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Tiaprofenic acid |
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indicationTiaprofenic acid is used to treat pain, especially arthritic pain.pharmacologyTiaprofenic acid is a non-steroidal anti-inflammatory drug of the arylpropionic acid (profen) class, used to treat pain, especially arthritic pain. The typical adult dose is 300mg twice daily. It is not recommended in children.mechanism of actionTiaprofenic acid belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). It works by blocking the production of a chemical (prostaglandin) which the body produces in response to injury or certain diseases. This prostaglandin would otherwise go on to cause swelling, pain and inflammation.biotransformationHepatic (10%). Sparingly metabolised in the liver to two inactive metabolites.absorptionBioavailability is 90% following oral administration.half life1.5-2.5 hoursdrug interactionsAcenocoumarol: Increased risk of bleeding.Acetylsalicylic acid: Increased risk of gastrointestinal bleeding. Aminosalicylic Acid: Increased risk of gastrointestinal bleeding. Cholestyramine: The bile acid sequestrant, Cholestyramine resin, may reduce Tiaprofenic acid absorption and therapeutic effect. Citalopram: Additive antiplatelet effects increase the risk of bleeding. Consider alternate therapy or monitor for increased bleeding. Colesevelam: The bile acid sequestrant, Colesevelam, may reduce Tiaprofenic acid absorption and therapeutic effect. Colestipol: The bile acid sequestrant, Colestipol, may reduce Tiaprofenic acid absorption and therapeutic effect. Cyclosporine: Tiaprofenic acid may increase the nephrotoxicity and/or the serum concentration of cyclosporine. Consider altnerate therapy or monitor for increased cyclosporine concentrations and nephrotoxicity during concomitant therapy. Escitalopram: Additive antiplatelet effects increase the risk of bleeding. Consider alternate therapy or monitor for increased bleeding. Fluoxetine: Additive antiplatelet effects increase the risk of bleeding. Consider alternate therapy or monitor for increased bleeding. Fluvoxamine: Additive antiplatelet effects increase the risk of bleeding. Consider alternate therapy or monitor for increased bleeding. Ginkgo biloba: Increased risk of bleeding due to additive antiplatelet properties of the two agents. Concomitant therapy should be avoided or monitored carefully for bleeding, bruising and altered mental status, which may be caused by CNS bleeds. Ginseng: Increased risk of bleeding due to additive antiplatelet properties of the two agents. Concomitant therapy should be avoided or monitored carefully for bleeding, bruising and altered mental status, which may be caused by CNS bleeds. Ketorolac: Concomitant therapy is contraindicated due to the risk of synergistic NSAID toxicity. Lithium: Tiaprofenic acid may increase the therapeutic/adverse effects of Lithium by increasing Lithium serum concentrations. Monitor for changes in the therapeutic/adverse effects of Lithium if Tiaprofenic acid is initiated, discontinued or dose changed. Methotrexate: Tiaprofenic acid may decrease renal excretion of methotrexate. Consider alternate therapy or monitor for methotrexate toxicity. Paroxetine: Additive antiplatelet effects increase the risk of bleeding. Consider alternate therapy or monitor for increased bleeding. Pemetrexed: Tiaprofenic acid may decrease Pemetrexed excretion. Tiaprofenic acid should not be used around the time when Pemetrexed is administered. Salsalate: Increased risk of gastrointestinal bleeding. Sertraline: Additive antiplatelet effects increase the risk of bleeding. Consider alternate therapy or monitor for increased bleeding. Telmisartan: Concomitant use of Telmisartan and Tiaprofenic acid may increase the risk of acute renal failure and hyperkalemia. Monitor renal function at the beginning and during treatment. Timolol: The NSAID, Tiaprofenic acid, may antagonize the antihypertensive effect of Timolol. Trandolapril: The NSAID, Tiaprofenic acid, may reduce the antihypertensive effect of Trandolapril. Consider alternate therapy or monitor for changes in Trandolapril efficacy if Tiaprofenic acid is initiated, discontinued or dose changed. Treprostinil: The prostacyclin analogue, Treprostinil, may increase the risk of bleeding when combined with the NSAID, Tiaprofenic acid. Monitor for increased bleeding during concomitant thearpy. Warfarin: The antiplatelet effects of tiaprofenic acid may increase the bleed risk associated with warfarin. Consider alternate therapy or monitor for signs and symptoms of bleeding during concomitant therapy. |