The U.S. Food and Drug Administration today approved Adempas (riociguat) to treat adults with two forms of pulmonary hypertension. Pulmonary hypertension is caused by abnormally high blood pressure in ...
Male patients are not enrolled in the Adempas REMS Program. Female patients of reproductive potential must comply with the pregnancy testing and contraception requirements. Pharmacies must be ...
WHIPPANY, N.J., Oct. 24, 2017 /PRNewswire/ -- Bayer announced today that data from its pulmonary disease franchise will be presented in scientific sessions at the 2017 annual meeting of the American ...
ADEMPAS (riociguat) tablets Bayer HealthCare announced that the FDA has approved Adempas (riociguat) tablets, a first-in-class drug, for the treatment of persistent/recurrent chronic thromboembolic ...
Bayer announced results from the phase IV REPLACE (Riociguat rEplacing PDE-5i Therapy evaLuated Against Continued PDE-5i thErapy) study, in which intermediate-risk adult patients with pulmonary ...
SILVER SPRING, Md. — The Food and Drug Administration today approved Adempas, also known as riociguat, to treat adults with two forms of pulmonary hypertension, which is caused by abnormally high ...
HealthDay News — The FDA has approved riociguat (Adempas, Bayer) to treat chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension (PAH) of various causes. The drug is ...
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