Sirturo 100 mg tablets

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

if you are allergic to bedaquiline or any of the other ingredients of this medicine (listed in section 6). Do not take SIRTURO if this applies to you. If you are not sure, talk to your doctor or pharmacist before taking SIRTURO.

Talk to your doctor, pharmacist or nurse before taking SIRTURO, if:

• you have had an abnormal heart reading on an electrocardiogram (ECG) or heart failure;
• you have a personal or family history of a heart problem called “congenital long QT syndrome”;
• you are taking any other medications, as some may increase the risk of side effects;
• you have a decreased thyroid gland function. This can be seen in a blood test;
• you have liver disease or you drink alcohol on a regular basis;
• you have a low level of potassium in the blood. This can be seen in a blood test;
• you have human immunodeficiency virus (HIV) infection.

If any of the above applies to you (or you are not sure), talk to your doctor, pharmacist or nurse before taking SIRTURO.

In adolescents weighing 30 to 40 kg, the levels of SIRTURO in the blood were predicted to be higher than in adults. This might be associated with an increased risk of abnormal heart reading on an ECG (called QT prolongation) or increased liver enzymes (shown in blood test). Talk to your doctor, pharmacist or nurse before taking SIRTURO.

Do not give this medicine to children under 5 years of age or weighing less than 15 kg because it has not been studied in these patients.

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

The following are examples of medicines patients with pulmonary tuberculosis due to M. tuberculosis resistant to at least rifampicin and isoniazid may take and that may potentially interact with SIRTURO:

Medicine (name of the active substance) Purpose of the medicine

rifampicin, rifapentine, rifabutin to treat some infections like tuberculosis (antimycobacterial)

efavirenz, etravirine to treat HIV infection (antiretroviral non-nucleoside reverse transcriptase inhibitors)

carbamazepine, phenytoin to treat epileptic fits (anticonvulsants)

St. John’s wort (Hypericum perforatum) an herbal product to relieve anxiety

You should not drink alcohol while taking SIRTURO.

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.

You may feel dizzy after taking SIRTURO. If this happens, do not drive or operate machinery.

SIRTURO contains “lactose” (a type of sugar). If you cannot tolerate or digest some sugars, talk to your doctor before taking this medicine.

How much to take

You take SIRTURO for a 24-week course.

First 2 weeks:

• Take 160 mg once a day.

From Week 3 to Week 24:

• Take 80 mg once a day for 3 days of each week only.
• There must be at least 48 hours in between each time you take SIRTURO. For example, you may take SIRTURO on Monday, Wednesday and Friday every Week from week 3 onwards.

How much to take

You take SIRTURO for a 24-week course.

First 2 weeks:

• Take 200 mg once a day.

From Week 3 to Week 24:

• Take 100 mg once a day for 3 days of each week only.
• There must be at least 48 hours in between each time you take SIRTURO. For example, you may take SIRTURO on Monday, Wednesday and Friday every week from Week 3 onwards.

How much to take

You take SIRTURO for a 24-week course.

First 2 weeks:

• Take 400 mg once a day.

From Week 3 to Week 24:

• Take 200 mg once a day for 3 days of each week only.
• There must be at least 48 hours in between each time you take SIRTURO. For example, you may take SIRTURO on Monday, Wednesday and Friday every week from Week 3 onwards.

You may need to keep taking your other medicines for tuberculosis for longer than 6 months. Check with your doctor or pharmacist.

• Always take SIRTURO with food. The food is important to get the right levels of medicine in your body.
• Swallow the tablets whole with water.

If you take more SIRTURO than you should, talk to a doctor straight away. Take the medicine pack with you.

During the first 2 weeks

• Skip the missed dose and take the next dose as usual.
• Do not take a double dose to make up for a forgotten dose.

From Week 3 onwards

• Take the missed dose as soon as possible.
• Resume the three times a week schedule.
• Make sure there is at least 24 hours between taking the missed dose and the next scheduled dose.
• Do not take more than the prescribed weekly dose in a 7-day period.

If you have missed a dose and you are not sure what to do, talk to your doctor or pharmacist.

Do not stop taking SIRTURO without first talking to your doctor.

Skipping doses or not completing the full course of therapy may:

• make your treatment ineffective and your tuberculosis could get worse, and;
• increase the chance that the bacteria will become resistant to the medicine. This means your disease may not be treatable by SIRTURO or other medicines in the future.

If you get any side effects, talk to your doctor or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via 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.

• The active substance is bedaquiline. Each tablet contains bedaquiline fumarate equivalent to 100 mg of bedaquiline.
• The other ingredients are: colloidal anhydrous silica, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, maize starch, microcrystalline cellulose, polysorbate 20.

Uncoated, white to almost white round biconvex tablet, 11 mm in diameter, with debossing of "T" over "207" on one side and "100" on the other side.

A plastic bottle containing 188 tablets.

A carton containing 4 push-through blister strips (containing 6 tablets per strip). Not all pack sizes may be marketed.