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
126776331 12677633 1 I 20160726 20160816 20160823 20160823 PER US-ACTELION-A-US2016-141157 ACTELION 38.00 YR A F Y 0.00000 20160823 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
126776331 12677633 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, UNK OP023P0101 21290 125 MG TABLET
126776331 12677633 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, UNK MA0299X 21779 5 UG INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126776331 12677633 1 Pulmonary arterial hypertension
126776331 12677633 2 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126776331 12677633 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126776331 12677633 Chest pain
126776331 12677633 Chronic respiratory failure
126776331 12677633 Pulmonary hypertension
126776331 12677633 Treatment noncompliance

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
126776331 12677633 1 20090721 0
126776331 12677633 2 20150408 0