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
123489674 12348967 4 F 20150516 20160801 20160509 20160811 EXP US-CELGENEUS-USA-2016050198 CELGENE 70.66 YR M Y 54.03000 KG 20160811 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
123489674 12348967 1 PS REVLIMID LENALIDOMIDE 1 Oral 21880 25 MG CAPSULES
123489674 12348967 2 SS REVLIMID LENALIDOMIDE 1 Oral 20 MILLIGRAM 21880 5 MG CAPSULES
123489674 12348967 3 SS VELCADE BORTEZOMIB 1 Intravenous drip 66188 3.5 MG UNKNOWN /wk
123489674 12348967 4 SS CYTOXAN CYCLOPHOSPHAMIDE 1 Oral 3.5 MILLIGRAM 21880 300 MG/M**2 UNKNOWN /wk
123489674 12348967 5 SS DECADRON DEXAMETHASONE 1 Oral 300 MILLIGRAM/SQ. METER 21880 20 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123489674 12348967 1 Plasma cell myeloma
123489674 12348967 3 Plasma cell myeloma
123489674 12348967 4 Plasma cell myeloma
123489674 12348967 5 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
123489674 12348967 OT
123489674 12348967 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123489674 12348967 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
123489674 12348967 1 20110802 20111219 0
123489674 12348967 2 20120416 20150219 0
123489674 12348967 3 20150430 20150618 0
123489674 12348967 4 20150430 20150618 0
123489674 12348967 5 20150430 20150618 0