Buy Metindol retard tablets 50 pcs

Metindol retard pills 50 pcs

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Active ingredients

Indomethacin

Release form

Pills

Composition

Deproteinized dialysate from the blood of healthy dairy calves (Bos Taurus), standardized chemically and biologically (in terms of dry substance) 2.125 mg, polydocanol 600 10 mg, preservatives methyl parahydroxybenzoate (E218) 1.8 mg, propyl parahydroxybenzoate (E216) 0.2 mg, excipients: sodium carboxymethylcellulose - 22.875 mg; peppermint oil - 2.925 mg; menthol - 0.075 mg. The basis of the paste: (sodium carboxymethylcellulose, gelatin, pectin, polyethylene 350000, liquid paraffin) - 960 mg

Pharmacological effect

Anti-inflammatory, antipyretic, analgesic, desensitizing. Blocks cyclooxygenase in the arachidonic acid cascade, inhibits PG biosynthesis

Pharmacokinetics

Absorption is fast. The bioavailability of the appointment inside the usual pills, pills or capsules - 90-98%, when using pills of prolonged action within 12 hours, 90% of the administered dose is absorbed. After ingestion, TCmax - 2 h, Cmax - 0.69 mcg / ml. Communication with plasma proteins - 90%. Metabolized mainly in the liver. T1 / 2 - 4-9 h (the indicator may vary depending on the severity of systemic metabolism, enterohepatic circulation and reabsorption). Excreted by the kidneys by 70%, with 30% unchanged, and the gastrointestinal tract - 30%. Penetrates into breast milk, when mother uses 200 mg of the drug per day in milk is determined from 0.5 to 2 mg. The drug is not removed during dialysis

Indications

Rheumatoid arthritis, ankylosing spondylitis, osteoarthritis, tendonitis, synovitis, acute gouty arthritis, reactive arthritis

Contraindications

Hypersensitivity, rhinitis, conjunctivitis or bronchospasm while taking NSAIDs, erosive and ulcerative lesions of the gastrointestinal tract, bleeding (especially intracranial or from the gastrointestinal tract), thrombocytopenia, hypocoagulation, suspected necrotizing enterocolitis, severe renal insufficiency, congenital heart disease, a rash heart (tethered mouse), a racer, a rash heart, a rash heart, a tetanus, a rash heart, a tetanus, a hysterocarditis, necrosis, necrosis, necrotizing enterocolitis, severe renal failure. ), proctitis (suppositories), pregnancy (teratogenicity may occur)

Precautionary measures

With caution should use the drug for ischemic heart disease, cerebrovascular diseases, disorders of blood formation (leukopenia and anemia), congestive heart failure, dyslipidemia / hyperlipidemia, thrombocytopenia,diabetes mellitus, peripheral arterial diseases, hypertension, smoking, liver cirrhosis with portal hypertension, QA less than 60 ml / min, immediately after surgery; in the presence of amnestic data on the development of ulcerative lesions of the gastrointestinal tract, in the presence of Helicobacter pylori infection, in the elderly, with prolonged use of NSAIDs, frequent use of alcohol, severe somatic diseases, concomitant therapy with the following drugs: anticoagulants (eg, warfarin), antiplatelet agents (eg, acetylsalicylic acid, clopidogrel), oral glucocorticosteroids (for example, prednisolone), selective serotonin reuptake inhibitors (for example, citalopram, fluoxetine, paroxetine, sertraline). akzhe should be careful in appointing metindol ointment in patients with mental disorders, depression, Parkinson's disease, epilepsy. To reduce the risk of adverse events, use the minimum effective dose with the shortest possible short course.

Use during pregnancy and lactation

Metindol Retard is contraindicated in pregnancy and lactation. Penetrates into breast milk, when mother uses 200 mg of the drug per day, 0.5 to 2 mg is determined in milk.

Dosage and administration

Inside, after eating. Adults are prescribed in an initial dose of 25 mg 2-3 times a day, with insufficient effect, 50 mg 3 times a day, retard pills (75 mg) 1-2 times a day, the maximum daily dose is 200 mg, with long-term use - should not exceed 75 mg. When effect is achieved, treatment is continued for 4 weeks. in the same or reduced dose. For the treatment of acute conditions or the relief of an exacerbation of a chronic process, 60 mg 1–2 times a day for 7–14 days are injected into the / m, after which they are transferred to pills or suppositories (0.05 or 0.1 g 2 times a day).

Side effects

Nausea, vomiting, epigastric pain, erosive and ulcerative lesions of the gastrointestinal tract, gastrointestinal bleeding, rectal bleeding, chronic hepatitis, constipation, hypertension, heart rhythm disorders, bone marrow hypoplasia, aplastic anemia, autoimmune hemolytic anemia, agranulocytosis, thrombocytopenia, impaired platelet function, fluid retention, hyperglycemia, glycosuria, hyperkalemia, pruritus, urticaria, exfoliative dermatitis, hair loss, erythema nodule, Stevens-Johnson syndrome, anaphilac tic shock, bronchospasm, vasculitis, pulmonary edema

Overdose

The clinical picture of Metindol Retard overdose is characteristic of indomethacin and includes the following symptoms: nausea, vomiting, severe headache, dizziness, memory impairment and disorientation. In more severe cases, paresthesias, numbness of the extremities and convulsions are observed. Treatment: Treatment consists in the rapid elimination of the drug from the body and the use of appropriate symptomatic agents. Indomethacin cannot be eliminated through hemodialysis.

Interaction with other drugs

Reduces the diuretic effect of potassium-sparing, thiazide and loop diuretics, hypotension caused by beta-blockers. Increases (mutually) the risk of side effects (first of all, gastrointestinal lesions) of other NSAIDs. Enhances the toxicity of methotrexate (reduces its tubular secretion). Causes an increase in plasma levels of lithium, digoxin

special instructions

When combined with cyclosporine, it is necessary to monitor renal function.

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