VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

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

Incidents per State

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

ID: 1349186
Sex: M
Age:
State:

Vax Date:
Onset Date: 02/01/2021
Rec V Date: 05/26/2021
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: diarrhea; feels kind of of weak; This is a spontaneous report from a Pfizer sponsored program. A contactable consumer (patient's wife) reported that a 77-year-old male patient received received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as first dose, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, on the day of his scheduled second dose, the patient experienced diarrhea and feels kind of of weak. The events were reported as non-serious. The outcome of the events was recovering (reported as symptoms were "a little bit now"). It was reported that the patient's area/city was under boil advisory for water, and was unsure if the patient's symptoms might be from bad water. The reporter was querying if the patient should get the second dose (reported as scheduled today) with symptoms. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1349187
Sex: M
Age:
State: MO

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: sore back; This is a spontaneous report from a Pfizer-sponsored program, received from a contactable consumer (patient). A male patient of an unspecified age (age: 65, unit: unknown) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as 1st dose, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient took 2 Tylenols about 8 hours prior to second dose of the Pfizer vaccine due to sore back from shoveling on an unspecified date. The Tylenol was not related to the first dose. Outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected

Other Meds:

Current Illness:

ID: 1349188
Sex: F
Age:
State: DE

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
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: My left arm is red where the shot; my arm is also sore; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot number and Expiration date were not reported), via an unspecified route of administration (administered on the left arm) on 19Feb2021 13:30 (at the age of 66-years-old) as 1st dose, single for COVID-19 immunisation. Medical history included multiple sclerosis (MS) from an unknown date. The patient was not pregnant at the time of vaccination. The patient has no known allergies. Concomitant medications included modafinil, anastrozole, colecalciferol (D3), calcium ascorbate (ESTER C), baclofen and pantoprazole sodium sesquihydrate (PANTOPRA) all taken for an unspecified indication, start and stop date were not reported. Prior to vaccination, the patient has not been diagnosed with COVID-19. The patient didn't receive any other vaccines within 4 weeks prior to COVID vaccine. On 20Feb2021 00:00, the patient experienced my left arm is red where the shot was given and my arm is also sore. Since the vaccination the patient has been tested for COVID-19. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: MODAFINIL; ANASTROZOLE; D3; ESTER C [CALCIUM ASCORBATE]; BACLOFEN; PANTOPRA

Current Illness:

ID: 1349189
Sex: F
Age:
State: MN

Vax Date: 02/16/2021
Onset Date: 02/16/2021
Rec V Date: 05/26/2021
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: itchy sensations all over body; tingling, prickly, itchy sensations all over body; This is a spontaneous report from a contactable consumer. A 62-year-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 16Feb2021 09:00 (Batch/Lot Number: EM9809) as SINGLE DOSE for covid-19 immunisation. Medical history included Hashimoto's thyroiditis. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Concomitant medications included levothyroxine sodium (SYNTHROID) taken for an unspecified indication, start and stop date were not reported; tocopherol (VITAMIN E) taken for an unspecified indication, start and stop date were not reported; vitamin d3 (VITAMIN D3) taken for an unspecified indication, start and stop date were not reported; ascorbic acid (VITAMIN C ASC ACID) taken for an unspecified indication, start and stop date were not reported; probiotics (PROBIOTICS) taken for an unspecified indication, start and stop date were not reported; zinc taken for an unspecified indication, start and stop date were not reported; calcium taken for an unspecified indication, start and stop date were not reported. The patient previously took Atovaquone / Proguanil, trimethoprim, acyclovir, bactrim, nitrofurantoin and cipro and had allergies. On 16Feb2021 18:00, patient experienced tingling, prickly, itchy sensations all over body with no visible rash started within 8-9 hours after injection and have persisted now for 5 days after injection; the sensations move around, have worsened as day proceeds; "I had the same reaction to Atovaquone/ Proguanil (malarone) 3 years ago", she added. The outcome of events was not recovered. Patient did not received any treatment for the events. Follow-up attempts are completed. No further information is expected.

Other Meds: SYNTHROID; VITAMIN E [TOCOPHEROL]; VITAMIN D3; VITAMIN C ASC ACID; PROBIOTICS; ZINC; CALCIUM

Current Illness:

ID: 1349190
Sex: M
Age:
State: MI

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 05/26/2021
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: Sore Arm; This is a spontaneous report from a contactable consumer. (patient) A 45-year-old male patient received bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE), dose 2 via an unspecified route of administration in the left arm on 19Feb2021 11:15 A.M (Batch/Lot Number: En6200) as 2ND DOSE, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient was not diagnosed with Covid-19 prior to vaccination. The patient has no known allergies. The patient received 1st dose of bnt162b2 (BNT162B2 reported as PFIZER COVID-19 VACCINE) at vaccination age of 45-year-old on 29Jan2021 (lot number: En5318) at 11:00 AM for covid-19 immunisation. The patient did not receive other vaccine in four weeks. On 19Feb2021 04:00 PM, the patient had a sore arm. No treatment was received for the adverse event. The patient has not been covid tested post vaccination. The outcome of the event was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1349191
Sex: M
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: fatigue; dizziness; This is a spontaneous report from a contactable consumer. A 67-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCIN), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as 1st dose, single (at the age of 67 years) for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. After the first dose of the vaccine, 3 days after experienced fatigue and dizziness. She was on the sofa all day. The dizziness and fatigue lasted on and off for 2 days but not the same degree. It was also reported that the patient received the 2nd dose of the Pfizer vaccine on 12Feb2021 (lot: EL9267). The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1349192
Sex: F
Age:
State: MO

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Fever; headache; swollen lymph node- left armpit; This is a spontaneous report from a contactable other health professional (patient). A 39-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in arm left on 19Feb2021 14:45 (Lot Number: EN5318) as 2ND DOSE, SINGLE for COVID-19 immunization. Medical history included allergy to red dye. Concomitant medications included amoxicillin, clavulanic acid (AUGMENTIN [AMOXICILLIN;CLAVULANIC ACID]) and birth control pills. The patient previously took tylenol with codeine and experienced allergy and first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3248) in the left arm on 29Jan2021 at 12:30 pm (age: 39 years) for COVID-19 immunization. On 20Feb2021 06:00, the patient experienced fever, headache, and swollen lymph node- left armpit. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: AUGMENTIN [AMOXICILLIN;CLAVULANIC ACID]

Current Illness:

ID: 1349193
Sex: M
Age:
State: VA

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 05/26/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: feeling of sharp pain, felt in the upper back-outer side of shoulder; pain starts at the top of the shoulder, and extends to the lower outer neck area; pain occurs if patient raise, or stretch arm(s) straight out or above the shoulder, or hold the outstretched arm up for more than a few seconds; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 19Jan2021 10:00 (Batch/Lot Number: ER4176) as 1st dose, single, then on the right arm on 09Feb2021 (lot number: EL9267), 2nd dose, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. No other vaccines were received in four weeks. The patient received first dose in left arm, and the second dose in right arm. The adverse effect, which was still being felt in left arm that started on 19Jan2021 17:00, led the patient to get second dose in other arm. The adverse event was still being experienced, and at the time of report, it was felt on both sides. It was a feeling of sharp pain, felt in the upper back-outer side of shoulder, above the location of each administered dose. The pain starts at the top of the shoulder, and extends to the lower outer neck area. The pain occurs if patient raise, or stretch arm(s) straight out or above the shoulder, or hold the outstretched arm up for more than a few seconds. The pain also occurs if patient contort his arm(s), such as putting on a dress shirt, or taking off a sweater. The pain will subside a few seconds after the arm has lowered back into a natural position. The sharp pangs of pain have continued, even over a month past the first dose. No treatment was given for the events. Outcome was not recovered. Patient did not had covid prior to vaccination and had undergone covid test: negative on 26Jan2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1349194
Sex: M
Age:
State: GA

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
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: little soreness in his right arm; right elbow was swollen profusely; This is a spontaneous report from a contactable consumer (patient). A 49-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in the right arm on 19Feb2021 (Lot Number: EL9264) as 1st dose, single for covid-19 immunisation. Medical history included diabetic. The patient's concomitant medications were not reported. The patient had a little soreness in his right arm on unknown date and yesterday (20Feb2021), when he was lying in bed, he noticed his right elbow was swollen profusely in the arm where he had got the shot on. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1349195
Sex: F
Age:
State: OH

Vax Date: 02/17/2021
Onset Date: 02/19/2021
Rec V Date: 05/26/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Dry Mouth; This is a spontaneous report from a contactable consumer (patient). A 76-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 17Feb2021 15:45 (03:45 PM) (Batch/Lot Number: EM9809) as 2nd DOSE, SINGLE for covid-19 immunisation. The patient is not pregnant at the time of vaccination. The patient had no other vaccine in four weeks and taking other medications in two weeks (unspecified medications). The patient has no covid prior vaccination and not covid tested post vaccination. Medical history included Osteoporosis, pre-COPD and allergy to dye used in treadmill test all from an unknown date and unknown if ongoing. The patient previously took vicodin and experienced allergies. The patient also previously took bnt162b2 (Lot: EL9262) first dose on 27Jan2021 15:45 (03:45 PM) administered in Arm Left for covid-19 immunisation. It was reported that the patient experienced Dry Mouth on 19Feb2021 12:00 PM. No treatment was given for the reported event. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1349196
Sex: F
Age:
State: WV

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 05/26/2021
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: My esophagus is inflamed and food is having a harder time going down. I have a diagnosis of Ineffective esophageal motility disorder; This is a spontaneous report from a contactable other healthcare professional (patient). A 55-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 intramuscular, administered in Arm Left on 28Jan2021 11:30 (Batch/Lot number was not reported) as 1st dose, single ( at the age of 55 years) for covid-19 immunisation. The patient's medical history included ineffective esophageal motility disorder, GERD and known allergies to numbing agent for upper endoscopy. The patient has not had covid prior to vaccination. Concomitant medications included cimetidine (TAGAMET [CIMETIDINE]) and Multi-vitamin taken for an unspecified indication, start and stop date were not reported. On 28Jan2021, 11:30, the patient experienced my esophagus was inflamed and food was having a harder time going down. She have a diagnosis of ineffective esophageal motility disorder. It was further reported that as soon as she was given the vaccine, her esophagus had a reaction. Her esophagus was inflamed and food was having a harder time going down. She had a diagnosis of ineffective esophageal motility disorder, and still having issues it has not cleared up, since the vaccination. It was reported that the event was treated with Carafate. The patient was not tested for Covid post vaccination. The outcome of the event was not recovered. Information on the Lot/Batch number has been requested.

Other Meds: TAGAMET [CIMETIDINE]

Current Illness:

ID: 1349197
Sex: M
Age:
State: TX

Vax Date: 02/20/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
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: Rash, inner thigh, both legs; This is a spontaneous report from a contactable consumer (patient). A 64-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 20Feb2021 at 10:30 (at the age of 64 years old) (Lot Number: EL9267, unknown expiration) as 1st dose, single for COVID-19 immunisation. Medical history included pre-diabetic and high cholesterol. No known allergies. Concomitant medications included rosuvastatin and metformin. The patient experienced rash, inner thigh, both legs on 20Feb2021 at 20:00. The patient did not receive treatment for the event. The patient has no COVID prior to vaccination and was not tested for COVID post vaccination. No other vaccine in four weeks. The patient had not yet recovered from the event. Follow-up attempts are completed. No further information is expected.

Other Meds: ROSUVASTATIN; METFORMIN

Current Illness:

ID: 1349198
Sex: F
Age:
State:

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 05/26/2021
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: Bad Chills; headache; This is a spontaneous report from a non-contactable consumer. An elderly female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) second dose via an unspecified route of administration on 17Feb2021 (Lot number was not reported) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received the first dose of BNT162B2 in Jan2021 for covid-19 immunisation. She had no COVID prior to vaccination and was not COVID tested post vaccination. It was unknown if patient received other vaccine in four weeks. On 17Feb2021, the patient experienced bad chills and headache. Treatment was not given. The patient recovered from the events. No follow-up attempts are possible. Information about Lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1349199
Sex: F
Age:
State: NJ

Vax Date: 02/06/2021
Onset Date: 02/08/2021
Rec V Date: 05/26/2021
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: tachycardia; sinus arrhythmia; heart palpitations; This is a spontaneous report from a contactable healthcare professional (patient). A 40-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), intramuscular, administered in the right arm on 06Feb2021 16:00 (04:00 PM) (Batch/Lot Number: EL9267) at the age of 40-years-old as unknown, single dose for COVID-19 immunization at a workplace clinic. The patient had no other vaccine in four weeks. The patient had no COVID prior vaccination. The patient had no medical history and no known allergies. Concomitant medications included daily multi-vitamin and an iron supplement, both taken for unspecified indications, start and stop date were not reported (reported as other medications in two weeks). The patient had heart palpitations beginning 08Feb2021 at 08:00 AM, then had an ECG with a sinus arrhythmia present on 10Feb2021, and then went to emergency room (ER) on 19Feb2021 for severe tachycardia. The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient did not receive treatment for the events. The patient was tested for COVID post vaccination which was a nasal swab (PCR) with a negative result on 10Feb2021. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: IRON

Current Illness:

ID: 1349200
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: UTI; bladder infection; This is a spontaneous report from a non-contactable consumer (patient) from a Pfizer Sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as 1st dose, single for COVID-19 immunisation. Medical history was not reported. The patient's concomitant medications were not reported. The patient reported that she may have a UTI or bladder infection. She wanted to know if she can take nystatin. She got the first shot and will be getting the second shot and she doesn't want to mess it up. She also wanted to know if she can get the antibiotic after the 2nd shot. She stated she also read about immunosuppressants. The outcome of the events 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: 1349201
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: big black and blue mark where they gave me the shot, I don't know if its from me taking off the bandage.; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot and expiry were not reported), via an unspecified route of administration on an unspecified date as 1 st dose, single for covid-19 immunisation. Medical history included cancer. The patient's concomitant medications were not reported. The patient got her first dose of vaccine "on the 3rd or 4th" (did not verify date before disconnecting call). Second dose was scheduled for 04March2021. After the first dose (on an unspecified date), she has big black and blue mark where they gave her the shot, she didn't know if its from her taking off the bandage. The patient took warfarin sodium (COUMADIN), "no pain with it at all". Asked if that was from the vaccine. The patient asked if she could get her "lung cancer shot" and the vaccine the following day. The patient did not know the lung cancer injection medication name or type. The patient's son that lived with her, tested positive for covid without symptoms. Asking, "could I get covid after vaccine? First dose?" Also asked if a person, who unknowingly has covid and got dose, if it would be safe or cause issues. Further asked if someone gets covid infection after the vaccine, if that would mean it didn't protect them. The patient stated, "why is it recorded where we are talking over each other-its driving me nuts. Its a shot in dark". The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1349202
Sex: M
Age:
State: NC

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
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: felt feverish (though temp was 97.3) more sluggish amd more brain fog than before injection (like I was getting a cold or flu). Symptoms less apparent today; felt feverish (though temp was 97.3) more sluggish amd more brain fog than before injection (like I was getting a cold or flu). Symptoms less apparent today; felt feverish (though temp was 97.3) more sluggish amd more brain fog than before injection (like I was getting a cold or flu). Symptoms less apparent today; felt feverish (though temp was 97.3) more sluggish amd more brain fog than before injection (like I was getting a cold or flu). Symptoms less apparent today; felt feverish (though temp was 97.3) more sluggish amd more brain fog than before injection (like I was getting a cold or flu). Symptoms less apparent today; felt feverish (though temp was 97.3) more sluggish amd more brain fog than before injection (like I was getting a cold or flu). Symptoms less apparent today; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration (at the age of 73-years-old), administered in Arm Left on 19Feb2021 13:30 (Batch/Lot number was not reported) as 1st dose, single for COVID-19 immunization. Medical history included Obstructive Sleep Apnea, ongoing sluggishness, ongoing brain fog, and COVID-19 ("If COVID prior vaccination: Yes"). Concomitant medications included armodafinil and doxepin hcl both taken for unspecified indications, start and stop dates were not reported. About 19 hours after injection (on 20Feb2021, 09:00 AM) felt feverish (though temp was 97.3), more sluggish and more "brain fog" than before injection ("like I was getting a cold or flu"). Symptoms less apparent today. No treatment received for the events. The patient underwent lab tests and procedures which included body temperature: 97.3 on 20Feb2021. The outcome of the events was Recovering/Resolving. Facility type vaccine was Public Health Clinic/Veterans Administration facility. No other vaccine in four weeks. Not COVID tested post vaccination. Information on the lot/batch number has been requested.

Other Meds: ARMODAFINIL; DOXEPIN HCL

Current Illness: Foggy feeling in head; Sluggishness

ID: 1349203
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: felt "achy"; This is a spontaneous report from a non-contactable consumer. A elderly male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as UNKNOWN, SINGLE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient received the COVID-19 shot and he felt "achy" on unspecified date. It was unknown if treatment was received. Prior to vaccination, it was unknown if the patient was diagnosed with COVID-19. It was unknown if the patient has been tested for COVID-19. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1349204
Sex: F
Age:
State: TN

Vax Date: 02/19/2021
Onset Date: 02/21/2021
Rec V Date: 05/26/2021
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: Sudden sensitivity; mild pain in jaws and lower lip area; mild pain in jaws and lower lip area; This is a spontaneous report from a contactable consumer (patient). A 72-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: EL9264, expiry date not reported), via an unspecified route of administration, administered in left arm on 19Feb2021 11:00 as first dose, single for covid-19 immunisation. Medical history included high blood pressure, low thyroid, and essential tremor. The patient had no known allergies. Concomitant medications included levothyroxine, hctz, trazodone, propranolol, and pravastatin, all taken for an unspecified indication, start and stop date were not reported. Patient was not pregnant at the time of vaccination and of the report. The patient had no other vaccine in four weeks. The patient had no covid prior vaccination. On 21Feb2021 16:30, the patient experienced sudden sensitivity and mild pain in jaws and lower lip area. No treatment received in response to the events reported. The patient was not tested for covid post vaccination. The patient was recovering from the events. Follow-up attempts are completed. No further information is expected.

Other Meds: LEVOTHYROXINE; HCTZ; TRAZODONE; PROPRANOLOL; PRAVASTATIN

Current Illness:

ID: 1349205
Sex: F
Age:
State: PA

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 05/26/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: I had swelling on my forehead, between my eyebrows, down the bridge of my nose, and, both sides of the bridge of my nose.; This is a spontaneous report from a contactable nurse (patient). A 49-year-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in left arm on 12Jan2021 09:30 (Batch/Lot Number: EJ1686) (at the age of 49 years old) as 1st dose, single for COVID-19 immunisation. The patient was not pregnant at the time of vaccination. Medical history included penicillin allergy. No other vaccine in four weeks and no other medications in two weeks. The patient experienced swelling on forehead between eyebrows, down the bridge of my nose, and both sides of the bridge of my nose on 13Jan2021 06:30. No treatment for the event. No COVID prior vaccination. The patient underwent lab tests and procedures which included Nasal Swab: negative on 12Feb2021. The outcome of the event was recovered on unspecified date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1349206
Sex: F
Age:
State: AZ

Vax Date: 02/15/2021
Onset Date: 02/01/2021
Rec V Date: 05/26/2021
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: a non-raised red rash appeared on chest and stomach area...also partially on my back; As the rash faded, I have an itch everywhere the rash existed; This is a spontaneous report from a contactable consumer (patient). A 73-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9267) at the age of 73-years-old, via an unspecified route of administration in right arm on 15Feb2021 at 12:15 at 1st dose, single for COVID-19 immunization. Medical history included being asthmatic. She has no other chronic health conditions, no known allergies, and has no COVID prior to vaccination. Concomitant medications included ascorbic acid, betacarotene, biotin, calcium, chloride, chromium, copper, folic acid, iodine, iron, magnesium, manganese, molybdenum, nickel, nicotinic acid, pantothenic acid, phosphorus, potassium, pyridoxine hydrochloride, riboflavin, selenium, silicon, thiamine, vanadium, vitamin b12 nos, vitamin d nos, vitamin e nos, vitamin k nos, xantofyl, zinc (CENTRUM SILVER WOMEN 50+) and acetylsalicylic acid (ASPIRIN). There were no other vaccines in four weeks. The facility where the vaccine was administered was reported as other. On Feb2021 (also reported as 11Feb2021 at 08:30), a non-raised red rash appeared on her chest and stomach area and also partially on her back; as the rash faded, she had an itch everywhere the rash existed. No treatment was given in response to the events. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: CENTRUM SILVER WOMEN 50+; ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 1349207
Sex: F
Age:
State: AL

Vax Date: 02/09/2021
Onset Date: 02/10/2021
Rec V Date: 05/26/2021
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: Swollen lymph node on left collar bone.; This is a spontaneous report from a contactable consumer (patient). A 39-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 09Feb2021 17:05 (at 39 years old, not pregnant) (Batch/Lot number was not reported) as 1st dose, single for covid-19 immunisation. The patient's medical history was not reported. Concomitant medication included losartan. On 10Feb2021 17:00, patient experienced Swollen lymph node on left collar bone. The outcome of the event was recovering. No treatment for the event. No covid prior vaccination. Not covid tested post vaccination. Follow-up attempts are completed. No further information is expected.

Other Meds: LOSARTAN

Current Illness:

ID: 1349208
Sex: F
Age:
State: FL

Vax Date: 02/15/2021
Onset Date: 02/16/2021
Rec V Date: 05/26/2021
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: Hint aches throughout body; very fatigued; This is a spontaneous report from a contactable consumer (patient). A 76-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 15Feb2021 12:30 (at 76 years old) (Batch/Lot Number: EN6201) as 1st dose, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On 16Feb2021, patient experienced Hint aches throughout body and very fatigued. No treatment for the events. The outcome of the events was not recovered. No other vaccine_in_four weeks. No covid_prior_vaccination. Not covid tested post vaccination.

Other Meds:

Current Illness:

ID: 1349209
Sex: F
Age:
State: MA

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 05/26/2021
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: I had a terrible smell of burnt toast, the day following the shot, then the next day, none, then yesterday once again. No other side effects. Strangely my sister 500 miles from me also had smells of; This is a spontaneous report from a contactable consumer (patient herself). A female patient (age not provided) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number not provided), via an unknown route in the right arm, on 16Feb2021 15:30 at single dose for COVID-19 immunisation. The patient was not pregnant. Relevant medical history included atrial fibrillation and asthma. Past drug history included allergy to penicillin. Relevant concomitant medications included phenobarbital, clonidine, levothyroxine sodium (SYNTHROID), and pantoprazole. The patient verbally reported ''I had a terrible smell of burnt toast, the day following the shot, then the next day, none, then yesterday once again''. No other side effects. The patient stated also ''strangely my sister 500 miles from me also had smells of burning and gasoline''. Pre and Post vaccination COVID tests were not performed. The patient was not treated for the event. The patient was recovering from the event. No follow-up attempts are possible. Information about Batch/Lot number cannot be obtained.

Other Meds: PHENOBARBITAL; CLONIDINE; SYNTHROID; PANTOPRAZOLE

Current Illness:

ID: 1349210
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: fast heart rate that lasted for 5 to 6 hours.; he felt a numb, tingling sensation down his arm, hands, palms, and fingers; he felt a numb, tingling sensation down his arm, hands, palms, and fingers; This is a spontaneous report from a non-contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Immediately after receiving the 1st dose of the Pfizer-BioNTech Covid-19 Vaccine, he experienced a fast heart rate that lasted for 5 to 6 hours. Then with the last 3 days, he felt a numb, tingling sensation down his arm, hands, palms, and fingers. He wants to know if this is a normal reaction to the vaccine, and if it is still safe for him to receive the 2nd dose of the vaccine. Outcome of the event fast heart rate was recovered; other events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1349211
Sex: F
Age:
State: WI

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
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: Itchy rash on back, stomach, wrists, ankles. Appeared about 36 hours post shot.; This is a spontaneous report from a contactable consumer A 43 -year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EN6200) on 19Feb2021 at 09:45 at single dose via an unspecified route of administration on right arm for COVID-19 immunization. Relevant medical history included migraines, depression, reynaud's syndrome, seasonal allergies, animal allergies and dust allergy. Concomitant medications included montelukast, escitalopram oxalate (LEXAPRO), trazodone, levocetirizine dihydrochloride (XYZAL). On 20Feb2021 at 17:00 the patient experienced itchy rash on back, stomach, wrists, ankles, appeared about 36 hours post shot. At the time of the reporting the patient had not yet recovered from the event Follow-up attempts are completed. No further information is expected.

Other Meds: MONTELUKAST; LEXAPRO; TRAZODONE; XYZAL

Current Illness:

ID: 1349212
Sex: F
Age:
State: PA

Vax Date: 02/11/2021
Onset Date: 02/01/2021
Rec V Date: 05/26/2021
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: tired; cold; head was in a fog; Staggering; Diarrhea; ears were ringing; arm was sore; body ache; neck was painful; back of head pain; This is a spontaneous report from a contactable consumer (Patient). A 79-year old female consumer reported that she received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number EL0140, Expiration Date Mar2021) into the left arm on 11Feb2021 at 4:00pm (at the age of 79-years-old) at single dose for COVID-19 immunization. Concomitant drugs included ciclosporin (RESTASIS) twice daily both eyes taken for dry eye; bimatoprost (LUMIGAN) one daily both eyes taken for glaucoma for 5-6 years, vitamin B complex 1 daily taken as supplement for 15-20 years; colecalciferol (D3) 2 daily during the winter and 1 daily in the summer taken as supplement for 3-4 years. She use to get a lot of sore throats. Her doctor suggested she take vitamins. Some that she took didn't help. On 11Feb2021 the patient experienced arm was sore not recovered, body ache recovered on 13Feb2021 and on 12Feb2021 she experienced tired recovered on 13Feb2021, cold recovered on 12Feb2021, head was in a fog not recovered, staggering recovered on 13Feb2021, ears were ringing recovered on 13Feb2021, Diarrhea recovered on 12Feb2021. Further reported the back of her head and neck was painful that was gone by 13Feb2021. Her arm was sore if she lays on it she can feel it. Unable to answer outcome of event for being tired,if she sits long enough she falls asleep. Her head still feels tender. She is no longer staggering. She feels comfortable going up and down stairs. The next dose is scheduled for 04Mar2021. She is considering not taking the second dose.

Other Meds: RESTASIS; LUMIGAN; VITAMIN B COMPLEX; D3

Current Illness:

ID: 1349213
Sex: F
Age:
State:

Vax Date: 02/01/2021
Onset Date: 02/18/2021
Rec V Date: 05/26/2021
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: a little bit of a Headache; This is a spontaneous report from a contactable consumer, based on information received by Pfizer from Eisai (manufacturer control number: EC-2021-088274). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration in Feb2021 (Batch/Lot number was not reported) as single dose (unknown if first or second dose) for COVID-19 immunisation and lenvatinib mesilate (LENVIMA) via an unspecified route of administration from 15Feb2021 at 20 mg daily for endometrial uterine cancer. Relevant medical history included ongoing malignant hypertension (blood pressure still runs high), 2 brain aneurysms, left thyroid lobe enlarged a number of years and endometrial uterine cancer. Concomitant medications were not reported. On 18Feb2021, the patient experienced a little bit of a headache. The patient stated she got a "COVID vaccine" last week (before starting LENVIMA) and patient's Doctor told her the "headache" cold be from the vaccine too. Cause unknown but occurred while on LENVIMA. The patient reported that her blood pressure was 149/82 on 18Feb2021 and it was 132/66 on 17Feb2021, which was low for her. The patient was instructed by her Doctor to notify her Doctor if blood pressure was ever "160/100, or higher." At the time of the report, the action taken with lenvatinib mesilate and the outcome of the event were unknown. No follow-up attempts are possible, information about batch number cannot be obtained.

Other Meds: LENVIMA

Current Illness: Malignant hypertension (Blood Pressure still runs high)

ID: 1349214
Sex: F
Age:
State: NY

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 05/26/2021
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: After the 1st shot, the muscle under my left thumb started to hurt; This is a spontaneous report from a non-contactable consumer. A 59-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3247) via an unspecified route of administration in left arm on 12Feb2021 03:00PM at single dose for COVID-19 immunisation. Relevant medical history was not reported, the patient did not receive any vaccine in four weeks and had allergy to codeine. The patient did not have COVID prior to vaccination and was not tested for COVID post vaccination. Concomitant medications were not reported. On 23Jan2021, after the first shot, the muscle under her left thumb started to hurt. The event was not treated, was non-serious and not resolved. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021218557 same patient/reporter, different AE/second dose

Other Meds:

Current Illness:

ID: 1349215
Sex: F
Age:
State:

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 05/26/2021
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: Sore Arm; This is a spontaneous report from a non-contactable Other HCP (patient herself). This 26-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EN5318), via an unknown route in the left arm, on 26Jan2021 (at the age of 26-year-old) at single dose for COVID-19 immunisation. No other vaccine was received in four weeks. Relevant medical history included COVID-19 (before vaccine). No relevant concomitant medications were provided. On 26Jan2021, the patient had sore arm. The event was reported as non-serious. No treatment was given for the event. Pre and Post vaccination COVID tests were not performed. The patient recovered from the event on unknown date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1349216
Sex: F
Age:
State:

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/26/2021
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: I experienced mild joint/muscle aches the day after receiving the 2nd shot. The side effect lasted for only 1 day.; I experienced mild joint/muscle aches the day after receiving the 2nd shot. The side effect lasted for only 1 day.; This is a spontaneous report from a non-contactable consumer. A 57-years-old, non-pregnant, female patient received the second dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine via an unspecified route of administration on 19Feb2021 (Batch/Lot Number: EL3247) as for COVID-19 immunization. The patient had no relevant medical history. The patient's concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination and was not tested for COVID after vaccination. The patient reported that, the day after receiving the 2nd shot, on 20Feb2021 08:00, she experienced mild joint/muscle aches. The side effect lasted for only 1 day. The events recovered on an unspecified date in Feb2021 without any treatment. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1349217
Sex: F
Age:
State: GA

Vax Date: 02/20/2021
Onset Date: 02/21/2021
Rec V Date: 05/26/2021
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: 24 hrs after vaccination I began to have a speckled rash; itchy skin on chest, back,arms; This is a spontaneous report from a Non-contactable consumer. A 75 year old female consumer received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3302) on 20Feb2021 at single dose via an unspecified route of administration for COVID-19 immunization. Relevant medical history and concomitant medications were not reported. On 21Feb2021 24 hours after vaccination patient began to have a speckled rash and itchy skin on chest, back, arms. No treatment received. At the time of the reporting the patient had not yet recovered from the events. No follow-up attempts are possible. No further information is expected

Other Meds:

Current Illness:

ID: 1349218
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: After the second dose, her platelet count dropped.; This is a spontaneous report from a contactable Nurse reporting for herself. A female patient of an unspecified age received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number unknown) via an unspecified route of administration on an unspecified date, at single dose for COVID-19 immunisation. Relevant medical history included idiopathic thrombocytopenic purpura (ITP). Concomitant medications were not reported. After the second dose, her platelet count dropped. Because of that, she was taking prednisone. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1349219
Sex: F
Age:
State: IN

Vax Date: 02/20/2021
Onset Date: 02/22/2021
Rec V Date: 05/26/2021
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: Swollen lymph nodes under right arm; This is a spontaneous report from a contactable Healthcare Professional reporting for herself. A 53-years-old, non-pregnant, female patient received the second dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine in Hospital, via an unspecified route of administration, administered in right arm on 20Feb2021 09:30 (Batch/Lot Number: EN6200) as single dose for COVID-19 immunization. The patient's medical history was not reported. Historical vaccine included the first dose of BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine in right arm on 25Jan2021 06:00 PM (Batch/Lot Number: EL8982) as single dose for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior vaccination and was not tested for COVID post vaccination. Concomitant medication included omeprazole taken for an unspecified indication, start and stop date were not reported. The patient experienced swollen lymph nodes under right arm on 22Feb2021 06:00. No treatment was administered for the event. The event had not resolved yet at the time of the report. No follow-up attempts are possible. No further information is expected.

Other Meds: OMEPRAZOLE

Current Illness:

ID: 1349220
Sex: F
Age:
State: NJ

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 05/26/2021
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: About 20 hrs after second dose, I experienced low grade fever (100.4 degree f).; chills; fogginess; This is a spontaneous report from a contactable consumer. A 30-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: En6201) on 16Feb2021 at 16:00 at single dose via an unspecified route of administration on left arm for COVID-19 immunization. The patient didn't have medical history. Concomitant drug included metformin and melatonin. The patient received first dose of BNT162B2 on 22Jan2021 at 04:00 pm on left arm. On 17Feb2021 at 13:00 about 20 hours after second dose, patient experienced low grade fever (100.4 degree f). The patient recovered from the events on an unspecified date. No follow-up attempts are possible. No further information is expected.

Other Meds: METFORMIN; MELATONIN

Current Illness:

ID: 1349221
Sex: F
Age:
State: IL

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 05/26/2021
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: if she pressed on the vaccine injection site, the vaccine injection site was slightly tender; This is a spontaneous report from a contactable consumer (patient herself). This 74-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number EL3247 with Expiration Date 31May2021), via intramuscular in the left upper arm, on 27Jan2021 15:00 (at the age of 74-year-old) at single dose for COVID-19 immunisation. No other vaccine was received in four weeks. No relevant medical history was provided. Relevant concomitant medications included levothyroxine. On 27Jan2021, the patient stated if she pressed on the vaccine injection site, the vaccine injection site was slightly tender. The patient had recovered from the event on 28Jan2021. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021183324 same patient, same product (second dose), different event

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1349222
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: fever; joint pain; headache; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as 1st dose, single for covid-19 immunisation. Medical history included gout and osteoarthritis. Concomitant medications included indomethacin [indometacin] and colchicine. The patient got the first dose of the covid vaccine and has developed fever, joint pain and headache. The patient has gout and osteoarthritis and she take indomethacin and colchicine however she has not taking those medications lately and she mentioned that she usually gets joint pain from her osteoarthritis. She went to her primary doctor and to the hospital and no one wanted to attend her since she has fever. She would like to know which medication she can take for her fever. The outcome of the events was unknown. No follow-up attempts are possible, information about lot number cannot be obtained. No further information is expected.

Other Meds: INDOMETHACIN [INDOMETACIN]; COLCHICINE

Current Illness:

ID: 1349223
Sex: F
Age:
State: MA

Vax Date: 02/06/2021
Onset Date: 02/08/2021
Rec V Date: 05/26/2021
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: Chills but no fever; Headaches for one and a half weeks; Dizziness; This is a spontaneous report from a contactable consumer reported for herself. A 94-year-old female consumer reported that received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number unknown), on 06Feb2021 12:00 AM (at the age of 94-years-old) at single dose for COVID-19 immunization. medical history included Allergies to Penicillin. Concomitant drugs were unknown. On 08Feb2021 the patient had chills but no fever. Headaches for one and a half weeks and Dizziness. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1349224
Sex: M
Age:
State: KY

Vax Date: 01/10/2021
Onset Date: 01/01/2021
Rec V Date: 05/26/2021
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: symptoms of nausea and lethargy; symptoms of nausea and lethargy; This is a spontaneous report from a contactable consumer reporting on behalf of the patient. A 75 (unspecified unit) old male patient (husband) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 10Jan2021 (Batch/Lot number was not reported) as 2nd dose, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient also received first dose of BNT162B2 on unspecified date (unknown lot number and expiration) for COVID-19 immunization. It was reported that the patient experienced symptoms of nausea and lethargy a week later in Jan2021. Outcome of the events was unknown. The events were assessed as non-serious. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1349225
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: just a sore arm; This is a spontaneous report from a Pfizer sponsored program from a non-contactable consumer reported for a female patient (friend) A female patient of an unspecified age received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. he patient medical history and concomitant medications were not reported. The patient experienced just a sore arm at the injection site on an unspecified date with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1349226
Sex: F
Age:
State: NY

Vax Date: 02/14/2021
Onset Date: 02/14/2021
Rec V Date: 05/26/2021
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: sore arm; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 14Feb2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. Patient reported that with the past flu shots that she has received she has experienced fever and body aches. The patient experienced a sore arm for around 5 hours a several hours after receiving the vaccine on 14Feb2021 with outcome of unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1349227
Sex: F
Age:
State: WI

Vax Date: 02/19/2021
Onset Date:
Rec V Date: 05/26/2021
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: I had a fever; weird strange dream; This is a spontaneous report from a contactable consumer (patient). A 82-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 19Feb2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced fever with outcome of unknown , weird strange dream with outcome of unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1349228
Sex: M
Age:
State:

Vax Date: 02/21/2021
Onset Date:
Rec V Date: 05/26/2021
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: experienced pain in his shoulder; This is a spontaneous report from a contactable consumer (patient himself). A male patient of unspecified age (reported as 'Age:68; Unit: Unknown') received received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 21Feb2021 (Batch/Lot number was not reported) as 2nd dose, single for COVID-19 immunisation. Medical history included injury unrelated to the COVID-19 vaccine. The patient's concomitant medications were not reported. The patient stated he only experienced pain in his shoulder on an unspecified date. He had several injuries unrelated to the COVID-19 vaccine and wanted to know how long he had to wait to take a pain pill for his other injuries. Outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1349229
Sex: M
Age:
State:

Vax Date: 01/19/2021
Onset Date: 01/01/2021
Rec V Date: 05/26/2021
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: gradually being short of breath/ huffing and puffing; This is a spontaneous report from a non-contactable consumer (patient's wife). A 72-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Jan2021 (Batch/Lot number was not reported) as 1st dose, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. About 8 days after the first dose in Jan2021, the patient started noticing gradually being short of breath. He would walk for 50 yards and he would be huffing and puffing which is unusual because he can walk a lot. It gradually got worse. Outcome of the event was not recovered. Patient received his second dose on 10Feb2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1349230
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: It's just a discomfort; pain; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support. A contactable consumer (patient herself) reported that a female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as 1st dose, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated she was due to receive the second dose on 25Feb2021. She wanted to go to the orthopedic doctor to discuss an underlying medical condition. She wanted to know in case she was to receive cortisone shot, if it would it impact the efficacy of the vaccine. She stated "I am going hold off going to the doctor. It's doesn't bother me as much. It's just a discomfort. I am not in excruciating pain. I will wait and take Tylenol for the pain. However I won't take Tylenol right before my shot." The events occurred on an unspecified date with outcome of unknown. Follow-up attempts are completed. No further information is expected. Information about the batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1349231
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: Affected my Menstrual cycle. Got my period 2 weeks early.; This is a spontaneous report from a non-contactable other healthcare professional. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EL9265) via intramuscular, administered in right arm, on an unspecified date, as 2nd dose, single, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient has no known allergies. Historical vaccine included 1st dose of COVID-19 vaccine on unspecified date. The patient had no COVID prior vaccination and she was not tested for COVID post vaccination. The patient was not pregnant at the time of report. It was reported that the patient's menstrual cycle was affected on unspecified date and got her period 2 weeks early. No follow-up attempts are possible. No further information is expected

Other Meds:

Current Illness:

ID: 1349232
Sex: M
Age:
State:

Vax Date: 01/23/2021
Onset Date:
Rec V Date: 05/26/2021
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: involuntary muscle twitching on the arm right after the 1st dose taken on 23Jan2021; This is a spontaneous report received from a contactable consumer (patient). A male patient with age reported as 39 (unit unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number not reported), via unspecified route of administration in right arm on 23Jan2021 as 1st dose, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient mentioned that he received both doses of the Pfizer COVID vaccine. He experienced muscle twitching on the arm right after the 1st dose taken on 23Jan2021. He was asking if that was reported as a common side effect. He was also asking if Amyotrophic Lateral Sclerosis (ALS) was a contraindication to vaccination or if it was reported to be a comorbidity in the clinical trials. The outcome of the event was unknown. Information about lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1349233
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/26/2021
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: after his dose he had a warm/burning sensation at the injection site; after his dose he had a warm/burning sensation at the injection site; This is a spontaneous report from a contactable consumer who reported on behalf of her husband. A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number was not reported), via an unspecified route of administration in his left arm on an unspecified date at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. About 1 to 2 hours after his dose, he had a warm/burning sensation at the injection site, which resolved on an unspecified date. Reporter was curious as to why the nurse told patient the vaccine goes in his left arm, even though he was left handed. No follow-up attempts are possible, information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1349234
Sex: F
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/11/2021
Rec V Date: 05/26/2021
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: I developed a dry cough 3 days after getting the 2nd dose of Pfizer vaccine; This is a spontaneous report from a contactable consumer(patient). A 59-year-old female patient (not pregnant) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number was not reported), via an unspecified route of administration, in left arm on 08Jan2021 (at 59 years) at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient had previous known allergy to flurbuprophen. Previously on 18Dec2020 at 14:45 (at 59 years) the patient took the first dose of the vaccine in left arm for covid-19 immunization. On 11Jan2021, 3 days after getting the 2nd dose of the vaccine, the patient developed a dry cough.The event required doctor or other healthcare professional office/clinic visit. Patient was tested negative for Covid (via Nasal Swab) on 05Feb2021; X-ray in Feb2021 was negative for pneumonia. Patient had a course of antibiotics, a corticosteroid and cough medicines. As of 23Feb2021 patient still had the cough. The final outcome of the event was not recovered. No follow-up attempts are possible, information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1349235
Sex: F
Age:
State:

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 05/26/2021
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: eyes were blood red; This is a spontaneous report received from a contactable consumer (patient). A female patient with age reported as 77 (unit unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number not reported), on 22Feb2021 as 1st dose, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that patient received the first dose of the vaccine the day before the present report (22Feb2021) in the afternoon. The day of this report (23Feb2021), she noticed her eyes were blood red. She also asked if there were any reports of eyes being blood red. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm