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
127222691 12722269 1 I 20150730 20160819 20160907 20160907 EXP CN-ELI_LILLY_AND_COMPANY-CN201608011967 ELI LILLY AND CO 58.00 YR M Y 0.00000 20160907 MD CN CN

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
127222691 12722269 1 PS CETUXIMAB CETUXIMAB 1 Unknown 8 DF, OTHER BIWEEKLY U U 209974 125084 8 DF INJECTION
127222691 12722269 2 C IRINOTECAN IRINOTECAN 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127222691 12722269 1 Colon cancer
127222691 12722269 2 Colon cancer

Outcome of event

Event ID CASEID OUTC COD
127222691 12722269 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127222691 12722269 Diarrhoea
127222691 12722269 Gastrointestinal mucosal disorder
127222691 12722269 Off label use

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
127222691 12722269 1 20150730 0