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Zonyra 0.005% Cream is a retinoid medication used to treat psoriasis and acne. It works by slowing down skin cell growth and reducing inflammation. Apply the gel as prescribed by your doctor, and use it for the recommended duration. You may experience mild side effects like dry skin or skin irritation, which usually resolve over time. Inform your doctor if you are allergic to Trifarotene or have certain skin conditions. Avoid using the gel during pregnancy and breastfeeding, and do not use it in children below 18 years. It's advisable to avoid driving while using Zonyra 0.005% Cream due to its unknown effect on driving ability.
No interaction found
There is no data available. Please consult a doctor before consuming the drug.
There is no data available. Please consult a doctor before using Zonyra 0.005% Cream.
There is no interaction between driving and consuming this drug. So dose alteration is not needed.
There is no data available. Please consult a doctor before use.
There is no data available. Please consult the doctor before use.
The precise mechanism of action of this medication has not yet been determined fully. According to studies, the active constituent of this medication when activated combines with all members of the receptor family, retinoic acids such as RARa, RARb, and RARg.
Trifarotene cream is a retinoid indicated for the topical treatment of acne vulgaris in patients 9 years of age and older.
Trifarotene is an agonist of retinoic acid receptors (RAR), with particular activity at the gamma subtype of RAR. Stimulation of RAR results in modulation of target genes which are associated with various processes, including cell differentiation and mediation of inflammation. The exact process by which Trifarotene ameliorates acne is unknown.
Pediatric Use:
Geriatric Use:
Pregnancy Category C. Available data from clinical trials with Trifarotene cream use in pregnant women have not identified a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for Trifarotene cream and any potential adverse effects on the breastfed infant from Trifarotene cream or from the underlying maternal condition.
Skin irritation: Patients using Trifarotene cream may experience erythema, scaling, dryness, and stinging/burning. Maximum severity of these reactions typically occurred within the first 4 weeks of treatment, and severity decreased with continued use of the medication. Depending upon the severity of these adverse reactions, instruct patients to use a moisturizer, reduce the frequency of application of Trifarotene cream or suspend use temporarily. If severe reactions persist the treatment may be discontinued. Avoid application of Trifarotene cream to cuts, abrasions, or eczematous or sunburned skin. Use of "waxing" as a depilatory method should be avoided on skin treated with Trifarotene cream.
Ultraviolet Light and Environmental Exposure: Minimize unprotected exposure to ultraviolet rays (including sunlight and sunlamps) during treatment with Trifarotene cream. Warn patients who normally experience high levels of sun exposure and those with inherent sensitivity to the sun to exercise caution. The use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided.
Do not store above 25°C. Protect from light. Keep out of reach of children.
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