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Roximstad

Document: Roximstad film-coated tablet ENG PL change

Package leaflet: Information for the user


Roximstad 150 mg film-coated tablets

Roximstad 300 mg film-coated tablets

roxithromycin


Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

  • Keep this leaflet. You may need to read it again.

  • If you have any further questions, ask your doctor or pharmacist.

  • This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.

  • If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.


What is in this leaflet

1. What Roximstad is and what it is used for

2. What you need to know before you take Roximstad

3. How to take Roximstad

4. Possible side effects

5. How to store Roximstad

6. Contents of the pack and other information


1. What Roximstad is and what it is used for


Roximstad film-coated tablets contain the active ingredient roxithromycin. Roxithromycin belongs to a group of medicines known as macrolide antibiotics. These are medicines used to fight infections caused by bacteria.


Roximstad is used to

treat bacterial infections of the airways including:

some types of a serious lung infection (pneumonia) caught in the community (community acquired pneumonia).


2. What you need to know before you take Roximstad


DO NOT take Roximstad


Warnings and precautions

Talk to your doctor before taking Roximstad if you have or have had any medical condition, especially the following:

However, your doctor may decide that you must take Roximstad to deal with your infection. In this case, your dose will be decreased.


Your doctor will check your liver function regularly if:

If your liver function gets worse during treatment, your doctor may tell you to stop taking Roximstad.


Pseudomembranous colitis: This is an infection causing inflammation of the large intestine. It can result in severe runny stools (diarrhoea) which can last for days or weeks, and can occur during or after treatment. If you have these symptoms:

Your doctor will prescribe another medicine to treat your symptoms.


Allergic (hypersensitivity) reactions: Some patients have had serious allergic reactions when taking roxithromycin. Reactions include a serious allergic reaction called anaphylaxis. Symptoms of anaphylaxis may include swelling of the skin, of the face, limbs, tongue or throat, and breathing difficulties. Occasionally these reactions can be life threatening. If you have an allergic reaction:


Irregular heartbeat (arrhythmia): If you develop signs of an irregular or rapid heartbeat during treatment:


A disorder causing muscle weakness (myasthenia gravis): If you suffer from myasthenia gravis your symptoms of myasthenia gravis may get worse. This may affect your breathing muscles and your breathing may get dangerously weak. If your symptoms get worse you should stop taking Roximstad and see your doctor immediately.


Children and patients weighing less than 40 kg: Roximstad should not be used by:


Blood and urine testing: If you need to take Roximstad for longer than two weeks your doctor will regularly check:


Other medicines and Roximstad

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.


DO NOT take Roximstad if you are already taking any of these drugs (see Section 2).


The effect of your Roximstad medicine can be affected by or can affect the following medicines:


Oral contraceptives: You should note that the oral contraceptive pill may be less effective when you take Roximstad.


Roximstad with food and drink

You should take Roximstad at least 15 minutes before a meal which ensures that your body absorbs the medicine rapidly. Take Roximstad with something to drink, e.g. a glass of water.


Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking any medicine.


Studies in animals have not shown any harmful effects of Roximstad. However, the use of Roximstad in pregnant or breast-feeding women has not been studied.

If you are pregnant, only use Roximstad if your doctor indicates it is absolutely necessary.

Breast-feeding

Roxithromycin passes into breast milk. If you are breastfeeding, only use Roximstad if your doctor indicates it is absolutely necessary.


Driving and using machines

When taking Roximstaddizziness and visual disturbance can occasionally occur. If you experience these symptoms you must not drive or use machines.


Roximstad contains milk sugar (lactose)

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.


3. How to take Roximstad


Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.


You should take Roximstad tablets at least 15 minutes before a meal with some liquid, e.g. water.


Adults, the elderly, and children weighing at least 40 kg


The recommended dose is 150 mg Roximstad twice a day (every 12 hours).


If you are being treated for pneumonia your doctor may tell you to take 300 mg Roximstad once a day.


If you have kidney or liver problems

If you have impaired kidney function your Roximstad dose will not need to be adjusted.


If you have mild to moderate liver disease your doctor will decide if you must take Roximstad or not.


If you have severe liver disease you should normally not take Roximstad. For example, if you have a scarred or fibrous liver (cirrhosis of the liver together with:

However, your doctor may decide that you must take Roximstad to deal with your infection. In this case, you will be given half of the usual dose per day. i.e. 150 mg roxithromycin.


Children

Children below 6 years of age should not use Roximstad tablets. Different forms of roxithromycin are available for young children. For example an oral suspension.


Duration of treatment

Your doctor will tell you for how long you should take Roximstad. For some infections treatment will last for at least 10 days.


You will usually be asked to take Roximstad for a further 3 or 4 days after your symptoms have improved.


It is important to always take the tablets for as long as your doctor tells you to.


If you take more Roximstadthan you should

If you have taken too many tablets contact your doctor or a pharmacist.


Remember to take the package and any remaining tablets with you.


Overdose with Roximstad may cause the following symptoms:


Your doctor will treat the symptoms of Roximstad overdose.


If you forget to take Roximstad

If you forget to take a dose of Roximstad, just take the next dose at the usual time. Do not take a double dose to make up for the missed one.


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 can cause side effects, although not everybody gets them.


Once-daily dosing (1 x 300 mg Roximstad tablets) gives more side effects than twice-daily dosing (2 x 150 mg Roximstad tablets).


Stop taking the medicine and contact your doctor immediately if you get:


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

Severe skin reactions such as

Erythema multiforme. This may cause spots, red welts or purple or blistered areas.


Rare (may affect up to 1 in 1,000 people):

Symptoms of angio-oedema (a life-threatening reaction), such as:

  • Swollen face, tongue or throat

  • Difficulty in swallowing

  • Hives and difficulty breathing


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

  • Inflammation of the bowel causing abdominal pain or diarrhoea (pseudomembranous colitis)

  • Severe skin reactions such as

  • Potentially fatal inflammation of the pancreas, characterised by abdominal pain, nausea, vomiting, diarrhoea, fever and shock (haemorrhagic pancreatitis)

  • Severe allergic (hypersensitivity) reactions (anaphylactic shock)

  • Severe reduction in number of white blood cells which makes infections more likely (agranulocytosis)



Roximstadcan also cause the following side effects:

Please consult your doctor in regular intervals as requested. This will help to detect possible side effects. Please inform your doctor during the routine examination, if you experience or experienced a possible side effect.


Common (may affect up to 1 in 10 people):


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


Rare (may affect up to 1 in 1,000 people):



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


Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly (see details below). By reporting side effects you can help provide more information on the safety of this medicine.

[To be completed nationally]


5. How to store Roximstad


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


Do not store Roximstad above 30 °C.


Do not use this medicine after the expiry date which is stated on the carton. The expiry date refers to the last day of that month.


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 Roximstadcontains

The active substance is roxithromycin.


One Roximstad 150 mg film-coated tablet contains 150 mg roxithromycin.

One Roximstad 300 mg film-coated tablet contains 300 mg roxithromycin.


The other ingredients in the tablet core are:


The other ingredients in the film coating are:


What Roximstad150 mg and 300 mg film-coated tablets look like and contents of the pack

Roximstad 150 mg film-coated tablets are white, with an off-white core, round and biconvex in shape and bevelled.


Roximstad 300 mg film-coated tablets are white, with an off-white core, oblong and capsule-shaped, with a break line on one side.


Roximstad film-coated tablets are packaged in PVC/aluminium blister packs containing:


150 mg tablets

5, 10, 12, 14, 16, 20, 28, 30, 50, 60, 90, 100, 250 and 500 tablets.


300 mg tablets

5, 6, 7, 10, 14, 16, 20, 28, 30, 50, 60, 90, 100, 250 and 500 tablets.


Not all pack sizes may be marketed.


Marketing Authorisation Holder and Manufacturer

[will be completed nationally]


This leaflet was last revised in 2014-02-10

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