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Reporte zur Charge ENG198

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

17Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 2 MN 2 VA 2 WA 2 CO 2 CA 2 MI 1 PA 1 IL 1 LA 1

VAERS 1073295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

schwer
Staat
FL
Alter
52,0
Geschlecht
F
Eingang
04.03.2021
Impfdatum
26.02.2021
Beginn
26.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Computerised tomogram head Contusion Diarrhoea Disorientation Fall Fatigue Head injury Headache Loss of consciousness Myalgia Nausea Neck injury Pyrexia Vomiting

Symptomtext

Day 1, 26 Feb 2021; headache began at noon; severe fatigue at 6:00 pm; 103 degree fever at midnight Day 2, 27 Feb 2021: 103 fever for 3 hours, reduced and maintained at 100 with alternating extra strength Tylenol with 800 mg Motrin every 4 hours; continued severe fatigue; continue headache, nausea started at 5:00 pm Day 3, 28 Feb 2021: Nausea, diarrhea, muscle pain, vomiting, headache, 100 degree fever for 24 hours, 6:00 pm passed out for less than 1 minute when standing to go to bathroom to vomit (aware, controlled fall); 2nd episode of passing out sometime after midnight, tried to stand, completely blacked out, woke up disoriented, called 911, transported to ER; bruised upper left arm, left side jaw/neck hitting furniture in fall, hit head on floor

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
CT for head injury at ER 1 March 2021, rehydrated via IV, IV meds for nausea; discharged at approximately 6:00 am
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma
Andere Medikamente
Allegra 180 mg, Singulair 10 mg, Effexor 37.5 mg
Allergien
NKDA, allergic to fruits and tree nuts
Vorherige Impfungen
-

VAERS 2108239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

moderat
Staat
MN
Alter
73,0
Geschlecht
M
Eingang
12.02.2022
Impfdatum
22.02.2021
Beginn
22.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood test Hypoaesthesia oral Pain in extremity Tremor

Symptomtext

quivering of his lower lip; numbness of his lower lip; slightly sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular, administered in arm left, administration date 22Feb2021 16:00 (Lot number: ENG198) at the age of 73 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Polio" (not ongoing), notes: victim of Polio in the 1950s. There were no concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 22Feb2021, outcome "recovered" (2021), described as "slightly sore arm"; TREMOR (non-serious) with onset 10Mar2021, outcome "recovering", described as "quivering of his lower lip"; HYPOAESTHESIA ORAL (non-serious) with onset 10Mar2021, outcome "recovering", described as "numbness of his lower lip". The events "slightly sore arm", "quivering of his lower lip" and "numbness of his lower lip" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, tremor, hypoaesthesia oral. Additional information: The patient received the 2nd dose of BNT162B2 (Lot number: EP7534) on 16Mar2021. The patient saw his physician on 05Apr2021 and had some bloodwork to make sure it was not post-polio syndrome. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
Test Date: 20210405; Test Name: bloodwork; Result Unstructured Data: Test Result:Unknown results; Comments: drew some bloodwork to make sure it was not post-polio syndrome
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Polio (victim of Polio in the 1950s)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1791803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

moderat
Staat
VA
Alter
38,0
Geschlecht
F
Eingang
16.10.2021
Impfdatum
27.02.2021
Beginn
27.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Nervousness Palpitations Tremor

Symptomtext

felt very jumpy.; Heart was racing; Shaky; This is a spontaneous report from a contactable consumer, the patient. A 38-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ENG198) via an unspecified route of administration in the left arm on 27Feb2021 at 13:15 (at the age of 38-year-old) as a single dose for COVID-19 immunisation. Medical history included lymphomatoid papulosis, raynauds, lactose intolerant (cream), allergic reaction to analgesics (allergy to pain relievers in the vicodin family) and fruit allergy (citric acid sensitivity). Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. On 27Feb2021 at 13:30, about 15-20 minutes after the vaccine, the patient felt very jumpy, she compared it to excessive caffeine jitters. The patient felt her heart was racing and like she was shaky. It subsided later that day. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the reported events. The clinical outcome of the events felt very jumpy, heart was racing and shaky was recovered on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergic reaction to analgesics (Known allergies: Pain relievers in the vicodin family); Fruit allergy (Known allergies: citric acid (sensitivity)); Lactose intolerant (Lactose intolerant (creams)); Lymphomatoid papulosis; Raynauds
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1426708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

moderat
Staat
MI
Alter
79,0
Geschlecht
F
Eingang
25.06.2021
Impfdatum
06.03.2021
Beginn
19.03.2021
Tage bis Beginn
13,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Cough Decreased appetite Diarrhoea Dyspnoea Fatigue Headache Illness Nasal congestion Pain

Symptomtext

loss of apatite/can't eat anything- everything tastes like soap; diarrhea; fatigue; body aches; difficulty breathing; congestion; feel sick; chills; cough; headache; This is a spontaneous report from a contactable consumer. This 79-year-old female consumer reported for herself that: A 79-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: ENG198, Expiration date: Unknown), via an unspecified route of administration with a needle into left upper arm on 06Mar2021 at 9:30 (at the age of 79-years) as (exact dose unknown) single dose for covid-19 immunization. The patient medial history included ongoing neuropathy pain, ongoing asthma (diagnosed when she was a kid), ongoing bladder problem/bladder infections (she kept getting bladder infections; went to a bladder specialist 6 months prior), ongoing high blood pressure (diagnosed for many years), ongoing arthritis (diagnosed for many years) and knee replacement in 2008. The patient had no history of previous immunization with the Pfizer vaccine considered as suspect, was not administered additional vaccines on the same date of the Pfizer vaccine, and did not receive any prior vaccinations within 4 weeks of Pfizer vaccine. The patient had no family history relevant to the adverse events. Concomitant medications included gabapentin (been taking that for years) from an unspecified date to ongoing for neuropathy pain, losartan potassium (been taking this for years) from an unspecified date to ongoing for high blood pressure, nitrofurantoin (MACRODANTIN) (about 6 months) from an unspecified date to ongoing for bladder infections, beclometasone dipropionate (QVAR REDIHALER) (been taking this for years) from an unspecified date to ongoing for asthma, Serevent Diskus (been taking this for years) from an unspecified date to ongoing for asthma, estradiol vaginal cream usp (about 6 months) for "bladder" (bladder disorder), and ibuprofen (if she needs it, but she doesn't always need it). The patient stated she was taking her usual medications-allergy medications, high blood pressure medicine and estrogen. The patient's historical vaccines included shingles vaccine in 2019 with sore arm as the reaction, pneumonia vaccine in 2019 with sore arm as the reaction and tetanus vaccine in 2019 with sore arm as the reaction. She did not have NDC/LOT/Expiration number of the historical vaccines. On 19Mar2021, the patient began to feel sick. She reported the following symptoms: chills, cough, headache, difficulty breathing and congestion starting on 19Mar2021 around noon time, fatigue and body aches starting on 20Mar2021 gradually throughout the day, and loss of appetite/ "can't eat anything- everything tastes like soap" gradually throughout the day and diarrhea starting on 21Mar2021. She thought it was going away, but it didn't. She stated that when the chills first started, she couldn't even hold her hand still, but that had improved. She stated that everything tasted like soap on the third day of the symptoms' onset on 21Mar2021. She stated that she made herself eat a little, but she just couldn't. She stated that she drank as much water as she could. She stated that the taste of soap was there before, but she didn't recognize it for what it was until it started to get worse. She stated that she needed to get her glasses to read the writing on her vaccination record card. She started that she did not want to get the second dose on Saturday, 27Mar2021. The patient inquired what she should do. She stated that to be able to talk on the phone, she had to take paracetamol (TYLENOL) 650 mg, and she had taken one tablet. The patient did not require emergency room or Physician office visit due to the events. She thought it would go away, so she didn't go see her doctor. Treatment received for the events included paracetamol (TYLENOL) 650 mg. The patient had undergone no investigations or relevant tests. The outcome of the event fatigue and loss of appetite was worsened. The outcome of the events difficulty breathing, body aches and diarrhea was not recovered. The outcome of the event chills, cough, headache and congestion was recovering. The outcome of the event "feel sick" was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Arthritis; Asthma; Bladder disorder; Bladder infection (She kept getting bladder infections); Blood pressure high; Neuropathic pain
Vorgeschichte
Medical History/Concurrent Conditions: Knee replacement
Andere Medikamente
GABAPENTINE; LOSARTAN POTASSIUM; MACRODANTIN; QVAR REDIHALER; ESTRADIOL
Allergien
-
Vorherige Impfungen
-

VAERS 1712521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
PA
Alter
59,0
Geschlecht
M
Eingang
18.09.2021
Impfdatum
01.03.2021
Beginn
02.03.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Back pain Lethargy Musculoskeletal stiffness Pain Pain in extremity

Symptomtext

Back Pain And Stiffness; Back Pain And Stiffness; Lethargy; General Aches And Joint Pain; General Aches And Joint Pain; Left Arm Soreness; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 01Mar2021 07:45 (at the age of 59-year-old) (Lot Number: ENG198) as dose 1, single for COVID-19 immunization. Medical history included high blood glucose increased, overweight, and COVID-19 (prior to vaccination). The patient did not have any known allergies. Concomitant medications included red rice yeast; cetirizine hydrochloride (ZYRTEC) and zinc, all taken for an unspecified indication, start and stop dates were not reported. The patient experienced left arm soreness, back pain and stiffness, lethargy, general aches and joint pain on 02Mar2021 06:00. The patient did not receive treatment for the events. The outcome of events was recovered. Since vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood sugar increased; COVID-19; Overweight
Andere Medikamente
RED RICE YEAST; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; ZINC
Allergien
-
Vorherige Impfungen
-

VAERS 1692635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
MN
Alter
70,0
Geschlecht
F
Eingang
11.09.2021
Impfdatum
25.02.2021
Beginn
01.02.2021
Tage bis Beginn
-
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pruritus Swelling

Symptomtext

itching face and neck; swelling itching welt kind of things; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Lot number: ENG198 and Expiration date: 30Jun2021) via an unspecified route of administration, administered on the left arm on 25Feb2021 16:00 (at the age of 70 years old) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were reported as none. On an unspecified date in Feb2021, the patient experienced an itching face and neck, a kind of "swelling itching welt kind of things". The patient tried not to touch it and took diphenhydramine hydrochloride (BENADRYL) as a treatment. The patient stated that the reaction was mostly on her neck, and it has gotten a little better, though she still has it. She says she has been drinking a lot of water to flush it out. The outcome of the reported events was recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1436672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
WA
Alter
64,0
Geschlecht
F
Eingang
30.06.2021
Impfdatum
11.03.2021
Beginn
11.03.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Body temperature Fatigue Headache Pain in extremity Pyrexia

Symptomtext

fatigue; temperature of 102F; headache; sore arm; This is a spontaneous report received from a contactable consumer, the patient. A 64-year-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: ENG198) via an unspecified route of administration in the left arm on 11Mar2021 at 11:00 (at the age of 64-years-old) as a single dose for COVID-19 immunisation. Medical history included breast cancer. The patient was allergic to erythromycin. The patient was diagnosed with COVID-19 prior to vaccination. The patient had not tested positive for COVID-19 since the vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included beclomethasone (QVAR), montelukast (MANUFACTURER UNKNOWN), olmesartan medoxomil (MANUFACTURER UNKNOWN), anastrozole (MANUFACTURER UNKNOWN) all for unknown indications and from an unknown date and unknown if ongoing. On 11Mar2021 at 15:00, the patient experienced fatigue, temperature of 102F, headache and sore arm. Fever lasted 24 hours and started 8 hours after shot. Fatigue started a few hours after shot and was severe for 24 hours (could not get out of bed) and gradually went away over a week. The adverse events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The patient did not receive treatment for the reported events. The clinical outcome of events fatigue, temperature of 102F, headache and sore arm was recovered on an unknown date in Mar2021. No follow up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
Test Date: 20210311; Test Name: Temperature; Result Unstructured Data: Test Result:102 Units:[degF]
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Breast cancer
Andere Medikamente
MONTELUKAST; OLMESARTAN MEDOXOMIL; ANASTROZOLE; QVAR
Allergien
-
Vorherige Impfungen
-

VAERS 1349407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
IL
Alter
60,0
Geschlecht
F
Eingang
26.05.2021
Impfdatum
03.03.2021
Beginn
03.03.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Fatigue Headache Herpes zoster Lymphadenopathy Malaise Myalgia Pain Urticaria

Symptomtext

tiredness; headache; muscle pain; feeling unwell; swollen lymph nodes; hives with pain in them; pain; I got Shingles; This is a spontaneous report from a contactable consumer (patient). A 60-year-old female patient received bnt162b2 (BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in right arm on 03Mar2021 13:15 (also reported 15Mar2021 13:30) (Batch/Lot Number: ENG198) (at the age of 60 years old) as 1st dose, single for COVID-19 immunisation. Medical history included stage 3 kidney disease and thyroid disorder. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 vaccine was administered was in doctor's office/urgent care. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that patient had other medications received within 2 weeks of vaccination (unspecified). On 03Mar2021, the patient experienced tiredness, headache, muscle pain, feeling unwell, swollen lymph nodes, hives with pain in them, pain and she got shingles. The events resulted in doctor or other healthcare professional office/clinic visit. The treatment received for the adverse event included Valtrex, anti biotic and creme. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The outcome of the event shingles was unknown; and not recovered outcome for the other events. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Chronic kidney disease stage 3; Thyroid disorder
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1123392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
FL
Alter
60,0
Geschlecht
F
Eingang
22.03.2021
Impfdatum
18.03.2021
Beginn
19.03.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site bruising Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

Injection site hot red swollen itchy burning

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site bruising
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1088845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
CO
Alter
75,0
Geschlecht
M
Eingang
10.03.2021
Impfdatum
25.02.2021
Beginn
02.03.2021
Tage bis Beginn
5,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Fatigue Mental impairment

Symptomtext

Very tried and very dizzy. My mind went blank. I could not spell my name.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Idiopathic pulmonary fibrosis
Andere Medikamente
Ofev, Levothyroxine sodium, Simvastatin, Fluorometholone,
Allergien
-
Vorherige Impfungen
-

VAERS 1079622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
VA
Alter
54,0
Geschlecht
M
Eingang
07.03.2021
Impfdatum
02.03.2021
Beginn
02.03.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site pain Insomnia Sensory disturbance Sensory overload

Symptomtext

1. Muscle soreness at injection site, lasting 2 days. Currently resolved. 2. Feeling of overstimulation throughout day and evening, and difficulty falling asleep at night. "Buzzing" feeling similar to drinking too much coffee. Lasting 3-4 days. Currently resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none
Vorgeschichte
moderate asthma
Andere Medikamente
Bupropion XL 300mg, men's multivitamin, calcium/magnesium zinc, vitamin d, glucosamine/chondroitin, msm
Allergien
sulfa, tree nuts
Vorherige Impfungen
-

VAERS 1069994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

mild
Staat
LA
Alter
53,0
Geschlecht
F
Eingang
03.03.2021
Impfdatum
02.03.2021
Beginn
02.03.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Eye pain Fatigue Headache Pain Pyrexia

Symptomtext

Body aches, fatigue, mild headache, eyes hurt. Feel feverish but have no fever

Weitere VAERSDATA-Felder
Praegender Schweregrund
Eye pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none
Vorgeschichte
DJD DDD Bulging disc sciatica HTN
Andere Medikamente
Losarten 50 mg daily HCTZ 25 mg/daily Tramadol 50 mg TID Prem-pro daily Multivitamin daily Calcium Vit D 600mg/400/BID Vit D3 2000IU BID
Allergien
Voltaren
Vorherige Impfungen
-

VAERS 2312555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Eng198

gering
Staat
-
Alter
52,0
Geschlecht
F
Eingang
08.06.2022
Impfdatum
19.03.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Mar2021 as dose 2, single (Lot number: Eng198) at the age of 52 years, in right arm for COVID-19 immunisation; COVID-19 vaccine MRNA (MRNA 1273) (MODERNA COVID-19 VACCINE), on 18Dec2021 as dose 3 (booster), single (Lot number: T60h21a), in right arm for COVID-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1791608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

gering
Staat
CA
Alter
43,0
Geschlecht
F
Eingang
16.10.2021
Impfdatum
27.02.2021
Beginn
28.02.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pre-existing condition improved Therapeutic response unexpected

Symptomtext

"I" have Rheumatoid Arthritis. It's been3 days since "my" vaccine and all of "my" RA symptoms are gone!!! "I" haven't felt this good for about a year!! "My" inflammation is completely nonexistent right now!; "I" have Rheumatoid Arthritis. It's been3 days since "my" vaccine and all of "my" RA symptoms are gone!!! "I" haven't felt this good for about a year!! "My" inflammation is completely nonexistent right now!; This is a spontaneous report from a contactable consumer, the patient. A 43-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ENG198) via an unspecified route of administration in the left arm on 27Feb2021 at 11:30 (at the age of 43-years-old) as a single dose for COVID-19 immunisation. Medical history included rheumatoid arthritis, degenerative disc disease and known allergies to penicillin. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient received unspecified medication within two weeks of vaccination. On 28Feb2021, It was reported that the patient had rheumatoid arthritis. It had been 3 days since her vaccine and all of her rheumatoid arthritis symptoms were gone (pre-existing condition improved and unexpected therapeutic benefit). The patient had not felt this good for about a year. Her inflammation was completely non-existent at the time of reporting. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. No therapeutic measures were taken as a result of the reported events. The clinical outcome of the events patient had rheumatoid arthritis. It had been 3 days since her vaccine and all of her rheumatoid arthritis symptoms were gone (pre-existing condition improved and unexpected therapeutic benefit). The patient hadn't felt this good for about an year. Her inflammation was completely non-existent right now was unknown at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pre-existing condition improved
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Degenerative disc disease; Penicillin allergy (known allergies: Penicillin); Rheumatoid arthritis
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1677924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

gering
Staat
CA
Alter
48,0
Geschlecht
F
Eingang
07.09.2021
Impfdatum
17.03.2021
Beginn
15.04.2021
Tage bis Beginn
29,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Herpes zoster

Symptomtext

A month after the second Pfizer vaccine came down with shingles.; This is a spontaneous report from a contactable consumer, the patient. A 48-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ENG198) via an unspecified route of administration in the left arm on 17Mar2021 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. Medical history included allergies to sulfa. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medication included norethisterone acetate, ethinylestradiol, ferrous fumarate (LARIN FE) from an unknown date for an unknown indication and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9266) via an unspecified route of administration in the left arm on 24Feb2021 at 15:00 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. On 15Apr2021, a month after the second Pfizer vaccine, the patient came down with shingles. This was the first time the patient had shingles. The patient was not sure if they're connected, but thought it was best to report it. The event resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were taken as a result of the event which included treatment with unspecified medication. The clinical outcome of the event shingles was not recovered at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Herpes zoster
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente
LARIN FE
Allergien
-
Vorherige Impfungen
-

VAERS 1129588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

gering
Staat
CO
Alter
41,0
Geschlecht
F
Eingang
02.07.2021
Impfdatum
20.02.2021
Beginn
26.02.2021
Tage bis Beginn
6,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Full blood count Immune thrombocytopenia Platelet count decreased

Symptomtext

Platelets of 19, Idiopathic thrombocytopenic purpura

Weitere VAERSDATA-Felder
Praegender Schweregrund
Immune thrombocytopenia
Hospital-Tage
-
Labordaten
CBC
Aktuelle Erkrankungen
None
Vorgeschichte
Meningioma, Brain Hashimoto Thyroiditis Rosacea Vocal Cord Dysfunction Spontaneous intracranial Hypotension
Andere Medikamente
Retin-A, Metrocream
Allergien
No known food/drug allergies
Vorherige Impfungen
-

VAERS 1436632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ENG198

gering
Staat
WA
Alter
48,0
Geschlecht
F
Eingang
30.06.2021
Impfdatum
26.02.2021
Beginn
14.03.2021
Tage bis Beginn
16,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Herpes zoster

Symptomtext

Shingles; This is a spontaneous report from a contactable consumer, the patient. A 48 year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: ENG198) via an unspecified route of administration in left arm on 26Feb2021 at 12:00 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient was allergic to penicillin. The patient did not receive any other medication within two weeks of vaccination. The patient did not receive any other vaccines within two weeks prior to the vaccination. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EL9262) via an unspecified route of administration in the left arm on 01Feb2021 at 16:00 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 14Mar2021, the patient experienced shingles which was diagnosed on 19Mar2021. Therapeutic measure for shingles included treatment with valacyclovir and prednisone. The event resulted in doctor or other healthcare professional office/clinic visit. The clinical outcome of shingles was not recovered at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Herpes zoster
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-