Budoster spray 100mcg/dose 10ml

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Budoster user manual

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Budoster eliminates the symptoms of a cold with an allergic nature. The drug is able to suppress the early and late stages of an allergic response.
Budoster stops the inflammatory process in the airways. The medicine inhibits the influx of leukocytes to the area of ​​allergic inflammation.
After ingestion, only 20% of the dose passes into the bloodstream. The maximum concentration of the substance in the plasma is reached after 42 minutes, it is 1 nmol / L.
The active substance is well distributed and bound to proteins, the volume is about 300 liters.
The bioavailability of the active element is low, more than 92% after metabolic processes are inactivated in the liver.
The elimination period is two to three hours. It leaves through the intestinal tract.

Indications

Budoster is indicated for preventive purposes, as well as as part of complex therapy for a cold of an allergic nature. In addition, the drug helps with diseases:
    vasomotor rhinitis;
    polyps in the nose.

Dosage and administration

The best result from treatment with Budoster will appear if the instructions for the drug are strictly observed.
Method of use for adults, the elderly and children over six years of age:
    Use only under the supervision of parents or other adults.
    Therapy begins with a dose of 100 mcg in each nostril in the morning and evening.
    The prophylactic dosage is 50 mcg in both nostrils in the morning and evening, or 100 mcg in both nasal passages immediately after waking up. A prophylactic dose is the minimum dosage that helps to cope with a runny nose.
    The maximum allowable dose is 200 micrograms per dose (total in both nostrils), no more than 400 micrograms of the drug can be taken per day. Continuous course - no more than three months.
With prolonged treatment of the child with a Budoster spray, it is recommended to regularly conduct control measurements of growth. If growth retardation is detected, the doctor should reduce the dosage. Adults need to constantly monitor the condition of the nasal mucosa.
If you skip a dose, you can take it later, but between doses should be at least one hour.
In case of an allergic rhinitis, the remedy should be used on a regular basis.

Release form, composition

Budoster is available in the form of a spray for the nose. In a glass bottle with a dosing system is a liquid homogeneous substance of white color with a subtle floral smell.
One pack contains two hundred doses. In a single dose of 50 μg of the active substance budesonide. The bottle is placed in a cardboard box, instructions are attached to it.
In the manufacture of the drug additional substances are used:
    specially prepared water 48 mg;
    hydrochloric acid;
    disodium edetate;
    polysorbate 80;
    potassium sorbate;
    avicel;
    dextrose.


Interaction with other drugs

When using phenytoin, refampicin and phenobarbital simultaneously with Budoster, the effectiveness of the latter may be reduced. Ketoconazole, estrogens, methandienone produce the opposite effect. They are able to increase the effectiveness of Budoster.
Budoster is safe for drivers of vehicles and for managers of other mechanisms and equipment. The drug does not change the reaction rate, does not negatively affect attention and thought processes.

Side effects

The following side effects of the drug are possible:
    burning and pain in the nasopharynx;
    sneezing and dry throat;
    mucosal irritation;
    crusts inside the nasal cavity;
    dizziness.
Side effects are much less common in practice:
    cough, difficulty breathing;
    acute desire to sleep;
    distinctly felt pulse;
    vomiting and nausea, stomach problems;
    skin rashes, redness of the skin;
    mucosal atrophy, ulcers, anosmia;
    nosebleeds;
    violation of the microflora of the nasal mucosa (with prolonged treatment).
In the early days of therapy, the development of rhinorrhea is possible, which quickly passes. It is important to remember the systemic effect of Budoster: suppression of the adrenal glands, decreased bone density, impaired visual function, delayed normal growth of children.

Overdose

Significant excess doses for a long time can lead to acne, dysmenorrhea and Cushing's syndrome. In these cases, the drug must be withdrawn gradually.

Contraindications

Budoster treatment cannot be started in the following cases:
    active tuberculosis;
    fungal infection of the lungs;
    bacterial or viral infections of the lungs;
    individual sensitivity to any component of the drug.
In pediatrics, the use of Budoster should be agreed with a specialist. Contraindicated in young children (up to six years). Under constant medical supervision Budoster is taken by people who have had surgery on the nasal cavity and injured their nose. This is due to the fact that the drug inhibits the process of regeneration of wounds.
It is required to avoid getting the spray on the shell of the eyes.
The drug is canceled if the symptoms after three months of treatment do not change. The first results usually appear five to seven days after the start of therapy.
Patients who have been treated with systemic glucocorticosteroids before Budoster are at risk for adrenal insufficiency. It is important to exercise increased caution and attention during the restoration of the adrenal system. The transition should be gradual.
At the same time, patients may be disturbed by pain in the muscle fibers, joint pain, loss of strength, depressive and apathetic state. Such symptoms are eliminated by increasing doses of systemic glucocorticosteroids, and then slowly withdrawing them.


During pregnancy and lactation

In any trimester of pregnancy, taking the drug is possible, but under the supervision of a gynecologist. It is necessary to assess the need to use the medicine in a particular case.
With breastfeeding, it is better not to start therapy. If there is an urgent need for taking Budoster, you need to temporarily stop feeding.
Such caution is associated with a lack of necessary research. Tests have not been conducted confirming the safety of the active substance for a pregnant woman and fetus.

Terms and conditions of storage

Do not store the vial in the freezer. The ambient temperature should not be higher than 25 degrees. Keep out of the reach of children. Use a sealed vial within 24 months after manufacture. An opened bottle is suitable for three months. When the expiration date is over, discard the bottle. Do not use at expiration.

Reviews

The drug received many positive ratings and reviews online from consumers and doctors. A noticeable result appears on 3-4 days of treatment. Many also note the pleasant aroma of the spray, the ease of use.
Some have side effects in the form of a mild headache, but the overall impression of Budoster remains positive.
Doctors and patients confirm the high effectiveness of Budoster in case of allergic rhinitis and vasomotor rhinitis.

Terms of sell

A prescription is not required to buy Budoster online.