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Package Leaflet: Information for the Patient
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/10 mg
film-coated tablets EFG
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/20 mg
film-coated tablets EFG
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/40 mg
film-coated tablets EFG
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/80 mg
film-coated tablets EFG
ezetimibe/atorvastatin
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Ezetimibe/Atorvastatin Sandoz Pharmaceutical is a medicine that lowers high cholesterol levels. Ezetimibe/Atorvastatin Sandoz Pharmaceutical contains ezetimibe and atorvastatin.
Ezetimibe/atorvastatin is used in adults to lower the levels of total cholesterol, "bad" cholesterol (LDL cholesterol) and certain fats (triglycerides) that are found in the blood. It also raises the levels of "good" cholesterol (HDL cholesterol).
Ezetimibe/atorvastatin works by reducing cholesterol in two ways. It reduces the amount of cholesterol absorbed in the gut and the amount of cholesterol produced by the body.
Cholesterol is one of the fatty substances that can be found in the bloodstream. Your total cholesterol 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, which can reduce or block the flow of blood to vital organs such as the heart and brain. This blocking of the flow of blood can lead to 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 found in the blood that can increase the risk of heart disease.
Ezetimibe/atorvastatin is used in patients who cannot control their cholesterol levels by diet alone. While you are taking this medicine, you should also follow a low-cholesterol diet.
Ezetimibe/atorvastatin is used in addition to your diet to lower cholesterol if you have:
Ezetimibe/atorvastatin does not help you lose weight.
Do not take Ezetimibe/Atorvastatin Sandoz Pharmaceutical if:
Warnings and precautions
Tell your doctor or pharmacist before you start taking ezetimibe/atorvastatin if:
Contact your doctor as soon as possible if you experience unexplained muscle pain, tenderness or weakness while taking ezetimibe/atorvastatin.This is because, on rare occasions, muscle problems can be serious, including muscle breakdown resulting in kidney damage. Atorvastatin can cause muscle problems and muscle problems have also been reported with ezetimibe.
Also, tell your doctor or pharmacist if you experience persistent muscle weakness. You may need further tests and additional medicines to diagnose and treat this condition.
Tell your doctor or pharmacist before you start taking ezetimibe/atorvastatin:
If you are in any of the above situations (or are unsure), consult your doctor or pharmacist before taking ezetimibe/atorvastatin, as your doctor will need to perform a blood test before starting your treatment and possibly during treatment to predict the risk of muscle side effects. It is known that the risk of muscle side effects, e.g. rhabdomyolysis (breakdown of skeletal muscle tissue), increases when certain medicines are taken at the same time (see section 2 "Other medicines and Ezetimibe/Atorvastatin Sandoz Pharmaceutical").
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 sugar and fats in the blood, are overweight, and have high blood pressure.
Tell your doctor about all your medical problems, including allergies.
The combined use of ezetimibe/atorvastatin and fibrates (medicines used to lower cholesterol) should be avoided, as the combined use of ezetimibe/atorvastatin and fibrates has not been studied.
Children
Ezetimibe/atorvastatin is not recommended for children and adolescents.
Other medicines and Ezetimibe/Atorvastatin Sandoz Pharmaceutical
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including those obtained without a prescription.
There are some medicines that can affect the way ezetimibe/atorvastatin works, or their effects can be altered by ezetimibe/atorvastatin (see section 3). This type of interaction could decrease the effectiveness of one or both medicines. On the other hand, it could also increase the risk or severity of side effects, including a serious disorder in which muscle tissue is destroyed, known as "rhabdomyolysis", which is described in section 4:
**If you have to take fusidic acid by mouth to treat a bacterial infection, you will have to stop using this medicine temporarily. Your doctor will tell you when you can restart treatment with ezetimibe/atorvastatin. The use of this medicine with fusidic acid can rarely cause muscle weakness, tenderness, or pain (rhabdomyolysis). For more information on rhabdomyolysis, see section 4.
Taking Ezetimibe/Atorvastatin Sandoz Pharmaceutical with food and alcohol
See section 3 for instructions on how to take ezetimibe/atorvastatin. Please note the following:
Grapefruit juice
Do not drink more than one or two small glasses of grapefruit juice per day, as large amounts of grapefruit juice can alter the effects of ezetimibe/atorvastatin.
Alcohol
Avoid excessive alcohol consumption while taking this medicine. For more details, see section 2 "Warnings and precautions".
Pregnancy and breast-feeding
Do not take ezetimibe/atorvastatin if you are pregnant, think you may be pregnant, or are planning to become pregnant. Do not take ezetimibe/atorvastatin if you can become pregnant, unless you use reliable contraception. If you become pregnant while taking ezetimibe/atorvastatin, stop taking it immediately and tell your doctor.
Do not take ezetimibe/atorvastatin if you are breast-feeding.
The safety of ezetimibe/atorvastatin during pregnancy and breast-feeding has not been established.
Ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines
Ezetimibe/atorvastatin 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/atorvastatin.
Ezetimibe/Atorvastatin10mg/10mg, 10mg/20mg, and 10 mg/40 mg
Ezetimibe/Atorvastatin Sandoz Pharmaceuticalcontains lactose
The tablets of Ezetimibe/Atorvastatin Sandoz Pharmaceutical contain a sugar called lactose. If your doctor has told you that you have an intolerance to some sugars, contact them before taking this medicine.
Ezetimibe/Atorvastatin Sandoz Pharmaceutical contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Follow the instructions for administration of this medicine exactly as told by your doctor. Your doctor will determine the appropriate dose of tablets for you, depending on your current treatment and your personal risk situation. If in doubt, consult your doctor or pharmacist again.
How much to take
The recommended dose is one ezetimibe/atorvastatin tablet by mouth once a day.
When to take it
Take ezetimibe/atorvastatin at any time of the day. You can take it with or without food.
If your doctor has prescribed ezetimibe/atorvastatin with colestyramine or any other bile acid sequestrant (medicines that lower cholesterol levels), you should take ezetimibe/atorvastatin at least 2 hours before or 4 hours after taking the bile acid sequestrant.
If you take more Ezetimibe/Atorvastatin Sandoz Pharmaceutical than you should
Consult your doctor or pharmacist.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, telephone: 91 562 04 20, indicating the medicine and the amount taken.
If you forget to take Ezetimibe/Atorvastatin Sandoz Pharmaceutical
Do not take a double dose to make up for forgotten doses. Take the normal dose at the usual time the next day.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
If you experience any of the following serious adverse effects or symptoms, stop taking your tablets and inform your doctor immediately, or go to the emergency department of the nearest hospital.
Consult your doctor as soon as possible if you experience problems associated with the unexpected or unusual appearance of bleeding or bruising, as this fact may be indicative of liver disease.
The following frequent adverse effects were reported (may affect up to 1 in 10 people):
The following infrequent adverse effects were reported (may affect up to 1 in 100 people):
Additionally, the following adverse effects have been reported in people taking ezetimibe/atorvastatin, or ezetimibe or atorvastatin tablets alone:
Possible adverse effects observed with some statins:
Consult your doctor if you experience weakness in your arms or legs that worsens after periods of activity, double vision, or drooping eyelids, difficulty swallowing, or breathing difficulties.
Adverse Effect Reporting
If you experience any type of adverse effect, consult your doctor or pharmacist, 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 that appears on the packaging after CAD/EXP. The expiration date is the last day of the month indicated.
This medicine does not require special storage conditions.
Medicines should not be thrown away through wastewater or household waste. Deposit the packaging and medicines you no longer need at the SIGRE Point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medicines you no longer need. This way, you will help protect the environment.
Composition ofEzetimibe/Atorvastatin Sandoz Pharmaceutical
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/10 mg: each film-coated tablet contains 10 mg of ezetimibe and 10 mg of atorvastatin (as atorvastatin calcium trihydrate).
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/20 mg: each film-coated tablet contains 10 mg of ezetimibe and 20 mg of atorvastatin (as atorvastatin calcium trihydrate).
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/40 mg: each film-coated tablet contains 10 mg of ezetimibe and 40 mg of atorvastatin (as atorvastatin calcium trihydrate).
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/80 mg: each film-coated tablet contains 10 mg of ezetimibe and 80 mg of atorvastatin (as atorvastatin calcium trihydrate).
The other components are:
Tablet core:
Microcrystalline cellulose 101 (E460), mannitol (E421), calcium carbonate (E170), sodium croscarmellose (E468), hydroxypropylcellulose (E463), polysorbate 80 (E433), yellow iron oxide (E172), magnesium stearate (E470b), povidone K29/32 (E1201), sodium lauryl sulfate (E487).
Tablet coating
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/10 mg, 10 mg/20 mg, 10 mg/40 mg:
Opadry white OY-L28900 consisting of:
Lactose monohydrate,
Hypromellose 2910 (E464),
Titanium dioxide (E171),
Macrogol 4000 (E1521).
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/80 mg: DrCoat FCU consisting of:
Hypromellose 2910,
Titanium dioxide (E171),
Talc (E553b),
Macrogol 400,
Yellow iron oxide (E172).
Product Appearance and Package Contents
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/10 mg:
white, round, biconvex film-coated tablets with a diameter of approximately 8.1 mm.
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/20 mg:
white, oval, biconvex film-coated tablets with dimensions of approximately 11.6 x 7.1 mm.
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/40 mg:
white, capsule-shaped, biconvex film-coated tablets with dimensions of approximately 16.1 x 6.1 mm.
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/80 mg:
yellow, oblong, biconvex film-coated tablets with dimensions of approximately 19.1 x 7.6 mm.
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/10 mg, 10 mg/20 mg, 10 mg/40 mg:
Packaging of 30, 90, and 100 film-coated tablets in OPA/Al/PVC//Al blisters.
Packaging of 30x1, 90x1, and 100x1 film-coated tablets in single-dose OPA/Al/PVC//Al blisters.
Ezetimibe/Atorvastatin Sandoz Pharmaceutical 10 mg/80 mg:
Packaging of 30, multiple packaging of 90 (2 packages of 45) and 100 (2 packages of 50) film-coated tablets in OPA/Al/PVC//Al blisters.
Packaging of 30x1, multiple packaging of 90x1 (2 packages of 45x1) and 100x1 (2 packages of 50x1) film-coated tablets in OPA/Al/PVC//Al blisters.
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Sandoz Farmacéutica, S.A.
Centro Empresarial Parque Norte
Edificio Roble
C/ Serrano Galvache, 56
28033 Madrid
Spain
Manufacturer
ELPEN Pharmaceutical Co. Inc.
Marathonos Avenue 95
Pikermi Attiki, 19009
Greece
or
Lek Pharmaceuticals d.d
Verovskova ulica 57
1526 Ljubljana
Slovenia
or
ELPEN Pharmaceutical Co. Inc.
Zapani, Block 1048,
Keratea, 190 01
Greece
Date of the Last Revision of this Leaflet:March 2024
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es.
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