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Sofosbuvir/velpatasvir, sold under the brand name Epclusa among others, is a fixed-dose combination medication for the treatment of hepatitis C in adults. [2] [5] [6] [7] It combines sofosbuvir and velpatasvir. [2] [5] [6] It is more than 90% effective for hepatitis C genotypes one through six. [2]
[6] [1] [5] The immediate-release form has an elimination half-life of 2.5 hours [6] [2] while the half-life of the extended-release form is 7 hours. [1] Viloxazine was first described by 1972 [10] and was marketed as an antidepressant in Europe in 1974. [6] [11] It was not marketed in the United States at this time. [12]
Download as PDF; Printable version; In other projects ... This is a complete list of clinically approved prescription antidepressants ... (Qelbree, formerly Vivalan ...
(Reuters) -The U.S. Food and Drug Administration on Monday delayed traditional approval for Liquidia Corp's inhaled drug for types of lung disorders, and allowed only tentative clearances, sending ...
Pirepemat (IRL-752) – "cortical enhancer" / serotonin 5-HT 7 receptor antagonist and α 2C-adrenergic receptor antagonist, other actions [96] [97] Pozanicline (A-87089.0, ABT-089) – α 4 β 2 nicotinic acetylcholine receptor agonist [98] SEP-225432 – serotonin–norepinephrine–dopamine reuptake inhibitor [99]
(Reuters) -The U.S. Food and Drug Administration has granted approval to a treatment from Verona Pharma for a chronic lung disease that commonly affects smokers, the U.K.-based company said on ...
The PDUFA date serves as a good first approximation of when a final decision on drug approval can be expected. Sponsors frequently publish PDUFA dates for their pending applications, [ 1 ] and while there is no official list of PDUFA dates, [ 10 ] several websites collect PDUFA dates from press announcements in a calendar form.
The U.S. Food and Drug Administration (FDA) on Friday approved a new drug used for treating schizophrenia in adults, according to a press release. “This drug takes the first new approach to ...
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