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: 1405950
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: experienced some fatigue after the first injection; This is a spontaneous report from a contactable consumer or other non hcp (patient's mother) Pfizer sponsored program. A 12-years-old male patient received BNT162B2, (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: was not reported) via an unspecified route of administration on an unspecified date as 1st dose, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced some mild fatigue after the first injection on an unspecified date. The reporter wanted to know why the Pfizer covid-19 vaccine dose was being used in kids only 10 mcg while the dose used in 12?15-year-old is the same as the adult dose, 30 mcg. The outcome of the event was unknown. No further information was provided or obtained.

Other Meds:

Current Illness:

ID: 1405951
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Some blood trickled down the arm; Mom is concerned that he may have not received the entire dose of the vaccine, because he is not complaining of much pain to injection site or arm; Mom is concerned that he may have not received the entire dose of the vaccine, because he is not complaining of much pain to injection site or arm; This is a spontaneous report from a contactable consumer (patient's mother). A 13-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number was not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: not reported), via an unspecified route of administration on an unspecified date, as a single dose for COVID-19 immunisation. Reporter was a mother of a 13-year-old who received the second shot of the Pfizer COVID vaccine and some blood trickled down the arm. Reporter was concerned that patient might have not received the entire dose of the vaccine, because he was not complaining of much pain to injection site or arm. The patient's mother reported events are non-serious. No product quality complains. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1405952
Sex: F
Age:
State: MT

Vax Date: 03/19/2021
Onset Date: 03/01/2021
Rec V Date: 06/17/2021
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: had the feeling that my right ear had a bit of pressure in it; This is a spontaneous report from a contactable consumer. A 56-years-old female (not pregnant) patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE); Lot/batch no: EN6205) via unspecified route in the right arm, as a single dose on 19Mar2021 at 09:15 for COVID-19 immunization (at the age of 56-years). The patient's medical history included drug hypersensitivity, penicillin allergy from an unknown date and unknown if ongoing. Concomitant medication included estradiol, estriol (BI EST) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had tested for COVID-19. The patient stated that after first dose of the vaccine I felt fine but had the feeling that my right ear had a bit of pressure in it. The clinical outcome for the event was not recovered. Information on Lot/Batch number is available; Further information has been requested.

Other Meds: BI EST

Current Illness:

ID: 1405953
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Gradually increasing weakness and pain in the leg; Gradually increasing weakness and pain in the leg; liver hepatic enzymes were elevated; Aldolase elevated; This is a spontaneous report from a contactable physician reported for a patient via medical information team. A 48-year-old male patient BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number and expiration date: Unknown), via an unspecified route of administration on unknown date as 1st dose, single dose and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number and expiration date: Unknown), via an unspecified route of administration on unknown date as 2nd dose, single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Consumer sated that they had a patient who was in the hospital who had both doses of the Pfizer-BioNTech COVID-19 vaccine and they were tracing his symptoms. Patient experienced a gradually increasing weakness and pain in the leg. They did not find an infection and the final cause of these symptoms. They conducted a muscle biopsy and no result provided. Aldolase and liver hepatic enzymes were elevated. Consumer wanted to know if there have been similar reports and how are patients treated and what could be done. Response: There are no information regarding how the vaccine affects test results or liver enzymes, and antipyretic. Also, pain relieving medications were used on the clinical trials, but Pfizer cannot give medication recommendations. The outcome of the events was unknown. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 1405954
Sex: F
Age:
State: PA

Vax Date: 06/07/2021
Onset Date: 06/01/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Her voice was a little rasped which may have been allergies; Her voice was a little rasped which may have been allergies; Felt bad; Hives on her left wrist, which was the arm of the vaccine; Feel a little stressed at the vaccination site due to poor safety precautions; This is a spontaneous report from a contactable consumer (patient herself) via Medical Information Team. A 61-year-old female received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration on 07Jun2021 as 2nd dose, single dose for COVID-19 immunization. Patient medical history included allergies to trees, cats, and several foods. The concomitant medications were not reported. Historical vaccine included BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration on 10May2021 as 1st dose, single dose for COVID-19 immunization. Patient received her first Pfizer Covid 19 Vaccine on 10May2021. She took the second Pfizer Covid-19 Vaccine on 07Jun2021. On an unspecified date in Jun2021, her voice was a little rasped which may have been allergies. Within one hour of receiving the vaccine she felt bad and experienced hives on her left wrist, which was the arm of the vaccine. She reports eating a hamburger prior to her appointment yesterday (07Jun2021). Voiced she was not allergic to anything on the burger. She did feel a little stressed at the vaccination site due to poor safety precautions. She was not sure if the hives came from stress or not. Patient asked if hives have been reported. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1405955
Sex: F
Age:
State: DE

Vax Date: 05/21/2021
Onset Date: 06/08/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: rash; dry, itchy scalp and hair loss; dry, itchy scalp and hair loss; dry, itchy scalp and hair loss; tired; shingles; This is a spontaneous report from a contactable consumer or other non hcp. A 64-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID VACCINE, solution for injection, Batch/Lot Number: EW0185), via an unspecified route of administration on 21May2021 (64-year-old at the time of vaccination) as a 2nd dose, single dose for COVID-19 immunization. Patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID VACCINE, solution for injection, Batch/Lot Number: EW0158), via an unspecified route of administration on 20Apr2021, as a 1st dose, single dose for COVID-19 immunization. The patient's medical history included take blood pressure medicine for high blood pressure daily and also takes vitamins, but other than that she wasn't sick and she wasn't taking anything else. She was allergic to shellfish. On 08Jun2021, the patient experienced shingles, she says that the shingles happened yesterday and she thought that it was just a rash and then she decided to call the dermatologist. It got worse today and it was also painful. That's how she figured it out that it was shingles, on an unspecified date, rash, dry, itchy scalp and hair loss then she started seeing hair loss and she was also a little itchy but now it was worse than it has ever been. She has put on coconut oil to soothe it but it has been going on for about the last week or week and a half, and tired. The dermatologist told her it was due to the Pfizer vaccine and told to take Valtrex and use a Silvadene cream topical and other stuff for her head. Her main concern was that her doctor told her that this was a side effect and she was just going by what the doctor had said. She was not under stress, she has been tired for a long time and she lives a good life. She was lucky but it just popped up and she knows that shingles was related to stress and other issues but the doctor said that the COVID vaccine does bring it out. The outcome of the event tired was unknown and all the other events were not recovered. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1405956
Sex: F
Age:
State: IL

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 06/17/2021
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: mark on her arm/"divit" in her arm; mark on her arm/"divit" in her arm and pain/The pain is getting worse; Is an indentation, like a divet, in the arm at the injection site; arm pain; everything is tanning except for that spot on left arm; crying; This is a spontaneous report from a contactable consumer (patient). A 59-years-old female patient received BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL1284; Expiration Date: Apr2021), via an unspecified route of administration, administered in left arm on 27Jan2021 10:30 as 1st dose, single dose(at the age of 59-years-old) for COVID-19 immunization. The patient medical history and concomitant medications were not reported. No history previous immunizations, and vaccinations within 4weeks. The patient experienced mark on arm, is an indentation, like a divet, in the left arm at the injection site and reported the mark was for a week or two after; and had arm pain, this is the same arm where the pain is. Patient started to get tan and everything is tanning except for that spot on her left arm. The pain has been worse, It hurts her so bad she wakes up in pain crying. In her opinion, the divot looks like it is getting bigger. Patient reported she visited to emergency room or physician office, and also reported she had a bloodwork but that was after and in opposite arm, in the right arm not the left and mammogram done last month. Patient refused to take the second dose of vaccination. The outcome of events was unknown. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1405957
Sex: F
Age:
State: TN

Vax Date: 03/21/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: pain in her arms and shoulders; pain in her arms and shoulders; pain "started under her left arm and left side of her breast"; swelling under left arm; weak in left arm; problems sleeping; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received second dose bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL9266 expiry date: unknown), via an unspecified route of administration on 21Mar2021 as a SECOND DOSE SINGLE DOSE for covid-19 immunisation. Patient did not receive any other products prior to 4 weeks of vaccination. Patient previously received her first dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: unknown), via an unspecified route of administration on 27Feb2021 as a FIRST DOSE SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date the patient experienced pain in her arms and shoulders, pain in her arms and shoulders), pain started under her left arm and left side of her breast, swelling under left arm, weak in left arm, problems sleeping. On 11May2021,after the second dose She called her doctor because she was going to the store was unable to get out of the car because her arm was throbbing.On 12May2021doctor had prescribed a treatment some kind of anti inflammatory, therapeutic measures was taken Meloxicam 15mg, once a day tablets She had started taking the Meloxicam 15mg. She had developed severe swelling in her feet. She was unable to put her shoes on and had stopped taking it on 18May2021.The outcome of the events was unknown. Information on batch/Lot number was received. Further information has been requested.

Other Meds:

Current Illness:

ID: 1405958
Sex: M
Age:
State: CA

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Brain fog; Nausea; weakness; Weird sensation on [his] tongue 5-10 mins; Weird taste in [his] mouth soon after that/funny taste in mouth; Shortness of breath/difficulty in breathing; Dizziness/Light headedness; Weakness in his upper chest and in both arms; Weakness in his upper chest and in both arms; Diarrhoea; Headache; felt like my throat is gonna close, I won't say I had any difficulty in swallowing, but it was not normal; This is a spontaneous report from a contactable consumer (patient). A 55-years-old male patient received BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number, Expiration date, NDC and UPC number was unknown), via an unspecified route of administration on 06Jun2021 at 11:30 hours as 1st dose, single dose (at the age of 55-years-old) for COVID-19 immunisation. Regarding lot number patient stated that it looks like EW, patient thought he was not sure if it was 6185 or 0185, not sure it looks like 0 but it looks like 6 too but patient think it was 0. The patient medical history included shortness of breath, sleep apnea and kidney disease (from an unknown date and unknown if ongoing). Patient sees a doctor for lot of conditions one was for shortness of breath and sleep apnea and sees a neurologist for Bph. The patient concomitant medications were not reported. Patient explained he was reluctant from getting vaccinated and nervous before the shot. On 06Jun2021, after patient took the shot, probably around 11:30 in the morning, patient was same, soon after 5 min maybe more, patient got a sensation on the left side of his tongue 5-10 mins, then kind of a weird taste came to his mouth, patient started to get a little dizzy, a little light headedness, weakness in his chest and both his arms, got shortness of breath but had been seeing a doctor for shortness of breath prior taking the Covid shot and had kind of reluctant of taking the shot but some other issues going on side, patient decided to take it, a couple of hours after the shot, patient had a headache, had the diarrhea. Patient described the weird taste like having a penny in his mouth. Patient explained he consulted a doctor on that Monday (07Jun2021), who said she encountered patients who also had the sensation on their tongues following vaccination, and that it was normal. Today (08Jun2021) patient had feeling just a little bit of nausea and patient kind a feel like a little brain fog, it was just his head doesn't feel right, the major concern was says some things risks factors and some of them had severe reactions, patient had a reaction difficulty in breathing, dizziness and feel little bit weakness, patient kind of a felt like his throat was going to close and he won't say he had any difficulty in swallowing, but it was not normal. Patient developed symptoms which spooked and scared him. Patient did not have his lab test but was constantly going to patient had just had right heart catheter right two weeks ago, you know last for him, patient was supposed to take another lab test to conduct at the end of the month for cholesterol, but patient saw neurologist for kidney disease. Events did not improve, patient just had this brain fog you know. Patient had to call a doctor after he got home, they did not prescribe him anything, patient mean he did bunch of appointment with doctor with the phone as soon as he got home from taken a Covid shot he was little worried. Patient stated he was concerned about getting the second dose of vaccine scheduled on 27Jun2021. Patient stated he will not be able to consult his doctor before the vaccination appointment and was not able to get further assistance from a pharmacist. Patient repeated he does not know what to do about the second dose. Patient was kind of reluctant taking the next shot, if he was going to feel the something like this again, he don't want to, as he already had uneasy you know just had and patient did not had difficulty in breathing all of time this comes and go, from the sentence he described it says on pamphlet that there was severe reaction to the shot and don't want to take the second shot and then end up in hospital because patient had more from it so his question was he was afraid to take the second shot. Patient don't had answer to that he means he would like to talk to somebody who can give him information kind of help me to relax little bit if it was normal and in in response it was responded that decision to receive the second dose for any other reason cannot be made by the company. Patient was referred to speak to his healthcare provider about the risks of the vaccine compared to the risks of potentially not being fully protected against COVID-19 infection, as healthcare provider knows his health situation and had access to information that can better help inform this decision. The outcome of brain fog was not recovered and outcome for other events was unknown. Information about lot/batch number is requested.

Other Meds:

Current Illness:

ID: 1405959
Sex: F
Age:
State: CA

Vax Date: 05/03/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital: Y

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Severe continous headache; This is a spontaneous report from a contactable consumer, (the patient reported for self) A 49-years-old (non-pregnant) female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), via an unspecified route of administration, administered in left arm on 03May2021 at 14:00 (at the age of 49-years-old) as a single dose for COVID-19 immunization. Reason why batch/lot was Unknown: Not available/provided to reporter at the time of report completion (Unable to locate or read the details). Medical history included rheumatoid arthritis from an unspecified date and unknown if ongoing. Concomitant medication and List of any other medications the patient received within 2 weeks of vaccination included: celecoxib (CELEBREX) taken for adenomatous polyposis coli; pregabalin (LYRICA); embril; duloxetine hydrochloride (CYMBALTA); hydrocodone bitartrate, paracetamol (NORCO); albumin human (MO) all taken at unknown doses from unspecified dates and for unspecified indications and unknown if ongoing. The patient had no other vaccine within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. On 16Apr2021 14:00, the patient experienced severe continuous headache and this adverse event resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient received treatment for the adverse event which includes: pain management, steroids. The patient was hospitalized for severe continuous headache for 3 days. Since the vaccination, the patient had not been tested for COVID-19. The seriousness was considered as hospitalization, disability by reporter. Outcome of the event was reported as not resolved. Device Date : 08Jun2021 Information about lot/batch number cannot be obtained. Follow up attempts are possible, additional information has been requested.

Other Meds: Celebrex; Lyrica; NORCO; MO; CYMBALTA

Current Illness:

ID: 1405960
Sex: F
Age:
State:

Vax Date: 05/13/2021
Onset Date:
Rec V Date: 06/17/2021
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: headaches; I had nausea; This is a spontaneous report from a contactable consumer(patient). A 34-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number not provided), via an unspecified route of administration on 13May2021 as a single dose for COVID-19 immunization. Patient medical history included vomiting before the covid vaccine when gave blood. It's been over 3 weeks of being nauseous and enquired Should I go get a covid test and had some diarrhea. Concomitant medication was not reported. On an unspecified date, Patient stated that I'm having side effects that's not on the pamphlet I received. Is there a way to know if that side effect can be more severe than normally. Do you have any recommendations to alleviate my symptoms. I received first dose on 13MAY and 2nd dose 3JUN2021. I have bad nausea, to top it off I can't eat a whole lot or sleep. Everything has a funny taste to it. taste like pennies. It doesn't matter what it is (it has a metallic taste; drink/liquids too). It's like when orange juice mixes with toothpaste. a nasty taste. I did have headaches when I got it initially. After the first dose I had nausea and headaches. Both worsened after 2nd dose (more with the nausea headaches isn't too too bad). The nausea was unbearable. I had nausea after first shot; worse with the 2nd one. My voice is raspy. My sinus is swollen too. I had vomiting before the covid vaccine when I gave blood. It's been over 3 weeks of being nauseous. Should I go get a covid test. You are the first person I called. To be honest I actually got your number from your cousin. I got a front and back information sheet. Not everyone is getting the same information; that needs to be corrected. My cousin asked me about different things. My paper was about wearing masks only have information on side effects: fever, diarrhea. I haven't had fever; I had nausea (which wasn't mentioned on my information sheet). Even when I asked the nurse about it she said fever but not nausea. We all don't have the same reactions like others. I had some diarrhea. This nausea is annoying. The pamphlet they give are different depending on which clinic/site you go to. I didn't get the same information sheet (fact sheet) you are mentioning. It was reported that side effects after your second shot may be more intense than the ones you experienced after your first shot. These side effects are normal signs that your body is building protection and should go away within a few days. I got a front and back information sheet. Not everyone is getting the same information; that needs to be corrected. My paper was about wearing masks only have information on side effects: fever, diarrhea. I haven't had fever; I had nausea (which wasn't mentioned on my information sheet). Even when I asked the nurse about it she said fever but not nausea. We all don't have the same reactions like others. I had some diarrhea. This nausea is annoying. The pamphlet they give are different depending on which clinic/site you go to. I didn't get the same information sheet (fact sheet) you are mentioning. The outcome of the events was reported as unknown. Follow attempts are needed; Information about lot number/batch number can be requested.

Other Meds:

Current Illness:

ID: 1405961
Sex: F
Age:
State:

Vax Date: 04/15/2021
Onset Date: 06/02/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: rashes; hives; itching; headache; swollen lymph nodes; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 15Apr2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 for COVID-19 immunization. On 02Jun2021, patient experienced rashes, hives, itching, headache and swollen lymph nodes. The outcome of events was unknown. Information about batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1405962
Sex: F
Age:
State: CA

Vax Date: 05/07/2021
Onset Date: 05/01/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Injured shoulder; She has chronic fatigue syndrome (CFS) for many years and has had bad flare ups; Tendinitis in her shoulder/which "hurts quite a bit"; Tendinitis in her shoulder; Wort headaches that "she ever had".; This is a spontaneous report from a contactable consumer (patient). A 60-year-old female patient received first dose of BNT162B2 (Formulation for injection; Batch/Lot number: unknown) via an unspecified route of administration on 07May2021 as single dose for COVID-19 immunisation. Medical history included chronic fatigue syndrome from an unknown date and unknown if ongoing for many years. The patient's concomitant medications were not reported. On an unspecified date of May2021 patient explained chronic fatigue syndrome (CFS) for many years and has had bad flare ups. She added she also has tendinitis in her shoulder, which hurts quite a bit. She mentioned 2.5-3 weeks post vaccination she had her CSF flare up and the worst headaches that she ever had. She added she will be consulting her neurologist on the 17th (failed to confirm the month), which will approach the 42 days mark post vaccination. She explained she would like to wait for this consultation before getting the second dose. She asked if the second dose can be administered beyond the 42 days. Upon follow up, she also reported that, her shoulder was injured and at the very least has tendonitis. She was 32 days out from receiving the first injection, but she wanted to know if it's okay to get the second shot to complete the vaccination series. The outcome of the events was unknown. Follow-up (08Jun2021): This is a follow-up spontaneous report from a Pfizer sponsored program Support via consumer (patient) which included new information such as: She is 32 days out from receiving the first injection, but she wants to know if it's okay to get the second shot to complete the vaccination series/ she has had chronic fatigue syndrome for years, but she had a bad fare up. Her shoulder is also injured and at the very least has tendonitis" No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1405963
Sex: F
Age:
State: IL

Vax Date: 06/07/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: MY arm is a tad swollen; It kinda hurt. It doesn't hurt unless I lay or press on it/Arm was aching a little bit; headache; was actually worried of getting the shot because I am on 3 different main pill (Unspecified medications) that I take every day and now I have not taken them; This is a spontaneous report from a contactable consumer (patient) from a Pfizer- sponsored program. A 59-years-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: UNKNOWN), via an intramuscular route on 07Jun2021 (at the age of 59-years) as 1st dose, single dose in the right arm for covid-19 immunisation. The patient medical history included COPD, high blood pressure, chronic lung disease (e.g., emphysema and chronic bronchitis, idiopathic pulmonary fibrosis, and cystic fibrosis), moderate to severe asthma, smoker. When confirmed if the patient had any vaccination 4 weeks prior to Pfizer COVID 19 Vaccine, patient stated, "I am supposed to go back as far as I know for second dose, 3 weeks on 28th". The patient concomitant medications were not reported. On unspecified date, the patient experienced arm was a tad swollen. It kinda hurt. It doesn't hurt unless she lay or press on it and arm was aching a little bit. Other than that she took it pretty well. She had a headache but didn't last too long. Patient stated that she has heart pills that she takes twice a day. She stopped taking it yesterday. She stated, I didn't know if it would interfere/ how it would interact with it. She also has blood thinner and acid reflux. Patient wants to knew when she can continue taking her medications. Patient was actually worried of getting the shot because she was on 3 different main pill (Unspecified medications) that she take every day and now she had not taken them. Patient stated that she didn't underwent any lab test but she took a scan like 3 or 4 month since she had anything like that then. The patient took Tylenol as a treatment for events. The outcome of the events was unknown. Follow-up attempts are needed. Information about lot/batch number requested.

Other Meds:

Current Illness:

ID: 1405964
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: Initially just a bit tired/ felt fatigued/ exhausting; Excruciating back pain; Pain shooting down her left leg/ foot was hurting; Pfizer vaccine has effected her soft/sore spots areas of her body that were weakened previous to getting the vaccine/ weak part of her body; Couldn't walk; Low grade fever; HA (headache); Stuffy nose; Dry cough; Still feeling some of the pain; Depressed; This is a spontaneous report from a contactable consumer (patient herself) via a medical information team. A 70-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number and expiration date were unknown), via an unspecified route of administration in right arm on 03Mar2021 as a single dose for COVID-19 immunization. The patient's medical history included ongoing stenosis, ongoing allergy to penicillin and clindamycin, surgery (patient had surgery 30 years ago on her foot), areas of her body that were weakened previous to getting the vaccine. 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 and expiration date were unknown), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. Patient states she received her 2nd Pfizer vaccine dose on 03Mar2021 in "her right arm." Patient states she was initially just a bit tired on an unspecified date in 2021." Patient states 2 months later, (end of April), "she began having excruciating back pain on an unspecified date in 2021 and pain shooting down her left leg on an unspecified date in 2021. Patient went for an MRI and she have had stenosis for years, but it doesn't act up like this. Patient foot was hurting on an unspecified date in 2021 and then her back. Patient had surgery 30 years ago on her foot and the Pfizer vaccine has effected her soft/sore spots on an unspecified date in 2021," areas of her body that were weakened previous to getting the vaccine. Patient states it has been like an inflammation. "Patient think she had a response, and it took 2 months, on an unspecified date in 2021, the patient experienced the weak part of her body, she couldn't walk, low grade fever, HA (headache), stuffy nose, dry cough." She states an allergy to penicillin and clindamycin and "she have sensitivity to medicines. Patient pain was getting less each day and she was taking Advil, she was still feeling some of the pain on an unspecified date in 2021 and it has been exhausting to her, patient was fatigue and depressed on an unspecified date in 2021." Enquired are these side effects even though there was a delay in the onset. Patient's healthcare professional state that she has experienced effects from the Pfizer vaccine. Enquired how long would these symptoms last. Sensitive to certain things, states that almost 2 months later, until this point, she was fine. Just tired after the vaccines, states in the last few days of Apr2021 all of a sudden, she got a back pain, states she has stenosis, the pain shot down her leg on the left side of her and then realized she had a dry cough the last month that came out of nowhere, states she has felt fatigued and depressed a little. States she has read this could be caused by the vaccine, wants to know if it was related to the vaccine. The patient underwent lab test and procedure which included MRI: Unknown results on an unspecified date. The patient was treated with Advil for the adverse events pain, back pain, pain shooting down her left leg, foot was hurting. The outcome of the events was unknown. Follow-up attempts are needed. information on Lot/Batch number can be requested.

Other Meds:

Current Illness: Drug hypersensitivity; Stenosis

ID: 1405965
Sex: F
Age:
State:

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

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

Allergies:

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

Symptoms: Sinus infection; there are allergies right now; I'm assuming she can't get the vaccine; This is a spontaneous report from a contactable pharmacist. A 15-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: 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 for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced sinus infection and assuming she can't get the vaccine, there are allergies right now on an unspecified date. The caller stated have a patient (female age unsure maybe 15 years) who was coming this friday for her vaccination and she had a sinus infection and on antibiotics. Pharmacist was assuming she can't get the vaccine. How long does she need to wait? It was her 2nd dose on Friday which will be at 3 weeks. She already got her first dose of the Pfizer covid vaccine. Pharmacist stated she need to talk to her patient more to find out if she was on any steroids and when her antibiotics ends. It makes sense to her that the immune system was fighting the infection. Caller stated she did not think the sinus infection was related (sounds like it was independent) to the Pfizer covid vaccine but she stated she will need to talk to her more and get more information from her patient. She stated she thinks she got the infection last week and she got her first dose of the Pfizer covid vaccine almost 3 weeks ago. She said in the withheld (where she was located) there are allergies right now. Therapeutic measures were taken as a result of sinus infection which include antibiotics. The outcome for event sinus infection was not recovered and rest of events outcome was unknown. Information on Batch/Lot Number has been requested.; Sender's Comments: Based on the information available and a close temporal association, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events of Sinusitis, hypersensitivity. The case will be reassessed once new information is available.

Other Meds:

Current Illness:

ID: 1405966
Sex: F
Age:
State: FL

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

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

Lab Data:

Allergies:

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

Symptoms: Stomach discomfort; Anxiety; Shortness of breath; This is a spontaneous report from a contactable consumer (patient) via medical information team. An unspecified age female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot number and Expiration date: Unknown), via an unspecified route of administration on an unknown date as 1st dose, single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. No investigation Assessment was provided. Patient was called about the Pfizer covid vaccine. It was a personal question, asking if everything that was happening to her was normal or not. If the things that she was experiencing, or feeling was normal. This was her first dose. She got the vaccine on Tuesday and by Thursday she started to have some stomach discomfort, it was not like diarrhea, it was just the feeling like she needed to go to bathroom. Friday, she started having anxiety. At times it was a thing that comes from time to time where she feels anxiety, shortness of breath and the need to deep breathe or take deep breaths and then it goes away and it comes back again. Reporter did not specify any seriousness. The outcome of shortness of breath, anxiety was reported as not resolved and stomach discomfort was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1405967
Sex: M
Age:
State: HI

Vax Date: 03/23/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Was much sicker when he was little and received small pox vaccine than with the Covid vaccine; Severe fever; Throwing up; This is a spontaneous report from a contactable consumer or other non hcp (patient). Communication: Report 2 of 2. A 61-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, FORMULATION: SOLUTION FOR INJECTION, LOT NUMBER: ER2613) via an unspecified route of administration in right arm on 23Mar2021 as single dose (age at vaccination 60-year-old )and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, FORMULATION: SOLUTION FOR INJECTION, LOT NUMBER: RE8736) via an unspecified route of administration in right arm on 29Apr2021 as single dose (age at vaccination 61-year-old ) for covid-19 immunisation. The patient's medical history was none, and concomitant medications were not reported. At age of 8-year-old, patient took smallpox vaccine on an unspecified date in 1968 in left arm for immunization and experienced sickness. When reporting on wife to agent, caller mentioned that he was much sicker when he was little and received the smallpox vaccine than with the Covid vaccine. Patient was sick for only a few days after he had the smallpox vaccine. Patient had severe fever and was throwing up. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 1405968
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: High blood pressure readings; This is a spontaneous report from a non-contactable consumer Pfizer-sponsored program Support. A male patient of an unspecified age received second dose of BNT162B2 (COVID-19 VACCINE, Solution for injection) via an unspecified route of administration on an unspecified date (Lot number and expiry date was not reported) as single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took BNT162B2 for Covid-19 immunization. Caller had his second shot and since had high blood pressure readings. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1405969
Sex: F
Age:
State: PA

Vax Date: 05/21/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Joint pain/knee pain; trouble walking; This is a spontaneous report from a Pfizer sponsored program COVAX US Support from a contactable consumer (patient). A 52-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, lot number was not reported), via an unspecified route of administration, on 21May2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that patient received first dose of COVID vaccine on 21May2021 and due for next dose on 11Jun2021. On an unspecified date in 2021, the patient experienced joint pain, knee pain, trouble walking. Reporter seriousness for Joint pain, knee pain and trouble walking were unspecified. Patient informed everything when she was leaving the doctor's office and heading to work, he had no time to answer question. She would just like to know if she should get the second shot on Friday. She stated that she understands about giving the information in the hopes to collect more data because she works in the medical field, but she is just not a registered nurse or Practitioner. Patient wanted the number for Medical information, and she will call them at another time. The outcome of events was unknown. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1405970
Sex: F
Age:
State: NC

Vax Date: 04/01/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Palpatition/It has gotten worse over the past few days; This is a spontaneous report from a Pfizer sponsored program Pfizer RxPathways via a contactable consumer (patient, self-reported). A 47-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on 01Apr2021, 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 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on an unknown date, as a single dose for COVID-19 immunization. The patient reported that, after having the vaccine, she had noticed palpatition on an unknown date. It has gotten worse over the past few days. The patient asked to have you come across any similar cases and did you have any advice. Outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1405971
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: Injection site pain; headache; body aches; This is a spontaneous report from a contactable consumer or other non hcp. A 48-years-old female patient received bnt162b2 (BNT162B2, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as 2ND DOSE, SINGLE DOSE for covid-19 immunization. Historical vaccine included BNT162B2, first dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced injection site pain, headache and body aches. The clinical outcome of events was unknown. Information about lot/batch number requested.

Other Meds:

Current Illness:

ID: 1405972
Sex: F
Age:
State: VA

Vax Date: 04/20/2021
Onset Date: 04/23/2021
Rec V Date: 06/17/2021
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: This is a spontaneous report from a contactable consumer (patient, self-reported). A 32-year-old non-pregnant female patient received BNT162B2 (BNT162B2, Formulation: Solution for injection, Lot number: EN0153 and Expiration date: unknown), dose 1 via an unknown route of administration, in left arm on 20Apr2021 at 13:45 as single dose, dose 2 via an unknown route of administration, in left arm on 20Apr2021 (Batch/Lot Number: EN0175) as single dose for COVID-19 immunization (at the age of 31-years-old). The patient's medical history included hypothyroidism. Concomitant medication included levothyroxine sodium 88ug taken for an unspecified indication. The patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. On 23Apr2021 at 10:00, the patient experienced pain and swelling of supraclavicular lymph nodes. The patient was not tested for COVID-19 since the vaccination. No treatment was received for events. Outcome of events was not recovered.

Other Meds: LEVOTHYROXINE SODIUM

Current Illness:

ID: 1405973
Sex: U
Age:
State:

Vax Date: 06/04/2021
Onset Date: 06/05/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Hives; rashes from head to my toe.; This is a spontaneous report from a contactable consumer. A 25-year-old patient of an unspecified gender received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Batch/Lot number: EW0172), dose 1 via an unspecified route of administration, in Arm Right on 04Jun2021 (at the age of 25-year-old), as 1st dose, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient told the person about the allergic reactions she had to an antibiotic (name unspecified) and she think it was okay to get the vaccine. The reactions she had with the antibiotic was hives in her body, nothing life threatening. The patient got the vaccine on Friday (04Jun2021) and she felt fine no pain, no headache nothing. she was perfectly fine but Saturday afternoon (05Jun2021). The patient started getting rashes from head to toe and started feeling the same hives again, no other symptoms other than hives. she got it from her hip all the way to waist completely covered hives. Patient asked if they can get second dose of vaccine. The outcome of the event hives was not resolved and unknown for rash. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1405974
Sex: F
Age:
State:

Vax Date: 02/16/2021
Onset Date:
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Took away the pain she had; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (COVID VACCINE, formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 26Jan2021 as 1ST DOSE, SINGLE DOSE and via an unspecified route of administration on 16Feb2021 (Batch/Lot number was not reported) as 2ND DOSE, SINGLE DOSE for covid-19 immunisation. Medical history included coma when she was 19, father passed away from arthritis in 2002 and mother passed away from heart palpitations in 2003. The patient's concomitant medications were not reported. The patient reported that, vaccine took away the pain she had. The patient reported that, she took the COVID shot, and the COVID shot released the blocks and she felt the covid shot stopped at all different points inside her body after it was given to her. Outcome of the event was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1405975
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: Headache; This is a spontaneous report from A contactable consumer (patient) reported that a female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number and expiration was not reported), via an unspecified route of administration on 08Jun2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced headache on 08Jun2021. It was reported that caller on the line that got the Pfizer COVID vaccine today and is experiencing a headache. Caller stated she has no information and has been on the call for 15 minutes. Caller stated the reason for the call is so she could get information. Caller stated she read and listened to the recording already and read everything on her paperwork. Caller stated she just wanted to see if it was ok to take Ibuprofen since everything, she sees says take Tylenol and she does not have Tylenol. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1405976
Sex: F
Age:
State: MI

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

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Allergies acting up right now; This is a spontaneous report from a contactable consumer (patient's husband). A 44-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: Not reported) via an unspecified route of administration on Mar2021 and first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: Not reported) via an unspecified route of administration on Feb2021 both as a single for COVID-19 immunization. The medical history was not reported. Concomitant medications included antihistamine for allergies, over the counter. Reporter stated that the patient started having symptoms about three weeks ago. The patient got her shots in February and March and her allergies acting up right now. Patient stated that she was fine, it's just her allergies, it's allergy season right now: ragweed, pollen, and mold was high. The outcome of the event was unknown. Information about lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 1405977
Sex: F
Age:
State: LA

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

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: body covered in rash/every time they try to stop the Prednisone the rash comes back; This is a spontaneous report from a Pfizer sponsored program COVAX US support. This consumer reported for a female patient (reporter's mother-in-law). An unspecified age female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: unknown; formulation: solution for injection; expiration date: unknown), via an unspecified route of administration on an unspecified date as second dose, single dose for covid-19 immunisation. prednisone (PREDNISONE), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. The patient medical history and concomitant medications were not reported. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; lot number: unknown; formulation: solution for injection; expiration date: unknown), dose 1 via an unspecified route of administration on an unspecified date as first dose, single dose for covid-19 immunisation. Patient reported that after getting the second Covid shot, her body was covered in a rash. They had been able to control it mildly with Prednisone, but every time they try to stop the Prednisone the rash came back. Looking for advice on treatment. They took her to the doctor, and he was the one to prescribe the Prednisone and then given loratadine for the rash, it was a pill and there was an ointment prescription also. consumer tried Calamine and some Neosporin where she had scratched it to like a blister. They will be done with the second dose of the Prednisone soon. She was to take 3 of the 5mg once a day the first time. Consumer wanted to know what they should did since had been done with the second dosed of prednisone. consumer Declined to provide further report details and would like to know what to do, what was next step. Recommended for patient to see further medical advice from medical provider since Pfizer was unable to provide medical advice. consumer stated that he will just be had to get her to see a specialist or allergist and thought that Pfizer could refer her or recommend one. Maybe there have been other people who had this rash. No further details provided. Action taken for prednisone was unknown. The outcome of event was unknown. Information regarding the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1405978
Sex: F
Age:
State: FL

Vax Date: 05/20/2021
Onset Date: 05/20/2021
Rec V Date: 06/17/2021
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: fatigue ahttp://argus.pfizer.com/img/tabs/tab_left_move.gifnd really feeling down, really like heavy, like tired and did not want to do anything; fatigue and really feeling down, really like heavy, like tired and did not want to do anything; The third day was like some symptoms of fever; sleeping all day; was feeling really headaches; The next day the same thing and all day feeling sick; Was having some pain in the night; Was a little dizzy; stomach ache all night; high blood pressure; This is a spontaneous report from a contactable consumer (patient). A 48-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0172) via an unspecified route of administration, administered in left arm on 20May2021 at 15:00 (at the age of 48-years) as 1st single dose for COVID-19 immunisation. Patient medical history included high blood pressure which was diagnosed 3 years ago and Covid-19 which made patient feel really bad on 18Mar2021 which was recovered a month later. The patient's concomitant medications were not reported. The patient did not receive any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. Patient was not administered with additional vaccines on same date of the pfizer suspect. On 20May2021, after administration of first dose of vaccine, the patient was dizzy and was having some pain in the night, she had a stomachache all night and woke up at 01:00 and 05:00 for taking milk or water as the pain was really bad in her stomach. On 21May2021, the next day patient had same events and all day feeling sick. On 23May2021, the third day was like some symptoms of fever and sleeping all day and was feeling headaches. The day after this, 24May2021, was fatigue and really feeling down, really like heavy, like tired and did not want to do anything. The patient reported that she never had any event prior to vaccine administration. It was reported that patient was having some pain in the night went away the third day after it began and recovered like 10 days after and was feeling normal again. The patient reported that she had high blood pressure and thinks that was the reason of the headaches. Patient informed all day feeling sick went away after taking two Aleve, fever and sleeping all day and headaches went away completely. Fatigue and really feeling down, really like heavy, like tired and did not want to do anything was going away little by little, day by day and was getting better. It was also reported that patient was to get the second dose Pfizer Covid 19 Vaccine this week. The patient underwent lab tests and procedures which included X-ray on her thorax for lungs and results were unknown, which was taken after receiving the first dose Pfizer Covid 19 Vaccine. Treatment for event feeling sick included two Aleve. Outcome of the event Fatigue and really feeling down, really like heavy, like tired and did not want to do anything was recovering, high blood pressure and little dizzy was unknown and outcome of rest all events was recovered on an unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness: Blood pressure high (Verbatim: she was diagnosed with high blood pressure like 3 years ago.)

ID: 1405979
Sex: F
Age:
State: DE

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

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: felt a little tired; This is a spontaneous report from a contactable consumer. A female patient (reporter's sister) of unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot number and expiry date was unknown), via unspecified route of administration, on an unknown date, as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. It was reported that patient had no side effects. Patient felt a little tired but other than that she was okay. Outcome of the event was unknown. No further details were provided or able to be obtained from caller due to her requesting to be transferred to USMI for her question.

Other Meds:

Current Illness:

ID: 1405980
Sex: U
Age:
State: CA

Vax Date: 06/07/2021
Onset Date: 06/01/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: Mild headache; Ache; Joint pain; Nausea; Little bit of dizziness; This is a spontaneous report from a contactable consumer (patient) reported for self. A 25-years-old patient of an unspecified gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EW0178, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 07Jun2021 at around 15:00 to 16:00 pm (age at vaccination was 25 years) as 2nd dose, single dose for COVID-19 immunization. The patient did not have any medical history. Concomitant medications were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EW0185, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on an unknown date (age at vaccination was unknown) 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. On an unspecified date in Jun2021, the patient had mild headache, some aches and some joint pains and nausea and little bit of dizziness as well. The patient just took the Pfizer vaccine yesterday the second dose and the patient was experiencing a couple of side effects and wondered if it was okay for the patient to take Ibuprofen. The patient was informed about Pfizer Medical Information Department. The patient stated that the patient did actually take Ibuprofen yesterday but found out today that the patient might not, shouldn't have taken it that's why the patient was a bit concerned the patient wanted to know if that was okay for the patient to do. The outcome of events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1405981
Sex: F
Age:
State: NC

Vax Date: 05/13/2021
Onset Date: 05/13/2021
Rec V Date: 06/17/2021
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: Diarrhea; Pain in the lower right side of my back; This is a spontaneous report from a contactable consumer (patient, self-reported). A 17-year-old female patient (age at vaccination: 17 year) received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0179 and expiry date was not reported), via an unspecified route of administration, in Arm Right, on 13May2021 at 12:30 PM, as a single dose for COVID-19 immunization. The patient was not pregnant at the time of vaccination. The patient's medical history included allergy to Biotin (big amounts of Biotin). Concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID. The patient reported that on 13May2021 at 16:00, she had diarrhea and pain in the lower right side of her back, the first few days after the first dose. There was no prolonged hospitalization. The patient did not receive any treatment for the events. Outcome of the events was resolved on an unknown date in May2021. Follow-up attempts are needed. Further information is expected.

Other Meds:

Current Illness:

ID: 1405982
Sex: F
Age:
State: NY

Vax Date: 04/05/2021
Onset Date: 04/19/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Both knees started aching, they were painful at the same time and My knee still aches at times in the beginning it was very painful and it is less painful today; This is a spontaneous report from a contactable consumer (patient). A 80-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection Batch/lot number: Unknown and expiry date was not provided), via an unspecified route of administration, in the left arm, on 05Apr2021 at 13:10 (at the age of 80-years-old) as a single dose for covid-19 immunisation. Medical history and concomitant medication were not reported. Patient had previously taken first dose of vaccine on 14Mar2021 at 10:00. No other vaccine has been administered within 4 weeks prior to COVID shot. On 19Apr2021, patient had both knees started aching, they were painful at the same time and for his knee still aches at times in the beginning it was very painful and it was less painful today. They slowly started getting better but they aren't 100 percent yet patient was little concerned that will never get back to normal. Patient still experiencing less pain, both knees are the same slightly improved but not completely. On 18May2021, patient had complete blood count as routine lab tests and result was normal. Reporter seriousness for both knees started aching, they were painful at the same time and for my knee still aches at times in the beginning it was very painful and it was less painful today was unspecified. No treatment was received. The outcome of event was recovering. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1405983
Sex: F
Age:
State: NC

Vax Date: 06/03/2021
Onset Date: 06/04/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: headaches with dizziness; headaches with dizziness; felt feverish; itchiness we're I got my 2nd shot; Diarrhea; stomachache; This is a spontaneous report from a contactable consumer (patient). A 17-year-old non-pregnant female patient received bnt162b2 (BNT162B2), dose 2 (Age at vaccination: 16 years) via an unspecified route of administration, administered in Arm Right on 03Jun2021 12:00 (Batch/Lot Number: EW0179 and Expiry date:Unknown) as 2ND DOSE, SINGLE for Covid-19 immunization. Medical history included allergy of big amounts of biotin. The patient concomitant medications was not reported. Historical vaccination included previously the patient received bnt162b2 (BNT162B2), dose 1 (Age at vaccination (years): 16) via an unspecified route of administration, administered in Arm Right on 13May2021 12:30 PM (Batch/Lot Number: EW0179 and Expiry date:Unknown) as 1st DOSE, SINGLE for Covid-19 immunization. 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 04Jun2021, after second dose, first day diarrhea and stomachache. On 05Jun2021 (2nd day) she felt feverish but was not too bad and also itchiness where she got her 2nd shot. On 06Jun2021,(on the 3-4 day) the patient had headaches with dizziness .The patient did not received treatment for the events. The outcome of the events was resolved on an unspecified date in 2021. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1405984
Sex: F
Age:
State:

Vax Date: 06/07/2021
Onset Date: 06/08/2021
Rec V Date: 06/17/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: breast are hurting; arm sore; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiry date were not reported) via unspecified route of administration on an unknown date (age at vaccination: 68-year-old) as 2nd dose, single dose for COVID-19 immunisation. Medical history and concomitant medication were not reported. Previously patient took first dose of bnt162b2 (Lot number EDOR76) via unspecified route for COVID-19 immunisation. The patient experienced breast was hurting and arm sore on 08Jun2021. Reporter states she took the shot yesterday and her breast are hurting. Would it make her breast hurt? she stated the second one. She had to look at the paper. It's got her arm sore and her pain in her breast. It was stated breast was hurting today, this morning it was hurting now the 8th. It keeps on hurting. she took two Tylenol as treatment for breast pain. The outcome of event was not resolved. PSCC Communication: Provided caller with report reference. The caller was provided with phone number for safety if she would like to call back at a later time, option 3 for safety, and hours of operation. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1405985
Sex: U
Age:
State: NJ

Vax Date: 04/03/2021
Onset Date:
Rec V Date: 06/17/2021
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: My sugar started running a little bit lower but not dangerous; I got the first shot it further gone down into the 110 which is where the warning and I kept going okay taking medicine working better; This is a spontaneous report from a contactable consumer or other non-hcp (Patient). A 52-year-old patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection; Batch/Lot Number: Unknown, Expiration date: Unknown) via an unspecified route of administration (Age at vaccination 52 years) in Left Arm on 03Apr2021 as 1st dose, single dose for COVID-19 immunization. The patient's medical history included ongoing stage 4 non-alcoholic cirrhosis of the liver, the patient was diagnosed with a stage 4 non-alcoholic cirrhosis of the liver and they were just about they put me on a transplant now that all sudden was now the stage 2 and ongoing brittle diabetic, the patient had from a last 3 years I became very brittle diabetic they have been trying all the medication. Concomitant medications included dapagliflozin propanediol monohydrate 10mg (FARXIGA) and semaglutide 1 mg (OZEMPIC) taken for an unspecified indication. It was reported that prior to taking the first vaccine the patient had been stable and was on to medication. The patient knew their sugar started running a little bit lower but not dangerous, so something they don't know if anyone else have had experiences with blood sugars with taking this vaccine or not, you know sometimes they say unintended things affects you to medication, so they figured was this worth calling let me know about this in case is having in people and maybe whatever if getting again. Before the patient had the vaccine their sugars were very out of control, they were 200 and they had the patient on medications and was maintaining like 150 all the time. So, the patient got the first shot it further gone down into the 110 which is where the warning and they kept going okay taking medicine working better. The patient underwent lab tests and procedures which included blood glucose decreased: hypoglycemia on an unspecified date. The seriousness of the event was reported as non-serious. The outcome of the events was unknown. Follow up attempts are needed. Further information has been requested.

Other Meds: FARXIGA; OZEMPIC

Current Illness: Cirrhosis liver; Diabetic

ID: 1405986
Sex: U
Age:
State: AK

Vax Date:
Onset Date:
Rec V Date: 06/17/2021
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: Strange sensation in my mouth/It still kind of feels numb, a little bit.; This is a Spontaneous case report received from a Pfizer Sponsored Program. A 30-years-old contactable consumer (patient) of an unspecified gender reported that to receive first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: Unknown, and Expiration date: Unknown), via an unspecified route of administration on an unspecified date as 1st dose, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that the patient took the Pfizer COVID vaccine number one shot and on an unspecified date experienced a strange sensation in mouth. She visits the dentist, and they give the shots to numb certain areas of the mouth when they go to work on the tooth or something like that. It felt just like that earlier. It still kind of feels numb, a little bit. But not as bad as 5 days earlier. The patient had this strange sensation. The events assessed as non-serious. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1405987
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: After the first dose I had nausea and headaches. Both worsened after 2nd dose; I can't eat a whole lot or sleep; I can't eat a whole lot or sleep; Everything has a funny taste to it/taste like pennies/it has a metallic taste/It's like when orange juice mixes with toothpaste/a nasty taste; My sinus is swollen too; After the first dose I had nausea and headaches. Both worsened after 2nd dose; My voice is raspy; had some diarrhea; This is a spontaneous report from a contactable consumer (Patient). A 34-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Solution for injection, via an unspecified route of administration on 03Jun2021 as 2nd dose, single dose for covid-19 immunisation. Medical history included, vomiting from. The patient's concomitant medications were not reported. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) received on 13-MAY-2021 and experienced nausea and headache. On an unspecified date in Jun2021, the patient experienced bad nausea, can't eat a whole lot or sleep, everything had a funny taste to it/taste like pennies/it had a metallic taste/it was like when orange juice mixes with toothpaste/a nasty taste, sinus was swollen too, headaches, voice was raspy and had some diarrhea. Patient had side effects that was not on the pamphlet she received. She received first dose on 13MAY and 2nd dose 3Jun2021. She had bad nausea, to top it off she could not eat a whole lot or sleep. Everything had a funny taste to it. taste like pennies. It did not matter what it was (it had a metallic taste; drink/liquids too). It was like when orange juice mixes with toothpaste. a nasty taste. she did have headaches when she got it initially. After the first dose she had nausea and headaches. Both worsened after 2nd dose (more with the nausea headaches was not too too bad). The nausea was unbearable. She had nausea after first shot; worsen with the 2nd one. Her voice was raspy. Her sinus was swollen too. She had vomiting before the covid vaccine when she gave blood. It had been over 3 weeks of being nauseous. She wanted to know if she should get a covid test done? She told that, she got a front and back information sheet. Not everyone was getting the same information; that needed to be corrected. Her cousin asked her about different things. Her paper was about wearing masks only have information on side effects: fever, diarrhea. She had no fever; had nausea (which wasn't mentioned on her information sheet). Even when she asked the nurse about it, she told her fever but not nausea. We all don't have the same reactions as others. She had some diarrhea. This nausea was annoying. The pamphlet they gave were different depending on clinic/site. She didn't get the same information sheet. The outcome of events was unknown. Information about lot/batch number is requested.

Other Meds:

Current Illness:

ID: 1405988
Sex: F
Age:
State:

Vax Date: 05/07/2021
Onset Date: 05/08/2021
Rec V Date: 06/17/2021
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: Severe headache; sore arm.; This is a spontaneous report from a non contactable consumer (patient). A 31-year-old non pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: solution for injection, Lot Number: EW0165) via an unspecified route of administration, administered in Arm Left on 07May2021 at 17:30 (at the age of 31 years old) as 1ST DOSE, SINGLE DOSE for COVID-19 immunization. The patient's past drug history included previously took Norco for allergy from an unknown date and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient reported that after first dose, she had a severe headache the second day (08May2021) and a sore arm. The clinical outcome of the events was recovered. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds:

Current Illness:

ID: 1405989
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 06/17/2021
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: Rash; Had a reaction; This is a spontaneous report received from Pfizer sponsored program. A contactable female consumer reported for her daughter. A female patient with unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, (Lot number and expiry was not reported) 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 rash, a week afternoon her arm and had a reaction. The patient didn't know what it was until her husband looked it up. It said that 7-10 days after the shot a rash can occur. No investigations were reported. Outcome of the events was unknown. Follow-up attempts are completed; information about lot/batch number are requested.

Other Meds:

Current Illness:

ID: 1405990
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: very dejected; he's very, very sick; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number, Expiration date, NDC and UPC number was not reported), via an unspecified route of administration on an unspecified date as 2nd dose, single dose for covid-19 immunisation. The patient's medical history and concomitant medications was not reported. Historical vaccine received BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration on an unspecified date as 1st dose, single dose for covid-19 immunisation. On an unspecified date, patient had no adverse effects to the COVID Vaccine after seven days that was patently false and knows a physician now after spending tens of thousands of dollars on a sick kid who was a star athlete in the state, who had not been able to find his butt with both hands after nine weeks after receiving the second COVID Vaccine and he was very, very sick and very dejected. Patient wanted to talk to a doctor who was studying the adverse effects report from the second virus from the second vaccine and wanted to talk to whoever was collecting information about the other people who had long term side effects from the COVID Vaccine. The outcome of both the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1405991
Sex: F
Age:
State:

Vax Date: 05/28/2021
Onset Date:
Rec V Date: 06/17/2021
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: Headache; Chills; Fever; No appetite; Tired; This is a spontaneous report from a non-contactable consumer. A 31-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Lot Number: EW0187) via an unspecified route of administration, administered in left arm on 28May2021 at 17:30 (at the age of 31-years-old) as a single dose for COVID-19 immunization. dose 1 via an unspecified route of administration, administered in left arm on 07May2021 at 17:30 (Batch/Lot Number: EW0165) as 1st single dose for COVID-19 immunization. Patients past medical history included severe headache from 07May2021 after first dose and sore arm from 08May2021 (second day). The patient's concomitant medications were not reported. The patient previously took norco. The patient was not pregnant at the time of vaccination. The patient had not been tested for COVID-19 nor before neither since the vaccination. Patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Facility where the most recent COVID-19 vaccine was administered was at the Pharmacy or Drug Store. On an unknown date, the patient experienced, headache the next day, chills, fever, no appetite for the entire day and tired. The clinical outcome for the events was recovered. Follow-up attempts needed. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1405992
Sex: U
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 06/17/2021
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: Seeing colors brilliantly.I wonder if it has somehow repaired my cones/rods. Also wondering if it has helped my blood pressure; This is a spontaneous report from a Pfizer sponsored program. A contactable consumer (patient) reported that an unspecified age and gender patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number Unknown), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. The patient's medical and concomitant medications were not reported. On an unspecified date, patient was seeing colors brilliantly. Patient knew that it was not something Pfizer has concerned with but was wondering if it has somehow repaired patient's cones/rods. Also wondering if it has helped blood pressure, of it was having started using progesterone. Prior to this, patient had very negative side effects from cardiac meds, so started progesterone and it seems to be helping. But was wondering if the shot was somehow fixing things. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1405993
Sex: F
Age:
State:

Vax Date: 04/15/2021
Onset Date: 05/16/2021
Rec V Date: 06/17/2021
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: Rashes; Hives; Itching; Headache; Fever; This is a spontaneous report from a contactable consumer (mother) reported for her daughter. A female patient of an unspecified age received second 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 15Apr2021 as 2nd dose, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient historical vaccine included first dose of BNT162B2 for COVID-19 immunization and reported that there is no reaction on previous exposure to vaccine. On 16May2021, the patient experienced rashes, hives, itching, headache, and fever (Reporter as the daughter's adverse events started on 16May2021). Caller wanted to know if these adverse events may be from the vaccine. She also wanted to know if other people have experienced their adverse events from the vaccine. The outcome of the events was reported as unknown. No PQC involved. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1405994
Sex: F
Age:
State: IL

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

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: she was very very tired; sleepy and weak; sleepy and weak; This is a spontaneous report from a contactable consumer (patient) received via medical information team. A 40-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: not reported) via an unspecified route of administration, administered in arm on an unspecified date in 2021 (at the age of 40-years-old) as 1st dose, single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient previously received Tylenol for an unspecified indication and had allergy. On an unspecified date in 2021, after receiving first dose of vaccination, the patient was very very tired, sleepy and weak was hesitant about getting the second shot because of what happened the first time. Patient states that the only reason she got the shot was because her baby has asthma. Reportedly, the first shot patient got the day after her birthday and she was tired and weak and even the patient's baby noticed that the patient was sleepy and then she got scared. Patient reports that she just turned 40, and she was a medical assistant, so she knows her body and knows what she was talking about. The outcome of the she was very very tired, sleepy and weak were unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1405995
Sex: F
Age:
State: VA

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

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Really bad headache; Nauseous; Diarrhea; Maybe she was hyperventilating; She's feeling a little sick; Having a problem breathing a little bit; This is a spontaneous report from a contactable consumer (patient). A 60-years-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EW0181), via an intramuscular route on 08Jun2021 at 10:45 (at the age of 60-years) as single dose in the right arm for covid-19 immunisation. The patient's medical history included high cholesterol, temporal arteritis. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included atorvastatin (LIPITOR) with dose 20 mg, daily for high cholesterol, Fish Oil with dose 2000 mg, daily for unspecified indication, venlafaxine hydrochloride (EFFEXOR) with dose 150 mg, daily for depression. The patient previously took Prednisone for temporal arteritis since 24Dec2020 and she had been holding off on getting the COVID 19 vaccine until she was taking a lower dose of the Prednisone. She's taking 8mg of Prednisone. The Prednisone is in a pharmacy bottle. The Prednisone 5mg tablet is in a yellow pharmacy bottle. She took her Prednisone every day at 2:30PM. Her doctor told her on 07Jun2021, that she was ok to get the COVID 19 vaccine. She was taking 60mg of Prednisone but she's weaning off of the Prednisone. She has gained weight while taking the Prednisone. On unspecified date at 14:30 (4 hours after vaccination), the patient experienced really bad headache, nauseous, having a problem breathing a little bit, maybe she was hyperventilating and She's feeling a little sick. She had diarrhoea when she first got home after getting the COVID 19 vaccine. She's scared. She hadn't reached out to her doctor or gone to the emergency room. She doesn't wanted to got the COVID 19 virus. She was been quarantined for a year. Patient reported that she took Ibuprofen and her headache is going away. She thinks she's feeling better now. She's still a little nauseous. And her breathing, maybe she was hyperventilating because of the nausea. She is starting to feel better. The outcome of the events really bad headache, breathing, maybe she was hyperventilating was recovering and other events was unknown. Information on Lot/Batch number was available. Additional information has been requested.

Other Meds: LIPITOR [ATORVASTATIN]; FISH OIL; EFFEXOR

Current Illness: High cholesterol (Verbatim: high cholesterol); Temporal arteritis (Verbatim: Temporal arteritis)

ID: 1405996
Sex: F
Age:
State: HI

Vax Date: 04/29/2021
Onset Date: 04/01/2021
Rec V Date: 06/17/2021
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Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: her hands started sweating again; After getting her second, some of her symptoms started to dissipate and her inflammation markers are coming down; After getting her second, some of her symptoms started to dissipate and her inflammation markers are coming down; This is spontaneous report from contactable consumer. This contactable consumer (patient's husband) reported for 60-year-old Female (patient) that who received first dose 23-MAR-2021 14:40 BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number ER2613 expiry date was unknown) at arm, second dose on 29Apr2021 (Age at vaccination 60-year-old), at arm left (Lot number: ER8736 and expiry date was unknown) via an unspecified route of administration as a single dose for COVID-19 immunisation. Medical history included covid-19 from an unknown date in Jan2021 to an unknown date got the covid infection in Jan2020 and is a long hauler, hyperhidrosis from an unknown date and unknown if ongoing her hands would sweat, but after having covid they stopped sweating, arthritis from an unknown date and unknown if ongoing has a lot of inflammation of her joints. Concomitant medication(s) included prednisone (PREDNISONE) taken for rheumatoid arthritis from Jan2021 to an unspecified stop date. She was given prednisone 5 mg for the inflammation and was on it when she got her first Pfizer covid vaccine. After getting her second, some of her symptoms started to dissipate and her inflammation markers are coming down and her hands started sweating again. On an unspecified date in 2021 patient experienced after getting her second, some of her symptoms started to dissipate and her inflammation markers are coming down (therapeutic response unexpected), after getting her second, some of her symptoms started to dissipate and on an unknown date in Apr2021 her inflammation markers are coming down and her hands started sweating again. The patient underwent lab tests and procedures which included inflammatory marker test: 2, inflammatory marker test: 8, rheumatoid arthritis: negative. Outcome of the events her hands started sweating again recovering, symptoms started to dissipate, and her inflammation markers are coming down (therapeutic response unexpected), after getting her second, some of her symptoms started to dissipate and on an unknown date in Apr2021 her inflammation markers are coming down was unknown.

Other Meds: PREDNISONE

Current Illness:

ID: 1405997
Sex: M
Age:
State: FL

Vax Date: 06/07/2021
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Rec V Date: 06/17/2021
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Symptom List: Injection site swelling, Limb discomfort

Symptoms: Stomach pain; fever for 101.5; Headache; 14 years patient received the BNT162B2 vaccine; This is a spontaneous report from a contactable consumer (patients Father). A 14-years-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on 07Jun2021 (Batch/Lot number was not reported) as 2ND DOSE, SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient previously received first dose of bnt162b2 (BNT162B2) on an unspecified date (3 weeks prior on Monday) for covid-19 immunisation. It was reported that his son who was 14 years old got the 2nd dose (Covid vaccine) of Pfizer yesterday around noon. So that was around something 17 hours ago, the reporter don't receive any information on how to handle any side effect. He apparently has headache and he has fever for 101.5 right now and he has stomach pain. But you said they were not open right now well that this was not very helpful at this point because its 5 eastern time right now. So where could get information on how to handle or what we should do with him to help him. If the reporter could go someplace for reference and couldnot contact at this point in time. Does not seem appropriate and especially giving that you know, you could do on a certain time. So pretty upset with that the reporter known it was recorded one. So, reporter hope someone on side does something about that because it was not very good practice he would try to find answers elsewhere. The outcome of the events were unknown. Follow-up attempts are needed; information abut lot/batch number has been requested

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Current Illness:

ID: 1405998
Sex: F
Age:
State: NY

Vax Date: 05/28/2021
Onset Date: 05/28/2021
Rec V Date: 06/17/2021
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Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: I still have a very mild sort of ache or very mild cramp sort of feeling in my left shoulder; I still have a very mild sort of ache or very mild cramp sort of feeling in my left shoulder; This is a spontaneous report from a contactable consumer (Patient) reported herself. A 28-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in Deltoid Left on 28May2021 09:45 (Batch/Lot Number: EW0183) as 2nd DOSE, SINGLE for covid-19 immunization. The patient medical history and concomitant medication was not reported. The patient did not receive any other vaccine within prior 4 weeks of vaccination. After the administration of 2nd dose of vaccine on 28May2021 like 11 days ago and she still have a very mild sort of ache or very mild cramp sort of feeling in her left shoulder it was a lot more severe and worsened, improved and persisting.it was faded away about 3 days and when she didn't notice it for several days and she started noticing it again about 2 to 3 days ago which would have been 04Jun or 05Jun. No treatment was received. The event outcome is not recovered. Follow up attempts are needed. Further information has been requested.

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Current Illness:

ID: 1405999
Sex: F
Age:
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Vax Date: 05/18/2021
Onset Date: 05/01/2021
Rec V Date: 06/17/2021
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Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: not feeling well; weak; in pain; This is a spontaneous report from a Pfizer sponsored program. A non-contactable consumer reported for a female patient of an unspecified age received BNT162B2 (Pfizer COVID-19 Vaccine, Solution for injection), dose 1 via an unspecified route of administration on 18May2021 (Batch/Lot number was not reported) as 1ST DOSE, SINGLE DOSE for covid-19 immunization. The patient medical history and concomitant medication was not reported. When caller wanted to reschedule the 2nd dose of vaccine, the patient experienced not feeling well, weak and pain on unspecified date in May2021. The clinical outcome of the events were unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am