Kapsikam ointment 50g №1

Name:
Capsic. Release formOintment for external use Dosage 50 g. Pack quantity: 1 pc. Manufacturer Tallinn Pharmaceutical Plant. FTG Local irritant.
Description:
Ointment white or white with a slightly yellowish tint, with the smell of camphor and turpentine. Composition of the drug 1 g of ointment contains (active substances): • nonivamide 2 mg • dimethyl sulfoxide 50 mg • racemic camphor 30 mg • gum turpentine 30 mg • benzyl nicotinate 20 mg excipients: • cetostearyl alcohol emulsifying (type A) • sodium cetylstearyl sulfate • polysorbate- 80 • bronopol • purified water Pharmacological properties Other agents for external use for pain in the joints and muscles. ATS code: M02AX10. Pharmacodynamics The ointment contains substances that have local irritating, vasodilating and analgesic effects. The local irritating effect changes and selectively improves the blood supply and trophism of those internal organs that are innervated by the corresponding nerves of the spinal cord segments. Additional stimulation of the corresponding segment of the spinal cord causes additional activation of the antinociceptive system, thus slowing down the conduction of a pain impulse to the cerebral cortex and helping to endure pain. Pharmacokinetics When applied topically to the skin, the ointment is rapidly absorbed, the skin temperature rises by 1-2 ° C, the effect lasts 2-3 hours. The analgesic effect occurs in 30-40 minutes and lasts up to 3-6 hours. With repeated use of the ointment, the effect persists for 10-14 days. Indications for use Pain reliever and warming agent for muscle and joint pain. Method of administration and doses It is applied externally. As a warming agent for athletes: 2-3 g of ointment is applied to the muscle area to be warmed up using an applicator and rubbed with light massaging movements into the skin until it is slightly reddened. After training, wash off the ointment from the skin with cool water (it is undesirable to leave it on the skin for a long time). For pain relief: 1-3 g of ointment is applied to the painful area with an applicator 2-3 times a day, depending on the intensity of the pain, and a bandage is applied to increase the thermal effect. The course of treatment consumes approximately 50-100 g of ointment. After each procedure, wash your hands with cool water and soap. The duration of the course of treatment depends on the nature and severity of the disease. There is no experience with the use of the drug in pediatrics (see section Precautions). If you miss another dose of the drug, take it immediately. Do not use a double dose to replace a missed one. Continue taking as directed by your doctor. Side effects Side effects are classified according to MedDRA organ system groups. Frequency classification is as follows: very common ≥ 1/10, common (≥ 1/100 to < 1/10), less common (≥ 1/1000 to < 1/100), rare (≥ 1/10,000 to < 1/10). 1000), very rare (< 1/10,000), not known (cannot be determined from available data). Immune system disorders Frequency unknown: hypersensitivity reactions. Damage to the skin and subcutaneous tissues Rare: itching. Frequency unknown: urticaria, edema, redness. Nervous system disorders Frequency unknown: burning sensation. With increased skin sensitivity to the components of the ointment, itching, swelling or urticaria may occur. The listed symptoms disappear in 8-12 hours after the termination of application of ointment. To avoid side effects, you should first apply a small amount of ointment to the skin to determine the sensitivity to the drug. If the listed adverse reactions occur, as well as if an adverse reaction occurs that is not mentioned in the instructions, you should consult a doctor. Contraindications Increased sensitivity of the skin to the components of the ointment. Tendency to convulsions, bronchospasm. Ulcers, skin diseases. During pregnancy and breastfeeding. Childhood and adolescence. Overdose When applying too much ointment to the skin, redness of the skin, slight transient itching or burning sensation may occur. In this case, wash off the ointment from the skin. Accidental ingestion of the ointment may cause gastrointestinal symptoms such as vomiting and diarrhea. Treatment is symptomatic. If the ointment is accidentally swallowed in large quantities, symptoms of acute poisoning may occur: nausea, vomiting, abdominal pain and headache, dizziness, feeling warm / hot, convulsions, respiratory depression and coma. In severe gastrointestinal and neurological symptoms of poisoning, patient monitoring and symptomatic treatment is necessary. You can't induce vomiting. Precautions The ointment should not be applied to damaged skin. To avoid severe irritation, avoid getting the ointment in the eyes and mucous membranes. Shortly before and after the use of the drug, it is not recommended to carry out thermal procedures (taking a bath, visiting a bath), as this causes the opening of skin pores and, as a result, a burning sensation of the skin. The ointment contains emulsifying cetostearyl alcohol (type A) and bronopol as excipients, which can cause local skin reactions (including contact dermatitis). To avoid side effects, you should first apply a small amount of ointment to the skin to determine the sensitivity to the drug. Elderly patients and patients with impaired liver and kidney function The drug should be used with caution due to the lack of data on its use in patients of these age groups. Pregnancy and lactation It is not recommended to use the drug during pregnancy and lactation due to the lack of data on the safety of its use during these periods. Children and adolescents It is not recommended to use the drug in children and adolescents due to the lack of sufficient data on its use in patients of these age groups. Influence on the ability to drive vehicles and maintain moving mechanisms No effect. Interaction with other medicinal products No interaction studies have been conducted with other medicinal products. Dimethyl sulfoxide promotes the penetration of other active substances through the skin. In order to avoid the negative consequences of the influence of these substances, the use of other drugs on the skin area treated with ointment should be avoided. Storage conditions and shelf lifeStore at a temperature not exceeding 25 °C. Do not freeze. Keep out of the reach of children. Shelf life - 2 years. Do not use after the expiry date stated on the packaging. Holiday conditions Without a prescription. Packing 30 g or 50 g in an aluminum tube in accordance with the nominal weight indicated on the package. 1 tube in a cardboard pack along with instructions for use and applicator. Buy Kapsikam ointment 50g №1 Price for Kapsikam ointment 50g №1Instruction for use for Kapsikam ointment 50g №1