Ospolot 20 mg/ml Oral suspension

• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor, pharmacist or nurse.
• 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, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

1. What Ospolot is and what it is used for
2. What you need to know before taking Ospolot
3. How to take Ospolot
4. Possible side effects
5. How to store Ospolot
6. Contents of the pack and other information

• is allergic to sulthiame or similar medicines (sulphonamides), to sodium methyl parahydroxybenzoate (E219), sodium propyl parahydroxybenzoate (E217) or any of the other ingredients in this medicine (listed in section 6)
• has an overactive thyroid
• has high blood pressure
• has a metabolic condition called acute porphyria.

Talk to your doctor before giving Ospolot,

• if the child has impaired kidney function,
• if the child is suffering from any psychiatric disorder.

Seek urgent medical advice if the child develops a fever, sore throat, rash with lymph node swelling and/or flu-like symptoms during treatment with Ospolot. These could be signs of an allergic, or other, reaction to the medicine which can become serious, in which case your doctor may decide to stop Ospolot.

Before treatment with Ospolot starts, blood tests will be carried out to check liver and kidney function. These will be repeated weekly for the first month of treatment then monthly up to six months after which they only need to be repeated two to four times a year.

A small number of patients being treated with anti-epileptics such as Ospolot have had thoughts of harming or killing themselves. If at any time such thoughts arise, immediately contact your doctor for advice.

Tell your doctor or pharmacist if the child is taking, has recently taken or might take any other medicines. Ospolot and the following medicines or groups of medicine may interact with each other during combined treatment.

• Phenytoin: Blood levels of phenytoin may be affected by Ospolot, especially if kidney function is reduced, so close monitoring will be carried out.
• Lamotrigine: Ospolot may increase lamotrigine blood levels. This will be carefully checked if this combination treatment is started.
• Primidone: This may worsen side-effects with Ospolot , particularly unsteadiness, dizziness and drowsiness.
• Carbamazepine: This may reduce levels of Ospolot in the blood.
• Topiramate: Side effects with Ospolot may be increased.
• Acetazolamide: Side effects with Ospolot may be increased.

Alcohol should be avoided during treatment with Ospolot as it can cause unpleasant symptoms which may include flushing, a throbbing headache, nausea and vomiting, palpitations and blurred vision. The symptoms can sometimes be more serious and include difficulty breathing, disturbances in heart rhythm and a fall in blood pressure with possible collapse and loss of consciousness. Seizures may also occur.

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.

Pregnancy

There is an increased risk that this medicine may harm your unborn baby. You should therefore not use this medicine during pregnancy unless it has been specifically prescribed by your doctor. If you are of childbearing age and are taking Ospolot, you must use an effective method of contraception. Do not interrupt your treatment with Ospolot before consulting with your doctor first. Any sudden discontinuation of treatment or unsupervised reduction of the dose may result in a return of epileptic seizures that may harm you and/or your unborn child.

Breast-feeding

It is not known whether the active substance contained in Ospolot passes into breast milk. For this reason, you should not take Ospolot while breast-feeding.

Even when used as directed, this medicine may affect your responsiveness to such an extent as to impair, for example, your ability to drive or use machines. In particular, this applies in combination with alcohol.

Sodium methyl parahydroxybenzoate (E219) and sodium propyl parahydroxybenzoate (E217) may cause allergic reactions (possibly delayed).

Sulphur dioxide (E 220) may rarely cause severe hypersensitivity reactions and bronchospasm.

This medicine contains 0.0026 mg fructose in each ml.

Glucose and sucrose: if you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine. Glucose, fructose and sucrose may be harmful to the teeth.

This medicine contains less than 1 mmol sodium (23 mg) per ml, that is to say it is essentially ‘sodium-free’.

There are three parts to the medicine kit:

1. A plastic adapter
2. A 10 ml oral dosing syringe which fits into the plastic adapter.

3. A bottle containing the oral suspension, with a child resistant cap. Always replace the cap after use.

1. Shake the bottle vigorously for 30 seconds in a bottom up position. If a sediment is detected at the bottom of the bottle, shake the bottle for another 30 seconds.
2. Open the child-resistant closure by firmly pressing it down and twisting it anti-clockwise (see top of cap).

Note: Keep the cap nearby to close the bottle after each use.

3. Hold the bottle upright on a table. Firmly push the plastic adapter with the oral syringe into the bottle opening, as far as you can.

Note: You may not be able to push the adapter down fully but it will be forced into the bottle when you screw the cap back on.

After the first use the adapter remains in the bottle.

4. Hold the oral syringe firmly and turn the bottle upside down carefully. Slowly pull out the plunger, so that the oral syringe fills up with the suspension. Then completely push the plunger back, in order to remove any large air bubbles that might be inside the oral syringe.

5. Drawing the prescribed dose: Slowly pull out the syringe plunger, until the top of the wider part of the plunger is exactly on a level with the marker on the oral syringe barrel that indicates the prescribed dose.

Ask your pharmacist if you are unsure.

6. Carefully turn the bottle and oral syringe the right way up. Remove the oral syringe by gently twisting it out of the adapter. The adapter must always stay in the bottle.

7. Administer the dose directly into the mouth of the patient, who should be sitting in an upright position. Press the plunger slowly in order to allow for easy swallowing. The patient should drink a glass of water, juice or milk directly after intake.

Also, the dose can be mixed preferably with a small amount of water, or alternatively with orange juice, milk, yoghurt or wheat porridge just prior to administration. Do not take carbonated beverages or hot food with the suspension to avoid eructation or slowed swallowing. Stir and take the entire mixture right away.

8. Replace the child resistant cap after use, leaving the adapter in place.
9. Cleaning: After each use, rinse the syringe thoroughly with running water and wipe the outside with a dry, clean tissue.

Ospolot may be taken with or without food. Ideally the same routine should be followed each day.

Ospolot may also be given via a feeding tube which should be rinsed with at least 15 ml of water immediately after giving the medicine. If given this way, the dose should be prepared as for oral use immediately before administration.

How long should Ospolot be taken?

Anti-epileptic treatment is essentially long-term therapy. In each individual case, a paediatric neurologist experienced in the treatment of epilepsy should decide how to adjust the treatment, how long it should last and when it should be discontinued. Ospolot should not be stopped suddenly.

Side-effects may be increased (see “Possible side effects”, below). Seek urgent medical advice and show this medicine and leaflet if possible.

Do not take a double dose to make up for a forgotten dose. Take the dose at your next scheduled time, as prescribed by your doctor. Your treating physician should be informed.

If you wish to interrupt or stop treatment with Ospolot, discuss it with your doctor first. Do not stop treatment with this medicine by yourself without medical advice, as it might cause the epileptic fits to return.

The length of treatment and the dose will vary depending on the individual patient and will be decided by your doctor.

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: Website: 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.

The active substance is sulthiame.

The other ingredients are: sodium methyl parahydroxybenzoate (E219), sodium propyl parahydroxybenzoate (E217), sucralose, docusate sodium, xanthan gum, sodium dihydrogen phosphate dihydrate, dipotassium phosphate, strawberry flavour, sweetness modulator flavour (containing fructose, glucose, sucrose and sulphur dioxide (E220)), masking flavour, phosphoric acid 85%, purified water

Ospolot is a white liquid with strawberry flavour.

The glass bottle with child-resistant closure contains 200 ml or 250 ml of Ospolot. It is packed in a cardboard box containing an oral syringe of 10 ml graduated every 0.25 ml and an adapter.

Not all pack sizes may be marketed.