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
125982731 12598273 1 I 20160714 20160727 20160727 EXP AU-CELGENEUS-AUS-2016073711 CELGENE 0.00 M Y 0.00000 20160727 PH AU AU

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
125982731 12598273 1 PS THALIDOMIDE THALIDOMIDE 1 Oral 100 MILLIGRAM U U 44320 100 MG CAPSULES QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125982731 12598273 1 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125982731 12598273 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125982731 12598273 Plasma cell myeloma
125982731 12598273 Renal disorder

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
125982731 12598273 1 2016 0