Movalis 15 mg 20 pcs

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Orally, during meals, with water or other liquid; rectally.

Osteoarthritis, rheumatoid arthritis: 7.5 mg/day. If necessary, this level may be increased to 15 mg/day. Depending on the wellness response, this level may be reduced to 7.5 mg/day.

Ankylosing spondylitis: 15 mg/day. Depending on the wellness response, this level may be reduced to 7.5 mg/day.

For patients with an increased risk of adverse reactions, it is recommended to initiate support with a level of 7.5 mg/day. For patients with severe renal insufficiency on hemodialysis, the level should not exceed 7.5 mg/day.

Adolescents

The maximum level for adolescents is 0.25 mg/kg.

As a general rule, this product should only be used in adolescents and adults (see Contraindications). The maximum recommended daily use is 15 mg.

Rectal suppositories are recommended at a level of 7.5 mg once daily. In more severe cases, suppositories at a level of 15 mg may be used.

Because the risk of adverse reactions depends on the level and duration of use, the product should be used for the shortest possible duration at the lowest effective level.

Combination use. The total daily level of Movalis®, whether administered as pieces, suppositories, or injections, should not exceed 15 mg.

Hypersensitivity to the active ingredient or any of the excipients. There is a possibility of cross-hypersensitivity to acetylsalicylic acid and other NSAIDs;
A history of asthma discomfort, nasal polyps, angioedema, or urticaria after taking acetylsalicylic acid or other NSAIDs;
Peptic ulcer condition/perforation of the stomach and duodenum in the acute stage or recent;
Crohn's condition or ulcerative colitis in the acute stage;
Severe liver failure;
Severe renal failure (unless hemodialysis is performed, creatinine clearance less than 30 ml/min, or with confirmed hyperkalemia), progressive kidney condition;
Acute gastrointestinal bleeding, recent cerebrovascular bleeding, or a confirmed assessment of a blood coagulation disorder;
Severe uncontrolled heart failure;
Pregnancy;
Breastfeeding;
Perioperative pain management during coronary artery bypass grafting.
Children under 12 years of age, except for use in juvenile rheumatoid arthritis (if this indication is approved).

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