Nizoral Anti-Dandruff Shampoo
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Nizoral™ Anti-Dandruff Shampoo
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Ketoconazole 2% w/w For excipients, see 6.1
3 PHARMACEUTICAL FORM
Pink viscous shampoo
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
In the prevention and treatment of the scalp condition dandruff.
4.2 Posology and method of administration
For topical administration.
Adults and adolescents aged over 12:
Wash affected areas and leave for 3 to 5 minutes before rinsing. Treatment:
Wash the hair every 3 or 4 days for 2 to 4 weeks.
Prophylaxis:
Use once, every 1 to 2 weeks.
Do not use more often than directed.
4.3 Contraindications
Known hypersensitivity to ketoconazole or any of the excipients.
4.4 Special warnings and precautions for use
Keep out of the eyes. If the shampoo should get into the eyes, they should be bathed with water.
In patients who have been on prolonged treatment with topical corticosteroids, it is recommended that the steroid therapy be gradually withdrawn over a period of 2 to 3 weeks, while using Nizoral Anti-Dandruff Shampoo, to prevent any potential rebound effect.
If the scalp has not cleared within 4 weeks, a doctor or pharmacist should be consulted.
4.5 Interaction with other medicinal products and other forms of interaction
None Known
4.6 Fertility, pregnancy and lactation
There are no adequate and well-controlled studies in pregnant or lactating women. Data on a limited number of exposed pregnancies indicate no adverse effects of topical ketoconazole on pregnancy or on the health of the foetus/newborn child. Animal studies have shown reproductive toxicity at doses that are not relevant to the topical administration of ketoconazole. No effects on the breastfed newborn/infant are anticipated. See Pharmacokinetic properties, section 5.2.
Plasma concentrations of ketoconazole were not detectable after topical administration of Nizoral anti-dandruff Shampoo to the scalp of non-pregnant humans. Plasma levels were detected after topical administration of Nizoral anti-dandruff Shampoo on the whole body. There are no known risks associated with the use of Nizoral anti-dandruff Shampoo in pregnancy or lactation.
4.7 Effects on ability to drive and use machines
None likely
4.8 Undesirable effects
The safety of Nizoral Anti-Dandruff Shampoo was evaluated in 2890 subjects who participated in 22 clinical trials. Nizoral Anti-Dandruff Shampoo was administered topically to the scalp and/or skin. Based on pooled safety data from these clinical trials, there were no ADRs reported with an incidence >1%.
The following table displays ADRs that have been reported with the use of Nizoral Anti-Dandruff Shampoo from either clinical trial or postmarketing experiences. The displayed frequency categories use the following convention:
Very common (>1/10); common (>1/100 to <1/10); uncommon (>1/1,000 to <1/100); rare (>1/10,000 to <1/1,000); very rare (<1/10,000); and not known (cannot be estimated from the available clinical trial data).
Table 1: Adverse Drug Reactions
|
System Organ Class |
Adverse Drug Reactions | ||
|
Frequency Category | |||
|
Uncommon (>1/1,000 to <1/100) |
Rare (>1/10,000 and <1/1,000) |
Not Known | |
|
Immune System disorders |
Hypersensitivity | ||
|
Nervous System Disorders |
Dysgeusia | ||
|
System Organ Class |
Adverse Drug Reactions | ||
|
Frequency Category | |||
|
Uncommon (>1/1,000 to <1/100) |
Rare (>1/10,000 and <1/1,000) |
Not Known | |
|
Infections and Infestations |
Folliculitis | ||
|
Eye Disorders |
Increased lacrimation |
Eye irritation | |
|
Skin and Subcutaneous Tissue Disorders |
Alopecia Dry skin Hair texture abnormal Rash Skin burning sensation |
Acne Dermatitis contact Skin disorder Skin exfoliation |
Angioedema Urticaria Hair colour changes |
|
General Disorders and Administration Site Conditions |
Application site erythema Application site irritation Application site pruritus Application site reaction |
Application site hypersensitivity Application site pustules | |
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 reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard
4.9 Overdose
In the event of accidental ingestion, supportive and symptomatic measures should be carried out. In order to avoid aspiration, neither emesis nor gastric lavage should be instigated.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Ketoconazole is a synthetic imidazole dioxolane antimycotic active against yeasts, including Malassezia, and dermatophytes. Its broad spectrum of activity is already well known.
Ketoconazole also has a direct anti-inflammatory action independent from its antifungal activity which may contribute to symptom relief in dandruff and seborrhoeic dermatitis.
5.2 Pharmacokinetic properties
Plasma concentrations of ketoconazole were not detectable after topical administration of Nizoral Shampoo on the scalp. Plasma levels were detected after topical administration of Nizoral Shampoo on the whole body.
5.3 Preclinical safety data
Effects in non-clinical studies were observed only at exposures considered sufficiently in excess of the maximum human exposure indicating little relevance to clinical use.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Sodium lauryl ether sulphate Disodium monolauryl ether sulphosuccinate Coconut fatty acid diethanolamide Laurdimonium hydrolysed animal collagen Macrogol 120 methyl glucose dioleate Sodium chloride Concentrated hydrochloric acid Imidurea
Sodium hydroxide Erythrosine sodium (E127)
Purified water
6.2 Incompatibilities
None known
6.3 Shelf life
3 years
6.4 Special precautions for storage
Store below 25°C
6.5 Nature and contents of container
High-density polyethylene bottle containing 60ml or 100ml Nizoral AntiDandruff Shampoo
Not all pack sizes may be marketed
6.6 Special precautions for disposal
Not applicable
7 MARKETING AUTHORISATION HOLDER
McNeil Products Limited
Foundation Park
Roxborough Way
Maidenhead
Berkshire
SL6 3UG
UK
8 MARKETING AUTHORISATION NUMBER(S)
PL 15513/0312
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
10/12/2010
10 DATE OF REVISION OF THE TEXT
08/07/2013