Desonide: Difference between revisions
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Revision as of 19:50, 23 March 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sheng Shi, M.D. [2]
Disclaimer
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Overview
Desonide is a corticosteroid that is FDA approved for the treatment of inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. Common adverse reactions include contact dermatitis, dry skin, pruritus, stinging of skin, burning sensation, irritation symptom.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Dermatoses
- Dosing information
- Desonide cream or ointment should be applied to the affected areas as a thin film two or four times daily depending on the severity of the condition.
- As with other corticosteroids, therapy should be discontinued when control is achieved. If no improvement is seen within two weeks, reassessment of diagnosis may be necessary.
- Desonide cream and ointment should not be used with occlusive dressings.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of desonide in adult patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of desonide in adult patients.
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
Safety and effectiveness in pediatric patients have not been established
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of desonide in pediatric patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of desonide in pediatric patients.
Contraindications
Desonide cream and ointment are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparations.
Warnings
There is limited information regarding Desonide Warnings' in the drug label.
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Desonide Clinical Trials Experience in the drug label.
Postmarketing Experience
There is limited information regarding Desonide Postmarketing Experience in the drug label.
Drug Interactions
There is limited information regarding Desonide Drug Interactions in the drug label.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA):
There is no FDA guidance on usage of Desonide in women who are pregnant.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Desonide in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Desonide during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Desonide in women who are nursing.
Pediatric Use
There is no FDA guidance on the use of Desonide in pediatric settings.
Geriatic Use
There is no FDA guidance on the use of Desonide in geriatric settings.
Gender
There is no FDA guidance on the use of Desonide with respect to specific gender populations.
Race
There is no FDA guidance on the use of Desonide with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Desonide in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Desonide in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Desonide in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Desonide in patients who are immunocompromised.
Administration and Monitoring
Administration
There is limited information regarding Desonide Administration in the drug label.
Monitoring
There is limited information regarding Desonide Monitoring in the drug label.
IV Compatibility
There is limited information regarding the compatibility of Desonide and IV administrations.
Overdosage
There is limited information regarding Desonide overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.
Pharmacology
There is limited information regarding Desonide Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Desonide Mechanism of Action in the drug label.
Structure
There is limited information regarding Desonide Structure in the drug label.
Pharmacodynamics
There is limited information regarding Desonide Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Desonide Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Desonide Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Desonide Clinical Studies in the drug label.
How Supplied
There is limited information regarding Desonide How Supplied in the drug label.
Storage
There is limited information regarding Desonide Storage in the drug label.
Images
Drug Images
{{#ask: Page Name::Desonide |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }}
Package and Label Display Panel
{{#ask: Label Page::Desonide |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}
Patient Counseling Information
There is limited information regarding Desonide Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Desonide interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Desonide Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Desonide Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.