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
125037352 12503735 2 F 20150105 20160706 20160628 20160719 EXP JP-ELI_LILLY_AND_COMPANY-JP201606008859 ELI LILLY AND CO 50.00 YR M Y 56.00000 KG 20160718 OT 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
125037352 12503735 1 PS ERBITUX CETUXIMAB 1 Unknown 250 MG/M2, WEEKLY (1/W) 776.316 MG/M2 U U 125084 250 MG/M**2 INJECTION /wk
125037352 12503735 2 SS CISPLATIN. CISPLATIN 1 Unknown 100 MG/M2, UNKNOWN U U 0 100 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125037352 12503735 1 Lip and/or oral cavity cancer
125037352 12503735 2 Lip and/or oral cavity cancer

Outcome of event

Event ID CASEID OUTC COD
125037352 12503735 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125037352 12503735 Dermatitis acneiform
125037352 12503735 Pigmentation disorder
125037352 12503735 White blood cell count decreased

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
125037352 12503735 1 20141215 20160205 0
125037352 12503735 2 20141215 20160205 0