The Safety Rates Drug Report

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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
125960512 12596051 2 F 20160523 20160726 20160922 PER US-AMGEN-USASP2016066166 AMGEN 0.00 F Y 0.00000 20160922 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
125960512 12596051 1 PS KYPROLIS CARFILZOMIB 1 Unknown UNK UNK, UNK U 202714 INTRAVENOUS INFUSION
125960512 12596051 2 SS NEUPOGEN FILGRASTIM 1 Unknown UNK UNK, UNK U 0 UNKNOWN FORMULATION
125960512 12596051 3 C DARATUMUMAB DARATUMUMAB 1 Unknown UNK 0
125960512 12596051 4 C POMALYST POMALIDOMIDE 1 UNK 0
125960512 12596051 5 C REVLIMID LENALIDOMIDE 1 UNK 0
125960512 12596051 6 C IXAZOMIB IXAZOMIB 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125960512 12596051 1 Plasma cell myeloma
125960512 12596051 2 Product used for unknown indication
125960512 12596051 3 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125960512 12596051 Disease progression
125960512 12596051 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