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
125895211 12589521 1 I 201606 20160720 20160725 20160725 EXP US-BAYER-2016-142625 BAYER 64.00 YR A M Y 73.92000 KG 20160725 OT US US

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
125895211 12589521 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 21923 400 MG FILM-COATED TABLET BID
125895211 12589521 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 21923 400 MG FILM-COATED TABLET BID
125895211 12589521 3 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
125895211 12589521 4 C LISINOPRIL. LISINOPRIL 1 0
125895211 12589521 5 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125895211 12589521 1 Hepatic cancer
125895211 12589521 2 Hepatic cancer

Outcome of event

Event ID CASEID OUTC COD
125895211 12589521 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125895211 12589521 Diarrhoea
125895211 12589521 Dysgeusia
125895211 12589521 Prostatic operation
125895211 12589521 Weight decreased

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
125895211 12589521 1 20160126 201606 0
125895211 12589521 2 201606 0