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Cosmetic brands
Septanazal nasal spray for children 0.05 mg + 0.005/dose 10ml
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NAME OF PREPARATION
SeptaName
QUALITY AND QUANTITATIVE COMPOSITION
Composition
Active ingredients: |
| 1 ml of spray contains: | 1 1 spray dose contains: |
Dexpanthenol |
| 50.00 mg | 5.00 mg |
Xylometazoline hydrochloride | 0.50 mg | 0.05 mg | |
Excipients: |
|
| |
Potassium dihydrophosphate | 9.00 mg | 0.90 mg | |
Sodium hydrophosphate dodecahydrate Purified water | 0.30 mg up to 1.00 ml | 0.03 mg up to 0.1 ml |
1 dose of the drug is 0.1 ml of solution.
The nominal number of doses of the drug in the vial - 90 doses
PHARMACEUTICAL FORM
Transparent, colorless solution.
PHARMACOLOGICAL PROPERTIES
Pharmacodynamics
Xylometazoline - local vasoconstrictor (decongestant) with alpha-adrenomimetic activity, causes narrowing of the blood vessels of the mucous membrane of the nasal cavity, restores the patency of the nasal passages, eliminates nasal congestion, facilitates nasal breathing. The effect of xylometazoline usually occurs within a few minutes after its use and lasts up to 10 hours. Dexapanthenol - vitamin B, a derivative of pantothenic acid. Dexpanthenol is converted into pantothenic acid in the body, which is a part of coenzyme A (CoA), and participates in acetylation processes, carbohydrate and fat metabolism, in the synthesis of acetylcholine, corticosteroids, porphyrins, stimulates the regeneration of the skin and mucous membranes, normalizes cellular metabolism, accelerates mitosis. increases the strength of collagen fibers. It has a regenerating, metabolic and weak anti-inflammatory effect.
Pharmacokinetics
Xylometazoline when applied topically, it is practically not absorbed. Concentrations in the blood plasma are so small that they can not be determined by modern analytical methods.
Dexapanthenol when applied topically, it is quickly absorbed by the skin and converted into pantothenic acid, binds to plasma proteins (mainly beta-globulin and albumin). Its concentration in the blood - 0.5-1 mg / ml, in the serum - 100 mcg / l. Pantothenic acid is not metabolized in the body (except for inclusion in CoA), it is excreted unchanged.
CLINICAL DATA
Indications for use
Acute respiratory diseases with rhinitis, acute allergic rhinitis, vasomotor rhinitis, sinusitis, otitis media (as part of combination therapy to reduce swelling of the nasopharyngeal mucosa), to facilitate rhinoscopy, restore impaired nasal breathing after surgical interventions in the nasal cavity.
Contraindications
Hypersensitivity to any of the components of the drug; arterial hypertension, tachycardia, marked atherosclerosis, glaucoma; atrophic rhinitis; hyperthyroidism, porphyria, prostatic hyperplasia, surgery on the meninges (in history), simultaneous use with monoamine oxidase inhibitors (MAO) and tricyclic antidepressants; pregnancy, breastfeeding period, children under 2 years old;
Carefully: Diabetes mellitus, pheochromocytoma, diseases of the cardiovascular system (including coronary heart disease, angina), hypersensitivity to the action of adrenergic drugs, accompanied by insomnia, dizziness, arrhythmia, tremor, increased blood pressure (BP).
Use during pregnancy and breastfeeding
The use of the drug SeptaNazal during pregnancy and during breastfeeding is contraindicated.
Dosage and administration
Intranasal.
For children from 2 to 6 years.
One metered injection in each nasal passage 3-4 times a day.
Remove the protective cap before use. Before the first use of the spray or after a long break, it is necessary to press the pump dispenser several times until uniform spraying appears. | |
Insert the tip of the bottle vertically in the nasal passage, take a slow breath through the nose, while simultaneously pressing the pump dispenser once. Repeat the procedure in the other nasal passage. After applying the tip should be wiped with a paper napkin and closed with a protective cap. |
Duration of therapy 5-7 days
Side effect
With frequent or long-term use: irritation and / or dryness of the nasal mucosa, burning, tingling, sneezing, hypersecretion, allergic reactions, swelling of the nasal mucosa, nausea, vomiting, headache, dry rhinitis, palpitations, increased blood pressure, tachycardia, insomnia, blurred vision, depression (with prolonged use of high doses).
Overdose
Symptoms:
In cases of overdose or accidental ingestion, the following symptoms may occur: mydriasis, nausea, vomiting, cyanosis, fever, convulsions, tachycardia, cardiac arrhythmias, vascular insufficiency, cardiac arrest, increased blood pressure, pulmonary edema, impaired respiratory function, hallucination.
Patients may also develop symptoms of depression from the central nervous system, accompanied by drowsiness, a decrease in body temperature, bradycardia, shock, cessation of breathing, and coma.
Treatment: the use of Activated carbon, gastric lavage, oxygen ventilation of the lungs. In order to reduce blood pressure, 5mg of phentolamine 0.9% sodium chloride solution is used by intravenous administration or 100mg of phentolamine inside. Vasoconstrictive drugs are contraindicated. If necessary, use antipyretic and anticonvulsant drugs.
Interaction with other drugs
Simultaneous use with inhibitors MAO and tricyclic antidepressants can lead to an increase in blood pressure due to the effects of these drugs on the cardiovascular system
Special notes
Before use, you must clean the nasal passages.
Do not use for more than 7 days. The duration of the drug in children is determined after consultation with the doctor.
Does not contain preservatives. After opening the bottle, the drug should be used within 12 weeks.
Impact on the ability to perform potentially hazardous activities that require special attention and quick reactions (for example, driving vehicles, working with moving machinery).
During the period of use of the drug should be precautionary measures, or avoid driving vehicles and occupations of other potentially hazardous activities that require high concentration of attention and speed of psychomotor reactions.
Release form
Spray nasal dosed (for children),
5 mg + 0.05 mg / dose.
10 ml (90 doses) of the drug in a vial of high-density polyethylene with a dosing device (pump) and a transparent protective cap of the combined material.
1 bottle together with the application instruction is placed in a pack cardboard.
Storage conditions
At a temperature not higher than 25 ° С, in the original package.
Keep out of the reach of children.