Adgar - Adapalene | VetSafeCare.Com

Gel

Adgar

Adapalene — ACI Limited
0.3% / gel · 0.1% / gel

Alternatives

6

Routes

TOP

Presentations

2

Generic profile Browse alternatives View combinations

Presentations

Gel · 0.3% / gel

10 gm

৳80.24

Gel · 0.1% / gel

10 gm

৳60.18

Dose rules

No structured dose rules are linked to this brand yet.

Dose reference

Human

Adapalene 0.1%: It should be applied to the affected areas of skin, once daily at night-time.Adapalene 0.3%: It should be applied to the entire face and any other affected areas of the skin, once daily in the evening.Children below 12 years of age: Safety and effectiveness in children below 12 years of age have not been established. Administration: A thin film of gel or cream should be applied to the skin areas where lesions present, using enough to cover the entire affected areas lightly.

Clinical notes

Applications:
  • Keratosis pilaris
Indication Notes:
Adapalene cream or gel is indicated for topical treatment of acne vulgaris.
Avoid In:

N/A

Contraindication Notes:
Adapalene should not be administered to individuals who are hypersensitive to Adapalene or any of its components.
Adapalene acts on retinoid receptors that are commonly found in the skin of face, back and chest. Biochemical and pharmacological studies have demonstrated that Adapalene is a modulator of cellular differentiation, keratinization, and inflammatory processes, all of that represent important features in the pathology of acne vulgaris. Adapalene binds with specific retinoic acid nuclear receptors that normalize the differentiation of follicular epithelial cells resulting in decreased microcomedone formation. Absorption of Adapalene through human skin is low.
Concomitant use of other potentially irritating topical products (medicated or abrasive soaps and cleansers, soaps and cosmetics that have a strong drying effect, products with high concentrations of alcohol, astringents, spices or lime) should be approached with caution. Exercise particular caution in using preparations containing sulfur, resorcinol or salicylic acid in combination with Adapalene. If any of these preparations have been used, it is advisable not to start therapy with Adapalene until the effects of such preparations in skin have subsided. If combined use of both medications is important, it is better to use in two different times.
Erythema, scaling, dryness, pruritus, burning sensation, skin irritation, stinging unburn, acne flares, etc. are commonly seen during the first month of therapy but usually lessen with continued use of the medication.
Use Adapalene during pregnancy only if the potential benefit justifies the potential risk to the fetus. It is not known whether this drug is excreted in breast milk. Exercise caution when administering Adapalene to a nursing mother.
Adapalene should not be applied to cuts, abrasions, eczematous or sunburned skin.