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
79575923 7957592 3 F 20160926 20110524 20160927 EXP FR-ROCHE-777314 ROCHE ASPESLAGH S, AWADA A, MATOS-PITA A, AFTIMOS P, BAHLEDA R, VARGA A AND SORIA J PHASE I DOSE-ESCALATION STUDY OF PLITIDEPSIN IN COMBINATION WITH BEVACIZUMAB IN PATIENTS WITH REFRACTORY SOLID TUMORS. ANTI-CANCER DRUGS 2016 SEP 08;:-. 0.00 Y 0.00000 20160927 OT FR FR

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
79575923 7957592 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) ON DAYS 1 AND 15 EVERY 4 WEEK U 125085 10 MG/KG SOLUTION FOR INFUSION
79575923 7957592 2 SS PLITIDEPSINE PLITIDEPSIN 1 Intravenous (not otherwise specified) ESCALATING DOSES: 2.8, 3.8 AND 4.8 MG/SQ M. U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
79575923 7957592 1 Neoplasm
79575923 7957592 2 Neoplasm

Outcome of event

Event ID CASEID OUTC COD
79575923 7957592 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
79575923 7957592 Alanine aminotransferase increased
79575923 7957592 Epistaxis
79575923 7957592 Fatigue
79575923 7957592 Headache
79575923 7957592 Myalgia
79575923 7957592 Nausea
79575923 7957592 Vomiting

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

no results found

Therapies reported

no results found