Tantum Verde 3mg eucalyptus-flavoured oral lozenges, 20pcs

Composition

Active ingredient: benzydamine hydrochloride 3 mg. Auxiliary substances: isomaltose-3183 mg; levomentol-4 mg;aspartame-3.5 mg; citric acid monohydrate-2 mg; mint flavor-5 mg;lemon flavor-1.5 mg; quinoline yellow dye (E 104) – 0.035 mg; indigo carmine dye (E 132) – 0.015 mg

Pharmacological action

Local analgesic, local anti-inflammatory.

Indications

Symptomatic therapy of pain syndrome of inflammatory diseases of the oral cavity and ENT organs (of various etiologies):

• gingivitis, glossitis, stomatitis (including after radiation and chemotherapy);
• pharyngitis, laryngitis, tonsillitis;
• candidiasis of the oral mucosa (as part of combination therapy);
• calculous inflammation of the salivary glands;
• condition after surgery and injuries (tonsillectomy, jaw fractures);
• condition after treatment and tooth extraction;
• periodontal disease.

For infectious and inflammatory diseases requiring systemic treatment, Tantum®should be used. Verde in combination therapy.

Contraindications

• Hypersensitivity to benzydamine or other components of the drug;
• fructose intolerance;
• children under 6 years of age.

With caution: hypersensitivity to acetylsalicylic acid or other NSAIDs; bronchial asthma (including in the anamnesis).

Side effects

WHO classification of side effects: very common – ≥1/10; common – ≥1/100 to <1/10; uncommon – ≥1/1000 to <1/100; rare – ≥1/10000 to <1/1000; very rare — In each group, undesirable effects are presented in decreasing order of severity. Local reactions: rarely-dry mouth, burning sensation in the oral cavity; frequency unknown-feeling of numbness in the oral cavity. Allergic reactions: infrequently-photosensitization; rarely-hypersensitivity reactions, skin rash, pruritus; very rarely-angioedema, laryngospasm; frequency unknown — anaphylactic reactions. If any of the side effects listed in the description get worse or any other side effects that are not listed in the description are noted, you should immediately inform your doctor.

How to take, course of use and dosage

Locally, after a meal. Tablets should be kept in the mouth until completely dissolved, do not swallow, do not chew. The duration of treatment should not exceed 7 days. If there is no improvement after treatment for 7 days or new symptoms appear, you should consult your doctor. The drug should be used only according to the method of use and in the doses indicated in the description. If necessary, you should consult your doctor before using the drug. Adults (including elderly patients) and children over 6 years of age: 1 tablet for resorption 3 times a day. Do not exceed the recommended dose. In children from 6 to 12 years of age, the use of the drug is carried out under the supervision of an adult.

Overdose

Currently, cases of overdose of Tantum®have been reported Verde was not informed. Symptoms: Overdose is unlikely if the drug is used as described. In case of accidental ingestion of the drug, vomiting, abdominal cramps, anxiety, fear, hallucinations, convulsions, ataxia, fever, tachycardia, respiratory depression are possible. Treatment: symptomatic; induction of vomiting or gastric lavage using a gastric tube (under the supervision of a doctor); provide medical supervision, supportive therapy, and adequate hydration. The antidote is unknown.

Special instructions

When using the drug Tantum® Verde may develop hypersensitivity reactions. In this case, it is recommended to stop treatment and consult a doctor to prescribe appropriate therapy. In a limited number of patients, the presence of ulcers in the throat and oral cavity may indicate the presence of a more serious pathology. If symptoms persist for more than 3 days, you should consult your doctor. Application of the drug Tantum® Verde is not recommended in patients with hypersensitivity to acetylsalicylic acid or other NSAIDs. Tantum®preparation Verde should be used with caution in patients with a history of bronchial asthma due to the possibility of developing bronchospasm while taking the drug. The drug contains isomaltose, and therefore it is not recommended for patients with hereditary fructose intolerance. The use of the drug in children is possible only under the supervision of adults in order to avoid swallowing the tablet. Influence on the ability to drive vehicles and mechanisms. It doesn’t affect you.

Form of production

Tablets for resorption.

Storage conditions

In a dark place, at a temperature not exceeding 25 °C. Keep out of reach of children.

Shelf

life is 4 years. Do not use after the expiration date.

Active ingredient

Benzydamine

Dosage form

tablets for resorption

Description

For adults and Children over 6 years of age

Indications

Pharyngitis, Laryngitis, Stomatitis, Oral inflammation, Tonsillitis, Gum inflammation, Sore throat