FINGOLIMOD SUN 0.5 MG HARD CAPSULES - patient leaflet, side effects, dosage

Patient leaflet - FINGOLIMOD SUN 0.5 MG HARD CAPSULES

Fingolimod SUN 0.5 mg hard capsules

fingolimod

This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. See the end of section 4 for how to report side effects.

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

1. what fingolimod sun is and what it is used forwhat fingolimod sun isthe active substance of fingolimod sun is fingolimod.

What Fingolimod SUN is used for

Fingolimod SUN 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

– patients who have rapidly evolving severe MS.

Fingolimod SUN 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.

What is multiple sclerosis

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.

How Fingolimod SUN works

Fingolimod SUN 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. This medicine also reduces some of the immune reactions of your body.

2. what you need to know before you take

Fingolimod SUN

Do not take Fingolimod SUN

– 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 this medicine
– 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, tell your doctor without taking Fingolimod SUN.

Warnings and precautions

Talk to your doctor before taking Fingolimod SUN: – 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, tell your doctor before taking Fingolimod SUN.

Slow heart rate (bradycardia) and irregular heartbeat At the beginning of treatment or after taking the first dose of Fingolimod SUN 0.5 mg when you switch from other fingolimod-containing medicinal products in a lower strength (0.25 mg daily dose), fingolimod 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 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.

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 SUN or after taking the first dose of Fingolimod SUN 0.5 mg when you switch from other fingolimod-containing medicinal products in a lower strength (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 SUN 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 this medicine after a break in treatment, depending on both how long the break was and how long you had been taking this medicine 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 may not be appropriate for you.

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

If you are taking medicines that can cause your heart rate to decrease, fingolimod 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 this medicine. If such a switch is impossible, the cardiologist will advise how you should start treatment with this medicine, 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. If this is the case, your doctor will delay the start of treatment with this medicine until one month after the full course of vaccination is completed.

Infections

Fingolimod lowers the white blood cell count (particularly the lymphocyte count). White blood cells fight infection. While you are taking this medicine (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, or have a headache accompanied by stiff neck, sensitivity to light, nausea, and/or confusion (these may be caused by a fungal infection and may be symptoms of meningitis), 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 ifyou 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 this medicine.

Human papilloma virus (HPV) infection, including papilloma, dysplasia, warts and HPV-related cancer, has been reported in patients treated with fingolimod. 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 SUN, 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 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 may cause swelling in the macula, a condition that is known as macular oedema. The swelling usually happens in the first 4 months of 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 this medicine.

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. This medicine 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 or unexplained nausea and vomiting, tell your doctor straight away.

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

During the first twelve months of 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 this medicine.

High blood pressure

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

Lung problems

Fingolimod 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 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 this medicine. 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 SUN, 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 this medicine.

Posterior reversible encephalopathy syndrome (PRES) A condition called posterior reversible encephalopathy syndrome (PRES) has been rarely reported in MS patients treated with fingolimod. 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 this medicine, because it could be serious.

Cancer

Skin cancers have been reported in MS patients treated with fingolimod. 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 this medicine, 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. 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.

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 SUN. In case of severe relapse, your doctor will consider performing MRI to evaluate this condition and will decide whether you need to stop taking this medicine.

Switch from other treatments to Fingolimod SUN Your doctor may switch you directly from beta interferon, glatiramer acetate or dimethyl fumarate to Fingolimod SUN 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 SUN. 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 SUN is appropriate for you.

Women of childbearing potential

If used during pregnancy, fingolimod can harm the unborn baby. Before you start treatment with Fingolimod SUN 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 this medicine. It also explains what you should do to avoid becoming pregnant while you are taking this medicine. 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 SUN treatment

Do not stop taking this medicine 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 this medicine. This could be serious (see „If you stop taking Fingolimod SUN“ in section 3, and also section 4, „Possible side effects“).

Elderly

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

Children and adolescents

Fingolimod SUN 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 SUN, 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 SUN can be started.
– The first time you take Fingolimod SUN, or when you switch from a 0.25 mg daily dose from other fingolimod-containing medicinal products to a 0.5 mg daily dose of Fingolimod SUN, 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 SUN, let your doctor know.
– If you suffer from depression or anxiety or if you become depressed or anxious while you are taking Fingolimod SUN, let your doctor know. You may need to be monitored more closely.

Other medicines and Fingolimod SUN

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 SUN together with such medicines as this could intensify the effect on the immune system (see also ‚Do not take Fingolimod SUN‘).
– 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 SUN, 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 SUN together with such medicines could intensify the effect on heartbeat in the first days after starting this medicine
– medicines for irregular heartbeat, such as quinidine, disopyramide, amiodarone or sotalol. You must not use Fingolimod SUN if you are taking such a medicine because it could intensify the effect on irregular heartbeat (see also ‚Do not take Fingolimod SUN‘)
– 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).

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 for advice before taking this medicine.

Pregnancy

Do not use Fingolimod SUN 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 this medicine 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 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 SUN 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 SUN and 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 SUN.

If you do become pregnant while taking this medicine, tell your doctor straight away. Your doctor will decide to stop treatment (see „If you stop taking Fingolimod SUN“ 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 SUN. This medicine can pass into breast milk and there is a risk of serious side effects for the baby.

Driving and using machines

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

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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 this medicine. Your ability to drive and use machines may be impaired during and potentially after this time period.

Fingolimod SUN contains potasssium

This medicine contains contains 0.013 mmol

(or 0.515 mg) potassium per capsule/ maximum daily dose. To be taken into consideration by patients with reduced kidney function or patients on a controlled potassium diet.

Fingolimod SUN contains sodium

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

3. how to take fingolimod sun

Treatment with Fingolimod SUN will be overseen by a doctor who is experienced in the treatment of multiple sclerosis.

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

The recommended dose is

Adults:

The dose is one Fingolimod SUN 0.5 mg hard capsule per day.

Children and adolescents (10 years of age and above):

The dose depends on body weight:

– children and adolescents with body weight equal to or below 40 kg : one 0.25 mg capsule per day. Fingolimod SUN 0.5 mg hard capsules are not suitable for paediatric patients with body weight equal to or below 40 kg. Other fingolimod-containing medicines are available in a lower strength (as 0.25 mg capsules).

– children and adolescents with body weight above

40 kg : one Fingolimod SUN 0.5 mg hard capsule per day.

Children and adolescents who start on one 0.25 mg capsule per day from other fingolimod-containing medicines and later reach a stable body weight above 40 kg will be instructed by their doctor to switch to one fingolimod 0.5 mg hard capsule per day. In this case, it is recommended to repeat the first-dose observation period.

Do not exceed the recommended dose.

Fingolimod SUN is for oral use.

Take Fingolimod SUN once a day with a glass of water. Fingolimod SUN capsules should always be swallowed intact, without opening them. Fingolimod SUN can be taken with or without food.

Taking Fingolimod SUN at the same time each day will help you remember when to take your medicine.

If you have questions about how long to take Fingolimod SUN, talk to your doctor or your pharmacist.

If you take more Fingolimod SUN than you should If you have taken too much Fingolimod SUN, call your doctor straight away.

If you forget to take Fingolimod SUN

If you have been taking Fingolimod SUN 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 SUN 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.

If you stop taking Fingolimod SUN

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

Fingolimod SUN 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 SUN you may have to wait for 6–8 weeks before starting a new MS treatment.

If you have to restart Fingolimod SUN 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 treatment with this medicine 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 treatment with this medicine. Tell your doctor straight away if you think your MS is getting worse after you have stopped treatment with Fingolimod SUN. This could be serious.

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

4. possible side effects in the early stages of infection, followed by numbness, itching or red patches with severe pain

– slow heartbeat (bradycardia), irregular heart rhythm
– a type of skin cancer called basal cell carcinoma (BCC) which often appears as a pearly nodule, although it can also take other forms
– depression and anxiety are known to occur with increased frequency in the MS population and have also been reported in paediatric patients treated with fingolimod
– weight loss.

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

– pneumonia with symptoms such as fever, cough, difficulty breathing
– macular oedema (swelling in the central vision area of the retina at the back of the eye) with symptoms such as shadows or blind spot in the centre of the vision, blurred vision, problems seeing colours or details
– reduction in blood platelets which increases risk of bleeding or bruising
– malignant melanoma (a type of skin cancer which usually develops from an unusual mole). Possible signs of melanoma include moles which may change size, shape, elevation or colour over time, or new moles. The moles may itch, bleed or ulcerate.
– convulsion, fits (more frequent in children and adolescents than in adults).

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

– a condition called posterior reversible encephalopathy syndrome (PRES). Symptoms may include sudden onset of severe headache, confusion, seizures and/or vision disturbances
– lymphoma (a type of cancer that affects the lymph system)
– squamous cell carcinoma: a type of skin cancer which may present as a firm red nodule, a sore with crust, or a new sore on an existing scar.

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

– electrocardiogram anomaly (T-wave inversion)
– tumour related to infection with human herpes virus 8 (Kaposi's sarcoma).

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

– allergic reactions, including symptoms of rash or itchy hives, swelling of lips, tongue or face, which are more likely to occur on the day you start fingolimod treatment
– risk of a rare brain infection called progressive multifocal leukoencephalopathy (PML). The symptoms of PML may be similar to an MS relapse. Symptoms might also arise that you might not become aware of by yourself, such as changes in mood or behaviour, memory lapses, speech and communication difficulties, which your doctor may need to investigate further to rule out PML. Therefore, if you believe your MS is getting worse or if you or those close to you notice any new or unusual symptoms, it is very important that you speak to your doctor as soon as possible.
– cryptococcal infections (a type of fungal infection), including cryptococcal meningitis with symptoms such as headache accompanied by stiff neck, sensitivity to light, nausea, and/or confusion
– Merkel cell carcinoma (a type of skin cancer). Possible signs of Merkel cell carcinoma include flesh-coloured or bluish-red, painless nodule, often on the face, head or neck. Merkel cell carcinoma can also present as a firm painless nodule or mass. Long-term exposure to the sun and a weak immune system can affect the risk of developing Merkel cell carcinoma.
– After fingolimod treatment is stopped, symptoms of MS can return and may become worse than they were before or during treatment.
– autoimmune form of anaemia (decreased amount of red blood cells) where red blood cells are destroyed (autoimmune haemolytic anaemia).

If you experience any of these, tell your doctor straight away.

Other side effects

Very common (may affect more than 1 in 10 people):

– infection from flu virus with symptoms such as tiredness, chills, sore throat, aching in the joints or muscles, fever
– feeling of pressure or pain in the cheeks and forehead (sinusitis)
– headache
– diarrhoea
– back pain
– blood testing showing higher levels of liver enzymes
– cough.

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

– ringworm, a fungal infection of the skin (tinea versicolor)
– dizziness
– severe headache often accompanied by nausea, vomiting and sensitivity to light (migraine)
– low level of white blood cells (lymphocytes, leucocytes)
– weakness
– itchy, red, burning rash (eczema)
– itching
– blood fat (triglycerides) level increased
– hair loss
– breathlessness
– depression
– blurred vision (see also the section on macular oedema under “Some side effects could be or could become serious")
– hypertension (this medicine may cause a mild increase in blood pressure)
– muscle pain
– joint 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, website: 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 fingolimod sun

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 carton and blister foil after EXP. The expiry date refers to the last day of that month.

Do not store above 30°C.

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 Fingolimod SUN contains

– The active substance is fingolimod. Each hard capsule contains 0.5 mg fingolimod (as hydrochloride).
– The other ingredients are:
- Capsule fill : magnesium stearate (E470b), polacrilin potassium (see section 2) , crospovidone (E1202), silica, colloidal anhydrous (E551)
- Capsule shell :

Capsule cap :iron oxide yellow (E172), titanium dioxide (E171), gelatin (E441), sodium laurilsulfate

Capsule body: titanium dioxide (E171), gelatin, sodium laurilsulfate

Printing ink : shellac (E904), propylene glycol (E1520), potassium hydroxide (E525), iron oxide black (E172).

What Fingolimod SUN looks like and contents of the pack

Fingolimod SUN 0.5 mg hard gelatin capsules have a yellow opaque cap and white opaque body, axially imprinted with ‚064‘ with black ink on cap and body.

Fingolimod SUN is available in blister packs.

Pack sizes: outer carton containing 7, 28, 56 or 98 hard capsules.

Not all pack sizes may be marketed in your country.

Marketing Authorisation Holder

Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87

2132 JH Hoofddorp

The Netherlands

Manufacturers

Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87

2132 JH Hoofddorp

The Netherlands

Terapia S.A.

Str. Fabricii nr 124

Cluj-Napoca, Jude^ul Cluj

Romania

This medicinal product is authorised in the Member States of the EEA under the following names

Germany:

Spain:

France:

Italy:

The Netherlands:

Poland:

United Kingdom:

Fingolimod Basics

Fingolimod SUN

Fingolimod SUN Fingolimod SUN Fingolimod SUN

This leaflet was last revised in April 2020.

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Some side effects could be or could become serious.