Properties
What is it?
International Nonproprietary Name - Tyrothricin, chlorhexidine, lidocaine Clinical-pharmacological group: Antiseptics → Antiseptics for topical use Composition Active substances in the preparation: Tyrothricin, Lidocaine hydrochloride, Chlorhexidine digluconate One lozenge contains: Tyrothricin 0.5 mg Lidocaine hydrochloride 1 H2O 1.0 mg Chlorhexidine gluconate 1.0 mg Excipients Sorbitol, magnesium stearate, flavoring agent One lozenge contains 0.69 g of sorbitol, which corresponds to 0.057 BU Indications Inflammatory and infectious diseases of the mouth and throat, such as: stomatitis, gingivitis, periodontitis, glossitis, tonsillitis and pharyngitis; dysphagia. For the prevention of infectious diseases in the oral cavity and throat before and after surgical interventions (tooth extraction, surgical treatment of gingivitis, tonsillectomy). Dosage and administration Adults should dissolve one lozenge every two hours, approximately 8 times a day, and children 6 times a day. With regular administration of the preparation, the symptoms usually disappear within a few days. To ensure long-term treatment success, continue taking TRRACHISAN® lozenges for an additional 2-3 days after symptoms have subsided. However, if no significant improvement is observed after 10 days, consult a doctor. TRRACHISAN® lozenges should not be used continuously for more than 2 weeks, unless otherwise prescribed by a doctor or dentist. Side effects Rarely, hypersensitivity reactions to tyrothricin may occur. TRRACHISAN® lozenges are generally well tolerated, but the preparation may cause a worsening of taste sensation and numbness of the tongue, which usually disappears completely. Discoloration of teeth, fillings, dentures or tongue with a yellowish-brown color, which occurs rarely with prolonged use of the preparation, disappears with proper oral hygiene; however, the discoloration itself disappears immediately after discontinuation of the preparation. Contraindications TRRACHISAN® lozenges should not be used in case of hypersensitivity to any of its active components, non-bleeding desquamation of the oral mucosa (erosive and desquamative changes), and relatively large, fresh wounds in the oral cavity and pharynx. Special precautions when using the preparation None.