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 concentration of the neurotransmitter acetylcholine (a substance that enables nerve cells to communicate with each other).
The action of rivastigmine is to block the enzymes that break down acetylcholine: acetylcholinesterase and butyrylcholinesterase. By blocking the action of these enzymes, Rivastigmin Orion allows the concentration of acetylcholine in the brain to increase, 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 inform their doctor and not take Rivastigmin Orion.
Before starting treatment with Rivastigmin Orion, the patient should discuss the following with their doctor:
If any of the above apply to the patient, the doctor may need to monitor them more closely during treatment.
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 inform 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 with other medicines that have 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 taken with 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 is to undergo surgery during treatment with Rivastigmin Orion, they should inform 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 taking 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 taking Rivastigmin Orion.
The doctor will inform the patient whether their condition allows them to drive or use machines safely. Rivastigmin Orion may cause dizziness and drowsiness, mainly during the initial treatment period or when increasing the dose. If the patient feels dizzy or drowsy, they should not drive, use machines, or perform any other tasks that require concentration.
This medicine should always be taken as directed by the doctor. If the patient has any doubts, they 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 taking 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 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 the patient experiences any of the above symptoms, they 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 inform their doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety, 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 this 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 on 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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