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
118887855 11888785 5 F 20150506 20160923 20160105 20160927 EXP CN-JNJFOC-20151224697 JANSSEN 42.23 YR A F Y 50.00000 KG 20160927 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
118887855 11888785 1 PS TRABECTEDIN TRABECTEDIN 1 Intravenous (not otherwise specified) N 4181;4182 207953 INTRAVENOUS INFUSION
118887855 11888785 2 SS TRABECTEDIN TRABECTEDIN 1 Intravenous (not otherwise specified) CYCLE 1 N 4181;4182 114938 1.65 MG INTRAVENOUS INFUSION
118887855 11888785 3 SS DOXIL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) N 14890;14891;14892 50718 LIPOSOME INJECTION
118887855 11888785 4 SS DOXIL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) CYCLE 1 N 14890;14891;14892 36778 45 MG LIPOSOME INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118887855 11888785 2 Neoplasm malignant
118887855 11888785 4 Neoplasm malignant

Outcome of event

Event ID CASEID OUTC COD
118887855 11888785 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118887855 11888785 Neutrophil count decreased
118887855 11888785 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
118887855 11888785 2 20150422 0
118887855 11888785 4 20150422 0