Stalevo 75 mg/18.75 mg/200 mg film-coated tablets

Spain
Brand name Stalevo 75 mg/18.75 mg/200 mg film-coated tablets
Form tablets, film-coated
Active substance / Dosage
LEVODOPA · 75,09 mg
CARBIDOPA · 18,75 mg
ENTACAPONE · 200 mg
Prescription type Prescription Only Medicine
Registration number 03260026
Manufacturer Orion Corporation
Stalevo 75 mg/18.75 mg/200 mg film-coated tablets tablets, film-coated

Package leaflet: Information for the user

Introduction

Package leaflet: information for the user

Stalevo 75mg/18.75mg/200mg film-coated tablets

Levodopa/carbidopa/entacapone

Read the entire leaflet carefully before you start taking this medicine, because it contains important information for you.

  • Keep this leaflet, as you may need to read it again.
  • If you have any questions, ask your doctor or pharmacist.
  • This medicine has been prescribed for you only, and you should not give it to other people, even if they have the same symptoms as you, because it could harm them.
  • If you experience any adverse effects, talk to your doctor or pharmacist, even if they are adverse effects not listed in this leaflet. See section 4.

Leaflet contents

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

1. What Stalevo is and what it is used for

Stalevo contains three active substances (levodopa, carbidopa, and entacapona) in a single film-coated tablet. Stalevo is used to treat Parkinson's disease.

Parkinson's disease is caused by low levels in the brain of a substance called dopamine. Levodopa increases the amount of dopamine and thereby reduces the symptoms of Parkinson's disease. Carbidopa and entacapona enhance the anti-Parkinson effects of levodopa.

2. What you need to know before taking Stalevo

Do not take Stalevo if:

  • you are allergic to levodopa, carbidopa or entacapone, or to any of the other ingredients of this medicine (listed in section 6)
  • you have narrow-angle glaucoma (an eye disorder)
  • you have a tumour of the adrenal glands
  • you are taking certain medicines to treat depression (combinations of selective MAO-A and MAO-B inhibitors, or non-selective MAO inhibitors)
  • you have ever had neuroleptic malignant syndrome (NMS – a rare reaction to medicines used in the treatment of serious mental disorders)
  • you have ever had non-traumatic rhabdomyolysis (a rare muscle disorder)
  • you have severe liver disease.

Warnings and precautions

Talk to your doctor or pharmacist before taking Stalevo if you have or have ever had:

  • a heart attack or any other heart or blood vessel disease, including arrhythmias
  • asthma or any other lung disease
  • a liver problem, as your dose may need to be adjusted
  • any kidney disease or hormone-related disorder
  • stomach ulcer or seizures
  • prolonged diarrhoea. Talk to your doctor, as this may be a sign of inflammation of the colon
  • any form of serious mental disorder, such as psychosis
  • open-angle glaucoma, as your dose may need to be adjusted and your intraocular pressure monitored.

Talk to your doctor if you are taking:

  • antipsychotics (medicines to treat psychosis)
  • any medicine that may cause a drop in blood pressure when standing up from a chair or bed. Be aware that Stalevo may worsen these reactions.

Talk to your doctor if, during treatment with Stalevo:

  • you experience marked muscle stiffness, violent muscle contractions, tremors, agitation, confusion, fever, rapid pulse or large fluctuations in blood pressure. If any of these occur, contact your doctor immediately
  • you feel depressed, have suicidal thoughts, or notice unusual changes in your behaviour
  • you start falling asleep suddenly or feel very drowsy. If this happens, do not drive or operate tools or machinery (see also section “Driving and use of machines”)
  • you begin to experience uncontrolled movements or they worsen. If this occurs, your doctor may need to change your dose
  • you experience diarrhoea; monitoring body weight is recommended to avoid potentially excessive weight loss
  • you experience progressive loss of appetite, asthenia (weakness, exhaustion), and weight loss over a relatively short period. In such cases, a full medical evaluation including liver function tests should be considered
  • you are considering stopping Stalevo; refer to the section "If you stop taking Stalevo".

Inform your doctor if you, or your family/caregiver, notice that you are developing addiction-like symptoms, leading to a desire for high doses of Stalevo and other medicines used to treat Parkinson’s disease.

Inform your doctor if you or your family/caregiver notice that you are developing urges or a tendency to behave in ways that are unusual for you or that you cannot resist the impulse, drive, or temptation to carry out certain activities that could harm you or others. These behaviours are known as impulse control disorders and may include gambling addiction, compulsive eating, spending sprees, or abnormally increased sexual drive or preoccupation with sexual thoughts or feelings. Your doctor may need to review your treatment.

During long-term treatment with Stalevo, your doctor may carry out regular blood tests.

If you are due to undergo surgery, you must tell your doctor that you are taking Stalevo.

Stalevo is not recommended for the treatment of extrapyramidal symptoms (e.g. involuntary movements, restlessness, muscle rigidity, and muscle contractions) caused by other medicines.

Children and adolescents

Experience with the use of Stalevo in patients under 18 years of age is limited. Therefore, Stalevo is not recommended for use in children or adolescents.

Taking Stalevo with other medicines

Tell your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines.

Do not take Stalevo if you are taking certain medicines to treat depression (combinations of selective MAO-A and MAO-B inhibitors, or non-selective MAO inhibitors).

Stalevo may increase the effect, and also the adverse effects, of certain medicines. These include:

  • medicines used to treat depression, such as moclobemide, amitriptyline, desipramine, maprotiline, venlafaxine and paroxetine
  • rimiterol and isoprenaline, used to treat respiratory diseases
  • adrenaline, used for severe allergic reactions
  • noradrenaline, dopamine and dobutamine, used to treat heart conditions and low blood pressure
  • alpha-methyldopa, used to treat high blood pressure
  • apomorphine, used to treat Parkinson’s disease.

Certain medicines may reduce the effects of Stalevo. These medicines are:

  • dopamine antagonists used to treat mental disorders, nausea and vomiting
  • phenytoin, used to prevent seizures
  • papaverine, used to relax muscles.

Stalevo may interfere with the gastrointestinal absorption of iron. Therefore, you should not take Stalevo at the same time as iron supplements. If you take either, you should wait at least 2 to 3 hours before taking the other.

Taking Stalevo with food and drink

  • Stalevo may be taken with or without food.
  • In some patients, Stalevo may not be well absorbed if taken with high-protein foods (meats, fish, dairy products, cereals and nuts) or shortly after eating them. Consult your doctor if you think this may be happening to you.

Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are planning to become pregnant, consult your doctor or pharmacist before taking this medicine.

You must not breast-feed while being treated with Stalevo.

Driving and use of machines

Stalevo may lower your blood pressure, which could cause dizziness or fainting. Therefore, take special care when operating tools or machinery.

If you feel very tired or notice that you sometimes fall asleep suddenly, wait until you are fully awake again before driving or doing anything else that requires alertness. Otherwise, you may put yourself and others at risk of serious or even fatal accidents.

Stalevo contains sucrose

Stalevo contains sucrose (1.4 mg/tablet). If your doctor has told you that you have an intolerance to certain sugars, consult him before taking this medicine.

3. How to take Stalevo

Follow exactly the instructions for use of this medicine given by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

Adults and elderly:

  • Your doctor will tell you the exact number of Stalevo tablets you should take each day.
    • The tablets must not be split or divided into smaller pieces.
    • Take only one tablet at a time.
    • Depending on how you respond to treatment, your doctor may instruct you to increase or decrease the dose.
    • If you are taking Stalevo tablets of 50 mg/12.5 mg/200 mg, 75 mg/18.75 mg/200 mg, 100 mg/25 mg/200 mg, 125 mg/31.25 mg/200 mg, or 150 mg/37.5 mg/200 mg, do not take more than 10 tablets per day.

Talk to your doctor or pharmacist if you think the effect of Stalevo is too strong or too weak, or if you experience possible adverse effects.

To open the bottle for the first time: press with the thumb on the seal until it breaks to open the closure. See Figure 1.

Figure 1

A hand squeezing a glass vial with fingers while a black arrow indicates the direction of downward pressure on the cap

If you take more Stalevo than you should

If you have accidentally taken more Stalevo tablets than you should, speak to your doctor or pharmacist immediately. In case of overdose, you may feel dizzy or agitated, your heartbeat may become slower or faster than normal, or you may notice a change in the colour of your skin, tongue, eyes, or urine.

If you forget to take Stalevo

Do not take a double dose to make up for forgotten doses.

If more than 1 hour remains until the next dose:

Take one tablet as soon as you remember, and take the next one at your usual time.

If less than 1 hour remains until the next dose:

Take one tablet as soon as you remember, wait 1 hour, and then take another tablet. After that, continue as usual.

There must always be an interval of 1 hour between Stalevo tablets to avoid possible adverse effects.

If you stop taking Stalevo

Do not stop taking Stalevo unless your doctor tells you to. In such a case, your doctor may need to adjust the dose of your other Parkinson's medications, especially levodopa, to ensure adequate symptom control. If you abruptly stop taking Stalevo and other Parkinson's medications, you may experience unwanted adverse effects.

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

4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them. Many of these can be relieved by adjusting the dose.

If you experience any of the following symptoms during treatment with Stalevo, contact your doctor immediately:

  • Severe muscle stiffness or violent muscle contractions, tremors, agitation, confusion, fever, rapid pulse, or large fluctuations in blood pressure. These may be symptoms of neuroleptic malignant syndrome (NMS, a rare but serious reaction to medicines used to treat disorders of the central nervous system) or rhabdomyolysis (a rare and serious muscle disorder).
  • Allergic reaction with signs such as hives, itching, rash, and swelling of the face, lips, tongue, or throat. This reaction may cause difficulty breathing or swallowing.

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

  • Uncontrolled movements (dyskinesias)
  • Feeling unwell (nausea)
  • Harmless brownish-red discoloration of the urine
  • Muscle pain
  • Diarrhea

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

  • Fainting or collapse due to low blood pressure, hypertension
  • Worsening of Parkinsonism symptoms, dizziness, drowsiness
  • Vomiting; abdominal pain and discomfort; heartburn; dry mouth; constipation
  • Difficulty sleeping; hallucinations; confusion; abnormal dreams (with nightmares); fatigue
  • Changes in mental state, including memory problems, anxiety, and depression (possibly with suicidal thoughts)
  • Heart or artery problems (e.g., chest pain), irregular heart rate
  • Increased frequency of falls
  • Shortness of breath
  • Increased sweating, rashes
  • Muscle cramps, swelling of the legs
  • Blurred vision
  • Anaemia
  • Decreased appetite, weight loss
  • Headache, joint pain
  • Urinary tract infections

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

  • Heart attack
  • Intestinal bleeding
  • Changes in blood cell counts that may lead to bleeding; abnormalities in liver function tests
  • Seizures
  • Feeling of restlessness
  • Psychotic symptoms
  • Colitis (inflammation of the colon)
  • Skin, nail, hair, or sweat discoloration different from that of urine
  • Difficulty swallowing
  • Inability to urinate

Frequency not known (cannot be estimated from available data):

A desire to take high doses of Stalevo exceeding those required to control motor symptoms, known as dopamine dysregulation syndrome. Some patients may experience severe abnormal involuntary movements (dyskinesias), mood changes, or other adverse effects after taking high doses of Stalevo.

The following adverse effects have also been reported:

  • Hepatitis (inflammation of the liver)
  • Itching

You may experience the following adverse effects:

  • Inability to resist the impulse to carry out an action that could be harmful, which may include:
    • A strong urge to gamble excessively despite serious personal or family consequences
    • Increased or altered interest in sexual activity and behaviour that is concerning to you or others, such as heightened sexual drive
    • Excessive or uncontrolled shopping or spending
    • Excessive (eating large amounts of food in short periods of time) or compulsive eating (eating more food than usual and more than needed to satisfy hunger).

Inform your doctor if you experience any of these behaviours: they will discuss how to manage or reduce these symptoms.

Reporting of adverse effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this leaflet. You can also report them directly through the national reporting system listed in Annex V. By reporting adverse effects, you can help provide more information on the safety of this medicine.

5. Storage of Stalevo

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

Do not use this medicine after the expiry date stated on the packaging after EXP. The expiry date is the last day of the month indicated.

No special storage conditions are required.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of any unused medicines or packaging. This will help protect the environment.

6. Contents of the pack and other information

Composition of Stalevo

  • The active substances in Stalevo are levodopa, carbidopa and entacapone.
  • Each Stalevo 75 mg/18.75 mg/200 mg tablet contains 75 mg of levodopa, 18.75 mg of carbidopa and 200 mg of entacapone.
  • The other components of the tablet core are croscarmellose sodium, magnesium stearate, maize starch, mannitol (E 421) and povidone (E 1201).
  • The components of the film coating are glycerol 85 percent (E 422), hypromellose, magnesium stearate, polysorbate 80, iron oxide red (E 172), sucrose and titanium dioxide (E 171).

Appearance of the product and contents of the pack

Stalevo 75 mg/18.75 mg/200 mg: light reddish-brown, oval-shaped tablets, with "LCE 75" engraved on one side.

There are five different pack sizes for Stalevo 75 mg/18.75 mg/200 mg (containing 10, 30, 100, 130 or 175 tablets). Not all pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Orion Corporation

Orionintie 1

FI-02200 Espoo

Finland

For further information about this medicinal product, please contact the local representative of the Marketing Authorization Holder.

Belgium/Belgium/Belgium

Orion Pharma BVBA/SPRL

Tel/Tel: +32 (0)15 64 10 20

Lithuania

UAB Orion Pharma

Tel.: +370 5 276 9499

Finland

Orion Corporation

Tel.: +358 10 4261

Luxembourg/Luxembourg

Orion Pharma BVBA/SPRL

Tel/Tel: +32 (0)15 64 10 20

Czech Republic

Orion Pharma s.r.o.

Tel: +420 234 703 305

Hungary

Orion Pharma Kft.

Tel.: +36 1 239 9095

Denmark

Orion Pharma A/S

Tlf: +45 8614 0000

Malta

Orion Corporation

Tel: +358 10 4261

Germany

Orion Pharma GmbH

Tel: +49 40 899 6890

Netherlands

Orion Pharma BVBA/SPRL

Tél/Tel: +32 (0)15 64 10 20

Estonia

Orion Pharma Eesti OÜ

Tel: +372 66 44 550

Norway

Orion Pharma AS

Tlf: +47 40 00 42 10

Greece

Orion Pharma Hellas M.E.Π.E

Tel: +30 210 980 3355

Austria

Orion Pharma GmbH

Tel: +49 40 899 6890

Spain

Orion Pharma S.L.

Tel: +34 91 599 86 01

Poland

Orion Pharma Poland Sp z.o.o.

Tel.: +48 22 8333177

France

Centre Spécialités Pharmaceutiques

Tel: +33 (0)1 47 04 80 46

Portugal

Orionfin Unipessoal Lda

Tel: +351 21 154 68 20

Croatia

Orion Pharma d.o.o.

Tel: +386 (0)1 600 8015

Romania

Orion Corporation

Tel: +358 10 4261

Ireland

Orion Pharma (Ireland) Ltd.

c/o Allphar Services Ltd.

Tel: +353 1 428 7777

Slovenia

Orion Pharma d.o.o.

Tel: +386 (0)1 600 8015

Iceland

Vistor hf.

Tel: +354 535 7000

Slovakia

Orion Pharma s.r.o

Tel: +420 234 703 305

Italy

Orion Pharma S.r.l.

Tel: +39 02 67876111

Finland/Sweden

Orion Corporation

Puh./Tel: +358 10 4261

Cyprus

Lifepharma (ZAM) Ltd

Tel.: +357 22056300

Sweden

Orion Pharma AB

Tel: +46 8 623 6440

Latvia

Orion Corporation

Orion Pharma parstavnieciba

Tel: +371 20028332

United Kingdom

Orion Pharma (UK) Ltd.

Tel: +44 1635 520 300

Date of the most recent review of this leaflet:

Other sources of information

Detailed information on this medicinal product is available on the website of the European Medicines Agency http://www.ema.europa.eu