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The product code(s) for this leaflet is: PL 00063/0767.
Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges
Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges
Contains Flurbiprofen
1. What Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges is and what it is used for
2. What you need to know before you use Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges
3. How to use Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges
4. Possible side effects
5. How to store Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges
6. Contents of the pack and other information
This medicine contains flurbiprofen. Flurbiprofen is a non-steroidal anti-inflammatory drug (NSAID) which has analgesic, antipyretic and anti-inflammatory properties. Flurbiprofen 8.75 mg lozenges are used for the short-term relief of symptoms of sore throat such as throat pain, soreness and swelling, and difficulty in swallowing in adults and adolescents over the age of 12 years.
You must talk to a doctor if you do not feel better or if you feel worse after 3 days.
are allergic (hypersensitive) to Flurbiprofen or to any of the other ingredients of this medicine (listed in section 6); have ever had asthma, unexpected wheezing or shortness of breath, a runny nose, facial swelling or itchy rash (hives) after taking acetylsalicylic acid (aspirin) or any other NSAID medicine; currently have or have ever had two or more episodes of a stomach ulcer, intestinal ulcers, or gastrointestinal bleeding; have had gastrointestinal bleeding or perforation, severe colitis (inflammation of the bowel) or bleeding disorders when taking NSAID medicines in the past; are in the last 3 months of pregnancy; have severe heart, severe kidney or severe liver failure
Talk to your doctor or pharmacist before taking Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges if you: have ever had asthma or suffer from allergies; have tonsillitis (inflamed tonsils) or think you may have a bacterial throat infection (as you may need antibiotics); you have an infection - please see heading “Infections” below; have heart, kidney or liver problems; have had a stroke; have a history of bowel disease (ulcerative colitis, Crohn’s disease); suffer from chronic autoimmune disease such as systemic lupus erythematosus and mixed connective tissue disease; are elderly, as you are more likely to experience the side effects listed in this leaflet; are in the first 6 months of pregnancy or breastfeeding; If you have high blood pressure; If you have analgesic-induced headache
At the first sign of any skin reaction (rash, peeling, blistering) or other sign of an allergic reaction, stop using the lozenge and consult a doctor at once. Report any unusual abdominal symptoms (especially bleeding) to your doctor. If you do not get better, you get worse, or develop new symptoms, talk to a doctor. The use of medicines containing flurbiprofen may be associated with a small increased risk of heart attack (myocardial infarction) or stroke. Any risk is more likely with high doses and prolonged treatment. Do not exceed the recommended dose or duration of treatment (3 days).
This medicine should not be used by children under the age of 12 years.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicine. In particular, tell them if you are taking:
low dose acetylsalicylic acid (aspirin) (up to 75 mg daily); medicines for high blood pressure or heart failure (antihypertensives, cardiac glycosides); water tablets (diuretics, including potassium sparing drugs); medicines for thinning the blood (anticoagulants, antiplatelet agents); medicines for gout (probenecid, sulfinpyrazone); other NSAIDs including cyclooxygenase-2 selective inhibitors or corticosteroids (such as celecoxib, ibuprofen, diclofenac sodium or prednisolone); mifepristone (a medicine used for pregnancy termination); quinolone antibiotics (such as ciprofloxacin); cyclosporine or tacrolimus (to suppress the immune system); phenytoin (to treat epilepsy); methotrexate (to treat autoimmune diseases or cancer); lithium or SSRIs (for depression); oral antidiabetics (to treat diabetes); zidovudine (to treat HIV)
Alcohol should be avoided during treatment with this medicine as it increases the risk of bleeding in the stomach or intestines.
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Do not take this medicine if you are in the last 3 months of pregnancy. If you are in the first 6 months of pregnancy or are breast-feeding, speak to your doctor before taking these lozenges.
Flurbiprofen belongs to a group of medicines which may impair fertility in women. This effect is reversible on stopping the medicine. It is unlikely that the lozenges, used occasionally, will affect your chances of becoming pregnant; however, tell your doctor before taking this medicine if you have problems becoming pregnant.
Non-steroidal anti-inflammatory drugs (NSAIDs) may hide signs of infections such as fever and pain. This may delay appropriate treatment of infection, which may lead to an increased risk of complications. If you take this medicine while you have an infection and your symptoms of the infection persist or worsen, consult a doctor or pharmacist without delay.
No studies on the effects on the ability to drive and use of machines have been performed. However, dizziness and visual disturbances are possible side effects after taking NSAIDs. If affected, do not drive or operate machinery.
Strefen Eucalyptus and Manuka Honey Flavour 8.75mg Lozenges contains Isomalt (E953) 2032.18 mg/lozenge and Liquid
Maltitol (E965) 509.03 mg/lozenge.
May have a mild laxative effect.
Calorific value 2.3 kcal/g maltitol or isomalt.
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product. Anise Alcohol, Benzyl Alcohol, Benzyl Benzoate, Benzyl Cinnamate, Benzyl Salicylate, Cinnamal, Cinnamyl Alcohol, Citral, Citronellol, d-Limonene, Geraniol, Limonene and Linalool may cause allergic reactions.
This medicine contains 0.00169 mg benzyl alcohol in each lozenge. Ask your doctor or pharmacist for advice if you have a liver or kidney disease or if you are pregnant or breast-feeding (see section 2. Pregnancy, breast-feeding and fertility). This is because large amounts of benzyl alcohol can build-up in your body and may cause side effects (called“metabolic acidosis”).
Benzyl alcohol may cause mild local irritation.
Always use this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.
Take one lozenge by mouth and suck slowly. Always move the lozenge around whilst sucking. The lozenges should start to work within 30 minutes. Then take one lozenge every 3-6 hours, if needed.
Do not take more than 5 lozenges in a 24 hour period.
Do not give to children under 12 years.
These lozenges are for short-term use only. The lowest effective dose should be used for the shortest duration necessary to relieve symptoms. If you have an infection, consult a doctor or pharmacist without delay if symptoms (such as fever and pain) persist or worsen (see section 2). If mouth irritation occurs, flurbiprofen treatment should be withdrawn.
Do not take this medicine for more than 3 days unless your doctor tells you to. If you do not get better, you get worse, or if you develop new symptoms, talk to a doctor or pharmacist.
Talk to a doctor or pharmacist or go to your nearest hospital straight away. Symptoms of overdose include: feeling sick or being sick, stomach ache or, more rarely, diarrhoea. Ringing in the ears, headache and gastrointestinal bleeding is also possible.
If you have any questions on the use of this product, ask your doctor or pharmacist.
Do not take a double dose to make up for a forgotten dose.
Like all medicines this medicine can cause side effects, although not everybody gets them.
signs of an allergic reaction such as asthma, unexplained wheezing or shortness of breath, itchiness, runny nose, skin rashes, etc.; swelling of the face, tongue or throat causing difficulty in breathing, racing heart and drop in blood pressure leading to shock (these can happen even on the first use of the medicine.); severe skin reactions such as peeling, blistering or flaking skin.
Common (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
drowsiness; blistering in the mouth or throat, numbness in the throat; stomach bloating, abdominal pain, wind, constipation, indigestion, vomiting; dry mouth; burning sensation in the mouth, altered sense of taste; skin rashes, itchy skin; fever, pain; feeling sleepy or difficulty in falling asleep; worsening of asthma, wheezing, shortness of breath; reduced sensation in the throat
Rare (may affect up to 1 in 1000 people)
anaphylactic reaction
Frequency not known (cannot be estimated from the available data) anaemia, thrombocytopenia (low platelet count in the blood that can give rise to bruising and bleeding); swelling (oedema), high blood pressure, heart failure or attack; severe forms of skin reactions such as bullous reactions, including Stevens-Johnson syndrome and Lyell’s syndrome and toxic epidermal necrolysis; hepatitis (inflammation of the liver)
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.
Medicines should not be disposed of via waste water or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
The active ingredient (the ingredient which makes the medicine work is flurbiprofen 8.75 mg. The other ingredients are: macrogol 300, potassium hydroxide (E525), ammonia caramel (E150c), curcumin (E100) (contains propylene glycol (E1520) and polysorbate 80), Honey and Eucalyptus flavour (contains Flavouring preparations, natural flavouring substances, Flavouring substances, Triacetin (E1518), Propylene Glycol (E1520), Anise Alcohol, Benzyl Alcohol, Benzyl Benzoate, Benzyl Cinnamate, Benzyl Salicylate, Cinnamal, Cinnamyl Alcohol, Citral, Geraniol, Limonene and Linalool), acesulfame potassium (E950), maltitol liquid (E965) and isomalt (E953).
The lozenges are circular in shape with an embossed brand logo and a pale brown to yellow colour, in opaque, white PVC/PVdC/Aluminium blisters and packed into cardboard cartons.
The pack contains 8 or 16 lozenges. Not all pack sizes may be marketed.
Produce licence number: PL 00063/0767
Date of revision: March 2025
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