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
125775141 12577514 1 I 20160715 20160720 20160720 PER US-CELGENEUS-USA-2016074299 CELGENE 0.00 M Y 0.00000 20160720 OT US US

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
125775141 12577514 1 PS REVLIMID LENALIDOMIDE 1 Oral N U A2088N 21880 25 MG CAPSULES QD
125775141 12577514 2 SS REVLIMID LENALIDOMIDE 1 Oral N U A2088N 21880 10 MG CAPSULES QD
125775141 12577514 3 SS REVLIMID LENALIDOMIDE 1 Oral N U A2088N 21880 5 MG CAPSULES
125775141 12577514 4 SS VELCADE BORTEZOMIB 1 Unknown N U 0 UNKNOWN
125775141 12577514 5 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125775141 12577514 1 Plasma cell myeloma
125775141 12577514 4 Product used for unknown indication
125775141 12577514 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125775141 12577514 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125775141 12577514 Fatigue

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
125775141 12577514 1 201308 0
125775141 12577514 2 201309 0
125775141 12577514 3 201605 0