


Ask a doctor about a prescription for EZETIMIBE/SIMVASTATIN RATIO 10 mg/20 mg TABLETS
Package Leaflet: Information for the User
Ezetimibe/Simvastatinratio10 mg/20 mg EFG tablets
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the package leaflet
This medicine contains the active substances ezetimibe and simvastatin. It is used to reduce the levels of total cholesterol, "bad" cholesterol (LDL cholesterol) and substances called triglycerides in the blood. It also increases the levels of "good" cholesterol (HDL cholesterol).
Ezetimibe/simvastatin works by reducing cholesterol in two ways. The active substance ezetimibe reduces the cholesterol absorbed in the gut. The active substance simvastatin, which belongs to a group of medicines called "statins", inhibits the production of cholesterol made by the body itself.
Cholesterol is one of the fatty substances that occur naturally in the blood. Your total cholesterol level is made up mainly of LDL and HDL cholesterol.
LDL cholesterol is often called "bad" cholesterol because it can build up in the walls of your arteries, forming plaques. Over time, this can lead to a narrowing of the arteries. This narrowing can reduce or completely block the flow of blood to vital organs such as the heart and brain. This blockage can cause a heart attack or stroke.
HDL cholesterol is often called "good" cholesterol because it helps prevent "bad" cholesterol from building up in the arteries and protects against heart disease.
Triglycerides are another type of fat in the blood that can increase the risk of heart disease.
Ezetimibe/simvastatin is used in patients who cannot control their cholesterol levels by diet alone. While taking this medicine, you should also follow a low-cholesterol diet.
Ezetimibe/simvastatin is used, along with a low-cholesterol diet, if you have:
This medicine does not help you lose weight.
Do not take Ezetimibe/Simvastatin ratio if
Do not take more than 10/40 mg of ezetimibe/simvastatin if you are taking lomitapide (used to treat rare and severe genetic cholesterol disorders).
Consult your doctor if you are not sure if your medicine is mentioned above.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Ezetimibe/Simvastatin ratio:
Your doctor will do a blood test before you start taking ezetimibe/simvastatin and also if you have any symptoms of liver problems while taking ezetimibe/simvastatin. This is to check how well your liver is working.
Your doctor may also want to do blood tests to check how well your liver is working after you start treatment with ezetimibe/simvastatin.
While you are taking this medicine, your doctor will check if you have diabetes or are at risk of developing diabetes. This risk of diabetes increases if you have high levels of sugars and fats in the blood, are overweight and have high blood pressure.
Talk to your doctor if you have severe lung disease.
The combined use of ezetimibe/simvastatin and fibrates (certain medicines used to lower cholesterol) should be avoided, as the combined use of ezetimibe/simvastatin and fibrates has not been studied.
Tell your doctor immediately if you experience muscle pain, tenderness or weakness. This is because, on rare occasions, muscle problems can be serious, including muscle breakdown, which can cause kidney damage; and very rarely, deaths have occurred.
The risk of muscle breakdown is greater with higher doses of ezetimibe/simvastatin, especially the 10/80 mg dose. The risk of muscle breakdown is also greater in certain patients. Tell your doctor in the following situations:
Also, tell your doctor or pharmacist if you experience persistent muscle weakness. Further tests and additional medications may be needed to diagnose and treat this problem.
Children and adolescents
Taking Ezetimibe/Simvastatin ratio with other medicines
Tell your doctor if you are taking, have recently taken or might take any other medicines with any of the following active substances. Taking ezetimibe/simvastatin with any of the following medicines can increase the risk of muscle problems (some of these are already included in the "Do not take Ezetimibe/Simvastatin ratio if" section).
As well as the medicines mentioned above, tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including those obtained without a prescription. In particular, tell your doctor if you are taking any of the following:
You should also tell any doctor who prescribes you a new medicine that you are taking ezetimibe/simvastatin.
Taking Ezetimibe/Simvastatin ratio with food and drink
Grapefruit juice contains one or more components that alter the metabolism of some medicines, including ezetimibe/simvastatin. You should avoid drinking grapefruit juice, as it can increase the risk of muscle problems.
Pregnancy and breast-feeding
Do not take ezetimibe/simvastatin if you are pregnant, trying to become pregnant or think you may be pregnant. If you become pregnant while taking ezetimibe/simvastatin, stop taking it immediately and tell your doctor. Do not take ezetimibe/simvastatin if you are breast-feeding, as it is not known whether this medicine passes into breast milk.
Consult your doctor or pharmacist before taking any medicine.
Driving and using machines
Ezetimibe/simvastatin is not expected to affect your ability to drive or use machines. However, it should be noted that some people experience dizziness after taking ezetimibe/simvastatin.
Ezetimibe/Simvastatin ratio contains lactose
If your doctor has told you that you have an intolerance to some sugars, consult him before taking this medicine.
Ezetimibe/Simvastatin ratio contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is essentially "sodium-free".
Your doctor will determine the appropriate dose of tablets for you, depending on your current treatment and your personal risk situation.
The tablets are not scored and should not be divided.
Follow exactly the instructions of administration of this medicine indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Adults: the dose is 1 tabletof ezetimibe/simvastatin once a day by mouth.
Use in adolescents(10 to 17 years of age): the dose is 1 tabletof ezetimibe/simvastatin once a day by mouth (do not exceed a maximum dose of 10 mg/40 mg once a day).
The dose of ezetimibe/simvastatin 10 mg/80 mg is only recommended for adult patients with very high cholesterol levels and a high risk of heart disease who have not reached the treatment goal with lower doses.
Take ezetimibe/simvastatin in the evening. You can take it with or without food.
If your doctor has prescribed ezetimibe/simvastatin along with another cholesterol-lowering medicine that contains the active substance cholestyramine or any other bile acid sequestrant, you should take ezetimibe/simvastatin at least 2 hours before or 4 hours after taking the bile acid sequestrant.
If you take more Ezetimibe/Simvastatin ratio than you should
In case of overdose or accidental ingestion, consult the Toxicology Information Service. Telephone: 91 562 04 20, consult your doctor or pharmacist
If you forget to take Ezetimibe/Simvastatin ratio
Do not take a double dose to make up for forgotten doses, take your normal dose of Ezetimibe/Simvastatin ratio at the usual time
If you stop taking Ezetimibe/Simvastatin ratio
Talk to your doctor or pharmacist because your cholesterol levels may increase again.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them (see section 2 "What you need to know before taking Ezetimibe/Simvastatin ratio").
The following frequent adverse effects have been reported (may affect up to 1 in 10 people):
The following infrequent adverse effects have been reported (may affect up to 1 in 100 people):
Additionally, the following adverse effects have been reported in people taking ezetimibe/simvastatin or medications containing the active ingredients ezetimibe or simvastatin:
The following additional adverse events have been reported with some statins:
Consult your doctor immediately if you experience pain, sensitivity to pressure, or unexplained muscle weakness. This is because, in rare cases, muscle problems can be serious, including muscle failure, which can cause kidney damage; and very rarely, deaths have occurred.
Consult your doctor if you experience weakness in the arms or legs that worsens after periods of activity, double vision, or drooping eyelids, difficulty swallowing, or difficulty breathing.
Reporting of Adverse Effects:
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect that is not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children
Do not use this medicine after the expiration date stated on the box, bottle, or blisters after [CAD]. The expiration date is the last day of the month indicated.
Do not store above 25°C.
Medicines should not be disposed of via wastewater or household waste. Deposit the packaging and any unused medicines in the SIGRE collection point at the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and any unused medicines. This will help protect the environment.
Composition of Ezetimibe/Simvastatin ratio 10 mg/ 20 mg
Appearance of the Product and Package Contents
Ezetimibe/Simvastatin ratio 10 mg/ 20 mg EFG tablets are round, biconvex, light brown, speckled tablets, 8 mm in diameter, engraved with "512" on one side.
Package sizes:
Blister pack:
28, 30, 50, 90, 98, and 100 tablets
HDPE bottle:
28, 30, 90, and 100 tablets.
The HDPE bottles contain a desiccant capsule. This capsule should not be removed from the bottle.
Not all package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Holder
ratiopharm España, S.A.
C/Anabel Segura, 11. Edificio Albatros B, 1ª planta.
Alcobendas, 28108 - Madrid
Manufacturer
Balkanpharma-Dupnitsa AD
3 Samokovsko Shosse Str., Dupnitsa 2600
Bulgaria
Date of the Last Revision of this Leaflet:April 2021
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/
The average price of EZETIMIBE/SIMVASTATIN RATIO 10 mg/20 mg TABLETS in December, 2025 is around 32.72 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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