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
127608311 12760831 1 I 201605 20160816 20160919 20160919 EXP AR-ELI_LILLY_AND_COMPANY-AR201608011438 ELI LILLY AND CO 41.00 YR F Y 0.00000 20160915 MD AR AR

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
127608311 12760831 1 PS CETUXIMAB CETUXIMAB 1 Unknown UNK, UNKNOWN U 125084 250 MG/M**2 INJECTION /wk
127608311 12760831 2 C PACLITAXEL. PACLITAXEL 1 Unknown 80 MG/M2, UNKNOWN U 0 80 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127608311 12760831 1 Head and neck cancer
127608311 12760831 2 Head and neck cancer

Outcome of event

Event ID CASEID OUTC COD
127608311 12760831 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127608311 12760831 Blister
127608311 12760831 Dermatitis acneiform
127608311 12760831 Eye infection staphylococcal
127608311 12760831 Impetigo
127608311 12760831 Rash pustular
127608311 12760831 Scab
127608311 12760831 Skin infection

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
127608311 12760831 1 20151217 0