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
126247691 12624769 1 I 20160621 20160729 20160805 20160805 EXP GB-AMGEN-GBRCT2016099076 AMGEN 60.00 YR A F Y 0.00000 20160805 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
126247691 12624769 1 PS carfilzomib CARFILZOMIB 1 Intravenous (not otherwise specified) 20/36 MG/M2, PER CHEMO REGIM 202714 INTRAVENOUS INFUSION
126247691 12624769 2 SS lenalidomide LENALIDOMIDE 1 Oral 25 MG, PER CHEMO REGIM 0 25 MG CAPSULE
126247691 12624769 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 40 MG, PER CHEMO REGIM 0 40 MG
126247691 12624769 4 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 500 MG, PER CHEMO REGIM 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126247691 12624769 1 Plasma cell myeloma
126247691 12624769 2 Plasma cell myeloma
126247691 12624769 3 Plasma cell myeloma
126247691 12624769 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126247691 12624769 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126247691 12624769 Anaemia
126247691 12624769 Diarrhoea
126247691 12624769 Duodenitis
126247691 12624769 Gastritis

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
126247691 12624769 1 20150923 20160127 0
126247691 12624769 2 20150923 0
126247691 12624769 3 20150923 0
126247691 12624769 4 20150923 0