VAERS 2021 Database www.vaers.hhs.gov

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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: 1773790
Sex: F
Age:
State: SC

Vax Date: 03/20/2021
Onset Date: 03/21/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data: Test Name: Feeling a like little feverish; Result Unstructured Data: Test Result: I do not think I have a temperature; Comments: I do not think I have a temperature; Test Name: weight; Result Unstructured Data: Test Result: 199 lbs.; Comments: I think I am at 199 (pounds).

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Slight pain on the site of injection; Lymph node might be little bit swollen and that's what I am experiencing right now; Lymph node under the arms where I got the vaccine, It was hurting; Feeling a like little feverish, I do not think I have a temperature; This is a spontaneous report from a contactable Consumer or other non-health professional (patient). A 51-years-old female patient received BNT162B2 (Batch/Lot Number: ER2613; Expiration Date: Jul2021, NDC number and UPC number were unknown), dose 1 via an unspecified route of administration, administered in Arm on 20Mar2021 (Age at vaccination 51 years-old) as dose 1, single for covid-19 immunisation. Medical history included hypertension Verbatim Blood pressure high from unknown start date and unknown start date. Concomitant medication(s) included amlodipine besilate (NORVASC) it's 5, omeprazole (OMEPRAZOLE) it's 40, cevimeline (CEVIMELINE) 30 mg start date and stop dates were not reported. The patient reported that I got the first COVID vaccine this past Saturday and I did not have really any feeling for anything on Saturday, but Sunday on 21Mar2021 the patient experienced slight pain on the site of injection (injection site pain) which was then cleared up but then I read on the sheet that I was given that, well the pain of the site, I do not have that pain anymore, lymph node might be little bit swollen and that's what I am experiencing right now; lymph node under the arms where i got the vaccine, it was hurting, the patient stated that I noticed that my lymph node under the arms where I got the vaccine, It was hurting, it's not hurting as much as it was, it seems like it starting to go down and I just feel, feeling a like little feverish, i do not think i have a temperature, But he was just calling to see you know like how long these symptoms should last 21Mar2021. The patient underwent lab tests and procedures which included weight: 199 lbs on I think I am at 199 (pounds). The outcome of the event slight pain on the site of injection and lymph node might be little bit swollen and that's what I am experiencing right now was recovering, while the outcome of the event feeling a like little feverish, I do not think I have a temperature was unknown No follow up attempts are possible. No further information is expected.

Other Meds: Norvasc; Omeprazole; Cevimeline

Current Illness:

ID: 1773791
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/09/2021
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: just got a little rash on my hand; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; batch/lot number, NDC number, UPC number, expiry date was reported as 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 received the first shot at job and experienced a side effect from the shot. Patient had little rash on hand. It was not all over the body. The patient was concerned and asked if it was going to go away. Consumer was informed about the role of Pfizer drug safety and Pfizer medical information. The patient might get the second shot. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773792
Sex: M
Age:
State: PA

Vax Date: 03/11/2021
Onset Date: 03/11/2021
Rec V Date: 10/09/2021
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: Start to getting 'twig' on the back of my throat; I thought like I had a full blow taste of flu; All the symptoms of the flu and what you guys got down on that paper for COVID symptoms, but I know I don't have COVID; Headache; Muscle pain; Chills; swelling at injection site; Nauseated; Coughing; Sore throat; I just didn't feel right; I had injection at the pain site; Sore arm; Aching joints/Joint pain; Tired; This is a spontaneous report from a contactable consumer (patient). A 74-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA vaccine, Solution for injection) via an unspecified route of administration, administered in left arm on 11Mar2021 (Batch/Lot Number: EN6207) (at the age of 74-year-old) as dose 1, single for COVID-19 immunization. Medical history included thyroid, macular degeneration and patient had a hearing problem from an unknown date and it is ongoing. Concomitant medication(s) included paracetamol (TYLENOL); levothyroxine sodium (L-THYROXINE [LEVOTHYROXINE SODIUM]); ascorbic acid, cupric oxide, dl-alpha tocopheryl acetate, xantofyl, zeaxanthin, zinc oxide (PRESERVISION AREDS 2) taken for macular degeneration prescribed by eye doctor, start and stop date were not reported; levothyroxine sodium (SYNTHROID) taken for thyroid prescribed by his family doctor because of his thyroid is out of way, start and stop date were not reported. The symptoms started on 11March2021. On 11Mar2021, the patient experienced sore arm and achy joints and he was tired, reporter stated he had injection at the pain site, he was tired, he had headache, did have muscle pain but he does not know, chills, joint pain, he had swelling at the injection site, it was times that he was nauseated, he just didn't feel right, he had cough, sore throat. 3 days after injection, on 14Mar2021, he started to getting 'twig' on the back of his throat and by that night which was Sunday (on 14Mar2021) night he thought like he had a full blow taste of flu, that he have it till today but not quite as bad. All the symptoms of the flu but he knew he didn't have COVID. Patient was asked was it possible for him to had a reaction to that shot. Patient was due for his second shot on 02April2021 and enquired if he should get that shot. The outcome of the events tired, headache and cough was not recovered and for the remaining events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: TYLENOL; L-THYROXINE [LEVOTHYROXINE SODIUM]; PRESERVISION AREDS 2; SYNTHROID

Current Illness: Hearing impaired

ID: 1773793
Sex: F
Age:
State: MS

Vax Date: 03/16/2021
Onset Date:
Rec V Date: 10/09/2021
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: Discomfort on the right arm; fever; chill; This is a spontaneous report reported by a consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported, via an unspecified route of administration, on 16Mar2021 as DOSE 1, SINGLE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that she had first shot 16Mar and was scheduled to take second shot on 08Apr. On an unspecified date, the patient experienced discomfort on the right arm. She was also experiencing fever and chill. The patient wanted to know if she needed to take second shot. Outcome of the event was not recovered. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1773794
Sex: F
Age:
State:

Vax Date: 03/22/2021
Onset Date:
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Pain in arm; Stiffness in arm; swollen fingers/ swollen hands; puffy face; This is a spontaneous report received from a contactable consumer (patient). A 79-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: unknown, Expiration date was not reported), via an unspecified route of administration on 22Mar2021 at 15:20 (at the age of 79-years-old) as a dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that, on an unspecified date in 2021, the patient experienced pain in arm, stiffness in arm, swollen fingers, swollen hand, puffy face. The consumer stated that, yesterday, on 22Mar2021, she went to get the first dose of the Pfizer vaccine around 03:20pm and when she got home there was no problem. Stated that, she went to bed at 11pm and woke up at 02:30am with pain in her arm, it was stiff and swollen. Stated that, her hand was swollen, fingers were swollen and her face was a little puffy. Stated that, initially she had swelling in her arm but clarified that, she had pain in her arm and not swelling. Only her hand, fingers and face were swollen and puffy. Stated that, she was scared to take the second shot and enquired, whether that was a normal reaction. The swelling lasted for 4 hours and now it was normal. At 06:30 am, she was already normal. Stated that, the pain was no problem. The swelling scared her. This was on her left side. Stated that, everybody that she heard of had something. Stated that, she knows everyone had a reaction or small problem with stiffness. No other details were provided. Stated that, her son said maybe she should not take the second dose and to call and inquire about this. She asked whether the second dose was safe and if she can take it or not. Stated that, she asked whether that would be safe. Stated that, she can deal with the puffiness. Everybody had issues in their arms, it was like having Covid. Stated that, she only called to ask whether it was normal and safe to take. The outcome of the events for swollen fingers/ swollen hands was recovered on an unspecified date in 2021 while for the other events was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773795
Sex: F
Age:
State: FL

Vax Date: 02/26/2021
Onset Date:
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: I broke with itchy rash all over my body; then another patch on my arm that actually black; I broke with itchy rash all over my body; then another patch on my arm that actually black; I had rash, red spot, or other rash all over my body; it's most severe on my right arm; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female patient received BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EN6198 and expiry date was not reported), via an unspecified route of administration, on 26Feb2021 (age at vaccination was 68 years), as a dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The reporter stated that she like to report the side effect of Covid-19 vaccination. On an unspecified date, the patient broke with itchy rash all over my body, then another patch on her arm that actually black. When paraphrased the above concern, the patient stated that she had rash, red spot, or other rash all over my body and it's most severe on her right arm. Reportedly the patient was still little itchy. The patient received treatment with Lotrimin for events. Outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773796
Sex: F
Age:
State: FL

Vax Date: 03/20/2021
Onset Date: 03/21/2021
Rec V Date: 10/09/2021
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: the very next day and I am still little itchy; This is a spontaneous report from a contactable consumer (Patient). A 68-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot Number: EN6198) via an unspecified route of administration on 20Mar2021 (at the age of 68-year-old) as dose 2, single 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: EN6198) via an unspecified route of administration on 26Feb2021 (at the age of 68-year-old) as dose 1, single for COVID-19 immunisation and experienced itchy rash all over her body and then another patch on her arm that actually black, patient had rash, red spot, or other rash all over her body and it was most severe on her right arm. On 21Mar2021, after second shot, the very next day, patient was still little itchy, the patch on her right arm appears to be getting better, that was improving. Patient's husband had some Lotrimin [corrective treatment], patient put that on there and that helps it. The outcome of event was recovering. No follow-up attempts are possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1773797
Sex: F
Age:
State:

Vax Date: 02/25/2021
Onset Date: 03/22/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Feeling sick; Runny nose; Itchy eyes; feels like she has the flu; This is a spontaneous report from a non-contactable consumer (Patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Lot Number: Not reported; Expiration date: Not reported) via an unspecified route of administration, administered on 25Feb2021 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 22Mar2021, the patient experienced feeling sick, runny nose, itchy eyes, feels like she has the flu. The patient is calling about the Pfizer covid vaccine. The patient got the first dose of the vaccination at (Facility name) in (name) on 25Feb2021. Today the patient is supposed to get the second shot but she woke up feeling sick, has a runny nose, itchy eyes and feels like she has the flu. This actually started yesterday. The patient wants to know if she should get her second dose of the vaccine at 2:00pm as scheduled. The outcome of all the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. Follow-up attempts not completed; information about lot/batch number cannot be obtained. No further information expected.

Other Meds:

Current Illness:

ID: 1773798
Sex: U
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: rash on the opposite side arm; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient developed a rash on the opposite side arm after receiving the COVID vaccine first dose on an unspecified date. The outcome of the event was unknown. No follow-up attempts are possible; information about batch/lot number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773799
Sex: F
Age:
State: CA

Vax Date: 03/12/2021
Onset Date: 03/01/2021
Rec V Date: 10/09/2021
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: she experienced a slight pain on the injection site; on the next morning she felt a pain on the left side of her neck/It was a little painful on the injection site; She feels it went to another site or the left side again at the back of her arm; She can't lift her arms because it was very painful/ I can't lift up my arm with there being an excruciating pain; if I sleep on it hurts; I tried to lift it up it hurts; I had stiffness and pain in my left side of neck; Pain moved to right side of my neck down to backside of my shoulders; now it is in the front of my shoulders; my muscles and my joints and it's so painful; in my muscles and my joints and its so painful that I cant lift up my arm; in my muscles and my joints and its so painful that I cant lift up my arm; This is a spontaneous report from a contactable consumer (patient herself) from Pfizer- sponsored program. A 63-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EN6203; Expiration Date: Jun2021), via an unspecified route of administration, administered in Arm Left on 12Mar2021 as DOSE 1, SINGLE for covid-19 immunisation (at the age of 63 years). Medical history included hypertension, hypothyroidism and Heart Issue all from an unspecified date unknown if was ongoing. Concomitant medications included lisinopril, 20 mg 2xdaily Tablet orally taken for hypertension, and metoprolol tartrate, 25 mg half tablet twice a day orally taken for cardiac disorder (Heart Issue) both from an unspecified date unknown if was ongoing. The patient reported that, she experienced she experienced a slight pain on the injection site; on the next morning she felt a pain on the left side of her neck/It was a little painful on the injection site, She feels it went to another site or the left side again at the back of her arm, She can't lift her arms because it was very painful/ I can't lift up my arm with there being an excruciating pain; if I sleep on it hurts; I tried to lift it up it hurts, I had stiffness and pain in my left side of neck, Pain moved to right side of my neck down to backside of my shoulders; now it is in the front of my shoulders; my muscles and my joints and it's so painful, in my muscles and my joints and it was so painful that I cannot lift up my arm on unspecified date in Mar2021. It was reported that consumer had received the Pfizer shot on 12Mar2021 on left arm, it was a little painful on the injection site reported as a slight pain on the injection site; on the next morning she felt a pain on the left side of her neck. Next morning she had stiffness and pain in left side of neck, she thought she slept on the wrong position but the next day it moved to right side and then pain moved to right side of neck down to backside of the shoulders, now it is in the front of my shoulders and in my muscles and my joints and it's so painful that she cannot lift up the arm with there being an excruciating pain , if I sleep on it hurts, I tried to lift it up it hurts. Patient reported problem she received her 1st shot, So, basically, she experienced a slight pain on the injection site but on the next morning she felt a pain on the left side of her neck, thinking that she slept on the wrong position but after that she feels it went to another site or the left side again at the back of her arm and she said that she cannot lift her arms because it was very painful. Reporter stated, I just did not know what to do to it, either something I can do for it, I mean it was in joints and in muscles. Due date of second shot of vaccine was reported as 02Apr2021. Reporter stated, it was bearable before but now it was worsening. Treatment received was Tylenol 500 mg (2 tablets), Tiger Balm (Ointment). Reporter seriousness for the events were unspecified. The clinical outcome of the events was not resolved. No follow-up attempts are needed. No further information is expected.

Other Meds: LISINOPRIL; METOPROLOL TARTRATE

Current Illness: Heart disorder (Verbatim: Heart Issue); Hypertension (Verbatim: Hypertension); Hypothyroidism (Verbatim: Hypothyroidism)

ID: 1773800
Sex: F
Age:
State: TN

Vax Date: 03/22/2021
Onset Date: 03/23/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:99.9-degree

Allergies:

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

Symptoms: she had a 99.9 degree fever; she felt really cruddy today; This is a spontaneous report from a contactable consumer or other non-healthcare professional reported for herself. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID -19 VACCINE, Formulation: solution for injection, Batch/Lot number: not reported and Expiry date: Unknown) via an unspecified route of administration on 22Mar2021 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 23Mar2021, the patient experienced she felt really cruddy today, and she had a 99.9 degree fever so she didn't feel really good. She said she was going to celebrate her grandson's second birthday on 26Feb2021. She said she read the pamphlets for the Pfizer COVID-19 Vaccine, but the pamphlets didn't say anything about if she would be contagious after getting the COVID-19 Vaccine. She said she didn't want to expose her 2-year-old grandson, if she was. On an unspecific date the patient underwent lab tests and procedures which included body temperature: 99.9-degree. 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: 1773801
Sex: U
Age:
State: PA

Vax Date:
Onset Date: 02/23/2021
Rec V Date: 10/09/2021
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: night sweats; nausea; body aches; chills; sleepiness; severe with slight fever; shakiness; brain fog; weakness; loss of weight; anxiety; This is a spontaneous report from a contactable consumer or other non hcp. A 76-years-old patient of an unspecified gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number -not reported), dose 2 via an unspecified route of administration on an unspecified date as DOSE 2, SINGLE (at 76-years age) for covid-19 immunisation. Medical history included celiacs, RA (rheumatoid arthritis), anemia, osteo-sarthritis, allergies all from an unknown date and unknown if ongoing. Concomitant medications included amlodipine (AMLODIPINE), fluticasone (FLUTICASONE), lamotrigine (LAMOTRIGINE), leflunomide (LEFLUNOMIDE) all were taken for an unspecified indication, start and stop date were not reported. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, lot number-unknown) via unspecified route of administration time in Left arm on 21Feb2021 at 06: 45 pm as DOSE 1, SINGLE for covid-19 immunization. The patient received vaccine at hospital. The patient not diagnosed with covid-19 prior to vaccination and did not tested post vaccination. The patient did not receive other vaccine in four weeks. The patient experienced night sweats, nausea, body aches, chills, sleepiness. for around 2 days after with lingering symptoms for a few days second shot, same reactions only more severe with slight fever and shakiness, have something like a brain fog, weakness, loss of weight, still experiencing symptoms but not as severe with anxiety and weakness on 23Feb2021 02:30 PM. The patient did not received treatment for all events. The outcome of all events was resolving. No follow-up attempts are Possible. Information on lot/batch cannot be obtained.

Other Meds: AMLODIPINE; FLUTICASONE; LAMOTRIGINE; LEFLUNOMIDE

Current Illness:

ID: 1773802
Sex: M
Age:
State: CT

Vax Date: 03/05/2021
Onset Date: 03/01/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data: Test Name: Hearing test; Result Unstructured Data: Test Result:unknown results; Test Name: Balance test; Result Unstructured Data: Test Result:unknown results; Test Name: Blood test; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:bad sinus infection

Allergies:

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

Symptoms: pretty bad sinus infection; dizziness, felt like he was drunk; throat started to swell up; Difficulty breathing/ shortness of breath; allergic reaction; Headache; the swelling of his lymph nodes in his throat and neck; Chills; This is a spontaneous report from a contactable consumer (patient). A 70-year-old male patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6198) via intramuscular on 05Mar2021 at 11:45 in left arm (at the age of 70-year-old) as single dose for covid-19 immunisation. The patient also received unspecified vaccine (NDC number, UPC number, Lot Number, expiry date was reported as unknown). Medical history (including any illness at time of vaccination) included that the patient had been dizzy since November. So December, January, and February, he did not drive a vehicle because the dizziness was so bad. He never had this before, but he thought he might have had the virus last February. He doesn't know for sure. His son's house had it and he live right beside him. He had something for like 4 or 5 days, but he didn't know if it was the flu or COVID. Back in Feb2020, they didn't know too much about the virus. Whatever it was, it went away. He was a smoker, but it's been a year since he stopped, He stopped last year, 13Mar2020. In Dec2019, his ENT doctor did do a sinus surgery, he doesn't know what the procedure was, but his drains weren't draining in his sinuses, the procedure went alright. All of a sudden in Nov2020, he started getting the dizziness. He doesn't get the flu shots only because he gets sick after he gets them anyway. History of all previous immunization with the Pfizer vaccine considered as suspect was reported as none. No prior vaccinations within 4 weeks and no adverse events following prior vaccinations. The patient's concomitant medications were not reported. The patient had dizziness and swelling of his lymph nodes in his throat and neck. He had been seeing the ENT and his family doctor for 3 months, and no one can come up with an answer. He was driving his car at the end of February. For 3 weeks, he was actually started to drive because the dizziness had improved some. He explains on a scale of 1-10, his dizziness was about 1.5-2 driving to the vaccination facility on 05Mar2021. He commented that shot wasn't in him for more than a minute, minute and a half. He clarified that when he got the shot, he was lit up to like a 10 or 11 in a matter of a minute and a half. His throat started to swell up. His dizziness was off the charts. He felt totally drunk, the best way he could explain it. He doesn't know how he walked out of that place without somebody stopping him because he was sure he was walking as he was drunk. He explained he didn't say anything to the nurses when he got the vaccine because he didn't want to go to the ER or anything like that. It was 20 degrees out that day so he walked outside and thought maybe the temperature might waking him up a little bit. He was sitting in his car for 30 minutes because he didn't want to drive. He stated his throat swelled, he meant right at the base of his neck, to the left- and right-hand sides was what he was told was fatty tissues and these areas swelled right up, it's hard as a freak in rock, it was hard to call it fatty tissue. Throat started to swell up at the base of his neck and up towards like the back of ears to back of skull; throat was still swelled up after 3 weeks. His doctor had given him a prescription, Meclizine 25mg which he took. When probed for , Lot number or expiry date of the bottle of Meclizine, he confirmed it was a (pharmacy name) bottle. He only sees Rx Expires: 06Dec2021. The dizziness was up at a high level which lasted a good 2 or 3 days. The other side effects he had with the vaccine were headaches and chills. He explained the whole thing lasted about 4 days. He also had allergic reaction, difficulty breathing, shortness of breath. He felt a little better on day 5 or 6. He has been seeing 2 doctors (ENT and family doctor) to figure his dizziness out but hasn't been having too much luck. He clarified that he started seeing the two doctors prior to receiving his Covid-19 vaccine. His biggest concern was getting the second shot or not. The way he lit up the first time, he knows the second shot is supposed to be more intense. He doesn't want this to happen with the second shot. He asked if Pfizer have any advice or whether or not to take the second vaccine. According to the MRI, he had a pretty bad sinus infection. He explained they were looking for the worst when he was sent for the MRI, but it was only found he had a bad sinus infection. He was looking on the adverse reactions sheet and noticed some of the side effects listed include dizziness from the virus itself. His doctor does not recommend him taking the second shot as he had difficulty breathing, shortness of breath, swelling of throat, severe dizziness and according to healthcare provider, he either would have called or drove to the hospital or either one, but he didn't. The dizziness went away after 4 or 5 days, but the throat was swelled up after 3 weeks. He was worried about his throat swelling up again and not being able to breathe. His second dose was scheduled for 26Mar2021. The patient underwent lab tests and procedures which included acoustic stimulation tests, balance test, blood test: results were unknown and magnetic resonance imaging on an unknown date in 2021: bad sinus infection. The outcome of the events dizziness, headache, and chills was recovered in 2021, for throat swelling was not recovered and for all other events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1773803
Sex: F
Age:
State: KS

Vax Date: 03/22/2021
Onset Date: 03/22/2021
Rec V Date: 10/09/2021
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: area across shoulders and down back hurts a lot, felt pressure in this area; area across shoulders and down back hurts a lot, felt pressure in this area; dry sore throat- feels like someone threw sand in her throat; Feeling achy, it was worse when she got up this morning; Feeling achy; This is a spontaneous report from a contactable consumer (patient). A 29-year-old female patient received BNT162B2 (BNT162B2, Solution for injection, PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: ER8727) via an unspecified route of administration, administered in right arm on 22Mar2021 12:00 as dose 1, single for COVID-19 immunization (Clinic) (at the age of 29-year-old). Medical history included flu shot over six months ago from an unknown date. Family history of heart disease and dementia, Grandma and great grandma had dementia on father's side. Mother's side- grandma had heart disease. There were no concomitant medications. The patient experienced feeling achy on 22Mar2021 Around 3:00 PM or 4:00 PM (15:00 or 16:00), patient thought it was the weather, feeling achy about two or three hours after the shot, feeling achy, it was worse when she got up this morning on 23Mar2021 it was ten times worse- she had never felt like this before, area across shoulders and down back hurts a lot, felt pressure in this area, dry sore throat- felt like someone threw sand in throat both on 23Mar2021 07.30. Relevant tests were none. Patient wanted to lay down so didn't feel the pressure across shoulders and down her back. Patient scheduled to receive the second dose on 12Apr2021. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773804
Sex: F
Age:
State: AZ

Vax Date: 03/22/2021
Onset Date: 03/22/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: It has bruising on the injection site; Muscle spasm; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: ER2613, Expiration date: Unknown), dose 1 via an unspecified route of administration, administered in Arm Left on 22Mar2021 at 14:00 (at the age of 42-years-old) as Dose 1, Single for Covid-19 immunization. Vaccination facility type was reported as sports facility. The patient's medical history included ongoing migraine headache. The patient's concomitant medication included brivaracetam (BRIVIACT) taken for migraine headache, start and stop date were not reported. On 22Mar2021 at 22:00, the patient experienced bruising on the injection site, it had bruise. Next day, she stated that yes bruise was lesser than yesterday. On an unspecified date in 2021, the patient had muscle spasm. It was reported that, patient had her cholesterol, blood test and calcium test 2 months ago, so nothing in the last month. Patient was taking medication of other vaccine (unspecified vaccine) and cyclobenzaprine (medication) for muscle spasm. She was concerned about her bruise and queried if she should check with her nurse or her doctor. Due date of second vaccination was reported as 12Apr2021 at 10:39 PM. Outcome of events were unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: BRIVIACT

Current Illness:

ID: 1773805
Sex: U
Age:
State:

Vax Date: 03/17/2021
Onset Date: 03/17/2021
Rec V Date: 10/09/2021
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 consumer (patient). A patient, of an unspecified gender and age, received the 2nd dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, solution for injection, batch/lot# unknown), via an unspecified route of administration, on Mar 17, 2021, single dose, for COVID-19 immunization. The patient previously received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine), via an unspecified route of administration, on Feb 20, 2021, single dose, for COVID-19 immunization. Medical history and concomitant medications not reported. On Mar 17, 2021, patient experienced diarrhea, headache, vomiting, muscle pain, tiredness and a little bit of fever (not much). The evening of the Mar 17, 2021, adverse events took place. The patient did not want to know anything and just wanted to inform of the adverse effects after getting the second shot. The patient just wanted to report illness/ill effects after the 2nd shot. They experienced mostly everything on list: diarrhea, vomiting, headache, muscle pain, tiredness and little bit of fever (not much). The outcome of the events: unknown. No follow-up attempts needed. Information about batch/lot number cannot be requested. No further information expected.

Other Meds:

Current Illness:

ID: 1773806
Sex: F
Age:
State:

Vax Date: 03/16/2021
Onset Date: 03/18/2021
Rec V Date: 10/09/2021
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: post nasal drip; Eczema; Rash; Pressure behind ear/some pressure in her ear; underneath chin swelling; This is a spontaneous report from a contactable Consumer or other non-health professional (Patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Lot number: not reported, Expiry date: not reported) via an unspecified route of administration on 16Mar2021 as a dose number unknown, single for COVID-19 immunization. The patient medical history included dermatitis, seasonal allergies (that are pretty bad), ear infections all are from an unknown date unknown if ongoing. Concomitant medication included Zyrtec (Lot number and expiration date: unknown via unspecified route of administration from an unknown date indicated for allergy to an unspecified stop date. Allegra 180mg once daily via unspecified route of administration from a specified date in 2021 indicated for allergy unknown if ongoing (Count size is 90 and there was no seal). Patient stated this was keeping her from panicking. She just started taking Allegra for 3 days. The Zyrtec maybe was not helping, and the doctor said maybe she should change so she did. They switched her allergy medication from Zyrtec to Allegra. It was reported that on 18Mar2021 patient felt like she had some pressure in her ear and underneath chin swelling. On an unspecified date It might have felt like it was, but they said it was postnasal drip. On 24Mar2021, patient woke up with a rash and a lot of pressure in her ear. The rash was not spreading on her neck. It was just one side and one spot on chest below her neck. It almost looked like Eczema. Her ENT did not think they are related. He does not think ears are related to red splotches because she has had ear infections in the past. She has a blocked tube in ear. It did not look like she had an ear infection. But there is fluid in it. This was after the vaccine. She went in this morning. She has not taken an Allegra today because she was not sure what the doctors would have her take when she went to see them today. He said it looked like Eczema. She has not been diagnosed with Eczema but does have contact dermatitis. Patient would like to know if she should take second one. It was not really a rash. There was a Product Complaint. It was reported that, she could not see anyone and someone said to take Benadryl, but it did not help. She did not change anything. She provided Lot SFM061, Expiration May2022. Dose is 5-10 mg. She took 10 ml. Total size in 1 bottle is 118ml. She would be willing to send a sample. She would be willing to send a sample. It was sealed and intact. Outcome of all the events were unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds: ALLEGRA ALLERGY

Current Illness:

ID: 1773807
Sex: F
Age:
State: NC

Vax Date: 03/22/2021
Onset Date: 03/23/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: High fever; Extreme shaking; Sore arm; Extreme chills; Swollen lymph nodes under arms; This is a spontaneous report received from a contactable consumer. A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration on 22Mar2021 as a dose 2, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration on an unspecified date as a dose 1, single for COVID-19 immunization. It was reported that, the consumer would like to report an adverse event for the COVID-19 vaccine (dose 2). Stated that, this was reported last night by the patient to the reporter. Stated that, she did not report adverse side effects with dose 1. On 23Mar2021 (starting 24 hours after treatment), the patient experienced high fever, extreme shaking (starting 24 hours after injection, subsided after overnight rest) and sore arm, extreme chills, swollen lymph nodes under arms starting (24 hours after injection, ongoing). The outcome of the events for high fever, extreme shaking was recovered on an unspecified date in Mar2021 while for the other events was not recovered. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1773808
Sex: M
Age:
State: NY

Vax Date: 03/17/2021
Onset Date: 03/01/2021
Rec V Date: 10/09/2021
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: in his mouth it is like very sensitive where his teeth would meet; have little pimples coming out; oral sores in his mouth that he can feel like they are poking out.; in his nostrils there are little bumpy areas that come out; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 48-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, batch/lot number: EN6Z04 and NDC/expiry date were unknown) via intramuscular route of administration, administered in left arm on 17Mar2021 11:30 as single for COVID-19 immunization. Medical history and concomitant medication were not reported. On an unspecified date in Mar2021 patient experienced little pimples coming out which are not a big deal but he wanted to see if this is from the vaccine; states he also has oral sores in his mouth that he can feel like they are poking out. Patient states that he has pimples and they are kind of more on his chest and stomach and there are some pimples on his arms and he noticed in his mouth it is like very sensitive where his teeth would meet; caller states this could be natural or related to the vaccine or could be a rash effect; states in his nostrils there are little bumpy areas that come out and are not crazy but he messes with them but maybe they are there because he has gotten the vaccine; states the pimples began this weekend and he just recognized them a couple of days ago on Saturday or Sunday and the pimples and sensitivity where his teeth would meet started probably on Friday 19Mar2021. Patient had no family medical history relevant to adverse events. Patient did not had any treatment for the reported events but it was just him picking at the pimples and squeezing them out and they are tiny and not a big deal but he wanted to see if this was normal. The patient had not received any other vaccine within 4 weeks. The outcome of events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1773809
Sex: M
Age:
State: TX

Vax Date: 03/21/2021
Onset Date: 03/01/2021
Rec V Date: 10/09/2021
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: skin flaking around hair follicles most noticeably around facial hair; mild headaches; Occasional nerve pain/tingling in left arm; Occasional nerve pain/tingling in left arm; joint pain more pronounced after second dose lasted about 3 days; This is a spontaneous report received from a contactable 35-year-old male consumer (patient) that reported. A 35-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in Left arm on 21Mar2021 at 02:00 Pm (at the age of 35-years-old) as dose 2, single for covid-19 immunisation. The medical history included Ehlers-Danlos Syndrome from an unknown date and unknown if ongoing, (POTs) postural orthostatic tachycardia syndrome from an unknown date and unknown if ongoing, High blood pressure from an unknown date and unknown if ongoing, (CACS) arteriosclerosis coronary artery from an unknown date and unknown if ongoing Coronary Artery Calcium score, thoracic outlet syndrome from an unknown date and unknown if ongoing, chronic fatigue syndrome (CFS) from an unknown date and unknown if ongoing, (OA) osteoarthritis from an unknown date and unknown if ongoing, Allergy to Neoprene and Legumes from an unknown date and unknown if ongoing. The concomitant medications included paracetamol (TYLENOL) taken for an unspecified indication, start and stop date were not reported, ibuprofen (IBUPROFEN) taken for an unspecified indication, start and stop date were not reported, hydroxychloroquine (HYDROXYCHLOROQUINE) taken for an unspecified indication, start and stop date were not reported and meloxicam (MELOXICAM) taken for an unspecified indication, start and stop date were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: Unknown), via an unspecified route of administration, administered in Arm Left on 28Feb2021 09:15 am (at the age of 35-years-old) as dose 1, single for covid-19 immunisation and experienced skin flaking around hair follicles, headache and joint pain. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 21Mar2021, the patient experienced skin flaking around hair follicles most noticeably around facial hair, mild headaches, Occasional nerve pain/tingling in left arm. On an unspecified date on Mar2021, the patient experienced joint pain more pronounced after second dose lasted about 3 days. The patient reported that Occasional nerve pain/tingling in left arm that lasted about 2 hours after second dose, skin flaking around hair follicles most noticeably around facial hair occurred with both doses last around three days, mild headaches with both doses lasted only one day, joint pain more pronounced after second dose lasted about 3 days. The patient did not receive any treatment. The l outcome of the events was recovered on an unspecified date in Mar2021. No follow-up attempts needed. No further information is expected.

Other Meds: TYLENOL; IBUPROFEN; HYDROXYCHLOROQUINE; MELOXICAM

Current Illness:

ID: 1773810
Sex: F
Age:
State: FL

Vax Date: 02/16/2021
Onset Date: 02/01/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Rash, palms of both hands and around fingers; Peeling of skin on palms of both hands and around fingers; Itching to palms of both hands and around fingers; This is a spontaneous report from a contactable consumer (patient). A 24-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, Lot Number: E19269) via an unspecified route of administration in right upper arm on 16Feb2021 at 13:00 (age at vaccination 24 year) as dose 1, single for COVID-19 immunization. Vaccine was offered to her. First week at new company they offered it and she said yes. she wasn't on any medications that she wasn't already taking for years already, so no concomitant medications. Medical history was not reported. Prior Vaccinations (within 4 weeks) , AE(s) following prior vaccinations, Family Medical History Relevant to AE(s) were reported as None. On an unspecified date in Feb2021, the patient experienced rash, palms of both hands and around fingers, peeling of skin on palms of both hands and around fingers and itching to palms of both hands and around fingers. Therapeutic measures were taken as a result of rash, palms of both hands and around fingers, peeling of skin on palms of both hands and around fingers and itching to palms of both hands and around fingers. The patient went to the doctor that day who gave her a steroid cream (Triamcinolone 0.1 percent cream to use three times a day) to put on the peeling skin to help with the itching. NDC: 67877-251-30. Lot and Expiration date unknown. Patient visited physician office. The doctor was also the one who recommended that she call and report this event because it seemed related to the vaccine. she called because she just wants to report a reaction. States that when it appeared after her first vaccine she thought maybe she had gotten into something that caused it. Now that the rash has improved her skin was peeling in the area where the rash was on the palms of both hands and around the fingers. States after the first shot it was a small rash. Relevant Tests were reported as None. The outcome of the events rash, palms of both hands and around fingers and itching to palms of both hands and around fingers was recovering while the outcome of the rest of the event was not recovered. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773811
Sex: M
Age:
State: CT

Vax Date: 03/22/2021
Onset Date: 03/23/2021
Rec V Date: 10/09/2021
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: light cough; nausea; sore arm; Headache; This is a spontaneous report from a contactable consumer or other non hcp (parent). A 16-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number EP6955, Expiry date was not reported) via an unspecified route of administration, administered in Arm Left on 22Mar2021 15:45 (at the age of 16 years old) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications and were not reported. Patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient had not received any other vaccine within 4 weeks. The patient had not received any other medications within 2 weeks. On 23Mar2021 at 06:30, the patient experienced light cough, nausea, sore arm and headache. The reporter reported that, the patient on 23Mar2021 6:30a.m. woke up this morning with light cough, nausea and sore arm. 12pm - cough and nausea are resolved, but he has a headache. The patient did not received treatment for events. The reporter informed that the reporter became aware of the event on Tuesday, 23Mar when he awoke in the morning at approximately 6a.m. Outcome of cough and nausea was resolved on ??-???-2021 and that of other events was recovering. Follow-up (26Mar2021): This is a follow-up spontaneous report received in response to the mail trail sent regarding the confirmation below mentioned query. The response included information about date and time of vaccination and clinical information. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773812
Sex: M
Age:
State: MS

Vax Date: 03/24/2021
Onset Date: 03/24/2021
Rec V Date: 10/09/2021
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: short of breath; got weak and lightheaded like he could not go on; got weak; he did not know what was going on; pain through arm; could feel the pain where they stuck him; could feel the pain where they stuck him, this morning, it is now from his arm to his back; having back spasms and he is feeling that again; throwing up/threw up what he ate this morning/threw up twice; This is a spontaneous report from a contactable consumer, patient. A 31-years-old male patient received first dose of bnt162b2 (PFIZER BIONTECH COVID 19 VACCINE, formulation: solution for injection, lot number was not reported) via an unspecified route of administration, in arm left on 24Mar2021 at 10:00 as dose 1, single (age at vaccination 31 years) for covid-19 immunisation. Medical history included high blood pressure, that was taken care of, it was under control and was diagnosed around 2013, illness, he had covid, he was having back spasms. The history of previous immunizations was none. Concomitant medication(s) included cetirizine that he was taking for the illness, he started taking the same day as the other ones, he was not sure the exact date; amoxicillin that he was only on for probably 2 or 3 days, taken for illness; benzonatate taken for illness, it was reported that amoxicillin he took only once, and the other medication only twice and added this was for the same thing when he got sick. On 24Mar2021 the patient experienced pain through arm, once they gave him the shot, he came back and sat down and could feel the pain where they stuck him. This morning, it was now from his arm to his back on an unknown date in 2021. He added that it was like when he had covid he was having back spasms and he was feeling that again on an unknown date in 2021. It was off and on, he still felt it in his arm. Clarified as left arm. The patient reads gas meters, he was walking and got weak and lightheaded like he could not go on. He sat on the ground before it got worse on 25Mar2021. Someone had to come pick him up because he did not know what was going on, on 25Mar2021. Being lightheaded is still going on. It was the same because he was just lying in bed and not doing anything. On 25Mar2021 the patient was short of breath. When he sat down, everything calmed down. This was not still going on. Clarified that this occurred around 9 am today. On an unknown date in 2021 caller added that they came and picked him up and he had to walk to his vehicle to return the vehicle that he has for the company. As he was getting ready to leave, he threw up twice. He has not thrown up since. The patient stated they put him on antibiotics right before he got the vaccine. He added that he stopped taking those before he got the shot because he did not want to mix it. He stopped taking the mediations more than 2 weeks prior to him getting the vaccine. No therapeutic treatment was taken in response to the events. No additional vaccines were administered on same date as suspect. The events did not require visit to ER or physician office. There were no adverse evets following prior vaccinations. The patient was a military veteran. There were no relevant lab tests. The outcome of the events pain from his arm to his back and having back spasms was unknown, for rest of the events was not recovered and for short of breath and throwing up was recovered on an unknown date in 2021. No follow-up attempts are needed. information about lot/batch number cannot be obtained.

Other Meds: CETIRIZINE; AMOXICILLIN; BENZONATATE

Current Illness:

ID: 1773813
Sex: F
Age:
State: PA

Vax Date: 02/15/2021
Onset Date: 02/01/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Diffuse bumpy intensely itchy rash on left shin and calf after first vaccine/Rash continued to spread, right leg; Diffuse bumpy intensely itchy rash on left shin and calf after first vaccine/Rash continued to spread, right leg; This is a spontaneous report from a contactable consumer (patient). A 65-years-old non pregnant female patient received bnt162b2(PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection; lot number: EL9269and expiration date was not reported) via an unspecified route of administration in the left arm on 15Feb2021 09:45 (at the age of 65-year-old) as dose 1, single for covid-19 immunization. Medical history included hypertension and fibromyalgia. Concomitant medication included atenolol, simvastatin and diphenhydramine Hydrochloride, all for an unknown indication. The patient had history of erythromycin allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19 and did not receive any other vaccine within four weeks. The patient was not pregnant at the time of vaccination. After taking the first dose of vaccination, on an unspecified date of Feb2021 the patient experienced diffuse bumpy intensely itchy rash on left shin and calf after first vaccine/rash continued to spread, right leg. Patient was not tested positive for COVID-19 since the vaccination. Therapeutic measures in response to the events included, topical and oral steroids. The outcome of the events was not resolved at the time of report. Follow-up attempts are completed. No further information is expected.

Other Meds: SIMVASTATIN; ATENOLOL; DIPHENHYDRAMINE HCL

Current Illness:

ID: 1773814
Sex: F
Age:
State: CA

Vax Date: 02/06/2021
Onset Date:
Rec V Date: 10/09/2021
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: Itching all over the body/experienced this after getting the first vaccine; This is a spontaneous report from a contactable consumer (Patient) via a Pfizer. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number was not reported), dose 1 via an unspecified route of administration on 06Feb2021 as dose 1 single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date in 2021, the patient experienced itching all over the body and it became worse after receiving the second dose. On an unspecified date in 2021, the patient received the second dose. She thought that it was not a side effect of the COVID vaccine. Caller was asking about the side effects of the vaccine. The clinical outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1773815
Sex: F
Age:
State: CT

Vax Date: 03/22/2021
Onset Date: 03/22/2021
Rec V Date: 10/09/2021
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: Woke up at 5:45 with a headache; intermittent fever; feeling very tired; This is a spontaneous report from a contactable Consumer or other non-HCP (Parent). A 20-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Lot number: EP6955) via an unspecified route of administration, administered on Right arm on 22Mar2021 at 12 pm as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient was not pregnant at the time of vaccination. Medical history included Atopic Dermatitis. Patient had no known allergies. Concomitant medications were not reported. The patient had not received any other vaccine within 4 weeks. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 23Mar2021 at 05:45, the patient experienced "woke up at 5:45 with a headache" on 22Mar2021 at 12:00 am intermittent fever and feeling very tired. Patient did not receive any treatment for the events. Outcome of the event headache was recovered on 23Mar2021, outcome of other events was recovering. Follow-up (24Mar2021): This is a follow-up spontaneous report from a contactable consumer. This consumer reported for a patient included Information about adverse events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773816
Sex: F
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 10/09/2021
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: itching all over the body/experienced this after getting the first vaccine and it became worse after receiving the second dose; This is a spontaneous report from a contactable consumer (patient) via the Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (BNT162B2), via an unspecified route of administration on 06Feb2021 (Batch/Lot number was not reported) as DOSE 1, SINGLE; and via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE, 2 SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient received the second dose of Covid-19 vaccine already and said she is itching all over the body. She mentioned that she experienced this after getting the first vaccine (06Feb2021) and it became worse after receiving the second dose. She thought that it was not a side effect of the Covid vaccine. The outcome of the event unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1773817
Sex: M
Age:
State: FL

Vax Date:
Onset Date: 03/20/2021
Rec V Date: 10/09/2021
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: watery eyes itching redness in both eyes; watery eyes itching redness in both eyes; watery eyes itching redness in both eyes; blurred vision; This is a spontaneous report received from a contactable consumer (patient's spouse) for a male patient of unspecified age received bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number was not reported, 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 and concomitant medications were not reported. On 20Mar2021 the patient experienced watery eyes itching redness in both eyes, and blurred vision. Patient started with eye drops and by Tuesday vision was restored to normal. The outcome of the event blurred vision was recovered on an unspecified date, and other events was unknown. No follow-up attempts are needed. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021324852 Same reporter/ drug /AE, different patient

Other Meds:

Current Illness:

ID: 1773818
Sex: M
Age:
State:

Vax Date: 03/10/2021
Onset Date:
Rec V Date: 10/09/2021
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: Test Name: Body temperature; Result Unstructured Data: Test Result:had a temperature; Comments: had a temperature

Allergies:

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

Symptoms: Terrible smell in nose; Had a temperature; This is a spontaneous report from a contactable consumer or other non hcp (wife of the patient). A 75-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported, Expiry date was not reported) via an unspecified route of administration, administered on 10Mar2021 (at the age of 75 years old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included cancer from an unknown date and unknown if ongoing. The patient did not have constipation. The patient's concomitant medications were not reported. The reporter reported that on an unspecified date, the patient experienced terrible smell in nose and had a temperature. The patient had not been tested COVID yet. The patient had a temperature. Also mentioned for like five days he had a smell in his nose. No other symptoms. The patient received the shot on 10Mar2021. The second vaccine would be supposed to be the following Monday on 29Mar2021. The first symptoms started on Monday. He also has chemo and radiation, and it could be related according to caller. The issue that was bothering them was the event related to the smell. He was not losing his sense of smell, he has a smell in his nose that was now less. This started on Monday. The patient underwent lab tests and procedures which included body temperature which results into had a temperature on unspecified date. The outcome for the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1773819
Sex: F
Age:
State: CA

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

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: arm soreness; arm swollen; rash; This is a spontaneous report from a Pfizer sponsored program from a contactable consumer or other non hcp (Patient). A female patient of an unspecified age received bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, batch/Lot number and expiration date was not reported) via an unspecified route of administration on 09Mar2021 as dose number unknown, single for COVID-19 immunization. Medical history included diabetes mellitus and she had broken blood vessels in her eye on the side that she got the vaccine. Concomitant medication(s) included clopidogrel bisulfate (PLAVIX) taken for she had broken blood vessels in her eye on the side that she got the vaccine. The patient had arm soreness and arm swollen and rash lasted few days on an unspecified date in Mar 2021. The event outcome for soreness in arm, arm swollen, and rash was reported as recovered on unspecified date of 2021. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds: PLAVIX

Current Illness:

ID: 1773820
Sex: F
Age:
State: MA

Vax Date: 03/20/2021
Onset Date: 03/22/2021
Rec V Date: 10/09/2021
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: 202012; Test Name: Covid test; Result Unstructured Data: Test Result:Negative; Comments: pretty sure she had Covid, but the test came back negative, she had all the symptoms.

Allergies:

Symptom List: Injection site pain

Symptoms: Both hands swelled up; Hives; Lip swelled; Tongue swelled up a little; Couldn't talk; Muscle pain and aches, ached all over; Didn't feel so good; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received bnt162b2 (PFIZER BIONTECH COVID-19 vaccine, Formulation: Solution for injection, Lot number: EP6955, Expiration date: unknown) via an unspecified route of administration, administered in arm left on 20Mar2021 (at the age of 67-year-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history included COVID (patient dad died of COVID and other family members had covid) from an unknown date and unknown if ongoing. There were no concomitant medications reported. The patient had no prior vaccinations within 4 weeks. The patient did not administer any additional vaccines on same date of the pfizer suspect. Historical vaccine included flu vaccine which led to arm ached and muscle ached from an unspecified date in Sep2020 (at the age of 66-year-old). On 22Mar2021, the patient didn't feel so good. On the same day at 01:00, the patient experienced muscle pain and aches, ached all over. On 23Mar2021, she was there alone with nobody to talk to during the day. She went to facetime one of her sister's and she could hardly talk. On the same day at 10:00 in the morning, the patient's lip swelled and tongue swelled up a little. On 24Mar2021, around 8 to 9 o'clock, in the morning, the patient both hands swelled up and hives. Caller stated that on monday, she didn't feel so good, but she said that was expected. She reported on tuesday, her lip swelled up and her tongue swelled up a little. She couldn't talk in the afternoon, for some reason, her voice, she didn't know. By 5 pm, her voice got better. Yesterday, her hand swelled up, later clarified as both her hands swelled up. She also had hives. Caller asked, OK, she wanted to make sure she could get the second shot, should she be worried about getting the second shot. The patient underwent lab tests and procedures which included SARS-CoV-2 test: negative (she was pretty sure she had covid, but the test came back negative, she had all the symptoms) on an unspecified date in Dec2020. The patient did not visited emergency room and physician office for the adverse events. The patient was treated with benadryl (Lot: 1805142 & Expiration: Aug2022) last night as a therapeutic measure of hives. On 23Mar2021, the patient recovered from didn't feel so good, muscle pain and aches, ached all over, lip swelled, tongue swelled up a little and couldn't talk. The outcome of the events both hands swelled up and hives was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773821
Sex: M
Age:
State: SC

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 10/09/2021
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: it was like a vagal reaction; gets confused at times; felt nauseous and wanted to vomit; Weaker; Blood pressure dropped; This is a spontaneous report from a contactable Nurse. This Nurse reported for a 90-year-old male patient (husband) that he received bnt162b2 (BNT162B2 Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 10Mar2021 13:30 (Batch/Lot number was not reported) as 1st dose, single for covid-19 immunisation (90-years at the age of vaccination). Medical history included ongoing diabetes mellitus Verbatim: Diabetes Additional Information for Other Conditions: Started 30-40 years ago , ongoing hypertension Verbatim: High Blood Pressure Additional Information for Other Conditions: Started 30-40 years ago. There were no concomitant medications. The patient experienced felt nauseous and wanted to vomit, weaker and blood pressure dropped on 10Mar2021, it was like a vagal reaction and gets confused at times on an unspecified date. He received his first Covid shot on 10Mar2021. Reporter states five minutes after the shot the patient said he felt nauseous and wanted to vomit and his blood pressure dropped. Reporter states the patient ended up in the ER. Reporter states that the patient is on hospice at home. Reporter states they took him to the pharmacy for the first vaccine and he has another appointment to go on 31Mar2021. Reporter asks for the number of the pharmacy vaccination site to call to see if they can call and delay the second vaccine The outcome of the events felt nauseous and wanted to vomit, Blood pressure dropped was resolved on 10mar2021, Weaker was resolving and other events was Unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness: Blood pressure high (Verbatim: High Blood Pressure Additional Information for Other Conditions: Started 30-40 years ago); Diabetes (Verbatim: Diabetes Additional Information for Other Conditions: Started 30-40 years ago)

ID: 1773822
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/09/2021
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: Nosebleed; nausea; muscle soreness; This is a spontaneous report from a contactable consumer (patient). A 29-year-old male patient received BNT162B2 (Pfizer-BioNTech COVID-19 vaccine), via an unspecified route of administration on an unspecified date (lot number was not reported) as dose number unknown, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced nosebleed, nausea and muscle soreness 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. No further information is expected.

Other Meds:

Current Illness:

ID: 1773823
Sex: F
Age:
State:

Vax Date: 03/24/2021
Onset Date: 03/25/2021
Rec V Date: 10/09/2021
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: 20210325; Test Name: body temperature; Result Unstructured Data: Test Result:100.8; Comments: 100.8

Allergies:

Symptom List: Tremor

Symptoms: severe headache; fever of 100.8; chills; joint aches; swollen lymph nodes on left side neck; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EK5730), via an unspecified route of administration, administered in Left arm on 24Mar2021 11:15 (at the age of 58 year) as dose 2, single for COVID-19 immunisation. Medical history included, allergies to sulpha drugs. Concomitant medications included carvedilol, losartan, and levothyroxine, all for an unspecified indication. The patient was not pregnant at the time of vaccination. Prior vaccination, patient did not receive any other vaccines within four weeks and had not diagnosed COVID-19. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number EJ1685, via an unspecified route of administration in left arm, on 04Mar2021 11:00 (at the age of 58 year), as single dose for COVID-19 immunization. On 25Mar2021, patient had severe headache, fever of 100.8, chills, joint aches, and her lymph nodes on left side neck swollen. Since vaccination, patient had not been tested COVID-19. No treatment was given in response to the events. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: CARVEDILOL; LOSARTAN; LEVOTHYROXINE

Current Illness:

ID: 1773824
Sex: F
Age:
State: CA

Vax Date: 03/22/2021
Onset Date: 03/23/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: fatigue.; Fever; aches; dizzy; This is a spontaneous report from a contactable consumer. An adult female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number, expiration date was not reported) via an unspecified route of administration, on 22Mar2021, at dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number, expiration date was not reported) via an unspecified route of administration, on an unspecified date, at dose 1, single for covid-19 immunization. The patient experienced fatigue, fever, aches, dizzy on 23Mar2021 02:00. The outcome of the events was recovering. Follow-up (26Mar2021): New information received from same contactable consumer includes: The event awareness date confirmed as 23Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773825
Sex: F
Age:
State: ME

Vax Date: 02/22/2021
Onset Date: 02/25/2021
Rec V Date: 10/09/2021
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: feeling under the weather; has this hoarseness in her voice whenever she speaks; coughing; not feeling well during the morning; This is a spontaneous report from a contactable consumer or other non hcp (patient) from Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: not reported), dose 2 via an unspecified route of administration on 22Feb2021 as dose 2, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: not reported), via an unspecified route of administration, administered on 01Feb2021 as dose 1, single for COVID-19 immunisation. received her 1st vaccine on 01Feb2021 and her 2nd vaccine on 22Feb2021. On 25Feb2021, the patient experienced feeling under the weather, has this hoarseness in her voice whenever she speaks, coughing. On an unspecified date in 2021, the patient was not feeling well during the morning. However, upon talking reported that she experienced feeling under the weather after 3 days of receiving the 2nd vaccine.she was not feeling well during the morning. However, that did not last very long as she felt a little better later that afternoon. Consequently, had this hoarseness in her voice whenever she speaks accompanied by coughing. Referred to the local health authority/vaccination facility for her lost card. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773826
Sex: F
Age:
State: DE

Vax Date: 03/05/2021
Onset Date:
Rec V Date: 10/09/2021
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: Chest Xray; Test Result: Negative ; Comments: My family doctor who ordered a chest Xray; Test Name: Xrays; Test Result: Negative ; Comments: My dentist, who did Xrays

Allergies:

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

Symptoms: Developed swelling of my cheeks and under my chin; This is a spontaneous report from a contactable consumer (patient) received via program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number was not reported), via an unspecified route of administration on 05Mar2021 as dose 2, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number unknown, via an unspecified route of administration on 12Feb2021, as single dose for COVID-19 immunization. On an unspecified date, patient had developed swelling of cheeks and under the chin, looks like, chip monk cheeks. The patient saw her family doctor. The patien underwent lab tests and procedures which included on an unspecified date, chest x-ray and x-ray, both were negative. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773827
Sex: F
Age:
State: KS

Vax Date: 03/18/2021
Onset Date: 03/19/2021
Rec V Date: 10/09/2021
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: 20210319; Test Name: fever; Result Unstructured Data: Test Result:99.4; Test Date: 20210320; Test Name: fever; Result Unstructured Data: Test Result:went up to 99.6

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: I am little bit kind of blurred vision because I normally look at my key board and I do not need my glasses until I look at the computer screen; I thought I almost had the flu then having this looming tension headache on the left side in my temporal area and on the right of the forehead or top of the crown; I am not back to myself physically and I also feel little foggy in the head; I thought I almost had the flu then having this looming tension headache on the left side in my temporal area and on the right of the forehead or top of the crown; I don't feel my energy has come back; ache and pain; I have began having a fever about 99.4 which went up to 99.6 on Saturday; I just also had diarrhea and I just do not feel well; I was extremely tired and my equilibrium was off on Friday; I just also had diarrhea and I just do not feel well; I was extremely tired and my equilibrium was off on Friday; This is a spontaneous report from a contactable consumer (Patient reported for herself). A 59-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: EN6206; Expiration date: 30-JUN-2021) via unspecified route of administration, on 18Mar2021 (at the age of 59-year-old) as a dose 1, single for COVID-19 immunization. The patient medical history included occasional cold or may be sinus infection. The concomitant medication of the patient was not reported. On 19Mar2021 the patient experienced diarrhea and patient just do not feel well. Patient stated that she was extremely tired and her equilibrium was off on Friday. On 20Mar2021 the patient begun having a fever about 99.4 which went up to 99.6 on Saturday. Patient also reported that on an unspecified date she almost had flu then having this looming tension headache on the left side in her temporal area and on the right of the forehead or top of the crown. Patient stated that she was not back to herself physically and also feel little foggy in the head and this could be surprise to her which tributary to the vaccination. Patient wanted to wait it out and see how her headache was going away. Patient was taking Tylenol every day, 6 hours part and was even awakened in the night to make sure to take the Tylenol. Patient was getting little bit of relief tension headache and felt like it gets little better and it comes on again. Patient reported that she started feeling achy and pain and took Advil (liquid gel) 200 mg each. Patient stated that she don't feel her energy has come back, patient felt like she was exerting herself because her room was on the second level of school and after come up the stairs she was gasping more, its consistent and felt more tired like yesterday. Patient came home and tried to cook dinner and started feeling light headed and wanted to lay down. Patient also reported that she had little bit kind of blurred vision because she normally looked at her key board and do not need her glasses until patient look at the computer screen but even the computer board and print patient needed to put glasses on now so patient was having a little bit of what she called blurred vision. The patient received the treatment of Tylenol capsule 500 mgs primarily for the headache, twice a day and Advil (liquid gel) 200mg each for ache and pain. The patient underwent lab tests and procedures which included Body temperature: on 19Mar2021 it was 99.4 and on 20Mar2021 it was 99.6. 2nd shot was due on 08Apr2021. Outcome of the event tiredness was not recovered and that of the other events were unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773828
Sex: F
Age:
State:

Vax Date: 03/25/2021
Onset Date: 03/01/2021
Rec V Date: 10/09/2021
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 all over/I am itching/My feet itch, my leg itch, my head itch, my arm itch, and my back itch; feeling like I am itching all over; feels a little sluggish; just getting little anxious; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 69-year-old female patient received BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot/batch number: ER8730 and expiry date was not reported), via an unspecified route of administration, on 25Mar2021 at 02:00 PM, as a dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unknown date in Mar2021 the patient experience itching all over and she feels a little sluggish. It was reported that the patient felt like she was having a bit of allergic reaction or something because she was itching. The patient reported that she did not had any redness at the site or anything, but she woke up last night about at 2 o'clock and even still this morning she felt like she was having a bit of allergic reaction or something because she was itching. Reportedly her feet, leg, head, arm and back itch. The patient reported that she was feeling like she was itching all over. The patient stated that she was just getting little anxious. In response to further probing, the patient queried can you tell me are these side effects from this? The patient did not understand what they were saying. It makes her itch; The patient was just getting little anxious because she can't understand what they were asking her. She needs to know how she should know about the side effects if these are normal or not. 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: 1773829
Sex: F
Age:
State:

Vax Date: 03/19/2021
Onset Date: 03/01/2021
Rec V Date: 10/09/2021
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: Test Date: 202103; Test Name: Fever; Result Unstructured Data: Test Result:99.9 Fahrenheit

Allergies:

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

Symptoms: Dry heavy cough; Fever; This is a spontaneous report from a non-contactable consumer (patient) from medical information team. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number, expiration date was not reported) via an unspecified route of administration, on 19Mar2021, at dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number, expiration date was not reported) via an unspecified route of administration, on an unspecified date, at dose 1, single for covid-19 immunization. The patient experienced dry heavy cough and fever on Mar2021. The patient underwent lab tests and procedures which included body temperature: 99.9 Fahrenheit on Mar2021. The outcome of the event was unknown. Follow-up (26Mar2021): No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773830
Sex: F
Age:
State: TX

Vax Date: 03/18/2021
Onset Date: 03/18/2021
Rec V Date: 10/09/2021
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: joint pain; bone pain; muscle pain; tiredness; fever; feeeling of warm from inside out the body; irritation in the throat and the sensation of a foreign body in the throat; irritation in the throat and the sensation of a foreign body in the throat; nausea; headache; eye pain; general discomfort; This is a spontaneous report from a contactable consumer (patient). A 57-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection and batch no, lot number and expiration date was not reported), first dose via an unspecified route of administration on 18Mar2021 (at the age of 57 year) as for covid-19 immunization. Medical history included cancer (patient was cancer survivor), ongoing osteoporosis. Concomitant medications included ergocalciferol (VIT D) and calcium taken for osteoporosis. Since vaccination, on 18Mar2021, patient has been presenting with joint pain, bone pain, muscle pain, tiredness, fever and the feeling of warm from inside out the body, throat irritation and the feeling of foreign body in the throat, nausea, headache, eyes pain and general discomfort. Patient reported she has been taking Tylenol at nights to manage the symptoms but as the evening arrives, symptoms are coming back and 8 days after vaccination has not disappeared. Patient reported she has not gone to the physician for management of prior symptoms. Therapeutic measures were taken as a result of all events and included treatment with Tylenol. The outcome of the events was unknown. No follow-up attempts are possible;information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: VIT D; CALCIUM

Current Illness: Osteoporosis (taked several medications to treat Osteoporosis)

ID: 1773831
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: Soreness on her arm; A little tiny rash (6 little dots that felt itchy.); Feel an itchy sensation on her leg, and arm; This is a spontaneous report from a contactable consumer or other non-healthcare professional (Patient herself). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number-UNKNOWN) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced those 2 days after receiving the 1st dose of the Pfizer-BioNTech Covid-19 Vaccine soreness on her arm, A week later a little tiny rash (6 little dots that felt itchy), feel an itchy sensation on her leg, and arm. Reporter wants to know how effective the Pfizer-BioNTech Covid-19 Vaccine would be with just one dose and if she could still receive the 2nd dose of the Pfizer-BioNTech Covid-19 Vaccine later than the recommended 3-week-interval if in case she decides to postpone her original schedule. The outcome of event soreness on her arm, feel an itchy sensation on her leg, and arm was unknown, a little tiny rash (6 little dots that felt itchy) was recovered. No follow-up attempts are Possible. Information on lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1773832
Sex: F
Age:
State: AZ

Vax Date: 03/21/2021
Onset Date: 03/24/2021
Rec V Date: 10/09/2021
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: pressure headache; cause her pain in her ears; cause her pain in her eyes; cause her pain in her neck; Sore Throat; coughing; sneezing; sinus infections; This is a spontaneous report from a contactable consumer (Patient). A 69-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on 21 Mar2021 as dose second, single for COVID-19 immunization. The patient medical history included sinus infection. Concomitant medications were not reported. On 24Mar2021, the patient experienced sinus Infections which cause her pain in her ears, eyes, neck, sore throat and coughing and sneezing. The patient reported that, that she had chronic recurring sinus infections for the last 25 years and she believes that she was having a sinus infection right now. She felt that her sinus infection was related to the Pfizer COVID-19 vaccine, however, she would like to know if she can take Augmentin or if it will interact with the vaccine causing it to be less effective. Has one pill left over from a previous time and wanted to go ahead and start taking something for her sinus infection while she was waiting for her doctor to call back but did not want to deactivate the vaccine. She also stated that she had a pressure headache and would like information on taking Tylenol or Naproxen to help with her headache. She states she did not feel like her headache from receiving the second dose of the vaccine, but rather, pressure from her sinuses. Outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773833
Sex: F
Age:
State: NY

Vax Date: 03/14/2021
Onset Date:
Rec V Date: 10/09/2021
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 Date: 202011; Test Name: Colonoscopy; Result Unstructured Data: Test Result:Unknown; Comments: Diverticulitis causing wall of descending loop to inflame.; Test Date: 202103; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: Normal; Test Date: 202103; Test Name: HDL; Test Result: 75 mg/dl; Test Date: 202103; Test Name: LDL; Test Result: 225 mg/dl; Test Date: 202011; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Unknown; Comments: Negative

Allergies:

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

Symptoms: SLE flare up; pressure went up; Face got red; This is a spontaneous report from a contactable consumer. A 69-year-old female patient received BNT162B2 (Batch/Lot Number: EN6205; Expiration Date: Jun2021), intramuscular, administered in Deltoid Left arm on 14Mar2021 11:30 as dose 2, single for COVID-19 immunisation. Medical history included systemic lupus erythematosus from 2011, intestinal blockage from Jul2019 to Sep2019 (had surgery to repair intestinal damaged septum; Hospital 1 month, ICU 10 days), diverticulitis from Sep2020. Concomitant medications included ongoing metoprolol succinate for heart beat from 2014; ezetimibe for cholesterol from 2020; pantoprazole for stomach from 2019; and 2 weeks prior to 2nd dose for a week, she took metronidazole; dicyclomine and ciprofloxacin for an unspecified indication. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number 21Feb2021, intramuscular, in left arm, as single dose for COVID-19 immunization and the patient experienced on and off diverticulitis flare up, SLE flare up, red face, BP high, Burning sensation in Face and trembling. On an unspecified date, after second dose of vaccine, her pressure went up, face got red but not bad as before (when he had after first dose) and also reported that she had a minor flare up from her lupus. The patient underwent lab tests and procedures which included on Nov2020, colonoscopy had done and found polyps, diverticulitis causing wall of descending loop to inflame, and took COVID test where result was negative, on Mar2021 her electrocardiogram showed normal , where HDL was 75 mg/dl, and LDL was 225 mg/dl. The events resulted in physician office visit. The patient was put on antibiotics for diverticulitis flare up. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: METOPROLOL SUCCINATE; EZETIMIBE; PANTOPRAZOLE; METRONIDAZOLE; DICYCLOMINE; CIPROFLOXACIN

Current Illness: SLE flare (Really had flare on day of 1st vaccine still going on.)

ID: 1773834
Sex: F
Age:
State: NY

Vax Date: 03/19/2021
Onset Date: 03/19/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Saw some sparkles; Red veins arounds her eyes; Hot like burning on the eyes; This is a spontaneous report from a contactable consumer (patient). A 38-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection,Lot Number: ER8727 ), dose 1 via an unspecified route of administration on 19Mar2021 (at the age of 38-years-old) as dose 1, single for covid-19 immunization at hospital. Relevant medical history was reported as None. History of all previous immunization with the Pfizer vaccine considered as suspect was reported as none.Concomitant medications were not reported. Patient did not have family history. Prior to vaccinations (within 4 weeks) patient received MMR vaccine three weeks ago for immunization (at the age of 37-years-old). It was reported that vaccine was not administered at military facility.On 19Mar2021, after having the vaccine, patient saw some sparkles for just a few seconds and felt some hot like burning on the eyes just at that moment and then red veins arounds her eyes appeared. Now she was having red veins around the eyes that were not going away. None of the AE required patient to visit emergency room or physician office. Patient was asking for someone to explained to her what happened. she was scheduled to received the next dose of the vaccine on 09Apr2021. The outcome of event for red veins around her eyes was not recovered. The outcome of the rest of the events was recovered on 19March2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773835
Sex: F
Age:
State: PA

Vax Date: 03/23/2021
Onset Date: 03/23/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data: Test Date: 20210324; Test Name: fever; Result Unstructured Data: Test Result:103 Fahrenheit

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: her upper arm became swollen and red.3 inches x 3 inches; her upper arm became swollen and red.3 inches x 3 inches; fever; chills; Her arm, at the injection site has a big, red ring, it's hot and swollen; Her arm, at the injection site has a big, red ring, it's hot and swollen; Her arm, at the injection site has a big, red ring, it's hot and swollen; arm was burning when shot went in; weakness; wakes up sweating, like her clothes are drenched; tired; body aches; This is a spontaneous report from a contactable consumer (patient). A 60-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number ER8730 and expiry date not reported ),via an unspecified route of administration, administered in Arm Left on 23Mar2021 11:30 (at the age of 60 years old)as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications was not reported. Family medical history to any adverse event is no. The patient did not receive any other vaccine in last 4 weeks except Pfizer dose 1. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number Lot#EN6199 and expiry date not reported ),via an unspecified route of administration, administered in Arm Left on 02Mar2021 (at the age of 60 years old)as dose 1, single for COVID-19 immunization. After first dose she had a sore arm for about 3 days, that's it, nothing else .The patient had vaccination for prevention from Covid. She got the Covid 19 vaccine at 11:30AM on 23Mar2021. The patient had experienced on an unspecified date her upper arm became swollen and red.3 inches x 3 inches, on 23Mar2021 10:30PM fever, chills, her arm, at the injection site has a big, red ring, it's hot and swollen, arm was burning when shot went in, weakness, body aches, wakes up sweating, like her clothes are drenched, tired. The patient reported that she had fever and body aches at 10:30PM and she knows that's normal in the night at 4:00AM the next morning, 24Mar2021 it was up to 103F. She had chills also but figures the chills went with the fever. She also reports when the Covid 19 vaccine first went in her arm, her arm was burning. It lasted around a few minutes then the burning feeling went away. She told the employee at the facility where she received the vaccine that her arm burned. After the 15 minute waiting period was over, the employee asked if her arm was still burning and she said no, it's better. She had the fever for 2 full days and hasn't had one since. She feels like if she does something she'll get tired. She wakes up sweating, like her clothes are drenched. In the daytime she gets tired, if she tries to do something she has this weakness. She has a picture of her arm if we need it. Her arm was hurting a lot the night after she received the Covid 19 vaccine. It started that night about 12 hours afterwards. Her arm hasn't changed at all. She's been putting ice on it hoping it will go away. When you touch her arm it's hot. Her arm, at the injection site has a big, red ring, it's hot and swollen. Is that normal. She's heard it's called the Covid arm. She's been waiting every day for her arm to get better. Sometimes during the day she feels a little sweaty. The patient did not visit physician office or emergency room nor hospitalized. The patient experienced Fever from 23Mar2021 to 25Mar2021,body aches from 23Mar2021,chills from 23Mar2021 to 25Mar2021,Her arm, at the injection site has a big, red ring, it's hot and swollen from 23Mar2021,arm was burning when shot went in from 23Mar2021 to 23Mar2021,weakness from 23Mar2021 ,wakes up sweating, like her clothes are drenched from 23Mar2021,tired from23Mar2021. The patient underwent lab tests and procedures which included body temperature: 103 Fahrenheit on 24Mar2021. The patient did not visited emergency room and physician office. The outcome of the events her upper arm became swollen and red.3 inches x 3 inches was unknown, fever, chills on 25Mar2021 was recovered, her arm, at the injection site has a big, red ring, it's hot and swollen was not recovered, arm was burning when shot went in on 23Mar2021 was recovered, weakness, body aches was recovering, wakes up sweating, like her clothes are drenched, tired was not recovered. Follow-up (26Mar2021)This is a follow-up spontaneous report from a contactable consumer A 60-year-old female patient includes: Suspect dose start date added, New events added, Clinical information, patient age added. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1773836
Sex: F
Age:
State: OK

Vax Date: 02/04/2021
Onset Date: 02/11/2021
Rec V Date: 10/09/2021
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: Test Name: Calcium; Result Unstructured Data: Test Result:decreased; Comments: Calcium decreased Onset Date: Age 73; Test Name: Electrolytes; Result Unstructured Data: Test Result:ok; Comments: Age 73 Can't take calcium because it causes constipation.; Test Name: Chest X-Ray; Result Unstructured Data: Test Result:Ok; Comments: Age 46 Chest hitting Steering wheel; Test Name: CAT Scan; Result Unstructured Data: Test Result:ok; Comments: Age 46 Subdural Hematoma due to severe seizure; Test Name: EEG; Result Unstructured Data: Test Result:Unknown results; Comments: Age 4; Test Name: EEG; Result Unstructured Data: Test Result:Unknown results; Comments: Age 10; Test Name: EEG; Result Unstructured Data: Test Result:Unknown results; Comments: Age 18; Test Name: CBC chem 12; Result Unstructured Data: Test Result:ok; Comments: Cholesterol increased, Onset Date: Age 73

Allergies:

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

Symptoms: itching; Got a bad rash all over my body; This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number: EL9264, expiration date was not reported) via intramuscular route, in left arm, on 04Feb2021 15:00 (at the age of 74-years-old), at dose 1, single for covid-19 immunization. Medical history included epilepsy from 1950 and ongoing (age 4- 1950), ongoing blood pressure increased (onset age: 45-50), ongoing increased cholesterol (onset Age: 60-65), ongoing hypothyroidism (onset age:70), Epileptic Seizures from an unknown date to 18Feb2020; had a lot of seizures but haven't had any since 18Feb2020, last year 2020, subdural hematoma. Concomitant medications included atorvastatin taken for cholesterol from 2007 and ongoing; clonidine taken for blood pressure from 2004 and ongoing; gabapentin taken for Epileptic Seizures from 13Mar2019 and ongoing; levetiracetam taken for Epileptic Seizures from 13Mar2019 and ongoing; levothyroxine taken for hypothyroidism from 2007 and ongoing; metoprolol tartrate taken for blood pressure from 2004 and ongoing; primidone taken for Epileptic Seizures from 20May1964 and ongoing. The patient experienced got a bad rash all over the body on 11Feb2021, itching on an unspecified date. The event rash all over the body resulted in physician office visit on 12Feb2021. The patient underwent lab tests and procedures which included blood electrolytes: ok; at age 73; could not take calcium because it causes constipation (as reported). , chest x-ray: ok on age 46; chest hitting steering wheel, CAT (computerized tomogram): ok on Age 46; subdural hematoma due to severe seizure, EEG (electroencephalogram): unknown results on age 4 ;unknown results on age 10; unknown results on age 18, full blood count: ok on cholesterol increased, onset date a age 73 , blood calcium: decreased on age 73. All tests on an unspecified date. Therapeutic measures were taken included steroid shot and placed on Ciprofloxacin for 5 days for rash and for itching: Clindamycin, Ciprofloxacin, antibiotics but neither this has done any good, also with 2 tubes of Hydrocortisone. The patient had his second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EN6202) on 25Feb2021 at 13:30-14:00 and had arm sore. The outcome of the events was not recovered. Follow-up (13May2021): New information received from same contactable consumer which includes: concomitant drug details added (Primidone, Clonidin, Metoprolol Tart, Atorvastatin, Levothyroxine, therapy details for Levetiracetam and gabapentin), RMH details, lab data, event details (physician office visit details), treatment details. Follow-up attempts are completed. No further information is expected.

Other Meds: ATORVASTATIN; CLONIDINE; GABAPENTIN; LEVETIRACETAM; LEVOTHYROXINE; METOPROLOL TARTRATE; PRIMIDONE

Current Illness: Blood cholesterol increased (Onset Age: Age 60-65); Blood pressure increased (Onset Age: Age 45-50); Epilepsy (Age 4- 1950); Hypothyroidism (Onset Age: Age 70)

ID: 1773837
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/09/2021
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: can the blood thinner with the vaccine cause a nosebleed; nosebleed off and on since [he] got the first dose; This is a spontaneous report from a contactable consumer or other non hcp. A 79-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID -19 VACCINE, formulation: solution for injection, Batch/Lot number was not reported, expiry date: unknown) via an unspecified route of administration on an unspecified date as dose, single for COVID-19 immunisation. Medical history included blood disorder. On an unspecified date the patient experienced "nosebleed off and on since [he] got the first dose, and "can the blood thinner with the vaccine cause a nosebleed. Patient stated that he got both doses of the Pfizer-BioNTech COVID-19 vaccine. He explained he had a "nosebleed off and on since [he] got the first dose", and he specified he "never had this before". He added he is on a blood thinner. He asked can the blood thinner with the vaccine cause a nosebleed. The outcome of the event was unknown. No follow up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1773838
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/09/2021
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: itchiness; This is a spontaneous report from a contactable consumer (patient). A 34-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for Covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient reported that she only experienced itchiness with the first dose on an unspecified date. Right after receiving the second dose of the vaccine, she started with an itchy arms, back and neck. She stated she had a scratchy throat 1-2 hours after receiving the second dose of vaccine on 25Mar2021. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1773839
Sex: F
Age:
State: NY

Vax Date: 03/19/2021
Onset Date: 03/20/2021
Rec V Date: 10/09/2021
Hospital:

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

Lab Data: Test Date: 20210320; Test Name: her daughter had a temperature of 100.2; Result Unstructured Data: Test Result:100.2

Allergies:

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

Symptoms: fever; patient is very nervous because of her auto immune; muscular discomfort; her daughter had a temperature of 100.2 but was okay by Sunday; This is a spontaneous report from a contactable consumer (parent). A 43-year-old female patient received bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), via an unspecified route of administration on 19Mar2021 as dose 2, single for COVID-19 immunisation. Medical history included pemphigus vulgaris (autoimmune disease). The patient's concomitant medications were not reported. The patient previously received bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date as dose 1, single for COVID-19 immunisation. The patient reported that her daughter had a temperature of 100.2 but was okay by Sunday (body temperature increased) on 20Mar2021, muscular discomfort on 22Mar2021, had fever and patient was very nervous because of her auto immune on an unspecified date. Seriousness of the events was reported as non-serious. The patient underwent lab tests and procedures which included body temperature increased: 100.2 on 20Mar2021. The patient received Tylenol as treatment for adverse events body temperature increased, myalgia and pyrexia. The event outcome for body temperature increased was reported as recovering, myalgia as not recovered, pyrexia as not recovered and nervousness as unknown. No follow-up attempts are needed; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am