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
125682381 12568238 1 I 2016 20160218 20160718 20160718 PER US-CELGENEUS-USA-2016024478 CELGENE 68.93 YR M Y 114.86000 KG 20160718 MD 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
125682381 12568238 1 PS REVLIMID LENALIDOMIDE 1 Oral Y U A2032A 21880 20 MG CAPSULES QD
125682381 12568238 2 SS REVLIMID LENALIDOMIDE 1 Oral Y U A2032A 21880 10 MG CAPSULES
125682381 12568238 3 SS REVLIMID LENALIDOMIDE 1 Oral 1 MILLIGRAM Y U A2032A 21880 10 MG CAPSULES
125682381 12568238 4 SS REVLIMID LENALIDOMIDE 1 Oral Y U A2032A 21880 10 MG CAPSULES
125682381 12568238 5 SS REVLIMID LENALIDOMIDE 1 Oral Y U A2032A 21880 10 MG CAPSULES
125682381 12568238 6 SS VELCADE BORTEZOMIB 1 Unknown U U 0 UNKNOWN
125682381 12568238 7 C COUMADIN WARFARIN SODIUM 1 Oral 0 1 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125682381 12568238 1 Plasma cell myeloma recurrent
125682381 12568238 6 Product used for unknown indication
125682381 12568238 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125682381 12568238 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125682381 12568238 Neutropenia
125682381 12568238 Pancytopenia
125682381 12568238 Pneumonia

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
125682381 12568238 1 201410 0
125682381 12568238 2 201412 0
125682381 12568238 3 20150709 0
125682381 12568238 4 20150917 20160531 0
125682381 12568238 5 201606 0