Neupane Purushottam, Thada Pawan Kumar, Singh Pramod, Faisal Abdul Rafae, Rai Niraj, Poudel Prabhat, Waleed Madeeha Subhan, Quinonez Jonathan, Ruxmohan Samir, Jain Esha
Medicine and Surgery, Punjab Medical College, Faisalabad, PAK.
Research and Academic Affairs, Larkin Community Hospital, Miami, USA.
Cureus. 2023 Jan 13;15(1):e33746. doi: 10.7759/cureus.33746. eCollection 2023 Jan.
The use of Edaravone, given orally, for the treatment of amyotrophic lateral sclerosis (ALS) was officially approved by the Federal Drug Association (FDA) in 2017. ALS is a rare and progressive degenerative disease that worsens over time. It attacks and destroys the nerve cells that control voluntary muscles, thus leading to weakness, eventual paralysis, and, ultimately death. Edaravone was given initially intravenously, but recent evidence shows better results with oral suspension. This narrative review is aimed to investigate the benefit of Edaravone for the management of ALS, compare it to Riluzole, discuss its mechanism of action, route of use, and side effects, and ultimately discuss future implications of this pharmacotherapy.
2017年,口服依达拉奉用于治疗肌萎缩侧索硬化症(ALS)获得了美国食品药品监督管理局(FDA)的正式批准。ALS是一种罕见的进行性退行性疾病,会随着时间的推移而恶化。它侵袭并破坏控制随意肌的神经细胞,从而导致虚弱、最终瘫痪,并最终导致死亡。依达拉奉最初是静脉给药,但最近的证据表明口服混悬液效果更好。这篇叙述性综述旨在研究依达拉奉治疗ALS的益处,将其与利鲁唑进行比较,讨论其作用机制、使用途径和副作用,并最终探讨这种药物治疗的未来意义。