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
93390463 9339046 3 F 20130530 20160901 20130610 20160915 EXP GB-CELGENEUS-167-20785-13060081 CELGENE 51.00 YR F Y 0.00000 20160915 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
93390463 9339046 1 PS THALIDOMIDE THALIDOMIDE 1 Oral 200 MILLIGRAM U 20785 200 MG CAPSULES QD
93390463 9339046 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral U 20785 500 MG TABLETS QD
93390463 9339046 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral U 20785 40 MG TABLETS QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93390463 9339046 1 Plasma cell myeloma
93390463 9339046 2 Plasma cell myeloma
93390463 9339046 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
93390463 9339046 LT
93390463 9339046 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
93390463 9339046 Deep vein thrombosis

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
93390463 9339046 1 20130430 0
93390463 9339046 2 20130430 0
93390463 9339046 3 20130430 0