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
127333651 12733365 1 I 20160826 20160909 20160912 20160912 EXP US-TAKEDA-2016MPI007945 TAKEDA 0.00 F Y 0.00000 20160912 CN 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
127333651 12733365 1 PS NINLARO IXAZOMIB 1 Oral UNK U 208462 CAPSULE
127333651 12733365 2 SS DARZALEX DARATUMUMAB 1 Unknown UNK U 0
127333651 12733365 3 SS BENDAMUSTINE BENDAMUSTINE 1 Unknown UNK U 0
127333651 12733365 4 SS BIAXIN CLARITHROMYCIN 1 Unknown U 0
127333651 12733365 5 SS THALIDOMIDE THALIDOMIDE 1 Unknown UNK U 0
127333651 12733365 6 SS REVLIMID LENALIDOMIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127333651 12733365 1 Plasma cell myeloma
127333651 12733365 2 Plasma cell myeloma
127333651 12733365 3 Plasma cell myeloma
127333651 12733365 4 Plasma cell myeloma
127333651 12733365 5 Plasma cell myeloma
127333651 12733365 6 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
127333651 12733365 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127333651 12733365 Alanine aminotransferase increased
127333651 12733365 Hepatotoxicity
127333651 12733365 Off label use

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
127333651 12733365 1 20160811 0