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Under the trade name Mircera, Roche Pharmaceuticals received approval from the U.S. Food and Drug Administration (FDA) in January 2008 to market a continuous erythropoiesis receptor activator (methoxy polyethylene glycol-epoetin beta) for the treatment of anemia in patients with chronic kidney disease, including in those undergoing dialysis.
A U.S. Federal Appeals Court ruled in September 2009, that Mircera infringed a patent held by Amgen Inc. The court refused to lift an injunction entered in the fall of 2008 which barred Roche from selling Mircera in the United States. [8] The injunction has since expired and Mircera has been available on the U.S. market since 2015. [9]
Mircera. The following types of ESAs are available: [citation needed] Erythropoietin (Epo) Epoetin alfa (Procrit, Epogen) Epoetin beta (NeoRecormon) Epoetin zeta (Silapo, Retacrit) Darbepoetin alfa (Aranesp) Methoxy polyethylene glycol-epoetin beta (Mircera)
The executive order gives the Domestic Policy Council 90 days to submit a list of policy recommendations. A collection of fertility treatment devices photographed on Friday, Oct. 11, 2024.
Despite Trump signing an executive order to make IVF more accessible and affordable, the overall state of affairs for women’s health and reproductive rights in America is dismal at best.
President Donald Trump's executive orders have begun to disrupt patient care in the United States, as some providers cannot access essential federal funding, according to interviews with a dozen ...
A liver support system or diachysis is a type of therapeutic device to assist in performing the functions of the liver. Such systems focus either on removing the accumulating toxins (liver dialysis), or providing additional replacement of the metabolic functions of the liver through the inclusion of hepatocytes to the device (bioartificial liver device).
The FDA on Thursday approved a new class of pain medication that provides an alternative to opioids. It will be sold under the brand name Journavx.