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
119287183 11928718 3 F 20160408 20160705 20160119 20160715 EXP US-ACTELION-A-US2016-129806 ACTELION 13.00 MON I M Y 0.00000 20160715 PH 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
119287183 11928718 1 PS TRACLEER BOSENTAN 1 Oral 15.625 MG, BID 8812 MG 21290 15.625 MG TABLET BID
119287183 11928718 2 C SILDENAFIL. SILDENAFIL 1 U 0
119287183 11928718 3 C REMODULIN TREPROSTINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119287183 11928718 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
119287183 11928718 DE
119287183 11928718 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119287183 11928718 Death
119287183 11928718 Gastrostomy
119287183 11928718 Mechanical ventilation
119287183 11928718 Pulmonary arterial hypertension
119287183 11928718 Tracheostomy

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
119287183 11928718 1 20150701 20160408 0