CLINDAMYCIN is a brand name for Clindamycin. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Clindamycin and Benzoyl Peroxide Gel is indicated for the topical treatment of mild to moderate acne vulgaris, particularly inflammatory lesions, in adults and adolescents aged 12 years and above. Consideration should be given to official guidance on the appropriate use of antibacterial agents.
Verbatim from this product's MHRA label. Tap a section to expand.
For cutaneous use only. Posology Adults and Adolescents (aged 12 years and above) Clindamycin and Benzoyl Peroxide Gel should be applied once daily in the evening, to the entire affected area. Patients should be advised that excessive application will not improve efficacy, but may increase the risk of skin irritation.
4). 1). The safety and efficacy of Clindamycin and Benzoyl Peroxide Gel has not been studied beyond 12 weeks in acne vulgaris clinical trials. Treatment with Clindamycin and Benzoyl Peroxide Gel should not exceed more than 12 weeks of continuous use.
Paediatric population The safety and efficacy of Clindamycin and Benzoyl Peroxide Gel has not been established in children under 12 years of age, therefore Clindamycin and Benzoyl Peroxide Gel is not recommended for use in this population.
Elderly patients No specific recommendations. Method of administration Clindamycin and Benzoyl Peroxide Gel should be applied in a thin film after washing gently with a mild cleanser and fully drying. If the gel does not rub into the skin easily, too much is being applied.
Hands should be washed after application.
Adverse drug reactions (ADRs) are summarised below for Clindamycin and Benzoyl Peroxide Gel as a combination including any additional ADRs that have been reported for the single topical active ingredients, benzoyl peroxide or clindamycin.
Adverse drug reactions are listed by MedDRA system organ class and by frequency. Frequencies are defined as: very common (≥1/10); common (1/100 and <1/10); uncommon (≥1/1,000 and <1/100); rare (≥1/10,000 and <1/1,000) and not known (cannot be estimated from the available data).
MedDRA SOC Very Common Common Uncommon Not known** Immune system disorders Allergic reactions including hypersensitivity and anaphylaxis Nervous system disorders* Paraesthesia Gastrointestinal disorders Colitis (including pseudomembranous colitis), haemorrhagic diarrhoea, diarrhoea, abdominal pain Skin and subcutaneous tissue disorders* Erythema, peeling, dryness (Generally reported as ‘mild’ in severity) Burning sensation Dermatitis, pruritus, erythematous rash, worsening of acne Urticaria General disorders and Administration site conditions Application site reactions including skin discoloration *At site of application.
**Based on post-marketing reports. Since these reports are from a population of uncertain size and are subject to confounding factors, it is not possible to reliably estimate their frequency however, systemic reactions are rarely seen.
In addition to the ADRs reported in the table above, in the pivotal trial conducted with topical clindamycin 1%/benzoyl peroxide 3% gel, application site photosensitivity reaction was also reported commonly. Also in addition to the ADRs reported above, in studies conducted with topical clindamycin alone, headache and application site pain were reported commonly.
Local Tolerability During the five clinical trials with Clindamycin and Benzoyl Peroxide Gel, all patients were graded for facial erythema, peeling, burning, and dryness on the following scale: 0 = absent, 1 = mild, 2 = moderate and 3 = severe.
The percentage of patients that had symptoms present before treatment (at baseline) and during treatment were as follows: Local Tolerability Assessments for Subjects (N=397) in the Clindamycin and Benzoyl peroxide Gel Group during the Phase 3 Studies: Before Treatment (Baseline) During Treatment Mild Moderate Severe Mild Moderate Severe Erythema 28% 3% 0 26% 5% 0 Peeling 6% <1% 0 17% 2% 0 Burning 3% <1% 0 5% <1% 0 Dryness 6% <1% 0 15% 1% 0 Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
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Contact with the mouth, eyes, lips, other mucous membranes or areas of irritated or broken skin should be avoided. Application to sensitive areas of skin should be made with caution. In case of accidental contact, rinse well with water.
Clindamycin and Benzoyl Peroxide Gel should be used with caution in patients with a history of regional enteritis or ulcerative colitis, or a history of antibiotic-associated colitis. Clindamycin and Benzoyl Peroxide Gel should be used with caution in atopic patients, in whom further skin drying may occur.
During the first weeks of treatment, an increase in peeling and reddening will occur in most patients. Depending upon the severity of these side effects, patients can use a non-comedogenic moisturiser, temporarily reduce the frequency of application of Clindamycin and Benzoyl Peroxide Gel or temporarily discontinue use; however, efficacy has not been established for less than once daily dosing frequencies.
Concomitant topical acne therapy should be used with caution because a possible cumulative irritancy may occur, which sometimes may be severe, especially with the use of peeling, desquamating, or abrasive agents. g. severe erythema, severe dryness and itching, severe stinging/burning) occurs, Clindamycin and Benzoyl Peroxide Gel should be discontinued.
As benzoyl peroxide may cause increased sensitivity to sunlight, sunlamps should not be used and deliberate or prolonged exposure to sun 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 Clindamycin and Benzoyl Peroxide Gel. If prolonged or significant diarrhoea occurs or the patient suffers from abdominal cramps, treatment with Clindamycin and Benzoyl Peroxide Gel should be discontinued immediately, as the symptoms may indicate antibiotic- associated colitis.
Suitable diagnostic methods, such as the determination of Clostridium difficile and toxin and, if necessary, colonoscopy should be employed and treatment options for colitis considered. The product may bleach hair or coloured fabrics.
Avoid contact with hair, fabrics, furniture or carpeting. 1). 5).
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Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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