RETIN-A is a brand name for Tretinoin, supplied as a cream. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: RETIN-A tretinoin is indicated for: topical application in the treatment of acne vulgaris. 1.1.1 Pediatrics Pediatrics (< 18 years of age): The safety and efficacy of RETIN-A in pediatric patients have not been established; therefore, Health Canada has not authorized an indication for pediatric patients (see…
Verbatim from this product's HC label. Tap a section to expand.
2 Recommended Dose and Dosage Adjustment Apply daily a pea-sized amount of RETIN-A to the affected areas after cleansing with a mild, non- medicated soap and water. Maintenance dose should be the least number of applications that will prevent recurrence of the condition.
Maintenance therapy should be administered daily for best results. Application of RETIN-A may cause a transitory feeling of warmth or slight stinging. When administered according to recommended guidelines, RETIN-A may produce a slight erythema similar to that of mild sunburn.
In cases where it is necessary to temporarily discontinue therapy or reduce the frequency of application, therapy should be resumed, or the frequency of application increased when the patient becomes able to tolerate the treatment.
Therapeutic effects may be noticed after two to three weeks of use, but more than six weeks of therapy may be required before definite beneficial effects are seen. During the early weeks of treatment, an apparent exacerbation of inflammatory lesions may occur.
This is due to the action of the medication on deep, previously unseen lesions and should not be considered a reason to discontinue therapy. Once a satisfactory response has been obtained, it may be possible to maintain this improvement with less frequent applications.
Discontinue treatment if a severe local inflammatory response is experienced. Reinstitute therapy PrRETIN-A® Product Monograph Page 4 of 21 when the reaction has subsided and apply preparation every other day or less frequently. Should discomfort still be experienced, stop treatment completely.
Excess application of RETIN-A does not provide more rapid or better results. In fact, marked redness, peeling or discomfort can occur. If excess application occurs accidentally or through over-enthusiastic use, RETIN-A should be discontinued for several days before resuming therapy.
4 Administration A pea-sized amount of RETIN-A should be squeezed onto a clean fingertip and a thin layer should be spread to the affected areas. The treated area should be washed no more than twice per day. After washing, the skin should be dried gently and completely without rubbing it.
Allow at least 20 to 30 minutes to dry before applying medication. Only a sufficient quantity of medication should be applied to cover the affected areas lightly, using a gauze swab, cotton wool or the tips of clean fingers. Over-saturation should be avoided since excess medication could run into the eyes, angles of the nose or other areas where treatment is not intended.
1 Adverse Reaction Overview True contact allergy to topical tretinoin is rarely encountered. Changes in the skin may be anticipated, indicating an active effect of the medication. Expected changes include mild erythema and flaking or peeling of the stratum corneum.
In certain very sensitive patients, the skin may become very erythematous, edematou s, blistered or crusted. In such cases, application of tretinoin should be discontinued until the skin has fully recovered. Further applications should be at a level that the individual can tolerate.
All adverse reactions observed are reversible when treatment is discontinued. Some degree of local irritation is expected. The most commonly reported undesirable effects are dry skin, burning, stinging, warmth, erythema, pruritus, rash, peeling and temporary hypo - and hyperpigmentation.
Rarely reported undesirable effects are blistering and crusting of the skin, eye irritation and edema. These reactions were usually mild to moderate in severity, generally well - tolerated and self-limiting, occurred early during the course of therapy and generally decreased over time with the exception of dry skin, which tended to persist.
General RETIN-A is for external use only. Not for ophthalmic use. Avoid contact with the eyes, eyelids, angles of the nose, lips, mucous membranes, severely inflamed skin or to open lesions or to other areas where treatment is not intended.
RETIN-A should be applied only to the affected areas. Excessive use should be avoided. Tretinoin may cause irritation of circumoral and other sensitive skin areas. Tretinoin should not be applied to severely inflamed skin or to open lesions.
Exposure to sunlight, including ultraviolet sunlamps, may provoke additional irritation. Therefore, exposure should be avoided or minimized during the use of tretinoin. A patient experiencing considerable sun exposure due to occupational duties, and/or any patient inherently sensitive to the sun, should exercise particular caution.
When exposure to sunlight cannot be avoided, use of sunscreen products and protective clothing over treated areas is recommended. Hyper- or hypopigmentation has occasionally been reported when the product is used to the point of producing severe irritation.
This is reversible when the medication is stopped. Cosmetics may be used, but the areas to be treated should be cleansed thoroughly before the medication is applied. Astringent toiletries should be avoided. Simultaneous use of harsh abrasives and other skin treatments, including sun lamp, should be avoided if possible.
g. plucking, electrolysis, depilatories) but should avoid these procedures at night before applying RETIN-A as they might result in skin irritation. Permanent wave solutions, waxing preparations, medicated soaps and shampoos can sometimes irritate even normal skin.
Caution should be used so that these products do not come into contact with skin treated with RETIN-A. In some patients temporary skin irritation may occur, especially in early weeks of treatment. Should these reactions occur to an excessive degree, and the skin becomes extremely red, swollen and crusted, use of tretinoin should be discontinued immediately.
RETIN-A is contraindicated in patients who have demonstrated a hypersensitivity to the drug or to any ingredient in the formulation, or any component of the container.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
Other brands of Tretinoin in Canada.
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Avoid eyes, mouth, paranasal creases, and mucous membranes. Not for ophthalmic, oral or intravaginal use.
An apparent exacerbation may develop due to the drug effect on previously seen deep lesions. This is an anticipated part of the therapeutic effect. Therapy should be continued. GELS ARE FLAMMABLE.
Note:
Keep away from heat and flame. Keep tube tightly closed. Skin Local Irritation Weather extremes, such as wind, cold and low humidity may be irritating to skin treated with RETIN-A and may increase its dryness. Tretinoin has been reported to cause severe irritation on eczematous skin and should be used with utmost caution in patients with this condition.
If a patient experiences severe or persistent irritation, the patient should be advised to discontinue application of RETIN-A completely, and if PrRETIN-A® Product Monograph Page 6 of 21 necessary, consult a physician. ) until these symptoms subside.
In certain sensitive individuals, RETIN-A may induce severe local erythema, swelling, pruritus, warmth, burning or stinging, blistering, crusting and/or peeling at the site of application. If the degree of local irritation warrants, the patient should be instructed to either apply the medication less frequently or discontinue its use temporarily.
1 Pregnant Women Topical tretinoin should be used by women of childbearing years only after contraceptive counselling. Topical tretinoin should not be used by pregnant women and by women planning a pregnancy. There have been a few reports of birth defects among babies born to women exposed to topical tretinoin during pregnancy.
To date, there have been no adequate and well-controlled prospective studies performed in pregnant women and the teratogenic blood level of tretinoin is not clear. However, a well-conducted retrospective cohort study of babies born to women exposed to topical tretinoin during the first trimester of pregnancy found n o excess birth defects among these babies when compared with babies born to women in the same cohort who were not similarly exposed.
Oral tretinoin has been shown to be teratogenic and fetotoxic in rats when given in doses 1000 and 500 times the topical human dose, respectively. In nine (9) out of ten (10) topical teratology studies of tretinoin conducted in rats and rabbits using several formulations, there has been no evidence of teratogenicity.
In one (1) out of ten (10) studies there was an increase in fetal malformations; however, a clear causal relationship of topical tretinoin in these findings could not be established. In a repeat of this study, there were no fetal malformations.
Topical tretinoin can produce treatment-related fetal effects (delayed ossification of bones and an increase in supernumerary ribs). 0 mg/kg/day (200 times the recommended clinical dose). 2 Breast-feeding It is not known whether RETIN-A are excreted in human milk.
Nevertheless, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother. Since many drugs are excreted in human milk, caution should be exercised when RETIN-A Cream and Gel are administered to a nursing mother.
3 Pediatrics Pediatrics (< 18 years): The safety and efficacy of RETIN-A in pediatric patients have not been established; therefore, Health Canada has not authorized an indication in children <18 years of age. 4 Geriatrics Geriatrics (> 65 years of age): A limited number of subjects aged ≥ 65 years have been treated with RETIN-A in clinical trials; therefore, the safety and efficacy of RETIN-A have not been established in this patient population.