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
122186686 12218668 6 F 20160315 20160805 20160329 20160810 EXP CN-JNJFOC-20160316280 JANSSEN 65.85 YR A F Y 59.00000 KG 20160810 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
122186686 12218668 1 PS TRABECTEDIN TRABECTEDIN 1 Intravenous drip Y N 4370045 207953 1.65 MG INTRAVENOUS INFUSION
122186686 12218668 2 SS TRABECTEDIN TRABECTEDIN 1 Intravenous drip Y N 4370045 114938 INTRAVENOUS INFUSION
122186686 12218668 3 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 Intravenous drip Y N 4371121 50718 45 MG LIPOSOME INJECTION
122186686 12218668 4 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 Intravenous drip Y N 4371121 36778 LIPOSOME INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122186686 12218668 1 Ovarian cancer
122186686 12218668 2 Ovarian cancer
122186686 12218668 3 Ovarian cancer
122186686 12218668 4 Ovarian cancer

Outcome of event

Event ID CASEID OUTC COD
122186686 12218668 HO
122186686 12218668 OT
122186686 12218668 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122186686 12218668 Alanine aminotransferase increased
122186686 12218668 Febrile neutropenia
122186686 12218668 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
122186686 12218668 1 20160308 0
122186686 12218668 3 20160308 0