VAERS 2021 Database www.vaers.hhs.gov

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VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

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

Incidents per State

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

ID: 1023355
Sex: M
Age:
State: FL

Vax Date: 01/12/2021
Onset Date: 01/27/2021
Rec V Date: 02/11/2021
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: Bell's Palsy right side of face; This is a spontaneous report from a contactable physician and consumer. An 80-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: unknown) via intramuscular first dose on 12Jan2021 14.00 at a single dose for COVID-19 immunisation. The patient medical history included DM (diabetes mellitus), hypertension, CAD (Coronary artery disease) and Atrial Fib (Atrial fibrillation). The patient concomitant medication was not reported. The patient visited physician office and it was reported that patient experienced bell's palsy right side of face on 27Jan2021 06.00. The patient did not receive therapeutic measures for the event. The patient did not have COVID prior vaccination and not tested COVID post vaccination. The patient had not received any vaccine in four weeks (as reported). The outcome of the event was not recovered. Information on the lot/batch number has been requested.; Sender's Comments: A possible contributory effect of suspect BNt162B2 on reported event cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1023356
Sex: F
Age:
State: KY

Vax Date: 01/16/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: Anaphylaxis; SOB (shortness of breath)/ difficulty breathing; Chest tightness; dizziness; Wheezing; Anxiety attack; Medication-induced allergic reaction; Blood pressure (BP) increased for 130/89; This is a spontaneous report received from a contactable pharmacist. A 64-year-old female patient (not pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL3249), intramuscular on left arm on 16Jan2021 at single dose for COVID-19 immunization. Medical history included HTN (hypertension), mopericarditis, anxiety and allergy to antihistamine tabs. The patient's concomitant medications were not reported. It was reported that, the patient was experiencing chest tightness, SOB (shortness of breath), and dizziness on 16Jan2021. 50 mg of Benadryl and 20 mg of famotidine was administered around 14:10. Patient was still experiencing chest tightness and was having difficulty breathing. 0.3 mg of epinephrine was administered at 14:20. EMS was called. Breathing improved. Pulse Ox 100%, HR (heart rate): 68, blood pressure (BP) increased for 130/89. EMS arrived and assumed patient care. ED COURSE: Patient was seen and examined with doctor. Patient developed of SOB, dizziness, wheezing after receiving first shot of Pfizer COVID vaccine. She received Benadryl upon development of symptoms, which actually made them worse given her allergy to antihistamine tabs, but her symptoms improved upon administration of 0.3 IM epinephrine shot. Differential diagnoses include but were not limited to anaphylaxis, anxiety attack, medication-induced allergic reaction on 16Jan2021. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was unknown whether the patient received any other medications within 2 weeks of vaccination. The patient visited emergency room/ department or urgent care due to the events. The patient was not diagnosed with COVID-19 prior to vaccination. It was unknown whether the patient has been tested for COVID-19, since the vaccination. The events were assessed as non-serious by the reporter. Therapeutic measures were taken as a result of events. The outcome of the events was reported as recovered on an unspecified date in Jan2021.; Sender's Comments: Based on the information provided and temporal relationship, a causal association between BNT162B2 and the reported events cannot be completely excluded. The treatment with Benadryl most likely contributed to the events as the patient is known allergic to antihistamine tabs. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1023357
Sex: F
Age:
State: IN

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 02/11/2021
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: rheumatoid and osteoarthritis. Always have some pain but it increased dramatically; rheumatoid and osteoarthritis. Always have some pain but it increased dramatically; This is a spontaneous report from a contactable nurse (patient). An 85-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: not reported), via an unspecified route of administration on right arm on 29Jan2021 08:00 at single dose for covid-19 immunisation. Medical history included ongoing rheumatoid arthritis, ongoing osteoarthritis, CAD (coronary artery disease), hypertension, GERD (gastrooesophageal reflux disease), osteoporosis, lumbar stenosis, lumbar degenerative disc and Allergies: Sulfa. Concomitant medication included carvedilol (COREG), prednisone, methotrexate, adalimumab (HUMIRA), fluoxetine hydrochloride (PROZAC) and risedronate sodium (RISEDRIN). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and not diagnosed with COVID-19 prior to vaccination. On 29Jan2021, 12:00 patient had rheumatoid and osteoarthritis. Always have some pain but it increased dramatically and almost unbearably. The patient pain med did help some. Lasted about 11 hours. The seriousness criteria were considered as non-serious. Since the vaccination, the patient been not tested for COVID-19. The outcome of the events was recovering. Information on the lot/batch number has been requested.; Sender's Comments: A possible contributory effect of suspect drug on reported Rheumatoid Arthritis aggravated cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds: COREG; PREDNISONE; METHOTREXATE; HUMIRA; PROZAC; RISEDRIN

Current Illness: Osteoarthritis (osteo arthritis); Rheumatoid arthritis

ID: 1023358
Sex: F
Age:
State: CA

Vax Date: 12/19/2020
Onset Date: 12/19/2020
Rec V Date: 02/11/2021
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: encephalitis-like symptoms; Hearing loss; memory loss; parathesias; visual disturbances; taste disturbances; dizziness; Lsided chest pain; staggering; elevated SBP 190-200; severe L-sided chest tightness; pre-syncope; elevated BP; DDimer was elevated; fell; intermittent memory lapses; nausea episodes; cant smell that last 1-2 hrs; L neck /head pain; L neck /head pain; Left axilla lymphadenopathy; rhinitis; lightheaded/lightheadedness; had an episode of pain all over; SOB; This is a spontaneous report from a contactable physician (patient). A 46-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date were unknown), via an unspecified route of administration from on 19Dec2020 at a single dose for COVID-19 immunization. Medical history included ovarian cancer at age 29, food allergy to clams and escargot, and allergy to sulfa. The patient's concomitant medications were not reported. The patient previously took bactrim and experienced allergies. On 19Dec2020, immediately after vaccine had rhinitis, lightheaded, given Zyrtec and water and observed for a duration of 30 min. Three hours postvaccination on 19Dec2020, at home had an episode of pain all over and SOB (shortness of breath). 3 days later (22Dec2020), patient had L (left) neck /head pain and left axilla lymphadenopathy. On 23Dec2020, she fell in the shower. On the same day (23Dec2020) the patient had intermittent memory lapses, lightheadedness, nausea episodes, can't smell that last 1-2 hours a few times a day. Symptoms worsened on 03Jan2021, with severe L-sided chest tightness, pre-syncope, was seen in the ER with elevated BP. DDimer was elevated, CT Scan of Chest/Abdomen showed L axilla lymphadenopathy, negative for PE. CBC, Electrolytes WNL (within normal limits), still on 03Jan2021. Observed in ER for 7 hrs. and then discharged home. Intermittent symptoms continued. On 08Jan2021, patient had another severe episode while at work. She was noted to be staggering, and again was complaining of left-sided chest pain. She was taken to the ER by her colleagues on 08Jan2021 and noted to have elevated SBP 190-200. On 08Jan2021, patient underwent CT head negative, MRI negative, w/u (workup) for pheochromocytoma negative and COVID negative. She was started on prednisone and Norvasc and discharged home. She continues to have intermittent episodes however they have decreased in intensity and last for about 1 hour. She described her symptoms as encephalitis-like symptoms. These include memory loss, paresthesia, visual disturbances, hearing loss, taste disturbances, and dizziness. These symptoms when severe have been incapacitating. She had been hospitalized for a neurological and infectious work up (including Brain MRI and multiple COVID tests) but no diagnosis has been yet identified. This symptom kcomplex (unspecified) has persisted to now. She has not received the second dose of vaccine. She is asking how long mRNA, the lipid nanoparticles and the protein spike lasts in the body. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on the limited information currently available, a possible contributory role of the suspect drug in the reported events cannot be completely excluded given the implied temporal association. However, underlying medical conditions may provide the alternate explanations. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regul atory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1023359
Sex: F
Age:
State: OK

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 02/11/2021
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: Seizure; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date not reported), via an unspecified route of administration on 28Jan2021 at a single dose for COVID-19 immunization. Medical history included being immunocompromised from an unknown date and was taking a lot of medications. Concomitant medication includes a lot of medications (unspecified). The patient was previously vaccinated with the first dose of BNT162B2 on an unspecified date. It was reported that the patient received the second dose of COVID-19 vaccine on the afternoon of 28Jan2021 and experienced seizure. The reporter wanted to know if he needed to seek a doctor early this morning for the patient. The outcome of the event was unknown. No follow-up attempts are possible. Information about batch/lot number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1023360
Sex: M
Age:
State: GA

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 02/11/2021
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: blood pressure (1:10 PM): 143/92; Syncopal episode; Patient was pale; Diaphoretic; feeling light-headed; This is a spontaneous report from a contactable nurse. A 38-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot: EL8982), intramuscularly into the left arm on 27Jan2021 13:00 at a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On 27Jan2021 13:05 patient had a syncopal episode but regained consciousness immediately and was assessed for injury and other reactions. The patient was pale, diaphoretic and reported feeling light-headed on 27Jan2021 13:05. The patient underwent lab tests and procedures on 27Jan2021 which included blood pressure measurement (units unspecified): 143/92 (1:10 pm), 125/90 (1:15 pm), 131/89 (1:20 pm), 135/81 (1:25 pm) and 130/89 (while standing upright); body temperature (unit unspecified): 98.6 (1:10 pm), 99.0 (1:25 pm) and 98.6 (oral; while standing upright); heart rate (unit unspecified): 74 (1:10 pm), 81 (1:15 pm), heart rate: 85 (1:20 pm), 79 (1:25 pm), 72 (while standing upright); oxygen saturation: 96% (1:10 pm), 99% (1:15 pm), 97% (1:25 pm), 96% (while standing upright); respiratory rate (unit unspecified): 20 (1:10 pm), 20 (1:15 pm), 20 (1:20 pm), 20 (1:25 pm), 18 (while standing up). Outcome of events recovered on an unspecified date.; Sender's Comments: Based on temporal association, the causal relationship between BNT162B2 and the event syncope cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1023361
Sex: F
Age:
State: CA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital: Y

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: tingling of lip and face; tingling of lip and face; numbness on left side of face/numbness was not in her throat but it was on her neck behind her ear; blood pressure spiked; tired; she didn't sleep well; Chest pain; This is a spontaneous report from a contactable nurse (patient herself). A 75-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number: lot number: E19262, via an unspecified route of administration, left arm, on 26Jan2021 10:00 at a single dose to not get Covid and to protect others around her. Medical history included mini stroke at least 8-10 years ago and neuropathy in face from ministroke. Concomitant medication included gabapentin for neuropathy in face from ministroke. The patient had no prior vaccinations (within 4 weeks). The patient previously took pregabalin (LYRICA): but was changed to gabapentin. On 26Jan2021, the patient experienced tingling of lip and face, numbness on left side of face, blood pressure spiked and chest pain. On 27Jan2021, the patient experienced tired. The events were described as: After getting the vaccine, she experienced tingling of the lip and left side of her face. She had numbness on the left side of her face. The numbness was not in her throat but it was on her neck behind her ear. Her blood pressure spiked. She drover herself to the emergency room. Her blood pressure was 160 something over 101. She was unable to specify the exact number. Then her blood pressure decreased to 104 over 80 something and it increased to 202 systolic. She was unable to specify the reading. She was tired on 27Jan2021 because she didn't sleep well in the hospital. She signed out against medical advice. The patient had a full work up to include a CT scan, MRI and doppler: results were not provided (unknown results). The patient wanted to know if recommendations were made in regard to taking the second dose if they have had adverse events. The patient was hospitalized from 26Jan2021 to 27Jan2021 (1 day) for tingling of lip and face, numbness on left side of face and blood pressure spiked. Chest pain was considered medically significant by the reporter. The outcome of she didn't sleep well was unknown. The patient was recovering from tingling of lip and face and tired. The patient has not recovered from numbness on left side of face. The patient recovered from blood pressure spiked and chest pain on 27Jan2021.; Sender's Comments: A possible contributory effect of suspect BNT162B2 on reported events cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds: GABAPENTIN

Current Illness:

ID: 1023362
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/16/2021
Rec V Date: 02/11/2021
Hospital: Y

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: dental pain; fatigue; headache; loss of taste; loss of smell; body aches; This is a spontaneous report from a contactable consumer. A 71-year-old female patient received bnt162b2 (BNT162B2), via intramuscularly on 13Jan2021 at single dose for covid-19 immunisation. Medical history included ongoing ankylosing spondylitis and potentially being exposed to COVID. The patient's concomitant medications was not reported. Patient began to have symptoms of COVID on 16Jan2021. The symptoms include Body aches, headache, loss of taste, loss of smell, dental pain, and fatigue. Hence on 22Jan2021 the patient hospitalized and same day had discharge, the patient had, blood sampling, X-ray, oxygen, and intravenous fluid. The patient underwent lab tests and procedures which included blood test: unknown result on 22Jan2021, x-ray: unknown result on 22Jan2021. The outcome of the events was recovering. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness: Ankylosing spondylitis

ID: 1023364
Sex: F
Age:
State: UT

Vax Date: 01/28/2021
Onset Date: 01/29/2021
Rec V Date: 02/11/2021
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: Blood pressure 170/84; lost ability to speak intelligibly; foggy; headache; scratchy throat; fatigue; Body aches; This is a spontaneous report from a non-contactable consumer. A 72-year-old female received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose on 28Jan2021, 11:00 AM (lot number:EL3249), via an unspecified route of administration in the left arm at single dose for COVID-19 immunization in Doctor's office/urgent care. The patient medical condition included right Bundle Branch Block, cardiac from an unknown date and unknown if ongoing. The patient had no known allergies. The patient concomitant medication included paracetamol (TYLENOL) and Upgraid. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) in the left arm on 06Jan2021, 02:00PM (lot number: EL3249) at the age of 72 years for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccination. The patient was not diagnosed with Covid-19 prior to vaccination and was not tested after the vaccination for covid-19. Twenty-four hours after vaccine received, on 29Jan2021 at 03:00 PM, the patient suddenly lost ability to speak intelligibly. The patient stated "I was completely aware though a little "foggy". Blood pressure 170/84. Friend present thought I was having a TIA and called 911. Ambulance came. Within 25 minutes, my ability to speak returned slowly. By the time I got to the ER, (45 minutes after onset), my ability to speak had mostly returned." Many blood labs were drawn, CT of head done, MRI of head done. EKG done. No cause of incident or evidence of TIA seen. After 5 hours, the patient was discharged with orders to come back if symptoms reoccurred. The patient had a headache, scratchy throat, fatigue and body aches in 2021. Since then the patient had a variety of tests, labs and Dr. visits. Blood pressure has been higher than her normal of 120/80, at intervals during the day in 2021. Since no evidence of TIA has been found, the patient was wondering if there have been any other reports of this loss of speaking ability (aphasia) occurring with any other vaccine recipients. The patient received treatment for the events. The consumer considered the events as non-serious. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: TYLENOL

Current Illness:

ID: 1023365
Sex: U
Age:
State:

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 02/11/2021
Hospital: Y

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: When got up I passed out; blood pressure shoot up to 180 over 100; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date were not reported), via an unspecified route of administration on 27Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient took the covid dose yesterday and after he/she took it, he/she sat there for few minutes and then when he/she got up he/she just passed out. The patient mentioned that they called the code blue in the hospital, they tried to, they were going to, he/she doesn't know what they were going to do but they ended up taking the patient to the emergency room where they ran every test possible blood work they did chest X-ray, they did EKG. The patient stated that the only thing that was consistent was that after the vaccine his/her blood pressure shot up to 180 over 100 and they were trying to get it down, they gave the patient some fluid (unspecified) which stayed for over two hours. The patient added that he/she have never had any blood pressure issues, as he/she was not even on any medications. The patient mentioned that he/she was now afraid to take the second dose. The events occurred on 27Jan2021 with outcome of unknown. Unknown results for blood work, EKG and chest X-ray. The reporter considered the events serious per hospitalization on 27Jan2021. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 1023366
Sex: F
Age:
State: MI

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/11/2021
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: numbness and heaviness in her whole arm/given in her right upper arm and that was the arm that was numb and heavy feeling; heaviness in her whole arm / discomfort at the site of injection; This is a spontaneous report from a contactable nurse (patient). An 84-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL1283), via an unspecified route of administration in the right upper arm on 21Jan2021 at 1:30 or 2pm at a single dose for COVID-19 immunization. Medical history included ongoing high blood pressure. Concomitant medication included medication for high blood pressure. The patient received the first dose on 21Jan2021 and has experienced numbness and heaviness in her whole arm on 25Jan2021. She was calling because she wanted to know what to should she do about it. She was leery about getting the second dose. The patient was asking if this is normal, it doesn't feel normal. She has called her doctor and was waiting to hear back from them. On 21Jan2021, on the day she got the injection, she noticed discomfort at the site of injection but that only lasted that day and that has resolved. Now she only has the heaviness and numbness, this started on 25Jan2021, 4 days later and was still ongoing. The vaccine was given in her right upper arm and that was the arm that was numb and heavy feeling. Outcome of the events was not recovered. The event numbness and heaviness in her whole arm was reported as serious (medically significant).; Sender's Comments: Based on temporal association, the causal relationship between bnt162b2 and the events vaccination site hypoaesthesia and vaccination site discomfort cannot be excluded. The information available in this report is limited and does not allow a medically meaningful assessment. This case will be reassessed once additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness: Blood pressure high

ID: 1023367
Sex: F
Age:
State: FL

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
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: she had a cut to the top of the roof of her mouth that had uncontrollable bleeding; she had a cut to the top of the roof of her mouth that had uncontrollable bleeding; right breast hurts; it radiates around to her back; Fatigue; and can't lift or pull anything and it really, really hurts; This is a spontaneous report from a contactable consumer. A 74-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9262), via an unspecified route of administration on 22Jan2021 at a single dose for COVID-19 immunisation. Medical history included sinus disorder from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient previously received a flu shot on an unspecified date. Consumer is calling about the Pfizer COVID-19 vaccine, and says she just spoke to a nurse who told her to call and find out if her experience for what she had after her first shot on Friday of the past week had been reported before. She says that on Saturday (23Jan2021), she woke up and her right breast hurt, there is something in there, it radiates around to her back, along with having fatigue. She says she was told to see if anyone else reported this, she expected normal stuff like, flu stuff, this is not that. She says she is on her way to urgent care to have that looked at. She asks if condition persists, she is supposed to get her second dose on 12Feb, does she get it? She got her first dose last Friday (22Jan2021) then woke up Saturday and can't lift or pull anything and it really, really hurts. She says to add to this, which she talked to two doctors (docs) who said it was unrelated, that night she had a cut to the top of the roof of her mouth that had uncontrollable bleeding, she went to the emergency room for that and got a shot to help her coagulate blood, and will be seeing an ENT so hopefully that will be under control. No further details provided about shot to help her coagulate blood. She got the flu shot but that was Thanksgiving, way back, not recent. She is going to get her sinuses checked out, they did a CAT scan yesterday, and is going to the doctor for that 1Feb. She is concerned that the breast pain started last Saturday and is still really painful, she doesn't know why all of a sudden that happened, so she is going to the urgent care to see if they can do something for it, and will be getting an appointment with her OBGYN. For her right breast hurting, she took Tylenol and Ibuprofen, that is all she has done. Tylenol, LOT: PPAO33, EXP: Sep2022. Ibuprofen, LOT: 113132. The patient underwent lab tests and procedures which included computerised tomogram: unknown results on 27Jan2021. Therapeutic measures were taken as a result of she had a cut to the top of the roof of her mouth that had uncontrollable bleeding she had a cut to the top of the roof of her mouth that had uncontrollable bleeding and right breast hurts. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1023368
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
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: cannot get flu shot, allergic to them; Initial information was received on 26-Jan-2021 regarding an unsolicited valid non-serious case from a consumer/non-healthcare professional (patient) via social media. This case involves a patient (unknown demographics) who could not get INFLUENZA VACCINE as he/she was allergic to it (allergy to vaccine). It was unknown if the patient had any concomitant disease or risk factor. The patient's medical history, past medical treatment(s), concomitant medications and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA VACCINE (produced by unknown manufacturer) (lot number and expiry date not reported) via an unknown route in an unknown administration site for prophylactic vaccination. On an unknown date, the patient developed allergy (allergy to vaccine) (unknown latency) following the administration of INFLUENZA VACCINE. It was unknown if there were lab data/results available. It was unknown if the patient experienced any additional symptoms/events. The details medication and reason for taking the medicine were not provided. It was not reported if the patient received a corrective treatment. At the time of reporting, the outcome was unknown for the event. There will be no information available on batch number for this case.

Other Meds:

Current Illness:

ID: 1023372
Sex: F
Age: 31
State: NJ

Vax Date: 01/03/2021
Onset Date: 01/04/2021
Rec V Date: 02/11/2021
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: INCREASED HEART RATE; NUMBNESS; TINGLING; SLURRED SPEECH; CONFUSION; OUT OF BREATH; A spontaneous report has been received from a consumer. The report concerns a female patient (age 31 years, height 60 in, weight 160 lb). No medical history was reported. Concomitant medication included Cosentyx for psoriatic arthritis, autoimmune condition. The patient received Flumist Quadrivalent (influenza virus vaccine live, intranasal) once/single administration, via nasal route, for prevention on 03-JAN-2021. On 04-JAN-2021, the patient experienced increased heart rate (preferred term: Heart rate increased), numbness (preferred term: Hypoaesthesia), tingling (preferred term: Paraesthesia), slurred speech (preferred term: Dysarthria) and confusion (preferred term: Confusional state). On an unknown date, the patient experienced out of breath (preferred term: Dyspnoea). At the time of reporting, the event of out of breath was ongoing. At the time of reporting, the event of increased heart rate was improving. The outcome of the event(s) of numbness, tingling, slurred speech and confusion was unknown. The events were considered non-serious. Laboratory values are available.

Other Meds:

Current Illness:

ID: 1023374
Sex: F
Age: 78
State: AZ

Vax Date: 01/08/2021
Onset Date: 01/12/2021
Rec V Date: 02/11/2021
Hospital: Y

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: Doesn't recognize Husband or family; Not eating much; Nausea; Headache; Diarrhea; Sleeping 24hs a day; A spontaneous report was received from a health care professional concerning a 78-year-old female patient who received Moderna's COVID-19 Vaccine (mRNA-1273) and developed diarrhea, nausea, headache, sleeping 24 hours a day, not eating, and didn't recognize husband or family. The patient's medical history included Alzheimer's disease. Products known to have been used by the patient, within two weeks prior to the event, included levothyroxine sodium. On 08 Jan 2021, approximately four days prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot 025J20-2A) intramuscularly in the left arm for prophylaxis of COVID-19 infection. On 12 Jan 2021, the reporter states the patient went into a sharp decline, diarrhea, nausea, headache and sleeping 24 hours a day. A few days later, the patient was not eating much and did not recognize her husband or family. Treatment for the event included paracetamol, emergency room visits, and nursing care center placement. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the events, developed diarrhea, nausea, headache, sleeping 24 hours a day, not eating, and didn't recognize husband or family, were considered unknown.; Reporter's Comments: This case concerns a 78-year-old, female patient with a medical history of Alzheimer's disease, who experienced unexpected events of diarrhea, hypersomnia, decreased appetite, confusional state and expected events of nausea and headache. The events of diarrhea, nausea, headache and hypersomnia occurred 5 days after the first dose of mRNA-1273 (Lot 025J20-2A) and, the events of decreased appetite and confusional state occurred unspecified number of days later. Treatment for the event included paracetamol, emergency room visits, and nursing care center placement. Very limited information regarding this event has been provided at this time. Alzheimer's disease is a confounding factor too. Based on temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Additional information has been requested.

Other Meds: SYNTHROID

Current Illness:

ID: 1023375
Sex: F
Age: 35
State: IA

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 02/11/2021
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: Became unresponsive; Looked like having a seizure; Felt light headed; BP extremely low; Profusely sweating; Heart rate extremely low; A spontaneous report was received from a pharmacist, concerning a 35-year-old female patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced felt light headed, became unresponsive, looked like having a seizure, BP extremely low, heart rate extremely low, and profusely sweating. The patient's medical history, as provided by the reporter, included high blood pressure. Products known to have been used by the patient, within two weeks prior to the event, included hydrochlorothiazide/lisinopril. On 29 Jan 2021, five minutes prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (Lot Number: 025L20A) intramuscularly in the right arm for prophylaxis of COVID-19 infection. On 29 Jan 2021, the patient felt light-headed five minutes after receiving the vaccine. He then became unresponsive but was breathing and had a pulse. The reporter stated it looked like the patient was having a seizure; his eyes rolled upward, his left arm shook, and he did not respond to touch or voice. It was reported that 911 was immediately called and responded within a couple of minutes. The patient's blood pressure and heart rate were extremely low, and he was profusely sweating. The reporter stated that the patient came to and still felt very light-headed. The patient was then taken to the emergency department. Medical tests and laboratory results were unknown, but the reporter stated that a magnetic resonance imaging (MRI) was possibly performed. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not provided. The outcome for the events, became unresponsive and looked like having a seizure, were resolved on 29 Jan 2021. The outcome for the events, felt light headed, BP extremely low, heart rate extremely low, and profusely sweating, was unknown.; Reporter's Comments: This case concerns a 35-year-old, female, with medical history of high blood pressure, who experienced a serious unexpected event of syncope, seizure, and non-serious unexpected events of dizziness, hypotension, hyperhidrosis, and heart rate decreased. The events occurred 1 day (5 min) after mRNA-1273 (Lot# 025L20A). Treatment information was not provided. Concomitant medications included: hydrochlorothiazide/lisinopril. Based on temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Additional information has been requested.

Other Meds: LISINOPRIL/HCTZ

Current Illness: Hypertension

ID: 1023376
Sex: F
Age:
State: AL

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/11/2021
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: fever; aches; chills; headache; This is a spontaneous report from a contactable other healthcare professional, the patient. This 51 year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EJ1686, dose 2, single dose via unknown route of administration in the left arm on 19Jan2021 at 09:15 AM (at the age of 51 years-old) for COVID-19 vaccination. Medical history included gastroesophageal reflux disease (GERD). Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EH9899, dose 1 via unknown route of administration in the left arm on an unknown date at 09: 45 AM. The patient was not pregnant at the time of vaccination. The patient had no known medication allergies. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included ibuprofen (MOTRIN), dextromethorphan, doxylamine, ephedrine, ethanol, paracetamol (NYQUIL) and omeprazole. On 19Jan2021 at 20:00, about twelve hours following the second injection, the patient developed a fever, aches, chills and headache that lasted for approximately 24 hours. The clinical outcome of fever, aches, chills and headache was recovered on an unknown date in Jan2021. Treatment received for fever, aches, chills and headache included an unknown over the counter medication without relief. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds: MOTRIN (IBUPROFEN); NYQUIL; OMEPRAZOLE

Current Illness:

ID: 1023377
Sex: M
Age:
State: CT

Vax Date: 01/23/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
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: Pain the next day at site of injection; This is a spontaneous report from a contactable consumer. A 75-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, via an unknown route of administration in the right arm on 23Jan2021 at 15:30 (at the age of 75-years-old) as a single dose for Covid-19 immunization. Medical history included aneurysm and pacemaker from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. It is unknown if patient received any other vaccines within four weeks prior to the vaccination. On 24Jan2021, the patient experienced pain at the site of injection. Treatment was not given for the event. The clinical outcome of the event vaccination site pain was recovering. It was reported that since the vaccination, the patient had not been tested for COVID-19. The batch/lot numbers for the vaccine, PFIZER-BIONTECH COVID-19 MRNA VACCINE, were not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1023378
Sex: F
Age:
State: NY

Vax Date: 01/21/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
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: severe tension/pain on left side of head; severe tension/pain on left side of head; This is a spontaneous report from a contactable healthcare professional. A 29-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration right arm on 21Jan2021 as single dose for covid-19 immunization. No medical history was noted. No allergies to medications, food, or other products. Concomitant medication included celecoxib (CELEXA). On 24Jan2021, at 08:00, the patient experienced severe tension/pain on left side of head. This was elaborated as behind the eye and above brow bone, radiates to back of neck. The events were non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of severe tension/pain on left side of head was not recovered.

Other Meds: CELEXA [CELECOXIB]

Current Illness:

ID: 1023379
Sex: M
Age:
State: TX

Vax Date: 01/22/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
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: Red mark on his shot mark; This is a spontaneous report from a contactable consumer. An 82-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Batch/lot number: EL9262, via an unspecified route of administration in the right arm on 22Jan2021 at SINGLE DOSE for covid-19 immunization. The patient has no other relevant medical history. The patient's concomitant medications were not reported. The patient experienced red mark on his shot mark on 24Jan2021. The mark was not raised, and it is about the size of a pencil eraser. Patient does not have any feeling or pain (in this mark). The outcome of event was not recovered. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1023380
Sex: F
Age:
State: NY

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 02/11/2021
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: This is a spontaneous report from a contactable other health professional (patient). A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number: ELO140, intramuscular in the left arm the age of 55-years on 30Dec2020 14:00 at SINGLE DOSE for COVID-19 immunization. Medical history included penicillin allergy, GERD (gastrooesophageal reflux disease), osteoarthritis and spinal stenosis. Prior to vaccination, the patient was diagnosed with COVID-19. Concomitant medications included dorzolamide hydrochloride, ketorolac tromethamine and timolol maleate. On 31Dec2020 08:00, patient woke up with muscle soreness in both quads it was a 4/10 pain. It lasted for 24 hours in the left. Since 31Dec2020, she still has soreness in the right quad, initially it was the entire muscle and then it settles to proximal & lateral to hip. The pain level was 2/10. Outcome of events was not recovered. The patient did not received treatment for the events. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: DORZOLAMIDE HYDROCHLORIDE; KETOROLAC TROMETHAMINE; TIMOLOL MALEATE

Current Illness:

ID: 1023381
Sex: F
Age:
State: VA

Vax Date: 12/23/2020
Onset Date: 01/03/2021
Rec V Date: 02/11/2021
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: back pain upper mid back, spread to left & right side; lower back muscles on the left & right side; This is a spontaneous report from a contactable healthcare professional. A 55-year-old female patient received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EK5730) on her right arm, via an unspecified route of administration on 23Dec2020 10:00 at a single dose for covid-19 immunization. Medical history included hypertension (HTN), asthma, obesity, postmenopause, hay fever, pre diabetic and allergy to sulfa. Concomitant medication included chlorthalidone, carvedilol (COREG), fexofenadine hydrochloride (ALLEGRA) and phytomenadione (VITAMIN K). The patient experienced back pain upper mid back, spread to left & right side and lower back muscles on the left & right side.; both on 03Jan2021 11:00 AM. The patient received lidocaine, methacarbamol, T3, prednisolone dosepak as treatment for the events. The outcome of the events was recovering.

Other Meds: CHLORTHALIDONE; COREG; ALLEGRA; VITAMIN K

Current Illness:

ID: 1023382
Sex: F
Age:
State: FL

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
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: severe contraction of chest muscles and neck lasting about 20 minutes; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL1283, expiry date unknown), via an unspecified route of administration on 25Jan2021 at 10:30 on the left arm at a single dose for COVID-19 immunization. Medical history included allergies to bee stings from an unknown date and unknown if ongoing. Concomitant medication included salbutamol sulfate (ALBUTEROL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that on 25Jan2021 at 11:30, one hour after injection the had severe contraction of chest muscles and neck lasting about 20 minutes. The patient did not receive treatment for the event. The outcome of the event was recovered. The event was reported as non-serious.

Other Meds: ALBUTEROL

Current Illness:

ID: 1023383
Sex: F
Age:
State: SD

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
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: Muscle aches; joints ache; slight head ache; This is a spontaneous report from a contactable consumer. A 21-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), via an unspecified route of administration in the left arm on 25Jan2021 at 13:15 (at the age of 21-years-old) as a single dose for COVID-19 immunisation. Medical history included asthma from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications included acetylsalicylic acid (ASPIRIN), montelukast (MANUFACTURER UNKNOWN), and omeprazole (MANUFACTURER UNKNOWN); all taken for unknown indications from unknown dates and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously took sulfamethoxazole/trimethoprim (BACTRIM) from unknown dates for an unknown indication and experienced drug allergy. On 25Jan2021 at 19:00, the patient experienced muscle aches, joints ache, and slight headache (reported as in the morning). The patient did not receive any treatment for the events. The clinical outcomes of muscle aches, joints ache, and slight headache were recovering. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; MONTELUKAST; OMEPRAZOLE

Current Illness:

ID: 1023384
Sex: F
Age:
State: NJ

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 02/11/2021
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: Fatigue for 12 days; severe pain to all joints especially knees and neck; severe pain to all joints especially knees and neck; weakness; nausea; headache; feverish; swelling of left arm; malaise for 12 days; symptoms of pain lasted 12 days-I still don't feel 100%; This is a spontaneous report from a contactable other healthcare professional (patient). A 50-year-old female patient received the first dose of bnt162b2 (Pfizer-Biontech COVID-19 Vaccine, Lot number: e1 3246), via an unspecified route of administration at the left arm on 11Jan2021 at single dose for COVID-19 immunization. The vaccine was received in a nursing home. Medical history included seasonal allergy. The patient was not pregnant at the time of vaccination. The patient's concomitant medications were not reported. On 11Jan2021 04:00 PM, the patient experienced fatigue for 12 days, severe pain to all joints especially knees and neck, weakness, nausea, headache, feverish, swelling of left arm, malaise for 12 days, symptoms of pain lasted 12 days- I still don't feel 100%.The events were assessed as non-serious, did not result in death, not life threatening, did not cause/prolonged hospitalization, not disabling/incapacitating, did not cause congenital anomaly/birth defect. Treatment was not received for the adverse events. Events resulted to Doctor or other healthcare professional office/clinic visit. The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination the patient was not diagnosed with COVID-19. The patient was tested for COVID-19 using Nasal Swab on 22Jan2021 and result was negative. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1023385
Sex: F
Age:
State:

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: severe chills; vomiting; Diarrhea; lots of nausea; her whole body was trembling violently; she was very cold; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received her second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 25Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient started experiencing severe chills and her whole body was trembling violently, she was very cold. Followed with vomiting, diarrhea and lots of nausea. The outcome of the events was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1023386
Sex: F
Age:
State: MN

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
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: first dose was administred on 28Dec2020 and second dose on 21Jan2021; Sore arm at injection site; body aches during the second shot for a full 24 hours; This is a spontaneous report from a contactable pharmacist (the patient). A non-pregnant 26-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL3302), via an unspecified route of administration, in the left arm on 21Jan2021 as a single dose for COVID-19 immunization. Medical history included asthma. The patient did not have any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications taken within two weeks of vaccination included spironolactone, ethinylestradiol, levonorgestrel (AVIANE), cholecalciferol. The patient did not receive any other vaccines within four weeks prior to the vaccination. Historical vaccine include the first dose of BNT162B2, lot #EK9231, intramuscular in the left arm on 28Dec2020 at the age of 26-year-old for COVID-19 immunization. On 22Jan2021, the patient experienced sore arm at injection site, (but not as severe in comparison to the flu shot), and body aches during the second shot for a full 24 hours. The events were reported as non-serious. Treatment for the events included acetaminophen 500 mg - 2 tablets by mouth twice daily. The clinical outcome of the events sore arm at injection site, and body aches during the second shot for a full 24 hours was recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds: SPIRONOLACTONE; AVIANE; CHOLECALCIFEROL

Current Illness:

ID: 1023387
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: Joint pain in her fingers, hands, and wrists; This is a spontaneous report from a contactable physician (patient). A 56-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 14Jan2021 at a single dose, with route of administration unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. In Jan2021, the patient had joint pain in her fingers, hands and wrists. The outcome of the event, pain in her fingers, hands and wrists, was unknown. Information regarding lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023388
Sex: M
Age:
State: FL

Vax Date: 01/19/2021
Onset Date: 01/21/2021
Rec V Date: 02/11/2021
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: Headache; Chills; Body aches; Nausea; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL8982), via an unspecified route of administration at left arm on 19Jan2021 08:28 at 0.3 mL, single for COVID-19 immunization. Medical history included Open heart surgery in Jan2003 and in Jan2018 (he had two open heart surgeries, the first one in Jan2003, and the last one in Jan2018);Stent placement (he has had 14 stents placed over a period of time, the last stents were done when open heart surgery was done, they put in 3 that time, in Jan2018); and Gallbladder removal on 16Jun2020. The patient's concomitant medications were not reported. The patient previously took influenza vaccine (flu vaccine) in Sep2020. The patient had a reaction to the COVID-19 vaccine two days (on 21Jan2021) after getting it. He had a really bad headache, chills, body aches and nausea, a whole series of things went wrong. He woke up at 04:00 21Jan2021 with an intense headache. The reaction happened all together, his headache, body aches, chills, and very bad nausea started about the same time, he contacted his doctor that day. At time of report was the first day he was starting to feel better. It was the first day he didn't have a headache, he was feeling better now, he was basically in bed from Thursday on. He got up a little bit yesterday, and at the time of report he was feeling much better, it lasted 4 to 5 days (as reported). He took Tylenol 500mg, two of them, and kept taking it 6 hours apart, it was all he had to take, and it barely touched it (UPC: 30043739 LOT SMA115, EXP Sep2022). The outcome of the event headache recovered on 26Jan2021; and recovering outcome for the other events.

Other Meds:

Current Illness:

ID: 1023389
Sex: F
Age:
State: MO

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: Anatomical site of vaccine administration: Left Arm, swelling on the arm like a hard notch/My arm is swelled up; Anatomical site of vaccine administration: Left Arm, There was really tender; Anatomical site of vaccine administration: Left Arm, swelling on the arm like a hard notch/My arm is swelled up; felt feverish; This is a spontaneous report from a contactable nurse (patient herself). A 63-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number EL8982), via an unspecified route of administration on 13Jan2021 at SINGLE DOSE (first dose, left arm) for covid-19 immunisation. Medical history included diabetes mellitus from an unknown date. The patient's concomitant medications were not reported. The patient received the first dose of the vaccine on 13Jan2021. Anatomical site of vaccine administration was the left arm. The patient experienced a reaction afterwards which made her miss 2 days of work and work with her patients as she do home care (Jan2021). She experienced swelling on the arm like a hard notch/arm is swelled up and felt feverish and by the next day she could not move her arm at all/move her arms up the following day. She reported that there was really tender. She was supposed to get the 2nd dose of the vaccine on 03Feb2021 and was asking if she can take it on the 05Feb2021 so as she cannot miss work in the event, she experiences the reaction again. No Physician Office/ Emergency Room visit involved. Treatment included Tylenol to help with the pain and then put ice on it to break it keep swelling down. Outcome of the events was unknown. The case was reported as non-serious.

Other Meds:

Current Illness:

ID: 1023390
Sex: M
Age:
State: FL

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
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: allergic reaction; redness at the injection site; swelling at the injection site; redness and swelling at the injection site that moved down his arm/then it traveled; redness and swelling at the injection site that moved down his arm/then it traveled; itching at injection site; pain at injection site; several hours before checking infection site; bump, it was typical like what it says in the brochure, as time went on, it got red, in a spot by injection site, then it traveled/middle of injection site there was a white area, raised; This is a spontaneous report from a contactable consumer (patient). This consumer reported similar events for two patients. This is the first of two reports. A 75-year-old male patient received his first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; unknown lot number and expiration date), via an unspecified route of administration on 22Jan2021 09:15 at a single dose for covid-19 immunization. Medical history included cholesterol (blood cholesterol abnormal) and blood pressure blood pressure abnormal). Concomitant medication included hydrochlorothiazide for blood pressure, atorvastatin for cholesterol, fish oil and vitamins NOS (MULTIVITAMIN). The patient reported that he got the first dose of the covid vaccine on Friday (22Jan2021) and he had symptoms following the injection which included redness and swelling at the injection site that moved down his arm. The patient also mentioned that he experienced like a bump, it was typical like what it says in the brochure, as time went on, it got red, in a spot by injection site, then it traveled. The patient mentioned that he was seen at his PCP and reports that he was told he had an allergic reaction to the shot, hopefully it would not spread any further, and states his doctor seemed to be very concerned his physician prescribed him with an epi pen to have for if he gets the second dose of the vaccine and the reporter stated that he has never diagnosed with allergies. The patient inquired if the injection wasn't put in correctly and it was put in the tissue and not the muscle. The reporter mentioned that his wife said the needle didn't go in as much as when she got her injection, so he was wondering if it was administered in the right way and also asking if part of the needle could have broken off and if that is what is causing the redness and swelling to his arm. His doctor assured him the needle could not break and stated that his said that it did not look like the injection was as deep as hers since she was watching him get his vaccine. The reporter also inquired if that could have caused an issue if it was not administered deep enough. He mentioned that he waited several hours before checking infection site [pending clarification] and noticing the swelling and redness. States it is also itchy and painful, not a painful to the touch but an itchy, knifey kind of pain, states sometimes it feels like he needs to rub it and sometimes it feels like someone is stabbing him. The outcome of the event allergic reaction was unknown while the outcome of the other events was not recovered. The following information on the batch/lot number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021077371 Same reporter/drug, similar events, different patient

Other Meds: HYDROCHLOROTHIAZIDE; ATORVASTATIN; FISH OIL; MULTIVITAMIN [VITAMINS NOS]

Current Illness:

ID: 1023391
Sex: F
Age:
State: TX

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
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: she needed to clear her throat a few times; felt dizzy; disoriented; foggy headed; mouth felt full; tongue was larger than normal and swollen; This is a spontaneous report from a contactable consumer (patient herself). A 37-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; batch/lot number and expiration date were unknown), via an unspecified route of administration on the left arm on 22Jan2021 at 09:45 at a single dose for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was reported as the clinic. The patient had no medical history; she had no allergies to medications, food, or other products. Concomitant medications included aloe ferox gum, aloe vera gum, atropa belladonna herb, peumus boldus leaf oil, rhamnus frangula (SPARK, "Advocare Spark") and "NLA for Her Shred Her" as diet supplement (sup). The patient was not pregnant at the time of vaccination. 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 had not been tested for COVID-19. On 22Jan2021 at 10:00, also reported as 10-13 minutes after vaccination, the patient needed to clear her throat a few times. Within seconds or minutes, she felt dizzy, disoriented, and foggy headed. Then her mouth felt full and she looked in the mirror and noticed her tongue was larger than normal and swollen. The reporter assessed the events as non-serious. The adverse events did result in a doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of all the events, which included a steroid and diphenhydramine (BENADRYL) shot. The patient recovered from all the events on an unspecified date. Information on the batch/lot number has been requested.

Other Meds: SPARK [ALOE FEROX GUM;ALOE VERA GUM;ATROPA BELLADONNA HERB;PEUMUS BOLDUS LEAF OIL;RHAMNUS FRANGULA]

Current Illness:

ID: 1023392
Sex: M
Age:
State: WA

Vax Date: 01/24/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
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: Testicular ache; chills; headache; SI joint pain bilaterally; Fatigue; This is a spontaneous report from a contactable 51-year-old male Health care professional reported for himself. A 51-year-old male patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number unknown), via an unspecified route of administration from 24Jan2021, 14:00 at SINGLE DOSE (second dose, left arm) for covid-19 immunisation, administered on a hospital. Medical history included history of chronic hives; no issues x 1 year from an unknown date. 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 had not been tested for COVID-19. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number unknown) on 03Jan2021 at 12:00 PM on the right arm for Covid-19 Immunization (Age of vaccination was 51 years old). The patient previously took Asa and experienced drug hypersensitivity and hives (known allergies: Asa - hives). Concomitant medication included celecoxib (CELEXA), and cetirizine hydrochloride (ZYRTEC), therapy dates and indication unspecified. The patient experienced testicular ache, chills, headache, si joint pain bilaterally, and fatigue on 25Jan2021 04:00. No treatment was given. Outcome of the events was recovered. Seriousness criteria was reported as non-serious. Information on the lot/batch number has been requested

Other Meds: CELEXA [CELECOXIB]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1023393
Sex: F
Age:
State: NC

Vax Date: 01/22/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
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: Runny nose; Fever; Lots of aches; Threw up; Headache; Extremely tired; This is a spontaneous report from a contactable consumer (patient) via the medical information team. A 71-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number not reported, expiration date: 31May2021), intramuscular (right arm) on 22Jan2021 at a single dose for COVID-19 vaccination. Medical history included hypertension, and cancer which was reported to have recovered from cancer twice. There were no concomitant medications. The patient was calling about BNT162B2 and reported that she had the vaccine on 22Jan2021. She reported that she was extremely tired Sunday, 24Jan2021, and Monday, 25Jan2021, and other than that, she started getting a runny nose on 25Jan2021. She reported that on 25Jan2021, she started running a fever of 100.2 to begin with and the morning of 26Jan2021 it was about that and it went up to 100.6. She reported that on evening of 25Jan2021 she had a lot of aches and went to bed early. Almost as soon as she got into bed before she took her temperature, she threw up. She also had a pretty bad headache. The patient was recovering from being extremely tired, and with unknown outcome from the rest of the events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023394
Sex: M
Age:
State: NY

Vax Date: 01/23/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
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: axillary lymphadenopathy; This is spontaneous report from a non-contactable consumer reporting for himself. A 30-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL324), via an unspecified route of administration on 23Jan2021 at SINGLE DOSE for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. 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 has no known allergies. The patient experienced axillary lymphadenopathy on 24Jan2021. No treatment was received. Outcome of the event was recovering. The reporter assessed the event as non-serious. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1023395
Sex: F
Age:
State: NC

Vax Date: 01/23/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: a sharp pain was coming from the side of my back and shooting to my left breast/ a muscle on the side going down of my back/ sharp pain when I make a turn or reach that goes to my breast; when she moves that she has a pain that goes through the lymph nodes or muscles behind her left breast; when she moves that she has a pain that goes through the lymph nodes or muscles behind her left breast; pain was either from something in her left shoulder, or the left side of her back, or a muscle; feeling a little down and out; she can't sleep in the heat at night; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: EL8982 ), via an unspecified route of administration at left upper arm on 23Jan2021 16:00 at single dose for COVID-19 immunization. There were on patient medical history and concomitant medications. No additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations (within 4 weeks).The patient said she did good on Saturday, 23Jan2021, saying her left arm didn't get sore. She said she did good on Sunday, 24Jan2021. She stated "I didn't get sore, but it just seemed like maybe a few days ago it seemed like a sharp pain was coming from the side of my back and shooting to my left breast (on 25Jan2021). It only does it when I am lying down and not when I am sitting down. I drank plenty of water and continue to drink plenty of water. Today, I am feeling a little down and out because of my breast (25Jan2021). My breast itself is not sore at all. It seems like maybe a muscle on the side going down of my back. There is a sharp pain when I make a turn or reach that goes to my breast. Well, if you have arthritis it could be that." She said it seemed when she moves or turns, she has a sharp pain in her left breast. The patient asked if the sharp pain she was experiencing in her left breast area were possibly her lymph nodes. She clarified her left breast was not sore, but the area behind her left breast has a pain go through it. She said it was just when she moves that she has a pain that goes through the lymph nodes or muscles behind her left breast. She said she normally doesn't sleep on her left side, but if she sleeps on her left side, the pain behind her left breast was better. She said she does not have big breasts and was not wearing a bra when she had the pain in her left breast area. She said she was wondering if the pain she has is from her lymph nodes or muscles in her back. She said the pain was either from something in her left shoulder, or the left side of her back, or a muscle. As treatment, patient reported that she has been holding her left breast area when she moves. She said holding the left breast area helps lessen the pain, but the pain was still there. She said she has been trying to troubleshoot her pain. She said she drinks coffee every day and thought maybe she was drinking too much caffeine. She said she can't sleep in the heat at night, so she turns the heat off in her house at midnight, but her house was still warm (70 degrees) when she wakes up in the morning. She said she thought that maybe the cold weather got into her back and left shoulder. She said she checked her left breast for lumps and didn't find any lumps. She said the only thing left for her to do was to contact her gynecologist and go have a mammogram. She doesn't take any medicine. She said she does take something for sleep as needed, but she would have to be going without sleep for a long time before she would take that medicine. She reported she is otherwise a healthy person. She said people talk about hormones changes after when a person used to have a period, and she sometimes doesn't know if her pain would be because of that. She said she may have irritation in her breasts from wearing a bra that may be too tight, but the pain she was experiencing now was different from that pain. The events did not require a visit to Emergency Room or Physician Office. The outcome of the events she can't sleep in the heat at night and feeling a little down and out was unknown; and not recovered outcome for the other events.

Other Meds:

Current Illness:

ID: 1023396
Sex: F
Age:
State: MN

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: chills; fever of 101 f; went to bed with an uneasy feeling; had a hard time sleeping; intermittent body aches; fatigue; This is a spontaneous report from a contactable nurse (patient). A 55-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: Ek9231 and expiry date: unknown), via an unspecified route of administration on the right arm, on 25Jan2021 11:00 at a single dose for COVID-19 immunization. The first dose was received on 04Jan2021 11:00 (lot number: Ek5730) on the left arm. Medical history included epilepsy. Patient was not pregnant at the time of vaccination. Concomitant medication included lamotrigine (LAMICTAL), and levetiracetam (KEPPRA) and unspecified multivitamin. There were no other vaccines received within 4 weeks prior to COVID vaccination. The patient previously took DILANTIN and experienced allergy. Patient went to bed with an uneasy feeling and had a hard time sleeping and had intermittent body aches on 25Jan2021 22:00. He woke up at 2am on 26Jan2021 with chills and a fever of 101 F. Patient took Acetaminophen and Iborprophin. The medications did get rid of the fever and body aches. Patient woke up at 4 feeling a little better but the body aches and fatigue on Jan2021 was still there. Patient called in sick to work on 26Jan2021. Outcome of the events was recovering. Case was considered non-serious. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination.

Other Meds: LAMICTAL; KEPPRA

Current Illness:

ID: 1023397
Sex: F
Age:
State: WI

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/11/2021
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: tingly, itchy, prickly feeling hands; tingly, itchy, prickly feeling hands; red blotches on her hands; This is a spontaneous report from a contactable nurse. A 62-year-old female patient received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3249), intramuscular on 21Jan2021 16:30 at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that 30 minutes after vaccination was administered, client stated she started tingly, itchy, prickly feeling hands. She did have red blotches on her hands. Public Health Nurse offered Benadryl which she accepted and was ok a half hour later. The outcome of the events was recovered on 21Jan2021 17:30.

Other Meds:

Current Illness:

ID: 1023398
Sex: F
Age:
State: NJ

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
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: Right arm was very sore; right hand felt numb; itchy on the right side of her back and her right arm; Itchy on the right side of my back; Rash with bumps; This is a spontaneous report from a contactable healthcare professional (patient). This 36-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9262 and expiry date unknown), via an unspecified route of administration on 22Jan2021 15:00 at a single dose on the right arm for COVID-19 immunization. The patient medical history was not reported. Concomitant medication included unspecified birth control pill. The patient was not diagnosed with COVID-19 prior to vaccination. Patient has not been tested for COVID-19 since the vaccination. Patient has no known allergies. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On day 2, 23Jan2021 17:00, the patient's right arm was very sore, right hand felt numb, itchy on the right side of her back and her right arm. The patient started to develop rash with bumps. Rash went away as soon as she took Benadryl. On Day 3, she was back to normal, no soreness, no numbness and no itchiness. The events were reported as non-serious. Outcome of the events was recovered on 24Jan2021.

Other Meds:

Current Illness:

ID: 1023399
Sex: F
Age:
State: TX

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/11/2021
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: Chills; fever lasted two days, temp ranges 99.1-100.5; Intense headache; Severe body aches; Dizziness; Loss of taste to everything except salt and lemon taste of cough drops; This is a spontaneous report from a contactable physician (patient). A 69-year-old female patient received the second dose of bnt162b2 (BNT162B2, lot number: EL9261, expiry date: not reported), via an unspecified route of administration, on 20Jan2021 12:00 AM at a single dose on the left arm for COVID-19 immunization. The most recent COVID-19 vaccine was administered at a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not pregnant at the time of vaccination. Medical history included hypertension. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included Valsartan, Metoprolol, Atorvastatin, Vitamin, Meth (unspecified). The patient previously took morphine and experienced drug allergy. The patient previously received the first dose of bnt162b2 (BNT162B2, lot number: EH9899, expiry date: not reported), via an unspecified route of administration, on 28Dec2020 12:15 AM at a single dose on the left arm for COVID-19 immunization (age at vaccination: 69-year-old). 16 hours later after vaccination, on 21Jan2021 04:00, the patient woke up with chills, fever, intense headache, severe body aches and dizziness. She noticed loss of taste to everything except salt and lemon taste of cough drops. Fever lasted two days, temp ranges 99.1-100.5. She cancelled clinic and stayed home. Due to loss of taste, she got tested for COVID infection on an unspecified date in Jan2021; result was negative. Body ache and loss of taste continued for 3 days. The reported adverse events resulted into doctor or other healthcare professional office/clinic visit. The patient underwent laboratory tests and procedures which included nasal swab on 07Jan2021 with result of negative. Therapeutic measures taken as a result of adverse events included Advil and Tylenol. Outcome of the events was recovered on unspecified dates in Jan2021. The reporter assessed the events as non-serious.

Other Meds: VALSARTAN; METOPROLOL; ATORVASTATIN

Current Illness:

ID: 1023400
Sex: F
Age:
State:

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/11/2021
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: Nausea; Weakness; High blood pressure; Fogginess; Shaking all over; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 15Jan2021 at a single dose, with route of administration unspecified, for COVID-19 immunization at the hospital. The patient's medical history and concomitant medications were not reported. On 15Jan2021, the patient had nausea; weakness; high blood pressure; fogginess; and was shaking all over. The outcome of the events, 'nausea', 'weakness', 'high blood pressure', 'fogginess' and 'shaking all over', was recovered on 15Jan2021 (17:00); blood pressure had come down to 136 (unit was not reported). Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023401
Sex: F
Age:
State: GA

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
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: injection site pain (current with itching); injection site pain (current with itching); tiredness/fatigue; tooth pain; joint pain; chills; low-grade fever (100.4); This is a spontaneous report from a contactable consumer (patient). A 52-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ELo142), via an unspecified route of administration in right arm on 21Jan2021 09:15 at single dose for COVID-19 immunization. The patient was not pregnant at time of vaccination. The facility where the most recent COVID-19 vaccine was administered was in the workpalce clinic. 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. Medical history included hypothyroidism and high blood pressure from an unknown date and unknown if ongoing. Concomitant medication included losartan and levothyroxine sodium (LEVOTHROID). On 22Jan2021, the patient experienced injection site pain (current with itching), three days of tiredness/fatigue, tooth pain, joint pain, chills and low-grade fever (100.4). The patient recovered on unspecified date. No treatment was given to the patient for the events. The events were considered non serious as it did not result in death, were not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and were not a congenital anomaly/birth defect.

Other Meds: LOSARTAN; LEVOTHROID

Current Illness:

ID: 1023402
Sex: F
Age:
State: CA

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/11/2021
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: Shortness of breath; chest tightness; dizziness; fatigue; joint and muscles pain; joint and muscles pain; headache; chills; injection site soreness; This is a spontaneous report from a contactable nurse (patient). A 46-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3249 and expiration date not provided), via an unspecified route of administration (left arm) first dose on 20Jan2021 09:15 at single dose for Covid-19 immunization. There was no medical history. The patient was not pregnant at time of vaccination. The patient's concomitant medication included losartan, citalopram hydrochloride (CITALOPRAM [CITALOPRAM HYDROCHLORIDE]), clonazepam, hydrocodone bitartrate, paracetamol (NORCO), carisoprodol (SOMA [CARISOPRODOL]), and hydrochlorothiazide. On 20Jan2021 09:15, the patient experienced Shortness of breath, chest tightness, dizziness, fatigue, joint and muscles pain, headache, chills, injection site soreness. The patient did not received treatment for the events. The outcome of the events was recovering. No other vaccine was given in four weeks. The patient was not tested positive post vaccination.

Other Meds: LOSARTAN; CITALOPRAM [CITALOPRAM HYDROCHLORIDE]; CLONAZEPAM; NORCO; SOMA [CARISOPRODOL]; HYDROCHLOROTHIAZIDE

Current Illness:

ID: 1023403
Sex: M
Age:
State: SC

Vax Date: 01/06/2021
Onset Date: 01/08/2021
Rec V Date: 02/11/2021
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: bakers cyst behind my right Knee; pain and swelling in my right knee/ calf and ankle/in the right leg/in left hand; pain and swelling in my right knee/ calf and ankle/in the right leg/in left hand; pain and swelling in my right knee/ calf and ankle/in the right leg/in left hand; pain and swelling in my right knee/ calf and ankle/in the right leg/in left hand; This is a spontaneous report from a contactable consumer (patient). A 48-years-old male patient received the first dose of BNT162B2 Pfizer-BioNTech COVID-19 Vaccine, lot number EH9899, via an unspecified route of administration in left arm on 06Jan2021 at 09:00 at single dose for COVID-19 immunization. The patient received vaccination in Doctor's office/urgent care. Medical history included bladder cancer from an unknown date, cancer treatment with tumor vaccine therapy BCG (Bacillus Calmette Guerin) on 23Dec2020, bone spur in right thumb from an unknown date, COVID-19 from an unknown date and drug allergy to amoxicillin/clavulanate potassium (AUGMENTIN). The patient has not been tested for COVID-19 since the vaccination. Concomitant medication included doxycycline. On 08Jan2021 (also reported 3 days after the vaccine) at 05:45 the patient experienced pain and swelling in his right knee/calf and ankle. Pain and swelling in the right knee, calf and ankle continued until 14Jan2021 when the patient went to the urgent care. He was sent to the emergency room with a suspected blood clot and ultrasound proved no clot was in the leg. On 15Jan2021 the patient went to a hematologist and had an additional ultrasound which found a bakers cyst behind his right knee. He continued to have pain and swelling in the right leg and left hand which had already arthritis and he suspected it was an immune response to the vaccine. Rest, ice, compression and elevation were suggested as therapeutic measures to treat the events. The reported events had not resolved yet at the time of the report.

Other Meds: DOXYCYCLINE

Current Illness:

ID: 1023404
Sex: F
Age:
State: NC

Vax Date: 01/07/2021
Onset Date: 01/09/2021
Rec V Date: 02/11/2021
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: menstrual cycle has been off and then it restarted with brown clotting old blood/her period was not due for another 10 days; This is a spontaneous report from a contactable nurse (patient). A 38-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EK9231), intramuscularly on the left arm, on 07Jan2021 10:30, at single dose, for covid-19 immunization. Medical history included thyroid cancer. Concomitant medication included thyroid (ARMOUR THYROID). The patient previously took hydromorphone (DILAUDID) and metaxalone (SKELAXIN) and experienced allergies to both. The vaccine was given at the hospital. The patient stated that her menstrual cycle has been off and then it restarted with brown clotting old blood on 09Jan2021 (also reported as 24Jan2021); her period was not due for another 10 days. She added that her cycles have never been off, and she has never had issues with her menstrual cycles or any female problems. The adverse event resulted in doctor or other healthcare professional office/clinic visit on 27Jan2021. Unspecified treatment was received for the adverse event. The outcome of the adverse event was unknown. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have COVID prior vaccination and have not been COVID tested post vaccination.

Other Meds: ARMOUR THYROID

Current Illness:

ID: 1023405
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
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: Some very bad gout; This is a spontaneous report from a contactable nurse. A patient of unspecified age and gender received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) at a single dose, with route of administration and therapy date unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on an unspecified date for COVID-19 immunization. On an unspecified date, the patient had some very bad gout. The outcome of the event was unknown. The reporting nurse would want to give the patient indomethacin for the gout, and wanted to know if it will be safe. Information about lot/batch number is requested.

Other Meds:

Current Illness:

ID: 1023406
Sex: F
Age:
State: OH

Vax Date: 01/22/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
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: my left knee started hurting/knee started screaming at me; This is a spontaneous report from a contactable consumer (patient). An 85-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration on 22Jan2021 at single dose for COVID-19 immunization. Medical history included knee replacement (her right knee was replaced years ago). Concomitant medications were not reported. The patient reported that after getting the vaccine, her left knee started hurting on an unspecified date in Jan2021. She took some pills over the weekend that helped. But she stood up that morning and that knee started screaming at her. This was further clarified as the left knee began hurting badly when standing this morning. Clinical outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023407
Sex: F
Age:
State: NC

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 02/11/2021
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: extreme fatigue; Headache; This is a spontaneous report from a contactable consumer. A 69-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EL1283), via an unspecified route of administration on 20Jan2021 at SINGLE DOSE at arm left for covid-19 immunisation. Medical history included none. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced extreme fatigue, and headache. The patient took Advil for the event headache. She says she has also had lots of rest and water. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1023408
Sex: F
Age:
State:

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
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: experienced rapid heartbeat; This is a spontaneous report from a non-contactable consumer reported for herself. This female patient of unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number and Expiration Date: Not Provided), via an unspecified route of administration on 25Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On 26Jan2021 13:30 she experienced rapid heartbeat for 4 hours. She said she feels better on 26Jan2021 and wanted advise on receiving 2nd dose. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1023409
Sex: F
Age:
State: VA

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
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: She said that she rarely gets sick; A soreness in her throat and it was hard to swallow; A soreness in her throat and it was hard to swallow; The feeling of a tooth ache/ having a toothache currently; Felt like someone punched her arm; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), intramuscular in upper right arm on 21Jan2021 at a single dose for COVID-19 immunization. Medical history included seasonal allergy. There were no concomitant medications. The patient experienced a soreness in her throat and it was hard to swallow, in which she had to get ice to help alleviate the pain in her throat. The pain in her throat resolved a couple of hours later (as reported). She wanted to know if these side effects were from the vaccine. She also reported the feeling of a tooth ache today (26Jan2021), in which she tried to medicate with Tylenol, but was not able to access any while at work. Patient asked what symptoms do people experience within 15 minutes if they have an allergic reaction to the vaccine. The patient got the vaccine 5-6 days ago, but today (26Jan2021) she was on the job in a group setting and was having difficulty swallowing and had a sore throat. She said that she treated it with ice and it is slowly subsiding. She noticed she almost had a like a headache type thing, but it was in the back of the throat. She has had tingling in the back of her throat from seasonal allergies, but nothing like this. Her temp was 97.9 and it was now 98.3. As she swallows, she is feeling pain. She said that the ice helped out. She is having a toothache currently too and stated that she needs to go to the dentist. She noticed her sore throat while she was talking and noticed the sore throat and it hurt and when swallowing. She said that after the injection, she felt like someone punched her in the arm the next day on 22Jan2021. This has resolved at this time. She said that she rarely gets sick. This is the second time she has had some type of symptoms within 2 years. She said that she has not been around anyone and is social distancing. Treatment received for "a soreness in her throat and it was hard to swallow" included ice. The outcome of the events "a soreness in her throat and it was hard to swallow" was recovering (as reported), for event "felt like someone punched her arm" was recovered on an unspecified date and the rest of the events was unknown. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm