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: 1752622
Sex: M
Age:
State: KY

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

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: loss of taste; his back throat hurts; felt there's a needle under his ear; This is a spontaneous report from a Pfizer Sponsored Program Support. A contactable male consumer of an unspecified age received bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration on 16Feb2021 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. He reported that he never got a schedule for the second dose because his vaccination card was switched with a different card. On an unspecified date in Feb2021, the patient experienced loss of taste, his back throat hurts and felt there's a needle under his ear. The events accessed as a non serious. The outcome of the events were unknown. No follow-up attempts are possible. Information about lot/batch number cannot been obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1752623
Sex: F
Age:
State: NY

Vax Date: 03/14/2021
Onset Date:
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: my hands got arthritis; This is a spontaneous report from a contactable consumer (patient). A 78-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number was not reported), via an unspecified route of administration on 14Mar2021 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient stated that she got the first shot yesterday, they put them down to 'Easter' to get and she didn't know that was the date on the 14th when they did and she can't get any help, her 'Ackey' will not come on that day, she is taking her family and she can't find anybody take my to take her place and she won't mean she will even get ambulance to go because very short of help that day. On an unspecified date, the patient hands got arthritis. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752624
Sex: M
Age:
State: TN

Vax Date: 03/10/2021
Onset Date: 03/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Tiredness; Slight fever; This is a spontaneous report from a contactable consumer (patient) reported for himself. A 45-years-old male patient received BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number: unknown, Expiry Date: unknown), via an unknown route of administration on 10Mar2021 (at the age of 45-years-old) as dose 1, single for COVID-19 immunization. Reason for no lot number of COVID 19 Vaccine consumer stated, "I don't know that it was not on my little card." The patient's medical history included asthma from an unknown date and unknown if ongoing. Consumer stated, "I don't have a Thyroid and I have occasional asthma." Concomitant medications included levothyroxine sodium (SYNTHROID), montelukast sodium (SINGULAIR), meloxicam (MELOXICAM); all were taken for an unknown indication from an unknown date. On an unknown date in Mar2021, the patient experienced tiredness and slight fever. The patient stated, "I was just wondering I had my first dose of Pfizer on Wednesday and had 2 days of tiredness and then Saturday and Sunday I have had like slight fever and I was trying to see if that's normal reaction for it to last this long." Patient stated, "It was 6th, no, it was 13Mar. I had tiredness 2 days before but (incomplete sentence)." Consumer stated that he was about 5 (Feet) 6 (inches) and 225 (pounds) (not sure hence not captured in tab)." No investigation assessment. Received Tylenol as treatment. The outcome of events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752625
Sex: F
Age:
State: TX

Vax Date: 03/07/2021
Onset Date: 03/11/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: allergic reaction; swollen lymph node glands; the swelling also was on side of my face all down to the jaw line; swelling above my ears and I can tell that the ear was swollen on the inside; I was had very sharp pain every so often in my ears; sharp pain in my throat; I wasn't able to do too much drinking or eating; under my jaw line was swollen and this was very uncomfortable it hurts; under my jaw line was swollen and this was very uncomfortable it hurts; This is a spontaneous report from a contactable Consumer or other non-HCP (patient). A 69-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EN6206 and Expiry Date of covid 19 vaccine: Unknown), dose 1 via an unspecified route of administration on 07Mar2021 (at the age of 69-year-old), as DOSE 1, SINGLE for COVID-19 immunisation. Medical history included Back problems (she had injection in my back probably 6 weeks ago), Aneurysm that she kept a watch on, High blood pressure, Cholesterol and Thyroid. The patient concomitant medications included a lot of other unspecified medicine. On 11Mar2021, the patient experienced allergic reaction, swollen lymph node glands, the swelling also was on side of her face all down to the jaw line, swelling above her ears and she can tell that the ear was swollen on the inside, very sharp pain every so often in her ears, sharp pain in her throat, she was not able to do too much drinking or eating, under her jaw line was swollen and this was very uncomfortable it hurts. The clinical details of the events as follows: consumer stated, she did not want to use the portal to report this but she wanted to talk about the side effects that she had only received the very first shot of the COVID vaccine and she felt like she had allergic reaction, so she also wondering should she even get the second shot, but her side effects was definitely the swollen lymph node glands, the swelling also was on side of her face all down to the jaw line and also swelling above her ears and she could tell that the ear was swollen on the inside and she was had very sharp pain every so often in her ears and she was not really able to do too much drinking or eating because every time she would swallow she would have sharp pain in her throat, yeah and her swelling lymph node gland was also from her ear down, neck and under her jaw line was swollen that did not take place until 4 days later after she took the shot, the first shot and this was very uncomfortable it hurts. Consumer stated, so she would like someone to basically call me and let her know is it safe for her to take second shot and she worried about it. There was no investigation Assessment provided. No treatment was received for the events. The patient outcome of the events was resolved on an unspecified date in Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752626
Sex: F
Age:
State: OH

Vax Date: 03/11/2021
Onset Date: 03/12/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 202103; Test Name: potassium; Result Unstructured Data: Test Result:Unknown results

Allergies:

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

Symptoms: Chills; sweats; red swollen arm; red swollen arm; This is a spontaneous report from a contactable consumer (Patient). A 66-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Batch/Lot Number: unknown), via an unspecified route of administration on 11Mar2021 at 08:30 (at the age of 66-years-old) as dose 2, single for COVID-19 immunisation at Health department in a tent by the fire department. Medical history included blood pressure high (Blood pressure high/Diagnosed a long time ago, may be 15 or 20 years ago). Concomitant medications were not reported. The family medical history relevant to AE included heart attacks, cancer, and stuff. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Batch/Lot Number: EN6202), via unspecified route of administration, administered in left arm on 18Feb2021 as dose 1, single for COVID-19 immunisation and did not have any problems, it was sore and red but not a big deal. The patient previously took flu shot (expiration date and Lot number: unknown) on an unspecified date (reported as October) and experienced arm gets red, a red dot and couldn't raise her arm. No additional vaccines administered on same date of the Pfizer Suspect. No prior vaccinations within 4 weeks. It was reported that the patient had her shot on Thursday, and on 12Mar2021 she had a reaction, her left arm became red arm and swelled. On an unspecified date, she also had chills and sweats on the first night. The patient was taking Benadryl, now the redness is spreading and blotchy, the redness is not going away. It was reported that a round circle began on the 12Mar2021, really big on the 13Mar2021, it looked like it spread but it was not as dark, still was fevery. The patient was expecting that her arm to be red where the injection went in, but not that its going to go clear across. The patient tried tylenol (Lot PLAO52, expiration Jun2023) but did not seem to be helping. The patient was seeing her Physician on the day of report. The patient wants to know if it is normal and what to do the patient gets a reaction from anything, she gets side effects from an aspirin. Is this a normal reaction. The patient reported that she was taking COVID-19 vaccine because everyone told her she had to and because she was old. Therapeutic measures were taken as a result of red swollen arm. The patient underwent lab tests and procedures which included blood potassium: unknown results on Mar2021. The outcome of the event red swollen arm was recovering and chills, sweats was unknown. The relatedness of drug to reaction red swollen arm was reported as related by primary source reporter with global introspection method of assessment. No follow-up attempts are possible; no further information is expected.

Other Meds:

Current Illness:

ID: 1752627
Sex: M
Age:
State: FL

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

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

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:Unknown result

Allergies:

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

Symptoms: I started having little problems with my shoulder neck muscle; I could not even move without shooting pain; My muscle are seized up; I have been aching and can't turn my head totally; My muscle are seized up; I have been aching and can't turn my head totally; I started having little problems with my shoulder neck muscle; I could not even move without shooting pain; I started having little problems with my shoulder neck muscle; I could not even move without shooting pain/muscle are seized up, have been aching, cannot turn my head totally; This is a spontaneous report from a contactable consumer. An 85-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EN6200), dose 2 via an unspecified route of administration on 04Mar2021 (at the age of 85 year) as dose 2, single for COVID-19 immunisation. Medical history included hypertension, stenosis (had some stenosis in the neck I guess about 8 years, 9 year earlier I had a nerve block injection which you know took care of the similar type of situation). There were no concomitant medications. The patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 on an unknown date (at the age of 85 year) for COVID-19 immunisation. On 04Mar2021, consumer started having little problems with shoulder neck muscle and then that got to the point where consumer could not even move without shooting pain through shoulder and consumer ultimately end up calling doctor and next day consumer said his muscle were seized up and what not and prescribed Baclofen, that was medication which was a muscle relaxant, which consumer took 10 mg twice a day for 10 days, that did not work. Consumer still getting the pain all it did, start easing a little bit but on the third day consumer could not stand the pain anymore so consumer took Aleve, took 2 tablets of NSAID like Aspirin consumer guess, and that relieved the shooting spasm pain but continued taking, consumer only took Aleve 1 more day and it stopped the spasm where consumer moved the shooting pain but the muscles in my neck like moving up side of my neck up to the skull and consumer do not know if you understand what he was referring to, neck muscles there, consumer have been aching and cannot turn his head totally, he can turn it now, it was a lot better, just want to let you know that what he has been, he would not been doing anything that would stress my neck at that time, however he wanted you to know that he had some stenosis in the neck he guess about 8 years, 9 year earlier he had a nerve block injection which you know took care of the similar type of situation. He was not sure if they correlated by he just thought he let you know since he has not had any problem recently with that. Product details (LOT# and expiration date) of Baclofen: Consumer stated, What he had, he still have, today was the last day for taking it, that was okay let me see here, 05Mar2021, was when it was filled. The day after my shot, it was the dispensed by (name), manufactured by pharma, shape round, color white, then it says side 1:E6, he do not know what that means, he do not see no lot number here. Consumer stated, Yeah the shooting pain was improved, definitely improved by using the Aleve the muscle relaxer consumer was sure that helped somewhat he still and it still has not totally eliminated the ache. He had blood work the day after the shot, no the day, the couple days before sorry, just around 01Mar he had the blood work. Consumer stated, Yes he believe he had them, what you need from them, there was lot of results, he meant you want cholesterol levels you talking about, yeah we will be spending whole lot time on that. The outcome of events was recovering. No follow-up attempts are possible. No further information is expected

Other Meds:

Current Illness:

ID: 1752628
Sex: U
Age:
State: AZ

Vax Date: 03/13/2021
Onset Date: 03/14/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Low grade fever; chills; headache; fatigue; some muscle soreness; nausea with stomach very painful; nausea with stomach very painful; earache; Crazy itching (whole body) like hives; hives; This is a spontaneous report from a contactable consumer (Patient). A 64-year-old patient of an unspecified gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6207) via an unspecified route of administration, administered in Arm Left on 13Mar2021 17:00 (Age at Vaccination 64-year-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history was none. Concomitant medications included Levothyroxine 50 MCG BIES 0.5 cream. The patient not aware of allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had covid prior vaccination and patient did not covid tested post vaccination. Doctor or other healthcare professional office/clinic visit. On 14Mar2021 09:00 the patient experienced Low grade fever, chills, headache, fatigue, some muscle soreness next day (whole body) nausea with stomach very painful earache Crazy itching (whole body) like hives. Patient received Ae treatment inflammatory. The outcome of events was not recovered. No follow-up attempts are Possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752629
Sex: F
Age:
State: OH

Vax Date: 03/12/2021
Onset Date: 03/12/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 201912; Test Name: tested positive for Covid; Result Unstructured Data: Test Result:Positive; Test Date: 20201210; Test Name: tested positive for Covid; Result Unstructured Data: Test Result:Positive

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: left lymph nodes swelling; sore; Low grade fever; Injection site swelling; Muscle pain; Joint pain; Chills; loss of appetite; Loss of taste; Injection site pain; Tiredness; Weakness; Headache; This is a spontaneous report from a contactable consumer (patient). A 62-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: EN6208; Expiration Date: 30Jun2021), via an unspecified route of administration, administered in arm right on 12Mar2021 at 10:30 (at the age of: 62-years-old) as dose 1, single for covid-19 immunisation at hospital. The patient medical history included ongoing arthritis (was diagnosed when she was in her late 30'S), ongoing osteoarthritis and ongoing degenerative joint disease (diagnosed 20 years ago at age 42). She was tested positive for Covid in Dec2019 and on 10Dec2020. She had all the minor side effects except for nausea and site redness. Concomitant medications was not reported. She took medications for arthritis and pain medication. Declines to provide further details. Patient did not receive any other vaccine within four weeks prior to vaccination. History of all previous immunization with the Pfizer vaccine considered as suspect was mentioned as none. Additional vaccines administered on same date of the Pfizer Suspect was mentioned as none. On 12Mar2021, the patient experienced loss of appetite, loss of taste, injection site pain, tiredness, weakness, headache and chills. On 13Mar2021, the patient experienced injection site swelling, low grade fever, muscle pain and joint pain. On 14Mar2021, the patient had sore. On 15Mar2021 the patient experienced left lymph nodes swelling. Caller received the Covid-19 vaccine on 12Mar2021. She had side effects that were bad and did not think she should get the second dose. She had a lot of muscle and joint pain. The next day she was sore. She felt her lymph nodes while reading the paperwork and discovered hers were swollen. The patient clarified that the lymph nodes on the left side were swollen instead of the right side. The outcome of the event low grade fever was recovered on 14Mar2021. The outcome of the event loss of appetite was recovered with sequelae on 15Mar2021 and muscle pain and joint pain was recovered on 15Mar2021. The outcome of the events loss of taste, injection site pain, tiredness, weakness, headache and chills were recovering. The outcome of the events injection site swelling and lymph nodes swelling were not recovered. The outcome of the event sore was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Arthritis (was diagnosed when she was in her late 30'S); Degenerative joint disease (Diagnosed 20 years ago at age 42); Degenerative joint disease

ID: 1752630
Sex: F
Age:
State: CT

Vax Date: 03/14/2021
Onset Date: 03/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 20210310; Test Name: double balloon teroscopy and enteroscopy; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Edema; big bags under her eyes; her legs are larger; A little left arm soreness; difficult to raise her left arm; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received bnt162b2 (PFIZER BIONTECH COVID-19 MRNA VACCINE Solution for injection Lot Number: EN6206) via an unspecified route of administration, administered in arm left on 14Mar2021 13:00 as dose 1, single (age at vaccination: 61 years) for COVID-19 immunisation. Medical history included GI procedure under general anesthesia from 10Mar2021 to 10Mar2021 Caller further described GI procedure as a double balloon teroscopy and enteroscopy-verified and documented as provided by reporter. Concomitant medications were not reported. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available). Additional Vaccines Administered on Same Date of the Pfizer Suspect: Vaccines, all vaccines administered on same date with the Pfizer vaccine considered as suspect was none. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) was none. The adverse event following prior vaccinations was none. Patients Medical History (including any illness at time of vaccination) Provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic / chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity was none. Family Medical History Relevant to adverse event, she was adopted, so no not that she is aware of. On 14Mar2021 19:00, about 6 hours after she was administered the Pfizer-BioNTech COVID-19 Vaccine, the patient experienced a little left arm soreness. Outcome is much better right now; but half of her arm was sore yesterday. At this time if she presses right on the injection site of her left arm it is still sore but it does not really hurt now. On an unspecified date Mar2021, yesterday it was difficult to raise her left arm, it just hurt. On 15Mar2021 08:00, had edema, described as big bags under her eyes and her legs are larger, seems to be staying the same. She is just sort of lying in bed and does not know if that is going to be helpful with the edema or not. She went to work today and figures the edema is going to go away, it is not causing discomfort. She experienced a little left arm soreness; but she also had edema which she does not know if is a reported side effect of the Pfizer-BioNTech COVID-19 Vaccine. She had not been able to find information about edema with the Pfizer-BioNTech COVID-19 Vaccine so she called to ask for information on the event relative to the vaccine. The adverse events did not require a visit to emergency room/physician office and was not hospitalized. The patient underwent lab tests and procedures which included double balloon teroscopy and enteroscopy resulted as unknown results on 10Mar2021. The clinical outcome of the event edema, big bags under her eyes, her legs are larger was not resolved, the event difficult to raise her left arm was unknown, and the event a little left arm soreness was resolving. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752631
Sex: M
Age:
State: IL

Vax Date: 02/19/2021
Onset Date: 03/12/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: dizziness; headache; weakness; joint pain; chills; since first dose (mild), but now following second dose is borderline debilitating; This is a spontaneous report from a contactable consumer or other non HCP (Patient) who reported for herself. A 56-years-old male received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was EN6199) via an unspecified route of administration on 12Mar2021 at 03:45, administered in left arm (age at the time of vaccination was 56-years-old) as a DOSE 2, single and first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was E29267) via an unspecified route of administration on 19Feb2021 at 03:45, administered in left arm (age at the time of vaccination was 56-years-old) as a DOSE 1, single for COVID-19 immunization. Medical history and Concomitant medications were not reported. The patient had no other vaccine in 4 weeks. The patient did not have COVID prior to vaccination and was not tested for COVID post vaccination. The consumer reported that, I've had headache, weakness, joint pain, chills and dizziness which has remained since first dose (mild), but now following second dose is borderline debilitating. No treatment was received for adverse events. The clinical outcome of the events was not recovered. No follow-up attempts are possible; no further information expected.

Other Meds:

Current Illness:

ID: 1752632
Sex: U
Age:
State: PA

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

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable consumer. This consumer reported that: A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: unknown), via an unspecified route of administration on an unspecified date as UNKNOWN, SINGLE for covid-19 immunisation. Medical history included hypothyroidism from an unknown date and unknown if ongoing (Optional Information: Hypothyroidism-NP). The patient's concomitant medications were not reported. The patient experienced headache, muscle aches, injection site pain, fever, joint pain on an unspecified date. Event took place after use of product. The outcome of events was unknown. No follow-up attempts are Possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752633
Sex: M
Age:
State: NC

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Tingling hands/feet; rashes over body; This is a spontaneous report from a contactable consumer or other non-health care professional (Patient himself). A 51-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection batch/lot Number: Not provided Expiration Date: Unknown) via unspecified route of administration, in left arm on 10Mar2021 05:00 PM (at the age of 51-year-old) as dose 1, single for COVID-19 immunization. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient is allergic to Penicillin. No other medical history or concomitant medications were reported. Patient did not receive any other medications within 2 weeks of vaccination. Prior to vaccination patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. On 10Mar2021 patient experienced Tingling hands/feet and rashes over body. Patient visited doctor for the same and received treatment, mentioned as Trying prednisone. Don't know what to try. Outcome of events was recovering. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1752634
Sex: F
Age:
State: CA

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

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable consumer (Patient). This 45-years-old female consumer reported that: A 45-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6198), dose 2 via an unspecified route of administration, administered in Arm Left on 04Mar2021 (at the age of 45 years old) as dose 2, single for covid-19 immunisation. The patient medical history was not reported. Concomitant medications included isotretinoin (Claravis) 60 mg, daily. The patient previously took historical vaccine bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9261), dose 1 via an unspecified route of administration on 02Feb2021, as dose 1, single for covid-19 immunisation and experienced Pain. On an unspecified date, the patient experienced rash on your body and for me it has been on my hand, i thought i had a flare up what i believe to be eczema on my hand but i am not really 100%. i was looking at the side effect and it says rash on your body and for me it has been on my hand. On 05Mar2021, the patient experienced soreness occurred at the injection site both times. On 08Mar2021, she had tired. The outcome of the events Tired and Soreness occurred at the injection site both times was recovered on an unspecified date and unknown for other events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752635
Sex: F
Age:
State: OH

Vax Date: 03/11/2021
Onset Date: 03/14/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Headache; nausea; vomiting; chills; sweats; things smell and taste off; things smell and taste off; This is a spontaneous report from a contactable consumer reported for herself that. A 61-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 11Mar2021 12:45 (Batch/Lot number was not reported) as DOSE 1 SINGLE for covid-19 immunization (Age at vaccination 61 years). The patient past Medical history included rheumatoid arthritis from an unknown date and unknown if ongoing 50 plus years rheumatoid arthritis high blood pressure from an unknown date and unknown if ongoing, digestive issues from an unknown date and unknown if ongoing, migraine from an unknown date and unknown if ongoing , anxiety from an unknown date and unknown if ongoing , depression from an unknown date and unknown if ongoing and fibromyalgia from an unknown date and unknown if ongoing. Concomitant medication(s) included losartan (LOSARTAN) taken for an unspecified indication, venlafaxine hydrochloride (EFFEXOR) taken for an unspecified indication, omeprazole (OMEPRAZOLE) taken for an unspecified indication, pravastatin (PRAVASTATIN) taken for an unspecified indication and gabapentin (GABAPENTIN) taken for an unspecified indication. 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 vaccine within 4 weeks prior to covid-19 vaccination. The patient has not received other medications in two weeks. The patient previously took morphine and experienced drug hypersensitivity. On 14Mar2021 16:00, the patient experienced headache, nausea, some vomiting, first night of symptoms, chills and sweats, things smell and taste off. No treatment was received. The event outcome was not recovered. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752636
Sex: F
Age:
State: CA

Vax Date: 02/06/2021
Onset Date: 02/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:high; Test Name: blood pressure; Result Unstructured Data: Test Result:usually it is no more than 125; Test Name: body temperature; Result Unstructured Data: Test Result:98.5 Fahrenheit; Comments: she developed a 98.5F fever

Allergies:

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

Symptoms: face was feeling hot and flushed; sore arm; Blood pressure high; face was flushed; 98.5F fever; felt jittery; 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, Batch/lot number: EL9265 and Expiration date: unknown) via an unspecified route of administration, in left arm on 06Feb2021 at 09:40 (at the age of 84-year-old) as dose 1, single for COVID-19 immunization. The patient medical history included high blood pressure diagnosed around 2010 and was under control with medication. Usually, blood pressure was no more than 125. The patient had no family medical history relevant to AE. Concomitant medication included blood pressure medication (unspecified) taken every day for high blood pressure. The patient had no prior vaccinations (within 4 weeks). It was stated that patient had no other additional vaccines administered on same date of the Pfizer suspect. The patient alerted the nurse that she was allergic to 2 antibiotics when she went to receive the vaccines. The doctors said it was no problem for the patient to receive the vaccine, but it was up to her. The patient was allergic to sulfameth something TMP, adenosine GISI something like that. The patient received her first shot on 06Feb2021. The patient was 85 and had always been in good health. The patient did not have any side effects except a sore arm the next day (07Feb2021). The next day (Feb2021) the patient's face was flushed and then she developed a 98.5F fever, felt jittery then it went away. This was with the first shot. The patient had a sore arm but went away after 2 days, she put a heating pad on it. The patient's face was feeling hot and flushed. The patient did not take her temp the first day she got the shot. For about a day or 2 days for her blood pressure was high. AE(s) did not require a visit to Emergency room or Physician's office. Outcome of the event sore arm was recovered on 09Feb2021, other events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1752637
Sex: F
Age:
State: IL

Vax Date: 03/12/2021
Onset Date: 03/13/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable nurse (patient, self-reported). A 35-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date was not reported), via an unspecified route of administration in Arm left, on 12Mar2021 at 5:45 PM, as dose 1, single for COVID-19 immunization at hospital. The patient was not pregnant at the time of vaccination. The patient medical history included COVID-19. The patient was diagnosed with COVID prior vaccination. The patient did not had known allergies. Concomitant medication included sertraline hydrochloride ( ZOLOFT). The patient did not receive any other vaccine in four weeks. On 13Mar2021 at 8:00 AM, the patient experienced Fever, muscle aches, stomach upset and weak. The patient was not tested for COVID post vaccination. The AE did not resulted in physician office visit or emergency room. The patient did not received any treatment for the events. Outcome of the events was recovered on an unspecified date in 2021. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1752638
Sex: M
Age:
State: NH

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

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

Lab Data:

Allergies:

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

Symptoms: intermittent fever; chills; intermittent fatigue; overnight muscles aches; This is a spontaneous report from a contactable Consumer (patient). A 47-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247), via an unspecified route of administration in left arm on 16Feb2021 at 11:15 (at the age of 47-year-old) as dose 2, single for COVID-19 immunisation at workplace clinic. The patient medical history was not reported. There were no concomitant medications. No other medications were administrated in two weeks. The patient had no known allergies. The patient did not diagnose with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously took bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3247), via an unspecified route of administration in left arm on 27Jan2021 (at the age of 47-year-old) as dose 1, single for COVID-19 immunisation and experienced slight ache around injection site. On 16Feb2021 at 18:00, the patient experienced intermittent fever, chills, intermittent fatigue, overnight muscles aches/ sensitivity (all body, not just at injection site). The patient did not receive any treatment for the events. The outcome of the events was reported as resolved on an unknown date. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752639
Sex: M
Age:
State: NJ

Vax Date: 03/03/2021
Onset Date: 03/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Name: Covid test; Test Result: Negative

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Chills; Did not feel good; Body aches; Fever; Whole time I felt that I was in a fog; Lethargic; Diarrhea; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 55-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EN6206 and expiry date: Jun2021), via an unspecified route of administration (at the age of 55-year-old), on 03Mar2021, as dose 1, single for COVID-19 immunization. The patient medical history included liver issue. Concomitant medication was not reported. The patient stated that he had received a Covid Vaccine shot on 03Mar2021. He still experiencing problems from the shot. He can go through the list of things that happened to him from 03Mar2021. On 03Mar2021, that evening he went through the chills, did not feel good, body aches. Went to work on Thursday, the 4th, did not feel good all day, came home that night from work and went to sleep, on Friday, did not feel good. I felt normal on Saturday 6th, felt good normal. He went up the chills and body aches and then he had a fever approximately for four days and whole time he felt that he was in a fog and had been lethargic the whole time, body ache, diarrhoea, you name every symptom he could have. When paraphrased the concern patient confirmed the same and stated, it has been two weeks and he was not feeling good and Right from the day one and he still have the problems. The patient stated that he had a Liver issue that is one of the reasons that he was eligible to take the shot. The patient went to two doctors. One he went to get a COVID test to make sure that he did not have Covid. Then he went to his regular primary Doctor because of all those symptoms. He did not run any lab or blood work or anything. The patient received treatment for the event fever with Tylenol and did not receive any treatment for other events. The patient underwent lab test and procedure include SARS-CoV-2 test with the result of negative on an unspecified date. Outcome of the events were not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752640
Sex: F
Age:
State: PA

Vax Date: 02/26/2021
Onset Date: 02/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: nausea; headache; The rash I had from first got worse. I had it everywhere on my limbs, body and my face was the worse; My face was very red and swollen.; My face was very red and swollen.; did not feel well.; This is a spontaneous report received from a contactable consumer (patient). A 65-years-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: EN6202) via an unspecified route of administration at left arm on 26Feb2021 09:30 as dose 2, single for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication included sertraline hydrochloride (ZOLOFT), lorazepam (ATIVAN) and Vitamins. Patient do not have any other medical history and known allergies. Patient was not pregnant at the time vaccination. Patient did not receive any other vaccines within 4 weeks of time. Patient did not have COVID-19 prior to vaccination. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: EL9266) via an unspecified route of administration at left arm on 05Feb2021 09:30 as dose 1, single for COVID-19 immunisation and experienced a mild rash on stomach and back. After second dose Feb2021, the patient experienced nausea, and headache for 4 days straight, the rash patient had from first got worse. patient had it everywhere on my limbs, body and her face was the worse. Her face was very red and swollen. It took almost 2 weeks for all symptoms to go away. During that two weeks, patient just did not feel well. Patient did not receive any treatment for the events. Since vaccination patient has not been tested for COVID-19. Outcome of event did not feel well was unknown and remaining all events was resolving. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752641
Sex: F
Age:
State:

Vax Date: 03/06/2021
Onset Date:
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: aches; headache; extreme nausea; fever; This is a spontaneous report from a non-contactable consumer or other non-health care professional (patient). A 48-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6201) via an unspecified route of administration, administered in left arm on 06Mar2021 17:15 (at the age of 48-year-old) as dose 2, single for covid-19 immunization. Patient's had known allergies to Nickel. The patient's concomitant medications were not reported. Historical vaccine included BNT162B2 (solution for injection, Lot number: EL9266) via an unspecified route of administration, administered in left arm on 13Feb2021 05:30 PM (at the age of 48-year-old) as dose 1 single for COVID-19 immunization. Patient has not received any other vaccines within four weeks prior to the COVID vaccine. Patient neither diagnosed with COVID-19 prior to vaccination nor tested post vaccination. On an unspecified date in 2021 the patient experienced aches, headache, extreme nausea, fever. No treatment was received for the events. Outcome of the events were resolved on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752642
Sex: F
Age:
State: NY

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

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

Lab Data: Test Date: 20210313; Test Name: Nasal Swab; Test Result: Negative ; Comments: Covid rapid test; Test Date: 20210315; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Pending; Comments: Covid pcr; Test Date: 20210315; Test Name: Nasal Swab; Test Result: Negative ; Comments: Rapid flu test

Allergies:

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

Symptoms: skin on back feels tight and sensitive; Fatigue; body aches; chills; low grade fever; skin on back feels tight and sensitive; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 64-years-old non-pregnant female patient received dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EN6203), via an unspecified route of administration (at the age of 64-years), administered in arm left on 04Mar2021 at 09:15 as dose number unknown, single for COVID-19 immunization. Medical history included diabetes, asthma, arthritis from an unknown date and unknown if ongoing. Concomitant medications included amoxicillin (AMOXICILLIN) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccine in four weeks. The patient was tested for COVID post vaccination. The patient had no known allergies. On 05Mar2021 at 16:00, the patient experienced skin on back feels tight and sensitive, fatigue, body aches, chills, low grade fever. The treatment was not received for all the adverse events. The patient underwent lab tests and procedures which included Nasal Swab test: negative on 13Mar2021 Covid rapid test, Nasal Swab test: pending Covid pcr, Nasal Swab test: negative both on 15Mar2021 Rapid flu test. The clinical outcome for the events was reported as not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752643
Sex: F
Age:
State: MA

Vax Date: 03/12/2021
Onset Date: 03/13/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: Injection site pain; Injection site swelling; Foggy brain; Mild fatigue; Sneezing; This is a spontaneous report from a Non-contactable Pharmacist. This 27-year-old female Pharmacist (patient) reported for herself). A 27-years-old non pregnant female patient received second dose of bnt162b2 (BNT162B2, solution for injection) via an unspecified route of administration, administered in Arm Left on 12Mar2021 11:30 AM (Lot Number: EN6208) (at the age of 27-years-old) as DOSE 2, SINGLE for covid-19 immunization at pharmacy or drug store. Historical vaccine included received first dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration administered in Arm Left on 17Feb2021 04:00 PM (Batch/Lot number: EN6201) (at the age of 27-years-old) as DOSE 1, SINGLE for covid-19 immunization. The patient was not pregnant at time of vaccination. The patient had no known allergies and also denies for any medical history. Patient denied for any other vaccine in four weeks. Patient did not had covid prior to vaccination neither tested for covid post the vaccination. The patient's concomitant medications were not reported. On 13Mar2021 12:00 PM, the patient experienced injection site pain and swelling, foggy brain, mild fatigue and had sneezing. Patient took 1000 mg Tylenol, x2 as a treatment received. The outcome of events was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected

Other Meds:

Current Illness:

ID: 1752644
Sex: F
Age:
State: AZ

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

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

Lab Data:

Allergies:

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

Symptoms: My arm became red and painful. Swollen 5 inch area.; My arm became red and painful. Swollen 5 inch area.; My arm became red and painful. Swollen 5 inch area.; This is a spontaneous report from a contactable consumer (patient).A 63-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number EN6206), via an unspecified route of administration, administered in Arm Left on 03Mar2021 at 18:45 (at the age of 63-year-old) as dose 1, single for COVID-19 immunization. Medical history included osteoporosis. Concomitant medications were not reported. The patient did not take no other vaccine in four weeks and other medications in two weeks. The patient had no known allergies. The patient did not had covid prior vaccination and not tested for Covid post vaccination. On 04Mar2021 at 07:00 the patient experienced Redness, Pain in arm and Swollen arm. The patient reporter her arm became red and painful. Swollen 5-inch area. Lasted 5 days. The patient did not receive any treatment for events. On 09Mar2021 the patient recovered from the events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752645
Sex: U
Age:
State:

Vax Date: 03/09/2021
Onset Date: 03/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 20210310; Test Name: Fever; Result Unstructured Data: Test Result:100.6; Comments: 100.6 off and on

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: felt hot and cold; sweating all that night; nausea; fever not rising above 100.6 off and on; chills; felt achy all over; sleeplessness; exhaustion; injection site tenderness; headache; shoulders ached and neck ache; shoulders ached and neck ache/severe joint pain; lymph node swelling under the injection site arm; lymph node swelling under the injection site arm. Painful and swollen; This is a spontaneous report from a contactable consumer (patient). A 40-year-old patient of unspecified gender received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EN6199) via an unspecified route of administration on 09Mar2021 11:30 as dose 2, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EN6201) via an unspecified route of administration on 16Feb2021 (age at the time of both vaccination was 40 years) as dose 1, single for covid-19 immunisation. She got the vaccine at 11:30am and later that afternoon (on 09Mar2021), she felt what she did after her first shot, injection site tenderness, headache, shoulders ached and neck ache. By 7:30pm, she had chills and felt achy all over. Through the night she had sleeplessness and severe joint pain (literally every joint she own, it felt like- fingers and toes included. But mostly hip joints), headache, felt hot and cold. The next day (Wednesday/ 10Mar2021) started off with a bit of nausea which thankfully resolved, but then she had a fever not rising above 100.6 off and on, joint aches, exhaustion, headache. She just tried to sleep all day. Some moments were worse than others. She slept better that night but still had joint pain and a headache. Thursday her fever came back in the morning time as her headache and joint pain persisted. She felt almost normal by mid-morning and thought she was past it. But Thursday night, her chills and achy feeling and fever returned. It went away with sweating all that night on 11Mar2021 and Friday she was back at work. By mid-day Friday, her knees were aching again. Advil helped but she felt a bit feverish off and on while working. By last night at about 7pm she felt normal again and had been since. Side note, she had lymph node swelling under the injection site arm. Painful and swollen. Not as bad on the day of reporting though, but still noticeable. The patient underwent lab test and procedure on 10Mar2021 included body temperature and resulted into 100.6 off and on. The outcome of sweating was recovered on 11Mar2021 and nausea in Mar2021, outcome of lymph node swelling under the injection site arm, painful and swollen was not recovered and outcome of other events was unknown. No follow-up attempts were possible. No further information was expected. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1752646
Sex: F
Age:
State: IL

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Headache; body aches; fever; stuffy nose; fatigue; muscle twitching in lower limbs mostly in the first 24 hours. 3 weeks later, and the muscle twitching has not stopped; This is a spontaneous report from a contactable consumer (patient). A 40-year-old non pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number and Expiry date: not reported), via an unspecified route of administration in left arm on 25Feb2021 15:30 (at age of 40-years-old) as single dose for COVID-19 immunisation in hospital. Medical history was reported as none. The patient had no known allergies. Concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number and Expiration Date: Not reported), via an unspecified route of administration in right arm on 04Feb2021 15:30 (at age of 40-year-old) as single dose for COVID-19 immunisation. The patient had not received any other vaccine within 4 weeks. The patient had not received any other medications within 2 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19 and post the vaccination, the patient was not tested for COVID-19. On 25Feb2021 at 23:00, the patient experienced headache, body aches, fever, stuffy nose, fatigue, muscle twitching in lower limbs mostly in the first 24 hours. 3 weeks later, and the muscle twitching has not stopped. Headache, body aches, fever, stuffy nose, and fatigue in the first 36 hours. Also, muscle twitching in lower limbs mostly in the first 24 hours. 3 weeks later, and the muscle twitching has not stopped, throughout various parts of the body. Legs, feet, stomach, hands, etc. Adverse events resulted in none. No therapeutic measures were taken as result of the adverse events. The outcome of all events was not resolved. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1752647
Sex: U
Age:
State: TN

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

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

Lab Data:

Allergies:

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

Symptoms: Slight swelling on one side of my face from the cheeks down to my chin and jawline; 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 mRNA VACCINE, formulation: solution for injection, lot number was unknown, expiration date was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that the patient do not want to report anything exactly, patient would like to ask a question or two. Patient got the Pfizer vaccine 2 weeks ago, the first dose and a couple of days after that patient noticed slight swelling on one side of patient face from the cheeks down to patient chin and jawline and patient was just wondering is that Covid vaccine related. Is that something that you have seen, or heard patient hesitate to get to the doctor because patient have not got patients second one. Do patient take the second one, can you advise me. The health department that gave the shot told patient to contact you. Patient have 2 questions to ask, is this a common side effect that patient should not be concerned about Is it something that will go away Is it safe to get a second vaccine. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752648
Sex: F
Age:
State: SC

Vax Date: 03/13/2021
Onset Date: 03/13/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: muscle soreness; tiredness; lack of sleep; Some buzzing in ears, and increased tinnitus (pre-existing) off and on; Soreness in arm, typical of other vaccinations ie., some soreness in arm at/around injection site; typical of other vaccinations (minimized bruising and soreness by rubbing arm during 15 min wait time to disperse serum and reduce bruising/soreness) and increasing overnight; typical of other vaccinations (minimized bruising and soreness by rubbing arm during 15 min wait time to disperse serum and reduce bruising/soreness) and increasing overnight; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 62-years-old non pregnant adult female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA vaccine, Solution for injection), dose 1 via an unspecified route of administration, administered in arm left on 13Mar2021 14:15 PM (Batch/Lot Number: en6199) as dose 1, single for covid-19 immunisation (at the age of 62-year-old). Medical history included fibromyalgia, arthritis, slightly high blood pressure, tinnitus, vertigo, gall stones, neuropathy, plantar fasciitis, heel spurs from an unknown date and unknown if ongoing. The concomitant medications were not reported. the patient had known allergies for food such as some herbs and spices, other allergies to cats, wool, soap, dust etc. and no known allergies to drugs other than intolerance of Sudafed. The patient did not received any other vaccines within 4 weeks prior to the Covid 19 vaccine. The patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. The patient received medications in two weeks of vaccination. On 13Mar2021 16:15 PM, 2-4 hours post dose the patient experienced tiredness (may have been unrelated and due to lack of sleep and activity that day); 4 hours post dose to 36 hours post: Soreness in arm, typical of other vaccinations i.e. some soreness in arm at/around injection site, typical of other vaccinations (minimized bruising and soreness by rubbing arm during 15 min wait time to disperse serum and reduce bruising/ soreness) and increasing overnight -feels much like exercise muscle soreness, still a bit tender to touch at site. The patient not received treatment. The outcome of the events was recovering. No follow-up attempts are possible; no further information expected.

Other Meds:

Current Illness:

ID: 1752649
Sex: F
Age:
State: ME

Vax Date: 03/11/2021
Onset Date: 03/13/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Itchy red welts on both arms, hands and rib cage; This is a spontaneous report from a contactable consumer. This female consumer (patient) reported that: A 36-years-old non-pregnant female patient (not pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot Number: Eng205), via an unspecified route of administration, administered in Arm Left on 11Mar2021 12:15 (36-year-old at the time of vaccination) as dose 1, single for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were reported as none. 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. The patient had no other medications in two weeks. On 13Mar2021 19:00, the patient experienced itchy red welts on both arms, hands and rib cage. No treatment was received for the event. The outcome of the event was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752650
Sex: F
Age:
State: CT

Vax Date: 03/06/2021
Onset Date: 03/15/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: itchiness; Itchy rash on left arm appeared on 14Mar and slight rash on right arm; This is a spontaneous report from a contactable consumer (Patient) or other non hcp. A 59-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: ENG205, Expiration date was not reported), dose 1 via an unspecified route of administration, administered in Arm Left on 06Mar2021, at 18:15 (at the age of 59-years-old) as dose 1, single for covid-19 immunisation. Medical history included obesity, blood pressure increased from an unknown date and unknown if ongoing. Concomitant medications included losartan, clonazepam, fluoxetine all taken for an unspecified indication, start and stop date were not reported. The patient previously took ampicillin and experienced drug hypersensitivity. The patient was not pregnant in that time. No treatment was received in response to the adverse events. The patient did not received any other vaccines within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 15Mar2021 at 03:00, the patient experienced itchiness, itchy rash on left arm appeared on 14March and slight rash on right arm. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752651
Sex: F
Age:
State: NJ

Vax Date: 03/12/2021
Onset Date: 03/12/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:101; Comments: fever of 101; Test Date: 20210312; Test Name: fever; Result Unstructured Data: Test Result:103; Comments: worst fever 103

Allergies:

Symptom List: Nausea

Symptoms: second shot my symptoms were worst fever 103 sever chills and horrible sweats, all my joint hurts, had nausea and my headache; second shot my symptoms were worst fever 103 sever chills and horrible sweats, all my joint hurts, had nausea and my headache; second shot my symptoms were worst fever 103 sever chills and horrible sweats, all my joint hurts, had nausea and my headache; second shot my symptoms were worst fever 103 sever chills and horrible sweats, all my joint hurts, had nausea and my headache; second shot my symptoms were worst fever 103 sever chills and horrible sweats, all my joint hurts, had nausea and my headache; second shot my symptoms were worst fever 103 sever chills and horrible sweats, all my joint hurts, had nausea and my headache; my appetite hasn't returned; my symptoms were worst; This is a spontaneous report from a contactable consumer (patient). A 49-years-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6205), via an unspecified route on 12Mar2021 (at the age of 49-years) as dose 2, single in the left arm for covid-19 immunisation. The patient medical history was not reported. The patient had no known allergies. The patient concomitant medications included Vitamin D, Vitamin c, Vitamin B12 from an unknown date and unknown if ongoing. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL9266), via an unspecified route on 20Feb2021 at 12:00 (at the age of 49-years) as dose 1, single in the left arm for covid-19 immunisation and experienced flu symptoms fever of 101 chills body aches for 12 hours. 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 12Mar2021at 22:00, the patient experienced after second shot her symptoms were worst fever 103 sever chills and horrible sweats, all her joint hurts, had nausea and her headache was so severe for 36 hours and her headache was the one that's lingering and her appetite had not returned. Patient did not received treatment for events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752652
Sex: F
Age:
State: OH

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 20210215; Test Name: Fever; Result Unstructured Data: Test Result:Low grade

Allergies:

Symptom List: Injection site pain

Symptoms: Vomiting in the middle of thr 3rd night; Exhaustion; underlying nausea; had to force myself to eat and drink.; Low grade fever and chills day 3-4.; Low grade fever and chills day 3-4.; Nights sweats for thr firstv3 nights.; This is a spontaneous report from a contactable Nurse (Patient). A 57-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6198), dose 1 via an unspecified route of administration, administered in Arm Left on 12Feb2021 15:30 (Age at Vaccination 57-year-old) as DOSE 1, SINGLE for COVID-19 immunization at clinic. Medical history were not reported. Concomitant medications included Low dose ASA, vit C & D, estroven, & multi vit. The patient has reported Known allergies: NKA. Patient had no other vaccine in four weeks. Patient did not covid prior vaccination and not covid tested post vaccination. On 12Feb2021 the patient experienced nights sweats for thr firstv3 nights, on 15Feb2021 03:30 vomiting in the middle of thr 3rd night, exhaustion, underlying nausea, had to force myself to eat and drink, low grade fever and chills day 3-4. The patient did not receive any treatment for the event. The patient underwent lab tests and procedures which included body temperature: low grade on 15Feb2021. Patient did not received treatment. The outcome of the events Nights sweats for there firstv3 nights was recovered on 15Feb2021. Vomiting in the middle of thr 3rd night, Exhaustion, underlying nausea, had to force myself to eat and drink, Low grade fever and chills day 3-4 and Low grade fever and chills day 3-4. was recovered in Feb2021 No follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752653
Sex: M
Age:
State: CT

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: inside upper side of your elbow I developed a rash there; right arm in the inside like high up on my arm where there is a fold the when you bend your arm. I got a mild rash; pain on left arm; This is a spontaneous report from a contactable consumer (patient). A 71-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EM981O) via an unspecified route of administration, administered in left arm on 26Feb2021 as dose 1, single (at the age of 71-year-old) for covid-19 immunisation. The patient medical history was not reported. Concomitant medication included sertraline hydrochloride (ZOLOFT) taken for depression and anxiety from an unspecified start date and ongoing. The patient experienced inside upper side of your elbow i developed a rash there; right arm in the inside like high up on my arm where there is a fold when you bend your arm. i got a mild rash and on 26Feb2021 pain on left arm. Patient stated, on 26Feb2021, he got his first vaccine and there was pain in left arm for about 3 days, on his right arm in the inside like high up on his arm where there is a fold the when you bend your arm, he got a mild rash, it didn't itch, it did not burn it did not spread, it just stood there for 3 days as long as the pain in arm had lasted and then it went away. No treatment was taken. On an unspecified date in 2021, outcome of the events was recovered. No Follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752654
Sex: F
Age:
State:

Vax Date: 03/14/2021
Onset Date: 03/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: She could not move her hand; Body aches; High fever; This is a spontaneous report from a non-contactable consumer or other non-healthcare professional (Reporter's Wife). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: Unknown), via an unspecified route of administration on 14Mar2021 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced she could not move her hand, body aches and high fever on Mar2021. This was the extent of the information that I have about this AE. The outcome of the events was reported as unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752655
Sex: F
Age:
State: RI

Vax Date: 02/24/2021
Onset Date: 02/25/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 20210225; Test Name: Fever; Result Unstructured Data: Test Result:100.6; Comments: Fever (up to 100.6)

Allergies:

Symptom List: Tremor

Symptoms: Fever (up to 100.6); headache; nausea; This is a spontaneous report from a non-contactable consumer or other non hcp. A 34-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: P270395-0068L, Expiration date: unknown) dose 2 via an unspecified route of administration, administered in Arm Left on 24Feb2021 14:30 (at 34-years age) as dose 2, single for covid-19 immunisation. Medical history included allergic to pencillin. Concomitant medication included levonorgestrel (KYLEENA), naproxen (NAPROXEN). Patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: P220395-0068L, Expiration date: unknown) dose 1 via an unspecified route of administration, in Arm Left on 02Feb2021 at 03:30 PM as dose 1, single for covid-19 immunisation. The patient underwent lab tests and procedures which included body temperature: 100.6 on 25Feb2021 Fever (up to 100.6). The patient not tested covid post vaccination. On 25Feb2021 12:00 the patient experienced fever (up to 100.6), headache, nausea. No treatment received for reported adverse events. The outcome of events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034; Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752656
Sex: F
Age:
State: TX

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

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

Lab Data: Test Name: Height; Result Unstructured Data: Test Result:She used to be 5ft 6.5in and now she is 5ft.; Test Name: weight; Result Unstructured Data: Test Result:147-148; Comments: she is not sure

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: left hip hurt then her right hip would start hurting; body aches/It would ache in one spot then another spot; hurt more at the shot site with the first Covid 19 vaccine/pain that day afterwards; on the whole left side where she had the first shot; This is a spontaneous report from a contactable consumer (patient) or other non HCP. A 89-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN6201, Expiration date not reported), via an unspecified route of administration, administered in left arm on an unknown date in Feb2021 as dose 1, single (at the age of 89-years-old) for covid-19 immunization. The patient's medical history included ongoing ankylosis spondylosis (when she was real young, a kid, first time it was noticed was when she was a child, exercising in PE she could not touch her toes, states it's autoimmune), ongoing GERD (gastrooesophageal reflux disease) 30-40 years, ongoing hiatus hernia 30-40 years, gradually gotten worse, has a lot of pain and restrictions with food intake, she should have had an operation, ongoing arthritis since childhood, ongoing venous insufficiency at least 25-30 years where her veins leak in her lower legs, ongoing high blood pressure since she was in her 20s, ongoing blood clotting 30-35 years, is in a blood thinner for a long time, and ongoing autoimmune since childhood, goes along with ankylosing spondylosis. concomitant medications she reports she has been on all her regular medications for years. Patient previously took flu vaccine in on an unknown date in. Prior vaccinations (within 4 weeks) covid 19 vaccine reported as only received the flu vaccine in Sep2020 for unknown indication. On an unknown date in Feb2021, the patient experienced body aches/it would ache in one spot then another spot, hurt more at the shot site with the first covid 19 vaccine/pain that day afterwards and on the whole left side where she had the first shot. On an unknown date, it was reported that, it was like if her left hip hurt then her right hip would start hurting. The patient underwent lab tests and procedures which included body height: she used to be 5ft 6.5in and now she is 5ft., weight: 147-148 she is not sure, both on an unknown date. The outcome of event body aches/it would ache in one spot then another spot was recovering, and outcome of other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Ankylosing spondylitis (real young, a kid, first time it was noticed was when she was a child); Arthritis (Since childhood); Autoimmune disorder (since childhood, goes along with ankylosing spondylosis); Blood pressure high (Since she was in her 20s); Clot blood (30-35 years, is in a blood thinner for a long time); GERD (30-40 years); Hiatal hernia (30-40 years, gradually gotten worse, has a lot of pain); Venous insufficiency (At least 25-30 years where her veins leak in her lower legs)

ID: 1752657
Sex: F
Age:
State: FL

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

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

Lab Data:

Allergies:

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

Symptoms: her arm was sore; her arm had like a black; her arm had like a black and blue to it on the injection site; she saw on her arm a 3-4 inch red spot; that was spread out and it was warm to touch; This is a spontaneous report from a contactable consumer or other non-Health Care Professional. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and Expiry date: Unknown), via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunization.The patient medical history was not reported.The patient's concomitant medications were not reported.On an unspecified date the patient experienced her arm was sore, her arm had like a black, her arm had like a black and blue to it on the injection site, she saw on her arm a 3-4 inch red spot, that was spread out and it was warm to touch. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752658
Sex: M
Age:
State: AZ

Vax Date: 03/07/2021
Onset Date: 03/10/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: mental confusion; Fever; chills; shaking/tremors; diarrhea; indigestion; joint pain; This is a spontaneous report from a contactable consumer (patient). A 71-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EN6205) via an unspecified route of administration, administered in Arm Right on 07Mar2021 (at the age of 71 years old) as dose 2, single for COVID-19 immunisation. Medical history included Coronary artery disease, high blood pressure, diabetes, all from an unknown date and unknown if ongoing. Concomitant medication(s) received within two weeks included irbesartan (IRBESARTAN), rosuvastatin (ROSUVASTATIN), both taken for an unspecified indication, start and stop date were not reported. The patient previously amoxicillin and experienced allergy (Known allergies: Amoxicillin). Patient historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL9269) via an unspecified route of administration, administered in Arm Left on 14Feb2021 19:45 (at the age of 71 years old) as single for COVID-19 immunisation. Patient did not received other vaccine within four weeks of COVID vaccine. Patient did not have COVID prior to vaccination. The patient experienced mental confusion, fever, chills, shaking/tremors, diarrhea, indigestion, joint pain on 10Mar2021 12:00. No treatment were given for the events. Patient did not tested for COVID post vaccination. Outcome of all the event were not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752659
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Fever; didn't feel well; This is a spontaneous report from a non-contactable Nurse. This female Nurse reported for herself. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: Unknown, and Expiration date: Unknown), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient medical history, family medical history relevant to adverse events and concomitant medications were unknown. The investigation assessment was unknown. History of all previous immunization with the Pfizer vaccine considered as suspect and additional vaccines administered on same date of the Pfizer suspect was unknown. Prior vaccination within 4 weeks and adverse events following prior vaccination was unknown. On an unspecified date, the patient experienced fever and didn't feel well for some time after the vaccination. It was unknown if any relevant tests were performed for the events. It was unknown if the patient visited emergency room of physician office for the events. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752660
Sex: F
Age:
State: NY

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

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

Lab Data:

Allergies:

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

Symptoms: itching on one side; This is a spontaneous report from a contactable consumer or other non hcp. This Consumer reported for 4 patients. This report is for 2nd of 4 patients. This consumer reported for a female patient. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number and Expiry date was not reported), via an unspecified route of administration on unspecified date as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications was not reported. On unspecified date, the caller is calling about the covid Pfizer vaccine. The caller mentioned that her primary care provider had an itch on one side but the caller has it on both after receiving the Pfizer Covid vaccine. The outcome for the event was unknown. No follow-up attempts are possible; information about lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1752661
Sex: F
Age:
State: CA

Vax Date: 03/14/2021
Onset Date:
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: caller asking if she can take stomach, cough, and allergy medication; caller asking if she can take stomach, cough, and allergy medication; caller asking if she can take stomach, cough, and allergy medication; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received bnt162b2 (BNT162B2, solution for injection, Lot number was unknown), via an unspecified route of administration on 14Mar2021 as dose number unknown, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced abdominal discomfort, cough, and hypersensitivity with outcome of unknown. On the 14Mar2021 the patient got the COVID 19 vaccination. She is calling to ask after she took the COVID 19 vaccination can she take her stomach, cough, and allergy medication. Her stomach medication is Omeprazole 20mg, she has bought any cough medication yet, and the allergy medication is Zyrtec. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752662
Sex: U
Age:
State:

Vax Date: 03/13/2021
Onset Date: 03/01/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Little bit of swelling in my throat; it is still 'stiff'; This is a spontaneous report from a contactable consumer. This consumer (patient) reported. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an 13Mar2021 as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date on Mar2021, the patient experienced little bit of swelling in throat and it is still stiff. The patient reported that the patient got the Pfizer vaccine yesterday. The reporter could tell after I left, the patient felt like a little swelling in throat. Is that normal. The patient took it yesterday and the patient had like a little bit of swelling in throat. It was yesterday (13Mar2021) when the patient took it, the patient stated that it is still 'stiff' a little bit and I was wondering is that normal or what is that. The outcome of the events were unknown. No follow up attempts are possible. Information about Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752663
Sex: M
Age:
State: NY

Vax Date:
Onset Date: 03/14/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 20210314; Test Name: Temperature; Result Unstructured Data: Test Result:99.9; Comments: Temperature has gone up to 99.9, It is raising up again this afternoon like 99.5, It is not super high; Test Date: 20210314; Test Name: Temperature; Result Unstructured Data: Test Result:99.5; Comments: Temperature has gone up to 99.9, It is raising up again this afternoon like 99.5, It is not super high

Allergies:

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

Symptoms: Temperature has gone up to 99.9, It is raising up again this afternoon like 99.5, It is not super high; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 56-years-old male patient received first dose of bnt162b2 ((PFIZER-BIONTECH COVID -19 VACCINE, Solution for injection, Batch/Lot number and Expiry date was not reported) via an unspecified route of administration, administered in left arm on an unspecified date as dose 1, single for COVID-19 immunization (age at vaccination: 56-years-old). Medical history included asthma from 2018 to an unknown date, and hypertension (last 30 years). Concomitant medications included atenolol and losartan taken for hypertension, budesonide, formoterol fumarate (SYMBICORT) taken for asthma from 2018 and ongoing. On 14Mar2021 the patient experienced temperature has gone up to 99.9, it is raising up again this afternoon like 99.5, it is not super high. The patient took the vaccine to prevent from Corona Virus pandemic. The patient had not received treatment for the event. On 14Mar2021 the patient underwent lab tests and procedures which included body temperature: 99.9 and 99.5 (Temperature has gone up to 99.9, It is raising up again this afternoon like 99.5, It is not super high). The outcome of the event was not recovered. No follow-up attempts are possible. Information about lot/ batch number cannot be obtained.

Other Meds: Pfizer, Inc. 027034; Pfizer, Inc. 27034; Pfizer, Inc. 027034

Current Illness:

ID: 1752664
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: she had some "sharp pain" under the scapula and didn't know why.; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for Injection, Batch/Lot number: EL9262; Expiration Date: 31May2021) via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6200, Expiration Date: 30Jun2021) via an unspecified route of administration on 05Mar2021 at single dose for covid-19 immunisation. The patient had rabies vaccine (She had a very bad experience 4 years ago when she got a rabies vaccine, it was given at 45?, the nurse gave the injection cutaneously, after 5 min she was so in pain.). The patient experienced some "sharp pain" under the scapula and didn't know why on an unspecified date. The outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1752665
Sex: M
Age:
State: NV

Vax Date: 03/06/2021
Onset Date: 03/07/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: broke out into hives; This is a spontaneous report from a contactable consumer (Patient). A 23-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: En6206) dose 2 via an unspecified route of administration, administered in right arm on 06Mar2021 at 13:30 (at the age of 23-year-old) at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: El9267) via an unspecified route of administration, on 12Feb2021 09:30 AM at single dose for COVID-19 immunisation. The patient was not COVID prior vaccination and did not test COVID post vaccination. After receiving the second dose, on 07Mar2021 at 12:00 AM, the patient broke out into hives and had them since. The patient did not receive any treatment for the vent. The clinical outcome of events was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1752666
Sex: M
Age:
State: IL

Vax Date: 03/10/2021
Onset Date: 03/14/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data: Test Date: 20210314; Test Name: body temperature; Result Unstructured Data: Test Result:101 degrees Fahrenheit; Comments: began having a fever of 101 degrees Fahrenheit

Allergies:

Symptom List: Vomiting

Symptoms: began having a fever of 101 degrees Fahrenheit; aches and chills; aches and chills; headache and all around feels horrible; headache and all around feels horrible; cough; scratchy throat; This is a spontaneous report from a contactable consumer (patient). A 56-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6206), via an unspecified route of administration, administered in Left Arm on 10Mar2021 (age at the time of vaccination was 56 years) at 16:00 as dose 1, single for covid-19 immunisation. Medical history and family medical history relevant to AE(s) was reported as none. There were no concomitant medications. Additional Vaccines administered on same date of the pfizer suspect were reported as none. Prior Vaccinations (within 4 weeks) were reported as none. The reporter stated he had the Pfizer COVID Vaccine on 10Mar2021 which was Wednesday and then began having a fever of 101 degrees Fahrenheit, aches and chills, a headache and all around feels horrible, had a cough and scratchy throat and all of the listed symptoms began on Sunday 14Mar2021. The reporter stated all of the symptoms were ongoing but he believes he was turning a corner and these symptoms have improved and are starting to improve. The reporter clarified to state he still does have a fever but the chills and aches and pains are not as bad as they were an hour ago which was how long he was waiting on the phone for DSU. He stated he had not had any treatment for the reported symptoms. The reporter stated that he has not had his 2nd dose of the Pfizer COVID vaccine but it was scheduled. The AE(s) did not require a visit to Emergency Room. He just called the HCP and the HCP told him to take Ibuprofen or Tylenol for fever, aches and pains and to drink plenty of water. On 14Mar2021, the patient underwent lab tests and procedures which included body temperature: 101 degrees fahrenheit (began having a fever of 101 degrees Fahrenheit). This report is not related to a study or program. No investigation Assessment was reported. The outcome of the event began having a fever of 101 degrees Fahrenheit was not recovered. The outcome of the events headache and all around feels horrible, cough and scratchy throat was unknown. The outcome of the events aches and chills was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1752667
Sex: F
Age:
State:

Vax Date: 03/14/2021
Onset Date: 03/13/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: I am hurting in between my breast like a type of soreness but yet sometimes I feel little pain is going between my two breasts; I am hurting in between my breast like a type of soreness but yet sometimes I feel little pain is going between my two breasts; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received bnt162b2 (BNT162B2) formulation solution for injection, unknown dose, via an unspecified route of administration on 14Mar2021 as a single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Consumer stated, she got the COVID Vaccine (reporting before day) yesterday and it may be about an hour and half she been having, they are not actual chest pain, but she was hurting in between her breast like a type of soreness but yet sometimes she feels little pain was going between her two breasts. She doesn't know that was why she called you. In response to further probing, consumer stated, "You know what never mind. She just holds it out." And hung up abruptly. Consumer hung up the call abruptly, hence, product details (LOT#, expiration date, NDC# and UPC#) reporter type and other details were unknown. Limited information was available over the call. Outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1752668
Sex: F
Age:
State: TX

Vax Date: 03/14/2021
Onset Date: 03/14/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Rash all over my body and it is really itchy; This is a spontaneous report from a contactable consumer or other non-HCP (Patient). A 44-years-old male received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was EN6207 and expiration date was 31Jul2021) via an unspecified route of administration on 14Mar2021 (age at the time of vaccination was 44-years-old) as a DOSE 1, SINGLE for COVID-19 immunization. Medical history was not reported. Concomitant medications included Lisinopril for an unspecified indication from an unspecified date. On 14Mar2021, the patient experienced Rash all over my body and it is really itchy. Additional Information: The consumer stated that she got a COVID shot today and had rash all over body and it was really itchy and she did not knew what to do. Vaccination date: The consumer stated that she got it 14Mar2021 and got the shot at 10 o clock this morning. Treatment: She I took some Benadryl to see if that would help but it did not helped. The clinical outcome of the event was Not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752669
Sex: F
Age:
State: CA

Vax Date: 03/08/2021
Onset Date:
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Getting like a hives or rash all over my legs and my arms; It was like the bumps like the color of my skin; Getting like a hives or rash all over my legs and my arms; This is a spontaneous report from a contactable consumer. This 37-year-old female consumer (patient) that she received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6199; Expiration Date: 30Jun2021; NDC number, UPC number: unknown), via an unspecified route of administration on 08Mar2021 (at the age of 37 years) as dose number unknow, single for covid-19 immunisation. Medical history included anxiety and panic attack. Concomitant medication(s) included escitalopram oxalate (LEXAPRO), once a day taken for anxiety, panic attack. No investigation assessment done. Consumer stated that she was not sure of her weight at the time of report but she thought she was 150, 155 pounds. She hadn't weigh in a while. She got her vaccine on 08th, Monday the 8th of this month. Two days ago, she started noticing that she got like a hives or rash all over her legs and her arms. It was like an over a week but it might be like 2-3 days ago, she started noticing that she got like a hives or rash all over her legs and rash like bumps, on her arms. It was kind of hives or rash on her arms or legs and they just felt like, they were getting worse at the time of report. She didn't notice it because when she first noticed it wasn't itchy at all. It was like the bumps like the color of her skin. They were not like inflamed or anything like that, not like red or anything. She just started feeling like bumps on her skin. She started noticing them like she wanted to say like Thursday or Friday. At the time of report, she still experiencing the events and it actually got more itchy. She was scratching her leg a minute ago and she realized they were coming out more. She took Benadryl (Batch/Lot number, NDC number, UPC number, Expiry date: Unknown) the other day like a day before but took the Benadryl on the day of report but it did not seem to be very helping. She did only took one. She took Benadryl but she thought it was supposed to take 2 but she only took one. The outcome of reaction/event at the time of last observation was not recovered/not resolved. No follow-up attempts are possible. No further information is expected. She did not know if it was just from the vaccine or what but she only know where else she had got them from. So she was calling for some advice. The patient experienced getting like a hives or rash all over my legs and my arms (rash) (non-serious) on an unspecified date with outcome of not recovered , it was like the bumps like the color of my skin (skin disorder) (non-serious) on an unspecified date with outcome of unknown , getting like a hives or rash all over my legs and my arms (urticaria) (non-serious) on an unspecified date with outcome of not recovered. The action taken in response to the event(s) for bnt162b2 was not applicable. Therapeutic measures were taken as a result of getting like a hives or rash all over my legs and my arms (rash).

Other Meds: Pfizer, Inc. EUA 027034

Current Illness:

ID: 1752670
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: fever; didn't feel well; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for Injection, Batch/Lot number: Unknown) via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced fever and did not feel well on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1752671
Sex: F
Age:
State: NC

Vax Date: 03/10/2021
Onset Date: 03/11/2021
Rec V Date: 10/01/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable consumer (patient). A 43-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EN6204 and expiry date was not reported), via an unspecified route of administration, in Arm Right, on 10Mar2021 (age at vaccination: 43 years), as a single dose for COVID-19 immunization. The patient took Covid-19 vaccine because to protect herself and others from Covid. The patient's medical history and concomitant medications were not reported. The patient reported that she thought 30 hours after getting the vaccine she had the typical normal thing she thought she would have the tiredness. On 11Mar2021, she started having pretty strong abdominal pain and then she had a nose bleed pretty heavy dripping for few minutes and then it just stopped. The patient did not receive any treatment for the events. The patient reported that he hasn't had it again, so a friend of mine was a doctor said that the nose bleed was not normal and she should probably call and report that. Outcome of events was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am