Instruction for use: Acenterine
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Active substance Acetylsalicylic acid
ATX code N02BA01 Acetylsalicylic acid
Pharmacological groups
NSAIDs - Salicylic acid derivatives
Nosological classification (ICD-10)
M00-M25 Arthropathy
M30-M36 Systemic involvement of connective tissue
Collagenoses
M45 Ankylosing spondylitis
Ankylosing spondylarthrosis, Marie-Strumpel disease, Ankylosing spondylitis, Pain syndrome in acute inflammatory diseases of the musculoskeletal system, Pain syndrome in chronic inflammatory diseases of the musculoskeletal system, Bechterew's disease, Ankylosing spondylitis, Diseases of the spinal column, Rheumatic spondylitis, Bechterew-Marie-Strumpel disease
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 with enteric coating contains acetylsalicylic acid 500 mg, in a package of 25 pcs.
pharmachologic effect
Pharmacological action - anti-inflammatory, antipyretic, analgesic.
Indications
Chronic polyarthritis, acute articular rheumatism, ankylosing spondylitis, collagenoses.
Contraindications
Hypersensitivity, gastric and duodenal ulcer, marked decrease in kidney function, diseases accompanied by bleeding, age (up to 10 years).
pregnancy and lactation
At pregnancy it is contraindicated, at feeding by a breast to consult with the doctor.
Side effects
Irritation of the stomach with burning sensation, ulcers, bleeding from the stomach or intestines, impaired liver function, bleeding from the nose and gums, increased blood loss during menstruation, decreased kidney function with a history of renal blood flow disorder, nephropathy, oliguria, tinnitus, hearing impairment, allergic reactions (runny nose, face and neck swelling, rash, asthmatic attacks, bronchospasm).
Interaction
Strengthens the effects of anticoagulants (increased risk of bleeding, especially from the stomach and intestines), sugar-containing drugs, methotrexate; weakens - diuretic and antihypertensive agents. Alcohol increases the likelihood of developing gastrointestinal side effects.
Dosing and Administration
Inside, not liquid, in between meals, squeezed a small amount of water. The daily dose of 6 table. on 500 mg in 3-4 reception. The dose is selected individually.
Overdose
Symptoms: headache, dizziness, tinnitus, confusion, sweating, thirst, breathing and blood composition disorders, nausea, vomiting, diarrhea, neurological disorders (central nervous system stimulation is replaced by progressive depression, with the possibility of transition to coma).
Treatment stationary: includes gastric lavage and reception of activated charcoal.
Precautionary measures
Be wary of patients suffering from asthma, stomach ulcers and duodenal ulcers, bleeding, gastric diseases, decreased kidney and liver function, and the elderly.
storage Conditions
At room temperature.
Keep out of the reach of children.