User:Mr. Ibrahem/Nimesulide

From Wikipedia, the free encyclopedia
Mr. Ibrahem/Nimesulide
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
By mouth, rectal, topical
Drug classNSAIDs
Legal status
Legal status
  • AU: S4 (Prescription only)
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Protein binding>97.5%
MetabolismLiver
Elimination half-life1.8–4.7h
ExcretionKidney (50%), fecal (29%)
Identifiers
  • N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
Chemical and physical data
FormulaC13H12N2O5S
Molar mass308.31 g·mol−1
3D model (JSmol)
  • [O-][N+](=O)c2cc(Oc1ccccc1)c(cc2)NS(=O)(=O)C
  • InChI=1S/C13H12N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h2-9,14H,1H3 checkY
  • Key:HYWYRSMBCFDLJT-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Nimesulide is a nonsteroidal anti-inflammatory drug (NSAID) used for acute pain and painful periods.[1][3] Use is recommended for less than 15 days.[1] There is no evidence of benefit over other NSAIDs and due to side effects it is considered a second line treatment.[2][1]

Side effects may include liver problems including those that result in the need for a liver transplant or death.[2][1][4] Other side effects may include stomach problems.[1] This issue occurs at a higher rate than other NSAIDs.[2] It works primarily by blocking the enzyme COX-2 that makes prostaglandins.[5]

Nimesulide has been approved for medical use in parts of Europe since 1985.[1] It has never been approved in the United States, United Kingdom, Canada, Australia, New Zealand, or Japan due to safety concerns.[2] Approval has been withdrawn in a number of countries including Spain, Ireland, and Finland.[2]

References[edit]

  1. ^ a b c d e f g "Nimesulide". European Medicines Agency. 2012. Archived from the original on 22 October 2020. Retrieved 27 October 2020.
  2. ^ a b c d e f "Nimesulide must be withdrawn worldwide due to serious liver damage". www.ti.ubc.ca. Archived from the original on 8 November 2020. Retrieved 27 October 2020.
  3. ^ "Nimesulide". Drugs.com. Archived from the original on 12 November 2020. Retrieved 27 October 2020.
  4. ^ Kwon, J; Kim, S; Yoo, H; Lee, E (2019). "Nimesulide-induced hepatotoxicity: A systematic review and meta-analysis". PloS one. 14 (1): e0209264. doi:10.1371/journal.pone.0209264. PMID 30677025.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  5. ^ Aronson, Jeffrey K. (2016). Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions. Elsevier. p. 738. ISBN 978-0-444-53716-4. Archived from the original on 10 November 2021. Retrieved 27 October 2020.