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Orbactiv is approved to treat patients with acute bacterial skin and skin structure infections (ABSS"...
Verdeso Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
Verdeso (desonide) Foam, 0.05% is a topical (for the skin) steroid used to treat the inflammation and itching caused by a number of skin conditions such as allergic reactions, eczema, and psoriasis. Common side effects include stinging, burning, irritation, dryness, or redness at the application site. Acne, new/unwanted hair growth, "hair bumps" (folliculitis), skin thinning/discoloration, or stretch marks may also occur.
Apply a thin layer dose of Verdeso Foam should to the affected area(s) twice daily. Verdeso may interact with other drugs. Tell your doctor all medications and supplements you use. During pregnancy, Verdeso Foam should be used only if prescribed. It is unknown if this drug passes into breast milk when applied to the skin. Similar medications pass into breast milk when taken by mouth. Consult your doctor before breastfeeding.
Our Verdeso (desonide) Foam, 0.05% Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What is Patient Information in Detail?
Easy-to-read and understand detailed drug information and pill images for the patient or caregiver from Cerner Multum.
Verdeso in Detail - Patient Information: Side Effects
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop using this medication and call your doctor at once if you have severe irritation of any treated skin, or if you show signs of absorbing desonide topical through your skin, such as:
- blurred vision, or seeing halos around lights;
- mood changes;
- sleep problems (insomnia);
- weight gain, puffiness in your face; or
- muscle weakness, feeling tired.
Less serious side effects may include:
- mild skin itching, redness, burning, or peeling;
- dryness or scaly skin;
- thinning or softening of your skin;
- skin rash or irritation around your mouth;
- swollen hair follicles;
- changes in color of treated skin;
- blisters, pimples, or crusting of treated skin; or
- stretch marks.
This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.
Read the entire detailed patient monograph for Verdeso (Desonide Foam) »
What is Patient Information Overview?
A concise overview of the drug for the patient or caregiver from First DataBank.
Verdeso Overview - Patient Information: Side Effects
Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.
Skin infections can become worse while you are using this medication. Tell your doctor promptly if redness, swelling, or irritation does not improve.
A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any symptoms of a serious allergic reaction, including: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.
This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.
In the US -
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.
Read the entire patient information overview for Verdeso (Desonide Foam)»
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Verdeso FDA Prescribing Information: Side Effects
Clinical Trial Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.
In a controlled clinical trial of 581 subjects aged 3 months to 17 years, adverse reactions occurred at the application site in 6% of subjects treated with VERDESO Foam and 14% of subjects treated with vehicle foam. Other commonly reported adverse reactions for VERDESO Foam and vehicle foam are noted in Table 1.
Table 1: Adverse Reactions in the Clinical Trial
|Adverse Reaction||VERDESO Foam
(N = 387)
(N = 194)
|Upper respiratory tract infection||37 (10%)||12 (6%)|
|Cough||14 (4%)||3 (2%)|
|Application site burning||11 (3%)||15 (8%)|
|Viral infection||6 (2%)||0 (0%)|
|Elevated blood pressure||6 (2%)||1 (1%)|
|Headache||7 (2%)||1 (1%)|
|Asthma||3 (1%)||0 (0%)|
|Irritability||2 (1%)||0 (0%)|
|Pharyngitis||2 (1%)||0 (0%)|
|Application site atrophy||5 (1%)||0 (0%)|
|Application site reactions (including atrophy, striae, telangiectasia, and pigmentation changes)||3 (1%)||6 (3%)|
Other local adverse events occurred at rates less than 1.0%. The majority of adverse reactions were transient and mild to moderate in severity, and they were not affected by age, race, or gender.
The following additional local adverse reactions have been reported with topical corticosteroids. They may occur more frequently with the use of occlusive dressings and higher potency corticosteroids. These reactions are listed in an approximate decreasing order of occurrence: folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, striae, and miliaria.
Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
The following adverse reactions have been identified during post-approval use of VERDESO Foam: application site irritation, application site erythema, application site reactions, skin reactions, and swelling face.
Read the entire FDA prescribing information for Verdeso (Desonide Foam) »
Additional Verdeso Information
Verdeso - User Reviews
Verdeso User Reviews
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Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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