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
125577723 12557772 3 F 2016 20160914 20160714 20160915 EXP US-BAYER-2016-110749 BAYER 0.00 E F Y 0.00000 20160915 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
125577723 12557772 1 PS NEXAVAR SORAFENIB 1 Oral 400 MG, BID 21923 400 MG FILM-COATED TABLET BID
125577723 12557772 2 SS NEXAVAR SORAFENIB 1 Oral 200 MG, QD 21923 200 MG FILM-COATED TABLET QD
125577723 12557772 3 SS NEXAVAR SORAFENIB 1 UNK 21923 FILM-COATED TABLET
125577723 12557772 4 SS NEXAVAR SORAFENIB 1 Oral 200 MG, QD 21923 200 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125577723 12557772 1 Hepatocellular carcinoma
125577723 12557772 2 Hepatocellular carcinoma
125577723 12557772 3 Hepatocellular carcinoma
125577723 12557772 4 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125577723 12557772 OT
125577723 12557772 DE
125577723 12557772 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125577723 12557772 Abdominal pain
125577723 12557772 Constipation
125577723 12557772 Death
125577723 12557772 Decreased activity
125577723 12557772 Eating disorder
125577723 12557772 Fatigue
125577723 12557772 Nausea
125577723 12557772 Toxicity to various agents
125577723 12557772 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
125577723 12557772 1 20160531 2016 0
125577723 12557772 2 2016 2016 0
125577723 12557772 3 2016 2016 0
125577723 12557772 4 20160603 0