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
125622171 12562217 1 I 20160202 20160701 20160715 20160715 EXP IT-ACTAVIS-2016-14725 ACTAVIS 64.80 YR M Y 88.00000 KG 20160715 CN 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
125622171 12562217 1 SS CAPECITABINE. CAPECITABINE 1 Oral 2000 MG, CYCLICAL UNKNOWN 0 2000 MG FILM-COATED TABLET
125622171 12562217 2 PS Oxaliplatin (Unknown) OXALIPLATIN 1 Intravenous (not otherwise specified) 160 MG, CYCLICAL UNKNOWN 78803 160 MG UNK

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125622171 12562217 1 Adenocarcinoma of colon
125622171 12562217 2 Adenocarcinoma of colon

Outcome of event

Event ID CASEID OUTC COD
125622171 12562217 OT
125622171 12562217 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125622171 12562217 Dizziness
125622171 12562217 Fall
125622171 12562217 Pain in extremity
125622171 12562217 Thrombocytopenia

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
125622171 12562217 1 20151009 0
125622171 12562217 2 20151009 0