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Alzero (Montelukast)

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Alzero is an oral medication used for allergies as well as long-term treatment of allergic asthma. Alzero doesn't work as well as some inhalers that are commonly used for asthma. It is usually an add-on treatment for asthma that is difficult to control.

Other names for this medication:
Admont, Afineday, Arogra, Breathezy, Coekastle, Deriphyllin, Emlucast, Ferodr, Fexoquin, Irmont, Kastzine, Lazine, Lelet, Letzit, Levasma, Levocet, Levodel, Levoler, Levotin, Lewlet, Luvle, Monamra, Monkezin, Montair, Montas, Montasma, Montelast, Montelukast, Montilife, Montolife, Nainmont, Nexofex, Novolen, Ontelio, Pulmokast, Romlist, Tastymont, Trimontemac, Ventyl, Vezomont, Xyvent

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Also known as: Montelukast


Alzero tablets, produced by Merck Sharp & Dohme, are indicated in the treatment of asthma as add-on therapy in those patients with mild to moderate persistent asthma who are inadequately controlled on inhaled corticosteroids. It helps prevent the wheezing, chest tightness, and shortness of breath caused by asthma and decreases the number of asthma attacks. The medicine is used to prevent exercise-induced bronchoconstriction (narrowing of the air passages in the lungs). It also helps treat seasonal and perennial allergic rhinitis. The active substance contained in the medication is Montelukast, a leukotriene receptor antagonist, that stops leukotrienes, chemical messengers in the immune system, from causing inflammation in the lungs and nose, preventing asthma symptoms and allergies.


Take Alzero chewable tablets (4 mg, 5 mg, 10 mg), granules, film-coated tablets orally with water. Usually Alzero is taken as a single dose at least two hours before you exercise. Do not take another dose of Alzero for at least 24 hours. Usually Alzero is taken once a day in the evening with or without food. Do not take Alzero for asthma attack treatment that has already begun. If you want to achieve most effective results do not stop taking Alzero suddenly.


If an overdose occurs and you are feeling unwell, you should seek emergency medical attention or contact your healthcare provider immediately.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) and away from excess moisture and heat. Keep your tablets in the blister pack until it is time to take them. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

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The most common side effects associated with Alzero 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 Alzero if you are allergic to its components or to aspirin. Do not take Alzero if you use Alzero while you are pregnant or have nurseling. You should not use Alzero for exercise-induced bronchoconstriction if you already take Alzero to prevent symptoms of allergy or asthma. Try to be careful using Alzero if you take phenobarbital (such as Solfoton, Luminal), rifampin (such as Rifamate, Rifadin, Rimactane, Rifater). It can be dangerous to use Alzero if you suffer from or have a history of phenylketonuria, liver disease. Avoid any activities such as driving or operating machinery while taking Alzero. It can be dangerous to stop Alzero taking suddenly.

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Reduced vaccination regimens such as the 2-1-1 have been proven to be efficient in raising protective antibody responses. In this work, we demonstrate that Mps, expressing functional muscarinic acetylcholine receptors, are able to proliferate in vitro in response to the muscarinic agonist carbachol. Researchers initially proposed the substitution of apoptotic chondrocytes in the superficial cartilage by injecting mesenchymal stem cells (MSCs) intraarticularly. However, deletion of Atalpha-DOX2 in Arabidopsis plants did not provoke any visible phenotypic alteration indicating that the relative importance of alpha-DOX2 in plant physiology is species specific. We studied, as a physiological benchmark, acute effects of right ventricular (RV) apical, RV outflow, and left ventricular (LV) pacing in children with normal cardiac function on LV and RV function and ventricular-ventricular interactions.

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This review presents an overview of current molecular epidemiology of bladder cancer and provides a useful resource for understanding the pathogenesis of bladder cancer. Differences in clinicopathologic features, relapse-free survival (RFS) rates, and cancer-specific survival (CSS) rates between the groups were evaluated. The concentrations of the major monoamine metabolites, homovanillic acid (HVA), 3-methoxy-4-hydroxyphenylethylene glycol (MOPEG), and 5-hydroxyindoleacetic acid (5-HIAA) in the cerebrospinal fluid (CSF), of platelet monoamine oxidase (MAO) and of dopamine beta-hydroxylase (DBH)-activity in serum and CSF were determined in pairs of healthy mono- and dizygotic twins, brothers and unrelated individuals. To highlight therapeutic controversies, and present a critical review of the most recent evidence on the management of heparin-induced thrombocytopenia (HIT). TSP-1 suppressed tumor growth at both primary and metastatic sites by inducing apoptosis in tumor-associated microvascular endothelial cells. I conclude that a small anastomosis may in some cases predispose to this problem.

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