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
124572426 12457242 6 F 20160805 20160610 20160810 EXP US-ACTELION-A-US2016-136838 ACTELION 64.00 YR A M Y 0.00000 20160810 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
124572426 12457242 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9X/DAY Y MA02A59 21779 5 UG INHALATION VAPOUR, SOLUTION
124572426 12457242 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 2.5 MCG, 6-9X/DAY Y 21779 2.5 UG INHALATION VAPOUR, SOLUTION
124572426 12457242 3 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 2.5 MCG, Q 2-3 HOURS Y 21779 2.5 UG INHALATION VAPOUR, SOLUTION
124572426 12457242 4 C OXYGEN. OXYGEN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124572426 12457242 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124572426 12457242 HO
124572426 12457242 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124572426 12457242 Disease progression
124572426 12457242 Drug hypersensitivity
124572426 12457242 Dyspnoea
124572426 12457242 Oxygen consumption increased
124572426 12457242 Pulmonary arterial hypertension
124572426 12457242 Pulmonary fibrosis
124572426 12457242 Tension
124572426 12457242 Ventilation perfusion mismatch

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
124572426 12457242 1 20160513 0
124572426 12457242 2 20160519 20160727 0