Product Information for the Patient
Arrox Plus 10 mg/10 mg Film-Coated Tablets
Arrox Plus 20 mg/10 mg Film-Coated Tablets
Arrox Plus 40 mg/10 mg Film-Coated Tablets
rosuvastatina/ezetimiba
Read this entire product information carefully before starting to take this medicine, as it contains important information for you.
Arrox Plus contains two different active principles in a film-coated tablet. One of the active principles is rosuvastatina, which belongs to the group of medications known as statins; the other active principle is ezetimiba.
Arrox Plus is a medication used in adult patients to reduce total cholesterol, "bad" cholesterol (LDL cholesterol), and certain fatty substances called triglycerides that circulate in the blood. Additionally, rosuvastatina/ezetimiba increases the concentrations of "good" cholesterol (HDL cholesterol).
Rosuvastatina/ezetimiba acts by reducing cholesterol in two ways. It reduces the cholesterol absorbed in the digestive tract as well as the cholesterol produced by the body itself.
Cholesterol is one of the many fatty substances that circulate in the blood. The total amount of cholesterol is composed mainly of LDL and HDL cholesterol.
For most people, high levels of cholesterol do not affect how they feel since they do not produce any symptoms. However, if left untreated, fatty deposits can accumulate in the walls of blood vessels and narrow them.
Sometimes, these narrowed blood vessels can become blocked, cutting off blood supply to the heart or brain, which would cause a heart attack or stroke. By reducing cholesterol levels, the risk of having a heart attack, stroke, or other related health problems can be reduced.
Rosuvastatina/ezetimiba is used in patients who cannot control their cholesterol levels solely with diet. While taking this medication, you must follow a cholesterol-reducing diet.Your doctor may prescribe this medication if you are already taking rosuvastatina and ezetimiba at the same dosage level.
Rosuvastatina/ezetimiba is used in combination with your cholesterol-reducing diet if you have:
This medication does not help with weight loss.
You must continue taking this medication, even if your cholesterol levels are within the normal range, as it prevents your cholesterol levels from rising again and causing the accumulation of fatty deposits.
However, you should stop taking it if your doctor instructs you to do so or if you are pregnant.
Do not take Arrox Plus if:
Also, do not take Arrox Plus 40 mg/10 mg (the highest dose):
If you find yourself in any of the above situations (or are unsure), consult your doctor.
Warnings and precautions
Consult your doctor or pharmacist before starting to take this medication if:
If you find yourself in any of these situations mentioned above (or are unsure): consult your doctor or pharmacist before starting to take any dose of this medication.
In a reduced 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 test) during treatment with this medication. It is essential that you visit your doctor for the tests.
While taking this medication, your doctor will closely monitor you if you have diabetes or are at risk of developing diabetes. You may be at risk of developing diabetes if you have high blood sugar and fat levels, are overweight, and have high blood pressure.
Severe skin reactions, including Stevens-Johnson syndrome and drug reaction with eosinophilia and systemic symptoms (DRESS), have been reported in association with rosuvastatin treatment. Stop using this medication and seek medical attention immediately if you notice any of the symptoms described in section 4.
Children and adolescents
The use of this medication is not suitable for children and adolescents under 18 years of age.
Other medications and Arrox Plus
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Inform your doctor if you are taking any of the following medications:
If you visit a hospital or receive treatment for another condition, inform the medical staff that you are taking this medication.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Do not take Arrox Plus if you are pregnant, think you may be pregnant, or intend to become pregnant. If you become pregnant while taking this medication, stop taking it immediately and inform your doctor. Women should use contraceptive methods during treatment with this medication.
Do not take Arrox Plus if you are breastfeeding, as it is unknown whether the medication passes into breast milk.
Driving and operating machinery
This medication is not expected to interfere with your ability to drive or operate machinery. However, some people may feel dizzy after taking this medication. If you feel dizzy, do not drive or operate machinery.
Arrox Plus contains lactose and sodium
This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
This medication contains less than 23 mg of sodium (1 mmol) per tablet; it is essentially "sodium-free".
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
You should continue to maintain a low-cholesterol diet and exercise while taking this medication.
The recommended dose for adults is one tablet per day.
You can take it at any time of the day, with or without food. Swallow the tablet whole with water.
Try to take the tablets every day at the same time, to help you remember.
This medication is not suitable for starting treatment. The start of treatment or dose adjustments, if necessary, should only be made by taking the components separately, and once the appropriate doses have been adjusted, it is possible to switch to the appropriate dose of rosuvastatin/ezetimiba.
If your doctor has prescribed rosuvastatin/ezetimiba along with another medication to reduce cholesterol that contains the active ingredient cholestyramine or any other medication that contains a bile acid sequestrant, you should take rosuvastatin/ezetimiba at least 2 hours before or 4 hours after these medications.
Regular Cholesterol Checks
It is essential that you visit your doctor regularly for cholesterol checks, in order to verify that your cholesterol levels have normalized and are maintained at appropriate levels.
If You Take More Arrox Plus Than You Should
Contact your doctor or the emergency department of the nearest hospital as you may need medical assistance.
In the case of overdose or accidental ingestion, consult
immediately with your doctor or pharmacist or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If You Forget to Take Arrox Plus
Do not worry, omit the missed dose and take the next scheduled dose at the planned time. Do not take a double dose to compensate for the missed dose.
If You Interrupt Treatment with Arrox Plus
Consult your doctor if you want to discontinue treatment with this medication. Your cholesterol levels may increase again if you stop taking this medication.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
It is important that you know which side effects may occur.
Stop taking Arrox Plus and seek medical help immediately if you experience any of the following symptoms:
Other side effects
Frequent side effects (may affect up to 1 in 10 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)
Unknown frequency (cannot be estimated from available data)
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for the Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
This medication does not require any special storage temperature.
Store in the original packaging to protect it from light and moisture.
Do not use this medication after the expiration date that appears on the box or blister pack after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or trash. Dispose of packaging and unused medications at the SIGRE drop-off point at the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medications. By doing so, you will help protect the environment.
Composition of Arrox Plus
Arrox Plus 10 mg/10 mg: Each film-coated tablet contains rosuvastatina calcium, equivalent to 10 mg of rosuvastatina, and 10 mg of ezetimiba.
Arrox Plus 20 mg/10 mg: Each film-coated tablet contains rosuvastatina calcium, equivalent to 20 mg of rosuvastatina, and 10 mg of ezetimiba.
Arrox Plus 40 mg/10 mg: Each film-coated tablet contains rosuvastatina calcium, equivalent to 40 mg of rosuvastatina, and 10 mg of ezetimiba.
Tablet core
Lactose monohydrate, croscarmelose sodium, povidone, sodium lauryl sulfate, microcrystalline cellulose, hypromellose, anhydrous colloidal silica, magnesium stearate.
Tablet coating
Arrox Plus 10 mg/10 mg: Hypromellose, titanium dioxide (E171), yellow iron oxide (E172), macrogol, talc.
Arrox Plus 20 mg/10 mg: Hypromellose, titanium dioxide (E171), talc, macrogol, yellow iron oxide (E172).
Arrox Plus 40 mg/10 mg: Lactose monohydrate, hypromellose, titanium dioxide (E171), macrogol.
Appearance of the product and contents of the package
Arrox Plus 10 mg/10 mg: Film-coated tablets, round, biconvex, beige-colored, with a diameter of approximately 10 mm, and the inscription "EL 4" on one face.
Arrox Plus 20 mg/10 mg: Film-coated tablets, round, biconvex, yellow-colored, with a diameter of approximately 10 mm, and the inscription "EL 3" on one face.
Arrox Plus 40 mg/10 mg: Film-coated tablets, round, biconvex, white-colored, with a diameter of approximately 10 mm, and the inscription "EL 2" on one face.
OPA/Al/PVC//Al blisters conditioned in cardboard boxes.
Packages of 30 film-coated tablets.
Marketing authorization holder
Laboratorios Alter, S.A.
C/ Mateo Inurria 30
28036 Madrid
Spain
Responsible for manufacturing
Elpen Pharmaceutical Co. Inc.
Marathonos Ave. 95
19009 Pikermi Attiki
Greece
or
Elpen Pharmaceutical Co. Inc.
Zapani, Block 1048
190 01 Keratea
Greece
Last review date of this leaflet:May 2023.
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)https://www.aemps.gob.es/.
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