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
127253451 12725345 1 I 20160830 20160908 20160908 EXP US-ELI_LILLY_AND_COMPANY-US201609001226 ELI LILLY AND CO 0.00 Y 0.00000 20160906 OT US US

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
127253451 12725345 1 PS Cetuximab CETUXIMAB 1 Unknown 400 MG/M2, UNKNOWN U U 125084 400 MG/M**2 INJECTION
127253451 12725345 2 SS Cetuximab CETUXIMAB 1 Unknown 250 MG/M2, UNKNOWN U U 125084 250 MG/M**2 INJECTION
127253451 12725345 3 SS CARBOPLATIN. CARBOPLATIN 1 Unknown 2 DF, UNKNOWN U U 0 2 DF
127253451 12725345 4 SS PACLITAX NAB PACLITAXEL 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
127253451 12725345 1 Squamous cell carcinoma of head and neck
127253451 12725345 3 Squamous cell carcinoma of head and neck
127253451 12725345 4 Squamous cell carcinoma of head and neck

Outcome of event

Event ID CASEID OUTC COD
127253451 12725345 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127253451 12725345 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found