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FLUCLOXACILLIN 250 MG / 5ML ORAL SOLUTION - patient leaflet, side effects, dosage

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Patient leaflet - FLUCLOXACILLIN 250 MG / 5ML ORAL SOLUTION

1. what your medicine is and what it is used for

Flucloxacillin is an antibiotic used to treat infections by killing the bacteria that can cause them. It belongs to a group of antibiotics called “penicillins”.

Flucloxacillin is used to treat:

  • chest infections
  • throat or nose infections
  • ear infections
  • skin and soft tissue infections
  • heart infections
  • bone and joint infections
  • meningitis
  • digestive system infections
  • blood infections
  • kidney, bladder or urethra (the tube which carries urine from the bladder) infections.

Flucloxacillin can also be used to prevent infections during major surgery, particularly heart or orthopaedic surgery.

2. what you need to know before you take your medicine

Do not take this medicine if:

  • You are allergic to flucloxacillin or any other penicillin antibiotics (see symptoms in section 4).
  • You are allergic to any of the other ingredients of this medicine (listed in section 6).
  • You have suffered previously from liver problems (e.g. jaundice) after taking flucloxacillin.
  • You have had an allergic reaction to p-lactam antibiotics (e.g. penicillins, cephalosporins).

Warnings and precautions

Talk to your doctor or pharmacist before taking this medicine if:

  • You suffer from kidney problems, as you may require a lower dose than normal (convulsions may occur very rarely in patients with kidney problems who take high doses)
  • You suffer from liver problems, as this medicine could cause them to worsen
  • You are 50 years of age or older
  • You have other serious illnesses (apart from the infection this medicine is treating)
  • You are taking this medicine for a long time as regular tests of liver and kidney function are advised
  • You have ever had swelling of the face or skin rash while taking an antibiotic
  • You are giving this medicine to a new born child
  • You are taking or will be taking paracetamol

There is a risk of blood and fluid abnormality (high anion gap metabolic acidosis) which occurs when there is an increase in plasma acidity, when flucloxacillin is used concomitantly with paracetamol, particularly in certain groups of patients at risk, e.g. patients with severe renal impairment, sepsis or malnutrition, especially if the maximum daily doses of paracetamol are used. High anion gap metabolic acidosis is a serious disease that must have urgent treatment.

The use of flucloxacillin, especially in high doses, may reduce the potassium levels in the blood (hypokalaemia). Your doctor may measure your potassium levels regularly during the therapy with higher doses of flucloxacillin.

Other medicines and Flucloxacillin Oral Solution

Check with your doctor or pharmacist before taking this medicine if you are taking any other medicines, especially:

  • Probenecid or sulfinpyrazone (used to treat gout).
  • Methotrexate (a chemotherapy drug)
  • Oral typhoid vaccine (antibiotics can make this less effective)
  • Sugammadex (used with general anaesthetics)
  • Piperacillin (an antibiotic taken by injection)
  • Warfarin (medicine to prevent blood clotting)
  • Paracetamol
  • Other types of antibacterial treatments such as bacteriostatic agents (e.g. chloramphenicol and tetracyclines).

Some medicines may affect the way others work. Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. This means medicines you have bought yourself as well as medicines on prescription from a doctor.

Pregnancy and breast-feeding

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.

Driving and using machines

Flucloxacillin Oral Solution may have insignificant or no influence on the ability to drive and use machines.

Tests

Regular monitoring of liver and kidney function should be performed whilst taking flucloxacillin for a long period of time. Tell your doctor that you are taking flucloxacillin if you are having urine tests or blood tests because it may affect the results.

Your medicine contains sucrose and sodium

This medicine contains up to 2.96g of sucrose (sugar) per 5ml dose. This should be taken into account in patients with diabetes mellitus. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

This medicine contains 24.09mg sodium (main component of cooking/table salt) in each 5ml spoonful of solution. This is equivalent to 1.20% of the recommended maximum daily dietary intake of sodium for an adult.

To be taken into consideration by patients on a controlled sodium diet.

3. how to take your medicine

Always take this medicine exactly as your doctor or pharmacist has told you. Their directions may differ from the information contained in this leaflet. The pharmacist’s label should tell you how much to take and how often. Check with your doctor or pharmacist if you are not sure.

Take your medicine on an empty stomach, at least 1 hour before or 2 hours after meals. It is important that you take your medicine at the right times.

To reduce the risk of pain in your oesophagus (the tube that connects your mouth with your stomach) take a full glass of water (250ml) after oral suspension intake and do not lie down immediately after oral suspension intake.

The dose will depend on the patient and will be decided by your doctor. However, the usual doses for each age group are:

Adults (including the elderly)

  • The usual dose is 250mg four times a day
  • Bone or heart infection: Up to 8g daily, in divided doses at six to eight hours apart.
  • Surgical prophylaxis: 1 to 2g IV at induction of anaesthesia followed by 500mg every six hours for up to 72 hours.

Use in children and adolescents

Children (10–18 years of age):

250mg four times daily

Children (2–10 years of age):

125mg four times daily

Children under 2 years of age:

  • 62.5mg four times daily

Patients with kidney problems

If you suffer from severe kidney failure your doctor will give you lower or fewer doses.

If you still feel unwell after finishing the treatment, speak to your doctor

If you take more of your medicine than you should

If you (or somebody else) takes too much of your medicine, or you think a child may have swallowed any contact your nearest hospital casualty department or speak to your doctor or pharmacist immediately. Gastrointestinal effects such as nausea, vomiting and diarrhoea may be evident and should be treated symptomatically.

If you forget to take your medicine

If you forget to take a dose, take it as soon as you remember, then carry on as before. Do not take a double dose to make up for a forgotten dose.

If you stop taking your medicine

Keep taking your medicine until your doctor tells you to stop. Do not stop taking it just because you feel better. If you stop taking the medicine, your infection may return or get worse. If you are still unwell after taking all the medicine, go and see your doctor.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. possible side effects

Like all medicines, this medicine may cause side effects, although not everybody gets them. If they occur, they are likely to be temporary, and not serious. However, some may be serious and need medical attention.

STOP taking flucloxacillin and contact your doctor if you experience:

  • allergy or hypersensitivity including itchy rash, itching, sore mouth or eyes, swelling of the face, lips, throat or tongue or breathing problems.
  • Severe, bloody diarrhoea (pseudomembranous colitis). If bloody diarrhoea develops, flucloxacillin treatment should be discontinued and appropriate therapy should be initiated.
  • Jaundice (yellow colour in the skin and whites of the eyes), hepatitis (liver inflammation) – sometimes these effects on the liver can be delayed for up to 2 months after finishing treatment.
  • Skin rash with circular, red patches (Erythema multiforme).
  • Severe skin rash with flushing, fever, blisters or ulcers (Stevens Johnson syndrome) or a severe rash with reddening, peeling and swelling of the skin that looks like a burn (toxic epidermal necrolysis).
  • A red, scaly rash with bumps under the skin and blisters (exanthematous pustulosis). The frequency of this is unknown.

Tell your doctor if you notice any of the following effects:

Common (may affect up to 1 in 10 people): Diarrhoea, stomach upset and feeling sick – Should be mild and wear off after a few days. If severe or lasting longer, tell your doctor.
  • Heartburn and indigestion.

Uncommon (may affect up to 1 in 100 people):

  • Hives

Very rare (may affect up to 1 in 10,000 people):

  • Kidney problems including inflammation (may result in difficulty passing water or blood in the urine)
  • Unexplained bleeding, bruising or skin discolouration (may be caused by changes in the numbers of blood cells)
  • Blood and lymphatic system disorders like neutropenia (reduction in white blood cells) including agranulocytosis (serious low level of white blood cells). People with this condition are at very high risk of serious infections due to their suppressed immune system. Patients are advised to report any signs and symptoms of infection to their doctor. Eosinophilia (an increased number of eosinophils in the blood)
  • Joint or muscle pains or fever (may develop 2 days after starting treatment).
  • Changes in liver function test results (reversible when treatment is discontinued).
  • Cases of blood and fluid abnormality (high anion gap metabolic acidosis) which occurs when there is an increase in plasma acidity, when flucloxacillin is used concomitantly with paracetamol, generally in the presence of risk factors (see section 2).

Not known (cannot be estimated from the available data):

  • Low potassium levels in the blood (hypokalaemia), which can cause muscle weakness, twitching or abnormal heart rhythm.
  • Pain in oesophagus (the tube that connects mouth with stomach) and other related symptoms, such as difficulties in swallowing, heartburn, throat irritation or chest pain.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the yellow card scheme at 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.

5. how to store your medicine

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the label. The expiry date refers to the last day of that month. Dry powder: Store below 25°C. Store in the original container in order to protect from light and moisture.

Do not open the foil pouch until ready to reconstitute the product.

Once opened the foil pouch may be discarded.

Reconstituted mixture: Store for 7 days at 2oC to 8oC in a refrigerator.

Once reconstituted (mixed) by the pharmacist, this medicine must be used within 7 days.

Return any left-over medicine to the pharmacist. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. contents of the pack and other information

What Flucloxacillin Oral Solution contains

The active substance is flucloxacillin as flucloxacillin sodium.

The other ingredients are sodium benzoate (E211), disodium edetate, saccharin sodium, monoammonium-glycyrrhizinate, sodium citrate, flavour pineapple, flavour menthol, RED FD&C No. 3 (E127) and sucrose.

Please see further information on sucrose in section 2.

What Flucloxacillin Oral Solution looks like and contents of the pack

Unconstituted powder: a pink granular powder with a characteristic odour of pineapple.

Reconstituted solution: a pink coloured solution with a characteristic odour of pineapple.

Flucloxacillin Oral Solution is available in size 100ml on reconstitution.

Marketing Authorisation Holder

Athlone Pharmaceuticals Limited, Ballymurray, Co. Roscommon, Ireland.

Manufacturer

Athlone Laboratories Limited, Ballymurray, Co. Roscommon, Ireland.

Distributed by:

Milpharm Limited, Ares Block, Odyssey Business Park, West End Road, South Ruislip, HA4 6QD, United Kingdom.

PL 30464/0168

This leaflet was last revised in February 2021.

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