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
125565161 12556516 1 I 20140730 20160711 20160714 20160714 PER US-CELGENEUS-USA-2016072724 CELGENE 60.00 YR F Y 61.10000 KG 20160714 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
125565161 12556516 1 PS REVLIMID LENALIDOMIDE 1 Oral 25 MILLIGRAM U U 21880 25 MG CAPSULES
125565161 12556516 2 SS VELCADE BORTEZOMIB 1 Subcutaneous U U 66188 1.3 MG/M**2 UNKNOWN BIW
125565161 12556516 3 SS DECADRON DEXAMETHASONE 1 Oral 1.3 MILLIGRAM/SQ. METER U U 66188 20 MG UNKNOWN
125565161 12556516 4 SS Panobinostat PANOBINOSTAT 1 Oral 20 MILLIGRAM U U 66188 10 MG UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125565161 12556516 1 Plasma cell myeloma
125565161 12556516 2 Plasma cell myeloma
125565161 12556516 3 Plasma cell myeloma
125565161 12556516 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125565161 12556516 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125565161 12556516 Pyrexia
125565161 12556516 Rash

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
125565161 12556516 1 20140717 20140730 0
125565161 12556516 2 20140717 20140727 0
125565161 12556516 3 20140717 20140728 0
125565161 12556516 4 20140717 20140728 0