• 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.

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

The active substance of Fingolimod Glenmark is fingolimod.

Fingolimod Glenmark is used in adults and in children and adolescents (10 years of age and above) with body weight above 40 kg to treat relapsing-remitting multiple sclerosis (MS), more specifically in:

• Patients who have failed to respond despite treatment with an MS treatment. or
• Patients who have rapidly evolving severe MS.

Fingolimod Glenmark does not cure MS, but it helps to reduce the number of relapses and to slow down the progression of physical disabilities due to MS.

MS is a long-term condition that affects the central nervous system (CNS), comprised of the brain and spinal cord. In MS inflammation destroys the protective sheath (called myelin) around the nerves in the CNS and stops the nerves from working properly. This is called demyelination.

Relapsing-remitting MS is characterised by repeated attacks (relapses) of nervous system symptoms that reflect inflammation within the CNS. Symptoms vary from patient to patient but typically involve walking difficulties, numbness, vision problems or disturbed balance. Symptoms of a relapse may disappear completely when the relapse is over, but some problems may remain.

Fingolimod Glenmark helps to protect against attacks on the CNS by the immune system by reducing the ability of some white blood cells (lymphocytes) to move freely within the body and by stopping them from reaching the brain and spinal cord. This limits nerve damage caused by MS. Fingolimod Glenmark also reduces some of the immune reactions of your body.

• if you have a lowered immune response (due to an immunodeficiency syndrome, a disease or to medicines that suppress the immune system).
• if you have a severe active infection or active chronic infection such as hepatitis or tuberculosis.
• if you have an active cancer.
• if you have severe liver problems.
• if, in the last 6 months, you have had heart attack, angina, stroke or warning of a stroke or certain types of heart failure.
• if you have certain types of irregular or abnormal heartbeat (arrhythmia), including patients in whom the electrocardiogram (ECG) shows prolonged QT interval before starting Fingolimod Glenmark.
• if you are taking or have recently taken medicine for irregular heartbeat such as quinidine, disopyramide, amiodarone or sotalol.
• if you are pregnant or a woman of childbearing potential not using effective contraception.
• if you are allergic to fingolimod or any of the other ingredients of this medicine (listed in section 6).

If this applies to you or you are unsure, talk to your doctor before taking Fingolimod Glenmark.

Talk to your doctor before taking Fingolimod Glenmark:

• if you have severe breathing problems during sleep (severe sleep apnoea).
• if you have been told you have an abnormal electrocardiogram.
• if you suffer from symptoms of slow heart rate (e.g. dizziness, nausea, or palpitations).
• if you are taking or have recently taken medicines that slow your heart rate (such as beta blockers, verapamil, diltiazem or ivabradine, digoxin, anticholinesteratic agents or pilocarpine).
• if you have a history of sudden loss of consciousness or fainting (syncope).
• if you plan to get vaccinated.
• if you have never had chickenpox.
• if you have or have had visual disturbances or other signs of swelling in the central vision area (macula) at the back of the eye (a condition known as macular oedema, see below), inflammation or infection of the eye (uveitis), or if you have diabetes (which can cause eye problems).
• if you have liver problems.
• if you have high blood pressure that cannot be controlled by medicines.
• if you have severe lung problems or smoker’s cough.

If any of these applies to you or you are unsure, talk to your doctor before taking Fingolimod Glenmark.

Slow heart rate (bradycardia) and irregular heartbeat

At the beginning of treatment or after taking the first dose of 0.5 mg when you switch from a 0.25 mg daily dose, Fingolimod Glenmark causes the heart rate to slow down. As a result, you may feel dizzy or tired, or be consciously aware of your heartbeat, or your blood pressure may drop. If these effects are pronounced, tell your doctor, because you may need treatment right away. Fingolimod Glenmark can also cause an irregular heartbeat, especially after the first dose. Irregular heartbeat usually returns to normal in less than one day. Slow heart rate usually returns to normal within one month. During this period, no clinically significant heart rate effects are usually expected.

Your doctor will ask you to stay at the surgery or clinic for at least 6 hours, with hourly pulse and blood pressure measurements, after taking the first dose of Fingolimod Glenmark or after taking the first dose of 0.5 mg when you switch from a 0.25 mg daily dose, so that appropriate measures can be taken in the event of side effects that occur at the start of treatment. You should have an electrocardiogram performed prior to the first dose of Fingolimod Glenmark and after the 6-hour monitoring period. Your doctor may monitor your electrocardiogram continuously during that time. If after the 6-hour period you have a very slow or decreasing heart rate, or if your electrocardiogram shows abnormalities, you may need to be monitored for a longer period (at least 2 more hours and possibly overnight) until these have resolved. The same may apply if you are resuming Fingolimod Glenmark after a break in treatment, depending on both how long the break was and how long you had been taking Fingolimod Glenmark before the break.

If you have, or if you are at risk for, an irregular or abnormal heartbeat, if your electrocardiogram is abnormal, or if you have heart disease or heart failure, Fingolimod Glenmark may not be appropriate for you.

If you have a history of sudden loss of consciousness or decreased heart rate, Fingolimod Glenmark may not be appropriate for you. You will be evaluated by a cardiologist (heart specialist) to advise how you should start treatment with Fingolimod Glenmark, including overnight monitoring.

If you are taking medicines that can cause your heart rate to decrease, Fingolimod Glenmark may not be appropriate for you. You will need to be evaluated by a cardiologist, who will check whether you can be switched to alternative medicine that does not decrease your heart rate in order to allow treatment with Fingolimod Glenmark. If such a switch is impossible, the cardiologist will advise how you should start treatment with Fingolimod Glenmark, including overnight monitoring.

If you have never had chickenpox

If you have never had chickenpox, your doctor will check your immunity against the virus that causes it (varicella zoster virus). If you are not protected against the virus, you may need a vaccination before you start treatment with Fingolimod Glenmark. If this is the case, your doctor will delay the start of treatment with Fingolimod Glenmark until one month after the full course of vaccination is completed.

Infections

Fingolimod Glenmark lowers the white blood cell count (particularly the lymphocyte count). White blood cells fight infection. While you are taking Fingolimod Glenmark (and for up to 2 months after you stop taking it), you may get infections more easily. Any infection that you already have may get worse. Infections could be serious and life-threatening. If you think you have an infection, have fever, feel like you have the flu, have shingles or have a headache accompanied by stiff neck, sensitivity to light, nausea, rash and/or confusion or seizures (fits) (these may be symptoms of meningitis and/or encephalitis caused by a fungal or herpes viral infection) contact your doctor straight away, because it could be serious and life-threatening.

If you believe your MS is getting worse (e.g. weakness or visual changes) or if you notice any new symptoms, talk to your doctor straight away, because these may be the symptoms of a rare brain disorder caused by infection and called progressive multifocal leukoencephalopathy (PML). PML is a serious condition that may lead to severe disability or death. Your doctor will consider performing an MRI scan to evaluate this condition and will decide whether you need to stop taking Fingolimod Glenmark.

Human papilloma virus (HPV) infection, including papilloma, dysplasia, warts and HPV-related cancer, has been reported in patients treated with Fingolimod Glenmark. Your doctor will consider whether you need to have a vaccination against HPV before starting treatment. If you are a woman, your doctor will also recommend HPV screening.

Macular oedema

Before you start Fingolimod Glenmark, if you have or have had visual disturbances or other signs of swelling in the central vision area (macula) at the back of the eye, inflammation or infection of the eye (uveitis) or diabetes, your doctor may want you to undergo an eye examination.

Your doctor may want you to undergo an eye examination 3 to 4 months after starting Fingolimod Glenmark treatment.

The macula is a small area of the retina at the back of the eye which enables you to see shapes, colours, and details clearly and sharply. Fingolimod Glenmark may cause swelling in the macula, a condition that is known as macular oedema. The swelling usually happens in the first 4 months of Fingolimod Glenmark treatment.

Your chance of developing macular oedema is higher if you have diabetes or have had an inflammation of the eye called uveitis. In these cases your doctor will want you to undergo regular eye examinations in order to detect macular oedema.

If you have had macular oedema, talk to your doctor before you resume treatment with Fingolimod Glenmark.

Macular oedema can cause some of the same vision symptoms as an MS attack (optic neuritis). Early on, there may not be any symptoms. Be sure to tell your doctor about any changes in your vision.

Your doctor may want you to undergo an eye examination, especially if:

• the centre of your vision gets blurry or has shadows;
• you develop a blind spot in the centre of your vision;
• you have problems seeing colours or fine detail.

Liver function tests

If you have severe liver problems, you should not take Fingolimod Glenmark. Fingolimod Glenmark may affect your liver function. You will probably not notice any symptoms but if you notice yellowing of your skin or the whites of your eyes, abnormally dark urine (brown coloured), pain on the right side of your stomach area (abdomen), tiredness, feeling less hungry than usual or unexplained nausea and vomiting, tell your doctor straight away.

If you get any of these symptoms after starting Fingolimod Glenmark, tell your doctor straight away.

Before, during and after the treatment your doctor will request blood tests to monitor your liver function. If your test results indicate a problem with your liver you may have to interrupt treatment with Fingolimod Glenmark.

High blood pressure

As Fingolimod Glenmark causes a slight elevation of blood pressure, your doctor may want to check your blood pressure regularly.

Lung problems

Fingolimod Glenmark has a slight effect on the lung function. Patients with severe lung problems or with smoker’s cough may have a higher chance of developing side effects.

Blood count

The desired effect of Fingolimod Glenmark treatment is to reduce the amount of white blood cells in your blood. This will usually go back to normal within 2 months of stopping treatment. If you need to have any blood tests, tell the doctor that you are taking Fingolimod Glenmark. Otherwise, it may not be possible for the doctor to understand the results of the test, and for certain types of blood test your doctor may need to take more blood than usual.

Before you start Fingolimod Glenmark, your doctor will confirm whether you have enough white blood cells in your blood and may want to repeat a check regularly. In case you do not have enough white blood cells, you may have to interrupt treatment with Fingolimod Glenmark.

Posterior reversible encephalopathy syndrome (PRES)

A condition called posterior reversible encephalopathy syndrome (PRES) has been rarely reported in MS patients treated with Fingolimod Glenmark. Symptoms may include sudden onset of severe headache, confusion, seizures and vision changes. Tell your doctor straight away if you experience any of these symptoms during your treatment with Fingolimod Glenmark, because it could be serious.

Cancer

Skin cancers have been reported in MS patients treated with Fingolimod Glenmark. Talk to your doctor straight away if you notice any skin nodules (e.g. shiny pearly nodules), patches or open sores that do not heal within weeks. Symptoms of skin cancer may include abnormal growth or changes of skin tissue (e.g. unusual moles) with a change in colour, shape or size over time. Before you start Fingolimod Glenmark, a skin examination is required to check whether you have any skin nodules. Your doctor will also carry out regular skin examinations during your treatment with Fingolimod Glenmark. If you develop problems with your skin, your doctor may refer you to a dermatologist, who after consultation may decide that it is important for you to be seen on a regular basis.

A type of cancer of the lymphatic system (lymphoma) has been reported in MS patients treated with Fingolimod Glenmark.

Exposure to the sun and protection against the sun

Fingolimod weakens your immune system. This increases your risk of developing cancers, in particular skin cancers. You should limit your exposure to the sun and UV rays by:

• wearing appropriate protective clothing.
• regularly applying sunscreen with a high degree of UV protection.

Unusual brain lesions associated with MS relapse

Rare cases of unusually large brain lesions associated with MS relapse have been reported in patients treated with Fingolimod Glenmark. In case of severe relapse, your doctor will consider performing MRI to evaluate this condition and will decide whether you need to stop taking Fingolimod Glenmark.

Switch from other treatments to Fingolimod Glenmark

Your doctor may switch you directly from beta interferon, glatiramer acetate or dimethyl fumarate to Fingolimod Glenmark if there are no signs of abnormalities caused by your previous treatment. Your doctor may have to do a blood test in order to exclude such abnormalities. After stopping natalizumab you may have to wait for 2-3 months before starting treatment with Fingolimod Glenmark. To switch from teriflunomide, your doctor may advise you to wait for a certain time or to go through an accelerated elimination procedure. If you have been treated with alemtuzumab, a thorough evaluation and discussion with your doctor is required to decide if Fingolimod Glenmark is appropriate for you.

Women of childbearing potential

If used during pregnancy, Fingolimod Glenmark can harm the unborn baby. Before you start treatment with Fingolimod Glenmark your doctor will explain the risk to you and ask you to do a pregnancy test in order to ensure that you are not pregnant. Your doctor will give you a card which explains why you should not become pregnant while taking Fingolimod Glenmark. It also explains what you should do to avoid becoming pregnant while you are taking Fingolimod Glenmark. You must use effective contraception during treatment and for 2 months after stopping treatment (see section “Pregnancy and breastfeeding”).

Worsening of MS after stopping Fingolimod Glenmark treatment

Do not stop taking Fingolimod Glenmark or change your dose without talking to your doctor first.

Tell your doctor straight away if you think your MS is getting worse after you have stopped treatment with Fingolimod Glenmark. This could be serious (see “If you stop taking Fingolimod Glenmark” in section 3, and also section 4, “Possible side effects”).

Experience with Fingolimod Glenmark in elderly patients (over 65 years) is limited. Talk to your doctor if you have any concerns.

Fingolimod Glenmark is not intended for use in children below 10 years old as it has not been studied in MS patients in this age group.

The warnings and precautions listed above also apply to children and adolescents. The following information is particularly important for children and adolescents and their caregivers:

• Before you start Fingolimod Glenmark, your doctor will check your vaccination status. If you have not had certain vaccinations, it may be necessary for you to be given them before Fingolimod Glenmark can be started.
• The first time you take Fingolimod Glenmark, or when you switch from a 0.25 mg daily dose to a 0.5 mg daily dose, your doctor will monitor your heart rate and heartbeat (see “Slow heart rate (bradycardia) and irregular heartbeat” above).
• If you experience convulsions or fits before or whilst taking Fingolimod Glenmark, let your doctor know.
• If you suffer from depression or anxiety or if you become depressed or anxious while you are taking Fingolimod Glenmark, let your doctor know. You may need to be monitored more closely.

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

• Medicines that suppress or modulate the immune system, including other medicines used to treat MS, such as beta interferon, glatiramer acetate, natalizumab, mitoxantrone, teriflunomide, dimethyl fumarate or alemtuzumab. You must not use Fingolimod Glenmark together with such medicines as this could intensify the effect on the immune system (see also ‘Do not take Fingolimod Glenmark’).
• Corticosteroids, due to a possible added effect on the immune system.
• Vaccines. If you need to receive a vaccine, seek your doctor’s advice first. During and for up to 2 months after treatment with Fingolimod Glenmark, you should not receive certain types of vaccine (live attenuated vaccines) as they could trigger the infection that they were supposed to prevent. Other vaccines may not work as well as usual if given during this period.
• Medicines that slow the heartbeat (for example beta blockers, such as atenolol). Use of Fingolimod Glenmark together with such medicines could intensify the effect on heartbeat in the first days after starting Fingolimod Glenmark.
• Medicines for irregular heartbeat, such as quinidine, disopyramide, amiodarone or sotalol.
  You must not use Fingolimod Glenmark if you are taking such a medicine because it could intensify the effect on irregular heartbeat (see also ‘Do not take Fingolimod Glenmark’).
• Other medicines:
  
  • protease inhibitors, anti-infectives such as ketoconazole, azole antifungals, clarithromycin or telithromycin.
  • carbamazepine, rifampicine, phenobarbital, phenytoin, efavirenz or St. John’s Wort (potential risk of reduced efficacy of Fingolimod Glenmark).

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine.

Pregnancy

Do not use Fingolimod Glenmark during pregnancy, if you are trying to become pregnant or if you are a woman who could become pregnant and you are not using effective contraception. If Fingolimod Glenmark is used during pregnancy, there is a risk of harm to the unborn baby. The rate of congenital malformations observed in babies exposed to Fingolimod Glenmark during pregnancy is about 2 times the rate observed in the general population (in whom the rate of congenital malformations is about 2-3%). The most frequently reported malformations included cardiac, renal and musculoskeletal malformations.

Therefore, if you are a woman of childbearing potential:

• before you start treatment with Fingolimod Glenmark your doctor will inform you about the risk to an unborn baby and ask you to do a pregnancy test in order to ensure that you are not pregnant. and,
• you must use effective contraception while taking Fingolimod Glenmark for two months after you stop taking it to avoid becoming pregnant. Talk to your doctor about reliable methods of contraception.

Your doctor will give you a card which explains why you should not become pregnant while taking Fingolimod Glenmark .

If you do become pregnant while taking Fingolimod Glenmark, tell your doctor straight away.

Your doctor will decide to stop treatment (see “If you stop taking Fingolimod Glenmark” in section 3, and also section 4, “Possible side effects”). Specialised pre-natal monitoring will be performed.

Breast-feeding

You should not breast-feed while you are taking Fingolimod Glenmark. Fingolimod Glenmark can pass into breast milk and there is a risk of serious side effects for the baby.

Your doctor will tell you whether your illness allows you to drive vehicles, including a bicycle, and use machines safely. Fingolimod Glenmark is not expected to have an influence on your ability to drive and use machines.

However, at initiation of treatment you will have to stay at the doctor’s surgery or clinic for 6 hours after taking the first dose of Fingolimod Glenmark. Your ability to drive and use machines may be impaired during and potentially after this time period.

If you have taken too much Fingolimod Glenmark, call your doctor straight away.

If you have been taking Fingolimod Glenmark for less than 1 month and you forget to take 1 dose for a whole day, call your doctor before you take the next dose. Your doctor may decide to keep you under observation at the time you take the next dose.

If you have been taking Fingolimod Glenmark for at least 1 month and have forgotten to take your treatment for more than 2 weeks, call your doctor before you take the next dose. Your doctor may decide to keep you under observation at the time you take the next dose. However, if you have forgotten to take your treatment for up to 2 weeks, you can take the next dose as planned.

Never take a double dose to make up for a forgotten dose.

Do not stop taking Fingolimod Glenmark or change your dose without talking to your doctor first.

Fingolimod Glenmark will stay in your body for up to 2 months after you stop taking it. Your white blood cell count (lymphocyte count) may also remain low during this time and the side effects described in this leaflet may still occur. After stopping Fingolimod Glenmark you may have to wait for 6-8 weeks before starting a new MS treatment.

If you have to restart Fingolimod Glenmark more than 2 weeks after you stop taking it, the effect on heart rate normally seen when treatment is first started may re-occur and you will need to be monitored at the doctor’s surgery or clinic for re-initiation of treatment. Do not restart Fingolimod Glenmark after stopping it for more than two weeks without seeking advice from your doctor.

Your doctor will decide whether and how you need to be monitored after stopping Fingolimod Glenmark. Tell your doctor straight away if you think your MS is getting worse after you have stopped treatment with Fingolimod Glenmark. This could be serious.

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: 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.

• Each hard capsule contains 0.5 mg of the active substance fingolimod (as hydrochloride).
• The other ingredients are:
  Capsule fill: calcium phosphate, stearic acid.
  Capsule shell: gelatin, titanium dioxide (E171), iron oxide yellow (E172).
  Printing ink: shellac (E904), iron oxide black (E172).

Fingolimod Glenmark 0.5 mg hard capsules are presented as white to off-white powder in a yellow opaque cap and white opaque body hard gelatin capsule with length 15.9 ± 0.3 mm, imprinted with “0.5 mg” on the cap with black ink.

Fingolimod Glenmark 0.5 mg capsules are packaged in a cardboard box containing the appropriate number of PVC/PE/PVDC aluminium foil blisters or PVC/PE/PVDC/aluminium foil perforated unit dose blisters with an appropriate number of capsules and an instruction leaflet.

Pack sizes:

Cartons containing 7, 7x1, 28, 28x1, 98 or 98x1 hard capsules or multipacks containing 84 capsules (3 packs of 28 capsules).

Not all pack sizes may be marketed.

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