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
125848332 12584833 2 F 20160721 20160722 20160727 EXP US-ACTELION-A-US2016-139697 ACTELION 49.00 YR A M Y 0.00000 20160727 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
125848332 12584833 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6-9X DAILY MA02A59 21779 5 UG INHALATION VAPOUR, SOLUTION
125848332 12584833 2 SS REVATIO SILDENAFIL CITRATE 1 Oral U U 0
125848332 12584833 3 C LETAIRIS AMBRISENTAN 1 U 0
125848332 12584833 4 C XARELTO RIVAROXABAN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125848332 12584833 1 Pulmonary arterial hypertension
125848332 12584833 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125848332 12584833 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125848332 12584833 Adverse reaction
125848332 12584833 Feeling hot
125848332 12584833 Fluid retention
125848332 12584833 Left ventricular failure
125848332 12584833 Oxygen saturation decreased
125848332 12584833 Petechiae
125848332 12584833 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
125848332 12584833 1 20160422 0