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
125968221 12596822 1 I 2016 20160418 20160726 20160726 EXP US-BAYER-2016-074773 BAYER 69.00 YR E M Y 0.00000 20160726 CN 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
125968221 12596822 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID BXH8GZ1 21923 400 MG FILM-COATED TABLET BID
125968221 12596822 2 SS NEXAVAR SORAFENIB 1 Oral 400 MG, BID BXH9XU1 21923 400 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125968221 12596822 1 Hepatocellular carcinoma
125968221 12596822 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125968221 12596822 HO
125968221 12596822 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125968221 12596822 Blood glucose decreased
125968221 12596822 Decreased appetite
125968221 12596822 Drug dose omission
125968221 12596822 Frequent bowel movements
125968221 12596822 Incorrect dose administered
125968221 12596822 Mood altered
125968221 12596822 Rash macular
125968221 12596822 Weight decreased

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
125968221 12596822 1 20160408 2016 0
125968221 12596822 2 2016 0