills ,temperature regulation disorder, peripheral swelling, lymphoedema, erythema was resolving and outcome of rash, neck pain , pain in extremity (arm), lethargy , fatigue, pruritus was resolved in may2021

Other Meds: METFORMIN; TOPROL XL; DILTIAZEM; FUROSEMID; LOSARTAN; LIPITROL [ATORVASTATIN CALCIUM]; VIT D; PRADAXA; NITROFURANTOIN

Current Illness: Diabetes

ID: 1381258
Sex: F
Age:
State: VA

Vax Date: 05/26/2021
Onset Date: 05/26/2021
Rec V Date: 06/08/2021
Hospital:

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

Allergies:

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

Symptoms: Feels hot but has no temperature/ She feels like warm; She was having a hot flash; Fever/ temperature was very high/ last night her temperature was 101.8/ high fevers like 101.2 in the morning and then in the afternoon it was 101.3, then in the evening it was 101.8.; Chills; Joint pain; Tiredness; Terrible headache; Muscle pain; Nauseated; Skin kind of hurt; Muscle pain in her arm where they gave her the injection; Yesterday in the shower she couldn't lift her arm; After the injection she staarted to hurt; Arm pain; This is a spontaneous report from a contactable consumer (patient, self-reported). A 59-year-old female patient (age at vaccination: 59 year) received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0185 and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 26May2021 at 13:05, as a single dose for COVID-19 immunization. The patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0167 and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 05May2021, as a single dose for COVID-19 immunization and had arm pain which was started to hurt that evening. It lasted probably 4 days. The patient took Pfizer COVID Second Shot because She didn't want the COVID. The patient's medical history and concomitant medications were not reported. The family medical history of the patient related to AE is reported as none. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient reported that on 26May2021, after the injection she started to hurt which included arm pain. On 27May2021, she experienced tiredness, terrible headache which was getting better. Yesterday it was horrible. She thought when she had a high fever, she got a headache. It was over on the left side of her head over her left eye. She took Advil yesterday morning at 07:00 and then Tylenol at 14:20 and then back to Advil. She had no NDC, lot, or expiration date available for the Advil or the Tylenol. They were both upstairs. She had muscle pain in her arm where they gave her the injection which was still sore. Yesterday in the shower she couldn't lift her arm. She thought it was slowly getting a little better. She woke up at 03:00 yesterday with chills. That has passed. It was completely gone now. She had joint pain which was also passed and was gone. She had fever with temperature was 101.8. Today she felt like she was nauseated this morning, but it seems to slowly be going away and which was getting better. Everything started yesterday. She had her second shot on Wednesday. With her first shot she had no side effects, just after the second shot she started having all the side effects. She had a headache this morning and took another Advil. She felt nauseous this morning, but she thought it was slowly passing. She feels hot but has no temperature today. She took her temperature, and it was normal, but she felt hot like she was having a hot flash. She feels like warm. Yesterday she was really hot with high fevers like 101.2 in the morning and then in the afternoon it was 101.3, then in the evening it was 101.8. It was even like her skin kind of hurt when she touched it. That has gone away too. On 28May2021, she felt hot but has no temperature/ She felt like warm which was just started today. She felt like hot now and then. When asked if it has improved, worsened, or is persisting, she stated when she went outside, she felt better, and when she came inside the house, she felt hot. She was right-handed so she had them both in her left arm. She did not know a dosage for either dose. It was provided by the Health Department. She had a lot of side effects yesterday after she received the shot. She didn't know if a lot of people had called. She asked if this was the right place to report her side effects too. Outcome of the events tiredness, chills, joint pain, Skin kind of hurt was recovered on 27May2021. Outcome of the events terrible headache, muscle pain, nauseated, arm pain, muscle pain in her arm where they gave her the injection, yesterday in the shower she couldn't lift her arm was recovering and for all other events, it was unknown.

Other Meds:

Current Illness:

ID: 1381259
Sex: F
Age:
State: SC

Vax Date: 05/21/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Sinus tachycardia; Edema; I had a 'tremor' and both of my legs; My heart rate has been a 140 ever since then; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 44-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: I38731) via an unspecified route of administration, administered in right arm on 21May2021 (at the age of 44 years old) as a single dose for COVID-19 immunization. Medical history included Long COVID, cardiac arrest (twice), bilateral pulmonary embolism, four upper extremity DVT (deep vein thrombosis), blood clot from an unknown date and unknown if ongoing. No family medical history of adverse effect. Concomitant medication included apixaban (ELIQUIS) 2.5 mg tablet in the morning and night to prevent blood clot, start and stop date were not reported. The patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EW6955) dose 1 via an unspecified route of administration on 28Apr2021 as 1st dose, single dose for COVID-19 immunization and it made her sick. The patient reported that she had a vaccine reaction that just needed to report. The patient had long COVID, tested positive in January. The patient waited for 90 days before she could be vaccinated for her first vaccine. The patient got her 2nd vaccine on 21May2021 4:30 in the evening and her heart rate had been 140 ever since then. She had a tremor and both of her legs. She went to cardiologist and doctor told to call and let Pfizer know about tachycardia. The patient stated that she woke up Saturday morning 22May2021 with tachycardia. He had done an EKG (electrocardiogram). It was just normal sinus tachycardia, there was no arrhythmia, heart rate was 68 to 78. The patient reported that it was the side effect of the vaccine. The patient stated that her cardiologist said there was nothing that can be done. The doctor told her to wear compression stroking for the edema which she had done since she follow him and her heart rate was coming down and it was down to like 120's now but doctor told her that it will eventually come down on its own, there was a medication and there was nothing to do. The doctor did have her on a heart monitor, so he can watch her rhythm and heart rate but stated there was a medication. The patient underwent lab tests and procedures which included electrocardiogram: normal on 28May2021 Normal sinus Tachycardia, heart rate: 140 on 28May2021, Cardiac magnetic resonance imaging: unknown on 28May2021. The clinical outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds: ELIQUIS

Current Illness:

ID: 1381260
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Having strange neurologic reaction; Burning sensation; Tingling; Sore Muscle; Sore Joint; Nervous sensation inside my body all the way from neck to my toe; Feeling like a nerve storm going on; This is a spontaneous report from a contactable consumer (Patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on an unspecified date as 1ST DOSE, SINGLE DOSE and dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as 2ND DOSE, SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unknown date the patient had having strange neurologic reaction, burning sensation, tingling, sore muscle, sore joint and nervous sensation inside my body all the way from neck to my toe; Feeling like a nerve storm going on. It was reported that patient received second vaccine shot on Wednesday and patient had very strange neurologic reaction, burning sensation, tingling, sore muscle, sore joint and just a nervous sensation inside body all the way from neck to my toe feeling like a nerve storm going on. It was reported that patient thought it started with the first shot and amplified (not clarified) with the second shot. patient need to get some immediate help (treatment). Reporter seriousness for events was Unspecified. The outcome of events was unknown. Information about lot/batch number has been be obtained.

Other Meds:

Current Illness:

ID: 1381261
Sex: U
Age:
State:

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 06/08/2021
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: Positive Covid after vaccine; Positive Covid after vaccine; This is a spontaneous report from a contactable other hcp. A patient of unspecified age and gender received BNT162b2 (COMIRNATY, Solution for injection; Batch/Lot number was not reported), via an unspecified route of administration on an unknown date in Jan2021 as unknown, single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced positive covid after vaccine. In an ongoing clinical trial the Pfizer BioNTech covid-19 vaccine has been shown to prevent covid-19 following two doses given to 3 weeks apart the duration of protection against covid-19 is currently unknown. When asked about risk of Pfizer biotech covid-19 vaccine, stated side effects that have been reported with pfizer biontech covid-19 vaccine includes: injection site pain, tiredness, headache, muscle pain , chills, joint pain, fever, injection site swelling, injection site redness, nausea, feeling unwell, swollen lymph nodes (lymphadenopathy). There is a remote chance that the pfizer biontech covid-19 vaccine could cause a severe allergic reaction. a severe allergic reaction would usually occur within a few minutes to 1 hour after getting a dose of pfizer biontech covid-19 vaccine. Signs of a serious allergic reactions can include difficulty breathing, swelling of the face and throat, fast heartbeat, a bad rash all over the body, dizziness and weakness, this may not be all the possible side effects of pfizer biontech covid-19 vaccine serious and unexpected side-effects may occur. Pfizer biontech covid-19 vaccine is still being studied in clinical trials. The outcome of event was unknown. Information on the lot/batch number has been requested.; Sender's Comments: As there is limited information in the case provided, the causal association between the event COVID -19 and the suspect drug BNT162b2 cannot be excluded. The case will be reassessed once new information is available

Other Meds:

Current Illness:

ID: 1381262
Sex: F
Age:
State: IL

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 06/08/2021
Hospital:

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

Allergies:

Symptom List: Nausea

Symptoms: both hands started itching; This is a spontaneous report from a contactable consumer (patient). A 71-years-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 29Mar2021 12:00 (Batch/Lot Number: ER8732, NDC 59267-1000-1) as, 0.3 ML SINGLE DOSE for covid-19 immunisation. The patient had no family medical history. Medical history included breast cancer from Sep2006; she completed 6 rounds of chemo and 37 days of radiation and finished in Aug2007; she had right mastectomy on 13Oct2006; she had 3 surgeries in 3 weeks and had 27 lymph nodes removed. Concomitant medication(s) included carvedilol (COREG) taken for arrhythmia (has been taking 14 years) start and stop date were not reported; lisinopril (LISINOPRIL) taken for blood pressure abnormal (has been taking 14 years) start and stop date were not reported. The patient previously took herceptin on Dec2006 and experienced cardiac failure congestive (she had heart damage from chemo and radiation, she had a reaction to Herceptin. They stopped it, stated she had congestive heart failure from it, but it did reverse and she still has that tagged on her. Caller stated she didn't die from breast cancer, but that's her history. Stated she previously had echos done monthly between chemo that was every 3 weeks to check the ejection fraction. Ejection fraction at some point started showing she was in trouble and he called the oncologists and said the Herceptin was done. Confirms she was told she had congestive heart failure, heart damage, but it was reversed now); Tylenol was like a big pain med for her, but it puts her to sleep; Aleve gave her hives and this occurred when it first came out, but she was not sure when that was. Caller stated both hands started itching at some point the evening of 29Mar2021, beginning around midnight, between midnight and 5 am on 30Mar2021. The patient didinot receive any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. Caller describes as kind of itch that is internally itching and cant scratch, it was inside of her itching. Caller stated it fully resolved by the time she woke up on 30Mar2021. The ouctome of th event was recovered on 30Mar2021. No treatment was received for the event.

Other Meds: COREG; LISINOPRIL

Current Illness:

ID: 1381263
Sex: M
Age:
State: KS

Vax Date: 05/26/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: throwing up every 10 minutes; diarrhea; This is a spontaneous report from a contactable consumer (patient wife). A 62-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), via an unspecified route of administration on 26May2021 (Batch/Lot number was not reported), as unknown, single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Reporter stated that patient took the Pfizer Covid vaccine. Reporter stated that her husband had not stopped throwing up since three o'clock this morning (28May2021) and had diarrhea on an unspecified date in May2021. She wanted to know how to get him to stop throwing up, that patient was throwing up every 10 minutes. Seriousness of the event was not reported. Outcome of the events was unknown. Communication: Caller was encouraged to reach out to her husbands healthcare provider, urgent care or emergency room for medical advice. Caller declines to provide further information and disconnects the call. No further information provided or obtained. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1381264
Sex: F
Age:
State: PA

Vax Date: 05/18/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
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: Big pimples on right side cheeks/Pimples on end of tongue; Lump in right side of throat; Chills; Weak; Dizziness; This is a spontaneous report received from a contactable consumer (Patient). A 55-year-old female patient received second dose of BNT162B2(PFIZER BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Right on 18May2021 (at the age of 55 years) (Batch/Lot Number: EW0176) as second dose, single dose for covid-19 immunisation. Medical history included ongoing asthma Diagnosed about 2 years ago. The patient's concomitant medications were not reported. Patient historic vaccine included first dose of BNT162B2 (PFIZER BIONTECH COVID-19 VACCINE, Lot Number: EW0162) received on 23Apr2021 (at the age of 55 years). Patient did not receive any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. Patient denied any family medical History Relevant to adverse event. On an unspecified date in May2021, the patient experienced big pimples on right side cheeks/pimples on end of tongue, lump in right side of throat, chills, weak and dizziness. She stated that she had the Covid Pfizer Vaccine, second dose, on 18May2021. She then travelled on 24May2021. She was having side effects and wanted to report them. She was currently out of the country. Stated that the symptoms started after the second dose of the vaccine; but before she travelled out of the country. She developed big pimples on the right side of her cheeks. then a lump in the right side of her throat. She thought these were going away, so she went ahead and travelled. She stated now they've gotten bigger. She also had pimples on the end of her tongue. States she also experienced chills, being weak, and dizziness but that was okay now. Now everyday she noticed something new. She would like to know if she should continue this way if symptoms persist. Should she go back and receive treatment, or she should wait. She called her healthcare provider, but she isn't working on Fridays. She denied any medications, labs, testing, or treatments relevant to events. She was not visited to either emergency room or physician's office. Relevant teste was reported as none. The outcome of event Big pimples on right side cheeks/Pimples on end of tongue was unknown, Lump in right side of throat was worsened and not recovered and chills, weakness and dizziness were recovered on an unspecified date in May2021.

Other Meds:

Current Illness: Asthma (Diagnosed about 2 years ago)

ID: 1381265
Sex: F
Age:
State:

Vax Date: 05/27/2021
Onset Date: 05/27/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: has been really shaky; has a headache; hasn't felt good; when she went to sleep she woke up 2 hours later; couldn't move her arm; cold chills; she believes she was running a fever last night because she was burning up but she couldn't find a thermometer though so she is not sure; she believes she was running a fever last night because she was burning up but she couldn't find a thermometer though so she is not sure; sharp pain throughout her arm; This is a spontaneous report from a contactable consumer (patient). A 20-years-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: UNKNOWN), via an unspecified route on 27May2021 (at the age of 20-years) as 1st dose, single dose in the left arm for covid-19 immunisation. The patient medical history and concomitant medications were not reported. patient side effects are that she has been really shaky, she has a headache, she hasn't felt good since yesterday, 27May2021, and she went to sleep yesterday, 27May2021, and woke up 2 hours later and couldn't move her arm at all and every time she did move it, it was shooting sharp pain throughout her arm, she has cold chills and she believes she was running a fever last night because she was burning up but she couldn't find a thermometer though so she is not sure. Clarified vaccine to the Pfizer COVID vaccine 1st dose. Reporter seriousness was Unspecified. She says they are all continuing to today except for she doesn't have the fever anymore and her arm is not shooting pain. But she does still have headache and cold chills every now and then and she's shaky. The outcome of the events Sleep disorder; Joint range of motion decreased; Fever; Burning sensation, Pain in arm was recovered in 2021. and rest of the events was not recovered. Information on the lot/batch number has been requested

Other Meds:

Current Illness:

ID: 1381266
Sex: U
Age:
State: NJ

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

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: I was looking a little drowsy or whatever and they refuse to give me my second shot; This is a spontaneous report from a contactable consumer (patient). An unspecified age and gender patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number and Expiration: Unknown), via an unspecified route of administration on unspecified date as 1st dose, single dose for COVID-19 immunisation. Medical history and concomitant medication were not reported. Patient reported that on an unknown date, went to get shot yesterday at the place where patient got it in and they refused. Patient was looking a little drowsy or whatever and they refuse to give the second shot. So, patient tried to figure out how would get the second shot. Patient informed that missed second shot of COVID-19 vaccine. Patient was informed about Pfizer Medical Information and provided the number and informed about the timings as 8 AM to 8 PM from Monday to Friday and 9 AM to 3 PM Saturday and Sunday as per EST. Limited information was available over the call. Reporter did not specify about seriousness. 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: 1381267
Sex: F
Age:
State:

Vax Date: 05/28/2021
Onset Date: 05/29/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Got the second dose and she was pregnant; Feeling tired; Headache; Chest pain; This is a spontaneous report from a contactable consumer (patient's husband). A female patient of an unspecified age received of bnt162b2 (COVID-19 VACCINE - MANUFACTURER UNKNOWN, Batch/Lot number was not reported) via an unspecified route of administration on 28May2021(Pregnant) as 2ND DOSE, SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took first dose of BNT162B2 (COMIRNATY, Solution for injection) on an unknown date for covid-19 immunization. Reporter reported for the side effect of his wife (consumer). It was reported that, She got the second dose yesterday and she was pregnant, she felt well yesterday last night after she got the vaccine. On 29May2021, she was kind of feeling tired, had headache but she felt like chest pain. Also reported that If she needed to go to the hospital or wait because she was feeling better now. The outcome of the events headache, feeling tired and chest pain was reported as recovering and for got the second dose and she was pregnant was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1381268
Sex: F
Age:
State: NC

Vax Date: 05/28/2021
Onset Date: 05/28/2021
Rec V Date: 06/08/2021
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: This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration date: unknown), via intramuscular route of administration, in the left arm on 28May2021 at 11:20 (at the age of 61-year-old) as 1st dose, single dose for COVID-19 immunization. The patient medical history includes thyroid and anaphylaxis. The concomitant medications include unspecified thyroid medications. The patient was allergic to shrimps and peanuts. No other vaccines were administered in in previous 4 weeks of vaccination. On 28may2021, almost immediately after the vaccination, the patient experienced hives on face and all over the body, rash and slightly elevated heartbeat. The patient treated the hives with a homeopathic treatment (capsicum) for allergic reactions. She used in the past that helps stop the progression of the allergic reaction. She denies any swelling of the lips, face or throat. No difficulty breathing. she was not sure if the elevated heartbeat was because she was nervous about the hives or if it was related to the vaccine. The patient stated that the hives resolved after 24 hours and are now completely gone. She wants to know if it was advisable to proceed with the second dose of the vaccine given the nature of her reaction. She did provide her health care provider information to DSU on Saturday when she filed the report. She saw what people report, also she doesn't know that she should have the second vaccine or not and she like to finish the vaccine but just don't know if that recommended if that's ok or not. she also called and reported this information to the CDC for statistical purposes. If she had a severe allergic reaction after a previous dose of the vaccine or if she had a severe allergic reaction to any ingredient of the vaccine. She referred her to speak to her health care provider about the risks of the vaccine compared to the risks of potentially not being fully protected against COVID-19 infection. Also used information from attached document to explain differences of non-severe allergic reaction versus severe allergic reaction. Also referred to HCP for further guidance on proceeding with second dose of the Pfizer COVID-19 vaccine. The second dose was scheduled on 18Jun2021. The reporter assessed all events as non-serious. The outcome of the events rash and urticaria was recovered on an unknown date in 2021, and the outcome of elevated heartbeat was unknown. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1381269
Sex: F
Age:
State: SC

Vax Date:
Onset Date:
Rec V Date: 06/08/2021
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: been sick/she is kind of halfway sick; been sick; lost a bunch of weight; already had three of her shots; This is a spontaneous report from a contactable consumer (Patient). A 94-years-old female patient received bnt162b2 (COVID-19 VACCINE - MANUFACTURER UNKNOWN, solution for injection, Batch/Lot Number: Unknown) via an unspecified route of administration on an unspecified date as unknown, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced seriousness for been sick, lost a bunch of weight and already had three of her shots, she is kind of halfway sick, she confirms she didn't have any experience to report. Patient states she is calling because they didn't give her a card. When probed for telephone number, the caller explains she doesn't have but one number, and she is kind of halfway sick. Patient already had three of her shots at (#) She doesn't know what happened but she doesn't have a card. She clarifies she took three shots already. She was looking through her purse and she doesn't have a card for that, but she has already had three shots already. She confirms she didn't have any experience to report. they said she already had two shots already, but she still couldn't understand that the last one she had was taken at #,that's the hospital where she goes. Reporter clarifies she doesn't know if she got the Pfizer COVID-19 vaccine. Patient thought everybody was getting one. Patient clarifies # is her regular hospital. She went there the first time, and she went there the second time, and the last time she went, she thought that was it. She kept seeing in the papers that they might give her another shot later. She didn't pay that much attention, but after she left one hospital, she didn't know where to go for another one. She clarifies it was in some papers that gave her and she didn't look at it. It was her fault. The first time, she went back to the hospital, and the last time was at hospital. She will be sure she look good next time. It was her fault. She is not able to provide an NDC/Lot/Expiry date. She mentions she might get her granddaughter to call. Her granddaughter lives in #. The patient thought she wouldn't take the Covid-19 shot, but her granddaughter told her to take it. Her granddaughter took her shot at the same the caller did, the same date. She said when she went to get her shot, the hospital staff asked her if she was coming to get her shot. After she got the shot, the staff told her she was through, and that was her last shot. She was born in that section of the hospital where she got her shot. Patient will contact her granddaughter in #and tell her what happened about her getting sent a card. She was reading in the paper, or book, that she was supposed to get another shot, but the caller doesn't know. She really doesn't want another shot, she's too old. She did good. Patient underwent lab test and procedures included weight. The outcome of events was unknown. Information about batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1381270
Sex: M
Age:
State: CT

Vax Date: 05/09/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
Hospital: Y

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Reflux and gastritis; 2 days later after his 2nd dose, he woke up in the middle of the night; 2 days later after his 2nd dose, he woke up in the middle of the night with stomach discomfort to the point that he is unable to eat solid foods./bad discomfort in his abdomen, upper abdomen area and you know it was actually worsening; bad discomfort in his abdomen, upper abdomen area and you know it was actually worsening; he is unable to eat solid foods/he can't eat; significant inflammation on the esophagus to stomach area that would be further confirmed by endoscopy by next week.; Mentioned that nausea and vomiting has been reported; Mentioned that nausea and vomiting has been reported; upper abdominal pain; Started to get abdominal pain; ends up with extreme pain; This is a spontaneous report from a contactable consumer (parent). A 16-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number: EW0176), via intramuscularly in left arm, on 09May2021 as a single dose for COVID-19 immunisation. The patient medical history included positive for Covid-19 in Feb2021. Concomitant medications were not reported. No other vaccinations within four weeks prior to the first administration. Previously the patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number: EW0170), via intramuscularly in left arm, on 18Apr2021 (at age 16-year-old) at 5:30 PM as a single dose for COVID-19 immunisation and experienced stomach upset, nausea, reflux and gastritis. It was reported that patient had experienced lasting side effect post-vaccination that even lead to 2 incidents of visiting the Emergency Room (ER). patient was positive for COVID way back February 2021. Also, it has been reported that 2 days later after his 2nd dose, he woke up in the middle of the night with stomach discomfort to the point that he was unable to eat solid foods all in May2021. This event led to the ER and his physician found out that the side effect reported was localized from the esophagus up to the lower abdomen. Their initial hunch was it could be a reflux or gastritis in May2021. Test results showed that EKG was fine and no inflammation on the heart but there was a significant inflammation on the esophagus to stomach area in May2021 that would be further confirmed by endoscopy by next week. Mentioned that nausea and vomiting has been reported in 2021. Caller also reiterated that nothing triggered the side effect except for the shots that was given prior. patient could be having intestinal reaction through the shot. He received his second shot on May 9th and a few days after he started to get abdominal pain, upper abdominal pain in 2021 and it has since now to a point where he can't eat, having very bad discomfort in his abdomen, upper abdomen area and you know it was actually worsening in May2021 and we don't know why and it hits him on after the shot. After 3 weeks later had his second shot and within like few days he started to have symptoms, waking up in the middle of night with discomfort. Since then you know he was been declining and now he was unable to get all his food down, if he does he ends up with extreme pain in 2021. We have been taking him to the hospital, they treating him for reflux and gastritis and they checked they did an EKG on him to make sure if there was any inflammation around heart. Treatment: Reporter stated, "He went to the ER twice, the emergency room twice and they are treating him with Prevacid medication and also treating him with medication called Carafate, they are waiting to do an endoscopy. Event reflux or gastritis was reported with seriousness of hospitalization. The outcome of the events abdominal discomfort, condition worsened, pain, reflux gastritis was not recovered, while for remaining events was unknown. Follow up attempts are needed; additional information has been requested.

Other Meds:

Current Illness:

ID: 1381271
Sex: U
Age:
State:

Vax Date: 05/28/2021
Onset Date: 05/29/2021
Rec V Date: 06/08/2021
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: Arm is getting sore; the arm where the shot was given was swollen and red; the arm where the shot was given was swollen and red; started feeling little warm; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported, NDC number, UPC number and Expiration date were Unknown), via an unspecified route of administration on 28May2021 as 2ND DOSE, SINGLE for covid-19 immunisation. Medical history included deafness (deaf, hard of hearing) from an unknown date. The patient's concomitant medications were not reported. The patient previously took first dose of historical vaccine, bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) on an unspecified date for covid-19 immunisation. It was reported that, the patient got the vaccination yesterday the second one, and felt fine but today on 29May2021, well all throughout the night the patient experienced arms were getting sore, that morning by time went to the store and got back home started feeling little warm and the arm where the shot was given was swollen and red. The Interpreter also asked, what can be done and if the patient can take Tylenol for that? Reporter seriousness for Arm is getting sore; started feeling little warm and the arm where the shot was given was swollen and red was Unspecified. The outcome of the events was not recovered. Information related to batch/Lot no. was requested.

Other Meds:

Current Illness:

ID: 1381272
Sex: U
Age:
State: CT

Vax Date: 05/01/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
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: This is a spontaneous report from a non-contactable consumer. This report was received via a sales representative. A patient of unspecified age and gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number and Expiration date was not reported), via an unspecified route of administration on an unknown date in May2021, as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date in May2021, after taking the vaccine, the patient experienced irregular heartbeat and went to clinic. It was reported that the doctors had not fully determined the cause but because he had his first COVID-19 shot last week, who said it was possibly due to that. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1381273
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: pain level was higher then normal; This is a spontaneous report from a contactable consumer or other non hcp from a Pfizer sponsored program. A female patient of an unspecified age received first dose and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on an unspecified date in May2021 (Batch/Lot number was not reported) as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that the patient had her 1st dose of the Pfizer vaccine 2 weeks ago (May2021). She said her pain level was higher than normal on the first day after vaccine and by the third day it was almost back to normal. Now (May2021) she had her second dose and her doctor wants too put her on immunosuppressant. Outcome of the event was recovered in May 2021. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1381274
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/08/2021
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: We keep smelling/tasting this funk; We keep smelling/tasting this funk; This is a spontaneous report from a contactable consumer or other non hcp (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as 2nd dose, single for covid-19 immunization. Medical history included, 4 of us had COVID-19 and lost our taste and smell. The concomitant medication was not reported. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as 1st dose, single dose for covid-19 immunization. The patient reported, was lucky to have received both doses of the Pfizer vaccine. However, they had a lingering side effect they can not find more information about. They keep smelling/tasting this funk, or something rotten can't really explain. Smell it randomly could be a bagel or egg or self. For the other girls, it's the same thing that has this smell/taste i.e. every time they drink tea or eat onions keep smelling/tasting this funk. The outcome of events was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 1381275
Sex: F
Age:
State:

Vax Date: 05/31/2021
Onset Date: 05/31/2021
Rec V Date: 06/08/2021
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; Chills; Nausea; Difficulty in breathing; She was very scared; This is a spontaneous report received from a non-contactable consumer (patient friend). A female patient of unspecified age received BNT162B2 (COVID-19 VACCINE - MANUFACTURER UNKNOWN), via an unspecified route of administration on 31May2021 (Batch number/Lot Number: UNKNOWN) as second dose single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported the patient previously received first dose of bnt162b2 on an unspecified date for covid-19 immunisation. Reporter stated, patient just got second vaccine (Unspecified Vaccine) and she did not feel anything horrible or bad at the first one, now after the second one she was having some side effects on 31May2021, like muscle pain, chills, nausea and difficulty in breathing. Patient does not wanted to go to ER. She was very scared. Reporter told her to take a pill of Allegra. Seriousness of the events was not reported. The outcome of all the events was reported as unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1381276
Sex: M
Age:
State:

Vax Date: 03/04/2021
Onset Date: 03/04/2021
Rec V Date: 06/08/2021
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: after the shot my smell and taste went away and I still haven't get it back; after the shot my smell and taste went away and I still haven't get it back; This is a spontaneous report from a contactable 28-year-old male consumer reported for himself. A 28-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: unknown, Expiration date: unknown), via an unspecified route, in right arm on 04Mar2021 (at the age of 28-year-old) as 1st dose, single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported.Prior to vaccination before 4 week, patient had never tested positive for covid .On 04Mar2021,hour after the vaccination, the patient smell and taste went away and still haven't got it back. The patient does not remember time of vaccination.No treatment was given. The patient asked about anything he can do to get smell and taste back. He also stated that his second dose is scheduled after 3 weeks. The outcome of the event was not recovered. Information on the lot/batch number has been requested

Other Meds:

Current Illness:

ID: 1381277
Sex: U
Age:
State:

Vax Date: 05/07/2021
Onset Date:
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Nausea; Had no appetite; Little bit tired; little red welt; Started developing little red welt or greyish circular spot on my neck and on the back of my calf on my right leg; it was very itchy and red and grey; it was very itchy and red and grey; This is a spontaneous report from a contactable consumer. A patient of an unspecified age and gender 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 07May2021 as a single dose and covid-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced nausea, had no appetite, little bit tired, little red welt, started developing little red welt or greyish circular spot on patient neck and on the back of patient calf on patient right leg, it was very itchy and red and grey. Patient called to doctor and he said it was a local reaction. And so it was very itchy and red and grey. And so patient put Calamine (further clarification unknown) on it but nobody was telling what more to do, it feels weird 3 weeks later. The outcome for all the events was unknown. No further information available over the call as the consumer hung up the call abruptly. Hence limited information available over the call. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1381278
Sex: F
Age:
State: WA

Vax Date: 05/29/2021
Onset Date: 05/29/2021
Rec V Date: 06/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Its peaceful; This is a spontaneous report from a contactable consumer. A 31-years-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, administered in Arm Left on 29May2021 17:00 as 1ST DOSE, SINGLE DOSE for covid-19 immunisation. The patient medical history were not reported. The patient's concomitant medications were not reported. No known allergies reported. On 29May2021 17:00, the patient experienced its peaceful. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No other medications the patient received within 2 weeks of vaccination. Prior to vaccination, it was unknown the patient diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No COVID tested post vaccination. The outcome of event was recovered. Information about Lot/batch number has been requested

Other Meds:

Current Illness:

ID: 1381279
Sex: F
Age:
State: TX

Vax Date: 05/24/2021
Onset Date: 05/25/2021
Rec V Date: 06/08/2021
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: Arm was very heated. Became red at the site, then spread from elbow to above site and covered 2/3 of upper arm.; Arm was very heated. Became red at the site, then spread from elbow to above site and covered 2/3 of upper arm.; Have a knot about size of ping pong ball; Had flu like symptoms; This is a spontaneous report from a contactable consumer (patient). A 78-years-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 24May2021 15:45 (Batch/Lot Number: EWOI86) as single dose for COVID-19 immunisation. Medical history included High blood pressure, high cholesterol, arthritis, nerve damage. Prior to vaccination, the patient was diagnosed with COVID-19. Concomitant medication(s) included benazepril (BENAZEPRIL) at 5mg; rosuvastatin (ROSUVASTATIN) at 5mg; mometasone furoate (NASONEX); gabap (as reported), all taken for an unspecified indication, start and stop date were not reported. The patient previously took vioxx, atorvastatin (LIPITOR) and chlorhexidine diacetate and experienced allergy. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that on 25May2021, 16.00, arm was very heated. Became red at the site, then spread from elbow to above site and covered 2/3 of upper arm. Have a knot about size of ping pong ball. Had flu like symptoms. The patient used Cold compresses, Tylenol to treat the events. Since the vaccination, the patient had not been tested for COVID-19. Outcome of the events was recovering.

Other Meds: BENAZEPRIL; ROSUVASTATIN; NASONEX

Current Illness:

ID: 1381280
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Pain in the armpit of the arm that had the shot; This is a spontaneous report from a non-contactable consumer or other non healthcare professional. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as UNKNOWN, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. It was not known if the patient was pregnant at time of vaccination. The patient experienced pain in the armpit of the arm that had the shot on an unspecified date. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1381281
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 06/08/2021
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: when he got his vaccine he got very ill from both shots; This is a spontaneous report from a contactable consumer (patients mother) reporting for A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number and Expiration date was not reported), dose 1 via an unspecified route of administration on an unspecified date as 1st dose, single dose, dose 2 via an unspecified route of administration on an unspecified date as 2nd dose, single dose for covid-19 immunization. The patient's medical history included Reporter stated that son (patient) had Covid, his wife and his son. He was very, very bad but he was quarantined and in the house, that had been a while back. and concomitant medications were not reported. On an unspecified date, the patient was very ill from both shots. When he got his vaccine he got very ill from both shots. The outcome of event was unknown. Patient relevant information added to the narrative and rest of the information was in cross linked case for the respective patient. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1381282
Sex: U
Age:
State:

Vax Date: 05/27/2021
Onset Date: 05/01/2021
Rec V Date: 06/08/2021
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: Fever; Headache; Body aches; Dizziness; got the shot my arm is very sore there is a lump there its red its hot; got the shot my arm is very sore there is a lump there its red its hot; got the shot my arm is very sore there is a lump there its red its hot; got the shot my arm is very sore there is a lump there its red its hot; I'm not feeling good; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 27May2021 as 1st dose, single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient got the shot, the first shot (unspecified shot) of the vaccine on Thursday (27May2021) and they said that patient had symptoms afterwards, first when he/she got it on Thursday, it was Thursday he/she do not know around may be 6'o clock or 7 somewhere around the very next day (28May2021), patient had started getting symptoms like fever, body aches, headache, dizziness. On an unspecified date of May2021, patient arm where he/she got the shot his/her arm was very sore there was a lump there its red its hot and was not feeling good. Patient stated that he/she was not going to start doing the survey when he/she was not feeling good. Patient still had a fever, arm where patient got the shot his/her arm was very sore there was a lump there it was red and its hot. Patient still had it and today was Monday, patient asked was that normal. The outcome of was not feeling good was unknown and not recovered for rest of the events. Information about batch/ lot number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am