Dermalog Cream 0.1% is a potent topical corticosteroid used to reduce inflammation and itching in various dermatologic conditions. It is applied directly to the skin in the form of creams, ointments, or lotions and is typically prescribed for short-term management of severe inflammatory skin conditions.
Dermalog Cream 0.1% is used to treat a variety of inflammatory skin disorders, including:
| Brand Name | Dermalog |
|---|---|
| Type | Cream |
| Weight | 0.1% |
| Generic | Halcinonide |
| Manufacturer | Jayson Pharmaceuticals Ltd. |
| Available in | English বাংলা |
Dermalog Cream 0.1% exerts its effects through binding to corticosteroid receptors within the cells, leading to decreased inflammation and immune response. This action reduces the production of inflammatory mediators, including prostaglandins and leukotrienes, thus alleviating symptoms such as redness, swelling, and itching.
The onset of action for Dermalog Cream 0.1% can vary, but improvement in symptoms is generally observed within a few days of starting treatment. The full therapeutic effects may take several days to a couple of weeks, depending on the severity of the condition and individual response to the medication.
Dermalog Cream 0.1% is absorbed through the skin upon topical application. Systemic absorption is minimal but can occur, especially if large areas of skin are treated or if occlusive dressings are used. The extent of systemic absorption can vary based on the condition of the skin and the vehicle used for the medication.
Dermalog Cream 0.1% is primarily metabolized in the liver. The metabolites are then excreted through the urine. The minimal systemic absorption typically leads to limited systemic metabolism and excretion.
The dosage of Dermalog Cream 0.1% depends on the specific formulation and the condition being treated:
To administer Dermalog Cream 0.1%:
Common side effects include:
Toxicity is rare with proper use but may occur with overuse or prolonged application, particularly under occlusive dressings. Symptoms of toxicity may include skin thinning, striae, or systemic effects like adrenal suppression. Seek medical attention if any severe symptoms develop.
Precautions include:
Topical corticosteroids like Dermalog Cream 0.1% may interact with other topical medications applied to the same area. Ensure to inform the healthcare provider of all concurrent topical treatments to avoid potential interactions.
Use Dermalog Cream 0.1% with caution in patients with:
Drug interactions are minimal with topical application. However, concurrent use with other corticosteroids or drugs that affect skin absorption or metabolism may require careful monitoring.
There are no specific food interactions reported with Dermalog Cream 0.1%. Maintaining a balanced diet supports overall health and can be beneficial during treatment.
Dermalog Cream 0.1% should be used during pregnancy only if clearly needed and prescribed by a healthcare provider. The potential risks and benefits must be weighed, as corticosteroids can affect fetal development.
Dermalog Cream 0.1% is generally considered safe for use during lactation when applied topically. However, avoid application to the breasts to prevent accidental ingestion by the infant. Consult a healthcare provider for personalized advice.
Acute overdose is unlikely with topical application. In case of accidental ingestion or significant overuse, seek medical attention immediately. Symptoms of overdose may include severe skin reactions or systemic effects.
Contraindications include:
Follow the prescribed dosage and application instructions carefully. Avoid using more than the recommended amount and do not apply to large areas of the body or under occlusive dressings unless directed by a healthcare provider.
Store Dermalog Cream 0.1% at room temperature, away from direct light and moisture. Keep the medication out of reach of children and ensure the container is properly sealed to maintain efficacy.
The volume of distribution for Dermalog Cream 0.1% is not typically measured in topical applications. The medication acts locally at the site of application with minimal systemic distribution.
The half-life of Dermalog Cream 0.1% in topical applications is not well-defined. The drug’s effects persist locally at the application site, and systemic half-life data may not be directly applicable.
Dermalog Cream 0.1% is cleared primarily through hepatic metabolism and renal excretion. The minimal systemic absorption associated with topical application generally results in limited systemic clearance.
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