Mefenamic acid drug data and news

Mefenamic acid drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Mefenamic acid
Brand Names/Synonyms AGN-1255; Acide Mefenamique; Bafameritin-M; Bafhameritin-M; Bonabol; CI 473; CI-473; CL 473; CN-35355; Coslan; HL 1; INF 3355; INF-3355; In-M; Lysalgo; Mefacit; Mefanamic Acid; Mefenacid; Mefenamic Acid; Mefenaminsaeure; Mephenamic Acid; Mephenaminic Acid; Methenamic Acid; Namphen; Parkemed; Ponalar; Ponstan; Ponstan Forte; Ponstel; Ponstil; Ponstyl; Pontal; Tamany Bonsan; Tanston; Vialidon
Indication For the treatment of rheumatoid arthritis, osteoarthritis, dysmenorrhea, and mild to moderate pain, inflammation, and fever.
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Description Not Available
Pharmacology Mefenamic acid, an anthranilic acid derivative, is a member of the fenamate group of nonsteroidal anti-inflammatory drugs (NSAIDs). It exhibits anti-inflammatory, analgesic, and antipyretic activities. Similar to other NSAIDs, mefenamic acid inhibits prostaglandin synthetase.
Mechanism Of Action Mefenamic acid binds the prostaglandin synthetase receptors COX-1 and COX-2, inhibiting the action of prostaglandin synthetase. As these receptors have a role as a major mediator of inflammation and/or a role for prostanoid signaling in activity-dependent plasticity, the symptoms of pain are temporarily reduced.
Mefenamic acid News
(When available)
In this article  Dec 30, 2005
Health24.com, Non-steroidal anti-inflammatory drugs (NSAIDs) such as mefenamic acid, ibuprofen and naproxen can also be used to treat certain cases of menorrhagia, as well ...

Dosage Forms BOLUS; CAPSULE; CAPSULE (ENTERIC-COATED); DROPS; LIQUID; LOTION; POWDER; POWDER FOR SOLUTION; SHAMPOO; SOAP BAR; SOLUTION; STICK; SYRUP; TABLET; TABLET (EXTENDED-RELEASE)
Drug_Category Anti-Inflammatory Agents, Non-Steroidal; Cyclooxygenase Inhibitors; ATC:M01AG01
Absorption Mefenamic acid is rapidly absorbed after oral administration.
Interactions Drug Interactions for Mefenamic acid:

Aspirin: As with other NSAIDs, concomitant administration of Ponstel and aspirin is not generally recommended because of the potential of increased adverse effects.

Methotrexate: NSAIDs have been reported to competitively inhibit methotrexate accumulation in rabbit kidney slices. This may indicate that they could enhance the toxicity of methotrexate. Caution should be used when NSAIDs are administered concomitantly with methotrexate.

ACE inhibitors: Reports suggest that NSAIDs may diminish the antihypertensive effect of ACE inhibitors. This interaction should be given consideration in patients taking NSAIDs concomitantly with ACE inhibitors.

Furosemide: Clinical studies, as well as post-marketing observations, have shown that NSAIDs can reduce the natriuretic effect of furosemide and thiazides in some patients. This response has been attributed to inhibition of renal prostaglandin synthesis. During concomitant therapy of Ponstel with furosemide, the patient should be observed closely for signs of renal failure, as well as to assure diuretic efficacy.

Lithium: NSAIDs have produced an elevation of plasma lithium levels and a reduction in renal lithium clearance. The mean minimum lithium concentration increased 15% and the renal clearance was decreased by approximately 20%. These effects have been attributed to inhibition of renal prostaglandin synthesis by the NSAID. Thus, when NSAIDs and lithium are administered concurrently, subjects should be observed carefully for signs of lithium toxicity.

Warfarin: The effects of warfarin and NSAIDs on GI bleeding are synergistic, such that users of both drugs together have a risk of serious GI bleeding higher than users of either drug alone.

Antacids: In a single dose study (n=6), ingestion of an antacid containing 1.7-gram of magnesium hydroxide with 500-mg of mefenamic acid increased the Cmax and AUC of mefenamic acid by 125% and 36%, respectively.¹

A number of compounds are inhibitors of CYP2C9 including fluconazole, lovastatin and trimethoprim. Drug interaction studies of mefenamic acid and these compounds have not been conducted. The possibility of altered safety and efficacy should be considered when Ponstel is used concomitantly with these drugs.

Toxicity Oral, rat LD50: 740 mg/kg. Symptoms of overdose may include severe stomach pain, coffee ground-like vomit, dark stool, ringing in the ears, change in amount of urine, unusually fast or slow heartbeat, muscle weakness, slow or shallow breathing, confusion, severe headache or loss of consciousness.
Organisms Affected Humans and other mammals
Chemical IUPAC Name 2-(2,3-dimethylphenyl)aminobenzoicacid
Chemical Formula C15H15NO2
Molecular Weight 241.285 g/mol
Smiles String CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C
Melting Point 230-231 °C
Water Solubility 20 mg/L
State Solid
LogP/Hphobicity 4.041
Isoelectric Point 4.2
Biotransformation Mefenamic acid undergoes metabolism by CYP2C9 to 3-hydroxymethyl mefenamic acid, and further oxidation to a 3-carboxymefenamic acid may occur. The activity of these metabolites has not been studied. Mefenamic acid is also glucuronidated directly.
Half Life 2 hours
Protein Binding [%] 90%
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Mefenamic_acid.html
http://www.rxlist.com/cgi/generic3/mefenamic.htm
Drug Type Approved Drug
Accession No APRD00730
CAS Registry Number 61-68-7
KEGG Compound ID C02168
PubChem ID SID:148984
PharmGKB ID PA450347
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2237826

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