VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

Total Manufacturer
199,106MODERNA
36,710JANSSEN
5,381PFIZER\BIONTECH
2,555GLAXOSMITHKLINE BIOLOGICALS
1,469UNKNOWN MANUFACTURER
897MERCK & CO. INC.
627SEQIRUS, INC.
112DYNAVAX TECHNOLOGIES CORPORATION
91SANOFI PASTEUR
75NOVARTIS VACCINES AND DIAGNOSTICS
40EMERGENT BIOSOLUTIONS
14PAXVAX
12TEVA PHARMACEUTICALS
12PROTEIN SCIENCES CORPORATION
9PFIZER\WYETH
4BERNA BIOTECH, LTD.
4SMITHKLINE BEECHAM
3INTERCELL AG
1MEDIMMUNE VACCINES, INC.
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL7,949
7,473
2,547
1,506
1,187
1,051
1,049
s0294561,043
866
IMM209861
816
UT7065MA766
657
579
U62828AA563
557
538
U6737AA516
515
S034636506
4F472471
458
P100253275449
444
276563436
429
418
4BH32414
MENVEO404
PP9L5362
UJ446AA337
319
306
290
271
49TM3270
R1B252M253
4F472179
933622147
C5763AA144
CW3116134
3Y7NL126
UNK114
113
ARBA141A105
104
103
96
300057A90
79
1F4EB73
R1B743M62
56
UJ090AA55
51
UH894AB46
45
UNK44
UNK42
42
EJ168638
Unknown36
35
34
32
32
26
el128424
24
A115A22
22
EN620222
21
UNK20
20
19
Z127A19
19
17
JEV18K95E15
12
111798PI12
10
A739088
No batch number8
3333324181078
6
6
TAR356
5
5
U6935AA5
UNK5
4
unknown4
3
2
55RB72
2
2
2
2
2
U7124AA2
JEV18A68E2
2
ABYB05BA1
1
1
1
1
AMVA436A1
1
1
TJ3521
A130A; VIS give1
1
U7140BB1
1
1
SP UP016AA1
1
1808P08802/ESV01
037K20A300,947
EL1284288,578
57,766
1,432

Incidents per State

State Total
82,750
CA62,821
FL38,209
TX36,512
NY34,921
PA23,646
IN23,622
IL20,597
MI19,590
OH19,426
NJ18,413
NC16,769
GA15,932
WA15,351
VA15,234
MA14,876
AZ14,206
MN12,940
MD12,656
CO11,908
WI11,425
MO10,240
TN9,685
OR8,768
KY8,437
CT8,300
SC6,700
OK6,293
AL5,692
LA5,025
IA4,825
KS4,821
UT4,637
NV4,374
NM3,967
AR3,807
ME3,161
NH3,096
NE2,918
MS2,859
ID2,785
WV2,469
HI2,459
PR2,417
MT2,414
RI2,076
DE1,868
AK1,830
VT1,734
DC1,715
ND1,388
SD1,269
WY866
GU118
VI69
AS47
MP29
MH8
XB6
FM4
QM3
XV2
XL1

ID: 1792819
Sex: F
Age:
State:

Vax Date: 04/02/2021
Onset Date: 04/02/2021
Rec V Date: 10/16/2021
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: Mild arm pain at injection site; This is a spontaneous report from a non-contactable pharmacist, the patient. An Adult non-pregnant female patient of unknown age received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP6955) via an unspecified route of administration on 02Apr2021 as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The patient did not receive any other medications within two weeks of vaccination. On 02Apr2021, the patient experienced mild arm pain at injection site. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event mild arm pain at injection site was resolved in April2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792820
Sex: M
Age:
State:

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 10/16/2021
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: Vasovagal without syncope; This is a spontaneous report from a non-contactable consumer, the patient. A 32-year-old male 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 07Apr2021 at 10:45 (at the age of 32-year-old) as a single dose for COVID-19 immunisation. Medical history included hypertension. Concomitant medications included lisinopril (MANUFACTURER UNKNOWN) and hydrochlorothiazide (MANUFACTURER UNKNOWN) from an unknown date for an unknown indication. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 07Apr2021 at 10:45, the patient experienced vasovagal without syncope. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of the events which included treatment with just water and ice packs on an unknown date. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event vasovagal without syncope was recovering at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: LISINOPRIL; HYDROCHLOROTHIAZIDE

Current Illness:

ID: 1792821
Sex: F
Age:
State: TX

Vax Date: 02/27/2021
Onset Date: 02/27/2021
Rec V Date: 10/16/2021
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: Felt dizziness vertigo on drive home; Extreme fatigue still; severe depression; headache; Felt dizziness vertigo on drive home; This is a spontaneous report from a contactable consumer (patient) via a Pfizer Sponsored program. An adult female (non-pregnant) patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 27Feb2021 10:00 (Batch/Lot Number: EM9810) as DOSE 1, SINGLE, for covid-19 immunisation. Medical history included fibromyalgia, osteoporosis, known allergies: Wheat, all from an unknown date and unknown if ongoing. On 06Feb2021, patient experienced, Allergies got worse since 30 years. Chills (gone). Concomitant medication included prednisone taken for an unspecified indication, start and stop date were not reported. Dose 2 of bnt162b2 was given on 30Mar2021 via an unspecified route of administration, administered in Arm Left (Lot Number: EN6202) for covid-19 immunisation. Facility type vaccine: Other. If other vaccine in four weeks: No. On 27Feb2021 10:00, patient Felt dizziness vertigo on drive home. Did not go away, she still felt it slightly, severe depression, Extreme fatigue still, headache. The outcome of the events was not recovered. No treatment for the events. Events were assessed as Important medical event by the reporter. No covid prior vaccination.Not covid tested post vaccination. No follow-up attempts are needed. No further information is expected.

Other Meds: PREDNISONE

Current Illness:

ID: 1792822
Sex: F
Age:
State: TN

Vax Date:
Onset Date: 04/07/2021
Rec V Date: 10/16/2021
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: This is a spontaneous report from a noncontactable nurse (patient). A 46-year-old (non-pregnant) female patient received BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, batch/lot: unknown), at the age of 46, via an unspecified route of administration, on an unknown date in 2021, single dose, for COVID-19 immunisation. No medical history reported. Prior to the vaccination, patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. The patient received unspecified medication within two weeks of vaccination. The patient previously received Tamiflu (oseltamivir phosphate) for unknown indication on an unknown date and experienced drug allergy. On Apr 7, 2021, patient experienced headache, body ache and extreme tiredness. Since the vaccination, patient has not been tested for COVID-19. Therapeutic measures taken as a result of reported events included treatment with Tylenol (paracetamol). The outcome of headache, body ache and extreme tiredness: not recovered at the time of this report. No follow-up attempts possible. Information about lot/batch number cannot be obtained. No further information expected.

Other Meds:

Current Illness:

ID: 1792823
Sex: M
Age:
State: TX

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 10/16/2021
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: my wound was bleeding and was in moderate to severe pain for the first time; Sore arm; tingling in the hand in the same arm after letting go of the steering wheel; I began to have pain in that wound for the first time; This is a spontaneous report from a contactable consumer (patient). A 19-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Lot number was not reported), via an unspecified route of administration, administered in arm left on 07Apr2021 at 15:00 as dose 1, single for COVID-19 immunization (at the age of 19-year-old) at Pharmacy or Drug Store. Medical history included ADHD, bipolar, anxiety disorder and neoplasm removal on foot of the pain (patient had a mole shaved off a one week ago from the vaccination on his foot) all from an unspecified date and unknown if was ongoing. Concomitant medications included lisdexamfetamine mesilate (VYVANSE), bupropion hydrochloride (WELLBUTRIN), isotretinoin (ACCUTANE), propranolol and lamotrigine (LAMICTAL) all from were taken from an unspecified indication from an unknown date and unknown if was ongoing. No other vaccine in four weeks. The patient did not had COVID prior vaccination and not tested for COVID post vaccination. On 07Apr2021 at 15:00, the patient experienced sore arm, tingling in the hand in the same arm after letting go of the steering wheel. He had a mole shaved off a one week ago from the vaccination on his foot. No bleeding or pain at first while applying Aquaphor and band-aid twice a day. The day of the vaccination 7 days after in the morning, he began to have pain in that wound for the first time. After he got the vaccine the pain in the foot was not as bad. When he woke up the next day, his wound was bleeding and was in moderate to severe pain for the first time. The patient did not received any treatment for adverse events. On an unspecified date in Apr2021, the patient recovered from all the events. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: VYVANSE; WELLBUTRIN; ACCUTANE; PROPRANOLOL; LAMICTAL

Current Illness:

ID: 1792824
Sex: M
Age:
State: OH

Vax Date: 04/06/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: Lost his voice completely; he had some chills; He is coughing so bad/ Patient had "dry cough/ coughing has worsened; has a sore throat; headache; This is a spontaneous report from a contactable consumer. This female consumer reported for her husband (patient). A 58-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: ET7534, NDC number and expiry date were reported as unknown) via unspecified route of administration on 06Apr2021 at 10:00 (at the age of 58-years-old) in left arm as dose 2, single for covid-19 immunisation in campus. Medical history included diabetes mellitus (diagnosed probably 20 years ago or more). Additional vaccines administered on same date of the Pfizer suspect and prior vaccinations (within 4 weeks) were reported as none. No adverse event following prior vaccinations. The patient's concomitant medications were not reported. The patient's historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EP7534; Expiry date: 31Jul2021) via intramuscular in left arm on 16Mar2021 for covid-19 immunisation. It was reported that the patient received the second dose on 06Apr2021. The first day on 06Apr2021, he was okay, he had some chills, but that was okay. The second day on 07Apr2021, he began to lose his voice, he had lost his voice completely. He was coughing so bad, had sore throat and dry cough. The reporter had been for the past 2 days, and she couldn't find any side effects like that, especially because he lost his voice. Coughing was worsened and sore throat had stayed about the same, he had complained about the coughing more. The adverse events did not require visit to emergency room or physician office. The reporter was planning to take the patient either to the doctor or the ER after she finishes talking to Pfizer. Relevant tests were reported as none. The patient was treated with Tylenol for chills and headache. The reporter wanted to know if the events were possible side effects of the vaccine. The clinical outcome of the events chills and headache was unknown and for all other events was not resolved. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792825
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: Lump on my left arm where my shot was given; it is hurting very bad and it got bigger; Lump on my left arm where my shot was given; it is hurting very bad and it got bigger; Nausea; Dizziness; Fever blisters around lips; Fever blisters around lips; Lymph node was inflamed; headaches; 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, Batch/Lot number and Expiration date: Unknown), via an unspecified route of administration, administered in left arm on an unspecified date in 2021 as dose 1, single for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unspecified dates in 2021, within one week of the vaccination, the patient experienced lump on left arm where shot was given; it was hurting very bad and it got bigger, and also experienced nausea, dizziness, fever blisters around lips, lymph node was inflamed and headaches. Patient didn't get any side effects other than nausea, dizziness and headaches for the first two days. But after a week, precise to a week the following Monday (unspecified date in 2021), patient experienced some sort of fever blisters around my lips and then following day, patient noticed, patient don't know when it started, underneath patient armpits where the shot was given. It's been almost two weeks and it has got a larger and larger and it hurts. Patient went through the center care yesterday (unspecified date) and they said there is a lymph node that was inflamed and also they gave some medication (for unspecified reason on unspecified date). That's just not the one, they said that's the largest one. Also, the ones on patients neck from left side, also got inflamed. Patient got the first shot vaccine around almost 3 weeks, tomorrow (at the time of report) would be 3 weeks ago, tomorrow patient was going for second shot. Patient don't know why it was a delayed reaction, patient don't know it has been persisting since the first week. Patient job was asking questions because they can't find a proof of side effects occurring after a week. Is it normal to have side effects after week. Patient believe events are related to the COVID vaccine. 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: 1792826
Sex: M
Age:
State: FL

Vax Date: 03/29/2021
Onset Date:
Rec V Date: 10/16/2021
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: throat was kind of sore; little light headedness; feeling pain in arm; tongue was sore; feeling a heat of rash where I had a surgery in the abdominal area; Ear ache; rash on my groin area; This is a spontaneous report from a contactable consumer (patient). A 62-year-old male patient received BNT162B2 (PFIZER-BIOTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EN6208) via an unspecified route of administration, administered in arm right on 29Mar2021 (at the age of 62 years old) as dose 1, single for COVID-19 immunisation. Medical history included hypertension, diabetes mellitus, and surgery in the abdominal area. Concomitant medications included glipizide taken for diabetes mellitus. On an unspecified date, the patient experienced throat was kind of sore, little light headedness, feeling pain in arm, tongue was sore, feeling a heat of rash where patient had a surgery in the abdominal area, earache, and rash on groin area. Treatment (cream) was received for the event rash. The outcome of the events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds: GLIPIZIDE

Current Illness:

ID: 1792827
Sex: F
Age:
State: NJ

Vax Date: 04/05/2021
Onset Date: 04/05/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210406; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Swollen lymph nodes, severe lymphadenopathy; This is a spontaneous report from a contactable consumer, the patient. A 16-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 05Apr2021 at 10:00 (at the age of 16-year-old) as a single dose for COVID-19 immunisation. Medical history included attention deficit disorder and shellfish allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included amfetamine (AMPHETAMINE) for attention deficit disorder (ADD) from an unknown date and unknown if ongoing. Concomitant medications also included sertraline hydrochloride (ZOLOFT) and lamotrigine (MANUFACTURER UNKNOWN) both for an unknown indication from an unknown date and unknown if ongoing. On 05Apr2021 at 12:00, the patient experienced swollen lymph nodes, severe lymphadenopathy. The event resulted in doctor or other healthcare professional office or clinic visit. Therapeutic measures were taken as a result of the adverse event and included treatment with steroids and MOTRIN started from an unknown date. Since the vaccination, the patient had been tested for COVID-19. On 06Apr2021, the patient underwent nasal swab test for SARS-CoV-2 and the result was negative. The clinical outcome of the event swollen lymph nodes, severe lymphadenopathy was recovering at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: ZOLOFT; AMPHETAMINE; LAMOTRIGINE

Current Illness:

ID: 1792828
Sex: F
Age:
State: KS

Vax Date: 04/09/2021
Onset Date: 04/09/2021
Rec V Date: 10/16/2021
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: Very tired; Body aches; Cannot stay awake; This is a spontaneous report from a contactable consumer, the patient. A 45-year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 09Apr2021 at 10:00 (at the age of 45-years-old) as a single dose for COVID-19 immunisation. Medical history included slight hypertension. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Concomitant medications included paracetamol (TYLENOL), lisinopril (MANUFACTURER UNKNOWN), gabapentin (MANUFACTURER UNKNOWN), vitamin D NOS (MANUFACTURER UNKNOWN) and lisdexamfetamine mesilate (VYVANSE); all for an unspecified indication from unknown date and unknown if ongoing. The patient previously received morphine (MANUFACTURER UNKNOWN) and azithromycin (ZITHROMAX) and experienced drug allergy. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 19Mar2021 at 17:00 (at the age of 45-years-old) as a single dose for COVID-19 immunisation. On 09Apr2021 at 10:15, the patient experienced very tiredness, body aches and cannot stay awake. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were not taken as a result of the events. The clinical outcome of the events tiredness, body aches and cannot stay awake were not resolved at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: TYLENOL; LISINOPRIL; GABAPENTIN; VITAMIN D NOS; VYVANSE

Current Illness:

ID: 1792829
Sex: F
Age:
State: WA

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: itching; just legs from the top of leg down to feet; knee has started puffing; knees started hurting and very red; knee has started puffing; knees started hurting and very red; it got really hot and then both of legs got very hot; knee got very big and puffed out; This is a spontaneous report from a contactable consumer (patient). An 84-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number:EP6955, Expiration Date was not reported), via an unspecified route of administration on 01Apr2021 10:00 (at the age of 84-year-old), as dose 2, single for COVID-19 immunisation. Medical history included knee that has got replaced 12-14 years ago. The patient's concomitant medications were not reported. Patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number, Expiration Date was not reported), via an unspecified route of administration on an unspecified date, as dose 1, single for COVID-19 immunization and experienced no adverse events (reported as everything was perfect). After the second dose, the patient experienced knee got very big and puffed out on 01Apr2021, itching; just legs from the top of my leg down to feet, knee has started puffing; knees started hurting and very red, it got really hot and then both of legs got very hot on an unspecified date. It was reported that patient have a knee that got replaced 12-14 years ago. So, she never had a problem with it. She had noticed that it got very big and puffed out and was also worried about the size of them . Within half hour, both of knees started itching, just the legs from the top of leg down to feet and it was so severe that at that time, patient just did not know what to do with herself. She then tried and put some stuff on it and rubbed on her legs. She did not know what to do. It was so severe. It finally calmed down after about half an hour and She went to bed. She woke up this morning and was fine and thought no more about it. She had never ever had anything like that, there were no itches on her hands, arms, face, body itself, just on her legs. So, she thought that maybe she just should report this as anybody else may have it. Now, her knee has started puffing up again right now. Patient also reported that after getting the shot yesterday, 01Apr2021, when the evening came, about in the 7 Hours and knees started hurting and very rare because it has been really build a long time ago and then all of a sudden it got really hot and then both of legs got very hot. Patient treated events with unspecified ointment on it thinking that it would help it. But patient said that she did not think that it did. She thought of washing it all off again and then washed the stuff off because it was all burning. The outcome of pruritus, knee pain was recovered on an unspecified date, knee swelling was not recovered, and the rest of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792830
Sex: F
Age:
State: MI

Vax Date: 03/24/2021
Onset Date: 03/24/2021
Rec V Date: 10/16/2021
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: Tongue swelling; Arm and shoulder hurt up to the neck; Arm and shoulder hurt up to the neck; Arm and shoulder hurt up to the neck; This is a spontaneous report from a contactable consumer or other non hcp (patient). An 80-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, Batch/Lot Number: EN6204), dose 1 via an unspecified route of administration, administered in Arm Left on 24Mar2021 (at the age of 80-year old) as DOSE 1, SINGLE for covid-19 immunization. Medical history included allergy to Bactrim from an unknown date and unknown if ongoing (found this allergy 20-30 years ago), breast cancer from an unknown date and unknown if ongoing and glaucoma from an unknown date and unknown if ongoing. Concomitant medications included brimonidine tartrate, timolol maleate (COMBIGAN) taken for glaucoma from an unspecified start date and ongoing (taken at least for 5 years), exemestane (EXEMESTANE) taken for breast cancer from an unspecified start date and ongoing. On 24Mar2021 the patient experienced tongue swelling, arm and shoulder hurt up to the neck on an unspecified date with outcome of unknown. She mentioned how she was upset but not sure if that was related or not but she experienced tongue swelling on 24Mar2021 in the evening after her first dose of the Pfizer vaccine. She stated it went away the next day. She stated, "It wasn't bad enough that she couldn't swallow but it was swollen; Not so bad that I couldn't eat, but it felt bigger. Outcome of the event swollen tongue was recovered on 25Mar2021. Outcome of other events was recovered on 28Mar2021. No follow-up attempts are needed. No further information is expected.

Other Meds: COMBIGAN; EXEMESTANE

Current Illness:

ID: 1792831
Sex: F
Age:
State: IL

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 10/16/2021
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: Severe bodyaches; Especially back & front thigh to below knee; Especially back & front thigh to below knee; Especially back & front thigh to below knee; Fatigue; Headache; This is a spontaneous report from a contactable consumer, the patient. A 58-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UUNKOWN) via an unspecified route of administration in the right arm on 07Apr2021 at 15:00 (at the age of 58-years-old) as a single dose for COVID-19 immunisation. Medical history included high blood pressure, high cholesterol, diabetes 2 and COVID-19. The patient had no known allergies. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications included multiple plus insulin (MANUFACTURER UNKNOWN) for an unknown indication from an unknown date and unknown if ongoing. On 07Apr2021 at 16:30, the patient experienced severe body aches especially back & front thigh to below knee, fatigue and headache. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19.The clinical outcome of the events severe body aches especially back & front thigh to below knee, fatigue and headache were not resolved at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792832
Sex: M
Age:
State: NC

Vax Date: 04/08/2021
Onset Date: 04/08/2021
Rec V Date: 10/16/2021
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: Swollen left hand and fingers; Swollen left hand and fingers; Tingling; This is a spontaneous report from a contactable consumer, the patient. A 55-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8737) via an unspecified route of administration in the left arm on 08Apr2021 at 17:15 (at the age of 55-years-old) as a single dose for COVID-19 immunisation. Medical history included cardiomyopathy. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. On 08Apr2021 at 17:45, the patient experienced swollen left hand, fingers and tingling. Less severe on right side. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events swollen left hand, fingers and tingling was resolving at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792833
Sex: F
Age:
State: NJ

Vax Date: 03/29/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: vomiting three times; Reached peak of pain; severe headache; monster headache due to all of the inflammation; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number: EP7533, expiration date: 31Jul2021) via an unspecified route of administration, administered in left upper arm on 29Mar2021 between 08:00 and 10:30 (age at the time of vaccination was 54 years) as dose 1, 0.3ML single for COVID-19 immunisation at hospital. The patient's medical history included she had a lot of spinal issues and neck issues, ongoing chronic inflammation, when she was 28, it could have been a little before that. The patient's concomitant medication were included celecoxib (CELEBREX) indicated for chronic pain. No other product. There was no history of all previous immunizations with the Pfizer vaccine considered as suspect and no additional Vaccines administered on same date of the Pfizer suspect. There were no other vaccinations within four weeks, prior to the first administration date of the suspect vaccine. No any illness at time of vaccination. There was no family Medical History relevant to adverse events and no relevant tests. The patient received the first dose of the Pfizer COVID-19 vaccine on 29Mar2021 and was scheduled to receive the second dose on 19Apr2021. She took Celebrex daily for chronic pain and her HCP (health professional) who prescribed the Celebrex advised her to hold her Celebrex 3 days prior to the vaccine, the day of the vaccine and 3 days after the vaccine because of the potential for decreased immune response. She stated that by the 6th day of holding her Celebrex she had a monster headache due to all of the inflammation and vomited. She developed a severe headache that resulted in vomiting three times. She stated she got headaches and she knew the differences in her types of headaches. Caller states well she has issues, lots of medical issues that bring about headache, so she cant tell me if its there because of the vaccine or if its there because of the other problems that she has. She stated it was clearly not a migraine. She stated that the headache was brought about by the discontinuation of the anti-inflammatory. The headache reached peak of pain somewhere around 16:00 and it just intensified and intensified until she finally started vomiting at 22:30 at night. She would like information on a different regimen for her Celebrex prior to taking the Pfizer COVID-19 vaccine so that it did not interfere with immune response but also did not cause the same issue as she had with the first dose. She had not notified her health professional of what happened when she stopped taking the Celebrex as directed. The patient stated she took ondansetron, which was prescribed for her and that helped and there was no more vomiting on Friday, 02Apr2021. She did not visit emergency room and physician office. The outcome of headache was recovering, outcome of vomiting was recovered on 02Apr2021, and outcome of other events was unknown No follow-up attempts were possible, Information about lot/batch number could not be obtained.

Other Meds: CELEBREX

Current Illness: Chronic inflammation of orbit, unspecified (when she was 28, it could have been a little before that.)

ID: 1792834
Sex: F
Age:
State: MA

Vax Date: 04/06/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: arm got sore; upset stomach; terrible taste on the mouth - metallic taste; does not have much of an appetite and gait is a little off; does not have much of an appetite and gait is a little off; chills; sweats; headache; feeling sick; 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 mRNA VACCINE, Solution for injection, Lot Number: ER8729), via an unspecified route of administration, administered in Arm Right on 06Apr2021 (at the age of 85-year-old) as single dose for COVID-19 immunization. Medical history included prior Covid virus survivor, that she was hospitalized in Apr2020 and intubated, states she had to have surgery a couple of weeks ago, had vocal cord surgery due to damage from being intubated, prior to vaccine. History of COVID 19 infection and was intubated 07Apr2021 (as reported)- Patient undergone surgery for removal of large cyst in the vocal cord last Mar2021. She had cellulitis in left arm around a year and a half ago so she got the vaccine in her right. Concomitant medication(s) included atorvastatin taken for cholesterol from an unspecified start date and ongoing. The patient experienced chills, sweats, headache, upset stomach, no appetite, terrible taste on the mouth - metallic taste and gait was off since 08Apr2021; arm got sore since 09Apr2021. Patient had the 1st dose of the PFIZER-BIONTECH COVID-19 VACCINE last 07Apr2021 (as reported) and she experienced feeling sick, chills, sweats, headache, arm got sore, upset stomach, terrible taste on the mouth - metallic taste. The patient stated she had her first dose of the Pfizer Covid vaccine on Tuesday morning 06Apr2021, states she had never been that sick, states she felt like she had every side effect she could possibly have. After the vaccine she was alright during the day and at home, states she then woke up in the early hours Thursday morning, 08Apr2021, states she had a headache, sweats, chills, that her arm did not bother her until this morning (09Apr2021), had upset stomach, the taste in her mouth was unbelievable, felt a little better, was improving, did not have much of an appetite and gait was a little off, but better. Asking if the 2nd dose will give her more side effects and if she could still get the 2nd shot because of the reactions. Caller wanted to know if she should have not gotten the vaccine since she had Covid last year. Outcome of the event sore arm, gait is off was not recovered; feeling sick was unknown; other events was resolving. No follow-up attempts are possible. No further information is expected.

Other Meds: ATORVASTATIN

Current Illness:

ID: 1792835
Sex: M
Age:
State: CA

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 10/16/2021
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: Arthritis in both right and left wrists; This is a spontaneous report from a contactable consumer, the patient. An 84-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the arm right on 29Jan2021 at 12:00 (at the age of 84-years-old) and the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 20Feb2021 (at the age of 84-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies to medications, food or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN), atorvastatin (MANUFACTURER UNKNOWN), tamsulosin hydrochloride (FLOWMAX) and metoprolol (MANUFACTURER UNKNOWN), all taken for an unspecified indication from an unknown date and unknown if ongoing. On 29Jan2021, the patient experienced arthritis in both right and left wrists. The event did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were taken as a result of the event and included treatment with naproxen sodium (ALEVE). Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event arthritis in both right and left wrists was not recovered at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: BABY ASPIRIN; ATORVASTATIN; FLOWMAX; METOPROLOL

Current Illness:

ID: 1792836
Sex: F
Age:
State: NY

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 10/16/2021
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: The toes with pain and numbness are more red than my other toes; feeling pain and numbness in the fifth toe on my right foot/pain and numbness in my second toe on my right foot; feeling pain and numbness in the fifth toe on my right foot/pain and numbness in my second toe on my right foot; There is also numbness, redness and tingling./the second toe on my right foot, beside my big toe, is also painful, red and tingling.; This is a spontaneous report from a contactable consumer (patient). A 24-years-old non-pregnant female patient BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: ER8734, Expiry date: unknown) via an unspecified route of administration as on 07Apr2021 (at the age of 24-year-old) dose 1, single for covid-19 immunization. Medical history included SLE (systemic lupus erythematosus). Patient had no known allergies. Patient was not pregnant. Concomitant medication (in two weeks) included hydroxychloroquine. Patient had not received any other vaccine in four weeks. Patient did not had any prior Covid-19 vaccination and was not tested to covid post vaccination. On 07Apr2021, around 4 to 5 hours after receiving shot she started feeling pain and numbness in the fifth toe on her right foot and her pinky toe on her right foot became painful. On 09Apr2021 morning, she started feeling the same pain and numbness in her second toe in her right foot. She stated that toes with pain and numbness are more red than her other toes. There was also numbness, redness and tingling. Patient had not received any treatment for the events reported. Outcome of all events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: HYDROXYCHLOROQUINE

Current Illness:

ID: 1792837
Sex: M
Age:
State: NJ

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 10/16/2021
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: weird low back pain; lot of joint pain; his left arm was sore; he could not lift his arm up over his head; pain in wrist; big toes hurt and throbbing; tiredness; everyone told caller he sounded terrible; muscle spasms; felt miserable; left shoulder pain; his left shoulder has been tingling on and off; This is a spontaneous report from a contactable consumer (patient) from a Pfizer sponsored program via medical information team. A 68-year-old male received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number EN6198; Expiration Date: 30Jun2021), via an unspecified route of administration, administered in arm Left (left shoulder by injection) on 26Feb2021 at 11.45 (at the age of 67-year-old) as dose 1, single for covid-19 immunisation. Medical history included ankylosing spondylitis from an unknown date and unknown if ongoing, ongoing elevated blood pressure from an unknown date and ongoing cholesterol from an unknown date. Concomitant medications included lisinopril was taken for elevated blood pressure, start and stop date were not reported (was taken for 8 months or 7 months), rosuvastatin calcium (ROSUVASTATIN PLUS PHARMA) taken for cholesterol, start and stop date were not reported (has been on for maybe a year), hydrochlorothiazide taken for elevated blood pressure water pill, start and stop date were not reported (has been on for about a year) and bunch of vitamins. Past drug included amlodipine for elevated blood pressure. The patient had only got his flu shot last Sep2020.On 27Feb2021, the patient experienced left arm was sore. On 06Apr2021, the patient experienced weird low back pain, lot of joint pain. On an unspecified date in 2021, the patient experienced he could not lift his arm up over his head, his left shoulder has been tingling on and off, pain in wrist, big toes hurt and throbbing, tiredness, everyone told caller he sounded terrible, muscle spasms, left shoulder pain and felt miserable. The patient reported that he got his first shot back in mid-Feb and he only had a reaction of a sore arm. The patient received his second shot of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: Lot EN6207, expiration date: 31JUL2021) via an unspecified route of administration, administered in arm Left (left shoulder by injection) on 19MAR2021 at 11:45 and did not really have any reaction. Caller confirmed this was the Pfizer Covid19 Vaccine. Caller added that he was fine up until a couple of days ago, when he was getting a lot of joint pain, particularly in his wrists. The patient's big toes were hurt, and he had a weird low back pain. The patient added that all of these symptoms started last Monday or Tuesday. For some reason, this morning he got up and he had a tingling in his shoulder. He added it was in his left shoulder where he got the shot, and it came and went. Caller added that it started tingling, went away, started tingling, and went away. Caller added that he did not know if this has something to do with the vaccine, but that was the only thing that he has done in the last few weeks. He has not really done anything else that could cause this. Caller added that his arm was sore the next day after he got the first shot. His arm was tender the next day, the next morning. Caller added that it was on 26FEB2021 that he received his first vaccine, and on the next day 27FEB2021 he had this soreness. Caller added that it went away. The only thing that he got after that was a tingling in his arm, like in the muscles. Refer to tingling in left arm and shoulder, caller added this was in his muscles. The pain went away but he had muscle spasms. It just kept on going, and it was not consistent. Like right now, it was not doing that but it would just start tingling and then it would go away. Caller confirmed this was after receiving his first vaccine when it started. The patient stated that he has left shoulder pain that seemed like it was in the morning. It went away this morning. Caller was wondering, it seemed like it was 2.5 weeks since his second shot and he had no symptoms before that. He did not know if it was from the shot or not. On 06APR2021, Tuesday, the patient had a lot of joint pain Now that he was thinking about it, it just suddenly shut off. Up until yesterday, he was miserable. His wrist was hurt his back was hurt. Caller stated that his right wrist was the worst and he could not open and close his hand or move his hand. Caller stated he had the vaccine on the left side. Caller. The patient reported that he felt miserable the last couple of days. Caller added that his symptoms came further out. Wrist hurt so bad he could not pick up glass of water, he had to use two hands. Caller added there was no pain there whatsoever now, it was just shut off. Just yesterday, he was having a hard time picking up a glass of water it hurt so bad and now the pain was gone. Weird low back pain: caller had trouble sitting, he was going from side to side because it just started and it was hurting. Caller added that it started on 06APR2021 but went away. Caller unsure dates on the events he listed, but he thought the low back pain was Tuesday, Wednesday, and Thursday. Caller did not clarify dates but states that yesterday was the worst, especially with the wrist. He still was having trouble lifting his arm up related to left shoulder pain. It subsided during the day, but in the morning he could not life his arm up. The patient added that the shoulder pain was his left, the wrist pain was his right. Unclear dates. Around Tuesday, the pain in his wrist was building and building until yesterday when he was really bad. This morning it went away, it went away when he woke up. Now, his wrist does not hurt at all. caller added he has been tired the last few days but today he was wide awake. He added he was kind of like, everybody kept saying what was the matter he sound terrible. The patient did not go to the physician's office or emergency room. He went to the chiropractor because he did not know where the pain was coming from or what was causing it and it came on suddenly and disappeared suddenly so he thought maybe it was a vaccine thing. The patient did not received any other vaccinations within four weeks prior to the first administration. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds: LISINOPRIL; ROSUVASTATIN +PHARMA; HYDROCHLOROTHIAZIDE; VITAMINS NOS

Current Illness: Cholesterol; Elevated blood pressure reading without diagnosis of hypertension

ID: 1792838
Sex: M
Age:
State: IL

Vax Date: 04/09/2021
Onset Date: 04/09/2021
Rec V Date: 10/16/2021
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: Dizziness; Vertigo; Sweating 2-3 min after injectionLasted 1-2 min; This is a spontaneous report from a contactable consumer, the patient. A 27-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 09Apr2021 at 14:45 (at the age of 27-year-old), as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. The patient did not receive any medications within two weeks of vaccination. On 09Apr2021 at 14:45, 2 to 3 minutes after the injection, the patient experienced dizziness, vertigo and sweating which lasted for 1 to 2 minutes. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events dizziness, vertigo and sweating was recovered on 09Apr2021. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792839
Sex: F
Age:
State: WI

Vax Date: 03/18/2021
Onset Date: 03/18/2021
Rec V Date: 10/16/2021
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: extreme nausea; fatigue; Repeated vomiting beginning at approximately the 25th hour and continuing for the next several hours / was unable to keep food or liquid down for another approximate 24 hours thereafter.; Sharp pain in toes began within hours of first injection; This is a spontaneous report from a contactable consumer, the patient. A 53-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER2613) via an unspecified route of administration in the left arm on 18Mar2021 at 15:30 (at the age of 53-years-old) as a single dose for COVID-19 immunisation. Patient was not pregnant. Medical history included asthma and hypertension. The patient had no known allergies to medications, food or other products. Prior to vaccination, it was unknown whether the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included acetylsalicylic acid (ASPIRIN), montelukast sodium (SINGULAIR) and hydrochlorothiazide (MANUFACTURER UNKNOWN); all for unknown indication from an unknown date and unknown if ongoing. On 18Mar2021, the patient experienced sharp pain in toes began within hours of first injection. On 19Mar2021 at 16:30 (as reported), approximately 22hours from first injection the patient experienced extreme nausea and fatigue, followed by repeated vomiting beginning at approximately the 25th hour and continuing for the next several hours. The patient was unable to keep food or liquid down for another approximate 24 hours thereafter. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of the events which included treatment with ondansetron (MANUFACTURER UNKNOWN). Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events sharp pain in toes, nausea, fatigue and vomiting were recovered on unknown date in 2021. The patient also received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0158) via an unspecified route of administration in the left arm on 08Apr2021 at 15:30 (at the age of 53-years-old) as a single dose for COVID-19 immunisation. No follow-up attempts are needed. No further information is expected. Amendment: This follow up report is being submitted to amend previously reported information: added Vaccination Facility information, revised narrative to add "patient was not pregnant", removed dose 2 from suspect dose regimen.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; SINGULAIR; HYDROCHLOROTHIAZIDE

Current Illness:

ID: 1792840
Sex: F
Age:
State: GA

Vax Date: 04/06/2021
Onset Date: 04/06/2021
Rec V Date: 10/16/2021
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: Dizzy; Congested; Upset stomach; Beginning of a migraine that did not develop; Fatigue; Constipation; This is a spontaneous report from a contactable consumer, the patient. A 58-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0151) via an unspecified route of administration in the right arm on 06Apr2021 at 15:00 (at the age of 58-years-old) as a single dose for COVID-19 immunisation. Medical history included menopause and osteopenia. The patient did not have allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included estrogens conjugated (PREMARIN) and ibandronate sodium (IBANDRONATE); both for unknown indications from unknown dates and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: En6204) via an unspecified route of administration in the left arm on 16Mar2021 at 10:15 (at the age of 58-years-old) as a single dose for COVID-19 immunisation. On 06Apr2021 at 22:00, the patient felt dizzy, congested, upset stomach, beginning of a migraine that did not develop, fatigue and constipation. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events dizzy, congested, upset stomach, beginning of a migraine that did not develop, fatigue and constipation was recovered on an unknown date in Apr2021. No follow-up attempts are needed. No further information is expected.

Other Meds: PREMARIN; IBANDRONATE

Current Illness:

ID: 1792841
Sex: F
Age:
State: MA

Vax Date: 04/04/2021
Onset Date: 04/09/2021
Rec V Date: 10/16/2021
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 muscle pain on arm, shoulders; Severe muscle pain on arm, shoulders; Severe muscle pain on arm, shoulders; This is a spontaneous report from a contactable consumer or other non hcp. A 62-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, Batch/Lot Number: EWO150), via an unspecified route of administration on 04Apr2021 (at the age of 62-year-old) as DOSE 1, SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. On 09Apr2021 the patient experienced severe muscle pain on arm, shoulders. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. Patient did not receive any treatment for the adverse event. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792842
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: Fever; This is a spontaneous report from a non-contactable consumer. A female patient of unknown age received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On an unknown date, the patient experienced fever after injection. The clinical outcome of the event fever after injection was unknown at the time of this report No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected. Amendment: This follow-up report is being submitted to amend previously reported information: Updated primary reporter information, patient details (country) and added Vaccination Facility Country. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792843
Sex: M
Age:
State: MT

Vax Date: 04/02/2021
Onset Date: 04/02/2021
Rec V Date: 10/16/2021
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: Sore arm, mild itching, both occurring at the injection site/Mild soreness at injection site (similar to flu shot), mild itching - nothing substantial; Sore arm, mild itching, both occurring at the injection site/Mild soreness at injection site (similar to flu shot), mild itching - nothing substantial; This is a spontaneous report from a contactable consumer or other non-healthcare professional. A 50-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: ER8727), via an unspecified route of administration, on 02Apr2021 09:30 AM (at the age of 50-year-old), in left arm as dose 1, single for COVID-19 immunization and also received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: ER8735), via an unspecified route of administration, on 23Apr2021 09:45 AM (at the age of 50-year-old), in left arm as dose 2, single for COVID-19 immunization. Medical history included Colitis ulcerative from an unknown date and unknown if ongoing. Allergies to medications, food, or other products reported as none known. Concomitant medications included balsalazide taken for an unspecified indication, start and stop date were not reported and tylenol taken for an unspecified indication, on day of vaccination only. Patient did not taken any other vaccine in four weeks. Patient had not diagnosed with COVID-19 Prior to vaccination and patient had not been tested for COVID-19 Since the vaccination. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. On 02Apr2021 the patient experienced sore arm, mild itching, both occurring at the injection site/mild soreness at injection site (similar to flu shot), mild itching - nothing substantial. Same events occurred after prime and boost and with roughly same time course. Soreness first apparent about 5 hrs post-injection reaching peak about 10 hrs post-injection, persisted for about 2.5 days. Itching first noticed approx. 24 hrs post-injection, disappeared after about 2.5 days. Patient was taken 3 max strength Tylenol/day (spaced morning, afternoon, night) on day of and day after each injection to mitigate side effects. Mild soreness at injection site (similar to flu shot), mild itching nothing substantial, disappeared after 2-3 days, patient took tylenol max strength (1 pill before inoculation, 1 pill in afternoon, 1 pill in evening) to help reduce any potential side effects. Treatment was not taken for the reported adverse events. The clinical outcome of event was recovered on unspecified date 2021. No follow-up attempts are needed. No further information is expected.

Other Meds: BALSALAZIDE; TYLENOL

Current Illness:

ID: 1792844
Sex: F
Age:
State: MN

Vax Date: 04/05/2021
Onset Date: 04/09/2021
Rec V Date: 10/16/2021
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: Swelling of eyelids and cheekbones; Swelling of eyelids and cheekbones; This is a spontaneous report from a contactable consumer (patient). A 57-year-old female patient first dose of received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6203) via an unspecified route of administration, administered in right arm on 05Apr2021 10:00 (at the age of 57-year-old) as dose 1, single for covid-19 immunisation. Patient was not pregnant at time of vaccination. Medical history included diabettes from an unknown date and unknown if ongoing and known allergies to chicken, cigarette and smoke from an unknown date and unknown if ongoing. Allergies to medications, food, or other products: Alergia pollo, humo de cigarro. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 09Apr2021 06:00, the patient experienced swelling of eyelids and cheekbones. No treatment received for the adverse event. Outcome of the event was not recovered at the time of reporting. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792845
Sex: M
Age:
State: KY

Vax Date: 04/08/2021
Onset Date: 04/08/2021
Rec V Date: 10/16/2021
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: Red Spotted rash on feet, legs, trunk, arms, neck and scalp; Red Spotted rash on feet, legs, trunk, arms, neck and scalp; Red Spotted rash on feet, legs, trunk, arms, neck and scalp; Red Spotted rash on feet, legs, trunk, arms, neck and scalp; Red Spotted rash on feet, legs, trunk, arms, neck and scalp; This is a spontaneous report from a contactable consumer (patient himself). A 62-year-old male patient received second dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: ER8737) via an unspecified route, administered in Left arm on 08Apr2021 at 08:15 (62-year-old at vaccination) as Dose 2, Single for Covid-19 immunization. The patient's medical history included hypothyroidism, Allergies to medications, food, or other products such as Amoxicillin. The patient's concomitant medications included sulfamethoxazole, trimethoprim oral tablet within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. Prior vaccination, the patient was not diagnosed with Covid-19 and since the vaccination the patient had not been tested for Covid-19. The patient previously received first dose of bnt162b2 (COMIRNATY, Solution for injection, Lot number: EN6208) via an unspecified route administered in left arm on 18Mar2021 at 07:45 (62-year-old at vaccination) as Dose 1, Single for COVID-19 immunization. On 08Apr2021, patient experienced red spotted rash on feet, legs, trunk, arms, neck and scalp. The patient did not receive any treatment medication for the adverse event. The outcome of the events was not recovered. No follow-up attempts are needed. No further information was expected.

Other Meds: Trimethoprim Sulfamethoxazole

Current Illness:

ID: 1792846
Sex: F
Age:
State: TX

Vax Date: 04/09/2021
Onset Date: 04/10/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210410; Test Name: Body temperature; Result Unstructured Data: Test Result:103.5; Comments: Very high fever (103.5)

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Very high fever (103.5); vomiting; Off label use; Drug use in unapproved population; This is a spontaneous report from a contactable consumer, the patient. A 39-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EP7533 and expiry date was not reported), via an unspecified route of administration, in Right Arm, on 09Apr2021 at 16:15 (at the age of 39-years-old), as dose 2, single dose for COVID-19 immunization. The patient's medical history included currently breast feeding. The patient had no known allergies to medications, food or other products. Concomitant medications included prenatal vitamins (MANUFACTURER UNKNOWN) from an unknown date and unknown if ongoing for an unknown indication. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EP6955 and expiry date was not reported), via an unspecified route of administration, in Right Arm, on 17Mar2021 at 16:30 (at the age of 39-years-old), as dose 1, single dose for COVID-19 immunization. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 10Apr2021 at 02:00, the patient experienced very high fever (103.5 UNSPECIFIED UNITS) and vomiting. It was not reported if the patient received any treatment for the re-ported events. There was an off label use and drug use in unapproved population as the patient had a maternal exposure during breast feeding since an un-known date in 2021. On 10Apr2021, the patient underwent body temperature measurement, and the result was found to be 103.5 (UNSPECIFIED UNITS). The events did not result in doctor or other healthcare professional office/clinic vis-it, emergency room/department or urgent care. The clinical outcome of the events very high fever (103.5), vomiting was recovering at the time of this re-port. The clinical outcome of the events off label use and drug use in unapproved population was unknown at the time of this report. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Breast feeding (Currently breastfeeding)

ID: 1792847
Sex: F
Age:
State: NJ

Vax Date: 04/10/2021
Onset Date: 04/10/2021
Rec V Date: 10/16/2021
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: Allergies; This is a spontaneous report from a contactable consumer (patient). A 37-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and expiration date not reported), via an unspecified route of administration, administered in left arm on 10Apr2021 08:15 (at the age of 37 years) as dose 1, single for covid-19 immunization. Medical history included allergy to vancomycin, cherries, and seasonal allergies, from an unknown date and unknown if ongoing. Concomitant medications included vitamin d [vitamin d nos] (VITAMIN D [VITAMIN D NOS]); and iron taken for an unspecified indication, start and stop date were not reported. Patient was not pregnant at the time of vaccination. No other vaccine in four weeks. No covid prior vaccination and not covid tested post vaccination. The patient experienced allergies on 10Apr2021 08:30. Therapeutic measures were taken as a result of event and patient received unspecified treatment. The outcome of event was recovering. Follow-up attempts completed. Information about lot/batch number cannot be obtained despite the follow-up attempts made. No further information is expected.

Other Meds: VITAMIN D [VITAMIN D NOS]; IRON

Current Illness:

ID: 1792848
Sex: M
Age:
State: NY

Vax Date: 04/02/2021
Onset Date: 04/02/2021
Rec V Date: 10/16/2021
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: Rashes on left leg/rash beginning on his left leg, above the knee going up to the groin; Itchy and has little bumps and it goes from knees to up to the groin/getting worse and it is very itching; Itchy and has little bumps and it goes from knees to up to the groin; This is a spontaneous report received from a contactable consumer (patient's wife). A 77-years-old male patient received BNT162b2 (Pfizer BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number, Expiration date, NDC and UPC number was unknown) via an unspecified route of administration on 02Apr2021 (Friday night) as dose 1, single (at the age of 77-years-old) for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 02Apr2021, Friday night, when he came home later, patient was very itchy, had little bumps and there was a rash beginning on his left leg, above the knee going up to the groin. Now, this reaction got worse yesterday (03Apr2021, Saturday) and it was worse today (04Apr2021, Sunday). Patient 's wife went to the store and brought some Cortisone cream, but the rash does not seem to be going away. And it was still very itching on it. Patient's wife stated that it seems to be getting worse and it was very itching. Patient's wife did not think at first that it had anything to do with the injection. Therapeutic measures were taken as a result of rash and itchy and treatment included cortisone cream. The outcome of rash and itchy was not recovered and unknown for had little bumps. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1792849
Sex: M
Age:
State:

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 10/16/2021
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: shortness of breath for 11 consecutive days; chest pain/ tightness; chest pain/ tightness; fatigue; This is a spontaneous report from a contactable patient or other non hcp (patient). A 40-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: not reported, Expiry Date: Unknown), dose 1 via an unspecified route of administration on 30Mar2021 (at the age of -years-old) as a DOSE 1, SINGLE for covid-19 immunisation at pharmacy. The patient medical history and concomitant medications were not reported. On 30Mar2021, the patient experienced shortness of breath for 11 consecutive days, chest pain/ tightness and fatigue. Patient received first dose of vaccine on 30Mar2021. Patient reported that he was experiencing side effects such as shortness of breath for 11 consecutive days, fatigue and chest pain/ tightness. Worried about the second dose due to side effects he was experiencing. Patient wanted to know if he should get second dose. Patient wanted to know if he does find that he is allergic to vaccine or has to wait to get second dose. Does he need to get two doses again in a year from now. Patient wanted know efficacy of vaccine after one dose. Patient stated, So, I am calling because I want to report some side effects that I have had received I was taking the vaccine of Pfizer (Unspecified Vaccine) on 30Mar2021 and I wanted to know if it is a good idea for me to actually take a second dosage because of the side effects I am presenting half last all this time and they have not gone away. PQC was not present. Outcome of all the events were unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1792850
Sex: F
Age:
State: OR

Vax Date: 01/09/2021
Onset Date: 01/16/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Name: allergy testing; Result Unstructured Data: Test Result:unknown; Test Name: Biopsy; Result Unstructured Data: Test Result:Urticarial Hypersensitivity Reaction; Comments: biopsy of the rash done. It showed "Urticarial Hypersensitivity Reaction

Allergies:

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

Symptoms: I developed areas of hives/rash over several parts of my body.; I developed areas of hives/rash over several parts of my body.; Urticarial Hypersensitivity Reaction; This is a spontaneous report from a contactable nurse (patient) and physician. A 64-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EK9231), via an unspecified route of administration, administered in arm left on 09Jan2021 at 19:00 (07:00 PM) as, dose 1, single for COVID-19 immunization. Second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9262), via an unspecified route of administration, administered in arm left on 30Jan2021 at 04:00 PM as dose 2, single for COVID-19 immunization. Medical history was reported as none. Patient had no known allergies. The patients took dietary supplement within in two weeks of vaccination. The patient did not receive any other vaccine in four weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 16Jan2021, the patient experienced I developed areas of hives/rash over several parts of my body, urticarial hypersensitivity reaction. Adverse events resulted in doctor or other healthcare professional office/clinic visit. Adverse event: I developed areas of hives/rash over several parts of my body. This began after the first vaccine (not immediately, days later) and became severe after the second vaccine dose. I saw my dermatologist DR. I also saw an allergist and had extensive allergy testing done. I eventually had a biopsy of the rash done. It showed Urticarial Hypersensitivity Reaction. It was reviewed by Dr. The patient underwent lab tests and procedures which included allergy testing was unknown; biopsy: urticarial hypersensitivity reaction. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. The patient received treatment for the events. The outcome of all the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792851
Sex: M
Age:
State: CO

Vax Date: 04/01/2021
Onset Date: 04/03/2021
Rec V Date: 10/16/2021
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: Rash in both arms; Red-blurred petechiae that are so uniforms and skin looks very red; Red-blurred petechiae that are so uniforms and skin looks very red; This is a spontaneous report from a contactable consumer (patient) and other-health care professional. A 46-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/lot number: Not Reported, Expiry Date: Not Reported), via an unspecified route of administration, administered in Arm right on 01Apr2021 16:15 (at the age of 46-year-old) as dose 1, single for covid-19 immunisation at hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and did not receive any other medications within 2 weeks of vaccination. The patient medical history concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has not been tested for COVID-19 since the vaccination. The patient did not have any known allergies to medications, food, or other products. On 03Apr2021 at 14:00, the patient experienced rash on both arms, red-blurred petechiae that are so uniforms and skin looks very red. The patient did not receive any treatment for the reported adverse event. As per the reporter, the seriousness criteria of the reported events were non-serious. The event does not lead to any of the seriousness criteria such death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, Congenital anomaly/birth defect. Outcome of the event was not recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792853
Sex: F
Age:
State: IL

Vax Date: 04/03/2021
Onset Date: 04/10/2021
Rec V Date: 10/16/2021
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: tight chest/dry or tight chest a week after receiving the 1st dose; low grade fever; body ache; chills; headaches; exhaustion and insomnia at the same time; exhaustion and insomnia at the same time; This is a spontaneous report from a contactable consumer. This female consumer (patient) of unspecified age reported for herself that she received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: UNKNOWN) via an unspecified route of administration on 03Apr2021 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 10Apr2021, the patient experienced tight chest/dry or tight chest a week after receiving the 1st dose, low grade fever, body ache, chills, headaches, exhaustion and insomnia at the same time. It was great. She had no repercussions. On 10Apr2021, she had a low-grade fever, body ache, chills, headaches, exhaustion and insomnia at the same time and tight chest. It was a week later/after she got the vaccine. Her husband (age: 65) received the Pfizer vaccine, had it 2 weeks before. His side effects were within the first 3 days which was normal. When she got her shot and did not feel anything for a week. then wham, he was sleeping on his. He was tired. He had low grade fever and chills for 5 days. Mine was later. Her dad (age 94) also received the Pfizer vaccine. He did not have any side effects and he did not even feel the needle and 2nd shot (he got on the 10th) he felt the shot this time. So far so good. He was feeling great. She wants to know if it was normal to experience fever, headache, insomnia and dry or tight chest a week after receiving the 1st dose. She received the 1st dose last 03Apr2021 and 2nd dose will be on 24Apr2021. Provided contact number and hours of operation. Unaddressed medical questions referred or forwarded to Medical Information. Outcome was unknown for all the events. Follow-up (12Apr2021): This is a follow-up spontaneous report from a contactable consumer reported verbatim and event description. No follow up attempts are possible. Information about lot/batch number cannot be requested. No further information is expected.

Other Meds:

Current Illness:

ID: 1792854
Sex: F
Age:
State: MA

Vax Date: 04/08/2021
Onset Date: 04/09/2021
Rec V Date: 10/16/2021
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: Severe headache; nausea; dizziness; joint pain; injection site swelling and redness; injection site swelling and redness; fatigue; fever; This is a spontaneous report received from contactable consumer (patient) reported for herself. A 44-year-old female patient received first dose of bnt162b2 (Pfizer COVID 19 vaccine, solution for injection, Lot number: ER8729), via an unspecified route on 08Apr2021 at 09:45 (age at vaccination: 44-year-old), as a single dose for covid-19 immunization. Medical history mentioned as none. The patient concomitant medications were not reported. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. No allergies were reported. Patient received any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not receive any other medications within 2 weeks of vaccination. On 09Apr2021 at 05:00, patient experienced severe headache, nausea, dizziness, joint pain, injection site swelling and redness, fatigue and fever. Patient did not receive any treatment for the events. The clinical outcome of the events was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792855
Sex: F
Age:
State: NV

Vax Date: 03/28/2021
Onset Date: 03/30/2021
Rec V Date: 10/16/2021
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: Zithromax Z-pack

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

Symptoms: This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, solution for injection, batch/lot# unknown), at the age of 61, via an unspecified route of administration, in left arm, on Mar 28, 2021, at 12:45, single dose, for COVID-19 immunisation. Medical history included diabetes and high cholesterol. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not tested for COVID-19. The patient previously took Zithromax Z-pack and experienced drug hypersensitivity. Other medications in two weeks reported as yes. On Mar 30, 2021, at 12:00, patient experienced muscles weakness, frequent chest pain and left arm weak/weakness in her left arm. No treatment received for the events. The outcome of the events: not recovered. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1792856
Sex: M
Age:
State: AZ

Vax Date: 02/03/2021
Onset Date:
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210303; Test Name: Negative spike antibody test; Test Result: Negative ; Comments: has had two antibody tests which came back negative; Test Date: 20210322; Test Name: SARS-CoV-2 antibody test negative; Test Result: Negative ; Comments: (SARS-CoV-2 antibody test negative)

Allergies:

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

Symptoms: headache; This is a spontaneous report from a contactable consumer (patient). A 75-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in the left arm on 03Feb2021 (at the age of 75 years old) (Lot Number: EL9264) as dose 2, single for COVID-19 immunisation. Medical history included chronic lymphocytic leukemia from an unknown date and unknown if ongoing (CLL, or chronic lymphocytic leukemia, which he is at stage zero, so requires no active treatment at all) and headache from an unknown date and unknown if ongoing (which started before he got the vaccine doses). Concomitant medications included acetaminophen taken for headache, start and stop date were not reported; ibuprofen (ADVIL [IBUPROFEN]) taken for headache, start and stop date were not reported; paracetamol (TYLENOL) taken for an unspecified indication, start and stop date were not reported. The patient previously took the first dose of BNT162B2 on 13Jan2021 for COVID-19 immunisation. On an unspecified date, the patient experienced headache. It was reported that the headaches probably started in April or May last year, it bothers him for a few weeks then went away then returned about a month ago after his second dose of the Pfizer COVID-19 vaccine, about 8 weeks ago. The patient underwent lab tests and procedures which included SARS-CoV-2 antibody test: negative on 03Mar2021 has had two antibody tests which came back negative and SARS-CoV-2 antibody test negative: negative on 22Mar2021 (SARS-CoV-2 antibody test negative). The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: ACETAMINOPHEN; ADVIL [IBUPROFEN]; TYLENOL

Current Illness:

ID: 1792857
Sex: F
Age:
State: OH

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
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: A burning pain in "my" shoulder after 2 weeks; "My" arm was sore after shot. Still sore arm at injection site; This is a spontaneous report from a contactable consumer, the patient. A 55-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 31Mar2021 at 15:30 (at the age of 55-years-old) as a single dose for COVID-19 immunisation. Medical history included blood pressure high and known allergies to peanuts and strawberry. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included lisinopril (MANUFACTURER UNKNOWN), potassium (MANUFACTURER UNKNOWN) and cetirizine hydrochloride (ZYRTEC); all for an unknown indication from an unknown date and unknown if ongoing. On 31Mar2021 at 20:00 the patient's arm was sore after shot. Still sore arm at injection site. On an unknown date in Apr2021 the patient experienced a burning pain in her shoulder after 2 weeks. The events resulted in doctor or other healthcare professional office/clinic visit. It was unknown whether any therapeutic measures were taken as a result of the events. The patient also reported she was going to doctor that week. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events arm was sore after shot, still sore arm at injection site and burning pain in shoulder after 2 weeks was not recovered at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: LISINOPRIL; POTASSIUM; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1792858
Sex: M
Age:
State: MI

Vax Date: 04/07/2021
Onset Date: 04/08/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210409; Test Name: Nasal Swab; Test Result: Negative

Allergies:

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

Symptoms: Vomiting and explosive diarrhoea for 4 hours; Vomiting and explosive diarrhoea for 4 hours; This is a spontaneous report from a contactable consumer, the patient. A 58-year-old male patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 07Apr2021 at 10:30 (at the age of 58-years-old) as a single dose for COVID-19 immunisation. Medical history included hernia. The patient had no known allergies to medications, food, or other products. Concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 08Apr2021 at 02:00, the patient experienced vomiting and explosive diarrhoea for 4 hours. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had been tested for COVID-19. On 09Apr2021, the patient underwent SARS-CoV-2 test via nasal swab and the result was negative. The clinical outcome of the events vomiting and explosive diarrhoea for 4 hours was resolving at the time of the report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792859
Sex: F
Age:
State: NJ

Vax Date: 04/09/2021
Onset Date: 04/10/2021
Rec V Date: 10/16/2021
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: Sore throat; Chest congestion; Immense muscle pain; Debilitation back pain; Over tiredness; Sleeping over 18 hours per day; Severe congestion; This is a spontaneous report from a contactable consumer, the patient. A 24-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: ER8731) via an unspecified route of administration in the left arm on 09Apr2021 at 15:15 (at the age of 24-year-old) as a single dose for COVID-19 immunisation. Medical history included allergy to just nickel metal. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. On 10Apr2021 at 16:00, the patient experienced severe congestion, sore throat, chest congestion, immense muscle pain, debilitation back pain, over tiredness and sleeping over 18 hours per day. The events did not result in doctor or other healthcare professional office or clinic visit, emergency room or department or urgent care. No therapeutic measures were taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events severe congestion, sore throat, chest congestion, immense muscle pain, debilitation back pain, over tiredness and sleeping over 18 hours per day were not recovered at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792860
Sex: M
Age:
State:

Vax Date: 04/03/2021
Onset Date: 04/03/2021
Rec V Date: 10/16/2021
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: his eyes got swollen, watery, swelling almost shut; his eyes got swollen, watery, swelling almost shut; This is a spontaneous report from a contactable Pharmacist received via Pfizer-sponsored program . A 26-years-old male patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 03Apr2021 (Age at vaccination 26 years old), as Dose 1, Single for covid-19 immunization. The patient's medical history included allergy to all types of pollen. The patient's concomitant medications were not reported. The reporter stated that the patient felt fine for the initial 30 minutes of observation. However, he informed the pharmacist that shortly after leaving his eyes got swollen, watery, swelling almost shut. He did not require the EpiPen he had at home. The patient said the following Monday went back to normal. The patient experienced his eyes got swollen, watery, swelling almost shut on 03Apr2021. Pharmacist had patient who received first dose of vaccine reported that 30 minutes after experiencing eyes swollen up to the point where almost swollen shut. The reporter said the following Monday went back to normal. The reporter wanted to know if swelling of the face was a common side effect. The reporter enquired if he patient should receive the 2nd dose of the covid vaccine. Outcome of the events was recovered on an unknown date in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792861
Sex: F
Age:
State: ID

Vax Date: 04/12/2021
Onset Date: 04/12/2021
Rec V Date: 10/16/2021
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: Projectile vomiting; Chills; Dizziness; Nausea; Headache; This is a spontaneous report from a contactable healthcare professional. A 51-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 12Apr2021 at 13:00 (at the age of 51-years-old) as a single dose for COVID-19 immunisation. Medical history included hypothyroidism. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the vaccination. The patient did not receive any concomitant medications. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 15Mar2021 at 12:15 (at the age of 51-years-old) as a single dose for COVID-19 immunisation. The patient previously took codeine (MANUFACTURER UNKNOWN) and vicodin (MANUFACTURER UNKNOWN) for an unknown indication on an unknown date and experienced drug allergy. On 12Apr2021 at 14:00, one hour after the booster shot the patient experienced nausea and headache. On 12Apr2021 at 17:00, 4 hours after the injection, the patient experienced chills and dizziness, then followed by projectile vomiting for 6 times on 12Apr2021 at 19:00, 5 hours after the injection. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events nausea, headache, chills, dizziness and projectile vomiting was recovering at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792862
Sex: F
Age:
State: CT

Vax Date: 04/11/2021
Onset Date: 04/12/2021
Rec V Date: 10/16/2021
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: Pain in the left arm where vaccine was injected; This is a spontaneous report from a contactable consumer. A 33-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 11Apr2021 (at the age of 33-years-old) as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. It was unknown, whether the patient received any other vaccines within four weeks prior to the vaccination. On 12Apr2021, the patient experienced pain in the left arm where vaccine was injected. The event did not result in doctor or other health care professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. The clinical outcome of the event pain in the left arm where vaccine was injected was unknown at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792863
Sex: F
Age:
State: TN

Vax Date: 04/06/2021
Onset Date: 04/07/2021
Rec V Date: 10/16/2021
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: Rash in various parts of the body; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 36-years-old female patient (patient was not pregnant at the time of vaccination) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: Ep7533, Expiration date: unknown) via an unspecified route of administration, administered in left arm on 06Apr2021 at 12:00 pm (age at vaccination was 36 years) as dose 2, single for COVID-19 immunization. The patient's medical history included Caesarean section performed. Concomitant medication included acetaminophen taken for an unspecified indication. The patient previously took NSAIDS and experienced allergy. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on an unspecified date (age at vaccination was unknown) as dose 1, single for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was Hospital. 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 07Apr2021 at 19:00 pm, the patient experienced rash in various parts of the body. No treatment was received for the adverse event. The outcome of event was not resolved. No follow-up attempts are possible. No further information is expected.

Other Meds: ACETAMINOPHEN

Current Illness:

ID: 1792864
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: This is a spontaneous report from a noncontactable consumer or other non-HCP (reporter's wife). A female patient, of an unspecified age, received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, solution for injection, batch/lot# and expiry date not reported), via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunization. The patient's medical history and concomitant medications not reported. On an unspecified date (one week after first dose), patient experienced nosebleed. Caller reported on behalf of wife who experienced nosebleed 7-8 days after the first dose. Unsure as their room is also humid. Asked if this is normal and if she should still get the second dose. Said in the news she heard that nosebleed is normal. Wanted to know if a nosebleed one week after the first Pfizer COVID-19 vaccine is an adverse event; and if you have this reaction, do you still get the second dose. The outcome of event: unknown. No follow-up attempts possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792865
Sex: M
Age:
State: MO

Vax Date: 04/10/2021
Onset Date: 04/10/2021
Rec V Date: 10/16/2021
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: Patient experienced slight fever and tiredness after second vaccine shot.; Patient experienced slight fever and tiredness after second vaccine shot.; This is a spontaneous report from non-contactable Non-healthcare Professional. This Non-healthcare Professional reporting for a 74-year-old male patient. A 74-year-old male patient received second dose of bnt162b2 (Pfizer Covid-19 Vaccine, solution for injection, Lot number: Not available), via an unspecified route on 10Apr2021 (age at vaccination: 74-year-old), as a single dose for covid-19 immunization. Medical history included cancer prostate. The patient concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 (Pfizer Covid-19 Vaccine, solution for injection, Lot number: Not available) at the age of 74-year, as a single dose for covid-19 immunization. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. On 10Apr2021, patient experienced slight fever and tiredness after second vaccine shot. It was unknown if patient received any treatment for the events. The clinical outcome of the events was recovered in 2021. No follow-up attempts possible. Information about Batch/ Lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792867
Sex: F
Age:
State: NJ

Vax Date: 03/30/2021
Onset Date: 04/03/2021
Rec V Date: 10/16/2021
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: Right eye seems to stay red; Daughter noticed that on the 3rd that my eye was red, that I felt it was itching; Wake up every day with my eye red; Right eye seems to stay red; Daughter noticed that on the 3rd that my eye was red, that I felt it was itching; Wake up every day with my eye red; This is a spontaneous report from a contactable consumer (patient). A 58-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Left on 30Mar2021 (Batch/Lot Number: ER8737) as dose number unknown, 0.3ml single (at the age of 58-year-old) for covid-19 immunisation. Medical history included high blood pressure for 15 years ago, Allergy, gout, asthma. Concomitant medication(s) included montelukast sodium (MONTELUKAST SODIUM) 10 mg, once a day, orally taken for asthma; hydrochlorothiazide, losartan potassium (LOSARTAN HCTZ) 100-25 mg, one tablet by mouth everyday taken for High Blood pressure. Historical vaccine included took allergy shots, so I took my two allergy shot 3 weeks ago from the shot for allergy. The patient experienced right eye seems to stay red; daughter noticed that on the 3rd that my eye was red, that I felt it was itching; wake up every day with my eye red on 03Apr2021. Treatment reported as No, I only take my daily medication, I don't take anything, my daily medications which is my high blood pressure, I think my gout medication. The outcome of event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: MONTELUKAST SODIUM; LOSARTAN HCTZ

Current Illness:

ID: 1792869
Sex: F
Age:
State: NY

Vax Date: 04/10/2021
Onset Date: 04/12/2021
Rec V Date: 10/16/2021
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: Redness, edema, rash and itchiness in nasal bridge and Eyelids; Redness, edema, rash and itchiness in nasal bridge and Eyelids; edema; rash and itchiness in nasal bridge and eyelids; Redness, edema, rash and itchiness in nasal bridge and eyelids; Redness, edema, rash and itchiness in nasal bridge and eyelids; Redness, edema, rash and itchiness in nasal bridge and eyelids; Redness, edema, rash and itchiness in nasal bridge and eyelids; This is a spontaneous report from a contactable consumer (patient). A 44-year old non-pregnant female patient (not pregnant at the time of vaccination) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration administered in Arm Left on 10Apr2021 12:30 (44-year-old at the time of vaccination) as dose 2, single for covid-19 immunization. Medical history included hypothyroidism from an unknown date and unknown if ongoing. The patient had no allergies to medications, food, or other products. Concomitant medications included quetiapine, lithium, drospirenone, ethinylestradiol (YASMIN); levothyroxine sodium (EUTIROX) all for unknown indications from unknown dates and unknown if ongoing. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration administered in Arm Left on 20Mar2021 as dose 1, single for COVID-19 immunization. The patient had not received any vaccine within four weeks. The patient had no covid prior to vaccination. The patient was not tested since vaccination. On 12Apr2021 01:00, the patient experienced redness, edema, rash and itchiness in nasal bridge and eyelids. Therapeutic measures were taken as a result of the events using Cetirizine 10mg. Adverse event resulted in: Doctor or other healthcare professional office/clinic visit. The outcome of the events was recovering. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: QUETIAPINE; LITHIUM; YASMIN; EUTIROX

Current Illness:

ID: 1792870
Sex: F
Age:
State: LA

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Name: Blood work; Result Unstructured Data: Test Result:Normal

Allergies:

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

Symptoms: little bumps when she scratches; continued itching on elbow, shoulder, legs, arms and a little on her back.; This is a spontaneous report from a contactable consumer. This 75-year old female consumer (patient) reported this report. A 75-year-old female patient received (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE: formulation: Solution for injection, Lot Number: unknown), via an unspecified route of administration, administered in Arm Right on Feb2021 (Batch/Lot number was not reported) as dose 2, single for covid-19 immunisation. The patient medical history included ongoing diabetes, Diagnosed when she was in her 50's. 51 or 52 years old, high blood pressure from 2000 and ongoing, cholesterol from 2000 and ongoing, cerebrovascular accident from 2000 to an unknown date States she had a stroke in 2000, ongoing cranial nerve neoplasm benign States she has had this since she was about 17 years old, ongoing Anxious feeling, Stated she has had this since she was about 17 years old, sore throat. Concomitant medications included minoxidil (Stated she started this medication a while ago; years ago) taken for blood pressure; pantoprazole (Stated has been on this medication for a long time.) taken for abdominal discomfort from an unspecified start date and ongoing; carvedilol taken for cardiac disorder, simvastatin taken for blood cholesterol, clopidogrel bisulfate taken for cerebrovascular accident, clonidine taken for cardiac disorder, hydralazine taken for cardiac disorder, digoxin taken for cardiac disorder all from 2000 to an unspecified stop date, lorazepam taken for cranial nerve neoplasm benign, anxiety; isosorbide mononitrate (ISOSORBIDE MN) taken for cardiac disorder, acetylsalicylic acid (ASPIRIN) and cilostazol taken for peripheral vascular disorder from 2000 and ongoing. amoxicillin trihydrate (AMOXICILLIN E), ongoing Furosemide for fluid and ongoing Nifedipine for Blood Pressure. The patient previously received historical vaccine BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: UNKNOWN), via an unspecified route of administration, administered in Arm Right in Jan 2021 as dose 1, single for covid-19 immunisation. The patient was scheduled for second dose on 19Feb2021, but they moved it and she did not remember what date it was moved to. The patient experienced "continued itching on elbow, shoulder, legs, arms and a little on her back in Feb2021, little bumps when she scratches on an unspecified date. She had little bumps when she scratches but stated that she was trying to not to scratch. She had been seen by her Primary Care Provider and a Dermatologist. She had been prescribed medications and creams (Betamethasone valerate 0.1% Cream and Hydroxyzine taken 25mg as needed at bedtime for itching) which she stated that they were not much effective. It was reported that it would get better for a little while but then it would come back. The patient was also seen using Gold Bond for Body Itch and Dry Skin and that was helping a little bit too. The patient last saw her Primary Care Provider 2 weeks ago and she did not have an appointment scheduled to see her Dermatologist next day evening. Itching all over legs to arms, shoulders to back was reported as worsened. Symptoms began a few days after the second vaccine; nothing like this happened after the first. The patient underwent lab tests and procedures which included blood test: normal on unspecified date. he patient wanted to know if this side effect has been reported by other people as well. Reporter seriousness for the events were unspecified. She reported her height as 5 foot ten and a half inches. She reported she was diabetic and takes a lot of medication, doesn't know if that has anything to do with her itching or not. The clinical outcome of the event little bumps when she scratches was unknown and that of continued itching on elbow, shoulder, legs, arms and a little on her back was not recovered. No follow up attempts are possible, no further information is expected.

Other Meds: MINOXIDIL; PANTOPRAZOLE; CARVEDILOL; SIMVASTATIN; CLOPIDOGREL BISULFATE; CLONIDINE; HYDRALAZINE; DIGOXIN; LORAZEPAM; ISOSORBIDE MN; ASPIRINE; CILOSTAZOL; AMOXICILLIN E; FUROSEMIDE; NIFEDIPINE

Current Illness: Anxious depression (States she has had this since she was about 17 years old.); Benign neoplasm of cranial nerves (States she has had this since she was about 17 years old.); Blood pressure; Cholesterol; Diabetes (Diagnosed when she was in her 50's. 51 or 52 years old.)

ID: 1792871
Sex: F
Age:
State: FL

Vax Date: 04/07/2021
Onset Date:
Rec V Date: 10/16/2021
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: chest congestion; a lot of pain in the joints; My body aches terrible, all body pains; coughing; sick; Feeling miserable; This is a spontaneous report from contactable female consumer (patient) via Pfizer sponsored program COVAX US Support. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: Unknown), via unspecified route of administration on 07Apr2021 as a dose 1, single for COVID-19 immunization. The patient medical history and concomitant medication were not reported. On an unspecified date in 2021, the patient experienced chest congestion, a lot of pain in the joints, body aches terrible with all body pain, coughing, sick and feeling miserable. Patient stated, after I got the vaccine Wednesday I felt terrible chest congestion, like I wanted to cough from the bottom of my stomach, something like that I felt, a lot of congestion, a lot of pain in the joints that I know is a part of side effects. But the problem congestion under my chest that is I am more concerned is that. My body aches terrible, all body pains. I think that the congestion is a more problem for me. I feel more of a concern because like coughing. I want to know what else I can take. Do I need to take some kind of medicine or something for this because I feel miserable. Patient further stated, this is a terrible service and I cannot believe I got sick and still do not have a help. Outcome of all the events was unknown. No follow-up attempts are possible. Information about lot/ batch no cannot be requested.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am