Ask a doctor about a prescription for ELECOR 50 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Elecor50 mg film-coated tablets
eplerenone
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack and other information:
Elecorbelongs to a group of medicines known as selective aldosterone blockers. These blockers inhibit the action of aldosterone, a substance produced by the body that controls blood pressure and cardiac function. High levels of aldosterone can cause changes in your body that lead to heart failure.
Elecoris used to treat heart failure to prevent worsening and reduce hospitalization if you have:
Do not take Elecor
Warnings and precautions
Talk to your doctor, pharmacist, or nurse before you start taking Elecor.
Children and adolescents
The safety and efficacy of eplerenone in children and adolescents have not been established.
Other medicines and Elecor
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Taking Elecor with food and drink
Elecorcan be taken with or without food.
Pregnancy and breast-feeding
If you are pregnant or breast-feeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. The effect of Elecorduring pregnancy in humans has not been evaluated.
It is not known whether eplerenone is excreted in breast milk. Your doctor will decide with you whether to discontinue breastfeeding or treatment.
Driving and using machines
After taking Elecor, you may feel dizzy. If this happens, do not drive or operate machinery.
Elecor contains lactose
Elecorcontains lactose (a type of sugar). If your doctor has told you that you have an intolerance to some sugars, consult with them before taking this medicine.
Elecorcontains less than 23 mg of sodium (1 mmol) per tablet; this is, essentially, "sodium-free".
Follow exactly the instructions of your doctor or pharmacist. If you are unsure, ask your doctor or pharmacist again.
Elecortablets can be taken with or without food. Swallow the tablets whole with plenty of water.
Elecoris usually given in combination with other medicines for heart failure, such as beta-blockers. The usual initial dose is one 25 mg tablet once daily, increasing after about 4 weeks to 50 mg daily (one 50 mg tablet or two 25 mg tablets). The maximum dose regimen is 50 mg per day.
Potassium blood levels should be determined before starting treatment with Elecor, during the first week, and one month after starting treatment or after a dose change. Your doctor may adjust the dose based on your potassium blood levels.
If you have mild kidney problems, you should start treatment with a 25 mg tablet per day, and if you have moderate kidney problems, you should start treatment with a 25 mg tablet every other day. These doses may be adjusted, if your doctor indicates, and according to your potassium blood levels.
Elecoris not recommended in patients with severe kidney disease.
No initial dose adjustment is necessary in patients with mild to moderate liver problems. If you have any liver or kidney disease, you may need to have potassium blood levels checked more frequently (see also "Do not take Elecor").
In elderly patients: no initial dose adjustment is required.
In children and adolescents: Elecoris not recommended.
If you take more Elecor than you should
If you take more Elecorthan you should, tell your doctor or pharmacist immediately. If you have taken too much medicine, the most likely symptoms will be low blood pressure (manifested as dizziness, blurred vision, weakness, sudden loss of consciousness) or hyperkalemia, high levels of potassium in the blood (manifested by muscle cramps, diarrhea, nausea, dizziness, or headache).
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take Elecor
If it is almost time for your next dose, skip the dose you missed and take the next dose at the right time.
Otherwise, take the dose as soon as you remember, provided that more than 12 hours have passed since the time you should have taken the dose. Take your medicine as usual.
Do not take a double dose to make up for forgotten doses.
If you stop taking Elecor
It is important to keep taking Elecoras your doctor has told you, unless your doctor tells you to stop.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If any of the following happen:
Seek medical attention immediately
These are symptoms of angioedema, a rare side effect (affecting up to 1 in 100 people).
Other side effects reported include:
Common side effects(may affect up to 1 in 10 people):
Uncommon side effects(may affect up to 1 in 100 people):
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly to the Spanish Medicines and Healthcare Products Agency (AEMPS) at www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
This medicine does not require any special storage conditions.
Do not use this medicine after the expiry date which is stated on the packaging and outer carton after EXP. The expiry date is the last day of the month shown.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to your pharmacist. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Composition of Elecor
The active substance of Elecorfilm-coated tablets is eplerenone. Each tablet contains 50 mg of eplerenone.
The other ingredients are lactose monohydrate, microcrystalline cellulose (E460), sodium croscarmellose (E468), hypromellose (E464), sodium lauryl sulfate, talc (E553b), and magnesium stearate (E470b).
The coating of Elecor 50 mg film-coated tablets contains hypromellose (E464), titanium dioxide (E171), macrogol 400, polysorbate 80 (E433), yellow iron oxide (E172), and red iron oxide (E172).
Appearance of Elecor and contents of the pack
The Elecor 50 mg tablet is a yellow film-coated tablet. It is marked with "NSR" above "50".
Elecor 50 mg film-coated tablets are available in packs with blisters containing 30, 50, or 200 tablets. Only some pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Almirall, S.A. General Mitre, nº 151 08022 – Barcelona (Spain).
Fareva Amboise. Zone Industrielle-29 route des Industries. 37530 Pocé-sur-Cisse (France)
Date of last revision of this leaflet: August 2022
Detailed and up-to-date information on this medicine is available on the website of the Spanish Medicines and Healthcare Products Agency (AEMPS) http://www.aemps.gob.es
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for ELECOR 50 mg FILM-COATED TABLETS – subject to medical assessment and local rules.