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
125824851 12582485 1 I 20160706 20160722 20160722 EXP US-ROCHE-1799503 ROCHE 69.00 YR F Y 46.40000 KG 20160722 MD 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
125824851 12582485 1 PS Vismodegib VISMODEGIB 1 Oral ASSIGNED CODE: TAC1, COURSE 2 203388 1000 MG QD
125824851 12582485 2 SS Vismodegib VISMODEGIB 1 Oral ASSIGNED CODE: TAC1, COURSE 3 203388 1000 MG QD
125824851 12582485 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) OVER 30 MINUTES ON DAYS 1, 8, AND 15. 0 1000 MG
125824851 12582485 4 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0 1000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125824851 12582485 1 Pancreatic carcinoma
125824851 12582485 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125824851 12582485 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125824851 12582485 Anaemia
125824851 12582485 Upper gastrointestinal haemorrhage

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
125824851 12582485 1 20120210 0
125824851 12582485 2 20120309 20120406 0
125824851 12582485 3 20120210 0
125824851 12582485 4 20120309 20120406 0