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Allrite (Montelukast)
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Allrite

Allrite is used to prevent wheezing, difficulty breathing, chest tightness, and coughing caused by asthma in adults and children 12 months of age and older. Allrite is in a class of medications called leukotriene receptor antagonists (LTRAs).

Other names for this medication:
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Also known as: Montelukast

Description

Target of Allrite is to treat symptoms of asthma, perennial and seasonal allergic rhinitis. Sometimes Allrite is taken to prevent exercise-induced bronchoconstriction in patients who take this medicine only for this condition.This remedy works by obstructing the activity of substances which cause symptoms of allergy and asthma. It is LTRA (leukotriene receptor antagonist). Allrite is also known as Montelukast sodium, Montair, Montus, Romilast.

Dosage

Asthma: - Adults (15 years of age and older): 10 mg a day. - Children (6 to 14 years of age): 5 mg a day. - Children (2 to 5 years of age): 4 mg a day. Allrite should be taken once a day in the evening. Exercise-Induced Bronchoconstriction (EIB): - Adults (15 years of age and older): 10 mg a day. - Children (6 to 14 years of age): 5 mg a day. - Children (2 to 5 years of age): 4 mg a day. For prevention of EIB, Allrite should be taken at least 2 hours before exercise. Do not take more than one dose in 24 hours. Allergic Rhinitis: - Adults (15 years of age and older): 10 mg a day. - Children (6 to 14 years of age): 5 mg a day. - Children (2 to 5 years of age): 4 mg a day. For allergic rhinitis, Allrite should be taken once a day. Patients with both asthma and allergic rhinitis should take only one Allrite dose daily in the evening. Pediatric patients are advised to take chewable tablets.

Overdose

If you overdose Allrite and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Allrite overdosage: stomach pain, agitation, insomnia, thirst, migraine, vomiting.

Storage

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.

Side effects

The most common side effects associated with Allrite 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 the Allrite if you are allergic to Montelukast or any of the other ingredients of this medicine. Do not use the tablets to treat an acute asthma attack, including Status Asthmaticus. Do not use the drug if you suffer from severe kidney failure. Do not combine the medication with drugs which induce the CYP450 enzyme system (phenobarbital and rifampin), as they may decrease the effects of Montelukast. Do not use the medication if you have a phenylketonuria, as Allrite contains phenylalanine. Do not take the medication tablets during pregnancy or while breastfeeding without consulting your doctor. Avoid drinking alcohol while taking Allrite tablets, as it may cause excessive drowsiness. Do not give this medicine to children less than 2 years of age.

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The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1. Considering that colony formation of in vitro retinoblastoma cells is completely suppressed by melphalan at 4 micrograms/ml concentration, an intravitreal application of melphalan could be used as a non-surgical treatment for retinoblastoma. The authors analysed their findings from four previously written articles based on qualitative interviews with 10 women with chronic pain, comparing the reported negative consultation experiences with the beneficial effects of good treatment experiences, in order to identify potentials for change. Automatic grunt detector and recognizer for Atlantic cod (Gadus morhua). Data were collected after single neurological and ophthalmological evaluations. In addition to improving our understanding of the etiology of these tumours, this accumulating knowledge of the oncogenic properties of these fusion proteins, their downstream targets, and cooperating genetic alterations will permit the development of a variety of novel approaches to improve the therapy of these cancers. Thus, BP serves as an important cardiovascular parameter during various stages in foreign spaceflight activities. Numerical computations are performed and analytic bounds are obtained on the excited spectrum of glueballs in SU(inifinity) gauge theory, by transverse lattice Hamiltonian methods.

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To determine whether immune activation and intestinal permeabilisation are more frequently observed in IBS patients compared with healthy controls. Since then, family physicians have been trained, employed and have gained experience of working in the district health services. In 125 patients treated with castration or maximal androgen blockage for at least 12 months, metabolic indicators were analyzed. Cultured synovium-derived MCs were generated by culturing synovial cells with stem cell factor, and receptor expression was analyzed using fluorescence-activated cell sorting. Sensitivity of human multiple myelomas and myeloid leukemias to the proteasome inhibitor I.

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The finding that cdx-2/3 mediates activation of the proglucagon promoter in both islet and enteroendocrine cells is consistent with the common endodermal lineage of these tissues and provides new insight into the coordinate regulation of genes expressed in both pancreatic and intestinal endocrine cell types. Later, the unique level of detail KIEs provided led to deeper questions about the potential role of protein motions in PTP catalysis. We find that de novo assembly and subsequent abundance ranking of repeats can successfully identify tandem repeats with homology to known tandem repeats. Intrarater and interrater reliabilities were examined and compared. The clinical features and tumor cells characteristics of splenic marginal zone lymphoma. We investigated whether a selective Syk inhibitor (GS-492429) could suppress antibody-mediated rejection (AMR) in a rat model of AMR in sensitized recipients. All patients remain alive without treatment-related mortality or evidence of disease.

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