pregabalin
type of chemical entity
subclass of3-(Aminomethyl)-5-methylhexanoic acid Sesa
has useaduro Sesa
stereoisomer ofCHEMBL167003 Sesa
chemical formulaC₈H₁₇NO₂ Sesa
canonical SMILESCC(C)CC(CC(=O)O)CN Sesa
isomeric SMILESCC(C)C[C@@H](CC(=O)O)CN Sesa
World Health Organisation international non-proprietary namepregabalin Sesa
pregnancy categoryAustralian pregnancy category B3, US pregnancy category C Sesa
LiverTox likelihood scoreLiverTox toxicity likelihood category C Sesa
subject has roleanalgesic, anticonvulsant agent, calcium channel blocker, anxiolytic Sesa

Pregabalin din a wɔde nim no wɔ dwa so ne Lyrica. Ɛyɛ aduro a nneɛma bi te sɛ an anticonvulsant, analgesic, ne anxiolytic amino acid wɔ mu. Wɔde sa ɛtweɛ yadeɛ. Wɔtumi nso de sa nyarewa bi te sɛ adwenemu yaw( neuropathic pain), fibromyalgia, restless legs syndrome, opioid withdrawal, ne generalized anxiety disorder (GAD).[1][2] Pregabalin alssan nso wɔ antiallodynic su.[3][4][5]

Baabi a Menyaa Mmoa Firiiɛ

sesa
  1. Frampton JE (September 2014). "Pregabalin: a review of its use in adults with generalized anxiety disorder". CNS Drugs. 28 (9): 835–854. doi:10.1007/s40263-014-0192-0. PMID 25149863. S2CID 5349255.
  2. Iftikhar IH, Alghothani L, Trotti LM (December 2017). "Gabapentin enacarbil, pregabalin and rotigotine are equally effective in restless legs syndrome: a comparative meta-analysis". European Journal of Neurology. 24 (12): 1446–1456. doi:10.1111/ene.13449. PMID 28888061. S2CID 22262972.
  3. Wyllie E, Cascino GD, Gidal BE, Goodkin HP (February 17, 2012). Wyllie's Treatment of Epilepsy: Principles and Practice. Lippincott Williams & Wilkins. p. 423. ISBN 978-1-4511-5348-4.
  4. Kirsch D (October 10, 2013). Sleep Medicine in Neurology. John Wiley & Sons. p. 241. ISBN 978-1-118-76417-6.
  5. Frye M, Moore K (2009). "Gabapentin and Pregabalin". In Schatzberg AF, Nemeroff CB (eds.). The American Psychiatric Publishing Textbook of Psychopharmacology. pp. 767–77. doi:10.1176/appi.books.9781585623860.as38. ISBN 978-1-58562-309-9. Archived from the original on February 27, 2024. Retrieved September 1, 2022.