1. What is Eplerenone Normon and what is it used for
2. What you need to know before starting to take Eplerenone Normon
3. How to take Eplerenone Normon
4. Possible adverse effects
5. Storage of Eplerenone Normon
6. Contents of the pack and additional information
EplerenonaNormonbelongs to a group of medicines known as selective aldosterone blockers. These blockers inhibit the action of aldosterone, a substance produced by the body, which controls blood pressure and cardiac function. Elevated levels of aldosterone can produce changes in the body that lead to heart failure.
EplerenonaNormonis used to treat heart failure to prevent worsening and reduce hospitalization if you have:
Do not take Eplerenona Normon
Warnings and precautions
Consult your doctor or pharmacist before starting to take Eplerenona Normon:
Children and adolescents
The safety and efficacy of eplerenone in children and adolescents have not been established.
Taking Eplerenona Normon with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Do not take Eplerenona Normon with the following medications (see "Do not take Eplerenona Normon"):
Inform your doctor if you are taking any of the following medications:
Taking Eplerenona Normon with food, drinks, and alcohol
Eplerenona Normon can be taken with or without food.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, or think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before using this medication.
The effect of Eplerenona Normon on pregnancy in humans has not been evaluated.
The elimination of eplerenone in breast milk is unknown. Your doctor will decide with you whether to stop treatment or breastfeeding.
Driving and operating machinery
After taking Eplerenona Normon, you may feel dizzy. If this happens, do not drive or operate machinery.
Eplerenona Normon contains lactose and sodium
This medication contains lactose. If your doctor has told you that you have a certain sugar intolerance, consult with them before taking this medication.
This medication contains less than 23 mg of sodium (1 mmol) per tablet; it is essentially "sodium-free".
Follow exactly the administration instructions for EplerenonaNormonas indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
EplerenonaNormontablets can be taken with or without food. Swallow the tablets whole with plenty of water.
EplerenonaNormonis usually taken together with other medications for heart failure, for example, beta-blockers. The usual initial dose is one 25 mg tablet once a day, increasing after 4 weeks to 50 mg daily (one 50 mg tablet or two 25 mg tablets). The maximum dosage regimen is 50 mg per day.
Blood potassium levels should be determined before starting treatment with EplerenonaNormon, during the first week, and one month after starting treatment or after a change in dose. Your doctor may adjust the dose based on your blood potassium levels.
If you have mild renal insufficiency, you should start treatment with one 25 mg tablet per day, and if you have moderate renal insufficiency, you should start treatment with one 25 mg tablet every other day. These doses may be adjusted, if your doctor indicates, and in accordance with your blood potassium levels.
EplerenonaNormonis not recommended for patients with severe renal disease.
No initial dose adjustment is necessary for patients with mild to moderate liver insufficiency. If you have any liver or kidney disease, you may need to have your blood potassium levels checked more frequently (see also “Do not take EplerenonaNormon”).
In the elderly: no initial dose adjustment is required.
In children and adolescents: EplerenonaNormonis not recommended.
If you take more Eplerenona Normonthan you should
If you take more EplerenonaNormonthan you should, inform your doctor or pharmacist immediately. If you have taken too much medication, the most likely symptoms will be low blood pressure (manifested as dizziness, blurred vision, weakness, acute 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 Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take Eplerenona Normon
If it is almost time to take the next tablet, skip the dose you forgot and take the next tablet at the usual time. Otherwise, take the tablet as soon as you remember, as long as more than 12 hours have passed since the usual time for taking the next tablet. Resume your medication as usual.
Do not take a double dose to compensate for the missed doses.
If you interrupt treatment with Eplerenona Normon
It is essential to continue taking EplerenonaNormonas indicated, unless your doctor tells you to stop treatment.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, EplerenonaNormoncan have side effects, although not everyone will experience them.
If you experience any of the followingseek medical attention immediately:
These are the symptoms of angioneurotic edema.
Other side effects reported include:
Frequent side effects(occur in 1 to 10 of every 100 patients):
Rare side effects(occur in 1 to 10 of every 1,000 patients):
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 prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use: 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.
Store below 30 °C.
Do not use this medication after the expiration date that appears on the packaging afterCad. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash.Deposit the packaging and medications you no longer need at the SIGRE collection pointat the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Eplerenona Normon
The active ingredient is eplerenone. Each tablet contains 50 mg of eplerenone.
The other components (excipients) are:
Core:Microcrystalline cellulose, lactose, sodium croscarmellose, sodium lauryl sulfate, hydroxypropyl methylcellulose, colloidal silica, and magnesium stearate.
Coating:Hydroxypropyl methylcellulose, titanium dioxide (E-171), talc, macrogol 6000, iron oxide red (E-172), and iron oxide yellow (E-172).
Appearance of the product and content of the packaging
Eplerenona Normon 50 mg is presented in the form of film-coated tablets. They are cream-colored, round, biconvex, and have the imprint “50”. Each package contains 30 tablets.
Holder of the marketing authorization and responsible manufacturer
Laboratorios Normon, S.A.
Ronda de Valdecarrizo, 6 – 28760 Tres Cantos – Madrid (SPAIN)
OTHER PRESENTATIONS
EplerenonaNormon25 mg film-coated tablets EFG
This prospectus was approved in June 2015
The detailed and updated information on this medication is available on the website ofthe Spanish Agencyof Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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