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
125821301 12582130 1 I 20110722 20160706 20160722 20160722 EXP US-ROCHE-1799531 ROCHE 78.00 YR M Y 80.50000 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
125821301 12582130 1 PS Vismodegib VISMODEGIB 1 Oral COURSE 1 203388 QID
125821301 12582130 2 SS Vismodegib VISMODEGIB 1 Oral COURSE 2, LAST TREATMENT ON 03/JUN/2011 203388
125821301 12582130 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) COURSE 2, LAST TREATMENT ON 03/JUN/2011 N 0 1000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125821301 12582130 1 Pancreatic carcinoma
125821301 12582130 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125821301 12582130 OT
125821301 12582130 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125821301 12582130 Death
125821301 12582130 Hyponatraemia
125821301 12582130 Hypophosphataemia

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
125821301 12582130 1 20110429 0
125821301 12582130 2 20110527 0
125821301 12582130 3 20110527 0