Neupro 1 mg/24 h parche transdermico

Prospecto: information for the user

Neupro 1 mg/24 h transdermal patch

Neupro 3 mg/24 h transdermal patch

Rotigotine

Read this prospectus carefully before starting to use the medication, as it contains important information for you.

• Keep this prospectus, as you may need to read it again.
• If you have any doubts, consult your doctor, pharmacist, or nurse.
• This medication has been prescribed only to you, and you should not give it to others, even if they have the same symptoms as you, as it may harm them.
• If you experience any adverse effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this prospectus. See section 4.

Contents of the prospectus:

1. What Neupro is and for what it is used
2. What you need to know before starting to use Neupro
3. How to use Neupro
4. Possible adverse effects
5. Storage of Neupro
6. Contents of the package and additional information

What is Neupro

Neupro contains the active ingredient rotigotine.

It belongs to a group of medicines known as “dopamine agonists”. Dopamine is an important messenger in the brain for movement.

What is Neupro used for

Neupro is used in adults to treat the symptoms of:

• Restless Legs Syndrome(RLS) – this syndrome can be associated with discomfort in thelegs or arms, need to move, sleep disturbances and a feeling of fatigue or sleepiness during the day. Treatment with Neupro reduces or decreases the duration of these symptoms.

Do not use Neupro if:

• You areallergicto rotigotine or any of the othercomponentsof this medication (listed in section 6)
• You are going to have amagnetic resonance imaging (MRI)scan (diagnostic images of the inside of the body, created using magnetic energy instead of X-ray energy)
• You need acardioversion(specific treatment for heart rhythm disorders)

Remove the Neupro patch just before having an MRI or cardioversion to avoid skin burns, as the patch contains aluminum. You can put a new patch on when these tests are finished.

Do not use Neupro if you experience any of the above. If you are unsure, talk to your doctor, pharmacist, or nurse first.

Warnings and precautions

Consult your doctor, pharmacist, or nurse before starting to use Neupro, as:

• You must control yourblood pressureperiodically while using Neupro, especially at the beginning of treatment. Neupro may affect your blood pressure.
• You should have youreyes checkedperiodically while using Neupro. If you notice any vision problems between check-ups, inform your doctor immediately.
• If you havesevere liver problems, your doctor may need to adjust the dose. If your liver problems worsen during Neupro treatment, inform your doctor as soon as possible.
• You may experienceskin reactionscaused by the patch – see ‘Skin problems caused by the patch’ in section 4.
• You may feelextremely drowsy or fall asleep suddenly– see ‘Driving and using machines’ in section 2.
• The symptoms ofRestless Legs Syndromemay start before treatment with Neupro, be more intense, or involve other parts of the body. If you experience these symptoms before or after starting Neupro treatment, contact your doctor, as you may need your treatment adjusted.

Medications used to treat Restless Legs Syndrome should be reduced or stopped gradually. Inform your doctor if you experience symptoms such as depression, anxiety, fatigue, sweating, or pain after stopping or reducing your Neupro treatment.

You may lose consciousness

Neupro may cause loss of consciousness. This can occur especially when starting Neupro treatment or when increasing the dose. Inform your doctor if you lose consciousness or feel dizzy.

Changes in behavior and abnormal thoughts

Neupro may produce adverse effects that change your behavior (how you act). If your family or caregiver, or your doctor, are concerned about changes in your behavior, it may be helpful to tell a family member or caregiver that you are using this medication and have them read the leaflet. Inform your doctor if you, your family, or caregiver notice that you are using the medication excessively or feel an urgent need to consume large doses of Neupro or other medications used to treat Restless Legs Syndrome.

For more information, see ‘Changes in behavior and abnormal thoughts’ in section 4.

Children and adolescents

This medicationshould not be administeredtochildrenunder 18 years of age, as its safety and efficacy in this age group are unknown.

Using Neupro with other medications

Inform your doctor or pharmacist if you areusing,have used recently, or may need to use any other medication. This includes over-the-counter medications and herbal remedies.

Do not take the following medications while using Neupro, as they may reduce its effect:

• ‘antipsychotic’ medications – used to treat certain mental illnesses
• metoclopramide – used to treat nausea and vomiting

Consult your doctor before using Neupro if you are taking:

• sedatives such as benzodiazepines or medications used to treat mental disorders or depression
• medications that lower blood pressure. Neupro may lower blood pressure when standing up – this effect may worsen when taking medications to lower blood pressure.

Your doctor will inform you if it is safe to take these medications while using Neupro.

Using Neupro with food, drinks, and alcohol

Since rotigotine enters the bloodstream through the skin, taking food or drinks does not affect how this medication is absorbed. Consult your doctor if you can drink alcohol while using Neupro.

Pregnancy and breastfeeding

Do not use Neupro if you are pregnant. This is because the effects of rotigotine on pregnancy and the fetus are unknown.

Do not breastfeed during Neupro treatment. This is because rotigotine may pass into breast milk and affect your baby. It is also likely to reduce milk production.

If you are pregnant, breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.

Driving and using machines

Neupro may make you feel extremely drowsy and you may fall asleep suddenly. If this happens, do not drive.

In rare cases, some people have fallen asleep while driving, resulting in accidents.

Do not use tools or machines if you feel extremely drowsy – or perform any activity that may put you or others at risk of serious injury.

Neupro contains sodium metabisulfite (E223)

Neupro contains sodium metabisulfite (E223), a substance that rarely may cause severe allergic reactions and bronchospasm (difficulty breathing due to narrowing of the airways).

Follow exactly the administration instructions of this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist.

What dose of patch to use

Neupro is available in patches of different doses that release the medication over 24 hours. The doses are 1 mg/24 h, 2 mg/24 h, and 3 mg/24 h for the treatment of Restless Legs Syndrome.

• Your starting dose of treatment will be a patch of 1 mg/24 h per day.
• From the second week, the daily dose will be increased by 1 mg weekly until the appropriate maintenance dose for you is reached. This is when you and your doctor confirm that your symptoms are adequately controlled and that the medication's side effects are acceptable.
• Follow the instructions indicated by your doctor carefully.
• The maximum dose is 3 mg per day.

If you have to stop taking this medication, see “If you interrupt treatment with Neupro”in section 3.

How to use Neupro patches

Neupro is a patch that is applied to the skin.

• Check that the used patch has been removed before putting on a new one.
• Put the new patch on a different area of the skin each day.
• Leave the patch on the skin for 24 hours, then remove it and put on a new one.
• Change the patchapproximately at the same time every day.
• Do not cut Neupro patches into pieces.

Where to place the patch

If you continue to have skin problems caused by the patch, see “Skin problems caused by the patch” in section 4 for more information.

To prevent the patch from peeling off or coming loose

• Do notput the patch in an area where it may be subjected tofriction from tight clothing.
• Do notusecreams, oils, lotions, powdersor any otherskin productwhere you will be putting the patch. Nor on top of or near another patch that you are already using.
• If you need to put a patch on an area of the skin where you have hair, at least3 days beforeputting it on that site, you shouldshave(depilate) the skin area.
• If the edges of the patch come loose, you can stick the patch with adhesive tape.

If the patch falls off, you should put a new one on for the rest of the day and the next day, put a new patch on at the usual time.

• You mustavoidthe area of thepatch from getting too hot- for example, too much sunlight, saunas, hot baths, hot compresses, or hot water bottles. This is because the medication could be released too quickly. If you think it has gotten too hot, contact your doctor or pharmacist.
• Always check that the patch has not fallen off after activities such asbathing, showering, or exercising.
• If the patch hasirritated your skin, you mustkeep the irritated areaprotected from direct sunlight. This is because exposure to the sun could cause changes in the skin color.

How to use the patch

• Each patch is individually packaged in a sachet.
• Before opening the sachet, you must decide where you will put the new patch and check thatthe used patch has been removed.
• When you have opened the sachet and removed the disposable cover from the patch, you must put the patch on the skin immediately.

How to remove the used patch

• Remove the used patch slowly and carefully.
• Wash the area gently with warm water and a mild soap. This way you will remove the remaining adhesive from the skin. You can also use a little baby oil to remove the remaining adhesive.
• Do not use alcohol or other solvents - such as nail polish remover. This could irritate your skin.

If you use more Neupro than you should

Using higher doses of Neupro than your doctor has indicated can cause side effects such as nausea or vomiting, decreased blood pressure, seeing or hearing things that are not real (hallucinations), confusion, extreme drowsiness, involuntary movements, and seizures.

Report this to your doctor or go to the hospital as soon as possible. They will tell you what to do.

If you forgot to change the patch at your usual time

• If you forgot to change the patch at your usual time, change it as soon as you remember. Remove the used patch and put on a new one.
• If you forgot to put on a new patch after removing the used patch, as soon as you remember, put on a new one.

In both cases, the next day put on a new one at the usual time. Do not use a double dose to make up for the missed doses.

If you interrupt treatment withNeupro

Do not stop using Neupro without first consulting your doctor. Sudden interruption could cause a condition called ‘neuroleptic malignant syndrome’ that can put your life at risk. The signs include: loss of muscle movement (akinesia), muscle rigidity, fever, unstable blood pressure, increased heart rate (tachycardia), confusion, decreased consciousness (e.g. coma).

If your doctor tells you to stop treatment with Neupro, thedaily doseof Neupro should begradually reduced:

• 1 mg every two days – if you use Neupro for Restless Legs Syndrome

If you have any other questions about the use of this medication, ask your doctor, pharmacist, or nurse.

Like all medicines, this medicine can cause side effects, although not everyone will experience them. Inform your doctor, pharmacist, or nurse if you notice any side effects.

Most likely side effects at the start of treatment

You may experiencenauseaandvomitingat the start of treatment. These side effects are usually mild or moderate and do not last long. You shouldconsult your doctorif the side effects last a long time or if they concern you.

Skin problems caused by the patch

• You may experience redness and itching in the area of the skin where the patch has been applied – these reactions are usually mild or moderate.
• These reactions usually disappear a few hours after removing the patch.
• Consult your doctorif you have a skin reaction that lasts more than a few days, is severe, or spreads beyond the area covered by the patch.
• Avoid exposure to the sun and sunlamps in areas of skin that show any type ofreaction caused by the patch.
• To help prevent skin reactions, the patch should be applied to a different site each day, and only use the same area again after 14 days.

You may experience loss of consciousness

Neupro can cause loss of consciousness. This can happen especially when you start treatment with Neupro or when your dose is increased. Inform your doctor if you lose consciousness or feel dizzy.

Changes in behavior and abnormal thoughts

Inform your doctor if you notice any change in behavior, thought, or both, as indicated below.

Your doctor will tell you how to manage or reduce the symptoms.

If your family or caregiver, or your doctor, are concerned about changes in your behavior, it may be helpful to tell a family member or caregiver that you are using this medicine and have them read this leaflet. Neupro can cause anxiety or an urgent need to behave in an unusual way and not be able to control the impulse, attack, or temptation to perform certain actions that may harm you or others.

These actions may include:

• Strong addiction to gambling – even seriously affecting you or your family
• Altered or increased sexual interest and behavior that causes great concern for you and others – for example, increased sexual desire
• Uncontrolled purchases or excessive spending
• Episodes of binge eating (eating large amounts of food in a short period of time) or compulsive eating (eating more food than normal or more than needed to satisfy your appetite).

Neupro can cause other abnormal behaviors and thoughts, which may include:

• Abnormal thoughts about reality
• Delusions and hallucinations (seeing or hearing things that are not real)
• Confusion
• Disorientation
• Aggressive behavior
• Restlessness
• Delirium.

Inform your doctor if you notice any change in your behavior, thought, or both, as indicated above.

Your doctor will tell you how to manage or reduce the symptoms.

Allergic reactions

Inform your doctor if you notice signs of an allergic reaction – which may include swelling of the face, tongue, or lips.

Side effects if using Neupro for Restless Legs Syndrome

Inform your doctor or pharmacist if you experience any of the following side effects:

Very common: may affect more than 1 in 10 patients

• Headache
• Nausea
• Feeling of weakness (fatigue)
• Irritations of the skin in the area of application of the patch, such as redness and itching

Frequent: may affect up to 1 in 10 patients

• Itching
• Feeling of irritability
• Allergic reaction
• Increased sexual desire
• Increased blood pressure
• Vomiting, heartburn
• Swelling in the legs and feet
• Drowsiness, falling asleep suddenly without warning, difficulty sleeping, unusual dreams, sleep problems
• Inability to control the impulse to perform a harmful action, including addiction to gambling, repetitive actions without sense, compulsive purchases or excessive spending
• Episodes of binge eating (eating large amounts of food in a short period of time), compulsive eating (eating more food than normal or more than needed to satisfy your appetite)

Uncommon: may affect up to 1 in 100 patients

• Feeling agitated
• Sensation of dizziness when standing up due to a drop in blood pressure

Rare: may affectup to 1 in 1,000 patients

• Aggressive behavior
• Disorientation

Unknown:not known how often they occur

• Anxiety about taking high doses of medicine like Neupro – more than needed for the treatment of the disease. This is known as ‘dopaminergic dysregulation syndrome’ and may lead to excessive use of Neupro.
• Seeing or hearing things that are not real (hallucinations)
• Nightmares
• Paranoia
• Confusion
• Psychotic disorders
• Delusions
• Delirium
• Dizziness
• Loss of consciousness, involuntary movements (dyskinesia)
• Involuntary muscle spasms (convulsions)
• Blurred vision
• Visual disturbances such as seeing colors or lights
• Dizziness (sensation of spinning)
• Increased heart rate (palpitations)
• Abnormal heart rhythm
• Drop in blood pressure
• Hypotension
• Constipation, dry mouth
• Abdominal discomfort and pain
• Diarrhea
• Redness, increased sweating
• Generalized itching, skin irritation
• Generalized rash
• Inability to achieve or maintain an erection
• Weight loss, weight gain
• Abnormal liver test results or elevated levels
• Increased heart rate
• Increased levels of creatine phosphokinase (CPK) (CPK is an enzyme mainly found in skeletal muscles)
• Falls
• Rhabdomyolysis (a rare and serious muscle disorder that causes muscle pain, sensitivity, and weakness and may lead to kidney problems)

Inform your doctor or pharmacist if you experience any of these side effects.

Reporting side effects

If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through thenational reporting system included in theAppendix V. By reporting side effects, you can contribute to providing more information about the safety of this medicine.

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

Do not use this medication after the expiration date that appears on the label and on the carton box.

Do not store above 86°F (30°C).

What to do with used and unused patches

• Used patches still contain the active ingredient, ‘rotigotine’, which can be hazardous to others. Fold the used patch with the adhesive side inwards. Place the patch in the original pouch and then dispose of it in a safe place, out of children's reach.

• Do not dispose of medications through drains or in the trash. Ask your pharmacist how to properly dispose of the packaging and unused medications. This will help protect the environment.

Composition ofNeupro

The active ingredient is rotigotine.

• 1 mg/24 h:

A patch releases 1 mg of rotigotine every 24 hours. Each patch of 5 cm2 contains 2.25 mg of rotigotine.

• 3 mg/24 h:

A patch releases 3 mg of rotigotine every 24 hours. Each patch of 15 cm2 contains 6.75 mg of rotigotine.

The other components are:

• Poly (dimethylsiloxane, trimethylsilyl silicate) copolymer, povidone K90, sodium metabisulfite (E223), ascorbyl palmitate (E304) and DL-α-tocopherol (E307).
• Protective coating:Polyester film, siliconized, aluminumized, colored with a layer of pigment (titanium dioxide (E171), yellow pigment 13, red pigment 166, yellow pigment 12) and printed (red pigment 146, yellow pigment 180, black pigment 7).
• Disposable coating:Transparent polyester film coated with fluoropolymer.

Appearance of the product and contents of the package

Neupro is a transdermal patch. It is thin and has three layers. It has a square shape with rounded corners. The outer part is brown and has the imprint Neupro 1 mg/24 h or 3 mg/24 h.

Neupro is available in the following formats:

Carton packs containing 7, 14, 28, 30 or 84 (multi-pack containing 3 packs of 28) patches, each patch is included in an individual sachet.

Only some package sizes may be marketed.

Marketing Authorization Holder

UCB Pharma S.A.

Allée de la Recherche 60

B-1070 Brussels

Belgium

Responsible for manufacturing

UCB Pharma S.A.

Chemin du Foriest

B-1420 Braine l’Alleud

Belgium

For more information about this medicine, please contact the local representative of the marketing authorization holder:

Last update of this leaflet:

Other sources of information

The detailed information about this medicine is available on the website of the European Medicines Agencyhttps://www.ema.europa.eu