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
126532781 12653278 1 I 20121105 20121105 20160815 20160815 EXP US-ACTELION-A-NJ2012-74342 ACTELION 88.00 YR E F Y 0.00000 20160815 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
126532781 12653278 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP021P0101,OP021P0101,OP023P01017 21290 125 MG TABLET BID
126532781 12653278 2 SS TYVASO TREPROSTINIL 1 Unknown 3 BREATHS U 0 QID
126532781 12653278 3 C COUMADIN WARFARIN SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126532781 12653278 1 Pulmonary arterial hypertension
126532781 12653278 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126532781 12653278 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126532781 12653278 Acute respiratory failure
126532781 12653278 Cardiac failure congestive
126532781 12653278 Coagulopathy
126532781 12653278 Dyspnoea
126532781 12653278 Fluid retention
126532781 12653278 Pleural effusion

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
126532781 12653278 1 20060518 0
126532781 12653278 2 20121102 0