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Deslor Syrup contains Desloratadine, which is classified as an antihistamine medication. It is primarily used to alleviate allergic symptoms associated with conditions like allergic rhinitis, including nasal congestion, itchy nose, repetitive sneezing, and red, watery, or itchy eyes. It can also be effective in treating urticaria, which is characterized by itchy raised patches on the skin.
Deslor Syrup is suitable for both adults and children aged 12 years and older. Unlike some other allergy medications, it does not typically cause drowsiness or sleepiness. Its effects can last up to 24 hours, allowing individuals to resume their regular daily activities and sleep patterns.
Prior to taking Deslor Syrup, it is important to inform your doctor if you have any kidney problems. Additionally, if you have a family history of seizures or epilepsy, it is recommended to disclose this information to your doctor as a precautionary measure.
Deslor Syrup is not recommended for use during pregnancy or while breastfeeding. The most commonly reported side effects of taking this medication include dry mouth, headache, and fatigue. If these side effects become troublesome, it is advised to consult your doctor for further guidance.
Avoid consumption of alcohol while taking Deslor Syrup.
Deslor Syrup is not recommended to take during pregnancy unless it is prescribed by your doctor.
Deslor Syrup should be avoided by breastfeeding mothers to reduce any chances of harm to the newborn baby. Take this medicine only if it is clearly needed and prescribed by your doctor.
Deslor Syrup does not affect your alertness or ability to drive as it does not make you sleepy. You may drive if you feel comfortable.
Deslor Syrup should be used with caution in patients with poor kidney function. Therefore, consult your doctor before taking it.
Deslor Syrup should be used with caution in patients with Liver Diseases. Therefore, consult your doctor before taking it.
Deslor 5 MG Tablet works by blocking the effects of a chemical messenger (histamine) in the body that causes allergic symptoms like itching and swelling, etc.
Allergic Rhinitis: Desloratadine is indicated for the relief of the nasal and non-nasal symptoms of allergic rhinitis (Both seasonal and perennial) in patients 2 years of age and older.
Chronic Idiopathic Urticaria: Desloratadine is also indicated for the symptomatic relief of pruritus, reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria 2 years of age and older.
Desloratadine, the primary active metabolite of Loratadine, is a non-sedating substance. It belongs to the class of long-acting tricyclic histamine antagonists and exhibits selective H1-receptor histamine antagonist activity. Desloratadine is effective in blocking the H1 receptors and preventing the effects of histamine in the body. Additionally, it can inhibit the release of histamine from mast cells in humans. This mechanism of action helps alleviate allergic symptoms without causing drowsiness.
Dosage instructions for the syrup form of the medication are as follows:
Some medicines can affect the way Deslor Syrup works or Deslor Syrup itself can reduce the effectiveness of other medicines taken at the same time. Tell your doctor about all the medicines, supplements, or herbals you are currently taking or might take to avoid any possible interaction.
Desloratadine is contraindicated in patients with known hypersensitivity to this medicine or to any of its ingredients or to loratadine.
The available data on the use of desloratadine in pregnancy are limited, and there is insufficient information to determine its potential risk for major birth defects and miscarriage. Adequate and well-controlled studies in pregnant women have not been conducted.
Regarding reproductive potential, there is no available data on the impact of desloratadine on human fertility. In studies conducted in rats, there were no clinically relevant effects on female fertility. However, in male rats, a decrease in fertility was observed at a high dose of desloratadine that was significantly higher than the recommended human dose.
Desloratadine and pseudoephedrine, another component of some formulations, can both pass into breast milk. There is not enough data on the effects of desloratadine on breastfed infants or its impact on milk production. The decision to continue breastfeeding or discontinue it should be made by considering the developmental and health benefits of breastfeeding, the clinical need of the nursing mother, and the potential adverse effects on the breastfed infant from the medication or the underlying maternal condition.
In adult patients with hepatic or renal impairment, it is recommended to start with a lower dose of desloratadine. A starting dose of one 5 mg tablet every other day is recommended based on pharmacokinetic data. This is done to account for the potential impact of impaired liver or kidney function on the clearance of the medication.
For patients with a medical or family history of seizures, caution should be exercised when prescribing desloratadine. Close monitoring may be necessary to assess the individual's response to the medication.
Desloratadine is not recommended for use in patients with severe renal or hepatic failure, children below 6 months of age, the elderly population, individuals with epilepsy, pregnant women, or breastfeeding mothers. The safety and effectiveness of desloratadine in these populations have not been established or sufficient data is not available.
Regarding lactation, it is unknown whether desloratadine is excreted in breast milk. Therefore, it is not recommended to use desloratadine during breastfeeding due to the lack of sufficient data on its effects on the breastfed infant.
Store in a cool & dry place, protected from light. Store below 30°C. Keep all medicines out of the reach of children.
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