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
125160162 12516016 2 F 20141115 20160627 20160630 20160708 EXP US-CELGENEUS-USA-2016066684 CELGENE 47.39 YR Y 0.00000 20160708 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
125160162 12516016 1 PS POMALYST POMALIDOMIDE 1 Oral U 204026 4 MG CAPSULES /wk
125160162 12516016 2 SS POMALYST POMALIDOMIDE 1 Oral 40 MILLIGRAM U 204026 5 MG CAPSULES
125160162 12516016 3 SS VELCADE BORTEZOMIB 1 Subcutaneous U U UNKNOWN 66188 1.3 MG/M**2 UNKNOWN /wk
125160162 12516016 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 1.3 MILLIGRAM/SQ. METER U U UNKNOWN 0 40 MG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125160162 12516016 1 Plasma cell myeloma
125160162 12516016 3 Plasma cell myeloma
125160162 12516016 4 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
125160162 12516016 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125160162 12516016 Engraftment syndrome
125160162 12516016 Febrile neutropenia

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
125160162 12516016 1 20140603 20141107 0
125160162 12516016 2 20150310 0
125160162 12516016 3 20140603 20141107 0
125160162 12516016 4 20140603 20141107 0