Instruction for use: Ortophen filmcoated tablets 0,025 g
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Active substance Diclofenac
ATX Code M01AB05 Diclofenac
Pharmacological group
NSAIDs - Acetic acid derivatives and related compounds
Nosological classification (ICD-10)
M00-M25 Arthropathy
M05 Seropositive rheumatoid arthritis
Rheumatoid arthritis seropositive
M15-M19 Osteoarthritis
M79.0 Other unspecified rheumatism
Degenerative rheumatic disease, Degenerative and rheumatic diseases of the tendons, Degenerative rheumatic diseases, Localized forms of rheumatism of soft tissues, Rheumatism, Rheumatism with a pronounced allergic component, Rheumatism of the articular and extraarticular, Rheumatic attack, Rheumatic complaints, Rheumatic diseases, Rheumatic disease of the spine, Relapses of rheumatism, Articular and extra-articular rheumatism, Articular and muscular rheumatism, Articular rheumatism, Articular syndrome with rheumatism, Chronic rheumatic pain, Chronic articular rheumatism, Rheumatoid diseases, Rheumatic diseases of the intervertebral disc
Composition and form of release
1 tablet, coated, contains diclofenac sodium 25 mg; in banks of 30 pcs. or in a blister 10 and 20 pcs., in a cardboard bundle of 1 can or 1 blister.
pharmachologic effect
Pharmacological action - anti-inflammatory, antipyretic, analgesic.
Inhibits cyclooxygenase, inhibits the synthesis of PG (prostaglandins).
Indications
Inflammatory and degenerative joint diseases, rheumatoid arthritis, rheumatism, osteoarthrosis.
Contraindications
Hypersensitivity, peptic ulcer of the stomach and duodenum, hepatic-renal failure, I trimester of pregnancy.
Side effects
Gastralgia, eructation, nausea, diarrhea, exacerbation of peptic ulcer of stomach and duodenum, dizziness, headache, arterial hypertension, allergic reactions.
Dosing and Administration
Inside, during or after a meal - 50 mg 1-6 times a day.
storage Conditions
In a dry place protected from light.
Keep out of the reach of children.
Shelf life
3 years.
Do not use after the expiry date printed on the package.