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Bronkonil (Albuterol)
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Bronkonil

Bronkonil is used to prevent and treat difficulty breathing, wheezing, shortness of breath, coughing, and chest tightness caused by lung diseases such as asthma and chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways).

Other names for this medication:
Aerotaz, Albuterol, Alernyl, Asmanil, Asthamol, Avasth, Bronkonat, Bronkonil, Bronsim, Codex, Derisone, Durabec, Durasal, Elkuf, Esmasol, Exporil, Ophyl, Respisol, Salbetol, Salbrosin, Salbusun, Salcare, Salvent, Spasomonyl, Sudex, Ventryl, Ventsolv, Vifex, Xputum, Zerfy, Zytus

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Also known as: Albuterol

Description

Bronkonil belongs to a class of drugs known as bronchodilators. Bronkonil is indicated for the relief and prevention of airway obstruction (bronchospasm) in patients with asthma and in patients with exercise-induced asthma. Bronkonil can also be used in treating patients with emphysema and chronic bronchitis when their symptoms are related to reversible airway obstruction. Albuterol, the active ingredient in Bronkonil is a selective beta-adrenergic bronchodilator used to treat severe acute asthma and chronic bronchospasm caused by other pulmonary obstructive disorders that have not responded to other forms of therapy. Generic names of Bronkonil are Albuterol, Salbutamol. Bronkonil is also known as Albuterol, Salbutamol, Ventorlin, Asthalin, Proventil, ProAir, Salamol, Aerolin.

Dosage

Follow the directions for using this medicine provided by your doctor. Use Bronkonil exactly as directed. Take this medication by mouth as directed by your doctor. Do not crush or chew it. Swallow the pill whole. Crushing or chewing Bronkonil will negate the delayed release mechanism of the medication. -The usual effective dose is 4mg, three or four times per day. -If adequate bronchodilation is not obtained, each single dose may be gradually increased to as much as 8mg. -Some patients obtain adequate relief with 2 mg three or four times daily. 2 - 6 years: The minimum starting dose is 1mg three times daily. This may be increased to 2mg (1 tablet), three or four times daily. 6 - 12 years: The minimum starting dose is 2mg three times daily. This may be increased to four times daily. Over 12 years: The minimum starting dose is 2mg three times daily. This may be increased to 4mg (2 tablets), three or four times daily. In elderly patients or in those known to be usually sensitive to beta-adrenergic stimulant drugs, it is advisable to initiate treatment with 2 mg salbutamol three or four times per day.

Overdose

If you overdose Bronkonil and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at a room temperature not exceeding 30 degrees C (86 degrees F) away from moisture, light and heat. Throw away the after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Bronkonil are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Bronkonil if you are allergic to Bronkonil components. It is not known whether Bronkonil will harm an unborn baby. Do not use this medicine without your doctor's advice if you are pregnant or breast-feeding. Be careful with Bronkonil if you have diabetes, heart disease, high blood pressure (hypertension), hyperthyroidism, irregular heart beats (arrhythmias). Bronkonil may make you dizzy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. Do not stop treatment, even if you are feeling better, unless your doctor tells you to. It may take 2 weeks or longer before you feel the full benefit of the medication. Avoid alcohol. Do not stop taking Bronkonil suddenly.

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Second, genetic manipulations altering nestin expression also exert the same effect on the expression of the RC2 antigen. Clinical observation on mild-warm moxibustion for treatment of diabetic peripheral neuropathy. The genetic and phenotypic characterization of poliovirus strain P3/Jinan/1/09, isolated from sewage sample in Jinan city, Shandong province, China, was described. In this unit, the gene of interest is inactivated by interrupting its coding sequence with a positive selectable marker (e.g., neo). 40 male patients with COPD (age 40 years or older) and with a significant smoking history (20 pack-years or more) were included in tofranil dosage the study. Soy isoflavones are natural products that could be used as an alternative to menopausal hormone therapy because they are structurally and functionally related to 17beta-estradiol.

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Elevated MPV might be considered as a marker of increased thromboembolic risk in patients with RMS. Colectomy with temporary ileostomy was performed for worsening symptoms and imminent perforation. However, overall survival (OS) appeared to plateau, even with the introduction and refinement of these regimens. Studies investigating only PTSD symptoms, trauma and physical disorders classified at the organ-system level were excluded. Similar cooling rates for all 3 conditions indicate that there is no benefit associated with wearing the PC17 or gel jacket. Effect of the estrous cycle stage on sensitivity to pheromone 2,5-dimethylpyrazine in the house mouse Mus musculus. Study of thermal properties of the metastable supersaturated vapor with the integral equation method. Twelve patients with anal cancer without evidence for inguinal LN involvement were included in the study. This work shows that the novel technology combines both advantages of the established practices: organic and inorganic pollutants are either destroyed or removed from the P containing material, and the P returned to the soil exhibits high plant-availability.

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