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
100824134 10082413 4 F 20140331 20140926 20140416 20140930 EXP GB-ONYX-2014-0737 ONYX 55.00 YR F Y 0.00000 20140930 N MD 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
100824134 10082413 1 PS carfilzomib CARFILZOMIB 1 INTRAVENOUS D 71057 INTRAVENOUS INFUSION
100824134 10082413 2 SS carfilzomib CARFILZOMIB 1 INTRAVENOUS D 71057 INTRAVENOUS INFUSION
100824134 10082413 3 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 ORAL D 0 TABLET
100824134 10082413 4 C lenalidomide LENALIDOMIDE 1 ORAL D 0 CAPSULE
100824134 10082413 5 C DEXAMETHASONE. DEXAMETHASONE 1 ORAL D 0 40 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100824134 10082413 1 Plasma cell myeloma
100824134 10082413 3 Plasma cell myeloma
100824134 10082413 4 Plasma cell myeloma
100824134 10082413 5 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
100824134 10082413 OT
100824134 10082413 LT
100824134 10082413 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100824134 10082413 Pulmonary embolism
100824134 10082413 Supraventricular tachycardia

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
100824134 10082413 1 20140320 20140321 0
100824134 10082413 2 20140327 0
100824134 10082413 3 20140320 0
100824134 10082413 4 20140320 20140330 0
100824134 10082413 5 20140320 0