PRODUCT INFORMATION ISOTREX GEL

Similar documents
PRODUCT INFORMATION Stieva-A Creams 0.025% w/w, 0.05% w/w and 0.1% w/w

AUSTRALIAN PRODUCT INFORMATION. STIEVA-A (tretinoin) cream

Stieva-A. Tretinoin Preparations

PRODUCT INFORMATION WARTEC SOLUTION

Summary of Product Characteristics

These metabolites are mainly excreted in the faeces and some oxidised metabolites are found in the urine.

50 microgram/g Calcipotriol and 500 microgram/g betamethasone (as dipropionate).

For the use only of a Registered Medical Practitioner or a Hospital or a Laboratory. Light Liquid Paraffin and White Soft Paraffin Cream

Chemical structure of calcipotriol

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

2 QUALITATIVE AND QUANTITATIVE COMPOSITION Metronidazole 7.5 mg/g

LUMACIP PLUS Cream (Fluocinolone acetonide 0.01% + Hydroquinone 4% + Tretinoin 0.05%)

1 g of white to slightly yellowish opaque cream contains 0.2 g (20 %) micronised azelaic acid.

APO-ACAMPROSATE ENTERIC COATED TABLETS

Campral is indicated as therapy to maintain abstinence in alcohol dependent patients. It should be combined with counselling.

MOVICOL Liquid Orange Flavour Concentrate for Oral Solution (macrogol 3350)

1. NAME OF THE MEDICINAL PRODUCT. Lamisil 1% cutaneous solution. 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

3 DOSAGE FORMS AND STRENGTHS

SUMMARY OF PRODUCT CHARACTERISTICS

Summary of Product Characteristics

For the use only of Registered Medical Practitioners or a Hospital or a Laboratory ZODERM E CREAM. Oxiconazole Nitrate Cream

Panretin (alitretinoin) gel 0.1% (For topical use only) Rx only DESCRIPTION

SUMMARY OF PRODUCT CHARACTERISTICS. Each gram of ointment contains 1 mg of mometasone furoate and 50 mg of salicylic acid

Summary of Product Characteristics

New Zealand Datasheet. 3 PHARMACEUTICAL FORM DIFFERIN topical cream is a smooth white cream containing 1 mg/g adapalene.

SUMMARY OF PRODUCT CHARACTERISTICS 2. QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

AUSTRALIAN PRODUCT INFORMATION RESOLVE PLUS 1.0 (MICONAZOLE NITRATE, HYDROCORTISONE) CREAM

SUMMARY OF PRODUCT CHARACTERISTICS

DOSAGE FORMS AND STRENGTHS Cream: Each gram contains 10 mg of ozenoxacin (1%) (3).

Immodium / loprarmide

SUMMARY OF PRODUCT CHARACTERISTICS. A 2.5ml single-dose bottle containing IU Cholecalciferol (equivalent to 625 micrograms vitamin D 3 )

DOVONEX (calcipotriene) Cream, 0.005% Rx only FOR TOPICAL DERMATOLOGIC USE ONLY. Not for Ophthalmic, Oral or Intravaginal Use.

Core Safety Profile. Pharmaceutical form(s)/strength: solution 1%, spray 1%, cream 1%, gel 1% SK/H/PSUR/0005/001 Date of FAR:

PRODUCT INFORMATION NAME OF THE MEDICINE DESCRIPTION PHARMACOLOGY. PATANOL * (Olopatadine) 0.1 % Eye Drops

SUMMARY OF THE PRODUCT CHARACTERISTICS

The Ointment is back!

MOVICOL Lemon-Lime Flavour Powder for Solution (macrogol 3350)

Acne vulgaris is a disease of the pilosebaceous unit (i.e., the sebaceous glands and adjacent hair follicle).

For topical use only. Not for oral, ophthalmic, or intravaginal use.

PRODUCT MONOGRAPH Pr TAZORAC

2 QUALITATIVE AND QUANTITATIVE COMPOSITION Metronidazole 7.5 mg/g

SUMMARY OF PRODUCT CHARACTERISTICS. for. Felden, gel

PRODUCT INFORMATION PANADOL COLD & FLU MAX HOT LEMON POWDER NAME OF THE MEDICINE. Chemical structure: CAS 2 Registry Number: DESCRIPTION

Body weight more than 30kg : 10ml (10mg) of the syrup once daily.

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

NEW ZEALAND DATA SHEET PEVARYL 1% w/w Foaming Solution

פורמט עלון זה נקבע ע"י משרד הבריאות ותוכנו נבדק ואושר SUMMARY OF PRODUCT CHARACTERISTICS

DESCRIPTION Locacorten-Vioform ear drops are a practically odourless clear, yellowish to brownish-yellow solution. Excipients: Macrogol 300

SUMMARY OF PRODUCT CHARACTERISTICS 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

PRODUCT INFORMATION. DESCRIPTION Addaven is a concentrated trace element solution for infusion which is clear and colourless to slightly yellow.

ACNE. What are the aims of this leaflet?

NEW ZEALAND DATA SHEET

AUSTRALIAN PRODUCT INFORMATION APO-BETAHISTINE (BETAHISTINE DIHYDROCHLORIDE) 2 AND 3 QUALITATIVE AND QUANTITATIVE COMPOSITION AND PHARMACEUTICAL FORM

PRODUCT INFORMATION CODAPANE XTRA Paracetamol 500 mg and Codeine Phosphate 15 mg Tablets

SUMMARY OF PRODUCT CHARACTERISTICS

PRODUCT INFORMATION VANIQA EFLORNITHINE CREAM, 11.5%

MOVICOL Junior Chocolate Flavour Powder for Solution (macrogol 3350)

SOLARAZE 3% gel. (diclofenac sodium)

NOVASONE CREAM, OINTMENT AND LOTION PRODUCT INFORMATION

SUMMARY OF PRODUCT CHARACTERISTICS

GlaxoSmithKline. Renal impairment. Hepatic impairment

PRODUCT INFORMATION. (RS)-N,N-Dimethyl-2-[(2-methylphenyl)phenylmethoxy]ethanamine dihydrogen 2-hydroxypropane-1,2,3-tricarboxylate

HIGHLIGHTS OF PRESCRIBING INFORMATION

3 PHARMACEUTICAL FORM Coated tablet Round, white to off-white, sugar coated tablets, plain on both sides.

AUSTRALIAN PRODUCT INFORMATION APOC-5FU CREAM (FLUOROURACIL)

MOVICOL Junior Powder for Solution (macrogol 3350)

Molecular formula: Molecular weight: C 8 H 9 NO 2 CAS Registry no.:

PRODUCT MONOGRAPH. (tretinoin gel, Manufacturer s Standard) 0.01% or 0.025% or 0.05% Gel TOPICAL ACNE THERAPY

Reference ID:

Betamethasone dipropionate

The chemical name of acyclovir, USP is 2-amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6Hpurin-6-one; it has the following structural formula:

PRODUCT INFORMATION H 2

LACIPIL QUALITATIVE AND QUANTITATIVE COMPOSITION

Prescribing Information

Package leaflet: Information for the patient. IsotrexIN Gel erythromycin 2% and isotretinoin 0.05%

MINIMS AMETHOCAINE EYE DROPS

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

PRODUCT INFORMATION. SUDAFED Sinus 12 Hour Relief Tablets

Ultravate (halobetasol propionate) Cream, 0.05% (halobetasol propionate) Ointment, 0.05% For Dermatological Use Only. Not for Ophthalmic Use.

WARNINGS AND PRECAUTIONS

0BCore Safety Profile. Pharmaceutical form(s)/strength: Cream 1% DK/H/PSUR/0009/005 Date of FAR:

LOPROX CREAM (ciclopirox) 0.77% FOR DERMATOLOGIC USE ONLY. NOT FOR USE IN EYES. Rx Only

SUMMARY OF PRODUCT CHARACTERISTICS

For the use only of Registered Medical Practitioners or a Hospital or a Laboratory GRISOVIN- FP. Griseofulvin Tablets I.P.

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

SUMMARY OF PRODUCT CHARACTERISTICS

TOPCORT Cream/Ointment (Mometasone furoate 0.1%)

Fluocinolone Acetonide 0.01% Topical Oil (Scalp Oil)

PRODUCT INFORMATION INTAL CFC-FREE INHALER AND INTAL FORTE CFC-FREE INHALER

Excipients with known effect: Each gramme of gel contains 1 mg methyl parahydroxybenzoate (E-218) and 0.5 mg propyl parahydroxybenzoate (E-216).

Summary of Product Characteristics

SUMMARY OF PRODUCT CHARACTERISTICS

NAME OF THE MEDICINAL PRODUCT IMODIUM CAPS. QUALITATIVE AND QUANTITATIVE COMPOSITION 2 mg loperamide hydrochloride (HCl) per capsule.

Package leaflet: Information for the user. Fluticrem 0.05% cream Fluticasone propionate

PHARMACOLOGY Class: Ketorolac trometamol is a member of the pyrrolo-pyrolle group of non-steroidal antiinflammatory

NEW ZEALAND DATA SHEET

Transcription:

PRODUCT INFORMATION ISOTREX GEL NAME OF THE MEDICINE Isotretinoin. DESCRIPTION Isotretinoin is a yellow to orange crystalline powder; it has the following chemical structure: Chemical name: 13-cis-retinoic acid; 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-y1)2-cis-4- trans-6-trans-8-trans-nonatetraenoic acid. CAS Number: 4759-48-2. Molecular formula: C 20 H 28 O 2. Molecular weight: 300.44. H 3 C CH 3 CH 3 CH 3 O OH Isotrex gel contains isotretinoin 0.05% w/w (0.05g per 100g gel). Excipients are butylated hydroxytoluene, hydroxypropylcellulose and ethanol. PHARMACOLOGY CH 3 Isotretinoin is structurally and pharmacologically related to Vitamin A, which regulates epithelial cell growth and differentiation. It is thought that topically applied isotretinoin acts in a comparable way to its stereoisomer, tretinoin, and: stimulates mitosis in the epidermis reduces intercellular cohesion in the stratum corneum contests the hyperkeratosis characteristic of acne vulgaris aids desquamation, preventing the formation of lesions mediates an increased production of less cohesive epidermal sebaceous cells, which appears to promote the initial expulsion of comedones and their subsequent prevention. Isotretinoin shows significant inhibition of leukotriene-b4-induced migration of polymorphonuclear leukocytes, which may contribute to its topical anti-inflammatory activity. Only a weak inhibition of polymorphonuclear leukocyte migration is produced by topical tretinoin. This may account for the reduced rebound effect seen with topical isotretinoin when compared with topical tretinoin. Pharmacodynamic effects The pharmacological action of isotretinoin remains to be fully elucidated. It has the following actions when given systemically: 1

suppresses sebaceous gland activity reduces sebum production; prevents or reduces comedogenesis, suppresses Propionibacterium acnes, and reduces inflammation. Studies in animal models have shown similar activity when isotretinoin is applied topically. Inhibition of sebum production by topical isotretinoin has been demonstrated in the ears and flank organs of the Syrian hamster. Topical application of isotretinoin has also been shown to have an effect on the epidermal differentiation of rhino mouse skin, resulting in a reduction in the size of the utriculi and superficial cysts which are hair follicle-derived squamous epithelium containing keratin, a feature of the skin of this animal model. Pharmacokinetics Absorption Following isotretinoin 0.05% gel application to acne patients at a daily dose of 20 g (equivalent to 10 mg of isotretinoin) to the face, chest and back for 30 days, plasma concentrations of isotretinoin and tretinoin were not measurable (< 20 ng/ml). Distribution Isotretinoin is more than 99.9% bound to plasma proteins, primarily albumin. Metabolism In vivo studies in humans showed that the three major metabolites identified in human plasma following oral administration of isotretinoin were 4-oxo-isotretinoin, retinoic acid (tretinoin), and 4-oxo-retinoic acid (4-oxo-tretinoin). In vitro studies indicated that all of these metabolites had retinoid activity. In vitro studies indicate that the major enzymes responsible for isotretinoin metabolism are cytochrome P450 isoenzymes 2C8 and 3A4 with additional smaller roles for 3A7, 4A11, 1B1, 2B6 and 2C19. Isotretinoin and its metabolites are further metabolized into conjugates and excreted in urine and faeces. INDICATIONS Isotrex gel is indicated for the topical treatment of mild to moderate acne vulgaris, characterised by comedones, papules and pustules. CONTRAINDICATIONS Isotrex Gel should not be used in patients with known hypersensitivity to any of the ingredients. Isotrex Gel should not be used in patients with a personal or family history of squamous cell or basal cell carcinoma. PRECAUTIONS Isotretinoin should be used with caution in patients with a history of local tolerability reactions or photoallergy. Contact with the mouth, eyes, mucous membranes, abraded or eczematous skin should be avoided. 2

Care should be taken not to let the medicine accumulate in skin fold areas and in the nasolabial folds. Due to the irritant nature of isotretinoin, caution should be used when applying to sensitive areas of skin, such as the neck, or in patients with concomitant rosacea or perioral dermatitis.concomitant topical acne therapy should be used with caution because a cumulative irritant effect may occur. If irritancy or dermatitis occur, reduce frequency of application or temporarily interrupt treatment and resume once irritation subsides. Treatment should be discontinued if irritation persists. Sensitivity to sunlight Albino mice treated with isotretinoin and exposed to ultraviolet light (artificial light) demonstrated an accelerated appearance of sunlight induced skin tumours; mice treated with isotretinoin but not exposed to ultraviolet light did not develop tumours. The significance of these findings as related to human beings is unknown. As isotretinoin may cause increased sensitivity to sunlight, sunlamps should not be used and deliberate or prolonged exposure to sunlight should be avoided or minimised. When exposure to strong sunlight cannot be avoided patients should be advised to use a sunscreen product and wear protective clothing. If a patient has sunburn, this should be resolved before using isotretinoin. Effects on fertility There are no data on the effect of topical isotretinoin on fertility in humans, but isotretinoin in oral therapeutic dosages does not affect the number, motility, and morphology of sperm. In rats, no adverse effects on gonadal function, fertility, conception rate, gestation or parturition were observed at oral dose levels of isotretinoin up to 32 mg/kg/day. In dogs, testicular atrophy and appreciable depression of spermatogenesis were noted after approximately 30 weeks at isotretinoin dose levels of 20 or 60 mg/kg/day given orally. However, in studies of men receiving oral isotretinoin, no significant effects have been seen on semen parameters. Use in pregnancy Pregnancy Category D Reproduction studies conducted in rabbits using isotretinoin gel applied topically at a dose of 0.5 mg/kg/day have revealed no harm to the fetus. This dose is approximately 19 times greater than the human dose of isotretinoin, based on body surface area and assuming use of 1 g gel by a 50 kg patient. However, isotretinoin has been shown to be teratogenic in multiple animal species (mice, rats, hamsters, rabbits and monkeys) following oral administration, and humans are recognised to be more sensitive to the teratogenic effects of isotretinoin than laboratory animal species. Teratogenicity has also been demonstrated with tretinoin an isomer and metabolite of isotretinoin, following topical administration in rats. Studies totalling almost 1600 women exposed to topical tretinoin (an isomer of isotretinoin) in early pregnancy did not provide evidence of an increased risk of congenital abnormalities, including retinoic acid embryopathy or major structural defects overall. A small number of temporally associated congenital abnormalities have been reported during clinical use of topical tretinoin. Although no definite pattern of teratogenicity and no causal association have been established from these cases, they include reports of the rare birth defect category, holoprosencephaly (defects associated with incomplete midline development of the forebrain). The significance of these reports in terms of risk to the foetus is uncertain, since these effects have not been reproduced. 3

Orally administered retinoids have been associated with congenital abnormalities. When used in accordance with the prescribing information, there is negligible systemic absorption from topically administered isotretinoin. However, risk cannot be excluded since there may be other factors that contribute to an increased systemic exposure such as: amount used; skin barrier integrity; concurrent use with other products; dietary intake of or ingestion of supplements containing vitamin A. Therefore, topical isotretinoin is not recommended during pregnancy or in women of childbearing potential not using an effective method of contraception properly. No specific contraceptive precautions are necessary for men using topical isotretinoin. Use during lactation There is insufficient information on the excretion of topically applied isotretinoin in human milk. A risk to the newborns/infants cannot be excluded. A decision must be made whether to discontinue breast-feeding or to discontinue /abstain from isotretinoin therapy taking into account the benefit of breast-feeding for the child and the benefit of therapy for the woman. Paediatric use The safety and efficacy of topical isotretinoin in children prior to puberty have not been established, therefore isotretinoin is not recommended for use in this population. Use in the elderly There are no specific recommendations for use in the elderly. Renal impairment No dosage adjustment is necessary. Renal impairment is not expected to result in systemic exposure to isotretinoin of clinical significance. This is because negligible percutaneous absorption of isotretinoin follows topical application (see Pharmacokinetics). Hepatic impairment No dosage adjustment is necessary. Hepatic impairment is not expected to result in systemic exposure to isotretinoin of clinical significance. This is because negligible percutaneous absorption of isotretinoin follows topical application (see Pharmacokinetics). Genotoxicity Isotretinoin was negative in assays for mutagenicity in bacteria (Ames test), chromosomal aberrations in vitro (Chinese hamster lung cells) and in vivo (mouse micronucleus test), and unscheduled DNA syntheseis in vitro (rat hepatocytes). Carcinogenicity In Fischer 344 rats given oral isotretinoin up to 32 mg/kg/day for 18 months or longer, there was an increased incidence of phaeochromocytomas relative to controls in both sexes at 32 mg/kg/day 4

and in males at 8 mg/kg/day. Given the high rate of spontaneous rate of occurrence of phaeochromoyctoma in Fischer 344 rats, the relevance of this finding to humans is uncertain. The tumourigenic potential of UV irradiation was increased with concurrent dermal exposure to isotretinoin at dose levels 100 mg/kgin hairless albino mice. Although the relevance of this finding to humans is not clear, patients should minimise exposure to sunlight or artificial UV sources (see also Sensitivity to sunlight). INTERACTIONS WITH OTHER MEDICINES Concomitant application of oxidising agents, such as benzoyl peroxide, should be avoided since they may reduce the efficacy of topical isotretinoin. If combination therapy is required, the products should be applied at different times of the day (eg, one in the morning and the other in the evening). ADVERSE EFFECTS The following convention is used for the classification of the frequency of an adverse reaction and is based on the CIOMS guidelines: Very common: 1/10 Common: 1/100 to <1/10 Uncommon: 1/1000 to <1/100 Rare: 1/10000 to <1/1000 Very rare: <1/10000 Not known*: (cannot be estimated from the available data) Clinical trial data Skin and subcutaneous tissue disorders Very common: Application site erythema, skin exfoliation, pain of skin, application site pruritus, skin irritation, skin tenderness, skin burning sensation, application site stinging, dry skin Post-marketing data Skin and subcutaneous tissue disorders Rare: skin hyperpigmentation, skin hypopigmentation, photosensitivity reaction DOSAGE AND ADMINISTRATION Adults and adolescents Apply Isotrex Gel sparingly over the whole affected area once daily, at night. Patients should be advised that 6-8 weeks of treatment may be required before a therapeutic effect is observed. The safety and effectiveness of Isotrex Gel have not been investigated in clinical studies for treatment periods longer than 14 weeks. Patients should be advised that excessive application will not improve efficacy, but may increase the risk of skin irritation. If undue irritation (redness, peeling, or discomfort) occurs, patients should reduce frequency of application or temporarily interrupt treatment. The normal frequency of application should be resumed once the irritation subsides. Treatment should be discontinued if the irritation persists. 5

OVERDOSAGE Symptoms and signs Oral ingestion of a 30g tube of topical isotretinoin would result in less exposure than achieved with the recommended dosage of oral isotretinoin. Consequently, the theoretical occurrence of symptoms of overdosage (e.g. hypervitaminosis A) is highly unlikely. The gel formulation contains more than 95% ethanol. Systemic absorption of this should be considered in the event of oral ingestion. Treatment Contact the Poisons Information Centre (telephone 13 11 26) for advice on overdose management. PRESENTATION AND STORAGE CONDITIONS Topical gel containing isotretinoin 0.05 % w/w (0.05 g per 100 g gel). Presented in aluminium tube, fitted with screw cap. Pack size is 30 g. Store below 25 C. NAME AND ADDRESS OF THE SPONSOR GlaxoSmithKline Australia Pty Ltd Level 4 436 Johnston Street Abbotsford Victoria 3067 POISON SCHEDULE OF THE MEDICINE Prescription only medicine. Date of first inclusion in the Australian Register of Therapeutic Goods (the ARTG): 30 November 1993 Date of most recent amendment: 24 May 2012 Version 4.0 6