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
126914601 12691460 1 I 20121130 20140808 20160826 20160826 PER US-CELGENEUS-163-21880-14082393 CELGENE 0.00 Y 0.00000 20160826 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
126914601 12691460 1 PS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 10 MG CAPSULES
126914601 12691460 2 SS REVLIMID LENALIDOMIDE 1 Oral 20 MILLIGRAM U UNKNOWN 21880 10 MG CAPSULES
126914601 12691460 3 SS REVLIMID LENALIDOMIDE 1 Oral U UNKNOWN 21880 10 MG CAPSULES
126914601 12691460 4 SS DECADRON DEXAMETHASONE 1 Oral U UNKNOWN 0 20 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126914601 12691460 1 Plasma cell myeloma
126914601 12691460 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126914601 12691460 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126914601 12691460 Urinary tract 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
126914601 12691460 1 20091231 0
126914601 12691460 2 20100120 20100322 0
126914601 12691460 3 20100422 20130524 0
126914601 12691460 4 20100528 20121130 0