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
125375912 12537591 2 F 2016 20160729 20160707 20160808 EXP US-BAYER-2016-091460 BAYER 65.00 YR E M Y 0.00000 20160808 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
125375912 12537591 1 PS NEXAVAR SORAFENIB 1 Oral 200 MG, BID 21923 200 MG FILM-COATED TABLET BID
125375912 12537591 2 SS NEXAVAR SORAFENIB 1 Oral 600 MG DAILY DOSE (200 MG IN THE MORNING AND 400 MG IN THE EVENING) 21923 600 MG FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125375912 12537591 1 Hepatocellular carcinoma
125375912 12537591 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125375912 12537591 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125375912 12537591 Diarrhoea
125375912 12537591 Dry skin
125375912 12537591 Dysphonia
125375912 12537591 Dyspnoea
125375912 12537591 Fatigue
125375912 12537591 Gait disturbance
125375912 12537591 Pain in extremity
125375912 12537591 Peripheral swelling

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
125375912 12537591 1 20160425 20160619 0
125375912 12537591 2 20160620 0