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
123187893 12318789 3 F 20160218 20160708 20160429 20160715 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-030871 BRISTOL MYERS SQUIBB 66.29 YR M Y 0.00000 20160715 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
123187893 12318789 1 PS SPRYCEL DASATINIB 1 Oral 140 MG, QD 61320 MG Y 21986 140 MG QD
123187893 12318789 2 SS SPRYCEL DASATINIB 1 Oral 140 MG, QD 61320 MG Y 21986 140 MG QD
123187893 12318789 3 SS SPRYCEL DASATINIB 1 Oral 140 MG, QD 61320 MG Y 21986 140 MG QD
123187893 12318789 4 C GABAPENTIN. GABAPENTIN 1 Oral 300 MG, QD U 0 300 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123187893 12318789 1 Chronic myeloid leukaemia
123187893 12318789 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123187893 12318789 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123187893 12318789 Ascites
123187893 12318789 Dyspnoea
123187893 12318789 Fatigue
123187893 12318789 Localised oedema
123187893 12318789 Mood altered
123187893 12318789 Pleural effusion
123187893 12318789 Pulmonary oedema
123187893 12318789 Weight decreased
123187893 12318789 Weight increased

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
123187893 12318789 1 20141209 0
123187893 12318789 2 20141208 20160507 0
123187893 12318789 3 20141112 0