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
125733991 12573399 1 I 20160706 20160720 20160720 EXP US-ROCHE-1797726 ROCHE 60.00 YR M Y 76.80000 KG 20160720 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
125733991 12573399 1 PS Vismodegib VISMODEGIB 1 Oral LAST TREATMENT DATE 21/SEP/2010 U 203388
125733991 12573399 2 SS Vismodegib VISMODEGIB 1 Oral U 203388
125733991 12573399 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) COURSE 2 U 0 1000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125733991 12573399 1 Pancreatic carcinoma
125733991 12573399 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125733991 12573399 DE
125733991 12573399 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125733991 12573399 Death
125733991 12573399 Hyponatraemia
125733991 12573399 Hypotension
125733991 12573399 Platelet count 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
125733991 12573399 1 20100713 0
125733991 12573399 2 20100921 0
125733991 12573399 3 20100810 0