Treprostinil sodium - @ Peripheral Vasodilators
Drug Name:
Treprostinil sodium - @ Peripheral Vasodilators
List Of Brands:
Indication Type Description:
Pharmacology/ Pharmacokinetics
Drug Interaction:
Anticoagulants- because treprostinil inhibits platelet aggregation there is a potential for inceased risk of bleeding, especially amongst patients maintained on anticoagulants Antihypertensive agents, diuretics or vasodilators- reduction in blood pressure caused by treprostinil may be exacerbated by drugs that by thmeselves alter blood presssure. such a hypertensive agents, diuretics or vasodilators
Indication:
Pulmonary arterial hypertension ( PAH )
Adverse Reaction:
CNS- dizziness ( 9%), headache (27%)
Dermatologic - pruritus (8% ), rash (14%),
GI - diarrhea (25%), nausea (22%), Miscellaneous- edema (9%) , hypotension (4%), infusion site pain (85%), infusion site reaction (83% ) jaw pain (13%), vasodilation (11%)
Contra-Indications:
Known hypersensitivity to the drug
Warnings/precautions-
Administration- Route- indicated for subcutaneous or IV use only Troprostinil should be used by clinician experienced in the diagnosis and treatment of PAH Renal and hepatic function impairment- use caution in patients with hepatic or renal function impairment
Dosages/ Overdosage Etc:
Pulmonary arterial hypertension (PAH ) -
Dosage-
Initial dose- Treprostinil can be administerd by continous infusion, preferably infused subcutaneously but can be administered by central IV line if subcutaneous rout is not tolerated he infusion rate is 1.25ng/kg/min. the rate can be reduced to 0.625ng/kg/mim in required
Patient Information:
Therapy with treprostinil will be needed for prolonged periods, possibly years.
Carefully consider the patients ability to accept and care for catheter and to use an infusion pump.
Pharmacology/ Pharmacokinetics:
Pharmacology-
Major pharmacologic actions of terprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds and inhibition of platelet aggregation
Pharmacokinetics-
Treprostinil is rapidly and completely absorbed after simultaneous infusion with an absolute bioavailability approximately 100% . Steady state concentration occured in approximately 10 hours Treprostinil is substantially metabolized by the liver. The elimination is biphasic with a terminal half life of appox. 4 hours
Pregnancy and lactation:
Pregnancy- Use treprostinil during pregnancy only if clearly needed.
Lactation- Excercise caution when treprostenil is administered to a beast feeding woman.
Children- safety and efficacy in children haved not been established
Elderly- use caution in dose selection, reflecting the greater frequency of decreased hepatic, renal or cardiac function and of concomittant disease or other drug therapy