EPLERENONE TARBIS 50 mg FILM-COATED TABLETS
How to use EPLERENONE TARBIS 50 mg FILM-COATED TABLETS
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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.
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Introduction
PACKAGE LEAFLET: INFORMATION FOR THE USER
Eplerenone Tarbis 50 mg film-coated tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
- Keep this leaflet, you may need to read it again.
- If you have any further questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
- If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.
Contents of the pack
- What Eplerenone Tarbis is and what it is used for
- What you need to know before you take Eplerenone Tarbis
- How to take Eplerenone Tarbis
- Possible side effects
- Storage of Eplerenone Tarbis
- Contents of the pack and other information
1. What Eplerenone Tarbis is and what it is used for
Eplerenone Tarbis belongs 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.
Eplerenone Tarbis is used to treat heart failure to prevent worsening and reduce hospitalization if you have
- A recent myocardial infarction, in combination with other medicines used to treat your heart failure or
- Mild persistent symptoms, despite the treatment you have been receiving so far.
2. What you need to know before you start taking Eplerenone Tarbis
Do not take Eplerenone Tarbis
- If you are hypersensitive (allergic) to eplerenone or any of the other ingredients of Eplerenone Tarbis.
- If you have high levels of potassium in your blood (hyperkalemia).
- If you are taking medicines that help eliminate excess fluid in the body (potassium-sparing diuretics) or "salt tablets" (potassium supplements).
- If you have severe kidney problems.
- If you have severe liver problems.
- If you are taking medicines used to treat fungal infections (ketoconazole or itraconazole).
- If you are taking antiviral medicines for the treatment of HIV (ritonavir or nelfinavir).
- If you are taking antibiotics used to treat bacterial infections (clarithromycin or telithromycin).
- If you are taking nefazodone for the treatment of depression.
- If you are taking medicines used to treat certain heart diseases or high blood pressure (such as ACE inhibitors and angiotensin receptor antagonists) at the same time.
Warnings and precautions
Consult your doctor or pharmacist before starting to take eplerenone:
- If you have kidney or liver disease (see "Do not take Eplerenone Tarbis")
- If you are taking lithium (used to treat manic-depressive disorders, also called bipolar disorder)
- If you are taking tacrolimus or cyclosporin (used to treat skin diseases such as psoriasis or eczema and to prevent organ transplant rejection)
Using Eplerenone Tarbis with other medicines
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
Eplerenone may affect other medicines. These, in turn, may affect the proper functioning of eplerenone.
Do not take Eplerenone Tarbis with the following medicines (see section "Do not use Eplerenone Tarbis"):
- Itraconazole or ketoconazole (used to treat fungal infections), ritonavir, nelfinavir (antiviral medicines for the treatment of AIDS), clarithromycin, telithromycin (used to treat bacterial infections), or nefazodone (used to treat depression), as these medicines reduce the metabolism of Eplerenone Tarbis, and thus prolong its effect in the body.
- Potassium-sparing diuretics (medicines that help eliminate excess fluid in the body) or potassium supplements (salt tablets), as these medicines increase the risk of high levels of potassium in the blood.
- ACE inhibitors and angiotensin receptor antagonists (used to treat high blood pressure, heart disease, or certain kidney diseases) at the same time, as these medicines may increase the risk of high levels of potassium in the blood.
Tell your doctor if you are taking any of the following medicines:
- Lithium (used to treat manic-depressive disorders, also called bipolar disorder). The use of lithium with diuretics and ACE inhibitors has been shown to cause high levels of lithium in the blood, which can cause the following adverse reactions: loss of appetite, vision changes, fatigue, muscle weakness, and muscle cramps.
- Cyclosporin or tacrolimus (used to treat skin diseases such as psoriasis or eczema and to prevent organ transplant rejection). These medicines can cause kidney problems and thus increase the risk of high levels of potassium in the blood.
- Non-steroidal anti-inflammatory drugs (NSAIDs - certain painkillers such as ibuprofen, used to relieve pain, stiffness, and inflammation). These medicines can cause kidney problems and thus increase the risk of high levels of potassium in the blood.
- Trimethoprim (used to treat bacterial infections) may increase the risk of high levels of potassium in the blood.
- Alpha-1 blockers, such as prazosin or alfuzosin (used to treat high blood pressure and certain prostate diseases), may lead to a decrease in blood pressure and dizziness when standing up.
- Tricyclic antidepressants such as amitriptyline or amoxapine (for the treatment of depression), antipsychotics (also known as neuroleptics) such as chlorpromazine or haloperidol (for the treatment of psychiatric disorders), amifostine (used during cancer chemotherapy), and baclofen (used to treat muscle spasms). These medicines may lead to a decrease in blood pressure and dizziness when standing up.
- Corticosteroids, such as hydrocortisone or prednisone (used to treat inflammation and certain skin diseases), and tetracosactide (mainly used to diagnose and treat adrenal cortex diseases), may reduce the blood pressure-lowering effect of Eplerenone Tarbis.
- Digoxin (used in the treatment of heart diseases). Blood levels of digoxin may increase when taken with Eplerenone Tarbis.
- Warfarin (an anticoagulant medicine): Caution is required when taking warfarin because high levels of warfarin in the blood may cause changes in the effect of Eplerenone Tarbis in the body.
- Erythromycin (used to treat bacterial infections), saquinavir (an antiviral medicine for the treatment of HIV infections), fluconazole (used to treat fungal infections), amiodarone, diltiazem, and verapamil (for the treatment of heart problems and high blood pressure) reduce the metabolism of Eplerenone Tarbis, thus prolonging its effect in the body.
- Hypericum perforatum or St. John's Wort (a medicinal plant), rifampicin (used to treat bacterial infections), carbamazepine, phenytoin, and phenobarbital (used, among others, to treat epilepsy) may increase the metabolism of Eplerenone Tarbis and thus reduce its effect.
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Taking Eplerenone Tarbis with food and drinks
Eplerenone Tarbis can be taken with or without food.
Pregnancy and breast-feeding
The effect of Eplerenone Tarbis during 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 breast-feeding or to stop treatment.
If you are pregnant or breast-feeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Driving and using machines
After taking Eplerenone Tarbis, you may feel dizzy. If this happens, do not drive or use machines.
Eplerenone Tarbis contains lactose
If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
3. How to take Eplerenone Tarbis
Follow exactly the administration instructions of Eplerenone Tarbis indicated by your doctor. Consult your doctor or pharmacist again if you have doubts.
The tablets of Eplerenone Tarbis can be taken with or without food. Swallow the tablets whole with plenty of water.
Eplerenone Tarbis is usually given together with other medicines for heart failure, for example, beta-blockers. The usual initial dose is one 25 mg tablet once a day, increasing later 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 levels in the blood should be measured before starting treatment with Eplerenone Tarbis, 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 potassium levels in the blood.
If you have mild kidney problems, you should start treatment with one 25 mg tablet per day, and if you have moderate kidney problems, you should start treatment with one 25 mg tablet every other day. These doses may be adjusted, if your doctor indicates, and according to your blood potassium levels.
Eplerenone Tarbis is 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 liver or kidney problems, it may be necessary to perform potassium blood tests more frequently (see also "Do not take Eplerenone Tarbis").
In elderly patients: no initial dose adjustment is required.
In children and adolescents: Eplerenone Tarbis is not recommended.
If you take more Eplerenone Tarbis than you should
If you take more Eplerenone Tarbis than you should, inform 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 Eplerenone Tarbis
If it is almost time to take the next tablet, skip the missed dose and take the next tablet at the corresponding time.
Otherwise, take the tablet as soon as you remember, provided that there are more than 12 hours left until the time to take the next tablet. Then, take your medicine as usual. Do not take a double dose to make up for the missed doses.
If you stop taking Eplerenone Tarbis
It is important to keep taking Eplerenone Tarbis as your doctor indicated, unless your doctor tells you to stop treatment. If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
4. Possible side effects
Like all medicines, Eplerenone Tarbis can cause side effects, although not everybody gets them.
If any of the following happen:
Seek medical attention immediately
- Swelling of the face, tongue, or throat
- Difficulty swallowing
- Blisters and difficulty breathing
These are symptoms of angioedema.
Other side effects reported include:
Common side effects(occur in 1 to 10 of every 100 patients):
- Myocardial infarction
- High levels of potassium in the blood (these symptoms include muscle cramps, diarrhea, nausea, dizziness, or headache)
- Dizziness
- Fainting
- Infection
- Cough
- Constipation
- Low blood pressure
- Diarrhea
- Nausea
- Abnormal kidney function
- Rash
- Itching
- Muscle spasms and pain
- Increased levels of urea in the blood
Uncommon side effects(occur in 1 to 10 of every 1,000 patients):
- Eosinophilia (increase in certain white blood cells)
- Dehydration
- High levels of cholesterol or triglycerides (fats) in the blood
- Low levels of sodium in the blood
- Insomnia (difficulty sleeping)
- Headache
- Heart problems such as irregular heartbeats, rapid heartbeats, and heart failure
- Inflammation of the gallbladder
- Low blood pressure that can cause dizziness when standing up
- Blood clots in the legs
- Sore throat
- Flatulence
- Vomiting
- Underactive thyroid
- Increased blood sugar levels
- Decreased sense of touch
- Increased sweating
- Back pain
- Weakness and general malaise
- Increased levels of creatinine in the blood, which may indicate kidney problems
- Kidney inflammation
- Enlargement of the breasts in men
- Changes in certain blood tests.
If you experience side effects, consult your doctor or pharmacist, even if it is a side effect not listed in this leaflet.
5. Storage of Eplerenone Tarbis
Keep this medicine out of the sight and reach of children.
Do not use Eplerenone Tarbis after the expiry date stated on the packaging after EXP. The expiry date is the last day of the month indicated.
No special storage conditions are required.
Medicines should not be disposed of via wastewater or household waste. Return the packaging and any unused medicine to a pharmacy for proper disposal. If you have any questions, ask your pharmacist. By doing this, you will help protect the environment.
6. Contents of the pack and other information
Composition of Eplerenone Tarbis
- The active substance is eplerenone. Each tablet contains 50 mg of eplerenone.
- The other ingredients are lactose monohydrate, microcrystalline cellulose (type 101), sodium croscarmellose, hypromellose (type 2910), microcrystalline cellulose (type 102), sodium lauryl sulfate, talc, magnesium stearate (core of the tablet);
Opadry II. white OY-L-28900: lactose monohydrate, hypromellose (Type 2910), titanium dioxide (E171), macrogol 4000 (tablet coating).
Appearance of the product and contents of the pack
50 mg tablet: white to almost white, round, biconvex, film-coated tablets marked "CG4" on one face of the tablet and smooth (unmarked) on the other face.
Eplerenone Tarbis 50 mg film-coated tablets EFG are available in blister packs of 30 and 50 tablets.
Marketing authorization holder and manufacturer
Marketing authorization holder:Tarbis Farma, S.L.
Gran Via Carlos III, 94
08028 Barcelona
Manufacturer:
Laboratorios LICONSA S.A.
Avenida Miralcampo 7, Polígono Industrial Miralcampo
19200 Azuqueca de Henares, Guadalajara
Spain
Date of the last revision of this leaflet:August 2012
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS)http://www.aemps.gob.es/
- Country of registration
- Average pharmacy price53.34 EUR
- Active substance
- Prescription requiredYes
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
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