Adult: Induction of remission in previously untreated patients and those who have relapsed from or refractory to standard chemotherapy: 45 mg/m2 daily in 2 equally divided doses, continued until complete remission. Max treatment duration: 90 days. Dose reduction, dosing interruption or re-initiation may be required according to individual safety and tolerability (refer to detailed product guideline). Child: 1-16 years Same as adult dose. Consider dose reduction to 25 mg/m2 if toxicity symptoms (e.g. intractable headache) occur.
Topical/Cutaneous Mottled hyperpigmentation, roughness and fine wrinkling of photodamaged skin
Adult: As 0.02% or 0.05% cream: Apply a pea-sized amount onto the face once daily at night or before bedtime, to cover the entire affected area lightly. Therapeutic effects may be observed after 6 months.
Topical/Cutaneous Acne vulgaris
Adult: As 0.01-0.05% gel/cream/lotion: Apply enough to the entire affected area once daily at night or before bedtime. Exacerbation of inflammatory lesions may occur in early weeks of treatment. Therapeutic effects may be observed after 2-3 weeks but may require >6 weeks of treatment to see consistent beneficial effects.
Reduce dose to 25 mg/m2 daily.
Reduce dose to 25 mg/m2 daily.
Should be taken with food.
Chống chỉ định
Pregnancy and lactation (oral). Concomitant use with tetracyclines, vitamin A, retinoids and anti-fibrinolytic agents (e.g. tranexamic acid, aminocaproic acid, aprotinin).
Patient with history of depression; eczema, sunburn, personal or family history of skin cancer, considerable sun exposure (e.g. due to occupation, inherent sensitivity to sunlight), fish allergies (topical). Avoid application to eyes, mouth and nose (topical). Lactation (topical). Children. Renal and hepatic impairment.
Phản ứng phụ
Significant: Venous thrombosis, MI, pseudotumor cerebri/benign intracranial hypertension (children), hypercholesterolaemia or hypertriglyceridaemia (reversible), hypercalcaemia, psychiatric disorders (e.g. depression, anxiety, mood alterations), elevated LFT, Sweet’s syndrome (acute febrile neutrophilic dermatosis); hypersensitivity reactions, photosensitivity (topical), skin irritation (e.g. excessive dryness, redness, swollen, blistered), application site reactions (e.g. feeling of warmth, dry skin, peeling, burning, stinging, pain). Blood and lymphatic system disorders: Thrombocytosis, basophilia. Cardiac disorders: Arrhythmia, chest pain. Ear and labyrinth disorders: Impaired hearing. Eye disorders: Visual disturbances, conjunctival disorders. Gastrointestinal disorders: Dry mouth, nausea, vomiting, diarrhoea, abdominal pain, constipation, pancreatitis, cheilitis. General disorders and administration site conditions: Chills, malaise. Investigations: Increased blood creatinine. Metabolism and nutrition disorders: Decreased appetite. Musculoskeletal and connective tissue disorders: Bone pain. Nervous system disorders: Headache, dizziness, paraesthesia. Psychiatric disorders: Confusional state, insomnia. Respiratory, thoracic and mediastinal disorders: Nasal dryness, asthma, respiratory failure. Skin and subcutaneous tissue disorders: Rash, pruritus, hyperhidrosis, erythema, alopecia, hypo-/hyperpigmentation (temporary). Vascular disorders: Flushing. Potentially Fatal: APL differentiation syndrome/retinoic acid syndrome, leukocytosis, QTc prolongation leading to torsade de pointes.
Oral: This drug may cause dizziness or severe headache, if affected, do not drive or operate machinery. Topical: Avoid or minimise exposure to sunlight (including sunlamps), if exposure cannot be avoided, use sunscreens or protective clothing over treated areas.
Perform bone marrow cytology to confirm t(15;17) translocation or presence of PML/RARα fusion protein; pregnancy test 1 week prior to therapy and every month during treatment. Monitor CBC with differential, coagulation profile, LFTs, triglycerides and cholesterol levels frequently. Closely monitor cardiac, CNS, and respiratory status frequently during treatment; signs of depression, and acute promyelocytic leukaemia (APL) differentiation syndrome (e.g. monitor volume and pulmonary status, temperature, respiration).
Symptoms: Oral: Reversible signs of hypervitaminosis A (e.g. headache, nausea, vomiting, mucocutaneous symptoms), transient headache, facial flushing, cheilosis, abdominal pain, dizziness, and ataxia. Topical: Marked skin redness, peeling, blistering, or discomfort. Management: Oral: Treat patient in a special haematological unit. Topical: Discontinue use and apply cold compress and a bland cream. If ingested, promote rapid gastric emptying by inducing emesis, gastric lavage and/or forced fluids.
Oral: May potentially alter pharmacokinetics with CYP450 inducers (e.g. rifampicin, glucocorticoids, phenobarbital, pentobarbital) and CYP450 inhibitors (e.g. ketoconazole, cimetidine, erythromycin, verapamil, diltiazem, ciclosporin). Topical: May increase risk of skin irritation with topical medications, medicated or abrasive soaps, shampoos, cleansers, permanent wave solutions, electrolysis, hair depilatories or waxes, cosmetics with strong drying effect, products with high concentrations of alcohol, astringents, spices or lime, and preparations containing sulfur, resorcinol, benzoyl peroxide or salicylic acid. Potentially Fatal: Oral: Increased risk of pseudotumour cerebri/intracranial hypertension with tetracyclines. Increased risk of symptoms suggestive of hypervitaminosis A with other retinoids and vitamin A. Increased risk of thrombotic complications with antifibrinolytic agents (e.g. tranexamic acid, aminocaproic acid, aprotinin).
Enhanced absorption with food. Rarely, may increase risk of vitamin A toxicity with cod liver oil or halibut fish oil.
Description: Tretinoin is a retinoid and an acid from of vitamin A. Topically, it modifies epithelial growth and differentiation; in acne treatment, it decreases the cohesiveness of follicular epithelial cells and microcomedo formation, stimulates mitotic activity, and increases the turnover of follicular epithelial cells resulting in the extrusion of comedones. Systemically, tretinoin specifically binds to 1 or more nuclear retinoic acid receptors (RAR), induces cellular differentiation, and decreases proliferation of acute promyelocytic leukaemia (APL) cells.
Synonym: All-trans retinoic acid (ATRA). Onset: Acne: ≥2 weeks, may take ≥7 weeks. Facial wrinkles: Up to 6 months. Pharmacokinetics: Absorption: Well absorbed from the gastrointestinal tract (oral); minimally absorbed from the skin (topical). Enhanced absorption with food (oral). Bioavailability: Approx 50% (oral). Time to peak plasma concentration: 1-2 hours (oral). Distribution: Plasma protein binding: >95%, mainly to albumin. Metabolism: Metabolised in the liver by CYP450 enzymes to form 4-oxo-trans-retinoic acid (primary metabolite); displays auto-metabolism. Excretion: Via urine (63%); faeces (30%). Terminal elimination half-life: 0.5-2 hours (oral).
Cap: Store between 20-25°C. Protect from light and moisture. Cream/gel/lotion: Store between 20-25°C. Do not freeze.
D10AD01 - tretinoin ; Belongs to the class of topical retinoid preparations used in the treatment of acne.
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