- Staat
- MN
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 22.12.2023
- Impfdatum
- 28.12.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Death
Symptomtext
The victim's teenage son shared this information via an online video. He dictated the dates, lot numbers and manufacturer of the COVID-19 EUA Countermeasure marketed as a vaccine. The son stated his father was inoculated as result of the attempted Mandate for employers with 100 employees or more. Other information was obtained through publicly available sources online. DOSE1 DATE 12/7/21 DOSE2 DATE 12/28/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNK
- Vorgeschichte
- UNK
- Andere Medikamente
- UNK
- Allergien
- UNK
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 14.09.2023
- Impfdatum
- 18.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Blood pressure measurement
Dental caries
Glaucoma
Ophthalmological examination
COVID-19
Investigation
Vaccination failure
Tooth fracture
Symptomtext
Her glaucoma eye pressure was elevated too/eye pressure was so high; she experienced elevated blood pressure (BP); experienced breaking her teeth and also cavities/one of my left real molars just the inside wall of my molar just shear glide of the tooth/had 4 more teeth cracked, the root had cracked; experienced breaking her teeth and also cavities; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 64-year-old female patient received bnt162b2 (BNT162B2), on 18Dec2021 as dose 3 (booster), single (Lot number: FL3197, Expiration Date: 31Dec2022) at the age of 64 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "glaucoma" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN taken for hypertension. Vaccination history included: bnt162b2 (DOSE 2, SINGLE, Pfizer COVID-19 Vaccine Second Dose:, Date: 08Mar2021, LOT#: EN6206, Expiration Date: 30Jun2021), administration date: 08Mar2021, when the patient was 64-year-old, for COVID-19 immunization; bnt162b2 (DOSE 1, SINGLE, Pfizer COVID-19 Vaccine First Dose : , Date: 12Feb2021, LOT#: EL9261, Expiration Date: 31May2021), administration date: 12Feb2021, when the patient was 64-year-old, for COVID-19 immunization. The following information was reported: TOOTH FRACTURE (medically significant) with onset Dec2021, outcome "unknown", described as "experienced breaking her teeth and also cavities/one of my left real molars just the inside wall of my molar just shear glide of the tooth/had 4 more teeth cracked, the root had cracked"; GLAUCOMA (medically significant) with onset Jan2022, outcome "unknown", described as "Her glaucoma eye pressure was elevated too/eye pressure was so high"; DENTAL CARIES (non-serious) with onset Dec2021, outcome "unknown", described as "experienced breaking her teeth and also cavities"; BLOOD PRESSURE INCREASED (non-serious) with onset Jan2022, outcome "unknown", described as "she experienced elevated blood pressure (BP)". The events "her glaucoma eye pressure was elevated too/eye pressure was so high", "experienced breaking her teeth and also cavities/one of my left real molars just the inside wall of my molar just shear glide of the tooth/had 4 more teeth cracked, the root had cracked", "experienced breaking her teeth and also cavities" and "she experienced elevated blood pressure (bp)" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: elevated; Ophthalmological examination: elevated. Therapeutic measures were taken as a result of glaucoma, tooth fracture, dental caries, blood pressure increased. Clinical course: A nurse practitioner called in as a patient. She has concerns about the Pfizer booster shot she received. Her 1st two doses of Pfizer Covid vaccines, she has no issues at all, she did not experience any adverse reactions. Her 3rd shot is a Pfizer Covid vaccine booster on 18Dec2021. She was not told if it was Bivalent or not. Her 4th shot was a Moderna Bivalent in Nov2022, she got no issues with that too. With regards to the booster though, after 3 weeks of getting it, she experienced elevated blood pressure (BP). Her glaucoma eye pressure was elevated too. Her specialist recommended surgery for the eye. After 1 week she experienced breaking her teeth and also cavities. She just wants to know if these are common side effects or related to the booster or not. She added that her medical condition was stable for 10 years with the medication she was taking, her BP was normal for 7 years with the medication she was taking as well. A specialist told her she can have laser treatment for her eyes to bring the pressure down. The last 18 months the same week the BP and eye press were up. She had put a crown on her left rear molar tooth the same week sheared the tooth. Since then, 5 teeth have cracked, and she never had that before. The consumer (Nurse Practitioner) further stated, "I have had a question about the Pfizer booster shot, I was able to get the first two Pfizer COVID-19 Vaccines without any reactions or side effect at all and I got the Bivalent without any reaction at all but when I got the COVID, the Pfizer COVID Booster shot and this was on 18Dec2021, three week after I got that shot, I was at my Cardiologist office and she noted that my blood pressure was very high and my blood pressure is not stable for several years, so she had to change blood pressure medication and increases, 5 weeks later I was at my glaucoma specialist office and they noted that my eye pressure was so high they wanted to do surgery on my eyes and my glaucoma pressure had been stable for about 10 years at that point and that same week I also one of my left real molars just the inside wall of my molar just shear glide of the tooth and I had to have the tooth cleaned and a crown put on it since then I have had 4 more teeth cracked, the root had cracked, the front teeth which never had cavity in gum ever, one chipped this summer and then about a month the other one chipped and so I am trying to figure out, have you heard of this happening to anyone else after a COVID booster or Pfizer Booster because I am an Oncology Nurse I know sometimes things can happen that are totally unrelated but I am just asking a question specially where you are at adverse reaction division have you heard of this happening to anyone else?". The consumer further stated, "the first and second Pfizer COVID-19 Vaccines were in Feb2021 and Mar2021 and then in Dec2021, I had the Pfizer Booster COVID-19 Vaccine and that was the one that I had the reaction right, everything seems to be changed after I had, three weeks after I had that shot, my blood pressure was very high, my eye pressure was very high, I started cracking teeth and still things to be happening over 18 months I have cracked 5 teeth, it never happened before and then Sep2022, I had the COVID Bivalent had no problem with that at all the first, second vaccines and the bivalent I was perfect after them but it was after the booster that is when I started, three weeks after that I started having all of these problems. Has anybody else reported these symptoms after getting the Bivalent because it did not happen right away like 3 weeks after the booster and all the problems started". Regarding the treatment, consumer stated, "the other thing I have is Glaucoma and my glaucoma pressure have been stable for 10 years and 3 weeks after the shot the booster, my eye pressure was so high they wanted to do surgery on my eye and I got a second opinion and I went to a specialist in and she said that I could do a laser treatment rather than a surgery which I was very happy about and so that is what I get and they added on another glaucoma medication, so I was taking 2 eye drops, one is Vyzulta and that is 1 drop in each eye at bed time and then the other one that they added on was Rhopressa and I do 1 drop in each eye at bed time".; Sender's Comments: Based on available information, the reported events are assessed as unrelated to BNT162B2: glaucoma aggravated and elevated blood pressure can be attributed to the course of the underlying glaucoma and hypertension, respectively; broken teeth and tooth cavity are intercurrent conditions. Case will be reassessed if additional information becomes available The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Glaucoma
- Hospital-Tage
- -
- Labordaten
- Test Name: blood pressure; Result Unstructured Data: Test Result:elevated; Test Name: eye pressure; Result Unstructured Data: Test Result:elevated
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Glaucoma; Hypertension
- Andere Medikamente
- LOSARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.08.2023
- Impfdatum
- 18.12.2021
- Beginn
- 17.01.2023
- Tage bis Beginn
- 395,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Deep vein thrombosis
Hypoxia
Pulmonary embolism
Symptomtext
SADDLE PULMONARY EMBOLISM ACUTE DVT OF BILAT LEGS, UNSPECIFIED VEINS ACUTE DVT, UNSPECIFIED VEIN ACUTE HYPOXEMIC RESPIRATORY FAILURE ACUTE PULMONARY EMBOLISM HYPOXEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 11.08.2023
- Impfdatum
- 30.12.2021
- Beginn
- 23.12.2022
- Tage bis Beginn
- 358,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Deep vein thrombosis
Obstructive sleep apnoea syndrome
Symptom recurrence
Symptomtext
OBSTRUCTIVE SLEEP APNEA ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN ACUTE DVT OF RIGHT FEMORAL VEIN ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/29/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 11.08.2023
- Impfdatum
- 31.12.2021
- Beginn
- 20.03.2023
- Tage bis Beginn
- 444,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 09.08.2023
- Impfdatum
- 16.01.2022
- Beginn
- 12.01.2023
- Tage bis Beginn
- 361,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypoxia
Symptomtext
ACUTE RESPIRATORY FAILURE HYPOXEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 22.12.2021
- Beginn
- 28.12.2022
- Tage bis Beginn
- 371,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypoxia
Myocardial ischaemia
Obstructive sleep apnoea syndrome
Symptomtext
OBSTRUCTIVE SLEEP APNEA DEMAND ISCHEMIA ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 13.01.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 106,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 03.01.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 151,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 20.04.2023
- Impfdatum
- 25.07.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Obstructive sleep apnoea syndrome
Symptom recurrence
Symptomtext
OBSTRUCTIVE SLEEP APNEA ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/13/2022 - RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 03.04.2023
- Impfdatum
- 07.01.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 447,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute myocardial infarction
Anticoagulant therapy
Arterial stent insertion
Atrioventricular block
COVID-19
Catheterisation cardiac abnormal
Pain
SARS-CoV-2 test positive
Sensory disturbance
Symptomtext
Discharge summary "Patient had recently suffered a NSTEMI. He had two stents placed there 1st diagonal and in LAD. He had been doing well and compliant with aspirin and plavix when he was awoken with sscp- squeezing. He was admitted and found at cath to have another blockage for which a third stent was placed in ostial diagonal branch. Pain resolved completely. He was stable overnight. He was stable for discharge to home on 3/31/23."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 1,0
- Labordaten
- COVID positive PCR test 3/31/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.02.2023
- Impfdatum
- 03.01.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 211,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
COVID-19
Cerebrovascular accident
Chronic kidney disease
Condition aggravated
Death
Gastrointestinal haemorrhage
SARS-CoV-2 test positive
Symptomtext
PATIENT ADMITTED TO HOSPITAL ON 7/9/22 FROM OUTSIDE FACILITY FOR AN AKI ON TOP OF HER CKD. SHE WAS COVID-19+ AT TIME OF ADMISSION AND REQUIRING OXYGEN. PATIENT HAD RECURRENT STROKES, GI BLEED, AND ACUTE ON CKD. PATIENT DECLINED DURING ADMISSION AND WAS TRANSITIONED TO DNR/DNI AND THEN MADE COMFORTABLE. PATIENT DIED 8/2/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- COVID-19 SPECIMEN COLLECTED ON 7/6/2022 - POSITIVE VIA PCR
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- PMH CAD; CHF; CKD; HTN; TYPE 2 DIABETES; HLD; ANEMIA; AND GALLBLADDER DISEASE;
- Andere Medikamente
- ASPIRIN; DICLOFENAC SODIUM; ALLOPURINOL; FERROUS SULFATE; NITROGLYCERIN; ATORVASTATIN; ATORVASTATIN; CITALOPRAM; COLESEVELAM; GLIPIZIDE; HYDRALAZINE; ISOSORBIDE MONONITRATE; METOPROIOL SUCCINATE; SITAGLIPTIN; ZETIA; TICAGRELOR;
- Allergien
- INFLUENZA VACCINE; PENICILLINS; POVIDONE-IODINE; SOAP; SULFAMETHOXAZOLE; TRIMETHOPRIM;
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 15.02.2023
- Impfdatum
- 10.01.2022
- Beginn
- 14.02.2023
- Tage bis Beginn
- 400,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acinetobacter test
Acute kidney injury
Acute respiratory failure
Agitation
Alanine aminotransferase normal
Ammonia increased
Anaemia
Angiogram pulmonary
Anion gap
Aspartate aminotransferase increased
Bacterial test positive
Band neutrophil percentage
Base excess
Basophil count decreased
Basophil percentage decreased
Bilirubin conjugated normal
Bilirubin urine
Blood albumin decreased
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on February 14, 2023 15:42 Verified By: MD on February 14, 2023 15:42 Encounter Info: Hospital, Inpatient, 02/14/23 - * Final Report * Document Has Been Revised History of Present Illness/Subjective This is a 62-year-old male who was brought in by the EMS from ECF for confusion and fever. In the ECF the patient was noted to have 1 or 2.9 ?F temperature this morning and was confused. On my evaluation the patient was alert and oriented x0 and agitated, in pain.In the ED patient was hypotensive, received for 3 L of fluid. Blood pressure stable now but has been persistently tachycardic since then it is sinus tachycardia with incomplete right bundle branch block. Labs were significant for leukocytosis anemia of 11.5, sedimentation rate of 111, dimers 5254, elevated C-reactive protein, patient has left leg wound x-ray was done which did not show erosive changes on the bone ultrasound left lower extremity did not show any DVT. CTA was done but cannot rule out PE because of motion. Patient's x-ray shows some pulmonary edema he is saturating 96% on room air but the leg is visibly swollen and erythematous. He is also noted to have AKI on CKD stage III. Review of Systems In point review of system was not possible due to patient's orientation Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) , O2Sat 94 (94-94) Patient Weight Patient Height None Reported Constitutional: acute distress Eyes: PERRLA, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: crepts Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: left lower leg, swollen, unable to open the bandage, he wouldnt let me Integumentary: Intact, warm, dry no rashes Neurologic: Alert but confused Psychiatric: agitated Assessment/Plan 1. Sepsis with acute hypoxic respiratory failure A41.9 - broad spectrum antibiotics - Follow lactate and procal - blood culture - acute resp failure secondary to pna, fluid overload, needs sleep study outpatient 2. Encephalopathy G93.40 - likely due to acute infective process - follow b12, tsh, ammonia - drug screen - Meningis is one of the differentials, given history of hallucinations, but there is a source of infection already 3. PNA (pneumonia) J18.9 - on broad spectrum due to PNA - de escalate once stablizes - f/u pna workup 4. Pulmonary edema J81.1 - mild pulmonary edema, - unable to diurese, at the moment due to severe sepsis 5. Left leg cellulitis L03.116 - xray not suggestive of osteo, - u/s lower ext: no dvt - continue broad spectrum antibiotics 6. Left renal stone N20.0 - out patient urology 7. Hypokalemia E87.6 - replete as per protocol 8. AKI (acute kidney injury) N17.9 - avoid nephrotoxins. - gentle hydration 9. Sinus tachycardia R00.0 - sinus, likely due to pain, -follow TSH, 10. Elevated d-dimer R79.89 - acute phase reactant, also other inflammatory markers elevated, including c reactive and esr - cta was non conclusive, will preemptively treat for PE , well - SCORE moderate risk and repeat cta WHEN MORE ALERT Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 02/14/23 14:59:00 azithromycin, 500 mg, IVPB, Injection, Q24H, Indication: Pneumonia - CAP, 02/15/23 15:00:00, for 3 Doses, 02/17/23 15:00:00, 250 mL/hr, Infuse Over 1 Hours, Total Volume (mL) = 250 cefePIME, 1 GM, IVPB, Injection, Q8H, Indication: Sepsis (Update Indication in 36-48 hrs), 02/14/23 23:00:00, 12.5 mL/hr, Infuse Over 4 Hours, Total Volume (mL) = 50 labetalol, 10 mg, IV Push, Injection, Q6H, PRN, Systolic Blood Pressure, 02/14/23 14:59:00 Lactated Ringers 1,000 mL, Total Volume (mL) = 1,000, IV, 02/14/23 14:59:00, for 1 Days, 02/15/23 14:58:00, 100 mL/hr, Clinical Weight magnesium sulfate, 4 GM, IVPB, Infusion, Q12H, PRN, Lab (Details Required), 02/14/23 15:33:00, 25 mL/hr, Infuse Over 4 Hours, Total Volume (mL) = 100 metroNIDAZOLE, 500 mg, IVPB, Infusion, Q8H, Indication: Sepsis (Update Indication in 36-48 hrs), 02/14/23 23:00:00, 100 mL/hr, Infuse Over 60 minutes, Total Volume (mL) = 100 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 02/14/23 14:59:00 potassium chloride, 30 mEq, Orally, Tab, Extended Rel, Unscheduled, PRN, Lab (Details Required), 02/14/23 15:33:00 potassium chloride, 40 mEq, Orally, Tab, Extended Rel, Unscheduled, PRN, Lab (Details Required), 02/14/23 15:33:00 sodium phosphate, 28 mmol, IVPB, Injection, Unscheduled, PRN, Lab (Details Required), 02/14/23 15:33:00, 37.5 mL/hr, Infuse Over 4 Hours, Total Volume (mL) = 150 sodium phosphate, 21 mmol, IVPB, Injection, Unscheduled, PRN, Lab (Details Required), 02/14/23 15:33:00, 50 mL/hr, Infuse Over 3 Hours, Total Volume (mL) = 150 sodium phosphate, 21 mmol, IVPB, Injection, Unscheduled, PRN, Lab (Details Required), 02/14/23 15:33:00, 50 mL/hr, Infuse Over 3 Hours, Total Volume (mL) = 150 traMADOL, 50 mg, Orally, Tablet, Q6H, PRN, Pain Moderate PO (4-6 out of 10), 02/14/23 15:41:00 Admit to Inpatient CAH Ammonia Pl QN Basic Metabolic Panel Basic Metabolic Panel Blood CX Blood CX Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature CBC w/Differential CBC w/Differential Collect Specimen Collect Specimen Collect Specimen Comp Metabolic Panel Comp Metabolic Panel DC SIRS Alert and Sepsis Screen Do Not (Specify) Drug Screen-Expanded, Urine Dysphagia Screen by RN Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol L pneumophila Ag Ur QL L pneumophila Ag Ur QL Lactate Pl Arterial QN Level of Care Message to Nursing Nasal Cannula Notify Provider Notify Provider Notify Provider Notify Provider NPO Advance as Tolerated OT Evaluation and Treatment Pain Assessment Peripheral IV Insertion Pharmacy Dosing Consult Procalcitonin Procalcitonin PT Evaluation and Treatment PTINR Resp Evaluation or Assessment Resuscitation Status Strep pneumoniae Ag Urine Titrate FiO2 to Keep O2 Sat TSH 3rd Gen SerPl QN Vancomycin Pharmacy Dosing Consult Vital Signs Vital Signs Vitamin B12 SerPl QN Weight Wound CX + Stn Code Status Resuscitation Status - Ordered -- 02/14/23 14:59:00, Full Code Chronic Problem List Adult BMI 30+ Allergic reaction Bilateral chronic knee pain Colonoscopy refused Hypertension Immunization refused Morbid obesity Obesity Osteoarthritis of right hip Osteoarthritis, chronic Prediabetes Procedure/Surgical History ?None Medications Home Medications (14) Active Aldactone 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily allopurinol 100 mg oral tablet 200 mg = 2 Tablet, Orally, Daily atenolol 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily Lasix 40 mg oral tablet 40 mg = 1 Tablet, Orally, Daily lisinopril 40 mg oral tablet 40 mg = 1 Tablet, Orally, Daily meloxicam 15 mg oral tablet 15 mg = 1 Tablet, Orally, Daily metFORMIN 500 mg oral tablet, extended release See Instructions, TAKE 1 TABLET BY MOUTH TWICE A DAY Pravachol 40 mg oral tablet 40 mg = 1 Tablet, Orally, Daily Probiotic Formula 1 Capsule, Orally, Daily Silvadene 1% cream 1 App, Topical, Daily traMADOL 50 mg oral tablet 50 mg = 1 Tablet, Orally, TID Tylenol Extra Strength 500 mg oral tablet 1,000 mg = 2 Tablet, Orally, Unscheduled, Tylenol Extra Strength (500MG Tablet, 1 Oral as needed) Active. Ventolin HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, Q6H Vitamin D3 (cholecalciferol) Active Scheduled Inpatient Medications azithromycin, Injection, 500 mg, IVPB, Q24H, Indication: Pneumonia - CAP, Start: 02/15/23 15:00:00 cefePIME, Injection, 1 GM, IVPB, Q8H, Indication: Sepsis (Update Indication in 36-48 hrs), Start: 02/14/23 23:00:00 metroNIDAZOLE, Infusion, 500 mg, IVPB, Q8H, Indication: Sepsis (Update Indication in 36-48 hrs), Start: 02/14/23 23:00:00 Lactated Ringers 1,000 mL IV 100 mL/hr One-Time Medications Given 02/13/23 00:00:00 TO 02/14/23 15:42:43 None Reported PRN Medications (0600 - 0559) from 02/13 - 02/14 acetaminophen, 650 mg, Orally, Q4H, 0 Dose(s) labetalol, 10 mg, IV Push, Q6H, 0 Dose(s) magnesium sulfate, 4 GM, IVPB, Q12H, 0 Dose(s) ondansetron, 4 mg, IV Push, Q6H, 0 Dose(s) potassium chloride, 30 mEq, Orally, Unscheduled, 0 Dose(s) potassium chloride, 40 mEq, Orally, Unscheduled, 0 Dose(s) sodium phosphate, 21 mmol, IVPB, Unscheduled, 0 Dose(s) sodium phosphate, 28 mmol, IVPB, Unscheduled, 0 Dose(s) traMADOL, 50 mg, Orally, Q6H, 0 Dose(s) Allergies Peanuts/Peanut Butter (Anaphylaxis) No Known Medication Allergies Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment home health, Lives with Alone. Substance Abuse Denies Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Family History Family history is negative Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 12.5 k/cumm High (02/14/23 03:52:00) RBC: 4.11 million/cumm Low (02/14/23 03:52:00) Hgb: 11.5 GM/dL Low (02/14/23 03:52:00) Hct: 35.1 % Low (02/14/23 03:52:00) MCV: 85 fL (02/14/23 03:52:00) MCH: 27.9 pg (02/14/23 03:52:00) MCHC: 32.7 GM/dL (02/14/23 03:52:00) RDW: 14.7 % High (02/14/23 03:52:00) Platelet: 224 k/cumm (02/14/23 03:52:00) MPV: 7.9 fL (02/14/23 03:52:00) Neutrophils %: 96 % (02/14/23 03:52:00) Lymphocytes %: 2 % (02/14/23 03:52:00) Monocytes %: 2 % (02/14/23 03:52:00) Eosinophils %: 0 % (02/14/23 03:52:00) Basophils %: 0 % (02/14/23 03:52:00) Absolute Neutrophil: 12.1 k/cumm High (02/14/23 03:52:00) Absolute Lymphocyte: 0.2 k/cumm Low (02/14/23 03:52:00) Absolute Monocyte: 0.2 k/cumm (02/14/23 03:52:00) Absolute Eosinophil: 0 k/cumm (02/14/23 03:52:00) Absolute Basophil: 0 k/cumm (02/14/23 03:52:00) Band: 14 % (02/14/23 03:52:00) Neutrophil: 81 % (02/14/23 03:52:00) Lymphocyte: 4 % (02/14/23 03:52:00) Monocyte: 1 % (02/14/23 03:52:00) RBC Morphology: Normal, (02/14/23 03:52:00) Sed Rate: 111 mm/hr High (02/14/23 03:52:00) Chemistry: Sodium SerPl QN: 135 mmol/L (02/14/23 03:52:00) Potassium SerPl QN: 2.9 mmol/L Critical (02/14/23 03:52:00) Chloride SerPl QN: 101 mmol/L (02/14/23 03:52:00) Carbon Dioxide SerPl QN: 20 mmol/L Low (02/14/23 03:52:00) Anion Gap: 14 mmol/L High (02/14/23 03:52:00) BUN SerPl QN: 50 mg/dL High (02/14/23 03:52:00) Creatinine SerPl QN: 1.71 mg/dL High (02/14/23 03:52:00) Estimated GFR (CKD-EPI, no race): 45 mL/min/1.73m2 Low (02/14/23 03:52:00) Estimated CRCL (CG): 61 mL/min (02/14/23 03:52:00) Glucose SerPl QN: 173 mg/dL High (02/14/23 03:52:00) Calcium Total SerPl QN: 8.7 mg/dL (02/14/23 03:52:00) Alkaline Phos SerPl QN: 74 Units/L (02/14/23 03:52:00) ALT SerPl QN: 28 Units/L (02/14/23 03:52:00) AST SerPl QN: 63 Units/L High (02/14/23 03:52:00) Bilirubin Direct SerPl QN: 0.3 mg/dL High (02/14/23 03:52:00) Bilirubin Total SerPl QN: 1 mg/dL (02/14/23 03:52:00) Total Protein SerPl QN: 6.9 GM/dL (02/14/23 03:52:00) Albumin SerPl QN: 3.4 GM/dL Low (02/14/23 03:52:00) Lipase SerPl QN: 12 Units/L (02/14/23 03:52:00) Lactate Venous Pl QN: 1.8 mmol/L (02/14/23 03:52:00) pH Bld Venous QN: 7.45 (02/14/23 03:52:00) PCO2 Bld Venous QN: 30 mmHg Low (02/14/23 03:52:00) PO2 Bld Venous QN: 51 mmHg High (02/14/23 03:52:00) Base Excess Bld Venous: -2 mmol/L (02/14/23 03:52:00) Bicarb Bld Venous Calc: 21 mmol/L Low (02/14/23 03:52:00) O2 Sat Bld Venous Calc: 88 % (02/14/23 03:52:00) Patient Temperature: 37 DegC (02/14/23 03:52:00) C-Reactive Prot SerPl QN: 49 mg/dL High (02/14/23 03:52:00) Coagulation: D-Dimer Pl QN: 5254 ng/mL DDU High (02/14/23 03:52:00) Urine Studies: Color: Yellow (02/14/23 04:14:00) Clarity: Clear (02/14/23 04:14:00) Specific Gravity: 1.025 (02/14/23 04:14:00) pH: 5.5 (02/14/23 04:14:00) Protein: 100 Abnormal (02/14/23 04:14:00) Glucose: NEGATIVE (02/14/23 04:14:00) Ketones: NEGATIVE (02/14/23 04:14:00) Bilirubin: NEGATIVE (02/14/23 04:14:00) Hgb Ur: SMALL. Abnormal (02/14/23 04:14:00) Nitrite: NEGATIVE (02/14/23 04:14:00) Urobilinogen: NormalUro (02/14/23 04:14:00) Leukocyte Esterase Ur: NEGATIVE (02/14/23 04:14:00) WBC: 0-5 (02/14/23 04:14:00) RBC: 0-2 (02/14/23 04:14:00) Bacteria: TRACE. (02/14/23 04:14:00) Squamous Epithelial: Few (02/14/23 04:14:00) Mucous: PRESENT. (02/14/23 04:14:00) Granular Casts: 3-5 Abnormal (02/14/23 04:14:00) Amorphous Crys Ur: PRESENT. (02/14/23 04:14:00) All Other Labs: COVID 19 Specimen Source: Nasal (02/14/23 03:55:00) Coronavirus SARS-CoV2 Rapid: Not Detected (02/14/23 03:55:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (02/14/23 03:55:00) Rapid Influenza A PCR: Not Detected (02/14/23 03:55:00) Rapid Influenza B PCR: Not Detected (02/14/23 03:55:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/14/2023 05:30 - XR Chest PA or AP Portable IMPRESSION:1. Question mildly increased interstitial opacities. This could berelated to poor penetration. Mild edema/vascular congestion oratypical infection is in the differential.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. 02/14/2023 07:10 - XR Tibia/Fibula Left Impression:1. Extensive soft tissue swelling of the foot. No underlying acutebony process seen. 02/14/2023 08:07 - Venous Duplex Scan LE Left IMPRESSION:1. Limited study due to overlying edema, with the deep calf veins notcompletely evaluated. No deep or superficial venous thrombosisevident in the visualized veins.2. Left inguinal lymphadenopathy.3. Diffuse soft tissue catheter edema.. 02/14/2023 08:43 - CTA Chest Pulm Embolism W/IV Contrast Impression:1. Nondiagnostic study for evaluation of pulmonary embolus due toextensive respiratory patient motion artifact and diminished overallenhancement of the pulmonary arteries. Pulmonary emboli would not beable to be excluded.2. No acute pulmonary process seen.3. Incidentally noted is a nonobstructing upper pole left renalcalyceal calculus. Signature Line Electronically Signed on 02/14/23 15:42 ________________________________________________________ MD Electronically Signed on 02/14/23 17:02 ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- Bacterial L pneumo Urine Ag QL Not Detected L pneumo Urine Ag QL Interp L pneumo Urine Ag QL Interp Strep pneumo Ag Ur Not Detected Strep pneumo Ag Ur Interp Negative Staphylococcus spp Not Detected Staphylococcus aureus Not Detected Staphylococcus epidermidis Not Detected Staphylococcus lugdunensis Not Detected Streptococcus spp (A) Detected Streptococcus agalactiae (Group B) Not Detected Streptococcus pneumoniae Not Detected Streptococcus pyogenes (Group A) Not Detected Enterococcus faecalis Not Detected Enterococcus faecium Not Detected Listeria monocytogenes Not Detected Enteric gram-negative bacilli Not Detected Enterobacter cloacae complex Not Detected Escherichia coli Not Detected Klebsiella aerogenes Not Detected Klebsiella oxytoca Not Detected Klebsiella pneumoniae group Not Detected Proteus spp Not Detected Salmonella spp Not Detected Serratia marcescens Not Detected Haemophilus influenzae Not Detected Neisseria meningitidis Not Detected Pseudomonas aeruginosa Not Detected Stenotrophomonas maltophilia Not Detected Acinetobacter baumannii cmplx Not Detected Bacteroides fragilis Not Detected CTX-M Test Not Performed IMP Test Not Performed KPC Test Not Performed mcr-1 Test Not Performed mecA/C Test Not Performed mecA/C and MREJ (MRSA) Test Not Performed NDM Test Not Performed OXA-48-like Test Not Performed vanA/B Test Not Performed VIM Test Not Performed Candida albicans Not Detected Candida auris Not Detected Candida glabrata Not Detected Candida krusei Not Detected Candida parapsilosis Not Detected Candida tropicalis Not Detected Cryptococcus neoformans/gattii Not Detected Blood Pathogen Interp * Blood Pathogen Interp
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 12.03.2021
- Beginn
- 26.09.2022
- Tage bis Beginn
- 563,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute myocardial infarction
Anticoagulant therapy
COVID-19
Chest X-ray abnormal
Electrocardiogram T wave abnormal
Fall
Haemoglobin decreased
Hypoxia
International normalised ratio increased
Lung disorder
Lymphocyte count decreased
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Tachycardia
Tachypnoea
Troponin
X-ray of pelvis and hip normal
Symptomtext
This is a 83y.o. male with PMH of CAD s/p CABG (1982, redo in 1992), CHF, ICM s/p ICD, T2DM, HLD, hypothyroidism, BPH who presented as a transfer from emergency room for management of NSTEMI and COVID-19 infection. He also has BLE pain after a fall three days prior. Pelvis XR was unremarkable. He tested positive for COVID-19. Workup revealed NSTEMI with troponin of 2.20. Of note, EKG revealed nonspecific t wave abnormalities however no evidence of St elevations or reciprocals. He received heparin bolus and started on heparin gtt. He was found to be hypoxic on room air which improved to 95% on 2L O2 NC. Patient was transferred to hospital for further management. In the ED, patient noted to be tachycardic in 120s, febrile (Tmax 100.5F), tachypneic, hypoxic in 80s. SpO2 currently maintained on 6L O2 NC. CXR shows mild coarsening of pulmonary interstitium - acute vs chronic. Labs significant for hgb 10.9, lymphocytes 0.8, INR 1.3. troponin 2.20 -- > 4.19. COVID-19 PCR detected. Patient was started on drcadron and remdesevir for 5 days. Patient was weaned off oxygen and passed home oxygen eval. Cleared by endocrine and pulmonary and discharged in a stable condition. Patient lives wife who can assist at home. Resume home Dm regimen per endo and follow up as outpatient. rx sent to pharmacy. Discussed with nursing staff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 5,0
- Labordaten
- 9/26 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 19.01.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 315,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Death on 11/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Positive COVID 19 test on 11/21/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COVID-19; OSC: COPD; DM2; CKD; CHF; CAD; HTN; HLD; obesity
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 29.04.2021
- Beginn
- 25.10.2022
- Tage bis Beginn
- 544,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Cerebrovascular accident
SARS-CoV-2 test positive
Symptomtext
Pt was admitted on 10/19 for CVA. She was due to be transferred to 3W for inpatient rehab and required a COVID test which was positive on 10/25. She is asymptomatic at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 24.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- UN / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Autopsy
Back pain
Condition aggravated
Cyanosis
Death
Dyspnoea
Fall
Pain in extremity
Pulmonary embolism
Skin discolouration
Swelling
Toxicologic test normal
Symptomtext
Two days after vaccination developed increased pain in the foot, extending into the calf ,associated with swelling and discoloration., Worsening over the next 10 days with subsequent death on 02/05/2022. Became weak, falling, back pain, shortness of breath, subsequently became cyanotic and arrested. At autopsy, found pulmonary emboli throughout. Suspected DVT not confirmed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Autopsy findings as noted. Toxicology unremarkable. No other lab findings available.
- Aktuelle Erkrankungen
- Long covid symptoms related to COVID-19 infection testing +09/30/2021. Persistent fatigue. Persistent foot pain diagnosed at one point as neuropathy.
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 12.01.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Sepsis
Staphylococcus test negative
Symptomtext
Severe sepsis causing acute hypoxic respiratory failure likely due to COVID 19 and possible HCAP. Patient was started on meropenem and vancomycin for possible hospital-acquired pneumonia. Patient continued to improve drastically so MRSA swab was negative so vancomycin was stopped. Patient continued to improve greatly so meropenem was switched to Levaquin and patient continued to feel fine. Patient has already completed 5-day course of antibiotics no further antibiotics are needed at this time. Patient was started on dexamethasone and will complete a 10-day course. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Amnesia
Anxiety
Asthenia
Blood test
Chest X-ray
Computerised tomogram head
Delirium
Disorientation
Dizziness
Dyspnoea
Electrocardiogram
Fatigue
Feeling abnormal
Headache
Hypoaesthesia
Impaired work ability
Injection site hypoaesthesia
Injection site paraesthesia
Symptomtext
Initially very tired, but was fine for a few days, and then I started to develop numbness and tingling in my throat and then numbness and tingling in my arm where the injection site was then it had spread to my left side of my body. I went to medical center and the doctors there laughed at me. After this I went home and I was still having trouble breathing, I started to develop bad panic attacks around January 11. I saw my family doctor she pond it off as panic attacks but then I began seeing stars regularly, muscle weakness in my whole body, shortness of breath, neurological symptoms such as: Brain fog, numbness, tingling, insomnia, headaches, waking up gasping for air, and I have now been diagnosed with pots, my life has been turned up side down. I am now going on a full month of severe symptoms, which symptoms are very similar to that of a blood clot, low oxygen levels, disorientation, and severe anxiety. After my second vaccine all of these symptoms have become more severe, I cannot work, and I cannot function normally. At times I have trouble breathing or as if I stop breathing while trying to fall asleep, this is lead to regular brain fog, delirium and anxiety. I have been referred to cardiology due to my symptoms following vaccination, the next referral will be neurology, I cannot function without being dizzy and near fainting. I regularly see stars and weird splotches in my vision, I feel disconnected from reality to the point by don?t even know who my family or friends are, almost as if all of my short term and now long-term memory are erased. I have a history of auto immune disease and in the past I have had Bell?s palsy which led to a a half paralyzed face. Since vaccination I have been very ill and I am so weak I cannot do my job and I barely leave my house.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- Pulmonary contrast scan, brain CT scan, bloodwork, Covid test, urine test, chest x-ray, EKG - 01/30/2022 at hospital EKG, lung x-ray - 01/8/2022 Medical center
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- Rheumatoid arthritis
- Andere Medikamente
- Vitamin D, atarax
- Allergien
- Pineapples, latex, metronidazole
- Vorherige Impfungen
- Pfizer/NBiotech
- Staat
- RI
- Alter
- 45,0
- Geschlecht
- U
- Eingang
- 27.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
We were notified the patient had passed away, cause of death unknown at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- History of substance use Well controlled HTN
- Vorgeschichte
- PTSD Anxiety Cocaine Use Disorder Transgender Impaired Glucose Metabolism Sleep Difficulties Rhinitis Hearing Loss of Left Ear Tension Headache
- Andere Medikamente
- Multivitamin- once daily Spironolactone 100mg-1 tablet twice daily Voltaren Arthritis Pain gel 1%- 1 application four times per day Fluticasone nasal spray- 1 spray in each nostril once per day Estradiol 2mg- 2 tablets twice per day Aze
- Allergien
- Seasonal allergies- itchy eyes
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cerebrovascular accident
Immunisation
Symptomtext
stroke; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A 55 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 29Dec2021 13:00 (Lot number: FL3197) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, LOT: EW0183, NDC, EXP: unknown, Route, Anatomical Location: right arm), administration date: 13May2021, for COVID-19 immunization; Bnt162b2 (Dose 2, LOT: EW0191, NDC, EXP: unknown, Route, Anatomical Location: right arm), administration date: 03Jun2021, for COVID-19 immunization. The following information was reported: IMMUNISATION (hospitalization, medically significant) with onset 29Dec2021 13:00, outcome "unknown", described as "Booster"; CEREBROVASCULAR ACCIDENT (hospitalization, medically significant) with onset 01Jan2022 12:23, outcome "unknown", described as "stroke". The patient was hospitalized for cerebrovascular accident (start date: 01Jan2022). The event "stroke" was evaluated at the emergency room visit. Therapeutic measures were taken as a result of cerebrovascular accident. Clinical course: The caller was the patients wife, reporting that her 55 years old husband who received the Pfizer covid vaccine Booster shot and 2 days later he had a stroke, he does not have any health issue, he was a very healthy person and doctors do not know the reason for stoke. She was calling to report it as advised by the doctor. She states that on Wednesday, they met with the doctor and they said there is no reason they can prove that this has something to do with her husband or his health. She states that he was perfectly fine and there was nothing wrong. She states that one of her friends who is a doctor, said to report this to Pfizer. Stroke occurred early Saturday morning at 12:23 in the morning. It was in the first few minutes of the new year, 01Jan2022. She states her husband is in critical condition and has been in the ICU since Saturday. He is not responsive and, they are saying his situation is getting very fast. Really bad things that usually go in like 6 days, is taking him hours. Treatment: Clarified that her husband has been in the hospital, in the ICU since 01Jan2022 and was still there now. She states she does not have any information with her regarding any treatments or mediations he has had. No prior vaccinations (within 4 weeks). No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No He does not have any health issues.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Bradycardia
Chest X-ray normal
Cold sweat
Computerised tomogram normal
Condition aggravated
Electrocardiogram abnormal
Grunting
Mydriasis
Nausea
Pallor
Respiratory arrest
Somnolence
Syncope
Unresponsive to stimuli
Yellow skin
Symptomtext
Patient received vaccine at 15:45. Ten minutes later at 15:55 the patient became unresponsive. He was pale sitting in chair and RN went to patient's side. He started experiencing "snorting" respirations which progressed to no breathing for approximately 4-6 secs. Vitals were O2 100% and HR 40. "Code Blue" was called. At 13:56, patient began to respond, but was still pale/yellow, pupils dilated, clammy, and nauseous. At 13:58 patient became unresponsive, stopped breathing for approximately 4-6 seconds. Vitals were BP 88/60 and HR 40. Patient was lowered to floor with legs raised. Skin still pale/yellow, pupils dilated, and clammy. At 15:39, patient began to respond. He could tell his name and where he was located. Pt assisted to sitting up position. Vitals: HR 48. Pt stated he felt "sleepy and that he felt it was about to happen again." He remained pale/yellow, skin cold and clammy. He was placed in supine position, again, and remained aware. Patient was lifted into stretcher and transported to Emergency Department at 16:05. In ED, patient reported that he had a similar syncopal episode about 4 years ago while accompanying his wife on an OB/GYN visit. Vital signs: HR 58-65, BP 125/69. EKG revealed sinus bradycardia. CT and CXR normal. ED provider's clinical impression was determined to be vasovagal syncope. Patient received 1 L of 0.9% Sodium Chloride and was discharged home with instructions to follow-up with PCP in 1-2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No past medical history; never smoker and never drinker
- Andere Medikamente
- Flonase 1 spray NS q day prn Azelastine 205.5 mcg nasal spray 2 spray NS q day prn Cetirizine 10 mg po q day prn Montelukast 10 mg qday prn
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Aphasia
Chest pain
Dyspnoea
Electrocardiogram abnormal
Emotional distress
Heart rate increased
Myocardial infarction
Myocardial injury
Nasopharyngitis
Pain
Pain in extremity
Palpitations
Paraesthesia
SARS-CoV-2 test negative
Symptomtext
I developed cold like symptoms December 24th. I got tested for covid December 27 about 4 pm (negative) My blood pressure was over 140 in one arm so she did it again in the other arm and it was 134. that was about 1 hour before the attack. After becoming emotionally upset my heart raced and pounded without slowing or decreasing in intensity for approximately 30 minutes and then flopped in my chest for about 30 seconds to a minute. I laid down in bed the whole time. I couldn't talk. Breathing was labored. I prayed and tried to slow heartbeat by calming down and relaxing through it all. afterwards I was afraid to move. I stayed in bed for about 14-16 hours and rested. I felt pains in my chest area on occasion when rolling over or moving. My left arm was tingly and achy until January 9, 2022. I had another racing heart incident that only lasted about 5 minutes but I layed down again. I took a baby aspirin the evening of January 8th. It hasn't hurt since then. I had an abnormal ekg on January 6 showing I had a heart attack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- -
- Labordaten
- EKG, Doppler 2D, asymptomatic heart attack with heart damage
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Strong histamine response to illness. I once broke out in hives during the flu to the point I had to go to the emergency room because the hives went down my throat. Hives, swollen air passageway, grass and pollen allergies
- Andere Medikamente
- Emergen-C vitamin C drink
- Allergien
- no
- Vorherige Impfungen
- Pfiizer sore arms where shot was
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Immunisation
Off label use
Product use issue
Symptomtext
off label use; Other vaccine same date vaccine date 27Dec2021; Patient died within 24 hrs of vaccination; booster; This is a spontaneous report received from contactable reporter(s) (Other HCP). A 68 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 27Dec2021 (Lot number: FL3197) at the age of 68 years as dose 3 (booster), single for covid-19 immunisation; hepatitis b vaccine rhbsag (yeast) (ENGERIX-B), administration date 27Dec2021 (Lot number: 5397F) as unk, single. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid (Dose Number: 2, Batch/Lot No: EN6204, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 19Mar2021, when the patient was 67 years old, for Covid-19 immunization; Covid (Dose Number: 1, Batch/Lot No: EN6203, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 26Feb2021, when the patient was 67 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (death, medically significant) with onset 27Dec2021, outcome fatal; OFF LABEL USE (death, medically significant) with onset 28Dec2021, outcome fatal; PRODUCT USE ISSUE (death, medically significant) with onset 28Dec2021, outcome fatal; DEATH (death, medically significant) with onset 28Dec2021, outcome fatal. It was unknown if therapeutic measures were taken as a result of immunisation, off label use, product use issue, death. The patient date of death was 28Dec2021. The reported cause of death was Unknown cause of death. It was not reported if an autopsy was performed. Additional Information: Patient died within 24 hrs of vaccination.; Sender's Comments: Based on the available information in the case, the causal association between the events immunization, off label use, product use issue, death and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.; Reported Cause(s) of Death: Unknown cause of death
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Cardiac arrest
Catheterisation cardiac normal
Ejection fraction decreased
Lung assist device therapy
Myocarditis
Symptomtext
myocarditis with cardiac arrest 1 day after receiving Pfizer COVID-19 booster, required VA ECMO support, initial EF < 5%, improved with solumedrol, no CAD on cardiac catheterization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 13,0
- Labordaten
- VA ECMO 12/25/21 - 12/30/21 solumedrol 1g IV qd x 3 doses (12/26/21 - 12/28/21)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 03.02.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 44,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Hypovolaemic shock
Symptom recurrence
Symptomtext
HYPOTENSION HYPOVOLEMIC SHOCK 5/1/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypovolaemic shock
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 21.12.2021
- Beginn
- 19.01.2023
- Tage bis Beginn
- 394,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Computerised tomogram
Ischaemic stroke
Magnetic resonance imaging
Syncope
Thrombectomy
Thrombosis
Symptomtext
Ischemic stroke, right side of the brain - collapsed at approximately 8:30am on 19-Jan-2023. Blood clot identified and removed by Dr at a HCF at approximately 11:30am
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- 5,0
- Labordaten
- CT scan, MRI, bloodwork
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Depression, anxiety, substance use (nicotine, cannabinoids)
- Andere Medikamente
- Prozac, Abilify, Buspirone, birth control
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 19.07.2022
- Impfdatum
- 29.12.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Heavy menstrual bleeding
Thrombosis
Symptomtext
My first period since getting shot (about 3 weeks later) was extremely heavy, so heavy to the point that no pad or tampon and need to wear adult diaper to stop bleeding. Also was more clotty then normal. I thought maybe it was just a one off but it's continued like that since. After 27 years of having the same period and then a few weeks after the shot it significantly gets heavier and has stayed that way points to the shot as a possible cause.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- None. I did not report to my doctor but also was not administered by their office. I just deal with it but this could be very concerning if i was planning on having more kids or had fertility issues.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal Vitamin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 17.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Embolic stroke
Muscle spasms
Muscle twitching
Muscular weakness
Symptomtext
Twitches/spasms and muscle weakness all over body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolic stroke
- Hospital-Tage
- -
- Labordaten
- neurologist full body exam and EMG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 19.06.2022
- Impfdatum
- 30.07.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 124,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Echocardiogram abnormal
Electrocardiogram abnormal
Postural orthostatic tachycardia syndrome
Sinus tachycardia
Syncope
Tilt table test positive
Ventricular extrasystoles
Symptomtext
vasovagal syncope, sinus tachycardia, PVCs, inappropriate tachycardia, POTS, all since vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- EKG, March, April, May, June 2022 Echocardiogram, April 2022 Tilt-table test, May 2022, positive result
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none before vaccination
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 10.06.2022
- Impfdatum
- 11.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antibody test
Antinuclear antibody
Antinuclear antibody increased
Blood pressure increased
Blood pressure measurement
Burning sensation
Cardiovascular insufficiency
Neuropathy peripheral
Paraesthesia
Haematoma
Heart rate
Heart rate increased
Hypoaesthesia
COVID-19
Vaccination failure
Insomnia
Laboratory test
Middle insomnia
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An adult patient received BNT162b2 (BNT162B2), on 14Mar2021 at 10:00 as dose 1, single (Batch/Lot number: unknown), in left arm, on 06Apr2021 at 10:00 as dose 2, single (Batch/Lot number: unknown), in right arm and on 11Jan2022 at 12:00 as dose 3 (booster), single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (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 vaccination failure, covid-19. Patient received the treatment of Antiviral paxlovid for COVID19 from 25May2022 till 29May2022. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 07.06.2022
- Impfdatum
- 22.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Computerised tomogram normal
Headache
Hypoaesthesia
Loss of consciousness
Magnetic resonance imaging
Migraine
Syncope
Urine analysis
Symptomtext
On 12/24/2021, she woke up with a headache with migraine like symptoms. That progressed like everyday, we would try TYLENOL and ALEVE. She went back to school January 8, 2022. We got her through four days and we had to take her out of school due to the headaches. In January, we took her to her first doctors visit at Dr.'s private practice. They didn't really run any test for the first visit. Dr. thought it was only migraines and prescribe her IMITREX. She took one dose and felt really weird so we discontinued that. On, 2/2/2022 we brought pt. to the hospital and they did a CAT Scan to rule out any tumors findings. On 2/4/2022 they did an MRI at an imaging center. We brought home and she started having vasovagal syncope and she would be sitting at the table eating dinner and her legs and arms would get numb and she would pass out. On, 2/9/2022, we brought her to the hospital. She saw another dr., and they did all sorts of test on her. They did blood work, urine test, and all test associated with MS. They gave her an IV of REGLAN and TORADOL as well. That helped but not completely. 2/15/2022, we saw the neurologist. She put pt. on naproxen 500 mg 1 a day for two weeks. After the two weeks they put her on riboflavin 400 mg and magnesium oxide 400 mg and she has continued to take that everyday since then. It seems to be working.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- 2/2/2022 CAT Scan was normal. 2/4/2022 MRI. 2/9/2022 blood work, urine test, and all test associated with MS and they gave her an IV of REGLAN and TORADOL as well. 2/15/2022 naproxen 500 mg 1 a day for two weeks. After the two weeks they put her on riboflavin 400 mg and magnesium oxide 400 mg and she has continued to take that everyday since then.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Slight allergy to gluten
- Vorherige Impfungen
- MMR Shot, she had a full body rash when she was little.
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 25.02.2021
- Beginn
- 17.05.2022
- Tage bis Beginn
- 446,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain lower
COVID-19
Chest pain
Cholelithiasis
Nausea
Pain
Syncope
Ultrasound abdomen abnormal
Vomiting
Symptomtext
Patient admitted 5/17. The patient complains of left and right lower abdominal pain associated with nausea and vomiting. She was evaluated in the ED and was found to have COVID-19 infection 5/17. Patient also complained of having chest pain. Patient describes that her chest pain started before the nausea and vomiting and feels like a sting and then the nausea and vomiting started. She describes having a syncopal event PTA. Patient does have a history of chronic abdominal pain. The patient underwent an ultrasound of the abdomen, which revealed findings consistent with cholelithiasis, no evidence of cholecystitis. No fevers, no chills. Dishcharged home 5/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 6,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- asthma, Mallory-Wiess tear, Acute focal neurological deficit Syncope Epistaxis, recurrent Symptomatic anemia Obesity (BMI 30-39.9) Chest pain NSTEMI (non-ST elevated myocardial infarction) S/P CABG (coronary artery bypass graft) Coronary artery disease involving native heart Essential hypertension Hyperlipidemia SOB (shortness of breath) CAD (coronary artery disease) Hematochezia Acute renal failure (ARF) Hematuria Essential hypertension, malignant
- Andere Medikamente
- albuterol (PROVENTIL, VENTOLIN, PROAIR), albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln amLODIPine (NORVASC) 10 MG PO Tab Ascorbic Acid 500 MG PO Tab aspirin (HALFPRIN) 81 MG PO Tablet Delayed Response ato
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 13.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Bell's palsy
Borrelia test negative
Symptomtext
Bell's palsy which started on 4/19, patient was seen in the emergency department and given steroids and symptoms resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- lyme test- negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 10.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac imaging procedure abnormal
Chest pain
Dizziness
Dyspnoea
Fluid retention
Magnetic resonance imaging abnormal
Magnetic resonance imaging heart
Myocarditis
Myopericarditis
Impaired work ability
Laboratory test
Scan with contrast abnormal
Symptomtext
Approximately 1 week after receiving her second Pfizer Booster (4th dose) the patient developed chest pain. Booster was given on 3/10/22 and chest pain began ~ 3/17/22. On 3/30/22 she was admitted for progressive chest pain. On 4/5/22 she had an MRI showing evidence of myocarditis. She was given a clinical diagnosis of myopericarditis. She does have connective tissue disease which is an alternate risk for myocarditis, but the timing with regards to her Pfizer booster made us concerned for possible Vaccine adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 9,0
- Labordaten
- See item 18 above - MRI showing myocardial late gadolinium enhancement in the basal inferolateral wall
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pulmonary Arterial Hypertension Mixed Connective Tissue Disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 08.05.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac monitoring
Dizziness
Echocardiogram
Presyncope
Syncope
Tilt table test
Symptomtext
Light-headed and dizzy, feeling like I would pass out. Within an hour of getting the vaccine call 911 after pulling over in my vehicle. Next day, still having the same symptoms visited ER. Symptoms occur many times a day and I am concerned for my long-term health. Diagnosed as "Vasovagal Syncope" by cardiologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Tilt table test, echocardiogram and heart monitor
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low-grade Age-appropriate high blood pressure
- Andere Medikamente
- Lisinopril 20mg.
- Allergien
- Erythromycin Penicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Immediate post-injection reaction
Syncope
Symptomtext
Vasovagal syncope 10-15 seconds after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 06.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest tube removal
Intensive care
Sternotomy
Thymectomy
Thymoma
Symptomtext
Thymoma - Median Sternotomy and Thymectomy - had a short stay in ICU for post operative management and was started on her Anti HTN Meds; Chest Tubes were removed without any complications and was discharged home. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 29.01.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Bell's palsy
Computerised tomogram head normal
Symptomtext
I HAVE DEVELOPED BELL'S PALSY INVOLVING THE LEFT SIDE OF MY FACE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- I WAS IN THE HOSPITAL ER ON 03/14/2022. HAD CT SCAN OF THE BRAIN, WHICH WAS NEGATIVE FOR STROKE.
- Aktuelle Erkrankungen
- HIGH CHOLESTEROL
- Vorgeschichte
- NONE
- Andere Medikamente
- SIMVASTATIN ZETIA
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 23.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fear
Seizure
Symptomtext
Seizure; I am scared now, if I have the side effect, it was bad and I don''t know, if I need to get more shot if you say, more difficult; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Dec2021 (Lot number: FL3197) at the age of 35 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: TROVAC. Vaccination history included: Bnt162b2 (DOSE: 1, Anatomical location: Left arm), for covid-19 immunization; Bnt162b2 (DOSE: 2, Anatomical location: Left arm), for Covid-19 immunization. The following information was reported: SEIZURE (medically significant), outcome "unknown", described as "Seizure"; FEAR (non-serious), outcome "unknown", described as "I am scared now, if I have the side effect, it was bad and I don''t know, if I need to get more shot if you say, more difficult". Clinical course: The patient did not receive any other vaccines within 3 weeks prior to the COVID vaccine. The patient had no family history for event related to the Covid-19 Vaccination. The patient had no medical problems. Consumer stated, "Yes I was taking one medication, I had only one medication "Trovac". Consumer stated, "I probably should have gone to the Hospital but I didn't go because I didn't know at that time what was the problem." No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- TROVAC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 06.03.2022
- Impfdatum
- 20.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal discomfort
Asthenia
Back pain
Balance disorder
Central nervous system inflammation
Computerised tomogram head
Demyelinating polyneuropathy
Dysstasia
Echocardiogram
Electrocardiogram
Electromyogram
Fall
Gait disturbance
Guillain-Barre syndrome
Hypoaesthesia
Immunoglobulin therapy
Impaired driving ability
Impaired work ability
Symptomtext
12/20/21 - I received the Pfizer COVID booster shot at the pharmacy at approximately 11:40 AM. 12/22/21 - I felt a tightness in my stomach, as if there was a tight band around it. 12/23/21 - I had numbness and tingling from my stomach down to my ankles which made it very difficult to walk, stay balanced and get up from a seated position. 12/24 - 12/26/21 - I had trouble standing, walking, walking up/down steps and getting up from a seated position. 12/26/21 - 1/5/22: I went to Urgent Care at approximately 8:00AM and was told to go to emergency room immediately. I went to the Hospital and was admitted. According to multiple Neurologists they determined it was an atypical case of Guillain-Barr? Syndrome and Acute Transverse Myelitis; typically both diagnoses start from the feet and work their way up, but mine did not - so the doctors were not fully sure of the cause. I was given a couple of different treatments that typically help with GBS and ATM. Treatments I received were 3 doses of gamma globulin injections, as well as 5 doses of Dexamethasone steroids. I received both physical and occupational therapy to help build my strength but since I did not have feeling in my knees and legs, I had randomly fallen while standing with a walker or while exercising. 1/5/22 - 2/4/22: I was then transferred to Rehab on 1/5/22. I was seen by their neurologist and team of doctors while receiving physical and occupational therapy. Starting on 1/8/22 I received 5 doses of Prednisone Steroids for Acute Transverse Myelitis. The neurologist could not exactly pinpoint what diagnosis I have but they believe that it is Acute Inflammatory Demyelinating Polyneuropathy / Paresthesia of the Lower Extremities which is a type of Guillain-Barr? Syndrome. 2/4/22 - Present: I left Rehab on was working with Home Care PT / OT from 2/4/22 - 2/16/22. I am going to outpatient neuro-PT, two times a week at (Privacy) Rehabilitation (my parents will be driving me), as well as exercising at home to regain strength. I am still feeling the numbness/tingling in my legs and knees, along with having back pain, difficulty going up and down stairs, difficulty walking smoothly with the walker, not being able to get up from a seated position, (especially seats without armrests), difficulty balancing and being unable to drive. I have not returned to work due to these circumstances and do not know when I will be able to return.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 11,0
- Labordaten
- Tests I received were: MRI Lumbar Spine with and without contrast on 12/27/21 MRI Thoracic Spine with and without IVC on 12/27/21 MRI Brain Scan with and without Contrast on 12/27/21 IR Lumbar Puncture on 12/28/21 CT Brain without contrast on 12/29/21 XR Portable Lspine AP and Knee AP Lateral/Bilateral on 12/30/21 due to a fall caused by buckling of knees while standing with walker Test I received were: ECG 12-Lead on 1/6/22 MRI Cervical Spine without contrast 1/10/22 MRI Thoracic Spine without Contrast on 1/10/22 MRI Lumbar Spine without Contrast on 1/10/22 MRI Brain without contrast on 1/12/22 MRI Pelvis without contrast on 1/12/22 MRI Brain without contrast on 1/13/22 EMG & NCV on 1/17/22 DX Knee RT on 1/18/22 due to a fall CV Duplex Lower extremity Venous Bilateral on 1/23/22 CV Transthoratic Echo-cardiogram on 1/23/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sesame, Tree Nuts, Cefprozil
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Electrocardiogram abnormal
Pericarditis
Troponin normal
Symptomtext
pericarditis- chest pain and EKG changes, resolved within 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- EKG- abnormal troponin normal
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Lexapro 20 mg/day Levora OCP one pill per day
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 19,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
3-Dimensional vasculography
Anticoagulant therapy
Computerised tomogram thorax abnormal
Deep vein thrombosis
Dyspnoea exertional
Fibrin D dimer increased
Heart rate increased
Lung opacity
Peripheral artery thrombosis
Pulmonary artery occlusion
Pulmonary thrombosis
Ultrasound Doppler abnormal
Symptomtext
Healthy, life time athlete: 10 days after Pfizer booster noticed heavier than normal breathing on intense workouts. Also noticed slight out of breath when talking to people while standing up. Check resting HR after 2 weeks of the above an notice my normal resting hr of 54 was now at 90 to 120. On this observation went into urgent care as I think I may have myocarditis from vaccine. Urgent Care doctors did not observe any immediate issues but ran d-dimer test which came back at 2,030 ng/mL. Sent immediately to ER. CT reviled large blood clot in lungs. Admitted to hospital. Heparin drip 2 days. Changed to oral Xarelto 15mg 2 times a day for next 6 months. Released home
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- CT Scan The pulmonary arteries are well opacified. Acute clot present distal aspect of the left main pulmonary artery. Clot are within at this level is significant and nearly occlusive. Clot extends into the proximal descending lower lobe pulmonary arteries. There is also some clot in the distal right main pulmonary artery as well as the proximal branch serving the right upper lobe. There is clot extending into the segmental branches of the medial right lower lobe. 3-D volumetric images also reviewed which shows the aforementioned clot. This also confirmed on the sagittal and coronal 2-D MIPS. Ultrasound onclusions: Sub - Acute deep vein thrombosis in the left distal femoral vein, popliteal vein and mid posterior tibial vein. No evidence of acute deep vein thrombosis in the right lower extremity and superficial venous thrombosis in the bilateral lower extremities. Triphasic arterial flow in bilateral posterior tibial artery in the distal segment. Critical Findings: Prelim results to both drs following exam
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- gout at random times. 1 time a year or 1 time in 2 years
- Andere Medikamente
- multi vitamins
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electric shock sensation
Occipital neuralgia
Pain
Sensitive skin
Symptomtext
Starting one day after vaccine, developed electrical pain starting behind left ear inferiorly and going up to near top of the ear then radiating back towards the back of the skull. Intermittently painful, shooting/zinging pain, severe. Also hypersensitivity of the skin behind the left ear. Sx c/w occipital neuralgia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- SLE;renal failure s/p transplant; HTN; recurrent UTI;anemia, HL; hypothyroidism; osteoporosis; hyperparathyroidism (secondary)
- Andere Medikamente
- Estradiol Cream; Levothyroxine; CA/Vit D; Denosumab; Mycophenolate Sodium; Omeprazole; Prednisone;, Ellura; Belacept
- Allergien
- Linezolid; Calcitonin; Codeine; Morphine; Oxycodone; Renvela; Sevelamer; Sulfa; Tramadol
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Confusional state
Hyperhidrosis
Nausea
Pallor
Syncope
Symptomtext
Within a couple minutes after the shot, patient fainted for a few minutes then he came back on his own. I can see the patient was pale, confused, sweating, nausea. I checked blood pressure and found that his BP was elevated 153/120 and pulse was 120. We did not give any medicines or epipen but just cold water. After 30 minutes of observation, i checked the BP again and it dropped back to 129/79, pulse was 70. Patient felt normal and was able to eat, drink and parent of patient decided to leave. Parent was advised to contact PCP for follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- no health conditions
- Vorgeschichte
- no
- Andere Medikamente
- n/a
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pain
Pyrexia
Syncope
Symptomtext
Syncope morning after received the vaccine. Also had fever, body aches and headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- Hydrocodone
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Symptomtext
Anaphylaxis reaction to 3rd dose of Pfizer personal epi-pen used 911 called EMS responded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- Unknown.
- Andere Medikamente
- Unknown.
- Allergien
- Stated has severe anaphylaxis to bee sting in August.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Asthenia
Diarrhoea
Dyspnoea
Ear disorder
COVID-19
Drug ineffective
Headache
Lymphadenopathy
Nasopharyngitis
Nausea
Pyrexia
Syncope
Vision blurred
Symptomtext
angina off and on; fever; headache; I'm still very weak I do get short of breath just walking from room to room; I'm still very weak I do get short of breath just walking from room to room; blurred vision off and on; her ear drums eardrums blew out; diarrhea; nausea; fainted; a cold feeling through body; lymph nodes swollen behind ears and in throat; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 69 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Dec2021 11:00 (Lot number: FL3197) as dose 1, single for covid-19 immunisation. Relevant medical history included: "herniated disc in back" (ongoing), notes: she needs surgery for it. Just had two more that blew out in Oct2021, but she has had herniated disc before. The patient took concomitant medications. The following information was reported: SYNCOPE (medically significant) with onset 28Dec2021, outcome "unknown", described as "fainted"; ANGINA PECTORIS (medically significant), outcome "unknown", described as "angina off and on"; NASOPHARYNGITIS (non-serious) with onset 28Dec2021, outcome "unknown", described as "a cold feeling through body"; EAR DISORDER (non-serious) with onset 01Jan2022, outcome "unknown", described as "her ear drums eardrums blew out"; VISION BLURRED (non-serious) with onset 02Jan2022, outcome "not recovered", described as "blurred vision off and on"; DIARRHOEA (non-serious) with onset 31Dec2021, outcome "not recovered", described as "diarrhea"; NAUSEA (non-serious) with onset 31Dec2021, outcome "unknown", described as "nausea"; LYMPHADENOPATHY (non-serious) with onset Dec2021, outcome "unknown", described as "lymph nodes swollen behind ears and in throat"; PYREXIA (non-serious), outcome "not recovered", described as "fever"; HEADACHE (non-serious), outcome "not recovered", described as "headache"; ASTHENIA (non-serious), DYSPNOEA (non-serious), outcome "not recovered" and all described as "I'm still very weak I do get short of breath just walking from room to room". Therapeutic measures were taken as a result of ear disorder. Clinical Course: She had it. At the time they gave her the shot she fainted and she had never fainted with a vaccine before. Her body got really cold and she could feel the cold spreading all through the body. When she got home she has fainted several times since the vaccine. Both ear drums blew out. She is having trouble with her vision. She has blurred vision off and on from it. She doesn't know what to do because her doctors said she has to have the at least two and a booster of the Pfizer vaccine or one of the vaccines or they won't see her anymore or see her in the office. She was afraid that she may end up having a heart attack or loosing her vision instead of blurred vision and busted ear drums and all. She had severe diarrhea and was still having severe diarrhea and nausea.She had scheduled to get the second one on 18Jan2022. She doesn't know. She won't be able to see the doctor for medical treatment. She had afraid something else might happen. Added that the report of her "eardrums blew out causes a loss of hearing", her blurred vision occurs "throughout the day and evening and night", she's "still having severe diarrhea, it hasn't gone away and I have to wear adult diapers. She added: "I still run a fever, and I have a headache everyday" I never had those problems before." which was not. Angina off and on: Date of Adverse Event: She had a little bit that day, 28Dec2021, but it didn't last but about 60 seconds the first time. About three days later she started experiencing it again. She hadn't any of that before. As time has passed it happens off and on and is getting more often and more painful when it happens. She was going to see her cardiologist because they are going to had to check her out. She hopes she didn't get myocarditis or pericarditis. Several people in her family had experienced things.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Herniated disc
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Syncope
Symptomtext
shortly after receiving the vaccine, as patient was leaving, she told her mother, she was going to pass out - then she passed out and fell to the floor. a cool pack was applied and juice given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Blood test
Chest pain
Computerised tomogram head normal
Computerised tomogram thorax abnormal
Echocardiogram
Electrocardiogram
Headache
Intensive care
Myocarditis
Pyrexia
SARS-CoV-2 test negative
Troponin increased
Vaccination complication
Symptomtext
Received MRNA Pfizer booster on Saturday, 1/8/22, at the Hospital Covid-19 popup vaccine clinic. Within 24 hours of booster he developed a headache and back pain, fever. Symptoms progressively got worse and developed a burning pain on the chest and severe headache. On Wednesday, 1/12/22 he went to ER around 4:30 am. They ordered Echocardiogram, EKG, CT of chest, blood tests, Covid test (negative)Troponin levels were elevated 76 and 99. Admitted to critical care. Dr of cardiology diagnosed patient with Myocarditis. Tropnin level went down to 86 and they release him. Said to take Tylenol as directed. Symptoms continued throughout the week. Saturday, 1/15/22 he went to his general practiconers office and saw Dr. for headache and chest pain. Later Saturday, 1/15/22 at 2:30pm patient went to ER for headache that persisted since 1/9/22. ER Dr. ordered CT of brain (unremarkable). Administered 3 prednisone tablets and fioricet. Headache and chest pain were bearable with medication until 1/21/22. On Friday, 1/21/22 he went to general practicer office to Dr. She has ordered a chest CT and to follow up with Dr of cardiology 2/7/22. This has been diagnosed at MRNA Booster induced Myocarditis. He took the vaccine because his school made it mandatory for a healthy (no negative health history) 20 yr old to get a booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 1,0
- Labordaten
- 1/12/ 22 EKG, Echocardiogram, Chest CT-normal, troponin levels 76,99,86 1/15/22 CT of head-normal
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamin
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Syncope
Symptomtext
PATIENT WAS VACCINATED AND BECAME LIGHTHEADED SEVERAL MINUTES AFTER THE VACCINATION. HE FAINTED AND FELL TO THE GROUND. HE WAS IMMEDIATELY HELPED AND WAS INSTRUCTED TO LIE FLAT, FEET WERE ELEVATED, AND WAS GIVEN AN ICE PACK. HE WAS QUICKLY LUCENT AND COHERENT WITH IS SURROUNDINGS. HE LAID THERE UNTIL HE FLET COMFORTABLE TO GET BACK IN A CHAIR WHICH HE SAT FOR APPROXIMATELY 30 MINUTES. HE REFUSED MEDICAL CARE FROM 911.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE LISTED
- Vorgeschichte
- NONE LISTED
- Andere Medikamente
- NONE LISTED
- Allergien
- NONE LISTED
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Approximately 5 minutes after vaccine administration, the patient's mother yelled for help whereupon the patient was observed in a state of syncope. The patient's mother had to hold her to prevent her from falling to the floor. First Aid was administered at this time and 911 was notified. Paramedics arrived shortly thereafter and patient was attended to. It was determined that patient was doing well enough to avoid going to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- medication history not maintained at this site
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Tachycardia
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Tachycardia-Mild, Additional Details: Patient fainted within 5 min of vaccine. We checked her BP and HR and had her sit so we could monitor her. She did not want to be seen by emergency dept or doctor. We monitored her for 15 min. She said she felt fine and called a friend to pick her up. We monitored her an addtional 10 min. and took down her phone number to check on her tonight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Confusional state
Diarrhoea
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Chills-Medium, Systemic: Confusion-Severe, Systemic: Diarrhea-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Weakness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pericarditis
Symptomtext
Pericarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Feeling hot
Syncope
Symptomtext
Patient received 1st COVID vaccine and was sitting in the waiting area afterward. He told his fiance that he felt "hot" and was going to the bathroom. While in there, he passed out and hit the bathroom wall. He was observed by EMTs and refused transport to the hospital. He left walking out with his fiance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None listed
- Vorgeschichte
- None listed.
- Andere Medikamente
- None listed
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Chest discomfort
Dyspnoea
Echocardiogram normal
Electrocardiogram normal
Myocarditis
Troponin increased
Vomiting
Symptomtext
On 1/13-1/14 patient had chest pressure and shortness of breath, 1 episode of vomiting. He was seen in the ED and was prescribed advil for 3 days and followup with cardiologist. avoid strenous physical activity for 2 weeks. Diagnosed with myocarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Troponin 0.38 (0.03 normal) 1/14 Echocardiogram , chest x ray, EKG reported WNL 1/14
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ADHD
- Andere Medikamente
- methylphenidate 37 mg daily
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Musculoskeletal stiffness
Neuralgia
Paralysis
Symptomtext
NERVE PAIN, STIFFNESS, PATIENT FELT PARALYZED COULDN'T MOVE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- NERVE PAIN
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 21,0
- Geschlecht
- U
- Eingang
- 13.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Syncope
Symptomtext
Patient received vaccination. After administration patient stood and waited several minutes for friend to get vaccine. Upon exiting vaccination room several minutes after vaccine patient fainted and fell to the ground. Patient quickly revived refusing medical treatment. Patient admits to being nervous about vaccine and admits after fainting that it happened once before when giving blood.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
C-reactive protein increased
Chest pain
Electrocardiogram abnormal
Myocarditis
Tachycardia
Troponin increased
Symptomtext
15 yo M, previously healthy, with 2 d of chest pain s/p COVID mRNA vaccine booster (3rd dose) on 1/8, with tachycardia, normotension, elevated CRP, significantly elevated troponin, and abnormal EKG, all most consistent with myocarditis, timing suggestive of COVID vaccine-associated myocarditis -- however, given other etiologies of myocarditis should also be considered, e.g. viral. Overall pattern of presentation less suggestive of MIS-C or systemic autoimmune disease.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 4,0
- Labordaten
- Lab 01/11/22 CRP 22.4* Troponin 1/10/22 - 12.61
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase increased
Angiogram cerebral normal
Aspartate aminotransferase increased
Blood bilirubin increased
Haematuria
Blood urine present
Chromaturia
Computerised tomogram head
Headache
Laboratory test
Haemoglobin decreased
Immune thrombocytopenia
Immunoglobulin therapy
Magnetic resonance imaging head normal
Magnetic resonance imaging head
Pain
Platelet disorder
Pyrexia
Symptomtext
after the covid 19 vaccine shot. my daughter started with fever and headache. I gave her Tylenol and the following day i did not send her to school due that she was in a lot of pain on her harm, fever, headache. On statuary 1/8/2022 i spotted blood clot on her lip and inside her mouth which I thought it was from the fever and her urine started changing color. Sunday morning 1/9/2022 i had to call her pediatrician and i explain to her what was happening to my daughter. i told her that she had more blood clots in her body and her urine look like blood. She told me to go straight to the emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- in the ER they did the following testes: Labs, imaging of her Brain, MRI, Head, CT scam, ultrasound, she still in the hospital. to many complications. with her Platelets and red blood cell. Blood transfusion, plasma transfusion etc.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Tylenol, vitamin c, d, and multivitamin
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient came in to get booster shot (3rd dose). He passed-out right when he opened the car door to go home. His dad called 911 and patient admitted to hospital. His dad came back to pharmacy to report incident at 12:45 pm. Around 4 pm, pharmacy gave him a callback to check on him. His mom said he was released from hospital and at home doing ok. The hospital said the shot might lower his blood pressure and that is why he passed-out (per mom). They will update us if there is anything further to happen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Disorientation
Fall
Loss of consciousness
Syncope
Symptomtext
Approximately 3.5 hours after getting his third COVID vaccine from Pfizer, patient fainted without much warning, never having had a history of this. He had eaten and hydrated normally that day, and after being unconscious on the floor for about 10 seconds and then confused and disoriented for about one minute, he behaved normally and reported that he felt okay. He was not injured in his fall.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Labs ordered by his nurse practitioner, include TSH, CBC, BMP, vitamin D, pre-albumin, LFT, and B12. Results pending.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Clonidine 0.3 mg once daily
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Loss of consciousness
Pallor
Syncope
Symptomtext
Patient passed out/fainted after giving 2nd vaccine. He came to a few seconds later and had pale and clammy skin for a few minutes. He sat there until he was failing better and then eventually left with his mother. I called a few hours later and patient was feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
Bradycardia
Electrocardiogram
Hypotension
Syncope
Symptomtext
Patient became very weak-Patient was placed in a dental chair with feet elevated Hypotentention- Provided patient with water and blood pressure was closely monitored Bradycardia - EKG showed sinus brady Syncope episode- patient was placed in dental chair and blood pressure was monitored
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- EKG 1-7 blood sugar level 1-7 Patient was transported to ER where further testing was completed.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Chronic pain total Hip arthroplasty hx of Cerebrovascular Accident Insomnia Generalized Anxiety HTN Hyperchlesterolemia Obesity Herniation of lumbar intervertebral disc with sciatica
- Andere Medikamente
- Amlodipine, ASA, acetaminophen, Buspirone, Ezetimbe, gabepentin, Hydrocodone-Acetaminophen, multivitamin, rosuvastatin, tizanidine, Vitamin C
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pericarditis
Pleuritic pain
Symptomtext
Pleuritic and positional pain over precordium, clinically consistent with pericarditis, starting about 24 hours after injection. Treatment includes aspirin and ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood pressure measurement
Body temperature
Body temperature decreased
Dizziness
Electrocardiogram
Extrasystoles
Fatigue
Feeling hot
Headache
Hypoaesthesia
Hypotension
Immunisation
Muscular weakness
Nasopharyngitis
Nausea
Product use issue
Syncope
Symptomtext
feeling weakening in her muscles; Product use for unapproved combination; Booster; found her on the bathroom floor last night; was very very nauseous; wanted to throw up; extreme hypotension; body temperature was a little low; was warm to the touch; really dizzy; shaking; really cold; super weak; her vision was super blurry but not blurry but it was dizziness; numb in her feet and hands and felt numbness in both hands and feet and felt the numbness a little bit in her hands but more in her feet; head hurts a little bit; was kind of tired/really tired and kind of weak; heart was also skipping a beat a few times; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 22 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 27Dec2021 11:30 (Lot number: FL3197) at the age of 22 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administered in arm left, administration date 27Dec2021 (Batch/Lot number: unknown) as dose number unknown, single for immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st dose, lot: EN6202), administration date: 23Feb2021, when the patient was 21 years old, for COVID-19 Immunization, reaction(s): "maybe really knocked down by the vaccine and it was also how she felt after the 1st and 2nd doses of the Pfizer Covid vaccine", "started feeling weakening in her muscles"; Bnt162b2 (2nd dose, lot: EN6207.), administration date: 16Mar2021, when the patient was 21 years old, for COVID-19 Immunization, reaction(s): "maybe really knocked down by the vaccine and it was also how she felt after the 1st and 2nd doses of the Pfizer Covid vaccine", "started feeling weakening in her muscles". The following information was reported: IMMUNISATION (medically significant) with onset 27Dec2021 11:30, outcome "unknown", described as "Booster"; SYNCOPE (medically significant) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "found her on the bathroom floor last night"; NAUSEA (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "was very very nauseous"; VOMITING (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "wanted to throw up"; HYPOTENSION (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "extreme hypotension"; BODY TEMPERATURE DECREASED (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "body temperature was a little low"; FEELING HOT (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "was warm to the touch"; MUSCULAR WEAKNESS (non-serious) with onset 27Dec2021 16:00, outcome "recovered" (Dec2021), described as "feeling weakening in her muscles"; DIZZINESS (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "really dizzy"; TREMOR (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "shaking"; NASOPHARYNGITIS (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "really cold"; ASTHENIA (non-serious) with onset 27Dec2021, outcome "not recovered", described as "super weak"; VISION BLURRED (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "her vision was super blurry but not blurry but it was dizziness"; HYPOAESTHESIA (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "numb in her feet and hands and felt numbness in both hands and feet and felt the numbness a little bit in her hands but more in her feet"; HEADACHE (non-serious) with onset 27Dec2021, outcome "recovered" (Dec2021), described as "head hurts a little bit"; FATIGUE (non-serious) with onset 27Dec2021, outcome "not recovered", described as "was kind of tired/really tired and kind of weak"; EXTRASYSTOLES (non-serious) with onset Dec2021, outcome "unknown", described as "heart was also skipping a beat a few times"; PRODUCT USE ISSUE (non-serious) with onset 27Dec2021 11:30, outcome "unknown", described as "Product use for unapproved combination". The patient underwent the following laboratory tests and procedures: blood pressure measurement: (Dec2021) 74/47; (Dec2021) skipping heart beats, notes: at one point the machine was showing she was skipping heart beats; (Dec2021) recovered pretty well, notes: took a series of blood pressure readings and the patient's blood pressure recovered pretty well; body temperature: (Dec2021) 93 or 96 degrees, notes: was a little low at 93 or 96 degrees; electrocardiogram: (28Dec2021) it was fine, notes: today at 1:00am or 2:00am. Therapeutic measures were taken as a result of syncope, nausea, vomiting, hypotension, body temperature decreased, feeling hot, muscular weakness, dizziness, tremor, nasopharyngitis, asthenia, vision blurred, hypoaesthesia, headache, fatigue, extrasystoles. Clinical course: Caller states his name is withheld and his daughter received the Pfizer Booster shot yesterday and it has on her patient card CPT # with Pfizer NDC 59267-1000-03 and lot number FL3197 and he will put his daughter on the line and let her speak; states the patient got the Pfizer Booster dose around 11:00am yesterday blood pressure reading of 74/47 and they measured the blood pressure a couple of times and then called the nurse that is on their health plan and the nurse helped the patient through this situation and they almost took the patient to the emergency room but instead pumped a lot of fluids in her and took a short walk outside and got the blood pumping a little bit and replenished her fluids. States they took a series of blood pressure readings and the patient's blood pressure recovered pretty well and it got to within normal range and did a round with an EKG unit and it looked good and said the patient was normal and that was today at 1:00am or 2:00am. The daughter who was the patient was provided with the call recording notification and she provided the rest of the report information. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): Caller states she got the flu shot at the exact same time in her other arm and states on 27Dec2021 she had the PFizer Covid booster shot in her right arm on her tricep near the shoulder and it had lot FL3197 and NDC 59267-1000-03 and no expiry date written on her patient card; states she also had the influenza flu shot administered to her left arm on 27Dec2021 but she has no flu shot name or lot number to provide. States she had the 1st dose of the Pfizer Covid vaccine on 23Feb2021 with lot EN6202 and the 2nd dose of the Pfizer Covid vaccine on 16Mar2021 with lot EN6207 and states her patient card has no expiry date or NDC number written on it for the 1st two doses of the Pfizer Covid vaccine. Caller states her heart was also skipping a beat a few times like when they took the EKG it was fine but when they took her blood pressure at one point the machine was showing she was skipping heart beats. Caller states it was 11:30am when she got the booster dose and when she got the vaccine but was maybe really knocked down by the vaccine and it was also how she felt after the 1st and 2nd doses of the Pfizer Covid vaccine and after the booster she woke up and was not feeling well. States her symptoms are not ongoing and she just feels way better today and her head hurts a little bit and she took Tylenol for that and was kind of tired and wiped out from everything last night and no nothing really and no numbness or anything today but is really tired and kind of weak. States for the Tylenol was brand and took one last night at 1:30am and took two 500mg at 1:30am and then took two more 500mg this morning at 8:30am or 9:00am and the Tylenol has at lot number that the patient's father said small numbers and caller states the lot is 1DV2110 with expiry date 20Dec2022 and for the UPC number she states she is not seeing that on the bottle or a bar code. Caller states the facility where she got the Pfizer Booster dose of the covid vaccine was one that her brother got off of withheld and on the calendar of events it was an event at withheld and thought it was a state or county regulated thing. Additional Vaccines Administered on Same Date of the Pfizer Suspect: states she also had the influenza flu shot administered to her left arm on 27Dec2021 but she has no flu shot name or lot number to provide. Adverse Event (AE) Details: Caller states it was 11:30am when she got the booster dose and when she got the vaccine and started feeling weakening in her muscles around 4:00-5:00pm but was maybe really knocked down by the vaccine and it was also how she felt after the 1st and 2nd doses of the Pfizer Covid vaccine and after the booster she woke up and was not feeling well and just really dizzy, super weak and shaking, was really cold and her vision was super blurry but not blurry but it was dizziness and was also numb in her feet and hands and felt numbness in both hands and feet and felt the numbness a little bit in her hands but more in her feet. Adverse Event (AE) Details: Caller states it was 11:30am when she got the booster dose and when she got the vaccine and started feeling weakening in her muscles around 4:00-5:00pm but was maybe really knocked down by the vaccine and it was also how she felt after the 1st and 2nd doses of the Pfizer Covid vaccine and after the booster she woke up and was not feeling well and just really dizzy, super weak and shaking, was really cold and her vision was super blurry but not blurry but it was dizziness and was also numb in her feet and hands and felt numbness in both hands and feet and felt the numbness a little bit in her hands but more in her feet.AE(s) did not require a visit to Emergency Room or Physician Office, but did call the nurse and was getting her input. Prior Vaccinations (within 4 weeks) was None. Description of complaint: Vaccine Supplemental Form completed in additional context. States her symptoms are not ongoing and she just feels way better today and her head hurts a little bit and she took Tylenol for that and was kind of tired and wiped out from everything last night and no nothing really and no numbness or anything today but is really tired and kind of weak. States for the Tylenol is is Kroger brand and took one last night at 1:30am and took two 500mg at 1:30am and then took two more 500mg this morning at 8:30am or 9:00am and the Tylenol has at lot number that the patient's father said is small numbers and caller states the lot is 1DV2110 with expiry date 20Dec2022 and for the UPC number she states she is not seeing that on the bottle or a bar code.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Test Date: 202112; Test Name: Blood pressure; Result Unstructured Data: Test Result:74/47; Test Date: 202112; Test Name: Blood pressure; Result Unstructured Data: Test Result:skipping heart beats; Comments: at one point the machine was showing she was skipping heart beats; Test Date: 202112; Test Name: Blood pressure; Result Unstructured Data: Test Result:recovered pretty well; Comments: took a series of blood pressure readings and the patient's blood pressure recovered pretty well; Test Date: 202112; Test Name: body temperature; Result Unstructured Data: Test Result:93 or 96 degrees; Comments: was a little low at 93 or 96 degrees; Test Date: 20211228; Test Name: EKG; Result Unstructured Data: Test Result:it was fine; Comments: today at 1:00am or 2:00am.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other history: No Family Medical History Relevant to AE(s): None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Electric shock sensation
Lip haemorrhage
Muscle twitching
Pharyngeal haemorrhage
Rash
Secretion discharge
Seizure
Sleep disorder
Tremor
Upper respiratory tract infection
Symptomtext
I received the Pfizer vaccine on 12/27/2021, two hours after receiving the vaccine, my lip started bleeding and filled my mouth with blood and I had to apply pressure to the opening on my lip for 5 minutes to get it to stop bleeding. I did not cut my lip, it started bleeding without prior trauma. Over the next 2-5 days after the vaccine, I kept tasting blood in my mouth and looked at my throat with a flashlight and found an area in the back of my throat, a capillary bleeding. I drank cold water to have it stop bleeding. 7 days after the vaccine, I got an upper respiratory infection with lots of thick yellow/brown mucus produced over the next 4 days and still ongoing. On day 7 after the vaccine, I started experiencing muscle twitching throughout my body, a sensation of full body tremors, and electric current feeling in my body all day and night. When falling asleep and during sleep, the muscle twitching's are quite large and wake me throughout the night and cause my entire lower body to convulse. I have also broke out in rashes throughout my body since the day of the injection. I had none of these symptoms prior to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- I have a scheduled appointment with my doctor on 2/7/2022 for lab work and a referral to a neurologist. If the bleeding continues or the muscle twitching progress, I will go to urgent care. However, am in between jobs and do not have insurance until 2/1/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Meniere's Disease
- Andere Medikamente
- Zinc 15 mg once daily Magnesium 500 mg once daiy Vitamin C 500 mg once daily
- Allergien
- Augment, Cipro, Flu Vaccine, Naproxen, MSG
- Vorherige Impfungen
- Flu vaccine- rash, upper respiratory congestion/high fever
- Staat
- VA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
PATIENT had a seizure episode for about 15 seconds near the inside of the pharmacy. After patient had come back with consciousness, he explained that this hasnt happened since he was 15. Patient did not acknowledge that he had a history of seizures on the pre-check health list.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- received a vaccination (couldn't remember name" at 15 that this has happened
- Staat
- IN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Flushing
Hyperhidrosis
Hypotension
Syncope
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: fainted on 2 separate occasions and vomited-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Vomiting-Mild, Additional Details: called 911 and she was taken to hospital by ambulance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Head injury
Hyperhidrosis
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting/Unresponsive-Mild, Systemic: Flushed/Sweating-Mild, Additional Details: Patient fainted after vaccine administration. Bumped head; cleaned area; Band-Aid provided. Patient refused EMT service. Friend drove him home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose normal
Dyskinesia
Eye movement disorder
Loss of consciousness
Feeling abnormal
Feeling hot
Syncope
Symptomtext
10 minutes after shot eyes rolled back into head and arms drew up and went unconscious for 5 seconds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Blood sugar 82 and vitals by EMS
- Aktuelle Erkrankungen
- Na
- Vorgeschichte
- Na
- Andere Medikamente
- Na
- Allergien
- Na
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mental impairment
Seizure
Speech disorder
Thinking abnormal
Symptomtext
couldn't think and progress my speech and thoughts; had a few seizures; couldn't think and progress my speech and thoughts; couldn't think and progress my speech and thoughts; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 21Dec2021 14:45 (Lot number: FL3197) at the age of 37 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Epilepsy" (unspecified if ongoing). There were no concomitant medications. The following information was reported: MENTAL IMPAIRMENT (non-serious), SPEECH DISORDER (non-serious), THINKING ABNORMAL (non-serious) all with onset 22Dec2021 07:00, outcome "recovered with sequelae" and all described as "couldn't think and progress my speech and thoughts"; SEIZURE (non-serious) with onset 22Dec2021 07:00, outcome "recovered with sequelae", described as "had a few seizures". Therapeutic measures were not taken as a result of mental impairment, seizure, speech disorder, thinking abnormal. The patient had no covid prior vaccination, covid tested post vaccination and known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Epilepsy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Dizziness
Syncope
Symptomtext
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Immunisation
Loss of consciousness
Lymph node pain
Lymphadenopathy
Myalgia
Symptomtext
Nearly passed out the following morning; headache; muscle aches; chills; fatigue; swollen and painful lymph nodes under left arm and collar bone; swollen and painful lymph nodes under left arm and collar bone; booster; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 12:45 (Lot number: FL3197) at the age of 45 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "anxiety disorder" (unspecified if ongoing); "Acid reflux (oesophageal)" (unspecified if ongoing). Patient did not have known allergies. Concomitant medication(s) included: PROZAC; DEXILANT; CLARITINE, unspecified birth control and unspecified vitamines. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: EP6955, in arm left), administration date: 12Apr2021, when the patient was 45 years old, for COVID-19 immunisation; Bnt162b2 (Dose 1, Batch/Lot No: EP6955, in arm left), administration date: 22Mar2021, when the patient was 45 years old, for COVID-19 immunisation. The following information was reported: LOSS OF CONSCIOUSNESS (medically significant) with onset 17Dec2021, outcome "recovering", described as "Nearly passed out the following morning"; HEADACHE (medically significant) with onset 17Dec2021, outcome "recovering", described as "headache"; MYALGIA (medically significant) with onset 17Dec2021, outcome "recovering", described as "muscle aches"; CHILLS (medically significant) with onset 17Dec2021, outcome "recovering", described as "chills"; FATIGUE (medically significant) with onset 17Dec2021, outcome "recovering", described as "fatigue"; LYMPH NODE PAIN (medically significant), LYMPHADENOPATHY (medically significant) all with onset 17Dec2021, outcome "recovering" and all described as "swollen and painful lymph nodes under left arm and collar bone"; IMMUNISATION (non-serious) with onset 16Dec2021 12:45, outcome "unknown", described as "booster". Therapeutic measures were not taken as a result of loss of consciousness, headache, myalgia, chills, fatigue, lymph node pain, lymphadenopathy. Additional information: the patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination the patient has not been diagnosed with COVID-19. Since the 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
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acid reflux (oesophageal); Anxiety disorder
- Andere Medikamente
- PROZAC; DEXILANT; CLARITINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fatigue
Loss of consciousness
Vomiting
Symptomtext
Patient passed-out twice after administration, then vomited. She felt very weak and tired until she vomited then she began to feel better. I talked to the patient about an hour later when she was at home and feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Thimerosal--was fine after getting first 2 doses of Pfizer
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
COVID-19
Intensive care
Obstructive airways disorder
SARS-CoV-2 test positive
Stridor
Wheezing
Symptomtext
Pt presented for her third Pfizer vaccine. Almost immediately after vaccination, pt c/o Wheezing. On assessment, pt had audible stridor, could not speak a sentence. Pt treated with albuterol and epi-pen. Due to concern for airway, rapid response called and pt taken to the ER. Patient is currently in ICU
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- Covid positive test on admission found incidentally 12/29/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Loss of consciousness
Syncope
Symptomtext
Patient fainted while sitting next to her mother after vaccine administration. Patient was unconscious for about 5 seconds in her mother's arm. Patient came to again quickly. No treatment was necessary. Patient stated that she faints after all vaccines before the vaccine was administered so staff and mother were ready to deal with the situation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- No known
- Vorherige Impfungen
- Fainting after all vaccines
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted while waiting for 15 min required observation period, became alert a few seconds later, declined going to ER. Patient reported being tired and dizzy a few hours after receiving 1st dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- After 1st covid vaccination patient felt tired and dizzy hours later.
- Staat
- IL
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Injection site swelling
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Site: Swelling at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Shakiness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Chest discomfort
Chest pain
Dizziness
Dyspnoea
Hypotension
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Mild, Additional Details: Patient felt lightheaded and had shortness of breath, BP was 83/42, called EMS they evaluated her heart, patient was feeling better and blood pressure increased prior to leaving. Did not need to go to hospital or in ambulance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Loss of consciousness
Symptomtext
Patient went temporarily unconscious and pulse ox went down to 74. Nurses triaged and pharmacy manager called Ems
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling abnormal
Loss of consciousness
Seizure
Symptomtext
Thirty-six hours after booster shot (around 3:30 a.m. on Dec. 20), I passed out after feeling dizzy and a few minutes after regaining consciousness, I had a seizure that my husband witnessed. Had a strange feeling throughout my body. Should have gone to hospital but did not. Went to bed and never followed up with doctor/hospital because of my busy holiday schedule.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- None
- Allergien
- Demerol makes me nauseous.
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Disorientation
Dizziness
Loss of consciousness
Muscle twitching
Symptomtext
Patient had no reaction with the 1st dose but had fever and chills and body aches with 2nd. She received the Moderna booster 0f 0.25ml and was asked to sit for 15 min, her mother was with her. Within 5 min after receiving the booster shot, her mom came to the counter and told us my daughter is passing out. Her daughter was sitting on the floor and seem to have twitched a little and mom went to allow her daughters head to rest on her leg. Meanwhile we called 911 and EMS immediately sent emergency personelle while one the phone questioning if the patient has any existing heart condition or stomach issues. We were adviced by the EMS not to give patient anything to drink or eat in case she seizes. Patient came to within couple minutes but seemed disoriented. She said she feels light headed. EMS arrived and took her vitals at that time and all were within normal range. They sat and took down patient history and monitored the patient and had her sit by the pharmacy for 30 min. During questioning, they discovered patient has not had anything to eat or drink since the day before which may have contributed to her adverse reaction. They checked her vitals again and all were within normal range after 30 minutes then she was given the ok to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Nausea
Syncope
Symptomtext
Received first dose of the Pfizer vaccine LOT: #FL3197 at 1635. Patient experienced a syncopal episode that lasted approximately 3 seconds in the vaccination chair. Patient did not fall to the ground during syncopal episode and did not hit his head. Head was being supported by his mom who was standing behind him. After syncopal episode patient felt nauseous but did not vomit. Patient stated that he has a history of syncope with needles. Patient stated that he is not on any medications. Patient stated the last time he had a syncopal episode was two years ago. EMT took patients vital signs at 1640. BP: 144/81, HR: 80, RR: 16, O2: 99%. Patient was then moved to observation area. Patient was able to walk unassisted and with a steady gait. Patient was asked to wait in observation area for 30 minutes. EMT reassessed and retook patients vital signs. BP: 138/82, HR: 93, RR: 16, O2: 99%. Patient stated that he was "feeling a lot better" and was not experiencing new symptoms. EMT retook patients vital signs. BP: 136/82, HR: 82, RR: 16, O2: 98% at 1710. RN reassessed patient. Patient was not experiencing any new symptoms. RN educated patient on adverse symptoms of COVID vaccine and when to seek EMS. Patient verbalized understanding. Patient left vaccination site after completing observation time with his mom unassisted and with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Disorientation
Seizure
Symptomtext
Very shortly after getting the vaccine the patient was in the post-vaccine waiting area and had a seizure that lasted about 30 seconds to 1 minute. EMS was called and patient was still very disoriented when EMS arrived and took him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- None performed by me.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None documented
- Andere Medikamente
- None documented on pt consent form, but unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Head injury
Seizure
Syncope
Symptomtext
patient passed out in chair, fell forward, hit head against the wall. patient had 2 seziures. 911 was called
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein increased
Cardiac imaging procedure abnormal
Chest pain
Echocardiogram abnormal
Electrocardiogram ST segment elevation
Immunoglobulin therapy
Immunosuppressant drug therapy
Laboratory test
Left ventricular dilatation
Left ventricular dysfunction
Left ventricular hypertrophy
Myalgia
Myocarditis
Red blood cell sedimentation rate normal
Respiratory viral panel
SARS-CoV-2 antibody test negative
Troponin increased
Vaccination complication
Symptomtext
Admission Date/Time: 12/19/2021 12:11:00 Discharge Date/Time: 12/21/2021 12:13:10 Chief Complaint chest pain Patient Narrative Patient is a previously healthy 16yM w/ GERD p/w 1d chest pain and ST elevations on EKG at urgent care.Patient was in USOH when he got his COVID booster vaccine 5d ago (12/14). Afterwards, he had a day of muscle soreness similar to the symptoms he had after his 2nd COVID vaccine. Because of the chest pain, patient went to outside urgent care where he was found to have ST elevations on inferior leads and troponins elevated to 12.5 (upper limit 0.05). Patient was then sent to ED. Labs showing elevated troponin 1.49, CRP 2.85, ESR 10. He was admitted to cardiology service with differential diagnosis of post covid vaccine myocarditis. He was started on immun suppresive treatment for presumed post vaccine myocarditis. Initial ECHO was consistent with Mild left ventricular dilatation. Mild left ventricular systolic dysfunction. Qualitatively normal right ventricular systolic function. No significant valve dysfunction. No pericardial effusion. He has completed a course of IVIG and started on 5 day course of methylprednisone. Currently, he is at his baseline and without symptoms. The ST segment elevation have nearly normalized with non-specific ST segment changes. Troponin levels downtrended to 0.95, with most recent one being 1.01 . Repeat ECHO was done on day 3 of admission that showed improved LV function compared to admission ECHO. His cardiac MRI changes was reviewed by radiology also found to be consistent with myocarditis. He is going to complete his 5 day steroid course at home and will be seen as outpatient for follow up on 12/29 with Dr. Tests Pending No tests pending at time of discharge These tests will be followed by the Primary Service at Discharge after Discharge Vitals and Discharge Physical T: 36.9 ?C (Temporal Artery) HR: 66 (Monitored) RR: 18 BP: 106/50 SpO2: 98% HT: 177.8 cm WT: 90.4 kg Discharge Physical Exam General: alert, no acute distress, normal hydration, not ill appearing Skin: no rash, warm, dry Head: atraumatic, normocephalic Eye: normal conjunctiva, sclera clear, no discharge, pupils equal, round, reactive, extraocular movements intact ENT: RTM normal, LTM normal, pharynx: normal, normal tonsils, mouth: moist mucus membranes, no lesions Neck: supple, trachea midline, no adenopathy, no tenderness Cardiovascular: regular rate and rhythm, no murmur, normal peripheral perfusion Respiratory: lungs CTA, respirations non labored Chest wall: no tenderness, no deformity Gastrointestinal: soft, nontender, nondistended, normal bowel sounds, no organomegaly Musculoskeletal: no deformity, no tenderness, normal range of motion, no joint swelling Diagnosis List 1. Adverse reaction to immunization, 12/19/2021 2. Chest pain, 12/19/2021 Procedure History No Procedure History Social History Smoking Status No Smoking Status Documented Allergies No known allergies Other Relevant Laboratory Results ECHO 12/19 Mild left ventricular dilatation. Mild left ventricular systolic dysfunction. Qualitatively normal right ventricular systolic function. No significant valve dysfunction. No pericardial effusion. ECHO 12/21 High-normal left ventricular size with low-normal systolic function - improved. Mild eccentric left ventricular hypertrophy. Qualitatively normal right ventricular systolic function. Normal valve function.? No pericardial effusion. Microbiology Results (Last 30 Days) Viral Respiratory panel negative, covid antibody negative Immunizations Covid booster on 12/14/202 Patient likely had myocarditis following his booster (3rd dose) of COVID-19 immunization that has low-normal function, but is currently asymptomatic. We will have him restricted from strenuous activity and competitive sports for 3 months. We will have him continue on the prednisone for 2 more days (5 total days) without a taper. He has follow-up in one week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- As above Troponin 1.75 ng/mL CRP 2.82 mg/mL Viral panel negative SARS-CoV-2 antibody negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD, Depression
- Andere Medikamente
- Fluoxetine 40 mg PO daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient passed out for 10-15 seconds a couple minutes after administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Syncope
Symptomtext
DIZZY, FAINTING, NAUSEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- no test per mom 12/22/2021
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- faint, dizzy, nausea
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Dizziness
Hypertension
Loss of consciousness
Neurological examination
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Hypertension-Medium, Additional Details: lost conciousness for about 5 seconds. RN did assessment including bp, pulse ox, and nero exam. 911 was called due to sustained elevated BP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Symptomtext
syncope within minutes of receiving booster shot. Patient lost consciousness for less than 1 minute
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Loss of consciousness
Seizure
Vision blurred
Symptomtext
Patient passed out, slight convulsions, blurred vision, general body weakness. Vaccine administered at 11:41am, reaction at 11:44am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Computerised tomogram head
Haematoma
Head injury
Nervousness
Syncope
Symptomtext
After patient was given the Pfizer booster in the morning, patient was told to stay for 15 minutes for observation in the post vaccination area. Per Rph, patient left after 5 minutes from the area, and the accompanying mother screamed that her son had collapsed. Police Department and Ambulance arrived 5-7 minutes after being called immediately. Firefighters say he had a hematoma around the head area. RPH called the father and CT scans came out normal. After everything had happened, mother of the patient said he was nervous and had not eaten anything night prior. RPH confirmed that patient had mild symptoms with the first two covid shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None reported
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Seizure
Symptomtext
Systemic: Seizure-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: Paramedics called due to the patient fainting and they cleared him. Patient felt dehydrated after, drank pedialyte and water and felt better after about 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient received 1st dose of her COVID vaccine. She fainted about 10 minutes after receiving the vaccine while sitting in the chair. EMS was called and she was taken to the emergency room in an ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Immediate post-injection reaction
Incoherent
Loss of consciousness
Posture abnormal
Respiration abnormal
Seizure like phenomena
Symptomtext
Vaccinator gave the IMZ (Pfizer). Immediately after, she sat down to write the IMZ on his personal IMZ record card. Vaccinator observed his head going forward, then leaning forward. His mom stepped out of the way and he fell out of the chair onto his head. He appeared to be having a seizure when he initially hit the ground and then when waking up. He was incoherent for about 10 seconds. We kept him on the floor and supported him while applying ice packs to the back of his neck. He was coherent and breathing normally within seconds. He could communicate his needs and told us he felt fine. We called EMS to have EMS evaluate him - because we thought he had a mild seizure and a possible concussion. EMS took over and took him to the hospital for further evaluation. His family will be contacted tomorrow to check on his condition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Dizziness
Fatigue
Feeling hot
Flushing
Hyperhidrosis
Lethargy
Nausea
Syncope
Tremor
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Medium, Systemic: Shakiness-Mild, Systemic: Vomiting-Medium, Additional Details: Patient has Hx of "wooziness/feeling faint" post injections/blood draws. Wife was with patient and me for entire event. Order of events: 1 - Discussed COVID-19 vax history w patient 2 - admin vax in patient's left arm while he was seated 3 - approximately 45 seconds post admin patient became: "green", sweating, overheated, vomiting, syncope. 911 responded. I spoke w/wife approx 45 min later; reports patient fine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Fall
Syncope
Unresponsive to stimuli
Symptomtext
Patient fell from a chair, he was found in prone position. Upon assessment patient did not respond to verbal commands, 911 was then called. After approximate five seconds patient was verbal and moving. He was coherent to person, place, time, and situation. Patients vitals post syncope episode were T. 98.2 R. 22 P. 96 B/P 131/71 spo2 96% on room air
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Patient transferred to hospital by fire department
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- Per patient this has happened when he sees needles.
- Staat
- IL
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
After vaccine patient passed out. Patient came to and drank some juice, then passed out again for a few seconds
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None listed
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal mass
Abdominal pain upper
Adnexa uteri pain
Amenorrhoea
COVID-19
Heavy menstrual bleeding
Pelvic mass
Computerised tomogram abnormal
Cyst
Cyst removal
Depressed mood
Dyspareunia
Fatigue
Fear
Feeling abnormal
Fluid retention
Haemorrhage
Hysterectomy
Symptomtext
mennorhagia, abdominal/pelvic mass
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- asthma
- Vorgeschichte
- asthma, PCOS
- Andere Medikamente
- Multivitamin
- Allergien
- Pine, Pet dander, Roaches PCN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 18.05.2023
- Impfdatum
- 26.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Angiogram cerebral
Arteriogram carotid
Back pain
Blood pressure increased
Blood test
Burning sensation
Fatigue
Hemiparesis
Hypoaesthesia
Lumbar puncture
Magnetic resonance imaging head
Magnetic resonance imaging spinal
Pain
Paraesthesia
Peripheral coldness
Scan with contrast
Sensitive skin
Spinal X-ray
Symptomtext
In the days and weeks following the adminstration of the Pfizer Covid booster vaccine on December 26, 2021, I experienced increasing tingling and numbness (parasthesia) in my right hand and arm. This was accompanied by a sore/throbbing spot on the right side of my back that moved around (initially it was in my lower back, then it moved up my back, then back down my back, then towards the right side of my lower back). The tingling eventually turned into burning on my right side, particularly in my right hand and arm, but also in the lower right side of my back and in my right hip and buttock. These symptoms persisted into mid-January 2022, so I decided to see a doctor. The earliest I could see a primary care physician was on March 1, 2022. The primary care physician referred me to a neurologist, who I first saw on April 14, 2022. Since then, I have seen two different neurologists (due to changes in my health insurance) on a number of different occasions. Over the course of the last year or so, my neurologists have ordered numerous tests described elsewhere in this report. Although they have been able to rule out various serious disorders like MLS, my case has perplexed them, and they have not been able to determine the cause of my symptoms. The burning on my right side, particularly in my hand and arm, continues to this day and can be intense at times. My neurologists have prescribed three different nerve pain medications, which have done little, if anything, to help. In addition to the burning symptoms, I now have almost no ability to sense heat or cold with my right hand (for example, I have to use my left hand to determine the temperature of water). I have also developed weakness on my right side. For example, my right arm will quickly fatigue after straining it (for example, when I use a screwdriver). My right hand also gets very cold sometimes (not just a perceived coldness, but actual coldness). And my right hand and arm are also highly sensitive to pain (for example, if I accidentally hit my hand against something, I feel a much sharper pain than I would have before the vaccine). I also experienced elevated blood pressure following the adminstration of the Pfizer Covid booster vaccine on December 26, 2021, and I am now taking blood pressure medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- 3/8/22: X-Ray Lumbosacral Spine 3/8/22: X-Ray Cervical Spine 3/8/22: MRI Brain without contrast 6/14/22: Lumbar Puncture 6/22/22: MRI Lumbar, Thoracic and Cervical Spine, with and without contrast 8/18/22: Ultrasound Kidney 10/31/22: MRI Brain and Brainstem 12/12/22: CT Angiogram Brain and Neck 2022: Various Blood Tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 30.12.2021
- Beginn
- 18.02.2022
- Tage bis Beginn
- 50,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypotension
Pain
Symptomtext
I95.9 HYPOTENSION 2/17/2022 CHRONIC PAIN TREATMENT PLAN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 24.04.2023
- Impfdatum
- 12.12.2021
- Beginn
- 09.04.2023
- Tage bis Beginn
- 483,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Condition aggravated
Diabetes mellitus
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Case was hospitalized on 04/09/2023 due to diabetes and weakness. On 04/18/2023 case had a fever and tested positive for COVID. Case was discharged the the following day 04/19/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 10,0
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- diabetes
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- F
- Eingang
- 02.03.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebral disorder
Dizziness
Heavy menstrual bleeding
Hypoaesthesia
Menstrual disorder
Palpitations
Polymenorrhoea
Symptomtext
I was just hospitalized for brain spasm; Numbness of my limbs, my arms; Lightheadedness/Dizziness; Heart palpitations; I have the heavy three menstrual cycle in a month; every single month for the last year and now I am not even having weekend between them I am on my 4th menstrual cycle for the month; patient just got off her period 5 days ago and nowhave it again; Two months after consistent bleeding; this is not normal; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 23-year-old female patient received BNT162b2 (BNT162B2), as dose 2, single (Lot number: FL3197), in arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose number: 1, Manufacture: unknown), for COVID-19 immunization. The following information was reported: CEREBRAL DISORDER (hospitalization), outcome "unknown", described as "I was just hospitalized for brain spasm"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "Numbness of my limbs, my arms"; DIZZINESS (non-serious), outcome "unknown", described as "Lightheadedness/Dizziness"; PALPITATIONS (non-serious), outcome "unknown", described as "Heart palpitations"; HEAVY MENSTRUAL BLEEDING (non-serious), outcome "unknown", described as "I have the heavy three menstrual cycle in a month; every single month for the last year and now I am not even having weekend between them I am on my 4th menstrual cycle for the month"; POLYMENORRHOEA (non-serious), outcome "unknown", described as "patient just got off her period 5 days ago and nowhave it again"; MENSTRUAL DISORDER (non-serious), outcome "unknown", described as "Two months after consistent bleeding; this is not normal". The event "two months after consistent bleeding; this is not normal" required physician office visit. Therapeutic measures were taken as a result of menstrual disorder. Clinical course: The patient was still experiencing side effects but on top of the side effects which were numbness of limbs/arms, lightheadedness, dizziness and heart palpitations. On top of that, had the heavy three menstrual cycle in a month, every single month for the last year and now not even having weekend between them and on her 4th menstrual cycle for the month and this all this Feb. The patient just got off her period 5 days ago and now have it again and she don't take medicine and don't take get vaccines the only vaccine she have had within the last 10 years of Pfizer. The patient went to an gynecologists like about two months after consistent bleeding and they are the ones that told me like that this was not normal. The patient ended up getting on birth control (Name could not be clarified hence, captured as unspecified medication) thinking it will stop the bleeding and they gave me signs of 'closure' before they gave me birth control things and she was bleeding three times a month before I even get birth control. On top of the bleeding there was another side effect, she was just hospitalized (Further hospitalization details were not available over the call hence, Seriousness criteria not checked) for heart spasm (Later clarified as brain spasm).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.03.2023
- Impfdatum
- 01.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 59,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blood test normal
Chills
Computerised tomogram abdomen normal
Condition aggravated
Coeliac disease
Fatigue
Feeling abnormal
Gastrointestinal disorder
Investigation
Defaecation urgency
Depression
Diarrhoea
Faeces soft
Feeling cold
Gastrointestinal pain
Headache
Hyperhidrosis
Symptomtext
fatigue; brain fog; celiacs; GI system is completely backwards. It became unbearably sensitive; whole year in pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), in Jan2022 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization Series Complete; Unknown Manufacturer), for COVID-19 immunization. The following information was reported: GASTROINTESTINAL DISORDER (non-serious) with onset Mar2022, 2 months after the suspect product(s) administration, outcome "unknown", described as "GI system is completely backwards. It became unbearably sensitive"; COELIAC DISEASE (medically significant) with onset Mar2022, 2 months after the suspect product(s) administration, outcome "unknown", described as "celiacs"; PAIN (non-serious) with onset Mar2022, 2 months after the suspect product(s) administration, outcome "unknown", described as "whole year in pain"; FEELING ABNORMAL (non-serious) with onset 2023, outcome "unknown", described as "brain fog"; FATIGUE (non-serious) with onset 2023, outcome "unknown". The patient underwent the following laboratory tests and procedures: tested: negative; negative; negative; negative; negative; negative; negative; negative; negative. Therapeutic measures were taken as a result of coeliac disease, gastrointestinal disorder, pain. Clinical course: 13 months ago (Jan2022), the patient got his/her booster. 2 months after (Mar2022), the patient started to develop some very worrying symptoms. His/her gastrointestinal (GI) system is completely backwards, became unbearably sensitive. It's almost like he/she have Celiacs. The patient spent the whole year in pain and on various probiotic strains, and bought so many supplements to combat it. The patient changed his/her whole diet around and even that only works a bit. Around now (2023), brain fog and fatigue were taking over the patient's life. The patient tested 9 times and all were negative. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative ; Test Name: tested; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 22.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Sleep disorder
Tremor
Symptomtext
Shaking woke me up 0400. For next couple hours intermittent shaking then would have shaking less often and Last event time at 1430 pm same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- calcium vitamin D, vitamin D3, Niacin Lisinopril, Lisinopril-HZT verapamil
- Allergien
- Statins Hmg-cna Rediclase inhibitors Zetia (Ezetimibe, Latex, Nitrate Analogues gloves
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Constipation
Delirium
Delusion
Diarrhoea
Fatigue
Headache
Mental impairment
Migraine
Muscle spasms
Nausea
Vomiting
Symptomtext
Headache started 4 hours after injection; intense muscle cramping for 6 hours; full body cramping; prescribe steroid booster; nausea and vomiting. Diarrhea and constipation; Prolonged migraine; delusions and delirium. Extreme fatigue. Over a period of weeks could not function in normal manner.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- Immunocompromised; Addison severe; CIRS; MS/CSF; Myasthenia Gravis; COPD; glial cellular priming; chelated; heavy metal poisoning; cadmium poisoning; mercury poisoning with mercury allergy; uranium ingested.
- Vorgeschichte
- Immunocompromised; Addison severe; CIRS; MS/CSF; Myasthenia Gravis; COPD; glial cellular priming; chelated; heavy metal poisoning; cadmium poisoning; mercury poisoning with mercury allergy; uranium ingested.
- Andere Medikamente
- IV saline; IV dextrose; IV heparin; injected B12; cephalexin; amino acid; atorvastatin; diazepam; ketoconazole; hydrocortisone; fludrocortisone; thyroxin; liothyronine; losartan
- Allergien
- Anaphylaxis severe; milk; shellfish; BOTOX; metal based multivitamin; metal based contrast imaging; barium; iodine; zinc
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 24.01.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 258,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Diarrhoea
Dyspnoea
Ear pain
Feeling abnormal
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I received my Covid-19 vaccine on 01/24/2022. On the evening of 10/09/2022 I started having horrible diarrhea. The next day's I experienced ear pain, sore throat fever and shortage of breath. On 10/12/2022 I tested positive for Covid-19 and contacted my doctor. I was not prescribed medication for Covid. Symptoms lasted about 2 weeks. After about 2 month I had Covid again with continuing on going symptoms of coughing, fever, brain fog, sore throat, ear pain, diarrhea, and congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Probiotic; Prenatal vitamin; Nasocort
- Allergien
- Mushroom; Latex; Mushroom
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 06.01.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 331,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Headache
Heart rate increased
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
Started having a sore throat and with body aches, headaches and slight chest pain; Took a Home COVID-19 test and it was positive; Called Doctor and was prescribed Paxlovid, though decided not to take it; Tested negative for COVID-19 one week later; Heart rate seems to have permanently increased since testing positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test - positive; Home COVID-19 test - negative.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Hashimotos's; Complex Regional Pain System
- Andere Medikamente
- MP Thyroid; Low dose Naltrexone; Multivitamin; Fish Oil; Vitamin D3; Vitamin K2.
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 14.01.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 50,0
- Dosis
- N/A
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Atrial flutter
C-reactive protein normal
Cardioversion
Carditis
Chest pain
Dizziness
Electrocardiogram abnormal
Palpitations
Supraventricular tachycardia
Symptomtext
I experienced chest pain and palpitations two weeks after receiving the Covid Booster on March 5th. I was found to have Aftrial Flutter and had to be Electrically Cardioverted. A second event happened on March 18th when I experienced chest pain and palpitations again and had to be brought into the ED via ambulance. I was found to have atrial flutter and also went into Supraventricular Tachycardia with a heart rate of 240 beats/min became dizzy and had a blood pressure of 74/55. I had to be chemically cardioverted with Adenosine .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -Electrocardiogram 3/5/22 -Atrial Flutter -Electrocardiogram 3/18/22-Atrial Flutter /Supraventricular Tachycardia (SVT) -Echocardiogram -3/9 /22 mild inflammation to right upper heart chamber -C-reactive Protien Lab work 3/22/22 elevated 0.8
- Aktuelle Erkrankungen
- Covid on 12/30/21
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Cephalosporin Antibiotics
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Chronic spontaneous urticaria
Paraesthesia
Temperature intolerance
Symptomtext
After much research I believe I have Chronic Spontaneous Urticaria Following Pfizer-BioNTech Coronavirus Disease 2019 Messenger RNA Vaccination. Not exactly sure when it started because I didn't record the exact date, but I had the first shot on 3-29-21 and the second on 4-19-21 and the booster on 12-22-21. When my body warms up, I get waves of pins and needles all over my body. There is no area that does not get it. I never had this before. I have always exercised and been an avid walker for 30 years. I am now 56 and every time I exercise or get hot for some other reason it always hits me. I do not get hives, just the overwhelming pins and needles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- I have discussed this with my primary care doctor and he has recorded this in my file. He just instructed me to take an antihistamine and maybe see an allergist doctor.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- simvastatin finasteride
- Allergien
- None other than slight reactions to some antibiotics
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 17.04.2021
- Beginn
- 29.07.2022
- Tage bis Beginn
- 468,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 8,0
- Labordaten
- POSITIVE COVID TEST 7/29/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Essential hypertension Chronic kidney disease, stage III Macroalbuminuric diabetic nephropathy Melanocytic nevus of left lower extremity Morbid obesity Type 2 diabetes mellitus with retinopathy of both eyes and macular edema
- Andere Medikamente
- atorvastatin (LIPITOR) 10 mg oral tablet bumetanide (BUMEX) 2 mg oral tablet carvedilol (COREG) 25 mg oral tablet cloNIDine HCL (CATAPRES) 0.2 mg oral tablet furosemide (LASIX) 20 mg oral tablet
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 12.01.2021
- Beginn
- 26.04.2022
- Tage bis Beginn
- 469,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest pain
Cough
Dyspnoea
Pneumothorax
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
Narrative: Patient received three doses of Pfizer COVID 19 Vaccine. The patient tested positive for COVID 19 on 26 April 2022. The patient presented to the ED with chest pain, shortness of breath, and cough. The patient was admitted to the hospital with respiratory failure with hypoxia, and chest pain. The patient was treated with IV antibiotics, steroids, and bronchodilators. The patient was discharged from the hospital on 27 April 2022 and then re-admitted to another hospital on 7 May 2022 with continued respiratory failure and pneumothorax. The patient was still in the hospital as of 17 May 2022. Reported per EUA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 06.01.2021
- Beginn
- 06.08.2022
- Tage bis Beginn
- 577,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
COVID-19
Confusional state
Dysarthria
Joint swelling
Lethargy
Pneumonia aspiration
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Pt to ED 8/3 for bilateral ankle swelling and pain. 8/4 pt is A&Ox4, cooperative. Respirations are even, unlabored. 8/5 Pt confused and lethargic. 8/6 pt COVID+. 8/7 Pt more oriented (x4) w/ intermittent confusion and slurred speech. Pt still lethargic, fever of 101.1. 8/11 Pt aox1,confused, on 3L 02 NC not in distress. 8/12 O2 requirements increased; possible component of aspiration pneumonia; remdesivir rx completed. 8/13 pt is aox3-4, with period of confusion. 8/15 Fever (resolved) likely secondary to COVID, now on RA O2 possible component of aspiration pneumonia.8/16 pt alert,orient x3. No distress noted. 8/17 pt is A&OX4, VSS no complaints or discomfort. Pt discharged 8/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia aspiration
- Hospital-Tage
- 15,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Alcoholic cirrhosis (CMS/HCC) ...
- Andere Medikamente
- acetaminophen (TYLENOL) suppository 650 mg ...
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 29.12.2021
- Beginn
- 22.07.2022
- Tage bis Beginn
- 205,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram pulmonary normal
COVID-19
Dyspnoea
Dyspnoea exertional
Gastrectomy
Hypoxia
Laparoscopic surgery
Malaise
SARS-CoV-2 test positive
Ultrasound Doppler normal
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 7/22/2022 Discharge Date: Jul 23, 2022 PRESENTING PROBLEM: Shortness of breath DOE (dyspnea on exertion) Hypoxia COVID-19 HOSPITAL COURSE: 32 year old female presented with history of transposition of the great vessels status post fontan procedure as an infant who underwent a laparoscopic gastric sleeve procedure on 5th July. She started having symptoms of covid on Tuesday followed by positive covid test. She was admitted to hospital on Saturday. She had CT angio done which was negative for PE though left pulmonary artery was non diagnostic. She is US venous duplex which was negative. She was evaluated by congenital heart. It was felt her symptoms were unlikely from PE. Her symptoms are felt from covid. She was not hypoxic even with exertion. She was discharged home with close follow up with PCP and congenital heart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- L-TGA, levo-transposition of great arteries with ventricular inversion S/P Fontan procedure DILV (double inlet left ventricle) Splenomegaly Status post endometrial ablation Morbid obesity Congenital heart disease Itchy skin Knee stiffness, unspecified laterality Elevated serum protein level Dehydration Increased anion gap metabolic acidosis Hypoglycemia after GI (gastrointestinal) surgery DOE (dyspnea on exertion) COVID-19 virus infection
- Andere Medikamente
- aspirin 81 MG tablet benzonatate (TESSALON) 100 MG capsule fluticasone (FLONASE) 50 MCG/ACT nasal spray levalbuterol (XOPENEX HFA) 45 MCG/ACT inhaler loratadine (CLARITIN) 10 MG tablet montelukast (SINGULAIR) 10 MG tablet omeprazole (
- Allergien
- Keflex [Cephalexin]Hives Reglan [Metoclopramide]Anxiety Contrast Dye [Ivp Dye, Iodine Containing]Other Medrol [Methylprednisolone]Rash, Joint Pain
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 21.01.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 137,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Cardiac monitoring
Dyspnoea
Laboratory test
Palpitations
Symptomtext
I received my 3rd dose on 01/21/2022. My symptoms started on 06/07/2022 I had heart palpation; I couldn't breath; I called my doctor and they did several tests also they put a heart monitor patch told me to go to a cardiologist. I have to wait for the cardiologist to see what is going on. I have low energy. I am not like the way I used to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Labs; Physical tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 24.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Computerised tomogram head normal
Dehydration
Dizziness
Fall
Symptomtext
Narrative: 81 year-old male patient with a PMH of Gi bleed, HTN, afib presented to outpatient hospital ED for weakness/dizziness and multiple falls. He received COVID 19 booster at a facility. In the ED, his BP 134/84, HR 125, RR 16. CT head was unremarkable. He was given fluids, decadron and meclizine for symptoms relief. The team believed the vaccine caused dehydration and worsening of his chronic condition. He was then deemed stable to discharge
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 22.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Condition aggravated
Ear, nose and throat examination
Tinnitus
Symptomtext
the ringing in my left ear has gotten worse and louder; the ringing in my left ear has gotten worse and louder; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Dec2021 at 12:30 as dose 3 (booster), single (Lot number: FL3197) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyrodism" (unspecified if ongoing). Concomitant medication(s) included: ATORVASTATIN; LEVOTHYROXINE; CALCIUM; BIOTIN. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EW0170, Location of injection: Arm Right, Vaccine Administration Time: 10:30), administration date: 24Apr2021, when the patient was 63-year-old, for covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: ER8737, Location of injection: Arm Right, Vaccine Administration Time: 14:15), administration date: 02Apr2021, when the patient was 63-year-old, for covid-19 immunization, reaction(s): "lost some hearing in the left ear", "ringing in my left ear/tinnitus". The following information was reported: TINNITUS (disability), CONDITION AGGRAVATED (disability) all with onset 2021, outcome "not recovered" and all described as "the ringing in my left ear has gotten worse and louder". The events "the ringing in my left ear has gotten worse and louder" required physician office visit. The patient underwent the following laboratory tests and procedures: Acoustic stimulation tests: (unspecified date) lost some hearing in the left ear, notes: He also performed an extensive hearing test and I have lost some hearing in the left ear; Ear, nose and throat examination: (05Oct2021) tinnitus, notes: I had an ENT confirm in an appt on 05Oct2021 that I have tinnitus. Therapeutic measures were not taken as a result of tinnitus, condition aggravated. Clinical course: The patient had not take any other vaccine in four weeks. The patient had not Covid prior vaccination and had not test Covid post vaccination. The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Name: hearing test; Result Unstructured Data: Test Result:lost some hearing in the left ear; Comments: He also performed an extensive hearing test and I have lost some hearing in the left ear.; Test Date: 20211005; Test Name: ENT; Result Unstructured Data: Test Result:tinnitus; Comments: I had an ENT confirm in an appt on 05Oct2021 that I have tinnitus.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism
- Andere Medikamente
- ATORVASTATIN; LEVOTHYROXINE; CALCIUM; BIOTIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 20.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Condition aggravated
Epstein-Barr virus infection
Epstein-Barr virus test positive
Fatigue
Feeling abnormal
Hyperhidrosis
Hypersomnia
Laboratory test abnormal
Thyroxine
Tri-iodothyronine decreased
Symptomtext
After dose 2 I had symptoms of extreme fatigue and reported on separate VAEARS. After dose 3, booster2, my fatigue was worse and continued. I wanted more lab work done because I didn't believe it was just my thyroid issue as determined by Dr. I saw my Natural Path Doctor. She ran T3T4 and looked more closely at my thyroid. My fatigue was really bad. I would come home from work, got to bed, and get up the next morning. I was tested for Lime Disease but it was negative. T3 was low and treated but stopped treatment because I couldn't tell any difference. After she ran more labs she found the Epstein Barr Virus had been reacted. My symptoms are sleeping 10-12 hours a day, sweating and brain fog. My treatment is Epstein Barr Virus drops. She advised me to eat Brazil nuts and seaweed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood panel
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Thyroid issues
- Andere Medikamente
- Adderall; Lisinopril; Levothyroxine; Vitamin D2; Calcium
- Allergien
- Seasonal environmental
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 17.12.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 135,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test normal
Electrocardiogram normal
Extrasystoles
Heart rate irregular
Pain
Palpitations
Pyrexia
Ventricular extrasystoles
Symptomtext
I had a normal reaction of little fever and achiness for a day or two, but then in early May I started having heart palpitations like I was having intense heartbeats 3-4 times in a row and then it would go away and come back. It lasted a week or two. I went to the Doctor and they did blood work and EKG to check for other causes and it was normal and it would happen intermittently. After about 3 weeks, they sort of went away on their own of occasional episodes of 3-4 beats. My pulse felt like my heart was skipping a beat and Doctor thought it was PVC's but it's not an official diagnosis. Doctor said to come back and I would do a 24-hour monitor but they ended up going away after 3 weeks and so I haven't done that. I was cleared to run and keep running after that but to keep an eye on it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Blood work, EKG (May 2022) Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac
- Andere Medikamente
- Multivitamin
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 05.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Abdominal tenderness
Anticoagulant therapy
Atrial fibrillation
Bladder catheterisation
Computerised tomogram abdomen abnormal
Computerised tomogram thorax abnormal
Culture urine positive
Drain placement
Escherichia test positive
COVID-19
COVID-19 pneumonia
Cholecystitis
Cholecystitis acute
Cholecystostomy
Gallbladder disorder
Gastrointestinal tube insertion
Haemoglobin normal
Symptomtext
Pfizer Dose 1 4/6/21 (EM9810) Pfizer Dose 2 5/11/21 (EM9810) Pfizer Dose 3 1/5/22 (FL3197) COVID Positive 1/8/22 COVID Positive 1/13/22 1/13/22: Patient has vascular dementia, altered mental status and is not a reliable historian. Most of the history is obtained by personal review of records. He is 68-year-old resident at nursing home. Past history of stroke, hemiplegia, dysphagia, aphasia, diabetes mellitus, status post craniotomy, status post PEG tube placement, neurogenic bladder and other medical problems. He also has atrial fibrillation and is on chronic Xarelto therapy. Is not known when he was last seen normal. He reportedly was more somnolent. Diagnosed with COVID on 1/8/2022. CT scan of chest shows bilateral pneumonia. He was on 2 L oxygen at the time of my examination. No witnessed seizures as per records. He has atrial fibrillation and is on Xarelto. CT scan of abdomen showed distended gallbladder with surrounding inflammatory changes. 1/22/22: Patient is a 68-year-old male with history of unspecified neurological injury, status post craniectomy, IDDM, neurogenic bladder with chronic Foley catheter, and chronic dysphagia who was admitted on 1/13/2022 with complicated UTI, bilateral COVID pneumonia, acute metabolic encephalopathy, and acute cholecystitis. He was admitted to the medical floor and was started on IV antibiotics, remdesivir, and dexamethasone. His Foley catheter was changed at that time. The general surgeon was consulted. On 1/17/2022 the patient had a CT-guided percutaneous cholecystostomy drain placed. His abdominal pain has essentially resolved since that time. The patient was noted to have some leukocytosis. He had a follow-up abdominal CT which did not show any acute processes. His urine culture grew E coli. He has completed an antibiotic regimen. The patient today is resting in bed and reports that he is feeling much better. He denies shortness of breath at rest, chest pain, palpitations. Still has mild tenderness to the right upper quadrant, but this has been associated to the site of the cystostomy tube. His tube feedings were resumed and he has been tolerating those well. His Xarelto was resumed and his hemoglobin has been stable. He was cleared by surgery for discharge this morning. The patient will be discharged back to long-term care center.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- stroke hemiplegia dysphagia aphasia DM s/p craniotomy s/p PEG neurogenic bladder a fib
- Andere Medikamente
- APAP 650 mg Gtube Q4h PRN bisacodyl 10 mg supp PR QD PRN calcium carbonate 1000 mg Gtube Q12h PRN carvedilol 3.125 mg Gtube BID insulin lispro sliding scale SQ lisinopril 2.5 mg Gtube QD magnesium citrate 17 gm Gtube PRN magnesium hydroxide
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.05.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dyspnoea
Ear pain
Fatigue
Feeling abnormal
Myalgia
Oropharyngeal pain
Oxygen saturation decreased
Pain of skin
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
The symptoms started with a sore throat, I then developed fatigue, brain fog, sore muscles, shortness of breath, low but not critical 02 stats, ear pain, runny nose, my skin felt bruised all over my body. Symptoms started on the 30th and lasted the 5/6th of June.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Covid test - positive until the 10th of June.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; Allergies
- Andere Medikamente
- Lisinopril; Loratadine; Pantoprazole
- Allergien
- NSAIDs; Betablockers; Sulfur drugs; Morphin; Peroxide.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 06.01.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 167,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Accelerated hypertension
Angiogram pulmonary
COVID-19
COVID-19 pneumonia
Chest X-ray normal
Condition aggravated
Inappropriate schedule of product administration
Renal impairment
SARS-CoV-2 test positive
Symptomtext
Patient received pfizer vaccine on 12/2/21 and 1/6/22. Presented to ER on 6/22/22 and found to be COVID positive. admitted on 06/22/2022 with COVID-19 pneumonia. Patient was started on dexamethasone therapy since he was requiring supplemental oxygen at admission (baseline is ambient air but he required as high as 4 L/min; remdesivir presumably contraindicated because of renal impairment). There was a suspicion for PE but CT Angio was inconclusive; a V/Q scan was ordered but patient declined this testing. Acutely accelerated hypertension was also noted and appropriate antihypertensive medication optimization initiated with good results. The patient's respiratory status remained stable. She was ultimately discharged back to his nursing home residence. He will follow-up with his PCP within 1 week. Discharged on 6/24/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accelerated hypertension
- Hospital-Tage
- 2,0
- Labordaten
- 6/22/22 COVID19: positive 6/22/22 chest xray: negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chest pain, Cocaine abuse, Equivocal stress test (8/27/2021), GERD with esophagitis, H/O chest pain, History of stomach ulcers, History of stomach ulcers, Hypertensive heart and kidney disease without heart failure and with stage 3a chronic kidney disease (8/27/2021), Noncompliance with medication regimen (8/27/2021), Other convulsions, Psychotic disorder, Schizoaffective disorder without good prognostic features, Seizures, Stroke, Unspecified essential hypertension, Unspecified essential hypertension, Unspecified psychosis, and Viral hepatitis C without hepatic coma.
- Andere Medikamente
- acetaminophen 325 MG Tabs Commonly known as: TYLENOL 650 mg, Oral, EVERY 4 HOURS PRN, instructions albuterol 108 (90 Base) MCG/ACT Aers Commonly known as: PROVENTIL HFA, VENTOLIN HFA 2 Puffs, Inhalation, EVERY 4 HOURS PRN ARIPiprazole 1
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 18.12.2021
- Beginn
- 18.04.2022
- Tage bis Beginn
- 121,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Dyspnoea
Malaise
SARS-CoV-2 test positive
Symptomtext
I started having symptoms on 4/18/2022 that kept worsening over the next couple of days, and I tested positive for COVID on 4/20/2022. I started having shortness of breath and tightness in my chest so I went to my Dr. at the dr.'s office. I don't remember the name of the Dr., but she gave me an albuterol Inhaler to use and I'm still using it now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Latex; estrogen
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 23.12.2021
- Beginn
- 13.06.2022
- Tage bis Beginn
- 172,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Atelectasis
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Fall
Hiatus hernia
Hypoxia
Lung opacity
Pleural effusion
Pneumonia
Rhabdomyolysis
SARS-CoV-2 test positive
Symptomtext
Patient received moderna vaccine on 3/18/21, 4/15/21 and pfizer vaccine on 12/23/21. Presented to ER on 6/11/22. Admitted due to fall. COVID test not done until 6/13/22 which was found to be COVID positive. She had mild hypoxia, which may be related to CHF as she was receiving fluids for rhabdomyolysis. She was started on remdesivir, steroids, she was also treated for community-acquired pneumonia. On room air starting 6/18/22 so remdesivir was stopped. Patient was discharged on 6/21/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 10,0
- Labordaten
- 6/13/22 COVID19: positive 6/13/22 chest xray: The patient has ground-glass opacity within the right lower lobe compatible with COVID pneumonia is difficult to see on chest radiography. Bibasilar atelectasis with bilateral effusions is again seen. The patient's large hiatal hernia is again demonstrated. The overall appearance of the aeration of the lungs is worse 6/17/22 chest xray: Interval improved aeration of the lungs with residual small right pleural effusion.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression, major, recurrent, severe with psychosis (HCC), GAD (generalized anxiety disorder), GERD (gastroesophageal reflux disease), Glaucoma, Hypertension, Hypokalemia (4/17), and MCI (mild cognitive impairment).
- Andere Medikamente
- Amitriptyline HCl 50 mg Oral NIGHTLY Brimonidine Tartrate 0.2 % 1 Drop Both Eyes 2 TIMES DAILY Cetirizine HCl 10 mg Oral DAILY Dexamethasone 6 mg Oral DAILY WITH BREAKFAST dilTIAZem HCl Coated Beads 300 mg Oral DAILY Escitalopram Oxala
- Allergien
- ciprofloxacin and ceftin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 22.12.2021
- Beginn
- 02.06.2022
- Tage bis Beginn
- 162,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood gases
Blood pH normal
Brain natriuretic peptide normal
C-reactive protein increased
COVID-19
Computerised tomogram thorax abnormal
Cough
Hypoxia
Infection
Lung disorder
Lung opacity
Organising pneumonia
Oxygen saturation decreased
PCO2 normal
PO2 decreased
Positron emission tomogram abnormal
Procalcitonin normal
Red blood cell sedimentation rate increased
Symptomtext
Patient received pfizer vaccine on 12/1/21 and 12/22/21. Presented to ER on 6/2/22 and found to be COVID positive. Patient has been having coughing spells since January . He had COVID infection in Sept 21, and again in Feb 22. He received Pfizer vaccine in December 21. A CT scan done in Feb 22 was unremarkable. He had a follow-up PET scan for his lymphoma with Dr. on May 9th 2022 which showed multicentric ground-glass opacities as well as airspace disease which are scattered in a multilobar fashion bilaterally. Patient has received at least 3 courses of different antibiotics (Z pack, Doxycycline and Ceftin) but continued to cough. Due to concern for drug-induced (Rituximab) pneumonitis, he was started on high-dose steroids which he has taken about 2 weeks without any improvement. Patient noted to be desatting to mid 80's at home with activity hence he presented to the ED on 6/2/22. Again he tested positive to COVID on 6/22. Work up done included BNP (wnl), CRP 50 (elevated ) ESR 37 (elevated ). procalcitonin wnl. ABG showed pH 7.45, PCO2 42, PO2 62. Patient did require 2 L of nasal cannula oxygen at first. He was started on doxycycline as well as short course prednisone taper. He was seen by ID, pulmonology and oncology services. CT chest wo contrast showed worsening bilateral ground-glass opacities probably organizing pneumonia or atypical infection. Work up for fungal infection and vasculitis was started. Results still pending as at time of discharge. Patient did well. Hypoxia resolved. On 6/6/22, he was discharged hoe in stable condition; plan to complete short course of prednisone taper and 3 more days lf antibiotics. 6 minute walk test showed he needed no oxygen. Discharged on 6/6/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Organising pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- 6/2/22 COVID19: positive 6/3/22 CT chest: Worsening bilateral ground-glass opacities. This could relate to organizing pneumonia or atypical infection. Eosinophilic pneumonia a consideration as well
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, morbid obesity, paroxysmal AFib, sleep apnea, port insertion, colonoscopy 2017, lymph node biopsy, right inguinal area, tonsillectomy.
- Andere Medikamente
- albuterol 108 (90 Base) MCG/ACT Aers Commonly known as: PROVENTIL HFA, VENTOLIN HFA 2 Puffs, Inhalation, EVERY 4 HOURS PRN carvedilol 25 MG Tabs Commonly known as: COREG 25 mg, Oral, 2 TIMES DAILY cetirizine 10 MG Tabs Commonly known a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 13.01.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 122,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest pain
Fatigue
Headache
Mobility decreased
Nasopharyngitis
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Her symptoms started with tiredness. She had no other symptoms but got a call from her friends that had tested positive. That day, she had symptoms of a cold of a runny nose, headache, sore throat, body aches, and a low grade fever. So she took an at home COVID-19 test that was positive. Her symptoms progressed. She was in bed for 1 week. She had to go to the urgent care due to pain in her chest. While there, her breathing was fine. She was prescribed a steroid for 3 days to help with the inflammation. And also took the prescribed Albuterol as well if needed. She still has lingering effects of the tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Fluoxetine 20mg once daily, Albuterol Inhaler taken prn
- Allergien
- Milk intolerance
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 04.01.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 88,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Blood test
COVID-19
Chest X-ray
Cough
Dyspnoea
Electrocardiogram
Fatigue
Gait disturbance
Heart rate increased
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I was at the airport getting ready to fly home so I had to take a test to get on my flight home. I tested positive but had no symptoms at the time. I went back to my host's apartment and the next day I was taken to the quarantine center the next day. I developed a sore throat and was very fatigued. I have a chronic cough so I did have a cough but I do not notice it from covid. The next day I was so exhausted I could not walk and had to be in a wheel chair- I was fighting to breath. My pulse and blood pressure were both high. I had started the meds for treatment after I arrived to the treatment center. I had my first negative test on April 8th and I was then able to travel home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- CoVID Test, Chest x-ray, blood test- not sure what but was used to see if I could take the antiviral meds, ECG,
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Bronchitis, Minor Mitrovalve regurgitation, High Cholesterol
- Andere Medikamente
- Albuterol, Celexa, Lipitor, Celexa, I take an allergy med but change it so it would have been Allergra, Zyrtec, or Clairton- No sure which one
- Allergien
- Flexeril
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 03.05.2021
- Beginn
- 17.05.2022
- Tage bis Beginn
- 379,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Atrial fibrillation
Dyspnoea
Laboratory test
Symptomtext
Pt came to ED c/o of SOB with new onset of AFib. Pt tested + upon discharge for placement to snf
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ETOH, HTN, HLD, PVD, Meniere's disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 14.04.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 273,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
COVID-19 pneumonia
Confusional state
Dizziness
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Symptomtext
Narrative: The patient received two doses of Pfizer COVID 19 Vaccine in April 2021 and Jan 2022. The patient tested positive for COVID 19 on 12 Jan 2022. The patient was admitted to a community hospital with dizziness and confusion due to COVID 19. The patient left the facility against medical advice and ended up admitted to another hospital on 19 Jan 2022 with covid pneumonia. The patient was treated with dexamethasone and discharged on 1 February 2022 in stable condition. Reported per EUA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 120,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dyspnoea
Hypoxia
Polyuria
Pyrexia
COVID-19
Chest X-ray abnormal
Chills
Chronic obstructive pulmonary disease
Condition aggravated
Respiratory disorder
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 5/3/2022 Discharge Date: 5/7/2022 PRESENTING PROBLEM: Acute exacerbation of chronic obstructive pulmonary disease (COPD) (HCC) [J44.1] COVID-19 virus infection [U07.1] Acute respiratory disease due to COVID-19 virus [U07.1, J06.9] HOSPITAL COURSE: Patient is a 57 y.o. male who presents today with dyspnea hypoxia cough and subjective fever and chills. He has had the symptoms for 2 days becoming progressively worse. He has a history of chronic obstructive pulmonary disease and came to the emergency department for evaluation. He was hypoxic and started on 2 L of supplemental oxygen. COVID-19 testing was positive. He is fully vaccinated with 3 doses. Chest x-ray showed possible airspace disease but pattern was not consistent with COVID. I was contacted by the emergency department staff agreed to admit him for acute respiratory disease secondary to COVID-19 and exacerbation chronic obstructive pulmonary disease. Continue aggressive pulmonary toilet monitor serial labs keep him diuresed well and monitor daily weights. Supplemental oxygen to maintain sats above 88%. Steroids and inhalers for chronic obstructive pulmonary disease. patient was admitted and treated with aggressive pulmonary toilet Remdesivir and dexamethasone. He responded well to therapy where the weaning of supplemental oxygen over the next couple of days. His chronic obstructive pulmonary disease stabilized as well he was seen on the day of discharge on room air anxious to go home. He was subsequently discharged home to return to his regular medication regimen as previously ordered. Diet and activity as tolerated. He was recommended follow-up with primary care provider in 7-10 days. He has recommended isolate until May 11th. He understood all these instructions and was discharged home in stable condition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Primary hypertension Type 2 diabetes mellitus without complication, without long-term current use of insulin (HCC) Dyslipidemia Fracture of proximal end of right humerus with routine healing Chest pain, unspecified type ASHD (arteriosclerotic heart disease) Fatigue Cough Sepsis due to pneumonia (HCC) Left subclavian artery occlusion Seizure disorder (HCC) Chronic obstructive pulmonary disease with acute lower respiratory infection (HCC) Chronic pain Stroke (HCC) Anxiety Acute respiratory failure with hypoxemia (HCC) Neurogenic orthostatic hypotension (HCC) Acute occlusion of aortoiliac artery due to thrombosis (HCC) Critical lower limb ischemia (HCC) Aortoiliac occlusive disease (HCC) Hypercholesterolemia Tobacco abuse Postoperative hypoxia Peripheral vascular disease (HCC) Unstable angina (HCC) Hypokalemia STEMI (ST elevation myocardial infarction) (HCC) Ischemic cardiomyopathy Long term current use of antiarrhythmic drug Gastro-esophageal reflux disease without esophagitis Paroxysmal atrial fibrillation (HCC) S/P drug eluting coronary stent placement Blood-tinged sputum Pulmonary nodule Congestive heart failure (HCC)
- Andere Medikamente
- ALPRAZolam (XANAX) 1 MG tablet amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 80 MG tablet clopidogrel (PLAVIX) 75 MG tablet empagliflozin (JARDIANCE) 10 MG tablet Fluticasone Furoate 100 MCG
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 28.01.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 20,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
Bronchitis
COVID-19
Carditis
Chest discomfort
Dyspnoea
Echocardiogram normal
Electrocardiogram normal
Vaccine breakthrough infection
X-ray normal
Symptomtext
Breakthrough of COVID after vaccines. I had pressure in my chest and difficulty breathing. I went to the ER where I was told I had Bronchitis and swollen of the heart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- EKG-normal, Echocardiogram-normal, X-ray-normal, Bloodwork - normal
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Prenatal vitamins, iron pills
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Angina pectoris
Arrhythmia
Chest discomfort
Defect conduction intraventricular
Dizziness
Dyspnoea
Echocardiogram normal
Electrocardiogram abnormal
Hypertension
Impaired work ability
Malaise
Symptomtext
Tightness in chest, Angina and troubles catching my breath. All symptoms occurred within a few days of booster shot. Similar symptoms after 2nd dose in series although not as acute and noticeable. Breathing issues and heart pain persisted for approximately 3-4 months. I was working in the operating room on Jan. 25th and could not catch my breath. The anesthesiologist took my BP. Blood pressure was high for me (~145/90). I was immediately relieved of my duties and wheeled to the E.R. A full EKG was performed and the E.R. doc noted Intraventricular conduction delay as well as high BP. This subsided after an hour or so. I was sent home 3 hours later feeling light-headed and not well. January 29th I was sent to the E.R. a 2nd time. This was at a different facility. A full lead EKG was performed. No signs of a heart attack and I was sent home 3-4 hours later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Early February I had a visit with Cardiologist. Confirmed heart arrhythmia. Feb. 11th - Visit with Cardiology clinic Feb. 18th - Echo March 9th - Stress echo Results within normal limits. Symptoms subsided in April.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Treated for Lyme disease in 2014
- Andere Medikamente
- Lamictal, Lyrica, Propecia prescription. Baclofen/Diazapam as needed (last taken 8 months ago). Multivitamins Omega 3/6. Resveratrol. Pepsid AC
- Allergien
- Cox2 inhibitors Walnuts and Pinneapples
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 17.12.2021
- Beginn
- 08.03.2022
- Tage bis Beginn
- 81,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac monitoring abnormal
Chest pain
Electrocardiogram normal
Heart rate increased
Palpitations
Tachycardia
Symptomtext
Started feeling that my heart was racing. I have a watch that reads my heart rate and it was saying that my heart rate was evaluated. Then, a few hours later, I started having chest pains. I went to the ER. They did an EKG, normal results. They referred my to a cardiologist. The cardiologist gave me a heart monitor to wear for a few days. That showed that I had tachycardia but he don't think that it is anything serious. The tachycardia is still ongoing as of today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lepro
- Allergien
- Celery
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 24.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Chest pain
Ear pain
Electrocardiogram normal
Symptomtext
Child presented to Urgent Care on 4/20/22 for ear pain. Pulse was 130 -140 (persistent) Mom stated child had one dose of vaccine at their primary care provider in January and developed chest pain a few days later. Never evaluated previously. Referred child to primary care provider for more complete evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG: NSR CXR: WNL 4/20/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- club right and left foot
- Andere Medikamente
- Benadryl ; topical steroid cread
- Allergien
- No known drug or food allergy
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 17.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Alopecia
Band sensation
Blood test normal
Fatigue
Headache
Inflammation
Paraesthesia
Thyroid function test normal
Tinnitus
Symptomtext
About 4 days after the third Pfizer shot, I started having a constant head humming, tingling in my head, intermittent headaches and inflammation in my head. This has been ongoing for four months now. Only about 4 weeks ago the tingling, inflammation and headache feeling in my head and face went away. I still have humming in my head. This became more intermittent; still a daily occurrence, but it's not constant. I've also had excessive fatigue and excessive hair loss. My hair has come out in clumps every day. I had bloodwork done. My thyroid is normal and so was my full blood panel.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Bloodwork done in January.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pantoprazole
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.01.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 42,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Angiogram normal
Chest X-ray normal
Cough
Echocardiogram abnormal
Hypoxia
Leukocytosis
Obesity
Oxygen saturation abnormal
Oxygen saturation decreased
Pulmonary hypertension
Pulmonary sepsis
Respiratory viral panel
Symptomtext
admitted 2/15 with cough, leukocytosis, chest x-ray unremarkable, CT angiogram without consolidation, ongoing desaturations hypoxia noted, findings of severe sepsis secondary to to this from presumed pulmonary origin. We initiated IV antibiotic therapy, pulmonary consulted, respiratory viral pathogen negative, echo showed mild pulmonary pretension, nocturnal hypoxia noted suspicious for OSA in setting of obesity. Will discharge on 2 L nocturnal, with upcoming OSA evaluation ordered. Patient improved through hospital course, was discharged home with nocturnal oxygen support given to find hypoxia on overnight oximetry study. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary hypertension
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 14.04.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 273,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
COVID-19 pneumonia
Confusional state
Dizziness
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Symptomtext
Narrative: The patient received two doses of Pfizer COVID 19 Vaccine in April 2021 and Jan 2022. The patient tested positive for COVID 19 on 12 Jan 2022. The patient was admitted to a community hospital with dizziness and confusion due to COVID 19. The patient left the facility against medical advice and ended up admitted to the hospital on 19 Jan 2022 with covid pneumonia. The patient was treated with dexamethasone and discharged on 1 February 2022 in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injected limb mobility decreased
Pain in extremity
Wrong technique in product usage process
Symptomtext
Almost 24 hours after vaccine booster, my arm started to hurt, I couldn't move it, I was in extreme pain, couldn't do anything. I went into the Dr. office on an emergency basis as it was very painful. The doctor pressed on my decollete in 3 different areas using her 2 index fingers. The first press was at the top of decollete and no pain, the second press was more inward then the first press and caused very bad pain. The doctor indicated the vaccine had gotten into my joints and gave me a shot of cortisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- I also had a Shingrix vaccine on the same date as the booster vaccine. The Shingrix was in the left arm and the booster was in the right arm. The right arm is where I had issues.
- Vorgeschichte
- Asthma Bronchitis High blood pressure High cholesterol
- Andere Medikamente
- 25 mg Hydrochlorothiazide in AM - Daily 25 mcg Levothyroxine in AM - Daily 20 mg Omprazole - AM & PM - Daily 2x/day 10 mg Montelukast in PM - Daily 30 mg Amitriptyline in PM - Daily 40 mg Pravastatin in PM - Daily
- Allergien
- Allergic to crab.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 28.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: ja
Arthralgia
Blood pressure fluctuation
C-reactive protein increased
Cognitive disorder
Condition aggravated
Head discomfort
Hyperacusis
Hypoaesthesia
Limb discomfort
Mobility decreased
Multiple sclerosis relapse
Muscle spasticity
Pain
Paraesthesia
Pyrexia
Tinnitus
Symptomtext
Autoimmune flare lasting seven weeks. Unable to function for seven weeks. Neuro: head pressure, blaring tinnitus,leg numb/heavy/spacticity, tingling extremities and face, cognitive dysfunction, extreme noise sensitivity,. Musculoskeletal: joint pain both hips, body aches,. Cardiac: blood pressure fluctuations to very low, low grade fevers 5 weeks after shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- C reactive protein 4.5
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- MS / autoimmune disease
- Andere Medikamente
- Low-dose naltrexone, medical marijuana, vitamin b complex, magnesium, alpha lipoid acid
- Allergien
- -
- Vorherige Impfungen
- Autoimmune flare first Covid dose
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Cold sweat
Dizziness
Hot flush
Nervousness
Palpitations
Tremor
Symptomtext
Heart racing 80 bpm resting cold sweats nervousness light headed and dizzy constant heart flutter !!! all the time shaky hands hot flashes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- artirial flutter started a week after 2nd dose
- Vorgeschichte
- none
- Andere Medikamente
- Diltiazam 30 mg metoproperol 25mg lisinopril 10mg buspirone 5mg
- Allergien
- none
- Vorherige Impfungen
- phyzer ep7533
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 03.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antibody test
Antinuclear antibody
Blood group B
Blood magnesium
Chills
Dry skin
Fall
Feeling abnormal
Muscle spasms
Muscle tightness
Myalgia
Neck pain
Night sweats
Pain
Pain in extremity
Paraesthesia
Pharyngeal enanthema
Rash
Symptomtext
tingly toes; The pain is like spasms; chills; night sweats; Hands/arms falling asleep; Shooting pain that felt like pulling in different directions in her arms, calf, and thigh/ It was a mild pain; it started to heel but skin was very dry for the next two weeks; Rash on her face, throat, chin, and around her eyes/rash all over her face; Rash on her face, throat, chin, and around her eyes; Tingling in feet & Hands; tingling in feet and hands; Back of her neck on one side was really tight; Pains in her muscles and nerves like they are pulling in different directions; There are pin points all over her body, like on her calves and the back of her arms; Neck pain; Arm was sore; zapping feeling in finger tips; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 30 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 14:30 (Lot number: FL3197) at the age of 30 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: RASH (non-serious) with onset 03Jan2022 21:00, outcome "recovered", described as "Rash on her face, throat, chin, and around her eyes/rash all over her face"; PHARYNGEAL ENANTHEMA (non-serious) with onset 03Jan2022 21:00, outcome "recovered", described as "Rash on her face, throat, chin, and around her eyes"; PARAESTHESIA (non-serious) with onset 03Jan2022 15:30, outcome "not recovered", described as "Tingling in feet & Hands"; MUSCLE TIGHTNESS (non-serious) with onset 03Jan2022, outcome "not recovered", described as "Back of her neck on one side was really tight"; PAIN (non-serious) with onset 04Jan2022, outcome "not recovered", described as "Shooting pain that felt like pulling in different directions in her arms, calf, and thigh/ It was a mild pain"; MUSCLE SPASMS (non-serious) with onset 05Jan2022 14:00, outcome "not recovered", described as "The pain is like spasms"; MYALGIA (non-serious) with onset 03Jan2022, outcome "unknown", described as "Pains in her muscles and nerves like they are pulling in different directions"; PARAESTHESIA (non-serious) with onset 03Jan2022, outcome "not recovered", described as "There are pin points all over her body, like on her calves and the back of her arms"; NECK PAIN (non-serious) with onset 03Jan2022, outcome "not recovered", described as "Neck pain"; PAIN IN EXTREMITY (non-serious) with onset 03Jan2022, outcome "recovering", described as "Arm was sore"; FALL (non-serious) with onset 04Jan2022, outcome "not recovered", described as "Hands/arms falling asleep"; PARAESTHESIA (non-serious) with onset 03Jan2022 15:30, outcome "not recovered", described as "tingling in feet and hands"; CHILLS (non-serious) with onset 05Jan2022, outcome "unknown", described as "chills"; NIGHT SWEATS (non-serious) with onset 04Jan2022, outcome "recovered" (07Jan2022), described as "night sweats"; PARAESTHESIA (non-serious) with onset 06Jan2022, outcome "not recovered", described as "tingly toes"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "unknown", described as "zapping feeling in finger tips"; DRY SKIN (non-serious) with onset 04Jan2022, outcome "not recovered", described as "it started to heel but skin was very dry for the next two weeks". The events "rash on her face, throat, chin, and around her eyes/rash all over her face", "rash on her face, throat, chin, and around her eyes", "tingling in feet & hands", "the pain is like spasms", "hands/arms falling asleep", "tingling in feet and hands", "chills", "night sweats", "tingly toes" and "zapping feeling in finger tips" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash, pharyngeal enanthema, muscle spasms (neurologist, allergist, PCP, Magnesium steroids), fall, paraesthesia. Therapeutic was taken by patient for events Hands/ Arms falling asleep (therapy included PCP, Neurologist, allergist), Face rash and Tingling in feet & hands. Additional information: Reporter reported that the tingles happened immediately afterwards when patient was in the car driving home. patient noticed that in her feet at that time. Later that night and into the next day it started pinpointing in different sections and patient felt like it was in her muscles or her nerves. Inquired for outcome and she says that the rash isn't as red today as it was yesterday but it was still there. Everywhere it was a little bit less red but the rest of her reactions are the same. Also, her arm was sore on that first day and yesterday but today it was less sore. For rash treatment Benadryl and it helped a bit. On 03Jan2022 patient had the first shot of Pfizer at 02:30 PM. Around 3 PM patient felt tingling in his feet & the back of my neck felt tight. That night around 9 PM patient developed a rash on his face & neck. It was raised, red & itchy. The next morning it was still there. Patient took Claritin and it started to heel but skin was very dry for the next two weeks my arm & hand fell asleep while sleeping 04Jan and that has never happened to me before. The next day on05Jan patient had chills and muscle spasm in his legs, feet and arm also had pain in his jaw. On 06Jan patient had tingly toes again and a zapping feeling in finger tips. On 07Jan patient started getting cramping in his toes and feet feel like she had an elbow in her throat. 04Jan-07Jan had night sweats 09Jan rash developed on his face again started to see within 1 day after, since patient have had persistent muscle spasm mainly in her feet 7& legs but really have them all over the body. Patient also have tingly feelings in her feet & readably his hands/ arms fall asleep every other night or so Patient had a bunch or blood work done, all looks normal. Patient saw a neurologist and they were not concerned & have an appointment with an allergist on 18Jan. she was taking magnesium but nothing else and have not noticed too much or a difference PCP & neuro did not have a diagnosis and dais it was a state to get 2nd shot would like more assurance before doing so as his worse rear this gets worse with 2nd shot. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220107; Test Name: Antibody; Test Result: Negative ; Test Date: 20220119; Test Name: Antibody; Result Unstructured Data: Test Result:Negative; Test Date: 20220107; Test Name: ANA; Test Result: Negative ; Test Date: 20220119; Test Name: ANA; Result Unstructured Data: Test Result:Negative; Test Date: 20220119; Test Name: ABO; Result Unstructured Data: Test Result:B+; Test Date: 20220107; Test Name: Magnesium; Result Unstructured Data: Test Result:1.9 mg/dL; Comments: Normal Low- 1.3 Normal High- 2.7; Test Date: 20220119; Test Name: ESR; Result Unstructured Data: Test Result:7 mm/hr; Comments: Normal Low-0 Normal High- 20; Test Date: 20220107; Test Name: B12; Result Unstructured Data: Test Result:1,236; Comments: Normal Low-211 Normal High- 911
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hypertension
Symptomtext
Dizziness, Patient reported history of hypertension and dizziness. BP: 160/80 Pulse: 62 RR: 19 After 15mins BP went down 128/74, Pulse 64, RR 18. Patient reported no more dizziness. Patient stable went home accompanied by wife.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Carditis
Chest discomfort
Chest pain
Chiropractic
Discomfort
Dyspnoea
Electrocardiogram
Feeling abnormal
Headache
Inflammation
Insomnia
Mental impairment
X-ray
Symptomtext
Inflammation around the heart, armpit, chest and back. Headaches, mental fog and unable to fully function before vaccine. Chest pain, struggle to breath, heaviness on the chest and neck. Unable to sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, blood work, X-ray, chiropractic care and over the counter meds.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Gait disturbance
Myalgia
Vaccination site pain
Symptomtext
now experiencing chest pain; he is having a hard time walking; muscle pain; pain at the injection site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 14 year-old male patient received bnt162b2 (BNT162B2), administration date 09Feb2022 (Lot number: FL3197) at the age of 14 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, ), administration date: 17May2021, when the patient was 14 years old, for Covid-19 immunization; Bnt162b2 (Dose: 2, ), administration date: 07Jun2021, when the patient was 14 years old, for Covid-19 immunization. The following information was reported: CHEST PAIN (non-serious) with onset 10Feb2022, outcome "not recovered", described as "now experiencing chest pain"; GAIT DISTURBANCE (non-serious) with onset 10Feb2022, outcome "unknown", described as "he is having a hard time walking"; MYALGIA (non-serious) with onset 10Feb2022, outcome "unknown", described as "muscle pain"; VACCINATION SITE PAIN (non-serious) with onset 10Feb2022, outcome "unknown", described as "pain at the injection site". Therapeutic measures were taken as a result of chest pain, gait disturbance, myalgia, vaccination site pain. Additional information: It was reported She says she does not have her son's vaccine card with her to provide NDC/LOT/EXP for the first two doses. Stated her son started having chest pain this morning, and when she called him he said he still has pain but did not say if it was worse or the same. She says she told him to take regular Tylenol that she has at home and put some ice on the pain on his leg, which is muscle pain on the right side. She says he is having a hard time walking and putting pressure on it, he has pain that is pretty bad pain. She says the chest pain, muscle pain, and injection site pain all started today because yesterday when she asked he said nothing hurt, it started this morning. She also stated that the whole family got COVID, and they had all got booster, and her son got to 6 months already so just in case, he got COVID booster. Caller clarifies that they had all gotten the booster dose last month except her son, and says then we all got infected, in the last couple weeks ago the family all tested positive except him. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 19.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Condition aggravated
Fatigue
Gait disturbance
Muscle spasms
Musculoskeletal stiffness
Nausea
Neuromyotonia
Pain
Pain in extremity
Pyrexia
Symptomtext
i can barely walk. severe muscle spasms and cramping. fever sore arm nausea and severe fatigue and overall pain. Such severe stiffness and cramping that it causes severe pain to move- body in lock down. Have not had this severe cramping in over 24 months when diagnosed with neuromyotonia. Started this morning around 10 and is worsening. Last 2 pfizer vaccines didnt give any other symptoms except mild soreness in arm and a liitle fatigue on second dose- July 3, 2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none - i have no insurance and no way to get to doctor
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- neuromyotonia with possible isaac?s disease HTN hashimotos thyroid Severe hearing loss from pencillen reaction reactive hypoglycemia PTSD
- Andere Medikamente
- levothyroxine
- Allergien
- Penicillin and pineapple- anaphylactic sulfa drugs and zonagran and tegretol- rash bleach, perfume, smoke- wheezes adhesive- blisters rash
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 15.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Audiogram normal
Condition aggravated
Hypoacusis
Sudden hearing loss
Tinnitus
Symptomtext
Sudden onset of hearing loss in both ears (left side more severe), distorted hearing, everything sounded muffled, unable to understand what teachers and classmates were saying, also had tinnitus, lasted for 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Able to see an audiologist and get audio gram two days after onset of symptoms (1/21/2022). By then all symptoms had resolved. Audiogram showed no difference from her baseline.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild to moderate hearing loss in left ear
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Eyelid irritation
Nausea
Vision blurred
Symptomtext
heart area/chest pain, sometime dull sometimes sharp pain and discomfort; heart area/chest pain, sometime dull sometimes sharp pain and discomfort; nausea; blurry vision developed and lasted for 2 weeks; felt very heavy impurity inside of upper eyelid; This is a spontaneous report received from contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 54 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 12Jan2022 10:30 (Lot number: FL3197) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing), notes: other medical history: asthma; "sulfite" (unspecified if ongoing), notes: known allergies: sulfite. Concomitant medication(s) included: PULMICORT. Past drug history included: Aspirin, reaction(s): "Allergy: aspirin", notes: known allergies: aspirin; Penicillin, reaction(s): "allergies: penicillin", notes: known allergies: penicillin. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6208, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 17Mar2021, when the patient was 53 years old, for Covid-19 Immunization, reaction(s): "heart area/chest pain, sometime dull sometimes sharp pain and discomfort ", "nausea"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0150, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 12Apr2021, when the patient was 53 years old, for Covid-19 Immunization, reaction(s): "heart area/chest pain, sometime dull sometimes sharp pain and discomfort ", "nausea". The following information was reported: CHEST PAIN (non-serious), CHEST DISCOMFORT (non-serious) all with onset 13Jan2022, outcome "recovered with sequelae" and all described as "heart area/chest pain, sometime dull sometimes sharp pain and discomfort"; NAUSEA (non-serious) with onset 13Jan2022, outcome "recovered with sequelae", described as "nausea"; VISION BLURRED (non-serious) with onset 13Jan2022, outcome "recovered with sequelae", described as "blurry vision developed and lasted for 2 weeks"; EYELID IRRITATION (non-serious) with onset 13Jan2022, outcome "recovered with sequelae", described as "felt very heavy impurity inside of upper eyelid". Therapeutic measures were not taken as a result of chest pain, chest discomfort, nausea, vision blurred, eyelid irritation. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination included ProAir Inhaler sometimes. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Device Date: 30Jan2022. It was reported that the patient experienced heart area/chest pain, sometime dull sometimes sharp pain and discomfort with nausea in all 3 stages of vaccine. In 3rd vaccine there were more symptom with her eyesight. She had blurry vision developed and lasted for 2 weeks. She felt very heavy impurity inside of upper eyelid. Adverse event resulted in none of the above. The reporter assessed the case as non-serious with no seriousness criteria of resulting in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, Congenital anomaly/birth defect. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (other medical history: asthma); Reaction to sulfites (known allergies: sulfite)
- Andere Medikamente
- PULMICORT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 17.12.2021
- Beginn
- 07.02.2022
- Tage bis Beginn
- 52,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood creatine phosphokinase increased
Blood creatinine increased
Blood culture negative
Blood lactate dehydrogenase increased
Blood sodium decreased
Brain natriuretic peptide increased
Culture urine negative
Echocardiogram normal
Enterovirus test negative
Fibrin D dimer
Full blood count abnormal
Human rhinovirus test
Hypotension
Laboratory test abnormal
Leukopenia
Lip erythema
Multisystem inflammatory syndrome in children
Ocular hyperaemia
Symptomtext
Patient received first dose 12/17/2021 and second dose1/7/2022. Developed URI between two vaccines. One month after URI and second dose, developed fever, rash, red eyes, red lips, hypotension and findings consistent with MIS-C
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- 2/13: CBC with elevated white count, leukopenia, creatinine 2.97, Troponin 2293, BNP 5357, chemistries with low sodium, DDimer 7.71, LDH 452 CK 980 Procalcitonin 65.37, RPP with rhino/enterovirus, blood and urine cultures negative, echocardiogram done-no failure, COVID-19 nucleocapsid IgG positive
- Aktuelle Erkrankungen
- URI after the vaccine dose 1 and before second dose
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 17.12.2021
- Beginn
- 07.02.2022
- Tage bis Beginn
- 52,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood creatine phosphokinase increased
Blood creatinine increased
Blood culture negative
Blood lactate dehydrogenase increased
Blood sodium decreased
Brain natriuretic peptide increased
Culture urine negative
Echocardiogram normal
Enterovirus test negative
Fibrin D dimer
Full blood count abnormal
Human rhinovirus test
Hypotension
Laboratory test abnormal
Leukopenia
Lip erythema
Multisystem inflammatory syndrome in children
Ocular hyperaemia
Symptomtext
Patient received first dose 12/17/2021 and second dose1/7/2022. Developed URI between two vaccines. One month after URI and second dose, developed fever, rash, red eyes, red lips, hypotension and findings consistent with MIS-C
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- 2/13: CBC with elevated white count, leukopenia, creatinine 2.97, Troponin 2293, BNP 5357, chemistries with low sodium, DDimer 7.71, LDH 452 CK 980 Procalcitonin 65.37, RPP with rhino/enterovirus, blood and urine cultures negative, echocardiogram done-no failure, COVID-19 nucleocapsid IgG positive
- Aktuelle Erkrankungen
- URI after the vaccine dose 1 and before second dose
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 26.12.2021
- Beginn
- 30.01.2022
- Tage bis Beginn
- 35,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
This was the Booster shot (3rd shot). I had the Exact same symptoms when I had the 2nd COVID-19 Pfizer dose/shot in my left arm. The 1st and 2nd vaccine shots were done in March 2021. With the 2nd shot, my left arm was achey/painful. With this 3rd shot that I'm reporting here- the Booster shot that I got 12/26/2021, my arm hurt even worse and felt like it was going to fall off. I had difficulty lifting my arm. That extreme pain lasted for a week. And then my arm started with slight soreness on the morning of 1/30/22 and then it felt the exact same (as the booster shot pain) later by mid-morning and throughout the day and through the week...like my arm was going to fall off. Again, it was difficult in lifting my arm. At this time, the major pain is primarily gone but there is the slight soreness I feel at times. I did take tylenol once.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure; Sciatica & chronic low back pain
- Andere Medikamente
- Prescription high blood pressure meds; other Prescriptions include Potassium pills, Vitamin D3 pills, Iron pills, Birth control pills; Vitamins taken daily include Centrum Women's Multivitamin & Emergen-C vitamins
- Allergien
- Have allergic reactions to Chamomile foods/products
- Vorherige Impfungen
- 2nd COVID-19 Pfizer Vaccine, I had chills, body aches, slight fever, nausea. 3rd COVID-19 Pfizer Booster Vaccine, I had the extr
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 30.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Symptomtext
Client presented to the vaccine site for 2nd dose COVID Pfizer vaccine on 1/20/2022. Client received 1st dose COVID Pfizer vaccine on 12/30/2021 and reported that she experienced "sharp chest pain" rated 9/10 3 days after receiving the vaccine. Client described the pain as "sharp and heavy" and explained that she continues to experience this intermittently, approximately 2-3 times per week lasting for 2 minutes at a time. Client reported to Lead RN that she had not followed up with her PCP. Client disclosed that she had an IUD inserted on 12/29/21. Client reported NKDA and no chronic health conditions. Lead RN submitted medical consult for guidance on administration of 2nd dose COVID Pfizer vaccine. Vaccine Operations Lead forwarded guidance from MD with approval for Pfizer 2nd dose and recommendation for "f/u with provider re other health issues". Lead RN advised the client to follow up with PCP regarding chest pain. At 1348 client received the 2nd dose COVID Pfizer vaccine (lot #FJ6369) in the L deltoid. No adverse reaction was reported by client during her 15 minute observation. Client left vaccine site with a steady and symmetrical gait at 1405.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Hyperhidrosis
Tremor
White blood cell count abnormal
Symptomtext
severe chills shaking throughout the night Profuse sweating Headache All these lasted for 3days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Blood test - White blood cell was abnormal
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- U
- Eingang
- 13.02.2022
- Impfdatum
- 05.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heat therapy
Injected limb mobility decreased
Injection site pain
Massage
Pain
Symptomtext
- L shoulder pain - point tenderness to posterior deltoid - soreness and pain with abduction greater than 100 degrees also extension greater than 30 degrees - Treating w/ Ibuprofen, heat, rest, massage
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -seasonal allergies -asthma -Dermographism
- Andere Medikamente
- Zyrtec turmeric Flonase albuterol
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injected limb mobility decreased
Injection site pain
Symptomtext
Very sore shoulder (area where shot was administered) for 2 days..could hardly raise or move arm. Extreme fatigue starting that evening until Saturday night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 2 Diabetes, Idiopathic Pulmonary Fibrosis
- Andere Medikamente
- 1 - Fenobibric Morning 145mg 1 - Atorvastatin Calcium Morning 40mg 2 - Carvedilol (1 Morning & 1 Night) 12.5mg Basaglar 150 units daily (75 ? morning/75 - evening) Budesonide/Formoterol Fumarate Dihydrate 160-4.5 INH1 - (2 spray
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Pain
Symptomtext
Patient waited at Pharmacy for 15 minutes then checked out groceries. Went to car & developed severe chest pain, SOB & pain on left side. Went home. Pain lasted until 3AM 12-29-21. after 3 pfizer shots did not cause this
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Bursitis
Injected limb mobility decreased
Injection site pain
Symptomtext
Site: Pain at Injection Site-Severe, Additional Details: Patient states that she has been experiencing severe pain at the site of injection since the day of administration. She is unable to lift her arm. After doctor visits and tests, her physicians have determined that she has bursitis related to the injection and needs to have a procedure done. The pharmacist that administered the vaccine was informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Chills
Decreased appetite
Headache
Hyperhidrosis
Illness
Oxygen therapy
Pain
Pyrexia
Tremor
Symptomtext
I was sick for 5 days; The booster put me in bed for 5 days; I had 102 degree fever for 3 days; chills; Body ache; Headaches; shaking really hard; No appetite; I had profuse sweating; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), administered in arm left (Lot number: FL3197) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Sjogren's syndrome" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "High blood pressure" (unspecified if ongoing); "Connective tissue disease" (unspecified if ongoing); "Aneurysm" (unspecified if ongoing), notes: I have an aneurysm on my heart.; "AFib" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "thyroid" (unspecified if ongoing), notes: I had have to my thyroid remove so that's why I take it.; "lung cancer" (unspecified if ongoing), notes: I had a lung cancer but I am a lung cancer survivor. Concomitant medication(s) included: LISINOPRIL taken for blood pressure abnormal; LORATADINE taken for hypersensitivity; TOPROL taken for atrial fibrillation; LIPITOR; XARELTO; LEXAPRO taken for anxiety; LEVOTHYROXINE taken for thyroid disorder. Vaccination history included: Bnt162b2 (Dose:1, Lot:EN6205, my first vaccine I didn't have any symptoms), administration date: 11Mar2021, when the patient was 60 years old, for Covid-19 Immunization, reaction(s): "I didn't have any symptoms"; Bnt162b2 (Dose:2, Lot:ER2613), administration date: 01Apr2021, when the patient was 60 years old, for Covid-19 Immunization, reaction(s): "I had chills and body ache for 24 hours", "I had chills and body ache for 24 hours". The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "booster"; PYREXIA (non-serious), outcome "recovered", described as "I had 102 degree fever for 3 days"; CHILLS (non-serious), outcome "recovered", described as "chills"; PAIN (non-serious), outcome "recovered", described as "Body ache"; HEADACHE (non-serious), outcome "recovered", described as "Headaches"; TREMOR (non-serious), outcome "recovered", described as "shaking really hard"; DECREASED APPETITE (non-serious), outcome "recovered", described as "No appetite"; HYPERHIDROSIS (non-serious), outcome "recovered", described as "I had profuse sweating"; ILLNESS (non-serious), outcome "recovered", described as "I was sick for 5 days; The booster put me in bed for 5 days". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, chills, pain, headache, tremor, illness. COVID-19 Vaccine is a Pfizer product, COVID-19 Vaccine manufacturer Unspecified, Dates for COVID-19 Vaccine (Start Unspecified Stop Unspecified), unknown NDC and UPC number of COVID-19 Vaccine, Expiry Date of COVID-19 Vaccine Unknown. Additional information; Treatment: The patient stated "Tylenol." LOT for the Tylenol:, "The patient don't have that, the patient at work right now and my bottle of Tylenol at home. I can't take anything because I am on a blood thinner, so that's the only thing I can take is Tylenol. But the Tylenol did help but when the Tylenol start 'wearing' off I can really feel it because the chills start coming back really hard again. I was sick for 5 days, for last 2 days I had fever for 3 days and then the last 2 days after my fever broke I had profuse sweating, I mean bad like I couldn't sleep dry 'clothed', just like profuse sweating." The patient further stated, "I have had, when I got my first vaccine I didn't have any symptoms at all, the second vaccine, I had chills and body ache for 24 hours and but then the booster put me in bed for 5 days." When probed if the patient had not any other vaccination 4 weeks prior to COVID 19 Vaccine, the patient stated, the first two were like in a hospital and the last one was done at withheld. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Name: Fever; Result Unstructured Data: Test Result:102; Comments: had 102 degree; Test Name: Oxygen supply; Result Unstructured Data: Test Result:Decreased; Comments: decreased oxygen supply at night time.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: AFib; Allergy NOS; Aneurysm (I have an aneurysm on my heart.); Anxiety; Blood pressure high; Connective tissue disorder; Fibromyalgia; Lung cancer (I had a lung cancer but I am a lung cancer survivor.); Sjogren's syndrome; Thyroid disorder (I had have to my thyroid remove so that's why I take it.)
- Andere Medikamente
- LISINOPRIL; LORATADINE; TOPROL; LIPITOR; XARELTO; LEXAPRO; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Axillary pain
Injection site pain
Interchange of vaccine products
Musculoskeletal chest pain
Fatigue
Insomnia
Pain
Pain in extremity
SARS-CoV-2 test
Swelling
Vaccination site pain
Tenderness
Symptomtext
began to feel pain in my armpit; Experienced pain at injection sight approximately 12 hrs; my first 2 were Moderna; Arm pain; It now stretches from my wrist in one painful line up to my armpit and down along my ribs; along with fatigue which was consistent with 2nd dose of previous shot; I could not sleep.; By morning, the pain spread from armpit down to each rib which was sensitive to the slightest touch and visibly swollen; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A 48 year-old patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 14Jan2022 10:00 (Lot number: FL3197) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "seasonal allergies" (unspecified if ongoing). Concomitant medication(s) included: ZYRTEC [CETIRIZINE HYDROCHLORIDE] taken for seasonal allergy (ongoing). Vaccination history included: Moderna (Dose: 2, Anatomical site of injection: Left arm, Route of administration: intramuscular, Batch/lot number: 039K20A), administration date: 10Feb2021, for COVID-19 immunization; Moderna (Dose: 1, Anatomical site of injection: Left arm, Route of administration: intramuscular, Batch/lot number: 039K20-2A), administration date: 13Jan2021, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 14Jan2022 10:00, outcome "unknown", described as "my first 2 were Moderna"; PAIN IN EXTREMITY (non-serious) with onset Jan2022, outcome "recovered" (2022), described as "Arm pain"; PAIN (non-serious) with onset Jan2022, outcome "recovered" (2022), described as "It now stretches from my wrist in one painful line up to my armpit and down along my ribs"; FATIGUE (non-serious) with onset Jan2022, outcome "unknown", described as "along with fatigue which was consistent with 2nd dose of previous shot"; AXILLARY PAIN (non-serious) with onset 15Jan2022 22:00, outcome "recovered" (2022), described as "began to feel pain in my armpit"; SWELLING (non-serious) with onset Jan2022, outcome "unknown", described as "By morning, the pain spread from armpit down to each rib which was sensitive to the slightest touch and visibly swollen"; VACCINATION SITE PAIN (non-serious) with onset 15Jan2022, outcome "recovered" (2022), described as "Experienced pain at injection sight approximately 12 hrs"; INSOMNIA (non-serious) with onset Jan2022, outcome "unknown", described as "I could not sleep.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, pain, axillary pain, vaccination site pain. Additional information: Experienced pain at injection sight approximately 12 hrs. later, along with fatigue which was consistent with 2nd dose of previous shot. Approximately 10 pm the next day, began to feel pain in my armpit. By morning, the pain spread from armpit down to each rib which was sensitive to the slightest touch and visibly swollen. Drug name: Kirkland Glucosamine Chondroitin,Drug name: Kirkland multivitamin Route: oral. That evening the pain spread all the way from my wrist (inside) all the way to the last rib on my inner left side to the point where I could not sleep. The most sensitive spots were the inside bend at my elbow, armpit and ribs. By day 5 the pain was entirely gone. Tylenol helped significantly. Follow-up attempts completed. No further information expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210526; Test Name: PCR; Test Result: Negative ; Comments: Comments: For travel to/from (city-withheld)travel; Test Date: 20210904; Test Name: Rapid test; Test Result: Negative ; Comments: Comments: For travel to/from (city-withheld)travel
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Seasonal allergy
- Andere Medikamente
- ZYRTEC [CETIRIZINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Mobility decreased
Pyrexia
Symptomtext
Fever of 101 for 24 hours then terrible really bad (couldn't hardly get out of bed) headache for 3 more days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Celexa 20mg/day
- Allergien
- -
- Vorherige Impfungen
- First two doses of Pfizer covid vacinne were even worse with fever of 101 or higher for 48 hours then terrible really bad headac
- Staat
- MN
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Adenovirus test
Angiogram pulmonary normal
Blood creatine phosphokinase increased
Blood lactate dehydrogenase increased
C-reactive protein increased
Chest pain
Echocardiogram normal
Electrocardiogram ST segment abnormal
Epstein-Barr virus test negative
Fibrin D dimer increased
Full blood count normal
HIV test negative
Headache
Herpes simplex test negative
Influenza virus test negative
Metabolic function test normal
Mycoplasma test negative
Symptomtext
Patient presented to the ED with 1 day history of chest and abdominal pain on 2/3/2022. States the pain lasts for around 30 minutes. The first 10 minutes described as 10/10 and then subsides to 3/10 over the course of 30 minutes. Pain located in the center of chest that radiates down to abdomen. Pain does not radiate to arms, back, or neck. Does not feel the pain is related to movement or eating but it does get better when passing gas or burping. He vomited once yesterday morning, no diarrhea. Endorses pleuritic chest pain. He received his COVID-19 immunization 4 days ago, and has had headache and body ache since for which he has taken ibuprofen regularly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- 2/3: Labwork revealed d-dimer elevated to 0.75, CRP 4.9, troponin 8.1 ng/mL, normal CBC and CMP. CT pulmonary angiogram was obtained however was negative for PE, pericardial effusion, or other thoracic abnormality. EKG with some diffuse ST segment changes. 2/4: echocardiogram normal, troponin continues to be elevated 27,578 ng/L (different scale), CK 1426 U/L, LDH 427; extensive viral workup (influenza, COVID, RSV, adenovirus, HIV, HSV, HHV6, mycoplasma pneumoniae, parainfluenza, EBV) negative 2/5: troponin 13,793 2/6: troponin 20,842
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, HTN, prediabetes
- Andere Medikamente
- Metformin 1000 mg BID
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Complement factor C2
Complement factor C3
Cough
Histamine level
Laboratory test
Nausea
Paraesthesia
Paraesthesia oral
Throat irritation
Tongue disorder
Total complement activity test
Tryptase
Symptomtext
Lips tingling Face tingling Throat scratchy Thickness of tongue feeling Nauseous Dry cough Elevated blood pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Tryptase- 14.0 mcg/L Histamine Plasma - 116 nmol/L C3-160 mg/dl C2- 4.2 mg/dl Factor H - 70.3 mg/dl CH50 - 78
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Health issues: POTS High blood pressure Asthma Allergies Type 1 Diabetes -March 8, 2019 -( Oct 6, 2016 - type 2) Chronic uticaria Urticaria pigmentosa cholinergic urticaria urticaria Exercise induced anaphylaxis Fibromyalgia Arthritis
- Andere Medikamente
- Breo ~Trulicity 4.5 mg ~Allegra 1 tab twice daily ~Singular (montelukast) 10 mg 1 tab -pm ~Hydroxyzine HCL 25 mg Tab -every 6 hrs ~Lo Loesterin Fe ~ Vascepa ( cholesterol) 2 capsules twice a day ~IC Diltiazem ER (CD) 180 mg CP 1X AM ~
- Allergien
- Allergic to: Latex NSAIDS Sulfa Metronidazole Percocet Vicodin / Hydrocodone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Back pain
Blood culture
Blood test
Chest X-ray
Chills
Computerised tomogram
Dehydration
Electrocardiogram
Hallucination
Infection
Influenza like illness
Liver disorder
Pyrexia
Renal disorder
Ultrasound scan
Urine analysis
Vomiting
Symptomtext
5 to 6 days of 102-104 fever, pain to back and stomach, flu-like body aches, hallucinations, chills, vomiting, severe dehydration, impact to liver and kidneys (including infection)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 4,0
- Labordaten
- Feb 2 CT-scan, EKG, chest x-rays, blood culture, ultra sound, urine sample, blood work
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- seasonal allergies since the 1990s, possible recent polycythemia
- Andere Medikamente
- Vitamin C, D, Zinc, baby aspirin, metropolol, and ibuprofen 600mg
- Allergien
- none
- Vorherige Impfungen
- In August 2020, patient received first dose of shingles vaccine and suffered high fever and large swelling to the injection sect
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 26,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Anxiety
Chest pain
Influenza A virus test
Influenza B virus test
Pain in extremity
SARS-CoV-2 test
Symptomtext
anxiety, chest pain, and pain in her left leg
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Hypoaesthesia
Insomnia
Myalgia
Paraesthesia
Symptomtext
Tingling and numbness started with my feet a few days after injection. This tingling and numbness travel up my body and currently my legs, stomach, back, arms, and hands/fingers are all numb and tingling. s; Tingling and numbness started with my feet a few days after injection. This tingling and numbness travel up my body and currently my legs, stomach, back, arms, and hands/fingers are all numb and tingling. a; In addition, my stomach and calf muscles are aching s; In addition, my stomach and calf muscles are aching; I cannot sleep at night; This is a spontaneous report received from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 20Jan2022 at 17:30 (Lot number: FL3197) at the age of 46 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). Concomitant medications included: GOLI and unspecified multivitamin. Past drug history included: Sulfur, reactions: "Drug allergy". Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: UNKNOWN; Route of administration: Unspecified; Anatomical site: Left arm; Administration time: 09:00), administration date: 26Apr2021, when the patient was 45 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: UNKNOWN; Route of administration: Unspecified; Anatomical site: Left arm; Administration time: 09:00), administration date: 17May2021, when the patient was 45 years old, for COVID-19 immunisation. The following information was reported: PARAESTHESIA (non-serious) with onset 22Jan2022 at 20:00, outcome "not recovered", described as "Tingling and numbness started with my feet a few days after injection. This tingling and numbness travel up my body and currently my legs, stomach, back, arms, and hands/fingers are all numb and tingling"; HYPOAESTHESIA (non-serious) with onset 22Jan2022 at 20:00, outcome "not recovered", described as "Tingling and numbness started with my feet a few days after injection. This tingling and numbness travel up my body and currently my legs, stomach, back, arms, and hands/fingers are all numb and tingling"; ABDOMINAL PAIN UPPER (non-serious) with onset 22Jan2022 at 20:00, outcome "not recovered", described as "In addition, my stomach and calf muscles are aching"; MYALGIA (non-serious) with onset 22Jan2022 at 20:00, outcome "not recovered", described as "In addition, my stomach and calf muscles are aching"; INSOMNIA (non-serious) with onset 22Jan2022 at 20:00, outcome "not recovered", described as "I cannot sleep at night". The events "Tingling and numbness started with my feet a few days after injection. This tingling and numbness travel up my body and currently my legs, stomach, back, arms, and hands/fingers are all numb and tingling", "Tingling and numbness started with my feet a few days after injection. This tingling and numbness travel up my body and currently my legs, stomach, back, arms, and hands/fingers are all numb and tingling", "In addition, my stomach and calf muscles are aching", "In addition, my stomach and calf muscles are aching" and "I cannot sleep at night" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of paraesthesia, hypoaesthesia, abdominal pain upper, myalgia and insomnia. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that the patient could not sleep at night because the numbness seemed to intensify when she laid down, but during day, bearable because she was moving around. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- GOLI
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Feeling abnormal
Hypoaesthesia
Immunisation
Limb discomfort
Malaise
Muscular weakness
Pain
Paraesthesia
Poor peripheral circulation
Neck pain
Vaccination site pain
X-ray normal
Symptomtext
I have had numbness, tingling, and weakness in my left arm and hand for four weeks after my COVID booster. It feels like there is a band constricting around my deltoid and is cutting off circulation to my arm and hand but there is no visible damage. I have been prescribed Gabapentin 200mg tid and this has numbed the pain but hasn't solved the problem. My insurance has denied both a ct-scan and an MRI. I have no diagnosis or treatment plan.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- X-ray was inconclusive. All other tests denied by insurance.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Feeling abnormal
Hypoaesthesia
Immunisation
Limb discomfort
Malaise
Muscular weakness
Pain
Paraesthesia
Poor peripheral circulation
Neck pain
Vaccination site pain
X-ray normal
Symptomtext
I have had numbness, tingling, and weakness in my left arm and hand for four weeks after my COVID booster. It feels like there is a band constricting around my deltoid and is cutting off circulation to my arm and hand but there is no visible damage. I have been prescribed Gabapentin 200mg tid and this has numbed the pain but hasn't solved the problem. My insurance has denied both a ct-scan and an MRI. I have no diagnosis or treatment plan.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- X-ray was inconclusive. All other tests denied by insurance.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Chest pain
Computerised tomogram coronary artery abnormal
Constipation
Fall
Feeding disorder
Hypophagia
Loss of personal independence in daily activities
Mobility decreased
Muscle contracture
Myalgia
Pollakiuria
Thirst
Tremor
Symptomtext
He got his vaccine, got it at 11:00 AM at pharmacy, came home and worked around the house, took care of the horse and came in the house about 7:00 PM, and wasn't in the house 15 minutes and started shaking violently with tremors. Tried to make it stop and his muscles were jerking all of the place. He then got real thirsty and would open a bottle of water and opened it and could not drink it due to the tremors, was slopping it on the floor, and unable to do so. Went up the stairs and fell down twice trying to get to the bed, and got in the bed. The shaking stopped about an hour later, his temp was 104.3. He did not eat or drink anything and then went to sleep. In the morning it was 104.1, and it took 4 days to get down below 100. He was not able to do anything for days, muscle pains, and abnormal bodily functions, and now has constipation and it is still not right. He is having chest pains, muscle soreness and bowel movement issues (constipation). He has frequency of urination now. He saw his PCP and is going to see a cardiologist next week. Had a calcium score done after this and it was 2842 was his level.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Above.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Vitamins.
- Allergien
- Cats, Epinephrine.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Disturbance in attention
Feeling abnormal
Interchange of vaccine products
Memory impairment
Symptomtext
intense brain fog, concentration, and memory issues beginning 2 days post vaccine. It has been way more intense than after my first two doses of Moderna in spring 2021. Last time, it lasted 5 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- There are no tests.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- melatonin
- Allergien
- penicillin, iodine, propylene glycol, formaldehyde
- Vorherige Impfungen
- hair loss and same cognitive issues after Moderna last year
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angioedema
Arthropathy
Blood test
Bone swelling
Condition aggravated
Erythema
Full blood count
Hypersensitivity
Joint effusion
Mass
Peripheral swelling
Skin warm
Swelling face
Ultrasound scan abnormal
Symptomtext
After receiving the vaccine I was having issues with redness, hotness, and swelling in my arm. The swelling did go down, but the issues with my shoulder is ongoing. Then I thought I was good, but then January 8, 2022 I started to develop puffy cheek bones. My cheeks just puffed up like I had an allergic reaction, but I haven't ate anything new or out of the ordinary. My face is still not better. My primary doctor offered to give me a steroid but I declined to take it. My doctor told me I had angioedema. Then the allergist told me I did not have angioedema. A week later I started to develop lumps in my joints of my hands and feet. I have 8 lumps now. I am still able to work for now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood work (1/28/2022), CBC (1/28/2022), Ultrasound showed fluid in the joints (1/14/2022)
- Aktuelle Erkrankungen
- My arm was still bothering me from the 1st dose.
- Vorgeschichte
- None
- Andere Medikamente
- Magnesium; zinc; vitamin C; vitamin D
- Allergien
- None
- Vorherige Impfungen
- Covid (1st Dose) I had problems with my arm and shoulder. I also had a rash after getting the vaccine. (11/5/2021).
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Laboratory test
Lymphadenopathy
Migraine
Motion sickness
Nausea
Pain
Pyrexia
Vertigo
Symptomtext
01/21/2022 Friday the night next day 01/22/2022, not able to get out of bed low grade fever 101.8 highest and severe body arches and joint pain, did not notice the dizziness 01/24/2022 Monday, unable to move without extreme nausea, migraine and motion sickness of vertigo. Tele-visit on Tuesday and was given directive of if not better to come to the office. On Friday 01/28/2022, went to doctor office as symptoms was not improving. Prescribed medication that current is not working and contact the doctor on 01/31/2022 and new prescriptions was prescribed and supposed to pick up new medication today. Diagnosed with vertigo and extreme enhanced migraines. Was prescribed exercised for inter ear issue and the motion system is proving to be difficult in the exercise process. Swollen lymph node under left arm side of vaccination and that occurred with vaccination 1 and two as well 101.8 temp.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Regular blood oxygen level test, blood pressure test and evaluated for stroke evaluation
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Migraines but not to the level,degree , or frequency after the vaccination . Random joint pains. Taken the vaccination increased migrains and added virtego.
- Andere Medikamente
- Only medication onboard at time of vaccination Birth control -Simpesse no birth control in system on filler bills 01/15/2022 last time taken prior vacation then the first time of taken after the vaccination in 01/23/2022 at 10:00PM .
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Cough
Interchange of vaccine products
Throat clearing
Throat irritation
Throat tightness
Symptomtext
The patient was seen in clinic for a COVID booster vaccine. Patient stated she received J&J on 04-11-2022 at local facility. She stated that 35 minutes after she received her vaccine she started to have itching and tightness to her throat. Per her Allergist, she was recommended to receive Pfizer or Moderna as her booster and to take an extra dose of Zyrtec prior to vaccination. Patient reported taking extra dose of Zyrtec prior to vaccination. Per Allergist, patient was recommended to come to a Public Health Center for Pfizer vaccination. The patient's history was reviewed with providers and was OK to give vaccine. The patient received Pfizer on left arm at 12:54 pm and was instructed to wait for one hour to be monitored. At 1:21 pm, patient noted having mild itchiness to her throat, but was not c/o SOB. She was still awake, alert, able to speak, and answer questions. At 1:26 pm, patient was coughing and clearing her throat. She stated she felt her throat a little tight with a little more itchiness. MD was notified at 1:29 of the patient's symptoms. At 1:32 pm, MD assessed patient and instructed Benadryl 50 mg to be administered. Benadryl 50 mg was given at 1:38 pm to right arm. Patient was monitored and at 2:00 pm, patient was stating that she has feeling less itchiness to her throat. At 2:15 pm, the patient continue to state she was feeling better. By 2:31 pm, she no longer felt any more symptoms. MD was notified and patient was assessed again before being discharged. Patient was advised to call husband to pick her up. She left the clinic at 2:45 pm, with her husband she was awake, alert, and orient. Was instructed if she had any more symptoms to go to ER. Patient and husband verbalized understanding. VS Time BP P O2 sat 1:32 pm 151/85 78 100% 1:40 pm 123/95 62 100% 1:54 pm 125/82 64 99% 2:19 pm 125/81 65 99%
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Zyrtec
- Allergien
- Multiple environmental and food products
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Dizziness
Dyspnoea
Fibrin D dimer
Fibrin D dimer increased
Nausea
Vomiting
Symptomtext
Dizziness, nausea, vomiting, weakness, shortness of breath, elevated D dimer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 01/29/2022 at 2300hrs D dimer 0.53 (ref <= 0.49)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Breast oedema
Chest pain
Ear swelling
Erythema
Bone swelling
Breast swelling
COVID-19
Face oedema
Hypoaesthesia
Localised oedema
Lymphadenopathy
Musculoskeletal pain
Oedema peripheral
Pain
Pain in extremity
Swelling
Peripheral swelling
Symptomtext
covid test result: Positive; covid test result: Positive; Chest pain; left arm edema and pain; left arm edema and pain; lymphadenopathy; adenopathy; swelling to left side of body from waist to head; swelling to left side of body from waist to head i.e. arm; swelling to left side of body from waist to head i.e. arm, shoulder; swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast; swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck; swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck, ear; swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck, ear, scapula; severe pain; Numbness to left arm; Numbness to left arm, finger; Numbness to left arm, finger and hand; swelling to left side of body from waist to head i.e. arm, shoulder, clavicle; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Dec2021 09:30 (Lot number: F13197) at the age of 55 years as dose 2, single and administered in arm left, administration date 01Dec2021 09:30 (Lot number: FF2590) as dose 1, single for covid-19 immunisation. Relevant medical history included: "HTN" (unspecified if ongoing); "latex" (unspecified if ongoing). Concomitant medication(s) included: FLU, administration date 10Nov2021; LOTREL [AMLODIPINE BESILATE;BENAZEPRIL HYDROCHLORIDE]. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 28Dec2021, outcome "unknown" and all described as "covid test result: Positive"; CHEST PAIN (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "Chest pain"; OEDEMA PERIPHERAL (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 22Dec2021 22:45, outcome "recovering" and all described as "left arm edema and pain"; LYMPHADENOPATHY (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "lymphadenopathy"; LYMPHADENOPATHY (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "adenopathy"; SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head"; PERIPHERAL SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm"; SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm, shoulder"; SWELLING (non-serious) with onset 22Dec2021 12:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle"; BREAST SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast"; SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck"; EAR SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck, ear"; BONE SWELLING (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck, ear, scapula"; PAIN (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "severe pain"; HYPOAESTHESIA (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "Numbness to left arm"; HYPOAESTHESIA (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "Numbness to left arm, finger"; HYPOAESTHESIA (non-serious) with onset 22Dec2021 22:45, outcome "recovering", described as "Numbness to left arm, finger and hand". The events "chest pain", "left arm edema and pain", "left arm edema and pain", "lymphadenopathy", "swelling to left side of body from waist to head", "swelling to left side of body from waist to head i.e. arm", "swelling to left side of body from waist to head i.e. arm, shoulder", "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle", "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast", "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck", "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck, ear", "swelling to left side of body from waist to head i.e. arm, shoulder, clavicle, breast, neck, ear, scapula", "severe pain", "numbness to left arm", "numbness to left arm, finger" and "numbness to left arm, finger and hand" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (28Dec2021) positive, notes: Nasal Swab. Therapeutic measures were taken as a result of chest pain, oedema peripheral, pain in extremity, lymphadenopathy, lymphadenopathy, swelling, peripheral swelling, swelling, swelling, breast swelling, swelling, ear swelling, bone swelling, pain, hypoaesthesia, hypoaesthesia, hypoaesthesia. Clinical course: AE treated with Antihistamines, prednisone, antibiotics. The patient did not have covid prior to vaccination. The patient was tested with covid post vaccination. The patient was not sure for Covid test name post vaccination. Other vaccine 4weeks details: other vaccine 4weeks product: Flu.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine can not be excluded for the reported events of COVID-19 and Vaccination failure due to temporal relationship
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211228; Test Name: Nasal swab; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Latex allergy
- Andere Medikamente
- LOTREL [AMLODIPINE BESILATE;BENAZEPRIL HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chest pain
Electrocardiogram Q waves
Influenza A virus test negative
Influenza B virus test
Influenza virus test negative
Interchange of vaccine products
Pain
SARS-CoV-2 test negative
Symptomtext
Patient developed chest tightness and pain after exerting himself yesterday moving boxes in his garage. Interestingly he got the J&J shot last year. Three weeks ago he got the Pfizer booster shot. We evaluated patient in the urgent care for chest pain. Advised no strenuous activity. Advised rest and NSAID for pain. If worse to go to the ED.. F.u with PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID rapid antigen negative Flu A and B negative EKG shows Q-waves but not obvious ST/T elevations
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizures
- Andere Medikamente
- Lamotrigine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electrocardiogram
Extrasystoles
Heart rate increased
Immediate post-injection reaction
Palpitations
Symptomtext
Immediately after receiving vaccine, patient started to have a racing heart beat, felt like it was skipping beats. Heart was elevated to 115. Patient was given water, an EKG was performed, Heart rate lowered to 75
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- depression, anxiety
- Andere Medikamente
- lorazepam, venlafaxine
- Allergien
- Bee venom, mold, percocet, pollen/tree extract
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chest pain
Dyspnoea
Gait disturbance
Immunisation
Pain in extremity
Pyrexia
Symptomtext
Severe chest pains; Trouble walking and breathing; Trouble walking and breathing; got the booster shot; Running fever; Pain in arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 12 year-old male patient received bnt162b2 (BNT162B2), administration date 07Jan2022 (Lot number: FL3197) at the age of 12 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Attention deficit hyperactivity disorder" (unspecified if ongoing), notes: ADHD; "Learning disability" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (dose 1), for covid 19 immunization; Bnt162b2 (dose 2), for covid 19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 07Jan2022, outcome "unknown", described as "got the booster shot"; CHEST PAIN (non-serious) with onset 08Jan2022, outcome "not recovered", described as "Severe chest pains"; GAIT DISTURBANCE (non-serious), DYSPNOEA (non-serious) all with onset 08Jan2022, outcome "unknown" and all described as "Trouble walking and breathing"; PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Running fever"; PAIN IN EXTREMITY (non-serious) with onset Jan2022, outcome "unknown", described as "Pain in arm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, pain in extremity. Additional information: the patient just got the booster shot on Friday(07Jan2022) and yesterday(08Jan2022) the reporter (patient's parent) was just watching like around 3 o'clock in the morning, the patient had severe chest pains and had trouble walking and breathing and it was a hard time for him to walk or breathe. The reporter was asking if this a side effect and should he/she take the patient to the emergency room and get this checked up. The reporter asked what was going on because the patient was still having it. It is not severe but he was still having chest pains. Reporter stated the only thing patient took was Tylenol as he was running fever, reporter did not give him more medication. The only thing was Tylenol that was for the fever and for the pain in the arms. Reporter stated the dosage and frequency of Tylenol as follows: It was 15 ml, the thing was that the patient did not take the form, reporter gave it to patient in liquid. It was a 160 mg and what it was given as 15 ml every 6 hours. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: running fever; Result Unstructured Data: Test Result:running fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADHD; Learning disability.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram
Asthenia
Blood test
Chest X-ray
Chest discomfort
Chest pain
Dyspnoea
Echocardiogram
Electrocardiogram ambulatory
Fatigue
Fibrin D dimer increased
Gastrooesophageal reflux disease
Nausea
Tachycardia
Symptomtext
Tachycardia, shortness of breath, chest pain, chest tightness, GI reflux, elevated D-dimer, nausea, fatigue, weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- CTA, chest xray, echocardiogram, bloodwork, 48 hr Holter
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Hyperhidrosis
Tremor
Visual impairment
Symptomtext
I woke up the next day feeling weak and light headed. Just within minutes of waking up and getting out of bed to urinate, I felt even more light headed. Right after exiting the bathroom my vision was blacking out as if there was no blood flow going to my head. So I rushed over to lay down and maybe narrowly avoided the possibility of going unconscious. After I laid down I was shaking and sweating which is something I did not experience when I first woke up. 10 min later I get out of bed again and I feel much better as if nothing had happened. I have no history of blacking out and it was the first time I had ever experienced such a side effect in all my life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Blood iron
Blood iron decreased
Blood pressure measurement
Cardiac function test
Condition aggravated
Disease recurrence
Dizziness
Dyskinesia
Electrocardiogram ambulatory
Fall
Immunisation
Investigation
Tardive dyskinesia
Symptomtext
dizziness; falling; dyskinesia; had again a deep increase in falling, dizziness, and dyskinesia symptoms; tardive dyskinesia; the tardive dyskinesia was diagnosed and was really increased and is terrible since the patient had the Pfizer covid vaccine 2nd and 3rd doses; iron level was very low; booster dose 30Dec2021; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 71 year-old male patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 30Dec2021 11:15 (Lot number: FL3197) at the age of 71 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Parkinson's disease", start date: 2017 (ongoing); "tardive dyskinesia" (ongoing). Concomitant medication(s) included: RYTARY taken for parkinson's disease; REGLAN [METOCLOPRAMIDE] taken for parkinson's disease, start date: 2017. Vaccination history included: Bnt162b2 (Dose 1, lot EL3248 and expiry date Apr2021, at approximately 08:30am), administration date: 22Jan2021, when the patient was 70 years old, for COVID-19 immunization; Bnt162b2 (Dose 2, Batch/lot number: EL3247, administered upper left arm, at approximately 11:15am), administration date: 12Feb2021, when the patient was 70 years old, for COVID-19 immunization, reaction(s): "dizziness", "falling", "dyskinesia". The following information was reported: IMMUNISATION (disability, medically significant) with onset 30Dec2021 11:15, outcome "unknown", described as "booster dose 30Dec2021"; DIZZINESS (disability), outcome "not recovered", described as "dizziness"; FALL (disability), outcome "not recovered", described as "falling"; DYSKINESIA (disability), outcome "not recovered", described as "dyskinesia"; DISEASE RECURRENCE (disability), outcome "not recovered", described as "had again a deep increase in falling, dizziness, and dyskinesia symptoms"; TARDIVE DYSKINESIA (disability, medically significant), outcome "not recovered", described as "tardive dyskinesia"; CONDITION AGGRAVATED (disability), outcome "not recovered", described as "the tardive dyskinesia was diagnosed and was really increased and is terrible since the patient had the Pfizer covid vaccine 2nd and 3rd doses"; BLOOD IRON DECREASED (non-serious), outcome "unknown", described as "iron level was very low". The events "dizziness", "falling", "dyskinesia", "had again a deep increase in falling, dizziness, and dyskinesia symptoms", "tardive dyskinesia" and "the tardive dyskinesia was diagnosed and was really increased and is terrible since the patient had the pfizer covid vaccine 2nd and 3rd doses" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: iron: (2021) very low, notes: iron level was very low; blood pressure: (2021) very low, notes: low very very low blood pressure; cardiac workup: (2021) everything was normal; holter monitor: (2021) fine; other workup: (2021) fine. Therapeutic measures were taken as a result of blood iron decreased. Patient that received the Pfizer Covid vaccine primary series in January and again in February and that was followed by an increased dizziness, falling and dyskinesia and the patient is also a Parkinson's patient; events subsided after 6 months and the patient got the Pfizer Booster covid vaccine last Thursday on 30Dec2021 and he had again a deep increase in falling, dizziness, and dyskinesia symptoms. Neurologist had stated there was no link to vaccine. The patient's dyskinesia and dizziness lasted and the patient started feeling good around Aug2021 or Sep2021 and then he had been really feeling good and now he got the 2nd vaccine and it started all over again; clarified later that the symptoms began after the 2nd dose of the vaccine and then again after the 3rd or booster dose of the vaccine; stated the patient cannot tolerate physical therapy at this point without getting dizzy and she told the transferring agent the patient had tardive dyskinesia. None vaccines administered on same date of the Pfizer suspect. The dizziness began and started the week right after the 2nd vaccine that week and she never made the connection and nobody listed to her and now the patient's symptoms are ongoing and stopped and then the symptoms resumed because he had the Pfizer covid booster vaccine and the symptoms began within a couple of days after the 2nd dose and a couple of days after the 3rd dose of the vaccine. The tardive dyskinesia was diagnosed and was really increased and is terrible since the patient had the Pfizer covid vaccine 2nd and 3rd doses; states the tardive dyskinesia was ongoing and was the same. For seriousness criteria, it was disabling and the patient also went to the hospital a few times and clarified to state it was not an overnight admission to the hospital but emergency room visits. The cardiac workup and he saw the neurologists and had everything done trying to figure out why he was getting dizzy and falling and they adjusted his medications and then said he seems to have resolved and then the symptoms began again with the Pfizer booster vaccine. Caller states for the cardiac workup and everything was normal and the only thing the patient did was have his iron level was very low and he had the iron infusions and everything else was fine and the holter monitor was fine and the other workup was fine and he had low very very low blood pressure and that blood pressure was not really ongoing and his pressure came up.; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events with the suspect drug Comirnaty cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: iron; Result Unstructured Data: Test Result:very low; Comments: iron level was very low; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:very low; Comments: low very very low blood pressure; Test Date: 2021; Test Name: cardiac workup; Result Unstructured Data: Test Result:everything was normal; Test Date: 2021; Test Name: holter monitor; Result Unstructured Data: Test Result:fine; Test Date: 2021; Test Name: other workup; Result Unstructured Data: Test Result:fine
- Aktuelle Erkrankungen
- Parkinson's disease; Tardive dyskinesia
- Vorgeschichte
- -
- Andere Medikamente
- RYTARY; REGLAN [METOCLOPRAMIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test
Chest X-ray
Chest pain
Fibrin D dimer
Pleurisy
Dental caries
Headache
Hyperaesthesia teeth
Tooth discolouration
X-ray dental abnormal
Symptomtext
Headache with high sensitivity in teeth. All teeth were sensitive to cold and heat. This has never happened before. Noticed that one of my teeth was turning grey and went to the Dentist. Physical exam of teeth and X rays showed the tooth was dying and was fine during my last visit with xrays in December 2021. Topical medication applied to teeth to help with sensitivity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- X rays- tooth and full set on 21January2022
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- COVID 19 from January 2021 with long effects
- Andere Medikamente
- Yes
- Allergien
- No
- Vorherige Impfungen
- Pfizer COVID-19 second shot on 15Apr2021
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dyspnoea
SARS-CoV-2 test
Symptomtext
shortness of breath and difficulty breathing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- SARS-CoV-2 (COVID-19) by NAA, Micro
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- obesity, pulmonary hypertension, paroxysmal atrial fibrillation, non-ischemic cardiomyopathy, mitral valve regurgitation, hypertension, congestive heart failure, and COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blindness
Condition aggravated
Metamorphopsia
Visual field defect
Vitreous disorder
Vitreous floaters
Symptomtext
distorted vision in left eye, loss of vision, floaters, peripheral vision loss and its continued to get worse, went to eye specialist at Clinic he could not see anything wrong. Doctor who is an ophthalmologist only thing he said was the vitreous had loosened some due to age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Had Covid-19 May 25,2021 on respirator then a tracheostomy all of June got out of hospital July 11, 2021 I have long haul covid dizziness very weak took PTdid not help.sleep all the time after vaccine lost and distorted vision in left eye specialist was know help
- Andere Medikamente
- machine 25mg, quetiapine 100mg, tamsulosino .4mg, meloxicam 15mg sertraline 100mg, amlodipine 10mg,
- Allergien
- Reception, valproic acid
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Dizziness
Dyspnoea
Echocardiogram
Electrocardiogram
Electrocardiogram ambulatory
Flushing
Heart rate increased
Laboratory test
Tachycardia
Symptomtext
Sat down after booster, had tachycardia with heart rate increase, flushing and dizziness. Pharmacy tech gave me Gatorade and monitored for an additional 10 minutes until I felt safe to leave and heart rate had returned to normal. About 5 days later I started having shortness of breath and bouts of tachycardia. This has persisted to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- ER visit 1/13/22 - labs, EKG, chest xray 24 hour Holter monitor from Cardiologist 1/11/22 Echocardiogram at Cardiologist office on 1/15/22 Followup with Cardiologist to review results on 1/18/22 GI consult on 1/17/22 Labwork ordered by GI that will be performed in next 1-2 days for review
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Klein-Waardenburg syndrome
- Andere Medikamente
- None
- Allergien
- Dilaudid Imitrex Fentanyl Dairy
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Dyspnoea
Pain
Symptomtext
Systemic: Body Aches Generalized-Mild, Systemic: Chest Tightness/Heaviness/Pain-Medium, Additional Details: Patient reported chest tightness and generalized body aches beginning 2 days after receiving booster dose of Pfizer/BioNTech vaccine. Patient stated chest tightness made it difficult to take a deep breath or even yawn. She described the tightness as "crushing," but said it resolved quickly. She has continued to improve back to baseline. All adverse effects reported resolved at the time of patient report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Dysphagia
Fluid retention
Hypoaesthesia
Lymphadenopathy
Mobility decreased
Pain
Peripheral swelling
Tenderness
Wheezing
Symptomtext
The left side of the patient's face, left side of neck, left leg, and left foot became numb. The patient's face and neck felt as if she she had gotten novocaine at the dentist. The patient's neck was tender and lymph nodes swollen. The patient's whole body was sore and she had difficulty moving, along with leg swelling and retaining water in extremeties. The patient had difficulty swallowing , mouth felt like it had a metallic taste, and the lungs felt like they were impacted and may start wheezing. The patient had to use her albuterol inahler more than normal to help with breathing. Symptoms lasted about a day and a half before starting to improve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Benign tumor of pituitary gland and craniopharyngeal duct, Asthma, Migraine
- Andere Medikamente
- Progesterone capsule 125mg daily, Estradiol Patch 0.1 mg twice a week, Flovent inhaler 2 times a day, Albuterol inhaler as needed, Vitamin D3 1000 IU daily, Zinc 30 mg daily
- Allergien
- Ciprofloxacin, amoxicillin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Flushing
Malaise
Paraesthesia oral
Pharyngeal paraesthesia
Symptomtext
About 5 minutes after the vaccine was administered, the patient reported tingling in the mouth, throat, and flushing and just "not feeling right". We were worried about anaphylaxis due to the mouth and throat involvement and decided to have paramedics come evaluate her. After they were called patient said she had not eaten much today. We were also concerned about hypoglycemia as a result, but the paramedics took her blood sugar upon arriving and it was normal. She decided to go with them to the ER to be evaluated. We have tried to follow up with the patient many times after the incident, but she hasn't responded. We do not believe it resulted in a serious event as it seemed to be resolving while she was still here and never progressed to anaphylaxis to our knowledge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling abnormal
Headache
Lymphadenopathy
Pain
Pain in extremity
Paraesthesia
Pruritus
Rash
Urticaria
Symptomtext
Patient reported to me on 1/14/22, that on 12/21/21, only 90 minutes after having received her pfizer covid-19 vaccination (dose 1), she began experiencing side effects, including a full body prickly sensation, which developed later (not sure of timing) into a rash, with hives and itching, in multiple body locations. Her lymph nodes swelled, she experienced normal side effects such as arm pain, but ended up with a red ring around her arm (she says she has complete documentation and even took pictures). She also experienced shooting pains that extended up into the back of her head. As she no longer has a PCP, she contacted her OB/GYN office, explained the situation to them; they recommended she not get her second dose presently and make an appt with an allergist/immunologist to further test for exact allergy. Patient is having trouble finding an appt with such a specialist. It is 3 weeks past her vaccine date and she still reports not feeling back to her normal self.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of vulvular cancer due to HPV in her 20's, recent diagnosis of rheumatoid arthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Dizziness
Fatigue
Feeling abnormal
Feeling hot
Injection site pain
Loss of personal independence in daily activities
Mobility decreased
Sitting disability
Symptomtext
I recieved my covid-19 booster (3rd shot) on 1/4/2022 at 11:15am. The only effect of the shot immediately after (15 minutes) was a bit of dizziness that subsided within 15-20minutes. I went home and laid down for around 4 hours. I felt groppy, tired and a bit warm, with soreness at the injection site, expected after vaccination. I tried getting up after 4 hours and felt soreness and pain in my lower back. I chalked it up to an immune response and continued resting for the next 24 hours. For days after vaccination all other symptoms subsided, but the back pain increased and persisted for 3-4 days. It gradually reduced in pain after a week but has returned at the same intensity after over a week after injection. Pain in very severe making it difficult or not possible to conduct some tasks and bend over. I would rate the pain 2/10 standing, 3/10 sitting, 6/10 bending at the waste or handing leg off something. Most painful period was around 7/10. Treatment has been self administered. Rest and stretching. 400mgs of Ibuprofen once daily for pain, twice daily when working. Ibuprofen provides significant, but not complete relief. Contacted the Clinic about the symptoms 1/14/2022. Symptoms still persist 11 days after vaccination as of this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic lower back pain, degenerative disk disease. Started initially during time served in the Army from 2007-2012. Vertigo, stress related (personal opinion) , medically diagnosed. Vitamin D deficiency, discovered early 2021, completed a prescribed regime. Levels are barely above minimum as of last test (7-8 months ago).
- Andere Medikamente
- Tylenol (standard over the counter dose) for headaches.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Angina pectoris
Dyspnoea
Flatulence
Heart rate abnormal
Heart rate increased
Palpitations
Symptomtext
About 18-20 hours after receiving the booster (3rd shot in the series), I had an elevated heart rate between 120-130bpm which is abnormal for just waking up in bed. My resting heart rate will range from 55-75 bpm. Throughout the next two days I felt my heart pumping much harder and faster than ever before, almost feeling like my heart was aching/sore from abnormal activity. I had periods where I felt shortness of breath and some difficulty breathing (heavy breathing). Subsequently, I also experienced stomach pains plus abnormal passing of gas frequently. The stomach pains continue two weeks later and counting, though this may not be directly tied to the booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Tylenol and ginger-lemon tea.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 23,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Blood test normal
Chest pain
Electrocardiogram normal
X-ray normal
Symptomtext
Continues Chest Pain , sharpness . Have gone to ER and made appts with Dr. They say it's notmal for teen boys to have chest pain. It's not normal
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Ekg text, xray test, and blood work. All 1/14/21 Doctors concluded they found nothing abnormal. Still has chest pain .
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Fatigue
Feeling of body temperature change
Pyrexia
Tremor
Symptomtext
Elevated usual temp by 4.3 degrees (97.4 to 101.7). ALL large & small joints very painful Whole body shaking & teeth chattering uncontrollably Feeling hot & cold at once Fear Lasted through the night By 7am fever reduced to 99.9 By about 5pm symptoms gone but I was ?wiped out? Used Tylenol 500mg in early morning with Gatorade. When most needed I couldn?t ?think? to take any Tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Dilaudid.
- Vorherige Impfungen
- Pfizer Covid 19
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dizziness
Dyspnoea
Feeling hot
Lip dry
Throat tightness
Symptomtext
Patient received her booster (pfizer) vaccine at 15:10, patient initially received Janssen as her first vaccine. 1512 patient came back to vaccinator's table stated she is having SOB "tightness in her chest", dizziness and light headedness and feeling warm. 1512 initial vitals taken as follow HR80 RR 18 BP 158/97 SAT 100%. 1514 water provided no signs of aspiration, patient still stated she is feeling warm and the feeling comes and goes. 1517 retook VS HR71 RR 19 BP 153/105 sat 100%. pt stated she felt like her throat is closing. 1527 HR 88, RR 18, BP 162/93 SAT 100% 1528 called 911. 1532 hr80, RR 18, BP 174/93 SAT 100% pt stated her thought is closing up again. stated her lips felt dry. 1542 EMS arrived and assessed patient. 1557 patient was taken out by EMS. PT A/O x 4 , ambulatory.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
complaint of chest pain - sharp, stabbing type of pain at the sternum which radiated outwards with movements and deep breaths. Currently on day 3 of pain - has lessened at this point compared to days 1 and 2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 1 visit to pediatrician for assessment. No medical tests or laboratory results completed at this time. Pediatrician recommended to monitor for a few days and assessed as potential costochondritis. If symptoms worsened or did not improve within 2-3 days, recommended a Chest X ray, EKG, and potential echocardiogram
- Aktuelle Erkrankungen
- none at the time of vaccination, common cold 2 weeks prior
- Vorgeschichte
- none
- Andere Medikamente
- Sertraline 25mg once daily; Junel Fe 1/20 once daily
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chest pain
Lymphadenopathy
Swelling
Symptomtext
PAINFUL SWELLING IN ARMPIT AND SIDE OF CHEST
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- anaplasma-lyme
- Vorgeschichte
- none
- Andere Medikamente
- herbal desbio treatment for lyme disease, tumeric, adrenal support and spanish radish
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest pain
Diarrhoea
Dyspnoea
Headache
Myalgia
Joint stiffness
Joint swelling
Lymphadenopathy
Nausea
Pain
Rash
Vomiting
Paraesthesia
Symptomtext
After receiving vaccine and waited 15 min I went home and started feeling nausea, diarrhea, body ache, joint stiffness, swelling, pain, head ache, swollen neck gland, shortness of breath, chest pain, tingling of arms and legs and a rash. Rash lasted 3 days but other symptoms are still there, some come and go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- I am schedule for an EKG and labs tomorrow. Currently advised by medical provider to take Tylenol and Ibuprofen as needed until test results are received and reviewed.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Multi - Vitamin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest pain
Diarrhoea
Dyspnoea
Headache
Myalgia
Joint stiffness
Joint swelling
Lymphadenopathy
Nausea
Pain
Rash
Vomiting
Paraesthesia
Symptomtext
After receiving vaccine and waited 15 min I went home and started feeling nausea, diarrhea, body ache, joint stiffness, swelling, pain, head ache, swollen neck gland, shortness of breath, chest pain, tingling of arms and legs and a rash. Rash lasted 3 days but other symptoms are still there, some come and go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- I am schedule for an EKG and labs tomorrow. Currently advised by medical provider to take Tylenol and Ibuprofen as needed until test results are received and reviewed.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Multi - Vitamin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Heart rate increased
Migraine
Oropharyngeal pain
Palpitations
Pyrexia
Urinary tract infection
Symptomtext
Uti day after getting vaccine and I don?t normally get them. Sore throat heart palpitations fast heart rate fever chills severe migraine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Muscular dystrophy
- Andere Medikamente
- None
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Feeling abnormal
Hypertension
Palpitations
Vision blurred
Symptomtext
BG over 200 during fasting. Normally it is 80-100. High blood pressure and heart racing/pounding. Blurry vision due to the high BG. Problem is all these effects have lasted over two weeks despite my attempts to fix it by increasing diabetes medication and keep to an even stricter diet: 0 carbs < 500 calorie meals. 2 day intermittent fasting has no effect which usually gets my BG back in gear if I eat something bad. It seemed to get a little bit better just before my last shot, but now I'm back where I was. Feeling like I'm going to die. I'm on day 2, hopefully these symptoms will go away someday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- type 2 diabetes
- Andere Medikamente
- Metformin, Glyburide, Pravstatin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Chills
Headache
Hyperhidrosis
Illness
Immunisation
Movement disorder
Respiratory tract congestion
Symptomtext
chills so bad that no one could not her touch skin; sweats; Chest congestion; severe headaches; Chest pain; not able to make it to the bathroom; Pfizer Covid-19 Booster dose; sick; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 47 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 20Dec2021 (Lot number: FL3197) at the age of 47 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "allergies" (ongoing), notes: she had been diagnosed since a kid. The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (first dose with a lot of EW0158. Stated that it was 0.3ml via fatty tissue to the left arm., Manufacture unknown), administration date: 07Apr2021, when the patient was 46 years old, for Covid-19 immunization; Covid-19 vaccine (second dose with a lot of EW0172. Stated that it was 0.3ml via fatty tissue to the right arm., Manufacture unknown), administration date: 28Apr2021, when the patient was 46 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 20Dec2021, outcome "unknown", described as "Pfizer Covid-19 Booster dose"; CHILLS (medically significant) with onset 21Dec2021, outcome "recovered" (25Dec2021), described as "chills so bad that no one could not her touch skin"; HYPERHIDROSIS (medically significant) with onset 21Dec2021, outcome "recovered" (25Dec2021), described as "sweats"; RESPIRATORY TRACT CONGESTION (medically significant) with onset 21Dec2021, outcome "recovering", described as "Chest congestion"; HEADACHE (non-serious) with onset 21Dec2021, outcome "recovered" (27Dec2021), described as "severe headaches"; CHEST PAIN (non-serious) with onset 21Dec2021, outcome "recovering", described as "Chest pain"; MOVEMENT DISORDER (non-serious) with onset 21Dec2021, outcome "recovered" (26Dec2021), described as "not able to make it to the bathroom"; ILLNESS (non-serious) with onset Dec2021, outcome "not recovered", described as "sick". The events "chills so bad that no one could not her touch skin", "sweats", "chest congestion", "severe headaches", "chest pain", "not able to make it to the bathroom" and "sick" were evaluated at the emergency room visit. Therapeutic measures were taken as a result of chills, hyperhidrosis, respiratory tract congestion, headache, chest pain. Clinical course: Patient received other Products as Immunotherapy shot, Dates for Concomitant Products Immunotherapy shot: (Start: May2019 Stop: Ongoing). Why was the patient taking Concomitant Products Immunotherapy shot (Verbatim): allergies, Dosage text: shot to fatty part of upper arm alternate arms weekly on Mondays. Additional Information for Other Conditions: Stated that she had been diagnosed since a kid. Pfizer Medical Information has a patient reporting an adverse event after her booster dose of Pfizer Covid 19 on 20Dec. Treatment: Stated that she had a steroid injection for chills were so bad that no one could not touch her skin and sweats. Stated that she had migraine medication for the sever headaches. Stated that she has been taking Albuterol nebulizer, Advair, cough suppressant and Hall's for chest congestion. Stated that she took pain medicine, steroid and Advair for the chest pain. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy (she had been diagnosed since a kid)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Dizziness
Fatigue
Immunisation
Interchange of vaccine products
Lymphadenopathy
Migraine
Nausea
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Dec2021 11:30 (Lot number: Fl3197) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "IgA nephropathy" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 026b21a, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 13Apr2021, for Covid-19 immunization; Moderna (Dose Number: 1, Batch/Lot No: 008c21a, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 11May2021, for COVID-19 immunization.The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 18Dec2021 11:30, outcome "unknown", described as "Dose 1: Moderna; Dose 2: Moderna"; IMMUNISATION (non-serious) with onset 18Dec2021 11:30, outcome "unknown", described as "Booster"; MIGRAINE (non-serious) with onset 19Dec2021 08:00, outcome "recovering", described as "Migraine"; LYMPHADENOPATHY (non-serious) with onset 19Dec2021 08:00, outcome "recovering", described as "Swollen lymph node in underarm"; FATIGUE (non-serious) with onset 19Dec2021 08:00, outcome "recovering", described as "Extreme fatigue"; DIZZINESS (non-serious) with onset 19Dec2021 08:00, outcome "recovering", described as "Light headedness"; NAUSEA (non-serious) with onset 19Dec2021 08:00, outcome "recovering", described as "Nausea"; DECREASED APPETITE (non-serious) with onset 19Dec2021 08:00, outcome "recovering", described as "Loss of appetite". Therapeutic measures were not taken as a result of migraine, lymphadenopathy, fatigue, dizziness, nausea, decreased appetite.Additional Information:Prior vaccination within 4 weeks was reported as none. Prior vaccination patient was not diagnosed with COVID-19 and since the vaccination the patient had not been tested for COVID-19.No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: IgA nephropathy.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Nausea
Palpitations
Symptomtext
Woke up morning after, heart racing and nausea. Later in the day noticed swollen lymphnode in armpit and painful
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Hasn't see healthcare provider yet as I looked on EUA and says may take a few weeks to subsode and is normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Heart palpitations and high resting pulse. Had cardiology work up last year and was cleared as having no issues other than hypermobile joints.
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Chills
Immunisation
Lymph node pain
Lymphadenopathy
Pain
Symptomtext
For 2.5 days had body aches and chills, all worst in first night; For 2.5 days had body aches and chills, all worst in first night; Some chest pain; Very swollen lymph node in armpit; Very swollen lymph node in armpit painful; Primary immunisation: BNT162b2; Booster: COMIRNATY; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. A 35-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 05Jan2022 at 09:00 (Lot number: FL3197) at the age of 35 years as dose 3 (booster), single for COVID-19 immunisation. The patient did not have any relevant medical history. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EK8734; Route of administration: unspecified; Anatomical site: Left arm; Administration time: 09:00), administration date: 02Apr2021, when the patient was 34 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: ER8737; Route of administration: unspecified; Anatomical site: Left arm; Administration time: 09:00), administration date: 23Apr2021, when the patient was 35 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 at 09:00, outcome "unknown", described as "Primary immunisation: BNT162b2; Booster: COMIRNATY"; PAIN (non-serious), CHILLS (non-serious) all with onset 05Jan2022 at 21:00, outcome "recovered" (18Jan2022), and all described as "For 2.5 days had body aches and chills, all worst in first night"; CHEST PAIN (non-serious) with onset 05Jan2022 at 21:00, outcome "recovered" (an unknown date in Jan2022), described as "Some chest pain"; LYMPHADENOPATHY (non-serious) with onset 05Jan2022 at 21:00, outcome "recovered" (an unknown date in Jan2022), described as "Very swollen lymph node in armpit"; LYMPH NODE PAIN (non-serious) with onset 05Jan2022 at 21:00, outcome "recovered" (an unknown date in Jan2022), described as "Very swollen lymph node in armpit painful". Therapeutic measures were not taken as a result of pain, chills, chest pain, lymphadenopathy and lymph node pain. Additional Information: Patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- 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
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Dyspnoea
Hypotension
Symptomtext
The patient was given their Pfizer booster around 12:34pm, around 12:39pm the patient reported feeling dizzy. We asked him to lie down on several chairs. He said he did not have any difficulty breathing and we took his blood pressure, which was relatively low (103/72), then called EMS. The fire department arrived around 1:01pm, and EMS left with the patient around 1:06pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient does not know
- Vorgeschichte
- Patient does not know
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- Patient mentioned fainting when having blood drawn
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia oral
Lip swelling
Pharyngeal hypoaesthesia
Pharyngeal paraesthesia
Symptomtext
Client presented to the vaccination site with her sons. Client received Pfizer booster, LOT# FL3197 (left arm) at 10:45 on 01/05/2022. Client received the 1st dose Pfizer Lot# EW0183 on 05/14/2021 and 2nd dose Pfizer Lot# EW0178 on 06/08/2021. At approximately 1055, client complained of tingling, numbness in throat. RN 1 responded. Client was alert and oriented to person, place, time and situation and sitting in chair. Client's vital signs were obtained by RN 2: BP 162/99, P 66, O2 99%. Client reported, "My lips are numb and swelling." Client denied shortness of breath, dizziness, headache. Client has no history of allergies. RN 3 assessed client and prepared 50mg/1ml diphenhydramine. Diphenhydramine 50mg/ml was given IM (right arm) by RN 1 with patient permission at 1110. Client's vital signs were obtained at 1115: BP 141/97, P 65, R 16, O2 99%. Client stated that her lips were better, no tingling, her throat remained numb. Client was able to breath and swallow. Client was not taking any medications. Client denied any allergic reactions with her 1st and 2nd dose of Pfizer Covid vaccines. Client's vital signs at 11:20 AM: BP 157/107, P 74, R 16, O2 99%. Client stated that her throat was still numb and denied difficulty breathing, chest pain or other symptoms. RN 1 educated client on side effects of diphenhydramine, signs and symptoms of when to seek care, follow up with PCP and use of V-safe. Client verbalized understanding. Client's vital signs at 11:30 AM: 156/98, P 66, R 16, 02 99%. Client reported, "I'm feeling better, my throat was less tingling". Client stated that her son will drive her home. Client left facility with unlabored respirations and a steady gait at 1152.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Hyperhidrosis
Paraesthesia
Throat irritation
Symptomtext
Patient had an allergic reaction response to the vaccine. She started sweating and flushing 3 mins post giving her the vaccine. At 1:28 PM on 01/09/2022; patient reported tingling sensation around the mouth, scratching in her throat. We administered an Epinephrine pen at 1:32 PM and called 911. At 1:33 PM we took her vitals and they were as follow BP: 125/83, Pulse: 80, RR: 18 and O2:96. EMS arrived at 1:45PM and she was doing okay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Chest discomfort
Discomfort
Dyspnoea
Tachycardia
Symptomtext
The client reported that 3 days after receiving the vaccine, they developed chest pressure, tachycardia, and mild shortness of breath. The client also reported feeling, "like I wanted to get out of my body" and stated her body felt uncomfortable. The client described these symptoms as "anxiety," but denied any history of anxiety or these symptoms prior to receiving the vaccine. The symptoms lasted 1.5 days. The client didn't take any medications or follow up with any providers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- Vitamins and supplements
- Allergien
- The client reported a history of her "eyes rolling back" after taking compazine.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Induration
Palpitations
Peripheral swelling
Pruritus
Symptomtext
ABOUT 20 MINUTES AFTER VACCINATION, MY HEART WAS RACING . I WASN'T UNCOMFORTABLE, JUST AWARE OF IT...THIS CONTINUED UNTIL ABOUT 7PM WHEN I WENT TO BED...MY ARM STARTED TO ITCH AND SWELL ABOUT 3 HRS AFTER THE VACCINATION...AT FIRST IT WAS A BUMP ABOUT THE SIZE OF A MOSQUITO BITE. OVER TIME IT BECAME BIGGER...BY THE NEXT MORNING, 12/21 IT WAS THE SIZE OF A SILVER DOLLAR AND IT WAS A HARD LUMP THAT PROTRUDED ABOUT1/2 IN FROM MY ARM..IT BECAME BIGGER FOR THE NEXT WEEK OR SO ABOUT THE SIZE OF A GOLF BALL...
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE...JUST SEASONAL ALLERGIES
- Andere Medikamente
- ZYRTEC...WAS NOT TAKEN ON DAY BEFORE OR DAY OF VACCINATION
- Allergien
- PENICILLIN, SULFA DRUGS, VARIOUS FOODS, LATEX...
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Lymphadenopathy
Musculoskeletal discomfort
Symptomtext
My lymph nodes are still swollen and causing mild discomfort in my left chest and shoulder as well as making it a little hard to breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Women?s multivitamin with calcium and iron, over the counter acid reflux medicine
- Allergien
- Soy
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Injection site pain
Movement disorder
Symptomtext
At 3:00am on 1/9/2022, patient woke with chest pain, difficult to move entire body, and difficulty breathing. Pain at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Unknown, recommended patient go to hospital.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Back pain
Breast pain
Ear pain
Mobility decreased
Neck pain
Pain
Pain in extremity
Pain in jaw
Symptomtext
Severe pain in axilla, which progressed to include pain in left arm, left breast, neck/jaw/ear and left upper back. Pain is constant in nature and movement aggravates the pain. Use of left arm is limited due to pain with exertion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None as of yet. I will contact my healthcare provider tomorrow.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Neuropathy, fibromyalgia, central processing disorder, central pain syndrome, POTS, GERD, depression, PTSD
- Andere Medikamente
- Pregabalin, Amitriptyline, Omeprazole, Zoloft, Vitamin D, Furosemide, Potassium
- Allergien
- PCN, Enbrel
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Dyspnoea
Symptomtext
client stated that she was having a hard time deep breathing that lasted about 3 min, no other symptoms noted. Stated that during her first and second vaccine she also had adverse reaction. Denies symptoms of her throat closing or chest tightness. Client is being observed in post vac for 30 min. She is stable and breathing fine with no distress noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- endometriosis
- Vorgeschichte
- -
- Andere Medikamente
- meloxicam, benadryl, effexor, hydroxyzine, orilissa , allegra
- Allergien
- none
- Vorherige Impfungen
- pfizer
- Staat
- ND
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Dizziness
Feeling hot
Nausea
Paraesthesia
Symptomtext
Within first couple of minutes receiving the vaccine pt came back to registration to state she was feeling weak and lightheaded and sat down at the table put her head down on the table. Pt then states she is feeling warm and nauseated. Bag given to pt to get sick in if needed and ice packs applied to forehead and back of neck while she sat in a chair and laid her head on the table. Vitals signs were 138/90, pulse 82 and sats 97%. Pt given water bottle to drink from as well. Pt continued to report feeling hot and started with tingling all over and wanted to lay down on floor. A blanket was used to lay pt on floor and bunched up to support her head. Benadryl was given at 1325 50 mg orally. After some time pt went back and forth with being hot then chilled and nauseated and not. Pt had been given snack of some pop tarts as well at some point and vitals were retaken before pt left. 124/78 with a pulse of 76 and sats o 99%. Pt reports feeling a little better and states she is just going to go home and take some Tylenol. Pt's husband was here with her and drove her home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- cephalosporins, pin, biaxin, hydroxyzine, dicyclomine
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site paraesthesia
Paraesthesia
Symptomtext
Left arm tingling from shoulder through left thumb
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid+ 12/16/21 COVID negative 12/29/21
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol and ibuprofen
- Allergien
- Sulfur, penicillin, bacitracin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Atrial fibrillation
Balance disorder
Computerised tomogram
Fatigue
Gait inability
Tremor
Symptomtext
On the 25th, I woke up completely exhausted. On 12/26/2021 I woke up and I was very shaky and weak, no headache, it felt like I could not walk. I asked my doctor if this could be a reaction, and they stated it may. On 12/27/2021 I went to the doctor and saw that when I was walking I was extremely wobbly. Found that I was in A-Fib. Currently I still feel fatigued, and have low strength in my legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- CT Scan scheduled for 1/6/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin, Saline Spray, Flonase, Turmeric, Fish Oil, Potassium Chloride, Olmesartan, Montelukast, Prednisone, Eliquis
- Allergien
- Mold allergy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Injection site pain
Injection site swelling
Malaise
Nausea
Pyrexia
Tremor
Symptomtext
Symptoms began about 11 hours post injection. Started with general feeling of malaise, followed by uncontrollable shaking/shivering. Progressed to severe headache that did not subside with Ibuprofen and lasted 18 hours or more. Fever of about 100, severe nausea that prevented me from laying on my side (could only lay on my back). Severely tired. Strong pain at injection site, along with swelling. Continued tenderness at injection site 4 days post injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Probiotic and Sulferzyme (Young Living)
- Allergien
- sulfa drugs
- Vorherige Impfungen
- 2nd shot of Pfizer given in April; report filed previously Temporary VAERS E-Report No: 508807
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest X-ray normal
Chest discomfort
Computerised tomogram normal
Electrocardiogram normal
Feeling hot
Limb discomfort
Migraine
Pain
Pain in extremity
Sleep disorder
Symptomtext
Pt says migraines got more intense and longer duration. Lasted 5 days and actually woke up from the pain. Felt uncomfortable tightness in chest with warmth and leg started to ache and feel very heavy. went to ER on 1/3/2022 where did Cat scan, chest x-ray, ekc and bloodwork. Everything came out ok and pt was released with symptoms abating. Did not take any Tylenol or motrin. Says had some chest discomfort for 1st 2 doses but only last 2 days and stopped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Cat scan, chest x-ray, EKG, bloodwork
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- migraine medication
- Allergien
- none
- Vorherige Impfungen
- chest discomfort/tightness but only for 2 days
- Staat
- IL
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 01.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Gastrointestinal pain
Joint stiffness
Mobility decreased
Pain
Vomiting
Symptomtext
Woke up in the middle of the night with all over body pain and stiffness in joints like I couldn't move, diarrhea and vomiting and pain and burning sensation in digestive bowel. I couldn't keep anything down from water, Pedialyte, ice chips. my mom took me to doctor this morning on Tuesday 4, 2022 and was given anti-nausea medicine .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Dr performed a Covid test to be on safe side
- Aktuelle Erkrankungen
- Influenza A
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- gluten
- Vorherige Impfungen
- 5/01/21 covid Pfizer
- Staat
- OR
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Condition aggravated
Impaired quality of life
Tinnitus
Symptomtext
Tinnitus. I had my first dose on 04/27/2021 of the COVID-19 Pfizer shot. Tinnitus began with this vaccination. The ringing was in both ears and loud enough to be heard during normal conversation. Similar to the ringing after attending a loud concert without ear protection. No loss of hearing occurred. The ringing did not improve with my second dose on 05/25/2021. I visited a health care provider who examined my ears and confirmed that there were no other causes (structural, ear infection, etc.). I worked with HCP and was able to finally begin to reduce the volume of the ringing using ketotifen and cromolyn. It had improved to no ringing in left ear and a ring that could only be heard in the quiet in the right ear. However, with my booster shot, the ringing returned within the day to full strength again. We are very confident the tinnitus is due to the COVID vaccination. While not life threatening, it does substantively impact my quality of life, such as hearing my young children's voices clearly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Ear examination and hearing test May 10, 2021
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- allergies (environmental and food)
- Andere Medikamente
- Benedryl, iron, ketotifen
- Allergien
- none
- Vorherige Impfungen
- COVID Vaccine 1 04/27/2021; COVID Vaccine 2 05/25/2021
- Staat
- GA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Blood pressure increased
Chest pain
Computerised tomogram normal
Cough
Dyspnoea
Electrocardiogram normal
Swelling
X-ray normal
Symptomtext
I began to have severe left chest pain. I then began having trouble breathing. It comes and goes for about 8 minutes. I drove to the hospital. I began to have trouble swelling and coughing. It seems that when I moving it gets worst. They checked my vitals and I had elevated blood pressure. They did an EKG, normal result. I had heart pain so they did an X-ray, normal. They did a CT scan, normal results. They said that I could go home and was unsure what was causing. They gave me a prescription for a medicine for my throat. I still have left chest pain and it is starting to decreased each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG X-ray CT scan
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Post-concussive symptom (PCS)
- Andere Medikamente
- Spintex
- Allergien
- Pollen, Cat
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- JET / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Condition aggravated
Dizziness
Injection site rash
Injection site reaction
Nausea
Pain in extremity
Rash pruritic
Somnolence
Symptomtext
she became, dizzy, weak, nauseous, sleet long, long hours and is still sleepy. had and has a itchy rsh about the size of a playing around injection site. A sore arm. She is feeling better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none, slight high blood pressure, medicine keeps it in normal range
- Andere Medikamente
- metoprolol tartrate 25 MG - 1/2 tablet by mouth twice daily
- Allergien
- none
- Vorherige Impfungen
- sore arm only
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Hypoacusis
Hypoaesthesia
Paraesthesia
Sedation
Symptomtext
Right sided facial numbness and tingling, possible decreased hearing acuity of right ear only, accompanied by moderate headache, sedation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Chest pain
Feeling abnormal
No adverse event
Symptomtext
Fluttering heart - "felt like a butterfly moving across chest" , chest pain Brain fog *Pfizer booster - other shots were Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- * Did have flu shot about a month before. No adverse effects.
- Aktuelle Erkrankungen
- Dehydration from diarrhea - week or two before
- Vorgeschichte
- Depression/Anxiety Arthritis IBS
- Andere Medikamente
- Sertralin- Zoloft Arthritis Strength Tylenol Women's One a Day Probiotic
- Allergien
- Tetracycline Food sensitivities to : gluten, dairy, eggs, greasy items
- Vorherige Impfungen
- Flu shot when made in eggs
- Staat
- IL
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypertension
Malaise
Symptomtext
Systemic: Hypertension-Severe, Additional Details: Patient presented to pharmacy on 12/31 and wanted to report a side effect he though was related to his first dose of pfizer. Patient had previously had Covid twice before being vaccinated on 12/21. He said about 2 hours after vaccination he was not feeling well and had is BP checked and in came out to 250/125. He was rechecked 5 hours after this and everything had normalized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dysuria
Feeling cold
Immunisation
Irritability
Pyrexia
Tremor
Symptomtext
strong chills; shaking; cold; feverish irritated; hurt to pee; feverish irritated; dose received 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). A 57 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Dec2021 10:00 (Lot number: FL3197) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: GABAPENTIN; TIZANIDINE; ZOMIG; EXCEDRIN ASPIRIN FREE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955), administration date: 12Apr2021, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955), administration date: 22Mar2021, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 10:00, outcome "unknown", described as "dose received 3"; CHILLS (non-serious) with onset 17Dec2021 01:00, outcome "recovered" (Dec2021), described as "strong chills"; TREMOR (non-serious) with onset 17Dec2021 01:00, outcome "recovered" (Dec2021), described as "shaking"; FEELING COLD (non-serious) with onset 17Dec2021 01:00, outcome "recovered" (Dec2021), described as "cold"; PYREXIA (non-serious), IRRITABILITY (non-serious) all with onset 17Dec2021 01:00, outcome "recovered" (Dec2021) and all described as "feverish irritated"; DYSURIA (non-serious) with onset 17Dec2021 01:00, outcome "recovered" (Dec2021), described as "hurt to pee". Therapeutic measures were not taken as a result of chills, tremor, feeling cold, pyrexia, dysuria, irritability. Additional information: 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. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- GABAPENTIN; TIZANIDINE; ZOMIG; EXCEDRIN ASPIRIN FREE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Impaired driving ability
Injection site pain
Mobility decreased
Pain
Symptomtext
Pain in left arm (injection site) is so severe that patient cannot lift arm above 45 degrees and cannot drive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None yet, primary physician has been notified of event.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypersensitivity
Paraesthesia
Paraesthesia oral
Pharyngeal swelling
Urticaria
Symptomtext
Patient reported Hives and tingling in neck. Reaction worsening with continued hives and feeling of throat thickening up, and tingling tongue. Patient went to the ER and wad diagnosed with allergic reaction. Patient was given prednisone and diphenhydramine and told to follow up with primary next week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Supraventricular tachycardia
Symptomtext
Supraventricular tachycardia beginning at approximately 7:30am local time. Heartrate at beginning in upper 150s/lower 160s. Episode has continued for more than one hour, and still continues at this time of writing. Average heartrate of 139 over past hour with 43 readings (both measured manually at the carotid and electronically using finger sensor while in the supine position). Highest reading was 164, lowest reading was 119. Last reading above 150 was at 8:22am local time. Last reading above 130 was at 8:32am local time. Current time is 8:58am. Prior to episode, no lightheadedness noted. Following beginning of episode, increasing lightheadedness. Moderate headache prior to episode; unsure if episode has exacerbated or not.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Supraventricular tachycardia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Supraventricular tachycardia - almost always short episodes lasting <10 minutes, sporadic in nature (sometimes multiple months with no episodes, sometimes multiple episodes in one month)
- Andere Medikamente
- OTC Ibuprofen
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hypoaesthesia
Migraine
Muscular weakness
Nausea
Symptomtext
PATIENT EXPERIENCED LIGHTHEADENESS, NAUSEAU, WEAKNESS TO LEFT ARM, NUMBNESS TO LEFT ARM, AND PATIENT STATED "IT IS HER SEVERE MIGRAINE" 15 MIN POST VACCINATION WITH PFIZER COVID DOSE. PATIENT EXPERIENCED SIMILAR EFFECTS 2 DAYS AFTER SHE RECEVIED HER 1ST DOSE OF JANNSSEN VACCINE on June 18, 2021. NOT A NEW ONSET. PATIENT STATED FORGOT MIGRAINE MED AT HOME. 911 WAS CALLED HOWEVER PATIENT REFUSED TO GO TO ED. HUSBAND PICKED UP PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Condition aggravated
Dizziness
Palpitations
Symptomtext
Patient. Received Pfizer booster COVID vaccine (LOT#:FL3197) on 12/30/21 at 1647. Patient alerted EMT and stated that she felt heart palpitations and tightness in her chest. Patient stated that this happened to her about 3 weeks ago when she took melatonin. Patient stated that she went to the ED and Doctor told her she was experiencing an allergic reaction to the melatonin. The Doctor stated that her chest wall was swelling and was causing her heart palpitations. EMT took patients vital signs at 1706. BP: 124/77 HR: 63, O2: 98%. Patient stated that her heart palpitations and chest tightness comes and goes. RN's arrived on scene at 1707. EMT retook vital signs at 1711. BP: 122/76, HR:79, O2: 98%. Patient stated that her chest tightness was a 9/10. RN called EMS at 1713. Other RN gave patient Benadryl 50mg/mL at 1715. RN asked patient to stay an extra 30 minutes for observation. EMT retook patients vital signs at 1717. BP: 128/97, HR: 78, O2: 99%. EMS arrived at 1725. EMS assessed patient. Patient signed AMA. EMS left vaccination site at 1730. RN educated patient on worsening adverse symptoms from COVID Pfizer vaccine and when to seek EMS. RN recommended that patient go see PCP about heart palpitations. Patient verbalized understanding of education. Patient stated that palpitations are "getting better" and that her dizziness is now at a 4/10. Patient completed her observation time at 1747. Patient left vaccination site with her mom unassisted and with a steady gait at 1747.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Hypotension
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Paraesthesia oral
Symptomtext
Pt received Pfizer vaccine and was told to wait on the bench for 15 minutes. After 5 minutes, pt stated that she had a headache and her tongue was tingling but her throat was not swelling. After 10 more minutes, I checked on the patient and she said there was still a little tingling in her tongue. I gave her benadryl and asked again about her throat swelling. I made the patient wait 10 more minutes and she said she was ok to go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Gave pt benadryl
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Cough
Fatigue
Migraine
Pyrexia
Symptomtext
Fever, headache (migraine), coughing, fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Migraine headache
- Vorgeschichte
- Migraine headache
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Symptomtext
Tingling in the left hand since she got the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Not known
- Allergien
- NKA
- Vorherige Impfungen
- age 32; pfizer vaccine 1st dose- felt a lot of pain in her arm. pfizer second dose- felt the worst headache of her life. do not
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Dysgeusia
Paraesthesia oral
Rash
Sleep disorder
Tongue disorder
Symptomtext
Tingling on lips, thick tongue, rash on neck and chest, metallic taste on tongue within 1 hour of injection. Pain in both knees which would wake me up at night lasted for 3 days. Metallic tasted lasted for 2 days. Today is day 7 and I am free from symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- When I got home I took a Pepcid, Benadryl, and 81 mg Asa.
- Allergien
- Garlic and Levaquin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Condition aggravated
Diarrhoea
Fatigue
Headache
Nausea
Oropharyngeal pain
Pain
Respiratory tract congestion
Vomiting
Symptomtext
chills--lasted 36 hours, body aches, headache, sore throat, congestion, nausea, fatigue--continuing 72 hours later vomiting, diarrhea--30 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Will be getting a PCR test 12/24/21 (today) to rule out COVID since I have many of the symptoms
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hypothyroid, hypertension, GERD, pre-diabetes, depression
- Andere Medikamente
- levothyroxine, losartan, pantoprazole, furosemide, KLC, metformin, wellbutrin, Vitamin B12, Vitamin B6, fexofenamide
- Allergien
- NKA
- Vorherige Impfungen
- fatigue after the second COVID vaccine
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac stress test
Echocardiogram
Electrocardiogram ambulatory
Heart rate irregular
Palpitations
Symptomtext
Irregular heart beat/palpitations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Holter monitor, echo and stress test ordered. Results pending.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Neomycin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Booster shot, previous 2 doses were also Pfizer with no adverse effects. Waited at facility the required 15 minutes and left. About 5 minutes after that (about 20 minutes after receiving dose), part of the left side of my face back to my ear (same side as vaccine) started feeling tingly and partially numb. I can still feel things and there isn't any weakness or non-response from that side of my face, and I otherwise feel normal. I am still feeling this a couple hours later (as of 1:55pm).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ADHD and mild anxiety
- Andere Medikamente
- Lexapro 5mg, Adderall 10mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 18.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Electrocardiogram ambulatory
Heart rate irregular
Palpitations
Symptomtext
Heart Palpitation. I experience irregular heartbeats. Faster heartbeats. No treatments yet. But seeing a doctor about it. Everything started this year. I have never experienced this before. I cannot say exactly when it started this year. I am not sure if it started before I received my early vaccine doses or after. I did not report it because I was not sure of the start date and did not know heart palpitations were linked to Pfizer vaccines. I learned later that it was a side effect. But I had my booster shot on 12/16/2021 and I experienced heartbeat pacing faster and irregular this evening (12/18/2021).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I had a wearable device on for 14 days. Awaiting results.
- Aktuelle Erkrankungen
- High Blood pressure, Chronic Hepatitis B, Glaucoma, Chronic fatigue Asthma, Fibromyalgia, Muscular pains, Heart palpitations (started this year not sure if it started before my vaccination or after).
- Vorgeschichte
- Chronic Fatigue, BP, Hep. B, Fibromyalgia, chronic pain.
- Andere Medikamente
- Vemlidy, Clonidine tab., Amiloride, Olmesartan medoxomil tab., Vitamin D2 Caps., Latanoprost ophth., Dorzolamide Timolol ophth., Fluticasone Propionate nasal spray, Ipratropium bromide nasal spray, Advair HFA.
- Allergien
- Develop pimples from peanuts.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Dizziness
Dyspnoea
Feeling cold
Headache
Pain
Pain in extremity
Symptomtext
Freezing feeling throughout body. Whole body aches. No energy. Dizzy Really bad headache. Arm hurts for couple days . Breathing was hard to do
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None. Stayed home and took aspirin and drank plenty of liquids
- Aktuelle Erkrankungen
- Nothing
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Codeine, broccoli,beef, citrus, cauliflower, beans
- Vorherige Impfungen
- Pfizer 1 & 2 shots
- Staat
- OH
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 10.10.2023
- Impfdatum
- 08.10.2023
- Beginn
- 09.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Fatigue
Swelling face
Urticaria
Lip dry
Lymphadenopathy
Rash
Swelling
Symptomtext
Patient stats about 24 hours after receiving both COVID and Flu vaccine to left deltoid she started to develop rash to chest, neck and face, arms. She states she had slight swelling and feeling of dry lips. She took a benadrly took a nap and woke up with rash going to abdomen and legs. She took benadryl this morning due to worsening rash,. She reports never having allergic reaction to anything before. Assessment- Hives throughout upper body and now legs- Lymph node swelling to left cervical - left deltoid was where both Flu and COVID vaccines were given. 10/8- Vaccines given 10/9- rash develops 10/10 seen at Clinic- given Prednisone 40 mg x 5 days and instructed to take benadryl OTC - if symptoms do not improve or worsen after starting treatment follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- presumptive spider bite to right forearm- was treated with clindamycin starting 9/28/2023 she denies any recent COVID, or Flu illness. has taken both COVID and Flu vaccines in past without any reactions. Denies any recent respiratory illness.
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Lexapro 10 mg Tretinoin (Retin-A) 0.05% cream to face Last day of Clindamycin 300 mg every 6 hours for presumptive infected spider bite.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 30.12.2021
- Beginn
- 08.11.2022
- Tage bis Beginn
- 313,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
End stage renal disease
Malaise
Obstructive sleep apnoea syndrome
Upper gastrointestinal haemorrhage
Symptomtext
G47.33 OBSTRUCTIVE SLEEP APNEA 4/23/2023 COVID-19 DISEASE G47.33 OBSTRUCTIVE SLEEP APNEA 4/23/2023 MALAISE G47.33 OBSTRUCTIVE SLEEP APNEA 4/23/2023 ESRD (END STAGE RENAL DISEASE) G47.33 OBSTRUCTIVE SLEEP APNEA 4/23/2023 UPPER GI HEMORRHAGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.04.2023
- Impfdatum
- 23.04.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Diarrhoea
Dysphonia
Fatigue
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Urinary tract infection
Symptomtext
I first time experienced hoarseness and that progressed into congestion. I had a low-grade fever at 100.5 degrees. I also had fatigue. The second time was more significant, I felt much worse It started with sore throat congestion and low-grade fever at 100.4 degrees. The fever the lasted over several days. I also had significant fatigue. I also had a UTI type of symptoms, diarrhea. I was prescribed Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 10JUN2022 COVID-19 test - Positive; 11APR2023 COVID-19 test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bicuspid Aortic valve; Mild Asthma
- Andere Medikamente
- Valsartan; Atorvastatin; Ibuprofen; Xyzal
- Allergien
- Penicillin; Sulfa; Medrol; IV contrast; Allergies; Eggs; Nuts; Animal dander
- Vorherige Impfungen
- I had a rash on my left arm after the first COVID-19 vaccine.
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 12.04.2022
- Beginn
- 01.04.2023
- Tage bis Beginn
- 354,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I tested positive for Covid-19 on April 01, 2023 I experienced sore throat, & cough. I was taking Day quil and was prescribed Paxlovid had side effects with Paxlovid nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Covid testing
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine; Zetia; Calcium; Vitamin D; Aspirin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 29.03.2023
- Impfdatum
- 14.01.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 305,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropathy
Injection site pain
Periarthritis
X-ray limb abnormal
Symptomtext
Started feeling twinges in right shoulder joints. Two months later I started to feel pain in my right shoulder. Went to my doctor the next month and received an X-ray. Afterwards I was referred to a Physical Therapist. Was found that I have a frozen shoulder. Am still going to Physical Therapy and was told that it takes a few months to repair it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- 15NOV2022 X-ray, frozen shoulder.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma
- Andere Medikamente
- CLARITIN; omeprazole; fish oil; vitamin C.
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.02.2023
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Fatigue
Headache
Laboratory test abnormal
Pain
Pain in extremity
Protein total increased
Red blood cell sedimentation rate increased
Symptomtext
Within 2-3 hours Am a little fatigued, and a headache. Most days pain is 5-6/10 but with medication it can be as low as 4/10. Sharp pains in legs cause falls. About 4 falls, worse in the morning. When standing after sitting for a prolonged period or in the morning getting out of bed is when pain is at its worst. Finally sought Doctor's advice. He ran a test showing elevated protein markers, T reactive and ESR elevated. He referred to Rheumatologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- protein markers, T reactive and ESR elevated. Actual values unknown.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine
- Allergien
- Eggs; Latex; Orange Juice; Bactrim
- Vorherige Impfungen
- Flu shot triggered egg allergy, 2004 30 years old
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Fatigue
Heavy menstrual bleeding
Menstrual disorder
Pain
Symptomtext
I started feeling very tired and lightheaded. I was not due for my period, and I started my period, and it was very heavy. I had body aches and chills as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- TYLENOL; emergency vitamin powder
- Allergien
- NORCO
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 23.12.2021
- Beginn
- 14.12.2022
- Tage bis Beginn
- 356,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Diarrhoea
Dizziness
Feeling abnormal
Feeling hot
Nasopharyngitis
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Sneezing
Symptomtext
My symptoms began on December 14th with diarrhea and fever. I had chills during the night. The next day I had a slight fever, and my back was very hot. The next night I had chills. The following day I had runny nose and sneezing and slight sore throat. These symptoms lasted for 5 days. I took PAXLOVID beginning December 15th. I felt better and tested negative. But three days later I began to feel weird and tested positive again. I then had chills and cold-like symptoms. I also felt lightheaded and had diarrhea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive, 12/15/2022; Home COVID-19, negative, 12/20/2022; Home COVID-19, positive, 12/12/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 17.01.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 298,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Malaise
Symptomtext
Symptom onset 11/11/22. Treatment includes oxygen, medication, and admission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- -
- Allergien
- Effexor
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 28.08.2022
- Impfdatum
- 28.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose decreased
Blood test abnormal
Borrelia test
COVID-19
Cardiac monitoring
Cardiac stress test
Constipation
Dizziness
Electromyogram
Fatigue
Feeling abnormal
Headache
Laboratory test
Laboratory test abnormal
Nerve conduction studies
Poor peripheral circulation
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Initial Headache & fatigue. Always has allergies & congestion in and off so hard to tell if congestion worse. About 1 month later occasional brain-fog, light-headedness, constipation, extreme fatigue started. Sometimes call after lunch to pickup at school, come home & sleep. 05/16/22 went to PCP for symptoms. Bloodwork + Allergy meds/sinus infection. Never got better. Tested for Lyme, thyroid, etc. 06/16/22 labs came back good except slightly low sugar. Dr. Did a POTS test (-) & referred to Cardiologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 05/16/22- Bloodwork (-) except low sugar. 07-16/22- (+) CoVID , worse headaches & congestion, blood pooling in hands & feet 08/01/22- Dr. @ local Heart Institute- (in-house tests & bloodwork w/Flow Symmetry) 08/02/22- Stress Test (passed & Dr. Signed off on Sports Form to play Field Hockey) Took home 24 Hr. Heart Monitor & jug for 24 Hr. Urine sample 08/04/22- 21 Vials w/in 6 hours of bloodwork taken at local Hospital Center 08/09/22- Autonomic Test 08/12/22- Neurocognitive Test 08/16/22- Nerve Conduction/EMG 08/17/22- Tilt Table 08/26/22- Stopped playing field hockey BC makes symptoms worse. Nurse gave patient a pass for year to use whenever needed. Local Counselor rearranged classes so harder (AP) in mornings and gym & Study Hall in afternoons in case we need to move to Virtual Learning due to symptoms.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None. (Born 5 weeks early w/jaundice & ??Murmur. Outgrew by 9 months old)
- Andere Medikamente
- Childrens Benadryl, SmartyPants Multivitamin, Tretinol Topical cream (acne)
- Allergien
- Cats, dogs, horses, mold, dust & seasonal environmental
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 20.01.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 193,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Heart rate decreased
Heart rate irregular
Pruritus
Symptomtext
Patient came in today to get preventive vaccines. While discussing vaccination, patient states her blood pressure went up, had low pulse rate, irregular heart beat, occasional itchiness on injection arm since 2nd dose of pfizer in 1/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acne
Dermatitis
Erythema
Flushing
Hyperhidrosis
Inflammation
Rash
Symptomtext
Systemic: Allergic: Rash (specify: facial area, extremities)-Severe, Systemic: Flushed/Sweating-Severe, Additional Details: After receiving the Pfizer vaccines, patient's face broke-out in acne like blemishes. Patient's face is red and inflamed. He went to the dermatologist. They diagnosed him with dermatitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 03.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chiropractic
Head discomfort
Headache
Intervertebral disc degeneration
Intervertebral disc protrusion
Magnetic resonance imaging head abnormal
Magnetic resonance imaging spinal abnormal
Meningeal thickening
Musculoskeletal stiffness
Neck pain
Pain
Venogram normal
White matter lesion
Symptomtext
Patient is a 41-year-old who developed an abrupt onset headache in January after having a booster of COVID Pfizer vaccine. She recalls the headache onset approximately 10 days after the vaccine. With a rapid head turning she felt there was a pain in the neck as well. She was seen by a chiropractor with a couple of manipulations complicated by echo in her ear but with significant resolution of the neck pain. The headache now is described as right frontal pressure-like with stiffness of the neck improved with yoga exercises. There is no associated light or noise sensitivity. She categorically denies any positional headache, headache worsened by coughing and sneezing and by bowel movement. Visual obscuration is also not reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- MRI brain from Facility was personally reviewed. Pachymeningeal thickening is seen. This is diffuse without any nodules and is symmetric. Outside images from country were reviewed it appears the pachymeningeal thickening seems to be resolving but still persistent and bilateral frontal convexity. Outside images from country also included an MR venogram which was normal Chiari malformation or a pituitary descent was not seen. Mild to moderate white matter changes were seen MRI Brain: MRI Brain (6/22/2022) Impression: 1. Numerous bilateral primarily subcortical white matter T2/flair hyperintense foci, typically the result of chronic microvascular ischemia and can be seen in patients with migraine. Otherwise normal. MRI C Spine: MRI C-Spine (6/2022) Impression: 1. Multilevel degenerative disc disease of the cervical spine, as described in detail above, demonstrating 2mm disc bulges at C3-C4 and C5-C6, without canal or foraminal stenosis. 2. No abnormal signal or enhancement with the cervical or upper thoracic cord to suggest demyelination.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 03.08.2022
- Tage bis Beginn
- 224,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Dizziness
Fatigue
Oropharyngeal pain
Respiratory tract congestion
Symptomtext
Fatigue, congestion, sore throat, cough and lightheadedness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 03.08.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
Sore arm only, no other reactions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Bowel- constipation
- Andere Medikamente
- melatonin, fiber, multivitamins
- Allergien
- N.K.D.A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Came down with COVID two months after my second and last booster which was indicated above. Symptoms included, congestion, sore throat and tired. Tested positive using a home kit. Went to Urgent Care on 6/22/2022 and was prescribed Paxlovit. Took all dosages and after two days felt better. Tested negative on June 29. Retested July 1st and was positive with the same symptoms as before though milder. Finally tested negative July 12 2022 and have been negative since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home test using iHealth COVID-19 Antigen Rapid Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, high cholesterol
- Andere Medikamente
- Gingko, Multi Vitamin
- Allergien
- Motrin, Sulfa Drugs, Clindamycin
- Vorherige Impfungen
- Hives when I took a standard flu vaccine
- Staat
- CT
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 11.01.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 168,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Lower respiratory tract congestion
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Starting 06/28/2022, she had a fever, body aches, chest congestion and runny nose. It mimicked allergies but with a high fever and body aches. We did at an at home test the same day and it was positive. We called the doctor the same day and they advised me how to treat symptoms at home and advised me to seek care if it progresses. Within 48 hours, she woke up completely normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (06/28/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 09.01.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 182,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Fatigue
Nasopharyngitis
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had congestion and fatigue so I tested with my home COVID-19 test that came back positive. I then went to the local hospital and had the PCR COVID-19 test that also came back positive. I have a telehealth visit with my Primary Care Physician July 12, 2022. I feel fatigued and as if I have a pretty bad cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test PCR COVID -19 Test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Hydrochlorothiazide; Omeprazole; Losartan
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 06.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Headache
Tenderness
Symptomtext
5 minutes post injection patient complained of slight headache, neck tenderness on left side. BP 102/78, HR 51, RR 16 oxygen saturation 97% on room air. Instructed patient to increase hydration, rest. Reviewed adverse reaction with patient. Instructed patient to contact her physician if headache does not resolve or improve. Patient verbalized understanding. Pt admits to being anxious about vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 04.01.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 178,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
COVID-19
Cough
Fatigue
Feeling abnormal
Headache
Pyrexia
SARS-CoV-2 test positive
Symptomtext
By having a primary vaccination and a Pfizer Booster, I got a case of COVID-19 on July 1, 2022 and my symptoms were more than mild. I had joint pain, fever, headache, brain fog, exhaustion, coughing. I am a lot better but tested positive today, July 6, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 Tests, July 1, 2022 and July 6, 2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mild Asthma
- Andere Medikamente
- Zoloft; Women's Multivitamin
- Allergien
- Ceflacor; Seasonal Allergies; Mold
- Vorherige Impfungen
- Johnson and Johnson COVID- 19 Dose 1 on April 12, 2021, 40 years old, numbness on left side of face, tingling into face and jaw,
- Staat
- CT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Disturbance in attention
Eye irritation
Headache
Lymphadenopathy
Myalgia
Pain in extremity
Symptomtext
arm aching; my hand with arthritis aching; joints ache; muscles ache; head hurts; eyes burn; Lymph nodes swollen; Cannot focus, do not want to hold my head up; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Jun2022 at 09:15 as dose 4 (booster), single (Lot number: fl3197) at the age of 55 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Breast Cancer", start date: Sep2018 (unspecified if ongoing), notes: Breast Cancer; "low HDL" (unspecified if ongoing); "basal joint arthritis" (unspecified if ongoing), notes: basal joint arthritis; "Known allergies: Sulfa drugs" (unspecified if ongoing), notes: Known allergies: Sulfa drugs. Concomitant medication(s) included: LIPITOR; CELEBREX; TAMOXIFEN; TRIAMTERENE HYDROCHLORIDE; TYLENOL. Past drug history included: Levaquin, reaction(s): "Drug allergy", notes: Known allergies:levaquin; Erythromicin, reaction(s): "Drug allergy", notes: Known allergies:erythromicin. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: fh8027, Location of injection: Arm Right, Vaccine Administration Time: 10:00 AM), administration date: 12Dec2021, when the patient was 55-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: ep6955, Location of injection: Arm Right), administration date: 22Apr2021, when the patient was 54-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: el3247, Location of injection: Arm Right), administration date: 28Feb2021, when the patient was 54-year-old, for COVID-19 immunization. The following information was reported: DISTURBANCE IN ATTENTION (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "Cannot focus, do not want to hold my head up"; LYMPHADENOPATHY (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "Lymph nodes swollen"; PAIN IN EXTREMITY (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "arm aching"; EYE IRRITATION (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "eyes burn"; HEADACHE (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "head hurts"; ARTHRALGIA (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "joints ache"; MYALGIA (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "muscles ache"; ARTHRITIS (non-serious) with onset 21Jun2022 at 20:30, outcome "not recovered", described as "my hand with arthritis aching". Therapeutic measures were not taken as a result of pain in extremity, arthritis, arthralgia, myalgia, headache, eye irritation, lymphadenopathy, disturbance in attention. Additional information: Started on Wednesday evening around 8:30 pm with arm aching, and my hand with arthritis aching. Woke up today and joints ache, muscles ache, head hurts, eyes burn. Cannot focus, do not want to hold my head up, Lymph nodes swollen, particularly under arms. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not tested for COVID-19. Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine was no. List of any other medications the patient received within 2 weeks of vaccination: Lipitor, Celebrex, Tamoxifen, Triamterene HCL, Tyl. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis single joint (basal joint arthritis); Breast cancer female (Breast Cancer); Low HDL; Sulfonamide allergy (Known allergies: Sulfa drugs)
- Andere Medikamente
- LIPITOR; CELEBREX; TAMOXIFEN; TRIAMTERENE HYDROCHLORIDE; TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Vaccination site pain
Vaccination site swelling
Symptomtext
experienced swelling, soreness and redness at the site of injection; experienced swelling, soreness and redness at the site of injection; experienced swelling, soreness and redness at the site of injection; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). A 35-year-old female patient received BNT162b2 (BNT162B2), on 14Jan2022 at 15:00 as dose number unknown (booster), single (Lot number: FL 3197) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE # and MANUFACTURER UNKNOWN), for COVID-19 immunization. The following information was reported: VACCINATION SITE SWELLING (non-serious), VACCINATION SITE PAIN (non-serious), INJECTION SITE ERYTHEMA (non-serious) all with onset 15Jan2022, outcome "unknown" and all described as "experienced swelling, soreness and redness at the site of injection". Description of Event: 35-year-old female patient received booster Pfizer-BioNTech Covid-19 vaccine around 3pm Friday 14Jan2022. The day after she experienced swelling, soreness and redness at the site of injection. No fever and site was not warm to the touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 05.03.2021
- Beginn
- 29.06.2022
- Tage bis Beginn
- 481,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Fatigue
Malaise
Myalgia
Productive cough
SARS-CoV-2 test positive
Symptomtext
Pt has a history of bladder cancer, DVT/PE, COPD/emphysema, and is a direct admit from an outlying hospital. She reported that she had not been feeling well over the last 7 days with fatigue, muscle aches, cough and sputum production. She was found to be COVID positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 28.12.2021
- Beginn
- 19.06.2022
- Tage bis Beginn
- 173,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Chills
Cough
Fatigue
Heart rate decreased
Myalgia
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On Sunday night I had a bit of sore throat and fatigue. Monday again sore throat and fatigue. Monday night I started to get shivers, fever and cough. Then on Tuesday I had muscle soreness and more significant fever and cough with a heavy chest. Wednesday was the peek infection and I did video call with physician because my temperature was 103.8. My heart rate was 120 resting. My fever decreased during the day. Heart rate decreased day 4. Symptoms began to improve and by Friday just lingering fatigue and heavy cough; no more fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Home nasal swab test, negative; Urgent care rapid test, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Atorvastatin
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 16.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chest X-ray
Mammogram
Pain in extremity
Ultrasound scan
Symptomtext
Caller had a little pain after receiving each dose, couldn't extend arm for 24 hours, that's one side effect caller got from all doses caller received of the vaccine. This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 58-year-old female patient received BNT162b2 (BNT162B2), on 19Dec2020 as dose 1, 0.3 ml single (Lot number: EK5730, Expiration Date: 19Dec2020) intramuscular, on 08Jan2021 as dose 2, single (Lot number: EL1284) and on 16Jan2022 at 17:45 as dose 3 (booster), 0.5 ml single (Lot number: FL3197, Expiration Date: 30Jun2022) at the age of 58 years intramuscular, in left deltoid for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Caller had a little pain after receiving each dose, couldn't extend arm for 24 hours, that's one side effect caller got from all doses caller received of the vaccine.". Relevant laboratory tests and procedures are available in the appropriate section. Started having pinpoint under her armpit, a shooting pain under her armpit, pain was spreading under caller's armpit What was the dose, dosage units, formulation, route of administration and frequency when the adverse event occurred? 3rd dose, booster dose; intramuscular in left deltoid, dose unknown, thinks 0.5ml Indication Healthcare worker; Additional Information: Caller is calling about the Pfizer covid-19 vaccine booster dose. Caller is a Registered Nurse. Caller received the 1st and 2nd dose of the vaccine and was doing a traveling assignment in (withheld), and caller was requested to get the booster dose, which caller received 16Jan2022 in caller's left arm. Caller confirmed this was her 3rd dose of the vaccine. In Feb2022 caller started having pinpoint under her armpit, a shooting pain under her armpit. Came back in Mar2022 to start a new job and the pain was spreading under caller's armpit. Caller has a job and insurance, brought this up to the doctor, had an ultrasound of her left armpit and mammogram of left breast. HCP information: Caller saw the doctor once, doesn't remember the name of HCP, knows HCP is with (withheld). HCP address, phone number, email address: Unknown. Event details: Only reason caller is calling is when she went to get the ultrasound and mammogram they asked caller if caller got the vaccine and if caller got the booster dose of the vaccine. Then caller looked at the date she got the vaccine and the date she had the pain. Caller went online this morning and saw where there was mentioned that some people are having swollen lymph nodes after the booster, says some people when they go do mammograms, think it is cancer, doctors say no, they are saying the swollen lymph nodes should disappear in 4-6 weeks but caller's pain has not, caller doesn't think her lymph node is swollen. Caller can feel where the pain has initially started and the pain is spreading under caller's armpit. Caller didn't know about this, did the mammogram and ultrasound yesterday and the technician kept asking caller the same questions about the vaccine booster so caller went to see when she received the booster dose and when she stated having the pain, caller received the booster dose 16Jan2022 and then the pain started Feb2022. Started having pinpoint under her armpit, a shooting pain under her armpit, pain was spreading under caller's armpit: Start date of adverse event: Unknown specific date, sometime in Feb2022. Stop date of adverse event: The dull pain is ongoing, but the shooting pain is not constant. Seriousness criteria: Very dull pain, a 1 or 2, can feel the discomfort, but sometimes the pain can increase like a shooting pain. When the pain is shooting, the pain goes towards caller's breast. Caller confirms the pain is under caller's armpit on the left side. COVID-19 vaccine: All 3 doses caller received were the Pfizer COVID-19 vaccine. 1st dose: Date: 19Dec2020, NDC number, lot number, expiration date: Says Pfizer COVID-19 vaccine, 0.3ml, says BUD1500, expiration date: 19Dec2020, lot number: EK5730. Dose and route: 0.3ml, intramuscular in deltoid but doesn't say that on the card. 2nd dose: Date: 08Jan2021, NDC number, lot number, expiration date: Lot number: EL1284, this one does not have an expiration date written on the card. Dose and route: No dose written on the card. 3rd dose, booster dose: Date: 16Jan2022 NDC number, lot number, expiration date: Says Pfizer COVID-19 vaccine BNT162B2, lot number: FL3197, expiration date: 30Jun2022. Dose and route: Intramuscular in left deltoid, dose unknown, thinks 0.5ml. Causality: Thinks so, because didn't have any pain before and when caller went for tests the technician asked caller if caller received the booster dose, that's when caller put 1 and 1 together and read about it online. If caller had known caller wouldn't have taken the booster dose, had to take the booster dose for job. The pain doesn't go away. Tests: Caller did the ultrasound, mammogram, and chest x-ray, hasn't gone to the doctor yet. Said they don't see anything when caller had the tests done, maybe caller needs as CT scan to see what's going on. Confirmed caller didn't see the doctor yet, the person who did the tests said they don't see anything and that caller needs to go to the doctor to have other things done. Caller had a little pain after receiving each dose, couldn't extend arm for 24 hours, that's one side effect caller got from all doses caller received of the vaccine. Vaccine Supplemental Form: 1. Patient Details: Patient Last Name: (name withheld) First Name: (name withheld) Address: withheld Phone: # 2. Patient Age at Time of Vaccination in Months: or Years: 58 3. Pfizer Suspect Vaccine and Vaccination Details: NDC number, lot number, expiration date: Says Pfizer COVID-19 vaccine BNT162B2, lot number: FL3197, expiration date: 30Jun2022. Dose and route: Intramuscular in left deltoid, dose unknown, thinks 0.5ml. Time the Vaccination Was Given: About 5:45PM Anatomical Location of Administration of Pfizer vaccine considered as suspect: Left deltoid 4. Only: Vaccination Facility Type: Hospital, Vaccine Administered at Military Facility? : No Vaccination Facility Address: Facility Name: (withheld) Address: Unknown Phone: Unknown 5. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): All 3 doses caller received were the Pfizer COVID-19 vaccine. 1st dose: Date: 19Dec2020, NDC number, lot number, expiration date: Says Pfizer COVID-19 vaccine, 0.3ml, says BUD1500, expiration date: 19Dec2020, lot number: EK5730. Dose and route: 0.3ml, intramuscular in deltoid but doesn't say that on the card. 2nd dose: Date: 08Jan2021, NDC number, lot number, expiration date: Lot number: EL1284, this one does not have an expiration date written on the card. Dose and route: No dose written on the card. Route, Anatomical Location: Caller thinks she alternated deltoids for previous doses because caller had a little pain after receiving each dose, couldn't extend arm for 24 hours, that's one side effect caller got from all doses caller received of the vaccine. 6. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect: No 7. Adverse Event (AE) Details: Provide the time of onset of AE(s): Adverse Event: Started having pinpoint under her armpit, a shooting pain under her armpit, pain was spreading under caller's armpit. Confirmed caller's left armpit. 8. Additional Information: Did any AE(s) require a visit to: Emergency Room? No Physician Office? Was on traveling assignment, when caller got a new job and came back that's when caller went to the doctor. 9. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): No 10. AE(s) following prior vaccinations: Had a little pain after receiving each dose, couldn't extend arm for 24 hours, that's one side effect caller got from all doses caller received of the vaccine. 11. Patients Medical History (including any illness at time of vaccination)? None 12. Family Medical History Relevant to AE(s): Not provided 13. Relevant Tests: Caller did the ultrasound, mammogram, and chest x-ray, hasn't gone to the doctor yet. Said they don't see anything when caller had the tests done, maybe caller needs as CT scan to see what's going on. Confirmed caller didn't see the doctor yet, the person who did the tests said they don't see anything and that caller needs to go to the doctor to have other things done.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- Test Name: Chest x-ray; Result Unstructured Data: Test Result: Unknown Results; Test Name: Mammogram; Result Unstructured Data: Test Result: Unknown Results; Comments: left breast; Test Name: Ultrasound; Result Unstructured Data: Test Result: Unknown Results; Comments: left armpit.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patients Medical History (including any illness at time of vaccination)? None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 21.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
COVID-19
Fatigue
Feeling abnormal
Headache
Impaired work ability
Influenza like illness
Nasopharyngitis
Nausea
Oropharyngeal pain
Pain
Pain in extremity
SARS-CoV-2 test positive
Symptomtext
After the booster I had a feeling like a terrible flu and I had to take off work for 2 days. Then I got COVID-19 with headaches, extreme tiredness, sore throat, nauseous, and body aches. I received a positive COVID-19 PCR test at an urgent care. My symptoms lasted for about 3 days. After the 3rd day, I was feeling somewhat better. After COVID-19 in late March, I noticed that pain that shoots down my legs from my back. I have always had lower back pain but this is different with the leg pain. I feel like I get more colds and feeling bad more lately. I have to take off work more often since having COVID-19. It is like my immune system is weaker. It is like the degree of my symptoms are much more stronger. When I get a headache it is more extreme than normal and with body aches as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pace Maker; Low Back Pain
- Andere Medikamente
- Breo Ellipta; Spiriva; Bupropion; Amlodipine; Albuterol; Carvedilol; Sertraline; Multivitamins; Vitamin B6; Vitamin B12; Vitamin D3
- Allergien
- Ace Inhibitors
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 18.12.2021
- Beginn
- 13.05.2022
- Tage bis Beginn
- 146,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Ear pain
Fatigue
Feeling abnormal
Headache
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID case: both ears ache, significant cough, headache, and exhaustion from coughing. Zero energy, brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- 05/13/2022: Covid test - positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Knee replacement in June
- Andere Medikamente
- ARMOUR THYROID; TOPROL XL; simvastatin; amlodipine; vitamin D3; coQ10; niacin; zinc; vitamin C
- Allergien
- COMPAZINE; sulfa; LIPITOR; LEVAQUIN; ARIMIDEX; CELEBREX; ZETIA; corn
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 24.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Arthralgia
Computerised tomogram head
Fatigue
Inflammation
Malaise
Pyrexia
Sinusitis
X-ray
Symptomtext
Within an hour after I began experiencing pain in shoulder, fatigue, fever, and feeling very unwell. Shoulder was so painful I had to go to Illinois bone and joint. I was diagnosed with inflammation of the shoulder and given steroid shots. The shots improved symptoms but have worn off. Developed an acute sinus infection in March and I have taken 3 rounds of antibiotics with no improvement. Currently on 3rd round of steroid and antibiotics. If that doesn't work surgery is an option. In March I also stopped menstrual cycle. Waiting on an appointment to see OB/GYN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Performed x-ray. Performed CT scan of head.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 05.05.2022
- Tage bis Beginn
- 140,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Malaise
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
May 5, 2022 felt ill sore throat, runny nose. Used home covid test kit tested positive contacted my Primary Care doctor who prescribed Paxlovid for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- May 5, 2022 Home Covid Test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diverticulitis; Asthma; Sleep Apnea; Spinal Stenosis; Degenerative Dish Disease; Sjogren Syndrome; High Cholesteral; PTSD; Anxiety; Depression.
- Andere Medikamente
- Atorvastatin; Probiotx; Vitamin D; fish oil.
- Allergien
- Niacin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 05.06.2022
- Tage bis Beginn
- 171,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Oropharyngeal pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Almost 6 months after vaccination, on 6-4-2022, the patient started having a sore throat. On 6-5-2022, we tested the patient with a home Covid test with a positive result. We called pharmacy clinic for a telemedicine visit. He was not prescribed any medications. We did give him ibuprofen, tylenol, mucinex, sudafed sinus and a bunch of vitamins. He is perfectly fine today with no symptoms. I am reporting his breakthu case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- one at home Covid test on 6-5-2022 with positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Myalgia
Pain
Pyrexia
Symptomtext
Chills; mild fever; Very very very bad muscle aches; pains; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 50-year-old female patient received BNT162b2 (BNT162B2), on 08Jun2022 at 09:45 as dose 4 (booster), single (Lot number: FL3197, Expiration Date: 30Jun2022) at the age of 50 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 3, Single, LOT: FH8027), administration date: 09Dec2021, when the patient was 50-year-old, for covid-19 immunization; BNT162b2 (Dose 2, Single, LOT: EP6955), administration date: 30Mar2021, when the patient was 49-year-old, for covid-19 immunization; BNT162b2 (Dose 1, Single, LOT: EL3247 (handwriting is hard to read)), administration date: 09Mar2021, when the patient was 49-year-old, for covid-19 immunization; Flu shot, administration date: Oct2021, reaction(s): "sore arm". The following information was reported: CHILLS (non-serious) with onset 08Jun2022, outcome "recovered" (Jun2022); MYALGIA (non-serious) with onset 08Jun2022, outcome "recovered" (Jun2022), described as "Very very very bad muscle aches"; PYREXIA (non-serious) with onset 08Jun2022, outcome "recovered" (Jun2022), described as "mild fever"; PAIN (non-serious) with onset 08Jun2022, outcome "recovered" (2022), described as "pains". Additional information: No additional vaccines administered on Same Date of the Pfizer Suspect and no prior vaccinations (within 4 weeks). No emergency room visit, and physician office visit required for AEs. The patient stated that she did not feel great, but it wasn't that bad. After second booster shot about 0945 yesterday morning. Late last evening, started feeling chills, mild fever, very very very bad muscle aches and pains that persisted throughout the course of the evening.All symptoms have completely resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- 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
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- 08.04.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Cough
Headache
Myalgia
Pyrexia
Rhinorrhoea
Symptomtext
myalgias 31May2022; fevers 01Jun; cough; Rhinorrhea; HA; This is a spontaneous report received from a non-contactable reporter(s) (Nurse). A 60-year-old male patient received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4 (booster), single (Lot number: FL3197) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (prev dose product: COVID 19, prev dose brand: Pfizer, prev dose brand unknown: False, prev dose lot number: EL3247, prev dose lot unknown: False, prev dose administration date: 17Mar2021 prev dose dose number: 2), administration date: 17Mar2021, when the patient was 59-year-old, for Covid-19 immunization; BNT162b2 (prev dose product: COVID 19, prev dose brand: Pfizer, prev dose brand unknown: False, prev dose lot number: EL3247, prev dose lot unknown: False, prev dose administration date: 23Feb2021 prev dose dose number: 1), administration date: 23Feb2021, when the patient was 59-year-old, for Covid-19 immunization; Covid-19 vaccine (prev dose product: COVID 19, prev dose brand unknown: True, prev dose brand name unknown: COVID19 Vaccine, prev dose lot unknown: True, prev dose lot unknown reason: Not available/provided to reporter at the time of report completion, prev dose dose number: 3), for Covid-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 31May2022, outcome "unknown", described as "HA"; RHINORRHOEA (non-serious) with onset 31May2022, outcome "unknown", described as "Rhinorrhea"; COUGH (non-serious) with onset 31May2022, outcome "unknown"; PYREXIA (non-serious) with onset 31May2022, outcome "unknown", described as "fevers 01Jun"; MYALGIA (non-serious) with onset 31May2022, outcome "unknown", described as "myalgias 31May2022". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of myalgia, pyrexia, cough, rhinorrhoea, headache. Additional information: Patient took Paxlovid for the adverse events of myalgia, pyrexia, cough, rhinorrhoea, headache. Patient did not have covid prior vaccination. Patient had a positive nasal swab covid test post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220601; Test Name: Fever; Result Unstructured Data: Test Result:Fevers; Comments: fevers 01Jun
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- 27.12.2021
- Beginn
- 30.03.2022
- Tage bis Beginn
- 93,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropathy
Hip arthroplasty
Hypersensitivity
Immunisation reaction
Irritable bowel syndrome
Nerve compression
Oropharyngeal pain
Psoriasis
Sinus congestion
Sinus operation
Skin plaque
Skin weeping
Urticaria
Symptomtext
irritable bowel syndrome; Vaccination adverse reaction; Hives; Pinched nerve; hip replacement; joint did not fit properly on the socket; increased environmental allergies; Sinus congestion; sinus drainage; Sore throat; oozing of liquid on ears/skin oozing; psoriasis scale on both ears/psoriasis in ears with Humira; plaque on thumb/ plaque on right thumb; FACILITATED COLLECT This is a solicited report received from contactable reporter(s) (Consumer or other non HCP) for a sponsored program. The reporter is the patient. Other Case identifier(s): 22K-163-4236033-00. A 56-year-old male patient received BNT162b2 (BNT162B2), on 27Dec2021 as dose 3 (booster), single (Lot number: FL3197) at the age of 56 years intramuscular for covid-19 immunisation; adalimumab (HUMIRA), on 05Apr2012 (Batch/Lot number: unknown), in Jul2014 as 40 mg (1 in 2 wk) (Batch/Lot number: unknown), in 2017 (Batch/Lot number: unknown), on 18Sep2021 (Batch/Lot number: unknown) and on 07May2022 (ongoing) as 40 mg (1 in 2 wk) (Batch/Lot number: unknown), all subcutaneous for psoriasis. The patient's relevant medical history included: "Hip replacement", start date: 12Aug2021, stop date: 12Aug2021; "Moderate to severe chronic plaque psoriasis" (unspecified if ongoing); "Sleep apnea", start date: 1999 (unspecified if ongoing); "First left knee surgery", start date: 2015, stop date: 2015; "Abstains from alcohol" (unspecified if ongoing); "Nonsmoker" (unspecified if ongoing); "Gluten allergy" (unspecified if ongoing); "Egg allergy" (unspecified if ongoing); "Graft allergy" (unspecified if ongoing); "Trees allergy" (unspecified if ongoing); "Molds allergy" (unspecified if ongoing); "Dove allergy" (unspecified if ongoing); "Cat allergy" (unspecified if ongoing); "Dog allergy" (unspecified if ongoing); "Fish allergy" (unspecified if ongoing); "Allergic rhinitis" (unspecified if ongoing); "Grass allergy" (unspecified if ongoing); "Shrub pollen allergy" (unspecified if ongoing); "Dry eyes" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "Inflammation" (unspecified if ongoing); "Meniscus injury", start date: 2018, stop date: 2018; "Fall", start date: 2018 (unspecified if ongoing); "Hip replacement", start date: Nov2021, stop date: Nov2021. Concomitant medication(s) included: XIIDRA taken for dry eye; SINGULAIR taken for hypersensitivity; MONTELUKAST SODIUM AND LEVOCETIRIZINE DIHYDROCHLORIDE; DICLOFENAC SODIUM & MISOPROSTOL taken for inflammation; DAILY VITE [ASCORBIC ACID;COLECALCIFEROL;CYANOCOBALAMIN;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE]; FISH OIL; GLUCOSAMINE; PATADAY; REFRESH TEARS LUBRICANT; VITAMIN D3 1000; XYZAL. Vaccination history included: BNT162b2 (Dose 1, Intra-muscular, Lot number: ER8731), administration date: 18Apr2021, when the patient was 55-year-old, for Covid-19 immunisation, reaction(s): "Difficulty in walking", "Hip replacement", "Irritable bowel syndrome", "Skin oozing", "Skin plaque", "Vaccination adverse reaction", "Hives", "Pinched nerve", "Joint disorder", "Allergy aggravated", "Psoriasis", "Sinus congestion", "Nasal sinus discharge", "Sore throat"; BNT162b2 (Dose 2, Intra-muscular, Lot number: EW0185), administration date: 08May2021, when the patient was 55-year-old, for Covid-19 immunisation, reaction(s): "Difficulty in walking", "Hip replacement", "Irritable bowel syndrome", "Skin oozing", "Skin plaque", "Vaccination adverse reaction", "Hives", "Pinched nerve", "Joint disorder", "Allergy aggravated", "Sinus congestion", "Nasal sinus discharge", "Sore throat", "Psoriasis". The following information was reported: SKIN PLAQUE (medically significant) with onset 30Mar2022, outcome "recovered" (2022), described as "plaque on thumb/ plaque on right thumb"; PSORIASIS (medically significant) with onset Apr2022, outcome "not recovered", described as "psoriasis scale on both ears/psoriasis in ears with Humira"; SKIN WEEPING (medically significant) with onset May2022, outcome "unknown", described as "oozing of liquid on ears/skin oozing"; IRRITABLE BOWEL SYNDROME (medically significant), outcome "unknown"; IMMUNISATION REACTION (medically significant), outcome "recovering", described as "Vaccination adverse reaction"; URTICARIA (medically significant), outcome "unknown", described as "Hives"; NERVE COMPRESSION (medically significant), outcome "unknown", described as "Pinched nerve"; HIP ARTHROPLASTY (medically significant), outcome "recovered", described as "hip replacement"; ARTHROPATHY (medically significant), outcome "unknown", described as "joint did not fit properly on the socket"; HYPERSENSITIVITY (medically significant), outcome "unknown", described as "increased environmental allergies"; SINUS CONGESTION (medically significant), outcome "unknown"; SINUS OPERATION (medically significant), outcome "unknown", described as "sinus drainage"; OROPHARYNGEAL PAIN (medically significant), outcome "unknown", described as "Sore throat". The action taken for adalimumab was dosage not changed. The reporter considered "irritable bowel syndrome", "hip replacement", "oozing of liquid on ears/skin oozing" and "plaque on thumb/ plaque on right thumb" not related to BNT162b2. The reporter considered "vaccination adverse reaction" related to BNT162b2. The reporter's assessment of the causal relationship of "hives", "pinched nerve", "joint did not fit properly on the socket", "increased environmental allergies", "sinus congestion", "sinus drainage", "sore throat" and "psoriasis scale on both ears/psoriasis in ears with humira" with the suspect product(s) BNT162b2 was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. Solicited report by a consumer of a 52 year old male with events of hard time walking, puts pressure on the legs, torn cartilage wen patient was knocked down and hip replaced and non-serious irritable bowel syndrome, oozing of liquid on ears/skin oozing, plaque on thumb, plaque on right thumb, side effects from covid shots and booster, hives off and on possibly caused heat, pinched nerve in back, torn cartilage wen patient was knocked down, joint did not fit properly on the socket, increased environmental allergies, sinus congestion, sinus drainage, sore throat and psoriasis scale on both ears/ psoriasis in ears with Humira 40mg/0.4ml (adalimumab). Information was also received from a healthcare professional. On unknown dates, the patient experienced irritable bowel syndrome, side effects from covid shots and booster, hives off and on possibly caused heat, pinched nerve in back, joint did not fit properly on the socket, increased environmental allergies, sinus congestion, sinus drainage and sore throat. In 2018, the patient experienced torn cartilage wen patient was knocked down and torn cartilage wen patient was knocked down. In 2018, the torn cartilage wen patient was knocked down resolved. On 12Aug2021, the patient experienced hard time walking, puts pressure on the legs. In Sep2021, the hard time walking, puts pressure on the legs resolved. On 22Nov2021, the patient experienced hip replaced. On 30Mar2022, the patient experienced plaque on thumb. In Apr2022, the patient experienced psoriasis scale on both ears/ psoriasis in ears. In May2022, the patient experienced oozing of liquid on ears/ skin oozing and plaque on right thumb. In 2022, the plaque on thumb resolved. On an unknown date, hip replaced resolved. Pfizer biontech covid-19 vaccine (tozinameran) was also considered suspect. The patient had second left knee surgery in 2018, the procedure was to scope the remaining cartilage that was torn when he was knocked down. He had left hip replaced on 12Aug2021, because he had difficulty walking, puts pressure on the legs. He mentioned that the joint did not fit properly on the socket. He had Irritable bowel syndrome. He had side effects from covid shots and booster. He had hives off and on possibly caused heat and Pinched nerve in back. He had to stopped Humira for six months because of a hip replacement. He also mentioned he has spinal injection every six months for the pinched nerve on his back. the alternative etiology for the event hard time walking, puts pressure on the legs was reported as pinched nerve on the back. He moved about two years ago and has been having increased environmental allergies since moving. He had sinus congestion, drainage and sore throat and had psoriasis in his ears and it had now gone away since restarting injections. His skin was cracking and oozing. It was unknown if patient was enrolled in a Covid-19 Vaccine Trial. Change History: On 25May2022, received updates to patient demographics, medical history, event information, reporter opinion of causality, company opinion of causality, company alternative etiology, suspect drug information, concomitant drug information and narrative description. The events of "torn cartilage wen patient was knocked down", "hip replaced", "oozing of liquid on ears", "plaque on thumb", "plaque on right thumb", "psoriasis scale on both ears", "torn cartilage wen patient was knocked down" and "joint did not fit properly on the socket" were added. The event of "left hip replaced" was amended to "hard time walking, puts pressure on the legs". On 25May2022, received updates to medical history, event information, reporter opinion of causality, company opinion of causality, company alternative etiology, suspect drug information, concomitant drug information and narrative description. The events of "increased environmental allergies", "sinus congestion", "sinus drainage", "sore throat" and "psoriasis scale on both ears/ psoriasis in ears" were added. The event of "oozing of liquid on ears" was amended to "oozing of liquid on ears/ skin oozing". The event of "psoriasis scale on both ears" was removed. The reporter's causality for the event(s) of left hip replaced, irritable bowel syndrome, side effects from covid shots and booster, hives off and on possibly caused heat and pinched nerve in back with humira (Adalimumab) was no reasonable possibility. The reporter's causality for event vaccination adverse reaction with Pfizer biontech covid-19 vaccine was possible. Drug: Humira 40mg/0.4ml (40 milligram, solution for injection in pre-filled pen) (adalimumab), 1151223, unknown, 1159670, 1159670, 1159670. Causality: Irritable bowel syndrome (Irritable bowel syndrome): Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine) and Causality as per Mfr. (Drug/Vaccine): No reasonable possibility. Dechallenge: N/A. Skin oozing (Skin weeping), Action(s) taken with drug: Drug discontinued. Causality as per reporter (Drug/Vaccine): Related, Causality as per Mfr. (Drug/Vaccine): Reasonable possibility. Dechallenge: No. Skin plaque (Skin plaque), Action(s) taken with drug: Drug discontinued. Causality as per reporter (Drug/Vaccine): Not related, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: Yes. Skin plaque, Causality as per reporter (Drug/Vaccine): Related, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: Yes. Vaccination adverse reaction (Immunization reaction), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): No reasonable possibility, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: N/A. Hives (Urticaria), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): No reasonable possibility, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: N/A. Pinched nerve (Nerve compression), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): No reasonable possibility, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: N/A. Joint disorder (Arthropathy), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not Reported, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: Unk. Allergy aggravated (Hypersensitivity), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility. Dechallenge: N/A. Sinus congestion, Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Causality as per Mfr. (Drug/Vaccine): No reasonable possibility, Dechallenge: N/A. Nasal sinus discharge (Paranasal sinus hypersecretion), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Causality as per Mfr. (Drug/Vaccine): Not assessable, Dechallenge: N/A. Causality for Humira 40MG/0.4ML (adalimumab): The reporters causality for the event(s) of hard time walking, puts pressure on the legs, torn cartilage wen patient was knocked down onset in 2018, hip replaced, irritable bowel syndrome, plaque on thumb, side effects from covid shots and booster, hives off and on possibly caused heat and pinched nerve in back with humira 40mg/0.4ml (adalimumab) was no reasonable possibility. The reporters causality for the event(s) of oozing of liquid on ears/ skin oozing and plaque on right thumb with humira 40mg/0.4ml (adalimumab) was a reasonable possibility. The reporter's causality for the event(s) of torn cartilage wen patient was knocked down onset in 2018, joint did not fit properly on the socket, increased environmental allergies, sinus congestion, sinus drainage, sore throat and psoriasis scale on both ears/ psoriasis in ears was not provided. Agency opinion is that there is no reasonable possibility that the events of hard time walking, puts pressure on the legs, torn cartilage wen patient was knocked down onset in 2018, hip replaced, irritable bowel syndrome, plaque on thumb, plaque on right thumb, side effects from covid shots and booster, hives off and on possibly caused heat, pinched nerve in back, torn cartilage wen patient was knocked down onset in 2018, joint did not fit properly on the socket, increased environmental allergies and psoriasis scale on both ears/ psoriasis in ears are related to humira 40mg/0.4ml (adalimumab). Agency opinion is that there is a reasonable possibility that the event of oozing of liquid on ears/ skin oozing is related to humira 40mg/0.4ml (adalimumab). AgencY opinion is that the events of sinus congestion, sinus drainage and sore throat are not assessable. Drug: Pfizer Biontech Covid-19 Vaccine (tozinameran) (tozinameran), ER8731, EW0185, FL3197. Causality: Irritable bowel syndrome, Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: N/A. Skin oozing (Skin weeping), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: N/A. Skin plaque (Skin plaque), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: N/A. Vaccination adverse reaction (Immunization reaction), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Related, Dechallenge: N/A. Hives (Urticaria), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A. Pinched nerve (Nerve compression), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A, Joint disorder (Arthropathy), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A. Allergy aggravated (Hypersensitivity), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A. Sinus congestion, Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A. Nasal sinus discharge (Paranasal sinus hypersecretion), Action(s) taken with drug: Unknown, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A. Did event abate after stopping drug: NA. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected. Follow-up (01Jun2022): This is a solicited follow-up report based on the information received by Pfizer from Agency (Mfr Control No.: 22K-163-4236033-00). A contactable 56-year-old male consumer reported for himself that: Updated Information included: Patient Details (weight, height) added. Other Relevant History (historical vaccine notes, age, RMH) added. BNT162B2 Dosage Regimens (lot number) added. Humira Substance Information (strength) added. Humira Dosage Regimens (start date, slider #02-slider#05) added. Concomitant drugs added. New events added. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender's Comments: Based on the information available, the causal relationship between the reported events (except irritable bowel syndrome", "hip replacement", "oozing of liquid on ears/skin oozing", "plaque on thumb/ plaque on right thumb" and "skin plaque (skin plaque)) and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate Events irritable bowel syndrome", "hip replacement", "oozing of liquid on ears/skin oozing", "plaque on thumb/ plaque on right thumb" and "skin plaque (skin plaque) are considered unrelated to suspect product BNT162B2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Abstains from alcohol; Allergic rhinitis; Allergic to dogs; Allergy; Allergy to animal; Allergy to molds; Allergy to plants; Dry eyes; Egg allergy; Fall; Fish allergy; Food allergy; Graft infection; Grass allergy; Hip replacement; Inflammation; Knee surgery NOS; Meniscus injury; Nonsmoker; Plaque psoriasis; Pollen allergy; Sleep apnea; Soap allergy
- Andere Medikamente
- XIIDRA; SINGULAIR; MONTELUKAST SODIUM AND LEVOCETIRIZINE DIHYDROCHLORIDE; DICLOFENAC SODIUM & MISOPROSTOL; DAILY VITE [ASCORBIC ACID;COLECALCIFEROL;CYANOCOBALAMIN;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLO; FISH OIL; GLUCOSAMINE; PATADAY;
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Limb discomfort
Musculoskeletal stiffness
Myalgia
Symptomtext
stiffness in shoulder and arm/stiffness; fatigue; muscle pain; soreness in shoulder and arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 31Mar2022 as dose 4 (booster), single (Lot number: FL3197, Expiration Date: 30Jun2022) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hernia" (unspecified if ongoing), notes: Hernia Was in his belly; "prostate" (unspecified if ongoing); "Blood pressure" (unspecified if ongoing); "thyroid" (unspecified if ongoing). Concomitant medication(s) included: TAMSULOSIN HCL taken for prostate ablation; LISINOPRIL taken for blood pressure abnormal; LEVOTHYROXINE taken for thyroid disorder; FINASTERIDE taken for prostate ablation. Vaccination history included: covid-19 vaccine (First Dose: 24Feb2021 Pfizer LOT: EM9810 Caller states it does not say lot number but has the number listed next to it. NDC: unknown EXP: 30Jun2021), administration date: 24Feb2021, when the patient was 68-year-old, for Covid-19 immunization; covid-19 vaccine (Second Dose: 17Mar2021 LOT: EN6208 EXP: 30Jun2021 NDC: Unknown It was 2 weeks later. 11:40AM), administration date: 17Mar2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (First Booster: 29Sep2021 Pfizer LOT: FF2589 EXP: Unknown NDC: unknown), administration date: 29Sep2021, when the patient was 68-year-old, for COVID-19 immunization. The following information was reported: MUSCULOSKELETAL STIFFNESS (non-serious), outcome "unknown", described as "stiffness in shoulder and arm/stiffness"; FATIGUE (non-serious), outcome "unknown"; MYALGIA (non-serious), outcome "unknown", described as "muscle pain"; LIMB DISCOMFORT (non-serious), outcome "unknown", described as "soreness in shoulder and arm". Additional information: Caller said he had no trouble from his first 3 doses of Pfizer covid vaccine, but with this 2nd booster dose, caller said he is experiencing a persistent stiffness in shoulder and arm. Caller wants to know if this side effect is associated with the booster and that others reported of having this as well. Caller is asking, if for his future boosters, could the vaccine be administered in his right arm instead of the left arm. Call is regarding the Pfizer Covid-19 second booster. He had the 2 regular shots and the first and second booster. He had no trouble at all with the first 3 shots. The second booster, the last shot, he had 1Apr2022 and has had a lot of stiffness and soreness in his shoulder and arm. It has persisted until now. He is calling to see if that happens. Reporter details: Email: Does not have email to provide Primary / Prescribing Healthcare Professional Info: Address, telephone, email: Unknown Event Details: Stiffness: It occurred probably within 2 weeks of the last shot which was around 1Arp2022. Caller then states it was actually 31Mar2022 that he got the last shot, the second booster and not 1Apr2022 as previously stated. Does not know exactly when he noticed it. It was within 2 weeks of the shot. Had surgery on 20May2022 and when he was going into surgery, he was aware of them. Outcome: Was really a weird thing that was couple of times, he thought. Thought he was coming out of it persisted and he thought he was coming out of it. It is a hard thing to describe. It progressed from stiffness to soreness and has been a really weird thing. He sleeps on his side and when he had surgery, he had to sleep on that sore shoulder all the time. It was hernia surgery and he couldn't sleep o the right side. Clarified that it was his left arm, that had the stiffness and soreness in the shoulder. His left side has taken a beating. Soreness in shoulder and arm: He states that when they test the arm and stuff and when he has a check up, they have to put out his arms to see how much he can lift with his arm. They put their arm on his arm arm and when he puts his arm straight, that is where he really feels it, when his arms are straight out and he is trying to push his arm up. It is like trying to lift something with his arm. When his arm is straight out, he can really feel it. He is doing it right now and he can't do it. It is just not right. Treatment: None Suspect products Covid-19 vaccine: First Dose: 24Feb2021 Pfizer LOT: EM9810 Caller states it does not say lot number but has the number listed next to it. NDC: unknown EXP: 30Jun2021 Second Dose: 17Mar2021 LOT: EN6208 EXP: 30Jun2021 NDC: Unknown It was 2 weeks later. 11:40AM First Booster: 29Sep2021 Pfizer LOT: FF2589 EXP: Unknown NDC: unknown Second booster: 31Mar2022 LOT: FL3197 EXP: 30Jun2022 NDC: unknown Indication: Trying to stay on top of it and stay immunized as he can vaccine supplemental form 1. patient details: patient last name; first name: withheld. Additional information: Call is regarding the Pfizer Covid-19 second booster. He had the 2 regular shots and the first and second booster. He had no trouble at all with the first 3 shots. The second booster, the last shot, he had 1Apr2022 and has had a lot of stiffness and soreness in his shoulder and arm. It has persisted until now. He is calling to see if that happens. Reporter details: Email: Does not have email to provide Primary / Prescribing Healthcare Professional Info: Address, telephone, email: Unknown Event Details: Stiffness: It occurred probably within 2 weeks of the last shot which was around 1Arp2022. Caller then states it was actually 31Mar2022 that he got the last shot, the second booster and not 1Apr2022 as previously stated. Does not know exactly when he noticed it. It was within 2 weeks of the shot. Had surgery on 20May2022 and when he was going into surgery, he was aware of them. Outcome: Was really a weird thing that was couple of times, he thought. Thought he was coming out of it persisted and he thought he was coming out of it. It is a hard thing to describe. It progressed from stiffness to soreness and has been a really weird thing. He sleeps on his side and when he had surgery, he had to sleep on that sore shoulder all the time. It was hernia surgery and he couldn't sleep o the right side. Clarified that it was his left arm, that had the stiffness and soreness in the shoulder. His left side has taken a beating. Soreness in shoulder and arm: He states that when they test the arm and stuff and when he has a check up, they have to put out his arms to see how much he can lift with his arm. They put their arm on his arm arm and when he puts his arm straight, that is where he really feels it, when his arms are straight out and he is trying to push his arm up. It is like trying to lift something with his arm. When his arm is straight out, he can really feel it. He is doing it right now and he can't do it. It is just not right. Treatment: None Suspect products Covid-19 vaccine: First Dose: 24Feb2021 Pfizer LOT: EM9810 Caller states it does not say lot number but has the number listed next to it. NDC: unknown EXP: 30Jun2021 Second Dose: 17Mar2021 LOT: EN6208 EXP: 30Jun2021 NDC: Unknown It was 2 weeks later. 11:40AM First Booster: 29Sep2021 Pfizer LOT: FF2589 EXP: Unknown NDC: unknown Second booster: 31Mar2022 LOT: FL3197 EXP: 30Jun2022 NDC: unknown Indication: Trying to stay on top of it and stay immunized as he can vaccine supplemental form 1. patient details: patient last name; first name: withheld. Caller states it does not say lot number but has the number listed next to it. NDC: unknown EXP: 30Jun2021 Second Dose: 17Mar2021 LOT: EN6208 EXP: 30Jun2021 NDC: Unknown It was 2 weeks later. 11:40AM First Booster: 29Sep2021 Pfizer LOT: FF2589 EXP: Unknown NDC: unknown 6. Additional Vaccines Administered on Same Date of the Pfizer Suspect: No 7. The adverse event required any visit to emergency room not provided 9. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): Possibly the flu vaccine. Believes it would be the only one. He takes other vaccines before this fall and the flu vaccine was the only one before Covid. It very well may have been within 4 weeks. Maybe a little soreness but, nothing like this. Clarified that the caller was referring to just in general, not to any specific vaccines. It may have been the pneumonia vaccine or something. He has gotten all kinds of vaccines. NDC, LOT, EXP Pneumonia vaccine. Maybe a little soreness but, nothing like this. Clarified that the caller was referring to just in general, not to any specific vaccines. It may have been the pneumonia vaccine or something. He has gotten all kinds of vaccines. NDC, LOT, EXP Pneumonia vaccine. Medicinal Product Name as Reported by the Primary Source for Other medicines Tamsulosin HCL: Has been taking 2 or 3 years. Lost track of everything before epidemic. Has probably been 3 or 4 years for both Tamsulosin and Finasteride. Additional Information for Other medicines Lisinopril: has been taking for years. Additional information on drug: Additional Information for Other medicines Levothyroxine: Has been taking more years than the Lisinopril, has been a long time. 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: Blood pressure abnormal; Hernia (Hernia Was in his belly); Prostate ablation; Thyroid disorder
- Andere Medikamente
- TAMSULOSIN HCL; LISINOPRIL; LEVOTHYROXINE; FINASTERIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pain
Vaccination site pain
Symptomtext
minor aches; Slight soreness at injection site; Sudden onsite of moderate chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old male patient received BNT162b2 (BNT162B2), on 01Jun2022 at 09:15 as dose 4 (booster), single (Lot number: FL3197) at the age of 44 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunisation series complete(First, second and third dose), MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 01Jun2022 at 23:00, outcome "recovering", described as "Slight soreness at injection site"; CHILLS (non-serious) with onset 01Jun2022 at 23:00, outcome "recovering", described as "Sudden onsite of moderate chills"; PAIN (non-serious) with onset 02Jun2022, outcome "recovering", described as "minor aches". Therapeutic measures were not taken as a result of vaccination site pain, chills, pain. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient stated he had slight soreness at injection site, sudden onsite of moderate chills at approx. 14hrs with minor aches at approx. 24hrs. The patient was not diagnosed with COVID-19, prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Nausea
Poor quality sleep
Pyrexia
Vaccination site pain
Vomiting
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old male patient received BNT162b2 (COMIRNATY), as dose number unknown (booster), single (Lot number: FL3197, Expiration Date: 30Jun2022) for covid-19 immunization. The patient's relevant medical history included: "elevated blood pressure" (unspecified if ongoing), notes: elevated blood pressure. Concomitant medication(s) included: LISINOPRIL AND HYDROCHLORTIAZIDE taken for blood pressure increased. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer.), for COVID-19 Immunization; Covid-19 vaccine (Dose number unknown first Booster, unknown manufacturer.), for COVID-19 Immunization. The following information was reported: POOR QUALITY SLEEP (non-serious), outcome "recovering", described as "A very restless night of sleep was experienced"; VACCINATION SITE PAIN (non-serious), outcome "recovering", described as "developed soreness at the injection site"; CHILLS (non-serious), outcome "recovering"; NAUSEA (non-serious), outcome "recovering", described as "very nauseous/bit of nausea"; VOMITING (non-serious), outcome "unknown", described as "became very nauseous, which led to vomiting"; PYREXIA (non-serious), outcome "recovering", described as "fever"; HEADACHE (non-serious), outcome "recovering", described as "a persistent headache". Additional information: Several hours after receiving the 2nd booster of Comirnaty, patient developed soreness at the injection site. 12 hours after the dose, patient experienced chills. 14 hours after dose, patient developed a fever and became very nauseous, which led to vomiting. A very restless night of sleep was experienced. He awoke to a bit of nausea and a persistent headache. Symptoms at the 25 hour point (post dose) are improving substantially. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure increased (elevated blood pressure.)
- Andere Medikamente
- LISINOPRIL AND HYDROCHLORTIAZIDE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Pain
Symptomtext
Soreness in arm was achy and tired; Soreness in arm was achy and tired; Soreness in arm was achy and tired; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old male patient received BNT162b2 (BNT162B2), on 01Jun2022 at 09:00 as dose 4 (booster), single (Lot number: FL3197) at the age of 65 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ELIQUIS; ATORVASTATIN; DILTIAZEM. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for Covid-19 Immunization; Covid-19 vaccine (Dose 3, Unknown Manufacturer), for Covid-19 Immunization. The following information was reported: ARTHRALGIA (non-serious), PAIN (non-serious), FATIGUE (non-serious) all with onset 01Jun2022 at 20:00, outcome "recovered" (Jun2022) and all described as "Soreness in arm was achy and tired". Therapeutic measures were not taken as a result of arthralgia, pain, fatigue. Additional information: It was reported that the patient had received no other vaccines within 4 weeks prior to covid vaccine. The patient had not diagnosed with covid prior vaccination and the patient had not tested to covid post vaccination. The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ELIQUIS; ATORVASTATIN; DILTIAZEM.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- -
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
Soreness in arm at injection site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An elderly female patient (not pregnant) received BNT162b2 (BNT162B2), on 27May2022 at 11:45 as dose 4 (booster), single (Lot number: FL3197) intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, unknown manufacturer), for Covid-19 immunization; Covid-19 vaccine (Dose 2, unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose 3, unknown manufacturer), for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 27May2022 at 22:00, outcome "recovering", described as "Soreness in arm at injection site". Therapeutic measures were not taken as a result of vaccination site pain. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- 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
- -
- Staat
- SC
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
COVID-19
Epistaxis
Feeling abnormal
Influenza A virus test positive
Oropharyngeal pain
Pulmonary congestion
SARS-CoV-2 test positive
Sinus congestion
Urinary tract infection
Symptomtext
On May 18, 2022 I started to feel bad had a sore throat. On May 20, 2022 I took a home COVID-19 Test that came back positive, so I went to were I volunteer, to take a PCR COVID-19 Test. They called me back to tell me the COVID-19 Test came back negative but I tested positive for Influenza A. I was instructed to quarantine for five days and take over the counter medications. On May 25, 2022 I took a home COVID-19 Test that came back positive. I went back to retake the COVID-19 Test. I was called back later and informed that I was positive for COVID-19 but no longer positive for Influenza A. They recommended Mucinex and over the counter cough syrup. I got an UTI from the Mucinex and had to be prescribed Nitrofurantoin. I was instructed to start taking Coricidin HBP but I ended up with extreme head and chest congestion. I ended up with a nose bleed that resulted with me having to go to the emergency room and having to get a balloon up my nose to stop the bleeding because I am on blood thinners. I will be seeing an Ear Nose and Throat Specialist this Friday to remove the balloon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 PCR COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Headache
Nasopharyngitis
Oropharyngeal pain
Oxygen saturation abnormal
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I woke up on 01/10/22 with a sore throat and I was starting to have symptoms of a cold. It got progressively worse over the day and feverish. I took medicine to try and help with it. I was monitoring my oxygen saturation on the phone and when I would walk it would go below 90%. By 01/16/22 I started to feel a little bit better but within a couple weeks after my joint pain got worse and since then my oxygen saturations have been up and down. The lowest was 81%, I could be sitting and will drop. I been fatigued. I still have the symptoms. The joint pain is not as bad as it was but still there. I believe it is lung COVID. I did see a Dr. without much help. I did take a COVID test at home and it was negative. I have been taking Tylenol for the headaches and joint pain. Recently I have had sore throat pain on the right side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID test- negative
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- orthostatic hypotension, fibromyalgia, cavernous angioma, Ehlers dahs syndrome
- Andere Medikamente
- Tylenol, Allegra
- Allergien
- Codeine, Amitriptyline, Sulfa, Ampicillin, Vicodin, Aleve, Aspirin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
Fatigue
Headache
Symptomtext
Headache; stomach pain; tired; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2 (BNT162B2), on 18May2022 at 11:45 as dose 4 (booster), single (Lot number: FL3197) at the age of 56 years intramuscular, in right arm for covid-19 immunization. The patient's relevant medical history included: "seasonal allergies" (unspecified if ongoing). Concomitant medication(s) included: AZELASTINE; QNASL; PEPCID [FAMOTIDINE]. Past drug history included: Sulfa, reaction(s): "Known allergies: sulfa drugs", notes: Known allergies: sulfa drugs; Clindamycin, reaction(s): "Known allergies: clindamycin", notes: Known allergies: clindamycin. Vaccination history included: Covid-19 vaccine (Dose 1, Primary immunization series completed but unknown manufacturer), for Covid-19 immunization; Covid-19 vaccine (Dose 2, Primary immunization series completed but unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose 3, Unknown manufacturer), for COVID-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 19May2022 at 06:00, outcome "recovered"; ABDOMINAL PAIN UPPER (non-serious) with onset 19May2022 at 06:00, outcome "recovered", described as "stomach pain"; FATIGUE (non-serious) with onset 19May2022 at 06:00, outcome "recovered", described as "tired". Therapeutic measures were not taken as a result of headache, abdominal pain upper, fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Seasonal allergy.
- Andere Medikamente
- AZELASTINE; QNASL; PEPCID [FAMOTIDINE].
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 05.01.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 125,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Malaise
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
I attended a school event on 5/7 with around 60-70 people that took place in a large tent. I began having symptoms, like a sore throat, fever, and chills on 5/10. The fever lasted around 3 days, the highest the temperature got was 38.5 degrees Celsius. I also experienced some runny nose and coughing. The fever broke 60 hours later and the sore throat only lasted around 48 hours. The coughing has lingered and still persists today. I did not take any medication other than some vitamins and supplements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- At home antigen test- mixed results, PCR test-positive
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pain
Vaccination site pain
Symptomtext
Fatigue; body aches; Soreness in the arm around injection area; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41-year-old male patient received BNT162b2 (BNT162B2), on 12May2022 at 10:30 as dose 3 (booster), single (Lot number: FL3197) at the age of 41 years, in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 10:30 AM), administration date: 04May2021, when the patient was 40-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 13Apr2021, when the patient was 40-year-old, for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 13May2022 at 06:00, outcome "recovering", described as "Soreness in the arm around injection area"; FATIGUE (non-serious) with onset 14May2022, outcome "recovering"; PAIN (non-serious) with onset 14May2022, outcome "recovering", described as "body aches". Therapeutic measures were not taken as a result of vaccination site pain. Additional information: The patient had received no other vaccines within 4 weeks prior to COVID vaccine. The patient had not diagnosed with COVID prior vaccination and the patient had not tested to COVID post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Headache
Pain
Pyrexia
Vaccination site pain
Symptomtext
PCR test result at 7pm on 16-May came to be COVID +ve.; PCR test result at 7pm on 16-May came to be COVID +ve.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2 (BNT162B2), on 07Apr2022 at 11:00 as dose 4 (booster), single (Lot number: FL3197) at the age of 56 years intramuscular, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "high LDL-C" (unspecified if ongoing). Concomitant medication(s) included: LIPITOR. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset May2022, outcome "recovering", COVID-19 (medically significant) with onset 16May2022, outcome "recovering" and all described as "PCR test result at 7pm on 16-May came to be COVID +ve.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14May2022) Negative, notes: At home kit gave me COVID -ve result on 14th; (16May2022) Positive, notes: PCR test result at 7pm on 16May came to be COVID +ve. Therapeutic measures were not taken as a result of drug ineffective, covid-19. Clinical Course: If other vaccine in four weeks was reported as no. Other medications in two weeks were reported as Lipitor 20 mg and multi vitamins. If covid prior vaccination was reported as no. If covid tested post vaccination was reported as no. No Known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220514; Test Name: PCR Test; Test Result: Negative ; Comments: At home kit gave me COVID -ve result on 14th; Test Date: 20220516; Test Name: PCR Test; Test Result: Positive ; Comments: PCR test result at 7pm on 16May came to be COVID +ve.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: LDL cholesterol increased
- Andere Medikamente
- LIPITOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Headache
Pain
Pyrexia
Vaccination site pain
Symptomtext
PCR test result at 7pm on 16-May came to be COVID +ve.; PCR test result at 7pm on 16-May came to be COVID +ve.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2 (BNT162B2), on 07Apr2022 at 11:00 as dose 4 (booster), single (Lot number: FL3197) at the age of 56 years intramuscular, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "high LDL-C" (unspecified if ongoing). Concomitant medication(s) included: LIPITOR. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset May2022, outcome "recovering", COVID-19 (medically significant) with onset 16May2022, outcome "recovering" and all described as "PCR test result at 7pm on 16-May came to be COVID +ve.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14May2022) Negative, notes: At home kit gave me COVID -ve result on 14th; (16May2022) Positive, notes: PCR test result at 7pm on 16May came to be COVID +ve. Therapeutic measures were not taken as a result of drug ineffective, covid-19. Clinical Course: If other vaccine in four weeks was reported as no. Other medications in two weeks were reported as Lipitor 20 mg and multi vitamins. If covid prior vaccination was reported as no. If covid tested post vaccination was reported as no. No Known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220514; Test Name: PCR Test; Test Result: Negative ; Comments: At home kit gave me COVID -ve result on 14th; Test Date: 20220516; Test Name: PCR Test; Test Result: Positive ; Comments: PCR test result at 7pm on 16May came to be COVID +ve.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: LDL cholesterol increased
- Andere Medikamente
- LIPITOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dysphonia
Feeling abnormal
Headache
Oropharyngeal pain
SARS-CoV-2 test
Vaccination failure
Symptomtext
07May2022 AG test (Positive); 07May2022 AG test (Positive); sore throat; cough; headache; hoarse voice; squeezing; This is a spontaneous report received from a contactable reporter(s) (Nurse) from product quality group. A 52-year-old female patient received BNT162b2 (BNT162B2), on 22Feb2021 as dose 1, single (Lot number: EL3247), on 15Mar2021 as dose 2, single (Lot number: EL3247), on 23Nov2021 as dose 3 (booster), single (Lot number: FF2589) and on 08Apr2022 as dose 4 (booster), single (Lot number: FL3197) at the age of 52 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 07May2022, outcome "recovering" and all described as "07May2022 AG test (Positive)"; COUGH (non-serious) with onset 07May2022, outcome "recovering"; HEADACHE (non-serious) with onset 07May2022, outcome "recovering"; DYSPHONIA (non-serious) with onset 07May2022, outcome "recovering", described as "hoarse voice"; OROPHARYNGEAL PAIN (non-serious) with onset 07May2022, outcome "recovering", described as "sore throat"; FEELING ABNORMAL (non-serious) with onset 07May2022, outcome "recovering", described as "squeezing". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (07May2022) Positive, notes: 07May2022 AG test (positive). It was unknown if therapeutic measures were taken as a result of vaccination failure, covid-19, oropharyngeal pain, cough, headache, dysphonia, feeling abnormal. Clinical course: Facility type vaccine reported as Workplace clinic. If other vaccine in four weeks reported as Unknown. If other vaccine in four weeks reported Unknown. If COVID tested post vaccination reported as Unknown. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information provide and plausible temporal association, the causality between BNT162B2 and events cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220507; Test Name: 07May2022 AG test (positive); Test Result: Positive ; Comments: 07May2022 AG test (positive)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 22.12.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 140,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient stated today that she believes that her skin is breaking out after having received the above vaccine on 12/22/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Headache
Vaccination site pain
Symptomtext
Soreness at injection site about 5 hours after injection; Chills; joint aches; headache about 10 hours; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), on 04May2022 at 11:15 as dose 4 (booster), single (Lot number: FL3197) at the age of 60 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "sulfa and ceftan based antibiotics" (unspecified if ongoing), notes: Known allergies: sulfa and ceftan based antibiotics. Concomitant medication(s) included: NASONEX; ESOMEPRAZOLE; LORAZEPAM; CENTRUM SILVER +50. Past drug history included: Sulfa and ceftan based antibiotics, reaction(s): "Known allergies: sulfa and ceftan based antibiotics", notes: Known allergies: sulfa and ceftan based antibiotics. Vaccination history included: Bnt162b2 (Dose 1, Lot No.: EL3247, Anatomical Location: Arm left), for COVID-19 immunization; Bnt162b2 (Dose 2, Lot No.: EP6955, Anatomical Location: Arm left), for COVID-19 immunization; Bnt162b2 (Dose 3, Lot No.: FH8027, Anatomical Location: Arm left), for COVID-19 immunization. The following information was reported: CHILLS (non-serious) with onset 04May2022, outcome "recovering"; VACCINATION SITE PAIN (non-serious) with onset 04May2022, outcome "recovering", described as "Soreness at injection site about 5 hours after injection"; HEADACHE (non-serious) with onset 04May2022, outcome "recovering", described as "headache about 10 hours"; ARTHRALGIA (non-serious) with onset 04May2022, outcome "recovering", described as "joint aches". Therapeutic measures were not taken as a result of vaccination site pain, chills, arthralgia, headache. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and patient received Nasonex, Esomeprazole, Lorazepam, Centrum Silver within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with Covid-19 and since the vaccination, the patient has not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Sulfonamide allergy (Known allergies: sulfa and ceftan based antibiotics.)
- Andere Medikamente
- NASONEX; ESOMEPRAZOLE; LORAZEPAM; CENTRUM SILVER +50.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Loss of personal independence in daily activities
Nausea
Pain
Pyrexia
Sleep disorder
Vomiting
Symptomtext
Client called and reported about 11 pm the night of the vaccine waking up with severe nausea and little vomiting (described vomiting more as spitting up). Client had experienced severe nausea for about 3-4 days, but without vomiting (described if she could vomit thinking it would have helped). Client also experienced; body aches, low grade fevers the first two days, and headache. Client called doctor and was prescribed Ondansetron (Zofran). Client reports that is helping with the nausea. Client reported on day seven finally able to resume normal daily activities. Client reported daughter in law came over to feed dogs and assist with daily activities during this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Client reports being diagnosed with blood cancer; Myelodysplastic syndrome (MDS), back in December AFib Hypothyroid GI issues client reported happens to her about three times a year and unknown of the cause
- Andere Medikamente
- Paroxetine (Paxil) 20 Mg Diltiazem 180 Mg Levothyroxine 150 Mcg Emergen-C Ibuprofen *All medication verbally reported by client on phone
- Allergien
- Erythromycin client states, "she thinks is what it is called."
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 13.01.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 77,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Activated partial thromboplastin time shortened
Alanine aminotransferase increased
Aspartate aminotransferase increased
Biopsy liver abnormal
Blood alkaline phosphatase increased
Blood bilirubin increased
Blood glucose normal
Blood immunoglobulin A
Blood immunoglobulin A increased
Blood iron increased
Blood thyroid stimulating hormone
Computerised tomogram abdomen normal
Full blood count
Gamma-glutamyltransferase
Globulins increased
Haematocrit decreased
Haemochromatosis
Symptomtext
Significantly elevated hepatic functions, nausea and vomiting and abdominal pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 3/31/22 - CMP (glucose 116, protein 9.6, globulin 5.8, bilirubin 2.6, alk phos 132, AST 908, ALT 954). CBC (leukocytes 4.1, Erythrocytes 3.69, hemoglobin 11.4, hematocrit 33.9, erythrocyte distribution width SD 52.5, erythrocytes distribution width CV 15.8, monocytes 15, neutrophils absolute 1.73 4/1/22 - lipase and hepatitis acute panel normal 4/5/22 - CBC, CMP abnormal like above 4/7/22 - PTT 35, INR 1.5, NASH fibrosure unable to calculate, celiac panel showed elevated IgA at 416, smooth muscle 85, iron 246, IGG 4841, ferritin 312, GGT 112, acetaminophen , TSH, hemochromatosis, seruloplasmin, AMA, and A1A normal, 4/1/22 CT abd/pelvis normal 4/6/22 US abd nonspecific findings that could be associated with hepatitis 4/11/22 Liver biopsy positive for autoimmune hepatitis
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Scoliosis, Chiari I malformation, migraine, obesity
- Andere Medikamente
- Omeprazole, Rizatriptan PRN, acetaminophen PRN, melatonin PRN
- Allergien
- Amoxicillin, adhesive tape
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Myalgia
Vaccination site pain
Symptomtext
Pain at injection site; muscle aches; headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old male patient received BNT162b2 (BNT162B2), on 27Apr2022 at 10:00 as dose 4 (booster), single (Lot number: FL3197) at the age of 64 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ATORVASTATIN; LISINOPRIL. Vaccination history included: Covid-19 vaccine (Dose: 01, Unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose: 02, Unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose: 03, Unknown manufacturer), for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 27Apr2022 at 22:00, outcome "recovering", described as "Pain at injection site"; HEADACHE (non-serious) with onset 27Apr2022 at 22:00, outcome "recovering"; MYALGIA (non-serious) with onset 27Apr2022 at 22:00, outcome "recovering", described as "muscle aches". Therapeutic measures were not taken as a result of vaccination site pain, myalgia, headache. Additional information: No other vaccine in four weeks. Other medications in two weeks: Atorvastatin and Lisinopril. No covid prior vaccination. No covid tested post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ATORVASTATIN; LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Limb mass
Nausea
Pain
Symptomtext
very bad headache; body aches; lump under left arm; Nauseous; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Apr2022 at 11:30 as dose 4 (booster), single (Lot number: FL3197) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Chronic lymphocytic leukaemia" (unspecified if ongoing). Concomitant medication(s) included: VIT C. Vaccination history included: Covid-19 vaccine (Dose 1, Unknown Manufacturer), for Covid-19 Immunization; Covid-19 vaccine (Dose 2, Unknown Manufacturer), for Covid-19 Immunization; Covid-19 vaccine (Dose 3 (BOOSTER), Unknown Manufacturer), for Covid-19 Immunization. The following information was reported: NAUSEA (non-serious) with onset 26Apr2022 at 18:00, outcome "recovering", described as "Nauseous"; PAIN (non-serious) with onset 26Apr2022 at 18:00, outcome "recovering", described as "body aches"; LIMB MASS (non-serious) with onset 26Apr2022 at 18:00, outcome "recovering", described as "lump under left arm"; HEADACHE (non-serious) with onset 26Apr2022 at 18:00, outcome "recovering", described as "very bad headache". Therapeutic measures were not taken as a result of headache, pain, limb mass, nausea. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: CLL
- Andere Medikamente
- VIT C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 15.01.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain upper
COVID-19
Cough
Diarrhoea
Fatigue
Feeling abnormal
Feeling hot
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 04/04/2022 with a at home test. My symptoms were slow and mild. First, I had a dry cough and it went from my stomach started hurting really bad. The pains were very severe, and it went to diarrhea. The diarrhea continued and I had a mid-grade fever. My body was very feverish, I had to turn on the air. I could still do some things, I just felt bad with the dry cough still. I didn't lose my taste or smell. I was very fatigue and a little tried. My diarrhea continued and I had to take Azithromycin for travelers' diarrhea. I went to my doctor, and she confirmed that I had COVID-19 on 04/06/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test COVID-19 PCR
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Nuvaring Birth Control and Flonase.
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Chills
Headache
Lethargy
Pyrexia
Symptomtext
Chills; Fever; Body aches particularly in my back and hips; Body aches particularly in my back and hips; Headache; Lethargy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20Apr2022 as dose 3 (booster), single (Lot number: FL3197) at the age of 55 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "Known allergies: Contrast dye" (unspecified if ongoing); "Covid-19" (unspecified if ongoing), notes: If covid prior vaccination: Yes. Concomitant medication(s) included: METOPROLOL SUCCINATE; ESCITALOPRAM; ATORVASTATIN. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EN6203), administration date: 23Mar2021, when the patient was 54-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EN6203), administration date: 01Mar2021, when the patient was 54-year-old, for Covid-19 immunization. The following information was reported: ARTHRALGIA (non-serious), BACK PAIN (non-serious) all with onset 21Apr2022, outcome "recovered" (2022) and all described as "Body aches particularly in my back and hips"; CHILLS (non-serious) with onset 21Apr2022, outcome "recovered" (2022); PYREXIA (non-serious) with onset 21Apr2022, outcome "recovered" (2022), described as "Fever"; HEADACHE (non-serious) with onset 21Apr2022, outcome "recovered" (2022); LETHARGY (non-serious) with onset 21Apr2022, outcome "recovered" (2022). Therapeutic measures were not taken as a result of chills, pyrexia, arthralgia, back pain, headache, lethargy. Additional information: The patient did not receive any other vaccine with in 4 weeks of covid-19 vaccination. Prior to the vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Contrast media allergy; COVID-19 (If covid prior vaccination: Yes); High cholesterol; Hypertension
- Andere Medikamente
- METOPROLOL SUCCINATE; ESCITALOPRAM; ATORVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature fluctuation
Exercise tolerance decreased
Exposure to SARS-CoV-2
Fatigue
Feeling cold
Pain
SARS-CoV-2 test positive
Symptomtext
Dose 4 vaccination 04/01/2022, FL3197 Pfizer BioNTech. Normally have a temperature of 95.6 but had a increase of 97.8 significant change body temperature and I was having issues of feeling not being able to get warm all day, with aches and pains and temperature fluctuation not able to regulate the temperature. I also had the Hep A and B combo 04/12/2022 and MMR 04/12/2022. I also had positive COVID-19 diagnosis on March 15, 2022. I had a telehealth visits. I had exposure by family member who tested positive for COVID-19 and was confident with at home test. I used to be able to get 12,000 steps regularly still experience issue with fatigue no longer able to handle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test and phone call observation.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- Vitamins; 81 aspirin; Glucosamine; Chondroitin; Magnesium; Vitamin E; COQ10; Omeprazole 20mg once nightly; Atorvastatin 10mg once nightly at bedtime
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Neck pain
Pain
Symptomtext
Client presented at the vaccination site on 12.23.21. Client reported he received first dose of Moderna COVID vaccine on 03/27/21 and received second dose of Moderna COVID vaccine on 04/24/21 both at the facility. Client reported with first dose of Moderna COVID vaccine, he had neck pain, body pain, and weakness 12 hours after received the vaccine lasted eight to 10 hours and with the second dose of Moderna COVID vaccine on 04/24/21, he had the same neck pain, body pain, and weakness 12 hours after received the vaccine lasted six hours. Client reported he took Tylenol with help with both doses. He denied any known allergy. Client told he has HTN controlled with Losartan and arthritis controlled with pain medication (unknown name). Client is requesting for the booster dose of Pfizer COVID vaccine today. PHN submitted a medical consult via text message to clinical project coordinator, requesting to proceed with the booster dose of Pfizer COVID vaccine. Per the doctor, approval to proceed with the booster dose of Pfizer COVID vaccine was obtained via text message from clinical project coordinator. Client received the booster dose of Pfizer COVID vaccine, LOT#: FL3197 on 12/23/21 at 1530 by RN. The client did not report any symptoms during the 30-minute observation period. PHN educated client on possible adverse reactions and when to seek EMS. Client verbalized understanding. Client left vaccination site at 1400 unassisted and with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN (Losartan) Arthritis (medication-unknown name)
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Lymphadenopathy
Symptomtext
Fatigue/tiredness; Fatigue/tiredness; Swollen lymph nodes in the left armpit; This is a spontaneous report received from a 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 15Apr2022 at 11:15 as dose 4 (booster), single (Lot number: FL3197) at the age of 53 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: FF2589, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM, Route of Administration: Intramuscular), administration date: 16Nov2021, for Covid-19 Immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 01:30 PM, Route of Administration: Intramuscular), administration date: 24Mar2021, for Covid-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 01:30 PM, Route of Administration: Intramuscular), administration date: 03Mar2021, for Covid-19 Immunization. The following information was reported: FATIGUE (non-serious), FATIGUE (non-serious) all with onset 15Apr2022 at 21:00, outcome "recovered" and all described as "Fatigue/tiredness"; LYMPHADENOPATHY (non-serious) with onset 15Apr2022 at 21:00, outcome "recovered", described as "Swollen lymph nodes in the left armpit". Therapeutic measures were not taken as a result of fatigue, fatigue, lymphadenopathy. Additional information: The patient was not pregnant during the vaccination. The most recent COVID-19 vaccine was administered at workplace in clinic. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any treatment for the adverse events. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Tinnitus
Vomiting
Symptomtext
5 days vomiting and diarrhea Tinnitus ongoing 4 months following first Pfizer Vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD, Arthritis
- Andere Medikamente
- Lamictal, Lithium, Clonazepam
- Allergien
- Dairy
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Injection site bruising
Mass
Symptomtext
Patient reported to pharmacy on 4/21/22 she experienced bruising around the injection site and into the back side of her arm. She has developed a "lump" on the interior side of her arm. Instructed patient to contact PCP for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- Tramadol, Morphine
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dry skin
Pruritus
Purpura
Rash
Rash erythematous
Symptomtext
Itching continued on my face, palms, head, back and scalp then it went to my arm. Then it went to my torso and my boobs all this happened with the first dose and it never went away and continued to the second dose and it didn't go away and here we are at the booster I got a rash from head to toe my literally entire body, my private areas, shoulders, neck, my arms, my thighs. It keeps getting progressively worse my eyes my lips mouth. They are large red itchy spots dry up and sometimes it bleeds depending on how dry it gets or how much I scratch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes, COPD, CHF, High Blood Pressure
- Andere Medikamente
- Humalog injection, Tresiba injection, Torsemide, Glimepiride, Carvedilol, Lisinopril, Tramadol, Pravastatin, Simvastatin, Dhea biotin, Omega 3, Tylenol, Gabapentin, body -ketoconazole 2%, Betamethasone, Dipropionate .05%
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Differential white blood cell count
Fatigue
Full blood count
Glycosylated haemoglobin increased
Hypothyroidism
Laboratory test abnormal
Lipids
Muscular weakness
Myalgia
Pain
Symptomtext
02/2022 I had muscle and joint pain with fatigue that right sent me doctor. I only had a physical at that time and was advised to take OTC pain med and start exercises. On April 7, had lab work done and it was discovered that I had hypothyroidism that was causing my muscle and joint weakness and pain. Was prescribed levothyroxine and continue with exercises to work the muscles. I have issue with pain when I move a certain way with my right arm but otherwise better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 04/07/2022 CBC w/diff (Labs are normal, except for elevated lipid A1C 7 and underactive thyroid).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HCL; HBP; Diabetes Type 2; Arthritis
- Andere Medikamente
- Lisinopril; Atenolol; B-12; Farxiga; Pravastatin; Claritin; Protonix
- Allergien
- Metformin; Morphine; Tomato; Milk; Latex
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Night sweats
Vaccination site pain
Symptomtext
Night sweats; soreness at injection site; light headed; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Apr2022 at 11:30 as dose 4 (booster), single (Lot number: fl3197) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing). Concomitant medication(s) included: ADVIL [IBUPROFEN]; TYLENOL. Vaccination history included: Covid-19 vaccine (Dose 1, primary series immunization completed but manufactured name unknown), for COVID-19 Immunization; Covid-19 vaccine (Dose 2, primary series immunization completed but manufactured name unknown), for COVID-19 Immunization; Covid-19 vaccine (Dose 3, Manufactured name unknown), for COVID-19 Immunization. The following information was reported: NIGHT SWEATS (non-serious) with onset 14Apr2022 at 22:00, outcome "recovering"; DIZZINESS (non-serious) with onset 14Apr2022 at 22:00, outcome "recovering", described as "light headed"; VACCINATION SITE PAIN (non-serious) with onset 14Apr2022 at 22:00, outcome "recovering", described as "soreness at injection site". Therapeutic measures were not taken as a result of night sweats, vaccination site pain, dizziness. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received Advil, Tylenol within 2 weeks of vaccination. The patient was not tested since the vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer
- Andere Medikamente
- ADVIL [IBUPROFEN]; TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 20.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Insomnia
Pain
Symptomtext
insomnia; severe chills; bodyaches; This is a spontaneous report received from a non-contactable reporter(s) (Nurse). A 47-year-old male patient received BNT162b2 (BNT162B2), on 12Apr2022 as dose 3 (booster), single (Lot number: FL3197) at the age of 47 years intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EL3247, Route of Administration: Intramuscular, Manufacturer: Pfizer), administration date: 23Feb2021, when the patient was 46-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3247, Route of Administration: Intramuscular, Manufacturer: Pfizer), administration date: 03Feb2021, when the patient was 46-year-old, for COVID-19 immunization. The following information was reported: PAIN (non-serious) with onset 12Apr2022, outcome "unknown", described as "bodyaches"; INSOMNIA (non-serious) with onset 12Apr2022, outcome "unknown"; CHILLS (non-serious) with onset 12Apr2022, outcome "unknown", described as "severe chills". It was unknown if therapeutic measures were taken as a result of insomnia, chills, pain. Additional information: Patient had vaccine at workplace clinic. He did not take other vaccine in four weeks. He was not tested covid positive prior to vaccination and was not tested positive after vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
COVID-19
Immunisation
Off label use
Pyrexia
SARS-CoV-2 test
Vaccination failure
Symptomtext
Covid test result= Positive; Covid test result= Positive; Fevers; Off label use; booster; This is a spontaneous report received from a non-contactable reporter(s) (Nurse) from product quality. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4 (booster), single (Lot number: FL3197) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: FF2589), administration date: 22Oct2021, when the patient was 59-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EL3247), administration date: 17Feb2021, when the patient was 59-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL3247), administration date: 28Jan2021, when the patient was 58-year-old, for Covid-19 immunization. The following information was reported: OFF LABEL USE (medically significant) with onset 08Apr2022, outcome "unknown"; IMMUNISATION (medically significant) with onset 08Apr2022, outcome "unknown", described as "booster"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 10Apr2022, outcome "unknown" and all described as "Covid test result= Positive"; PYREXIA (non-serious) with onset 10Apr2022, outcome "unknown", described as "Fevers". The patient underwent the following laboratory tests and procedures: Body temperature: (10Apr2022) Unknown results; SARS-CoV-2 test: (10Apr2022) Positive, notes: Nasal Swab; (11Apr2022) Positive. It was unknown if therapeutic measures were taken as a result of vaccination failure, covid-19, pyrexia. Clinical course: Facility type vaccine was Workplace clinic. It is unknown if the patient received other vaccine in four weeks. No covid prior vaccination. 08Apr22 got dose 4 COVID dose and then out to lunch and massage next day 09Apr22.- symptoms started Sunday night 10Apr22 fevers HA + ag test 10Apr night and 11Apr am. Treatment for AE was reported as unknown. No follow-up attempts are possible. No further information is expected.; Sender's Comments: The reported COVID-19 positive after both the doses of COVID-19 immunization is considered as vaccination failure of BNT162B2, and the Company cannot completely exclude the possible causality between the reported events and BNT162B2 administration. The at risk events Off label use and immunisation assessed as NA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220410; Test Name: Fevers; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220410; Test Name: Home Ag; Test Result: Positive ; Comments: Nasal Swab; Test Date: 20220411; Test Name: Home Ag; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Influenza like illness
Pain in extremity
Pyrexia
Symptomtext
Arm pain; flu-like symptoms; low grade fever (99.8-100.1); This is a spontaneous report received from a 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 05Apr2022 at 11:30 as dose 4 (booster), single (Lot number: FL3197) at the age of 53 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: shellfish" (unspecified if ongoing), notes: Known allergies: yes - shellfish. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for Covid-19 immunization; Bnt162b2 (DOSE 2, SINGLE), for Covid-19 immunization; Bnt162b2 (DOSE 3 (BOOSTER), SINGLE), for Covid-19 immunization. The following information was reported: OFF LABEL USE (non-serious) with onset 05Apr2022 at 11:30, outcome "unknown", described as "dose received More than 3 / dose number: 4"; PAIN IN EXTREMITY (non-serious) with onset 05Apr2022 at 16:00, outcome "recovered" (2022), described as "Arm pain"; INFLUENZA LIKE ILLNESS (non-serious) with onset 05Apr2022 at 16:00, outcome "recovered" (2022), described as "flu-like symptoms"; PYREXIA (non-serious) with onset 05Apr2022 at 16:00, outcome "recovered" (2022), described as "low grade fever (99.8-100.1)". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, influenza like illness, pyrexia. Additional Information: No other vaccine in four weeks. No COVID prior to the vaccination. No COVID tested post vaccination. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220405; Test Name: fever; Result Unstructured Data: Test Result:99.8-100.1; Comments: low grade
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Shellfish allergy (Known allergies: yes - shellfish)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Symptomtext
red circle at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- congestive heart failure, high cholesterol, fibromyalgia
- Andere Medikamente
- -
- Allergien
- opiodes, penicillin, sulfer
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Extra dose administered
Headache
Muscle spasms
Nausea
Pain
Pyrexia
Symptomtext
chills within 30 minutes, then headache, fever (102), arms and legs muscle spasms, overall pain, nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes type 2 hypothyroidism depression OCD edema
- Andere Medikamente
- Aspirin 81mg Bupropion HCL XL 300mg Trulicity 0.75mg Emgality 120 mg/ml Furosemide 40 mg Levothyroxine 100 mcg Amphetamine Salts ER 25 mg Estradiol 2mg
- Allergien
- none
- Vorherige Impfungen
- covid vaccination and booster but not as severe
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 03.04.2022
- Impfdatum
- 03.03.2021
- Beginn
- 23.01.2022
- Tage bis Beginn
- 326,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Dizziness
Rhabdomyolysis
SARS-CoV-2 test positive
Symptomtext
Narrative: Patient received three doses Pfizer COVID 19 vaccine Mar 2021/13 Jan 2022. The patient tested positive for COVID 19 on 23 Jan 2022. The patient presented to the ED with cough, dizziness, and rhabdomyolysis. The patient was admitted on 23 Jan 22 and treated with fluids, magnesium, potassium, dexamethasone. The patient was discharged on 25 Jan 2022 in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 03.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Nausea
Vomiting
Symptomtext
Patient experienced nausea and vomiting after receiving the booster Pfizer vaccine for COVID 19. The patient was treated with ondansetron and released home from the ED. The patient still required ondansetron on 4 February 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- 21.04.1951
- Beginn
- 16.03.2022
- Tage bis Beginn
- 25.897,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Pain
Symptomtext
Muscle aches and joint pain and aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Insomnia
Joint range of motion decreased
Lymphadenopathy
Muscular weakness
Pain assessment
Pain in extremity
Symptomtext
intense continuous pain in my upper back/pain with each deep breath; constantly in pain and weak/ lost range of motion in my left arm; constantly in pain and weak/ lost range of motion in my left arm; lymph nodes under my left arm are still swollen; Sleeping is fitful; arm started to feel very sore; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Dec2021 16:15 (Lot number: FL3197) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0180, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 02Jun2021, when the patient was 55 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0182, Location of injection: Arm Left, Vaccine Administration Time: 04:30 PM), administration date: 12May2021, when the patient was 55 years old, for Covid-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 22Dec2021 21:30, outcome "not recovered", described as "arm started to feel very sore"; BACK PAIN (non-serious) with onset 23Dec2021, outcome "recovered" (Dec2021), described as "intense continuous pain in my upper back/pain with each deep breath"; MUSCULAR WEAKNESS (non-serious), JOINT RANGE OF MOTION DECREASED (non-serious) all with onset 22Dec2021 21:30, outcome "not recovered" and all described as "constantly in pain and weak/ lost range of motion in my left arm"; LYMPHADENOPATHY (non-serious) with onset 22Dec2021 21:30, outcome "not recovered", described as "lymph nodes under my left arm are still swollen"; INSOMNIA (non-serious) with onset 22Dec2021 21:30, outcome "not recovered", described as "Sleeping is fitful". The events "arm started to feel very sore", "constantly in pain and weak/ lost range of motion in my left arm", "constantly in pain and weak/ lost range of motion in my left arm" and "sleeping is fitful" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, muscular weakness, joint range of motion decreased, lymphadenopathy, insomnia. Therapeutic measures were taken as a result of back pain. Additional information: The patient did not receive other vaccine in four weeks and other medications in two weeks. Facility where the most recent COVID-19 vaccine was administered was Administration facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not received any other medications within 2 weeks of vaccination. On the evening of my booster at 9.30pm my arm started to feel very sore. Next morning around 11.30am I felt intense continuous pain in my upper back-level 9 pain. I had pain with each deep breath. I called the nurse hotline. The nurse told me to take ibuprofen. After two days of pain and ibuprofen it subsided. However the pain in my left arm has not gone away. It is constantly in pain and weak. I have lost range of motion in my left arm, a problem I have never had before. It has been three months and the pain is still constant. The lymph nodes under my left arm are still swollen. Sleeping is fitful because I can't sleep on my left side and the pain in my left arm wakes me up at night. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211223; Test Name: Pain level; Result Unstructured Data: Test Result:9; Comments: level 9 pain
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: No other medical history: None.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Hypoaesthesia
Hypoaesthesia oral
Nausea
Pyrexia
Vaccine positive rechallenge
Symptomtext
By the time I left the parking lot I started feeling numbness starting on left side of face between hairline and left eye all the way to my lip, and down to my chin, drove home as fast as I could. By the time I got home, I had chills, nausea. A very mild numbness persisted for a few days. I had powdered Tylenol by my bed that I consistently took every 6 hours, fevers still reached 104. These symptoms lasted full 3 days, just a little longer than the first two. I still had numbness for two months afterwards, for it slowly going away. Similar to coming off of Novocain. I still have some numbness in left side area by my lip.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Requested an antibody test be done before booster to have on my record because of my previous reactions.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis, Two Artificial Knees, 3 Back surgeries, Chronic Constipation, pain, Abdominal surgeries, Hysterectomy
- Andere Medikamente
- Arthrotec, Prilosec, Metformin 500 once a day, PRN Inhaler
- Allergien
- Environmental Allergies (Pollen), also allergic to Amoxicillin
- Vorherige Impfungen
- similar reactions to first and second dose of Covid-19 Pfizer vaccine
- Staat
- AZ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 20.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Decreased appetite
Dry throat
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I had sore throat, dry throat, fatigue, and loss of appetite. These symptoms lasted for about a month. On Jan 14th, I tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- Upper respiratory infection
- Vorgeschichte
- Asthma; Osteoarthritis
- Andere Medikamente
- Asthma medicine
- Allergien
- Nitroglycerin; dairy; Walnuts; Pecan
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Lymph node pain
Lymphadenopathy
Myalgia
Neck pain
Symptomtext
The patient called today 3/28/22 to complain that since getting her vaccine, she is having right-sided muscular pain and aches. This pain is between her neck and extends down to her shoulder on the right side where we administered her COVID vaccine. She said that she had swollen lymph nodes initially but that has gotten better and this pain has gotten worse. The pain is only slightly relieved with Advil. She has not seen a medical provider for this pain and thinks that it could be either from the vaccine or from her physically demanding job. She is able to use that extremity and has full feeling (denies numbness or tingling) in that lower extremity. I encouraged her to visit a medical provider to evaluate this problem.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- No labs or tests done
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid Reflux
- Andere Medikamente
- Alive, Omeprazole, Vitamin D3, Vitamin C, Fenugreek, Hair/Skin/Nails vitamins, Alka-Seltzer cold, pharmagaba
- Allergien
- Azithromycin, Inapsine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 21.12.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
COVID-19
Cough
Exercise tolerance decreased
Fatigue
Headache
Loss of personal independence in daily activities
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Contracted covid in January. Cough, sore throat, congestion, headache, fatigue Still have not recovered and am not able to return to normal activities. Symptoms return if I do not rest every few days. Unable to exercise as I did before contracting covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Routine blood work conducted and all results were normal.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma Urticaria Environmental allergies
- Andere Medikamente
- Allegra 180mg twice daily
- Allergien
- Penicillin NSAIDs
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 24.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Headache
Pain
Pyrexia
Symptomtext
tiredness; Fever; chills; headache; body ache; light headed; dizziness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An adult male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 23Feb2022 (Lot number: FL3197) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing), notes: other medical history: Diabetes; "fatty liver disease" (unspecified if ongoing), notes: other medical history: fatty liver disease. Concomitant medication(s) included: METFORMIN; CELECOXIB; LISINOPRIL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Right, Route of Administration: Intramuscular), administration date: 01Apr2021, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 11Mar2021, for Covid-19 Immunization. The following information was reported: FATIGUE (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "tiredness"; PYREXIA (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "chills"; HEADACHE (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "headache"; PAIN (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "body ache"; DIZZINESS (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "light headed"; DIZZINESS (non-serious) with onset 23Feb2022 14:30, outcome "recovering", described as "dizziness". The events "tiredness", "fever", "chills", "headache", "body ache", "light headed" and "dizziness" were evaluated at the physician office visit. Therapeutic measures were taken as a result of fatigue, pyrexia, chills, headache, pain, dizziness, dizziness. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Treatment received for the adverse event was Tylenol. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes (other medical history: Diabetes); Fatty liver (other medical history: fatty liver disease)
- Andere Medikamente
- METFORMIN; CELECOXIB; LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Confusional state
Fatigue
Pyrexia
Symptomtext
Fever, tired, confusion 3 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, thyroid,migraine, htn,hyperlipedema,vit d dificiency
- Andere Medikamente
- Vit c,atorvastatin,fioracet,vit d3,pristiq,synthroid,losartin,metformin,methocarbamal,omeprazole,topamax,tramadol,zinc,hair skin nails
- Allergien
- Ceclor,codeine,imatrex
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Headache
Hyperhidrosis
Musculoskeletal stiffness
Nausea
Pallor
Symptomtext
Immediate headache; nauseous; couldn't walk without support; fingers in extension and couldn't bend; started sweating; hands pale and face pale; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 12 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Dec2021 16:00 (Lot number: FL3197) at the age of 12 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: HEADACHE (non-serious) with onset 21Dec2021 16:00, outcome "unknown", described as "Immediate headache"; NAUSEA (non-serious) with onset 21Dec2021 16:00, outcome "unknown", described as "nauseous"; GAIT DISTURBANCE (non-serious) with onset 21Dec2021 16:00, outcome "unknown", described as "couldn't walk without support"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 21Dec2021 16:00, outcome "unknown", described as "fingers in extension and couldn't bend"; HYPERHIDROSIS (non-serious) with onset 21Dec2021 16:00, outcome "unknown", described as "started sweating"; PALLOR (non-serious) with onset 21Dec2021 16:00, outcome "unknown", described as "hands pale and face pale". Therapeutic measures were not taken as a result of headache, nausea, gait disturbance, musculoskeletal stiffness, hyperhidrosis, pallor. Additional information: Facility where the most recent COVID-19 vaccine was administered: facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Serious: No. Reported Event: Immediate headache, felt nauseous, started sweating, couldn't walk without support, fingers in extension and couldn't bend, hands pale and face pale. Had to be monitored after shot and check vitals. Device Date : 21Dec2021 No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 21.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
experiencing a lot of itching; Rash; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 21Jan2022 (Lot number: FL3197) at the age of 74 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing); "Thyroid" (unspecified if ongoing). Concomitant medication(s) included: GLIPIZIDE taken for diabetes mellitus; METFORMIN taken for diabetes mellitus; LOSARTAN; SIMVASTATIN; METHIMAZOLE taken for thyroid disorder. The following information was reported: PRURITUS (non-serious) with onset Jan2022, outcome "not recovered", described as "experiencing a lot of itching"; RASH (non-serious) with onset Jan2022, outcome "unknown", described as "Rash". Therapeutic measures were taken as a result of pruritus, rash. Additional information: Today, patient took an allergy pill (Further clarification unknown, hence suspect captured conservatively as unspecified medication). Patient put a little Cortisone (Suspect captured as per verbatim; further not clarified hence Pfizer not checked) cream on it but the itching is still there and now the rashes. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes; Thyroid disorder
- Andere Medikamente
- GLIPIZIDE; METFORMIN; LOSARTAN; SIMVASTATIN; METHIMAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.03.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Pyrexia
Symptomtext
fever on and off; I''ve been having a low grade and a high grade fever; it''s been more than 24 hours that I''ve had fever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2) (Lot number: FL3197) as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1), for COVID-19 immunization. The following information was reported: PYREXIA (non-serious), outcome "not recovered", described as "fever on and off; I''ve been having a low grade and a high grade fever; it''s been more than 24 hours that I''ve had fever". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was stated, Basically patient was just concerned about that have been having a fever on and off since patient got 2nd dose of Pfizer. Patient got it on Thursday and then started feeling fever around 10 O' Clock that night and patient have been having a low grade and a high grade fever like ever since then. It was stated, Yeah, patient just wanted to know was it normal that it was been going on for now like more patient would say more than a day because it was been more than 24 hours that have had fever. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: Fever; Result Unstructured Data: Test Result:low grade/ high grade; Comments: fever on and off; I've been having a low grade and a high grade fever; it's been more than 24 hours that I've had fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 27.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial infection
COVID-19
Drug ineffective
Dysphonia
Fatigue
Nasopharyngitis
SARS-CoV-2 test
Secretion discharge
Unevaluable event
Symptomtext
Unevaluable event; Fatigue aggravated; Voice disturbance; Mucus discharge; COVID-19; COVID-19; Common cold; Bacterial infection; This is a solicited report received from contactable reporter(s) (Consumer or other non HCP) from product quality group for a sponsored program. The reporter is the patient. A 62 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administration date 27Dec2021 (Lot number: FL3197) at the age of 62 years as dose 3 (booster),single for covid-19 immunisation; adalimumab (HUMIRA), first regimen subcutaneous from Aug2021 (Batch/Lot number: unknown) to Dec2021 at 40 mg (citrate free (40 mg,1 in 2 wk)), second regimen subcutaneous from 15Dec2021 (Batch/Lot number: unknown) to 05Jan2022 at 40 mg (citrate free (40 mg,1 in 1 wk)), third regimen subcutaneous since 12Jan2022 (ongoing) (Batch/Lot number: unknown) at 40 mg (citrate free (40 mg,1 in 1 wk)) and fourth regimen subcutaneous (Batch/Lot number: unknown) at 0.4 mL for rheumatoid arthritis. Relevant medical history included: "Tobacco use", stop date: 2010; "Fibromyalgia", start date: 2020 (unspecified if ongoing); "Memory issues" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing); "Alcohol use wine occasionally" (unspecified if ongoing); "Rheumatoid arthritis" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "for sleep" (unspecified if ongoing); "Stomach issues" (unspecified if ongoing). Concomitant medication(s) included: CELECOXIB taken for rheumatoid arthritis; PRILOSEC [OMEPRAZOLE] taken for abdominal discomfort; METHOTREXATE taken for rheumatoid arthritis; PREDNISONE taken for rheumatoid arthritis; MELATONIN taken for sleep disorder; CLONAZEPAM taken for sleep disorder; VITAMIN D [COLECALCIFEROL] taken for supplementation therapy; FOLATE taken for rheumatoid arthritis; VITAMIN C [ASCORBIC ACID;ROSA CANINA] taken for immune complex level increased; ZINC taken for immune complex level increased; CALCIUM taken for supplementation therapy; MAGNESIUM taken for supplementation therapy; BACLOFEN taken for rheumatoid arthritis; ZYRTEC [CETIRIZINE HYDROCHLORIDE] taken for hypersensitivity. Past drug history included: Codeine, reaction(s): "Codeine allergy Manifestation by hives and itching"; Codeine, reaction(s): "Codeine allergy Manifestation by hives and itching"; Tetracycline, reaction(s): "Tetracycline allergy". Vaccination history included: Bnt162b2 (On 06Apr2021, she received 2nd dose covid-19 Vaccine manufactured by Pfizer/Biontech, lot number EN6204), administration date: 06Apr2021, when the patient was 62 years old, for covid-19 immunization; Bnt162b2 (On 17Mar2021, she received 1st dose covid-19 Vaccine manufactured by Pfizer/Biontech, lot number EL9263), administration date: 17Mar2021, when the patient was 62 years old, for covid-19 immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 31Dec2021, outcome "unknown" and all described as "COVID-19"; NASOPHARYNGITIS (non-serious) with onset 31Dec2021, outcome "recovered" (Jan2022), described as "Common cold"; BACTERIAL INFECTION (non-serious) with onset 31Dec2021, outcome "recovering", described as "Bacterial infection"; UNEVALUABLE EVENT (non-serious), outcome "unknown", described as "Unevaluable event"; FATIGUE (non-serious) with onset 31Dec2021, outcome "recovering", described as "Fatigue aggravated"; DYSPHONIA (non-serious) with onset 31Dec2021, outcome "not recovered", described as "Voice disturbance"; SECRETION DISCHARGE (non-serious) with onset 31Dec2021, outcome "recovered", described as "Mucus discharge". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (31Dec2021) positive. The action taken for adalimumab was unknown. Investigation results for lot EN6204 (Dose 2) and Dose 3 (FL3197). The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EN6204 and was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EN6204, fill lot EN5335, and the formulated drug product lot EN5325. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE INJECTABLE lot FL3197 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FL3197, fill lot FJ8803, and the formulated drug product lot FL3180. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Clinical Course: It was unknown if patient was enrolled in a Covid-19 Vaccine Trial. The patient was treated with Tylenol. The Reporter Causality for the all the events for suspect Bnt162b2 was not reported and for another suspect, ADALIMUMAB for the events (Mucus discharge, Fatigue aggravated, Covid-19, Nasopharyngitis and Bacterial infection it was reported as unrelated. It was not reported for the event unevaluable event. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on temporal association, there is reasonable possibility of causal association between the Reported events and the suspect drug BNT162B2. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211231; Test Name: Nasal swab test; Result Unstructured Data: Test Result:Positive
- Aktuelle Erkrankungen
- Tobacco user
- Vorgeschichte
- Medical History/Concurrent Conditions: Alcohol use; Allergy; Fibromyalgia; Memory disturbance; Penicillin allergy; Rheumatoid arthritis; Sleep disorder; Stomach discomfort
- Andere Medikamente
- CELECOXIB; PRILOSEC [OMEPRAZOLE]; METHOTREXATE; PREDNISONE; MELATONIN; CLONAZEPAM; VITAMIN D [COLECALCIFEROL]; FOLATE; VITAMIN C [ASCORBIC ACID;ROSA CANINA]; ZINC; CALCIUM; MAGNESIUM; BACLOFEN; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; HUMIRA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chills
Headache
Lymphadenopathy
Pyrexia
Symptomtext
chills/freezing cold; pain in left arm pit; Left arm pit is slightly swollen; feverish; Headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). Other Case identifier(s): US-PFIZER INC-202101814636 (Pfizer). A 16 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Dec2021 14:00 (Lot number: FL3197) at the age of 16 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Yes - allergic to certain tree nuts: allergy to legumes" (unspecified if ongoing), notes: Yes - allergic to certain tree nuts. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 16Jun2021, when the patient was 16 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 26May2021, when the patient was 16 years old, for COVID-19 Immunization. The following information was reported: HEADACHE (non-serious) with onset 16Dec2021 22:00, outcome "recovered" (17Dec2021 11:00), described as "Headache"; PYREXIA (non-serious) with onset 17Dec2021 02:30, outcome "recovered" (17Dec2021 11:00), described as "feverish"; CHILLS (non-serious) with onset 17Dec2021 09:30, outcome "recovered" (17Dec2021 11:00), described as "chills/freezing cold"; AXILLARY PAIN (non-serious) with onset 17Dec2021 02:30, outcome "not recovered", described as "pain in left arm pit"; LYMPHADENOPATHY (non-serious) with onset 17Dec2021 02:30, outcome "not recovered", described as "Left arm pit is slightly swollen". Therapeutic measures were not taken as a result of headache, pyrexia, chills, axillary pain, lymphadenopathy. Clinical course: Headache starting at 10 pm on 16Dec2021; then feverish; at 2:30 am on 17Dec2021 chills/freezing cold, headache; at 9:30am on 17Dec2021 chills, feverish, headache; At 11am on 17Dec2021 felt fine and no more symptoms. Adverse event start date: 16Dec2021 at 10:00 PM. If covid prior vaccination: No. If covid tested post vaccination: No. Additional symptom of pain in left arm pit which started 2:30am on 17Dec2021 and has not resolved. Left arm pit is slightly swollen. This symptom was not previously reported. Adverse event start date: 17Dec2021, Adverse event start time: 02:30 PM. Additional information: The patient received no other vaccines within 4 weeks prior to the COVID vaccine. The patient received no other medications within 2 weeks of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination and had not been tested for COVID-19 since the vaccination. Known allergies: Allergy to some tree nuts Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to nuts (Yes - allergic to certain tree nuts)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 12.03.2022
- Impfdatum
- 21.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymphadenopathy
Pain in extremity
SARS-CoV-2 antibody test
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection.; Followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection.; Followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection.; Severe swelling/pain in both axillary lymph nodes starting a few days after 3rd (booster) injection; Severe swelling/pain in both axillary lymph nodes starting a few days after 3rd (booster) injection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Dec2021 11:30 (Lot number: FL3197) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing), notes: other medical history No. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8731, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 16Apr2021, when the patient was 42 years old, for Covid-19 Immunization, reaction(s): "Covid test result=Positive", "Covid test result=Positive"; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Left Arm , Vaccine Administration Time: 01:00 PM), administration date: 28Mar2021, when the patient was 42 years old, for Covid-19 Immunization, reaction(s): "Covid test result=Positive", "Covid test result=Positive". The following information was reported: PAIN IN EXTREMITY (non-serious), AXILLARY PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 23Dec2021, outcome "not recovered" and all described as "Followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection."; LYMPHADENOPATHY (non-serious), AXILLARY PAIN (non-serious) all with onset 23Dec2021, outcome "not recovered" and all described as "Severe swelling/pain in both axillary lymph nodes starting a few days after 3rd (booster) injection". The events "followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection.", "followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection.", "followed by dull ache in armpits and intermittent pain in hands and feet (most severe in left, injection-side hand) that still persists at time of reporting 2 months after injection.", "severe swelling/pain in both axillary lymph nodes starting a few days after 3rd (booster) injection" and "severe swelling/pain in both axillary lymph nodes starting a few days after 3rd (booster) injection" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, axillary pain, pain in extremity, lymphadenopathy, axillary pain. Follow-up (23Feb2022): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220118; Test Name: UK NHS Rapid Test; Test Result: Positive ; Comments: covid test type post vaccination=Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No, Comment: other medical history No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 05.03.2022
- Impfdatum
- 16.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Some type of skin rash (big red/purple lesions all over neck and chest); This is a spontaneous report received from contactable consumer. The reporter is the patient. A 42 year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in arm left, administration date 16Dec2021 20:30 (Lot number: FL3197) at the age of 41 years as dose 1, single and administered in arm left, administration date 21Jan2022 08:30 (Lot number: FJ6369) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Antiphopholipid Syndrome" (unspecified if ongoing). Concomitant medications included: WARFARIN; SERTRALINE. The following information was reported: RASH (non-serious) with onset 26Dec2021 07:00, outcome "not recovered", described as "Some type of skin rash (big red/purple lesions all over neck and chest)". The event "some type of skin rash (big red/purple lesions all over neck and chest)" was evaluated at the physician office visit. Therapeutic measures were taken as a result of rash. Additional information: some type of skin rash (big red/purple lesions all over neck and chest) appeared 10 days after 1st dose and also again 10 days after 2nd dose. Prior to vaccination, the patient was not diagnosed with COVID-19, and since the vaccination, has not been tested for COVID-19. The were no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Antiphospholipid syndrome
- Andere Medikamente
- WARFARIN; SERTRALINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blister
Blister rupture
Contusion
Injection site bruising
Injection site swelling
Burning sensation
Burns second degree
Pain
Scar
Lymphadenopathy
Wound
Symptomtext
9 to 10 hour after getting the shot a 3 inches by 2 inches blister developed with fluid inside and very painful with burning effects, which later developed to open wound it took about 8 days to heal; and very painful/ and till this day I still have occasional sharp pain from the site.; with burning effects; which later developed to open wound it took about 8 days to heal; The scar resembles second degree burn; The scar resembles second degree burn; This is a spontaneous report received from contactable reporter (Other HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Jan2022 11:30 (Lot number: FL3197) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The patient had no known allergies. There were no other vaccines received in four weeks and no other medications in two weeks. The vaccine was administered in a doctor's office/ urgent care. The patient did not have COVID prior to vaccination. Vaccination history included: Bnt162b2 (DOSE 2, lot number: EL3249, at 10:00 AM, in Left arm), administration date: 26Jan2021, when the patient was 63 years old, for Covid-19 immunization; Bnt162b2 (DOSE 1, lot number: EL0140, at 09:45 AM in left arm), administration date: 05Jan2021, when the patient was 63 years old, for COVID-19 Immunization. The following information was reported: BLISTER (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "9 to 10 hour after getting the shot a 3 inches by 2 inches blister developed with fluid inside and very painful with burning effects, which later developed to open wound it took about 8 days to heal"; PAIN (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "and very painful/ and till this day I still have occasional sharp pain from the site."; BURNING SENSATION (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "with burning effects"; WOUND (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "which later developed to open wound it took about 8 days to heal"; SCAR (disability), BURNS SECOND DEGREE (disability) all with onset 04Jan2022 22:00, outcome "recovered with sequelae" and all described as "The scar resembles second degree burn". The events "9 to 10 hour after getting the shot a 3 inches by 2 inches blister developed with fluid inside and very painful with burning effects, which later developed to open wound it took about 8 days to heal", "and very painful/ and till this day i still have occasional sharp pain from the site.", "with burning effects", "which later developed to open wound it took about 8 days to heal", "the scar resembles second degree burn" and "the scar resembles second degree burn" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of blister, pain, burning sensation, wound, scar, burns second degree. The patient was not tested for COVID after vaccination.; Sender's Comments: Based on the information provided and plausible temporal association, the causality between the suspect drug and the events cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- 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
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blister
Blister rupture
Contusion
Injection site bruising
Injection site swelling
Burning sensation
Burns second degree
Pain
Scar
Lymphadenopathy
Wound
Symptomtext
9 to 10 hour after getting the shot a 3 inches by 2 inches blister developed with fluid inside and very painful with burning effects, which later developed to open wound it took about 8 days to heal; and very painful/ and till this day I still have occasional sharp pain from the site.; with burning effects; which later developed to open wound it took about 8 days to heal; The scar resembles second degree burn; The scar resembles second degree burn; This is a spontaneous report received from contactable reporter (Other HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Jan2022 11:30 (Lot number: FL3197) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The patient had no known allergies. There were no other vaccines received in four weeks and no other medications in two weeks. The vaccine was administered in a doctor's office/ urgent care. The patient did not have COVID prior to vaccination. Vaccination history included: Bnt162b2 (DOSE 2, lot number: EL3249, at 10:00 AM, in Left arm), administration date: 26Jan2021, when the patient was 63 years old, for Covid-19 immunization; Bnt162b2 (DOSE 1, lot number: EL0140, at 09:45 AM in left arm), administration date: 05Jan2021, when the patient was 63 years old, for COVID-19 Immunization. The following information was reported: BLISTER (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "9 to 10 hour after getting the shot a 3 inches by 2 inches blister developed with fluid inside and very painful with burning effects, which later developed to open wound it took about 8 days to heal"; PAIN (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "and very painful/ and till this day I still have occasional sharp pain from the site."; BURNING SENSATION (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "with burning effects"; WOUND (disability) with onset 04Jan2022 22:00, outcome "recovered with sequelae", described as "which later developed to open wound it took about 8 days to heal"; SCAR (disability), BURNS SECOND DEGREE (disability) all with onset 04Jan2022 22:00, outcome "recovered with sequelae" and all described as "The scar resembles second degree burn". The events "9 to 10 hour after getting the shot a 3 inches by 2 inches blister developed with fluid inside and very painful with burning effects, which later developed to open wound it took about 8 days to heal", "and very painful/ and till this day i still have occasional sharp pain from the site.", "with burning effects", "which later developed to open wound it took about 8 days to heal", "the scar resembles second degree burn" and "the scar resembles second degree burn" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of blister, pain, burning sensation, wound, scar, burns second degree. The patient was not tested for COVID after vaccination.; Sender's Comments: Based on the information provided and plausible temporal association, the causality between the suspect drug and the events cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- 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
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Dizziness BP: 170/88 Pulse: 74. After 15mins no complain of dizziness BP: 146/78 Pulse: 68 As per patient, patient had fell in october 2021 since then her B.P remains high. Patient stayed extra 15mins for observation. Advised to notify PHP about reactions. Patient left with assistant, no more dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension, stroke
- Vorgeschichte
- -
- Andere Medikamente
- Diovan, some other hypertension medication
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Headache
Pain in extremity
Taste disorder
Symptomtext
Headaches= next day Lower back pain= excruciating pain the next day Arm pain lasted for a week. Bad taste in the mouth. For all these symptoms over the counter medications were taken such as advil or Tylenol as needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal X-ray
Abdominal pain upper
Catheterisation cardiac
Chest discomfort
Computerised tomogram normal
Constipation
Electrocardiogram normal
Flatulence
Stent placement
Troponin increased
Symptomtext
escalating constipation throughout the next week, having to strain to have a BM, culminating in gas pain in upper abdomen and chest pressure on 2/20/22. Went to ER, found Triponon significantly elevated. Admitted for trending, etc. Had a Cardiac Cath procedure where stents were placed. I am reporting this because the timing is suspicious and I am aware that there can be cardiac related adverse events with the Mrna vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- 2,0
- Labordaten
- 2/20-2/21/22 High sensitivity Troponin over 2000, unremarkable EKG's, abdominal xray and CT scan to check for blockage or infection, clear.
- Aktuelle Erkrankungen
- High blood pressure managed with meds
- Vorgeschichte
- -
- Andere Medikamente
- Hydrochlorothiazide
- Allergien
- Penecillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Incorrect dose administered
Medication error
Symptomtext
MD Called 1/25/22, medication error Adult Pfizer Dose given to patient Inform parents of error Pediatrician also Called - Dr. (Privacy) Patient c/o headache and fatigue VS Stable BP 104/80 P80 Oxygen Saturation 97% Patient received Tylenol X 1 dose Patient monitored for at least 30 minutes Patient felt better and back to baseline after eating and discharge Pediatrician followed up that evening, marked improvement noted Patient seen in clinic the next day w/ Pediatrician Called (Privacy), spoke to (Privacy) , refer to CDC Appendix A, Medication Error Patient to obtain Dose #2 as scheduled Precaution Advised
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 21.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Lipase increased
Pancreatitis acute
Vomiting
Symptomtext
Pt with abdominal pain and vomiting, admitted via the ED with acute pancreatitis without clear etiology
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Lipase 1360
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- MVI
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Asthma
Bone pain
Burning sensation
COVID-19
Chest discomfort
Cough
Fatigue
Frustration tolerance decreased
Headache
Hyperhidrosis
Lung disorder
Pain
Pleural effusion
Pneumonitis
SARS-CoV-2 test
X-ray
Symptomtext
felt frustrated; asthma; inflammation in her lungs; pleural effusion; COVID PCR test.it was positive; Sweating; burning up; lost taste in her mouth; her lungs were "brutal"; Headache; severe pain in the front and back of her body; chest felt awful; exhaustion; pain in bones; Aches and pains in front and back of body; cough; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 63 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Jan2022 14:20 (Lot number: FL3197) at the age of 63 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Environmental toxins mold exposure", start date: 2015 (unspecified if ongoing); "Known allergy:Sulfa" (unspecified if ongoing), notes: Allergic to Codeine, Sulfa and Toradol. She does not remember the dates but it was prior to 2015. Some time in her 40's. She does not have the manufacturer, lot or expiration of those products.; "Respiratory issues related to toxic mold exposure", start date: 2015 (unspecified if ongoing), notes: Respiratory issues related to toxic mold exposure in 2015.; "COPD from cigarette smoking and cancer." (unspecified if ongoing), notes: COPD from cigarette smoking and cancer. The patient's concomitant medications were not reported. Past drug history included: Codeine for Drug allergy, notes: Allergic to Codeine, Sulfa and Toradol. She does not remember the dates but it was prior to 2015. Some time in her 40's. She does not have the manufacturer, lot or expiration of those products.; Toradol for Drug allergy, notes: Allergic to Codeine, Sulfa and Toradol. She does not remember the dates but it was prior to 2015. Some time in her 40's. She does not have the manufacturer, lot or expiration of those products. The following information was reported: COVID-19 (Non-serious) with onset 25Jan2022, outcome "unknown", described as "COVID PCR test.it was positive"; PAIN (non-serious) with onset 16Jan2022 18:30, outcome "unknown", described as "severe pain in the front and back of her body"; CHEST DISCOMFORT (non-serious) with onset 16Jan2022 18:30, outcome "not recovered", described as "chest felt awful"; AGEUSIA (non-serious) with onset 17Jan2022, outcome "not recovered", described as "lost taste in her mouth"; LUNG DISORDER (non-serious) with onset 17Jan2022, outcome "unknown", described as "her lungs were "brutal""; HEADACHE (non-serious) with onset 16Jan2022 18:30, outcome "not recovered", described as "Headache"; FRUSTRATION TOLERANCE DECREASED (non-serious), outcome "unknown", described as "felt frustrated"; BONE PAIN (non-serious) with onset 16Jan2022 18:30, outcome "recovering", described as "pain in bones"; PAIN (non-serious) with onset 16Jan2022 18:30, outcome "recovering", described as "Aches and pains in front and back of body"; ASTHMA (non-serious), outcome "unknown", described as "asthma"; FATIGUE (non-serious) with onset 16Jan2022 18:30, outcome "unknown", described as "exhaustion"; COUGH (non-serious) with onset 16Jan2022, outcome "not recovered", described as "cough"; FATIGUE (non-serious) with onset 24Jan2022, outcome "unknown", described as "feels tired"; HYPERHIDROSIS (non-serious) with onset 21Jan2022, outcome "recovering", described as "Sweating"; BURNING SENSATION (non-serious) with onset 21Jan2022, outcome "unknown", described as "burning up"; PNEUMONITIS (non-serious), outcome "unknown", described as "inflammation in her lungs"; PLEURAL EFFUSION (non-serious), outcome "unknown", described as "pleural effusion". The events "severe pain in the front and back of her body", "chest felt awful", "lost taste in her mouth", "her lungs were "brutal"", "headache", "felt frustrated", "pain in bones", "aches and pains in front and back of body", "asthma", "exhaustion", "cough", "feels tired", "sweating", "burning up", "inflammation in her lungs" and "pleural effusion" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (25Jan2022) positive, notes: On 25Jan2021, she got report that it was positive; x-ray: (unspecified date) like a pleural effusion, notes: X-ray of chest front and back lateral - unremarkable cardio mediastinal silhouette. It did show visible Costophrenic angles. Therapeutic measures were taken as a result of lung disorder, cough. Clinical Course: Reported as, later that day at 6:30 pm she went into severe pain in the front and back of her body, her chest felt awful (she had environmental toxic exposure to mold, so her lungs tend to have issues regularly). The next day she claims she lost taste in her mouth and her lungs were "brutal". On Tuesday 18th she called her doctor and she gave her a prescription for prednisone and antibiotic for "doxicilin" (not sure about this antibiotic). On Friday she still had some headaches but no fever and yesterday she got and X-Ray test for her lungs and she was placed with more Prednisone. She stated that this "triggered" the whole thing.The pain in bones and everything else started at 6:30 pm. It set her body off. This thing just nailed her body and came out of nowhere and was progressive. Headaches are still coming though. Her Lungs have been exposed to environmental toxins from mold and her body is kind of like when it has asthma. The lungs react. This thing went right to her lungs. She has been put on antibiotics and was in ER yesterday and the doctor said it would take a long time. Headaches are not as frequent but still there. Her body was in total exhaustion and she just had to try and sleep. On Monday, 17 she lost taste. She could smell but had no taste. Lungs were progressing. Tuesday, she did a Telehealth with her doctor because of her lungs and all of the symptoms that she mentioned, so they put her on Prednisone and Doxycycline. On 24Jan2022, she did a telehealth visit because of the ongoing issue with her lungs, exhaustion and cough. Her body feels tired. Checked vitals, they did an x-ray front and lateral of chest, and gave prescription Medrol dose pack 4mg, 21 tablets, She has not picked it up yet. Also gave prescription for Tessalon Pearls 100mg, 3 times daily for cough. She has picked those up yet. Telehealth visit on 24Jan2022. They prescribed Prednisone 20mg twice daily and Doxycycline. They told her to get a COVID test on 24Jan2021, she got a COVID PCR test at 15:30. On 25Jan2021, she got report that it was positive. It was so amazing because she had no symptoms or anything from 16Jan2022 to 24Jan2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220125; Test Name: COVID PCR test; Test Result: Positive ; Comments: On 25Jan2021, she got report that it was positive.; Test Name: X-ray; Result Unstructured Data: Test Result:like a pleural effusion; Comments: X-ray of chest front and back lateral - unremarkable cardio mediastinal silhouette. It did show visible Costophrenic angles.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COPD (COPD from cigarette smoking and cancer.); Exposure to mold; Respiratory disorder (Respiratory issues related to toxic mold exposure in 2015.); Sulfonamide allergy (Allergic to Codeine, Sulfa and Toradol. She does not remember the dates but it was prior to 2015.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Pyrexia
Symptomtext
Per mom: inflammation in armpit wrapped around to the front of his ribs. It looked like a flattened water balloon under his skin. No lymph node inflammation or pain. He could feel it when his arms were down near his body. He also had a fever, which resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Fatigue
Full blood count abnormal
Headache
Inflammation
Lymphadenopathy
Metabolic function test
Myalgia
Pain
Pain in extremity
Pyrexia
Thyroid function test
Symptomtext
The day after the vaccine I had a fever of 101. I had chills and body aches. That lasted about 24 hours. I also had headaches affecting the front of my head and my temples. I also felt full body muscle and joint pains for about 24 hours. The pain lingered mostly in my hips and legs. After that subsided I noticed I was getting more and more tired throughout the day. It was hard to function. If I sat still for a few mins I would start to fall asleep. I went to the Dr. and had labs done and they showed I had an elevated thyroid. Every morning after that, even until now, I wake up in the morning with really swollen lymph nodes. Especially on the right side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 01/26/2022: Bloodwork for Thyroid: elevated CBC and CMP: Shows mild inflammation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth Control
- Allergien
- Bee allergy Melons
- Vorherige Impfungen
- Flu Vaccine. I now only get the Flu block. MMR: I break out in hives. 10/2019 33yrs old.
- Staat
- FL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 13.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
Sweating, lightheadedness, dizziness within 5 minutes of administration. Patient requested medical attention and to lay down. Paramedics were requested and , upon arrival took care of patient. Once stable and feeling better, patient went home by himself ( 40 min aprox after symptoms started)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bursitis
Fatigue
Headache
Joint swelling
Oral herpes
Pain
Rash
Swelling
Symptomtext
Cold sores / herpes simplex virus (HSV-1), resolved about 3 weeks after booster; Large swelling, left armpit, starting day following and lasting over a week; Swelling and rash at joints, may be 3 days following; Swelling and rash at joints, may be 3 days following; Swelling/bursitus in left elbow, still present 1- month following booster; Headache; Body ache; Tiredness; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Jan2022 at 11:15 (Lot number: FL3197) at the age of 63 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1, MANUFACTURER UNKNOWN), for COVID-19 immunisation and Covid-19 vaccine (DOSE 2, MANUFACTURER UNKNOWN), for COVID-19 immunisation. The following information was reported: ORAL HERPES (non-serious) with onset an unknown date in Jan2022, outcome "recovered" (an unknown date in Jan2022), described as "Cold sores / herpes simplex virus (HSV-1), resolved about 3 weeks after booster"; SWELLING (non-serious) with onset an unknown date in Jan2022, outcome "not recovered", described as "Large swelling, left armpit, starting day following and lasting over a week"; JOINT SWELLING (non-serious), RASH (non-serious) all with onset an unknown date in Jan2022, outcome "not recovered", and all described as " Swelling and rash at joints, may be 3 days following"; BURSITIS (non-serious) with onset an unknown date in Jan2022, outcome "not recovered", described as "Swelling/bursitus in left elbow, still present 1- month following booster"; HEADACHE (non-serious) with onset an unknown date in Jan2022, outcome "not recovered", described as "Headache"; PAIN (non-serious) with onset an unknown date in Jan2022, outcome "not recovered", described as "Body ache"; FATIGUE (non-serious) with onset an unknown date in Jan2022, outcome "not recovered", described as "Tiredness". The event "Swelling/bursitus in left elbow, still present 1- month following booster" was evaluated at the physician office visit. It was unknown whether any therapeutic measures were taken as a result of the reported events. Additional Information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Headache
Insomnia
Movement disorder
Panic attack
Pyrexia
Somnolence
Symptomtext
She gets panic attacks at night time; She wasn't able to sleep; She hasn't been able to really move until now.; really high fever between 103-104; Headache; fell asleep a couple of hours; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 13Jan2022 19:00 (Lot number: FL3197) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE: 1, Her First COVID vaccine was given at (Withheld), on 08Apr2021; lot EW0153.), administration date: 08Apr2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "After the first COVID vaccine, she just had pain in her arm, and she had to hold her arm"; Bnt162b2 (DOSE: 2, Her second COVID vaccine was given on 01May2021, at (Withheld), the Lot is either EW0170 or EW0179.), administration date: 01May2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "she had a fever"; Bnt162b2 (DOSE: 2, Her second COVID vaccine was given on 01May2021, at (Withheld), the Lot is either EW0170 or EW0179.), administration date: 01May2021, when the patient was 49 years old, for Covid-19 Immunization, reaction(s): "This time time her fever has been way worse to the point she hasn't been able to work". The following information was reported: PYREXIA (non-serious) with onset 14Jan2022, outcome "not recovered", described as "really high fever between 103-104"; HEADACHE (non-serious) with onset 14Jan2022, outcome "not recovered", described as "Headache"; SOMNOLENCE (non-serious) with onset 14Jan2022, outcome "unknown", described as "fell asleep a couple of hours"; PANIC ATTACK (non-serious), outcome "unknown", described as "She gets panic attacks at night time"; INSOMNIA (non-serious), outcome "unknown", described as "She wasn't able to sleep"; MOVEMENT DISORDER (non-serious), outcome "not recovered", described as "She hasn't been able to really move until now.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, headache, panic attack, insomnia. Additional information: NDC number and Expiry Date of COVID 19 vaccine was unknown. No other products.Patient was no history. No investigation assessment.The fever has been really hard to break down. Patient consulted with doctor virus to 1.5 months get over she is good to go with booster. She got the pfizer booster. Then, during the night about 1:30-2 am, she started feeling like she had a fever. She took 3 pills total. The first time, she took Aleve, almost right after she woke up with the fever. Then she was waited and fell asleep a couple of hours. When she woke up she had terrible headaches. She had a really high fever / temperature. Her thermometer might now be really accurate. It was 103.7 or something like that. After she woke up, she took her temperature again and it was between 103-104. She took another Aleve this time and waited about an hour. Then, maybe around 10 am she took an Ibuprofen gel. It didn't help really. Her headache and fever were still going. Her mom was thinking of calling emergency services because the fever wouldn't break down. Her mom was sitting right next to her, and noticed she was calming down . She fell asleep an hour ago, and now her temperature is down to 100. She really can't see the UPC/lot/expiration on the bottles of Aleve and Ibuprofen. She would need her glasses. She hasn't been able to really move until now. She only take Alprazolam , 0.5mg once at night. She gets panic attacks at night time. She wasn't able to sleep, and the doctor prescribed this to help her sleep through the night. It helped. Vaccine was not administered at military facility. Additional Vaccines were not administered on same date of the pfizer suspect. No any prior vaccinations (within 4 weeks). Patients medical history (including any illness at time of vaccination): provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity was not. No any relevant tests and List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging (e.g. chest X-ray, MRI).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220114; Test Name: Fever; Result Unstructured Data: Test Result:down to 100; Comments: now her temperature is down to 100; Test Date: 20220114; Test Name: Fever; Result Unstructured Data: Test Result:103-104; Comments: really high fever between 103-104; Test Date: 20220114; Test Name: Fever; Result Unstructured Data: Test Result:103.7; Comments: It was 103.7 or something like that
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
CD4 lymphocytes
Epistaxis
Fatigue
Gingival swelling
Haemoptysis
Headache
Lethargy
Neck pain
Pyrexia
Symptomtext
Right gums swollen; Nose bleeds; Neck is sore; Headache; Fever of 101.8 degrees Fahrenheit; Feels lethargic/lethargy; tired; cleared his throat and tried to expel sputum and had blood/clear mucous; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 13Jan2022 13:00 (Lot number: FL3197) at the age of 47 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "HIV" (unspecified if ongoing), notes: Verbatim: HIV, He is now probably 15 years since being diagnosed. Family history included: "Alpha 1 antitrypsin deficiency" (unspecified if ongoing), notes: Verbatim: Alpha 1 antitrypsin deficiency, Diagnosed 4 years ago. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1, Lot: FA7484, expiration unknown, injected in right arm), administration date: 19Jul2021, when the patient was 47 years old, for Covid-19 immunization; Bnt162b2 (Dose: 2, Lot: FC3181, expiration unknown. Injected in right arm), administration date: 16Aug2021, when the patient was 47 years old, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 14Jan2022, outcome "recovered" (16Jan2022), described as "Fever of 101.8 degrees Fahrenheit"; LETHARGY (non-serious) with onset 14Jan2022, outcome "recovering", described as "Feels lethargic/lethargy"; GINGIVAL SWELLING (non-serious) with onset 17Jan2022, outcome "recovering", described as "Right gums swollen"; EPISTAXIS (non-serious) with onset 17Jan2022, outcome "not recovered", described as "Nose bleeds"; NECK PAIN (non-serious) with onset 17Jan2022, outcome "not recovered", described as "Neck is sore"; HEADACHE (non-serious) with onset 17Jan2022, outcome "not recovered", described as "Headache"; FATIGUE (non-serious) with onset Jan2022, outcome "recovering", described as "tired"; HAEMOPTYSIS (non-serious) with onset Jan2022, outcome "not recovered", described as "cleared his throat and tried to expel sputum and had blood/clear mucous". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Additional information: It was reported that on Friday evening, he had a fever of 101.8 degrees Fahrenheit that lasted for about 2 days. It was daytime fever as well. It was controlled with Tylenol. On Sunday, the fever broke, but he felt lethargic and still had residual energy and he woke up with right gums swollen and nose bleeds. The lethargy started on Friday. He was still tired, but improving. He cleared his throat and tried to expel sputum and had blood. It was not coming from chest, it was from nasal passage, and is clotty. When he tried to expel it in a tissue through mouth, it was blood and clear mucous. He was still clearing throat and still bleeding. He just takes his normal medication and his infusion treatment, but nothing different. He does not had any lymph node involvement, but both sides of his neck are very sore. Vaccine not administered at Military Facility. Vaccines Administered on Same Date of the Pfizer Suspect, all vaccines administered on same date with the Pfizer vaccine considered as suspect was none. Fever of 101.8 degrees Fahrenheit, felt lethargic - Before bedtime around 19:30-20:00, right gums swollen, Neck is sore at morning time, nose bleeds and headache at afternoon. The adverse event did not require visit to Emergency Room and virtual visit with physician and no treatment offered. The other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) was none. AE(s) following prior vaccinations was None. The other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity Illness/AE: Compromised immune and genetic abnormalities: He was diagnosed HIV 15 years ago and has Alpha 1 antitrypsin deficiency. Relevant Tests was None. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220114; Test Name: Body temperature; Result Unstructured Data: Test Result:101.8 Fahrenheit; Comments: Fever; Test Name: CD4 count; Result Unstructured Data: Test Result:1400
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Alpha-1 antitrypsin deficiency (Verbatim: Alpha 1 antitrypsin deficiency Diagnosed 4 years ago.); HIV infection (Verbatim: HIV He is now probably 15 years since being diagnosed.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site pain
Vaccination site swelling
Symptomtext
swelling, soreness and redness at the site of injection; swelling, soreness and redness at the site of injection; swelling, soreness and redness at the site of injection; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). A 35 year-old female patient received bnt162b2 (COMIRNATY), administration date 14Jan2022 15:00 (Lot number: FL 3197) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for COVID-19 immunization; Bnt162b2 (DOSE 2, SINGLE), for COVID-19 immunization. The following information was reported: VACCINATION SITE SWELLING (non-serious), VACCINATION SITE PAIN (non-serious), VACCINATION SITE ERYTHEMA (non-serious) all with onset 15Jan2022, outcome "unknown" and all described as "swelling, soreness and redness at the site of injection". Additional information: 35 year old female patient received booster Pfizer-BioNTech Covid-19 vaccine around 3pm Friday 14Jan. The day after she experienced swelling, soreness and redness at the site of injection. No fever and site was not warm to the touch. Event took place after use of product. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Musculoskeletal stiffness
Pain
Vaccination site pain
Vaccination site reaction
Symptomtext
Discomforts subside; General stiffness; Mild aches; Soreness and stiffness at injection site; Soreness and stiffness at injection site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 12Jan2022 10:15 (Lot number: FL3197) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EL3247; Administration Time: 13:00; Anatomical Location: Right leg; Route of Administration: Intramuscular), administration date: 04Mar2021, when the patient was 58 years old, for COVID-19 immunisation, reaction(s): "Vaccine administered at inappropriate site"; Bnt162b2 (DOSE 2, SINGLE; Lot Number: EP6955; Administration Time: 11:00; Anatomical Location: Right arm; Route of Administration: Intramuscular), administration date: 26Mar2021, when the patient was 58 years old, for COVID-19 immunisation. The following information was reported: MUSCULOSKELETAL STIFFNESS (non-serious) with onset 12Jan2022 19:00, outcome "recovered" (13Jan2022 12:00), described as "General stiffness"; PAIN (non-serious) with onset 12Jan2022 19:00, outcome "recovered" (13Jan2022 12:00), described as "Mild aches"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE REACTION (non-serious) all with onset 12Jan2022 19:00, outcome "recovered" and all described as "Soreness and stiffness at injection site"; DISCOMFORT (non-serious) with onset 13Jan2022 19:00, outcome "recovered", described as "Discomforts subside". Therapeutic measures were taken as a result of musculoskeletal stiffness, pain, vaccination site pain, vaccination site reaction, discomfort. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four 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. The events did not result in doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Prior vaccinations (within 4 weeks) was none. Specific relevant test for thromboembolic events with thrombocytopenia was none. Only treatment (13Jan) was 400 mg Advil. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- 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
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Injection site pain
Symptomtext
Patient received an expired dose of Pfizer Covid-19 vaccine. It was out of the refrigerator at 1700 on 2/8/22 at 1700, expired at 2300, then administered 2/9/22 at 0915-0930. Patient so far does not c/o of any adverse symptoms other than expected pain at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Calcipotriene topical, Clobetasol topical, Desonide topical, Allopurinol
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Neck pain
Pain
Symptomtext
Site: Pain at Injection Site-Severe, Additional Details: Patient is complaining of severe pain radiating from the left neck down to the injection site. Patient claims it started two days after getting the vaccine and has not went away since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Ear discomfort
Fatigue
Feeling abnormal
Head discomfort
Headache
Lymph node pain
Magnetic resonance imaging
Malaise
Oropharyngeal discomfort
Photophobia
Tinnitus
Symptomtext
I now am certain that these symptoms in my case are due to MRNA covid vaccines. 2nd shot with Mod created the same reactions. Current unresolved symptoms include tender nodes and awful pressure in head and throat, and TINNITUS, and 1- I feel pressure in my head, behind my ears, and pressure, on and off, at different nodes/locations around my head and throat. The nodes are very tender. This increases and decreases with intensity and can make me feel sick and dizzy. 2- Sharp pain comes and goes in my head. Bad headaches. 3- I hear a very high frequency sound that I can best describe as "old tv static", heard from both ears, from inside my head. 4- Light sensitivity which lasts approx 1 week. 5- Fatigue. Brain fog. Having now experienced this adverse reaction twice, as a 51 year old, who was pro vaccine, now there is no doubt in my mind that the MRNA vaccines are causing unacceptable adverse reactions in a small percentage but SIGNIFICANT number of people. I believe, as a statistician, that these adverse reactions are significantly underreported due to this climate where doctors, in my experience, seem to want to believe and convince patients that it was a coincidence and the highly unusual and awful things going on in your body must be something like late onset allergy (at the age of 50) or tell you to stop eating gluten rather than give any weight to the highly unusual event (receiving an MRNA vaccine) that you feel caused the highly unusual to you reaction which is occurring in your body. For me it took over 9 months for the Moderna side affects to just start waring off. I was maybe 65% better when I took the Pfizer vaccine (3rd dose) which threw me back to the same awful side effects created by the Moderna vaccine in my body. This made it clear to me that the head pressure / head tenderness/ headaches/ high frequency static Tinnitus/ fatigue were a direct cause of these vaccines in my case. My body (unlike I understand my husbands and many others has a terrible negative response to these vaccines which I have never experienced with any other vaccine) I don't have any allergies to regular foods etc that I have experienced my entire life. This reaction was foreign to me and took away my ability to do much of what is required to live as I had been living. The constant pressure and buzz and headaches are debilitating and feel never ending. As a statistician I was open to the small possibility that it was a coincidence early in 2021 when I first experienced this, even though my gut felt what was going on in my body was absolutely directly caused by the MRNA covid vaccine. I am pro vaccine. I took the booster because I believe in the greater good and trusted the advice given and the fear in my mind was overcome by the medical community and doctors dismissing a connection, the general environment, and the idea that the Pfizer vaccine will be different to the Moderna ( which I was too fearful to take again), not knowing anything about it, but hopeful that it was different. However now I believe it is unacceptable to allow, whilst some may argue is a small percentage but still are a significant number of people, to be dismissed and the obvious (really awful which takes away any normal life) adverse reactions not to be taken seriously. (There must be a significant statistical bias where the real number of adverse reactions in the MRNA / and or covid vaccines are substantially underreported due to the environment and medical professional dismissals of any connection) . If the obvious is continued to be dismissed I fear for the long term consequences of loss of trust by the general public and the anti vaccine community growing due to people like me losing any trust and confidence in the system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 1- VAERS report submitted 07/22/21 VAERS ID: private E-Report Number: private after similar adverse reaction with Moderna 2nd vaccine detail and include MRI performed previously.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- Liothyronine 15 mcg/day started Oct'21 due to vaccine reaction
- Allergien
- NONE
- Vorherige Impfungen
- Always take required vaccines (flu/travel etc) NEVER had adverse affect until the MRNA vaccines above
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 28.12.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Symptomtext
Shoulder joint pain on left arm and deltoid muscle soreness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- melatonin
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash macular
Symptomtext
Red rash on face that comes on after washing face and stays for about 30 mins. Blotchy spots when face is touched
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- rosacea and acne
- Andere Medikamente
- doxycycline
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Pruritus
Rash
Symptomtext
The client reported that they received a first dose of Sinovac COVID vaccine (Lot# 6-202102005) on 03/21/21. The client states she received a second dose of Sinovac COVID vaccine, but does not have documentation of the second dose. The client presented to clinic on 12/29/21 where she was advised to start the Pfizer series over and received a fist dose of Pfizer COVID vaccine (Lot# FL3197). The client stated that 4 hours after the Pfizer dose she developed itching and a rash dispersed on her body. The client stated these symptoms lasted two days. The client took Benadryl which helped her symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Insulin and Metformin
- Allergien
- The client reported a history of developing a rash and itching after taking penicillin.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 01.08.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial infection
COVID-19
Dysphonia
Fatigue
Nasopharyngitis
SARS-CoV-2 test
Secretion discharge
Vaccination failure
Symptomtext
vaccination failure; COVID-19; Mucus discharge; Fatigue aggravated; Common cold; Voice disturbance; Bacterial infection; FACILITATED COLLECT This is a solicited report received from non-contactable reporter(s) (Consumer or other non HCP) from product quality group for a Pfizer sponsored program (NOT PROVIDED). The reporter is the patient. Other Case identifier(s): 21K-163-4216546-00. A 62 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administration date 27Dec2021 (Lot number: FL3197) at the age of 62 years as dose 3 (booster), single for covid-19 immunisation; adalimumab (HUMIRA), first regimen subcutaneous from Aug2021 (Batch/Lot number: unknown) to Dec2021 at 40mg/0.4ml/ citrate free (40 mg,1 in 2 wk), second regimen subcutaneous from 15Dec2021 (Batch/Lot number: unknown) to 05Jan2022 at 40mg/0.4ml/ citrate free (40 mg,1 in 1 wk) and third regimen subcutaneous since 12Jan2022 (ongoing) (Batch/Lot number: unknown) at 40mg/0.4ml/ citrate free (40 mg,1 in 1 wk) for rheumatoid arthritis. Relevant medical history included: "TOBACCO USE", stop date: 2010, notes: TOBACCO USE (Stopped 2010); "FIBROMYALGIA", start date: 2020 (unspecified if ongoing), notes: Fibromyalgia (Started 2020); "MEMORY ISSUES" (unspecified if ongoing); "PENICILLIN ALLERGY" (unspecified if ongoing); "CODEINE ALLERGY" (unspecified if ongoing), notes: Codeine allergy manifestation by hives and itching.; "TETRACYCLINE ALLERGY" (unspecified if ongoing); "ALCOHOL USE WINE" (unspecified if ongoing), notes: occasionally. Concomitant medication(s) included: CELEBREX taken for rheumatoid arthritis; PRILOSEC [OMEPRAZOLE MAGNESIUM] taken for gastritis; PREDNISONE taken for rheumatoid arthritis; MELATONIN taken for somnolence; CLONAZEPAM taken for sleep disorder; VITAMIN D [COLECALCIFEROL] taken for supplementation therapy; FOLATE taken for rheumatoid arthritis; BACLOFEN taken for rheumatoid arthritis; ZYRTEC ALLERGY taken for hypersensitivity; METHOTREXATE SODIUM taken for rheumatoid arthritis; MAGNESIUM SULFATE taken for supplementation therapy; ZINC CHLORIDE taken for immune enhancement therapy; CALCIUM taken for supplementation therapy; VITAMIN C [ASCORBIC ACID;ROSA CANINA] taken for immune enhancement therapy. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number EL9263), administration date: 17Mar2021, for COVID-19 immunization; Bnt162b2 (DOSE 2, SINGLE, Lot number EN6204), administration date: 06Apr2021, for COVID-19 immunization. The following information was reported: VACCINATION FAILURE (medically significant) with onset 31Dec2021, outcome "unknown", described as "vaccination failure"; COVID-19 (medically significant) with onset 31Dec2021, outcome "unknown", described as "COVID-19"; SECRETION DISCHARGE (non-serious) with onset 31Dec2021, outcome "recovering", described as "Mucus discharge"; FATIGUE (non-serious) with onset 31Dec2021, outcome "recovering", described as "Fatigue aggravated"; NASOPHARYNGITIS (non-serious) with onset 31Dec2021, outcome "recovered" (Jan2022), described as "Common cold"; DYSPHONIA (non-serious) with onset 31Dec2021, outcome "not recovered", described as "Voice disturbance"; BACTERIAL INFECTION (non-serious) with onset 31Dec2021, outcome "recovering", described as "Bacterial infection". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (31Dec2021) positive, notes: Positive for Covid-19. The action taken for adalimumab was unknown. Clinical information: The patient was treated with Tylenol. Causality as per reporter for Humira was Not Related. Causality as per reporter for bnt162b2 was Not Reported. As part of the simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according. Investigation result: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE INJECTABLE lot EL9263 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot EL9263, fill lot EL9254, and the formulated drug product lot EL9245. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. When more than one investigation is found in the family, the Conclusion field could result in repeating rows for the CR in the table. If the Conclusion is blank in the table above, then the investigation record is likely an Offline Contractor Investigation and the conclusion must be obtained directly from the child investigation record(s) of the linked Complaint Record. No follow-up attempts are possible. No further information is expected. Follow-Up (28Jan2022): Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information provided and known drug safety profile the lack of efficacy of the vaccine and the events fatigue, secretion discharge and nasopharyngitis with the suspect drug BBNT162B2 cannot be excluded. The events dysphonia and bacterial infection were considered as an intercurrent illness and hence were assessed as unrelated to the suspect vaccine BNT162B2. Case will be reassessed if any new information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211231; Test Name: NASAL SWAB TEST; Result Unstructured Data: Test Result:Positive; Comments: Positive for Covid-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Alcoholism (occasionally); Allergy (Codeine allergy manifestation by hives and itching.); Allergy to antibiotic; Amnesia; Fibromyalgia (Fibromyalgia (Started 2020)); Penicillin allergy; Tobacco user (TOBACCO USE (Stopped 2010))
- Andere Medikamente
- CELEBREX; PRILOSEC [OMEPRAZOLE MAGNESIUM]; PREDNISONE; MELATONIN; CLONAZEPAM; VITAMIN D [COLECALCIFEROL]; FOLATE; BACLOFEN; ZYRTEC ALLERGY; METHOTREXATE SODIUM; MAGNESIUM SULFATE; ZINC CHLORIDE; CALCIUM; VITAMIN C [ASCORBIC ACID;ROSA CANINA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Decreased appetite
Illness
Nausea
Ocular hyperaemia
Somnolence
Vomiting
Symptomtext
nausea; has been sleeping; she started throwing up; she lost her appetite/not able to eat anything; became sick; a red eye on the right side; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. Other Case identifier(s): US-PFIZER INC-202200063664 (Pfizer). A 62 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 04Jan2022 09:30 (Lot number: FL3197) at the age of 62 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Mentally challenged" (unspecified if ongoing), notes: Diagnosis date: 20 years ago; "Blood pressure" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing), notes: Investigation Assessment: No. Concomitant medication(s) included: RISPERIDONE; SERTRALINE; LISINOPRIL; ATORVASTATIN; LISINOPRIL HCTZ. Vaccination history included: Bnt162b2 (dose 1, lot number unknown), for covid 19 immunization, reaction(s): "did not have no side effects"; Bnt162b2 (dose 2, lot number unknown), for covid 19 immunization, reaction(s): "did not have no side effects". The following information was reported: SOMNOLENCE (non-serious) with onset 04Jan2022, outcome "unknown", described as "has been sleeping"; VOMITING (non-serious) with onset 04Jan2022, outcome "recovering", described as "she started throwing up"; DECREASED APPETITE (non-serious) with onset 04Jan2022, outcome "recovered" (2022), described as "she lost her appetite/not able to eat anything"; ILLNESS (non-serious) with onset 04Jan2022, outcome "unknown", described as "became sick"; OCULAR HYPERAEMIA (non-serious) with onset 2022, outcome "not recovered", described as "a red eye on the right side"; NAUSEA (non-serious) with onset 04Jan2022 17:00, outcome "recovered" (2022), described as "nausea". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of somnolence, vomiting, decreased appetite, illness, nausea. Therapeutic measures were taken as a result of ocular hyperaemia. Additional information: Vaccination anatomical site was right shoulder. Reporter mentioned that his wife received booster dose on Tuesday morning (04Jan2022), she was fine until Tuesday evening when she started throwing up, mentioned that she lost her appetite and has been sleeping since then. She did not want to eat anything and was still throwing up but not as bad. He mentioned that she cannot say what's wrong because she was mentally challenged, and mentioned that she had no fever, with her temperatures as 98 F yesterday and 99 F this morning. She had no problem with her first 2 doses, and it was a breeze, reporter was asking whether this is temporary. The patient was mentally challenged, so reporter must do and talk for her, as she was not able to do that. She had the reaction from Booster one, with the other two shot she did not have no side effects with them, but this Booster shot was taken Tuesday (04Jan2022) morning later the day she became sick, and she began to vomit and that's why right now she was not able to eat anything since Tuesday. Right now, she was just sick. She hasn't eaten many times since then, reporter tried to get her to eat something, but she has thrown up. Took her temperature yesterday and it was 98 point something, so it was okay and took her temperature this morning and it was still Ok; it was 99 so she had no running nose, not temperature anything but she still has not eat many times. Right now, she was just sleeping, she just meaning sleep ever since. Reporter just wanted to report it right now, reporter was just watching her fearful condition and just wanted to get some information from Pfizer like she has for just a day, two or just wait to see just will go away but reporter wanted to let it be known. Reporter stated, she never had no problem. Patient reported nausea, being sick and she could not eat along with a red eye on the right side which would be the side that she received the shot. The patient received the shot around 9:30 AM and the nausea started around 5 PM in the afternoon where the nausea got bad, and she started throwing up. Reporter stated for the next two days, she had no appetite and anything she ate, she would throw it up; the nausea has passed but the red eye remained, however it does not hurt or anything. Reporter had been putting over the counter eye drops (treatment for a red eye on the right side) for his wife, later clarified that she had nausea and could not eat but that has passed; also clarified that it is for the right eye. When probed for treatment for adverse events, reporter stated, this happened just yesterday, so we did nothing. Nobody did anything, we first called Pfizer, and nothing been done. The patient was still having the problems (event). Later stated that the nausea has passed, stated that on the side that she got the shot in that her eye is red. Stated that she got shot last Tuesday and the side effects started that afternoon. Later clarified that she had nausea and could not eat but that has passed. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- Test Name: body temperature; Result Unstructured Data: Test Result:98 Fahrenheit; Test Name: body temperature; Result Unstructured Data: Test Result:99 Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood cholesterol abnormal (Investigation Assessment: No); Hypertension; Mental disorder (Diagnosis date: 20 years ago)
- Andere Medikamente
- RISPERIDONE; SERTRALINE; LISINOPRIL; ATORVASTATIN; LISINOPRIL HCTZ
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Lymphadenopathy
Symptomtext
Swollen lymphnodes- arm pit and neck(three days).; Headaches; fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 31Dec2021 08:45 (Lot number: FL3197) at the age of 60 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Fibromyalgia" (unspecified if ongoing); "spinal stenosis" (unspecified if ongoing); "Degenerative disk dz" (unspecified if ongoing); "Known allergies: Latex" (unspecified if ongoing), notes: Known allergies: Latex, steroids. Concomitant medication(s) included: SINGULAIR. Past drug history included: Steroids, reaction(s): "Known allergies: steroids", notes: Known allergies: Latex, steroids. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 31Dec2021 12:00, outcome "not recovered", described as "Swollen lymphnodes- arm pit and neck(three days)."; HEADACHE (non-serious) with onset 31Dec2021 12:00, outcome "not recovered", described as "Headaches"; FATIGUE (non-serious) with onset 31Dec2021 12:00, outcome "not recovered", described as "fatigue". Therapeutic measures were not taken as a result of lymphadenopathy, headache, fatigue. Additional information: The patient did not take any other vaccine in four weeks prior COVID -19 vaccine. The patient was not diagnosed with COVID prior vaccination and not tested with COVID post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Degenerative disc disease; Fibromyalgia; Latex allergy (Known allergies: Latex, steroids); Spinal stenosis
- Andere Medikamente
- SINGULAIR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Headache
Loss of personal independence in daily activities
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Received booster vaccine without symptoms and positive antibody serology test. Day 3 after vaccination had headache, fever (100 F), sore throat, body aches and inability to perform ADLs. Day 3 after vaccination + COVID antigen test, continuation of same symptoms. Day 4 after vaccination, + COVID PCR test, continuation of same symptoms. Day 5 - continuation of same symptoms. Day 6 and 7 (today) - no fever, however continuation of body aches, headache and new onset chest discomfort.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID antigen test 02/01/2022 (positive), COVID-19 PCR test 02/02/2022 (positive).
- Aktuelle Erkrankungen
- Possible COVID-19 infection without symptoms at the time of vaccination. Positive antibody serology COVID-19 test IgG/IgM on 01/24/2022.
- Vorgeschichte
- Bilateral hearing impairment
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Diarrhoea
Fatigue
Headache
Hot flush
Injection site pain
Myalgia
Nausea
Pain of skin
Pyrexia
Symptomtext
Severe pain in head, muscles, joints. Severe fatigue with chills and hot flashes. Air hurts my skin. When I am cold it feels like daggers piercing my skin. Nauseous. Diarrhea. Injection site tenderness. Fever up to 102.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Other viral infection two weeks prior always tested negative for covid
- Vorgeschichte
- Allergies environmental, GERD, asthma
- Andere Medikamente
- Adderall, omeprazole, baclofen, gabapentin
- Allergien
- Walnuts, melons, sometimes avocado,
- Vorherige Impfungen
- Pfizer covo
- Staat
- IL
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 31.12.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Oral pain
Symptomtext
She received Pfizer COVID-19 vaccine on 12/31/2021. On 1/3/22 she noted a metal taste in her mouth which was followed by severe pain in her mouth. This has slowly started improving, but is still quite painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pain
- Hospital-Tage
- -
- Labordaten
- Timing seems related to COVID-19 vaccination - will need to report as potential side effect. Rx for viscous lidocaine. - lidocaine viscous (LIDOCAINE VISCOUS) 2 % oral solution; Take 5 mLs by mouth every 6 hours as needed for pain Resolved after use of Viscous Lidocaine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, Hypothyroidism, Vaginal vault prolapse s/p hysterectomy, insomnia
- Andere Medikamente
- Vitamin D 1000 units daily, Estardiol 1mg PO daily, Gabapentin 300mg TID, HCTZ 12.5mg PO Daily, Levothyroxine 75mcg PO Daily, Meloxicam 15mg PO daily, Metoprolol tartrate 50mg PO BID, Oxycodone/APAP 7.5mg PO Q4-6HR PRN, Ocuvite 2 tabs PO
- Allergien
- Penicllin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Hot flush
Pyrexia
Symptomtext
Headache fever heat flush
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID two weeks ago
- Vorgeschichte
- Psoriasis psoriatic arthritis
- Andere Medikamente
- Tylenol
- Allergien
- Pcn , humeria
- Vorherige Impfungen
- COVID and flu
- Staat
- PA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 31.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Diarrhoea
Gingival discolouration
Lip swelling
Peripheral swelling
Rash
Rash pruritic
Symptomtext
1 day after immunization administration onset of itchy rash that progressively spread throughout the body. Was seen at an ER 1/30/22 for worsening itchy rash, was given Benadryl and hydrocortisone and sent home. Reported to our office for worsening symptoms with bilateral hand swelling, lip swelling and gum discoloration. Also reported diarrhea yesterday and spreading itchy/painful rash. Vital signs were stable. Was given PO Benadryl in the office and sent to the ER for further evaluation for potential reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- ADHD
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Dermatitis
Diarrhoea
Fatigue
Headache
Herpes virus infection
Influenza virus test
Pain
Pyrexia
SARS-CoV-2 test
Symptomtext
1/26 - Developed fever of tmax 102.8F (resolved on 1/28); having persistent fatigue, body aches, headache, decreased appetite. On 1/28 had four episodes of diarrhea; also developed herpes vesicular dermatitis to right and left upper and lower lips, right upper gum, and right cheek.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Obtaining COVID/influenza testing to r/o current infection due to prolonged symptoms.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol, Cymbalta, Neurontin, Robaxin, Ditropan, Vagifem, Elavil, vitamin D2, baclofen, Dulera
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash
Symptomtext
Rash all over body, still going on
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Urgent care visit
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Fish
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site scab
Symptomtext
Patient developed a very light scab on the injection site area about one week after receiving the vaccine. No further adverse events associated. The scab began to go away after a couple weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site scab
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Oligomenorrhoea
Vaginal haemorrhage
Symptomtext
Irregular vaginal bleeding potentially related to menstrual cycle. Mild lightheadedness due to blood loss. Bleeding has continued on/off for the last 29 days forcing the patient to seek treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Fatigue
Myalgia
Pyrexia
Symptomtext
had fever/chills - this continued into the following morning (temperature peaking at 1:30am at 100.3degrees); had fever/chills - this continued into the following morning (temperature peaking at 1:30am at 100.3degrees); experienced muscle aches; feeling very fatigued; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 33-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 13Jan2022 10:00 (Lot number: FL3197) at the age of 33 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hashimoto's thyroiditis" (unspecified if ongoing); "Lichen simplex chronicus" (unspecified if ongoing). Concomitant medication(s) included: JUNEL taken for contraception; LEVOTHYROXINE. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247), administration date: 14Jan2021, when the patient was 32 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, Vaccine Administration Time: 03:00 PM), administration date: 04Feb2021, when the patient was 33 years old, for COVID-19 Immunization. The following information was reported: FATIGUE (non-serious) with onset 13Jan2022 21:30, outcome "recovering", described as "feeling very fatigued"; CHILLS (non-serious), PYREXIA (non-serious) all with onset 13Jan2022 22:30, outcome "recovering" and all described as "had fever/chills - this continued into the following morning (temperature peaking at 1:30am at 100.3degrees)"; MYALGIA (non-serious) with onset 13Jan2022 21:30, outcome "recovering", described as "experienced muscle aches". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of fatigue, chills, pyrexia, myalgia. Additional details: Patient did not receive any other vaccine in four weeks. List of other medications received in two weeks include: JUNEL 1/20 for birth control and LEVOTHYROXINE 25mcg. Patient did not have covid prior vaccination. Patient did not test for covid, post vaccination. Patient had no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220114; Test Name: Fever; Result Unstructured Data: Test Result:100.3; Comments: degrees
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's thyroiditis; Lichen simplex chronicus
- Andere Medikamente
- JUNEL; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site warmth
Sleep disorder
Symptomtext
18 days post injection (COVID booster) presented to clinic with continual worsening of pain, redness, and warmth to injection site (left deltoid). ROM and CMS intact, afebrile, no systemic effects. Started on course of with keflex Q6H X7 days today for possible cellulitis to injection site. Reports symptoms have been so bothersome it is impacting his sleep and ADLs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic low back pain
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Vaccinated on the 14th. Painful rash spreading over body began on the 24th. Patient came to urgent care. Will start on a high-dose steroid taper. Will follow-up with PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Hyperhidrosis
Influenza like illness
Nausea
Neck pain
Pain
Pyrexia
Symptomtext
Flu like symptoms; Fever; Bad headache; Severe body aches; Sweats; Neck and back pain; Neck and back pain; Nausea; This is a spontaneous report received from a contactable reporter (consumer). The reporter is the patient. A 27-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 13Jan2022 (lot number: FL3197) at the age of 27-years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing). Concomitant medication included: ESCITALOPRAM taken for anxiety. Vaccination history included: BNT162B2 (as dose 1, single), for COVID-19 immunisation and BNT162B2 (as dose 2, single), for COVID-19 immunisation. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset 14Jan2022, outcome "recovering", described as "Flu like symptoms"; PYREXIA (non-serious) with onset 14Jan2022, outcome "recovering", described as "Fever"; HEADACHE (non-serious) with onset 14Jan2022, outcome "recovering", described as "Bad headache"; PAIN (non-serious) with onset 14Jan2022, outcome "recovering", described as "Severe body aches"; HYPERHIDROSIS (non-serious) with onset 14Jan2022, outcome "recovering", described as "Sweats"; NECK PAIN (non-serious) and BACK PAIN (non-serious) all with onset 14Jan2022, outcome "recovering" and all described as "Neck and back pain"; and NAUSEA (non-serious) with onset 14Jan2022, outcome "recovering", described as "Nausea." Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety
- Andere Medikamente
- ESCITALOPRAM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Vomiting
Symptomtext
Patient received dose at 1720. Reported nausea 1740 and went to the bathroom to vomit. Blood pressure112/80 oxygen sat 98%. Patient sat down for observation. Reported feeling dizzy. Felt better after being monitored for 45 minutes. Repeat blood pressure 120/80
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes type 2
- Andere Medikamente
- -
- Allergien
- Reported having nausea and vomiting after receiving first two doses of Pfizer vaccine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Fatigue
Headache
Immunisation
Nausea
Pain in extremity
Symptomtext
very sharp pains in the side of my head; i had a pain between my pinky toe and my left hope going up my foot for a little bit which stopped; nausea; Her stomach is extremely queasy/stomach was turning; booster; little tired; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 28Dec2021 12:40 (Lot number: FL3197) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU taken for immunisation, administration date 30Nov2021. Past drug history included: Amoxicillin, reaction(s): "she felt like she could not breathe", notes: she took Amoxicillin, she had to take a Benadryl because she felt like she could not breathe. She does not have a lot or expiration for the Amoxicillin. It was many years ago. Vaccination history included: Bnt162b2 (Dose 1 of the Pfizer COVID Vaccine , Lot number: CG6955, Injected in right upper arm, she reported the headaches after first or second dose of the Pfizer COVID vaccine), administration date: 20Mar2021, when the patient was 39 years old, for COVID-19 Immunization, reaction(s): "Headache"; Bnt162b2 (Dose 2 of the Pfizer COVID Vaccine , Lot number: EW0151, Injected in right upper arm, she reported the headaches after first or second dose of the Pfizer COVID vaccine), administration date: 10Apr2021, when the patient was 39 years old, for COVID-19 Immunization, reaction(s): "Headache", "Sharp pains". The following information was reported: IMMUNISATION (non-serious) with onset 28Dec2021, outcome "unknown", described as "booster"; HEADACHE (non-serious) with onset 29Dec2021 01:00, outcome "recovering", described as "very sharp pains in the side of my head"; PAIN IN EXTREMITY (non-serious) with onset 29Dec2021, outcome "recovering", described as "i had a pain between my pinky toe and my left hope going up my foot for a little bit which stopped"; NAUSEA (non-serious) with onset 29Dec2021, outcome "not recovered", described as "nausea"; ABDOMINAL DISCOMFORT (non-serious) with onset 29Dec2021, outcome "unknown", described as "Her stomach is extremely queasy/stomach was turning"; FATIGUE (non-serious) with onset Dec2021, outcome "unknown", described as "little tired". Therapeutic measures were taken as a result of headache. Additional information: The patient had a very sharp pain in head more towards the top of ear to head and it lasted about 7 hours. It would go away, but it continued through the night and was very sharp. Yesterday, it went away after the morning. She only had it once or twice throughout the day and then it was gone. She had another weird pain, and does not know if it is related. She had pain between two of toes going up her left foot. It happened 3-4 times and it stopped and she never had it before. This was in the middle of the night. She was up all night. Patient was also very nauseous. Yesterday, pretty much since midday up until today. Her stomach was extremely queasy. It was fine the night before. She was hungry and ate but had just been nauseous. She had not thrown up and feels like her stomach was turning. She was able to keep food down and just felt like she needed ginger ale. After vaccination, the patient had minor headache prior, but did not take anything. She had her period and was really heavy on that day. This was her third one. Nausea was mild and she was not vomiting, it's guessing around noon. The patient had Flu vaccine exactly 4 weeks before this. Headache the next day that was cured with the tylenol. Was a little tired the next day. It was nothing odd. It was only because it was a sharp pain. She heard regular headaches were common and she would not have reported it had it not been sharp. No patient history. No investigation assessment. Vaccine was not administered at Military facility. Vaccination facity type was Pharmacy. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect was reported as none. No visit to emergency room or physician office. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Symptomtext
Pain/burning sensation at injection site, pain around rotator cuff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Induration
Pyrexia
Symptomtext
FOLLOWING DAY PATIENT CALLED PHARMACY TO REPORT HIGH FEVER, AND HARD BUMP ON HER ARM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Lymphadenopathy
Nausea
Symptomtext
swollen lymphnodes, shoulder pain, naseau
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Discomfort
Symptomtext
Pain in armpit of vaccinated arm. Advised using OTC for discomfort and to follow-up in 3 days sooner if symptoms worsen or new symptoms develop.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Lymphadenitis
Pyrexia
Tonsillitis
Symptomtext
Chills, lymph nodes flared up, tonsillitis, and fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Throat culture 1/3/2022
- Aktuelle Erkrankungen
- Cold ( not Covid)
- Vorgeschichte
- Graves? disease
- Andere Medikamente
- Birth control, multi vitamin, and iron
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Pain in extremity
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Throat clearing
Symptomtext
She received her vaccine on 12/28/2021. After the vaccine, her right arm arm was extremely sore and then around 01/07/2022 she started having mild headaches and a bit of a cough. She felt like she needed to clear her throat and felt fatigued. I took her to a local health care facility. No exams were performed. She tested positive for Covid on 01/15/2022 and retested on 01/20/2022 where she tested negative. As for today, she has severe headaches and extremely fatigued, coughs and gets congested out of the blue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- No exams performed.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol
- Allergien
- Cantaloupe; watermelon; pistachios
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Body temperature
Chills
Decreased appetite
Dizziness postural
Erythema
Fatigue
Gait disturbance
Headache
Hyperhidrosis
Immunisation
Nausea
Pain
Photophobia
Pyrexia
Sinus headache
Somnolence
Vaccination site pain
Symptomtext
severe headache; Pain, swelling and redness at injection site; Pain, swelling and redness at injection site; Pain, swelling and redness at injection site; Pain, swelling and redness at injection site; tiredness; weakness; sensitive to light; pain at location of a sinus headache; pain at location of a sinus headache; dizzy and nauseated when sitting or standing; dizzy and nauseated when sitting or standing; chills; Fever 99.8; lose of appetite; vomited; sweating; not steady on my feet; slept for over 12 hours; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 05Jan2022 10:00 (Lot number: FL3197) at the age of 69 years as dose 3 (booster) , single for covid-19 immunisation. Relevant medical history included: "Breast cancer survivor" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Known allergies: aspirin, reaction(s): "Known allergies: aspirin". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 06Apr2021, when the patient was 68 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 18Mar2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "severe headache"; IMMUNISATION (non-serious) with onset 05Jan2022 10:00, outcome "unknown", described as "Booster"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE SWELLING (non-serious), ERYTHEMA (non-serious), VACCINATION SITE REACTION (non-serious) all with onset 06Jan2022 07:00, outcome "recovering" and all described as "Pain, swelling and redness at injection site"; FATIGUE (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "tiredness"; ASTHENIA (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "weakness"; PHOTOPHOBIA (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "sensitive to light"; PAIN (non-serious), SINUS HEADACHE (non-serious) all with onset 06Jan2022 07:00, outcome "recovering" and all described as "pain at location of a sinus headache"; DIZZINESS POSTURAL (non-serious), NAUSEA (non-serious) all with onset 06Jan2022 07:00, outcome "recovering" and all described as "dizzy and nauseated when sitting or standing"; CHILLS (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "chills"; PYREXIA (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "Fever 99.8"; DECREASED APPETITE (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "lose of appetite"; VOMITING (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "vomited"; HYPERHIDROSIS (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "sweating"; GAIT DISTURBANCE (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "not steady on my feet"; SOMNOLENCE (non-serious) with onset 06Jan2022 07:00, outcome "recovering", described as "slept for over 12 hours". The patient underwent the following laboratory tests and procedures: body temperature: 96, notes: Fever 99.8 usually temperature is 96; 99.8, notes: Fever 99.8 usually temperature is 96. Therapeutic measures were not taken as a result of headache, vaccination site pain, vaccination site swelling, erythema, vaccination site reaction, fatigue, asthenia, photophobia, pain, sinus headache, dizziness postural, nausea, chills, pyrexia, decreased appetite, vomiting, hyperhidrosis, gait disturbance, somnolence. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: temperature; Result Unstructured Data: Test Result:96; Comments: Fever 99.8 usually temperature is 96; Test Name: temperature; Result Unstructured Data: Test Result:99.8; Comments: Fever 99.8 usually temperature is 96
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Burning sensation
Cardiac flutter
Erythema
Immunisation
Rash
Skin burning sensation
Urine odour abnormal
Symptomtext
I am worried for my wellbeing now; Booster; fluttering feelings in my chest and all over my torso; I turned red like a tomato; rash going up my entire neck and scalp that burned; rash going up my entire neck and scalp that burned; rash going up my entire neck and scalp that burned; urine also smells like chemical; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Jan2022 18:00 (Lot number: FL3197) at the age of 34 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines in four weeks or any other medications in two weeks. Past drug history included: Topamax, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0182, Location of injection: Arm Left), administration date: 12May2021, when the patient was 34 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8731, Location of injection: Arm Left), administration date: 21Apr2021, when the patient was 34 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 05Jan2022, outcome "not recovered", described as "Booster"; CARDIAC FLUTTER (medically significant) with onset 05Jan2022, outcome "not recovered", described as "fluttering feelings in my chest and all over my torso"; ERYTHEMA (non-serious) with onset 05Jan2022, outcome "not recovered", described as "I turned red like a tomato"; RASH (non-serious), BURNING SENSATION (non-serious), SKIN BURNING SENSATION (non-serious) all with onset 05Jan2022, outcome "not recovered" and all described as "rash going up my entire neck and scalp that burned"; URINE ODOUR ABNORMAL (non-serious) with onset 05Jan2022, outcome "not recovered", described as "urine also smells like chemical"; ANXIETY (non-serious), outcome "unknown", described as "I am worried for my wellbeing now". The events "booster", "fluttering feelings in my chest and all over my torso", "i turned red like a tomato", "rash going up my entire neck and scalp that burned", "rash going up my entire neck and scalp that burned", "rash going up my entire neck and scalp that burned" and "urine also smells like chemical" were evaluated at the physician office visit. The clinical course was reported as follows: "Well, immediately I turned red like a tomato and developed a rash going up my entire neck and scalp that burned. That night I started to get fluttering feelings in my chest and all over my torso. The fluttering has got worse. I am worried for my wellbeing now, but all the urgent cares are packed with covid patients. My urine also smells like chemical. It is hard to take care of my kids." The patient was not tested for COVID-19 post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Vaccination site mass
Vaccination site pain
Vaccination site pruritus
Symptomtext
She stated it hurt a lot yesterday; Booster; lump underneath the site of the injection; itchy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 33 year-old female patient received bnt162b2 (BNT162B2), administration date 05Jan2022 (Lot number: FL3197) at the age of 33 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: VALIUM taken for lower limb fracture; GABAPENTIN taken for lower limb fracture. Vaccination history included: Bnt162b2 (Dose 1, she was taking a muscle relaxer, Valium and gabapentin for her leg), administration date: Mar2021, for Covid-19 immunization, reaction(s): "She broke her leg severely in Sep"; Bnt162b2 (Dose 2, she was taking a muscle relaxer, Valium and gabapentin for her leg), administration date: Apr2021, for Covid-19 immunization, reaction(s): "She broke her leg severely in Sep". The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022, outcome "unknown", described as "Booster"; VACCINATION SITE MASS (non-serious) with onset Jan2022, outcome "unknown", described as "lump underneath the site of the injection"; VACCINATION SITE PRURITUS (non-serious) with onset Jan2022, outcome "unknown", described as "itchy"; VACCINATION SITE PAIN (non-serious) with onset 06Jan2022, outcome "unknown", described as "She stated it hurt a lot yesterday". Additional information: She broke her leg severely in September. Now she was taking a muscle relaxer, Valium, and gabapentin for her leg. She stated she has not had a reaction in the past so she was not sure if she should take those medications today. The caller stated she had her 3rd dose of the Pfizer-BioNTech COVID-19 vaccine and it was a little sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- VALIUM; GABAPENTIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Vomiting
Symptomtext
vomiting with in 24 hours; dose_received: 03; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 22 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 05Jan2022 17:00 (Lot number: FL3197) at the age of 22 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0178), administration date: 18May2021, when the patient was 21 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0168), administration date: 09Jun2021, when the patient was 21 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 17:00, outcome "unknown", described as "dose_received: 03"; VOMITING (non-serious) with onset 06Jan2022 11:30, outcome "not recovered", described as "vomiting with in 24 hours". Therapeutic measures were not taken as a result of vomiting. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination and Since the vaccination, patient was not tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No known allergies: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Body temperature
Decreased appetite
Fatigue
Headache
Immunisation
Pain
Pyrexia
Symptomtext
Felt like death; Body aches; Headaches; Fever 100.7; Loss appetite; Fatigue; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 12:00 (Lot number: FL3197) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing), notes: other medical history: Anxiety MItral valve prolapse; "MItral valve prolapse" (unspecified if ongoing), notes: other medical history: Anxiety MItral valve prolapse. Concomitant medication(s) included: SERTRALINE; INDERAL. Past drug history included: Vancomycin, reaction(s): "known allergies: Vancomycin", notes: known allergies: Vancomycin. Vaccination history included: Bnt162b2 (prev dose product=COVID 19,, prev dose brand=Pfizer,, prev dose brand unknown=False,, prev dose lot number=EP6198,, prev dose lot unknown=False,, prev dose administration date= 25Mar2021,, prev dose administration time=01:00 PM, prev dose number=2, prev dose vaccine location=Left arm), administration date: 25Mar2021, for COVID-19 immunization; Bnt162b2 (prev dose product=COVID 19,, prev dose brand=Pfizer,, prev dose brand unknown=False,, prev dose lot number=EP8730,, prev dose lot unknown=False,, prev dose administration date= 04Mar2021,, prev dose administration time=01:00 PM, prev dose number=1,, prev dose vaccine location=Left arm), administration date: 04Mar2021, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 29Dec2021 12:00, outcome "unknown", described as "Booster"; ANXIETY (non-serious) with onset 29Dec2021 19:00, outcome "unknown", described as "Felt like death"; PAIN (non-serious) with onset 29Dec2021 19:00, outcome "unknown", described as "Body aches"; HEADACHE (non-serious) with onset 29Dec2021 19:00, outcome "unknown", described as "Headaches"; PYREXIA (non-serious) with onset 29Dec2021 19:00, outcome "unknown", described as "Fever 100.7"; DECREASED APPETITE (non-serious) with onset 29Dec2021 19:00, outcome "unknown", described as "Loss appetite"; FATIGUE (non-serious) with onset 29Dec2021 19:00, outcome "unknown", described as "Fatigue". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of anxiety, pain, headache, pyrexia, decreased appetite, fatigue. No follow-up attempts are possible. No further information is expected. Additional information: Patient was not received any treatment for adverse event. Covid prior vaccination was reported as no. Covid tested post vaccination was reported as no. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211229; Test Name: Fever; Result Unstructured Data: Test Result:100.7; Comments: Fever 100.7
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety (other medical history: Anxiety MItral valve prolapse); Mitral valve prolapse (other medical history: Anxiety MItral valve prolapse)
- Andere Medikamente
- SERTRALINE; INDERAL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Pruritus
Symptomtext
All over itchiness, almost like an allergic reaction, that comes and goes throughout the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Ear infection and UTI
- Vorgeschichte
- None
- Andere Medikamente
- Mirena
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye pain
Fatigue
Headache
Influenza like illness
Malaise
Myalgia
Nausea
Pain
Paranasal sinus discomfort
SARS-CoV-2 test
Symptomtext
A couple of hours following the vaccination I felt general myalgias, headache, nausea, sinus pressure, and general malaise. These flu-like symptoms persisted all the following day. On 16Jan2022 many of the myalgias went away but the headache persisted, and most of all I experienced a sharp pain in my eyes and forehead/brow area any time I moved my eyes. This continues the next several days and at the time I?m writing this continues to be uncomfortable. A week after my vaccine my complaints are fatigue, random onset of nausea intermittent throughout day, headache, and eye pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- oropharyngeal covid test administered 20Jan2022 at 0830. Results pending
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- GERD
- Andere Medikamente
- Pantoprazole 20mg Magnesium
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hyperaesthesia
Lip swelling
Rash
Sleep disorder
Symptomtext
Awoke in am with swelling of lips, especially upper and rash on upper thighs and left arm - with hyperaesthesia in areas of rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Golabi-Behmel Syndrome - Overgrowth syndrome ADHD Kidney stones
- Andere Medikamente
- none
- Allergien
- Pineapple, red sauce - swelling of lips and tongue
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Immunisation
Muscular weakness
Neuralgia
Pain
Rash
Rash papular
SARS-CoV-2 test
Symptomtext
raised rash; nerve psi / Nerve pain; Arm weakness; Body aches; Rash turned into large red patch before fading; Rash turned into large red patch before fading; 3rd dose; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm right, administration date 21Dec2021 10:45 (Lot number: FL3197) at the age of 58 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Breast cancer" (unspecified if ongoing); "Known allergies: Sulfur" (unspecified if ongoing). Concomitant medication(s) included: TAMOXIFEN. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8735, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 20Apr2021, when the patient was 58 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8732, Location of injection: Arm Left, Vaccine Administration Time: 01:15 PM), administration date: 30Mar2021, when the patient was 58 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 21Dec2021 10:45, outcome "recovered", described as "3rd dose"; RASH PAPULAR (non-serious) with onset 21Dec2021 18:00, outcome "recovered", described as "raised rash"; NEURALGIA (non-serious) with onset 21Dec2021 18:00, outcome "recovered", described as "nerve psi / Nerve pain"; MUSCULAR WEAKNESS (non-serious) with onset 21Dec2021 18:00, outcome "recovered", described as "Arm weakness"; PAIN (non-serious) with onset 21Dec2021 18:00, outcome "recovered", described as "Body aches"; RASH (non-serious), ERYTHEMA (non-serious) all with onset 21Dec2021 18:00, outcome "recovered" and all described as "Rash turned into large red patch before fading". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of immunisation, rash papular, neuralgia, muscular weakness, pain, rash, erythema. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. The AE treatment was given with gabapentin. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211224; Test Name: Quick vue; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer; Sulfonamide allergy
- Andere Medikamente
- TAMOXIFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Immunisation
Malaise
Urticaria
Symptomtext
hives reaction throughout the body; Booster / 3rd dose of Pfizer vaccine; Headache; not feeling well; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 16 year-old male patient received bnt162b2 (BNT162B2), administration date 16Dec2021 16:00 (Lot number: FL3197) at the age of 16 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "known allergies: Lactose intolerant" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0161, Vaccine Administration Time: 04:00 PM), administration date: 16Apr2021, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0167, Vaccine Administration Time: 04:00 PM), administration date: 07May2021, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 16:00, outcome "unknown", described as "Booster / 3rd dose of Pfizer vaccine"; HEADACHE (non-serious) with onset Dec2021, outcome "unknown", described as "Headache"; MALAISE (non-serious) with onset Dec2021, outcome "unknown", described as "not feeling well"; URTICARIA (non-serious) with onset 23Dec2021 08:00, outcome "unknown", described as "hives reaction throughout the body". The events "headache", "not feeling well" and "hives reaction throughout the body" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of headache, malaise, urticaria. Additional Information: It was reported that, the patient had headache the first day after vaccine, not feeling well for next 5 days and hives reaction throughout the body today (7th day after vaccine). The patient did not have COVID prior vaccination. The patient was not tested for COVID post vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Lactose intolerant
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site mass
Injection site pain
Injection site pruritus
Injection site warmth
Pain in extremity
Symptomtext
Hard and hot lump with redness, itching, and aching around injection site ~2 inches in diameter, with aching going down the arm into the hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic migraines, tendinitis in arms
- Andere Medikamente
- Valproic acid, lamotragine, rosuvastatin, zyrtec, fluoxetine, vitamin d, acetaminophen, ibuprofen
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Injection site pain
Mouth swelling
Swelling face
Swelling of eyelid
Swollen tongue
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Severe, Systemic: cough-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Injection site pain
Lymphadenopathy
Malaise
Pain
Pyrexia
Swelling
Symptomtext
Systemic: Body Aches Generalized-Mild, Systemic: Fever-Medium, Systemic: Lymph Node Swelling-Medium, Additional Details: Patient stated arm was squeezed and it hurt being administered. Patient said it was deep, not subcutaneous. Her arm did not hurt at injection site, it hurt under arm and was swollen. Fever was 104. She will take covid test. Felt sick for about 5 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Intervertebral disc protrusion
Lumbar puncture normal
Magnetic resonance imaging spinal abnormal
Muscular weakness
Pain
Pyrexia
SARS-CoV-2 test positive
Sensory loss
Symptomtext
Patient presented to hospital with history of fever, chills and body aches. Her symptoms started 5 days ago, she tested positive for COVID two days after developing the symptoms. One day after testing postive, she gradually developed bilateral lower extremity weakness and loss of sensation. Conservative treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 2,0
- Labordaten
- Lumbar puncture unremarkable. MRI spinal survey showed C5-C6 central protrusion, L5-S1 protrusion.
- Aktuelle Erkrankungen
- UTI
- Vorgeschichte
- UTI
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Musculoskeletal stiffness
Myalgia
Symptomtext
waking up with a crick in neck first 3 days. Both neck glands feel swollen. All muscles ache while in use.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- pre diabetes and thyroid goiters
- Andere Medikamente
- no
- Allergien
- Bactrim
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Chills
Headache
Pain
Swelling face
Tenderness
Symptomtext
Started with chills, headache, puffy/swollen face to blisters on my inner thighs which have now popped and are extremely painful and very tender to the touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- HTN
- Andere Medikamente
- Synthnroid HctZ Vitamins Lexapro
- Allergien
- PCN Clindamycin
- Vorherige Impfungen
- Chills, body aches, headache on the first and second vaccine
- Staat
- FL
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Myalgia
Pain
Pyrexia
Symptomtext
fever high of 104.2 degrees F. body aches, muscle aches, fatigue, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Environmental allergies
- Vorgeschichte
- environmental allergies
- Andere Medikamente
- Flonase
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphthous ulcer
Headache
Lymphadenopathy
Pain
Pyrexia
Vomiting
Symptomtext
three days of fever. Highest 102.2, vomiting, severe body aches, headache, swollen glands and multiple canker sores in my mouth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Had a cold the week before Christmas that was negative for COVID using an antigen test.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Fatigue
Headache
Vision blurred
Head discomfort
Immunisation
SARS-CoV-2 test
Symptomtext
Fatigue, severe headache, headache continued to intensify (causing vision to become blurry), chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Fatigue
Headache
Vision blurred
Head discomfort
Immunisation
SARS-CoV-2 test
Symptomtext
Fatigue, severe headache, headache continued to intensify (causing vision to become blurry), chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure increased
Feeling of body temperature change
Hot flush
Nausea
Pain
Vomiting
Symptomtext
The patient said the day after he felt nausea throwing up cold and hot flashes aches and pains. when he went to the er the dr said his blood pressure was elevated and gave him bp meds. today he said his blood pressure is almost back to normal. diastolic was a little high at 90. He said other pts and dr complained of similar symptoms with flu /covid combination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- no known
- Aktuelle Erkrankungen
- hypertension, anxiety pain
- Vorgeschichte
- hypertension, anxiety pain
- Andere Medikamente
- lorazepam lovastatin/ metoprolol
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site induration
Injection site mass
Symptomtext
Extremely large hard lump on arm near site of injection. Appeared within 1 day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lethargy
Pyrexia
Symptomtext
Fever letharhic Narriative: N/A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oropharyngeal pain
Pain
Rash
Throat irritation
Urticaria
Symptomtext
Pts husband reports pt had a sore throat and body aches yesterday (1/12/22) about 4 hours after receiving Pfizer booster started at about 1:40 on 1/13/22 pt had a rash develop on L and R arms. Almost looked like welts and pt's throat was scratchy but otherwise feels okay. Asked if benadryl was ok
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- Diabetes, Asthma
- Andere Medikamente
- unknown
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Urinary incontinence
Symptomtext
Pt felt dizzy about 30 seconds after the pfizer vaccines was administered. Pt lost control bladder control as well. After moving patient to lie on the floor and elevating her legs, patient regained consciousness. Blood pressure was checked - wnl - 107/80. Paradmedics were called per pt's guardian request. Heart monitor showed normal heart rhythum and blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none.
- Aktuelle Erkrankungen
- NONE - PT HAD A PHYSICAL a few months ago. Dad said pt had no issues
- Vorgeschichte
- none
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye injury
Fall
Haemorrhage
Head injury
Headache
Hyperhidrosis
Unresponsive to stimuli
Symptomtext
Client presented receive Pfizer Booster .Client stated she has a history of fainting with vaccines. She declined to sit in zero gravity chair for vaccination and reported to Vaccinator that ?it hasn't happened with other vaccines in a while. I should be ok?. Client was at vaccination table and received Pfizer COVID vaccine Booster. While still in chair client fell on floor face forward. Client had loss of responsiveness for about 30 seconds. Client was moved over on her back and legs were elevated by RN .. Client was AAOx3. Client was speaking normally and denied dizziness, or blurriness, no double vision. Client was sweating, and no pallor was observed on face, arms or neck. Vitals taken by RN at 1225 Vitals . Client stated she felt better and didn't feel like she was going to faint again. Client stated she had a mild headache pain scale 1/10 on the left side of where she bumped her head. Client had a scrape on left upper side of eye with mild bleeding. Scrape was cleaned and covered by RN. Client was informed that EMS were going to be called due to bumping her head. Client verbalized understanding. EMS was activated .. Client denies being on blood thinners. No other medical history was reported. Client was advised to follow up with her Primary care provider and seek emergency care for any other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- penicillin, ,acetaminophen
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Erythema
Fatigue
Feeling cold
Headache
Impaired work ability
Pain
Pain in extremity
Skin swelling
Symptomtext
A few hours after the shot, I started becoming very tired and weak, Body aches pains. A bad severe headache. I kept getting sharp stabbing pains on my upper left back all the next day after the shot. I believe was my kidneys. I have 3 kidneys, (NO typo, 3 kidneys) I have two half size kidneys on my left side. I have had stones in past, but never sharp pain like this. I missed work on Thursday. Had no energy all day. Slept wrapped in blanket. I was constantly cold on Thursday. My arm is sore with red spot and bump under skin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- No tests, Just stayed home. Felt better by Friday.
- Aktuelle Erkrankungen
- Diabetes, moderate cholesterol.
- Vorgeschichte
- Bronchitis ( weak lungs from multiple pneumonia over the years.) I have had kidney stones in past, required procedure. Diagnosed with Ramsey Hunt syndrome in past. I have had shingles at about age 30. I have severe headaches occasionally.
- Andere Medikamente
- Metforman 2-500 mg. , Rosuvastin, B12 vitamin, Biotin Vitamin, Multi Vitamin
- Allergien
- Allergic to Cain, balsam, cobalt, latex, nickel, fragrance, some herbs
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness postural
Pyrexia
Symptomtext
Cyclical fever, rigors, orthostatic dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Eggs
- Vorherige Impfungen
- Fever, rigors w/ Pfizer Covid Vaccine (Lot EL3246)
- Staat
- CT
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Immunisation
Interchange of vaccine products
Off label use
Symptomtext
has stomach cramps becoming more severe; His first two shots were Moderna; His first two shots were Moderna; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 24 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 09:30 (Lot number: FL3197) at the age of 24 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Moderna (1st dose date 28May2021 Lot 047C21A, expiration is unknown. Injected in left arm), administration date: 28May2021, when the patient was 24 years old, for Covid-19 immunization; Moderna (2nd dose date 25Jun2021, Lot 033C21A, expiration is unknown.Injected in left arm.), administration date: 25Jun2021, when the patient was 24 years old, for Covid-19 immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 03Jan2022 09:30, outcome "unknown" and all described as "His first two shots were Moderna"; IMMUNISATION (non-serious) with onset 03Jan2022 09:30, outcome "unknown", described as "booster"; ABDOMINAL PAIN UPPER (non-serious) with onset 04Jan2022 10:00, outcome "not recovered", described as "has stomach cramps becoming more severe".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeling abnormal
Headache
Pericardial effusion
Pyrexia
Symptomtext
PER PATIENT: SHE HAD FEVER, HEADACHE, VERY TIRED ON 12/26/2021 AT 4:30PM SHE WAS HOME NOT FEELING GOOD. ON 01/04/2022 SHE WENT TO THE HOSPITAL AND AT THE DR. SAID SHE HAS FLUID IN HEART. SHE WAS IN THE HOSPITAL UNTIL 01/09/2022 MORNING. SHE SAID SHE DID CALL HER DR. TO LET DR. KNOW WHAT TOOK PLACE ON 01/04/2022,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- UNKNOWN ANY Medical tests and laboratory results related to the adverse event.
- Aktuelle Erkrankungen
- ASTHMA, SEIZURES RESULED
- Vorgeschichte
- N/A
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- SEIZURES
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Client presented to receive Pfizer Booster. After receiving vaccine Client informed vaccinator, she was feeling a little ?woozy?. Client stated this happens to her after getting a vaccine. Client moved to zero gravity chair. A bottled water was given. Client had some sips of water. Client rested in chair. At 1715 client was asked by Nurse how she was feeling. Client stated she ?felt fine?. Client declined to have her vitals taken by EMT. Client had no Shortness of breath. Client was AAOx3. Client stood out of zero gravity chair without assistance and sat in chair while waiting in observation area. Before leaving vaccination, client was asked by nurse how she was feeling, and client said she felt good. Client left vaccination area at with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Discomfort
Erythema
Fatigue
Injection site erythema
Injection site pain
Injection site swelling
Lymphadenopathy
Pain
Pyrexia
Skin warm
Symptomtext
24 hours after vaccination patient was running a fever of 102, fatigued, and had body aches. Injection site was sore and armpit was sore and slightly swollen. Managed symptoms with tylenol and ibuprofen and cold packs. About 48 hours after vaccination we noticed more swelling and redness at injection site and a lot more swelling and redness underarm and in armpit and it was hot to the touch. Over the next several hours the redness and swelling continued to get worse, and redness was spreading to chest and back from armpit. Area was hot and swollen and uncomfortable. Patient was around 100 all day. Symptoms were managed with ibuprofen and cold packs. That evening we went to an urgent care facility to make sure there was not an infection. They suggested monitoring closely and watching for more spreading or swelling. By following day fever was gone and redness had not gotten worse. 96 hours after vaccination redness and swelling started to go away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- skin sensitivity reactions to some skin products, insect bites and stings
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Decreased appetite
Oedema peripheral
Pain
Pyrexia
Tenderness
Symptomtext
Intermittent fever of 99.0-100.1 persisting 3 days after dose was received Body aches and chills persisting 3 days after dose was received Egg sized area of swelling to the right axillary area with tenderness noted approximately 2 days after dose received Decreased appetite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec Benadryl Ibuprofen Tylenol Aleve Vitamin C Olly brand sleep gummy supplement Olly brand stress relief gummy supplement
- Allergien
- None
- Vorherige Impfungen
- Generalized weakness/fatigue after receiving first Pfizer covid vaccine on 12/17/2020
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain lower
Blister
Erythema
Erythema of eyelid
Eyelids pruritus
Herpes zoster
Ophthalmic herpes zoster
Rash
Sleep disorder
Swelling of eyelid
Symptomtext
I felt pain in the left lower abdomen in a small area which severely affected my sleep on the night of 12/30. Small amount of rashes were noticed in the morning of next day 12/31. The red blisters were expanding to form a horizontal belt in my left side for the coming 3 days. I visited facility in 1/4 and Dr. made the diagnosis of Shingles. While rashes appeared in my left side, my left eye upper lid felt itchy too; the lid got red and a little swell with a few small blistered. Dr. told me that what is in my eye is also shingles. Dr. prescribed 3 days antivirals medicine Valacyclovir. While taking this medicine the symptom was getting better with less pain, rashes were turning to darker in color and not spreading. At this time, the pain on my side remains but much less severe and the rashes are getting much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- cold sore occurred about three weeks ago. It is over when I had booster.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Nausea
Skin warm
Symptomtext
5 minutes after receiving vaccine 12 yo male feeling "like I'm going to be sick". Skin warm and clammy, BP = 108/62; RR = 22; HR= 86; 02 sat = 98-100%. Laid down on cot for 10 minutes at which time male stated "I'm feeling better now" Sat up for 10 minutes with no further symptoms. BP = 110/64 RR = 20 HR = 82. Escorted patient and Pt parent to door. Reviewed s/s of adverse reaction and provided instructions for further action if needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Skin warm
Symptomtext
Patient came 1/7/2022 to get Pfizer booster. Patient called Monday 1/10 to report sore arm and her arm was hot. A pharmacist talked with her to recommend Tylenol. Pharmacist also advised patient if it got worse to seek medical assistance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 12.01.2022
- Tage bis Beginn
- 23,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pain
Symptomtext
Patient given adult dose of Pfizer. Patient experienced feeling soreness all over the day after getting the vaccination and now issues after that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known Drug Allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Injection site erythema
Vaccination site oedema
Vaccination site pain
Vaccination site warmth
Symptomtext
Symptoms: edema, redness, warmth, and pain surrounding vaccine site increasing in intensity. Symptoms first noticed by patient approximately 18 hours post injection. Warm compresses, ice packs, and ibuprofen were initial treatment but were not helpful as symptoms continued to intensify. Patient was seen by PCP on 4th day of symptoms and diagnosed with cellulitis and given antibiotic treatment. Treatment is currently ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension (controlled), Endometriosis
- Andere Medikamente
- Propranolol, Pantoprazole, Duloxetine, Vitamin D3, Zyrtec OTC, Prenatal Vitamins
- Allergien
- Nifedipine, Sulfa
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Immunisation
Nasal congestion
Pain
Pain in extremity
Symptomtext
Overall body soreness particularly in the right arm; Soreness particularly in the right arm; Tiredness; Stuffy nose; Dose received:3/ Dose number = 3; This is a spontaneous report from a contactable reporter (consumer or other non hcp). The reporter is the patient. A 26-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in right arm, administration date 05Jan2022 at 11:00 (Lot number: FL3197) at the age of 26 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: EL3247, Route of Administration: Intramuscular), administration date: 11Feb2021, when the patient was 26 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot number: EL3247, Administration time: 10:30, Route of Administration: Intramuscular), administration date: 05Mar2021, when the patient was 26 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 at 11:00, outcome "unknown", described as "Dose received:3/ Dose number = 3"; PAIN (non-serious) with onset 06Jan2022, outcome "unknown", described as "Overall body soreness particularly in the right arm"; PAIN IN EXTREMITY (non-serious) with onset 06Jan2022, outcome "unknown", described as "Soreness particularly in the right arm"; FATIGUE (non-serious) with onset 06Jan2022, outcome "unknown", described as "Tiredness"; NASAL CONGESTION (non-serious) with onset 06Jan2022, outcome "unknown", described as "Stuffy nose". Therapeutic measures were not taken as a result of pain, pain in extremity, fatigue and nasal congestion. Additional information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Myalgia
Symptomtext
Headache, Myalgia, Chills Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Injection site pain
Muscle spasms
Myalgia
Symptomtext
Myalgia, Arthralgia, Injection site soreness and hands cramping Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Headache
Injection site pain
Myalgia
Symptomtext
Headache, Myalgia, Injection site soreness and back shoulder pain Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Headache
Injection site pain
Lymphadenopathy
Myalgia
Pyrexia
Symptomtext
Headache, Myalgia, Fever, injection site soreness, Left lymph nodes swollen, back pain Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Fatigue
Headache
Injection site pain
Lymphadenopathy
Myalgia
Nausea
Pyrexia
Vomiting
Symptomtext
Headache, Myalgia, Fever, NauseaVomiting, chills, lymph node swelling L armpit, injection site soreness, fatigue Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchospasm
Lymphadenopathy
Menstrual disorder
Pain
Symptomtext
Missed menstrual cycle: one week as of reporting Swallon gland on left clavicle: causes serve pain and sensation of restricted breathing pathway
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Lactose
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain in extremity
Vomiting
Symptomtext
vomiting, headache, soreness in arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- aspirin, cinammon, atorvastatin, omeprazole, amlodepine, atenelol, losartan, metformin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Retching
Vomiting
Symptomtext
vomiting, stomah pain, dry heaving
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- amatriptoline, levothyroxine, prozac, atorvastatin, aspirin, probiotic, glucosamine, magnesium
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test
Asthenia
Colonoscopy
Cough
Fatigue
Oesophagogastroduodenoscopy
Symptomtext
1ST DOSE - 04/21/21 - PFIZER LOT# ER8731 2ND DOSE - 05/12/21 - PFIZER LOT# EW0170 3RD DOSE - 12/27/21 - PFIZER LOT# FL3197 I have had a cough every day since 05/13/21 after my 2nd dose of the Pfizer vaccine, and I have been feeling rundown and worn out with no energy every day since then.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Allergy tests, and began getting allergy shots in July 2021. Esophagogastroduodenoscopy and Colonoscopy on 11/19/21. No issues detected.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Prozac Adderall Nexium Vitamin C Vitamin D Probiotics
- Allergien
- Phenergen
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Injection site pain
Myalgia
Pyrexia
Symptomtext
Headache, Myalgia, Fever, Injection site soreness Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Headache
Myalgia
Symptomtext
Headache, Myalgia, Fatigue Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Throat irritation
Symptomtext
Skin itching, itchy throat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Sjogrens Syndrome and Fibromyalgia
- Andere Medikamente
- Plaquenil, Multi- vitamins, Tumeric, Flaxseed Oil, Magnesium Sulfate.
- Allergien
- Sulfa and shellfish
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Disturbance in attention
Dizziness
Headache
Lethargy
Nausea
Vertigo
Vomiting
Symptomtext
Nausea Vomiting Headaches Vertigo Dizziness Spins Light headed Weak Lethargic Lack of focus Scattered brain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Atorvastatin Spironolactone
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Insomnia
Pruritus
Symptomtext
Itchiness starting about 7 days after first dose mild during the day but very hard to sleep at night itches all over body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Spironolactone
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chills
Headache
Pain
Pyrexia
Symptomtext
Chills Fever Body aches Join pain Weakness Headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 09.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Pruritus
Rash macular
Symptomtext
Approximately 8 hours after receiving the second dose, I noticed my forehead started to itch. After looking into the mirror, I observed red dots all over my forehead. I received the dosage on 12/27/21. Today is 01/09/22, and I still have the itchiness and dots present on my face/forehead. I have also noticed prolonged pain in my arm that this same dosage was received in.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None.
- Allergien
- Augementin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 09.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Heart rate increased
Myalgia
Urticaria
Symptomtext
In addition to expected fatigue, muscle and joint pain, in the morning of 1/8/22 I developed a rapid heartbeat. My resting HR was between 110 and 120 bpm over the course of the day, then in the evening of 1/8/22, I developed hives over my whole torso, arms and face. They did not itch and were not painful but were quite extensive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- No known Allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Dysmenorrhoea
Heavy menstrual bleeding
Injection site pain
Lymphadenopathy
Menopausal symptoms
Menstruation irregular
Muscle spasms
Myalgia
Symptomtext
I am perimenopausal, so my periods are neither regular nor (lately) heavy (I use tracking software for my periods-- in 2021, other than some occasional light spotting, I had periods on Aug. 1, July 6, May 3, Mar 29, and Feb. 12). My adverse event that I believe is vaccine-linked is my current period, in which I am experiencing an exceptionally heavy flow, compared to what is usual for me. I started experiencing normal vaccination side effects (slightly elevated temperature of 99.1F, injection site soreness, general muscle aches, swollen lymph nodes under armpit and in neck on side of injection) by early evening the day of my vaccination (1/5/22). Just after midnight on 1/6, my period started accompanied by moderate cramping. Within a couple of hours I was also experiencing back cramping, which is not usual for me. I had to change my pad in the middle of the night, again in the morning. Today it's been three times so far-- I've been experiencing a MUCH heavier flow than usual.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypothyroidism, obesity.
- Andere Medikamente
- Levothyroxine 0.150 mcg (prescription) Vitamin D3 5000 IU softgels (OTC, but by doctor's prescription) Super B Energy Complex softgels (OTC) Claritin Liqui-Gels (loratadine 10mg)
- Allergien
- None. (Lactose intolerant.)
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Vomiting
Symptomtext
Patient vomited immediately following her injection. Thirty minutes after vaccinated, pt. feels fine and she was discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Zoloft. Lomotrin
- Allergien
- NKA
- Vorherige Impfungen
- Vagal response frequently w/ vaccinations
- Staat
- IN
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Feeling abnormal
Loss of personal independence in daily activities
Pain in extremity
Vomiting
Symptomtext
Vomited once, temp rose during the day to 100F, sore arm, felt generally bad, missed school
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- Albuterol inhaler as needed
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Headache
Immunisation
Pyrexia
Symptomtext
Fever; Chills; Headache; Little energy; Dose number 3; This is a spontaneous report received from a non-contactable reporter (Consumer or other non HCP). The reporter is the patient. A 18 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 16:45 (Lot number: FL3197) at the age of 18 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Lot Number: EP6955), administration date: 04Apr2021, when the patient was 17 years old, for COVID-19 immunisation, reaction(s): "Inappropriate schedule of vaccine administered"; Bnt162b2 (DOSE 1, SINGLE, Lot Number: EP6955), administration date: 27Mar2021, when the patient was 17 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 16:45, outcome "unknown", described as "Dose number 3"; PYREXIA (non-serious) with onset 17Dec2021, outcome "recovered" (Dec2021), described as "Fever"; CHILLS (non-serious) with onset 17Dec2021, outcome "recovered" (Dec2021), described as "Chills"; HEADACHE (non-serious) with onset 17Dec2021, outcome "recovered" (Dec2021), described as "Headache"; ASTHENIA (non-serious) with onset 17Dec2021, outcome "recovered" (Dec2021), described as "Little energy". Therapeutic measures were taken as a result of pyrexia, chills, headache, asthenia. Additional Information: 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. Therapeutic measures taken as a result of reported events included treatment with Tylenol. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Fall
Limb injury
Tinnitus
Vision blurred
Symptomtext
Please received Pfizer booster. Within 2 minutes of observing pt felt dizzy, Blurry vision, anxious. Ringing in the ears, and light headed. Per mom, "pt started to lean to the right side then fell out of chair landing on rt shoulder." @ 1643. pt while being observed was given ice pack, head positioned on yoga mat, vitals taken, pt Denies pain. EMS called at 1648 and arrived at 1657. EMS assessed pt, vital signs taken also. EMS had pt sit up first then stand up and walked with her to sit in a chair. Pt declined additional care and mom declined as well. Mom will contact HCP if additional care is needed per Mom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 02.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Decreased appetite
Fatigue
Headache
Pain
Somnolence
Symptomtext
I had pain for a few days from the shot. The day after I slept all day. And the next day I was extremely fatigued, no appetite, and extreme body chills. After sleeping an additional day, I began to feel better and normal, however I had lots of fatigue, chills on and off, headache on and off, and in general it was taking longer than normal to bounce back. Pain was about an 8/10. I am gaining more strength now, eating more, headaches are no longer there and chills are no longer there. First two doses of Pfizer no issues in comparison.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Severe Vertigo; Neuropathy
- Andere Medikamente
- Venlafaxine; Lamotrigine; Oxybutynin; Rosuvastatin; Propranolol; Baby aspirin
- Allergien
- Promethazine; REGLAN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Gait disturbance
Vaginal ulceration
Vulvovaginal pain
Symptomtext
Extremely painful vaginal ulcers.. Patient was taken to hospital. Needed to be admitted for pain control but no beds were available. Two weeks later, they are still there and very painful. Patient can't walk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vulvovaginal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dysautonomia
- Vorgeschichte
- exercise induced asthma
- Andere Medikamente
- Abilify, Trazadone, Fludrocortisone
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Injection site pain
Injection site swelling
Lymph node pain
Lymphadenopathy
Symptomtext
Four days later and I still have very swollen painful deltoid and underarm/lymphnode.... very swollen breast tissue and left scapular area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acupuncture
Arthralgia
Fatigue
Headache
Impaired work ability
Massage
Symptomtext
Joint pain 12/29/2021-1/1/2022, rest and sleep, Advil Headache not staying in any one place 12/30/2021, 1/2/2022, 1/5/2022, rest, sleep, Advil Headache not staying in any one place, mostly in front near eyebrows and forehead, 1/3/2021-1/4/2022, Acupuncture helped a lot Fatigue, ongoing for days, 12/29/2022-1/6/2022, staying home from work, resting as needed (I experienced fatigue for more than two months after my second Covid shot on 4/9/2021, Acupuncture and massage, and time off work helped)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Benign neoplasm of liver
- Andere Medikamente
- SCDophilus 10+ probiotic (from GI Pro Health); Betaine HCL Pepsin (Pure Encapsulations); CoQ10 Ubiquinol 200mg (Bluebonnet); Liquid Vitamin D3 (Ortho Molecular Products); Quercetin Phytosome (Thorne); Algae Omega (Nordic Naturals); Sodium B
- Allergien
- Penicillin, Tramodol, Wheat, dairy, yeast, apples, mushrooms, celery
- Vorherige Impfungen
- Fatigue, headaches from second Covid dose, age 47, vaccination date 4/9/2021 in right arm, Pfizer vaccine lot ER8733
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test
Symptomtext
Fatigue, fever 101 and sore throat 6 hours after booster Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test only.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Vitamins, BP medication
- Allergien
- NKDA, no food allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Symptomtext
Patient with immediate dizziness after receiving the vaccine. Patient was observed for 45 minutes. Patient was lying supine the entire time. After providing patient with 3 cups of water, and him eating candy that he brought along, patient was still not improving much. Doctor was brought into the exam room to access.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Headache
Insomnia
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had fever, chill, cough, serve headache, congestive and unable to sleep. These lasted for about a week. I call my healthcare provider. She wanted to have the antibody fusion. On Jan 2nd, I got test for Covid-19, positive result.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid-19 test
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site erythema
Injection site induration
Injection site mass
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Interchange of vaccine products
Vaccination complication
Symptomtext
About 12 hours after the vaccine, I started getting redness, swelling and a hard lump at the site of the vaccine. It also felt warm to the touch. About 24 hours later, it was about 2-3 inch in diameter and was very red, itchy and hot. About 48 hours later, it was still the same. I called the doc on tele doc, where I was told that I may have a strong reaction to the vaccines and I could take a steroid or use cream. Over the next few days, it decreased in swelling, redness went down and it wasn't as hard as before. As of yesterday, the pain seems to have subsided. It appears today as a mild bruise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hives from second dose of Moderna
- Andere Medikamente
- Loratadine
- Allergien
- Dust mites, pollen, cats, NSAIDs
- Vorherige Impfungen
- Still experiencing symptoms from the 1st and 2nd dose of Moderna.
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Ear discomfort
Fatigue
Lymphadenopathy
Tenderness
Tinnitus
Symptomtext
Typical arm tenderness for 3-4 days, and fatigue. However, continued on day 5 with swollen lymph nodes under left arm pit (the left arm was where the vaccine was administered). Ear fullness, clogging, fluttering sounds and popping started around day 5 and continue to the present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No illnesses
- Vorgeschichte
- Migraines
- Andere Medikamente
- Vitamins, Claritin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Lip pruritus
Lip swelling
Mouth swelling
Pruritus
Rash
Swelling face
Swollen tongue
Throat irritation
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash Generalized-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Additional Details: Vaccine received on 01/03/2022 at 6:53pm, patient's mother arrived in drive-thru on 01/04/2022 in the afternoon stating that pt had itching and swelling of lips and itchy throat since 01/03/2022 in the evening. Mother had already contacted MD office and was waiting on call back. I told her to call MD office back to express urgency, and for pt to go to urgent care clinic after leaving my pharmacy, and that pt should administer Auvi-Q (on hand) if needed. Attempted to f/u but reached VM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Pain
Pyrexia
Symptomtext
Fever, joint pain, fatigue, body ache, lung discomfort? I rested and used emergency inhaler.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Methylphenidate,, AG-1, Myco-brain, vitamin D,
- Allergien
- -
- Vorherige Impfungen
- 2nd dose of Pfizer vaccine
- Staat
- MN
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Mouth swelling
Pruritus
Urticaria
Symptomtext
All over body itching, hives, swelling of eyes and mouth started overnight after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 35,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Skin warm
Symptomtext
01/05/2022 Woke up to rash on front of neck from chin to top of chest, hot and itchy, 4" x 6"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UTI, sore throat
- Vorgeschichte
- Hypothyroidism, GERD, high blood pressure, high cholesterol, mild asthma
- Andere Medikamente
- Levothyroxine, Pantopazole, Lisinopril, Atorvastatin, Albuterol Hfa Inh
- Allergien
- latex, sulfa, bees, some shell fish
- Vorherige Impfungen
- Moderna 002A21A 03/03/2021 dermis numb on injection side (left) for 28 days. Moderna 020B21A 03/31/2021 Painful headache for 2 d
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bone pain
Bone swelling
Discomfort
Insomnia
Lymphadenitis
Lymphadenopathy
Neck pain
Nervousness
Pain in extremity
Swelling
Symptomtext
I received the Pfizer booster along with the flu shot in the same left arm (bicep location) on 12/30. I had the usual soreness in the arm on 12/30. However on 12/31 when I awoke, my entire collarbone was swollen, lumpy and extremely painful. The swollen supraclavicular lymph nodes were inflamed and at least 1-2 inches. The entire left side of the collarbone to the neck was swollen and extremely sore. Anything touching the collarbone & lymph nodes and area near the carotid artery resulted in discomfort and extreme pain. I was more alarmed on how huge my lymph nodes had swelled to. It was impossible to get any rest the night of 12/31-1/1 since the arm and lymph nodes were giving me so much pain. I was extremely nervous that this could be a clot but after checking out the collarbone and touching it in various areas, I felt it was lymphnodes. I did an internet search and saw that this was a normal effect response so didn't seek urgent care. It is 1/4 and my collarbone is still swollen but not painful. The lymphnodes are not as huge as they were on 12/31 through 1/3. I feel you should know about this reaction I had. I didn't have any adverse extreme side effect with my Pfizer vaccines1 & 2. Only the booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- some thyroid issues
- Andere Medikamente
- None
- Allergien
- Allergic to morphine, surgical adhesive bandaging, some bandaids
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Urticaria
Symptomtext
SEVERE HIVES TO B/L UPPER EXTREMITIES,POSSIBLE EXACERBATION OF PSORIATIC CONDITION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HISTORY OF PSORIASIS
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- JANSSEN COVID VACCINE 3/24/2021
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angioedema
Urticaria
Symptomtext
Diffuse Urticaria and L upper face angioedema starting about 2 days after vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Upper Respiratory Infection symptoms at time of Vaccination
- Vorgeschichte
- none
- Andere Medikamente
- Trazodone 100mg nightly as needed for sleep
- Allergien
- Penicillins Hydrocodone/APAP causes nausea/vomiting
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Fatigue
Influenza like illness
Nausea
Oropharyngeal pain
SARS-CoV-2 test positive
Vision blurred
Symptomtext
I was out of town but was tired with sore throat and blurry vision on 12/28. The next day I went to a nearby Urgent Care and was feeling fatigued with flu-like symptoms. COVID test first and it was positive on the PCR test. Was told to quarantine for 10 days even though the quarantine guideline at the time was 5 days. Was given prescription cough medicine, Albuterol, and nausea medicine. Is still under quarantine. Not yet recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 12/29 COVID Test (positive).
- Aktuelle Erkrankungen
- Migraine
- Vorgeschichte
- None
- Andere Medikamente
- VitaFusion Adult gummy
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Axillary pain
Back pain
Fatigue
Neck pain
Pain in extremity
Pyrexia
Rash
Swelling
Symptomtext
Fever over 101 from 2pm on 12-31 until around 11am on 1/2, swollen armpit with pain to the underarm, shoulder, neck and back, fatigue. Rash also developed on thigh, not sure if that?s related. Fever is now gone but armpit is still swollen with arm and back pain. Rash mostly went down when fever did.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None, treated at home
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- OTC allergy med, daily vitamin, collagen
- Allergien
- Light sensitivity to some lotions
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Symptomtext
Patient felt dizzy,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- not known
- Andere Medikamente
- unknown
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Axillary pain
Diplopia
Strabismus
Symptomtext
Day one after dose Lt axilla pain. Day two after dose started with vision changes (diplopia), possibly ocular nerve palsy. Day three after dose left eye drifting to towards my nose and vision worsened. Day four after dose vision worsened. Day five after dose slight vision correction. Day six after dose some improvement, but not totally resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None. Went to the ER on day four with fear of losing my sight and they did nothing.
- Aktuelle Erkrankungen
- Fibromyalgia
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Ibuprofen 800mg prn pain
- Allergien
- PCN and Sulfa
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Dizziness
Facial pain
Fatigue
Feeling abnormal
Head discomfort
Headache
Injection site erythema
Injection site induration
Injection site mass
Injection site swelling
Memory impairment
Nausea
Pain
Pallor
Pruritus
Somnolence
Symptomtext
I remember going to get the shot and felt perfectly fine. I know within an hour of the shot 12/23/2021 I started to feel itching and pain. I then started to feel nauseated, chills, and light headed. The site where they injected the shot it was very hard, large lump and instead of getting smaller, it got larger within 3 hours the lump was huge and really red. I went to the doctor the 26th to a walk-in clinic and I told them what happened and the provider said I could go to the hospital or use OTC medication for itchiness and allergies. I bought OTC Benadryl cream and then the Claritin pills the day after on the 27th. Right now I still have a little lump. The itching has gone away. The Provider at walk-in advised me to go to hospital if I needed to or follow-up with PCP in 5 days. They did say if I felt short of breath or fever to go to hospital immediately. I also could not remember things I did the day of my shot. My son and sister-in-law told me I got very pale and I didn't feel good but could not remember a lot of what I did. I had a very bad throbbing pressure headache from forehead to front of my nose. Constant pain and the pain lasted until the 1st of January New Year's day. I kept taking Motrin and it wouldn't go away. Also some joint pain I still have. I was also really tired and all I wanted to do is sleep. But they did tell me that could happen and I was aware of that part. I have recovered except the joint pain, the drip, and a little lump.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, Neuropathy
- Andere Medikamente
- Motrin; Allergy medication; Benadryl Topical Cream; Claritin; Novolog; Lantus; B12; Vitamin D; Gabapentin; medication for kidney/blood in urine
- Allergien
- I do have Allergies to BYETTA (Insulin)
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Axillary pain
Lymph node pain
Lymphadenopathy
Pain in extremity
Symptomtext
I noticed a lot of pain in right arm up into armpit 24 hours after my Pfizer Booster shot that was given to me on 12/30. Today on 01/01 I was in the shower and noticed a very enlarged lymph node in my right arm pit, the same arm as I received my booster shot. The size of the swollen area is about 4.5" inches long by 2.5" wide. It is sore to the touch. I have never had an adverse reaction like this from my first two covid shots or any other vaccines I have received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- I have not had a visit to my doctor yet.
- Aktuelle Erkrankungen
- None at time of vaccination. I did have a cold over the week of Nov 23-Nov 31
- Vorgeschichte
- None
- Andere Medikamente
- Birth Control Pill-Sprintec, Multi Vitamin Daily gummy
- Allergien
- None that I know of for food and medication. Slightly allergic to some metals/jewerely on skin/ scented laundry detergent.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Sensitive skin
Symptomtext
PATIENT SAID RIGHT EAR WAS HURTING AND SENSITIVE. SHE SAID IBUPROFEN HELPED WITH PAIN. I ADVISED HER TO SEEK URGENT CARE IF PAIN WORSENED AND TO KEEP TREATING HER SYMPTOMS WITH OVER THE COUNTER PAIN THEARPY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 01.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Injection site swelling
Lymphadenopathy
Oropharyngeal pain
Symptomtext
Site: Swelling at Injection Site-Mild, Systemic: Lymph Node Swelling-Medium, Additional Details: pt states he has a large lump under left arm and sore throat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Immunisation
Nausea
Symptomtext
Nausea; Headache; Chills; Tiredness; Dose number: 3; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. An adult female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Dec2021 (Lot number: FL3197) as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EL3247; Route of Administration: Unspecified), administration date: 03Feb2021, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EL3247; Route of Administration: Unspecified), administration date: 24Feb2021, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021, outcome "unknown", described as "Dose number: 3"; NAUSEA (non-serious) with onset 23Dec2021 at 01:30, outcome "recovered" (23Dec2021), described as "Nausea"; HEADACHE (non-serious) with onset 23Dec2021 at 01:30, outcome "recovered" (23Dec2021), described as "Headache"; CHILLS (non-serious) with onset 23Dec2021 at 01:30, outcome "recovered" (23Dec2021), described as "Chills"; FATIGUE (non-serious) with onset 23Dec2021 at 01:30, outcome "recovered" (23Dec2021), described as "Tiredness". Therapeutic measures were taken as a result of nausea, headache, chills and fatigue. Additional Information: Treatment for the events included IBUPROFEN. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- 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
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Pruritus
Swelling
Vaccination site erythema
Vaccination site mass
Vaccination site swelling
Symptomtext
itching; booster; redness past the injection site/ red way past the injection site; Swollen and red way past the injection site; swelling; Right on the top of the arm where I got injection it is hard and big; This is a spontaneous report received from a contactable Consumer or other non HCP from medical information team. The reporter is the patient. A 53 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 (Lot number: FL3197) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Osteoarthritis" (ongoing), notes: Osteoarthritis; "Hypertension" (ongoing), notes: Diagnosed in her late thirties. Maybe when she was between the ages 37-38. There were no concomitant medications. Vaccination history included: Bnt162b2 (First Dose: , Lot: ER8737), administration date: 01Apr2021, for COVID-19 immunization; Bnt162b2 (Second Dose: , Lot: EWO169), administration date: 22Apr2021, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021, outcome "unknown", described as "booster"; SWELLING (non-serious) with onset Dec2021, outcome "unknown", described as "swelling"; VACCINATION SITE ERYTHEMA (non-serious) with onset 16Dec2021, outcome "not recovered", described as "redness past the injection site/ red way past the injection site"; PRURITUS (non-serious) with onset 19Dec2021, outcome "not recovered", described as "itching"; VACCINATION SITE MASS (non-serious) with onset Dec2021, outcome "unknown", described as "Right on the top of the arm where I got injection it is hard and big"; VACCINATION SITE SWELLING (non-serious) with onset 16Dec2021, outcome "not recovered", described as "Swollen and red way past the injection site". Therapeutic measures were taken as a result of swelling, vaccination site erythema. Additional information: No other product has been mentioned. Diagnosed in her late thirties. Maybe when she was between the ages 37-38.First it was supposed to be rheumatoid arthritis. Then she had tests done a year ago and was told it's definitely osteoarthritis. It's confusing to her but they keep changing the name. She just knows it hurts like heck .Clarified she is reporting about her third dose, COVID-19 Vaccine. The lady who administered her booster dose, wouldn't give caller her name, it made her uncomfortable. She went with her family members and the nurse did theirs. The nurse that did her family member, he is fine. He doesn't have this and his is great. No further details provided.Has been keeping up per the CDC and this new variant. Trying to do the right thing. She has doubts. The myths are just horrible. Has high regards to Dr. and medical staff. Prayed to God that this is being used for the right thing. Got it to be whole and healthy and do the right thing at the right time. Was taking a baby Aspirin, but quit taking it the same day as the booster dose COVID-19 Vaccine or the next day. NDC/LOT/EXP for baby Aspirin not probed over call. The lady administering caller's COVID-19 vaccine booster dose was acting and looking a certain way. She wouldn't give caller her name, only stating they call her. Caller states this is an important shot and the administering person was acting weird. The patient visited neither Emergency Room nor Physician Office.States when she first started getting the Flu shot, she would swell up. Told this to the nurse and it was put in her chart. The nurse stated it would be necessary to warm up the spot first before injection. Clarified the swelling was specific to the injection site of the Flu vaccine. Has had swelling and redness at injection site of COVID-19 vaccine. Was advised by a Pharmacist to take 2 Benadryl. It has continued for 4 days and caller feels it is worse. It is now starting to itch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension (Diagnosed in her late thirties. Maybe when she was between the ages 37-38); Osteoarthritis (Osteoarthritis)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Pyrexia
Rash erythematous
Rash papular
Skin warm
Symptomtext
Fever of 103.9 for 3+ hours; took 2 doses of Tylenol and 1 dose of Motrin to bring down below 101. Large, red, raised, warm rash at sign of injection which I am now on day 3 of. The rash continues to get larger by the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- Avocado
- Vorherige Impfungen
- Rash on left arm from 2nd Pfizer dose; still 29; same symptoms of current rash; lasted 15 days
- Staat
- KY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Diarrhoea
Nausea
Vomiting
Symptomtext
Severe diarrhea and vomiting for 2 days 19 hours post vaccination 1st dose pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- vitamic C, D and E
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Diarrhoea
Nausea
Vomiting
Symptomtext
Severe diarrhea and vomiting for 2 days 19 hours post vaccination 1st dose pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- vitamic C, D and E
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Diarrhoea
Dissociation
Feeling abnormal
Musculoskeletal stiffness
Neck pain
Rash
Symptomtext
Diarrhea/ rash on neck / pain and stiffness in neck / fogginess and zoned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Pain
Symptomtext
The site got swollen, red, and itchy. It also hurt a lot to move the arm or touch the area. The red mark was about 2 by 2 and a half inches in an oval shape. This whole thing was swollen. The itchiness started two days later but is persistent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Prilosec
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site erythema
Injection site swelling
Injection site vesicles
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: A GRANULE BLISTER AT SITE OF INJECTION WITH REDNESS AND SWELLING IN THE SURROUNDING AREA-Mild, Additional Details: Patient reported a blister with fluid the size of granule at the injection site with redness and swelling at the surrounding area. Pt will monitor and report if there is any worsening or no improvement after a few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Myalgia
Pyrexia
Symptomtext
Myalgia, Fever, chills Narrative: N/A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
Fatigue
Headache
Symptomtext
I feel tired and headache after around 10h after vaccination and I can see gross blood in my urine after 24h. This also happened after I received my second dose of the Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- chronic kidney diseases
- Vorgeschichte
- chronic kidney diseases
- Andere Medikamente
- lisinopril 20mg
- Allergien
- -
- Vorherige Impfungen
- Pfizer\BioNTech second dose
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Feeling hot
Nervousness
Symptomtext
Client received the Booster COVID vaccine (Pfizer, Lot #FL3197) at approximately 1235. At 1238,Observation RN was alerted by client, that she was feeling lightheaded and warm. Client was moved to anti-gravity chair and provided snacks and water. Co-lead was requested by Observation RN. At 1241, vitals assessed (BP 123/71, P 67, color wnl). Client reports feeling nervous and a little lightheaded. Client also reports she had not eaten anything recently. At 1256 vitals assessed (BP 125/86, P 68, color wnl). Client reports that she is feeling better. Client continues to eat snacks and drink water. Client has hypothyroidism and currently taking 60mg armour thyroid daily. No known Allergies. At 1303 client reports feeling good and feels ready to leave. Vitals assessed (BP 127/88, P 69, color wnl). Client educated on signs/symptoms when to seek medical care and to follow-up with primary care provider. Client left with steady gait and with husband present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- Armour Thyroid 60mg
- Allergien
- KNA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear discomfort
Myalgia
Pain in extremity
Tinnitus
Symptomtext
Tinnitus, ringing in the ear, feeling clogged, since waking up the day after the vaccine; Soreness in the arm, and other muscles starting the evening of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Symptomtext
Severe low back pain stretching length entire low back. Most severe day after but has continued to present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cold 12/16-12/18. Symptoms (sneezing, congestion) resolved 12/19. Tested negative for COVID via at home test on 12/18. Had a cold a month or month and half prior.
- Vorgeschichte
- Asthma
- Andere Medikamente
- Vitamin C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Diarrhoea
Malaise
Symptomtext
Chills, feeling unwell and diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- none
- Allergien
- no known allergy
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Symptomtext
Approx a couple minutes after vaccination, patient complained of dizziness and nausea symptoms. Patient was resting on pharmacy bench post vaccination. Offered patient cold water and they accepted and relaxed on bench. After 15 minutes patient reported that symptoms went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Patient reported to RN a reaction to the second dose of Moderna COVID vaccine (LOT# 004M20A, exp. 07/10/2021) on 02/12/2021. Patient reported no allergic reaction with the first dose of Moderna COVID vaccine (LOT# 027L20A, exp. 06/30/2021). Patient reported hives on "abdomen, chest, and upper extremities" the morning after her vaccination. Patient reported no itchiness, swelling, and difficulty breathing. Patient contacted PCP and was prescribed a topical cream and steroid medication. Patient took medications for one week. Patient reported no known allergies, no chronic conditions, and no current medications. RN elevated situation to Clinical Supervisors. Clinical Supervisors elevated to medical consult team. Medical consult team approved patient for a Pfizer COVID vaccine booster dose. Patient reported she will return on 12/23/21 due to work schedule. On 12/23/2021, at approximately 0900, patient returned to facility. RN advised patient to wait for 30 minutes in observation and educated patient on signs/symptoms of when to alert observation staff. At 0924, patient received Pfizer COVID booster vaccine (LOT# FL3197, exp. 06/30/2022). At approximately 0939, RN assessed patient. Patient denied rashes, itchiness, and difficulty breathing. At approximately 0954, RN reassessed patient. Patient denied rashes, itchiness, and difficulty breathing RN educated patient on signs/symptoms of when to seek emergency care, to follow up with PCP, and to sign up on V-safe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Symptomtext
Systemic: Nausea-Medium, Additional Details: Patient felt nauseous ~5mins after vaccine. She laid on the floor which she said helped, she did not feel lightheaded or other symptoms. Pharmacist sat with her for 15 mins and she said she felt better and went home, no ambulance required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Dizziness
Hyperhidrosis
Pallor
Staring
Unresponsive to stimuli
Symptomtext
within 3 minutes of vaccine patient was lightheaded and sat down. by the time I walked out to check on the patient he was pale, not responsive and eyes were wide and up to the right as if he was going to have a seizure I ran to get the emergency cart and water while the mom braced the child's head. He was responsive and able to drink by the time I returned and was able to drink water and take 10ml of benadryl. We walked him back into the clinic room to get blood pressure and removed his shirt that was soaked in sweat. His reading was 68/29. I gave him a bottle of water and had the technicians get chips for him while I was getting his reading. We had dialed 911 in the meantime and the mom wanted the paramedics to come to check him out. His blood pressure went up to 137/68 , blood sugar was 117 and he was fine by the time the paramedics got there. He stayed another 30 minutes then left to get food with parents who decided not to take him to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- BLOOD PRESSURE 68/29, THEN 137/68 AFTER FLUIDS AND FOOD. BLOOD SUGAR 117 AFTER EATING CHIPS
- Aktuelle Erkrankungen
- NONE, BUT GAVE BLOOD AND HAD A VAGAL RESPONSE AS WELL, BUT THEY DID NOT PUT ON THE FORM AND DID NOT DISCLOSE UNTIL AFTER THIS REACTION
- Vorgeschichte
- NONE
- Andere Medikamente
- ADDERALL 20MG
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Fatigue
Headache
Injection site discolouration
Injection site erythema
Injection site pain
Injection site pruritus
Nausea
Pain
Symptomtext
Later that night of the vaccination, I was very tired and 2:00AM I woke up with headache, chilis, nausea and body ache. Later in the afternoon the next day my left arm was red and there was oval around the shot area, it was very sore. It was also a little itchy so that is when I called my doctor and had a consultation over the phone spoke to his nurse, she said it'll improve in a couple of days and to ice it 4 times a day for 20 minutes each time. It is improving some but it still sore and there is discolor around the site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- N/A
- Andere Medikamente
- Claritin; Multivitamin
- Allergien
- Seafood; Environmental Allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Feeling of body temperature change
Headache
Injection site rash
Nausea
Pain
Peripheral swelling
Pruritus
Rash erythematous
Symptomtext
1 day post injection. ( 14 hrs after injection) Severe headache. (Migraine level) nausea. Fatigue. By that evening. Also had chills. Was hot but so cold but no fever. Body aches. Symptoms are better (but not gone) by day three. Still very tired. Nausea is only there after I eat. Headache is mild. But now I have a huge red rash at injection site. Bicep is swollen and hit. I noticed it when it itched.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hashimotos hypothyroidism. Rosacea.
- Vorgeschichte
- Hypothyroidism. Hashimoto. Rosacea.
- Andere Medikamente
- Levithyroxine. Ibuprophen.
- Allergien
- None that I know of.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Body temperature increased
Myalgia
Symptomtext
Elevated temperature 103 + F Severe body (muscle & joint) pain Symptoms started approx 12 hrs after injection and subsided approx 40 hrs after injection. Partially responded to treatmen with acetaminophen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- seasonal allergies, depression (mild), hx of afib (successful treated 3 yrs prior with left atrial ablation)
- Andere Medikamente
- Multivitamin, Zyrtec, Sertraline, Fish Oil, Move Free (otc joint health), vitamin D3, magnesium
- Allergien
- None
- Vorherige Impfungen
- Covid Biontech
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Body temperature
Chills
Immunisation
Pyrexia
Symptomtext
Shivering/ Chills; High Fever (100 deg. F); Slight pain in joints due to the shivering; Dose received: 3; This is a spontaneous report received from contactable reporter (consumer or other non-HCP). A 66-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in left arm, administration date 20Dec2021 (Lot number: FL3197) at the age of 66 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Hyperthyroidism" (unspecified if ongoing) and "Graves' disease" (unspecified if ongoing), notes: Graves disease. Concomitant medication included: METHIMAZOLE. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: Unknown), for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: Unknown), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021, outcome "unknown", described as "Dose received: 3"; CHILLS (non-serious) with onset 21Dec2021, outcome "not recovered", described as "Shivering/ Chills"; PYREXIA (non-serious) with onset 21Dec2021, outcome "not recovered", described as "High Fever (100 deg. F)"; ARTHRALGIA (non-serious) with onset 21Dec2021, outcome "not recovered", described as "Slight pain in joints due to the shivering". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of chills, pyrexia and arthralgia. Additional Information: The patient had no known allergies. 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-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211221; Test Name: Body temperature; Result Unstructured Data: Test Result:100 Units:[degF]; Comments: High Fever (100 deg. F)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Graves' disease (Graves disease); Hyperthyroidism
- Andere Medikamente
- METHIMAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye pain
Fatigue
Headache
Immunisation
Lymphadenopathy
Pain in extremity
Pyrexia
Vomiting
Symptomtext
Fever; Headache; Vomiting; Fatigue; Pain behind eyes; Sore arm; Swollen lymph nodes over 48 hours; dose received :3; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 18Dec2021 at 10:30 (Lot number: FL3197) at the age of 31 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Sulfonamide allergy" (unspecified if ongoing), notes: known allergies: Sulfa drugs. The patient did not receive any concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: ER8735, Anatomical site: Left arm; Administration time: 17:00), administration date: 30Mar2021, when the patient was 31 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot number: ER8731, Anatomical site: Left arm, Administration time: 17:00), administration date: 20Apr2021, when the patient was 31 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 18Dec2021 at 10:30, outcome "unknown", described as "dose received :3"; PYREXIA (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Fever"; HEADACHE (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Headache"; VOMITING (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Vomiting"; FATIGUE (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Fatigue"; EYE PAIN (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Pain behind eyes"; PAIN IN EXTREMITY (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Sore arm"; LYMPHADENOPATHY (non-serious) with onset 18Dec2021 at 21:00, outcome "recovering", described as "Swollen lymph nodes over 48 hours". Therapeutic measures were not taken as a result of pyrexia, headache, vomiting, fatigue, eye pain, pain in extremity and lymphadenopathy. Additional Information: 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. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Sulfonamide allergy (known allergies: Sulfa drugs)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pyrexia
Symptomtext
Mild fever and headache for 8 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Colitis
- Andere Medikamente
- Paxil, general vitamin, vitamin e
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling hot
Headache
Immunisation
Pain in extremity
Symptomtext
chills and sore calves starting midnight; chills and sore calves starting midnight; headache morning of 17- Dec-2021; Felt warm; dose number = 3; This is a spontaneous report from a contactable reporter (consumer or non-HCP). A 17-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 16Dec2021 at 10:00 (Lot number: FL3197) at the age of 17 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE Lot number: EP6955 Route of administration: unspecified), administration date: 12Apr2021, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE Lot number: DP6955 Route of administration: unspecified), administration date: 22Mar2021, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 at 10:00, outcome "unknown", described as "dose number = 3"; FEELING HOT (non-serious) with onset 16Dec2021 at 22:00, outcome "recovered" (an unknown date in Dec2021), described as "Felt warm"; CHILLS (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 17Dec2021 at 00:00, outcome "recovered" (17Dec2021), and all described as "chills and sore calves starting midnight"; HEADACHE (non-serious) with onset 17Dec2021, outcome "recovered" (17Dec2021), described as "headache morning of 17-Dec-2021". Therapeutic measures were not taken as a result of feeling hot, chills, pain in extremity and headache. Additional Information: On 16Dec2021 at midnight, the patient experienced chills and sore calves and on 17Dec2021 at morning, the patient experienced headache. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- -
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Immunisation
Pyrexia
Rash
Symptomtext
Tired; Low grade fever within 24 hour.; Rash covering torso and face; headache after 24 hours; Dose received 3; This is a spontaneous report from a contactable reporter (consumer or non HCP). A female patient of unknown age (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in left arm, administration date 16Dec2021 at 11:30 (Lot number: FL3197) as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: ER8734, vaccine location: Left arm, administration time: 09:45 , route of administration: intramuscular), administration date: 27Mar2021, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot number: EW0162, vaccine location: Left arm, administration time: 09:45, route of administration: intramuscular), administration date: 17Apr2021, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 at 11:30, outcome "unknown", described as "dose received 3"; FATIGUE (non-serious) with onset 17Dec2021 at 08:00, outcome "not recovered", described as "Tired"; PYREXIA (non-serious) with onset 17Dec2021 at 08:00, outcome "not recovered", described as "Low grade fever within 24 hour"; RASH (non-serious) with onset 17Dec2021, outcome "not recovered", described as "Rash covering torso and face"; HEADACHE (non-serious) with onset 17Dec2021, outcome "not recovered", described as "headache after 24 hours". Therapeutic measures were not taken as a result of fatigue, pyrexia, rash and headache. Additional information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive other vaccines within four weeks prior to COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Pyrexia
Symptomtext
Chills, fatigue, temperature high of 104.1, 103.6, 102.7, 100.9, 99.8, for 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None, just rested, stayed hydrated and let it run its course.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Leiden Factor 5
- Andere Medikamente
- Yes
- Allergien
- No
- Vorherige Impfungen
- Had effects after 2nd covid vaccination with chills, fatigue and temperature for 30 hours.
- Staat
- IN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Asthenia
Balance disorder
Chills
Headache
Pain
Pyrexia
Vomiting
Symptomtext
Headache, chills, very slight fever 99.4 (my normal temperature runs around 97.1) terrible body aches, weakness, unsteady walking, upset stomach, vomiting. This lasted for 12 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- conjunctivitis from my senior flu shot on 12/15/21
- Vorgeschichte
- -
- Andere Medikamente
- propranolol 80 mg, oxybutynin 5 mg, triamterene/hctz 75-50 mg, estradiol/norethindrone acetate 0.5 mg/0.1, zyrtec turmeric 1500 mg, magnesium citrate 250 mg, vitamin d3
- Allergien
- penicillin
- Vorherige Impfungen
- conjunctivitis 12/15/2021 age 72
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Fatigue
Headache
Injection site pain
Vomiting
Symptomtext
Pt. states that after receiving the 3rd dose of Phizer 12/22/2021, started experiencing symptoms 12/23/2021 early morning of loose stool, vomiting, headache, chills, fatigue, and injection arm pain. Vomiting and loose stools have subsided, no noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- IBS
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypersensitivity
Injection site erythema
Injection site induration
Injection site mass
Injection site pruritus
Injection site swelling
Symptomtext
Booster shot, Pfizer, same brand as first two shots in April/May 2021. No reactions or major symptoms from first two shots. This Pfizer booster shot on 12/18, I had an allergic reaction only at the site of the shot on my left arm. It swelled up into a hard lump that I could feel below the surface of my skin within 24 hours after the booster shot. My skin turned red around the area of the shot (about the size of the palm of my hand), and that area was itchy. It did not spread anywhere else on my body, so it was localized to the site of the shot. It was more itchy the first 24 hours. I took one benadryl that night. Have not taken anything else since. The itchiness has slowed and redness is slowly subsiding and lump is slowly getting smaller.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Metronidazole Tobramycin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Feeling hot
Symptomtext
Client obtained his first dose and second COVID vaccines (first dose Pfizer COVID vaccine lot: EW0182 on 05/12/2021 and second dose Pfizer COVID vaccine lot: EW0187 on 06/02/2021 both). Client received his Pfizer Booster COVID vaccine lot: FL3197 exp: 06/30/2022 today at 12:02PM. Ancillary was approached by client's family member. Family member reported that client got vaccinated earlier, feeling dizzy and is lying on the floor. Ancillary then reported it to RN. RN then instructed Ancillary to call the RN Leads. RN and Ancillary approached client and client was sitting in the back seat of the their car drinking water. RN and RN responded as well. Ancillary assisted with translating from another language for client's family members during entire conversation. Client reported that he got vaccinated earlier and that he finished his 15 minutes observation with no issues. Client reported that he felt dizzy 5 minutes ago, which was around 1:14PM, felt anxious and hot, so he took off his shirt and started walking around, he then sat down and laid on the ground. Client denied falling on the ground. Client reported that he did eat earlier at around 10am, but has not been drinking water and that he only had coffee this morning. Client has no medical condition, no known allergies, and is currently taking any medications. Client reported that he's feeling okay now. RN and Co Lead RN educated client to ensure to drink water, rest, on ER precautions and when to contact MD and client verbalized understanding. Client left with family at 1:24PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Not taking any medications
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gingival ulceration
Pain
Stomatitis
Tongue ulceration
Symptomtext
Painful sores in mouth, on tongue, cheek, gums. Has been there got worse on day 5 after vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None aware of
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Injection site reaction
Rash
Rash erythematous
Rash pruritic
Skin warm
Symptomtext
An after hour receiving vaccine booster my left arm at the injection site and left side of my chest and neck broke out into a very itchy bright red hot rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Xanax .50 3 times a day as needed for anxiety
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dizziness
Throat tightness
Symptomtext
Around minute 13, I developed dizziness and sensation of throat/chest tightening
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- vitals: all normal
- Aktuelle Erkrankungen
- URI November 25th
- Vorgeschichte
- asthma anxiety PCOS
- Andere Medikamente
- Benadryl Allegra buspirone vitamin D albuterol phenylephrine omeprazole Pepcid Tums
- Allergien
- none
- Vorherige Impfungen
- Pfizer, 2/12/21, covid 19 vaccine
- Staat
- MO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Pruritus
Skin warm
Symptomtext
About 24-30 hours after I got the shot, my arm got very itchy and a red spot formed that is warm to the touch and red and raised. The spot is about 1.5 inches in diameter. It?s itchy and sore. I?ve put hydrocortisone cream on it and taken Tylenol. The whole arm hurts.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None except allergies
- Vorgeschichte
- Allergies, arthritis, restless legs, thyroid disease, high BP
- Andere Medikamente
- Levothyroxine, gabapentin, ropinirole, fiber gummies, chlorthalidone, escitalopram, omeprazole, potassium ER, Qsymia, restasis, cranberry, vitamins, aloe Vera capsules, Zyrtek, xyzal
- Allergien
- All outdoor allergies, levaquin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Pruritus
Symptomtext
When patient received the 1st dose of Pfizer, she began complaining of itchiness on her right arm and felt lightheaded. As a result, we provided client with Benadryl. At 15:01, she received 50mg Benadryl by mouth. Her vitals: temp 97.9, pulse 95, R 14, O2 97%, BP 90/60. Injection site: no sign of redness. At 15:15: Temp 97.9; Pulse 82; R 12; 02 99%; BP 100/60. And at 15:15, patient stated she has a history of fainting after receiving vaccines. Still no signs of redness at injection site. At 15:30: Temp 97.9; Pulse 78; R 12; 02 99%; BP 100/60. Patient stated she felt better, and her daughter can drive her home. At 15:30, we advised if she still doesn't feel well to seek medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown.
- Aktuelle Erkrankungen
- History of hypothyroidism and ulcerative colitis.
- Vorgeschichte
- History of hypothyroidism and ulcerative colitis.
- Andere Medikamente
- Thyroid medication taken last night 12/20/2021. Patient could not remember the dose.
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient stated before administration he had a severe phobia of needles. Following administration, he said he felt dizzy and lightheaded. The patient was certain that the event was brought on by his phobia of needles. He remained seated to be observed until he felt better. He checked with staff stating he felt better and left shortly after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / 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 reaction
Injection site swelling
Lymphadenopathy
Rash erythematous
Rash pruritic
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient called today, 12/21/21, to report of what she called "Covid arm." She has a 2inch circular rash where she was injected that is red, itchy, and swollen. Also, she said she has swollen lymph nodes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -