DESOGRACE LOTION contains Desonide which belongs to a group of medicines called Topical Corticosteroids. DESOGRACE LOTION is used to relieve inflammatory and pruritic manifestations of corticosteroid-responsive dermatosis.
Along with this treatment, your doctor might advise you to take a urinary-free cortisol and ACTH (adrenocorticotropic hormone) stimulation test to evaluate HPA axis suppression (a condition that causes poor body defence against infection) especially in children to prevent its effect in the body.
Before applying DESOGRACE LOTION, inform your doctor if you are allergic to Desonide or any other ingredients in the medicine, and or have concomitant skin infections (infections caused by parasites).
DESOGRACE LOTION should be used in pregnant and breastfeeding women only if it is necessary. Consult your doctor for advice.
DESOGRACE LOTION is not recommended for use in children (less than 2 years of age). Consult your doctor before applying DESOGRACE LOTION.
The most common side effects of applying DESOGRACE LOTION are application site reactions such as burning, irritation, itching and redness, headache. Contact your doctor if any of the side effects get worse.
DESOGRACE LOTION works by the induction of lipocortins (inflammatory enzyme) that results in the decreased biosynthesis of prostaglandins and leukotrienes (potent mediators of inflammation) which prevents the release of arachidonic acid (hormone responsible for inflammatory process in the skin) thus providing relief from the inflammation, redness, and itching sensation.
Apply DESOGRACE LOTION as directed by your doctor. It is for external use only. Avoid contact of this medicine in your eyes, ears, nose, mouth, or mucous membrane. Your doctor will decide the duration of treatment depending on the severity of the condition.
Stop applying DESOGRACE LOTION and contact your doctor immediately if you experience any of the following side effects:
Headache:
If DESOGRACE LOTION cause headache, then take rest and drink plenty of fluids. Try to avoid drinking alcohol. Ask your doctor to recommend a painkiller. Headaches should usually go away after the first week of applying DESOGRACE LOTION. If headaches last more than a week or severe, inform your doctor.
DESOGRACE LOTION should be used in pregnant women only if it is clearly advised by your doctor. Consult your doctor before using DESOGRACE LOTION.
DESOGRACE LOTION should be used in breastfeeding women only if clearly advised by your doctor. Do not apply DESOGRACE LOTION to the breasts during lactation since it might lead to risk of ingestion by the neonate. Consult your doctor before applying DESOGRACE LOTION.
DESOGRACE LOTION does not interfere with your ability to drive or use heavy machines. Consult your doctor before applying DESOGRACE LOTION.
Avoid or limit the consumption of alcohol while applying DESOGRACE LOTION. Consult your doctor for advice.
Do not use DESOGRACE LOTION if you are allergic to Desonide or any other ingredients in the medicine. Consult your doctor before applying DESOGRACE LOTION.
DESOGRACE LOTION is not recommended for use if you:
Before applying DESOGRACE LOTION, inform your doctor if you have:
Use in pediatrics:
DESOGRACE LOTION is not recommended for use in children (less than 2 years of age). Your doctor will prescribe the right dose depends on your child’s age, body weight and disease condition. Consult your doctor before applying DESOGRACE LOTION.
Use in geriatrics:
DESOGRACE LOTION should be used with caution in elderly patients (above 65 years of age). Consult your doctor before applying DESOGRACE LOTION.
A. Drug-Drug Interactions:
Before applying DESOGRACE LOTION, inform your doctor, if you are taking or using prescription, non-prescription and herbal medicines.
Overdosage:
If you or anyone else accidentally uses too much DESOGRACE LOTION, consult your doctor immediately or visit the nearby hospital.
Drug | : | Desonide |
Pharmacological Category | : | Topical Corticosteroids |
Therapeutic Indication | : | Corticosteroid-responsive dermatoses (skin disorder characterized by itchy scalp and red skin) |
Dosage Forms | : | Cream, Lotion, Gel |
What DESOGRACE LOTION is used for?
DESOGRACE LOTION is used to relieve inflammatory and pruritic manifestations of corticosteroid-responsive dermatosis.
How DESOGRACE LOTION is applied on the affected site?
Apply DESOGRACE LOTION as directed by your doctor. It is for external use only. Wash your hands before and after use to ensure hygiene is maintained. Your doctor will decide the duration of treatment depending on the severity of the condition.
What are the side effects of DESOGRACE LOTION?
The most common side effects of applying DESOGRACE LOTION are application site burning and irritation, headache, high blood pressure, and red skin. Contact your doctor if any of the side effects worsen.
Is DESOGRACE LOTION safe to use in children?
DESOGRACE LOTION is not recommended for use in children (less than 2 years of age) and is advised to be used with caution in children (above 2 years) and adolescents (less than 18 years) after consult your doctor before applying DESOGRACE LOTION who might check for any occurrence of side effects.
1. KD. Tripathi. Drugs Acting on Skin and Mucous Membranes. Essentials of medical pharmacology. Seventh edition. 2013. Page – 895.
2. Wake Forest University. Efficacy of Desonide (Desonatetm) Gel 0.05% in Younger and Older Subjects with Atopic Dermatitis. NIH U.S. National Library of Medicine. ClinicalTrials.gov. [Revised in September 2018] [Accessed on 6th May 2022] https://clinicaltrials.gov/ct2/show/NCT00690833
3. Sarah Gabros; Trevor A. Nessel; Patrick M. Zito. Topical Corticosteroids. NIH National Library of Medicine. National Center for Biotechnology Information. StatPearls. November 2021 [Accessed on 6th May 2022] https://www.ncbi.nlm.nih.gov/books/NBK532940/
4. Galderma Australia Pty Ltd. DESOWEN. [Revised in August 2018] [Accessed on 6th May 2022] https://www.galderma.com/au/sites/default/files/inline-files/Desowen%20PI_7%20Aug%202018_0.pdf
5. Stiefel Laboratories, Inc. U.S. Food & Drug Administration. [Revised in April 2013] [Accessed on 6th May 2022] https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021978s010lbl.pdf
6. Bayer HealthCare Pharmaceuticals Inc. U.S. Food & Drug Administration. [Revised in July 2014] [Accessed on 6th May 2022] https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021844s008lbl.pdf
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