The Safety Rates Drug Report

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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
125553691 12555369 1 I 20160629 20160714 20160714 EXP IT-CIPLA LTD.-2016IT09531 CIPLA AGLIETTA M, BARONE C, SAWYER MB, MOORE MJ, MILLER WH, BAGALA C ET AL.,. A PHASE I DOSE ESCALATION TRIAL OF TREMELIMUMAB (CP-675,206) IN COMBINATION WITH GEMCITABINE IN CHEMOTHERAPY-NAIVE PATIENTS WITH METASTATIC PANCREATIC CANCER. ANNALS OF ONCOLOGY. 2014;25:1750 TO 1755 0.00 Y 0.00000 20160714 OT IT IT

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
125553691 12555369 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown 1000 MG/M2, ON DAYS 1, 8, AND 15, EVERY 28 DAYS U U 78759 1000 MG/M**2
125553691 12555369 2 SS Tremelimumab TREMELIMUMAB 1 Intravenous (not otherwise specified) 10 MG/KG, ON DAY 1 OF EACH 84-DAY CYCLE U U 0 10 MG/KG INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125553691 12555369 1 Pancreatic carcinoma metastatic
125553691 12555369 2 Pancreatic carcinoma metastatic

Outcome of event

Event ID CASEID OUTC COD
125553691 12555369 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125553691 12555369 Dehydration

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found