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
125864391 12586439 1 I 20160629 20160715 20160725 20160725 EXP US-UNITED THERAPEUTICS-UNT-2016-011388 UNITED THERAPEUTICS 0.00 A F Y 0.00000 20160725 CN 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
125864391 12586439 1 PS ORENITRAM TREPROSTINIL 1 Oral 0.125 MG, BID 203496 .125 MG TABLET BID
125864391 12586439 2 SS ADCIRCA TADALAFIL 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125864391 12586439 1 Pulmonary arterial hypertension
125864391 12586439 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125864391 12586439 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125864391 12586439 Blood pressure decreased
125864391 12586439 Dehydration
125864391 12586439 Diarrhoea
125864391 12586439 Dysgeusia
125864391 12586439 Oedema peripheral
125864391 12586439 Oxygen saturation decreased
125864391 12586439 Vision blurred

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
125864391 12586439 1 20160608 0