Fenbid
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Fenbid Forte 10% Gel
AAH Pharmaceutical’s Ibuprofen pain relief gel maximum strength 10% w/w Tesco’s Ibuprofen pain relief gel maximum strength 10% w/w Lloydspharmacy’s Maximum strength Ibuprofen 10% gel Ibuprofen 10% gel
Numark’s Ibuprofen Pain Relief Gel Maximum Strength 10% w/w Morrison’s Ibuprofen Pain Relief Gel Maximum Strength 10% w/w Thornton &Ross’s Ibuprofen 10% gel Phorpain gel maximum strength Boots Ibuprofen Max Strength 10% Gel
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Ibuprofen Ph. Eur. 10% Gel
3 PHARMACEUTICAL FORM
Gel for topical application
4 CLINICAL PARTICULARS
4.1 Therapeutic indications Prescription Only indication
For the relief of pain and inflammation associated with backache, mild to moderate arthritic conditions, rheumatic and muscular pain, sprains, strains, sports injuries and neuralgia.
Pharmacy Only indication
For the relief of pain and inflammation associated with backache, rheumatic and muscular pain, strains, sprains, neuralgia and sports injuries. For the relief of pain of non-serious arthritic conditions.
4.2 Posology and method of administration
Method of administration
For topical application to the skin.
Dosage
Adults, the elderly and children over 14 years: Squeeze 50 to 125mg (2 to 5cm) of the gel from the tube and lightly rub into the affected area until absorbed.
The dose should not be repeated more frequently than every four hours and no more than 4 times in any 24 hour period.
Wash hands after each application. Do not exceed the stated dose. Review treatment after 2 weeks, especially if the symptoms worsen or persist.
Children under 14years: Do not use on children 14 years of age, except on the advice of a doctor.
4.3 Contraindications
Hypersensitivity to any of the constituents. Hypersensitivity to aspirin, or other non-steroidal anti-inflammatory drugs, asthma, rhinitis or urticaria.
Not to be used on broken or damaged skin.
4.4 Special warnings and precautions for use
Apply with gentle massage only. Avoid contact with eyes, mucous membranes and inflamed or broken skin.
Discontinue if rash develops.
Hands should be washed immediately after use.
Not for use with occlusive dressings.
The label will state:
Do not exceed stated dose Keep out of reach of children For external use only
If symptoms persist consult your doctor or pharmacist.
Do not use if you are allergic to Ibuprofen or any of the ingredients, aspirin, or any other painkillers.
Consult your doctor or pharmacist before use if:
- you are taking aspirin or any other pain relieving medication
- you are pregnant
Not recommended for children under 14 years.
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, patients with an active peptic ulcer, a history of kidney problems or asthma should seek medical advice before using Ibuprofen gel as should patients already taking other painkillers.
Patients should seek medical advice if symptoms worsen or persist.
Patients should be advised against excessive exposure to sunlight of area treated in order to avoid possibility of photosensitivity.
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. Concurrent aspirin or other NSAIDS may result in an increased incidence of adverse reactions.
4.6 Pregnancy and lactation
Not to be used during pregnancy or lactation.
Pregnancy:
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.
Lactation:
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 reaction and anaphylaxis (b) respiratory tract reactivity comprising of asthma, aggravated asthma, brochospasm or dyspnoea, or (c) assorted skin disorders, including rashes of various types, pruritis, urticaria, purpura, angioedema and less commonly, bullous dermatoses (including epidermal necrolysis and erythema multiforme).
Gastro-intestinal: Side effects such as abdominal pain and dyspepsia have been reported.
Renal: Renal impairment can occur in patients with a history of kidney problems.
4.9 Overdose
Overdosage with a topical presentation of Fenbid Forte Gel is 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
ATC code: M02A A13, Anti-inflammatory preparations, non-steroids for topical use.
The gel is for topical application. It contains the active ingredient, ibuprofen, a phenylpropionic acid derivative which exerts its anti-inflammatory and analgesic effects directly in inflamed tissues underlying the site of application, mainly by inhibiting prostaglandin biosynthesis. Because it is formulated in an aqueous/ alcoholic gel, the preparation 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 (approximately 22% of a finite dose within 48 hours), achieving high, therapeutically relevant local concentrations in underlying soft tissues, joints and the 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.
5.3 Preclinical safety data
There is no new data published on the active ingredient.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Hydroxyethyl cellulose EP Sodium Hydroxide EP Benzyl alcohol EP Isopropyl alcohol BP Purified water
6.2 Incompatibilities
None known
6.3 Shelf life
36 months
6.4 Special precautions for storage
Store below 25°C
6.5 Nature and contents of container
Collapsible aluminium tubes with internal protective lacquer with polypropylene screw caps.
P:30g,50g POM: 30, 50 & 100g
6.6 Special precautions for disposal
No special instructions
7 MARKETING AUTHORISATION HOLDER
Mercury Pharma Group Ltd No. 1 Croydon,
12-16 Addiscombe Road,
Croydon CR0 0XT,
UK
8 MARKETING AUTHORISATION NUMBER(S)
PL 10972/0082
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
05/12/2005
10 DATE OF REVISION OF THE TEXT
06/09/2013