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Betameson Ointment (Betamethasone 0.05%) is indicated for Atopic eczema, contact dermatitis, and other inflammatory and itchy manifestations of severe or resistant corticosteroid-responsive dermatitis.
No interaction found/established
Betameson Ointment should be used with caution in pregnant women. Consult your doctor before using Betameson Ointment.
Betameson Ointment should be used with caution in breastfeeding women. Consult your doctor before using Betameson Ointment.
No interaction found/established
No interaction found/established
No interaction found/established
Betameson Ointment works by acting inside skin cells and preventing the release of certain chemical messengers in the body that cause redness, itching, and swelling. When the skin reacts to any kind of allergens, such chemicals are released normally.
Betameson Ointment is used to treat a variety of skin conditions (such as eczema, dermatitis, allergies, and rash). Betamethasone reduces the swelling, itching, and redness that can occur in these types of conditions.
Betamethasone is a glucocorticoid-primarily corticosteroid. It prevents and regulates inflammation by regulating protein synthesis, inhibiting polymorphonuclear leukocyte and fibroblast migration, and reversing capillary permeability and lysosomal stabilization.
A topical corticosteroid with anti-inflammatory, anti-pruritic, and vasoconstrictive properties is betamethasone dipropionate. A peptide known as lipocortin is induced by betamethasone dipropionate. Phospholipase A2, an enzyme that leads to the breakdown of leukocyte lysosomal membranes and the release of arachidonic acid, is inhibited by lipocortin. This has the effect of reducing the production and release of inflammatory mediators from within the body (including prostaglandins, kinins, and histamine).
In terms of pharmacokinetics, intact, healthy skin can absorb betamethasone dipropionate. To varying degrees, corticosteroids bind to plasma proteins. The liver and kidneys are where corticosteroids are primarily metabolized and eliminated.
Apply a thin film to the affected area once or twice each day to completely cover it. Patients with chronic psoriasis who have experienced at least a noticeable improvement in their psoriatic lesion (i.e., about 80% improvement) with Betamethasone Dipropionate may be kept in remission with a pulse dosing regimen consisting of three consecutive applications of up to 3.5 g of each Betamethasone Dipropionate cream and ointment, spaced out by twelve hours (e.g., morning, evening, next morning), The previously affected and treated lesion sites should be covered with Betamethasone Dipropionate cream and ointment for this reason. Patients who experience a relapse while on this pulse dose regimen should switch back to the standard dosing regimen.
Always apply Betameson Ointment as directed by your physician. It is for external use only. Apply a thin layer of Betameson Ointment to the affected area. Avoid applying this medicine around your eyes, including your eyelids. Your doctor will decide the correct dose and duration of Betameson Ointment depending on your age, weight, and health condition.
There is no evidence of any kind of interaction.
Allergic to betamethasone dipropionate, other corticosteroids, or any component of this preparation. Like other topical corticosteroids, betamethasone dipropionate is contraindicated for viral skin infections such as vaccinia, chickenpox, and herpes simplex, as well as tuberculosis, rosacea, fungal skin infections (candidiasis), perioral dermatitis and ulcers sick.
The safety of using the ointment during pregnancy is not established as there is not enough data to identify the potential risk of birth defects, miscarriage, or adverse outcomes for the mother and the fetus. Studies conducted on animals suggest that the use of ointment during pregnancy may increase the risk of malformations in the fetus. Pregnant women should use the ointment on the smallest possible skin area for the shortest duration possible to reduce the risk of low birth weight infants.
The safety of using the ointment during breastfeeding is not established as there is not enough data to determine the presence of the drug in human milk and the potential adverse effects on the breastfed infant. The benefits of breastfeeding should be considered along with the mother's need for the therapy and the potential adverse effects on the infant. Breastfeeding women should use the ointment on the smallest possible skin area for the shortest duration possible and avoid direct application to the nipple and areola to minimize exposure to the breastfed infant.
Keep the temperature below 30°C, and protect from light and moisture. Keep out of reach of children.
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