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
122969696 12296969 6 F 20151112 20160819 20160422 20160902 EXP GB-CELGENEUS-GBR-2015114821 CELGENE 57.65 YR M Y 0.00000 20160902 OT GB GB

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
122969696 12296969 1 PS POMALIDOMIDE POMALIDOMIDE 1 Oral U 0 4 MG CAPSULES
122969696 12296969 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown U 0 40 MG UNKNOWN
122969696 12296969 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown U 0 40 MG UNKNOWN
122969696 12296969 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122969696 12296969 1 Plasma cell myeloma
122969696 12296969 2 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
122969696 12296969 DE
122969696 12296969 HO
122969696 12296969 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122969696 12296969 Neutropenic sepsis
122969696 12296969 Plasma cell myeloma
122969696 12296969 Renal failure

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
122969696 12296969 1 20150818 20150901 0
122969696 12296969 2 20150818 20150909 0
122969696 12296969 3 201409 0
122969696 12296969 4 201101 0