Nimesulide

From Wikipedia, the free encyclopedia - View original article

Nimesulide
Systematic (IUPAC) name
N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
Clinical data
AHFS/Drugs.comInternational Drug Names
Pregnancy cat. ?
Legal statusPrescription Only (S4) (AU) Usually prescription only
RoutesOral, rectal, topical
Pharmacokinetic data
Protein binding>97.5%
MetabolismHepatic
Half-life1.8–4.7h
ExcretionRenal (50%), fecal (29%)
Identifiers
CAS number51803-78-2 YesY
ATC codeM01AX17 M02AA26
PubChemCID 4495
DrugBankDB04743
ChemSpider4339 YesY
UNIIV4TKW1454M YesY
KEGGD01049 YesY
ChEBICHEBI:44445 N
ChEMBLCHEMBL56367 YesY
Chemical data
FormulaC13H12N2O5S 
Mol. mass308.311 g/mol
 N (what is this?)  (verify)
 
Jump to: navigation, search
Nimesulide
Systematic (IUPAC) name
N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
Clinical data
AHFS/Drugs.comInternational Drug Names
Pregnancy cat. ?
Legal statusPrescription Only (S4) (AU) Usually prescription only
RoutesOral, rectal, topical
Pharmacokinetic data
Protein binding>97.5%
MetabolismHepatic
Half-life1.8–4.7h
ExcretionRenal (50%), fecal (29%)
Identifiers
CAS number51803-78-2 YesY
ATC codeM01AX17 M02AA26
PubChemCID 4495
DrugBankDB04743
ChemSpider4339 YesY
UNIIV4TKW1454M YesY
KEGGD01049 YesY
ChEBICHEBI:44445 N
ChEMBLCHEMBL56367 YesY
Chemical data
FormulaC13H12N2O5S 
Mol. mass308.311 g/mol
 N (what is this?)  (verify)

Nimesulide is a relatively COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic properties. Its approved indications are the treatment of acute pain, the symptomatic treatment of osteoarthritis and primary dysmenorrhoea in adolescents and adults above 12 years old. It has a multifactorial mode of action and is characterized by a fast onset of action.

History[edit]

It was launched in Italy for the first time as Aulin and Mesulid in 1985 and is presently available in more than 50 countries worldwide, among others France, Portugal, Greece, Switzerland, Belgium, Russia and Brazil. Nimesulide has never been filed for Food and Drug Administration (FDA) evaluation in the United States, where it is not marketed.[1] Due to concerns about the risk of hepatotoxicity, Nimesulide has been withdrawn from market in many countries.

Advantages[edit]

Availability[edit]

100mg Nimesulide pills

It is available in a variety of forms: tablets, powder for dissolution in water, suppositories, mouth dissolving tablets and topical gel (Sulidin Gel).

A recent evaluation from EMEA (the European Medicines Agency) concluded that the overall benefit/risk profile of nimesulide is favourable and in line with that of the other NSAIDs (such as for example, diclofenac, ibuprofen, naproxen).

Trade names[edit]

Nimesulide is available through the world as original product with the following trademarks: Sulide, Nimalox, Mesulid (Novartis, Brazil, Boehringer Ingelheim, Greece), Coxtal (Sanofi, China, Czech, Bulgaria),Sintalgin (Abbott, Brazil), Eskaflam (GSK, Brazil, Mexico), Octaprin, Nimside (Teva,Pakistan), Nise (Dr. Reddy’s Laboratories, India, Russia, Venezuela, Vietnam, Ukraine), Nilsid (Egypt); Aulin, Ainex, Drexel, Donulide, Edrigyl, Enetra, Heugan, Mesulid, Minapon, NeRelid, Nexen, Nidolon, Nilden (Mexico); Nimed, Nimedex, Nimesil, Nimulid, Nimutab, Nimdase, Nimopen-MP (India), Nisulid, Nodard Plus, Nicip, Nimcap, Nic-P, Nic-Spas (India); Novolid, Relmex (Ecuador); Remisid (Ukraine); Scaflam, Scaflan, Sulidin (Turkey); Modact-IR (Pakistan);[2] Sulidene and Zolan for veterinary use. Many generic and copy-products also exist (Lusemin, Medicox, Nidol, Nimalox, Nimesil, Nimotas, Nimulid, Nizer, Sorini, Ventor, Vionim, Neolide, Willgo among others), new-aid (S.A.R.), Nims (Nepal).

Pharmacokinetics[edit]

Nimesulide is rapidly absorbed following oral administration.[3]

Nimesulide undergoes extensive biotransformation, mainly to 4-hydroxynimesulide (which also appears to be biologically active).[3]

Food, gender and advanced age have negligible effects on nimesulide pharmacokinetics.[3]

Moderate renal impairment does not necessitate dosage adjustment while patients with severe renal impairment or hepatic impairment are contraindicated.[4]

Nimesulide has a relatively rapid onset of action, with meaningful reductions in pain and inflammation observed within 15 minutes from drug intake.[5][6]

The therapeutic effects of Nimesulide are the result of its complete mode of action which targets a number of key mediators of the inflammatory process such as: COX-2 mediated prostaglandins, free radicals, proteolytic enzymes and histamine.[5] Clinical evidence is available to support a particularly good profile in terms of gastrointestinal tolerability.[7]

Nimesulide Events[edit]

Madras High Court revokes ban on manufacture and sale of Nimesulide[edit]

On September 13, 2011 Madras High Court has revoked a ban on manufacture and sale of paediatric drugs nimesulide and phenylpropanolamine (PPA).[8]

EMEA re-confirms efficacy of Nimesulide[edit]

On 23 June 2011, the European Medicines Agency concluded the review of systemic nimesulide-containing medicine. They concluded that the benefits of systemic nimesulide continue to outweigh their risks in the treatment of patients with acute pain and primary dysmenorrhea.

Central Drugs Standard Control Organization of India Restricts use of Nimesulide under 12 years of age.[edit]

Several reports have been made of adverse drug reactions in India.[9][10][11][12] On Feb 12, 2011, Express India that the Union Ministry of Health and Family Welfare had finally decided to ban the pediatric use of the analgesic, Nimesulide suspension.[13] From 10 March 2011 onwards Nimesulide formulations for human use in children below 12 years of age has been banned[14]

EMA confirms the positive benefit/risk ratio[edit]

On September 21, 2007 the EMA released a press release on their review on the liver-related safety of nimesulide. The EMA has concluded that the benefits of these medicines outweigh their risks, but that there is a need to limit the duration of use to ensure that the risk of patients developing liver problems is kept to a minimum. Therefore the EMA has limited the use of systemic formulations (tablets, solutions, suppositories) of nimesulide to 15 days.[15]

Irish Medicines Board (IMB) suspends Nimesulide containing drugs (15 May 2007)[edit]

The Irish Medicines Board (IMB) has decided to suspend Nimesulide from the Irish market and refer it to the EU Committee for Human Medicinal Products (CHMP) for a review of its benefit/risk profile. The decision is due to the reporting of six (6) cases of potentially related liver failures to the IMB by the National Liver Transplant Unit, St Vincent Hospital. These cases occurred in the period from 1999 to 2006.[16]

Delhi High Court verdict[edit]

In response to a petition against Nimesulide filed in May 2004, the Delhi High Court passed a verdict that Nimesulide will continue to be marketed in India since the concerns over its side effect profile are unsubstantiated. The High court sought the help of leading pediatricians and medical agencies from India to arrive at the conclusion that Nimesulide is a safe NSAID with a side effect profile that is comparable to the other NSAIDs.

Bribes allegedly paid in Italy to spare few drugs from official scrutiny[edit]

In May 2008, Italy's leading daily paper Corriere della Sera and other media outlets reported that a top-ranking official at Italy's medicines agency AIFA had been filmed by police while accepting bribes from employees of pharmaceutical companies.[17][18] The money was allegedly being paid to ensure that certain drugs would be spared scrutiny from the drugs watchdog. The investigation had started in 2005 following suspicions that some AIFA drug tests had been faked. Eight arrests were made. Presently[when?], nimesulide can be bought carrying a prescription from a physician, that is kept as a receipt at the chemist shop, nominally allowing strong control over selling.

The original manufacturer of Nimesulide is Helsinn Healthcare SA, Switzerland, which acquired the rights for the drug in 1976. After the patent protection had terminated, a number of other companies have started production and marketing of Nimesulide.

European Medicines Agency reports favourable benefit/risk ratio[edit]

On August 1, 2003 the Committee for Proprietary Medicinal Products (CPMP) of the European Medicines Agency (EMA) reported that the benefit/risk profile of nimesulide containing medicinal products (Aulin, Mesulide, Nimed and associated product names) for systemic and topical use is favourable and that Marketing Authorisations should be maintained/granted. The CPMP recommended to restrict the use of nimesulide to the indications of treatment of acute pain, symptomatic treatment of painful osteoarthritis and primary dysmenorrhoea for the systemic formulations and symptomatic relief of pain associated with sprains and acute tendinitis for the topical formulation.[19]

Alembic Ltd. issued a circular asking wholesalers and retailers to withdraw all stocks of Nimegesic Drops (a pediatric dosage form of nimesulide) in 2003, consistent with the fact that nimesulide is, like most NSAIDs, not indicated in children.[20]

Side effects[edit]

Nimesulide is known to be hepatotoxic (damaging to the liver). The use of nimesulide in children under the age of 12 is contraindicated.

The drug has certain side effects, that can affect individuals in different ways. The following are some of the side effects, that are often associated with the drug:

Women should use the drug with caution during lactation and it is contraindicated during pregnancy.[21]

References[edit]

  1. ^ Traversa G, Bianchi C, Da Cas R, Abraha I, Menniti-Ippolito F, Venegoni M (July 2003). "Cohort study of hepatotoxicity associated with nimesulide and other non-steroidal anti-inflammatory drugs". BMJ 327 (7405): 18–22. doi:10.1136/bmj.327.7405.18. PMC 164233. PMID 12842950. 
  2. ^ [1]
  3. ^ a b c Bernareggi A (October 1998). "Clinical pharmacokinetics of nimesulide". Clin Pharmacokinet 35 (4): 247–74. PMID 9812177. 
  4. ^ Microsoft Word - opnh.P.Nimesulide .EMEA-CPMP-3086-03-en-Final.doc
  5. ^ a b Rainsford KD (June 2006). "Nimesulide – a multifactorial approach to inflammation and pain: scientific and clinical consensus". Curr Med Res Opin 22 (6): 1161–70. doi:10.1185/030079906X104849. PMID 16846549. 
  6. ^ Bianchi M, Broggini M (2003). "A randomised, double-blind, clinical trial comparing the efficacy of nimesulide, celecoxib and rofecoxib in osteoarthritis of the knee". Drugs 63 (Suppl 1): 37–46. PMID 14506910. 
  7. ^ Laporte JR, Ibáñez L, Vidal X, Vendrell L, Leone R (2004). "Upper gastrointestinal bleeding associated with the use of NSAIDs: newer versus older agents". Drug Saf 27 (6): 411–20. PMID 15144234. 
  8. ^ http://www.scribd.com/doc/64907025/Madras-High-Court-Revokes-Ban-on-Manufacture-and-Sale-PPA
  9. ^ Safety of nimesulide. CD ROM, Appropriate Use of Antipyretics / Analgesics in Children, Health Informatics, New Delhi, 2004.
  10. ^ Rahman SZ, Khan RA (2004). "Is nimesulide safe in a cardiovascular-Compromised patient?". Indian J Pharmacol 36: 252–3. 
  11. ^ Khan RA, Rahman SZ (2004). "A Case Report on Nimesulide and its Relation with Angina". J Pharmacovigilance Drug Safety 1: 19–21. 
  12. ^ Khan RA, Rahman SZ (2004). "Nimesulide Induced Coronary Artery Insufficiency – A Case Report". J Pharmacovigilance Drug Safety 1: 11–3. 
  13. ^ http://www.expressindia.com/latest-news/Nimesulide-for-kids-to-be-banned-finally/749147/
  14. ^ CDSCO website-wide gazette notification GSR 82(E) dated 10.03.2011.
  15. ^ EMA press release on nimesulide September 2007
  16. ^ IMB Announces Immediate Suspension of the Marketing of Medicines Containing Nimesulide
  17. ^ «Mazzette per evitare i controlli sull'Aulin». Mario Pappagallo, Corriere della Sera, 23 May 2008
  18. ^ Italian medicines agency officials arrested in corruption probe. Manufacturing Chemist
  19. ^ European Commission CPMP favourable opinion on nimesulide
  20. ^ The end begins
  21. ^ http://www.pharmaceutical-drug-manufacturers.com/pharmaceutical-drugs/nimesulide.html

External links[edit]