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
119021575 11902157 5 F 20160725 20160108 20160804 EXP US-ACTELION-A-NJ2015-129484 ACTELION 75.00 YR E F Y 0.00000 20160804 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
119021575 11902157 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP060P0101,OP021P0101,OP023P0101 21290 125 MG TABLET BID
119021575 11902157 2 SS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP026P0101 21290 125 MG TABLET BID
119021575 11902157 3 C SILDENAFIL. SILDENAFIL 1 U 0
119021575 11902157 4 C TYVASO TREPROSTINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119021575 11902157 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
119021575 11902157 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119021575 11902157 Blood count abnormal
119021575 11902157 Dizziness
119021575 11902157 Haemorrhoidal haemorrhage
119021575 11902157 Transfusion

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
119021575 11902157 1 20130205 0