Oral Pain and inflammation associated with musculoskeletal and joint disorders
Adult: Dosage is individualised depending on the severity of symptoms. Usual dose: 60 mg tid. May give up to 120 mg as a single dose for the treatment of severe symptoms. Max: 180 mg daily. Elderly: Initiate at the lowest effective dose.
Các sản phẩm có chứa hoạt chất Loxoprofen tại Việt Nam?
Hypersensitivity to loxoprofen. History of hypersensitivity, history of or existing NSAID-induced (e.g. aspirin) asthma; severe cardiac function failure, severe blood disorders, active peptic ulcer. Severe renal and hepatic impairment. Concomitant use with other NSAIDs.
Thận trọng
Patient with a history of peptic ulcer including peptic ulcer associated NSAID use; blood disorders; bronchial asthma; ulcerative colitis, Crohn's disease. May mask the signs and symptoms of infection. Mild to moderate renal and hepatic impairment. Elderly. Pregnancy and lactation.
Tác dụng không mong muốn
Significant: Gastrointestinal bleeding, gastrointestinal perforation, small and/or large intestinal stenosis and/or obstruction; CHF; hypersensitivity reactions, shock, anaphylaxis; Stevens-Johnson syndrome, toxic epidermal necrolysis, erythema multiforme; agranulocytosis, haemolytic anaemia, leucopenia, thrombocytopenia, aplastic anaemia; interstitial pneumonia, asthmatic attack; acute kidney injury, nephrotic syndrome, interstitial nephritis; hepatic function disorder, jaundice, increased transaminases; aseptic meningitis; rhabdomyolysis; drowsiness. Blood and lymphatic system disorders: Eosinophilia. Cardiac disorders: Palpitations. Gastrointestinal disorders: Constipation, heartburn, stomatitis, peptic ulcer, dyspepsia, thirst, abdominal distention, small and/or large intestine ulcer. General disorders and administration site conditions: Malaise. Nervous system disorders: Headache, numbness, dizziness, somnolence. Renal and urinary disorders: Haematuria, proteinuria, dysuria. Respiratory, thoracic and mediastinal disorders: Chest pain.
Chỉ số theo dõi
In patients receiving long-term therapy, monitor urinalysis, haematological tests, and LFTs.
Tương tác
May enhance the anticoagulant effect of coumarin anticoagulants (e.g. warfarin). May increase the risk of bleeding with factor Xa inhibitor. May enhance the hypoglycaemic effect of sulfonylureas (e.g. glimepiride, tolbutamide). May enhance the convulsant effect of quinolone antimicrobial agents (e.g. levofloxacin). May increase the plasma concentration of methotrexate and lithium. May reduce the diuretic antihypertensive effect of thiazide diuretics (e.g. hydrochlorothiazide). May worsen the renal function and decrease the therapeutic effect of antihypertensive drugs (e.g. ACE inhibitors, angiotensin II receptor antagonists). Potentially Fatal: May increase the risk of adverse effects with other NSAIDs (e.g. mefenamic acid, aspirin).
Tương tác với thức ăn
May enhance toxic effects with alcohol.
Ảnh hưởng đến kết quả xét nghiệm
May result in false-positive aldosterone/renin ratio (ARR).
Tác dụng
Description: Mechanism of Action: Loxoprofen is a propionic acid-based nonsteroidal anti-inflammatory drug (NSAID). After absorption, it is rapidly metabolised to an active metabolite (trans-alcohol form) which potently prevents prostaglandin biosynthesis by nonselective inhibition of cyclooxygenase (COX) enzymes, thus resulting in its anti-inflammatory and analgesic effects. Pharmacokinetics: Absorption: Rapidly absorbed from the gastrointestinal tract. Time to peak plasma concentration: Approx 30 minutes (loxoprofen); approx 50 minutes (active metabolite). Metabolism: Rapidly metabolised in the liver by carbonyl reductase into the trans-alcohol form (active metabolite). Excretion: Via urine (approx 50%). Elimination half-life: Approx 75 minutes.
Đặc tính
Loxoprofen Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 3965, Loxoprofen. https://pubchem.ncbi.nlm.nih.gov/compound/Loxoprofen. Accessed Jan. 31, 2024.