Package Leaflet: Information for the User
Simvastatina STADA 10 mg Film-Coated Tablets
Simvastatina STADA 20 mg Film-Coated Tablets
Simvastatina STADA 40 mg Film-Coated Tablets
Read this leaflet carefully before you start taking this medicine because it contains important information for you.
-Keep this leaflet, as you may need to read it again.
-If you have any questions, ask your doctor or pharmacist.
-This medicine has been prescribed for you only. Do not pass it on to others even if their symptoms are the same as yours. It may harm them.
-If you get any side effects, talk to your doctor or pharmacist. See section 4.
1.What Simvastatina Stada is and what it is used for
2.What you need to know before you take Simvastatina Stada
3.How to take Simvastatina Stada
4.Possible side effects
5.Storage of Simvastatina Stada
6.Contents of the pack and additional information
Simvastatina Stada contains the active ingredient simvastatina. Simvastatina is used to reduce total cholesterol, "bad" cholesterol (low-density lipoprotein, LDL) and fatty substances called triglycerides that circulate in the blood. Additionally, simvastatina increases the levels of "good" cholesterol (high-density lipoprotein, HDL). Simvastatina is a member of a class of medications called statins.
Cholesterol is one of the fatty substances that are found in the bloodstream. Its total cholesterol is composed mainly of LDL and HDL.
LDL cholesterol is often referred to as "bad" cholesterol because it can accumulate in the walls of your arteries forming plaques. Over time, this accumulation of plaque can cause a narrowing of the arteries. This narrowing can make the blood flow to vital organs such as the heart and brain slower or interrupted. This interruption of blood flow can cause a myocardial infarction or a stroke.
HDL cholesterol is often referred to as "good" cholesterol because it helps to prevent "bad" cholesterol from accumulating in the arteries and protects them from cardiovascular diseases.
Triglycerides are another type of fat in your blood that can increase the risk of cardiovascular disease.
While taking this medication, you must follow a cholesterol-reducing diet.
Simvastatina is used, along with a cholesterol-reducing diet, if you have:
Most people do not have immediate symptoms of high cholesterol. Your doctor may measure your cholesterol with a simple blood test. Visit your doctor regularly, monitor your cholesterol, and discuss your goals with your doctor.
Do not take more than 40 mg of simvastatin if you are taking lomitapide (used to treat rare and severe genetic cholesterol disorders).
Consult your doctor if you are unsure if your medicine is on the above list.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Simvastatin Stada.
Inform your doctor:
Your doctor will do a blood test before you start taking simvastatin and also if you have any symptoms of liver problems while taking 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 taking 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 sugar and fat in your blood, being overweight, and high blood pressure.
Inform your doctor if you have a severe lung disease.
Consult your doctor immediately if you experience unexplained muscle pain, tenderness, or weakness. This is because, in rare cases, muscle problems can be severe, including muscle failure that causes kidney damage; and very rarely, deaths have occurred.
The risk of muscle failure is higher with high doses of simvastatin, especially with the 80 mg dose. The risk of muscle failure is also higher in certain patients. Talk to your doctor if any of the following situations affect you:
Also inform your doctor or pharmacist if you experience persistent muscle weakness. Further tests and additional medicines may be needed to diagnose and treat this problem.
Children and adolescents
The effectiveness and safety of simvastatin treatment were studied in boys aged 10 to 17 years and in girls who had their first menstrual period (menstruation) at least one year earlier (see section 3). Simvastatin has not been studied in children under 10 years of age. For more information, consult your doctor.
Other medicines and Simvastatin Stada
Inform your doctor or pharmacist if you are using or have used recently or may need to use any other medicine.
Taking simvastatin with any of the following medicines may increase the risk of muscle problems (some of these are already included in the section above "Do not take simvastatin").
As with the medicines mentioned above, inform your doctor or pharmacist if you are taking or have taken recently other medicines, even those purchased without a prescription. In particular, inform your doctor if you are taking medicines with any of the following active ingredients:
You should also inform any doctor who prescribes a new medicine that you are taking simvastatin
Simvastatin Stada with food, drinks, and alcohol
Simvastatin can be taken with or without food.
Avoid consuming grapefruit juice while taking simvastatin, as this juice increases simvastatin levels in the blood.
Simvastatin should be administered with caution in patients who consume alcohol. If you drink alcohol regularly, consult your doctor.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Simvastatin is contraindicated during pregnancy.
In the event of pregnancy or suspected pregnancy, you should discontinue treatment and inform your doctor as soon as possible.
Do not take simvastatin if you are breastfeeding, as it is unknown whether this medicine passes into breast milk.
Driving and operating machines
At normal doses, simvastatin does not affect the ability to drive or operate machines. However, if you experience dizziness, do not drive or operate machines until you know how you tolerate the medicine.
Simvastatin Stada contains lactose
This medicine contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.
Follow exactly the administration instructions of this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Remember to take your medication.
Your doctor will indicate the duration of your treatment with simvastatin. Do not discontinue treatment before.
Before starting to take simvastatina, you must be following a diet to reduce cholesterol.
Dosage
The recommended dose is one tablet once a day by oral route.
Adults
The recommended starting dose is10 to40 mg per day, administered in a single dose at night.
After at least 4 weeks, your doctor may adjust your dose up to a maximum of 80 mg per day, administered in a single dose at night.Do not take more than 80 mg per day.
Your doctor may prescribe lower doses, especially if you are taking certain medications indicated earlier or have certain kidney disorders.
The 80 mg dose is only recommended for adult patients with very high cholesterol levels and a high risk of heart disease problems who have not achieved their cholesterol goal with lower doses.
Use in children and adolescents
In children and adolescents aged 10 to 17 years, the recommended daily dose for starting treatment is 10 mg, at night. The maximum recommended daily dose is 40 mg.
Older patients
No dose adjustment is necessary.
Administration form
The tablets should be taken at night and can be administered with water and with or without food.
If your doctor has prescribed simvastatina along with another cholesterol-lowering medication that contains a bile acid sequestrant, you should take simvastatina at least 2 hours before or 4 hours after taking the bile acid sequestrant.
The groove is only for breaking the tablet if it is difficult to swallow whole.
If you take more Simvastatina Stada than you should
If you have taken moresimvastatinathan you should, consult your doctor or pharmacist immediately and/or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
If you forgot to take Simvastatina Stada
Do not take a double dose to compensate for the missed doses.
Take the next dose at your usual time.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
The following terms are used to describe how often side effects have been reported:
??Rare (may affect up to 1 in 1,000 people).
??Very rare (may affect up to 1 in 10,000 people).
??Frequency not known (cannot be estimated from available data).
If any of the serious side effects mentioned below occur, stop taking the medicine and inform your doctor immediately or go to the nearest hospital emergency department.
The following serious side effects have been reported:Rare:
The following serious side effects have been reported:Very rare:
Rarely, the following side effects have also been reported:
The following side effects have also been reported, but the frequency cannot be estimated from the available data (frequency not known):
Consult your doctor if you experience weakness in the arms or legs that worsens after periods of activity, double vision, eyelid drooping, difficulty swallowing, or difficulty breathing.
Possible additional side effects reported with some statins:
Additional tests
In some blood tests, elevated liver function (transaminases) and a muscle enzyme (creatine kinase) were observed.
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 inthis leaflet. You can also report them directly through the Spanish System for the Vigilance 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.
Store in the original packaging.
Do not use Simvastatina Stada after the expiration date that appears on the packaging, after CAD. The expiration date is the last day of the month indicated.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and medicines you no longer need atPunto SIGREof the pharmacy. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. In this way, you will help protect the environment.
Composition of Simvastatina Stada
The active ingredient is simvastatina.
Simvastatina 10 mg: Each tablet contains 10 mg of simvastatina.
Simvastatina 20 mg: Each tablet contains 20 mg of simvastatina.
Simvastatina 40 mg: Each tablet contains 40 mg of simvastatina.
The other components (excipients) are lactic acid, microcrystalline cellulose, pregelatinized cornstarch, butylhydroxyanisole (E320), magnesium stearate, talc, hypromellose, hydroxypropylcellulose, and titanium dioxide (E171).
Appearance of the product and contents of the package
Simvastatina Stada 10 mg is presented in the form of film-coated tablets, white, oblong, biconvex, with a notch on one face. The tablets are marked with “SVT” on the unnotched face and with “10” on the notched face. Each package contains 28 or 500 (clinical package) tablets.
Simvastatina Stada 20 mg is presented in the form of film-coated tablets, white, oblong, biconvex, with a notch on one face. The tablets are marked with “SVT” on the unnotched face and with “20” on the notched face. Each package contains 28 or 500 (clinical package) tablets.
Simvastatina Stada 40 mg is presented in the form of film-coated tablets, white, oblong, biconvex, with a notch on one face. The tablets are marked with “SVT” on the unnotched face and with “40” on the notched face. Each package contains 28 or 500 (clinical package) tablets.
Only some package sizes may be commercially available.
Holder of the marketing authorization and responsible for manufacturing.
Holder of the marketing authorization
STADA, S.L.
Frederic Mompou, 5
08960 Sant Just Desvern (Barcelona) Spain
Responsible for manufacturing
Synthon Hispania S.L
Castelló 1, Polígono Las Salinas
08830 Sant Boi de Llobregat (Barcelona)
Spain
or
STADA Arzneimittel AG
Stadastraße 2 – 18
D-61118 Bad Vilbel
Germany
or
STADA M&D SRL
Str. Trascaului nr. 10,
Municipiul Turda,
Judet Cluj 401135,
Romania
Last review date of this leaflet:October 2023
The detailed information of this medication is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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