VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
PLEASE CHECK BACK SOON
Download the files above while you wait.







Manufacturers

Total Manufacturer
46,870MODERNA
532GLAXOSMITHKLINE BIOLOGICALS
353PFIZER\BIONTECH
231MERCK & CO. INC.
221UNKNOWN MANUFACTURER
62SEQIRUS, INC.
25DYNAVAX TECHNOLOGIES CORPORATION
13EMERGENT BIOSOLUTIONS
12SANOFI PASTEUR
9NOVARTIS VACCINES AND DIAGNOSTICS
5PFIZER\WYETH
5PAXVAX
2TEVA PHARMACEUTICALS
2PROTEIN SCIENCES CORPORATION
1BERNA BIOTECH, LTD.
1INTERCELL AG
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL1,906
1,575
289
IMM209286
252
236
229
s029456178
171
UT7065MA166
155
149
145
S034636133
107
U62828AA103
100
98
P10025327596
U6737AA85
UJ446AA79
78
78
59
57
4BH3254
4F47253
52
27656352
50
PP9L548
49TM346
42
40
38
MENVEO38
4F47237
R1B252M36
34
C5763AA30
93362229
25
300057A24
UNK24
22
CW311621
18
17
15
UH894AB15
3Y7NL12
R1B743M12
EJ168611
el128410
10
10
10
9
ARBA141A9
UNK9
8
UNK8
8
1F4EB8
Unknown7
7
No batch number6
5
5
UJ090AA5
5
5
4
4
4
UNK4
JEV18K95E4
UNK3
A115A3
Z127A3
3
3333324181073
2
2
2
TAR352
1
1
1
1
1
A739081
1
1
1
1
1
037K20A68,542
EL128447,700
133

Incidents per State

State Total
15,185
CA14,096
NY7,507
TX7,196
FL6,939
IN5,527
PA4,560
IL4,179
OH4,054
AZ3,856
MI3,771
NJ3,411
MA3,278
VA3,208
NC3,114
WA3,034
GA2,864
MD2,652
MN2,534
CO2,532
WI2,457
MO2,029
OR1,943
TN1,715
CT1,693
KY1,603
OK1,226
AL1,201
KS1,162
IA1,157
SC1,106
NM1,065
UT973
AR951
LA945
NE829
NV797
ME795
MT789
NH756
ID674
AK661
WV661
PR650
MS585
HI536
RI510
VT441
SD361
ND356
DE350
DC239
WY209
GU32
AS16
VI13
MP9
MH3
FM2
QM1
XB1

ID: 1015661
Sex: F
Age:
State: KY

Vax Date: 01/09/2021
Onset Date: 01/14/2021
Rec V Date: 02/09/2021
Hospital: Y

Lab Data: Test Name: Tested; Test Result: Negative ; Test Name: Tested; Test Result: Negative

Allergies:

Symptoms: took 1st dose of Covid vaccine and then ended up in the hospital with fluid around her heart; took 1st dose of Covid vaccine and then ended up in the hospital with fluid around her heart which they said came out to be a virus; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program Pfizer First Connect. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE)on 09Jan2021 at single dose for COVID-19 immunization. The patient medical history included lost her taste and had a low grade fever. Concomitant medications were not reported. This patient reported for a day and a half she lost her taste and had a low grade fever. So she went the next week (date unspecified) and was tested 2 times and came out negative (clarification of test type not provided). So on 09Jan2021 she got her first dose of the vaccine. On 14Jan2021 she ended up in the hospital with fluid on her heart which they said came out to be a virus. Outcome of the event was unknown.She was due for her second dose of the vaccine on 30Jan2021. Patient called to ask if she should or should not still get the second shot as scheduled. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1015662
Sex: F
Age:
State: VT

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: black outs; Severe migraine; full body shakes; soured; delayed jumbled speech; loss of memory; nausea; motor control issues; This is a spontaneous report from a contactable consumer reported for herself. A 31-year-old female patient (not pregnant at the time of vaccination and event onset) received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number: EL3249, via an unspecified route of administration on 25Jan2021 10:00AM at single dose in right arm for covid-19 immunization, immunized in hospital. Medical history included obesity, anxiety, post-traumatic stress disorder (PTSD), insomnia, allergy to walnuts pecans. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included sertraline hydrochloride (ZOLOFT), clonidine, fish oil and multi vitamin. The patient previously received the first dose of bnt162b2 lot number: EL1284, on 04Jan2021 12:00 PM at single dose in left arm for COVID-19 immunization. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously also received morphine and codeine, experienced allergy. The patient experienced sever migraine, black outs, full body shakes, soured, delayed jumbled speech, loss of memory, nausea and motor control issues, from 26Jan2021 11:30 PM. The events resulted in emergency room/department or urgent care. It was unknown if treatment was received. The outcome of the events was recovering. Since the vaccination, the patient had not been tested for COVID-19. The case was reported as non-serious.

Other Meds: ZOLOFT; CLONIDINE; FISH OIL

Current Illness:

ID: 1015663
Sex: F
Age:
State: WA

Vax Date: 01/03/2021
Onset Date: 01/01/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: Test Name: COVID virus; Test Result: Positive ; Comments: Her sister has tested positive for the third time for the COVID virus; Test Name: COVID virus; Test Result: Positive ; Comments: Her sister has tested positive for the third time for the COVID virus; Test Date: 20210118; Test Name: COVID virus; Test Result: Positive

Allergies:

Symptoms: tested positive for covid-19; tested positive for covid-19; Dementia; This is a spontaneous report from a Pfizer sponsored program. A contactable consumer reported for her sister that a 73-year-old female patient received first dose BNT162B2 (Pfizer BioNTech Covid 19 vaccine), via an unspecified route of administration on 03Jan2021 at single dose for COVID-19 immunization. The medical history and concomitant medications were not reported. The patient had tested positive for the third time for the COVID virus. The patient had Dementia in Jan2021. The patient had first dose of BNT162B2 on 03Jan2021 and tested positive for COVID on 18Jan2021. Patient was scheduled for the second dose for Thursday 28Jan2021. Since patient had an active case with symptoms the reporter was assuming patient won't get the second dose on 28Jan2021. Since patient had already had the first dose, currently in quarantine until after 01Feb, the reporter wanted to know if patient would have to start all over with getting the vaccine. The patient underwent lab tests and procedures, which included COVID virus positive twice on an unknown date, positive once on 18Jan2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1015664
Sex: M
Age:
State:

Vax Date: 01/23/2021
Onset Date: 01/24/2021
Rec V Date: 02/09/2021
Hospital: Y

Lab Data:

Allergies:

Symptoms: chest pain; This is a spontaneous report from a non-contactable Consumer. A male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) on 23Jan2021 at single dose for covid-19 immunization. The patient medical history was not reported. There were no concomitant medications. The patient experienced chest pain on 24Jan2021 . The patient was hospitalized for chest pain on an unknown date. No follow up attempts are possible. Information on lot/batch cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1015665
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: her face got swollen; lymph node right there it was extremely swollen and very tender and very painful; She had a lump at the site of the injection; chills; headache; flu like symptoms; This is a spontaneous report from a contactable consumer. A 60-years-old female patient received the second dose of bnt162b2 (BNT162B2; Lot # EL8982) vaccine , via an unspecified route of administration on 20Jan2021 at single dose for covid-19 immunisation . Medical history included hypertension. Concomitant medication included telmisartan (MICARDIS). On 30Dec2021 the patient received the first dose of BNT162B2 vaccine. The patient experienced her face got swollen on an unspecified date with outcome of unknown , lymph node right there it was extremely swollen and very tender and very painful on an unspecified date with outcome of unknown , she had a lump at the site of the injection on an unspecified date with outcome of unknown , chills on an unspecified date with outcome of unknown , headache on an unspecified date with outcome of unknown , flu like symptoms on an unspecified date with outcome of unknown. The events swollen face and lymph adenopathy were considered important medical Events. The remaining events were considered non serious. The patient stated she got the second vaccine shot of Pfizer on Wednesday the 20Jan2021. She got like a weird side effect like under her armpit it got really swollen and painful, like the lymph node right there it was extremely swollen and very tender and very painful. It still is but not as much. The next day the right side of her face was swollen The patient received Tylenol as treatment for the events. Follow up information has been requested.

Other Meds: MICARDIS

Current Illness:

ID: 1015666
Sex: F
Age:
State: GA

Vax Date: 12/28/2020
Onset Date: 01/08/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: patient was pregnant while taking BNT162B2; patient was pregnant while taking BNT162B2; Miscarriage 11 days post vaccine; This is a spontaneous report from a contactable Nurse. A 39-year-old female nurse reported that she received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EL0142), into the left arm on 28Dec2020 at 07:30 AM at single dose for COVID-19 immunization. Medical history included asthma and eosinophilic esophagitis and allergies to Keflex ASA. Concomitant drugs were none. At the time of vaccination the patient was pregnant, her last menstrual date was on 20Nov2020, gestational period 6. The patient reported that on 08Jan2021 at 12:00 PM she had miscarriage 11 days post vaccine. The patient was seen at Doctor or other healthcare professional office/clinic visit. At the time of reporting the patient was recovering.; Sender's Comments: Based on temporal association, a possible contributory role of BNT162B2 cannot be completely excluded for reported miscarriage. However, information is limited, and miscarriage is multifactorial event. In the general population, the estimated background risk of miscarriage in clinically recognized pregnancies is 15% to 20%. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1015667
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: diarrhea (7+ loose stools each day starting on this day); headache; severe nausea; worsened muscle pain; new joint pain morning after (Included in aforementioned, but significant stiff neck.); new joint pain morning after (Included in aforementioned, but significant stiff neck.); fatigue/malaise; fatigue/malaise; This is a spontaneous report from a contactable other HCP report for self. This 30-year-old not pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3302) Intramuscular at left arm on 20Jan2021 at single dose for COVID-19 immunization. Medical history included Asthma, anxiety, allergies to Acetaminophen (seizure like activity and fainting). No COVID prior vaccination. No other vaccine in four weeks. Other medications in two weeks includes fluoxetine, lorazepam, and Ibuprofen. Patient received first dose of bnt162b2 (lot number: EL0140) on 30Dec2020 and experienced injection sight tenderness, severe headache and fatigue. On 20Jan2021 5:00 PM after the second dose, patient experience headache, severe nausea, diarrhea (7+ loose stools each day starting on this day), worsened muscle pain several hours later, new joint pain morning after (Included in aforementioned, but significant stiff neck), fatigue/malaise. Patient received Ibuprofen and rest, supportive care due to events. The outcome of event was not recovered. Rapid Nasal Swab tested Negative on 21Jan2021.; Sender's Comments: The reported event diarrhea was likely causally related to the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) due to temporal relationship, and considering no alternative cause reported currently. The case will be reassessed should additional information become available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.

Other Meds: FLUOXETINE; LORAZEPAM; IBUPROFEN

Current Illness:

ID: 1015668
Sex: F
Age:
State: NJ

Vax Date: 01/21/2021
Onset Date: 01/23/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: localized injection site reaction: redness, swollen and warm to the touch; localized injection site reaction: redness, swollen and warm to the touch; localized injection site reaction: redness, swollen and warm to the touch; This is a spontaneous report from a contactable nurse. A 73-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular on 21Jan2021 at SINGLE DOSE vaccine location: left arm, dose number:1 for covid-19 immunisation. Medical history and concomitant medications were none. The patient experienced localized injection site reaction: redness, swollen and warm to the touch on 23Jan2021 with outcome of not recovered considered as important medical event. The physician recommended Tylenol and cold compress as treatment. The action taken was not applicable. Caller works in an assisted living facility. Information on the lot/batch number has been requested.; Sender's Comments: Based on temporal association, a possible contributory role of BNT162B2 cannot be excluded for reported vaccination site events. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1015669
Sex: F
Age:
State: NJ

Vax Date: 01/21/2021
Onset Date: 01/01/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swelling and significant bruise at injection site; swelling and significant bruise at injection site; This is a spontaneous report from two contactable nurses. A 78-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number unknown), intramuscular into the left arm on 21Jan2021 at single dose for COVID-19 immunization. Medical history and concomitant drugs were none. The patient developed swelling and a pretty significant bruise where the injection was given in her left arm. The caller noticed the bruise and swelling on 25Jan2021 but states it could be older. The events were reported as medically significant. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: A causal association between administration of BNT162B2 and the onset of vaccination site swelling and bruise cannot be excluded, considering the temporal association and the known adverse event profile of the suspect product.

Other Meds:

Current Illness:

Date Died: 01/18/2021

ID: 1015670
Sex: F
Age:
State: KY

Vax Date: 12/29/2020
Onset Date: 01/02/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: Test Date: 20210102; Test Name: Covid test; Result Unstructured Data: Test Result:Positive; Test Date: 20210115; Test Name: Xrays; Result Unstructured Data: Test Result:covid Poss pockets all in her lungs

Allergies:

Symptoms: Xrays showed covid Poss pockets all in her lungs on 15Jan; Xrays showed covid Poss pockets all in her lungs on 15Jan; This is a spontaneous report from a contactable consumer. An 85-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 29Dec2020 at single dose for covid-19 immunisation. Medical history included dementia. Concomitant medications were not reported. Patient popped hot 02Jan2021 along with 4 others on the hall she lived. Within 9 days 50+ patients were positive. All had the vaccine the same day. Patient was test positive on 02Jan2021. She was on day 12 of her quarantine when she started to get worse. She was unresponsive by 16Jan2021 and passed 18Jan2021. We were with her from 14Jan2021 to 18Jan2021. But had not been allowed to visit with her since Mar2020. And what post treatment pairs well with it? Publicly we hear Remdesivir and Bamlanivimab but these patients only received a general antibiotic and some vitamins. Death cause was Xrays showed covid Poss pockets all in her lungs on 15Jan2021. No autopsy was performed. Information on the lot/batch number has been requested.; Sender's Comments: Based on the information available, a possible contributory role of the suspect products cannot be excluded for the reported event of positive for corona virus infection for the lack of efficacy of the vaccine. However, based on the mechanism of action of the vaccine, it is unlikely the patient would have fully developed immunity for the vaccine to be effective, due to the number of days passed since the vaccine is given. Case will be reevaluated based on follow-up information; Reported Cause(s) of Death: Xrays showed covid Poss pockets all in her lungs on 15Jan

Other Meds:

Current Illness:

Date Died: 01/20/2021

ID: 1015671
Sex: F
Age:
State: KY

Vax Date: 01/13/2021
Onset Date: 01/18/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: CT; Result Unstructured Data: Test Result:bowel perforation; Comments: CT showed a bowel perforation in the small bowel

Allergies:

Symptoms: bowel perforation; pain in her upper abdomen; This is a spontaneous report from a contactable consumer. An 86-year-old female patient received the 2nd dose of bnt162b2 (BNT162B2) at single dose on 13Jan2021 for Covid-19 immunisation, administerd at nursing home/senior living facility Medical history included dementia, arthritis. No known allergies. Patient was not pregnant. Patient had not COVID prior vaccination. Concomitant medication in 2 weeks included: memantine (manufacturer unknown) 10 mg BID, diclofenac (manufacturer unknown) BID, carbidopa, levodopa (manufacturer unknown) 25-100 mg TID, quetiapine (manufacturer unknown) 12.5 mg q HS, escitalopram oxalate (LEXAPRO) 10 mg q HS, paracetamol (TYLENOL) 650 mg BID, glucosamine (manufacturer unknown) drink. The patient received the 1st dose of bnt162b2 (BNT162B2) at single dose on 24Dec2020 for Covid-19 immunisation. No other vaccine received in 4 weeks. The patient experienced bowel perforation and pain in her upper abdomen on 18Jan2021 07:30. The events resulted in Emergency room/department or urgent care, Life threatening illness (immediate risk of death from the event), and death. On 18Jan2021 07:30 AM, less than a week after the second shot, she had pain in her upper abdomen and was taken to the ER on 18Jan2021. CT showed a bowel perforation in the small bowel. She had never had bowel surgery or diverticulitis. She had been healthy other than her dementia and arthritis. Patient received treatment for the events: hospice and pain management. COVID-19 was not tested post vaccination. The cause of death was bowel perforation. An autopsy was not performed. Information about lot/batch number has been requested.; Reported Cause(s) of Death: bowel perforation

Other Meds: MEMANTINE; DICLOFENAC; CARBIDOPA/LEVODOPA; QUETIAPINE; LEXAPRO; TYLENOL; GLUCOSAMINE

Current Illness:

ID: 1015672
Sex: F
Age:
State: MA

Vax Date: 01/08/2021
Onset Date: 01/13/2021
Rec V Date: 02/09/2021
Hospital: Y

Lab Data:

Allergies:

Symptoms: my body collapsed and I had a Pulmonary embolism/I have clot in my lung; I have behind my knee like a deep wide black spot and it is hard; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 at single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medication included amlodipine, metformin and propranolol. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 18Dec2020 at single dose for COVID-19 immunization and experienced severe headache and diarrhea. On 13Jan2021, the patient reported that: "my body collapsed, I had a pulmonary embolism. I had to go to the hospital in ambulance. When I was there, they find out that I have clot in my lung. I was in an intensive care for 2 days or 3 days and about 5 days in the hospital (from 13Jan2021 to 17Jan2021). I have behind my knee like a deep wide black spot and it is hard, my body did not have anything like that". Therapeutic measures were taken as a result of event pulmonary embolism/ clot in lung and included treatment with "some medications", one of which ELIQUIS. The patient outcome of pulmonary embolism and "clot in lung" was recovered on an unspecified date and of deep wide black spot was unknown. The information on the batch number has been requested.

Other Meds: AMLODIPINE; METFORMIN; PROPRANOLOL

Current Illness:

ID: 1015673
Sex: M
Age:
State: NC

Vax Date: 01/27/2021
Onset Date: 01/30/2021
Rec V Date: 02/09/2021
Hospital: Y

Lab Data: Test Date: 20210130; Test Name: Sodium level; Result Unstructured Data: Test Result:Low; Test Date: 20210201; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Confusion; General "Don't feel right"; Seizure; Low Sodium level; This is a spontaneous report from a contactable consumer (reported for himself). A 71-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL3247), via an unspecified route of administration on 27Jan2021 11:15 at single dose in left arm for COVID-19 immunization. Medical history included High Cholesterol; No known allergies. Concomitant medication in two weeks included atorvastatin. Facility type vaccine was Hospital. No other vaccine in four weeks. On 30Jan2021 23:00, the patient experienced Seizure, Low Sodium level, Confusion, General "Don't feel right". The events resulted in Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). The number of days hospitalization was 3 (from unspecified date in 2021 to an unspecified date in 2021). It was unknown if treatment received. No covid prior vaccination. Covid tested post vaccination: Nasal Swab tested on 01Feb2021 with the result of Negative. The outcome of the events was recovered on an unspecified date in 2021.

Other Meds: ATORVASTATIN

Current Illness:

ID: 1015674
Sex: F
Age:
State: FL

Vax Date: 01/19/2021
Onset Date: 01/01/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: Test Name: pathology; Result Unstructured Data: Test Result:skin eruptions she is having is from Ibrance

Allergies:

Symptoms: She confirms the rash started after receiving the covid vaccine/terrible rash is up and down both arms, the crown of her head, and on her scalp; Pfizer covid vaccine: nausea; Pfizer covid vaccine: chills; Pfizer covid vaccine: hurting at the injection site; Pfizer covid vaccine: headaches/on and off headaches; She cannot speak this morning; Pfizer covid vaccine: vomiting; This is a spontaneous report from a contactable Nurse (patient). A 71-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EL8982, expiry date: 31May2021) intramuscular injection in right upper arm on 19Jan2021 10:00 at single dose for COVID-19 immunisation. Her second dose is scheduled on 10Feb2021. Medical history included stage 4 metastatic breast cancer. There were no concomitant medications. The patient previously took Ibrance for stage 4 metastatic breast cancer and experienced broken out in terrible rash. She is taking Ibrance for cancer, she has been taking it for a while. The past few weeks she has broken out in terrible rash. She went to a dermatologist that stated the rash was from Ibrance. She cannot speak this morning (Jan2021). Her doctors are speaking to each other and she is being told not take Ibrance by the dermatologist and to continue taking from her oncologist. Reports she had a pathology report and it showed her skin eruptions she is having is from Ibrance. She clarifies that her terrible rash is up and down both arms, the crown of her head, and on her scalp. She took the first dose of the COVID-19 vaccine a couple of weeks ago. She is having quite a bunch of side effects from the injection. The side effects she is experiencing after the COVID vaccine are nausea, vomiting, chills, hurting at the injection site which is not terrible, and on and off headaches. Events did not require a visit to emergency room or physician office. Nausea started 3 days after the receiving the vaccine on 22Jan2021. Vomiting is still ongoing on and off and started about a week and half after receiving the vaccine (Jan2021). Chills started right away and she still has the chills. It has not changed. The chills started maybe a day after receiving the vaccine (20Jan2021). Hurting at the injection site started the day after (20Jan2021) and lasted for two or three days and is still ongoing, reports it goes on and off. Reports the hurting at the injection site is not terrible. Headaches started a day or so after receiving the vaccine (20Jan2021) and is still ongoing, on and off. Reporter seriousness for events nausea, vomiting, chills, hurting at the injection site, headaches were reported as medically significant. She is currently taking Ibrance since her oncologist told her not to stop taking Ibrance. The dermatologist said her rash is related to Ibrance. When querying causality she reported that she is not sure because she has been taking Ibrance for a while. She confirms the rash started after receiving the COVID vaccine. Events outcome of nausea, vomiting, chills, hurting at the injection site, headaches was not recovered (nausea and vomiting was reported as worsened), while for others was unknown. Relatedness of drug Pfizer COVID vaccine to events for nausea, vomiting, chills, hurting at the injection site, headaches were reported as related.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of serious events cannot be excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1015675
Sex: M
Age:
State: AR

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

Lab Data:

Allergies:

Symptoms: I faint anf fell twice hurt my back once; I faint anf fell twice hurt my back once; hurt my back once; Dizzy spells; Constipation; This is a spontaneous report from a contactable consumer (patient). A 91-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284) via an unspecified route of administration in Jan2021 (a week before reporting) at single dose in left shoulder for COVID-19 immunisation. Age at vaccination was 91 years. The patient's medical history and concomitant medications were not reported. About 24 hours after shot he started having some dizzy spells and then fainted and fell a couple of times and hurt his back once. He stated he also had had constipation since the shot and do not know if that is related or not. The patient wanted to talk to see if he could get his second shot. He is taking some pain killers for his back. With regards to Physician Office/ Emergency Room: patient stated, 'This for my back and nothing else of that'. The outcome of the events was unknown. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1015676
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: tongue is a lot swollen; Dizziness; Nausea; feeling weak; tired and washed out; swollen glands; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date at single dose for COVID-19 immunisation. The patient medical history and the concomitant medications were not reported. The patient was experiencing dizziness and right after the vaccine had dizziness and nausea. She said that the nausea went away after eating something. She said that he also feels like his tongue was swollen. The patient said that he feels like his tongue is a lot swollen. He stated that he had the shot 4 hours and when he gets up off of the chair, he can barely stand up because he is so dizzy. He said that he is also feeling weak, tired, and washed out. He said that he also has swollen glands. The event tongue is a lot swollen was serious as Life threatening, and Emergency Room Visit and Physician Office Visit. The outcome was unknown. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1015677
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: get sick from the flu vaccine; Initial information received on 29-Jan-2021 regarding an unsolicited valid non-serious case received from a consumer (patient). This case involves a patient of an unknown age and gender who was sick (illness), while he/she received INFLUENZA VACCINE. The patient's medical treatments, vaccinations, concomitant medications and family history were not provided. It is unknown if the patient had any medical history, concomitant disease or risk factor. On an unknown date, the patient received a dose of suspect INFLUENZA VACCINE produced by unknown manufacturer (batch number and expiry date not reported) via an unknown route in unknown administration site for prophylactic vaccination. On an unknown date, the patient was sick (illness) (Unknown latency, non-serious event) following the administration of INFLUENZA VACCINE. It is unknown if the patient experienced any additional symptoms/ events. Medication Details and reason for taking the medicine: not provided. There were no lab data/results available. It was not reported if the patient received a corrective treatment. The event outcome was reported as unknown for event illness. There will be no information on the batch number for this case.

Other Meds:

Current Illness:

ID: 1015678
Sex: F
Age: 12
State: TN

Vax Date: 11/03/2020
Onset Date: 11/03/2020
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: A 12 year old received Flublok and not the prescribed Fluarix, no AE; A 12 year old received Flublok and not the prescribed Fluarix, no AE; Initial information regarding an unsolicited valid non-serious case was received from a Nurse via regulatory authority (Reference number- 00444333) and transmitted to Sanofi on 25-Jan-2021. This case involves a 12 years old female patient who received 0.5 ml dose of suspect INFLUENZA QUADRIVALENT RECOMBINANT VACCINE (lot QFAA2037, expiry: 30-Jun-2021) via unknown route in the right deltoid for prophylactic vaccination on 03-Nov-2020, instead of INFLUENZA VACCINE INACT SPLIT 3V (FLUARIX) (Wrong product administered and Product administered to patient of inappropriate age) Medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HPV VACCINE VLP RL1 4V (YEAST) (GARDASIL), MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA) and DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS) for prophylactic vaccination. The Nurse reported that error was found out two months after administration. It was a case of an actual medication error due to Inappropriate age at vaccine administration and Wrong vaccine administered (latency same day). At the time of report, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Other Meds: GARDASIL; MENACTRA; DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS

Current Illness:

ID: 1015679
Sex: M
Age: 63
State: TX

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: The patient received an expired vaccine, no AE; Initial information regarding an unsolicited valid non-serious case was received from a other health care professional via Medical Information (Reference number- 00453109) and transmitted to Sanofi on 29-Jan-2021. This case involves a 63 years old male patient who received 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT [TENIVAC] (lot C5578AA, expiry date: 28-Jan-2021, injection) via intramuscular route in the left deltoid for prophylactic vaccination on 29-Jan-2021 (Expired product administered) Medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had no other vaccines. It was a case of an actual medication error due to Expired vaccine used (latency same day). The reporter stated that he gave an injection of an expired Tenivac vaccine and wanted to know what to do now. The health care professional asked for appropriate follow-up after expired vaccine was given At the time of report, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Other Meds:

Current Illness:

ID: 1015681
Sex: F
Age: 63
State: PA

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

Lab Data: none

Allergies: none

Symptoms: Pain in right side of neck,nausea, No treatment, went away within 45 mins

Other Meds:

Current Illness: none

ID: 1015682
Sex: F
Age: 73
State: CA

Vax Date: 01/29/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: N/A

Allergies: None known

Symptoms: Itching, hard lump swelling, rash at injection site 8 days after 1st shot.

Other Meds: Synthroid 88

Current Illness: None

ID: 1015683
Sex: M
Age: 34
State:

Vax Date: 02/08/2021
Onset Date: 02/08/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: None

Allergies: Doxicyclin

Symptoms: Joint Ache at 2000 hours followed a small headache and fever followed shortly by extreme chills, shivering, and exhaustion at 2100 hours. Next morning fever and chills were gone, but headache, joint ache, sore arm, and exhaustion remains.

Other Meds: Multivitamin

Current Illness: None

ID: 1015684
Sex: F
Age: 70
State: FL

Vax Date: 02/08/2021
Onset Date: 02/08/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: Penicillin

Symptoms: Client verbalized feeling dizzy after receiving the vaccine. She was evaluated by onsite nurse practitioner. Client was advised to seek additional evaluation. Client declined to be transported to the hospital for elevated blood pressure. Client was released out at 3:51 pm accompanied by co-worker.

Other Meds: none

Current Illness: unknown

ID: 1015685
Sex: M
Age: 71
State: FL

Vax Date: 02/08/2021
Onset Date: 02/09/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: None

Allergies: Cipro, Amlodipine

Symptoms: Yesterday around 1:30PM I received my 2nd dose of the Moderna vaccine. All went well between the time I got the shot to the time I went to bed at about 10PM. I thought I had it made. At midnight I awoke with intense shivering. I absolutely couldn't stop. I wasn't cold as my body was hot. I had plenty of covers, but I was hot and shivering cold. Include a severe headache in this picture. This went on for a good hour and I finally settled down and dozed off again. This morning I have a mild headache and a really sore shoulder where I received the vaccine.

Other Meds: Metoprolol, Alopurinol, Tamsulosin, Finasteride, Trazodone, Benedryl, Livalo, Baby Aspirin

Current Illness: None

ID: 1015686
Sex: F
Age: 20
State: IN

Vax Date: 01/26/2021
Onset Date: 01/31/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: NKDA

Symptoms: Rash/hives started 1/31/2021. Seen in clinic for this 2/2/2021 and Rx Prednisone and antihistamine and H2 blocker. Then developed angioedema and went to ED on 2/3/2021.

Other Meds: Maxalt prn, Topamax, Tri-sprintec

Current Illness: No illnesses.

Date Died: 02/09/2021

ID: 1015687
Sex: M
Age: 62
State: OH

Vax Date: 02/08/2021
Onset Date: 02/08/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: nknda or food allergies

Symptoms: Almost immediate headache per wife. Developed fever around 4 pm. Headache all day. Took Tylenol at 4 and 10 pm. Gradual development of SOB and cough. Temp of 101.4 at 10 pm. pulse ox 92% at 10 pm. Went to sleep, woke up at 0050 with increasing SOB. Pulse ox 82%. Used albuterol inhaler, wife called emergency services at 0113. EMS arrived around 0130 to patient's home. pulse ox 86%, coughing, sob, hard time breathing. Walked to stretcher. Became unresponsive. Found to have no pulse, stopped breathing. CPR initiated at about 0140. King airway placed in field, I/O in left tibia. Patient from PEA to asystole, to vfib, to asystole. ACLS followed. Unrecoverable asystole and patient time of death 0213.

Other Meds: lipitor, pepcid, uloric, prozac, synthroid, lisinopril, troprol xl, multivitamin, niacin, nifedical xl, ranexa, demadex, xarelto

Current Illness: none

ID: 1015688
Sex: F
Age: 90
State: IN

Vax Date: 01/31/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Redness and swelling noted underneath upper right arm from elbow to armpit. Light pink in color. Denies any pain and occasional itching noted.

Other Meds:

Current Illness:

ID: 1015689
Sex: F
Age: 37
State: AZ

Vax Date: 02/06/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: None

Allergies: Codeine, Latex

Symptoms: First day: Fatigue Extreme Restless Leg (Advil calmed) Fever (101.4 at highest, Advil, damp washcloth on forehead) Chills Muscle ache in hips (hot rice pillow, Advil) Pain at injection site 2nd day: Lower fever (99.7, Advil, no damp wash cloth, seemed too cold) Chills Muscle ache in hips and hands (hot rice pillow, Advil) Fluttering under right breast (about 2 seconds long, happened 6 times) Start of migraine (Aleve, took edge off but not completely gone) Pain at injection site Day 3: Migraine (Aleve) Muscle aches in hands (Advil) Late in day, around 2pm, migraine turns into headache in left eye socket by around 7pm pain feels more like congestion in same area. (Aleve, doesn't seem to help much, neither does Advil) Day 4 (Morning): Headache/congested feeling in left eye socket continues (Aleve or Advil, neither help so far)

Other Meds: None

Current Illness: None

ID: 1015690
Sex: F
Age: 58
State: OH

Vax Date: 02/07/2021
Onset Date: 02/07/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: NSAIDs PCN

Symptoms: fever, weakness, chills, shakiness, body aches

Other Meds: Xhance montekulast vitamin E

Current Illness:

ID: 1015691
Sex: F
Age: 70
State: FL

Vax Date: 02/06/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: none

Allergies: none

Symptoms: fatigue, headache, muscle & joint aches, mental fog

Other Meds: Verapamil, HCTZ, Losartan, Claritin, Calcium, Atorvastatin, Trazadone, baby aspirin, Pepcid, Aldactone

Current Illness: none

ID: 1015692
Sex: M
Age: 82
State: IN

Vax Date: 01/27/2021
Onset Date: 02/05/2021
Rec V Date: 02/09/2021
Hospital: Y

Lab Data: 2/8/21 1241 CBC WBC 7.2 RBC 5.26 Hemoglobin 16.2 Hematocrit 49.0 MCV 93.2 MCH 30.8 Platelets 1 (THOUS/uL)

Allergies: Latex allergy

Symptoms: Patient received first dose of Moderna vaccine 1/27/21 and presented to urgent care 2/8/21 with complaint of sores on inside of lower lip. Patient reported that sores started on 2/5/21 and seem to be growing in size. Patient did not recall any injury and sees dentist regularly for annual cleaning. Patient also does not smoke or chew tobacco. Patient was referred to his dentist who was able to get patient in and felt that lesions and ulcerations were not infectious or cancerous. The NP ordered lab work and recommend patient follow up with PCP. Labs came back two hours later and showed patient had a platelet count of 1 (THOUS/uL). Patient was sent to ER at Hospital 1 and was transferred to Hospital 2 for a hematology work-up. Patient is currently admitted and receiving IVIG and steroids

Other Meds: Aspirin 81mg daily Levothyroxine 50 mcg daily Multi-vitamin daily

Current Illness: None

ID: 1015693
Sex: F
Age: 30
State:

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: None

Allergies: Penicillin

Symptoms: Vaccine #1: Sore, tender at injection site. Symptoms start two hours post injection and resolved 24 hours post injection. No treatment. Vaccine #2: Sore, tender, swollen at injection site; headache; body aches; chills; fatigue. Symptoms started 2-3 hours post injection and resolved 43 hours after symptoms started. No treatment.

Other Meds: Lisinopril 5mg oral NORGEST/EE 0.3 MG-30 MCG ORAL TAB

Current Illness: None

ID: 1015694
Sex: F
Age: 79
State: PA

Vax Date: 01/28/2021
Onset Date: 02/03/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: none

Allergies: none known

Symptoms: Rash at injection site started approximately 1 week following injection and is ongoing. Rash has increased in size and intensity over a period of 1 week. Rash at 1 week is approximately 8" x 5", quite red and itchy.

Other Meds: calcium+d3

Current Illness: none

ID: 1015695
Sex: F
Age: 54
State: IN

Vax Date: 02/06/2021
Onset Date: 02/07/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: None.

Allergies: None

Symptoms: Fever, chills, dizziness, muscle aches and pains, extreme fatigue. Treated with extra strength Acetaminophen. Symptom relief after 48 hours.

Other Meds: Vitamin D, Fish oil, Claritin

Current Illness: None.

ID: 1015696
Sex: F
Age: 47
State: IL

Vax Date: 01/27/2021
Onset Date: 01/28/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: none

Allergies: no

Symptoms: My left arm is painful, red, swollen and bruised. The pain only lasted for one day but the redness, swelling and bruising is still here after 13 days but it has improved a lot.

Other Meds: lipitor, norvasc, olmesartan medoxomil, multivitamin, cinnamon tablet, fish oil capsules, naturelo probiotic, cider& vinegar with mother tablets.

Current Illness: none

ID: 1015697
Sex: M
Age: 63
State: NJ

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: N/A

Allergies: none

Symptoms: head hurts swollen lymph nodes

Other Meds: Blood pressure medication men's one a day vitamin

Current Illness: none

ID: 1015698
Sex: F
Age: 57
State: MN

Vax Date: 01/31/2021
Onset Date: 02/07/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: none

Allergies:

Symptoms: Exactly one week after receiving the first dose of the vaccine, a rash appeared at the injection site. It was raised, red, a little itchy, slightly warm to the touch, and a little tender. It is not bothersome, but it has gotten a little larger. As of today I still have the reaction.

Other Meds: Imvexxy-estradiol 10mcg

Current Illness:

ID: 1015699
Sex: F
Age: 70
State: OH

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

Lab Data: None

Allergies: None

Symptoms: Injection was at noon. Six PM - left arm was extremely painful, (not "achy"), feverish and tender. Fatigue had set in. By 9PM migraine headache and extreme nausea . Midnight brought shivering chills. By 3AM had a fever of 102.4 and nausea had worsened. Throughout the next 48 hours the symptoms continued but slowly subsided: by noon (24 hours after inoculation) the fever was 100. Nausea subsided to allow broth and crackers by 30 hours after injection. Within 60 hours symptoms were gone except for the arm. On day three I did develop "Covid arm". The red tender patch is still visible (one week after injection) but the rash is slowly diminishing.

Other Meds: 12.5 mg Hydrochlorothiazine and 15mg Lisinopril, 82mg aspirin and Centrum multi-vitamin for Women

Current Illness: Although I had no symptoms, I did have an anitbody test (Whitmire ) for Covid on January 29, 2021. Per the pharmacist who interrupted the results, I had strong IgG and IgM antibodies. He suggested I had had Covid up to 4 weeks prior. I did not get a Covid test to confirm these findings.

ID: 1015700
Sex: F
Age: 82
State: HI

Vax Date: 01/31/2021
Onset Date: 02/01/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Moderna COVID-19 Vaccine EUA. Muscle aches, joint aches. Personal physician contact on 2nd day of symptoms and recommended 2 Bufferin tablets every 6 hours. Symptoms began diminishing after first ingestion of Bufferin.

Other Meds: Losartan Potassium and Pravastatin Sodium

Current Illness:

ID: 1015701
Sex: F
Age: 71
State: OH

Vax Date: 02/01/2021
Onset Date: 02/07/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Itchy rash at injection site

Other Meds:

Current Illness:

ID: 1015702
Sex: F
Age: 26
State: MN

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: n/A

Allergies: Allergic to Z-pack Allergic to Bee venom

Symptoms: The day of the vaccine my left arm hurt, and I got a red and itchy circle around the injection site, this lasted about 4 days. On day 8 of post vaccine, the red circle appeared again, this time bigger, and more itchy than before. I went to the doctor following the return of the red ring and it being bigger, and was told to take some benadryl/cetrizine and that would help, I continued to take Benadryl for 3 days and it went away completely.

Other Meds: TUMS as needed Tylenol as needed Nyquil as needed Mirena- constantly

Current Illness: N/A

ID: 1015703
Sex: F
Age: 80
State: FL

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: Reported to primary doctor but no solution offered.

Allergies: Many including Naproxen, Sulpher, Tetracycline, Ciproflaxan, Levoquin, Bactrim Major itchy rash reaction all over body after Moderna vaccine shot

Symptoms: Day after Moderna shot major rash breakout over body. Very itchy for first day and not as itchy second day but still very visible and new rash continuing to show up on body on day 5 after shot.

Other Meds: Lisinipril, Allegra

Current Illness: Neuropathy, Lymphedema

ID: 1015704
Sex: M
Age: 21
State: WA

Vax Date: 01/18/2021
Onset Date: 02/03/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: Two weeks ago I received a varicella vaccine for work and now I am experiencing swelling/redness in the area I got the shot. I also have blisters I believe that have popped up all over my body. Location Left upper arm with swelling that started 2 weeks after getting the shot, overnight started to get vessicular lesions about 30-40 all over the body. + itching

Other Meds: None

Current Illness: None

ID: 1015705
Sex: F
Age: 65
State: OR

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

Lab Data: None

Allergies: sulfa dris

Symptoms: I had the shot at 12:30pm. I went bed about 10pm, and woke up to my right arm having a series of tiny shooting pain tingling (at specific spots, as if it were a pin prick traveling up and down my arm; pinging randomly across the arm). This was accompanied by an extreme desire to scratch/itch my arm where the pin pricks were being felt. I found myself scratching my arm in my sleep. There didn't seem to be a discernable rash of any color, but by the next day, i was seeing slight welts at various points along my upper and lower outer arm. I would feel a sharp pin-prick/tingle and instantly would feel the urge to scratch it. The scratching continued -- but not consistently. Sometimes for an hour or two at a time, seemingly coming out of no where. The arm was fine and then I'd wake up or be jolted by the sharp pin prick accompanied by the insane desire to scratch my arm. These 'spells' of tingling and itching have continued until today (one week and one day after getting the #2 Moderna shot. I have managed this with Benedryl (it worked by addressing the itching somewhat and provided relief from the tingling - it made me sleepy); anti-itch creams (soothed the skin topically), ice (to take the sting/itch sensation away) and calamine lotion (didn't really work). Tonight (1/8/2021 I cannot sleep. Although the itching and sensations seem to be intermittent, I have woken up the last couple of nights with intense itching and tingling to the point I couldn't sleep Usually Benedryl calms everything down, but tonight it isn't helping at all and I am crawling out of my skin. I have not gone to my Primary Care Physician, but will call and go in tomorrow.

Other Meds: Prilosec, Wellbutrin (generic), Benedryl, Vitamin D

Current Illness: Periodontal Surgery - January 2021 Back Pain - January 2021

ID: 1015706
Sex: F
Age: 78
State: FL

Vax Date: 09/30/2020
Onset Date: 11/24/2020
Rec V Date: 02/09/2021
Hospital:

Lab Data: NA

Allergies: NA

Symptoms: Patient just wanted us to know that she passed out in the AM and woke up around 1PM on 11/24/2020, but her vaccinations was on 09/30/2020. She said she was ok when she woke up and that she did not need any medical attention.

Other Meds: NA

Current Illness: NA

ID: 1015707
Sex: F
Age: 74
State: FL

Vax Date: 01/29/2021
Onset Date: 02/07/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: sulfur

Symptoms: Red, itchy rash at vaccination site (on left arm). Ongoing for 3 days now.

Other Meds: atorvastatin, magnesium, vitamin D3

Current Illness: none

ID: 1015708
Sex: F
Age: 67
State: MD

Vax Date: 01/27/2021
Onset Date: 02/09/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies: codeine

Symptoms: flat, red rash on left upper arm

Other Meds: multi-vitamin, collagen supplement

Current Illness: none

ID: 1015709
Sex: F
Age: 76
State: MA

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: none

Allergies: Norvasc, codeine

Symptoms: flu like symptoms--aches, chills, headache, fatigue, followed by red rash over left chest area, with itching Treated with benadryl with little effect. Received Rx for dosepack Prednisone. Also applied cortizone OTC to rash area. Flu like symptoms abated wtihin 36 hours; rash improving more slowly.

Other Meds: Lisinopril, Omeprazole, Pravastatin, HCTZ, Red Yeast Rice, Fish Oil, Calcium, Vitamin D, AREDS eye caps, Vitamin C, Tylenol, Dorzolomide eye gtts, Latanaprost eye gtts

Current Illness: glaucoma

ID: 1015710
Sex: F
Age: 40
State: VT

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data:

Allergies:

Symptoms: on the morning on 2/6/2021 at 6am, swollen lymph nodes under left arm, migraine, vomiting and diarrhea, fever 99.8. Did not feel well through 2/8/2021.

Other Meds:

Current Illness:

ID: 1015711
Sex: F
Age: 41
State: MD

Vax Date: 01/29/2021
Onset Date: 02/06/2021
Rec V Date: 02/09/2021
Hospital:

Lab Data: None

Allergies: Very minor allergies to melons and avocado.

Symptoms: A week after receiving my 1st shot , had redness, swelling, fever at sight and muscle fatigue, Sunday redness got worse and had some itching

Other Meds: One a day vitacraves

Current Illness: No

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm