Zurueck zur Suche

Reporte zur Charge UJ882AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

36Reporte angezeigt
0Todesfaelle
5Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
WA 5 CA 5 OH 3 WI 2 IN 2 WV 2 VA 2 PA 1 NJ 1 MI 1 MS 1 ND 1

VAERS 2530085

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

kritisch
Staat
-
Alter
73,0
Geschlecht
F
Eingang
13.12.2022
Impfdatum
13.09.2022
Beginn
22.11.2022
Tage bis Beginn
70,0
Dosis
UNK
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Activated partial thromboplastin time normal Anion gap Anticoagulant therapy Basophil count decreased Basophil percentage decreased Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium decreased Blood urea normal Brain natriuretic peptide normal Carbon dioxide normal Cardiac monitoring Chest discomfort Coagulation test Colonoscopy

Symptomtext

Document Type: ED Physician Progress Note Document Subject: ED Progress Note Performed By: on November 22, 2022 09:50 Verified By: on November 22, 2022 14:29 Encounter Info: Emergency, 11/22/22 - 11/22/22 * Final Report * Basic Information Time Seen: 11/22/2022 09:44 Chief Complaint Shortness of breath (Complaint of) History of Present Illness Patient seen: 11/22/22 09:53:52 A 73 year old female with Hx of HTN and T2DM, presents to the ED via private vehicle c/o shortness of breath. Patient presents from outpatient CT found bilateral lower lobe PEs. She does not wear oxygen at home. Denies long car rides, swelling in legs, or calf pain. Chart Review: Patient had an outpatient CT scan today that showed bilateral lower lobe PEs. He was seen by NP yesterday for shortness of breath on exertion for 3 weeks that has been worse over the past week. He also reported questionable chest pressure. Review of Systems Constitutional: No fever, no chills Skin: No rash, no lesions Eyes: No recent vision problems, no icterus ENT: No ear pain, no sore throat, no sinus pain Resp: +SOB, no cough Cardio: No chest pain, no palpitations, no peripheral edema Gastro: No abdominal pain, no nausea, no vomiting, no diarrhea, no constipation Back: No back pain, no joint pain Neuro: No headache, no dizziness, no altered LOC, no numbness, no tingling Psych: No anxiety, no depression Additional ROS info: Except as noted in the above Review of Systems and in the History of Present Illness, all other systems have been reviewed and are negative or noncontributory. Physical Exam/Objective Vitals & Measurements last 24 hours VITAL SIGNS Temp C: 36.5 DegC Heart Rate: 102 bpm Resp Rate: 22 br/min BP: 194 / 86 mmHg SpO2 (%): 88 % O2 Device: Room air Height CM: 162.2 cm Weight KG: 97.7 kg Ideal Body Weight: 54.37 kg General: Alert, no acute distress, elevated BMI Skin: Warm, dry, intact Head: Normocephalic, atraumatic ENT: Oral mucosa moist, no pharyngeal erythema or exudates Neck: Supple, no tenderness Cardiovascular: Regular rate and rhythm, no murmur, no lower extremity edema or asymmetric swelling, symmetric distal pulses Respiratory: Lungs CTA, non-labored respirations, breath sounds equal, no wheezes, rales, or rhonchi. 88% on RA. upper 90s on 2L. Musculoskeletal: No tenderness or deformity Abdomen: Soft, non-tender, non-distended Back: Non-tender, normal ROM Neuro: No focal neuro deficits, normal sensory, normal motor, normal speech, normal coordination Psych: Cooperative, appropriate mood Medical Decision Making Notes reviewed: ED nurse, prior ED, prior records Diagnostic results: Labs: Reviewed Diagnostic imaging: Reviewed 11/22/22 11:37:12 Sent a message for bed request. 11/22/22 11:46:39 Dr. agrees to admit patient to inpatient Med/Surg for pulmonary embolism. 11/22/22 13:32:20 Spoke with Dr. At this time they are not recommending transfer for intraarterial treatment, but if patient begins to decline they would reconsider. Re-Assessment 11/22/22 11:39:12 Discussed plan for admission. Patient is agreeable with plan, all questions addressed. Condition Stable Disposition: 11/22/22 11:47:02 Admit to, Location: Med/Surg Scribe Attestation I, acting as a scribe for on 11/22/22 09:47:15. Signed, 11/22/22 09:47:15. I, MD, attest that the scribe's documentation has been prepared under my direction and personally reviewed by me in its entirety. I confirmed that the note above accurately reflects all work, treatment, procedures, and medical decision-making preformed by me. Assessment/Plan Pulmonary embolism I26.99 Orders: heparin 25,000 Units + Sodium Chloride 0.45% 250 mL, Total Volume (mL) = 250, IV, 11/22/22 9:47:00, Per Nomogram heparin infusion bolus dose, Per STANDARD Dose Heparin Nomogram, Via Infusion Pump, Infusion, Unscheduled, PRN, Other-See Comments, 11/22/22 9:47:00 **Coronavirus SARS-CoV2 Rapid aPTT Pl QN Auto Diff Basic Metabolic Panel Bed Request (Decision to Admit) BNP Pl QN Call Bleeding Call PTT Results Cardiac Monitor CBC w/Differential Collect Specimen Collect Specimen Collect Specimen Continuous Oxygen Saturation COVID 19 PCR Diagnosis Electrocardiogram Height and Weight PP Required: Initiate only Troponin-I High Sensitivity Chronic Problem List CTS (carpal tunnel syndrome) Diabetic neuropathy Essential hypertension Hyperlipidemia Left otitis media Major depression Major depression, recurrent Onychogryphosis Onychomycosis Pre-ulcerative calluses Type 2 diabetes mellitus without complication Procedure/Surgical History ?Colonoscopy (11/03/2022) ?EGD (esophagogastroduodenoscopy) gastric outlet reduction (11/03/2022) ?Colonoscopy (08/24/2011) ?Removal of toenail ?right knee replacement ?surgery from mrsa Surgical History Internal 11/03/2022 Colonscpy Diagnostic/Screen 06/17/2015 Knee Arthroplasty (Right) Medications Home Medications (10) Active FreeStyle Test Strips Check up to 3 times daily, Other, TID, E11.9, on insulin HumULIN N (insulin NPH) human recombinant 100 units/mL subcutaneous injection See Instructions, INJECT 50 UNITS IN THE AM AND 30 UNITS IN THE PMDx E11.9 Hyzaar 100 mg-25 mg oral tablet 1 Tablet, Orally, Daily Lexapro 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily Lipitor 80 mg oral tablet 80 mg = 1 Tablet, Orally, Daily metFORMIN 500 mg (Eqv-Glumetza) oral tablet, extended release 1,000 mg = 2 Tablet, Orally, Daily Norvasc 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily omeprazole 20 mg oral delayed release capsule 20 mg = 1 Capsule, Orally, Daily Pen Needles - Insulin Check up to 2 times daily, Other, Unscheduled, E11.9 traZODONE 50 mg oral tablet 50 mg = 1 Tablet, PRN, Orally, At Bedtime Medication Administration Given heparin additive (intermittent) 25,000 Units + Sodium Chloride 0.45% 250 mL, IV heparin infusion bolus dose (Freetext), 6000 Units, Via Infusion Pump Allergies NKA Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Work/School description: homemaker. Home/Environment widow, 2 children Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Heart disease..: Father. Ovarian cancer..: Mother. Lab Results Hemogram-Platelets-WBC Differential FS LATEST RESULTS HISTORICAL RESULTS WBC 11/22/22 10:02 7.5 06/07/22 9.5 RBC 11/22/22 10:02 4.39 06/07/22 4.47 Hgb 11/22/22 10:02 12.0 06/07/22 12.3 Hct 11/22/22 10:02 36.4 06/07/22 37.6 MCV 11/22/22 10:02 83 06/07/22 84 MCH 11/22/22 10:02 27.3 06/07/22 27.4 MCHC 11/22/22 10:02 32.9 06/07/22 32.6 RDW 11/22/22 10:02 14.2 06/07/22 13.9 Platelet 11/22/22 10:02 243 06/07/22 386 MPV 11/22/22 10:02 8.0 06/07/22 8.6 Neutrophils % 11/22/22 10:02 54 06/07/22 53 Lymphocytes % 11/22/22 10:02 36 06/07/22 38 Monocytes % 11/22/22 10:02 8 06/07/22 6 Eosinophils % 11/22/22 10:02 2 06/07/22 3 Basophils % 11/22/22 10:02 1 06/07/22 0 Absolute Neutrophil 11/22/22 10:02 4.0 06/07/22 5.1 Absolute Lymphocyte 11/22/22 10:02 2.7 06/07/22 3.6 High Absolute Monocyte 11/22/22 10:02 0.6 06/07/22 0.5 Absolute Eosinophil 11/22/22 10:02 0.2 06/07/22 0.3 Absolute Basophil 11/22/22 10:02 0.0 06/07/22 0.0 Routine Coagulation Studies FS LATEST RESULTS aPTT 11/22/22 10:02 31.2 Routine Chemistry Tests FS LATEST RESULTS HISTORICAL RESULTS Sodium SerPl QN 11/22/22 10:02 133 Low 06/07/22 141 Potassium SerPl QN 11/22/22 10:02 3.8 06/07/22 4.0 Chloride SerPl QN 11/22/22 10:02 102 06/07/22 103 Carbon Dioxide SerPl QN 11/22/22 10:02 25 06/07/22 26 Anion Gap 11/22/22 10:02 6 06/07/22 12 High BUN SerPl QN 11/22/22 10:02 18 06/07/22 14 Creatinine SerPl QN 11/22/22 10:02 0.88 06/07/22 0.90 Estimated GFR (CKD-EPI, no race) 11/22/22 10:02 69 06/07/22 68 Estimated CRCL (CG) 11/22/22 10:02 64 06/07/22 61 Glucose SerPl QN 11/22/22 10:02 153 High 06/07/22 81 Calcium Total SerPl QN 11/22/22 10:02 9.6 06/07/22 8.6 Troponin-I High Sensitivity 11/22/22 10:02 19 High BNP Pl QN 11/22/22 10:02 70 Molecular Diagnostic Tests LATEST RESULTS COVID 19 Specimen Source 11/22/22 10:02 Nasal Coronavirus SARS-CoV2 Rapid 11/22/22 10:02 Not Detected Diagnostic Results No qualifying data available. EKG Time: 11/22/2022 09:53 Rate: 89 bpm Rhythm: normal sinus rhythm Axis: normal ST-T segments: no changes T waves: normal Ectopy: none P waves and PR interval: within normal limits QT interval:within normal limits QRS interval: within normal limits Previous EKG:none available Interpretation Signature Line Electronically Signed on 11/22/22 11:47 ________________________________________________________ Electronically Signed on 11/22/22 13:33 ________________________________________________________ Electronically Signed on 11/22/22 14:29 ________________________________________________________

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

VAERS 2594868

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

moderat
Staat
CA
Alter
73,0
Geschlecht
M
Eingang
10.03.2023
Impfdatum
08.09.2022
Beginn
01.03.2023
Tage bis Beginn
174,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Blood test abnormal COVID-19 Cardiac failure Chest X-ray abnormal Diuretic therapy Dyspnoea Fluid retention SARS-CoV-2 test positive

Symptomtext

I went to the hospital, because I had shortness of breath the night before. When I got to the hospital, I was put on an IV and underwent bloodwork. A routine COVID-19 test was done, and the result was positive. I was then admitted on COVID-19 precautions. They gave me one dose of IV remdesivir and treated me for heart failure. I was also given a diuretic to get rid of the fluid buildup. I was discharged the next day. After that, everything was fine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
1,0
Labordaten
01MAR2023 - Bloodwork - Heart Failure; 01MAR2023 - COVID-19 Test - Positive Result; 01MAR2023 - Chest X-Ray - Heart Failure Detected
Aktuelle Erkrankungen
None
Vorgeschichte
Atrial Fibrillation; Hypertension
Andere Medikamente
Benecar; Bystolic; Magnesium; Vitamin D; Baby Aspirin
Allergien
Hydrochlorothiazide; Lipitor
Vorherige Impfungen
-

VAERS 2506630

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

moderat
Staat
OK
Alter
74,0
Geschlecht
F
Eingang
12.11.2022
Impfdatum
29.10.2022
Beginn
30.10.2022
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Arrhythmia Diarrhoea Heart rate decreased Mobility decreased Muscular weakness

Symptomtext

Patient reports diarrhea, muscle weakness, low pulse, arrhythmias starting the day after her vaccines. Says she could barely move enough to get out of bed. Patient went to the Emergency room because of her low pulse and arrhythmias. She was put on Metoprolol to control her arrhythmia.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arrhythmia
Hospital-Tage
-
Labordaten
Unknown, Patient went to Medical Center Emergency Room
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Unknown
Andere Medikamente
Eplerenone, Potassium, Montelukast, Lisinopril, Hydrochlorothiazide
Allergien
None
Vorherige Impfungen
-

VAERS 2491791

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

moderat
Staat
IN
Alter
79,0
Geschlecht
F
Eingang
27.10.2022
Impfdatum
12.10.2022
Beginn
13.10.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Diarrhoea Mobility decreased Pyrexia

Symptomtext

Patient experienced diarrhea, fever, limited range of arm mobility, and a sore shoulder that "feels like it has been wrenched out of the socket". She states it is slowly getting better.

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

VAERS 2491408

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

moderat
Staat
CA
Alter
65,0
Geschlecht
M
Eingang
27.10.2022
Impfdatum
20.10.2022
Beginn
22.10.2022
Tage bis Beginn
2,0
Dosis
N/A
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Angiogram normal Atrial flutter Blood test Brain natriuretic peptide increased Cardiac stress test abnormal Chest X-ray Chest discomfort Dyspnoea Echocardiogram Electrocardiogram Malaise Myocardial necrosis marker Pyrexia Sleep disorder

Symptomtext

25-30 hours later woke up with shortness of breath and chest pressure in night. Next am 99.4 fever, general malaise. Next night woke up again with shortness of breath, chest pressure. Fever of 100.4 in am. Urgent care that afternoon sent me to the ER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
4,0
Labordaten
Ekg, chest X-ray, blood tests performed. Cardiac enzyme was .06 BNP was 498. Hospitalized for 4 nights. Had stress test which showed a-flutter, echocardiogram, and CTA scan (no embolism). Still in hospital.
Aktuelle Erkrankungen
None
Vorgeschichte
Aortic valve replaced 2008 (congenital)
Andere Medikamente
Rosuvastatin 10 mg Magnesium 200 mg Multi vitamin
Allergien
None
Vorherige Impfungen
-

VAERS 2464695

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

moderat
Staat
WV
Alter
76,0
Geschlecht
F
Eingang
29.09.2022
Impfdatum
12.09.2022
Beginn
12.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Cough Dyspnoea Myalgia Oropharyngeal pain Pain Pharyngeal erythema SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

Patient called and reported muscle and body aches, chills, red and sore throat, cough, and shortness of breath that started about 6 hours after receiving her vaccine. Her symptoms lasted for about 2 weeks. She was started on Augmentin 875 and Albuterol HFA 10 days after her vaccine. She was tested for COVID and Strep, both were negative.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
COVID one month prior to vaccination
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2441023

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

moderat
Staat
WV
Alter
69,0
Geschlecht
M
Eingang
12.09.2022
Impfdatum
10.09.2022
Beginn
11.09.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Burning sensation Dry mouth Dyspnoea Mass Pain Throat tightness

Symptomtext

Cotton mouth Felt like mouth/throat were closing Trouble breathing Sore all over - burning sore

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Iodine Morphine
Vorherige Impfungen
-

VAERS 2430952

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

moderat
Staat
TX
Alter
68,0
Geschlecht
F
Eingang
07.09.2022
Impfdatum
06.09.2022
Beginn
06.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Migraine Nausea Peripheral swelling

Symptomtext

Migraine, dizziness, swollen left arm, nausea

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

VAERS 2608495

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
MN
Alter
66,0
Geschlecht
M
Eingang
03.04.2023
Impfdatum
07.09.2022
Beginn
03.01.2023
Tage bis Beginn
118,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Headache Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

I started to feel like I was catching a cold, possibly the fl. I had a small headache. I took a home COVID-19 test, it did come back positive. I called my doctor to let them know I tested positive for COVID-19, I was prescribed the Paxlovid. I started taking it immediately. I was feeling better within a day of taking the medication.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
3JAN2023 Home COVID-19 test - positive
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
Levothyroxine; Lipitor; Vitamin D3; Centrum Multivitamin; Lutein Xanthinin; CoQ10; Glucosamine/Chondroitin
Allergien
No
Vorherige Impfungen
-

VAERS 2606293

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
CA
Alter
67,0
Geschlecht
F
Eingang
29.03.2023
Impfdatum
25.09.2022
Beginn
20.03.2023
Tage bis Beginn
176,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Discomfort Headache Nasal congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a headache, cough, stuffy nose, pressure, and running nose. I took a COVID-19 test and I tested positive. I messaged my doctor and she prescribed PAXLOVID. It really helped with my symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
03/21/2023, COVID-19 test, positive
Aktuelle Erkrankungen
N/A
Vorgeschichte
Congestive Heart Failure; Type 2 Diabetic Controlled
Andere Medikamente
Metformin; bupropion; carvedilol; ENTRESTO; furosemide; LIVALO; vitamin D3; coQ10; omega
Allergien
CECLOR
Vorherige Impfungen
-

VAERS 2545267

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

mild
Staat
KS
Alter
67,0
Geschlecht
F
Eingang
28.12.2022
Impfdatum
27.10.2022
Beginn
27.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Pain in extremity

Symptomtext

patient said arm has been sore since getting vaccine, however the arm does not hurt at injection site but only as patient moves arm backwards

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

VAERS 2520518

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
-
Alter
64,0
Geschlecht
F
Eingang
01.12.2022
Impfdatum
09.09.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest X-ray Pain in extremity Tuberculin test

Symptomtext

little soreness in her arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (little soreness in her arm) in a 64-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) for COVID-19 prophylaxis. Co-suspect products included non-company products VARICELLA ZOSTER VACCINE RGE (CHO) (SHINGRIX) for an unknown indication and INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) for an unknown indication. The patient's past medical history included Welts (Twenty-flve or thirty years ago she had a TB test with ppd. After that test, her entire arm "blew up" instantly with a giant welt.). Previously administered products included for Drug use for unknown indication: Flu Shots, TD and Typhoid. Past adverse reactions to the above products included No adverse event with TD and Typhoid; and Pain in extremity with Flu Shots. Concomitant products included CORTISONE ACETATE (CORTISONE [CORTISONE ACETATE]) for an unknown indication. On 09-Sep-2022, the patient received dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) (unknown route) at an unspecified dose. On an unknown date, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and dose of VARICELLA ZOSTER VACCINE RGE (CHO) (SHINGRIX) (unknown route) at an unspecified dose. On an unknown date, the patient experienced PAIN IN EXTREMITY (little soreness in her arm). At the time of the report, PAIN IN EXTREMITY (little soreness in her arm) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Chest X-ray: Negative. On an unknown date, Tuberculin test: test was contaminated with something. Patient dermatologist gave her a shot Of cortisone and she took antihistamines. Both her dermatologist and internist were not sure if the Fluzone HD could be the cause, especially with the 4-day delay Of onset, however the patient could not think of anything else that she might had been exposed to that would have caused the hives. When the hives began, they started in the armpit of her right arm at that same level as the injection site. She discussed her previous experience with other vaccines as to how it was so unusual for her to had hives after Fluzone HD QIV. She received Moderna Covid vaccines. The bivalent Covid booster a week ago caused her to have a little soreness in her arm. All of the other Covid boosters did not cause problems for her. She has taken vaccines against pneumonia without problems. Twenty-five or thirty years ago she had a TB test with ppd. After that test, her entire arm blewed up instantly with a giant welt. She was told at first that she had T B. A follow-up chest x-ray was negative. It was realized that she did not have TB and that instead something was wrong with that test. She later had subsequent ppd tests without reactions. No treatment medications were provided. This case was linked to MOD-2022-679659 (Patient Link).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
Test Name: chest x ray; Test Result: Negative ; Test Name: PPD; Result Unstructured Data: test was contaminated with something
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Welts (Twenty-five or thirty years ago she had a TB test with ppd. After that test, her entire arm "blew up" instantly with a giant welt).
Andere Medikamente
CORTISONE [CORTISONE ACETATE]
Allergien
-
Vorherige Impfungen
-

VAERS 2505051

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

mild
Staat
CA
Alter
66,0
Geschlecht
F
Eingang
10.11.2022
Impfdatum
27.08.2022
Beginn
27.08.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bursitis Cartilage injury Injection site pain Magnetic resonance imaging abnormal Musculoskeletal discomfort Pain Rotator cuff syndrome Tendonitis

Symptomtext

I have experienced a sore left upper arm consistently since August 27 date of vaccine (it is now Nov. 10), sharp pain in left shoulder, burning discomfort below left scapula. I have taken ibuprofen, received massage therapy. I experience some relief from ibuprofen and somewhat from rolfing massage therapy

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
MRI 11/9/22 showed rotator cuff tendinitis, mild subacromial subdeltoid bursitis; degenerative tearing superior labrum biceps anchor, tendinitis long biceps tendon; normal deltoid muscle, no axillary adenopathy.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Pexeva, Deplin, vitamin D3, magnesium, multi-vitamin, iron, lion's mane mushroom caplets
Allergien
none
Vorherige Impfungen
-

VAERS 2490892

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
-
Alter
64,0
Geschlecht
F
Eingang
27.10.2022
Impfdatum
09.09.2022
Beginn
13.09.2022
Tage bis Beginn
4,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Depressed level of consciousness Tenderness Urticaria

Symptomtext

kind of knocked me out a little bit; she came down with a severe case of hives. The hives covered from her chest down to her ankles, and part of her back.; little soreness in her arm; Initial information received on 14-Oct-2022 regarding an unsolicited valid serious case received from a consumer/non-hcp. This case involves a 64 years old female patient who experienced kind of knocked me out a little bit, she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back. and little soreness in her arm while receiving vaccines moderna covid-19 vaccine, shingrix and influenza quadrival a-b high dose hv vaccine [fluzone high-dose quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included CORTISONE (CORTISONE). On 09-Sep-2022, the patient received a dose of suspect influenza quadrival a-b high dose hv lot UJ882AB via unknown route in the right arm. from prophylactic vaccination. On an unknown date, the patient received a dose of suspect shingrix not produced by Sanofi Pasteur lot number not reported via unknown route in unknown administration site from prophylactic vaccination. On an unknown date, the patient received a Booster dose of suspect moderna covid-19 vaccine not produced by Sanofi Pasteur lot number not reported via unknown route in unknown administration site from prophylactic vaccination. On an unknown date the patient developed a serious kind of knocked me out a little bit (depressed level of consciousness) (unknown latency) following the administration of influenza quadrival a-b high dose hv, shingrix, moderna covid-19 vaccine. This event was assessed as medically significant. On 13-Sep-2022 the patient developed a non-serious she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back. (urticaria) and little soreness in her arm (tenderness) 4 days following the administration of quadrival a-b high dose hv, shingrix, moderna covid-19 vaccine. It was reported "She received Fluzone HD QIV for the first time on 09Sep2022. She has received flu shots for many years in the past without any problems other than a sore arm. This year, four days after the Fluzone HD QIV was administered in her right arm, she came down with a severe case of hives. The hives covered from her chest down to her ankles, and part of her back. They were so severe that she could not function. Her dermatologist gave her a shot of cortisone and she took antihistamines. Both her dermatologist and internist were not sure if the Fluzone HD QIV could be the cause, especially with the 4-day delay of onset, however the patient cannot think of anything else that she might have been exposed to that would have caused the hives. When the hives began, they started in the armpit of her right arm at that same level as the injection site. She discussed her previous experience with other vaccines as to how it is so unusual for her to have hives after Fluzone HD QIV. She received Moderna Covid vaccines. The bivalent Covid booster a week ago caused her to have a little soreness in her arm. When she received the second full dose of the initial series of Moderna Covid vaccine, that dose "knocked me off my feet and I could not get out of bed for 24 hours". All of the other Covid boosters did not cause problems for her. She has taken vaccines against typhoid, Td, and pneumonia without problems. The Shingrix vaccine "kind of knocked me out a little bit. I was told by other people that Shingrix really hurts." (see #01322462 for report for "other people"). Twenty-five or thirty years ago she had a TB test with ppd. After that test, her entire arm "blew up" instantly with a giant welt. She was told at first that she had TB. A follow-up chest x-ray was negative. It was realized that she did not have TB and that instead something was wrong with that test. She later had subsequent ppd tests without reactions. She says, "I suspect that test was contaminated with something". Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events (she came down with a severe case of hives. The hives covered from her chest down to her ankles, and part of her back., little soreness in her arm, kind of knocked me out a little bit). At time of reporting, the outcome was Recovering / Resolving for the event she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back., was Recovering / Resolving for the event little soreness in her arm and was Unknown for the event kind of knocked me out a little bit.; Sender's Comments: Sanofi company comment dated 24-Oct-2022: This case concerns 64 years old female patient who experienced kind of knocked me out a little bit, she came down with a severe case of hives. the hives covered from her chest down to her ankles, and part of her back. and little soreness in her arm while receiving vaccines moderna covid-19 vaccine, shingrix and influenza quadrival a-b high dose hv vaccine [fluzone high-dose quadrivalent]. Based on information provided, the causal role of company suspect cannot excluded. Case will be re-evaluated post further update on information regarding underlying disease, risk precipitating factor, past medical history and patient lifestyle which will preclude a comprehensive assessment of this case. Based upon the reported information, the role of the suspect vaccine cannot be assessed.

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

VAERS 2472622

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

mild
Staat
OH
Alter
68,0
Geschlecht
F
Eingang
08.10.2022
Impfdatum
04.10.2022
Beginn
04.10.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Pain in extremity

Symptomtext

Patient reported painful throbbing radiating down her right arm starting a couple hours after the shot on 10/4 and said it is still continuing on 10/8. Suggested she go to the MD on Monday to get checked out.

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

VAERS 2469973

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
IN
Alter
65,0
Geschlecht
F
Eingang
05.10.2022
Impfdatum
26.09.2022
Beginn
27.09.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site exfoliation Injection site haemorrhage Injection site infection Injection site pain Injection site reaction

Symptomtext

PATIENT'S ARM APPEARED TO BE INFECTED AT INJECTION SITE OR TO HAVE AN INJECTION SITE REACTION THAT CAUSED SKIN TO BECOME RED AND PEEL. IT WAS ABOUT THE SIZE OF A SILVER DOLLAR AND HAD BEEN BLEEDING AT ONE POINT. PATIENT STATES IT STARTED THE DAY AFTER THE VACCINE AND DID NOT APPEAR TO GO AWAY. SHE FINALLY WENT TO THE DOCTOR TODAY (10/5) AND THE DOCTOR IS TREATING IT WITH AN ANTIBIOTIC. I ASKED HER TO LET ME KNOW IF IT DID NOT END UP BEING AN INFECTION. SHE STATED THAT IT HURT TO TOUCH

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
NONE
Vorgeschichte
-
Andere Medikamente
BUPROPION, DHEA, FAMOTIDINE, HYDROCHLOROTHIAZIDE, LISINOPRIL, PANTOPRAZOLE
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2463202

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
TN
Alter
91,0
Geschlecht
F
Eingang
28.09.2022
Impfdatum
26.09.2022
Beginn
26.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Nausea Pyrexia

Symptomtext

Patient received one dose of Fluzone HD at approximately 12:30pm on 9/26/22. Patient called on 9/27/22 at approximately 2:45 pm to report the side effects, including fever, extreme chilling, nausea that she states began in the evening and lasted throughout the night. Pharmacist recommended that she seek care from a physician, but the patient stated that her symptoms have now resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
Demerol, Penicillin
Vorherige Impfungen
-

VAERS 2463160

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
ND
Alter
67,0
Geschlecht
F
Eingang
28.09.2022
Impfdatum
14.09.2022
Beginn
28.09.2022
Tage bis Beginn
14,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Injection site erythema Injection site pruritus Injection site swelling

Symptomtext

patient reported redness, itching, and swelling of her arm at her covid injection site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
No acute illnesses.
Vorgeschichte
hypothyroidism, osteoporosis, reactive airway disease.
Andere Medikamente
tretinoin cream, levothyroxine, montelukast, prolia, tizanidine, pepcid, pantoprazole, flovent HFA, tessalon, hydromet, albuterol HFA, calcium plus D, lutein, multivitamin, ibuprofen.
Allergien
bees,bactrim, formaldehyde, golytely, hydrocodien, molds,
Vorherige Impfungen
-

VAERS 2461101

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
WA
Alter
76,0
Geschlecht
F
Eingang
27.09.2022
Impfdatum
18.09.2022
Beginn
19.09.2022
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site rash Rash Rash pruritic

Symptomtext

Patient said that one day after she got two vaccines she noticed rash on injection site, then it spreads all over the body. It is not painful but itchy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
hypothyroidism
Andere Medikamente
Atorvastatin, Alprazolam
Allergien
No known allergy
Vorherige Impfungen
Tetanus

VAERS 2451261

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
WA
Alter
58,0
Geschlecht
M
Eingang
19.09.2022
Impfdatum
17.09.2022
Beginn
17.09.2022
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 erythema Pain

Symptomtext

Patient said his symptoms were the same as what he had with the COVID vaccine (body aches, soreness, redness at injection)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
COVID vaccine- said he had same symptoms (body aches, redness)

VAERS 2450644

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

mild
Staat
CA
Alter
79,0
Geschlecht
F
Eingang
18.09.2022
Impfdatum
13.09.2022
Beginn
14.09.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site warmth

Symptomtext

Site: Redness at Injection Site-Medium, Systemic: warm to the touch at injection site-Medium

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2450227

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882ab

mild
Staat
OH
Alter
73,0
Geschlecht
F
Eingang
17.09.2022
Impfdatum
16.09.2022
Beginn
16.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Pain in extremity Peripheral swelling

Symptomtext

Patient came back to pharmacy next day after shot complaining of sore arm, arm swelling, and redness around injection site. Patient has been using ibuprofen and cold compresses to help.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Nothing filled at this pharmacy of record
Allergien
Penicillin, sulfa
Vorherige Impfungen
-

VAERS 2449275

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj882AB

mild
Staat
WI
Alter
69,0
Geschlecht
F
Eingang
17.09.2022
Impfdatum
15.09.2022
Beginn
16.09.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pruritus Injection site rash

Symptomtext

Patient was fine for the day and evening of the vaccine. The next morning when she woke up, her arm below the injection site had a rash about 2 inches x 4 inches but was not itching. Two days post vaccine, the area is itching and getting larger. Patient will be following up with her medical doctor.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
None at this time
Aktuelle Erkrankungen
None
Vorgeschichte
High Blood Pressure
Andere Medikamente
Multivitamin, Atenolol, ASA 365mg, Calcium, Lisinopril
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2447913

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
ID
Alter
90,0
Geschlecht
F
Eingang
16.09.2022
Impfdatum
02.09.2022
Beginn
02.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Dizziness Flushing Nausea

Symptomtext

Patient reported feeling faint, flush, nausea, and chills several hours after hours.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
No other illness reported
Vorgeschichte
-
Andere Medikamente
Unknown for this patient/no medication list provided
Allergien
No known allergies reported by patient
Vorherige Impfungen
-

VAERS 2447771

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
WI
Alter
79,0
Geschlecht
F
Eingang
16.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Injection site erythema Limb discomfort Oropharyngeal discomfort Throat irritation

Symptomtext

Pt got vaccines in AM. Has had multiple flu and 4 other covid vaccines in past with no issue. Noted a couple hours later her left arm felt heavy and "clogged". Noted her throat felt itchy and funny. Called and was advised to be evaluated for possible reaction. Took benedryl prior to ER. By the time she got to ER, felt at baseline and no worsening symptoms. Today was called to check in. She is feeling totally fine. Left arm has redness at injection site of flu shot but no pain or itching. Denies any other symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
none just ER visit and evaluation.
Aktuelle Erkrankungen
none
Vorgeschichte
Hyperlipidemia PMR (polymyalgia rheumatica) Osteoarthritis of multiple joints Seasonal allergic rhinitis History of colonic polyps Diverticulosis of colon (without mention of hemorrhage) Urinary incontinence, unspecified type Uterine prolapse GERD (gastroesophageal reflux disease) Unilateral primary osteoarthritis, left knee
Andere Medikamente
?Albuterol Sulfate HFA 108 (90 Base) mcg/act aerosol solution 2 puffs as needed Inhalation every 4 hrs ?Aspirin 81 MG Tablet Chewable 1 tablet Orally Once a day ?Flonase(Fluticasone Propionate) 50 MCG/ACT Suspension 2 spray in each no
Allergien
Naproxen: hives Mucinex DM: lip/tongue swelling Methylprednisolone: rash face throat tight
Vorherige Impfungen
-

VAERS 2443943

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
WA
Alter
72,0
Geschlecht
M
Eingang
13.09.2022
Impfdatum
10.09.2022
Beginn
01.09.2022
Tage bis Beginn
-
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Pyrexia

Symptomtext

Patient reported that he developed a high grade fever and had to go to the hospital. He did not give any additional information

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unknown
Vorgeschichte
T2DM Tremors Dyslipidemia Hypertension Hypercholesterolemia
Andere Medikamente
Propranolol 40mg tab Lipitor 10mg tab Gabapentin 300mg cap Tamsulosin 0.4mg cap Losartan 100mg tab Bydureon BCise ER 2mg/0.85 Primidone 50mg tab
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2441099

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

mild
Staat
WA
Alter
67,0
Geschlecht
F
Eingang
13.09.2022
Impfdatum
12.09.2022
Beginn
12.09.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site swelling

Symptomtext

SWELLING AND RAISED INJECTION SITE (ABOUT 2 INCHES IN DIAMETER)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site swelling
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NO
Vorgeschichte
UNKNOWN
Andere Medikamente
UNKNOWN
Allergien
SULFA ANTIBIOTICS
Vorherige Impfungen
-

VAERS 2688262

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
VA
Alter
82,0
Geschlecht
M
Eingang
28.09.2023
Impfdatum
21.09.2023
Beginn
21.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

expired dose of FLUZONE HD QIV was administered to a patient/dose expired on 30JUN2023 with no reported adverse event; Initial information was received on 22-Sep-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 82 years old male patient who received expired dose of influenza quadrival a-b high dose hv vaccine [Fluzone HIGH-DOSE QUADRIVALENT] was administered to a patient/dose expired on 30jun2023 with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 21-Sep-2023, the patient received a dose of 0.7 ml of suspect influenza quadrival a-b high dose hv vaccine (lot UJ882AB, Expiry date : 30-Jun-2023, frequency : once, formulation, strength was unknown) via unknown route in the right deltoid for Influenza and Immunization and expired dose of fluzone hd qiv was administered to a patient/dose expired on 30jun2023 with no reported adverse event (expired product administered) (latency : same day). Action taken with QUADRIVALENT influenza vaccine (Fluzone HIGH-DOSE QUADRIVALENT) was not applicable. At time of reporting, the outcome was Unknown for the event expired dose of fluzone hd qiv was administered to a patient/dose expired on 30jun2023 with no reported adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2503944

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
MS
Alter
62,0
Geschlecht
F
Eingang
10.11.2022
Impfdatum
01.11.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product use issue

Symptomtext

fluzone hd qiv was given to a 62 year old patient in error with no reported adverse event; Initial information was received on 01-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 62 years old female patient who stated influenza quadrival a-b high dose hv vaccine [Fluzone HIGH-DOSE QUADRIVALENT] was given in error with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 01-Nov-2022, the patient received a suspect influenza quadrival a-b high dose hv vaccine at a dose of 0.7 ml once (lot UJ882AB, expiry date - 30-Jun-2023) via intramuscular route in the left deltoid for Immunization. On an unknown date the patient stated a non-serious event of influenza quadrival a-b high dose hv vaccine was given in error with no reported adverse event (product use issue) (unknown latency) following the administration of vaccine. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the guidelines. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product use issue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2490204

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882ab

gering
Staat
WA
Alter
64,0
Geschlecht
F
Eingang
26.10.2022
Impfdatum
25.10.2022
Beginn
26.10.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Circumstance or information capable of leading to medication error Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Pt reported her age as 65 on her Consent for Immunization. As insurance was down, shot dose was provided to her based on her age. Fluzone HD was given instead of Flublok

Weitere VAERSDATA-Felder
Praegender Schweregrund
Circumstance or information capable of leading to medication error
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2483766

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
MI
Alter
76,0
Geschlecht
M
Eingang
20.10.2022
Impfdatum
13.10.2022
Beginn
13.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered No adverse event

Symptomtext

received a /2 to 1/3 of vaccine dose with no adverse event; Initial information received on 13-Oct-2022 regarding an unsolicited valid non-serious case from other health professional. This case involves a 76 years old male patient who received a 1/2 to 1/3 of vaccine dose with no adverse event while receiving vaccine influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s), concomitant medication and family history were not provided. On 13-Oct-2022, the patient received suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE at a 1/2 to 1/3 of vaccine dose (0.7 ml) (lot UJ882AB, expiry date: 30-Jun-2023) via intramuscular route in the right deltoid for Immunization. On 13-Oct-2022 the patient developed a non-serious received a 1/2 to 1/3 of vaccine dose with no adverse event (incorrect dose administered) (same day latency) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. Action taken: Not applicable. Outcome: Unknown. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the guidelines. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2480271

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
NJ
Alter
72,0
Geschlecht
F
Eingang
17.10.2022
Impfdatum
07.10.2022
Beginn
07.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

patient received the high dose flu on 9/28/2022 and then requested again and received the same medication on 10/7/2022. Patient has reported no adverse effects following the second dose

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
HTN, lambda light chain myeloma
Andere Medikamente
eliquis, carvediolol, daratumumab, folbic, lasix, lisinopril, simvastatin
Allergien
cipro
Vorherige Impfungen
-

VAERS 2477001

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
PA
Alter
66,0
Geschlecht
M
Eingang
13.10.2022
Impfdatum
07.10.2022
Beginn
07.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

instead of asking them for the pneumonia shot he asked for a flu shot so they gave him the Adjuvanted Flu with no reported adverse event; Initial information received on 07-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 66 years old male patient who experienced instead of asking them for the pneumonia shot he asked for a flu shot so they gave him the adjuvanted flu with no reported adverse event while receiving vaccine influenza quadrival a-b high dose hv vaccine [fluzone high-dose quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2022, the patient received a dose of suspect influenza quadrival a-b high dose hv vaccine at dose of 0.7ml lot UJ882AB expiration date:30-Jun-2023 via intramuscular route in Left Deltoid site for Immunization. On 07-Oct-2022 the patient developed a non-serious instead of asking them for the pneumonia shot he asked for a flu shot so they gave him the adjuvanted flu with no reported adverse event (wrong product administered) following the administration of influenza quadrival a-b high dose hv vaccine. It was reported "Medical Assistant says the consumer received the FLUZONE HIGH DOSE QUADRIVALENT at their office and wanted to get the pneumonia 20 but they do not carry that. He went to the pharmacy next door to them and instead of asking them for the pneumonia shot he asked for a flu shot so they gave him the Adjuvanted Flu Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Unknown for the event instead of asking them for the pneumonia shot he asked for a flu shot so they gave him the adjuvanted flu with no reported adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2472467

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
GA
Alter
76,0
Geschlecht
M
Eingang
08.10.2022
Impfdatum
12.09.2022
Beginn
12.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered Needle issue Syringe issue

Symptomtext

while administering a dose of fluzone high dose quadrivalent the needle popped off of the prefilled syringe resulting in about 1/2 of the medication to leak out with no reported adverse event; Initial information received on 04-Oct-2022 regarding an unsolicited valid non-serious case received from a other health care professional. This case involves a 76 years old male patient and while administering a dose of fluzone high dose quadrivalent the needle popped off of the prefilled syringe resulting in about 1/2 of the medication to leak out with no reported adverse event while receiving vaccine influenza quadrival A-B high dose HV vaccine [Fluzone high-dose quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 12-Sep-2022, the patient, while administering a dose of fluzone high dose quadrivalent the needle popped off of the prefilled syringe resulting in about 1/2 of the medication to leak out at dose of 0.7 mL TOTAL via intramuscular route in the left deltoid (lot - UJ882AB, expiry date: 30-Jun-2023) for Immunization with no reported adverse event (incorrect dose administered) (latency : same day) Caller reporting while administering a dose of fluzone high dose quadrivalent the needle popped off of the prefilled syringe resulting in about 1/2 of the medication to leak out of the syringe. Caller reporting they have since discarded that entire batch of needles and have not had any further issues. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2469672

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
VA
Alter
75,0
Geschlecht
M
Eingang
05.10.2022
Impfdatum
04.10.2022
Beginn
04.10.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Patient was to receive MODERNA BIVALENT booster but received Moderna NON-BIVALENT booster.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2466861

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ882AB

gering
Staat
OH
Alter
75,0
Geschlecht
F
Eingang
02.10.2022
Impfdatum
28.09.2022
Beginn
29.09.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Blood magnesium decreased Blood pressure increased Electrocardiogram normal Feeling abnormal Heart rate increased Laboratory test normal

Symptomtext

9-29 felt bad, 9-30 went to ER with increased heart rate and blood pressure. ER found her having low magnesium levels, administerer magnesium and HR and BP lowered. Stayed in hospital for 1 day then released

Weitere VAERSDATA-Felder
Praegender Schweregrund
Blood magnesium decreased
Hospital-Tage
1,0
Labordaten
Patient said EKG and ECC were normal.
Aktuelle Erkrankungen
diabetic, heart disease
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-