Tantum Verde tablets d / rassas. orange honey, no. 20

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SKU
BIDL3181769
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Expiration Date: 11/2025

Russian Pharmacy name:

Тантум Верде таблетки д/рассас. апельсин-мед, №20

Tantum Verde tablets d / rassas. orange honey, no. 20

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

  • gingivitis, glossitis, stomatitis (including after radiation and chemotherapy);

  • pharyngitis, laryngitis, tonsillitis;

  • oral mucosa candidiasis (as part of combination therapy);

  • calculous inflammation of the salivary glands;

  • after surgical interventions and injuries (tonsillectomy, jaw fractures);

  • after treatment and tooth extraction;

  • periodontal disease.

For infectious and inflammatory diseases requiring systemic treatment, it is necessary to use TantumЃ Verde as part of a combination therapy.

The drug is used topically after meals. The tablets should be kept in the mouth until completely dissolved, do not swallow or chew.

Adults (including elderly patients) and children over 6 years of age are prescribed 1 tab. for resorption 3 times / day. Do not exceed the recommended dose.

In children aged 6 to 12 years, the use of the drug is carried out under the supervision of an adult.

The duration of treatment should not exceed 7 days. If after treatment within 7 days there is no improvement or new symptoms appear, the patient should consult a doctor.

Orange-yellow orange-honey-flavored lozenges, translucent, square, with a depression in the center, with a characteristic smell of orange and honey.

1 tab. benzydamine hydrochloride 3 mg

Excipients: isomaltose - 3073.53 mg, citric acid monohydrate - 44.82 mg, acesulfame potassium - 1.28 mg, orange flavor - 9.287 mg, honey flavor - 2.32 mg, levomenthol - 1.707 mg, quinoline yellow dye (E104) - 0.034 mg, solar dye sunset yellow (E110) - 0.017 mg.

  • Fructose intolerance;

  • children under 6 years of age;

  • hypersensitivity to benzydamine or other components of the drug.

Precautions: hypersensitivity to acetylsalicylic acid or other NSAIDs; bronchial asthma (including history).

pharmachologic effect

Benzydamine is a non-steroidal anti-inflammatory drug (NSAID), belongs to the indazole group. It has an anti-inflammatory and local anesthetic effect, has an antiseptic effect against a wide range of microorganisms.

The mechanism of action of the drug is associated with the stabilization of cell membranes and inhibition of prostaglandin synthesis.

Benzydamine has an antibacterial and specific antimicrobial effect due to the rapid penetration of microorganisms through the membranes with subsequent damage to cellular structures, disruption of metabolic processes and cell lysosomes.

Has antifungal activity against Candida albicans. It causes structural modifications of the cell wall of fungi and their metabolic chains, thus interfering with their reproduction, which was the basis for the use of benzydamine in inflammatory processes in the oral cavity, including infectious etiology.

Pharmacokinetics

When applied topically, the drug is well absorbed through the mucous membranes and penetrates into the inflamed tissues, is found in the blood plasma in an amount insufficient to obtain systemic effects.

Excretion of the drug occurs mainly by the kidneys, in the form of inactive metabolites or conjugation products.

Side effect

In each group, adverse effects are presented in order of decreasing severity.

Local reactions: rarely - dry mouth, burning sensation in the mouth; frequency unknown - feeling of numbness in the mouth.

Allergic reactions: infrequently - photosensitivity; rarely - hypersensitivity reactions, skin rash, pruritus; very rarely - angioedema, laryngospasm; frequency unknown - anaphylactic reactions.

If any of the side effects indicated in the instructions are aggravated or any other side effects not indicated in the instructions are noted, the patient should immediately inform the doctor about it.

Application during pregnancy and lactation

The drug TantumЃ Verde should not be used during pregnancy and during breastfeeding.

Application in children

The use of the drug is contraindicated in children under the age of 6 years.

Use in elderly patients

Prescribed according to indications.

special instructions

The drug should be used only according to the method of administration and in those doses indicated in the instructions. If necessary, the patient should consult a doctor before using the medicinal product.

When using TantumЃ Verde, hypersensitivity reactions may develop. 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 sores in the throat and mouth may indicate a more serious pathology. If symptoms persist for more than 3 days, the patient should consult a doctor.

The use of TantumЃ Verde is not recommended in patients with hypersensitivity to acetylsalicylic acid or other NSAIDs.

The drug TantumЃ 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; therefore, it is not recommended to use TantumЃ Verde in patients with hereditary fructose intolerance.

Use in pediatrics

The use of the drug in children is possible only under the supervision of adults to avoid swallowing the tablet.

Influence on the ability to drive vehicles and use mechanisms

The drug does not affect the ability to drive vehicles and work with mechanisms.

Overdose

Currently, no cases of overdose of TantumЃ Verde have been reported. When using the drug in accordance with the instructions, an overdose is unlikely.

Symptoms: if the drug is accidentally swallowed, the following symptoms are possible - vomiting, abdominal cramps, anxiety, fear, hallucinations, convulsions, ataxia, fever, tachycardia, respiratory depression.

Treatment: carrying out symptomatic therapy; induce vomiting or gastric lavage using a gastric tube (under medical supervision); it is necessary to provide medical supervision, supportive therapy and the necessary hydration. The antidote is unknown.

Drug interactions

Interaction studies with other medicinal products have not been conducted.

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