Label: information for the user
galantamine
Read this label carefully before starting to take this medicine, as it contains important information for you.
Reminyl contains the active ingredient “galantamine”, an anti-dementia medication. It is used in adults to treat the symptoms of mild to moderately severe Alzheimer's disease, a type of dementia that alters brain function.
Alzheimer's disease causes an increase in memory loss, confusion, and changes in behavior, making it increasingly difficult to perform routine daily activities.
It is thought that these effects are caused by a lack of “acetylcholine”, a substance responsible for transmitting messages between brain cells. Reminyl increases the amount of acetylcholine in the brain and thereby treats the signs of the disease.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Reminyl. This medication should only be used for Alzheimer's disease and is not recommended for other types of memory loss or confusion.
Severe side effects
Reminyl may cause severe skin reactions, heart problems, and seizures. You should be aware of these side effects while taking Reminyl. See section4 “Be aware of severe side effects”.
Before starting treatment with Reminyl, your doctor must know if you have or have had any of the following conditions:
Your doctor will decide if Reminyl is suitable for you or if the dose needs to be changed.
Also, inform your doctor if you have recently had surgeryin the stomach, intestine, or bladder.Your doctor will decide if Reminyl is suitable for you.
Reminyl may cause weight loss.Your doctor will check your weight regularly while you are taking Reminyl.
Children and adolescents
Reminyl is not recommended for children or adolescents.
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Reminyl should not be taken with medications that work in the same way. These include:
Some medications may cause side effects more likely in people taking Reminyl. These include:
If you are taking any of these medications, your doctor may give you a lower dose of Reminyl.
Reminyl may affect some anesthetics. If you are undergoing general anesthesia, inform your doctor, in advance, that you are taking Reminyl.
Consult your doctor or pharmacist if you have any doubts.
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Do not breastfeed while taking Reminyl.
Reminyl may make you feel dizzy or drowsy, especially during the first few weeks of treatment. If Reminyl affects you, do not drive or operate tools or machines.
Reminyl oral solution contains methylo- and propylparahydroxybenzoates.
These may sometimes cause allergic reactions (possibly delayed).
Reminyl oral solution contains sodium
This medication contains less than 1mmol of sodium (23mg) per 6ml of Reminyl 4mg/ml oral solution (equivalent to the maximum daily dose of Reminyl); this is essentially “sodium-free”.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
How much to take
You will start treatment with Reminyl at a low dose. The usual initial dose is 4mg (1mL of solution), taken twice a day (a total of 8mg per day). Your doctor will gradually increase your dose, every 4weeks or more, until you reach the most suitable dose for you. The maximum dose is 12mg (3ml of solution), taken twice a day (a total of 24mg per day).
Your doctor will explain with which dose you should start and when to increase it.If you are unsure of what to do or find that the effect of Reminyl is too strong or weak, inform your doctor or pharmacist.
Your doctor needs to see you regularly to check that this medication is working and to discuss with you how you feel.
If you have liver or kidney problems,your doctor may give you a reduced dose of Reminyl or decide if this medication is not suitable for you.
How to take it
Take your Reminyl dose twice a day, in the morning and at night, with water or other liquids. Try to take Reminyl with food.
Drink plenty of liquid while taking Reminyl, to stay hydrated.
The solution comes with a syringe, with which you can extract the exact amount needed from the bottle.
Instructions for opening the bottle and using the syringe
Fig. 1: The bottle has a child-resistant cap and must be opened as follows: -Push the cap down while turning it counterclockwise. -Once unscrewed, remove the cap. Fig. 2: Insert the syringe into the bottle. While holding the lower ring, pull the upper ring down to the mark corresponding to the number of milliliters you want to administer. Fig. 3: Hold the lower ring and remove the syringe completely from the bottle. Empty the syringe into any non-alcoholic beverage by sliding the upper ring down and drink immediately. Close the bottle. Wash the syringe with water. |
If you take more Reminyl than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or
call the Toxicological Information Service, phone: 91 562 04 20 indicating the medication and the
amount ingested. Bring the remaining solution bottle with you. The signs of an overdose may include:
If you forget to take Reminyl
If you forget to take a dose, leave that dose and continue treatment as usual with the next scheduled dose.Do not take a double dose to compensate for missed doses.
If you forget to take more than one dose, consult your doctor.
If you interrupt treatment with Reminyl
Consult with your doctor before interrupting treatment with Reminyl. It is essential to continue taking this medication to treat your disease.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Be aware of severe side effects
Stop taking Reminyl and consult a doctor or go to the nearest emergency service immediatelyif you notice any of the following side effects
Skin reactions,including:
These skin reactions are rare in people taking Reminyl (they can affect up to 1 in 1,000 people).
Heart problemsincluding changes in heart rhythm (such as slow heartbeat or extra beats) or palpitations (feeling a rapid or irregular heartbeat). Heart problems can be seen as an abnormal tracing on an electrocardiogram (ECG), and may be common in people taking Reminyl (they can affect up to 1 in 10 people).
Seizures. This is rare in people taking Reminyl (they can affect up to 1 in 100 people).
You should stop taking Reminyl and seek help immediatelyif you notice any of the mentioned side effects.
Other side effects
Frequent side effects(they can affect more than 1 in 10 people):
Common side effects(they can affect up to 1 in 10 people):
Rare side effects(they can affect up to 1 in 100 people):
Very rare side effects(they can affect up to 1 in 1,000 people):
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through theSpanish System for Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es/.By reporting side effects, you can contribute to providing more information on 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 after CAD. The expiration date is the last day of the month indicated.
Do not freeze.
Reminyl oral solution should not be used once 3 months have passed since the bottle was first opened.
Medicines should not be thrown down the drains or in the trash.Dispose of the containers and medicines you no longer need at theSIGREpharmacy drop-off point.Ask your pharmacist how to dispose of the containers and medicines you no longer need. This will help protect the environment.
Parahydroxybenzoate of methyl (E218), parahydroxybenzoate of propyl (E216), purified water, sodium saccharin, and sodium hydroxide.
Appearance of the product and contents of the packaging
Reminyl is a transparent and colorless oral solution that comes in a 100 ml container.
The solution comes with a syringe with which the exact amount needed can be drawn from the bottle.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Essential Pharma Limited,
Vision Exchange Building,
Triq it-Territorjals, Zone 1,
Central Business District,
Birkirkara, CBD 1070,
Malta
Responsible for manufacturing
Janssen-Pharmaceutica, N.V.
Turnhoutseweg, 30
B-2340 Beerse
Belgium
This medicine is authorized in the Member States of the European Union with the following names:
AustriaReminyl4mg/ml- oral solution
BelgiumReminyl 4mg/ml, oral solution
DenmarkReminyl4mg/ml oral solution
FinlandReminyl 4mg/ml oral solution
FranceReminyl 4mg/ml, oral solution
GreeceReminyl 4mg/mlsolubleformulation
IrelandReminyl4mg/ml oral solution
ItalyReminyl4mg/mloral solution
NorwayReminyl4mg/ml mixture, solution
PortugalReminyl 4mg/mloral solution
SpainReminyl4mg/ml oral solution
SwedenReminyl4mg/ml oral solution
United Kingdom (Northern Ireland)Reminyl4mg/ml oral solution
This leaflet has been approved in:October 2021.
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) (http://www.aemps.gob.es/).
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