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
120369804 12036980 4 F 20160315 20160711 20160208 20160724 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-006073 BRISTOL MYERS SQUIBB 43.00 YR F Y 0.00000 20160724 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
120369804 12036980 1 PS COUMADIN WARFARIN SODIUM 1 Unknown U 00014802 9218
120369804 12036980 2 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD SBFX 0 10 MG TABLET QD
120369804 12036980 3 SS REVATIO SILDENAFIL CITRATE 1 Unknown U 0
120369804 12036980 4 SS REMODULIN TREPROSTINIL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120369804 12036980 1 Product used for unknown indication
120369804 12036980 2 Product used for unknown indication
120369804 12036980 3 Product used for unknown indication
120369804 12036980 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120369804 12036980 HO
120369804 12036980 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120369804 12036980 Cellulitis
120369804 12036980 Diarrhoea
120369804 12036980 Headache
120369804 12036980 Infusion site cellulitis
120369804 12036980 Syncope

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
120369804 12036980 2 20150902 0