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
124658703 12465870 3 F 20160601 20160701 20160614 20160713 EXP US-ACTELION-A-NJ2016-137424 ACTELION 65.00 YR E F Y 0.00000 20160713 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
124658703 12465870 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 272000 MG OP023P0101 21290 125 MG TABLET BID
124658703 12465870 2 C FLOLAN EPOPROSTENOL SODIUM 1 U 0
124658703 12465870 3 C WARFARIN WARFARIN 1 U 0
124658703 12465870 4 C TREPROSTINIL DIOLAMIN TREPROSTINIL DIOLAMINE 1 U 0
124658703 12465870 5 C SILDENAFIL. SILDENAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124658703 12465870 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124658703 12465870 HO
124658703 12465870 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124658703 12465870 Fall
124658703 12465870 Joint injury
124658703 12465870 Loss of consciousness
124658703 12465870 Pulmonary hypertension

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
124658703 12465870 1 20130628 20160620 0