Rosuvastatin + Ezetimibe
Ezehron Duo contains two different active substances in one tablet. One of the active substances is rosuvastatin, which belongs to a group of medicines known as statins, and the other active substance is ezetimibe. Ezehron Duo is used to lower the level of cholesterol in the blood, specifically "bad" cholesterol (LDL cholesterol) and a type of fat called triglycerides, and to increase the level of "good" cholesterol (HDL cholesterol). The medicine works in two ways: it reduces the amount of cholesterol absorbed in the gut and the amount of cholesterol produced in the body. In most people, high cholesterol does not affect their well-being, as it does not cause any symptoms. However, if left untreated, it can cause fatty deposits to build up in the walls of blood vessels, leading to their narrowing. As a result of the narrowing, it is possible for the blood vessel to become blocked, cutting off blood flow to the heart or brain, which can lead to a heart attack or stroke. By lowering cholesterol levels, the risk of heart attack, stroke, or other similar health problems can be reduced. Ezehron Duo is used in patients for whom diet alone is not enough to maintain a healthy cholesterol level. During treatment with this medicine, the patient should continue to follow a low-cholesterol diet. The doctor may prescribe Ezehron Duo if the patient is already taking rosuvastatin and ezetimibe in the same doses as in the combination medicine. The medicine is used in patients with:
Ezehron Duo does not help with weight loss.
If any of the above situations apply to the patient (or if the patient is unsure), they should consult their doctor.
If any of the above situations apply to the patient (or if the patient is unsure), they should consult their doctor again.
Before taking Ezehron Duo, the patient should discuss it with their doctor or pharmacist if:
the patient has kidney problems; the patient has liver problems; the patient has experienced recurring or unexplained muscle pain, or if they or their family members have had muscle diseases or have had muscle problems while taking other cholesterol-lowering medicines. If the patient experiences unexplained muscle pain, especially if accompanied by a feeling of illness or fever, they should immediately consult their doctor. The patient should also inform their doctor or pharmacist about persistent muscle weakness; the patient is of Asian origin (Japanese, Chinese, Filipino, Vietnamese, Korean, or Indian). The doctor will determine the appropriate dose of Ezehron Duo for the patient; the patient is taking antiviral medicines, including those used to treat HIV or hepatitis C infection, such as ritonavir with lopinavir and/or atazanavir or simeprevir (see "Ezehron Duo and other medicines"); the patient has severe respiratory failure; the patient is taking other cholesterol-lowering medicines, such as fibrates. The patient should read the leaflet carefully, even if they have taken other cholesterol-lowering medicines before; the patient regularly consumes large amounts of alcohol; the patient has been diagnosed with hypothyroidism (underactive thyroid); the patient is over 70 years old (as the doctor will need to choose a suitable dose of Ezehron Duo); the patient is taking or has taken fusidic acid (an antibiotic) in the last 7 days. Taking fusidic acid and Ezehron Duo at the same time may lead to serious muscle problems (rhabdomyolysis); the patient has or has had myasthenia gravis (a disease that causes general muscle weakness, including muscles involved in breathing) or ocular myasthenia (a disease that causes muscle weakness in the eyes), as statins may sometimes worsen the symptoms of the disease or lead to the development of myasthenia (see section 4); the patient has ever experienced a severe skin rash or skin peeling after taking rosuvastatin or other similar medicines. If any of the above situations apply to the patient (or if the patient is unsure), they should not take Ezehron Duo, 40 mg + 10 mg (the highest dose), and should consult their doctor or pharmacist before starting treatment with Ezehron Duo. In rare cases, statins may affect liver function. This can be detected by a simple blood test that checks for increased liver enzyme activity. Therefore, the doctor will recommend regular blood tests while taking Ezehron Duo. It is essential for the patient to attend these tests as scheduled. During treatment with this medicine, the doctor will closely monitor patients with diabetes or at risk of developing diabetes. There is a high risk of developing diabetes if the patient has high blood sugar and fat levels, is overweight, and has high blood pressure. Rosuvastatin has been associated with the development of severe skin reactions, including Stevens-Johnson syndrome and drug reaction with eosinophilia and systemic symptoms (DRESS). If the patient experiences any of the symptoms described in section 4, they should stop taking Ezehron Duo and seek medical attention immediately.
Ezehron Duo should not be used in children and adolescents under 18 years of age.
The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take. The patient should tell their doctor about taking any of the following medicines:
If the patient is to be hospitalized or treated for another condition, they should inform the medical staff that they are taking Ezehron Duo.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a baby, they should consult their doctor or pharmacist before taking this medicine.
Ezehron Duo should not be takenif the patient is pregnant, trying to become pregnant, or thinks they may be pregnant. If the patient becomes pregnant while taking Ezehron Duo, they should stop taking the medicine immediatelyand inform their doctor. During treatment with Ezehron Duo, women should use effective methods of contraception (see "Pregnancy and breastfeeding").
Ezehron Duo should not be takenduring breastfeeding, as it is not known whether the medicine passes into breast milk.
Ezehron Duo is unlikely to affect the patient's ability to drive or use machines. However, the patient should be aware that Ezehron Duo may cause dizziness. In this case, the patient should consult their doctor before driving or using machines.
If the patient has been diagnosed with intolerance to some sugars, they should consult their doctor before taking Ezehron Duo.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially "sodium-free".
This medicine should always be taken exactly as prescribed by the doctor or pharmacist. In case of doubt, the patient should consult their doctor or pharmacist. During treatment with Ezehron Duo, the patient should continue to follow a low-cholesterol diet and maintain physical activity. The recommended daily dose for adults is one tablet of the prescribed strength.
The medicine can be taken at any time of day, with or without food. The tablets should be swallowed whole, with a glass of water. The patient should take the medicine at the same time every day. Ezehron Duo is not suitable for starting treatment. If treatment is started or the dose needs to be changed, the patient should take each active substance separately and then switch to Ezehron Duo at the prescribed strength. The maximum daily dose of rosuvastatin is 40 mg, which is used in patients with high cholesterol levels and a high risk of heart attack or stroke, for whom a dose of 30 mg was not sufficient to lower cholesterol levels.
It is essential for the patient to attend regular check-ups with their doctor to ensure that their cholesterol levels are under control.
In case of overdose, the patient should consult their doctor or the emergency department of the nearest hospital, as medical attention may be necessary.
If the patient misses a dose, they should take the next tablet at the scheduled time. The patient should not take a double dose to make up for the missed dose.
The patient should inform their doctor if they want to stop taking Ezehron Duo. After stopping Ezehron Duo, cholesterol levels may rise again. If the patient has any further doubts about taking this medicine, they should consult their doctor or pharmacist.
Like all medicines, Ezehron Duo can cause side effects, although not everybody gets them. It is essential for the patient to know what side effects may be associated with taking Ezehron Duo. The patient should stop taking Ezehron Duo and seek medical attention immediatelyif they experience any of the following:
The patient should consult their doctor immediatelyif they experience any unusual, persistent muscle pain. This condition may rarely progress to a life-threatening muscle injury (known as rhabdomyolysis), causing illness, fever, and kidney problems. To determine the frequency of side effects, the following classification has been used:
headache; constipation; nausea; muscle pain; muscle tenderness; feeling weak; dizziness; increased protein in the urine. This usually resolves on its own and does not require stopping Ezehron Duo (only applies to the 40 mg dose of rosuvastatin); diabetes - this is more likely in patients with high blood sugar and fat levels, who are overweight, and have high blood pressure. The doctor will monitor the patient's condition during treatment with this medicine; stomach pain; diarrhea; bloating (excess gas in the intestines); feeling tired; increased results of some blood tests that assess liver function (aminotransferase activity)
rash, itching, hives; increased protein in the urine, which usually resolves on its own, without the need to stop taking Ezehron Duo (applies to the 15 mg and 30 mg doses of rosuvastatin); increased results of some blood tests that assess muscle condition (creatine kinase activity); cough; indigestion; heartburn; nausea; joint pain; muscle spasms; neck pain; decreased appetite; pain; chest pain; hot flushes; high blood pressure; tingling; dry mouth; stomach inflammation; back pain; muscle weakness; pain in the arms and legs; swelling, especially of the hands and feet
pancreatitis, causing severe abdominal pain that may radiate to the back; increased tendency to bleed or bruising due to low platelet count.
jaundice (yellowing of the skin and eyes); liver inflammation; trace amounts of blood in the urine; nerve damage in the arms and legs (e.g., numbness); memory loss; breast enlargement in men (gynecomastia)
shortness of breath; swelling; sleep disorders, including insomnia and nightmares; sexual disorders; depression; respiratory disorders, including persistent cough and/or shortness of breath or fever; tendon damage; persistent muscle weakness; red, raised rash, sometimes with lesions in a target shape (erythema multiforme); muscle tenderness; gallstones or cholecystitis (which can cause abdominal pain, nausea, vomiting); myasthenia gravis (a disease that causes general muscle weakness, including muscles involved in breathing); ocular myasthenia (a disease that causes muscle weakness in the eyes); The patient should talk to their doctor if they experience weakness in their arms or legs, worsening after periods of activity, double vision, or drooping eyelids, difficulty swallowing, or shortness of breath.
If the patient experiences any side effects, including any side effects not listed in the leaflet, they should inform their doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, more information can be collected on the safety of the medicine.
The medicine should be stored in its original packaging to protect it from light. There are no special storage temperature requirements. The medicine should be kept out of sight and reach of children. Do not use this medicine after the expiry date stated on the carton and blister pack after EXP. The expiry date refers to the last day of the month. Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substances of Ezehron Duo are rosuvastatin (in the form of rosuvastatin calcium) and ezetimibe. The tablets contain rosuvastatin calcium equivalent to 15 mg, 30 mg, or 40 mg of rosuvastatin. Each tablet contains 10 mg of ezetimibe. The other ingredients are lactose monohydrate, microcrystalline cellulose type 102, sodium croscarmellose, crospovidone type A, povidone K-30, sodium lauryl sulfate, and magnesium stearate.
Ezehron Duo, 15 mg + 10 mg: white or almost white, hexagonal, biconvex, uncoated tablet, approximately 9 x 8 mm in size, with a double-sided engraving "E3". Ezehron Duo, 30 mg + 10 mg tablets: white or almost white, biconvex, uncoated tablet, rectangular in shape, approximately 12 x 6 mm in size, with a double-sided engraving "X". Ezehron Duo, 40 mg + 10 mg tablets: white or almost white, elliptical, biconvex, uncoated tablet, approximately 13 x 6 mm in size, with a double-sided engraving "E6". The packaging contains 28, 30, 56, 60, 90, or 100 tablets in a blister pack of PA/Aluminum/PVC/Aluminum foil, placed in a cardboard box with a patient information leaflet. Not all pack sizes may be marketed.
Adamed Pharma S.A., Pieńków, ul. M. Adamkiewicza 6A, 05-152 Czosnów, tel.: +48 22 732 77 00
Adamed Pharma S.A., ul. Marszałka J. Piłsudskiego 5, 95-200 Pabianice
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