VAERS 2021 Database www.vaers.hhs.gov

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

Total Manufacturer

Incidents per State

State Total
92,076
AK1,880
AL6,345
AR4,151
AS46
AZ14,991
CA66,887
CO12,550
CT8,943
DC1,795
DE2,009
FL42,724
FM4
GA17,031
GU124
HI2,580
IA4,919
ID2,892
IL22,128
IN24,197
KS5,047
KY9,111
LA5,500
MA15,718
MD13,434
ME3,351
MH8
MI20,971
MN13,585
MO10,747
MP30
MS3,198
MT2,477
NC18,051
ND1,501
NE3,109
NH3,218
NJ20,216
NM4,218
NV4,728
NY37,667
OH20,793
OK6,692
OR9,244
PA25,607
PR2,588
QM2
RI2,163
SC7,261
SD1,282
TN10,445
TX39,890
UT4,618
VA15,980
VI67
VT1,830
WA16,071
WI12,042
WV2,571
WY926
XB5
XL1
XV2

ID: 1426724
Sex: U
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Rec V Date: 06/25/2021
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Symptoms: Diarrhea; Stomach problem; This is a spontaneous report from a non-contactable consumer (patient). A patient of an unspecified age and gender received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number not reported) via an unspecified route of administration on an unspecified date, at single dose for COVID-19 immunisation. Relevant medical history and concomitant medications were not reported. On an unspecified date the patient had diarrhea and stomach problem. 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: 1426725
Sex: F
Age:
State:

Vax Date: 03/11/2021
Onset Date: 03/01/2021
Rec V Date: 06/25/2021
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Symptoms: having pain in hands shoulder and knees; having pain in hands shoulder and knees; This is a spontaneous report from a non-contactable consumer (patient) via a Pfizer-sponsored program. A 65-year-old female patient received bnt162b2 (Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 11Mar2021 (at the age of 65 years old) as single dose for covid-19 immunization; tofacitinib citrate (XELJANZ, Lot Number: DP7374), orally from an unspecified date to an unspecified date, at 1 Tablet by mouth daily for OTH Rheeumatoid Arthritis w Rheumatoid Fator mult site. Medical history included age-related Osteoporosis without current pathological fracture. Concomitant medications included ascorbic acid/ ferrous fumarate/ folic acid/retinol (PRENATAL), ertugliflozin pidolate (STEGLATRO), lisinopril, levothyroxine sodium (LEVO T), metformin hcl, flucytosine, curcuma longa (TURMERIC CURCUMIN), vitamins and minerals. The patient stated that she stopped taking the medication on 11Mar2021 due to receiving the COVID-19 vaccination, the MD told her to restart the medication 1 week after second vaccination scheduled for 09Apr2021, patient reported due to not being on medication, she was having pain in hands shoulder and knees, all questions and concerns addressed, patient agreed to follow up calls after she restarts the regimen. The action taken of tofacitinib citrate was unknown. The outcome of events was unknown No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: PRENATAL [ASCORBIC ACID;FERROUS FUMARATE;FOLIC ACID;RETINOL]; STEGLATRO; LISINOPRIL; LEVO T; METFORMIN HCL; FLUCYTOSINE; TURMERIC [CURCUMA LONGA]; Xeljanz

Current Illness:

ID: 1426726
Sex: F
Age:
State: MS

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 06/25/2021
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Symptoms: allergic reaction; This is a spontaneous report from a contactable consumer. A 71-years-old female patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection), dose 1 via an unspecified route of administration on 28Feb2021 (at a age of 71 year old) as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. On Mar2021 the patient experienced allergic reaction stated that between her first and second dose she had an allergic reaction to a different medication and was in the hospital. Last Friday (she said maybe it was the 25Mar2021) she went to get her second dose of the vaccine and they wouldn't give it to her, and she had to get confirmation from doctor that her reaction was not to the vaccine. Outcome of event was unknown. Follow-up attempts not completed; information about lot/batch number cannot be obtained. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021354364 similar report from same reporter

Other Meds:

Current Illness:

ID: 1426727
Sex: F
Age:
State: FL

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 06/25/2021
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Symptoms: the injection site is red and swollen/swelling with red silver dollar spots; arm is sore; she had a very red and tender arm; the injection site is red and swollen; This is a spontaneous report from a contactable consumer (patient herself). An 80-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6206), via an unspecified route of administration, administered in right arm on 29Mar2021 14:20 (reported as Monday) (age at vaccination: 80 years) as DOSE 2, SINGLE for covid-19 immunization at Physician Office. The patient medical history was not reported. Concomitant medication included levothyrxoine sodium (SYNTHROID). The patient said that she was basically healthy. Patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6202), via an unspecified route of administration, administered in his right arm on 08Mar2021 as DOSE 1, SINGLE for covid-19 immunization. Patient was was okay with the 1st Covid shot. The night after the second shot, she had a very red and tender arm. The next morning, it was red and swollen and redder. It has been the same for the last 2 days. The arm was sore with red patches the size of 2 silver dollars. Patient took a Benadryl thinking that would help and used an ice patch. The arm was a little redder this morning. Caller added that pain wise and everything, it was about the same. The discomfort was about the same. The area was redder and the redness has worsened as in bigger than it was last night.The patient had no prior vaccinations within 4 weeks. The outcome of the event was not recovered.

Other Meds: SYNTHROID

Current Illness:

ID: 1426728
Sex: F
Age:
State: MS

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 06/25/2021
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Symptoms: Itching; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 38-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EN6207, Expiration date: Jul2021), via an unspecified route of administration in the left arm on 30Mar2021 at 08:15 or 08:30 (at the age of 38-year-old) as single dose for COVID-19 immunisation. Medical history included high blood pressure and hypertension from Aug2015 and ongoing; COVID on an unknown date in Dec2020 and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient's concomitant medications were not reported. No investigation assessment was provided. The patient stated she had the 1st dose of the Pfizer vaccine ?yesterday', 30Mar2021 and itching began at 17:00 that ?same day yesterday evening' and she was just itching, and it was a lot of itching all over and could not find anything in her system and did not see anything anywhere and she was not allergic to anything. She was asking if this was a possible side effect of the vaccine. She said that the itching got worse and started at 17:00 yesterday and now was about the same as when it began. The patient stated she has not yet had treatment, has not gone to the emergency room or to the HCP (health care professional) and was hoping the itching would go away; stated she was taking Benadryl unsure of the dosage and was hoping the itching would go away with Benadryl. She did take the Benadryl before she went to bed last night and took one tablet but does not know the dosage. She got the Pfizer vaccine because she just wanted to hurry up and get it because she had COVID on an unknown date in Dec2020. She was fine yesterday and prior to this right now she was doing testing on her thyroid but has no results to provide; stated she has not seen a specialist yet and was still waiting to see the specialist; stated her last blood work was on Thursday, 25Mar2021 and they were checking her levels, but she has no results. The event was not resulted in emergency room nor physician's office visit. The patient underwent lab tests and procedures which included thyroid function test: no results on 25Mar2021 - checking her levels but she has no results. The outcome of the event was unknown. Follow-up attempts are needed. Further information is expected.

Other Meds:

Current Illness: Hypertension (high blood pressure and hypertension)

ID: 1426729
Sex: F
Age:
State:

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Rec V Date: 06/25/2021
Hospital: Y

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Symptoms: difficulty breathing/ issues breathing; hives; redness; Pressure on her chest; throat tightness; itching sensation in her skin and face/ itchy; burning sensation on her face; rash in her skin; mild discomfort on her throat; allergic reaction; she does not feel as bad as yesterday; chest pain has diminished; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration on an unspecified date as unknown, single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced pressure on her chest, throat tightness, hives, redness, difficulty breathing, itching sensation in her skin and face, burning sensation on her face, rash in her skin, allergic reaction, she does not feel as bad as yesterday, chest pain has diminished. Patient received the Pfizer COVID-19 vaccine and had a severe reaction and she was no longer in the hospital, indicated that she should use a Blue Epinephrine injector 0.3 mg two unites in case she required it. She wanted to know if this product could cause another major allergic reaction. She took Prednisone (still taking it today) and Benadryl, the chest pain has diminished but since 11:30-12:30 and mentioned that a normal allergic reaction usually gone away after a wile but this one was returned after her treatment. During the call she mentioned that she was worried that she might die sooner if she used the Epipen. It was reported that patient experienced allergic reaction to Pfizer Covid Vaccine with issues breathing, and itchy hives requiring having to the hospital. Events resulted in Emergency room visit. Patient received treatment with Prednisone and Benadryl for the events. Therapeutic measures were taken as a result of pressure on her chest, throat tightness, hives, redness, difficulty breathing, itching sensation in her skin and face, burning sensation on her face, rash in her skin, allergic reaction, she does not feel as bad as yesterday, chest pain has diminished. The outcome of chest pain has diminished was recovered on an unspecified date and other events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

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Current Illness:

ID: 1426730
Sex: F
Age:
State: VA

Vax Date: 03/21/2021
Onset Date: 03/01/2021
Rec V Date: 06/25/2021
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Symptoms: a large purple, hard area around the injection site; fingers on her right side were also swollen; a large purple, hard area around the injection site; stiffness in her fingers, legs, and neck; had scars on both arms where she received her covid vaccinations; tired; This is a spontaneous report from a contactable consumer (Patient, reported for self). This case is for the second dose of BNT162B2. A 40-years-old female patient received second dose of BNT162B2, (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Formulation: Solution for injection,Batch/Lot Number: EP6555), via an unspecified route of administration, administered in arm right on 21Mar2021 as single dose for covid-19 immunisation. Medical history included von willebrand's disease. The patient concomitant medications were not reported. The patient had earlier received first dose of BNT16B2 and experienced adverse events. The patient experienced bleeding with acupuncture on 23Mar2021. The patient experienced that her fingers on her right side were also swollen and stiff along with her right leg and right side of her neck on 30Mar2021. About a week later, she received regularly scheduled weekly allergy shots, one in each arm. After the allergy shot, she noticed that her right arm developed a large purple, hard area around the injection site on 31Mar2021. She mentioned also feeling very tired after getting the second vaccination and she had scars on both arms where she received her COVID vaccinations in Mar2021. She had called to see if these issues in her right side might be due to the fact that she had her second COVID vaccination in her right arm. She inquired if this reaction possibly due to receiving the allergy shot too close to the COVID injection site. She stated that she didn't re-ally bleed like a fountain but it was unexpected and surprising to the acupuncturist. She did bleed but it stopped. She has had acupuncture in the past and had a small amount of bleeding in the past. Pa-tient clarified that she received her first dose of the Pfizer COVID 19 vaccine on 01Mar2021 in the afternoon in the right arm; and the second dose on 21Mar2021 at an unknown time on the left arm. She added that she was tired after the first dose and after the second dose. She thinks the allergist inject-ed too close to the COVID 19 vaccination site and that caused the bruise. She stated that her arm was swollen and that has made it stiff. Her doctor didn't warn her about the von willebrand's disease possibly being activated by the vaccine. The scars she noticed from the COVID 19 vaccine are very tiny and one was close to the small pox scar. She mentioned that she got a B12 injection on the other arm and it was fine. The outcome of tired and had scars on both arms where she received her COVID vaccinations was unknown. The outcome of a large purple, hard area around the injection site was not recovered and stiffness in her fingers, legs, and neck was recovering. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1426731
Sex: F
Age:
State: CA

Vax Date: 03/24/2021
Onset Date: 03/01/2021
Rec V Date: 06/25/2021
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Symptoms: fast heart beat/occasional fast heartbeat, feels it for a second then goes away; her pressure and was 166/81. Caller states it had went up a little bit; dizziness/little bit dizzy for a few seconds; blurry vision/looked away and had blurry vision, like grayness; hearing that sounds far/hearing is a little bit far; some nervousness and anxiety; some nervousness and anxiety; a fast palpitation; his is a spontaneous report from a contactable consumer. A 48-year-old female patient received first dose of BNT162B2 (Pfizer-BioNTech Covid-19 Vaccine: Solution for injection; Batch/Lot Number: ER8730), dose 1 via an unspecified route of administration, administered in Arm Left on 24Mar2021 14:30 HR as dose 1, single for COVID-19 immunization. Medical history included ongoing Hashimoto thyroid maybe from 4 or 5 years ago, ongoing multiple spinal stenosis degeneration, joint disease, maybe from 3 or 4 years ago. Concomitant medications included levothyroxine (LEVOTHYROXINE) 75mcg once daily, in the morning taken for thyroid disorder, paracetamol (TYLENOL A) 500 mg, as needed taken for neck pain, back pain, cefixime (FLEXERIL [CEFIXIME]) 5 mg or 10mg by mouth taken for muscle relaxant therapy, sulfamethoxazole, trimethoprim (MORTIN) taken for spinal stenosis, ibuprofen (ADVIL [IBUPROFEN]) 400 mg as needed taken for spinal stenosis, start and stop date were not reported. Caller stated that she would like to mention a side effect. She was concerned. Caller stated she got her first shot at local pharmacy on 24Mar2021. Caller stated after maybe ten minutes of waiting there at the pharmacy, on 24Mar2021 she started getting a little bit dizzy for a few seconds, then it would go away and had blurry vision, also had an occasional fast heartbeat that would like, like it would happen with a fast heartbeat and she feels it for a second and then it would go away. Caller states her hearing is a little bit far. Had blurry vision then got better. Caller stated she told the Pharmacist, they took her pressure and was 166/81. It was reported that it had gone up a little bit and she stated he said it could be normal. Caller stated there was some nervousness and anxiety, which she has both. Caller stated she came back home and occasionally throughout the day, it was happening, not the dizziness, but the heartbeat would come back and go away at night and then around 600AM, then it would go away. Occasional fast heartbeat that has continued, it was more than a couple of hours. She noticed it when she went to go to bed then early that woke her up around 60:0AM for the next two nights. Caller states occasionally she thinks it's still happening, but it's very mild. Caller stated she would get a fast palpitation and then it would go away. Caller stated she doesn't know if it's because of her coffee, then it would go away. Caller stated it's much less when she goes to bed or when she wakes up it is mild. Thinks it was from the vaccine. Caller states it is between improved and it went away, it comes for a few seconds then it goes away, but it hasn't happened. It happened a couple of days she felt the palpitations then it went away after a few seconds. Caller verified that her other symptoms had recovered completely. On 24Mar2021 patient underwent lab tests and procedures which included blood pressure measurement: 166/81 mmhg. The outcome of the events was recovered for fast heartbeat/occasional fast heartbeat, feels it for a second then goes away, her pressure and was 166/81. Caller stated it had went up a little bit, dizziness/little bit dizzy for a few seconds, blurry vision/looked away and had blurry vision, like grayness, hearing that sounds far/hearing is a little bit far and unknown outcome for events nervousness, anxiety and fast palpitation. Follow up attempts are completed. No further information is expected.

Other Meds: LEVOTHYROXINE; TYLENOL A; FLEXERIL [CEFIXIME]; MORTIN; ADVIL [IBUPROFEN]

Current Illness: Hashimoto's disease (maybe 4 or 5 years ago); Spinal stenosis (maybe 3 or 4 years ago)

ID: 1426732
Sex: F
Age:
State: FL

Vax Date: 03/27/2021
Onset Date: 03/01/2021
Rec V Date: 06/25/2021
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Symptoms: high fever; body and muscle pain; body and muscle pain; Looks like she has Covid; This is a spontaneous report from a contactable consumer (husband). A 59-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in left arm on 27Mar2021 14:45 (Batch/Lot Number: EN6208; Expiration Date: 30Jun2021) as single dose for COVID-19 immunisation. Medical history included ongoing diabetes and high blood pressure. Concomitant medication included metformin taken for diabetes, ongoing from an unknown date. It was reported that consumer and his wife received the COVID-19 vaccine. consumer is fine. He is reporting on his wife. On Saturday, she felt well. 24 hours later on 28Mar2021, patient experienced high fever, had body and muscle pain. Patient still has fever and pain that comes and goes. On an unknown date in Mar2021, patient looks like she has COVID and it is not good. On 24Mar2021 patient had COVID-19 test, which shows negative results, which was prior to vaccination. These adverse events did not require any visit to emergency Room nor physician office. The patient did not receive any prior vaccinations within 4 weeks. The outcome of the event looks like she has COVID was unknown. The outcome of rest all the events was recovering. Description of Product Complaint: Description of complaint: wife looks like she has Covid and it is not good. Was tested prior to getting the vaccine and was negative QA Review & Rationale: The complaint and its classification have been reviewed. No immediate containment action is required. The complaint, its priority, and its classification have been reviewed and determined to be appropriate. A full investigation will be performed. This is a complaint for lack of effect of lot EN6208 of the Pfizer-BioNTech Covid-19 Vaccine Injectable. The initial scope of this investigation is limited to the reported finished goods lot EN6208 pending review of lot genealogy. The investigation will include a review of the returned complaint sample (if received) and reserve samples, if necessary. Investigation findings: Summary of Investigation: The initial scope of the investigation was limited to the reported finished goods lot EN6208, fill lot EN5338, and the bulk formulated drug product lot EN5329. Based on the results of the investigation, the scope was not expanded. Manufacturing and packaging batch records were examined for the reported complaint batch. Pfizer (Site name) did not receive photographs or a complaint sample for examination. The complaint was not confirmed. No probable root cause for the complaint related to the manufacturing process of the reported lot was identified. There were no corrective actions taken as a result of this complaint investigation. No related quality issues were identified during the investigation. There were no planned or unplanned deviations recorded during the manufacture of the complaint lot and associated manufacturing lots that may have caused a complaint of this nature. A review of the manufacturing records confirmed processing steps were performed within pre-established parameters. All raw materials and amounts used in the manufacture of the batch were of the correct weight and identity. The drug product is stored at controlled refrigeration throughout the manufacturing process and a log is maintained documenting the elapsed time out of refrigeration. A review of the logs confirmed that all times were within allowable limits. The product also requires storage in ultra-low temperature freezers following the packaging of the product. A review of the freezer temperature log for the reported batch confirmed that all freezer temperatures were within allowable limits. The results of all analytical tests performed at the time of lot release confirmed that the batch meets potency specifications. There is no impact to the quality of the lot. It is unknown how the product was handled, stored, or administered after it left the (Site name). Root Cause Analysis/Identif: Pfizer (Site name) Quality Operations could not indicate a probable root cause for the complaint to be related to the production process of the involved batch. Review of the manufacturing and packaging batch records and release test results confirmed that the batch meets potency specifications. It is unknown how the product was handled, stored, or administered after it left the (Site name). Impact Analysis: Based on the final scope of the investigation, which was limited to the reported finished goods lot and associated fill and formulated drug product lots, and that a root cause related to the production process was not identified, the reported issue is not representative of the lot and does not indicate a negative impact on product quality. No regulatory notification is required. Root Cause Category (Tier 1): Non-assignable (Complaint Not Confirmed) Corrective / Preventive Action: There were no corrective actions as a result of this complaint investigation. The results of all tests, inspections, and in-process controls have been reviewed and all results met the established requirements prior to the release of the reported batch for distribution. Conclusion: The complaint for lack of effect of the Pfizer-BioNTech Covid-19 Vaccine Injectable lot EN6208 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot EN6208, fill lot EN5338, and the formulated drug product lot EN5329. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Scope of Compl. Investigation: The scope of this investigation included the reported finished goods lot EN6208, fill lot EN5338, and the bulk formulated drug product lot EN5329. Acceptable review of related documentation, including manufacturing and packaging batch records and review of release test results at the time of lot release confirmed that there were no issues which may have resulted in a complaint of this nature. Therefore, the scope was not expanded No follow-up attempts are possible. No further information is expected.

Other Meds: METFORMIN

Current Illness: Blood pressure high (Verbatim: high blood pressure); Diabetes

ID: 1426733
Sex: F
Age:
State: FL

Vax Date: 03/25/2021
Onset Date: 03/31/2021
Rec V Date: 06/25/2021
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Symptoms: I developed shingles , left side of my face, days after the first dose of the vaccine.; This is a spontaneous report from contactable consumer (patient herself). A 55-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number: EN6208, Expiry date: Unknown) via an unspecified route of administration in left arm on 25Mar2021 at 15:30 (at the age of 55-year-old) as 1st dose, single for COVID-19 immunization. Patient did not have any other medical history or known allergies to medications, food, or other products. Other medications (concomitant) the patient received within 2 weeks of vaccination included levothyroxine sodium (Synthroid 100 mcg) and escitalopram oxalate (Lexapro 10mg) both taken for unspecified indications. 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 and since the vaccination, the patient has not been tested for COVID-19. On 31Mar2021, days after the first dose of the vaccine, patient developed shingles, left side of face. Reporter considered the event as non-serious. Therapeutic measures taken in response to the event included Valacyclovir. The outcome of the event was recovering.

Other Meds: SYNTHROID; LEXAPRO

Current Illness:

ID: 1426734
Sex: F
Age:
State:

Vax Date: 03/31/2021
Onset Date: 04/01/2021
Rec V Date: 06/25/2021
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Symptoms: swelling on her armpit; This is the spontaneous report from a contactable consumer (Patient). A female patient of unknown age received bnt162b2 (Pfizer-Biontech COVID-19 Vaccine, Lot Number: unspecified), via an unspecified route of administration on 31Mar2021 (Wednesday), as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Yesterday, on 01Apr2021, the patient experienced that she had swelling on her armpit and wants to know if this was normal. The outcome of the event was unknown. Follow-up (05Apr2021): This is a follow-up spontaneous report in response to mail trail send to translate the attached report. No follow-up attempts are possible. Information about lot/ batch number cannot be requested.

Other Meds:

Current Illness:

ID: 1426735
Sex: M
Age:
State: NJ

Vax Date: 03/14/2021
Onset Date:
Rec V Date: 06/25/2021
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Symptoms: Received first dose on 14Mar. Tested positive. Finished isolation period.; Tested positive; This is Spontaneous report from a contactable consumer reported for himself via Pfizer sponsored program. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot number was not reported),via an unspecified route of administration on 14Mar2021 as 1st Dose, Single Dose for COVID-19 immunization. The patients medical history and concomitant medications were not reported. The patient received first dose on 14Mar2021,tested positive and finished isolation period. The patient underwent lab tests and procedures which included sars-cov-1 test resulted as positive. The outcome for the events was Unknown. No follow-up attempts are possible. Information about lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1426736
Sex: F
Age:
State: CA

Vax Date: 03/26/2021
Onset Date: 03/26/2021
Rec V Date: 06/25/2021
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Allergies:

Symptom List:

Symptoms: nosebleed; palpitations; extreme fatigue; my resting heart rate was 99BPM in the urgent care; Almost faint; This is a spontaneous report from a contactable other hcp (patient). A 47-year-old non-pregnant female patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: ER2613), via an unspecified route of administration on 26Mar2021 11:00 (Friday) as single dose for COVID-19 immunization. Medical history included diagnosed with ongoing MCAS (mast cell activation syndrome) 2 weeks ago. Concomitant medications included zinc, probiotics, ergocalciferol (VIT D), turmeric [curcuma longa rhizome], bacillus coagulans, bifidobacterium lactis, fructooligosaccharides, herbal nos, lactobacillus acidophilus, lactobacillus reuteri, minerals nos, vitamins nos (GUNDRY MD VITAL REDS); all taken for an unspecified indication, start and stop date were not reported. Patient had known allergy to pseudoephedrine, previously took pseudoephedrine and experienced rash. Patient reported she had no preexisting conditions, very healthy and active. 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. On 26Mar2021, within 1 minute after vaccination, patient felt like almost faint. 24 hours later on 27Mar2021 12:00, patient had a nose bleed, palpitations, and extreme fatigue etc. Resting heart rate was 99BPM in the urgent care on 27Mar2021. The patient underwent lab tests and procedures which included heart rate: 99 beats per minute on 27Mar2021, sars-cov-2 test (Nasal swab): negative on 07May2021 and 27Mar2021. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Therapeutic measures were taken as a result of events with Antihistamines, supplements, Low Dose Naltrexone. Since the vaccination, patient not tested positive for Covid-19 . The outcome of heart rate was 99BPM was unknown and patient was recovering from rest all of the events.

Other Meds: ZINC; PROBIOTICS; VIT D; TURMERIC [CURCUMA LONGA RHIZOME]; GUNDRY MD VITAL REDS

Current Illness:

ID: 1426737
Sex: F
Age:
State: IL

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 06/25/2021
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Symptom List:

Symptoms: tingling and numbness in right foot developed in evening following vaccination; this has happened previously 4 years ago after an international flight; tingling and numbness in right foot developed in evening following vaccination; this has happened previously 4 years ago after an international flight; This is a spontaneous report from a contactable pharmacist. This pharmacist reported for a patient (family member) a 30-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: ER2613; Expiration date: unknown) via intramuscularly, administered in Arm Left on 30Mar2021 17:15 (at the age of 30-years-old) as first dose, single for COVID-19 immunization at Workplace clinic. The patient medical history and concomitant medications were not reported. Patient had not any allergies to medications, food, or other products. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No other medications the patient received within 2 weeks of vaccination. On 30Mar2021, patient had tingling and numbness in right foot developed in evening following vaccination and this has happened previously 4 years ago after an international flight. Patient had not received any treatment for the adverse events. Patient was not diagnosed with COVID-19 prior and since the vaccination. Seriousness was reported as No. The outcome of events was recovered on an unspecified date in 2021. No follow-up attempts are needed. No further information is expected. Amendment: This follow up report is being submitted to amend previously reported information: (To update the patient information.)

Other Meds:

Current Illness:

ID: 1426738
Sex: F
Age:
State:

Vax Date: 03/18/2021
Onset Date:
Rec V Date: 06/25/2021
Hospital:

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Symptom List:

Symptoms: flare up of the herpes virus; This is a spontaneous report from a non-contactable consumer. This female consumer reported for herself. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 18Mar2021 as 1ST dose, single for COVID-19 immunization. Medical history included ongoing herpes virus infection. The patient's concomitant medications were not reported. On an unspecified date in 2021, the patient stated that she had side effects from the first dose of the Pfizer vaccine which she received on 18Mar2021. Two weeks later she had a flare up of the herpes virus. She has not had any additional stress and was not been working. She wore her masks so she could only conclude the flare up (which she hasn't had in many years) occurred due to the vaccine. Her 2nd vaccine is scheduled for 09Apr2021. Treatment medication included an unknown antiviral and ongoing with it. Outcome of the event was reported as Unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness: Herpes virus infection

ID: 1426739
Sex: M
Age:
State: WI

Vax Date: 04/07/2021
Onset Date: 04/08/2021
Rec V Date: 06/25/2021
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Symptom List:

Symptoms: low grade fever ( 100 degrees F) developed; Rash/itching/hives, starting in groin area, moving to arms, then both sides of trunk, then behind knees.; Rash/itching/hives, starting in groin area, moving to arms, then both sides of trunk, then behind knees.; Rash/itching/hives, starting in groin area, moving to arms, then both sides of trunk, then behind knees.; Flushing and redness in face; Flushing and redness in face; This is a spontaneous report from a contactable consumer (patient). A 57-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0158), via an unspecified route of administration, administered in arm left on 07Apr2021 at 13:15 (at the age of 57-year-old) as a single dose for COVID-19 immunization at hospital. Medical history included pollen allergies and no known allergies with medications, food, or other products. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications included omeprazole 20 mg, atorvastatin 10 mg and tadalafil 5 (units not provided) (received within 2 weeks of vaccination). Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6199), via an unspecified route of administration, administered in left arm on 17Mar2021 at 10:45 as a single dose for COVID-19 immunization. On 08Apr2021 at 13:15, the patient experienced rash/itching/hives, starting in groin area, moving to arms, then both sides of trunk, then behind knees and had flushing and redness in face but no swelling/itching. As rash was subsided, low grade fever (100 degrees Fahrenheit) developed. Patient did not receive any treatments for the events. The events resulted in doctor or other healthcare professional office/clinic visit. The outcome of the event rash was recovered on an unspecified date in 2021 and the rest of the events was recovering. Information on Lot/Batch number was available.

Other Meds: OMEPRAZOLE; ATORVASTATIN; TADALAFIL

Current Illness:

ID: 1426740
Sex: M
Age: 27
State: PA

Vax Date: 05/26/2021
Onset Date: 06/12/2021
Rec V Date: 06/25/2021
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Allergies: None

Symptom List:

Symptoms: About two weeks after the vaccine I woke up with a brain fog that will not go away. It's been over a week and the brain fog still remains. Focusing, holding a conversation, and multitasking have turned into very difficult tasks. My body is fine but my brain fog makes me constantly feel lethargic even when I know I have energy.

Other Meds: None

Current Illness: None

ID: 1426741
Sex: F
Age: 55
State: TN

Vax Date: 03/25/2021
Onset Date: 03/27/2021
Rec V Date: 06/25/2021
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Lab Data:

Allergies: Codeine drugs

Symptom List:

Symptoms: I had really bad chills and fever I lost my taste and smell and started feeling extremely fatigued. I could not get out of bed. I went got 2 covid test, I got a rapid and a send off both came back negative. I stayed in bed for a week.

Other Meds:

Current Illness:

ID: 1426742
Sex: F
Age: 50
State: MD

Vax Date: 05/10/2021
Onset Date: 05/10/2021
Rec V Date: 06/25/2021
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Symptom List:

Symptoms: Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)

Other Meds:

Current Illness:

ID: 1426743
Sex: F
Age: 36
State: KY

Vax Date: 06/22/2021
Onset Date: 06/22/2021
Rec V Date: 06/25/2021
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Lab Data:

Allergies: No

Symptom List:

Symptoms: Immediately after shot was administered, my entire left arm started tingling down to my left pinky finger. I become overheated and had to sit down and fan myself from fainting. After 20 minutes, I was able to drive home. That evening, I wasn't able to sleep. My entire body was in severe pain, had a bad headache, and sweated through the sheets. The following day at work, I ran a low grade fever, was pale and felt like I didn't sleep for weeks. Ran a low grade fever all day. The following day, I took off work and tried to rest. On Friday morning, experienced chest pains. Took Ibuprofen and it subsided. Still have pain in left arm.

Other Meds: Sertraline 150mg; Vitamins: C, D, Turmeric, B12

Current Illness: No

ID: 1426744
Sex: M
Age: 42
State: SC

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 06/25/2021
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Symptom List:

Symptoms: My left arm injection site has never stopped hurting. It occasionally itches. It is sore in the muscle.

Other Meds:

Current Illness:

ID: 1426745
Sex: M
Age:
State: MS

Vax Date: 04/08/2021
Onset Date: 04/08/2021
Rec V Date: 06/25/2021
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Symptom List:

Symptoms: A rash broke out all over my body; This is a spontaneous report from a contactable consumer (patient). A patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number ER8733), via an unspecified route of administration, in arm left on 08Apr2021 at 14:45 as 1st dose single for COVID-19 immunisation. The patient had no medical history. The concomitant medications of the patient included bisoprolol fumarate, hydrochlorothiazide (BISOPROLOL /HCTZ) and allopurinol both taken for an unspecified indication received within 2 weeks of vaccination. The patient had no allergies to medications, food, or other products. 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 not been tested with COVID-19. On 08Apr2021 at 17:00, the patient experienced a rash broke out all over body. Therapeutic measures were taken as a result event that included over the counter Benadryl and Pepcid. The outcome of the event was not resolved. Information on Lot/Batch number was available. Follow up letter has been generated for further information.

Other Meds: BISOPROLOL /HCTZ; ALLOPURINOL

Current Illness:

ID: 1426746
Sex: M
Age: 40
State: KS

Vax Date: 06/25/2021
Onset Date: 06/25/2021
Rec V Date: 06/25/2021
Hospital:

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Allergies: none known

Symptom List:

Symptoms: Patient had vasovagal response to receiving the vaccine, became light-headed and briefly lost consciousness. We called Dr. in the attached office and his intern over to make sure Pt. was okay. Gave the pt water and he felt fine after sitting for ~15 minutes

Other Meds: none

Current Illness: none

ID: 1426747
Sex: F
Age: 53
State: MA

Vax Date: 06/09/2021
Onset Date: 06/10/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Allergies:

Symptom List:

Symptoms: Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Dizziness /Lightheadedness-Mild, Systemic: Exhaustion/Lethargy-Medium, Systemic: Fever-Mild, Systemic: burning sensation in skin-Mild, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extremities)-Medium, Systemic: Weakness-Mild, Additional Details: numbness and tingling in arm, back and spine. Patient states symptoms felt like shingles. Loss of feeling from mid-spine up. Burning sensation on upper, left shoulder.

Other Meds:

Current Illness:

ID: 1426748
Sex: F
Age: 23
State: NY

Vax Date: 06/24/2021
Onset Date: 06/24/2021
Rec V Date: 06/25/2021
Hospital:

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Symptoms: A-Team member stated they didn't feel good this morning and last night after taking the J&J vaccine. Around 8 am looked for the employee health nurse to get medication for nausea and headache. She was then making tea and was noted not to be feeling well and fainted. Another employee found her on the floor, and her heart rate was 115, and BP was 112/64 with a 100-degree temp Fahrenheit. A couple of hours prior, her temp was 97 degrees Fahrenheit. She looked diaphoretic, hypoglycemic, and was too weak to get off the floor, there was a maxi lift used to transfer to a wheelchair, and she was very dizzy. The only medicine taken was Pepto Bismol for nausea.

Other Meds:

Current Illness:

ID: 1426749
Sex: M
Age: 71
State: KS

Vax Date: 03/27/2021
Onset Date: 03/27/2021
Rec V Date: 06/25/2021
Hospital:

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Lab Data:

Allergies: Rosuvastatin, Simvastatin, Niacin

Symptom List:

Symptoms: Within 6 hours of getting his last COVID vaccine, he stated he knew he was in trouble. For 4 days he could not even function. He couldn't even use the phone to call for help. He stated his temperature was 104. Stated he continues to have shortness of breath all the time. He can't even walk the full length of his house without getting winded. He has no energy and feels tired all the time. He wakes up in the morning feeling tired. He feels like it is slowly getting a little better, but it has been over 2 months already. He denies having any further headaches. He still gets floaters in his left eye but feels like the flashes of light are getting less. This report 6/15/2021.

Other Meds: Vitamin E, Vitamin B-Complex, Semaglutide, KCL, Niacin, Multivitamin, Lisinopril, Glargine Insulin, Glimepiride, Garlic Oil, Lasix, Fluticasone Nasal spray, Ezetimibe, Diclofenac Ophthalmic solution, Coenzyme, Cinnamon, Carboxymethylcellulo

Current Illness: None

ID: 1426750
Sex: F
Age: 51
State: IL

Vax Date: 06/12/2021
Onset Date: 06/12/2021
Rec V Date: 06/25/2021
Hospital:

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Symptom List:

Symptoms: Patient received the dose after manufacturer recommended freezer storage duration.

Other Meds:

Current Illness:

ID: 1426751
Sex: F
Age:
State:

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Symptom List:

Symptoms: Menstrual spotting; bloody nose; headache; fatigue; This is a spontaneous report received from a non-contactable consumer, the patient. A 34-years-old non pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number unknown) via an unspecified route of administration in Arm Right on 07Apr2021 15:00 (age at vaccination 34years old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history included Ehlers Danlos syndrome from an unknown date and unknown if ongoing. Concomitant medication included naltrexone (NALTREXONE) taken for an unspecified indication, start and stop date were not reported. The patient had no allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested positive for COVID-19. Timeframe between vaccination and starting of symptoms was reported as 5Hours. On 07Apr2021 20:00, the patient experienced menstrual spotting, bloody nose, headache and fatigue. It was unknown if patient received any treatment for the adverse events. The clinical outcome of the events was reported as unknown. Information on the lot/batch number has been requested.

Other Meds: NALTREXONE

Current Illness:

ID: 1426752
Sex: M
Age: 61
State: FL

Vax Date: 03/30/2021
Onset Date: 04/01/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies: Penicillian

Symptom List:

Symptoms: Extreme soreness after first injection. After second injection, soreness moved to left shoulder which has been compromised as to motion. Unable to move shoulder as before injections.

Other Meds: Levothyroxin, Simvastatin, Amlodiprine/Benazepril

Current Illness: None

ID: 1426753
Sex: F
Age:
State: FL

Vax Date: 04/07/2021
Onset Date: 04/08/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Symptom List:

Symptoms: Swollen lymph node in arm pit; This is a spontaneous report from a contactable consumer, the patient. A 50-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER- BIONTECH COVID-19 m RNA vaccine; Lot number: Ew0151), via an unspecified route of administration to the left arm on 07Apr2021 at 1130 (at the age of 50-years-old), as a single dose for COVID-19 immunisation. Medical history included Hashimotos. The patient had an allergy to Penicillin. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: UNKNOWN), via an unspecified route of administration on an unknown date, as a single dose for COVID-19 immunisation. Concomitant medication included thyroid medications. The patient did not receive any other vaccine within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient experienced swollen lymph node in the arm pit on 08Apr2021, the size of a golf ball. Since the vaccination, the patient had not tested positive for COVID-19. The patient did not receive any treatment for the adverse event. The clinical outcome of the event of swollen lymph node was not recovered at the time of reporting. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426754
Sex: F
Age: 66
State: MI

Vax Date: 03/18/2021
Onset Date: 04/01/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies: Dust, Mold, Morphine, Betadine

Symptom List:

Symptoms: 2 weeks after getting the vaccine I had swollen lymph nodes in the top of my neck. I discussed it with the physician on 3/17/2021 and we decided to just continue to watch it without any treatment for now. I'm having blood work in about a month.

Other Meds: Levothyroxine , Fexofenadine, vitamin B, vitamin D, Turmeric, Cinnamon supplement, Centrum silver, 5HTP, Calcium, Magnesium

Current Illness: None

ID: 1426755
Sex: F
Age: 12
State: IL

Vax Date: 06/12/2021
Onset Date: 06/12/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Lab Data:

Allergies:

Symptom List:

Symptoms: Patient received the dose after manufacturer recommended freezer storage duration.

Other Meds:

Current Illness:

ID: 1426756
Sex: F
Age: 12
State: SC

Vax Date: 06/23/2021
Onset Date: 06/23/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List:

Symptoms: Systemic: Abdominal Pain-Medium, Systemic: Nausea-Medium, Systemic: Vomiting-Medium, Additional Details: patient vomiting within minutes of receiving injection

Other Meds:

Current Illness:

ID: 1426757
Sex: F
Age:
State: PA

Vax Date: 04/08/2021
Onset Date: 04/08/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List:

Symptoms: This is a spontaneous report from a contactable consumer, the patient. A 40-years-old non pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; lot Number: ER8734) via an unspecified route of administration in the left arm on 08Apr2021 at 08:15 (at the age of 40-years-old) as a single dose for COVID-19 immunisation. Medical history included palindromic rheumatism and sulfonamide allergy. Concomitant medications were not reported. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number; ER8727) via an unspecified route of administration in the left arm on 18Mar2021 at 08:15 (at the age of 40-years-old) as a single dose for COVID-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had not received any other vaccines within 4 weeks prior to the COVID-19 vaccine. Since the vaccination, the patient was not tested for COVID-19. The patient experienced swelling in ankles and in feet most severe on left side on 08Apr2021 at 17:00. The patient did not receive any treatment for the events. The clinical outcome for events swelling in ankles and in feet was resolved on unknown date in Apr2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1426758
Sex: F
Age: 27
State: NY

Vax Date: 04/01/2021
Onset Date: 04/02/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies: Amoxicillin

Symptom List:

Symptoms: Moderate lethargy, soreness, achyness, suspected mild hyperthermia

Other Meds: Lo lo earrings Fe SID Valcyclovir 500mg SID Allegra 180mg SID Famotidine 20mg SID

Current Illness: None

ID: 1426759
Sex: F
Age: 16
State: IL

Vax Date: 06/12/2021
Onset Date: 06/12/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

Symptom List:

Symptoms: Patient received the dose after manufacturer recommended freezer storage duration.

Other Meds:

Current Illness:

ID: 1426760
Sex: F
Age: 16
State: TX

Vax Date: 06/23/2021
Onset Date: 06/23/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Symptom List:

Symptoms: Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: Approxiamately 5 minutes after the vaccine the patient felt light headed and dizzy. She then fainted forward and her mom lifted her back and at that point she appeared to shake (2 jerking motions) and then became alert. The patient was instructed to lay down. Her blood pressure was taken and was normal. The ambulance was called due to the shaking motion which appeared to be a possible seizure. The patient and her mom did not wish to be taken to the hospital. Follow-up call not answered

Other Meds:

Current Illness:

ID: 1426761
Sex: F
Age: 45
State: PA

Vax Date: 05/19/2021
Onset Date: 06/02/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies: Penicillin Erythromycin Sulfa Spiro Drugs

Symptom List:

Symptoms: I went to hospital on 06/04/2021. They x-rayed it and wrapped it. I followed up with my rheumatologist. She put a drain in it but it came back that night. They diagnosed it as olecranon bursitis. All I have on now is a compression wrap.

Other Meds:

Current Illness:

ID: 1426762
Sex: M
Age: 26
State: IL

Vax Date: 06/12/2021
Onset Date: 06/12/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
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Lab Data:

Allergies:

Symptom List:

Symptoms: Patient received the dose after manufacturer recommended freezer storage duration.

Other Meds:

Current Illness:

ID: 1426763
Sex: F
Age: 47
State: PA

Vax Date: 06/02/2021
Onset Date: 06/02/2021
Rec V Date: 06/25/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List:

Symptoms: Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: patient said she had numbness occure 2 hours after first shot. numbness in left neck,left chest,left arm,left shoulder

Other Meds:

Current Illness:

ID: 1426764
Sex: F
Age: 37
State: IL

Vax Date: 06/08/2021
Onset Date: 06/09/2021
Rec V Date: 06/25/2021
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Symptoms: Sudden pain in the left lower part of of the abdomen, it started the next day at noon after the vaccine, it wasn't a continuous pain but more or less constant and suddenly and it kept me from doing what I was doing. Bloody diarrhea that's started 20 minutes after the initial stomach pain. I had about 6 bloody bowel movements during that day, the pain disappeared that same day during the evening, the bloody diarrhea stopped during the night and I had two more bloody bowel movements between 7 and 9am on the 10th of June.

Other Meds: Co Aprovel 150mg; Aspirin protect

Current Illness:

ID: 1426765
Sex: F
Age: 22
State: VA

Vax Date: 06/24/2021
Onset Date: 06/24/2021
Rec V Date: 06/25/2021
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Symptoms: fever>101.2 and dry heaving (unable to vomit due to lack of eating)

Other Meds:

Current Illness:

ID: 1426766
Sex: F
Age: 65
State: FL

Vax Date: 06/01/2021
Onset Date: 06/01/2021
Rec V Date: 06/25/2021
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Allergies: Narcotics

Symptom List:

Symptoms: Extreme fatigue, headache, sore throat, and high fever. The high fever ran for a few days. I had no appetite. I slept a lot.

Other Meds: Hydrocortisone, Metoprolol, Fludrocortisone, Cholesterol, Euthyrox,

Current Illness: None

ID: 1426767
Sex: M
Age: 74
State: NY

Vax Date: 04/13/2021
Onset Date: 06/25/2021
Rec V Date: 06/25/2021
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Allergies: NKA

Symptom List:

Symptoms: Patient has been feeling extremely fatigue, joints sore (knees, wrists), more depressed and has passed out twice since the 2nd Moderna vaccine. The patient has been seen by his PCP and has been tested for lyme as had a tick bite last year, but the bloodwork came back negative. Pt also feels his normal pain medication (oxycodone 5mg) is not working as well for his back pain. He said he will do yard work that he normally does, like mowing the lawn, and is extremely tired. No change in medication or health status other than noticing these symptoms. The patient passed out once while raking leaves and another time on the porch and stood up and passed out. The patient feels these symptoms are getting progressively worse and not getting any better.

Other Meds: Alprazolam 1mg, Citalopram 40mg, Gabapentin 300mg, Levothyroxine 100mcg, Oxycodone 5mg MDD 6 tabs,

Current Illness: none

ID: 1426768
Sex: M
Age: 39
State: IL

Vax Date: 06/12/2021
Onset Date: 06/12/2021
Rec V Date: 06/25/2021
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Symptoms: Patient received the dose after manufacturer recommended freezer storage duration.

Other Meds:

Current Illness:

ID: 1426769
Sex: F
Age: 40
State: PA

Vax Date: 06/23/2021
Onset Date: 06/23/2021
Rec V Date: 06/25/2021
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Symptoms: Systemic: Dizziness / Lightheadness-Mild, Additional Details: patietn said dizziness occurred within the 15 minutes while she was waiting post vaccine

Other Meds:

Current Illness:

Date Died: 05/13/2021

ID: 1426770
Sex: M
Age: 68
State: GA

Vax Date: 01/18/2021
Onset Date: 04/27/2021
Rec V Date: 06/25/2021
Hospital: Y

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Symptom List:

Symptoms: COVID-19 PNEUMONIA, ACUTE RESPIRATORY FAILURE WITH HYPOXIC

Other Meds:

Current Illness:

ID: 1426771
Sex: F
Age: 64
State: KY

Vax Date: 04/23/2021
Onset Date: 04/24/2021
Rec V Date: 06/25/2021
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Allergies: None

Symptom List:

Symptoms: Severe nausea Severe headache Severe chills Severe muscle aches Severe side effects lasted 6 hrs. Worse than the flu which I?ve had twice. After that in bed 2 more days but not severe

Other Meds: Amlodopine 5 mg Pristique lowest dose

Current Illness: None

ID: 1426772
Sex: F
Age: 52
State: WA

Vax Date: 05/17/2021
Onset Date: 06/11/2021
Rec V Date: 06/25/2021
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Allergies: None

Symptom List:

Symptoms: Lump on the lower left breast

Other Meds: Tapazole

Current Illness:

ID: 1426773
Sex: M
Age: 23
State: MS

Vax Date: 05/18/2021
Onset Date: 06/25/2021
Rec V Date: 06/25/2021
Hospital:

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Allergies: Penicillin

Symptom List:

Symptoms: Asymptomatic.

Other Meds: None.

Current Illness: None.

Total 2021 VAERS Injuries: 704,237

Page last modified: 03 October 2021 5:28pm