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
125501691 12550169 1 I 20160202 20160624 20160712 20160712 EXP IT-ELI_LILLY_AND_COMPANY-IT201607001813 ELI LILLY AND CO 71.00 YR M Y 68.00000 KG 20160711 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
125501691 12550169 1 PS ERBITUX CETUXIMAB 1 Intravenous (not otherwise specified) 330 MG, CYCLICAL U U 125084 330 MG INJECTION
125501691 12550169 2 SS FLUOROURACIL. FLUOROURACIL 1 Intravenous bolus 700 MG, CYCLICAL U U 0 700 MG
125501691 12550169 3 SS FLUOROURACIL. FLUOROURACIL 1 Intravenous (not otherwise specified) 4300 MG, CYCLICAL U U 0 4300 MG
125501691 12550169 4 C LEDERFOLIN LEUCOVORIN CALCIUM 1 Intravenous (not otherwise specified) 350 MG, UNK 0 350 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125501691 12550169 1 Adenocarcinoma of colon
125501691 12550169 2 Adenocarcinoma of colon
125501691 12550169 4 Adenocarcinoma of colon

Outcome of event

Event ID CASEID OUTC COD
125501691 12550169 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125501691 12550169 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
125501691 12550169 1 20150723 0
125501691 12550169 2 20150723 0
125501691 12550169 4 20150723 0