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Reporte zur Charge UT7682LA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

27Reporte angezeigt
0Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
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VAERS 2536088

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut7682la

kritisch
Staat
IN
Alter
57,0
Geschlecht
F
Eingang
17.12.2022
Impfdatum
30.09.2022
Beginn
15.12.2022
Tage bis Beginn
76,0
Dosis
UNK
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Acinetobacter test Acute respiratory failure Anion gap Anticoagulant therapy Auscultation Bacterial test negative Base excess Blood bicarbonate normal Blood calcium normal Blood chloride normal Blood creatinine increased Blood culture positive Blood glucose normal Blood lactic acid normal Blood pH normal Blood potassium normal Blood sodium normal Blood thyroid stimulating hormone

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on December 15, 2022 17:24 Verified By: MD on December 15, 2022 17:24 Encounter Info: Inpatient, 12/15/22 - * Final Report * History of Present Illness/Subjective 57 year old female with Hx of COPD, OSA on CPAP and GERD presents to the ED via EMS c/o increased SOB and fevers onset 4 days ago. Patient reports to be apparently well until 4 days ago when she started noticing shortness of breath associated with cough productive of greenish sputum. 1 week prior to onset of shortness of breath patient had flu respiratory disease which is managed symptomatically and did not require to be in the hospital. Shortness of breath is associated with fever, cough, low urine volume, on and off chest pain and nausea. No vomiting, diarrhea, headache, constipation no recent travel history EMS gave breathing treatment, Solu-Medrol, en route. Pt denies tobacco or EtOH use. She states she has been around people with a cough. CODE STATUS-full code In the ER Vital signs In ED, pt's initial temperature was 40.2 C. Blood pressure 137/71, heart rate 95, respiratory rate 18, on 4 L of nasal cannula. She was noted to be in acute respiratory failure with increased work of breathing and has been on and off BiPAP throughout her hospital course in the ER. Labs WBC 19.1, hemoglobin 9.5, hematocrit 29.3, platelet 150, sodium 136, potassium 4.1, chloride 102, bicarb 23, BUN/creatinine 34/1.71, glucose 126 Troponin 4, lactate 0.7 Venous blood gas pH 7.36, PCO2 44, PO2 58, oxygen saturation 88 Urinalysis-WBC 11-20, moderate to high squamous epithelial cell Flu negative COVID-negative Imaging CT chest Multifocal airspace disease involving all lobes, including regions of frank consolidation involving both lower lobes, the lateral segment of the right middle lobe, and posterior left upper lobe as described above. Numerous smaller patchy foci of airspace disease as well. The appearance is nonspecific, with differential diagnosis including atypical infection and multifocal inflammatory lung disease. Borderline/mild mediastinal and supra clavicular adenopathy. No overt malignant findings. CXR Right hilar prominence with multiple bilateral nodular opacities may represent multifocal pneumonia but raises the possibility of metastatic malignancy Patient is admitted for acute respiratory failure secondary to multifocal pneumonia Review of Systems All 13 point review of systems were reviewed with the patient and are negative except as specified in the HPI Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.9 (36.9-36.9) Temp (FAHR) 98.4 (98.4-98.4), BP 149/77 (149-149)/(77-77), HR 95 (95-95), RR 18 (18-18), O2Sat 92 (92-92) Patient Weight Patient Height None Reported General: Alert and oriented, No acute distress. Eye: Normal conjunctiva. Cardiovascular: Regular rate, Normal rhythm, No murmur. Respiratory: Lungs are clear to auscultation, Respirations are non-labored. On 4 L of nasal cannula Gastrointestinal: Soft, Non-tender, Non-distended, Normal bowel sounds, No organomegaly. Neurologic: Alert, Oriented, non focal Psychiatric: Cooperative, Appropriate mood & affect. Musculoskeletal: No swelling, Assessment/Plan 57 year old female with Hx of COPD, OSA on CPAP and GERD presents to the ED via EMS c/o increased SOB and fevers onset 4 days ago 1. Pneumonia J18.9 Evidenced on chest imaging. Pneumonia is multifocal and given history of recent influenza infection, pneumonia is likely to be post influenza pneumonia which is usually caused by MRSA. We will give broad coverage antibiotics to include MRSA infection-cefepime and vancomycin -Send pneumonia labs -Continue oxygen supplementation to maintain SPO2 above 92% -Other respiratory protocol to continue -Get MRSA swab -Pharmacy to dose vancomycin 2. Sepsis A41.9 Meets SIRS criteria on admission with high-grade fever tachycardia, and leukocytosis. Lactate is normal so no severe sepsis. , imaging for multifocal infiltrate. Blood cultures pending, urinalysis appears weakly positive at this time URINE sample is dirty evidenced by squamous epithelium, procalcitonin pending, lactate repeat WNL. Continue empiric coverage with cefepime and vancomycin de-escalate therapy as appropriate. SARS CoV 2 negative. Continue IVF at 100cc/hr 3. Acute respiratory failure J96.00 Secondary to pneumonia Management as outlined in #1 4. Chronic kidney disease N18.9 Creatinine at baseline. Patient reports reduced urinary output, will monitor urinary output closely with IV hydration for response. Avoid nephrotoxic medications 5. Dependence on CPAP ventilation Z99.89 Due to OSA. Patient needs nightly CPAP for OSA To ensure continuation during hospitalization. 6. HTN (hypertension) I10 Chronic Continue home meds as blood pressure tolerates 7. Hyperlipidemia E78.5 Chronic Continue home meds 8. OSA on CPAP G47.33 Nocturnal CPAP to continue Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 12/15/22 15:42:00 albuterol-ipratropium, 3 mL, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q6H, 12/15/22 19:00:00 cefePIME, 1 GM, IVPB, Injection, Q8H, Indication: Pneumonia - CAP (MRSA/PSA Risk Factors), 12/15/22 20:00:00, for 14 Doses, 12/20/22 4:00:00, 12.5 mL/hr, Infuse Over 4 Hours, Total Volume (mL) = 50 heparin, 7,500 Units, Subcutaneous, Injection, Q8, Routine, 12/15/22 22:00:00 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 12/15/22 15:42:00 polyethylene glycol 3350, 17 GM, Orally, Powder, Daily, PRN, Constipation - Use First, 12/15/22 15:42:00 Sodium Chloride 0.9% 1,000 mL, Total Volume (mL) = 1,000, IV, 12/15/22 15:42:00, 100 mL/hr, Clinical Weight Sodium Chloride 0.9% 500 mL, Total Volume (mL) = 500, IV, 12/15/22 16:40:00, Other - See Comments, Clinical Weight vancomycin, 1.5 GM = 15 mL, IVPB, Injection, Q18H, Indication: Pneumonia - CAP (MRSA/PSA Risk Factors), 12/15/22 21:00:00 180 gm Carb per day Diet Admit to Inpatient 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 Comp Metabolic Panel CPAP Intermittent DC SIRS Alert and Sepsis Screen Do Not (Specify) Hgb A1C HPLC Bld QN Incentive Spirometry Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Respiratory Protocol Initiate Skin and Wound Care Protocol L pneumophila Ag Ur QL Level of Care Lipid Panel SerPl QN Medical Service MRSA PCR Mucous Clearance Device Nasal Cannula OT Evaluation and Treatment Peripheral IV Insertion Procalcitonin Procalcitonin PT Evaluation and Treatment Resp CX + Stn Resp Evaluation or Assessment Resuscitation Status RVP2 PCR Strep pneumoniae Ag Urine Titrate FiO2 to Keep O2 Sat TSH w FreeT4 reflex Vancomycin Pharmacy Dosing Consult Vital Signs Vital Signs Weight Greater than 60 minutes total with greater than 50% of time face-to-face with patient reviewing course, plan of care, and in care coordination Code Status Resuscitation Status - Ordered -- 12/15/22 15:42:00, Full Code Chronic Problem List Addison's disease Anxiety Anxiety and depression Breast cancer screening Chronic UTI Constipation COPD (chronic obstructive pulmonary disease) Depression GERD (gastroesophageal reflux disease) History of bariatric surgical procedure. History of kidney stones HTN (hypertension) Hydronephrosis Hyperlipidemia Hypothyroidism Knee pain Leg cramps Lesion of bladder Medicare annual wellness visit, subsequent Morbid obesity Nausea OA (osteoarthritis) OA (osteoarthritis) of knee OSA on CPAP RA (rheumatoid arthritis) Super obesity Tachycardia Procedure/Surgical History ?cystoscopy with stent placement (10/20/2022) ?cystoscopy (08/2022) ?cysto, bladder biopsy, fulguration, bilat retrograde pyelogram (01/17/2022) ?Colonoscopy (10/17/2018) ?History of laparoscopic adjustable gastric banding ?Hysterectomy ?Left knee surgery ?Surgery ?Tonsillectomy and adenoidectomy Surgical History Internal 11/11/2022 Ureteroscopy. 10/20/2022 Cystoscopy Insert Ureteral Stent or Cath (Right) 01/17/2022 Cystoscopy Bladder Biopsy 10/17/2018 Colonscpy Diagnostic/Screen Medications Home Medications (29) Active acetaminophen 650 mg oral tablet, extended release 1,300 mg = 2 Tablet, PRN, Orally Aldactone 50 mg oral tablet 50 mg = 1 Tablet, Orally, Daily amitriptyline 25 mg oral tablet 25 mg = 1 Tablet, Orally, At Bedtime amLODIPine 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily carvedilol 25 mg oral tablet 25 mg = 1 Tablet, Orally, BID Centrum Silver Ultra Women's 1 Tablet, Orally, QAM Colace 100 mg oral capsule 100 mg = 1 Capsule, Orally, BID Combivent Respimat CFC free 100 mCg-20 mCg/inh inhalation aerosol 1 Puff, Inhalation, 4 Times Daily Order Details or printed requisition for more information., This is a print requisition order, cannot be ePrescribed. Dulera 200 mCg-5 mCg/inh inhalation aerosol 2 Puff, Inhalation, BID estradiol topical 0.1 mg/gm cream See Instructions, Apply pea sized amt to vaginal opening nightly x 2 weeks, then 2x/week thereafter. Fasenra 30 mg, Subcutaneous, Every 8 Weeks fluticasone 50 mCg/inh nasal spray 100 mCg = 2 Spray, intraNASAL, BID hydrALAZINE 50 mg oral tablet 100 mg = 2 Tablet, Orally, TID hydroCODONE-acetaminophen 10 mg-325 mg oral tablet 1 Tablet, PRN, Orally, Q6H hydrOXYzine hydrochloride 25 mg oral tablet 25 mg = 1 Tablet, PRN, Orally, Q6H leflunomide 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily levothyroxine 100 mCg (0.1 mg) oral tablet 100 mCg = 1 Tablet, Orally, QAM losartan 100 mg oral tablet 100 mg = 1 Tablet, Orally, Daily Mucinex DM 30 mg-600 mg oral tablet, extended release 1 Tablet, Orally, Q12H Myrbetriq 50 mg oral tablet, extended release 50 mg = 1 Tablet, Orally, Daily omeprazole 40 mg oral delayed release capsule 40 mg = 1 Capsule, Orally, Daily sertraline 100 mg oral tablet 150 mg = 1.5 Tablet, Orally, Daily solifenacin 5 mg oral tablet 5 mg = 1 Tablet, Orally, Daily Spiriva Respimat 1.25 mCg/inh inhalation aerosol 2.5 mCg = 2 Puff, Inhalation, Daily theophylline 400 mg/24 hours oral tablet, extended release 400 mg = 1 Tablet, Orally, BID torsemide 20 mg oral tablet 20 mg = 1 Tablet, Orally, Unscheduled, as needed for shortness of breath zafirlukast 10 mg oral tablet 10 mg = 1 Tablet, Orally, BID Zofran 4 mg oral tablet 4 mg = 1 Tablet, PRN, Orally, Q6H Active Scheduled Inpatient Medications albuterol-ipratropium (albuterol-ipratropium inh soln 2.5 mg-0.5 mg/3 mL), Inhalation SOLN, 3 mL, Neb Inhal, Q6H, Start: 12/15/22 19:00:00 cefePIME, Injection, 1 GM, IVPB, Q8H, Indication: Pneumonia - CAP (MRSA/PSA Risk Factors), Start: 12/15/22 20:00:00 heparin (heparin 5,000 units/0.5 mL injectable solution), Injection, 7,500 Units, Subcutaneous, Q8, Start: 12/15/22 22:00:00 Vancocin, Injection, 1.5 GM, IVPB, Q18H, Indication: Pneumonia - CAP (MRSA/PSA Risk Factors), Start: 12/15/22 21:00:00 Lactated Ringers 1,000 mL IV 125 mL/hr Sodium Chloride 0.9% 1,000 mL IV 100 mL/hr Sodium Chloride 0.9% 500 mL IV Other - See Comments One-Time Medications Given 12/14/22 00:00:00 TO 12/15/22 17:24:12 None Reported PRN Medications (0600 - 0559) from 12/14 - 12/15 acetaminophen, 650 mg, Orally, Q4H, 0 Dose(s) ondansetron, 4 mg, IV Push, Q6H, 0 Dose(s) polyethylene glycol 3350, 17 GM, Orally, Daily, 0 Dose(s) Allergies Plaquenil (Difficulty Breathing) sulfa drugs (Difficulty Breathing) Augmentin (Hives) Ceclor (Hives) codeine (Itching) Social History Alcohol Past, 1-2 times per month Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Unemployed Home/Environment Lives with Spouse. Home equipment: CPAP/BiPAP. Other 2 children Substance Abuse Past, Marijuana Tobacco Tobacco Use: Former smoker, quit more than 30 days ago. Started age 13.0 Years. Stopped age 20 Years. Family History COPD - Chronic obstructive pulmonary disease: Mother, Father, Sister, Brother and Brother. Diabetes mellitus: Mother, Father, Brother and Grandmother (M). Diabetes mellitus type 1: Brother. Diabetes mellitus type 2: Sister and Child. ESRD - End stage renal disease: Brother. Heart attack: Father. Heart disease: Mother. Hypertension: Father. Kidney disease: Father. Kidney stone: Mother. Rheumatoid arthritis: Sister and Brother. Stroke: Father. Transplant of kidney: Brother. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 19.1 k/cumm High (12/15/22 05:27:00) RBC: 3.3 million/cumm Low (12/15/22 05:27:00) Hgb: 9.5 GM/dL Low (12/15/22 05:27:00) Hct: 29.3 % Low (12/15/22 05:27:00) MCV: 89 fL (12/15/22 05:27:00) MCH: 28.9 pg (12/15/22 05:27:00) MCHC: 32.6 GM/dL (12/15/22 05:27:00) RDW: 15.6 % High (12/15/22 05:27:00) Platelet: 150 k/cumm (12/15/22 05:27:00) MPV: 9.9 fL (12/15/22 05:27:00) Chemistry: Sodium SerPl QN: 136 mmol/L (12/15/22 05:27:00) Potassium SerPl QN: 4.1 mmol/L (12/15/22 05:27:00) Chloride SerPl QN: 102 mmol/L (12/15/22 05:27:00) Carbon Dioxide SerPl QN: 23 mmol/L (12/15/22 05:27:00) Anion Gap: 11 mmol/L (12/15/22 05:27:00) BUN SerPl QN: 34 mg/dL High (12/15/22 05:27:00) Creatinine SerPl QN: 1.71 mg/dL High (12/15/22 05:27:00) Estimated GFR (CKD-EPI, no race): 35 mL/min/1.73m2 Low (12/15/22 05:27:00) Estimated CRCL (CG): 55 mL/min Low (12/15/22 05:27:00) Glucose SerPl QN: 126 mg/dL High (12/15/22 05:27:00) Calcium Total SerPl QN: 9.2 mg/dL (12/15/22 05:27:00) Troponin-I High Sensitivity: 4 ng/L (12/15/22 05:27:00) Lactate Venous Pl QN: 0.7 mmol/L (12/15/22 05:27:00) pH Bld Venous QN: 7.36 (12/15/22 09:28:00) PCO2 Bld Venous QN: 44 mmHg (12/15/22 09:28:00) PO2 Bld Venous QN: 58 mmHg High (12/15/22 09:28:00) Base Excess Bld Venous: -1 mmol/L (12/15/22 09:28:00) Bicarb Bld Venous Calc: 25 mmol/L (12/15/22 09:28:00) O2 Sat Bld Venous Calc: 88 % (12/15/22 09:28:00) FIO2: Venous (12/15/22 09:28:00) Patient Temperature: 37 DegC (12/15/22 09:28:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (12/14/22 09:08:00) Rapid Influenza A PCR: Not Detected (12/14/22 09:08:00) Rapid Influenza B PCR: Not Detected (12/14/22 09:08:00) Diagnostics Radiology Results - Last 24 hours Across Visits 12/15/2022 08:20 - CT Chest W/O IV Contrast IMPRESSION: Limited exam in the absence of intravenous contrast.Multifocal airspace disease involving all lobes, including regions offrank consolidation involving both lower lobes, the lateral segmentof the right middle lobe, and posterior left upper lobe as describedabove. Numerous smaller patchy foci of airspace disease as well. Theappearance is nonspecific, with differential diagnosis includingatypical infection and multifocal inflammatory lung disease.Borderline/mild mediastinal and supra clavicular adenopathy.No overt malignant findings.Thank you for consulting with Radiology. Healthcare providerswishing to discuss this case further can contact. Signature Line Electronically Signed on 12/15/22 17:24 ________________________________________________________

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
-
Labordaten
COVID 19 Specimen Source Nasopharyngeal Coronavirus SARS-CoV2 Rapid * Not Detected Microbiology Studies - Bacterial Blood CX (+) POS In Progress NEG In Progress Resp CX + Stn NEG 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 Not 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 (A) 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 Viral FS Rapid Influenza Method PCR - Rapid Influenza A PCR * Not Detected Rapid Influenza B PCR * Not Detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2499353

SEQIRUS, INC. · INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) · Charge UT7682LA

schwer
Staat
WI
Alter
64,0
Geschlecht
F
Eingang
04.11.2022
Impfdatum
17.10.2022
Beginn
21.10.2022
Tage bis Beginn
4,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Cardiac flutter Computerised tomogram abdomen Electrocardiogram ambulatory Feeling abnormal Hypoacusis Impaired driving ability Laboratory test Nasal congestion Sleep disorder Syncope Viral infection

Symptomtext

States she had a syncope episode in the shower 10/21/22. Seen in UC and diagnosed with a viral infection. Continued to feel "off", had a friend take her to ED 10/28/22 due to "heart fluttering". Cardiac workup done including wearing a 24 hour Holter monitor and abdominal CT. Reports decreased hearing, her PCP is unsure of if she has a concussion from initial fall. States she has felt off since 10/17/22 COVID booster and flu vaccine. Did see PCP 11/3/22, told to take Sudafed for nasal congestion. Is also unable to sleep more than 2-3 hours per night. Has been working remotely as she does not feel it is appropriate to drive with decreased hearing. Does feel that she can work, but has a MD note stating she requires a flexible schedule. States her supervisor told her to call EHS, although has not missed 5 or more days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
24 hour holter monitor, abd CT scan, lab work
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
Unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2480332

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

schwer
Staat
WV
Alter
28,0
Geschlecht
F
Eingang
17.10.2022
Impfdatum
14.10.2022
Beginn
14.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Anaphylactic reaction Blood test Computerised tomogram abdomen Computerised tomogram head Hypoaesthesia Paraesthesia Rectal haemorrhage

Symptomtext

On 10/14/2022 I had an anaphylaxis reaction that was treated with 125mg solumedrol and 100mg benadryl at approximately 0940. The provider I saw had suggested I take another 100mg benadryl that same evening.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
I went to my local Emergency Department on 10/16/2022 for abnormal rectal bleeding, numbness and tingling in my hands and feet. CT Scans of head and abdomen were completed. Blood work was also completed at this time.
Aktuelle Erkrankungen
none
Vorgeschichte
Anxiety
Andere Medikamente
lexapro 20mg daily
Allergien
none
Vorherige Impfungen
-

VAERS 2607569

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

moderat
Staat
MN
Alter
32,0
Geschlecht
M
Eingang
31.03.2023
Impfdatum
16.02.2023
Beginn
16.02.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Acoustic stimulation tests abnormal Audiogram Condition aggravated Sleep disorder Tinnitus

Symptomtext

On my way home from the doctor's office, I heard pinging in my ears. I didn't think much of it at the time because there wasn't any use dwelling on it. That evening, about an hour after falling asleep, I was awakened by an intense perceived ringing in my ears that was significantly louder than my previous baseline tinnitus. I would describe the ringing as higher pitched than my normal tinnitus, and about three times louder at minimum. I can say the ringing was three times louder because I had to increase the volume on the device I use for masking by about three times just to begin to mask the new level of tinnitus. This lasted all night, and has since lessened to a degree, but not to my previous baseline. The perceived pitch has changed, and the perceived loudness has gone up in the month since vaccination. My tinnitus has been present since at least June of 2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
I had an audiogram, and a tympanogram hearing test on 03/29/23 which showed normal hearing bilaterally, largely stable since my last hearing test in July of 2021.
Aktuelle Erkrankungen
-
Vorgeschichte
tinnitus
Andere Medikamente
10mg Adderall XR once daily
Allergien
alkaseltzer
Vorherige Impfungen
I had the Janssen Covid-19 vaccination on 04/08/2021, intramuscular in left arm, and lot #043A21A. Sometime in June is when I fi

VAERS 2488589

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

moderat
Staat
NJ
Alter
21,0
Geschlecht
F
Eingang
25.10.2022
Impfdatum
17.10.2022
Beginn
17.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest discomfort Dyspnoea Electrocardiogram normal Hypoaesthesia Joint range of motion decreased

Symptomtext

Patient had decreased range of motion, left arm felt numb, and developed heavy breathing with chest discomfort.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
EKG done, was normal.
Aktuelle Erkrankungen
Denies
Vorgeschichte
Denies
Andere Medikamente
Denies
Allergien
Augmentin
Vorherige Impfungen
-

VAERS 2468150

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

moderat
Staat
MA
Alter
62,0
Geschlecht
F
Eingang
04.10.2022
Impfdatum
06.09.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Chest discomfort Chest pain Hepatic enzyme abnormal Hepatic enzyme increased Myalgia Myocardial necrosis marker increased Oropharyngeal pain Pyrexia Rash

Symptomtext

a bilateral rash on her trunk; chest discomfort with chest tightness; sore throat; myalgia; fever of 103.5; chest pain; elevated cardiac enzymes; abnormal liver enzymes; Initial information received on 23-Sep-2022 regarding an unsolicited valid serious case received from a consumer/non-hcp. This case involves a 62 years old female patient who experienced sore throat, a bilateral rash on her trunk, myalgia, fever of 103.5, chest discomfort with chest tightness, elevated cardiac enzymes and abnormal liver enzymes and chest pain after receiving vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 06-Sep-2022, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B VACCINE once (lot UT7682LA; 30-06-2022) via unknown route in unknown administration site for immunization. On an unknown date after 12 hours, the patient developed a serious events sore throat (oropharyngeal pain), bilateral rash on her trunk (rash), myalgia, fever of 103.5 (pyrexia), chest discomfort with chest tightness (chest discomfort) and chest pain (unknown latency) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. The patient was hospitalized for these events and discharged on 19-Sep-2022.On an unknown date the patient developed a serious events elevated cardiac enzymes (myocardial necrosis marker increased) and abnormal liver enzymes (hepatic enzyme abnormal) These events were assessed as medically significant. Relevant laboratory test results included: Hepatic enzyme increased - On an unknown date: [not available] Myocardial necrosis marker increased - On an unknown date: [not applicable] Pyrexia - On an unknown date: 103.5 UNK Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events (sore throat, a bilateral rash on her trunk, myalgia, fever of 103.5, chest discomfort with chest tightness, chest pain, hepatic enzyme abnormal, myocardial necrosis marker increased ). At time of reporting, the outcome was unknown for hepatic enzyme abnormal and Not Recovered / Not Resolved for rest of the events.; Sender's Comments: Sanofi Company Comment dated: 29-Sep-2022: This case involves a 62 years old female patient who experienced sore throat, a bilateral rash on her trunk, myalgia, fever of 103.5, chest discomfort with chest tightness, elevated cardiac enzymes, abnormal liver enzymes and chest pain after receiving vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV].Further information regarding medical history, concurrent condition during vaccination, previous vaccination, concomitant medication and tolerance, allergic history, laboratory investigations excluding alternative etiologies for the reported event are needed to fully assess this case. Based upon the reported information, the role of the individual suspect vaccine cannot be assessed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Test Name: abnormal liver enzymes; Result Unstructured Data: not available; Test Name: cardiac enzymes; Result Unstructured Data: not applicable; Test Name: fever of 103.5; Test Result: 103.5 {DF}
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2466867

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge Ut7682la

moderat
Staat
NJ
Alter
42,0
Geschlecht
F
Eingang
02.10.2022
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: nein
Condition aggravated Dehydration Migraine Vomiting

Symptomtext

Vomiting, to the point that nothing could be held down. Not even very small sips of clear liquid. Sever dehydration resulted, along with sever migraine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Migraines
Andere Medikamente
Trokendi, venlafaxine
Allergien
None
Vorherige Impfungen
-

VAERS 2516782

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge UT7682LA

mild
Staat
WI
Alter
28,0
Geschlecht
F
Eingang
25.11.2022
Impfdatum
29.09.2022
Beginn
01.10.2022
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exercise tolerance decreased Injection site pain Loss of personal independence in daily activities Pain

Symptomtext

Per employee "I received my influenza vaccine in my L upper arm on 9/30/22. A few months later I still have L upper arm pain at the site of the injection. It is a shooting pain with certain movements of my arm. It has limited my exercise and ADLs due to pain." Documented date was 09/29/22 in Employee Health records.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
Unknown to reporter
Vorgeschichte
Unknown to reporter
Andere Medikamente
Unknown to reporter
Allergien
Unknown to reporter
Vorherige Impfungen
-

VAERS 2509559

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

mild
Staat
KY
Alter
45,0
Geschlecht
F
Eingang
16.11.2022
Impfdatum
14.11.2022
Beginn
14.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Oedema peripheral Rash pruritic Urticaria

Symptomtext

Patient contacted office on 11/16/2022 and reported that in the afternoon of 11/14/2022 after receiving her Influenza vaccine she developed a hive like rash to bilateral hands/wrist area. Noted with small bumps, itching to areas. Moderate edema noted to right hand and mild edema noted to left hand. No issues at injection site. No fever or difficulty breathing. Patient has taken Benadryl without success at alleviating symptoms. Medrol dose pack has been prescribed that physician of vaccine clinic.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash pruritic
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
Carpal tunnel syndrome Cirrhosis Diabetes Depression Essential hypertension GAD (generalized anxiety disorder) GERD (gastroesophageal reflux disease) Gastritis Hypothyroid Major depress dis, severe Migraine Mitral regurgitation Mixed hyperlipidemia NASH (nonalcoholic steatohepatitis) Nightmares associated with chronic post-traumatic stress disorder Trauma and stressor-related disorder Tricuspid regurgitation
Andere Medikamente
Praluent Pen 150mg every 84 days, Amitriptyline 50mg daily, Aspirin 81 mg daily, Farxiga 10mg daily, Valium 2mg TID PRN, Lasix 20mg daily PRN, Laxis 40mg daily, Imdur 30mg daily, Synthroid 100mcg daily, Metformin 500mg BID, Metoprolol 25mg
Allergien
Clopidogrel (Plavix)-Severe leg pain
Vorherige Impfungen
-

VAERS 2489861

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

mild
Staat
NJ
Alter
57,0
Geschlecht
F
Eingang
26.10.2022
Impfdatum
20.09.2022
Beginn
07.10.2022
Tage bis Beginn
17,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Body temperature increased Bronchitis Cough Influenza virus test positive Pain SARS-CoV-2 test negative Streptococcus test positive Wheezing

Symptomtext

As of 10/07/2022, I experienced achiness, a low grade flu temperature, and cough. I tested negative for COVID-19 three times. But I tested positive for strep throat and flu on 10/09/2022. I was given AUGMENTIN steroids. I was also wheezing and I was given a 5 day course of steroids. My symptoms worsened and I went back to the doctor. I was given Z-PAK. I was diagnosed with Bronchitis as well.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
Oct2022 three COVID-19 tests negative; 09Oct22 strep throat positive; 09Oct22 flu positive; 12Oct22 Bronchitis.
Aktuelle Erkrankungen
None
Vorgeschichte
Sjogren's syndrome
Andere Medikamente
Losartan; AJOVY; multivitamin
Allergien
Sulfa drugs; CIPRO
Vorherige Impfungen
-

VAERS 2471584

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

mild
Staat
MN
Alter
48,0
Geschlecht
F
Eingang
07.10.2022
Impfdatum
05.10.2022
Beginn
06.10.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site swelling Injection site warmth Tenderness

Symptomtext

Patient presented with some slight redness and raised area on her injection site on 10/6/22. Slight pain to the touch. Later evening on 10/6/22 patient reported the site is warm to the touch and redness is increasing. Patient describes a reaction similar to this 2 years ago.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None noted
Aktuelle Erkrankungen
None stated
Vorgeschichte
Thyroid deficient. Elevated Blood pressure. Heart arrythmias.
Andere Medikamente
-
Allergien
None noted
Vorherige Impfungen
2 yrs ago to the Influenza vaccine.

VAERS 2427909

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7682la

mild
Staat
ND
Alter
4,0
Geschlecht
M
Eingang
02.09.2022
Impfdatum
02.09.2022
Beginn
02.09.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

Hives starting shortly after vaccination - L thigh and upper back. Self-resolved after ~ 5 minutes while still in clinic

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none
Vorgeschichte
History of prematurity
Andere Medikamente
PRN albuterol and topical triamcinolone, none recently
Allergien
Lorazepam - myoclonic jerks (in NICU)
Vorherige Impfungen
-

VAERS 2420144

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut7682la

mild
Staat
PA
Alter
4,0
Geschlecht
F
Eingang
25.08.2022
Impfdatum
25.08.2022
Beginn
25.08.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash Rash maculo-papular

Symptomtext

maculopapular rash on bil;ateral arms and legss and mildly also on abdomen, starting ~30mins after vaccines in left arm. No anaphylaxis (no hives, no hypotension, no GI sx, no wheezing). Rash started to fade over next 20-30. Not fully gone at 1hr when discharged

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
URI (cough and rhinorrhea) 3 weeks prior to vaccination
Vorgeschichte
autism
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2686507

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
IN
Alter
42,0
Geschlecht
F
Eingang
26.09.2023
Impfdatum
21.09.2023
Beginn
21.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered

Symptomtext

MA gave expired flu shot to patient. Patient notified, no signs or symptoms reported. Flu vaccine Expired 06/30/2023. Patient will return for another shot, due to expired vaccine possibly being not as effective.

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

VAERS 2549019

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
PA
Alter
37,0
Geschlecht
F
Eingang
03.01.2023
Impfdatum
12.10.2022
Beginn
12.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient given Moderna monovalent booster instead of Moderna bivalent booster. Patient notified.

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

VAERS 2548978

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) · Charge UT7682LA

gering
Staat
PA
Alter
59,0
Geschlecht
F
Eingang
03.01.2023
Impfdatum
12.10.2022
Beginn
12.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient given Moderna monovalent booster instead of Moderna bivalent booster. Patient notified.

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

VAERS 2540614

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
PA
Alter
51,0
Geschlecht
F
Eingang
22.12.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient was given Moderna Monovalent Booster dose instead of the Moderna Bivalent Booster. Patient notified.

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

VAERS 2540602

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
PA
Alter
46,0
Geschlecht
F
Eingang
22.12.2022
Impfdatum
10.10.2022
Beginn
10.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient was given Moderna Monovalent Booster dose instead of the Moderna Bivalent Booster. Patient notified.

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

VAERS 2540597

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
PA
Alter
56,0
Geschlecht
F
Eingang
22.12.2022
Impfdatum
10.10.2022
Beginn
10.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient was given Moderna Monovalent Booster dose instead of the Moderna Bivalent Booster. Patient notified.

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

VAERS 2540588

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
PA
Alter
61,0
Geschlecht
F
Eingang
22.12.2022
Impfdatum
10.10.2022
Beginn
10.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient was given Moderna Monovalent Booster dose instead of the Moderna Bivalent Booster. Patient notified.

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

VAERS 2507119

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
OH
Alter
29,0
Geschlecht
M
Eingang
14.11.2022
Impfdatum
03.11.2022
Beginn
03.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Patient expected to receive Tdap vaccine, but instead received the flu vaccine.

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

VAERS 2497634

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut7682la

gering
Staat
IN
Alter
58,0
Geschlecht
F
Eingang
03.11.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Goitre Thyroid mass Ultrasound Doppler abnormal Ultrasound thyroid abnormal

Symptomtext

Document Type: US Thyroid Document Subject: US Thyroid * Final Report * Reason For Exam enlarged thyroid Report EXAMINATION: Thyroid ultrasound EXAM Date: 10/11/2022 08:44 HISTORY: Enlarged thyroid. COMPARISON: None available. FINDINGS: Multiple grayscale and color Doppler ultrasound images of the thyroid gland are presented for interpretation. The right thyroid lobe measures 4.6 cm sagittal by 1.3 cm AP by 1.5 cm transverse. The left thyroid lobe measures 4.1 cm sagittal by 1.2 cm AP by 1.3 cm transverse. The isthmus demonstrates normal thickness measuring approximately 0.2 cm. The right lobe contains a 1.0 cm well-circumscribed hypoechoic and slightly heterogeneous nodule that appears mildly hypervascular. No other nodules are identified in the right or left lobes. IMPRESSION: A 1.0 cm nodule in the right thyroid lobe is a TR4 lesion for which follow-up ultrasound is recommended at 1, 2, 3 and 5 years according to current ACR guidelines. Dictated on: 10/11/2022 1:16 PM Signature Line This examination and reported findings have been reviewed and confirmed by the undersigned. Read By: MD Click VIEW IMAGE icon to Display Image This document has an image

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

VAERS 2475682

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UT7682LA

gering
Staat
IL
Alter
11,0
Geschlecht
F
Eingang
11.10.2022
Impfdatum
05.10.2022
Beginn
05.10.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event

Symptomtext

Expired COVID-19 vaccine given to patient. COVID vaccine lot FL2757 expired 09/30/2022 (also thawed on 09/30/2022) and was given on 10/5/2022. no adverse events reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Vesicoureteral reflux with nephropathy, unilateral
Vorgeschichte
-
Andere Medikamente
Pediatric multivitamin
Allergien
NKA
Vorherige Impfungen
-

VAERS 2465322

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
NJ
Alter
-
Geschlecht
U
Eingang
30.09.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Poor quality product administered Product storage error

Symptomtext

Temperature excursion at unknown temperature for 5 hours due to human error with no reported adverse event; Vaccine administered post temperature excursion with no reported adverse event; Initial information received on 27-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age and unknown gender patients who were administered vaccine post temperature excursion at unknown temperature for 5 hours due to human error with no reported adverse event while receiving vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the suspect INFLUENZA QUADRIVAL A-B VACCINE was exposed to a temperature excursion at unknown temperature for 5 hours due to human error with no reported adverse event (product storage error). On an unknown date, the patients received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UT7682LA and expiry date: 30-Jun-2023; formulation, strength, dose, route and administration site not reported) for prophylactic vaccination. On an unknown date, the patients were administered vaccine post temperature excursion with no reported adverse event (poor quality product administered) (unknown latency) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. It was reported, "Home health service were training someone new, they took 2 vaccines out of the refrigerator drove it to 2 patients houses and administered them but didn't take the typical transport device for storage". Action taken was not applicable. At time of reporting, the outcome was Unknown for both the events. 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
Poor quality product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2461857

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
NY
Alter
0,2
Geschlecht
M
Eingang
27.09.2022
Impfdatum
23.09.2022
Beginn
23.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age

Symptomtext

I had just clocked in for the day when Dr. came out of the patients room . He stated that patient needs some vaccines and had them on a tray already. I proceeded to my desk to log them in when I heard him call out add a flu shot as well. I said ok. I prepared the vaccines, went in the patient room. I went over the vaccines with The mom and dad before they signed the paper acknowledging what shots were being given. I administered the vaccinations I asked if they had any other questions or concerns. They said no and left the room. Later on Dr. reviewed the chart and realized I gave a flu shot and called to make the parents aware.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2455992

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
NJ
Alter
11,0
Geschlecht
F
Eingang
23.09.2022
Impfdatum
22.09.2022
Beginn
22.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product preparation error

Symptomtext

Covid 19 Vaccine 0.2ml was administered without being diluted in error

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none documented in EMR
Vorgeschichte
N/A
Andere Medikamente
none known
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2415731

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7682LA

gering
Staat
PR
Alter
-
Geschlecht
M
Eingang
19.08.2022
Impfdatum
16.08.2022
Beginn
16.08.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Accidental exposure to product Medication error No adverse event

Symptomtext

rest of the vaccine dripped down his arm with no reported adverse event; dose was supposed to 0.50 ml , however only about half was injected with no reported adverse event; Initial information received on 16-Aug-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 25 years old male patient and it was reported that dose was supposed to 0.50 ml , however only about half was injected with no reported adverse event and rest of the vaccine dripped down his arm with no reported adverse event , while receiving vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 16-Aug-2022, the patient was supposed to receive a dose of 0.5 ml of suspect , however only half was injected (incorrect dose administered) (latency: same day) and it involved vaccine INFLUENZA QUADRIVAL A-B VACCINE , prefilled syringe, (frequency: once) (lot : UT7682LA ; expiry date: 30-Jun-2023) via intramuscular route in the left upper arm for immunization. The reporter stated that she attempted to inject FLUZONE QUADRIVALENT PFS 0.5mL into a patient's left upper arm. She inspected the needle 3 times. During injection, approximately half of the FLUZONE QUADRIVALENT leaked out where the needle is attached. The patient stated that he could feel some of the vaccine going in. The rest of the vaccine dripped down his arm (accidental exposure to product) (latency: same day). She asks if the vaccine was valid or if she should reinject 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 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
Accidental exposure to product
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-