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Ovixan

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Document: Ovixan cutaneous solution ENG SmPC change

SUMMARY OF PRODUCT CHARACTERISTICS


1. NAME OF THE MEDICINAL PRODUCT


Ovixan 1 mg/g cutaneous solution


2. QUALITATIVE AND QUANTITATIVE COMPOSITION


One gram cutaneous solution contains 1 mg mometasone furoate

Excipients with known effect:

300 mg propylene glycol per gram solution.

For the full list of excipients, see section 6.1.


3. PHARMACEUTICAL form


Cutaneous solution

Colourless to slightly yellow low-viscous solution.


4. Clinical particulars


4.1 Therapeutic indications


Ovixan is indicated for the symptomatic treatment of inflammatory skin conditions which respond to topical treatment with glucocorticosteroids, such as atopic dermatitis and psoriasis (excluding widespread plaque psoriasis).


4.2 Posology and method of administration


Posology


Adults (including older people)and children (from 6 years):

Ovixan is applied in a thin film once daily on the affected areas of skin. The application frequency is then gradually decreased. Use of a less potent corticosteroid is often preferred when clinical improvement is achieved.


Ovixan cutaneous solution is intended for treatment of skin lesions on the scalp but it may also be used on other parts of the body.


As for all strong topical glucocorticoids Ovixan should not be applied on the face other than under close supervision by a doctor.


Ovixan should not be used for long periods (over 3 weeks) or on large areas (over 20% of body surface area). In children a maximum of 10 % of body surface area should be treated.


Paediatric population

Children below 6 years:

Ovixan is a strong glucocorticoid (group III) and it is usually not recommended for children below 6 years since relevant safety data are lacking (see section 4.4).


Method of administration

Topical use.

4.3 Contraindications


Hypersensitivity to the active substance, mometasone furoate, to other corticosteroids or to any of the excipients listed in section 6.1.


Ovixan is contraindicated for patients with facial rosacea, acne vulgaris, skin atrophy, perioral dermatitis, perianal and genital pruritus, napkin eruptions, bacterial infections (e.g. impetigo), viral infections (e.g. herpes simplex, herpes zoster and chickenpox) and fungal infections (e.g. candida or dermatophyte), varicella, tuberculosis, syphilis or post-vaccine reactions. Ovixan should not be used on wounds or on skin which is ulcerated.


4.4 Special warnings and precautions for use


If irritation or sensitisation develops with the use of Ovixan, treatment should be withdrawn and

appropriate therapy instituted.


Should an infection develop, use of an appropriate antifungal or antibacterial agent should be instituted. If a

favourable response does not occur promptly, the corticosteroid should be discontinued until the infection is

adequately controlled.


Systemic absorption of topical corticosteroids can produce reversible hypothalamic-pituitary-adrenal (HPA)

axis suppression with the potential for glucocorticosteroid insufficiency after withdrawal of treatment.

Manifestations of Cushing’s syndrome, hyperglycemia, and glucosuria can also be produced in some

patients by systemic absorption of topical corticosteroids while on treatment. Patients applying a topical

steroid to a large surface area or areas under occlusion should be evaluated periodically for evidence of HPA

axis suppression.



Local and systemic toxicity is common especially following long continued use on large areas of damaged

skin, in flexures and with polythene occlusion. If used on the face, occlusion should not be

used. If used on the face, courses should be limited to 5 days. Long term continuous therapy should be

avoided in all patients irrespective of age.


Topical steroids may be hazardous in psoriasis for a number of reasons including rebound relapses

following development of tolerance, risk of centralised pustular psoriasis and development of local or

systemic toxicity due to impaired barrier function of the skin. If used in psoriasis careful patient supervision

is important.


As with all potent topical glucocorticosteroids, avoid sudden discontinuation of treatment. When long term

topical treatment with potent glucocorticoids is stopped, a rebound phenomenon can develop which takes

the form of a dermatitis with intense redness, stinging and burning. This can be prevented by slow reduction

of the treatment, for instance continue treatment on an intermittent basis before discontinuing treatment.


Glucocorticoids can change the appearance of some lesions and make it difficult to establish ab adequate

diagnosis and can also delay the healing.


Ovixan should not be applied to the eyelids because of the potential risk of glaucoma simplex or

subcapsular cataract. Ovixan topical preparations are not for ophthalmic use.

Ovixan cutaneous solution contains propylene glycol that may cause skin irritation.


Paediatric population

Use with care in children. The side effects that have been reported during systemic use of corticosteroids,

including inhibition of adrenal cortex, may also appear with local use of corticosteroids, especially in

children. Children may be more sensitive to the influence of topical glucocorticoids on the hypothalamic-

pituitary- adrenal system (HPA-axis) and to Cushing’s syndrome than adults because the skin surface

is larger in relation to the body weight. Chronic treatment with glucocorticoids may influence the growth

and development in children (see section 4.8).


Treatment with occlusive dressing should not be used in the childhood.


As the safety and efficacy of mometasone furoate in paediatric patients below 2 years of age have not been

established, Ovixan is not recommended in this age group.


4.5 Interaction with other medicinal products and other forms of interaction


No interaction studies have been performed.


4.6 Fertility, pregnancy and lactation


Pregnancy

Corticosteroids passes the placenta. There are no clinical data from the use of mometasone furoate during pregnancy. Studies of mometasone furoate in animals following oral administration have shown teratogenic effects, see section 5.3. The potential risk for humans is unknown.Although systemic exposure is limited, Ovixan should only be used during pregnancy after careful consideration of risks and benefit.

During pregnancy corticosteroids with low potency should be prescribed for treatment of larger body surfaces during longer periods.


Breast-feeding

It has not been established if mometasone furoate passes over to maternal milk. Mometasone furoate should only be given to lactating mothers after careful consideration of risk and benefit. Ovixan should not be applied to the breast or adjacent skin during lactation.


Fertility

No known effects.


4.7 Effects on ability to drive and use machines


Not relevant.


Undesirable effects


The adverse events are presented according to MedRA system organ classification within each frequency

area and after decreasing degree of severity:

Very common (≥ 1/10)

Common (≥1/100 to <1/10)

Uncommon (≥ 1/1000 to < 1/100)

Rare (≥ 1/10,000 to < 1/1,000)

Very rare (< 1/10,000)

Not known (cannot be estimated from the available data)


Adverse events that have been reported during use of glucocorticoids for topical use include:


Treatment related adverse events reported according to system organ classification and frequency


Infections and infestations

Not known

Secondary infection, furuncolosis


Very rare

Folliculitis

Nervous system disorders

Not known

Paresthesia

Very rare

Burning sensation

Vascular disorders

Very rare

Telangiectasis


Skin and subcutaneous tissue disorders

Not known

Allergic contact dermatitis, perioral dermatitis, hypopigmentation, hypertrichosis, striae, maceration of skin, miliaria, acneiform reactions, local skin atrophy, irritation, papulous rosacea like dermatitis (facial skin), capillary sensitivity (ekkymosis), dryness, hypersensitivity (mometasone)


Very rare

Pruritus


General disorders and administration site conditions

Not known

Application site pain, application site reactions


Increased risk for systemic effects and local adverse events is present with frequent administration, when treating large areas or during long-term as well as during treatment of intertriginous areas or with occlusion. Hypo- or hyper-pigmentation has been reported in rare cases in connection with other cortisone medicines and may therefore appear with mometasone furoate.


Adverse events that have been reported during systemic treatment with glucocorticoids – including adrenal suppression- may also appear with topically applied corticosteroids.


Treatment of widespread psoriasis or sudden stopping of prolonged therapy with a potent corticosteroid may induce pustular or erythrodemic psoriasis.


Flare-up of eczema may be seen as a rebound phenomenon after abrupt stopping of therapy.


Paediatric populationPaediatric patients may demonstrate greater susceptibility to topical glucocorticoid-induced hypothalamic-pituitary-adrenal axis suppression and Cushing’s syndrome than mature patients because of a larger skin surface to body weight ratio. Chronic glucocorticoid therapy may interfere with the growth and development of children.

Intracranial hypertension has been reported in paediatric patients receiving topical glucocorticoids. Manifestations of intracranial hypertension include bulging fontanelles, headaches and bilateral papilloedema.


Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reaction via the national reporting system listed in Appendix V.


Overdose


Exaggerated long-term use of topical glucocorticosteroids may suppress the HPA-axis function and give rise to secondary adrenal cortex suppression. If suppression of the HPA-axis is reported, the number of applications times should be decreased or treatment should be stopped while observing necessary caution in these situations.


The steroid content of each container is so low as to have little or no toxic effect in the unlikely event of accidental oral ingestion.


5. PHARMACOLOGICAL PROPERTIES


5.1 Pharmacodynamic properties


Pharmacotherapeutic group: Corticosteroids, Dermatological preparations. Corticosteroids, Plain.

ATC code: D07AC13


Mechanism of action and pharmacodynamics effects

Mometasone furoate is a strong glucocorticoid, group III


The active substance, mometasone furoate, is a synthetic, non-fluorinated glucocorticoid with a furoate esther in position 17.


As for other corticosteroids for topical use mometasone furoate has anti-inflammatory, antipruritic and anti-allergic effects.


5.2 Pharmacokinetic properties


Absorption

Results from percutaneous absorption studies show that the systemic absorption is less than 1 %.


5.3 Preclinical safety data


Preclinical data reveal no special hazard for humans based on conventional studies of safety toxicology, genotoxicity and carcinogenicity (nasal administration) of mometasone furoate besides what is already known for corticosteroids.

Studies of corticosteroids in animals following oral administration have shown reproduction toxicity (cleft palate, skeletal malformations).


6. PHARMACEUTICAL PARTICULARS


6.1 List of excipients


Propylene glycol

Isopropyl alcohol

Hydroxypropylcellulose

Sodium dihydrogen phosphate dihydrate

Phosphoric acid, concentrated (for pH adjustment)

Water, purified


6.2 Incompatibilities


Not applicable.


6.3 Shelf life


30 months.


6.4 Special precautions for storage


Do not store above 30°C.


Nature and contents of container


White LDPE bottles of polyethylene with a white LDPE dropper, and a white HDPE, tamper proof screw cap of polyethylene.


Pack sizes:

30 ml, 100 ml, 2 x 100 ml


Not all pack sizes may be marketed.


6.6 Special precautions for disposal


No special requirements


7. MARKETING AUTHORISATION HOLDER


Galenica AB

P A Hanssons väg 41

SE-205 12 Malmö

Sweden


8. MARKETING AUTHORISATION NUMBER(S)


To be completed nationally


9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION


12 June 2012


10. DATE OF REVISION OF THE TEXT


2015-04-07

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