Rivastigmin Orion, 1.5 mg, hard capsules
Rivastigmine
The active substance of Rivastigmin Orion is rivastigmine.
Rivastigmin Orion belongs to a group of medicines called cholinesterase inhibitors. In patients with Alzheimer's disease or Parkinson's disease dementia, certain brain cells die, which reduces the 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 blocking the action of these enzymes, Rivastigmin Orion increases the levels of acetylcholine in the brain, which helps to alleviate the symptoms of Alzheimer's disease and Parkinson's disease dementia.
Rivastigmin Orion is used to treat adult patients with mild to moderate Alzheimer's disease, a progressive brain disease that causes gradual memory, intellectual, and behavioral disorders. The capsules can also be used to treat dementia in adult patients with Parkinson's disease.
If this situation applies to the patient, they should tell their doctor and not use Rivastigmin Orion.
Before starting to use Rivastigmin Orion, the patient should discuss it with their doctor:
If any of the above applies to the patient, the doctor may need to monitor them more closely while using the medicine.
If the patient has stopped taking Rivastigmin Orion for more than three days, they should not take the next dose until they have consulted their doctor.
Rivastigmin Orion should not be used in children and adolescents to treat Alzheimer's disease.
The patient should tell their doctor about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
Rivastigmin Orion should not be given at the same time as other medicines with similar effects.
Rivastigmin Orion may interact with anticholinergic medicines (medicines used to relieve stomach cramps or spasms, to treat Parkinson's disease, or to prevent motion sickness).
Rivastigmin Orion should not be used at the same time as metoclopramide (a medicine used to relieve or prevent nausea and vomiting). Taking these two medicines together may cause disorders such as stiffness of the limbs and hand tremors.
If the patient needs to undergo surgery while taking Rivastigmin Orion, they should tell their doctor about the use of rivastigmine before receiving any anesthetics, as Rivastigmin Orion may enhance the effect of certain muscle relaxants during anesthesia.
Care should be taken when Rivastigmin Orion is used with beta-adrenergic blockers (medicines such as atenolol, used to treat high blood pressure, angina, and other heart diseases). Taking these two medicines together may cause disorders such as slow heart rate (bradycardia) leading to fainting or loss of consciousness.
Care should be taken when Rivastigmin Orion is used with other medicines that may affect heart rhythm or the heart's conduction system (prolonged QT interval).
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.
If the patient is pregnant, the benefits of using Rivastigmin Orion should be weighed against the possible effects of the medicine on the unborn child. Rivastigmin Orion should not be used during pregnancy unless it is absolutely necessary.
The patient should not breastfeed while using Rivastigmin Orion.
The doctor will inform the patient whether their condition allows them to drive vehicles and operate machines safely. Rivastigmin Orion may cause dizziness and drowsiness, mainly during the initial treatment period or when increasing the dose. If the patient experiences dizziness or drowsiness, they should not drive vehicles, operate machines, or perform any other tasks that require concentration.
This medicine should always be used as directed by the doctor. If there are any doubts, the patient should consult their doctor, pharmacist, or nurse.
The doctor will regularly check if the medicine is working for the patient. During treatment with this medicine, the doctor will also monitor the patient's weight.
If the patient has stopped taking Rivastigmin Orion for more than three days, they should not take the next dose until they have consulted their doctor.
In case of unintentional ingestion of a higher dose of Rivastigmin Orion than recommended, the patient should inform their doctor, as medical attention may be necessary.
In some individuals who have accidentally taken too much Rivastigmin Orion, nausea (vomiting), vomiting, diarrhea, high blood pressure, and hallucinations have been observed. Slow heart rate and fainting may also occur .
If a dose of Rivastigmin Orion is missed, the patient should wait and take the next dose at the usual scheduled time. They should not take a double dose to make up for the missed dose.
If the patient has any further doubts about using this medicine, they should consult their doctor or pharmacist.
Like all medicines, Rivastigmin Orion can cause side effects, although not everybody gets them.
Side effects may occur more frequently during the initial treatment period or when increasing the dose. Side effects usually disappear slowly as the body adapts to the treatment.
Very common ( may affect more than 1 in 10 people)
Common ( may affect up to 1 in 10 people)
Uncommon ( may affect up to 1 in 100 people)
Rare ( may affect up to 1 in 1,000 people)
Very rare ( may affect up to 1 in 10,000 people)
Frequency not known ( cannot be estimated from the available data)
In these patients, some side effects occur more frequently. They may also experience additional symptoms:
Very common ( may affect more than 1 in 10 people)
Common ( may affect up to 1 in 10 people)
Uncommon ( may affect up to 1 in 100 people)
Frequency not known ( frequency cannot be estimated from the available data)
Common ( may affect up to 1 in 10 people)
Uncommon ( may affect up to 1 in 100 people)
Frequency not known ( cannot be estimated from the available data)
If any of the above symptoms occur, the patient should contact their doctor, as medical attention may be necessary.
If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products,
Aleje Jerozolimskie 181 C, 02-222 Warsaw, Tel.: +48 22 49 21 301,
Fax: + 48 22 49 21 309. Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help to gather more information on the safety of the medicine.
Hard capsule.
Rivastigmin Orion 1.5 mg hard capsule is yellow, 3 mg hard capsule is orange, 4.5 mg hard capsule is red, and 6 mg hard capsule is half red and half orange.
The hard, non-transparent capsules contain a powder that is white to pale yellow in color.
They are packaged in PVC/PVdC/Aluminum blisters. The packs contain 28, 56 hard capsules.
Additionally, only for Rivastigmin Orion 3 mg, 4.5 mg, and 6 mg hard capsules - a pack of 112 hard capsules.
Not all pack sizes may be marketed.
Orion Corporation
Orionintie 1
FI-02200 Espoo
Finland
Orion Corporation Orion Pharma
Orionintie 1
FI-02200 Espoo
Finland
Orion Corporation Orion Pharma
Joensuunkatu 7
FI-24100 Salo
Finland
To obtain more detailed information about this medicine, the patient should contact the local representative of the marketing authorization holder:
Orion Pharma Poland Sp. z o. o.
kontakt@orionpharma.info.pl
Denmark, Finland, Norway, Poland, Sweden: Rivastigmin Orion
Date of last revision of the leaflet:04.2025
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