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Cevimeline

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Cevimeline
Names
Pronunciationse vim' e leen[1]
Trade namesEvoxac
  • (2R,2R)-2'-Methylspiro[4-azabicyclo[2.2.2]octane-2,5'-[1,3]oxathiolane]
Clinical data
Drug classMuscarinic agonist[1]
Main usesDry mouth[1]
Side effectsIncreased sweating, runny nose, nausea, diarrhea, headaches, dizziness, visual disturbances, tiredness[1]
Pregnancy
category
  • C
Routes of
use
By mouth (capsules)
External links
AHFS/Drugs.comMonograph
MedlinePlusa608025
Legal
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetics
Protein binding<20%
Chemical and physical data
FormulaC10H17NOS
Molar mass199.31 g·mol−1
3D model (JSmol)
  • O1[C@H](SC[C@@]12CN3CCC2CC3)C
  • InChI=1S/C10H17NOS/c1-8-12-10(7-13-8)6-11-4-2-9(10)3-5-11/h8-9H,2-7H2,1H3/t8-,10-/m1/s1 checkY
  • Key:WUTYZMFRCNBCHQ-PSASIEDQSA-N checkY

Cevimeline, sold under the brand nameEvoxac, is a medication used to treatdry mouth due toSjögren's syndrome orradiation therapy.[1] It is similar topilocarpine.[2] It is taken by mouth.[1]

Side effects are usually mild and may include increased sweating, runny nose, nausea, diarrhea, headaches, dizziness, visual disturbances, and tiredness.[1] Safety in pregnancy is unclear.[2] It is amuscarinic agonist, which results in increased saliva production.[1]

Cevimeline was approved for medical use in the United States in 2000.[2] It is available as ageneric medication.[3] In the United States a month of medication costs about 52 USD as of 2021.[3]

Contents

Medical use

Dosage

The typical dose is 30 mg three times daily.[1]

Side effects

Known side effects includenausea,vomiting,diarrhea, excessivesweating,rash,headache,runny nose,cough,drowsiness,hot flashes,blurred vision, anddifficulty sleeping.[4]

Contraindications includeasthma andangle closure glaucoma.[citation needed]

Mechanism of action

By activating the M3 receptors of theparasympathetic nervous system, cevimeline stimulates secretion by thesalivary glands, thereby alleviating dry mouth.

See also

  • Pilocarpine — a similar parasympathomimetic medication for dry mouth (xerostomia)
  • Bethanechol — a similar muscarinic parasympathomimetic with longer-lasting effect

References

  1. 1.01.11.21.31.41.51.61.71.8"Cevimeline".LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. National Institute of Diabetes and Digestive and Kidney Diseases. 2012.Archived from the original on 6 May 2021. Retrieved3 January 2022.
  2. 2.02.12.2"Cevimeline Monograph for Professionals".Drugs.com.Archived from the original on 28 January 2021. Retrieved3 January 2022.Cite error: Invalid<ref> tag; name "AHFS2022" defined multiple times with different content
  3. 3.03.1"Cevimeline Prices, Coupons & Savings Tips - GoodRx".GoodRx.Archived from the original on 26 September 2016. Retrieved3 January 2022.
  4. [1]Archived 2017-09-30 at theWayback Machine MedicineNet: Cevimeline. Accessed 10/12/2007

External links

Identifiers:
mAChRs
Agonists
Antagonists
Precursors
(andprodrugs)

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