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
126032391 12603239 1 I 20160316 20160419 20160728 20160728 EXP DE-ACTELION-A-US2016-135235 ACTELION 0.00 M Y 0.00000 20160728 OT DE FR

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
126032391 12603239 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) 5 MCG, 6ID U 21779 5 UG INHALATION VAPOUR, SOLUTION
126032391 12603239 2 SS VENTAVIS ILOPROST 1 Respiratory (inhalation) 2.5 MCG, UNK U 21779 2.5 UG INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126032391 12603239 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
126032391 12603239 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126032391 12603239 Condition aggravated
126032391 12603239 Drug ineffective
126032391 12603239 Dyspepsia
126032391 12603239 Flushing
126032391 12603239 Headache
126032391 12603239 Intentional product misuse
126032391 12603239 Malaise
126032391 12603239 Nausea
126032391 12603239 Oedema peripheral
126032391 12603239 Pruritus

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
126032391 12603239 1 20160316 20160629 0