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
125730791 12573079 1 I 20160706 20160720 20160720 EXP US-ROCHE-1797679 ROCHE 65.00 YR M Y 85.40000 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
125730791 12573079 1 PS Vismodegib VISMODEGIB 1 Oral 20/JUN/2011, 18/JUL/2011 AND 10/OCT/2011 203388 1000 MG CAPSULE
125730791 12573079 2 SS Vismodegib VISMODEGIB 1 Oral 203388 500 MG CAPSULE
125730791 12573079 3 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 03/JAN/2011, 31/JAN/2011, 28/FEB/2011, 23/MAY/2011 AND 10/OCT/2011 0 1000 MG
125730791 12573079 4 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 15/AUG/2011 0 500 MG
125730791 12573079 5 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125730791 12573079 1 Pancreatic carcinoma
125730791 12573079 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
125730791 12573079 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125730791 12573079 Alanine aminotransferase increased
125730791 12573079 Neutrophil 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
125730791 12573079 1 20110523 20111024 0
125730791 12573079 2 20110815 0
125730791 12573079 3 20101108 20111024 0
125730791 12573079 4 20110620 0
125730791 12573079 5 20110718 0