Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Medical uses  





2 Side-effects  



2.1  Pregnancy  







3 Chemistry  





4 Mechanism of action  





5 Society and culture  



5.1  Brand names  







6 References  














Mesalazine






العربية
تۆرکجه
Català
Cymraeg
Deutsch
Español
فارسی
Français

Hrvatski
Italiano
עברית
Македонски
Nederlands

ି
Polski
Português
Русский
Slovenščina
Српски / srpski
Srpskohrvatski / српскохрватски
Suomi
Svenska
Türkçe
Українська
Tiếng Vit

 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 

(Redirected from Lialda)

Mesalazine
Clinical data
Trade namesAsacol, Lialda, Pentasa, Delzicol, others[1]
Other namesmesalamine, 5-aminosalicylic acid, 5-ASA, Mesalamine (USAN US)
AHFS/Drugs.comMonograph
MedlinePlusa688021
License data
Pregnancy
category
  • Routes of
    administration
    By mouth, rectal
    ATC code
    Legal status
    Legal status
    • AU: S4 (Prescription only)[3]
  • CA: ℞-only[4][5][6]
  • UK: POM (Prescription only)[7]
  • US: ℞-only[8][9][10]
  • EU: Rx-only[11]
  • Pharmacokinetic data
    Bioavailabilityorally: 20–30% absorbed
    rectally: 10–35%
    MetabolismRapidly & extensively metabolized intestinal mucosal wall and the liver
    Elimination half-life5 hours after initial dose.
    At steady state 7 hours
    Identifiers
    • 5-Amino-2-hydroxybenzoic acid

    CAS Number
    PubChem CID
    IUPHAR/BPS
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEBI
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.001.745 Edit this at Wikidata
    Chemical and physical data
    FormulaC7H7NO3
    Molar mass153.137 g·mol−1
    3D model (JSmol)
    Melting point283 °C (541 °F)
    • O=C(O)c1cc(ccc1O)N

    • InChI=1S/C7H7NO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,8H2,(H,10,11) checkY

    • Key:KBOPZPXVLCULAV-UHFFFAOYSA-N checkY

      (verify)

    Mesalazine, also known as mesalamineor5-aminosalicylic acid (5-ASA), is a medication used to treat inflammatory bowel disease, including ulcerative colitis and Crohn's disease.[1] It is generally used for mildly to moderately severe disease.[1] It is taken by mouth or rectally.[1] The formulations which are taken by mouth appear to be similarly-effective.[12]

    Common side-effects include headache, nausea, abdominal pain, and fever.[1] Serious side-effects may include pericarditis, liver problems, and kidney problems.[1][12] Use in pregnancy and breastfeeding appears safe.[12] In people with a sulfa allergy certain formulations may result in problems.[1] Mesalazine is an aminosalicylate and anti-inflammatory.[1][12] It works by direct contact with the intestines.[1]

    Mesalazine was approved for medical use in the United States in 1987.[1][8] It is on the World Health Organization's List of Essential Medicines.[13] It is available as a generic medication.[1][14][15][16] In 2021, it was the 239th most commonly prescribed medication in the United States, with more than 1 million prescriptions.[17][18]

    Medical uses

    [edit]

    It is used to treat inflammatory bowel disease, including ulcerative colitis and Crohn's disease (effective only in colonic diseases).[1]

    In 2022 Germany introduced guidance to use mesalamine to treat acute uncomplicated diverticulitis.[19]

    Side-effects

    [edit]

    Most often reported side-effects are gastrointestinal (GI) (but may also include headache), including: nausea, diarrhea, and abdominal pain.[7]

    Very rarely, use of mesalazine has been associated with an exacerbation of the symptoms of colitis, Stevens Johnson syndrome, and erythema multiforme.[7]

    Pregnancy

    [edit]

    There is no data on use in pregnant women, but the drug does cross the placenta and is excreted in breast milk. The drug should not be used in children under two years of age,[7] people with kidney disease,[7] or people who are allergic to aspirin.[7]

    Chemistry

    [edit]

    Mesalazine is the active moietyofsulfasalazine, which is metabolized to sulfapyridine and mesalazine.[20] It is also the active component of the prodrug balsalazide along with the inert carrier molecule 4-aminobenzoyl-beta-alanine.[21] It is in the category of disease-modifying antirheumatic drugs (DMARDs) family of medications.[22] It is unclear exactly how it works.[22] Mesalazine is claimed to be a PPAR-γ agonist.[23]

    Mechanism of action

    [edit]

    Exact mechanism of mesalazine is unknown, but is speculated that mesalazine decreases synthesis of prostaglandin and leukotriene, modulating the inflammatory response derived from the cyclooxygenase and lipooxygenase pathways.[24] It appears to act locally on colonic mucosa.[25]

    Society and culture

    [edit]

    Brand names

    [edit]

    Mesalazine is sold under various names including Apriso, Asacol, Asacol HD, Canasa, Delzicol, Fivasa, Lialda, Salofalk, Pentasa, Rowasa, Octasa, and Sfrowasa. In Europe, it is sold under the name Salofalk (rectal suppository). [26][27]

    References

    [edit]
    1. ^ a b c d e f g h i j k l "Mesalamine Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists.
  • ^ "Mesalamine Use During Pregnancy". Drugs.com. 18 September 2018. Retrieved 30 December 2019.
  • ^ "Mesalazine Sun/ Mesalz (Sun Pharma ANZ Pty Ltd)". Therapeutic Goods Administration (TGA). 13 January 2023. Retrieved 9 April 2023.
  • ^ "Product monograph brand safety updates". Health Canada. February 2024. Retrieved 24 March 2024.
  • ^ "Regulatory Decision Summary for Mezera". Drug and Health Products Portal. 5 February 2024. Retrieved 2 April 2024.
  • ^ "Drug and medical device highlights 2018: Helping you maintain and improve your health". Health Canada. 14 October 2020. Retrieved 17 April 2024.
  • ^ a b c d e f "Asacol 400mg MR Tablets - Summary of Product Characteristics (SmPC)". (emc). 14 April 2016. Retrieved 30 December 2019.
  • ^ a b "Asacol HD- mesalamine tablet, delayed release". DailyMed. 15 April 2018. Retrieved 30 December 2019.
  • ^ "Pentasa- mesalamine capsule". DailyMed. 8 November 2021. Retrieved 17 May 2022.
  • ^ "Lialda- mesalamine tablet, delayed release". DailyMed. 8 November 2021. Retrieved 17 May 2022.
  • ^ Human Medicines Evaluation Division (15 October 2020). "Active substance: mesalazine" (PDF). List of nationally authorised medicinal products. European Medicines Agency.
  • ^ a b c d British national formulary: BNF 76 (76 ed.). Pharmaceutical Press. 2018. pp. 39–41. ISBN 9780857113382.
  • ^ World Health Organization (2021). World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization. hdl:10665/345533. WHO/MHP/HPS/EML/2021.02.
  • ^ "ANDA Approval Reports - 2017 First Generic Drug Approvals". Food and Drug Administration (FDA). 3 November 2018. Retrieved 8 April 2019.
  • ^ "2022 First Generic Drug Approvals". U.S. Food and Drug Administration (FDA). 3 March 2023. Archived from the original on 30 June 2023. Retrieved 30 June 2023.
  • ^ "Competitive Generic Therapy Approvals". U.S. Food and Drug Administration (FDA). 29 June 2023. Archived from the original on 29 June 2023. Retrieved 29 June 2023.
  • ^ "The Top 300 of 2021". ClinCalc. Archived from the original on 15 January 2024. Retrieved 14 January 2024.
  • ^ "Mesalamine - Drug Usage Statistics". ClinCalc. Retrieved 14 January 2024.
  • ^ Peery AF (12 November 2022). "New German guidelines for the management of diverticulitis". United European Gastroenterology Journal. 10 (9): 913–914. doi:10.1002/ueg2.12331. PMC 9731652. PMID 36302089.
  • ^ Finkel R, Clark MA, Cubeddu LX (2009). Lippincott's Illustrated Reviews: Pharmacology (Fourth ed.). Lippincott Williams & Wilkins. ISBN 978-0-7817-7155-9.
  • ^ "Balsalazide: increasing the choice for patients with ulcerative colitis". Drugs & Therapy Perspectives. 19 (1–4): 1–4. 2003. doi:10.2165/00042310-200319100-00001. S2CID 195230977.
  • ^ a b "Sulfasalazine". The American Society of Health-System Pharmacists. Archived from the original on 21 December 2016. Retrieved 8 December 2016.
  • ^ Cevallos SA, Lee JY, Velazquez EM, Foegeding NJ, Shelton CD, Tiffany CR, et al. (January 2021). Ehrt S (ed.). "5-Aminosalicylic Acid Ameliorates Colitis and Checks Dysbiotic Escherichia coli Expansion by Activating PPAR-γ Signaling in the Intestinal Epithelium". mBio. 12 (1): e03227–20. doi:10.1128/mBio.03227-20. PMC 7845635. PMID 33468700.
  • ^ Nakashima J, Preuss CV (2022). "Mesalamine (USAN)". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 31869178. Retrieved 1 September 2022.
  • ^ Iacucci M, de Silva S, Ghosh S (February 2010). "Mesalazine in inflammatory bowel disease: a trendy topic once again?". Canadian Journal of Gastroenterology. 24 (2): 127–133. doi:10.1155/2010/586092. PMC 2852235. PMID 20151072.
  • ^ "Substance Name: Mesalamine [USAN:USP]". ChemIDplus. Retrieved 2 October 2020.
  • ^ "Mesalamine Uses, Side Effects & Warnings". Drugs.com. 30 August 2019. Retrieved 2 October 2020.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Mesalazine&oldid=1226561444"

    Categories: 
    Anilines
    Anti-inflammatory agents
    Antioxidants
    Gastroenterology
    Salicylic acids
    Drugs developed by AbbVie
    Drugs developed by Takeda Pharmaceutical Company
    Orphan drugs
    Hidden categories: 
    Articles with short description
    Short description is different from Wikidata
    Use dmy dates from November 2022
    Infobox drug with local INN variant
    Drugs with non-standard legal status
    ECHA InfoCard ID from Wikidata
    Drugboxes which contain changes to watched fields
    Wikipedia medicine articles ready to translate
     



    This page was last edited on 31 May 2024, at 12:42 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki