The Safety Rates Drug Report

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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
126650161 12665016 1 I 20160725 20160810 20160818 20160818 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-066157 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160818 CN 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
126650161 12665016 1 PS SPRYCEL DASATINIB 1 Oral 100 MG, QD U 21986 100 MG QD
126650161 12665016 2 SS SPRYCEL DASATINIB 1 Oral 70 MG, UNK U 21986 70 MG
126650161 12665016 3 C LASIX FUROSEMIDE 1 Unknown UNK U 0
126650161 12665016 4 C POTASSIUM POTASSIUM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126650161 12665016 1 Product used for unknown indication
126650161 12665016 3 Product used for unknown indication
126650161 12665016 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126650161 12665016 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126650161 12665016 Pulmonary oedema

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
126650161 12665016 1 201512 0