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
123884572 12388457 2 F 2016 20160727 20160520 20160805 EXP GB-BAYER-2016-093804 BAYER 46.00 YR A M Y 0.00000 20160805 OT GB GB

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
123884572 12388457 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID Y 21923 400 MG FILM-COATED TABLET BID
123884572 12388457 2 SS NEXAVAR SORAFENIB 1 Oral UNK Y 21923 FILM-COATED TABLET
123884572 12388457 3 SS NEXAVAR SORAFENIB 1 Oral REDUCED DOSE Y 21923 FILM-COATED TABLET
123884572 12388457 4 C TENOFOVIR TENOFOVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123884572 12388457 1 Hepatocellular carcinoma
123884572 12388457 2 Hepatocellular carcinoma
123884572 12388457 3 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
123884572 12388457 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123884572 12388457 Diarrhoea Diarrhoea
123884572 12388457 Hepatocellular carcinoma

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
123884572 12388457 1 201203 0
123884572 12388457 2 2013 0