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
89575312 8957531 2 F 20120716 20160811 20121210 20160823 EXP GB-CELGENEUS-167-21880-12072257 CELGENE 60.00 YR M Y 0.00000 20160823 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
89575312 8957531 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U 21880 10 MG CAPSULES
89575312 8957531 2 SS REVLIMID LENALIDOMIDE 1 Oral Y U 21880 10 MG CAPSULES
89575312 8957531 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 300 MILLIGRAM U 0 300 MG TABLETS
89575312 8957531 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 30 MILLIGRAM U 0 30 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89575312 8957531 1 Plasma cell myeloma
89575312 8957531 3 Plasma cell myeloma
89575312 8957531 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
89575312 8957531 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
89575312 8957531 Carpal tunnel syndrome
89575312 8957531 Fatigue
89575312 8957531 Malaise

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
89575312 8957531 1 20120527 0
89575312 8957531 2 20120723 0
89575312 8957531 3 20120705 0
89575312 8957531 4 20120526 0