VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
PLEASE CHECK BACK SOON
Download the files above while you wait.






Manufacturers

Total Manufacturer
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: 1364108
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: experienced chills, fatigue; experienced chills, fatigue; felt lousy/wasn't able to go to work because she doesn't feel well; muscle pain; she doesn't feel well; This is a spontaneous report from a Non-contactable consumer (Patient) via Pfizer sponsored program. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, lot number and Expiration Date: not reported), via unspecified route on an unknown date at single dose for covid-19 immunization. The patient's medical history and concomitant medication was not reported. It was reported that the patient got first shot last Saturday and after a few hours she experienced chills, fatigue and muscle pain and yesterday she felt lousy and got chills again. This morning she wasn't able to go to work because she doesn't feel well. 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: 1364109
Sex: F
Age:
State: IL

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 06/01/2021
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: body ache; mild chills; This is a spontaneous report from a contactable other healthcare professional (nurse, patient). A 62-year-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection) via an unspecified route of administration, administered in Arm Left on 13Jan2021 at 16:15 (at the age of 62-years-old) as single dose for covid-19 immunisation. The patient's medical history was not reported. The patient's concomitant medication included docusate and naproxen sodium (NAPROSYN). The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration, administered in Arm Left on 22Dec2020 at 16:15 (at the age of 62-years-old) as single dose for covid-19 immunisation. On 14Jan2021 at 19:00, the patient experienced body ache, mild chills and no fever. The patient took acetominophen with relief. The outcome of the event was recovered on an unknown date. Therapeutic measures were taken as a result of body ache and mild chills. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds: DOCUSATE; NAPROSYN [NAPROXEN SODIUM]

Current Illness:

ID: 1364110
Sex: M
Age:
State: VA

Vax Date: 01/08/2021
Onset Date: 01/01/2021
Rec V Date: 06/01/2021
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: diarrhea; Borborygmi; This is a spontaneous report from a contactable physician. This 87-year-old male physician reported for himself that an 87-year-old male patient received first dose of BNT162B2 (solution for injection, lot number: EL3302, Expiration Date: Unknown), via an unspecified route of administration on 08Jan2021 in his left arm at about 2:00PM at single dose for COVID-19 immunization. The Patient Medical history included Hypertension, GERD. Concomitant medications were not included. that the patient received second dose of BNT162B2 (solution for injection, lot number: EL9263, Expiration Date: Unknown), via an unspecified route of administration on 29Jan2021 in his left arm in his left arm at about 12:30PM. at single dose for COVID-19 immunization. On Jan2021 Borborygmi (clarified as belly gurgling) and he also experienced diarrhea. He said it is annoying to hear his belly gurgling. He said the Borborygmi and diarrhea started 10 days after his first COVID-19 Vaccine shot. The Patient reported he had a phone call with his doctor on Monday, 01Feb2021, due to snow, and his doctor put him on probiotics. He said he was getting better with taking the probiotic. The outcome of the event was resolving. Relatedness of drug to reactions was reported as related for diarrhea and Borborygmi. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364111
Sex: F
Age:
State:

Vax Date: 02/02/2021
Onset Date:
Rec V Date: 06/01/2021
Hospital:

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: I got the vaccine yesterday and I have only had arm soreness as a negative side effect.; Cough; breathing is very clear today even though I have asthma/My nose would frequently swell shut and now my nose is very clear/now after the vaccine the rash is gone/My eyes would water a lot and now my eyes feel almost normal today; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 02Feb2021 (Batch/Lot number was not reported) as UNKNOWN, SINGLE for covid-19 immunisation. Medical history included A\allergies, respiratory infection, asthma and rash. The patient's concomitant medications were not reported. The patient experienced "i got the vaccine yesterday and i have only had arm soreness as a negative side effect" cough and "breathing is very clear today even though i have asthma/my nose would frequently swell shut and now my nose is very clear/now after the vaccine the rash is gone/my eyes would water a lot and now my eyes feel almost normal today". It was reported that when the patient heard vaccines were being developed, she heard they were not including pregnant women or people with severe seasonal allergies. She informs that she might be an interest specifically for a study. Her allergies are in the 39,000 range. She got the vaccine yesterday and she has only had arm soreness as a negative side effect. However, she had had some very good side effects as well. Last night she coughed up a lot of old nodules from a respiratory infection she had a year ago. Her breathing is very clear today even though she has asthma. Her nose would frequently swell shut and now her nose is very clear. Her skin was broken out before the vaccine, so much so that she used a different arm because of the rash and now after the vaccine the rash is gone and is only a little pink where it was before. Her eyes would water a lot and now her eyes feel almost normal today. When she told her friend about this, she said her mom actually coughed up a lot of old infection nodules as well. Outcome of the events were unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364112
Sex: F
Age:
State:

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 06/01/2021
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: I got a rash on my chest, back, and neck. No other symptoms other than being about to see the rash; This is a spontaneous report from a contactable consumer (patient, self-reported). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number and Expiry date: not reported), dose 1 via an unspecified route of administration, on 07Jan2021, as single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 07Jan2021, about an hour after the vaccination, the patient experienced rash on her chest, back, and neck. No other symptoms other than being about to see the rash. On 04Feb2021, tomorrow, the patient due to get her second shot. The patient wanted to double check that it would be ok after having the reaction to the first one. The outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364113
Sex: M
Age:
State: FL

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 06/01/2021
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: Muscles hurt and was weak; Muscles hurt and was weak; got excited; tongue became swollen; fell down; felt so weak that he could not lift himself to get up; This is a spontaneous report from a contactable consumer or other non-hcp (Patient). A 78-year-old male 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 25Jan2021 as a single dose for COVID-19 immunization. Medical history included COVID-19 from Jul2020 to an unknown date; he also mentioned that he had COVID-19 back in July but has already recovered. The patient's concomitant medications were not reported. On an unspecified date in Jan 2021, the following day, he woke up and his tongue was swollen. He got excited and called doctor and he went in. He went to get dressed and as he went in, he fell down. Then he is trying to get up and cannot get up. He layed there for 1/2 hour. He could not get up. He was trying and trying. His wife had to call neighbors to help him get up. He did not want to go to the hospital and wait for 2-3 hours. He took some Benadryl and a couple of Aspirin and fell asleep. The following day when he woke up, his mouth was not swollen and he was able to get up and around. His muscles hurt and he felt like a weakling. The clinical outcome of tongue became swollen, fell down, felt so weak that he could not lift himself to get up was resolved and the outcome of other events was unknown. He is scheduled to get second dose on 24Feb2021. He would like to know if he should get it or not. He was an EMT in Fire Department before he retired. That day when it happened, he really felt old. No further details provided. The seriousness of the events was reported as non-serious. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364114
Sex: F
Age:
State: CA

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 06/01/2021
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: Her arm of course was aching, Sore arm; This is a spontaneous report received from a contactable consumer (patient). A 78-year-old female patient reported A 78-year-old female received 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, administered in upper left arm on 01Feb2021 (at the age of 78-year-old) as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On 01Feb2021, the patient experienced her arm was aching. The patient reported that she received the first dose of the Pfizer vaccine on 01Feb2021, but patient was questioning how many don't have any issues and no symptoms. Reporter stated, she thinks it was normal. It's not going to be effective, she was expecting something, That's kind a good. The patient had a sore arm on the first day, and it subsided, it went away. it's a tiny sore. The patient was a little concerned because she did not have a reaction, that tend to worry. she was not experienced any symptoms except for her arm of course was aching, it was gone away now, is it still effective if there are no symptoms. The patient clarified her arm aching is very slight now. The outcome of the event was resolving. Information about Lot and Batch has been requested. Follow-up: This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected

Other Meds:

Current Illness:

ID: 1364115
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: However after the second shot he had flu like symptoms for 24 hours; This is a spontaneous report from non-contactable consumer via Pfizer Sales Representative. This consumer (patient's daughter) reported. A 85-years-old male patient 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 an unspecified date as 2nd, dose single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported that patient received first dose of Pfizer COVID vaccine and had no symptoms. On an unspecified date 2021, after second shot, patient experienced flu like symptoms for 24 hours and then itself resolved. The outcome of the event was recovered on an unspecified date 2021. No follow-up attempts are possible. Information about lot/Batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1364116
Sex: F
Age:
State: AR

Vax Date: 02/02/2021
Onset Date: 02/02/2021
Rec V Date: 06/01/2021
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: nausea; vomiting; dizziness; rapid heart rate (139 beats/min)/heart rate was elevated; This is a spontaneous report from a contactable pharmacist. A 46-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN5813), intramuscularly in the left arm on 02Feb2021 at 11:00 as a single dose for COVID-19 immunization. The patient's medical history included history of reacting to flu vaccines and flu-like symptoms. The patient's concomitant medications were not reported. It was unknown whether the patient was pregnant at the time of the vaccination. It was unknown whether the patient received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient diagnosed with COVID-19. It was unknown if the patient tested positive for COVID-19. It was reported that, on 02Feb2021 at 11:00 PM, approximately 12 hrs after inoculation, the patient experienced nausea, vomiting, dizziness and rapid heart rate (139 beats/min). The patients heart rate was elevated for 2 hrs. The treatment received for the events was unknown. On 02Feb2021, the patient underwent lab tests and procedures which included heart rate and resulted as 139 beats/min, rapid. The outcome of the events was recovered. The reporter classified the events as non-serious and seriousness criteria that resulted in death, life threatening, caused/prolonged hospitalization, disabling/incapacitating and congenital anomaly/birth defect was reported as no. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364117
Sex: F
Age:
State: MI

Vax Date: 01/29/2021
Onset Date: 01/30/2021
Rec V Date: 06/01/2021
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: Rash on left forearm; Chills; swollen lymph nodes; Sore right arm; This is a spontaneous report from a contactable other hcp (patient herself). A 55-year-old non-pregnant female patient (not pregnant at the time of vaccination) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: Unknown), via an unspecified route of administration, administered in Left arm on 29Jan2021 at 13:30 (at the age of 55-years-old) as a single dose for covid-19 immunisation. Medical history included first dose of historical vaccine, bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: Unknown) administered in left arm on 08Jan2021 (at the age of 55-years-old) 13:30 for covid-19 immunisation, hypothyroidism, GERD, and unspecified allergies. Concomitant medication included levothyroxine (LEVOTHYROXINE) taken for an unspecified indication received within 2 weeks of vaccination on an unspecified date. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has not been tested for COVID-19 since the vaccination. On 30Jan2021 at 12: 00 AM, the patient experienced, Chills, swollen lymph nodes, Sore right arm, Rash on left forearm on day 4 and 5 post 2nd vaccine. No treatment was received for adverse event. The reporter assessed adverse events as non-serious with no seriousness criteria of resulting in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, Congenital anomaly/birth defect. The outcome of the events was not recovered. Information on the lot/batch number has been requested. This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1364118
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: extreme weakness and malaise; extreme weakness and malaise; inability to ambulate; no appetite; She requires complete assistance with even basic Activities of daily living; This is a spontaneous report from a contactable other hcp (nurse, patient's daughter). A female patient of an unspecified age received bnt162b2 (BNT162B2, Formulation: Solution for injection) via an unspecified route of administration on an unspecified date (Lot number and Expiry date was not reported) as 1st dose, single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, within 6 days the patient experienced extreme weakness and malaise, inability to ambulate, no appetite and she requires complete assistance with even basic activities of daily living. She was previously independent and ambulatory. The outcome of the events was unknown. Information about lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364119
Sex: F
Age:
State: VA

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts.; Sore arm at injection site with arm movement or palpation; Sore arm at injection site with arm movement or palpation; Sore arm at injection site with arm movement or palpation; This is a spontaneous report from a contactable other hcp. A 56-years-old female patient (non-pregnant at the time of vaccination) received first dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EU), via an unspecified route of administration, administered in Deltoid Left on 02Feb2021 at 13:15 as 1st dose single for COVID-19 immunization. Age at the time of vaccination was reported as 57. Other vaccine same date and details was reported as (02Feb2021, EU5318, Dose 1, L deltoid). Medical history included type 2 diabetes mellitus from an unknown date and unknown if ongoing DMII, hypothyroidism from an unknown date and unknown if ongoing hypothyroid, metabolic syndrome from an unknown date and unknown if ongoing, polycystic ovaries from an unknown date and unknown if ongoing PCOS. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, has the patient has not been tested for COVID-19. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took griseofulvin and wellbutrin and experienced drug hypersensitivity. Location of injection information is available for all vaccines received on the same date. On 03Feb2021 at 04:30 patient experienced itching at skin folds, palms of hands, scalp, eyelids, behind ears, followed by swelling and welts (Itchy skin, Itching both hands, Itchy scalp, Eyelids pruritus, Localized itching, Swelling and Urticaria) and Sore arm at injection site with arm movement or palpation (Vaccination site pain, Pain upon movement and Trigger point pain). Treatment received for the adverse event was unknown. Seriousness criteria was reported as No. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364120
Sex: F
Age:
State: KY

Vax Date: 01/29/2021
Onset Date: 01/31/2021
Rec V Date: 06/01/2021
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: She is feeling sick; her arm was very sore; headache; she doesn't feel good and is tired; she doesn't feel good and is tired; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect. A contactable 53-year-old female Nurse reported for herself. A 53-year-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Formulation: Solution for injection, Lot number: EL9265 and expiration date: 31May2021) via an unspecified route of administration, administered in left deltoid on 29Jan2021 at 10-10:30am (at the age of 53-year-old) as single dose for COVID-19 immunization. The patient medical history included a shingles in Nov2020, breast cancer, it is non-metastatic triple negative and Covid virus where she had headache, was sick for 2 full weeks and then on the 3rd week she felt better. The patient's concomitant medications were not reported. The patient did not had allergies. The patient did not have any illness at time of vaccination. On 30Jan2021, the patient's arm was sore and very sore when she touches it the first day after, she put a cold compress and felt much better the next day and headache is felt like when she had covid previously and feels like she is at the tail end of having the virus. She doesn't feel good and feeling so tired because of all of this. The patient has taken treatment of Excedrin migraine for the headaches also taken Tylenol and when she got desperate, she took a sumatriptan, a product used for migraines. The patient did not diagnose with COVID-19 since the vaccination. The outcome of event arm was very sore is recovering. The outcome of events Headache and doesn't feel good and tired is not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364121
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: Fatigue; sore arm; stiffness through out day; difficulty walking due to pain; This is a spontaneous report from a contactable consumer or other non hcp. A 72-year-old male patient received BNT162B2(BNT162B2, solution for injection, Batch/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 fatigue, sore arm, stiffness through out day, difficulty walking due to pain. The outcome of the events were unknown. No follow-up attempts are possible. Information about batch/Lot number can not be obtained.

Other Meds:

Current Illness:

ID: 1364122
Sex: F
Age:
State: AZ

Vax Date: 02/03/2021
Onset Date: 02/04/2021
Rec V Date: 06/01/2021
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: Severe chills; rapid heart rate; muscle aches; fever; insomnia; headache; This is a spontaneous report from a contactable pharmacist (patient) reporting herself. A 58-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL1283), dose 2 via intramuscular route of administration, administered in Arm Left on 03Feb2021 at 11:30 (at the age of 58-year-old) as SINGLE DOSE for covid-19 immunization. The patient received first dose of bnt162b2 (Lot number: unknown) on an unspecified date as SINGLE DOSE for covid-19 immunization. Medical history included hypothyroidism and seasonal allergy. The patient had no allergies to medications, food, or other products. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications included estradiol (ESTRADIOL); progesterone (PROGESTERONE); citalopram (CITALOPRAM); thyroid (ARMOUR THYROID); levocetirizine dihydrochloride (XYZAL). Patient was not diagnosed with COVID 19 prior to vaccination. On 04Feb2021 at 01:00, the patient experienced severe chills, rapid heart rate, muscle aches, fever, insomnia and headache. The patient reported the seriousness s as non-serious. The Patient has not received any treatment for the adverse event. Since the vaccination, patient not been tested for COVID-19. The outcome for the events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: ESTRADIOL; PROGESTERONE; CITALOPRAM; ARMOUR THYROID; XYZAL

Current Illness:

ID: 1364123
Sex: F
Age:
State: MN

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: under arm started to burn, went and looked and glands had swollen up to golf ball size; under arm started to burn; Pain in joints; headache on right side; This is a spontaneous report from a contactable other health care professional (patient). A 52-years-old non-pregnant female 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 administered in right arm on 02Feb2021 11:00 as a single dose for covid-19 immunization. Medical history included asthma, gluten allergy, fructose allergy, lactose allergy. Concomitant medications included calcium, tea, green, diindolylmethane (DIM), Asthma inhaler and Vit. 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. The patient previously took historical vaccine of first 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 unknown date as a single dose for covid-19 immunization. On 03Feb2021, the patient experienced pain in joints and headache on right side. In the evening at about 5:30, under arm started to burn, and glands had swollen up to golf ball size. No treatment was received for the adverse events. Seriousness of the events was assessed as non-serious by reporter. The outcome of the events was resolving. Follow-up attempts have been completed and no further information is expected. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds: CALCIUM; GREEN TEA; DIINDOLYLMETHANE

Current Illness:

ID: 1364124
Sex: M
Age:
State: TN

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: Swelling and pain to left arm from deltoid to fingertips; Swelling and pain to left arm from deltoid to fingertips; This is a spontaneous report from a contactable nurse (patient also). A 48-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number: EL3248) via Intramuscular route of administration, administered in left arm on 03Feb2021 at 08:45 AM as 1st dose single for covid-19 immunisation in hospital. The patient medical history included hypertension. The patient had allergies with eggs. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient not been tested for COVID-19. The patient's concomitant medications included lisinopril, HCTZ and fexofenadine (within 2 weeks). On 03Feb2021, 09:00 AM, the patient experienced swelling and pain to left arm from deltoid to fingertips. The patient did not receive treatment for the adverse event. At the time of this report events outcome was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: LISINOPRIL; FEXOFENADINE; HCTZ

Current Illness:

ID: 1364125
Sex: F
Age:
State: NJ

Vax Date: 01/24/2021
Onset Date: 01/26/2021
Rec V Date: 06/01/2021
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: Swollen lymph nodes; Nausea; vomiting; lack of appetite for 11 days; This is a spontaneous report from a contactable other health professional (patient) via COVID-19 Vaccine Adverse Event Self-Reporting Solution. A 29-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, /Lot Number: EL9262, expiration date not reported), via an unspecified route of administration, administered in left arm on 24Jan2021 14:45 (age at the time of vaccination 29-year-old) as 1st dose, single for covid-19 immunisation at workplace clinic. Patient had no medical history. The patient concomitant medications received within 2 weeks of vaccination include multivitamins. The patient had no allergies to medications, food, or other products. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 26Jan2021, the patient experienced swollen lymph nodes, nausea, vomiting, lack of appetite for 11 days. It was unknown if the patient was pregnant. The patient underwent lab tests and procedures which included sars-cov-2 test, nasal swab with negative result on 31Jan2021. The case was considered as non-serious with no seriousness criteria (Results in death/ Life threatening/Caused/prolonged hospitalization/Disabling/Incapacitating/ Congenital anomaly/birth defect). The patient did not receive any treatment for the events. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: MULTIVITAMINS [VITAMINS NOS]

Current Illness:

ID: 1364126
Sex: F
Age:
State: MO

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 06/01/2021
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: Eyelid twitch returned after the vaccine; Chills; headache; body aches; minor nausea; tiredness; weakness; This is a spontaneous report from a contactable other health professional(patient). A 30-year-old female patient received BNT162B2 (COMIRNATY, Solution for Injection, lot number: EN9581, Expiration date: unknown), via intramuscular route of administration on left arm on 01Feb2021 at 09:30 AM as unknown, single for covid-19 immunization. The patient medical history included a history of an eyelid twitch. The patient's concomitant medications included vitamin D3, zinc picolinate, vitamin C, vitamin A. On 01Feb2021 at 07:30 PM the patient experienced chills, headache, body aches, minor nausea, tiredness, and weakness were severe for about 24 hours. These symptoms were managed with extra strength Tylenol every 4 hours and sleep. The symptoms were lessened but remained for another 12 hours. A minor headache was still present 78 hours later. The twitch returned after the vaccine. The outcome of the event eyelid twitch returned after vaccine was unknown. Outcome of other events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: VITAMIN D3; ZINC PICOLINATE; VITAMIN C; VITAMIN A

Current Illness:

ID: 1364127
Sex: M
Age:
State: LA

Vax Date: 01/12/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: minor injection site discomfort; This is a spontaneous report from a contactable consumer (patient). A 71-year-old male patent received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EL 3246), via an unspecified route of administration n left arm on 12Jan2021 at 03:15 AM as 1st dose single for COVID-19 immunization. Medical history included HIV +, high blood pressure, shoulder replacement, hip replacement, knee replacement. Concomitant medications included dolutegravir sodium (TIVICAY), emtricitabine, tenofovir alafenamide fumarate (DESCOVY), hydrochlorothiazide, rosuvastatin. Facility where the most recent COVID-19 vaccine was administered was hospital. The patient dd not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. On 03Feb2021 at 08:00 AM (after first dose), patent experienced minor injection site discomfort. No treatment was received for the adverse event. Since the vaccination, the patient had not been tested for COVID-19. Patient also received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EL 82982), via an unspecified route of administration n left arm on 02Feb2021 at 03:00 PM as 2nd dose, single dose for COVID-19 immunization and experienced minor injection site discomfort, Joint pain, achy all over, weakness, little bit of fever, chills, no appetite. This lasted 1.5 days. The outcome of the event was recovered.

Other Meds: TIVICAY; DESCOVY; HYDROCHLOROTHIAZID; ROSUVASTATIN

Current Illness:

ID: 1364128
Sex: M
Age:
State: MI

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: fatigue; severe headache; light chills; This is a spontaneous report from a contactable consumer or other non health professional (Patient). A 21-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3248) dose 2, via an unspecified route of administration, administered in Arm Left on 02Feb2021 (at the age of 21-years-old) as single dose for covid-19 immunisation. The patient's medical history and concomitant medication was not reported. The patient had no allergies to medications, food, or other products. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient previously received INFLUENZA vaccines within 4 weeks prior to the COVID vaccine in left arm on 07Jan2021 for immunisation. The patient previously took first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3248) via an unspecified route of administration, administered in Left arm on 13Jan2021 02:45 pm (at the age of 21-years-old) as single dose for covid-19 immunisation. The patient wouldn't consider this adverse, just the predicted side effects, fatigue, severe headache, light chills on 03Feb2021 at 06:00 am. The headache was continued 2 days after vaccination. The patient not received treatment for the adverse event. Since the vaccination, the patient was not tested for COVID-19. The reporter assessed the events as non serious. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364129
Sex: M
Age:
State: LA

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: aches; fatigue; This is a spontaneous report from contactable consumer (patient) via Pfizer Sales Representative. A 48-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: unknown), via an unspecified route of administration on an unspecified date as 2nd dose, single for COVID-19 immunization. Patent previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: unknown), via an unspecified route of administration on an unspecified date as 1st dose, single for COVID-19 immunization. Medical history and concomitant medications were not reported. Patient experienced aches & fatigue same day that he received 2nd dose of vaccine. The outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1364130
Sex: M
Age:
State: WI

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: cold; runny nose; cough; This is a spontaneous report from a contactable consumer (patient) via Pfizer-sponsored program. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: Not reported), via an unspecified route of administration on an unspecified date as 1st dose, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date (a week after the vaccination), the patient experienced cold, runny nose and cough. The outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364131
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: He is asking if its okay for him to take Oxycontin for his back pain.; This is a spontaneous report received from a non-contactable consumer (patient) via Pfizer. A male patient of an unspecified age received the 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 an unspecified date at a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date after the vaccination, the patient experienced back pain. Patient enquired whether if its okay for him to take Oxycontin for his back pain. The outcome of the event was unknown. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1364132
Sex: M
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: Caller took Tylenol for his head before and after the 1st dose; This is a spontaneous report from a contactable consumer via Pfizer sponsored program Pfizer First Connect. A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on an unspecified date as first dose, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient took Tylenol for his head before and after the 1st dose. The outcome for the event was Unknown. The lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364133
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: other vaccine same date; other vaccine same date; Chills; upper arm soreness; This is a spontaneous report from a non-contactable consumer (patient) or other non hcp. A 29-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL3247), via an unspecified route of administration, administered on an unspecified date (at the age of 29-years-old) as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient took unknown vaccine of dose number 1 on same date as of COVID-19 vaccine administered on upper arm. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not diagnosed with COVID-19, prior vaccination. On an unknown date, the patient experienced chills, upper arm soreness and other vaccine administered on same date as of COVID-19 vaccine. The patient did not receive any treatment for adverse events. On an unspecified date, the patient underwent lab tests and procedures which included sars-cov-2 test found to be negative post vaccination via nasal swab. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1364134
Sex: F
Age:
State: CT

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: sore arm; This is a spontaneous report from a contactable consumer (patient). A 34-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: P220895-0068L), via an unspecified route of administration, in left arm on 02Feb2021 at 15:45 (at the age of 34-year-old) as 1st dose, single dose for covid-19 immunisation. Medical history included allergy to penicillin. Concomitant medications that patient received within 2 weeks of vaccination included naproxen (NAPROXEN) and levonorgestrel (KYLEENA). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not prior to vaccination and was not diagnosed with COVID-19. On 03Feb2021 at 07:00, the patient experienced sore arm. The patient did not receive treatment for the adverse event. Since the vaccination, the patient was not tested for COVID-19. The report was non-serious. Outcome of the event was recovered on an unknown date. Follow-up attempts are completed. No further information is expected.

Other Meds: NAPROXEN; KYLEENA

Current Illness:

ID: 1364135
Sex: F
Age:
State:

Vax Date: 01/01/2020
Onset Date: 01/21/2021
Rec V Date: 06/01/2021
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: NAUSEA; VOMITING; weak; tired, fatigue; This is a spontaneous report from a contactable consumer, based on information received by Pfizer from a company (manufacturer control number: EC-2020-085712), for BNT162B2. A non-pregnant female patient of an unspecified age received 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 unknown, single for COVID-19 immunization. Co-suspect drug included oral Lenvima 8mg daily from 21Jan2021 for liver cell carcinoma. The patient's medical history and concomitant medications were not reported. On an unspecified date, 2 weeks after COVID-19 vaccination, the patient experienced nausea, vomiting and fatigue. On 21Jan2021, she was feeling weak and tired and did not want to get up from bed. Patient missed 2 doses of Lenvima due to side effects and planned to see primary care physician. The clinical outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: LENVIMA

Current Illness:

ID: 1364136
Sex: U
Age:
State:

Vax Date: 01/30/2021
Onset Date:
Rec V Date: 06/01/2021
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: soreness at inj site 5/10; joint pain, mild; low appetite; mild headache; malaise; This is a spontaneous report from a contactable consumer (patient, self-reported). A 30-year-old patient of an unspecified gender 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 30Jan2021, as a single dose for COVID-19 immunization. The patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on 09Jan2021, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that on an unknown date, about 17 hours post injection, the patient had soreness at inj site 5/10, joint pain, mild, low appetite, mild headache, and malaise. The patient was not reported about nausea, vomiting, rash, fever, diarrhea or any other s/s. Duration of events was 24/30 hours. The patient took treatment as 400mg Advil 2x, most above s/s resolved, Inc fluid intake, and rest. Outcome of the events was resolved on an unknown date. Information on the lot/batch number has been requested. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364137
Sex: M
Age:
State: AR

Vax Date: 01/29/2021
Onset Date: 01/01/2021
Rec V Date: 06/01/2021
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: Caller stated he may have gotten the "water " not good or not have gotten the full dose.; he may have gotten a bad dose; He said he got the second dose on the 29Jan "felt the heat like alcohol burning"/Second dose burned a little; he may have gotten a bad dose; This is a spontaneous report from a contactable consumer (patient). An 85-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: EL3249), via an unspecified route of administration on 29Jan2021 as 2nd dose, single for COVID-19 immunization. The patient previously received first dose of BNT162B2 for COVID-19 immunisation and experienced sore arm, felt the fire chills and heat, arm pain for a couple days, felt the burning of it going in, little heat and a little chill but the next day he was on the way to being good. The patient medical history included really sick with the flu before getting the vaccine, it was just sick not really an event and was like he got the flu but in 2 hours. The concomitant medications were Advil and Tylenol. One Benadryl will knock him out. He said he gets sick with flu vaccine. On an unspecified date, the patient experienced felt the heat like alcohol burning when injecting but no sore arm nothing else, did feel the burn and it go into his arm but after an hour he left and has had no pain, none in his arm or hurting, nothing. His mind is going to go there and is thinking did he get a bad dose. He may have gotten the water not good or not have gotten the full dose. He wanted to know the proof that he has gotten the vaccine, are there any blood test or any test he could have to see if he got the vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds: ADVIL [IBUPROFEN]; TYLENOL

Current Illness:

ID: 1364138
Sex: M
Age:
State: GA

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 06/01/2021
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: Saying he could not breath; anxious; reported being cold; complained of Chest pain; began to shake; This is a spontaneous report from a contactable other hcp reported that a 58-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number: EL3302 and expiration date: unknown), via intramuscularly in Arm Left on 29Jan2021 at 09:45 (at the age of 58 years old) as a single dose for COVID-19 immunisation. Medical history included allergies to Sulfa drugs from an unknown date and unknown if ongoing, Cardiac stents from 2004 to an unknown date. Concomitant medications included Lipitor, Aspirin, Plavix, Nitroglycerine for an unspecified indication from an unspecified date. No other illness reported at the time of vaccination and up to one month prior. The patient was in observation for 30 minutes. At approximately 25 minutes post vaccination at 10:15am, Patient signaled that he wanted to leave and was instructed to stay 5 minutes. Patient anxious and began to shake, saying he could not breathe. Vitals were 147/88, HR 86, O2 98% on RA. Pt was reclined on floor and reported being cold and was striking his head on the blanket; head stabilized. Patient was alert and oriented X3 but complained of Chest pain. EMS called, arrived at 10:25, vitals: 144/92, HR83 O2 99% on 2L. Pt stable & transported by EMS at 10:35am. The patient underwent lab tests and procedures which included heart rate: 86, 83, investigation: 147/88, 144/92, oxygen saturation: O2 98% on RA , oxygen saturation: 99 % on 29Jan2021. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: LIPITOR [ATORVASTATIN]; ASPIRIN [ACETYLSALICYLIC ACID]; PLAVIX; NITROGLYCERIN

Current Illness:

ID: 1364139
Sex: F
Age:
State: CA

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 06/01/2021
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: Brain fog; feeling of sluggishness; annoyingly mild headache; Mildly sore left arm where injection was; Body felt warmer than usual when went to bed; This is a spontaneous report from a non-contactable consumer (patient herself). A 35-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EJ1686), via an unspecified route of administration in left arm on 14Jan2021 at 17:45 (at the age of 35-year-old) as a single dose for COVID-19 immunization. The patient's medical history was none. No allergies to medications, food, or other products/known allergies. Concomitant medications included ascorbic acid (VITAMIN C) and colecalciferol (VITAMIN D); Patient received both drugs within 2 weeks of vaccination. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL1284), via an unspecified route of administration in left arm on 24Dec2020 at 09:30 (at the age of 35-year-old) as a single dose for COVID-19 immunization and experienced sorest left arm where the injection was and very mild swelling of the area. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that, 14Jan2021 2nd dose. Later that night had a mildly sore left arm where injection was. Body felt warmer than usual when went to bed. Next morning, 15Jan2021, woke up with a brain fog, feeling of sluggishness. Mid-day, 15Jan2021 around noon, started having an annoyingly mild headache. Same night my body felt warmer than usual again. Next morning 16Jan2021 woke up feeling great and all symptoms resolved. Did not take any medications except for nature made Vitamin C and D. No treatment medications were received for the adverse events. On 22Jan2021, the patient underwent lab tests and procedures which included nasal swab: Negative, RT-PCR COVID-19 test: Negative. The events were considered as non-serious by the consumer. The outcome of the events was recovered on 16Jan2021.

Other Meds: VITAMIN C [ASCORBIC ACID]; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1364140
Sex: F
Age:
State: AZ

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 06/01/2021
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: body aches (like growing pains in the joints); I was fatigued; Arm where vaccine was given was sore; I was very cold; swollen lymph node in the armpit of the arm where vaccine was given.; Chills lasted until about 24 hours after vaccine was given; This is a spontaneous report received from a contactable consumer (patient). A 44-year-old adult female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL 9264), via unspecified route of administration in the left arm on 05Feb2021 at 06:30 PM, as single for COVID-19 immunization at Public Health Clinic. The patient's medical history included hypothyroidism, high cholesterol, acid reflux, gallbladder stone, overweight and seasonal allergies that last all year. The patient was not allergic to medications, food, or other products. The patient was not pregnant at the time of vaccination. Concomitant medications included levothyroxine sodium (SYNTHROID), omeprazole, montelukast sodium (SINGULAIR), levocetirizine. 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. Historical vaccination included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: E13247), via an unspecified route of administration in the left arm on 14Jan2021 at 06:30 PM, as single dose for COVID-19 immunisation. On 06Feb2021 at 07:30 AM, 12-13 hours after the vaccine: body aches (like growing pains in the joints), she was fatigued, was very cold. Arm where vaccine was given was sore and swollen lymph node in the armpit of the arm where vaccine was given. Chills lasted until about 24 hours after vaccine was given. Body aches went away about 30 hours after vaccine was given. Swollen lymph node still swollen 2.5 days after vaccine. Took Tylenol about 19 hours after vaccine and it seemed to take the edge off the aches. Took 1 more dose of Tylenol 6 hours later and that's all she needed. Since the vaccination, the patient had not been tested for COVID-19. The outcome of the events body aches (went away about 30 hours) and chills (was lasted until about 24 hours) was recovered on 07Feb2021; swollen lymph node was not recovered; for rest of events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: SYNTHROID; OMEPRAZOLE; SINGULAIR; LEVOCETIRIZINE

Current Illness:

ID: 1364141
Sex: F
Age:
State: SC

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 06/01/2021
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: Aches; Fever; Chills; Redness injection site swelling under arm; Redness injection site swelling under arm; This is a spontaneous report from a contactable consumer. A 57-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Batch/Lot number: EL1284, Expiration Date was not reported), via an unspecified route of administration, administered in right arm on 12Jan2021 (at the age of 57-year-old) as 2ND DOSE, SINGLE for covid-19 immunisation administered in Hospital. The medical history was not reported. Concomitant medications included levothyroxine sodium (SYNTHROID), started 10yrs; tamoxifen, started 4 yrs; vitamin c [ascorbic acid]; zinc all from an unspecified date to ongoing. Historical vaccine included BNT162B2 for covid-19 immunization. On 12Jan2021 23:00 after 2nd dose the patient experienced, fever, chills, aches and Redness injection site swelling under arm. Admission to hospital is not involved. Therapeutic measures were taken for the events with Anti-inflammatory + Benadryl and Naproxen Sodium for taking is Redness injection site swelling under arm, Chills, Fever, Aches, 25 mg twice daily from 31Dec2020 to an unspecified date. The outcome for the events was resolved. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds: SYNTHROID; TAMOXIFEN; VITAMIN C [ASCORBIC ACID]; ZINC

Current Illness:

ID: 1364142
Sex: F
Age:
State: NC

Vax Date: 02/02/2021
Onset Date: 02/01/2021
Rec V Date: 06/01/2021
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: little aching in the injection site(arm); This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect. A contactable consumer (patient) reported that: a female patient of an unspecified age received (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number and expiration date were not reported) dose 2 via an unspecified route of administration, administered in Arm on 02Feb2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that, the patient got the 2nd dose of Covid 19 Vaccine yesterday, she's feeling good and no side effects at all, a little aching in the injection site (arm) on an unknown date in Feb2021 but she said that it's fine. Want to know if she can take the prescription Cyclobenzaprine, just wondering if this drug will interfere with the vaccine. The outcome of the event resolved on unknown date in Feb2021. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364143
Sex: F
Age:
State: VA

Vax Date: 01/11/2021
Onset Date:
Rec V Date: 06/01/2021
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, fatigue for 24 hrs; body aches, fatigue for 24 hrs; This is a spontaneous report from a contactable Other HCP. A 26-year-old female received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL/284), via an unspecified route of administration on Right Deltoid on 11Jan2021 (Age at Time of Vaccination: 26 years) at single dose for COVID-19 immunization at hospital. The patient Medical history included ongoing allergies to Augmentin, strawberries, bananas from 2002. It was reported that patient was not deceased.Prior Vaccinations (within 4 weeks), any other vaccinations within four weeks prior to the first administration date of the suspect vaccine was reported as not applicable and there was no events following prior vaccinations. Family Medical History Relevant to adverse events was reported as not applicable.The concomitant medications included Cryselle from Mar2014 (daily dose and regimen including Formulation, Route, Frequency: Daily Tablet) for menses regulation. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EJ/685), via an unspecified route of administration on Right Deltoid on 21Dec2020 at single dose for COVID-19 immunization. On an unspecified date after second dose, the patient experienced body aches, fatigue for 24 hrs. It was reported that reaction recurred on re-administration of product. The events resulted in Emergency Room or Physician Office. The relevant lab tests was reported as none. The patient was not required any treatment for the events. The outcome of the events was resolved. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Drug allergy; Fruit allergy

ID: 1364144
Sex: F
Age:
State: TX

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 06/01/2021
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: Got really sick after getting vaccine; had diarrhea all day long; exhausted; Fever; This is a spontaneous report from a contactable consumer from a Pfizer sponsored program Pfizer First Connect. A 71-years-old female patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE: Solution for injection; Batch/Lot number: Unknown), dose 1 via an unspecified route of administration on 28Jan2021 as 1ST DOSE SINGLE for covid-19 immunisation. The patient's medical history included ongoing 2 arteries that are blocked, has post-traumatic stress syndrome, had stroke, only seemed to affect her emotions and nothing physical, was supposed to get blood work done and had infection. Was placed on anti-biotic. Same time as starting antibiotic she received 1st dose of covid vaccine. The doctor gave her an antibiotic that is the generic, Telocin, 300mg three times. Spelling of generic antibiotic documented as provided by caller. She takes it with food and a lot of water. Caller clarified that she is taking the antibiotic now, but she also got something to help the infection when she was seen at the doctor, ongoing nightmare. The patient's concomitant medications were not reported. On 28Jan2021 caller clarified that when she got home, she had diarrhea all day long, she was exhausted, and she had fever. She is scheduled to go back for her second shot on 18Feb2021. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness: Carotid artery disease (Has 2 arteries that are blocked); Nightmares; Post-traumatic stress disorder (post-traumatic stress syndrome); Post-traumatic stress disorder

ID: 1364145
Sex: F
Age:
State: WA

Vax Date: 02/03/2021
Onset Date: 02/05/2021
Rec V Date: 06/01/2021
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: Asthenia, Chills, Headache, Myalgia

Symptoms: sleep for two days; This is a spontaneous report from a contactable consumer or other non hcp (patient, self-reporting). A 77-years-old (non-pregnant) female patient received BNT162B2 (BNT162B2, Solution for injection, Batch/Lot number and expiration dates were not reported), via an unspecified route of administration in arm right on 03Feb2021 13:45 as unknown, single dose for COVID-19 immunization. Medical history included subclavian artery stenosis from an unknown date and unknown if ongoing, arteriosclerosis from an unknown date and unknown if ongoing and allergy to penicillin. No other vaccine in four weeks. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for covid post vaccination. The patient concomitant medications were not reported. On 05Feb2021, 36 hours after the injection and the patient experienced all the side effects except fever and nausea and needed bed rest and sleep for two days and was worried about what will happen with the second dose of the vaccine. Will she get all the unpleasant effects again and could it be worse enquired. The treatment was not received. The outcome of the event was recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1364146
Sex: F
Age:
State: LA

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 06/01/2021
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: scratchy nose/sinus and sore throat; scratchy nose/sinus and sore throat; This is a spontaneous report from a Pfizer-. A contactable consumer (patient) reported that a female patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: Unknown), via unspecified route of administration on an unknown date in Jan2021 (reported as first dose was 3 weeks ago), as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that she was scheduled to take the second dose of the COVID-19 vaccine today on 03Feb2021 and experiencing scratchy nose/sinus and sore throat on an unknown date in 2021 and she has been taking sinus medication for it. She wanted to know if she will take the second dose today. The outcome of the events was unknown. The lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364147
Sex: F
Age:
State: NY

Vax Date: 01/27/2021
Onset Date: 01/28/2021
Rec V Date: 06/01/2021
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: arm was so sore; arm was swollen; Event: Pain was reported as worsened; she cannot move 1 arm, being the left arm; Swollen lymph nodes; Pain; This is a spontaneous report from a contactable consumer (patient). A 36-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection, Lot Number: EN5318 and expiration date was not reported) via an unspecified route of administration in left arm on 27Jan2021 (at age of 36-years-old) as a single dose for COVID-19 immunization. Medical history included migraine pain. Concomitant medication included acetylsalicylic acid; caffeine; paracetamol (EXCEDRIN) for migraine pain, took it after the vaccine and takes birth control pills regularly. Patient had previously received first dose of vaccine (Lot EL3249) in left arm on 06Jan2021 and only had mild pain all over the body. It was reported that this time with the second dose she was having swollen lymph nodes and she cant move 1 arm, being the left arm. The Second Dose was on 27Jan2021 and the next day she had the pain from the shot, then last night her arm was so sore that she got up and saw that arm was swollen. This occurred on 28Jan2021 for swelling of the lymph nodes and the pain. She wants to know what she should do next and if this was a normal Side effect. Caller was frustrated asking how long she will have to wait for the other department, She waited 1 hour just to give all this information and now she was going to be transferred again. The outcome for events swollen lymph nodes and pain was not resolved and for other events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: EXCEDRIN [ACETYLSALICYLIC ACID;CAFFEINE;PARACETAMOL]

Current Illness:

ID: 1364148
Sex: F
Age:
State:

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 06/01/2021
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: This is a spontaneous report from a contactable consumer or other non hcp (patient herself) reported that a female patient of an unspecified age received unknown 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 in Arm Left on an unspecified date in Jan2021 as a single dose for COVID-19 immunisation. Medical history included ongoing arthralgia. The patient's concomitant medications were not reported. Caller states a week ago today she had the COVID 19 vaccine shot, and is calling to ask, she is having, not related to the shot, she has had this before, pain in her right shoulder, can she take Aleve? Clarifies she got the vaccine a week ago today, this just came because of the way she slept, she had it before, pain in her right shoulder, she got the vaccine in her left arm, she usually takes Aleve, and just wishes to know if she can take Aleve? States the pain is bad this morning. The outcome of the event was unknown. Information about batch/lot number has been requested. Follow-up (19Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness: Shoulder pain

ID: 1364149
Sex: F
Age:
State:

Vax Date: 01/15/2021
Onset Date:
Rec V Date: 06/01/2021
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: increased drainage since getting the vaccine; increased drainage since getting the vaccine; sore arm for one day; This is a spontaneous report from a contactable other hcp. A 66-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration on 15Jan2021 (Batch/Lot Number: EL3302) as a Single dose for covid-19 immunization. The patient past medical history included Sinus node dysfunction, neurological condition were the heart rate goes low, She has a pace maker (pacemaker insertion), flu vaccine, Tetanus vaccine, menopause and drainage. The patient's concomitant medications were not reported. on an unspecified date the patient reported increased drainage since getting the vaccine and sore arm for one day. They were vaccinated on 15Jan2021 with first dose. The Wednesday after which was about 5 days after the vaccine her husband got chills, sneezing, and fatigue. He did not call the doctor and did not get tested. About a week later her son had nasal congestion and cough. This was the third day for that. Called her son's doctor since this was the second person in the house to have symptoms. The patient son had COVID test and it came back positive. The patient enquired was the COVID vaccine enough to give a positive test. She had symptoms too, but she normally get sinusitis this time of year. No one in her family had a fever. She was at a quandary. She has to quarantine in case it was. The patient enquired could the vaccination cause a positive COVID test result. She thought the symptoms should show up in 1 to 3 days. A week in between her husband and son and it was hard to believe. It should have been her to get it worse since she sleeps with her husband. Praise the Lord she has not. She and her husband have not been tested for COVID. Only her son was COVID tested.Her drainage started in Oct2020. It could be dust in the house. She had increased drainage since vaccination. She didn't think much of it. She had sore arm for one day. It was worse than after the flu vaccine because she was over 60 and they give her the enhanced version. With this last flu vaccine her arm was more sore than with the Tetanus vaccine.She wants everyone to wear a mask in the house. If she had been thinking straight she would have had them wearing mask sooner. The patient underwent lab tests low density lipoprotein (LDL): result:34 and Sars-Cov-2 Test: Negative on an unspecified date. The event outcome is Unknown for increased drainage since getting the vaccine and recovered for sore arm for one day on an unspecified date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364150
Sex: F
Age:
State: NJ

Vax Date: 02/02/2021
Onset Date:
Rec V Date: 06/01/2021
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: Sinusitis; headache; ear ache; dizziness; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer reported that a female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 02Feb2021 (Lot number, expiration date: unknown) as unknown dose number, single dose for covid-19 immunisation. The patients medical history and concomitant medications were not reported. The patient experienced sinusitis, headache, ear ache, dizziness on an unspecified date. She took Tylenol and wants to know if she can take other medications. Therapeutic measures were taken as a result of the events. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364151
Sex: F
Age:
State: FL

Vax Date: 02/01/2021
Onset Date: 02/02/2021
Rec V Date: 06/01/2021
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: More sore with second vaccine, within a handswidth of injection site; Intermittent runny nose/sneezing; Intermittent runny nose/sneezing; This is a spontaneous report from a contactable consumer or other non hcp. A 65-years-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported and expiry date: unknown), via an unspecified route of administration, administered in Arm Left on 01Feb2021 16:30 as SINGLE DOSE for covid-19 immunization. Medical history included osteoporosis, stroke at 35 yrs old, lactose intolerance, significant lactose intolerance and gastrointestinal (GI) issues and allergic to caine family of drugs from an unknown date and unknown if ongoing. Concomitant medications included evolocumab (REPATHA SURECLICK) and lorazepam; both taken for an unspecified indication, start and stop date were not reported. The patient's historical vaccine included received first dose of BNT162B2 via an unspecified route of administration, administered in Arm Left on 11Jan2021 12:00 PM as SINGLE DOSE for covid-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient not been tested for COVID-19. The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. On 02Feb2021 at 12:00 AM, the patient developed more sore with second vaccine, within a handswidth of injection site. Intermittent runny nose/sneezing. It was unclear if related to vaccine. I was asked by Pfizer to report, since I am on a bi-monthly dose of injectable Repatha. The patient did not received any treatment. The outcome of the events was recovered in Feb2021. Follow-up attempts have been completed. No further information was expected.

Other Meds: REPATHA SURECLICK; LORAZEPAM

Current Illness:

ID: 1364152
Sex: F
Age:
State: GA

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 06/01/2021
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: Both cheeks both side left and right but left more very red, as was my forehead, which was also slightly red, looked like a rash; look like a sunburn; Both cheeks both side left and right but left more very red, as was my forehead, which was also slightly red, looked like a rash; look like a sunburn; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported a female patient of an unspecified age received first dose of bnt162b2 (Pfizer BioNTech Covid 19 vaccine, Solution for injection, Lot Number: EN9581), via an unspecified route of administration on 03Feb2021 17:15 as 1st dose, single dose for I don't want get covid. The patient's medical history and concomitant medication were not reported. On 03Feb2021, the patient experienced both cheeks both side left and right but left more very red, as was my forehead, which was also slightly red, looked like a rash; look like a sunburn. Consumer stated, I had my first dose of Pfizer vaccine yesterday and 5:15 PM , okay at 5:15 PM 03Feb2021 (yesterday). Felt fine, looked fine, got home and of course everyone worldwide is wearing a mask now so when I got home and took the mask off, my both cheeks both side left and right but left more very red, as was my forehead, which was also slightly red, it looked like a rash and I thought well maybe because I had the mask on, you know all day long and so got that, well it really look like a sunburn, so you know when you are out in the sun too long and your skin gets burned instead getting brown, so I monitored it all night it never improved, again this morning after lying down seems like it improved, but within minute after being upright again it gets bad again so this morning again I have what looks like a red rash or sunburn on my left cheek and on right cheek and my forehand, left cheek worse, it's very modeled looking and needless to say I am little bit concerned, so what you can tell me about this kind of reaction, has it been reported before, or is this the first time you are hearing about it. Still experiencing the event: consumer stated, yes this morning, still. Outcome of event: consumer stated, it persisting and it's little bit better, than it was last night when I went to bed, but the longer I am awake the more it is looking like it did yesterday. Treatment: consumer stated, no, I did not take anything because I was not sure if I should or what I should, so that's another question can I take advil or something or does that think can help, advil is over the counter I am sure you know, so what you recommending it terms of over the counter, okay I need to talk to the medical people. The patient did not receive any treatment for the events. The clinical outcome of the both cheeks both side left and right but left more very red, as was my forehead, which was also slightly red, looked like a rash, look like a sunburn were not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364153
Sex: F
Age:
State: MA

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 06/01/2021
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: Slight pressure like ears and eyes; Slight headache but it had become so bad that I never had; Did not feel well; Vision was blur; Hard to open eyes; it is like a pressure; Still I had at back of my head like a pressure little bit; concentration, everything was gone within like so fast; This is a spontaneous report from a Contactable consumer (patient). A 48-Years-old female consumer received bnt162b2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration on 28Jan2021 as an 1ST DOSE, SINGLE for COVID-19 immunization (age a vaccination 48-Years-old). Medical history and concomitant medications of the patient were none. On 28Jan2021 around one hour after vaccination, the patient had slight pressure like ears and eyes, slight headache but it had become so bad that she never had, hard to open eyes; it was like a pressure, did not feel well, vision was blur, concentration, everything was gone within like so fast, Still I had at back of my head like a pressure little bit. Clinical course was provided as follows: She had her first dose and started having some symptoms right like within an hour or so. It was a slight pressure like ears and eyes and little like slight headache but then it had become like at the end of the day, it was so bad that she never had, (intensity was more than before). It was sudden, and she could not keep her eyes open. It was to that point like hard to open her eyes and it was like a pressure. She went back to the site and checked blood pressure, she recorded it was fine, '100.2 and over' (not further clarified), pulse and everything was fine, but she did not feel well. Even she felt like her vision was blur her concentration, everything was gone within like so fast." She did not receive any medication, but she had sat down and was laid on until she felt normal. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364154
Sex: F
Age:
State:

Vax Date: 01/30/2021
Onset Date:
Rec V Date: 06/01/2021
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: lost a filling and will need dental work done; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection) via an unspecified route of administration on 30Jan2021 as single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient took vaccine on the 30th. On an unspecified date, she just lost a filling and will need dental work done and was wondering if she can take antibiotics. The outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1364155
Sex: F
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: Implant site swelling to face; This is a spontaneous report based on the information received by Pfizer from a contactable other healthcare professional. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Expiration date: UNKNOWN), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received hyaluronic acid (RESTYLANE) for an unspecified indication on an unspecified date. On an unspecified date the patient experienced Implant site swelling to face post Restylane Lyft injection. Patient received Pfizer COVID 19 Vaccine 1 week prior to injection. Outcome of the event Implant site swelling to face is unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1364156
Sex: F
Age:
State: SC

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: nauseous; chills; brain fog/really felt stuff going on throughout my blood vessels; sneezes; Hot and cold body aches overnight; took Ibuprofen which made me feel better but super tired all day; This is a spontaneous report from a contactable nurse (patient) received by Pfizer . A female patient of an unspecified age received bnt162b2 (Pfizer Covid-19 Vaccine, Solution for injection, Lot number was not reported), dose 2 via an unspecified route of administration on an unspecified date at 8.30 as second dose, single for covid-19 immunisation. The patient medical history was and concomitant medications were not reported. The reporter reported that patient received her second round of the vaccine. The patient got shot at 08:30 in the morning. Round 2 of Pfizer and feel "yucky" for 12-24 hours later. Also asked if us did not know what yucky means, reporter would said "nauseous, chills, brain fog, sneezes and I really felt stuff going on throughout my blood vessels". Hot and cold body aches overnight. The patient took Tylenol 12 hours after, nada. 24 hours later when woke up the next day at 08:30am, thankfully patient was not working at the hospital, took Ibuprofen which made feel better but super tired all day. By 48 hours, patient was good to go. The microchip has successfully in filtrated body". There was no contact information available for the patient. No PQC reported. Therapeutic measures were taken as a result of nauseous, chills, brain fog/really felt stuff going on throughout my blood vessels, sneezes, hot and cold body aches overnight, took ibuprofen which made me feel better but super tired all day. The outcome of events was resolved. Information about Batch/Lot number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1364157
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 06/01/2021
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: caught a cold; cough type symptoms; This is a spontaneous report from a Pfizer Sponsored Program. A contactable consumer (patient) reported that: a female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that, received "first dose and then caught a cold and cough type symptoms on an unknown date and now her HCP has prescribed to her a steroid Prednisone to assist". Therapeutic measures were taken as a result of caught a cold cough type symptom. Outcome of the events was unknown. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm