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
125870192 12587019 2 F 20160721 20160725 20160729 EXP CN-BAYER-2016-139541 BAYER 0.00 M Y 0.00000 20160729 CN CN CN

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
125870192 12587019 1 PS NEXAVAR SORAFENIB 1 Oral UNK 21923 FILM-COATED TABLET
125870192 12587019 2 SS NEXAVAR SORAFENIB 1 Oral UNK 21923 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125870192 12587019 1 Hepatocellular carcinoma
125870192 12587019 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125870192 12587019 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125870192 12587019 Abdominal discomfort
125870192 12587019 Adverse reaction
125870192 12587019 Ascites
125870192 12587019 Blood pressure increased
125870192 12587019 Hair colour changes
125870192 12587019 Hiccups
125870192 12587019 Palmar-plantar erythrodysaesthesia syndrome
125870192 12587019 Peripheral swelling
125870192 12587019 Vomiting

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
125870192 12587019 1 2010 2012 0
125870192 12587019 2 201606 0