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
126850251 12685025 1 I 20160506 20160822 20160825 20160825 PER US-CELGENEUS-USA-2016085961 CELGENE 74.75 YR Y 0.00000 20160825 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
126850251 12685025 1 PS REVLIMID LENALIDOMIDE 1 Oral 10 MILLIGRAM U U UNKNOWN 21880 10 MG CAPSULES
126850251 12685025 2 SS ELOTUZUMAB. ELOTUZUMAB 1 Intravenous drip U U 0 1690 MG UNKNOWN /min
126850251 12685025 3 SS DECADRON DEXAMETHASONE 1 Oral 1690 MILLIGRAM U U 0 28 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126850251 12685025 1 Plasma cell myeloma
126850251 12685025 2 Plasma cell myeloma
126850251 12685025 3 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
126850251 12685025 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126850251 12685025 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
126850251 12685025 1 20140319 20160420 0
126850251 12685025 2 20140319 20160420 0
126850251 12685025 3 20160319 20160420 0