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
125307481 12530748 1 I 20141118 20141121 20160706 20160706 EXP GB-CELGENEUS-GBR-2014120312 CELGENE 85.00 YR M Y 0.00000 20160706 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
125307481 12530748 1 PS REVLIMID LENALIDOMIDE 1 Oral 25 MILLIGRAM U 21880 25 MG CAPSULES
125307481 12530748 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral U 0 500 MG TABLETS
125307481 12530748 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 500 MILLIGRAM U 0 20 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125307481 12530748 1 Plasma cell myeloma
125307481 12530748 2 Plasma cell myeloma
125307481 12530748 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125307481 12530748 DE
125307481 12530748 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125307481 12530748 Infection

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
125307481 12530748 1 20141102 20141119 0
125307481 12530748 2 20141102 0
125307481 12530748 3 20141102 20141119 0