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
115528906 11552890 6 F 20150812 20160705 20150925 20160708 EXP CO-BAYER-2015-421472 BAYER 58.00 YR A F Y 0.00000 20160708 CN CO CO

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
115528906 11552890 1 PS NEXAVAR SORAFENIB 1 Oral 200 MG, BID 24000 MG 21923 200 MG FILM-COATED TABLET BID
115528906 11552890 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 24000 MG 21923 400 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115528906 11552890 1 Hepatocellular carcinoma
115528906 11552890 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
115528906 11552890 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115528906 11552890 Abasia
115528906 11552890 Alopecia
115528906 11552890 Blood pressure increased
115528906 11552890 Hepatomegaly
115528906 11552890 Hypertension
115528906 11552890 Limb mass
115528906 11552890 Rash

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
115528906 11552890 1 20150801 2015 0
115528906 11552890 2 20150809 20151020 0