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
127599011 12759901 1 I 2016 20160902 20160919 20160919 PER ID-BAYER-2016-171692 BAYER 50.00 YR A F Y 0.00000 20160919 CN ID ID

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
127599011 12759901 1 PS NEXAVAR SORAFENIB 1 Oral 1X200 MG DAILY DOSE 21923 200 MG FILM-COATED TABLET
127599011 12759901 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, BID (2X200 MG) 21923 200 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127599011 12759901 1 Hepatocellular carcinoma
127599011 12759901 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
127599011 12759901 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127599011 12759901 Dry skin
127599011 12759901 Erythema
127599011 12759901 Generalised erythema
127599011 12759901 Haematochezia
127599011 12759901 Pruritus
127599011 12759901 Pruritus generalised

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
127599011 12759901 1 20160802 20160804 0
127599011 12759901 2 20160805 0