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
121733437 12173343 7 F 2016 20160811 20160311 20160816 EXP DE-ACTELION-A-US2016-132392 ACTELION 42.00 YR A M Y 0.00000 20160816 OT DE KR

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
121733437 12173343 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK Y 21779 INHALATION VAPOUR, SOLUTION
121733437 12173343 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK Y 21779 INHALATION VAPOUR, SOLUTION
121733437 12173343 3 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) UNK Y 21779 INHALATION VAPOUR, SOLUTION
121733437 12173343 4 C SILDENAFIL. SILDENAFIL 1 U 0
121733437 12173343 5 C WARFARIN WARFARIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121733437 12173343 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
121733437 12173343 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121733437 12173343 Concomitant disease aggravated
121733437 12173343 Drug ineffective
121733437 12173343 Dyspnoea
121733437 12173343 Hypoaesthesia
121733437 12173343 Inappropriate schedule of drug administration
121733437 12173343 Nausea
121733437 12173343 Pulmonary oedema

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
121733437 12173343 1 20151231 201606 0
121733437 12173343 2 201603 0