TREPULMIX

This brand name is authorized in Austria, Croatia, Estonia, Ireland, Italy, Lithuania, Poland, Romania, Spain.

Active ingredients

The drug TREPULMIX contains one active pharmaceutical ingredient (API):

1
UNII 7JZ75N2NT6 - TREPROSTINIL SODIUM
 

Treprostinil is a vasodilator that is used for the treatment of pulmonary arterial hypertension. Treprostinil is a potent oral antiplatelet agent. The major pharmacologic actions of treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds and inhibition of platelet aggregation. Other studies have shown that treprostinil causes a dose-related negative inotropic and lusitropic effect. Treprostinil had high affinity for the Prostaglandin D2 receptor (DP1), Prostaglandin E2 receptor EP2 subtype (EP2) and Prostaglandin D2 receptor (IP) receptors (Ki 4.4, 3.6 and 32 nM, respectively), low affinity for EP1 and EP4 receptors and even lower affinity for EP3, Prostaglandin F (FP) and thromboxane (TP) receptors. Treprostinil has demonstrated a unique effect on PPAR gamma, a transcription factor important in vascular pathogenesis as a mediator of proliferation, inflammation and apoptosis.

 
Read more about Treprostinil

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 TREPULMIX Solution for infusion MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
B01AC21 Treprostinil B Blood and blood forming organs → B01 Antithrombotic agents → B01A Antithrombotic agents → B01AC Platelet aggregation inhibitors excl. heparin
Discover more medicines within B01AC21

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1815601, 1815612, 1815623, 1815634
ES Centro de información online de medicamentos de la AEMPS 1191419001, 1191419002, 1191419003, 1191419004
IT Agenzia del Farmaco 048724013, 048724025, 048724037, 048724049
LT Valstybinė vaistų kontrolės tarnyba 1089836, 1089837, 1089838, 1089839
PL Rejestru Produktów Leczniczych 100436680, 100436697, 100436705, 100436711
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W66823001, W66824001, W66825001, W66826001

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