Exelon 3 mg hard capsules
Spain
Table of Contents
Package leaflet: Information for the user
Introduction
Package leaflet: information for the user
Exelon 1.5 mg hard capsules
Exelon 3.0 mg hard capsules
Exelon 4.5 mg hard capsules
Exelon 6.0 mg hard capsules
rivastigmine
Read the entire leaflet carefully before you start taking this medicine, because it contains important information for you.
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Keep this leaflet, as you may need to read it again.
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If you have any questions, ask your doctor, pharmacist or nurse.
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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.
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If you experience any adverse effects, consult your doctor, pharmacist or nurse, even if the effects are not listed in this leaflet. See section 4.
Contents of the leaflet
- What Exelon is and what it is used for
- What you need to know before taking Exelon
- How to take Exelon
- Possible adverse effects
- How to store Exelon
- Contents of the pack and other information
1. What Exelon is and what it is used for
The active substance in Exelon is rivastigmine.
Rivastigmine belongs to a group of substances called cholinesterase inhibitors. In patients with Alzheimer's dementia or dementia associated with Parkinson's disease, certain nerve cells in the brain die, resulting in low levels of the neurotransmitter acetylcholine (a substance that enables nerve cells to communicate with each other). Rivastigmine works by blocking the enzymes that break down acetylcholine: acetylcholinesterase and butyrylcholinesterase. By inhibiting these enzymes, Exelon increases the levels of acetylcholine in the brain, helping to reduce the symptoms of Alzheimer's disease and dementia associated with Parkinson's disease.
Exelon is used to treat adult patients with mild to moderately severe Alzheimer's dementia, a progressive brain disorder that gradually affects memory, intellectual capacity, and behavior. The capsules and oral solution can also be used for the treatment of dementia in adult patients with Parkinson's disease.
2. What you need to know before starting Exelon
Do not take Exelon
- if you are allergic to rivastigmine (the active substance in Exelon) or to any of the other ingredients of this medicine (listed in section 6).
- if you have a skin reaction that spreads beyond the size of the patch, if you experience a more intense local reaction (such as blisters, increasing skin inflammation, swelling), or if there is no improvement within 48 hours after removing the transdermal patch.
If you are in any of these situations, inform your doctor and do not take Exelon.
Warnings and precautions
Talk to your doctor before starting Exelon:
- if you have or have ever had an irregular or slow heart rate (pulse).
- if you have or have ever had an active stomach ulcer.
- if you have or have ever had difficulty urinating.
- if you have or have ever had seizures.
- if you have or have ever had asthma or a serious respiratory disease.
- if you have or have ever had (impaired) kidney function.
- if you have or have ever had (impaired) liver function.
- if you suffer from tremors.
- if you have low body weight.
- if you experience gastrointestinal reactions such as dizziness (nausea), vomiting, and diarrhea. You may become dehydrated (loss of large amounts of fluid) if vomiting or diarrhea is prolonged.
If you are in any of these situations, your doctor may consider closer monitoring during treatment.
If you have not taken Exelon for more than three days, do not take the next dose until you have consulted your doctor.
Children and adolescents
Exelon should not be used in the pediatric population for the treatment of Alzheimer's disease.
Other medicines and Exelon
Tell your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines.
Exelon should not be administered at the same time as other medicines with effects similar to those of Exelon. Exelon may interfere with anticholinergic medicines (used to relieve stomach cramps or spasms, for the treatment of Parkinson's disease, or to prevent travel sickness).
Exelon should not be taken at the same time as metoclopramide (a medicine used to relieve or prevent nausea and vomiting). Taking both medicines together may cause problems such as stiffness in the limbs and hand tremors.
If you need to undergo surgery while taking Exelon, inform your doctor before receiving any anesthetic, as Exelon may intensify the effects of certain muscle relaxants used during anesthesia.
Caution is advised when using Exelon together with beta-blockers (medicines such as atenolol used to treat hypertension, angina, and other heart conditions). Taking both medicines together may cause complications such as a slowed heart rate (bradycardia), which may lead to fainting or loss of consciousness.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to become pregnant, consult your doctor or pharmacist before using this medicine.
If you are pregnant, the benefits of using Exelon must be weighed against the potential risks to the fetus. Exelon should not be used during pregnancy unless clearly necessary.
You should not breastfeed during treatment with Exelon.
Driving and using machines
Your doctor will advise you whether your condition allows you to drive or operate machinery safely. Exelon may cause dizziness and drowsiness, especially at the beginning of treatment or when the dose is increased. If you feel dizzy or sleepy, do not drive, operate machinery, or perform any other tasks requiring your full attention.
3. How to take Exelon
Follow exactly the instructions for using this medicine given by your doctor. If in doubt, consult your doctor, pharmacist, or nurse again.
Starting treatment
Your doctor will tell you what dose of Exelon you should take.
- Treatment usually starts with a low dose.
- Your doctor will slowly increase your dose depending on how you respond to treatment.
- The highest dose you will take is 6.0 mg twice daily.
Your doctor will regularly monitor whether the medicine is working for you. Your doctor will also monitor your weight while you are taking this medicine.
If you have not taken Exelon for more than three days, do not take the next dose until you have consulted your doctor.
Taking this medicine
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Inform your caregiver that you are taking Exelon.
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To benefit from your medicine, take it every day.
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Take Exelon twice a day (in the morning and at night), with meals.
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Swallow the capsule whole with liquid.
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Do not open or crush the capsule.
If you take more Exelon than you should
If you accidentally take more Exelon than you should, inform your doctor. You may require medical attention. Some people who have accidentally taken higher doses have experienced nausea, vomiting, diarrhea, high blood pressure, and hallucinations. Slowing of the heart rate and fainting may also occur.
If you forget to take Exelon
If you forget your dose of Exelon, wait and take your next dose at the usual time. Do not take a double dose to make up for forgotten doses.
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 experiences them.
You may experience adverse effects more frequently when starting treatment or when your dose is increased. Generally, adverse effects will gradually disappear as your body gets used to the medicine.
Very common (may affect more than 1 in 10 people)
- Dizziness
- Loss of appetite
- Stomach problems such as feeling sick (nausea), vomiting, diarrhoea
Common (may affect up to 1 in 10 people)
- Anxiety
- Sweating
- Headache
- Indigestion
- Weight loss
- Stomach pain
- Feeling restless
- Feeling tired or weak
- Feeling generally unwell
- Tremor or feeling confused
- Decreased appetite
- Nightmares
Uncommon (may affect up to 1 in 100 people)
- Depression
- Difficulty sleeping
- Fainting or accidental falls
- Changes in liver function
Rare (may affect up to 1 in 1,000 people)
- Chest pain
- Skin rash, itching
- Epileptic seizures (convulsions)
- Ulcers in your stomach or intestine
Very rare (may affect up to 1 in 10,000 people)
- High blood pressure
- Urinary tract infection
- Seeing things that are not there (hallucinations)
- Problems with your heart rhythm such as fast or slow heartbeat
- Gastrointestinal bleeding – manifested as blood in the stools or vomiting blood
- Inflammation of the pancreas – signs include severe pain in the upper abdomen, often with nausea or vomiting
- Worsening of signs of Parkinson’s disease or development of similar symptoms – such as muscle stiffness, difficulty performing movements
Not known (cannot be estimated from available data)
- Severe vomiting that may cause a tear in the part of the digestive tract connecting your mouth to your stomach (oesophagus)
- Dehydration (loss of large amounts of fluid)
- Liver disorders (yellowing of the skin, yellowing of the whites of the eyes, abnormally dark urine, or unexplained nausea, vomiting, tiredness and loss of appetite)
- Aggression, feeling of restlessness
- Irregular heartbeat
Patients with dementia or Parkinson’s disease
These patients experience certain adverse effects more frequently and may also have additional adverse effects:
Very common (may affect more than 1 in 10 people)
- Tremor
- Fainting
- Accidental falls
Common (may affect up to 1 in 10 people)
- Anxiety
- Feeling of restlessness
- Slow and fast heart rate
- Difficulty sleeping
- Excessive saliva and dehydration
- Abnormally slow movements or uncontrollable movements
- Worsening of signs of Parkinson’s disease or development of similar symptoms – such as muscle stiffness, difficulty performing movements and muscle weakness
Uncommon (may affect up to 1 in 100 people)
- Irregular heartbeat and loss of movement control
Other adverse effects observed with Exelon transdermal patches and which may also occur with hard capsules:
Common (may affect up to 1 in 10 people)
- Fever
- Severe confusion
- Urinary incontinence (inability to properly control urine)
Uncommon (may affect up to 1 in 100 people)
- Hyperactivity (high level of activity, restlessness)
Not known (cannot be estimated from available data)
- Allergic reaction at the site where the patch was applied, such as blisters or skin inflammation
If you experience any of these adverse effects, contact your doctor, as you may require medical attention.
Reporting of adverse effects
If you experience any adverse effect, talk to your doctor, pharmacist or nurse, even if it is a possible adverse effect not listed in this leaflet. You can also report them directly through the national reporting system included in Appendix V. By reporting adverse effects, you can help provide more information on the safety of this medicine.
5. Storage of Exelon
- 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 refers to the last day of the month indicated.
- Do not store above 30°C.
- Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of any unused medicine and its container. This will help protect the environment.
6. Contents of the pack and other information
Composition of Exelon
- The active substance is rivastigmine hydrogen tartrate.
- The other components are hypromellose, magnesium stearate, microcrystalline cellulose, colloidal anhydrous silica, gelatin, iron oxide yellow (E172), iron oxide red (E172), titanium dioxide (E171) and shellac.
Each Exelon 1.5 mg capsule contains 1.5 mg of rivastigmine.
Each Exelon 3.0 mg capsule contains 3.0 mg of rivastigmine.
Each Exelon 4.5 mg capsule contains 4.5 mg of rivastigmine.
Each Exelon 6.0 mg capsule contains 6.0 mg of rivastigmine.
Nature of the product and pack contents
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Exelon 1.5 mg hard capsules contain a white to almost white powder and have a yellow cap and body with a red imprint “EXELON 1.5 mg” on the body.
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Exelon 3.0 mg hard capsules contain a white to almost white powder and have an orange cap and body with a red imprint “EXELON 3 mg” on the body.
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Exelon 4.5 mg hard capsules contain a white to almost white powder and have a red cap and body with a white imprint “EXELON 4.5 mg” on the body.
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Exelon 6.0 mg hard capsules contain a white to almost white powder and have a red cap and an orange body with a red imprint “EXELON 6 mg” on the body.
The product is packaged in blisters and is available in three different pack sizes (28, 56 or 112 capsules) and in plastic bottles containing 250 capsules. Not all pack sizes may be available in your country.
Marketing Authorization Holder
Novartis Europharm Limited
Vista Building
Elm Park, Merrion Road
Dublin 4
Ireland
Manufacturer
Novartis Farmacéutica, S.A.
Production Plant
Ronda de Santa Maria 158
E-08210 Barberà del Vallès, Barcelona
Spain
For further information on this medicinal product, please contact the local representative of the Marketing Authorization Holder:
Belgium/Belgium/Belgium Novartis Pharma N.V. Tel/Tel: +32 2 246 16 11 | Lithuania SIA „Novartis Baltics“ Lithuania Branch Tel: +370 5 269 16 50 |
Bulgaria Novartis Bulgaria EOOD Tel: +359 2 489 98 28 | Luxembourg/Luxembourg Novartis Pharma N.V. Tel/Tel: +32 2 246 16 11 |
Czech Republic Novartis s.r.o. Tel: +420 225 775 111 | Hungary Novartis Hungária Kft. Tel.: +36 1 457 65 00 |
Denmark Novartis Healthcare A/S Tlf: +45 39 16 84 00 | Malta Novartis Pharma Services Inc. Tel: +356 2122 2872 |
Germany Novartis Pharma GmbH Tel: +49 911 273 0 | Netherlands Novartis Pharma B.V. Tel: +31 26 37 82 111 |
Estonia SIA Novartis Baltics Estonia Branch Tel: +372 66 30 810 | Norway Novartis Norge AS Tlf: +47 23 05 20 00 |
Greece Novartis (Hellas) S.A.E. Tel: +30 210 281 17 12 | Austria Novartis Pharma GmbH Tel: +43 1 86 6570 |
Spain Novartis Farmacéutica, S.A. Tel: +34 93 306 42 00 | Poland Novartis Poland Sp. z o.o. Tel.: +48 22 375 4888 |
France Novartis Pharma S.A.S. Tél: +33 1 55 47 66 00 | Portugal Novartis Farma - Pharmaceutical Products, S.A. Tel: +351 21 000 8600 |
Croatia Novartis Hrvatska d.o.o. Tel. +385 1 6274 220 | Romania Novartis Pharma Services Romania SRL Tel: +40 21 31299 01 |
Ireland Novartis Ireland Limited Tel: +353 1 260 12 55 | Slovenia Novartis Pharma Services Inc. Tel: +386 1 300 75 50 |
Iceland Vistor hf. Tel: +354 535 7000 | Slovakia Novartis Slovakia s.r.o. Tel: +421 2 5542 5439 |
Italy Novartis Farma S.p.A. Tel: +39 02 96 54 1 | Finland Novartis Finland Oy Puh/Tel: +358 (0)10 6133 200 |
Cyprus Novartis Pharma Services Inc. Tel: +357 22 690 690 | Sweden Novartis Sverige AB Tel: +46 8 732 32 00 |
Latvia SIA “Novartis Baltics” Tel: +371 67 887 070 | United Kingdom Novartis Pharmaceuticals UK Ltd. Tel: +44 1276 698370 |
Date of the most recent review of this leaflet:
Other sources of information
Detailed information on this medicine is available on the website of the European Medicines Agency: http://www.ema.europa.eu