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
107025995 10702599 5 F 20141223 20160923 20150109 20160930 EXP GB-AMGEN-GBRCT2015000464 AMGEN 66.00 YR E M Y 0.00000 20160930 OT GB GB

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
107025995 10702599 1 PS carfilzomib CARFILZOMIB 1 Intravenous (not otherwise specified) 20 MG/M2, PER CHEMO REGIM Y 202714 20 MG/M**2 INTRAVENOUS INFUSION
107025995 10702599 2 SS lenalidomide LENALIDOMIDE 1 Oral 25 MG, PER CHEMO REGIM Y 0 25 MG CAPSULE
107025995 10702599 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 500 MG, PER CHEMO REGIM 0 500 MG
107025995 10702599 4 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 40 MG, PER CHEMO REGIM 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107025995 10702599 1 Plasma cell myeloma
107025995 10702599 2 Plasma cell myeloma
107025995 10702599 3 Plasma cell myeloma
107025995 10702599 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
107025995 10702599 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
107025995 10702599 Infection

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
107025995 10702599 1 20141222 0
107025995 10702599 2 20141222 0
107025995 10702599 3 20141222 0
107025995 10702599 4 20141222 0