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Tantum Verde oral solution 150mg/100ml 120 ml

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Tantum Verde oral solution 150mg/100ml 120 ml
Tantum Verde oral solution 150mg/100ml 120 ml
Tantum Verde oral solution 150mg/100ml 120 ml
Tantum Verde oral solution 150mg/100ml 120 ml
Tantum Verde oral solution 150mg/100ml 120 ml
Tantum Verde oral solution 150mg/100ml 120 ml
In Stock
467.39 грн.
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Active ingredient:Benzydamine hydrochloride
Adults:Can
ATC code:A AGENTS AFFECTING THE DIGESTIVE SYSTEM AND METABOLISM; A01 AGENTS FOR USE IN DENTAL TECHNOLOGY; A01A AGENTS FOR USE IN DENTAL TECHNOLOGY; A01A D Other agents for topical use in dentistry; A01A D02 Benzydamine
Country of manufacture:Italy
Diabetics:Can
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Tantum Verde oral solution 150mg/100ml 120 ml
467.39 грн.
Description

Instructions Tantum Verde oral solution 150mg/100ml 120 ml

Composition

active ingredient: benzydamine hydrochloride;

100 ml of solution contain 0.15 g of benzydamine hydrochloride;

excipients: ethanol 96%, glycerin, methyl parahydroxybenzoate (E 218), flavoring (menthol), saccharin, sodium bicarbonate, polysorbate 20, quinoline yellow (E 104), patent blue V (E 131), purified water.

Dosage form

Oral solution.

Main physicochemical properties: clear green liquid with a typical mint flavor.

Pharmacotherapeutic group

Means for use in dentistry. Other means for local use in the oral cavity.

ATX code A01A D02.

Pharmacological properties

Pharmacodynamics

Benzydamine is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and antiexudative properties.

In clinical studies, benzydamine has been shown to be effective in relieving symptoms associated with localized irritant pathologies in the oral cavity and pharynx. In addition, benzydamine has anti-inflammatory and local analgesic effects, and has a local anesthetic effect on the oral mucosa.

Pharmacokinetics

The fact of absorption through the mucous membrane of the oral cavity and pharynx has been proven by the presence of measurable amounts of benzydamine in human blood plasma. However, this is not sufficient to exert any systemic pharmacological effect. Excretion occurs mainly in the urine, mainly in the form of inactive metabolites or conjugated compounds.

It has been shown that topical application achieves the accumulation of effective concentrations of benzydamine in inflamed tissues due to its ability to penetrate the mucous membrane.

Indication

Symptomatic treatment of irritations and inflammations of the oropharynx; pain caused by gingivitis, stomatitis, pharyngitis; in dentistry after tooth extraction or for prophylactic purposes.

Contraindication

Hypersensitivity to the active substance or to other components of the drug.

Interaction with other medicinal products and other types of interactions

No interaction studies have been conducted.

Application features

In cases of sensitivity during long-term use, treatment should be discontinued and a doctor should be consulted to prescribe appropriate treatment.

In some patients, buccal/pharyngeal ulcers may be due to serious pathological processes. Therefore, patients whose symptoms worsen or do not improve within 3 days, or who develop a fever or other symptoms, should seek advice from a physician or dentist as appropriate.

Benzydamine is not recommended for use in patients with hypersensitivity to acetylsalicylic acid or other nonsteroidal anti-inflammatory drugs.

The use of the drug may cause bronchospasm in patients with bronchial asthma or with a history of bronchial asthma. Such patients should be warned about this.

For athletes: the use of medicines containing ethyl alcohol may give a positive result in an anti-doping test, taking into account the limits set by some sports federations.

Use during pregnancy or breastfeeding

There are currently no adequate data available on the use of benzydamine in pregnant or breastfeeding women. The ability of this drug to pass into breast milk has not been studied. Animal data are insufficient to draw any conclusions regarding the effects of this drug during pregnancy or breastfeeding. The potential risk to humans is unknown.

Tantum Verde® should not be used during pregnancy or breastfeeding.

Ability to influence reaction speed when driving vehicles or other mechanisms

When used in recommended doses, the drug has no effect on the ability to drive vehicles and operate machinery.

Method of administration and doses

From the bottle, using a measuring cup, measure 15 ml of Tantum Verde® solution and rinse the oral cavity with the undiluted or diluted (15 ml of the measured solution can be diluted with 15 ml of water) preparation. Rinsing should be carried out

2-3 times a day. Do not exceed the recommended dose.

Children

The drug should not be used in children under 12 years of age due to the possibility of swallowing the solution while rinsing the mouth.

Overdose

There have been no reports of overdose with topical benzydamine.

However, it is known that benzydamine, when taken internally in large doses (hundreds of times higher than the possible doses of this dosage form), especially in children, can cause agitation, convulsions, tremors, nausea, increased sweating, ataxia, vomiting. Such an acute overdose requires immediate gastric lavage, treatment of water and electrolyte imbalance and symptomatic treatment, adequate hydration.

Adverse reactions

Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.

Adverse reactions are classified according to frequency of occurrence: very common (≥ 1/10); common (≥ 1/100 to < 1/10); uncommon (≥ 1/1000 to < 1/100); rare (≥ 1/10,000 to < 1/1000); very rare (< 1/10,000); frequency unknown (cannot be estimated from the available data).

Gastrointestinal: rarely - burning sensation in the mouth, dry mouth; frequency unknown - oral hypoesthesia, nausea, vomiting, swelling and discoloration of the tongue, taste changes.

On the part of the immune system: rarely - hypersensitivity reaction; frequency unknown - anaphylactic reaction.

Respiratory, thoracic and mediastinal disorders: very rarely - laryngospasm; frequency unknown - bronchospasm.

Skin and subcutaneous tissue disorders: uncommon - photosensitivity; very rare - angioedema; frequency unknown - rash, itching, urticaria.

Nervous system: frequency unknown - dizziness, headache.

Tantum Verde® contains methyl parahydroxybenzoate, which may cause allergic reactions (also delayed reactions).

Expiration date

4 years.

Storage conditions

Store at a temperature not exceeding 25 ° C. Keep out of the reach of children.

Packaging

120 ml of solution in a bottle with a measuring cup; 1 bottle in a cardboard box.

Vacation category

Without a prescription.

Producer

Aziende Kimike Riunite Angelini Francesco A.K.R.A.F. S.p.A., Italy.

Location of the manufacturer and its business address

Via Vecchio Del Pinocchio, 22 – 60100 Ancona (AN), Italy.

Specifications
Characteristics
Active ingredient
Benzydamine hydrochloride
Adults
Can
ATC code
A AGENTS AFFECTING THE DIGESTIVE SYSTEM AND METABOLISM; A01 AGENTS FOR USE IN DENTAL TECHNOLOGY; A01A AGENTS FOR USE IN DENTAL TECHNOLOGY; A01A D Other agents for topical use in dentistry; A01A D02 Benzydamine
Country of manufacture
Italy
Diabetics
Can
Dosage
1.5 mg/ml
Drivers
Can
For allergies
With caution
For children
From the age of 12
Form
Liquids
Method of application
For the oral cavity
Nursing
It is impossible.
Pregnant
It is impossible.
Producer
Azienda Kimike Riunite Angelina Francesco
Quantity per package
120 ml
Series/Line
For children
Trade name
Tantum verde
Vacation conditions
Without a prescription
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