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
187,133MODERNA
33,878JANSSEN
2,321PFIZER\BIONTECH
1,091GLAXOSMITHKLINE BIOLOGICALS
983UNKNOWN MANUFACTURER
363MERCK & CO. INC.
229SEQIRUS, INC.
45DYNAVAX TECHNOLOGIES CORPORATION
41NOVARTIS VACCINES AND DIAGNOSTICS
29SANOFI PASTEUR
18EMERGENT BIOSOLUTIONS
8PAXVAX
7TEVA PHARMACEUTICALS
4PFIZER\WYETH
3BERNA BIOTECH, LTD.
2SMITHKLINE BEECHAM
2INTERCELL AG
2PROTEIN SCIENCES CORPORATION
1CSL LIMITED

Incidents per State

State Total
77,548
AK1,869
AL5,581
AR3,688
AS47
AZ14,288
CA61,984
CO11,665
CT8,149
DC1,663
DE1,807
FL37,749
FM5
GA15,058
GU120
HI2,453
IA4,625
ID2,692
IL20,334
IN24,007
KS4,615
KY7,696
LA4,887
MA14,654
MD12,514
ME3,129
MH11
MI18,739
MN12,528
MO9,710
MP29
MS2,790
MT2,375
NC16,368
ND1,356
NE2,880
NH3,100
NJ17,634
NM3,916
NV4,239
NY34,355
OH19,081
OK6,195
OR8,636
PA23,083
PR2,370
QM2
RI2,088
SC6,411
SD1,212
TN9,131
TX35,174
UT4,273
VA14,937
VI64
VT1,676
WA14,909
WI11,259
WV2,388
WY861
XB5
XL1
XV2

ID: 1277319
Sex: F
Age:
State:

Vax Date: 04/12/2021
Onset Date: 04/13/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Redness at injection site; shortness of breath; Feverish; lethargy; This is a spontaneous report from a non-contactable consumer (patient). A 34-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 via an unspecified route of administration, administered in Arm Left on 12Apr2021 13:15 (Batch/Lot Number: EW0162) as SINGLE DOSE for covid-19 immunisation in hospital. Medical history included, drug hypersensitivity (Penicillin allergy) from an unknown date and unknown if ongoing known allergies. The patient's concomitant medications were not reported. Patient previously took first dose of bnt162b2 for covid-19 immunisation. The patient was feverish and had lethargy on 13Apr2021, a day after receiving COVID-19 vaccine. The patient developed redness at injection site and shortness of breath on day 2. The patient did not receive treatment for the events. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive other medications within 2 weeks of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1277320
Sex: M
Age:
State: MD

Vax Date: 03/31/2021
Onset Date: 04/13/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: he has days when he can't hear, clarified as selective hearing; trouble finding veins/ he was stuck 20 times yesterday trying to get blood and find a vein; knot on face; his eyeball and bone around the eyeball hurts; jawbone hurts; inner ear and outer ear hurts all the way down to neck and shoulder; inner ear and outer ear hurts all the way down to neck and shoulder; inner ear and outer ear hurts all the way down to neck and shoulder; Headache; This is a spontaneous report from a contactable consumer (patient). A male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in left arm on 31Mar2021 at 18:00 (Batch/Lot Number: ER8732; expiration date not reported) at the age of at a single dose for COVID-19 immunisation. The vaccination facility type was pharmacy. Medical history included diabetic from 2006 and ongoing; heart patient, had first heart attack in 2006; kidney stones, diagnosed during end of last year 2020 or beginning of this year 2021. Patient had his 1st car accident when he was . Family medical history relevant to adverse events was reported as none. There is no history of previous immunization with the Pfizer vaccine, no additional vaccines administered on same date, no other vaccinations within four weeks prior to the first administration date of the vaccine and no adverse events following prior vaccinations. There were no concomitant medications. The patient stated that he got the COVID vaccine at the end of the last month, the 30Mar2021 or 31 Mar2021. Patient then confirmed it was 31Mar2021. Patient stated that he is diabetic and a heart patient. He has been having kidney stones that has nothing to do with vaccine. He was supposed to have a procedure for the kidney stones done yesterday, 13Apr2021. He drank a lot of water 3 days before but when he went in yesterday, 13Apr2021, they couldn't find a vein and usually he does not have trouble with people finding a vein. They did try to go in his neck a couple of times to place an IV and he did end up with a knot in his face. They couldn't find a vein that would hold an IV, so he was not able to have the procedure done. Patient reported that the knot was just a little knot on the jaw below the ear lobe, and so he went home but it kept getting bigger and hurting a lot more. He reported that the knot is now all the way to the center of his nose, his eyeball and bone around the eyeball hurts. The patient's jawbone hurts, inner ear and outer ear hurts all the way down to neck and shoulder. He went back to the surgical center yesterday, 13Apr2021, they told him there was no bleeding and that he could go home or do whatever he wanted to do. Patient stated that he ended up in emergency room on 13Apr2021. He reported that the emergency room ran some bloodwork but doesn't know what kind and that they had to stick him 4 or 5 times and then had to use a sonogram machine to find a vein. He stated that he was stuck 20 times yesterday trying to get blood and find a vein. He stated that finding a vein on him has never been that hard and that he does have tricky veins sometimes, but if someone is good enough, they can get it. Patient reported that the emergency room basically did a CAT or CT scan, it wasn't an MRI, but he thinks it was a CAT scan with contrast. He stated that the emergency room didn't find anything and that they told him it was his imagination but that it is not his imagination to see a knot on the side of his face. Patient stated that he could be wrong, but he thinks it is because of the COVID vaccine. He stated that he has had needles, surgeries, IVs before and never had this where they can't get a vein and have never had knots just pop up on his body. Patient commented he has days when he can't hear, clarified as selective hearing since an unknown date. Patient stated that he will not be getting that second COVID vaccine. He stated that last month he had no problems with his veins, so the only thing new since last month is the COVID vaccine he received on 31Mar2021. He stated that he thinks he received the COVID vaccine on the left side but everything he is experiencing is on the right side. Patient reported that trouble finding veins started at 7:00 AM, the knot showed up around 8:00 AM or 8:30 AM and that he has a headache that started on 13Apr2021, around 8:00 AM or 8:30 AM that is ongoing and staying about the same as a constant headache. Patient stated that he was told that the hospital isn't for what he has. The outcome of the events knot on face and headache was not recovered while the outcome of the other events was unknown.

Other Meds:

Current Illness: Diabetic

ID: 1277321
Sex: M
Age:
State: VA

Vax Date: 04/12/2021
Onset Date:
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: has fits at night nothing seems to change/ constantly chocking and coughing; has fits at night nothing seems to change/ constantly chocking and coughing; excess mucous was reported as worsened; he is not sleeping because he is constantly chocking and coughing every second; Feeling funny; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose via an unspecified route of administration, administered in the right arm on 12Apr2021 at 10:45 (batch/lot number: EW0162) as a single dose for COVID-19 immunization. The patient has no medical history and no concomitant medications. Historical vaccine included BNT162B2 first dose on 15Mar2021 at 11 am (lot number: EM6208) for COVID-19 immunisation and experienced excess mucous (started at the end of Mar2021 or beginning of Apr2021), has fits where he was trying to cough up mucous and allergies. The patient reported that he just got his second Pfizer shot Monday 12Apr2021, and he got his first one 15Mar2021. He wanted to report what he thinks was a side effect. He doesn't know if it was related or not, but at the end of Mar2021 or beginning of Apr2021, he started having excess mucous. He has fits where he was trying to cough up mucous for 45 minutes. Ever since it started there has been a lot of mucous. He has been taking Benadryl and stuff like that. He headed to urgent care Sunday 11Apr2021, but decided to go to the ER instead because he was having a mucous coughing spell. They checked for pneumonia, but it was negative. They were contributing it to allergies, but he has never had them this way before. He wanted to report because he was thinking maybe it was something from having the vaccine. He thinks the mucous first started the end of Mar2021 or the first day of Apr2021. He went to ER on 11Apr2021. He also went back and forth with the doctor. They gave him allergy medicine. The ER gave him codeine cough syrup and Allegra D. Her GP has him on Sudafed now, Flonase, Allegra, and Benadryl. They were saying it was allergies, but he has never had a reaction like this with mucous. He has been wearing his mask too. He knows the allergy season was supposed to be bad, but they said on the news the masks were actually helping with the allergies. That people were having less symptoms. On an unspecified date, excess mucous was reported as worsened. He has fits at night nothing seems to change. He was not sleeping because he was constantly chocking and coughing every second. Last night, he finally fell asleep at 3 am and woke up at 9 am. They don't want to give him prednisone yet. He would have to wait 2 weeks after his last shot for it. The patient also experienced "feeling funny" on an unspecified date. The patient underwent lab tests and procedures which included chest X-ray: negative for pneumonia on 11Apr2021; the chests X-ray was clear with no pneumonia. Vaccine was not administered at military facility. No additional vaccines administered on same date of the Pfizer suspect. The adverse events excess mucous, cough and not sleeping required a visit to the physician's office. No prior vaccinations (within 4 weeks). The outcome was not recovered for the events "has fits at night nothing seems to change/ constantly chocking and coughing", "excess mucous was reported as worsened" and "he was not sleeping because he was constantly chocking and coughing every second"; and unknown for the event "feeling funny". No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1277322
Sex: M
Age:
State: NY

Vax Date: 03/29/2021
Onset Date: 04/10/2021
Rec V Date: 05/01/2021
Hospital: Y

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: lower right side of his face drooping and unable to move it/ Bell's Palsy; This is a spontaneous report from a contactable consumer (patient). A 27-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: ER8733) via an unspecified route of administration, administered on the left arm on 29Mar2021 11:30 at a single dose for COVID-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. The patient previously took amoxicillin and experienced allergies. On 10Apr2021 09:00 AM, patient woke up with lower right side of his face drooping and unable to move it. Urgent care advised going to ER, he was put in a stroke protocol, MRI proved it to be Bell's Palsy; ruled out stroke, brain tumors, all blood work normal, echocardiogram normal. No Lyme. No other events or health issues, only change was taking the vaccine. The event resulted in emergency room/department or urgent care visit and hospitalization for 1 day. Therapeutic measures were taken as a result of the event which included valaciclovir (VALTREX) and prednisone (and lots of tests). COVID test post vaccination on 10Apr2021: nasal swab negative. The facility where the vaccine was administered was in a pharmacy or drug store. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There were no other medications the patient received within 2 weeks of vaccination. Outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1277323
Sex: F
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: fever 100.9; nausea; back pain; sleepiness; chills; fast heartbeat; This is a spontaneous report from a contactable consumer (parent) reporting for his daughter. A 17-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration as single dose and had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration as single dose for covid-19 immunization and stated was fine after the first dose. Patient was 17-years-old at the time of vaccination. The patient medical history and concomitant medications were not reported. The patient experienced fever 100.9, nausea, back pain, sleepiness, chills, fast heartbeat on an unspecified date. The outcome of event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277324
Sex: F
Age:
State:

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

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: hot flashes; body was hot all over; This is a spontaneous report from a non-contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and patient's concomitant medications were not reported. Patient got vaccine and got hot flashes and body was hot all over that night and was fine the next day. The event outcome for events was recovered. No follow up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277325
Sex: F
Age:
State: IL

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: she felt chills; feeling of tiredness; This is a spontaneous report from a contactable female consumer (patient) via Pfizer-sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on an unspecified date as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. Caller wants to check if she can have other vaccines for the 2nd dose instead of Pfizer since she got Pfizer for the first dose. She wants to know also why people are getting blood clots with other vaccines. She said she felt chills and a feeling of tiredness. The clinical outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277326
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Myalgia and fever lasting several days; Myalgia and fever lasting several days; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender 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 single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced myalgia and fever lasting several days. The outcome of the event was recovered. No follow-up attempts are needed, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277327
Sex: F
Age:
State: NJ

Vax Date: 04/13/2021
Onset Date: 04/13/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: I was on my 4th week pregnancy. The next day I took my second dose I had spotting and the third day I'm having a miscarriage. ( this is my third pregnancy); I was on my 4th week pregnancy. The next day I took my second dose; I was on my 4th week pregnancy. The next day I took my second dose; This is a spontaneous report from a contactable Other HCP (patient). A 43-year-old female patient (pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EP7534), second dose via an unspecified route of administration, administered in Arm Left on 13Apr2021 14:45 (at 43 years old, pregnant), single dose for covid-19 immunisation. The patient's medical history included that this was her third pregnancy. The patient's concomitant medications were not reported. The patient had his first dose of bnt162b2 on 23Mar2021 14:45 for covid-19 immunisation, left arm, lot number EP7534. Patient was on her 4th week pregnancy. The next day, she took her second dose, she had Spotting and the third day (also reported as 14Apr2021 15:00) she was having a miscarriage. Treatment was Received. The outcome of the event Miscarriage of pregnancy was recovering. No covid prior vaccination. 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. No Allergies to medications, food, or other products.; Sender's Comments: Based on the information currently available and known safety profile of the drug, a possible contributory role of suspect product Bnt162b2 to the reported events can not be ruled out. But product is not indicated in this population group. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1277328
Sex: F
Age:
State: NY

Vax Date: 03/01/2021
Onset Date: 03/18/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: She has not had the second dose. (1st dose 01Mar2021/PRD 15Apr2021); She has not had the second dose. (1st dose 01Mar2021/PRD 15Apr2021); received the first dose of the Pfizer COVID 19 vaccine on 01Mar. She tested positive for COVID on 18Mar; received the first dose of the Pfizer COVID 19 vaccine on March 1st. She tested positive for COVID on March 18; This is a spontaneous report from a Pfizer Sponsored Program. A contactable consumer (patient) reported that a 60-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number was not reported), via an unspecified route of administration on 01Mar2021 (at the age of 60-years-old) as a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that she received 1st Pfizer dose on 01Mar2021 and tested positive for Covid on 18Mar2021. On 22Mar2021 she received the antibody infusion and was wondering if she should receive the 2nd Pfizer shot. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1277329
Sex: F
Age:
State: ND

Vax Date: 03/17/2021
Onset Date: 03/18/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: hives; itching all over her body; This is a spontaneous report from a contactable consumer. A 51-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Left Arm on 17Mar2021 16:00 (Batch/Lot Number: EP7534) as SINGLE DOSE (at the age of 51 years) for covid-19 immunisation. Medical history included mycotic allergy from an unknown date, seasonal allergy from an unknown date ( Grass/ Weeds allergies), allergy to animal from an unknown (various animals), asthma from an unknown date, sinusitis from 2021 to an unknown date, fruit allergy from an unknown date (she has had reactions to strawberries, apples, basically every fruit except bananas). Concomitant medications included loratadine (LORATADINE) taken for outside allergies; triamcinolone acetonide (NASACORT) taken for sinus infection and budesonide, formoterol fumarate (SYMBICORT) taken for asthma. Patient states that she started immunotherapy around Oct2020 and gives herself unspecified "allergy shots" every other day. Dr. did not know how they would interact with Covid vaccine and sent her a letter advising her to stop allergy shots 48 hours before and 48 hours after receiving Pfizer COVID-19 vaccine, which she did. She started taking her allergy shots in 16Feb2021 and had no problems, no hives, no reactions, no itching until she got the Pfizer COVID-19 vaccine. The patient experienced hives on 18Mar2021 with outcome of recovering and itching all over her body on 18Mar2021 with outcome of not recovered. She had hives on her feet, neck, and legs. Therapeutic measures were taken as a result of hives and itching all over her body. She has taken Calamine lotion, oatmeal baths, and Benadryl (not brand name) to treat her symptoms. She has seen a doctor who prescribed steroids to take. She was prescribed Prednisone 20mg tablets twice a day on 13Apr2021. She states her doctor advised her to take a break on the allergy shots since on prednisone. She does have an Epi pen but didn't feel any kind of respiratory distress, she did not feel she needed to use it. No additional vaccines administered on same date of the Pfizer product. No other vaccines were given within 4 weeks of the Pfizer product. She states on 07Apr2021 she was supposed to get her second Pfizer COVID-19 vaccine, but she was advised not to take the second dose by her MD. She never had a reaction to any vaccination, and she has had unspecified pneumonia and flu vaccinations. No follow-up attempts are possible; No further information is expected.

Other Meds: LORATADINE; NASACORT; SYMBICORT

Current Illness:

ID: 1277330
Sex: F
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: sore arm; This is spontaneous report received from a non-contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced sore arm on an unspecified date with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277331
Sex: M
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: body aches; fatigue; sore ''armpit''; This is spontaneous report from a contactable consumer (Patient) reported for himself. A male patient of unspecified age received second dose of BNT162b2 (Pfizer-BioNTech COVID-19 Vaccine), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced body aches, fatigue, sore ''armpit'', all on an unspecified date with outcome of unknown. Event took place after use of product. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277332
Sex: U
Age:
State: CT

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Foggy head; lots of anxiety; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received bnt162b2 (BNT162B2), via an unspecified route of administration on an unspecified date (Lot number was not reported) as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced foggy head, lots of anxiety on an unspecified date. The outcome was unknown. Pfizer is a marketing authorization holder of BNT162B2 in the country of incidence or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of BNT162B2 has submitted the same report to the regulatory authorities. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277333
Sex: F
Age:
State: MA

Vax Date: 03/18/2021
Onset Date: 03/18/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Sore arm at injection; back ache; body aches; chills; swollen tongue; burning eyelids(inner); nausea; headache; fatigue; This is a spontaneous report from a contactable physician. A 68-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose intramuscular, administered in left deltoid on 18Mar2021 09:55 (Batch/Lot Number: Er2613) as single dose for covid-19 immunisation. Medical history low back pain, ACP (advance care planning), chronic constipation, allergic rhinitis caused by unspecified, postmenopausal asymptomatic status sp hysterectomy with BSO, osteoarthritis hands, other and unspecified hyperlipidemia, overweight (BMI 25.0-29.9), osteopenia, ex-cigarette smoker, fatigue. Concomitant medication(s) included atorvastatin calcium (LIPITOR) taken for hyperlipidaemia; biotin; colecalciferol (VITAMIN D3 1000); loratadine (CLARITIN ONCE-A-DAY) taken for allergy symptoms; melatonin taken for sleep; plantago afra (PSYLLIUM SEEDS) taken for constipation; ascorbic acid, cupric oxide, dl-alpha tocopheryl acetate, xantofyl, zeaxanthin, zinc oxide (OCUVITE LUTEIN & ZEAXANTHIN); vitamin b complex (B-COMPLEX). Patient previously took BNT162B2 first dose on 25Feb2021 21:00 (lot number: EN60205) experienced back ache, tired and fatigue, treatment received and went to chiropractor for back ache. The patient experienced back ache, body aches, chills, swollen tongue, burning eyelids(inner), nausea, headache, fatigue, all on 18Mar2021; sore arm at injection on unspecified date. The event outcome for sore arm at injection was recovered on unspecified date, for other events was recovered on 21Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: LIPITOR [ATORVASTATIN CALCIUM]; BIOTIN; VITAMIN D3 1000; CLARITIN ONCE-A-DAY; MELATONIN; PSYLLIUM SEEDS; OCUVITE LUTEIN & ZEAXANTHIN; B-COMPLEX [VITAMIN B COMPLEX]

Current Illness:

ID: 1277334
Sex: M
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: fever; chills; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), Lot number: Expiry date: Unknown, dose 1 via an unspecified route of administration on an unspecified date at SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified sate the patient experienced fever and chills. Outcome of the event was recovered on an unspecified date. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277335
Sex: M
Age:
State:

Vax Date: 04/03/2021
Onset Date: 04/13/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

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

Symptoms: caller got positive result of COVID 19 after first shot/tested positive; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 58-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot number: unknown), via an unspecified route of administration on 03Apr2021 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient stated that at first he had no side effects. Then, last Saturday on 10Apr2021, he started getting a headache and a cough. Sunday on 11Apr2021, it got worse. Monday on 12Apr2021 he had a fever. On 13Apr2021, Tuesday he was getting ready to go to work but he tested positive. He was still going through it but he's wondering if he can get the second dose. He also mentioned that they told to him to isolate for 10 days from the time he showed symptoms, then he can go get tested. He has to get 2 negative tests before going back to work. Patient got positive result of COVID 19 after first shot. The outcome of event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1277336
Sex: F
Age:
State:

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

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: allergic to the Pfizer covid vaccine; swollen lip; rash; few hives; This is a spontaneous report from a contactable consumer (Patient) via medical information team. A 55-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, lot number: unknown) via an unspecified route of administration on an unspecified date for COVID-19 immunization. Medical history and concomitant medication were not reported. On an unknown date, patient stated she was allergic to the Pfizer covid vaccine, from the first dose. She had swollen lip and a few hives. Her doctor prescribed her steroids and the hives/rash comes back once she finishes the steroids treatment. She wanted to know what she can do about her symptoms. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277337
Sex: F
Age:
State: PA

Vax Date: 04/10/2021
Onset Date: 04/10/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: stomach spasms; loose stools; This is a spontaneous report from contactable consumer (patient) via medical information team. A 73-year-old female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: Unknown), via an unspecified route of administration on 10Apr2021 at 10:50 (at the age of 73-years-old) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. No additional vaccines administered on same date of the Pfizer suspect. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, batch/Lot Number: EN6206) on 20Mar2021 (at the age of 73-years-old) for COVID-19 immunization. The patient received vaccine within 4 weeks prior to the next dose of vaccine. On 10Apr2021 at 23:30 the next night, she started to have "stomach spasms" that lasted all night and into the morning. She also reports some loose stools, but did not classify them as diarrhea. She reports that she is "still having terrible spasms". After she came home, she was ok, but then she was up all night going to the bathroom with severe stomach spasms. Patient reported severe stomach spasms and diarrhea and took Bentyl, Diarrhea medicine, Gaviscon, nothing seems to be working. A visit to emergency room and physician office not required for events. She should have went somewhere but she did not. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277338
Sex: F
Age:
State: MN

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

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data:

Allergies:

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

Symptoms: I got tested because of my job and I tested positive; I got tested because of my job and I tested positive; allergies; stuffy nose; This is a spontaneous report from a contactable consumer (Patient herself). A 43-year-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot/Batch number: Unknown, Expiration date: Unknown) via an unspecified route of administration on 01Apr2021 as single dose for covid-19 immunization. Medical history and Concomitant medication were not reported. The patient experienced allergies, stuffy nose on Apr2021 and on 14Apr2021 patient tested positive. The patient stated she had allergies and had them for three weeks and was around someone that tested positive and so got tested because of her job and tested positive. She had a stuffy nose but that was her only symptom and her 10 days of quarantine would be complete. Scheduled second dose on 23Apr2021. The outcome of the event allergies was recovered. and the outcome of all other events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277339
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: arm pain; This is a spontaneous report received from a non-contactable consumer (patient). A patient of unspecified age and gender received BNT162b2 (Pfizer-BioNTech COVID-19 Vaccine), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced arm pain on an unspecified date with outcome of unknown. Event took place after use of product. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277340
Sex: F
Age:
State: FL

Vax Date: 04/02/2021
Onset Date: 04/01/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (the patient) reported that a 47-year-old female patient received the first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6206; Expiration Date: 30Jun2021) via an unspecified route of administration in left arm on 02Apr2021 17:00 at age of 47-year-old at single dose for COVID-19 immunisation. Medical history was reported as "none". Concomitant medications included ergocalciferol (VIT D), collagen, biotin, curcuma longa (TURMERIC), aloe vera, malus domestica (VINEGAR APPLE CIDER PLUS), and all of the natural vitamins. The patient took these every singe day. She was taking all the above vitamins because she was 47 years old and she wanted her skin different and she wanted to prevent the COVID. She had oil essence that she put on every single day and she had for more than one year it was the essential oil that she put in her diffuser with water and it was to prevent sickness. None prior vaccination within 4 weeks prior. Relevant Family History related to AE(S) was none. The patient received her 1st dose of Pfizer vaccine on 02Apr2021. She received a positive COVID test result on 04Apr2021. After 10-11 days she felt really good, she had only mild symptoms. She just had one or two days of body aches and that's it. 2nd dose was due 23Apr2021. The patient said she did not get COVID from the vaccine but was positive because of her husband who has allergies and cough every day of the year. He caught COVID at the restaurant (One family had invited them to go to a restaurant with them and inside the restaurant it was crazy. There were more than 80 people in there and that's it, after that her husband got the positive COVID test and then her daughter and then finally her), but they did not know because the symptoms were exactly the same as his pollen allergy. When she had the vaccine she had COVID in her body already. The only thing that she felt after the vaccine was a little cold (Apr2021), but the weather in the city was crazy, the temperature was around 50 and she said "oh perfect," she was going to get a cold after the vaccine. She thought that it wasn't the vaccine that caused it, she caught a cold because suddenly the weather was around 50 and she told her daughter that she needed a sweater and she gave her sweater to her daughter and she thought that she got a cold, but that was the only thing she felt. Another thing, when they put the vaccine in the area where she got the vaccine it was a little pain after the vaccine and she could feel it in her muscle. That was the only thing. It was muscle pain but only a little one. She thinks that began around the second day, 03Apr2021. She confirmed that she has recovered completely and added that currently she felt perfect. Caller said that she didn't remember when her muscle pain ended, it disappeared. The person that is with the department of health said that the caller didn't need to repeat her COVID test but she said that she was going to repeat her test because she wanted a negative test result. The person she spoke to said to wait 19 days to do the test because she can get positive results and then after 10 days she would not be contagious anymore. She would be able to walk outside of her house because she would not be contagious but the caller said that she wanted to wait until she got a negative result because COVID had got all of her family, her little one, her husband and her. The person that entered the COVID virus in her house was her husband. But she was confused because every single day of his life he has a cough. She thought the pollen was heavy outside and he coughed from that and then the same day they she the vaccine they had the same appointment. She told her husband to go to the doctor and asked if he can still have the vaccine and see if he has allergies so hard and that is it. He wasn't having allergies, it was COVID. Probed if the caller's husband had the COVID vaccine the same day that she did and she said that her husband had cancelled his appointment. The only person that has received the COVID vaccine that day was her because she thought that she just had the same allergy that he was having. She felt something about two days ago and said "what?" but she had to attend to everyone in the house and honestly she didn't have enough. Just had one or two days of body aches: She got her vaccine Friday, 02Apr2021, she had the positive result on Sunday, 04Apr2021, but that Friday night, 02Apr2021, she had body aches in her legs only but she walked a lot. She felt tired and her legs had muscle pain (onset date unknown). She felt tired currently and that was the only thing. What she had wasn't chills, but it was weird she has never felt that kind of chill before, it was inside the muscles. It was weird. It was different. The next day she called the doctor and he told her that she was positive for COVID and then her symptoms started the night before that and he said to take some medicine and that is it. She took it and the second day she was perfect. Caller confirmed that it was either Tuesday, 06Apr2021, or Wednesday, 07Apr2021, that she felt better. She confirmed that she has recovered completely from the body aches. She cough likes (she gave an example of the cough) and that is it. Probed if she still has the cough currently and she said that she did not have it at the date of report. The only thing was that if she had to clean the house or exercise, she can feel a little bit tired and then she has to rest. No further details provided. The only thing was the day she got the first symptom her period appeared and it was different because she had a lot of pain and in all of her life she has never gotten pain. She had a lot, a lot of pain in her pelvic area and it was in the coccyx area. It was a discomfort pain, it was weird. The first day of the period with the pain was 08Apr2021. Probed for how long she had the pain and she said it was the day before her period, the day of her period and then it disappeared the next day. It was really weird pain but she supposed it was because she had COVID. Confirmed began on 07Apr2021 and it went away on 09Apr2021 which was the day after. She has recovered completely. She had a COVID test on 04Apr2021 and had a repeat test on 05Apr2021 and both were positive. Someone said to repeat the test because she had the vaccine on that Friday and maybe she had a false positive and she thought about how her daughter didn't get the COVID vaccine and she was positive so the caller thought that she has to be positive too. And that is it, she repeated it at the convention center and she received the positive result again. Someone said that she needed to retest in 19 days, she asked if it was correct. For question if any AE(s) require a visit to: emergency room or physician office, the patient said yes (as reported), she had an over the phone appointment with her doctor because she got the positive COVID result and she wanted to ask him about what happened to her body. She had the vaccine and then had COVID with no symptoms inside her body. She said what happened? And someone she spoke to said that she would have to call her doctor because they didn't know. Nothing happened and the doctor said that she could get COVID without the vaccine because she didn't have enough time to protect her body. If she had gotten COVID after the vaccine, about 10 days then she would feel less. The outcome of events "a little pain after the vaccine and she could feel it in her muscle/her legs had muscle pain", "just had one or two days of body aches/body aches in her legs only" was recovered in Apr2021, "her period appeared and it was different because she had a lot of pain and in all of her life she has never gotten pain", "pain in her pelvic area and it was in the coccyx area", " was recovered on 09Apr2021, the outcome of other events was unknown.

Other Meds: VIT D; COLLAGEN; BIOTIN; TURMERIC [CURCUMA LONGA]; VINEGAR APPLE CIDER PLUS

Current Illness:

ID: 1277341
Sex: F
Age:
State: IA

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Vasovagal; This is a spontaneous report from a contactable physician reported on behalf of the daughter(patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced vasovagal after injection on an unspecified date with outcome of unknown. Physician asked if Pfizer had any information on syncope in terms with Covid vaccines? He said his daughter had a vasovagal after injection. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277342
Sex: F
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: eosinophilia esophagitis; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on an unspecified date as SINGLE DOSE for covid-19 immunisation . The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced eosinophilia esophagitis on an unspecified date with outcome of unknown after full course of COVID vaccine and nothing else in her life changed. No follow-up attempts are possible. No further information is expected. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277343
Sex: M
Age:
State: MN

Vax Date: 03/31/2021
Onset Date: 04/15/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: positive Covid result; positive Covid result; This is a spontaneous report from a contactable consumer (patient). A 58-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, administered in left arm on 31Mar2021 11:00 (Lot Number: ER8734) as single dose for COVID-19 immunisation. Medical history included hyperlipidemia, essential hypertension, subarachnoid hemorrhage. No known allergies. Patient had no Covid prior vaccination. Concomitant medications included fenofibrate; losartan potassium (LOSARTIN). No other vaccine in four weeks. The patient started having flu-like symptoms 10 days after vaccine (10Apr2021), including low grade fever, body aches, exhaustion, difficulty breathing, cough, sore throat, upset stomach and bad headache. Blood tests on 14Apr2021 showed infection, inflammation and ultimately positive Covid result (Nasal Swab) on 15Apr2021. No treatment received. Adverse events resulted in Doctor or other healthcare professional office/clinic visit. Outcome of the events was recovering.

Other Meds: FENOFIBRATE; LOSARTIN

Current Illness:

ID: 1277344
Sex: F
Age:
State: WI

Vax Date: 03/31/2021
Onset Date: 04/06/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: headache; nausea; light headed/ dizziness; unsteady gait; vomiting; chills; sweats; superficial blood clot; pain to back of Rt knee; bruising; swelling; This is a spontaneous report from a contactable Nurse. A 57-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscularly, administered in Arm right on 31Mar2021 (Batch/Lot Number: EW0150) (at age of 57-year-old) as single dose for COVID-19 immunisation. Medical history included osteoarthritis, and migraines. The patient's concomitant medications were not reported. The patient previously took the first dose of BNT162B2, intramuscularly, administered in left Arm on 10Mar2021 (at age of 57-year-old) (Lot number: EN6207) for COVID-19 immunisation. It was unknown if other vaccine in four weeks. It was unknown if COVID prior vaccination. The patient experienced onset of pain to back of Rt knee, bruising, and swelling on 06Apr2021. She called doctor on 09Apr2021, provider diagnosed her with superficial blood clot. Treating with applying warm compress to area. Client had onset of headache, dizziness, nausea, light headed, unsteady gait, vomiting, chills and sweats on 10Apr2021. Patient called doctor on 14Apr2021, they recommended covid-19 testing, results are negative on 12Apr2021. Symptoms ongoing since 14Apr2021. The outcome of events was not resolved.; Sender's Comments: Based on plausible temporal association, a causal association between the reported event thrombosis and suspect drug bnt162b2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1277345
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: fever; chills; sweaty; This is a spontaneous report received from a contactable physician via a Pfizer sponsored program. A patient of an unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number and expiration Date not reported) via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. The patient experienced fever, chills and sweaty on an unspecified date. The outcome of the events was reported as unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1277346
Sex: M
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: contracted Covid 19; contracted Covid 19; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that the patient contracted Covid19 in between doses. They are asking if the patient can get the second dose, now that he shows no symptoms and has completed quarantine. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1277347
Sex: F
Age:
State: WA

Vax Date: 03/12/2021
Onset Date: 04/01/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: difficulty breathing/breathing problems; increased blood pressure/blood pressure really high; itching incessantly; This is a spontaneous report from a contactable other health professional (patient) received via Medical Information Team. A 58-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in arm right on 12Mar2021 at 09:30 (Lot Number: EN6198) (at the age of 58-year-old) as single dose for COVID-19 immunisation. Medical history included a couple of surgeries, prediabetic, breaking out with blisters on chin, hormone replacement, insomnia, muscle pain, blood pressure abnormal, depression, iron deficiency, allergies and itching, all from an unknown date and unknown if ongoing. Concomitant medications included metformin (formulation: tablet) oral at 500 mg once a day taken for prediabetic from 2019 and ongoing; acyclovir at 400 mg twice a day taken for breaking out with blisters on chin from an unspecified start date and ongoing; estradiol (formulation: tablet) at 1 mg once a day taken for hormone replacement from 2019 and ongoing; medroxyprogesterone acetate (PROVERA) at 2.5 mg once a day taken for hormone replacement therapy from 2019 and ongoing; trazodone HCl (formulation: tablet) at 100 mg once a day taken for insomnia from 2016 and ongoing; meloxicam at 15 mg once a day taken for muscle pain from 2016 to an unspecified stop date; hydrochlorothiazide at 50 mg once a day taken for blood pressure abnormal from 2016 and ongoing; buspirone (formulation: tablet) at 10 mg thrice a day taken for depression from 2016 and ongoing; ferrous sulfate (FEROSUL, formulation: tablet) at 65 mg twice a day taken for iron deficiency from 2016 and ongoing; cetirizine (formulation: tablet) at 10 mg once a day taken for allergies from Feb2021 and ongoing; hydroxyzine (formulation: tablet) oral at 25 mg taken for itching from Feb2021 and ongoing. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular, administered in arm left on 19Feb2021 (Lot Number: EN6200) (at the age of 58-year-old) as single dose for COVID-19 immunisation. The patient reported that blood pressure was really high on 09Apr2021. On 10Apr2021 she woke up from sleeping due to difficulty breathing/breathing problems and went to the emergency room (ER) at 03:00. Caller stated they found out in the ER that her blood pressure was high. She stated that in the ER they didn't do anything but took her blood pressure and watched her blood pressure. Caller stated she was not admitted, she was there for 4 hours and sent home. Caller stated her blood pressure was over 200 and they still let her go home. Caller stated she went into the doctor on 12Apr2021 at 15:00 and got some medicine for the itching, at that time her blood pressure was down. Patient stated that itching could have been a reaction from one of the drugs she was given. Therapeutic measures were taken as a result of the blood pressure, the patient started a new medication, LOSARTAN at 50mg one time a day and got some medicine for the itching. The patient outcome of difficulty breathing/breathing problems and increased blood pressure/blood pressure really high was recovering and of itching was not recovered. No follow-up attempts are needed. No further information is expected.; Sender's Comments: The contributory role of the suspect product BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot Number: EN6198), to reported events is possible. Tis case will be reassessed if follow-up information is received.

Other Meds: METFORMIN; ACYCLOVIR [ACICLOVIR]; ESTRADIOL; PROVERA; TRAZODONE HCL; MELOXICAM; HYDROCHLOROTHIAZIDE; BUSPIRONE; FEROSUL; CETIRIZINE; HYDROXYZINE

Current Illness:

ID: 1277348
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: slight headache; This is a spontaneous report from a Pfizer-sponsored program. A contactable nurse reported that a patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced slight headache for 5 minutes on unspecified date. The outcome of the event was resolved on unspecified date. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277349
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: chills overnight; FEVER; SWEATY; This is a spontaneous report from a received from Pfizer program. A contactable nurse reported that patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced chills overnight, fever, sweaty. Outcome of events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277350
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: This is an Initial spontaneous report from a Pfizer Sponsored Program COVAX US Support. A contactable nurse reported that a patient of unspecified age and gender received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced pain in injection arm. Outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277351
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: Sore; This is a spontaneous report from a received from Pfizer colleagues Immediate Family and household Vaccination program. A contactable nurse reported that a patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced sore on unknown date. Outcome of event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277352
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Muscle aches; This is a spontaneous report from a received from Pfizer colleagues Immediate Family and household Vaccination program. A contactable nurse reported that a patient of unspecified age and gender received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced muscle aches on an unspecified date. Outcome of event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277353
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: loss of appetite; This is a spontaneous report from a Pfizer Sponsored Program COVAX US Support from a contactable other hcp. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced loss of appite 24 hours on an unspecified date with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277354
Sex: U
Age:
State:

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

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

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

Symptoms: body aches; This is a spontaneous report received from a Pfizer sponsored program. The contactable nurse reported that a patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date as SINGLE DOSE for covid-19 immunisation . The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced body aches on an unspecified date with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277355
Sex: U
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: brain fog grassy; Feeling off; cold; This is a spontaneous report from a Pfizer-sponsored program, . A contactable nurse reported that a patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient had cold for 1 week (brain fog grassy feeling off) on unspecified date. He stated he felt the same way after a flu shot. The outcome of the events were unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277356
Sex: M
Age:
State: IL

Vax Date: 03/25/2021
Onset Date:
Rec V Date: 05/01/2021
Hospital: Y

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: he was in hospital at the intensive care for 3 weeks and he is still ill; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on 25Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient wants to cancel his 2nd dose appointment because was hospitalized and stayed 3 weeks in intensive care. Cannot take the 2nd shot because still ill. The patient was hospitalized for the event for 21 days. The outcome of the event was unknown. Information about lot/batch has been requested.; Sender's Comments: Linked Report(s) : PFIZER INC-2021421729 similar report from same reporter

Other Meds:

Current Illness:

ID: 1277357
Sex: F
Age:
State: IL

Vax Date: 03/18/2021
Onset Date: 03/23/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: allergic reaction; hives on the arm, described as rash down the arm where she received the injection; hives on the arm, described as rash down the arm where she received the injection; This is a spontaneous report from a contactable pharmacist. A 39-year-old female patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6201) on 18Mar2021 as single dose in deltoid right for covid-19 immunisation at the age of 39-year-old. The patient medical history and concomitant medications were not reported. The patient experienced hives on the arm, described as rash down the arm where she received the injection 5 days after receiving the vaccine, the pharmacist considered it as an allergic reaction. The second dose of vaccine was scheduled 28 days after the first vaccine, the patient was at risk for not getting the second dose of vaccine, due to previous reaction. The reporter considered the events were contraindicated and wanted to check with Pfizer to see if it is alright to get the second vaccine. Outcome of the events was unknown. The events were assessed as non-serious by pharmacist. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1277358
Sex: F
Age:
State: NY

Vax Date: 03/23/2021
Onset Date:
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: I had a headache for 10 days; 5 days were migraine-like'; This is a spontaneous report from a contactable consumer from a Pfizer sponsored program. A 56-year-old female (patient) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Formulation: Solution for injection, Batch/Lot Number: unknown; Expiration Date: unknown), via an unspecified route of administration on 23-MAR-2021 as single dose for covid-19 immunization. The patient medical history and concomitant medication were not reported.Caller reported that 'When I recieved the 1st vaccine, I had a headache for 10 days, 5 days were migraine-like'. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277359
Sex: F
Age:
State: GA

Vax Date: 03/23/2021
Onset Date: 03/23/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: low fever; diarrea; headache; fatigue; This a spontaneous report received from consumer (patient) via a Pfizer Sponsored program. A female patient of an unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot and expiration date was not reported) via an unspecified route of administration on 23Mar2021 as single dose for COVID-19 immunization. Medical history included acid reflux, other gastrointestinal issues, patient was allergic to bee stings, delayed allergic reaction to codeine medication, allergic to IV contrast, lactose intolerant and can't tolerate dairy products. Concomitant medications were not reported. Patient previously took probiotics, zinc, vitamins and minerals (prior to getting her first dose but would like to know if they interfere with the vaccine). On 23Mar2021, after first dose of vaccine patient experienced low fever, diarrhea, headache, and fatigue. Patient inquired about possible drug interactions between the vaccine and probiotics and vitamins they take for acid reflux and other gastrointestinal issues. Outcome for the events were unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1277360
Sex: F
Age:
State:

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Received their first doses/Tested positive for covid illness; Received their first doses/Tested positive for covid illness; This is a spontaneous report from a contactable consumer (patient). This consumer reported similar events for two patients (patient herself and husband). This is the first of two reports. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in Apr2021 (Batch/Lot number was not reported) as a single dose for COVID-19 immunisation. The patient's medical history included COVID-19 exposure. Concomitant medications were not reported. The patient and her husband received their first doses of COVID-19 vaccine in Apr2021, and both tested positive for COVID illness in Apr2021. They believe their exposure was the day they received their vaccination, as her husband came in contact with COVID-19 the same day. The patient had two negative tests for COVID-19 in Apr2021. Their second dose is scheduled on 23Apr2021. Outcome of the event was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021421935 Same reporter, product, event; different patient

Other Meds:

Current Illness:

ID: 1277361
Sex: M
Age:
State:

Vax Date: 04/01/2021
Onset Date: 04/15/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: Right in the center of chest is tender; feel like it's muscle pain when I push on it; This is a spontaneous report from a contactable consumer (patient). A 59-years-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration in Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. It was reported that the patient got his second shot Tuesday (Apr2021), woke up this morning (15Apr2021) and right in the center of chest is tender. He wanted to know this is because of the shot. It does feel like it's muscle pain when he pushed on it. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1277362
Sex: F
Age:
State: GA

Vax Date: 04/14/2021
Onset Date: 04/14/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

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

Symptoms: moderate nausea; severe headache; moderate joint pain; Muscle pain; So bad she cannot get up from the bed; pain at injection site; small redness at injection point; chills; fever 102 F; She couldn't sleep well due to fever and chills.; This is a spontaneous report from a contactable consumer and Follow-up (15Apr2021) received from same reporter processed together with initial information. A 49-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: ER8727) via an unspecified route of administration on 14Apr2021 at 10:00 as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 14Apr2021, 3-4 hours after the patient experienced pain at injection site, small redness at injection point, At night chills, fever 102 f, patient couldn't sleep well due to fever and chills and On 15Apr2021, moderate nausea, severe headache, moderate joint pain, muscle pain, so bad she cannot get up from the bed. The patient underwent lab tests and procedures which included body temperature increased: 102 Fahrenheit on fever 102 F. Outcome of the event's moderate nausea, severe headache, moderate joint pain and muscle pain was not recovered, and remaining events was unknown.

Other Meds:

Current Illness:

ID: 1277363
Sex: F
Age:
State: WI

Vax Date: 04/13/2021
Onset Date: 04/14/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: unconscious; seizure; throwing up while unconscious; This is a spontaneous report from a contactable other healthcare professional (patient). A 23-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: Ew0169), dose 1 intramuscular, administered in Arm Right on 13Apr2021 14:45 (at the age of 23years) as single dose for Covid-19 immunization. The patient is not pregnant at the time of vaccination. There were no medical history and concomitant medications. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that on 14Apr2021 (10:15 PM), the patient was unconscious for about 15 seconds, having a seizure for 5 seconds, and throwing up while unconscious. The adverse events resulted in Emergency room/department or urgent care. There was no treatment received for the adverse event. The patient has not been tested for COVID-19 since the vaccination. The outcome of events was recovering.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events loss of consciousness, seizure, vomiting and the suspect vaccine BNT162B2. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1277364
Sex: M
Age:
State: SC

Vax Date: 04/13/2021
Onset Date:
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: experienced a lymph node under his arm on the same side he got the shot/swollen lymph node; This is a spontaneous report from a contactable consumer or other non hcp. A 43-years-old male patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: Batch/Lot Number: unknown; Expiration Date: unknown), dose 1 via an unspecified route of administration on 13Apr2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced a lymph node under his arm on the same side he got the shot/swollen lymph node (lymphadenopathy). The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1277365
Sex: F
Age:
State: FL

Vax Date: 02/19/2021
Onset Date:
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: tested positive again for Covid 19 during pre-op labs/asymptomatic; tested positive again for Covid 19 during pre-op labs/asymptomatic; This is a spontaneous report from contactable consumers. A 67-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration on 19Feb2021 (Batch/Lot Number: EN6200; Expiration Date: Jun2021) at a single dose and dose 1 via an unspecified route of administration on 29Jan2021 (Batch/Lot Number: EL9262; Expiration Date: May2021) at a single dose, for COVID-19 immunization. Medical history included kidney disease, high blood pressure, and also had Covid in Dec2020. Concomitant medications included unspecified blood thinner, high blood pressure pills and a heart medication. The patient is a 67-year-old female who had Covid 19 in Dec2020, was vaccinated with both doses of the Pfizer Covid 19 vaccine, and just tested positive again for Covid 19 during pre-op labs. She was asymptomatic and doesn't know where she would have gotten it. It was also reported that, now, the patient caught Covid again which she doesn't know how. She was getting ready for open-heart surgery that week and they did pre-op and they said she was Covid positive again. She was also calling about her son and grandson who received the first doses of the Pfizer Covid 19 vaccine last week and have been exposed to her. She is afraid they might have Covid 19 now too and they are being tested for it. The patient also asked how it would affect their second dose that is scheduled for 27April2021. The patient underwent lab tests and procedures which included blood work with unknown results. She said her COVID-19 Virus RPR (rapid) test was also negative when she had it done on an unspecified date in 2021, and a Covid 19 positive test result on an unspecified date in 2021. She had 3 or 4 then on 9th on Saturday, the 9th that's when she found she was Covid positive. The event outcome was unknown.

Other Meds:

Current Illness:

ID: 1277366
Sex: F
Age:
State:

Vax Date: 01/18/2021
Onset Date: 01/28/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: she was tested positive for covid; This is a spontaneous report from a contactable nurse (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date unspecified), via an unspecified route of administration on 18Jan2021 as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 28Jan2021, 10 days later after she received her first dose, the patient was tested positive for covid. She stated she had not received her second dose of the vaccine and was asking when can she get it. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on 28Jan2021. Outcome of event was unknown. Information on lot number/batch number has been requested.

Other Meds:

Current Illness:

ID: 1277367
Sex: M
Age:
State: CT

Vax Date: 03/23/2021
Onset Date: 03/01/2021
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: tested positive for Covid; This is a spontaneous report from a contactable consumer (patient). A 52-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Mar2021 (Batch/Lot number was not reported) as single dose (dose 1) for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received first dose of Pfizer BioNTech Covid 19 vaccine on 23Mar2021 and then 3-4 days later tested positive for COVID and had it for 8 days (as reported, pending clarification). He was scheduled to receive second vaccine on 20Apr2021. The patient underwent lab tests and procedures which included SARS-COV-2 test: positive in Mar2021. The outcome of the event was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1277368
Sex: U
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 05/01/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

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

Symptoms: the platelet level was 101,000; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received the second dose of bnt162b2, via an unspecified route of administration on 31Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2, via an unspecified route of administration on 10Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Recently physician ordered screening labs prior to a medication initiation and the platelet level was 101,000. The platelets were noticed to be clumped in the lab tube, this is being repeated. Her physician is performing follow-up testing in 2 weeks. The outcome of the event was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm