Eslotin 5mg 2p x 10 tablets — Made in Turkey — Free Delivery

Eslotin assists in the elimination of symptoms associated with:

Active ingredient: desloratadine.

1 coated tablet contains desloratadine 5 mg.

Excipients: calcium hydrogen phosphate, dihydrate; talc starch corn cellulose microcrystalline magnesium stearate.

Hypersensitivity to desloratadine, loratadine or to any of the excipients of the preparation.

Adults and adolescents (over 12 years old) 1 tablet once a day, with or without food, to eliminate symptoms associated with allergic rhinitis (including intermittent and persistent allergic rhinitis) and urticaria.

Treatment of intermittent allergic rhinitis is carried out until the symptoms are resolved and can be resumed when they reappear (presence of symptoms more than 4 days a week and more than 4 weeks), patients can be offered long-term treatment during periods of exposure to the allergen.

Patients with renal insufficiency of a high degree of severity, the preparation should be administered under the supervision of a physician.

The preparation should be used with caution in patients with a personal and family history of conviction, especially young children, may be more sensitive to the development of a new seizure attack. If seizures develop, consider discontinuing the preparation.

A large amount of data on the use of pregnant women (more than 1000 proven results) does not indicate either congenital or feto-neonatal toxicity of desloratadine. Animal studies indicate neither direct nor indirect adverse effects on reproductive function. As a precautionary measure, you should avoid using the preparation during pregnancy.

The efficacy and safety of using desloratadine in children under 12 years of age has not been established. No data available.

Does not affect.

The profile of adverse reactions in case of overdose, established during post-registration use, corresponds to the profile when used in therapeutic doses, however, the degree of manifestation may be higher.

In clinical studies in which desloratadine was administered at doses of 45 mg (which is 9 times the recommended), clinically significant adverse reactions were not observed.

In case of overdose, apply standard measures to remove the unadsorbed active substance. Symptomatic and supportive treatment is recommended. Desloratadine is not removed by hemodialysis; the possibility of its removal during peritoneal dialysis has not been established.

From the side of metabolism and nutrition: the frequency is unknown - increased appetite.

From the side of the psyche: very rarely - hallucinations, the frequency is unknown - aggression, abnormal behavior.

From the side of the nervous system: often - headache; very rarely - dizziness, drowsiness, insomnia, psychomotor hyperactivity, convulsions.

From the side of the heart: very rarely - tachycardia, palpitations; frequency unknown - prolongation of the QT interval.

From the digestive tract: often - dry mouth; very rarely - abdominal pain, nausea, vomiting, indigestion, diarrhea.

On the part of the digestive system: very rarely - an increase in the level of liver enzymes, an increase in the level of bilirubin, hepatitis, the frequency is unknown - jaundice.

On the part of the musculoskeletal system and connective tissue: very rarely - myalgia.

On the part of the skin and subcutaneous tissues: frequency unknown - photosensitization.

From the side of the body as a whole: often - increased fatigue; very rarely - hypersensitivity reactions (for example, anaphylaxis, angioedema, shortness of breath, pruritus, rash and urticaria), the frequency is unknown - asthenia.

When desloratadine was used together with erythromycin or ketoconazole, no clinically significant interactions were observed.

Desloratadine did NOT enhance the negative effects of ethanol on psychomotor function. However, there have been cases of alcohol intolerance and alcohol intoxication with the use of desloratadine. In the case of alcohol consumption during the period of preparation use, caution should be exercised.

Store at a temperature not exceeding 25 ° C in a dry place out of the reach of children.

Shelf life is 3 years.