Cerner Multum, Inc. "Australian Product Information." Due to inconsistencies between the drug labels on DailyMed and the pill images provided by Indications, dose, contra-indications, side-effects, interactions, cautions, warnings and other safety information for ADAPALENE. 0781-7142-70 Side effects requiring immediate medical attention. Free E-newsletter Subscribe to Housecall. No effects of adapalene were found on the reproductive performance or fertility of the FThe safety and efficacy of once daily use of adapalene gel, 0.3% for treatment of acne vulgaris were assessed in one 12 week, multi-center, controlled, clinical study, conducted in a total of 653 patients 12 to 52 years of age with acne vulgaris of mild to moderate severity. Applying creams, lotions, or moisturizers as needed helps lessen these skin problems.During treatment with this medicine, avoid getting too much sun on treated areas and do not use sunlamps. Along with its needed effects, adapalene topical may cause some unwanted effects. Common side effects of Differin Gel 0.3% include:

If experienced, these tend to have a Severe expression. There are no adequate and well-controlled studies in pregnant women.

Copy the URL below and paste it into your RSS Reader application. Differin Gel 0.3% is available in generic form.

( Adapalene gel, 0.3% should not be administered to individuals who are hypersensitive to adapalene or any of the components in the gel vehicle. Do not use Adapalene Gel, 0.3% for a condition for which it was not prescribed. Our general interest e-newsletter keeps you up to date on a wide variety of health topics. Side effects. Side effects requiring immediate medical attention. It is also available combined with benzoyl peroxide under the brand names Epiduo and Tactupump. Adapalene is used to treat acne. Differin Gel is available in generic form. Particular caution should be exercised in using preparations containing sulfur, resorcinol, or salicylic acid in combination with adapalene gel, 0.3%.

You can also ask your doctor or pharmacist for information about Adapalene Gel, 0.3% that is written for health professionals.Inactive ingredients: carbomer 980, edetate disodium, methylparaben, poloxamer 182, propylene glycol, purified water and sodium hydroxide. Animal studies have shown an increased risk of skin neoplasms with the use of pharmacologically similar drugs (e.g., retinoids) when exposed to UV irradiation in the laboratory or to sunlight. You may report side effects to FDA at 1-800-FDA-1088.You may also report side effects to Sandoz Inc. at 1-800-525-8747.Medicines are sometimes prescribed for purposes other than those listed in a Patient Information Leaflet. These are not all the possible side effects of Adapalene Gel, 0.3%. All rights reserved. These were most likely to occur during the first four weeks of treatment, were mostly mild to moderate in intensity, and usually lessened with continued use of the medication. Information is for End User's use only and may not be sold, redistributed or otherwise used for commercial purposes.Mayo Clinic does not endorse companies or products. "Product Information. Adapalene Gel, 0.3%, is a retinoid, indicated for the topical treatment of acne vulgaris in patients 12 years of age and older. The incidence of local cutaneous irritation with adapalene gel, 0.3% from the controlled clinical study is provided in the following table:Table 1: Physician assessed local cutaneous irritation with adapalene gel* Total number of subjects with local cutaneous data for at least one post-Baseline evaluation.Table 2: Patient reported local cutaneous adverse reactions with adapalene gel* Selected adverse reactions defined by investigator as Possibly, Probably or Definitely RelatedRelated adverse reactions from the controlled clinical trial that occurred in greater than 1% of patients who used adapalene gel, 0.3% once daily included: dry skin (14.0%), skin discomfort (5.8%), pruritus (1.9%), desquamation (1.6%), and sunburn (1.2%). Because many drugs are excreted in human milk, caution should be exercised when adapalene gel, 0.3% is administered to a nursing woman.Safety and effectiveness have not been established in pediatric patients below the age of 12.Clinical studies of adapalene gel, 0.3% did not include subjects 65 years of age and older to determine whether they respond differently than younger subjects. Female patients who were pregnant, nursing or planning to become pregnant were excluded from the study.Patients enrolled in the study were Caucasian (72%), Hispanic (12%), African-American (10%), Asian (3%), and other (2%). For more information, ask your doctor or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. The following selected adverse reactions occurred in less than 1% of patients: acne flare, contact dermatitis, eyelid edema, conjunctivitis, erythema, pruritus, skin discoloration, rash, and eczema.In a one-year, open-label safety study of 551 patients with acne who received adapalene gel, 0.3%, the pattern of adverse reactions was similar to the 12-week controlled study.The following adverse reactions have been identified during post approval use of adapalene: skin irritation, application site pain, face edema, eyelid edema, lip swelling, and angioedema.

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