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
124575664 12457566 4 F 20160831 20160610 20160912 EXP US-ACTELION-A-NJ2016-137547 ACTELION 60.00 YR A F Y 0.00000 20160912 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
124575664 12457566 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP023P0101, OP021P0101, OP026P0101 21290 125 MG TABLET BID
124575664 12457566 2 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124575664 12457566 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124575664 12457566 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124575664 12457566 Cardiopulmonary failure
124575664 12457566 Chest pain
124575664 12457566 Drug dose omission
124575664 12457566 Dyspepsia
124575664 12457566 Dyspnoea
124575664 12457566 Heart valve incompetence
124575664 12457566 Stomatitis

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
124575664 12457566 1 20160309 0