Ibugel Forte 10%
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Ibugel Forte 10%
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Ibuprofen 10.0% w/w
3 PHARMACEUTICAL FORM
Gel
Aqueous-alcoholic, non-greasy, fragrance-free, clear or slightly hazy
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
For the topical treatment of rheumatic and muscular pain, sprains, strains, backache and neuralgia. Ibugel Forte 10% is also indicated for symptomatic relief of pain due to non-serious arthritic conditions.
4.2 Posology and method of administration
2 to 5cm gel (50 to 125mg ibuprofen) is to be applied to the affected area up three times daily, or as directed by the physician. The gel should be massaged well into the skin until completely absorbed, and hands washed after use unless being treated.
Treatment should not normally continue for more than a few weeks, unless recommended to do so by a doctor.
The same dosage and dosage schedule applies to all age groups, although Ibugel Forte 10% is not normally recommended for use on children under the age of 12 years, unless instructed by the physician.
4.3 Contraindications
Not to be used if allergic to any of the ingredients, or in cases of hypersensitivity to aspirin, ibuprofen or related painkillers (including when taken by mouth), especially where associated with a history of asthma, rhinitis or urticaria.
Not to be used on broken or damaged skin.
4.4 Special warnings and precautions for use
To be kept away from the eyes and mucous membranes.
Oral NSAIDs, including ibuprofen, can sometimes be associated with renal impairment, aggravation of active peptic ulcers, and can induce allergic bronchial reactions in susceptible asthmatic patients. Although the systemic absorption of topically applied ibuprofen is less than for oral dosage forms, these complications can occur in rare cases. For these reasons, caution should be exercised before prescribing Ibugel Forte 10% for patients with an active peptic ulcer, a history of kidney problems, asthma or intolerance to aspirin or ibuprofen taken orally.
Patients should seek medical advice if symptoms worsen or persist.
4.5 Interaction with other medicinal products and other forms of interaction
Non-steroidal anti-inflammatory drugs may interact with blood pressure lowering drugs, and may possibly enhance the effects of anticoagulants, although the chance of either of these occurring with a topically administered preparation is extremely remote. Where aspirin or other NSAID tablets are taken concurrently, it is important to bear in mind that these may increase the incidence of undesirable effects.
4.6 Pregnancy and lactation
Not to be used during pregnancy or lactation.
Although no teratogenic effects have been demonstrated, ibuprofen should be avoided during pregnancy. The onset of labour may be delayed, and the duration of labour increased. Ibuprofen appears in breast milk in very low concentrations, but is unlikely to affect breast fed infants adversely.
4.7 Effects on ability to drive and use machines
None known
4.8 Undesirable effects
Very rarely, susceptible patients may experience the following side effects with ibuprofen, but these are extremely uncommon when ibuprofen is administered topically. If they occur, treatment should be discontinued:-
Hypersensitivity: hypersensitivity reactions have been reported following treatment with ibuprofen. These may consist of (a) non-specific allergic reactions and anaphylaxis, (b) respiratory tract reactivity comprising asthma, aggravated asthma, bronchospasm, or dyspnoea, or (c) assorted skin disorders, including rashes of various types, pruritus, urticaria, purpura, angioedema and, less commonly, bullous dermatoses (including epidermal necrolysis and erythema multiforme).
Renal: renal impairment can occur in patients with a history of kidney problems.
Gastrointestinal: side effects such as abdominal pain and dyspepsia have been reported.
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
Not applicable. Any overdose with a topical presentation of ibuprofen is extremely unlikely.
Symptoms of severe ibuprofen overdosage (eg following accidental oral ingestion) include headache, vomiting, drowsiness and hypotension. Correction of severe electrolyte abnormalities should be considered.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Ibugel Forte 10% is a topical preparation which has anti-inflammatory and analgesic properties. It contains the active ingredient, ibuprofen, which exerts its effects directly in inflamed tissues underlying the site of application, mainly by inhibiting prostaglandin biosynthesis.
Because it is formulated in an aqueous/alcoholic gel, Ibugel Forte 10% also exerts a soothing and cooling effect when applied to the affected area.
5.2 Pharmacokinetic properties
Specially formulated for external application, the active ingredient penetrates through the skin rapidly and extensively, achieving high, therapeutically relevant local concentrations in underlying soft tissues, joints and synovial fluid, whilst producing plasma levels that are unlikely to be sufficient to cause any systemic side effects, other than in rare individuals who are hypersensitive to ibuprofen.
Furthermore, there do not appear to be any appreciable differences between the oral and topical routes of administration regarding metabolism or excretion of ibuprofen.
5.3 Preclinical safety data
Published information on subchronic toxicity studies confirms that topically applied ibuprofen is well tolerated both locally and by the gastro-intestinal tract. Any local erythema is only mild and no signs of mucosal lesions or ulcerogenic effects have been determined in the gastro-intestinal tract.
In the course of assessing mucosal tolerance, topical ibuprofen has been found to cause acute, but reversible, irritant reactions in the eyes and mucous membranes.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
IMS
Carbomers Diethylamine Purified Water
6.2 Incompatibilities
None known
6.3 Shelf life
36 months from the date of manufacture
6.4 Special precautions for storage
Do not store above 25°C
6.5 Nature and contents of container
1. Membrane sealed, epoxy resin coated, collapsible aluminium tube, fitted with a screw cap, containing 100g of product.
2. Membrane sealed, collapsible aluminium tube, fitted with a screw cap, containing 100g of product.
6.6 Special precautions for disposal
Not applicable
7 MARKETING AUTHORISATION HOLDER
Diomed Developments Limited
T/A Dermal Laboratories Tatmore Place Gosmore Hitchin
Herts SG4 7QR United Kingdom
MARKETING AUTHORISATION NUMBER
PL 00173/0175
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10
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
03/03/2000 / 24/06/2005
DATE OF REVISION OF THE TEXT
12/05/2015