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
126398081 12639808 1 I 20160706 20160810 20160810 EXP US-ROCHE-1809010 ROCHE 46.00 YR F Y 56.40000 KG 20160810 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
126398081 12639808 1 PS Vismodegib VISMODEGIB 1 Oral U 203388 1000 MG CAPSULE QD
126398081 12639808 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) NEXT DOSE ON: 01/OCT/2010, 29/OCT/2010, 26/NOV/2010, 27/DEC/2010, 21/JAN/2011 U 0 1000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126398081 12639808 1 Pancreatic carcinoma
126398081 12639808 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
126398081 12639808 LT
126398081 12639808 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126398081 12639808 Abdominal pain
126398081 12639808 Anaemia
126398081 12639808 CD4 lymphocytes decreased
126398081 12639808 Colostomy
126398081 12639808 Enterostomy

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
126398081 12639808 1 20101227 20110215 0
126398081 12639808 2 20100903 20110215 0