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
187,133MODERNA
33,878JANSSEN
2,321PFIZER\BIONTECH
1,091GLAXOSMITHKLINE BIOLOGICALS
983UNKNOWN MANUFACTURER
363MERCK & CO. INC.
229SEQIRUS, INC.
45DYNAVAX TECHNOLOGIES CORPORATION
41NOVARTIS VACCINES AND DIAGNOSTICS
29SANOFI PASTEUR
18EMERGENT BIOSOLUTIONS
8PAXVAX
7TEVA PHARMACEUTICALS
4PFIZER\WYETH
3BERNA BIOTECH, LTD.
2SMITHKLINE BEECHAM
2INTERCELL AG
2PROTEIN SCIENCES CORPORATION
1CSL LIMITED

Incidents per State

State Total
77,548
AK1,869
AL5,581
AR3,688
AS47
AZ14,288
CA61,984
CO11,665
CT8,149
DC1,663
DE1,807
FL37,749
FM5
GA15,058
GU120
HI2,453
IA4,625
ID2,692
IL20,334
IN24,007
KS4,615
KY7,696
LA4,887
MA14,654
MD12,514
ME3,129
MH11
MI18,739
MN12,528
MO9,710
MP29
MS2,790
MT2,375
NC16,368
ND1,356
NE2,880
NH3,100
NJ17,634
NM3,916
NV4,239
NY34,355
OH19,081
OK6,195
OR8,636
PA23,083
PR2,370
QM2
RI2,088
SC6,411
SD1,212
TN9,131
TX35,174
UT4,273
VA14,937
VI64
VT1,676
WA14,909
WI11,259
WV2,388
WY861
XB5
XL1
XV2

ID: 1023410
Sex: F
Age:
State: LA

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: chills; fever blisters; This is a spontaneous report from a contactable Consumer reporting for a patient. A female patient of an unspecified age (Age: 76, unit: unspecified) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on unspecified date at SINGLE DOSE (second dose) for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date for covid-19 immunisation. The reporter stated that her friend has had the second dose of the PFIZER COVID-19 vaccine and had chills the first night and at the end of the second week (14 days) she broke out in fever blisters in her mouth and is on an antibiotic because of the fever blisters. Outcome of the events was unknown. Reporter wanted to know if this is a side effect of the vaccine. Reporter considered the event was non-serious. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023411
Sex: F
Age:
State: NJ

Vax Date: 01/23/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: the red rash and hives maybe cellulitis; a red rash with hives at the COVID-19 Vaccine injection site; a red rash with hives at the COVID-19 Vaccine injection site; she felt red and itchy and noticed swelling at the injection site/ a red rash with hives at the COVID-19 Vaccine injection site; she felt red and itchy and noticed swelling at the injection site; she felt red and itchy and noticed swelling at the injection site/ a red rash with hives at the COVID-19 Vaccine injection site; she had experienced a red rash and hives at the vaccine injection site because the vaccine was administered at an incorrect location on her arm; arms soreness; This is a spontaneous report from a contactable nurse (patient). A 35-year-old female patient received the first dose of bnt162b2 (Pfizer-Biontech COVID-19 Vaccine, Lot number: Unknown), via an unspecified route of administration at the right deltoid on 23Jan2021 11:30 at a single dose for COVID-19 immunization. The vaccine was administered in a hospital; not in a military facility. Medical history included ongoing eczema since infant and childhood asthma. Her childhood asthma was exercised induced. She stated she has not had an occurrence of asthma since she was 10 years old. There were no concomitant medications. Felt fine, just had the normal arms soreness on Jan2021. But reports that around 36 hours later, she felt red and itchy and noticed swelling at the injection site on 24Jan2021. Reported on 24Jan2021 at about 6:00PM she developed a red rash with hives at the COVID-19 Vaccine injection site. She said she was trying to do research to see if what she was experiencing was an expected side effect of the COVID-19 Vaccine, and if so, how to treat the red rash and hives. She said she put a cold compress on the injection site and took Motrin. She said the injection site red rash with hives subsided. She said later on the night of 24Jan2021, at 11:00PM, the red rash and hives at the COVID-19 Vaccine injection site started up again. She reports that she took Benadryl and Motrin and applied some Cortisone cream. The red rash and hives subsided. She said last night, 25Jan2021, the red rash and hives happened again at the COVID-19 Vaccine injection site. She said the red rash and hives seems to only happen at night. She said she thought her COVID-19 Vaccine dose was administered a bit low on her arm. She said she thought maybe she had experienced a red rash and hives at the vaccine injection site because the vaccine was administered at an incorrect location on her arm. She said she felt fine after receiving the COVID-19 Vaccine and thought the red rash and hives maybe cellulitis. She said her throat was fine, and during the day the COVID-19 Vaccine injection site was fine. She said the red rash and hives at the COVID-19 Vaccine inject site only starts again at night. The events did not require Emergency Room nor No Physician Office visit. The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. The outcome of the event arm soreness was unknown and for the events she felt red and itchy and noticed swelling at the injection site/ a red rash with hives at the COVID-19 Vaccine injection site and the red rash and hives maybe cellulitis was recovering. Information about lot/batch number has been requested.

Other Meds:

Current Illness: Eczema

ID: 1023412
Sex: M
Age:
State:

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: UTI; fever; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age (age: 73, unit: unknown) received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number unknown), via an unspecified route of administration on 12Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced a reaction to the vaccine, a fever, the next day, 13Jan2021. He stated that the fever lasts 8 days and was "predictable" (started normal temperature in morning, then would increase as the day progressed). It was also reported that he was diagnosed with UTI on an unspecified date and was being treated for UTI and the fever subsided. The patient is scheduled to get the second dose on 02Feb2021 but was reluctant to have this dose if he had this reaction to the first one. He stated that he understands the reaction to booster is more significant to original. The outcome of the event fever was recovering while the outcome of the event UTI was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023413
Sex: F
Age:
State: NC

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: HR at 11:30 and it was 104; This is a spontaneous report from a contactable consumer (reported for herself). A 77-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date not reported), via an unspecified route of administration on 26Jan2021 10:00 at a single dose in the right arm for COVID-19 immunization. Medical history included Afib (atrial fibrillation) from an unknown date and unknown if ongoing. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient had no allergies to medications, food, or other products. The patient was not pregnant at the time of vaccination and reporting. Concomitant medications included apixaban (5 mg tab) at 5 mg, and atorvastatin calcium (10 mg tab) at 10 mg; both reported as other medications the patient received within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient checked her HR (heart rate) at 11:30 and it was 104, and at 12:30 it had come down to 90. No treatments received in response to the event reported. The event was reported as not serious (did not result in death, not life-threatening, did not cause/prolonged hospitalization, not disabling/incapacitating and not a congenital anomaly/birth defect). Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event "HR at 11:30 and it was 104" was recovering. Information on the lot/batch number has been requested.

Other Meds: APIXABAN; ATORVASTATIN CALCIUM

Current Illness:

ID: 1023414
Sex: F
Age:
State: MN

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: numbness in hands and feet; slight shortness of breath; This is a spontaneous report from a contactable nurse. A 32-year-old non-pregnant female patient received her first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; lot number: EL3248; expiration date: unknown), intramuscular left arm on 26Jan2021 12:15 at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took morphine and acetaminophen but had allergies. The patient did not receive other vaccine in four weeks. The patient received the vaccine in a public health clinic/veterans administration facility. The patient reported that she received vaccine and was waiting in the observation area. She complained of numbness in hands and feet and slight shortness of breath on 26Jan2021 12:30 PM. She was offered and ingested diphenhydramine 25 mg at 12:30 and another 25mg at 12:38. Patient's radial pulse was strong and regular. On examination, there was no rash, no swelling visible, no respiratory stridor and the patient was able to talk in complete sentence with one breath. The patient continued to feel symptoms (not better and not worse) so 911 ambulance was called. The patient's care was turned over to them when they arrived. It was mentioned that the patient received treatment that included diphenhydramine and ambulance to ETC. The adverse events resulted in emergency room/department or urgent care. It was unknown if the patient was with COVID prior vaccination and if the patient was COVID tested post vaccination. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1023415
Sex: F
Age:
State: MI

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Tightening of throat; Numbness in left thumb, arm, and jaw; Confused; Rapid heart rate; Nausea; Increased blood pressure; This is a spontaneous report from a contactable consumer (patient). A non-pregnant 46-year-old female patient received the first dose of BNT162B2 (PFIZER BIONTECH COVID-19 VACCINE; Lot Number: EL3248), via an unspecified route of administration in left arm, on 25Jan2021 at 11:30, at a single dose, for COVID-19 immunization. The patient's medical history included allergies to bees, penicillin, and dairy. The patient's concomitant medications included loratadine (CLARITIN) and paracetamol (TYLENOL). The patient was not diagnosed with COVID-19 prior vaccination. No other vaccine was administered in four weeks. The vaccine was administered in a school or student health clinic facility. Within 5 minutes of injection on 25Jan2021 (starting at 11:30), rapid heart rate, nausea, and increased blood pressure began, continued, and worsened. After an hour, these got worse and seen by medics. Then the patient was transported to emergency room (ER) by ambulance but could not be seen for 4 hours. About an hour and a half after the injection (13:00), the patient experienced tightening of throat and numbness in left thumb, arm, and jaw. The patient was also very confused at that point as well. After 2 hours in waiting room, the patient felt well enough to be taken home. The symptoms slowly improved on their own. The adverse events resulted in doctor or other healthcare professional office or clinic visit and emergency room or department or urgent care. No treatment was given for the events. The patient has not been tested for COVID-19 post-vaccination. The patient recovered from the events in Jan2021.

Other Meds: CLARITIN [LORATADINE]; TYLENOL

Current Illness:

ID: 1023416
Sex: F
Age:
State: AR

Vax Date: 01/21/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: fast heartbeat; increased BP; weak; dizziness; nausea; headache; confused; a little soreness in her arm; felt like she could pass out; didn't know who she was, she just kept walking and walking; funny feelings; This is a spontaneous report from a contactable consumer (patient). An 84-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0142, expiry date not reported), via an unspecified route of administration on the right upper arm on 21Jan2021 17:00 at single dose for covid-19 immunization. Medical history included oral cancer from an unknown date and unknown if ongoing. There were no concomitant medications. The patient previously received flu vaccine for immunization and reported that it made her sick for 10 days 4 or 5 years ago. The patient previously took Tylenol (takes 1 instead of 2, Everything she takes half the recommended dose). The patient experienced fast heartbeat, increased BP, weakness, dizziness, nausea and headache on an unspecified date in Jan2021. It was further reported that she had a fast heart beat, her blood pressure went real high, she was dizzy and weak. This was while she was there and being watched for the 15 minutes by a nurse. She is 84 years old and doesn't take any medication; she did have oral cancer but with no chemo as it had not spread and this was 2 years ago. It was explained that the patient didn't feel good about it but she drove home. When she got home she was confused and felt like she could pass out. She walked through the house didn't know who she was, she just kept walking and walking. It was a strange feeling that lasted 15-20 minutes. She called her son late in the afternoon and told him to check on her to make sure she made it through the night. She still had funny feelings over the next few days but at this point she only has the dizziness that happens occasionally. She notes also that her blood pressure was checked at home by her and was higher than normal the first few days after but is now normal. Over the next day she had a headache and a little nausea, but it was not severe. She also mentions having a little soreness in her arm but not bad. She did read about the side effects and states she had the elevated heart rate, increase in blood pressure and dizziness right after getting it. The patient wonders could she ask for smaller dose, she only weighs about 110lb. When she spoke with her doctor she was told that the COVID virus is worse than what she experienced after the vaccine. She has not been to the doctor since getting the vaccine, she just talked to them. The patient underwent lab tests and procedures which included blood pressure measurement: high and heart rate: fast on Jan2021. The patient was recovering from dizziness, the outcome of nausea was unknown and the patient recovered from the rest of the events on an unspecified date in Jan2021.

Other Meds:

Current Illness:

ID: 1023417
Sex: F
Age:
State:

Vax Date: 01/24/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Sore arm; This is a spontaneous report received from a contactable consumer (patient). A female patient of an unspecified age (reported as 70, unit not provided, pending clarification) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration, on 24Jan2021, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced sore arm from the injection in Jan2021. The patient was concerned as she stated that her shot did not even take a sec, it was quickly administered and she saw in the TV that it was given slowly. The patient wanted to know if it takes 2 weeks for the antibodies to be made after the first dose, wanted to know about new strain and if its covered by the vaccine, if she should continue to wear mask and social distancing after the vaccine, and how many ml/mg is the medication. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023418
Sex: F
Age:
State: PA

Vax Date: 01/20/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: swelling of lymph nodes on same arm of injection site; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0140, expiry date: not reported), via an unspecified route of administration, on 20Jan2021 14:30, at a single dose on the left arm for COVID-19 immunization. The vaccine was administered at a hospital. Medical history and concomitant medications were none. Family Medical History Relevant to the adverse event: Patient's mother has bad allergies and knows she is contraindicated to this vaccine, but patient has never experienced any allergic reaction to anything. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0140, expiry date: not reported), via an unspecified route of administration, on 30Dec2020 1:30 pm, at a single dose on the left arm for COVID-19 immunization (age at vaccination: 41-year-old). The patient was administered her first dose the vaccine on 30Dec2020. She was administered her second dose of Pfizer COVID-19 Vaccine 20Jan2021, completing treatment. On 23Jan2021 08:00, three days after receiving the second dose of the vaccine she experienced swelling of lymph nodes on same arm of injection site. She reported onset of swollen lymph nodes in left arm 23Jan2021 which is ongoing. The swollen lymph nodes are present in the same arm that she was administered both first and second doses. She looked on the CDC website and did not know that this was a reported a side effect of the vaccine. She assumes it will go away. She called to clarify if she should tell her healthcare provider about this or if there are any recommendations regarding this event. She has taken some Motrin to help with the swelling. The event did not require a visit to the emergency room of physician's office. Therapeutic measures taken as a result of the adverse event included Motrin. Outcome of the event was not recovered. The patient assessed the event as non-serious. She does believe the event was potentially caused by the vaccine.

Other Meds:

Current Illness:

ID: 1023419
Sex: F
Age:
State: NH

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: struggled to stay awake; achy; hot; couldn't get back to sleep; very tired; This is a spontaneous report from a contactable consumer. A 44-year-old female patient received the second dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number: EL3249) in the hospital, 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 was not diagnosed with COVID-19 prior to vaccination. It was unknown if the patient received other vaccines within 4 weeks prior to the COVID vaccine and it was also unknown if the patient received any other medications within 2 weeks of the vaccination. The patient received the first dose of BNT162B2 (lot number: EJ1685) in the hospital on 30Dec2020 for COVID-19 immunization. It was reported that on 21Jan2021, the patient struggled to stay awake. She took Tylenol and woke achy and hot at midnight and couldn't get back to sleep. She woke again at 2:30 AM and took Motrin and got back to sleep about 3:30 AM still hot and achy. By 5:30 AM, she said she was less hot and achy, but very tired. Treatment was recevied for events struggled to stay awake, achy, hot and couldn't get back to sleep. It was unknown if treatment was received for the event very tired. The outcome of the events was unknown. The events were reported as non-serious. Since the vaccination, it is unknown if the patient had been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1023420
Sex: M
Age:
State: TN

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Headache; This is a spontaneous report from a contactable consumer. A 35-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration in Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient experienced headache about 30 hours after receiving second vaccine dose (Jan2021). No treatment was received for the event. The outcome of the event was recovered in Jan2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1023421
Sex: M
Age:
State: CT

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Soreness at the site of injection; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient received BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number unknown) in the workplace clinic, via an unspecified route of administration on 22Jan2021 at 10:30 on the left arm at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced soreness at the site of injection during 12-24 hours post administration on 22Jan2021 at 22:00. The outcome of the event was recovered. The patient did not receive treatment for the event. The event was reported as non-serious. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023422
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: neuropathic pain; bilateral feet burning, burning in both calves and slight extent to both hands; This is a spontaneous report from a contactable healthcare professional (patient). A 57-year-old female patient [unknown age of vaccination] received bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; unknown lot number and expiration date), 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 she was experiencing neuropathic pain, bilateral feet burning, burning in both calves and slight extent to both hands on an unspecified date. She inquired if there were other reports like this. The outcome of the events was unknown. The following information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1023423
Sex: F
Age:
State:

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: really bad headaches; heart rate is a little higher than usual; numbness at the side of the shot; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age (reported as 45 [units unspecified]) received her first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; unknown lot number and expiration date), via an unspecified route of administration on 16Jan2021 at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. She had her first dose of the vaccine on 16Jan2021 and had no side effects, just "numbness at the side of the shot". She mentioned however, since Sunday (24Jan2021), she's been having "really bad headaches" and has noticed that her "heart rate is a little higher than usual". The patient reported she had headaches more than 1 week after receiving the vaccine. She added that she didn't really have any symptoms, but she know like the main symptoms were within like the 3 day period. She has been experiencing the symptoms now and she doesn't know if it could be like a delayed reaction to the vaccine but she had the curiosity and wanted to report if and see if it is the delayed reaction or something else. The outcome of the events was unknown. The following information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1023424
Sex: F
Age:
State: NY

Vax Date: 01/08/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: swelling of her lymph nodes; This is a spontaneous report from a contactable consumer (patient). A 27-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration, on 08Jan2021, at single dose, for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced swelling of her lymph nodes on 22Jan2021, 2 weeks after getting the vaccine. The outcome of the event was unknown. The patient wanted to know if this was a normal side effect of the vaccine. The patient also wanted to know the risks of the Pfizer-Biontech covid-19 vaccine and what should she do about the side effects. Information about the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023425
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: a real bad rash that was not severe, just red, sore, and irritating; a real bad rash that was not severe, just red, sore, and irritating; This is a spontaneous report from a consumer (patient). A female patient of an unspecified age received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient stated that after first dose, 3-4 days after she got a real bad rash that was not severe, just red, sore, and irritating. It started coming slowly. Rash was located on her neck. The patient was unsure if the rash was from the vaccine. The patient thought, maybe she put too much chemical on her hair/head. Clinical outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023426
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: sore arms; fever; body aches/pain; sore throat; diarrhea; This is a spontaneous report from a contactable consumer (patient) via a medical information team. A male patient of an unspecified age received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), 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. It was reported that during the first dose of BNT162B2, the patient experienced sore arms, fever, body aches, pain, sore throat, and diarrhea. The patient has tested negative for COVID on unspecified date. The patient stated, "Can I use Benadryl after getting vaccinated?" The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023427
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: I have some pain in my neck; This is a spontaneous report from a contactable consumer via the Medical Information Team. A female patient of an unspecified age received her 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. The patient's medical history and concomitant medications were not reported. It was reported by the patient that she has some pain in her neck unrelated to the vaccine. She is due to receive her steroid shot. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023428
Sex: F
Age:
State: TN

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Fatigue; Arm pain; Headaches; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on the right arm, on 25Jan2021 16:45 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient was not pregnant at the time of vaccination. There was no other vaccine received within four weeks prior to vaccination. The patient experienced fatigue, arm pain, headaches Jan2021. Outcome of the events was unknown and no treatment was given. Events were considered non-serious. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023429
Sex: F
Age:
State: NC

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Pain in arm; This is a spontaneous report from a contactable other health care professional (patient). A 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number el9261 and expiration date not provided), via an unspecified route of administration (left arm) first dose on 25Jan2021 15:00 at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at time of vaccination. On 26Jan2021 04:00, the patient experienced pain in arm. The patient did not received treatment for then event. The outcome of the event was recovering. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No medication was taken within 2 weeks of vaccination.

Other Meds:

Current Illness:

ID: 1023430
Sex: M
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Severe pain in upper left arm muscle (vaccine site); Severe pain in upper left arm muscle (vaccine site)/ also in my left shoulder joint; Severe pain in upper left arm muscle (vaccine site)/ also in my left shoulder joint/ unable to lift my left arm; This is a spontaneous report from a contactable consumer (patient). A 77-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 13Jan2021 12:45 at single dose for COVID-19 immunization. Medical history included high blood pressure and cholesterol from an unknown date and unknown if ongoing. Concomitant medication included medication for high blood pressure and cholesterol. 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 has not been tested for COVID-19. It was reported that initially, there was no adverse reaction, but 10 days later on 24Jan2021 07:00 AM, the patient stated, "I experienced severe pain in upper left arm muscle (vaccine site) and also in my left shoulder joint. Also unable to lift my left arm. The lower arm and fingers function normally. These symptoms continue through today 12 days after the vaccine ". The outcome of the events was not recovered. No treatment was given to the patient for the events. The events were considered non serious as it did not result in death, were not life threatening, did not cause/prolonged hospitalization, were not disabling/Incapacitating and were not a congenital anomaly/birth defect. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023431
Sex: F
Age:
State:

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: felt a very slight tingling on her lips; This is a spontaneous report from a non-contactable consumer (patient) via the Pfizer-sponsored program. A female patient of unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration, on an unspecified date in Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient received the 1st dose of the bnt162b2 a few days prior to the date of this report in Jan2021. However, after 5 minutes, she felt a very slight tingling on her lips that lasted for about 10 minutes. HCP wants to know if she should still receive the 2nd dose. Outcome of the event was recovered on an unspecified date in Jan2021. The reporter assessed the event as non-serious. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1023432
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Sore arm; Tiredness; This is a spontaneous report from a contactable consumer. An elderly female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) at a single dose, with route of administration and therapy date unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on an unspecified date for COVID-19 immunization. The patient was not pregnant at the time of vaccination. In Jan2021, the patient had sore arm and tiredness. The patient did not receive any treatment for the reported events. The outcome of the events, sore arm and tiredness, was recovered in Jan2021. The patient was not diagnosed with COVID-19 prior to vaccination, and had not been tested post-vaccination. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 1023433
Sex: F
Age:
State: PA

Vax Date: 01/22/2021
Onset Date: 01/01/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: It's the longevity of the side effects at a level preventing work and daily activities that is the biggest problem; fatigue; headaches; fevers; chills; dizziness; generalized pain; This is a spontaneous report from a contactable nurse (patient). A 47-year-old female patient received the second dose of bnt162b2 (BNT162B2, lot number: EL324, expiry date: not reported), via unspecified route of administration on 22Jan2021 05:00 PM at a single dose on the left arm for COVID-19 immunization. The vaccine was administered at a hospital. The patient did not receive any other vaccine in four weeks prior vaccination. Medical history included epilepsy and asthma. Concomitant medications included lamotrigine (LAMICTAL), escitalopram oxalate (LEXAPRO), riboflavin (VITAMIN b2), magnesium (MAGNESIUM), ascorbic acid, betacarotene, cupric oxide, manganese sulfate, selenium, tocopheryl acetate, ubidecarenone, zinc oxide (COQ10). The patient previously received the first dose of bnt162b2 (BNT162B2, lot number: EL1284, expiry date: not reported), via unspecified route of administration on 02Jan2021 07:00 PM at a single dose on the left arm for COVID-19 immunization (age at vaccination: 47-year-old). Past drug history included known allergies to Parafon forte and Macrobid. The patient stated that it's the longevity of the side effects at a level preventing work and daily activities that is the biggest problem. She stated that she's 5 days post injection at the time of report (26Jan2021), and the fatigue, headaches, fevers/chills, dizziness and generalized pain are not going away (started on an unspecified date in Jan2021). Her doctor told me to report this to the manufacturer and get advice. No treatment was received. The patient did not have covid prior vaccination and was not tested for covid post vaccination. Outcome of the events was recovering.

Other Meds: COQ10 [ASCORBIC ACID;BETACAROTENE;CUPRIC OXIDE;MANGANESE SULFATE;SELENIUM;TOCOPHERYL ACETATE;UBIDECA; LEXAPRO; LAMICTAL; MAGNESIUM; VITAMIN B2 [RIBOFLAVIN]

Current Illness:

ID: 1023434
Sex: F
Age:
State: MA

Vax Date: 01/24/2021
Onset Date: 01/24/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: felt sharp pain behind right ear which lasted 2 hours; headache; This is a spontaneous report received from a contactable other healthcare professional (who is also the patient). An 18-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN5318, expiry date: unknown), via an unspecified route of administration in the left arm, on 24Jan2021 13:00, at single dose, for COVID-19 immunization, at the workplace clinic. Medical history included depression. The patient was not pregnant at the time of vaccination. The patient has no known allergies. Concomitant medication included an unspecified birth control pill, melatonin and multivitamins. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686, expiry date: unknown), via an unspecified route of administration in the left arm, on 03Jan2021 12:00, for COVID-19 immunization. The patient did not receive any other vaccine in four weeks. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. On 24Jan2021 17:00, 4 hours after vaccination, the patient felt sharp pain behind right ear which lasted 2 hours. On 24Jan2021 15:00, a few hours after vaccination, the patient started having a headache which, as the patient reported, "hasn't gone away, even with a Tylenol, actually feels worse than when it started on Sunday". Treatment for the events included Tylenol, heat, and quiet and dark room. The outcome of the event "felt sharp pain behind right ear which lasted 2 hours" was recovered on 24Jan2021 at 19:00; and headache was not recovered.

Other Meds: MELATONIN; MULTIVITAMINS [VITAMINS NOS]

Current Illness:

ID: 1023435
Sex: F
Age:
State: NY

Vax Date: 01/24/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: fever chills/I recorded a temperature of 102 at 9pm; backache; Headache; swollen left underarm, same arm that she received the vaccine; same arm that she received the vaccine. Tender to touch; This is a spontaneous report from a contactable consumer. A 25-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EL9261), via an unspecified route of administration on 24Jan2021 17:30 at SINGLE DOSE in arm left for COVID-19 immunization. Medical history included eczema, migraine from an unknown date and unknown if ongoing. Concomitant medication included biotin (BIOTIN), rizatriptan benzoate (RIZATRIPTAN BENZOATE). The patient received first dose of BNT162B2 on 03Jan2021 10:00 AM in left arm for covid19 immunization. On 25Jan2021, the patient experienced Headache when she woke up at 8am, by 12pm she also had a fever chills and backache. Symptoms did not improve even after 6 ibuprofen throughout the day. The patient recorded a temperature of 102 at 9pm. None of the above symptoms on 26Jan. However, had a significantly swollen left underarm, same arm that she received the vaccine. Tender to touch. If the swelling doesn't go down in 1-2 days the patient will visit an urgent care. The patient underwent lab tests and procedures which included body temperature: 102 on 25Jan2021. Therapeutic measures were taken as a result of headache (headache), fever chills (pyrexia), backache (back pain). The patient did not receive treatment for the events vaccination site swelling, and vaccination site pain. The outcome of the events headache, fever chills was recovered on 26Jan2021, while unknown for the events vaccination site swelling, and vaccination site pain.

Other Meds: BIOTIN; RIZATRIPTAN BENZOATE

Current Illness:

ID: 1023436
Sex: M
Age:
State:

Vax Date: 01/21/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Positive PPD skin test/Skin test flaring and still growing 5 days after administered; Positive PPD skin test/Skin test flaring and still growing 5 days after administered; This is a spontaneous report from a non-contactable nurse. A 28-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not provided), intramuscular (left arm) first dose on 21Jan2021 12:00 at single dose for Covid-19 immunization. The patient's medical history includes PPD skin test positive from 21Jan2021 3 hours prior Pfizer covid 19 vaccine injection. The patient's concomitant medications were not reported. On 21Jan2021, PPD skin test done 3 hours prior Pfizer covid 19 vaccine injection on same left arm, Positive PPD skin test with clear x-ray with no history of positive PPD skin test. The patient had a separate negative PPD skin test in 2018 with negative results. On 23Jan2021 12:00, the patient skin test flaring and still growing 5 days after administered. Again the patient got the skin test the same day as the vaccine and have no history of a positive PPD skin test. The patient did not received treatment for the event. The outcome of the event was recovering. No follow-up attempts are Possible. Information on Lot/batch number cannot be obtained. No further information is expected

Other Meds:

Current Illness:

ID: 1023437
Sex: F
Age:
State: IN

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: her left arm tired more quickly; felt a deep radiating pain from her arm up to her shoulder; felt a deep radiating pain from her arm up to her shoulder/pain and discomfort up thru her shoulder into her neck; pain and discomfort up thru her shoulder into her neck; pain and discomfort up thru her shoulder into her neck; moderate fatigue; headache; took a nap on Friday afternoon for over an hour/Saturday for two hours in the afternoon; a service member was vaccinated subcutaneously instead of intramuscularly; This is a spontaneous report from a contactable consumer via a medical information team. A 34-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EL3302, expiration date: 31May2021), subcutaneously in the left arm (also reported as left upper arm) on 22Jan2021 at 08:00 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The reporter was asking if there were any data on a vaccinated person who could be a carrier of COVID and transmit the virus to someone else even though they had been vaccinated and did not get sick and also asked if there was any follow up if somebody vaccinated became positive, carried the virus, and spread the virus. The reporter was also looking for recommendations on what to do if the vaccine was inadvertently administered subcutaneously. It was further reported that the patient, a service member, was vaccinated subcutaneously instead of intramuscularly (IM) on 22Jan2021. The reporter said that the patient was injected 4 inches down from her shoulder and an inch towards back of her arm. The patient described the area being the fatty portion of her arm. The reporter said that the patient wrote up a statement for them and said after she got the vaccine, she massaged the injection site and didn't feel any discomfort. The reporter said that the patient reported that 5.5 hours after injection on 22Jan2021 at 13:30, she felt a deep radiating pain from her arm up to her shoulder, then in the next few hours she had pain and discomfort up thru her shoulder into her neck. The patient reported other symptoms such as moderate fatigue and a headache. The reporter said that the patient reported she took a nap on Friday afternoon (22Jan2021) for over an hour, and took ibuprofen before bed Friday night. The patient took a nap Saturday (23Jan2021) for two hours in the afternoon, then slept 14 hours Saturday night. On Sunday morning (24Jan2021), the patient had continued fatigue, and thru Sunday, her shoulder and neck pain didn't subside. On Monday (25Jan2021), the patient was concerned that the pain and discomfort had been there several days, so she called her normal primary care provider (PCP), and the on call nurse told her to go to the emergency room (ER). The patient reported that the ER doctor said it looked like a subcutaneous injection versus IM. This was the end of information the patient gave, other than the ER doctor told her to take ibuprofen more regularly since noon on 25Jan2021. The patient also said in the email on Monday (25Jan2021) that she was still having pain, headache, and fatigue. The patient reported that her left arm tired more quickly (from an unspecified date) and was trying to use it while typing the email, and she was having trouble. The reporter was asking on what to do moving forward, whether it was recommended that they restart vaccine process and do two rounds or add a booster. Therapeutic measures were taken as a result of felt a deep radiating pain from her arm up to her shoulder/pain and discomfort up thru her shoulder into her neck, moderate fatigue, and headache. The patient was not recovered from the events "moderate fatigue and headache," while the outcome of the rest of the events was unknown.

Other Meds:

Current Illness:

ID: 1023438
Sex: F
Age:
State: TN

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: fever; tiredness; muscle aches; chills; nausea; This is a spontaneous report from a contactable consumer. A 54-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3302), via an unspecified route of administration on 25Jan2021 at 10:10 at a single dose on left arm for COVID-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. This morning (26Jan2021), when the patient woke up, she had a fever. She was wondering if she would be contagious to her family. Confirmed she is not positive for COVID. She was just wondering if she would be contagious since she had a fever. She has experienced tiredness, muscle aches, fever, chills, and nausea this morning when she woke up. She is a little better at this point. She works at a doctor's office but is not a healthcare provider. The patient received the first dose of BNT162B2, lot number: EJ1686 on an unspecified date. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1023439
Sex: M
Age:
State: WA

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Pronounced soreness near injection site; Mild flu-like symptoms; vivid dream; This is a spontaneous report from a contactable consumer (patient). A 76-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9261), via an unspecified route of administration in left arm on 22Jan2021 21:30 at a single dose for COVID-19 immunization. Medical history included none. Concomitant medication included levothyroxine sodium (THYROXINE), vitamin D, tamsulosin. The patient experienced pronounced soreness near injection site, mild flu-like symptoms, and vivid dream on 23Jan2021 01:00. Pronounced soreness near injection site. Mild flu-like symptoms strong for two hours and then diminishing with time. Very, vivid dream, detail rich, color, flashing light. No treatment received for the events. The outcome of the events was recovered on an unspecified date. The events were assessed as non-serious. Facility where the most recent COVID-19 vaccine was administered was Hospital. No other vaccines received within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been been tested for COVID-19.

Other Meds: THYROXINE; VITAMIN D [VITAMIN D NOS]; TAMSULOSIN

Current Illness:

ID: 1023440
Sex: F
Age:
State: KY

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: Numbness and weakness in arm at injection site and below; Numbness and weakness in arm at injection site and below; Numbness and weakness in arm at injection site and below; This is a spontaneous report received from a contactable consumer (patient). A 24-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: el 3249, expiry date: unknown), via an unspecified route of administration in the arm, on 26Jan2021 10:45, at single dose, for COVID-19 immunization, at the hospital. Medical history included anxiety and depression. The patient was not pregnant at the time of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. Concomitant medication included vilazodone hydrochloride (VIIBRYD), lamotrigine, acetylcysteine (NAC), betaine, citric acid monohydrate, cobamamide, cocarboxylase, flavine adenine dinucleotide, folic acid, folinic acid, iron amino acid chelate, magnesium ascorbate, magnesium levomefolate, nadh, nutrients nos, phosphatidyl serine, pyridoxal phosphate, sodium citrate, zinc ascorbate (ENLYTE), and probiotics. The patient previously took cefaclor (CECLOR) and experienced allergy. The patient did not receive any other vaccines within 4 weeks prior to BNT162B2 vaccine. The patient experienced numbness and weakness in arm at injection site and below on 26Jan2021 10:45. No treatment for the events was given. The patient was recovering from the events.

Other Meds: VIIBRYD; LAMOTRIGINE; NAC [ACETYLCYSTEINE]; ENLYTE; PROBIOTIC

Current Illness:

ID: 1023441
Sex: F
Age:
State: ND

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Fever/Undocumented fever; Chills; Numbness left body; Metallic taste; Headache; Body aches; Diarrhea; Fatigue; This is a spontaneous report from a contactable consumer (patient herself). A 30-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number and expiration date were not reported), via an unspecified route of administration on 05Jan2021 16:45 at single dose on the left arm for COVID-19 immunization. The patient's medical history was not reported. The patient was not pregnant at the time of vaccination. The patient was taking an unspecified concomitant medication. The patient previously took first dose of BNT162B on 26Jan2021 at 16:15 for COVID-19 immunization. On 05Jan2021 at 18:00, the patient experienced every reaction that was possible to the vaccine including fever (also reported as undocumented fever), chills, numbness left body, metallic taste, headache, body aches, diarrhea, and fatigue. The events were reported as non-serious and no treatment was given to the patient. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has been tested for COVID-19 with unknown results at the time of the report. The patient recovered from all of the events on an unspecified date. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023442
Sex: F
Age:
State: CA

Vax Date: 01/25/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: left face and ear were red and hot; left face and ear were red and hot; She got scared; side where the injection was given on her face felt like NOVOCAINE wearing out after the dentist/left side of the face cheeks to eye felt numb tingling, it felt different/like it was numb but not numb; left side of the face cheeks to eye felt numb tingling, it felt different; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EZ9262), via an unspecified route of administration in the left arm on 25Jan2021 10:00 at a single dose for COVID-19 immunization. The patient's medical history included high cholesterol diagnosed a few years ago. Concomitant medication included atorvastatin for high cholesterol. The patient took the vaccine yesterday (25Jan2021) and the side where the injection was given on her face felt like procaine hydrochloride (NOVOCAINE) wearing out after the dentist and she doesn't see this listed on the sheet given. The left side of the face cheeks to eye felt numb tingling, it felt different. She wants to know if it's normal. She got the shot at 25Jan2021 10:00 and by 25Jan2021 17:00, her left face and ear were red and hot. Then, she felt her face. It felt like procaine hydrochloride wearing out after the dentist, like it was numb but not numb. She got scared and got up and looked at herself to see how it looked and there was no change. She scratched both sides of her face and they felt the same. It continued all night. This morning (26Jan2021), she thought it went away but she felt it all over again, not as much. She is not burning up, not like yesterday. She did not take her temperature; she should have to see if she had a low grade fever. Outcome of the event "she was scared" was unknown while of the remaining events was recovering.

Other Meds: ATORVASTATIN

Current Illness:

ID: 1023443
Sex: F
Age:
State:

Vax Date: 01/24/2021
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: I need to take Norco for a bad back/All I need you to tell me is if I can take Norco for my back pain, and coded to back pain; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot and expiration date unknown), via an unspecified route of administration on 24Jan2021 at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient need to take Norco for a bad back,and coded to back pain. She have had a very bad back. She had the Pfizer vaccine this past Sunday. And need to if she could take Norco for her back pain. The outcome of the event was unknown. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 1023444
Sex: M
Age:
State: OK

Vax Date: 01/13/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Lower abdominal pain; ringing in ears; aching joints, frontal headache, very tired/Felt like the worst flu ever; This is a spontaneous report from a contactable healthcare professional (patient). This 63-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL1283 and expiry date unknown), via an unspecified route of administration on 13Jan2021 10:30 at a single dose on the right arm for COVID-19 immunization. Medical history included asthma and allergies: sulfa drugs. The patient's concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. Patient has not been tested for COVID-19 since the vaccination. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did fine until 23Jan2021 09:00 through 25Jan2021 as the patient experienced lower abdominal pain, aching joints, frontal headache, ringing in ears, and very tired. The patient stated that it felt like the worst flu ever. He also stated that his concern was will it be worse on the second injection. He may not take it. Events resulted in doctor or other healthcare professional office/clinic visit. No treatment was received. Outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1023445
Sex: F
Age:
State: WA

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: hemoptysis; short breath; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL9262), via an unspecified route of administration (left arm), on 21Jan2021 18:00, at single dose, for covid-19 immunization. Medical history included osteoporosis; there were no known allergies. There were no concomitant medications. The patient had no Covid prior vaccination. The vaccine was given at the hospital. The patient stated that on the next day after having the Pfizer-BioNTech Covid-19 vaccine, on 22Jan2021 15:00 the patient had short breath. On the 2nd day, 23Jan2021, the patient had hemoptysis. The patient does not know whether hemoptysis has something to do with the vaccine injection. The patient never had short breath nor hemoptysis in her life. These adverse events resulted in emergency room/department or urgent care visit. No treatment was received for the adverse events reported. At the time of the report, the patient had not recovered from the adverse events. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was Covid-tested post vaccination via nasal swab PCR on 25Jan2021 with results of negative.

Other Meds:

Current Illness:

ID: 1023446
Sex: F
Age:
State: NC

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: dont want to eat anything; hot and cold chills; headaches; muscle pain; fever; joint pain; injection site swelling; redness; nauseated; swollen lymph nodes on throat; face swelling; fast heartbeat; body didn't feel well; chills; didn't feel like herself; light headed; felt weak; tired/slept all day; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient 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 22Jan2021 15:30 at a single dose on right arm for COVID-19 immunization. Medical history included breast cancer 16 years ago, patient on defibrillator from Oct2016 (it was reported that this past October2020 would have been 4 years since she had the defibrillator put in), ongoing congestive heart failure, ongoing (COPD) chronic obstructive pulmonary disease, sinuses problems, back and hip problems, positive for COVID-19 from 11Jan2021, and hurting. The patient's concomitant medications were not reported. The patient previously received flu shot for immunization on unspecified date. On Saturday (23Jan2021), the patient reported that she "slept all day, felt weak, light-headed, and tired". The patient stated, "I have problems breathing anyways". The patient stated she "doesn't want to eat anything". On Sunday (24Jan2021), the patient "felt good", then Monday (25Jan2021), "didn't feel too bad". On unspecified date, patient experienced hot and cold chills, body didn't feel well, and breathing problems. She has breathing problems because she has COPD. Other things in the list of the adverse events (from the paperwork she was given) that the patient experienced include tiredness, headaches, muscle pain, chills, fever, joint pain, injection site swelling, redness, nauseated, feeling unwell, swollen lymph nodes on throat, face swelling, a fast heartbeat, dizziness, and weakness. Right now (26Jan2021), the patient did not even feel like going to her doctor's appointment (on Thursday). She just didn't feel like doing anything. She didn't feel like herself on 26Jan2021. She clarified on 11Jan2021 (prior to vaccination), she went to hospital because she was hurting. She clarified it was in and out of the Emergency Room. She was never admitted into the hospital. They ran some tests urine, blood, EKG tests. All the tests came back good. The patient underwent COVID test on 11Jan2021: positive; and same test on 22Jan2021: negative. Outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness: Congestive heart failure; COPD

ID: 1023447
Sex: F
Age:
State: FL

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Dizziness lasting more than a day; very migraine like; slight nausea; light sensitivity; visual disturbances; This is a spontaneous report from a contactable consumer who reported for herself. A 73-year-old female patient received her first single dose of BNT162B2 (Pfizer-BioNTech Covid-19 vaccine, lot number EL8982) at left arm 04:00 PM on 25Jan2021 for Covid-19 immunization. The patient's medical history included diabetes, osteopenia, hematuria, irritable bowel syndrome (IBS), high cholesterol, migraine. The patient had known allergies to penicillin- diarrhea, lactose intolerant, extreme allergy to sesame seeds and sage family. Concomitant medications included cyanocobalamin (B12), metformin, levothyroxine, multi vit, and calcium. The patient had not received other vaccines within four weeks. Around 10:15 AM on 26Jan2021, the patient experienced dizziness which lasted more than a day, light sensitivity, visual disturbances, slight nausea- very migraine like. No treatment was received for the events. The outcome of the events was resolving at the time of reporting. The patient had no Covid prior vaccination and had not covid tested post vaccination.

Other Meds: B12 [CYANOCOBALAMIN]; CALCIUM; LEVOTHYROXINE; METFORMIN

Current Illness:

ID: 1023448
Sex: F
Age:
State:

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Sore arm; Slight fever; This is a spontaneous report from a non-contactable consumer (patient). This 59-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EL9262) via an unspecified route of administration on 25Jan2021 at 16:00 (at the age of 59-years-old) as a single dose in the left arm for COVID-19 immunization. The patient had no medical history. The patient had allergies to cashews and iodine. The patient was not pregnant at the time of vaccination. Prior to vaccination the patient was not diagnosed with COVID-19. Concomitant medications included ibuprofen from an unknown date for an unspecified indication. The patient did not receive any other vaccines within 4 weeks prior to BNT162B2. The patient experienced sore arm and slight fever on 26Jan2021 at 9:00. The patient did not receive any treatment for the events. The patient was not hospitalized for the events. The reporter's overall assessment of the events was non-serious. The outcomes of sore arm and fever were not recovered. It was also reported that 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: IBUPROFEN

Current Illness:

ID: 1023449
Sex: F
Age:
State: NM

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: dizziness; cold extremities; redness in left ear; rash on left shoulder; Mild anxiety; This is a spontaneous report from a contactable pharmacist. A 26-year-old female patient received the second dose of bnt162b2 (Pfizer-Biontech COVID-19 Vaccine, Lot number: EL3302), intramuscular at the left arm on 26Jan2021 11:00 at a single dose for covid-19 immunization. The vaccine was administered in a hospital. The patient's medical history and concomitant medications were not reported. It was unknown if the patient was pregnant at the time of vaccination. Historical vaccine includes first dose of bnt162b2 on 05Jan2021 10:15 AM, lot number: EL1284, intramuscular at the left arm for COVID-19 immunization at the age of 26 years. No reaction to first dose was reported. On 26Jan2021 11:00, the patient experienced dizziness, cold extremities, redness in left ear and rash on left shoulder noted and mild anxiety. Oral 25 mg Benadryl was administered. Returned to work at 10:25 am. The events were assessed as non-serious, did not result in death, not life threatening, did not cause/prolonged hospitalization, not disabling/incapacitating, did not cause congenital anomaly/birth defect. Since the vaccination the patient has not been tested for COVID-19. The outcome of the events was recovered on 26Jan2021.

Other Meds:

Current Illness:

ID: 1023450
Sex: M
Age:
State: TN

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Headache; This is a spontaneous report from a contactable consumer (patient). A 91-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL9261), intramuscular in left arm, on 21Jan2021 (Thursday) at 08:45, at a single dose, for COVID-19 immunization. The patient's medical history included ongoing diabetes (diabetic) diagnosed about 50 years ago (1971). The patient's concomitant medications included glipizide and insulin glargine (LANTUS), both were ongoing for diabetes. The patient previously took the first dose of BNT162B2 (Lot Number: EL3046) on 02Jan2021 around 09:00 AM for COVID-19 immunization (in right arm). The patient had no other prior vaccinations within 4 weeks. The vaccine was administered in a (public) health department facility. The patient had second dose of the Pfizer COVID-19 vaccine on Thursday (21Jan2021) and from Friday morning (22Jan2021), he started experiencing headache and he cannot get rid of it. It had been 5 days. The patient took paracetamol (TYLENOL) and it is not helping. Today (26Jan2021), the patient went to the hospital emergency room (ER) but they did not see him since the ER was so busy; he sat in ER waiting room for 6 hours and he never got waited on so he left. The patient did not have physician office visit but is going to see his doctor tomorrow (27Jan2021) for the headache. The patient had not recovered from the event.

Other Meds: GLIPIZIDE; LANTUS

Current Illness: Diabetes (Diabetic; diagnosed about 50 years ago)

ID: 1023451
Sex: F
Age:
State:

Vax Date: 01/16/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: tenderness in her arm; red patch at the injection site; This is a spontaneous report from a contactable consumer (patient) via a medical information team. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 16Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated her arm did not bother her much just tenderness in her arm. 10 days after the vaccine, on 26Jan2021, the patient developed a red patch at the injection site and wanted to know if this symptom has been reported this many days after the vaccine. The patient wanted to know if she should get the second dose of the vaccine after she experienced a red patch around the injection site 10 days after the first dose of the PFIZER-BIONTECH COVID-19 VACCINE. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1023452
Sex: F
Age:
State: GA

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: itching in her eardrums, her face, nose and everything/inside of her ears/between her fingers, hands, feet/back/sides/itching all day; one hive came up around the injection site; sneezed 3 or 4 times/sneezing 5-6 times all day/sneezing all day; arm was itching where she got the injection site at; This is a spontaneous report from a contactable consumer (patient). A 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL0142), intramuscularly on the upper left arm (also reported as in humerus area), on 23Jan2021 11:00, at single dose, for covid-19 immunization. Medical history included allergies to shellfish and medications; allergic to cats and dogs; had to go to the emergency room with an allergic reaction; hypothyroidism from 2008 and ongoing; asthmatic from an unspecified date and ongoing (diagnosed with asthma as a kid, (maybe at 5 years old); asthma was well controlled and she has an asthma inhaler she uses like once a month); light GERD from 2018 and ongoing; recovering from a meniscus tear in her knee that occurred on 21Aug2020 - she had surgery for it on 23Oct2020; anterior uveitis of the eyes and; partially blind in her eyes. Concomitant medications included adalimumab (HUMIRA) and methotrexate - both from an unspecified date and ongoing for anterior uveitis of the eyes which the patient clarified was a condition where her retina swells and its defined as an autoimmune problem. She informed that she was partially blind in her eyes but something about the methotrexate and Humira in which she was able to see now. The patient stated that she received the first dose of the COVID-19 vaccine last Saturday, 23Jan2021 at 11 AM. Later that evening of 23Jan2021, she started itching in her eardrums, her face, nose and everything, and one hive came up around the injection site. She has been extremely itchy since she took it. Also, she sneezed 3 or 4 times later that evening of 23Jan2021. It's pretty unusual for her to sneeze. She stated she used to take allergy shots, so she doesn't really sneeze at all. Between the time of 10:40- 10:45pm that night, on 23Jan2021 she sneezed three consecutive times. Then she went to lay down, and she noticed on 23Jan2021 that her arm was itching where she got the injection site at. She noticed she had one hive at the injection site. She confirmed she only had one hive. She did start to itch all over- her face and nose was itching. She has had an allergic reaction before, (medical history) and it wasn't a type of reaction where she needed more than one hand to scratch; it was just a subtle itch. She informed that she should have been aware when she started sneezing because she never sneezed. She has been sneezing 5-6 times all day. Then she took Benadryl at 18:00 which was helping. She waited the allotted 15 minutes after taking it and she was fine; she had no problems at all. But as soon as it wore out, she began itching and sneezing. After an hour she took another because the inside of her ears was still itching; the itching went deep down into her ears. She had itching of her face, arms in between her fingers, hands, her feet (only the top of her feet, not the bottom), and her back. She was itching a little bit on her sides. The itching was basically all over, but she only had one hive. She had one hive at the injection site, so she assumed it was probably due to the vaccination. Then the hive was gone. However, she still feels itching mainly in her nose, arm and back, just like that night following the injection. She was still itching for some reason. She got up on Sunday 24Jan2021 and everything was gone. She confirmed the hives, the itching, everything was gone. She didn't take anything on Sunday. Yesterday, 26Jan2021 she noticed a little slight itch, but she didn't pay any attention to it and didn't worry about taking any Benadryl. Today, 27Jan2021, she has been itching and sneezing all day. Like right now, her foot was itching but the itching has kind of subsided a little bit. But all day her nose has been a little itchy. She added that she was allergic to cats and dogs (she doesn't own any pets), so if she gets in the vicinity of any cats or dogs, her nose starts itching. Her nose has had the same kind of itching and sneezing all day long. She hasn't had any testing. She didn't go to an emergency room only because it wasn't bad enough. If her throat was itching or swelling, then she would have been ready to go to the ER at 1am. Also, if she would have had shortness of breathing or her throat/tongue started itching, she would have gone to the emergency room. She stated that once her ear stopped itching, she was fine. She wanted to know if her experience was reported as a side effect of the vaccine. She mentioned that she definitely wants to take the second dosage, but she was a little apprehensive. She was scared it may be worse with the second vaccine. Now that she received the vaccine, she was unable to access an HCP at her job and primary care facility. So, she called her primary care physician who prescribed her an EpiPen in case she receives the second dose of the vaccine. Her doctor also instructed her to take Benadryl a day or two after the injection. She did call (privacy) since they were the ones who did the injection. She informed that she did all her research beforehand because she was a little apprehensive to get the first vaccine. She already had to go to the emergency room with an allergic reaction before. She told one of the nurse practitioners about her itching all the time and; she was told that that was common. She explained that, everybody that she has come into contact with that has had this vaccine, no one has had any problems with itching. Itching was not mentioned on any of the information she has read, the research she has done, the news, or if she goes on the website there wasn't any mention of itching. There were things like headaches and other symptoms but nothing about itching and hives. She then requested to speak to someone about itching being a side effect of the vaccine. She was a little apprehensive about getting the second vaccine so she would like further information. The final outcome of the adverse events was unknown.

Other Meds: HUMIRA; METHOTREXATE

Current Illness: Asthmatic (diagnosed with asthma as a kid, (maybe at 5 years old); asthma was well controlled and she has an asthma inhaler she uses like once a month); GERD; Hypothyroidism

ID: 1023453
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: his wife took the shot and she had no reaction, just a little soreness; This is a spontaneous report from a contactable consumer (husband). This consumer reported similar events for two patients. This is the second of two reports. A female patient of an unspecified age received bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; unknown lot number and expiration date), 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 husband reported that his wife took the shot and she had no reaction just a little soreness. His wife also mentioned that his needle didn't go in as much as when she got her injection, so he was wondering if his vaccine was administered in the right way. The outcome of the event was unknown. The following information on the batch/lot number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021075865 Same reporter/drug, similar events, different patient

Other Meds:

Current Illness:

ID: 1023454
Sex: F
Age:
State: NV

Vax Date: 01/22/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: a rash on her chest/have a rash on her chest that itches; This is a spontaneous report from a contactable consumer (patient). A 76-year-old female patient received her first dose of bnt162b2 (BNT162B2 reported as PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; lot number: EK9231; expiration date: unknown), via an unspecified route of administration on 22Jan2021 at a single dose for covid-19 immunization. Medical history included blood pressure (blood pressure abnormal), borderline diabetes, hypertension, arrhythmia and cholesterol high. Concomitant medication included amlodipine besilate for blood pressure, metoprolol succinate (METOPROLOL SUCCER) for arrhythmia, metformin hcl and rosuvastatin calcium for cholesterol high. The patient reported that she received the first dose of the Pfizer vaccine on 22Jan2021 and two days later she noticed a rash on her chest. She mentioned that she has been using an anti-itch cream. She mentioned that she was supposed to schedule her second dose for 12Feb2021 but is unable access the website to schedule her appointment through. She mentioned that she had a rash on her chest that itches, and she have got some itching cream, but she keeps waiting for it to finally go away but so far it is still there. When asked about the treatment, she mentioned that she had Triamcinolone 0.1% for other usages from her skin doctor (her dermatologist). The outcome of the event was not recovered.

Other Meds: AMLODIPINE BESILATE; METOPROLOL SUCCER; METFORMIN HCL; ROSUVASTATIN CALCIUM

Current Illness:

ID: 1023455
Sex: F
Age:
State: NM

Vax Date: 01/23/2021
Onset Date: 01/23/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: began to cough; This is a spontaneous report from a contactable pharmacist reported that a 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN5318), intramuscular on 23Jan2021 12:30 at a single dose for Covid-19 immunization. The vaccine was administered at the clinic. Medical history included history of asthma attacks and has to occasionally use her epinephrine pen to aide in breathing due to a new onset of an allergy to salad dressing from an unknown date. Concomitant medication included epinephrine. On 23Jan2021 12:30, the patient began to cough. The patient was given water with no resolve to coughing. The patient went to first aid area assessed by Medic. The lungs were clear to auscultation and patient O2 saturation was 95% on RA on 23Jan2021. Patient denied any difficulty breathing. The provider evaluated patient and at 12:40 patient given 4 puffs of albuterol inhaler (patient's personal inhaler used). After reassessment/observation provider released patient home. The outcome of the event was recovered.

Other Meds: EPINEPHRINE

Current Illness:

ID: 1023456
Sex: F
Age:
State: SC

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: itchy feet and hands; This is a spontaneous report from a contactable healthcare professional (patient). A 54-year-old female received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL3246 and expiry date: unknown), via an unspecified route of administration on the right arm, on 13Jan2021 15:00 to 13Jan2021 15:00 at SINGLE DOSE for covid-19 immunisation. Medical history included high blood pressure and seasonal allergies. Patient was not pregnant at the time of vaccination. Concomitant medication included high blood pressure medication. There were no other vaccine received within 4 weeks prior to COVID vaccination. On 14Jan2021 13:00, patient woke up with itchy feet and hands. She also was experiencing what felt like a rubber and around her chest. The next day on 15Jan2021, it had spread to my legs and arms, and then the next day it was on my back and chest. As of 26Jan2021, it has moved to her neck and face. Patient had been using Benadryl orally, and Cortizone Topical in the areas. Outcome of the event was not recovered. Event was considered non-serious. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination.

Other Meds:

Current Illness:

ID: 1023457
Sex: F
Age:
State: FL

Vax Date: 01/21/2021
Onset Date: 01/25/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: lost her smell; extremely tired; bad headache; congestion/ felt like a really bad sinus infection; felt like a really bad sinus infection; This is a spontaneous report from a contactable healthcare professional (HCP, patient herself). A 22-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EL1283, expiration date was unknown), via an unspecified route of administration on the left arm on 21Jan2021 at 19:15 at a single dose for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was reported as the hospital. The patient had no medical history; she had no allergies to medications, food, or other products. The patient's 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. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On Monday, 25Jan2021 at 04:00, the patient woke up with a bad headache and congestion and it worsened up until Tuesday. It felt like a really bad sinus infection. Then on Tuesday night, 26Jan2021, the patient lost her smell and she was also extremely tired. The reporter assessed the events as non-serious. The patient did not receive any treatment for the adverse events. The patient was not recovered from all the events.

Other Meds:

Current Illness:

ID: 1023458
Sex: F
Age:
State: GA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Mild headache; chills; some joint pains; This is a spontaneous report from a contactable consumer (patient). A 78-year-old non-pregnant female patient received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: EL8982), via an unspecified route of administration in the left arm on 26Jan2021 11:15 at 0.3 mL, single for COVID-19 immunization. Medical history included hypertension and known allergies to penicillin. The patient is not pregnant at the time of vaccination. The patient has no COVID prior vaccination. The patient has not been tested for COVID post vaccination. Concomitant medications included atenolol, chlorthalidone, felodipine, losartan, and potassium acetate (POTASSIO ACETATO). On 26Jan2021 15:00, the patient experienced mild headache, chills, and some joint pains. The patient did not receive any treatment for the adverse events. The outcome of the events was not recovered.

Other Meds: ATENOLOL; CHLORTHALIDONE; FELODIPINE; LOSARTAN; POTASSIO ACETATO

Current Illness:

ID: 1023459
Sex: M
Age:
State: CT

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 02/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: headache; Left arm sore; This is a spontaneous report from a contactable consumer (patient) This 61-year-old male consumer received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) from Lot# EL3247 at left arm on 26Jan2021 11:00 at SINGLE DOSE for covid-19 immunisation . Facility where the most recent COVID-19 vaccine was administered:Workplace clinic. the patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine.Medical history :none. Concomitant medication included atorvastatin calcium (LIPITOR ) bupropion hydrochloride (WELLBUTRIN), acetylsalicylic acid (ASPIRIN) 81 mg.The patient experienced left arm sore and minor headache on 27Jan2021 06:00 .No treatment received.Events reported as non serious.Outcome of the event was recovering.No Prior to vaccination, was the patient diagnosed with COVID-19 .Since the vaccination, The patient hadn't been tested for COVID-19

Other Meds: LIPITOR (ATORVASTATIN CALCIUM); WELLBUTRIN; ASPIRIN (ACETYLSALICYLIC ACID)

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm