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Avihist (Albuterol)

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Avihist 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:
Albuterol, Alernyl, Asthacure, Avasth, Benylin, Broncof, Bronkonat, Bronkonil, Bronkotab, Brosol, Budesal, Codex, Derisone, Derivent, Durabec, Efflin, Elkof, Elkuf, Esmasol, Etobrom, Kofnil, Okaril, Pedex, Pencolin, Pherin, Proventil, Respisol, Salbair, Salbomin, Salsol, Salubril, Salvent, Servent, Spasmonyl, Suprivent, Synabron, Ventirex, Ventorlin, Ventosol, Ventosym, Ventplus, Ventryl, Viburil, Vifex, Viscodyne, Viscof, Vospire, Xputum, Zenovit

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Also known as: Albuterol


Avihist belongs to a class of drugs known as bronchodilators. Avihist is indicated for the relief and prevention of airway obstruction (bronchospasm) in patients with asthma and in patients with exercise-induced asthma. Avihist 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 Avihist 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 Avihist are Albuterol, Salbutamol. Avihist is also known as Albuterol, Salbutamol, Ventorlin, Asthalin, Proventil, ProAir, Salamol, Aerolin.


Follow the directions for using this medicine provided by your doctor. Use Avihist 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 Avihist 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.


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


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 Avihist 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.


Do not take Avihist if you are allergic to Avihist components. It is not known whether Avihist 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 Avihist if you have diabetes, heart disease, high blood pressure (hypertension), hyperthyroidism, irregular heart beats (arrhythmias). Avihist 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 Avihist suddenly.

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The N-terminal periactin dosing sequences up to residue 35, show that heterotepalins exhibit an high percentage identity with other type 1 RIPs isolated from Phytolaccaceae. Cholinergic and adrenergic interaction in the hypothalamic control of drinking and eating behavior. Based on this, the distribution of DEHP between water and bed sediment was investigated as a model of organic pollutant through both the field investigation and laboratory experiment. In order to understand whether there is a specific role for the posttranslational N-acetylglucosamine modification linked O-glycosidically (O-GlcNAc) to serine and threonine residues of proteins during development and/or ageing of the brain, we investigated the O-GlcNAc expression of early postnatal cerebellar neurons as well as of mouse brain of different ages. The present findings demonstrate that iron distribution in the brain is changed by transferrin deficiency and that iron abnormally accumulates in the brain of HP mice. An aggressive surgical approach is justified in patients with MPLC and offers the greatest chance for long-term survival even in the case of limited resection. Combining these two factors may increase the risk for postural complications in at-risk patients. Specifically, we first estimate the spatial quantile process for climate model output using nonlinear monotonic regression during a historical period. The adsorption of trichloroethylene, perchloroethylene, and p-xylene on a MFI (Mobile-FIve) zeolite is studied using in situ FTIR spectroscopy at 298 K.

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