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
125918471 12591847 1 I 201602 20160224 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-003089 UNITED THERAPEUTICS 74.27 YR M Y 83.45000 KG 20160726 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
125918471 12591847 1 PS ORENITRAM TREPROSTINIL 1 Oral 2 MG, TID Y 2100370 203496 2 MG TABLET TID
125918471 12591847 2 SS ORENITRAM TREPROSTINIL 1 Oral 1.75 MG, TID Y 2100370 203496 1.75 MG TABLET TID
125918471 12591847 3 SS ORENITRAM TREPROSTINIL 1 Oral UNK Y 2100397 203496 TABLET
125918471 12591847 4 SS ORENITRAM TREPROSTINIL 1 Oral UNK Y 2100477 203496 TABLET
125918471 12591847 5 SS BUMEX BUMETANIDE 1 Unknown UNK, TID 0 TID
125918471 12591847 6 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125918471 12591847 1 Pulmonary arterial hypertension
125918471 12591847 5 Product used for unknown indication
125918471 12591847 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125918471 12591847 Chills
125918471 12591847 Dyspnoea
125918471 12591847 Fatigue
125918471 12591847 Headache
125918471 12591847 Hypotension
125918471 12591847 Influenza like illness
125918471 12591847 Pain
125918471 12591847 Weight increased

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
125918471 12591847 1 20160120 0