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
127166461 12716646 1 I 20151205 20151210 20160906 20160906 EXP IR-BAYER-2015-487858 BAYER 56.00 YR A M Y 0.00000 20160906 MD IR IR

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
127166461 12716646 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 21923 400 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127166461 12716646 1 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127166461 12716646 DE
127166461 12716646 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127166461 12716646 Hepatocellular carcinoma
127166461 12716646 Palmar-plantar erythrodysaesthesia syndrome

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
127166461 12716646 1 20151205 20151210 0