The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
103841126 10384112 6 F 201406 20160711 20140814 20160714 EXP PHHY2014FR099012 NOVARTIS 70.00 YR M Y 0.00000 20160714 MD FR FR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
103841126 10384112 1 PS AFINITOR EVEROLIMUS 1 Unknown 10 MG, QD Y 22334 10 MG QD
103841126 10384112 2 SS AFINITOR EVEROLIMUS 1 Unknown UNK Y 22334

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103841126 10384112 1 Renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
103841126 10384112 LT
103841126 10384112 HO
103841126 10384112 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103841126 10384112 Acute kidney injury
103841126 10384112 Femoral neck fracture
103841126 10384112 Haematuria
103841126 10384112 Hypokalaemia
103841126 10384112 Hyponatraemia
103841126 10384112 Malignant neoplasm progression
103841126 10384112 Prostatic adenoma
103841126 10384112 Tumour haemorrhage
103841126 10384112 Urinary retention

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
103841126 10384112 1 201405 20140625 0