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10 mg
3 x 10
৳45.14

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Other brands with the same active ingredient

These brands contain the same active ingredient (Acitretin). Strength and form may differ — confirm substitution with your doctor or pharmacist before switching.

From ৳45.14 (3 x 10)
Available as: 10 mg · 3 x 10

Indications & Uses

Soritec is indicated for:

Dosage Reference

Reference Information Only

Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.

Adults:

Adult and elderly: Initial daily dose should be 25 mg or 30 mg for 2 to 4 weeks. After this initial treatment period the involved areas of the skin should show a marked response and/or side-effects should be apparent. In general, a daily dosage of 25-50 mg taken for a further 6 to 8 weeks to achieve optimal therapeutic results. However, it may be necessary in some cases to increase the dose up to a maximum of 75 mg/day.In patients with Darier’s disease a starting dose of 10 mg may be appropriate. The dose should be increased cautiously as isomorphic reactions may occur. Patients with severe congenital ichthyosis and severe Darier’s disease may require therapy beyond 3 months. The lowest effective dosage, not exceeding 50mg/day, should be given. Continuous use beyond 6 months is contra-indicated as only limited clinical data are available on patients treated beyond this length of time.Children: The daily dosage is about 0.5mg/kg. Higher doses (up to 1mg/kg daily) may be necessary in some cases for limited periods, but only up to a maximum of 35 mg/day.

Side Effects

Adverse effects occur in most people taking Soritin. Most of these side effects are dose-related and are generally well tolerated at the recommended doses. However, because the toxic dose of Soritin is close to its therapeutic dose, most patients notice some side effects during the initial period while the dose is being adjusted. The skin and mucous membranes are affected most often, and a temporary flare-up of psoriasis symptoms is sometimes seen at the start of treatment.

Cautions & Contraindications

Warnings & Precautions

The risk of giving birth to a deformed child is exceptionally high if Soritin is taken before or during pregnancy, no matter for how long or at what dosage. Women of childbearing potential must not receive blood from patients being treated with Soritin. Donation of blood by a patient being treated with Soritin is prohibited during and for two years after completion of treatment with Soritin. The effects of UV light are enhanced by retinoid therapy; therefore patients should avoid excessive exposure to sunlight. Hepatic function should be checked before starting treatment with Soritin, every 1-2 weeks for the first 2 months after commencement and then every 3 months during treatment. Serum cholesterol and serum triglycerides (fasting values) must be monitored before starting treatment, one month after the commencement and then every 3 months during treatment, especially in high-risk patients and during long-term treatment. Retinoids can alter glucose tolerance, blood sugar levels should therefore be checked. Patients should be warned of the possibility of alopecia. Decreased night vision has been reported with Soritin therapy. Patients with severe headache, nausea, vomiting, and visual disturbances should discontinue Soritin immediately.

Contraindications

Acitretin is highly teratogenic and must not be used by women who are pregnant. The same applies to women of childbearing potential unless strict contraception is practiced 4 weeks before, during and for 2 years after treatment. The use of Acitretin is contra-indicated in women who are breast feeding.Acitretin is contraindicated in patients with severe hepatic or renal impairment and in patients with chronic abnormally elevated blood lipid values. Concomitant administration of Acitretin with other retinoids or Vitamin A is contra-indicated due to the risk of hypervitaminosis A. Acitretin is contra-indicated in cases of hypersensitivity to the preparation (acitretin or excipients) or to other retinoids. Patients with rare glucose-galactosemalabsorption should not take this medicine.

Drug Interactions

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Major Methotrexate
Major Vitamin A
Moderate Progesterone
Moderate Phenytoin
Moderate Ethanol 70%
Moderate Warfarin Sodium
Last updated: 20 Aug 2026