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
127496421 12749642 1 I 20160714 20160912 20160916 20160916 EXP US-AMGEN-USACT2016123686 AMGEN 67.00 YR E M Y 104.30000 KG 20160916 OT 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
127496421 12749642 1 PS carfilzomib CARFILZOMIB 1 Intravenous (not otherwise specified) 36 MG/M2, PER CHEMO REGIM 202714 36 MG/M**2 INTRAVENOUS INFUSION
127496421 12749642 2 SS rituximab RITUXIMAB 1 Intravenous (not otherwise specified) 375 MG/M2, PER CHEMO REGIM 0 375 MG/M**2 INJECTION
127496421 12749642 3 SS lenalidomide LENALIDOMIDE 1 Oral 15 MG, PER CHEMO REGIM 0 15 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127496421 12749642 1 Mantle cell lymphoma
127496421 12749642 2 Mantle cell lymphoma
127496421 12749642 3 Mantle cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
127496421 12749642 HO
127496421 12749642 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127496421 12749642 Cardiac disorder
127496421 12749642 Dyspnoea

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found