Product Description
Azilsartan medoxomil (Edarbi, Takeda) is a new addition to the ARB class of antihypertensive agents. As an ARB, azilsartan medoxomil selectively inhibits angiotensin II from binding to the angiotensin II type-1 receptor (AT1). This receptor inhibition provides the antihypertensive activity of azilsartan medoxomil because it blocks the pressor effects of angiotensin II. (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278144/)
Mechanisms of Action: ARB Blocker
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Approved
Approved Countries: Austria | Bangladesh | Belgium | Canada | Croatia | Czech | Egypt | Estonia | European Medicines Agency | Finland | Greece | Hong Kong | Hungary | Iceland | India | Ireland | Italy | Jordan | Korea | Latvia | Lebanon | Lithuania | Mexico | Netherlands | Peru | Philippines | Poland | Portugal | Russia | Saudi Arabia | Slovakia | Spain | Sweden | Switzerland | Taiwan | Thailand | Ukraine | United Arab Emirates
Approved Indications: None
Known Adverse Events: None
Company: None
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
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