Loading…
STREFEN HONEY AND LEMON is a brand name for Flurbiprofen. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Strefen Honey and Lemon 8.75mg Lozenge are indicated for the short term symptomatic relief of sore throat in adults and children over the age of 12 years.
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Adults the elderly and children over the age of 12 years:
One lozenge sucked/dissolved slowly in the mouth every 3 - 6 hours as required. Maximum 5 lozenges in a 24 hour period. It is recommended that this product should be used for a maximum of three days Children: Not indicated for children under 12 years.
Elderly:
A general dose recommendation cannot be given, since to date clinical experience is limited. The elderly are at increased risk of the serious consequences of adverse reactions.
Impaired hepatic:
In patients with mild to moderate impairment of hepatic function no dose reduction is required. 3).
Impaired renal:
In patients with mild to moderate impairment of renal function no dose reduction is required. 3). Method of administration For oromucosal administration and short-term use only. 75mg Lozenge should be moved around the mouth whilst sucking.
4)
g. g. pruritus, urticaria, angioedema and more rarely exfoliative and bullous dermatoses (including epidermal necrolysis and erythema multiforme) Oedema, hypertension and cardiac failure have been reported in association with NSAID treatment.
4). 75 mg lozenges The following list of adverse effects relates to those experienced with flurbiprofen at OTC doses for short-term use. (Very common (≥1/10), Common (≥1/100 to <1/10), Uncommon (≥1/1000 to <1/100), Rare (≥1/10000 to <1/1000), Very rare (<1/10000), not known (cannot be estimated from the available data)) Blood and lymphatic system disorders: Not known: anaemia, thrombocytopenia.
Immune System disorders:
Rare: anaphylactic reaction Psychiatric disorders: Uncommon: insomnia Cardiovascular and cerebrovascular disorders Not known: Oedema, hypertension and cardiac failure Nervous System disorders: Common: dizziness, headache, parasthesia Uncommon: somnolence Respiratory, thoracic and mediastinal disorders: Common: throat irritation Uncommon: exacerbation of asthma and bronchospasm, dyspnoea, wheezing, oropharyngeal blistering, pharyngeal hypoaesthesia.
Gastrointestinal disorders:
Common: diarrhoea, mouth ulceration, nausea, oral pain, paraesthesia oral, oropharyngeal pain, oral discomfort (warm or burning feeling or tingling of the mouth). Uncommon: abdominal distension, abdominal pain, constipation, dry mouth, dyspepsia, flatulence, glossodynia, dysgeusia, oral dysaesthesia, vomiting Hepatobiliary disorders: Not known: hepatitis Skin and subcutaneous tissue disorders: Uncommon: various skin rashes, pruritus.
Not known: severe forms of skin reaction such as bullous reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis.
General disorders and administration site conditions:
Undesirable effects may be minimised by using the lowest effective dose for the shortest duration necessary to control symptoms. Elderly population The elderly have an increased frequency of adverse reactions to NSAIDs, especially gastrointestinal bleeding and perforation, which may be fatal.
Respiratory:
Bronchospasm may be precipitated in patients suffering from, or with a previous history of bronchial asthma or allergic disease. Flurbiprofen lozenges should be used with caution in these patients. 5). 8), however this effect is not usually seen with short term limited use products such as flurbiprofen lozenges.
Cardiovascular, Renal and Hepatic Impairment:
NSAIDs have been reported to cause nephrotoxicity in various forms including interstitial nephritis, nephrotic syndrome and renal failure. The administration of an NSAID may cause a dose dependent reduction in prostaglandin formation and precipitate renal failure.
Patients at greatest risk of this reaction are those with impaired renal function, cardiac impairment, liver dysfunction, those taking diuretics and the elderly, however, this effect is not usually seen with short term, limited use products such as flurbiprofen lozenges.
Cardiovascular and cerebrovascular effects:
Caution (discussion with doctor or pharmacist) is required prior to starting treatment in patients with a history of hypertension and/or heart failure as fluid retention, hypertension and oedema have been reported in association with NSAID therapy.
Clinical trial and epidemiological data suggest that the use of NSAIDs (particularly at high doses and in long term treatment) may be associated with a small increased risk of arterial thrombotic events (for example myocardial infarction or stroke).
Hypersensitivity to flurbiprofen or any of the excipients in the product. g. asthma, bronchospasm, rhinitis, angioedema, or urticaria) in response to acetylsalicylic acid or other NSAIDs. Active or history of recurrent peptic ulcer/haemorrhage (two or more distinct episodes of proven ulceration) and intestinal ulceration.
History of gastrointestinal bleeding or perforation, severe colitis, haemorrhagic or haematopoietic disorders related to previous NSAID therapy. Last trimester of pregnancy. 4)
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
Other brands of Flurbiprofen in United Kingdom.
Know a brand we are missing in United Kingdom? Suggest a brand →
Brand names are compiled from public regulatory records for active-ingredient mapping only. Drugvu is not affiliated with any manufacturer. This is not medical advice.
Uncommon: pyrexia, pain 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.
uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
There are insufficient data to exclude such a risk for flurbiprofen when given at a daily dose of no more than 5 lozenges. 8) Nervous System effects Analgesic induced headache - In the event of prolonged use of analgesics or use beyond the regulations headache may occur, which must not be treated with increased doses of the medicinal product.
8) Gastrointestinal bleeding, ulceration or perforation, which can be fatal has been reported with all NSAIDs at anytime during treatment, with or without warning symptoms or a previous history of serious GI events. 3), and in the elderly, however this effect is not usually seen with short term limited use products such as flurbiprofen lozenges.
Patients with a history of GI toxicity, particularly the elderly, should report any unusual abdominal symptoms (especially GI bleeding) to their healthcare professional. 5). If GI bleeding or ulceration occurs in patients receiving flurbiprofen, the treatment should be withdrawn.
8). Flurbiprofen lozenges should be discontinued at the first appearance of skin rash, mucosal lesions, or any other sign of hypersensitivity. g. development of necrotising fasciitis) has been described in temporal association with the use of systemic NSAIDs as a class, the patient is advised to consult a physician immediately if signs of a bacterial infection occur or worsen during the flurbiprofen lozenges therapy.
It should be considered whether initiation of an anti-infective antibiotic therapy is indicated.
Masking of symptoms of underlying infections:
Epidemiological studies suggest that systemic non-steroidal anti-inflammatory drugs (NSAIDs) can mask symptoms of infection, which may lead to delayed initiation of appropriate treatment and thereby worsening the outcome of the infection.
This has been observed in bacterial community acquired pneumonia and bacterial complications to varicella. 75mg Lozenge is administered while the patient suffers from fever or pain in relation to infection, monitoring of infection is advised.
Important Information about some of the ingredients of this medicine • This medicine contains only very low levels of gluten (from wheat starch). It is regarded as ‘gluten-free’ and is very unlikely to cause problems if you have coeliac disease.
38 micrograms of gluten. If you have wheat allergy (different from coeliac disease) you should not take this medicine. 069 g Glucose per lozenge. Patients with rare hereditary problems of fructose intolerance, glucose galactose malabsorption or sucrase isomaltase insufficiency should not take this medicine.
• This medicine contains sulphites, which may rarely cause severe hypersensitivity reactions and […]