Package Leaflet: Information for the User
Twicor 20mg/10mg film-coated tablets
rosuvastatin and ezetimibe
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
Twicor contains two different active substances in one film-coated tablet. One of the active substances is rosuvastatin, which belongs to a group of medicines called statins, the other active substance is ezetimibe.
Twicor is a medicine used in adult patients to lower high levels of cholesterol, the "bad" cholesterol (LDL cholesterol) and substances called triglycerides that circulate in the blood. It also raises the levels of the "good" cholesterol (HDL cholesterol). This medicine works by reducing cholesterol in two ways: it reduces the cholesterol absorbed in the gut and the cholesterol produced by the body itself.
For most people, high cholesterol does not affect how they feel, as it does not produce any symptoms. However, if left untreated, fatty deposits can build up in the walls of blood vessels and narrow them. Sometimes, these narrowed blood vessels can become blocked, cutting off the blood supply to the heart or brain, leading to a heart attack or stroke. By lowering cholesterol levels, you can reduce your risk of having a heart attack, stroke, or other health problems related to it.
This medicine is used in patients who cannot control their cholesterol levels by diet alone. While taking this medicine, you should follow a low-cholesterol diet. Your doctor may prescribe Twicor if you are already taking rosuvastatin and ezetimibe at the same dose level.
This medicine is used in patients with heart disease. Twicor reduces the risk of heart attack, stroke, surgery to increase blood flow to the heart, or hospitalization for chest pain.
This medicine will not help you lose weight.
Do not take Twicor if:
If you are in any of the above situations (or are unsure), consult your doctor.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Twicor if:
If you are in any of these situations mentioned above (or are unsure), consult your doctor or pharmacist before starting to take any dose of this medicine.
In a small number of people, statins can affect the liver. This is detected by a simple test that detects increased levels of liver enzymes in the blood. For this reason, your doctor will normally perform blood tests (liver function tests) during treatment with this medicine. It is essential that you go to the doctor for these tests.
While taking this medicine, your doctor will closely monitor you if you have diabetes or are at risk of developing diabetes. You are likely to be at risk of developing diabetes if you have high levels of sugar and fats in your blood, are overweight, and have high blood pressure.
Children and adolescents
This medicine is not recommended for use in children and adolescents under 18 years of age.
Other medicines and Twicor
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
Inform your doctor if you are taking any of the following medicines:
If you go to the hospital or receive treatment for another illness, tell the medical staff that you are taking Twicor.
Pregnancy and breast-feeding
Do not take Twicor if you are pregnant, think you may be pregnant, or plan to become pregnant. If you become pregnant while taking this medicine, stop taking it immediately and inform your doctor. Women must use contraceptive methods during treatment with this medicine.
Do not take Twicor if you are breast-feeding, as it is not known whether the medicine passes into breast milk.
Driving and using machines
This medicine is not expected to affect your ability to drive or use machines. However, some people may feel dizzy after taking this medicine. If you feel dizzy, do not drive or use machines.
Twicor contains sodium:this medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Follow the instructions for taking this medicine exactly as your doctor or pharmacist has told you. If you are unsure, consult your doctor or pharmacist again.
This medicine is not suitable for starting treatment. The start of treatment or dose adjustments, if necessary, should only be done by taking the active substances separately, and once the appropriate doses have been adjusted, it is possible to switch to the appropriate dose of Twicor.
You should follow a low-cholesterol diet and exercise while taking Twicor.
The recommended daily dose for adults is one film-coated tablet.
Take Twicor once a day.
You can take it at any time of day, regardless of meals. Take the medicine every day at the same time. Swallow the film-coated tablets whole with a glass of water.
Regular cholesterol level checks
It is essential that you regularly visit your doctor to have your cholesterol levels checked to ensure that your cholesterol levels have returned to normal and remain at appropriate levels.
If you take more Twicor than you should
Contact your doctor or the nearest hospital emergency department immediately, as you may need medical attention.
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 ingested.
If you forget to take Twicor
Do not worry, omit the missed dose and take the next scheduled dose at the planned time. Do not take a double dose to make up for missed doses.
If you stop taking Twicor
Consult your doctor if you want to stop taking this medicine. Your cholesterol levels may increase again if you stop taking this medicine.
If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
It is essential that you know what these side effects can be.
Stop taking Twicor and seek medical attention immediately if you experience any of the following side effects:
Rare side effects (may affect up to 1 in 1,000 people):
Allergic reactions such as swelling of the face, lips, tongue, and/or throat, which can cause difficulty breathing and swallowing, lupus-like syndrome (which includes skin rash, joint disorders, and effects on blood cells), and muscle rupture.
Unexplained muscle pain or cramp that lasts longer than expected. In rare cases, this can become a potentially life-threatening muscle damage known as rhabdomyolysis, leading to general discomfort, fever, and kidney failure.
Frequency not known (cannot be estimated from the available data):
Red patches on the trunk, red, target-like, or circular patches, often with central blisters, peeling of the skin, ulcers in the mouth, throat, nose, genitals, and eyes. These severe skin reactions can be preceded by fever and flu-like symptoms (Stevens-Johnson syndrome).
Widespread rash, high body temperature, and swollen lymph nodes (DRESS or drug hypersensitivity syndrome).
Other side effects
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
Rare side effects (may affect up to 1 in 1,000 people)
Very rare side effects (may affect up to 1 in 10,000 people)
Frequency not known (cannot be estimated from the available data)
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 difficulty breathing.
Reporting of side effects:
If you experience any side effects, talk to your doctor or pharmacist, even if it is possible side effects that are 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 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.
Do not use this medicine after the expiry date which is stated on the carton or blister after "EXP". The expiry date is the last day of the month shown.
Store in the original package to protect from light and moisture.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to a pharmacy for proper disposal. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Composition of Twicor
Rosuvastatin - Core
Pregelatinized starch (corn); Microcrystalline cellulose (E460); Meglumine; Dihydrate calcium hydrogen phosphate (E-341); Crospovidone (E-1202); Anhydrous colloidal silica (E-551); Sodium stearyl fumarate.
Ezetimibe - Core
Mannitol (E-421); Butylhydroxyanisole (E-320); Sodium lauryl sulfate (E-487); Croscarmellose sodium (E-468); Povidone (K-30) (E-1201); Red iron oxide (E-172); Magnesium stearate (E470 b); Sodium stearyl fumarate.
Coating
Hypromellose (E-464); Titanium dioxide (E-171); Macrogol 4000; Red iron oxide (E-172).
Product Appearance and Package Contents
Twicor 20 mg/10 mg are film-coated tablets of pink color, round, with a diameter of 10.7 mm, smooth on both sides.
Twicor is available in OPA/Al/PVC-Al blister packs of 10, 30, 60, 90 film-coated tablets.
Only some pack sizes may be marketed.
Marketing Authorization Holder
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
Dublin
Ireland
Manufacturer
Pharmadox Healthcare Ltd.
KW20A Kordin Industrial Park
Paola PLA3000
Malta
or
Mylan Hungary Kft.
Mylan utca 1
Komárom, 2900
Hungary
or
McDermott Laboratories Limited T/A Gerard Laboratories T/A Mylan Dublin
Unit 35/36 Baldoyle Industrial Estate
Grange Road
Dublin 13
Ireland
For further information about this medicinal product, please contact the local representative of the marketing authorization holder:
Viatris Pharmaceuticals, S.L.
C/ General Aranaz, 86
28027 - Madrid
Spain
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
ROSUVASTATINE/EZETIMIBE MYLAN HEALTHCARE Netherlands
ROSUVASTATINE/EZETIMIBE MYLAN Czech Republic
ROZOR
Bulgaria, Cyprus, Greece, Croatia, Hungary, Slovakia, Slovenia
ROZEIOND
Italy
TWICOR
Czech Republic, Denmark, Finland, France, Ireland, Malta, Portugal, Romania, United Kingdom, Spain
MYROSOR
Belgium, Luxembourg
Sorento
Poland
Date of last revision of this leaflet: May 2025
Detailed information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) https://www.aemps.gob.es/
The average price of TWICOR 20 mg/10 mg FILM-COATED TABLETS in October, 2025 is around 18.44 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.