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
119657754 11965775 4 F 20160801 20160127 20160803 EXP JP-ROCHE-1701041 ROCHE , IWASA S, FUKAHORI M, SUDO K, SASAKI Y, SHOJI H, HONMA Y, OKITA N, TAKASHIMA A, HAMAGUCHI T, BOKU N, SHIMADA Y, HONDA K, YAMADA T AND YAMADA Y. A PHASE I STUDY OF THE COMBINATION OF PANITUMUMAB AND BEVACIZUMAB IN KRAS WILD-TYPE COLORECTAL CANCER PATIENTS PREVIOUSLY TREATED WITH FLUOROPYRIMIDINE, OXALIPLATIN, IRINOTECAN AND BEVACIZUMAB. CANCER CHEMOTHERAPY AND PHARMACOLOGY 2016 JUN 20;:1-9. 72.00 YR F Y 0.00000 20160803 MD JP JP

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
119657754 11965775 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous drip ON DAY1 125085 5 MG/KG QOW
119657754 11965775 2 SS PANITUMUMAB PANITUMUMAB 1 Intravenous drip ON DAY1 U 0 6 MG/KG QOW
119657754 11965775 3 C MINOCYCLINE HYDROCHLORIDE. MINOCYCLINE HYDROCHLORIDE 1 Oral 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119657754 11965775 1 Colorectal cancer
119657754 11965775 2 Colorectal cancer
119657754 11965775 3 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
119657754 11965775 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119657754 11965775 Dermatitis acneiform

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

no results found

Therapies reported

no results found