Combined antiseptic preparation for topical use for throat infections.
Pharmacodynamics. The preparation has antiseptic properties. The effectiveness of the preparation is due to the presence of two antibacterial components of a wide spectrum of action - amylmetacresol and 2,4-dichlorobenzyl alcohol, which are active against a wide range of gram-positive and gram-negative microorganisms (staphylococcus, pneumococcus, fusobacteria and especially Staphylococcus aureus, Pseudomonas aerialr. and have antifungal effects. They prevent the attachment of a secondary bacterial infection in viral diseases of the upper respiratory tract. Amylmetacresol destroys the structure of bacterial proteins, provides a bactericidal effect. Alcohol 2,4-dichlorobenzyl has a bacteriostatic effect due to dehydration of the bacterial cell. Natural medicinal additives that are part of the preparation reduce pain in the throat, have a softening effect on the mucous membrane.
Pharmacokinetics. Systemic absorption of the preparation is low.
Symptomatic treatment for infectious and inflammatory diseases of the oral cavity and pharynx.
Adults and children over 6 years of age: it is recommended to take 1 Hexoral® Lorsept lozenge every 2-3 hours; the maximum daily dose is 8 lozenges.
Suck one lozenge slowly in your mouth. Do not chew or swallow whole candy.
The duration of the course of treatment is 5-7 days.
Hypersensitivity to any component of the preparation.
From the digestive system: stomatitis, burning sensation, tingling or pain in the mouth and throat, pain and swelling of the lips, tongue, throat, glossitis, glossodynia, dyspepsia, nausea.
From the immune system: hypersensitivity reactions, including skin rash, itching, angioedema, urticaria, erythema.
Hexoral® Lorsept with black currant flavor contains the dye carmoisin (E122), Hexoral® Lorsept with orange flavor contains the dye “sunset yellow” FCF (E110), which can cause allergic reactions.
If any adverse reactions occur, you must stop using the preparation and consult a doctor.
If the symptoms of the disease persist for more than 3-4 days and are accompanied by a high body temperature, headache, nausea, vomiting or other manifestations, you should consult a doctor. do not exceed the indicated dose.
Use with caution in patients with epilepsy, patients with impaired cardiac conduction, shock, liver disease.
Patients with diabetes mellitus should take into account that the preparation contains sucrose, glucose solution.
Patients with rare hereditary fructose intolerance, glucose-galactose malabsorption syndrome or sucrase-isomaltase deficiency should not use this preparation.
Use during pregnancy and lactation. Adequate and strictly controlled clinical studies of the use of a combination of 2,4-dichlorobenzyl alcohol and amylmetacresol during pregnancy and lactation have not been conducted, but an increased risk of malformations, spontaneous abortions or weight loss at birth is not expected. It has not been established whether 2,4-dichlorobenzyl alcohol and amylmetacresol or their metabolites penetrate into breast milk.
You should not use the preparation during pregnancy and lactation, unless the potential benefit of treatment for the mother outweighs the possible risks to the developing fetus or to the baby. You should consult your doctor before using the preparation during pregnancy and lactation.
Children. Do not use in children under 6 years of age.
The ability to influence the reaction rate when driving or working with other mechanisms. The use of the preparation in the recommended dosage does not affect the ability to drive vehicles or work with potentially dangerous machinery.
Unknown.
It manifests itself as symptoms of gastrointestinal discomfort (violation of taste sensitivity, nausea, vomiting, diarrhea). it is possible to increase the manifestations of adverse reactions. in this case, treatment should be discontinued.
Storage conditions
In the original packaging at a temperature not exceeding 30 ° C, out of the reach of children. shelf life is 4 years.
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