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: 1111344
Sex: F
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Chills; Fatigue; This is a spontaneous report from a contactable consumer. This consumer reported 2 reports for different patients (herself and her husband). This report is for herself. A 70-year-old female patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration, on an unspecified date, at single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced chills and fatigue the day after vaccination when she woke up for a few hours. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111345
Sex: M
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: a slight headache; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced a slight headache on an unspecified date. The patient reportedly took 2 tabs of paracetamol (TYLENOL) as treatment. Outcome of event was unknown. Information regarding lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111346
Sex: F
Age:
State:

Vax Date: 01/30/2021
Onset Date: 01/31/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Diarrhea; This is a spontaneous report from a contactable consumer (patient). This 34-year-old female patient received dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 30Jan2021 at 14:15 (at the age of 34-years-old) as a single dose in the left arm for COVID-19 immunization. The patient had no medical history. The patient was not pregnant at the time of vaccination. Prior to the vaccine, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the vaccine. The patient did not take any concomitant medications. The patient did not have any allergies to medications, food, or other products. On 31Jan2021 at 15:00 the patient experienced diarrhea going on 3 days. The event was reported as non-serious. The patient was not hospitalized for the event. The patient did not receive any treatment for the event. The outcome of diarrhea was not recovered. It was also reported that since the vaccine, the patient had not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1111347
Sex: F
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: had both doses of the COVID-19 vaccination, a couple weeks after, the patient tested positive for COVID-19; had both doses of the COVID-19 vaccination, a couple weeks after, the patient tested positive for COVID-19; This is a spontaneous report from a contactable consumer via a Pfizer-sponsored program. A female patient of an unspecified age started received first and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE); both via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had both doses of the COVID-19 vaccination, a couple weeks after, the patient tested positive for COVID-19 on unspecified date. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111348
Sex: F
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Got positive reading after her vaccination.; Got positive reading after her vaccination.; This is a spontaneous report from a contactable consumer (patient). This consumer reported similar events for two patients (herself and her husband). This is first (wife) of two reports. A female patient of an unspecified age received her first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that got positive reading after her vaccination on an unspecified date. She added that her husband got a bad covid outbreak after first dose and the location closed. The patient underwent lab tests and procedures which included covid-19 reading (sars-cov-2 test) was positive on an unspecified date. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111349
Sex: F
Age:
State: AR

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: mild arm pain; This is a spontaneous report from a contactable consumer (patient's husband). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date were unknown), via an unspecified route of administration on 20Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced mild arm pain on an unspecified date. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111350
Sex: F
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: headache; This is a spontaneous report from a sponsored program. A non-contactable consumer (patient) reported that a female patient of unspecified age received first dose of BNT162B2, via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient previously took dupilumab (DUPIXENT). The patient took dupilumab the day before the covid vaccine. She was concerned if it worked, is she can get the second dose. She experienced a headache after covid vaccine. The outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1111351
Sex: F
Age:
State: SC

Vax Date: 01/11/2021
Onset Date: 01/18/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Loss of taste; Loss of smell; she tested positive- 5/tested positive for COVID-19; This is a spontaneous report from a sponsored Program. A contactable female consumer (patient) reported that a 37-years-old female patient received bnt162b2 (BNT162B2; Batch/lot number: EL1284) first dose, intramuscular on 11Jan2021 between 9-9:30 a.m at SINGLE DOSE at Right upper arm for covid-19 immunisation. The patient medical history was not reported. Prior Vaccinations (within 4 weeks) was None. Additional Vaccines Administered on Same Date of the Pfizer Suspect was None. The patient's concomitant medications were not reported. The patient experienced she tested positive- 5/tested positive for covid-19 on 18Jan2021 with outcome of unknown, loss of taste on 18Jan2021 02:00 with outcome of recovered on 23Jan2021, loss of smell on 18Jan2021 02:00 with outcome of recovered 23Jan2021. The patient underwent lab tests and procedures which included sars-cov-2 test (COVID-19 Rapid Test): positive on 18Jan2021, sars-cov-2 test (COVID-19 Test): inconclusive on 29Jan2021. The action taken in response to the event(s) for bnt162b2 was not applicable. Caller was scheduled today for the 2nd dose of Pfizer vaccine. However, 2 weeks ago she tested positive- 5 days after the 1st dose of the vaccine. Today, she had no symptoms for over a week and she didn't know yet if she was still positive for COVID or not. Caller was asking if she can take the 2nd dose today or if she needed to wait for days/weeks before taking it. On 11Jan2021, the caller received her first dose of COVID-19. On 18Jan2021, the caller tested positive for COVID-19. She was symptom free after 5 days. She was scheduled to receive her second dose at 12:00pm today. She stated she has been getting conflicting information. She wanted to know can she receive the second vaccine? Since 23Jan2021, she has been symptom free. She mentioned she filled out a questionnaire online about and she did respond that she tested positive after receiving the first dose, but she never heard anything back. Caller stated she noticed probably around 2 am in the morning on 18Jan, she had that feeling in my throat where she was losing her sense of smell and taste. She woke up that morning around 8am, and these senses were completely gone. Caller stated it was the only symptom she had. She confirmed she had a COVID-19 Rapid test done on 18Jan2021. She actually went and got tested again on Friday, 29Jan2021, to see if she still had COVID. However, the person doing the test must not have done it right. The person only swabbed one nostril and the test came back inconclusive as of yesterday. The events not require a visit to Emergency Room and Physician Office. No further information was provided or obtained.

Other Meds:

Current Illness:

ID: 1111352
Sex: M
Age:
State: IL

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: he had a problem with his heart; neck pain/his neck on the left side, when he turn his head to the left side it hurts; muscle pain is from neck down to upper shoulder; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 28Jan2021 at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 28Jan2021, patient experienced neck pain; further reported as his neck on the left side, when he turn his head to the left side hurts and patient also experienced muscle pain from his neck down to the upper shoulder. It was also reported that the patient had a problem with his heart on an unspecified date. Outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111353
Sex: F
Age:
State: TX

Vax Date: 01/24/2021
Onset Date: 01/01/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Rash on my chest; I guess the rash joined one another on my chest, inside my legs and both my upper arms; Cough; My left arm where I got the shot that arm, it was feverish, it was very hot; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female patient received first dose of BNT162B2, lot no. EL9262, via an unspecified route of administration (left arm) on 24Jan2021 at a single dose for COVID-19 immunization at a hospital facility. They gave her a dose that was recommended. Medical history and concomitant medications were not reported. The patient reported a reaction that she had to her first vaccine. It was Pfizer BioNTech COVID-19 Vaccine EUA and she had that on 24Jan2021 and she had a little cough the following day (25Jan2021) which she did not have before and then she didn't recover from the cough but she woke up on the 27th with a little bit of rash on her chest and she just kind of ignored it but within four hours she had not just a rash, she had she guessed the rash joined one another on her chest, inside her legs and both her upper arms. She started taking Benadryl and it took about 125 mg of the Benadryl over 30 hours before she was able to get rid of the rash. It happened three days later at her house. She treated herself with Benadryl. She was not experiencing any kind of breathing problems or anything that she was alarmed about. She only took Benadryl 25 mg when she first saw it because the rash was not severe but within four hours even after she took the 25 mg, the rash became very severe and her left arm where she got the shot that arm, it was feverish, it was very hot on Jan2021. She didn't know next step with her second dose. She felt like rash was severe. Her rash took over 30 hours and taking 125mg Benadryl to get rid of it. So, she didn't know how to prepare or what to expect. She was due to get it on 14Feb. The patient recovered from rash generalized on Jan2021, not recovered from cough, while outcome of other event was unknown.

Other Meds:

Current Illness:

ID: 1111354
Sex: M
Age:
State: TX

Vax Date: 01/28/2021
Onset Date: 02/01/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: discomfort; did not sleep a wink last night; Nauseous; blood pressure elevated/139/94; heart rate elevated/His heart rate is currently 139; This is a spontaneous report from a contactable consumer (patient). A 56 -year-old male patient received his first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: EL9264), intramuscular (on left arm) on 28Jan2021 12:30 (at the age of 56 -years-old), single dose for COVID-19 immunization. No relevant medical history. The patient's concomitant medications were not reported. Patient is calling about the first dose of the Pfizer covid19 vaccine which he received on Thursday. Yesterday, he started getting nauseous, it is terrible and very strong. The nausea has been continuous since yesterday. His blood pressure and heart rate is pretty elevated. Declines any treatment. The nausea was bad yesterday and stayed bad, he did not sleep a wink last night. His last blood pressure taken about 10 minutes ago was 139/94. His blood pressure is normally 125 over 65 or 70. His heart rate is currently 139. His heart rate and blood pressure became elevated yesterday. States it might have to do with how much discomfort he is in. When querying other medications and medical conditions, he reports nothing out of the ordinary. The outcome of the events sleep disorder and discomfort was unknown, other events was not recovered. No Prior Vaccinations (within 4 weeks).No AE(s) following prior vaccinations.

Other Meds:

Current Illness:

ID: 1111355
Sex: F
Age:
State: FL

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Dizziness; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received first single dose of BNT162B2 (Solution for injection, lot number: EL9263, exp date not reported), via an unspecified route of administration (anatomical location: arm left) on 02Feb2021 11:00 as treatment first dose (COVID-19 immunisation). Vaccination Facility Type: at the mall. Vaccine was not administered at military facility. Medical history included diabetes type 1, from late 30s or 40s; and she had a stroke when she was 53 years old. Family history included sister with type 1 diabetes, other sister with hypogammaglobulin anemia. Concomitant medication included ongoing oral ramipril taking since she was 53 because she had a stroke as blood thinner. The patient had no prior vaccinations within 4 weeks. She thought she got Moderna but they sent her home with Pfizer paper. Asking how can she know which vaccine she had? Then states now she sees the name Pfizer on her vaccine card. Mentions that she had some dizziness in the last half hour on 02Feb2021. She was scheduled to receive the next dose of the vaccine 23Feb2021. No investigation assessment performed. The outcome of dizziness was recovering (ongoing at the time of reporting).

Other Meds: RAMIPRIL

Current Illness:

ID: 1111356
Sex: F
Age:
State: FL

Vax Date: 01/31/2021
Onset Date: 02/01/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: I got the first shot on 24Jan2021 and I got the second dose on 31Jan2021; I got the first shot on 24Jan2021 and I got the second dose on 31Jan2021; Have a lump on my arm and it's very itchy/lump where they give me the shot; Have a lump on my arm and it's very itchy/lump where they give me the shot; This is a spontaneous report from a contactable consumer. A 66-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9262), via an unspecified route of administration on 31Jan2021 at a single dose on arm for COVID-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. The patient received the first dose of BNT162B2 for COVID-19 immunisation on 24Jan2021. Consumer stated, "I took my second Covid shot on Sunday (31Jan2021) and I have a lump where they give me the shot. I have a lump on my arm and it's very itchy. So that's what I wanted to know that is why I have been hold for an hour to find out how you can assist me. I am asking you what you can do for me. I don't think you understand me. I have been holding an hour because my arm has a lump where I got the shot. Are they supposed to give the first shot and second shot in the same arm?" Event start date was reported as "Yesterday, 01Feb2021." The patient did not receive treatment for the events. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1111357
Sex: M
Age:
State: PA

Vax Date: 01/21/2021
Onset Date:
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: his arm was just sore for a day; This is a spontaneous report from a contactable healthcare professional (patient). A male patient of an unspecified age received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot and expiration date were not provided) solution for injection, via an unspecified route of administration on 21Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated that he received the first dose of the COVID vaccine on 21Jan2021 (12 days ago). He stated that he was fine, his arm was just sore for a day on an unspecified date in 2021. The outcome of the event was recovered on an unspecified date in 2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111358
Sex: U
Age:
State:

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Chills; Very tired; just don't feel well; Headache; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number unknown), via an unspecified route of administration on 2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced chills, very tired, just don't feel well all on 2021 with outcome of unknown and headache on 2021 with outcome of not recovered. The patient stated, "I am having some I think they are side effects, I had my injection for the vaccine (Clarified as COVID 19 vaccine Pfizer) Thursday last Thursday and I was wondering, I didn't had any side effect right away but I am having chills, no fever, very tired, just don't feel well, I didn't know (incomplete sentence), I read the list that's on the list headache but it still be 5 days later." On paraphrasing concern, patient stated, "Yeah, the chills are the worst more than the headache that is my question." Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111359
Sex: F
Age:
State: FL

Vax Date: 01/07/2021
Onset Date: 01/01/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: When she got the first dose it hurt a little, but didn't hardly feel anything.; This is a spontaneous report from a contactable consumer (patient). A 90-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot: Either EX3246 or EL3246) via an unspecified route of administration left arm, at the age of 90-year-old, on 07Jan2021 around 13:30-14:00, single dose, for covid-19 immunisation. Medical history included glaucoma and drip down her nose and sinus. The patient's concomitant medications were not reported. In Jan2021, when she got the first dose, it hurt a little but didn't hardly feel anything. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1111360
Sex: F
Age:
State: CA

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Bloating; Constipation; Gas; Headache; This is a spontaneous report from a contactable consumer reporting for himself and his wife. This consumer reported similar events for two patients. This is the second of two reports. A 66-year-old female patient (reporter's wife) received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL8982), intramuscular on 26Jan2021 at a single dose on the right arm for COVID-19 immunization. The patient had no medical history and there were no concomitant medications. The patient did not have prior vaccinations within 4 weeks of the COVID vaccine. The reporter called for himself and his wife. He reported that they looked at the at the symptoms on the vaccine fact sheet and they did not have any of those symptoms. They received the first dose of the vaccine on 26Jan2021. The first couple of days they had a little bit of a headache starting on 27Jan2021. The third day, 29Jan2021, they started having constipation and bloating which is not normal for them. They are having a lot of gas and are very bloated. The reporter and patient was asking if anyone else has reported this since it is unusual for them. The patient then stated that she had just a very mild headache. She has been able to go to the bathroom a little bit. Usually she is going to the bathroom a lot. The patient stated that the gas and bloating is unreal. All she had last night was chicken broth and a piece of toast for dinner. She took Tylenol for the headache. She is not taking anything for constipation. She is drinking caffeinated coffee which she never drinks or she would be going to the bathroom all day. She just wishes she could fart. The outcome of headache was recovered on 29Jan2021. The outcome of bloating, constipation and gas was not recovered.

Other Meds:

Current Illness:

ID: 1111361
Sex: F
Age:
State: SC

Vax Date: 02/16/2021
Onset Date: 02/16/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: My face went numb; Headache; This is a spontaneous report from a contactable consumer. A 67-years-old non-pregnant female patient received BNT162b2 (Pfizer-BIONTECH Covid-19 Vaccine), via an unspecified route of administration, in the left arm, on16Feb2021 at 10:15 (at the age of 67 years-old) as a single dose for covid-19 immunisation. Medical history included headache, anaphylaxis reactions to food allergies, Spinich, cabbage, sulfa based drugs diabetes, and asthma. The patient had not received any other vaccinations within 4 weeks and was not diagnosed with COVID-19. Concomitant medication included diabetes meds and insulin glargine (BASAGLAR). The patient reported on 16Feb2021, at 10:45 after waiting 30 as instructed, I had a reaction 5 - 10 minutes later. My face went numb, and then a headache started. I have had only 1headache in my life prior to this. The patient was not hospitalized for the events nor was treatment received. The clinical outcome of the event was recovered

Other Meds: BASAGLAR

Current Illness:

ID: 1111362
Sex: F
Age:
State: NC

Vax Date: 02/16/2021
Onset Date: 02/16/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: could taste metal in my mouth; get over heated and breathing slightly difficult; get over heated and breathing slightly difficult; This is a spontaneous report from a contactable consumer reported for herself. A 73-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand: Pfizer; lot number: EL8982) via an unspecified route of administration at left arm on 16Feb2021 at 01:15 PM at a single dose for COVID-19 immunization. Medical history included allergies to medications, food, or other products: dairy and pineapple. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand: Pfizer; lot number: EL8982) at left arm on 29Jan2021 at 01:15 PM for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications the patient received within 2 weeks of vaccination included acetylsalicylic acid (BABY ASPIRIN) and vitamin D nos. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 vaccine was administered was other. As soon as the nurse started to administer the shot the patient could taste metal in her mouth. Within minutes she started to get over heated and breathing slightly difficult. She opened all the windows in the car and reminded herself that she was breathing and could blow the horn at any time. Difficulty breathing lasted minutes but the overheating about 20 minutes. Once she cooled down all symptoms disappeared. Adverse event start date was reported as on 16Feb2021 at 01:15 PM. The events were reported as non-serious. No treatment received for events. The outcome of events was resolved on 16Feb2021. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds: BABY ASPIRIN; VITAMIN D NOS

Current Illness:

ID: 1111363
Sex: M
Age:
State: MO

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

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

Symptoms: Fever at 102.2; chills; stomach cramping; sore neck; sore at site of injection; minor headache; runny nose; This is a spontaneous report from a contactable consumer reported for self. This 37-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot#: EN 5318) at single dose on 16Feb2021 10:00 for COVID-19 immunisation. The first dose was on 26Jan2021 at 11:00 AM (Lot#: EN5318) in left arm. Medical history was not reported. Allergies to medications, food, or other products was none known. Concomitant medication included vitamin D. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient had fever at 102.2 and chills, stomach cramping, sore neck, sore at site of injection, minor headache and runny nose on 17Feb2021 12:00 AM. There was no treatment received for the adverse event. This was a non-serious report. The events did not result in death, not life threatening, not caused/prolonged hospitalization, no disabling/incapacitating, no congenital anomaly/birth defect. Patient was recovering from the events. No follow-up attempts are possible. No further information is expected.

Other Meds: VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 1111364
Sex: F
Age:
State: NJ

Vax Date: 02/13/2021
Onset Date: 02/13/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Lab Data:

Allergies:

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

Symptoms: Arm was sore for a day; This 66- year-old female patient contactable consumer (reported for herself) received the first dose BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration, on 13Feb2021 at 10:00 AM (at the age of 66-years-old) as a single dose for COVID-19 immunization, in left arm. The facility where COVID-19 vaccine was administered was at a Hospital. She has had no other vaccines on the same day or in the past 4 weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Medical history included: Thyroid problem. Concomitant medication included: Synthroid 88mcg, Synthroid 75mcg, Ibandronate. On 13Feb2021 at 5:00PM, the patient reported that her arm was sore for a day. The clinical outcome of the event arm sore was recovered. It was reported that since the vaccination, the patient had not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds: SYNTHROID; IBANDRONATE

Current Illness:

ID: 1111365
Sex: M
Age:
State: AK

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
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Allergies:

Symptom List: Unevaluable event

Symptoms: Really Big Headache; This is a spontaneous report from a contactable other health professional. A 19-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (batch/lot is unknown: Not available/provided to reporter at the time of report completion) via an unspecified route of administration on 16Feb2021 at single dose for COVID-19 immunization. Medical history included Covid-19. Prior to vaccination, the patient was diagnosed with COVID-19. No known allergies to medications, food, or other products. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received the first dose of BNT162B2 on an unspecified date for COVID-19 immunization. The patient experienced really big headache on 17Feb2021. Event did not result in Emergency Room Visit or Physician Office Visit. No treatment received for the adverse event. The event was considered non-serious per reporter. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1111366
Sex: F
Age:
State: GA

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

Vax Type:
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Allergies:

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

Symptoms: extremely weak; right shoulder pain; temp started rising & by 2PM it was up to 102.4; legs were like jelly; felt unsteady & like I would fall; felt so bad/felt awful/talking about end of life wishes; no appetite; chest tightness; This is a spontaneous report from a contactable other health care professional reported for herself. A 58-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number not available), via an unspecified route of administration on 09Feb2021 16:30 (at the age of 58-year-old) at single dose in left arm for covid-19 immunization. Medical history included Heart Failure, Sarcoidosis, Asthma, Obesity and Covid from Apr2020 to an unknown date. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19, since the vaccination, the patient had not been tested for COVID-19. Concomitant medications the patient received within 2 weeks of vaccination included prednisone, carvedilol (COREG), spironolactone (ALDACTONE), hydrochlorothiazide, lisinopril (LISINOPRIL/HCTZ). The day of injection on 09Feb2021 at 16:30 PM that same night 8 pm the patient started experiencing some chest tightness. Since the patient live in country when she left work(hospital). At that point she took 50mg of P.O. benadryl (diphenhydramine). So the patient just took time and hung around town. She went to family dollar then publix. She felt better at 9 pm so and went home. The next morning (on 10Feb2021 her legs were like jelly when she woke up to go to bathroom. She felt unsteady and like she would fall. Next thing she just felt so bad and no appetite so she ate nothing that day. Her temp started rising and by 2PM on 10Feb2021 it was up to 102.4, the patient felt so awful then the feeling of doom set in so she was talking about end of life wishes. She had Covid back in Apr2020 and it was like reliving it again. On 11Feb2021 she felt better but had to call out low grade 99.4 only she was able to eat some but extremely weak and right shoulder pain (moderate). Friday (on 12Feb2021) she went to work but still felt weak. She felt better over the weekend (Feb2021). Here we were 17Feb2021 and still not completely there but 90% better. The adverse events result in doctor or other healthcare professional office/clinic visit. No treatment received for other adverse event. The patient underwent lab tests and procedures which included body temperature: 102.4 on 10Feb2021, body temperature: 99.4 on 11Feb2021, Nasal Swab Covid-19/SARS: negative on 16Feb2021. The outcome of the events was reported as recovered in Feb2021. Information on the lot/batch number has been requested.

Other Meds: PREDNISONE; COREG; ALDACTONE; LISINOPRIL/HCTZ

Current Illness:

ID: 1111367
Sex: F
Age:
State: CA

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Fever 100.7; chills; headache; nausea; injection site pain redness & swelling; injection site pain redness & swelling; injection site pain redness & swelling; exhaustion; This is a spontaneous report from a contactable 65 reporting for herself. A 65-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number EN6201/expiration date: not provided), via an unspecified route of administration, on 12Feb2021 at 11:00 (at the age of 65 years old) as a single dose in the left arm for COVID-19 IMMUNIZATION. Relevant medical history included Hashimoto's hypothyroidism. The patient has allergies to halibut and sea kelp. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number EL8982/expiration date: not provided), via an unspecified route of administration, on 22Jan2021 at 03:30 PM (at the age of 65 years old) as a single dose in the left arm for COVID-19 IMMUNIZATION. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included levothyroxine sodium (SYNTHROID), rosuvistatin, acetylsalicylic acid (ASPIRIN), probiotic, and vitamin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 12Feb2021 at 23:00, the patient experienced fever 100.7, chills, headache, nausea, injection site pain redness and swelling, and exhaustion. The events did not require hospitalization. The outcome of the events fever 100.7, chills, headache, nausea, injection site pain redness and swelling, and exhaustion was recovering. Since the vaccination, the patient had not been tested for COVID-19.

Other Meds: SYNTHROID; ROSUVASTATIN; ASPIRIN; PROBIOTIC

Current Illness:

ID: 1111368
Sex: M
Age:
State: NY

Vax Date: 01/25/2021
Onset Date: 02/07/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Deep itching; dry cough in lungs; chest tightness, heaviness; shortness of breath for 4 days after; This is a spontaneous report from a contactable consumer reported for himself that a 42-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at Left arm on 25Jan2021 12:00 at single dose for covid-19 immunisation. The COVID-19 vaccine was administered at Hospital. Medical history included Seasonal allergies, various surgeries. Concomitant medication included levocetirizine dihydrochloride (LEVOCETIRIZIN). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced Deep itching dry cough in lungs and chest tightness, heaviness, shortness of breath for 4 days after, events start date provided as 07Feb2021 04:00 PM. No treatment received for the events. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient was not been tested for COVID-19. The outcome of the events was not recovered. The patient received the second dose of BNT162 on 13Feb2021 11:30 AM via an unspecified route of administration at Right arm for covid-19 immunization. Information on the lot/batch number has been requested.

Other Meds: LEVOCETIRIZIN

Current Illness:

ID: 1111369
Sex: F
Age:
State: AK

Vax Date: 02/16/2021
Onset Date: 02/16/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

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

Symptoms: Nausea; tiredness; headache; injection site tenderness; feeling unwell; chills; fever waves; This is a spontaneous report from a contactable consumer reported for self. This 52-year-old female patient (not pregnant at the time of vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose on 16Feb2021 11:00 AM in left arm for COVID-19 immunization. Medical history included HBP (Blood pressure high); thyroid issues; obesity; known_allergies: seasonal allergies; covid-19. Concomitant medications the patient received within 2 weeks of vaccination included levothyroxine, losartan, HCTZ, vitamin D NOS, paracetamol (TYLENOL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient experienced nausea, tiredness, headache, injection site tenderness, feeling unwell, chills/fever waves on 16Feb202112:00 PM. There was no treatment received for the adverse event. This was a non-serious report. The events did not result in death, not life threatening, not caused/prolonged hospitalization, no disabling/incapacitating, no congenital anomaly/birth defect. The outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds: LEVOTHYROXINE; LOSARTAN; HCTZ; VITAMIN D NOS; TYLENOL

Current Illness:

ID: 1111370
Sex: F
Age:
State: FL

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

Vax Type:
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Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: enlarge lymph node under left armpit detected in sonogram. Not visual to eye or felt with manual examination; This is a spontaneous report from a contactable consumer reported for herself. A 66-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, LOT# EL9262), via an unspecified route of administration in left arm on 03Feb2021 at second single dose for covid-19 immunisation. Medical history included high blood pressure, hypothyroidism, low vitamin D, breast cancer survivor since Jan2018. No allergies to medications, food, or other products. Patient was not pregnant at the time of vaccination. The patient previously took bnt162b2 (LOT# EL1284) in left arm on 13Jan2021 at first single dose for covid-19 immunisation. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was receiving yearly mammogram and sonogram for breast cancer survivor since Jan2018. Enlarge lymph node under left armpit was detected in sonogram. Not visual to eye or felt with manual examination. Event was considered as non-serious. It was unknown whether treatment was received. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1111371
Sex: F
Age:
State: CO

Vax Date: 02/15/2021
Onset Date: 02/16/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: Alt is at 148; my INR level went from 2.9 to 4.3; This is a spontaneous report from a contactable consumer, the patient. This 65-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: unknown), dose 1, single dose via an unspecified route of administration in the left arm on 15Feb2021 at 12:00 PM (at the age of 65-years-old ) for COVID-19 vaccination. Relevant medical history included asthma and chronic blood clot in heart. The patient was not pregnant. 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. The patient had no allergies to medications, food, or other products. Concomitant medications included amiodarone and warfarin. On 16Feb2021 at 15:00 the patient experienced alanine aminotransferase (ALT) at 148 and international normalized ratio (INR) went from 2.9 to 4.3. The events were reported as non-serious and required a doctor or other healthcare professional office/clinic visit. Treatment received for events alanine aminotransferase (ALT) at 148 and international normalized ratio (INR) went from 2.9 to 4.3 included reducing dosage of warfarin still working on the liver. The clinical outcome of alanine aminotransferase (ALT) at 148 and international normalized ratio (INR) went from 2.9 to 4.3 was unknown. Since the vaccination, the patient has not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds: AMIODARONE; WARFARIN

Current Illness:

ID: 1111372
Sex: F
Age:
State: FL

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

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

Symptoms: hoarse voice; felt like she had a big lump in her throat; difficulty swallowing; Allergic reaction; This is a spontaneous report from a contactable consumer (patient's daughter) received via Medical Information Team. An 85-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9265), via an unspecified route of administration on 04Feb2021 (at the age of 85 years) at single dose for COVID-19 immunisation. The patient medical history included allergic to different medications. The patient's concomitant medications were not reported. It was reported that on 04Feb2021, the patient an hour after the vaccine developed a hoarse voice and two hours later felt like she had a big lump in her throat and had difficulty swallowing, their healthcare provider said he didn't believe it was an allergic reaction and was leaving it up to her if she wants to get it or not. The reporter stated her mother is allergic to different medications and those allergic reactions started the same way this did. The patient outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1111373
Sex: F
Age:
State: CT

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: body aches; headache; nausea; a low-grade fever; This is a spontaneous report from a contactable consumer (patient). A 27-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247) via an unspecified route of administration on 16Feb2021 12:30 at single dose on left arm for covid-19 immunisation. The medical history was none. Historical Vaccine included first dose of of bnt162b2 (lot number: EL3247) on 26Jan2021 12:30 at single dose on left arm for covid-19 immunisation. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included vitamin D, and ethinylestradiol, ferrous fumarate, norethisterone acetate (JUNEL FE). The patient experienced body aches, headache, nausea and a low-grade fever on 17Feb2021. About 12 hours after the second dose, the patient started to have body aches, a headache, and nausea. This lasted for about 18 hours. At about 24 hours post-shot, she took her temperature and had a low-grade fever. She took 400 mg of ibuprofen at about 24 hours post-shot and that helped ease the side effects. By 30 hours post-shot, she was able to return to normal activies. Since the vaccination, the patient has not been tested for COVID-19. The outcome of events was recovered on 17Feb2021.

Other Meds: VITAMIN D; JUNEL FE

Current Illness:

ID: 1111374
Sex: F
Age:
State: NY

Vax Date: 02/08/2021
Onset Date: 02/01/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: headache; not feeling well; nausea; had a temperature of 100.4 and 100.2; weak and tired; weak and tired; sinuses became very dry; This is a spontaneous report from a Pfizer-sponsored program, COVAX Support. A contactable consumer (patient) reported that a 59-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot: EM9809, expiry: 30Jun2021), via an unspecified route of administration on the left arm on 08Feb2021 at 16:45 (at the age of 59years) at 0.3 mL, single because she didn't want to get the virus and wants to get the world back to normal. Medical history included obese, prophylaxis (reported as she takes as extra precaution during winter) and abdominal discomfort (reported as stomach). Concomitant medications included cyanocobalamin, ergocalciferol, nicotinamide, pyridoxine hydrochloride, retinol, riboflavin, sodium ascorbate, thiamine mononitrate (ONE A DAY), montelukast sodium (SINGULAIR), lansoprazole for stomach, sucralfate, piroxicam (ZICAM) for she takes as extra precaution during winter, calcium and bifidobacterium bifidum, bifidobacterium lactis, bifidobacterium longum, lactobacillus acidophilus, lactobacillus rhamnosus (PROBIOTIC). Historical vaccine included flu shot and experienced arm sore and bed for the weekend (first time she got the flu shot she was in bed. It was kind of the same thing. Everyone said with the first vaccine it would make her arm sore. She was in bed for the weekend. She has had the flu shot five times in her lifetime. Subsequent flu shots she has been fine with. She doesn't have NDC, lot, and expiry for flu shot as it was at least 27 or 28 years ago). She received Pfizer COVID19 vaccine on Monday 08Feb2021 and her "sinuses became very dry" (in Feb2021). The patient experienced not feeling well, headache, nausea, temperature of 100.4 and 100.2 on 09Feb2021. During the night probably early on the ninth (09Feb2021) she got a headache, was not feeling well, and had nausea. When she got out of bed she had a temperature of 100.4 and 100.2. She thought that was a regular reaction to the vaccine. She didn't go to work. She felt weak and tired. She was told that was not usual for first but was for the second. She had slight headache the next day. She had a light headache for a few days. On Tuesday when she had the fever, she took paracetamol (TYLENOL, extra strength) and it wasn't getting rid of the headache. The fever came down a little. She wouldn't call what she had a big fever. She took ibuprofen (ADVIL, regular strength) later in the day. She normally doesn't take ibuprofen, but she did because she needed relief and paracetamol wasn't doing it. Since Wednesday, she might have taken one or two paracetamol a day. Once her sinuses started to dry out she started taking paracetamol. On Friday night her sinuses felt very dry and she was thinking it was all from the vaccine. She had a three day weekend. On Monday, she couldn't go back to work because she was nasally. Her symptoms began on 11Feb2021 and the health department had her quarantining for 10 days. The doctor said she should get tested and she was she then tested positive for COVID-19 on 12Feb2021. Apparently she picked it up coincidently. She couldn't figure where she picked up COVID. She tested positive. There was nothing concrete on when she can go back to get second COVID vaccine. She knows she couldn't be sick and symptomatic. She has to follow quarantine. The second appointment was on 01Mar. The patient asked if there was any guidance regarding when could she get the next dose and if she could return to work on 23Feb2021. Also asked if how long she could go without losing the efficacy of the first dose. She felt better today. She took the COVID test on Monday 15Feb2021. It was the PCR test. The results came in an email at 05:00 on 16Feb2021. The patient has been isolating in her bedroom. Her daughter was home. Her husband's company paid for him to stay in a hotel. She has felt good today and got on the treadmill. Usually she was a very active person. The facility was a state-run vaccine site. The patient had no previous immunization with the Pfizer vaccine, no additional vaccines administered on same date of the Pfizer suspect and no prior vaccinations within 4 weeks. The outcome of the events was unknown.

Other Meds: ONE A DAY [CYANOCOBALAMIN;ERGOCALCIFEROL;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL;RIBOFLAVIN;SO; SINGULAIR; LANSOPRAZOLE; SUCRALFATE; ZICAM [PIROXICAM]; CALCIUM; PROBIOTIC [BIFIDOBACTERIUM BIFIDUM;BIFIDOBACTERIUM LACTIS;BIFIDOBACTERIUM

Current Illness:

ID: 1111376
Sex: F
Age:
State: OH

Vax Date: 02/04/2021
Onset Date: 02/11/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
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Lab Data:

Allergies:

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

Symptoms: positive COVID-19 test with symptoms; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program. This consumer reported that a 31-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 31-years, via an unspecified route of administration on 04Feb2021 at single dose for COVID-19 immunisation. Medical history included anxiety. Concomitant medication included venlafaxine hydrochloride (EFFEXOR) for anxiety. Patient stated that she started to show symptoms of COVID-19 on 10Feb2021 and tested positive for COVID-19 on 11Feb2021 and her quarantine is going to be over this weekend on 21Feb2021 and scheduled to get a second dose on 25Feb2021 (Thursday) and wondering if it is recommended that she gets the 2nd dose next week since had a positive COVID-19 test. No treatment received. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds: EFFEXOR

Current Illness:

ID: 1111377
Sex: M
Age:
State: FL

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

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

Allergies:

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

Symptoms: headaches; temp 99.4; neckache; tiredness; feeling unwell; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via an unspecified route of administration on 18Feb2021 at 02:15 (at the age of 66-years-old) in the left arm as a single dose for COVID-19 immunisation. Medical history included heart transplant on an unspecified date, immunosuppressed from an unspecified date and ongoing and COVID-19 in Jul2020. The patient stated that "heart transplant most significant but others". Concomitant medications (other medications taken in two weeks) included tacrolimus, mycophenolate mofetil (MYCOPHENOLATE), pravastatin and lisinopril, all taken for unspecified indications on unspecified dates. The patient did not receive another vaccine within 4 weeks prior to the COVID-19 vaccine. The patient previously received atorvastatin (LIPITOR) and experienced allergy. On 18Feb2021 at 06:00 the patient experienced headaches, temp 99.4, neckache, tiredness and feeling unwell. The patient reported that he was immunosuppressed and for him a 1 degree increase in temperature was significant. He stated that he was diagnosed with COVID-19 at the end of July of 2020 and had subsequently recovered. These were new symptoms. The patient did not receive treatment for the events. The clinical outcomes of the events headaches, temp 99.4, neckache, tiredness and feeling unwell were all not recovered/not resolved. It was also reported that since the vaccination, the patient had not been tested for COVID-19 The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds: TACROLIMUS; MYCOPHENOLATE; PRAVASTATIN; LISINOPRIL

Current Illness: Immunosuppression

ID: 1111378
Sex: F
Age:
State: CA

Vax Date: 01/22/2021
Onset Date: 01/24/2021
Rec V Date: 03/18/2021
Hospital:

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Allergies:

Symptom List: Tremor

Symptoms: Tightness in airways noted after 2 days from second dose.; This is a spontaneous report from a contactable Nurse reporting for herself. A 36-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL1284, expiration date unknown) intramuscular (arm left) on 22Jan2021 (12:45 AM) (age at vaccination of 36-years-old) at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL1824, expiration date unknown), intramuscular (arm left) on 04Jan2021 (12:45 PM) (age at vaccination of 36-years-old) at single dose for covid-19 immunisation. The patient experienced tightness in airways after 2 days from second dose on 24Jan2021, 12:00 AM; no hospitalization required. No treatment was administered in response to the event. The patient was not diagnosed with COVID-19 prior to vaccination and since vaccination the patient has not been tested for COVID-19. Outcome of the event was recovered on an unspecified date. .

Other Meds:

Current Illness:

ID: 1111379
Sex: F
Age:
State: NJ

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 03/18/2021
Hospital:

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Allergies:

Symptom List: Erythema, Pruritus

Symptoms: felt my left arm sour, heavy to lift; felt my left arm sour, heavy to lift; muscle ache on both shoulders; headache; fatigue; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EL3247), via an unspecified route of administration on 17Feb2021 13:15 at single dose for covid-19 immunization. Vaccine location was left arm and it was the second dose. Patient received the first dose of BNT162B2 on 27Jan2021 03:00 PM at left arm with lot number EL3247 for covid-19 immunization, also at age of 54 years old. Patient is not pregnant at the time of vaccination. The patient medical history was none, concomitant medications were not reported. No known allergies. Patient was not diagnosed with COVID-19 prior to vaccination nor tested for COVID-19 since the vaccination. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine nor received any other medications within 2 weeks of vaccination. Two hours after the 2nd dose, patient felt headache and fatigue. She took 500mg of Tylenol at 6 pm on 17Feb2021. The headache went away during the night. The next morning, she felt left arm sour, heavy to lift. Some level of muscle ache on both shoulders. Patient took another 500 mg of Tylenol. The arm sourness was much less in the afternoon on 18Feb2021, and totally disappeared on 19Feb2021. The outcome of event headache was recovered on 17Feb2021, events fatigue and "heavy to lift" were recovered in Feb2021, the other events were recovered on 19Feb2021. The events were reported as non-serious.

Other Meds:

Current Illness:

ID: 1111380
Sex: F
Age:
State: CT

Vax Date: 02/17/2021
Onset Date: 02/18/2021
Rec V Date: 03/18/2021
Hospital:

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Allergies:

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

Symptoms: Injection site soreness; body aches; fatigue; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration into the left arm on 17Feb2021 11:15 at a single dose for COVID-19 immunisation. Medical history included allergies. Patient was not pregnant. The patient was taking unspecified concomitant medications. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. On 18Feb2021, patient experienced injection site soreness, body aches and fatigue. The events were reported as non-serious and patient did not receive treatment. Outcome of events recovered on Feb2021. No follow up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1111381
Sex: M
Age:
State: CA

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 03/18/2021
Hospital:

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

Symptoms: Fever of greater than 101F, ranging as high as 102.6F persisted for roughly 31 hours.; This is a spontaneous report from a contactable consumer. A 28-years-old male patient started to receive second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Feb2021 10:00 in right arm at single dose for covid-19 immunisation. Medical history and concomitant medications were none. The patient did not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. No allergies to medications, food, or other products. Historical vaccine included first dose of BNT162B2 on 28Jan2021 12.00 PM in right arm. No vaccines within 4 weeks prior to the COVID vaccine received. The patient experienced fever of greater than 101f, ranging as high as 102.6f persisted for roughly 31 hours on 19Feb2021 21:00 with outcome of recovered. No treatment received. Seriousness was non serious. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1111382
Sex: F
Age:
State: CA

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 03/18/2021
Hospital:

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Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: right arm felt like needles and sensitive to the touch; all joints hurt more than usual; difficult to concentrate; The right arm felt a little dormant with a little tiredness and pain; The right arm felt a little dormant with a little tiredness and pain; This is a spontaneous report from a contactable female consumer reported for herself. A 55-year-old female patient received her second single dose of BNT162B2 (Pfizer-BioNTech Covid-19 vaccine, lot number EN5318) in left arm 14:15 on 17Feb2021 for Covid-19 immunization. The patient had her first injection (lot number EN5318) in left arm 2:15PM on 27Jan2021. The patient had a history of some age related arthritis and had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and had not received other medications within 2 weeks of vaccination. The vaccine was applied in the left arm, close to shoulder. About one hour later, the right arm felt a little dormant with a little tiredness and pain. 18 hours later the right arm felt like needles and sensitive to the touch. Additionally, all joints hurt more than usual and it was difficult to concentrate. No headache nor fever. After 48 hours patient felt normal. No Tylenol was taken. No treatment was received for the events. The patient had recovered from the events. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The reporter considered all events were non-serious.

Other Meds:

Current Illness:

ID: 1111383
Sex: F
Age:
State: NJ

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

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Allergies:

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

Symptoms: loss of appetite; spontaneous bleeding under skin by right eye; severe pain under arm in armpit with swelling; severe pain under arm in armpit with swelling; hot feeling on skin; extreme fatigue; had some itchy skin and redness an hour after shot, especially on both arms; had some itchy skin and redness an hour after shot, especially on both arms; Extremely nausea/Often nauseous; insomnia; mild diarrhea; This is a spontaneous report from a contactable Other HCP (patient). A 48-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EM9809; expiration date not provided), via an unspecified route of administration (anatomical location: arm right) on 09Feb2021 18:00 at SINGLE DOSE for COVID-19 immunisation. Medical history included asthma and known allergies to sulfa drug both from unknown dates and unknown if ongoing. The patient has no COVID prior vaccination. Patient is not pregnant. The patient's concomitant medications were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL9262; expiration date not provided) on 19Dec2020 02:30 pm (vaccination location: left arm) and experienced dizziness, extreme itchy skin, headache, and fatigue reported as 'After 1st shot had dizziness and extreme itchy skin 1 hour after shot for approx 2 hours before it ended, then headache and fatigue for 1-2 days. However, after 48 hours all effects from the 1st shot were gone'. The patient experienced spontaneous bleeding under skin by right eye on 14Feb2021. Patient's clinical course is as follows: After 2nd shot, patient had some itchy skin and redness an hour after shot, especially on both arms that lasted a couple hours (started at 7PM and stopped at 9PM). Patient also had extreme fatigue everyday since 11Feb2021, as well as insomnia especially during the first 48 hours. Also had total loss of appetite the past 8 days (17Feb2021), extremely nauseous and mild diarrhea everyday since immediately after 2nd shot until now (8 days later) with no improvement. Often nauseous until close to the point of vomiting. 2 days after 2nd shot started having severe pain under arm in armpit area with swelling and hot feeling on skin. Developed some spontaneous bleeding under skin by right eye about 5 days (14Feb2021) after shot which has now gone away. Fatigue and health is poor with no improvement; most effects seem to be getting worse instead of improving each day. Patient was not COVID tested post vaccination. It was reported that no treatment was provided for the events. Outcome of the event 'had some itchy skin and redness an hour after shot, especially on both arms' was recovered on 09Feb2021; outcome of the event 'spontaneous bleeding under skin by right eye' was recovered; outcome of the remaining events was not recovered.

Other Meds:

Current Illness:

ID: 1111384
Sex: F
Age:
State: CO

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 03/18/2021
Hospital:

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

Symptoms: Increased heart palpitations; almost passed out; This is a spontaneous report from a contactable healthcare professional (patient). A 40-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration on 21Jan2021 at a single dose for COVID-19 immunization. Medical history included allergies. The patient's concomitant medications were not reported. The patient had not been diagnosed with Covid prior to vaccination. She was not pregnant. On 21Jan2021, the patient experienced increased heart palpitations and almost passed out immediately after second shot. No treatment was received for the events. Events resulted to doctor or other healthcare professional office/clinic visit. Outcome of events was not recovered. The patient was not tested for Covid post vaccination. Information on the batch/ lot number has been requested.

Other Meds:

Current Illness:

ID: 1111386
Sex: M
Age:
State: IL

Vax Date: 02/17/2021
Onset Date: 02/01/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: I cannot move out of my bed; My vision is also blurred; It am dropping rather rapidly because I am not able to eat; It am dropping rather rapidly because I am not able to eat; This is a spontaneous report from a contactable consumer (patient). A 67-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot number EN6200 , on 17Feb2021 at single dose in arm for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (lot number ELI283) on 27Jan2021 and had no adverse effect. The patient was wondering if he hold the current record for the number of days consecutive for a person to have adverse reaction to the second vaccine because it was over a week and he could not move out of his bed. That almost killed him. His vision was also blurred. His weight was dropping rather rapidly because he was not able to eat. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1111387
Sex: F
Age: 31
State: FL

Vax Date: 03/12/2021
Onset Date: 03/14/2021
Rec V Date: 03/18/2021
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Allergies: none

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

Symptoms: Severe fatigue: Started 03/14/2021 the facility that gave the vaccine, and was advised to call the COVID-19 Hotline.

Other Meds: Trazodone 25-50 mg for sleep and anti-anxiety on an as needed basis. Pt denies taking Trazodone since the vaccine was administered.

Current Illness:

ID: 1111388
Sex: F
Age: 31
State: CO

Vax Date: 12/23/2020
Onset Date: 12/30/2020
Rec V Date: 03/18/2021
Hospital:

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Allergies: no

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

Symptoms: the first couple of days were fine, 1 week later Itwas a nasty rash a few inches around my arm, raised, hot, red, it looked like an infection and I went to the Dr they prescribed antibiotics, two days into medication it went away, the spot itches every now and then but it's not a rash anymore

Other Meds: foloxatine, I was breastfeeding

Current Illness: no

Date Died: 03/16/2021

ID: 1111389
Sex: M
Age: 80
State: NC

Vax Date: 02/24/2021
Onset Date: 03/05/2021
Rec V Date: 03/18/2021
Hospital: Y

Vax Type:
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Allergies: none

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

Symptoms: Cough started on 3/5. Hospitalization on 3/7, Expired 3/16. Doctor's Death Diagnosis: acute on chronic respiratory failure.

Other Meds: Proair, Xanax, Cardizem, Lasix, Insulin, Magnesium

Current Illness: PMH of Hypertension, H/o of HFpEF, PAF not on anticoagulation due to GI bleeding, Severe Pulmonary hypertension, T2DM, H/o of GI bleeding, ESRD on HD, Chronic hypoxic respiratory failure on home oxygen.

ID: 1111390
Sex: F
Age: 40
State: LA

Vax Date: 03/16/2021
Onset Date: 03/17/2021
Rec V Date: 03/18/2021
Hospital:

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Lab Data:

Allergies: none known

Symptom List: Vomiting

Symptoms: Moderna COVID-19 Vaccine EUA Began with headache and sweating around 9:45am, increased in intensity with generalized pain over the next hour. Intense migraine, nausea that lasted about 12 hours. Vomiting began about 6 hours in, two times. Received treximet for migraine and ondansetron for vomiting.

Other Meds: Adderal

Current Illness: UTI approx 1 month prior

ID: 1111391
Sex: M
Age: 50
State: SC

Vax Date: 03/17/2021
Onset Date: 03/18/2021
Rec V Date: 03/18/2021
Hospital:

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Allergies: nuts, raw fruit, raw vegetables

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Same day March 17th, by 2230 or 1030pm slight injection sight pain and minor head ache in temple area mostly. Today the 18th Awoke with much greater injection site pain in the arm in delt area but no swelling or rash. Still minor headache but around the whole head. Approximately 1000-1030-AM and through 1300 hours (pm), extreme headache but tolerable, EXTREME FATIGUE and SHORTNESS OF BREATH and DIZZINESS (ALL CONTINUING) post physical activity.....ie: bending, lifting, moving etc etc.....Sitting now for 30 minutes still have the above listed items in CAPS ongoing. Temp is good and pulse is good. Aside from increased arm pain I have been feeling incredible burning sensation going from injection site left arm across upper back to right side .....thats it so far

Other Meds: blood pressure medication

Current Illness: none

ID: 1111392
Sex: F
Age: 29
State: NE

Vax Date: 03/16/2021
Onset Date: 03/17/2021
Rec V Date: 03/18/2021
Hospital:

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Allergies: Neomycin

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

Symptoms: Sharp upper back pain that radiated into chest. Pleuritic in nature, seemed to be concentrated at base of lungs bilaterally. Slightly worse when taking deep breath. Not really associated with shortness of breath. No other associated symptoms. Made worse by lying down. Slightly alleviated by raising shoulder blades up and sitting with head in hands. Lasted approximately 1.5 hours with periods of worsening and getting slightly better. Was considering going to emergency room given severity of pain, but eventually resolved on its own with no further symptoms since that time. Have never experienced symptoms like that before. Pregnant at time of occurrence, 15 weeks 4 days along.

Other Meds: Prenatal vitamin Loratadine Cranberry supplement Docusate sodium

Current Illness: None

ID: 1111393
Sex: F
Age: 21
State: AZ

Vax Date: 03/16/2021
Onset Date: 03/18/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
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Lab Data:

Allergies: Na

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Shortness of breath. Happening 2 days after the shot. Been occurring for over an hour now. Can't even speak a sentence without getting out of breath

Other Meds: Birth control isibloom

Current Illness: I went to the doctor recently due to shortness of breath and was advised my lungs were very tight. Was on a z pack

ID: 1111394
Sex: F
Age: 36
State: CA

Vax Date: 03/09/2021
Onset Date: 03/15/2021
Rec V Date: 03/18/2021
Hospital:

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Manufacturer:
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Lab Data:

Allergies: No

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

Symptoms: Subconjunctival haemorrhage in right eye, itchiness in the eye. Ongoing on date of report. No treatment required.

Other Meds: No

Current Illness: No

ID: 1111395
Sex: M
Age: 74
State: CA

Vax Date: 03/02/2021
Onset Date: 03/15/2021
Rec V Date: 03/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
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Lab Data:

Allergies: None

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

Symptoms: Vertigo starting at 4 am on 3/15 and lasting all day. Had 2 quick episodes of vertigo (30 seconds) on 3/17.

Other Meds: Norvasc 10 mg , olmesartan 20 mg

Current Illness: None

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am