Simvagen 20,20 mg, coated tablets
Simvagen 40,40 mg, coated tablets
Simvastatin
Simvagen is used to lower the level of cholesterol and fats called triglycerides in the blood.
During treatment, you should follow a low-cholesterol diet. This medicine belongs to a group of medicines called statins.
Simvagen is used in combination with a diet in people:
Most people do not experience any symptoms related to high cholesterol levels.
The doctor or pharmacist can assess cholesterol levels with a simple blood test. High cholesterol levels in the blood can lead to coronary heart disease. It can clog blood vessels, leading to hardening of the arteries (atherosclerosis). Stiffened arteries have a reduced ability to supply blood to the heart and the entire body. This can cause chest pain (angina pectoris) and lead to a heart attack.
In people with high cholesterol levels, the likelihood of developing coronary heart disease is higher if they also have:
To get advice on the above factors, you should consult a doctor or pharmacist.
Simvagen should not be used in a dose greater than 40 mg if the patient is taking lomitapide (used to treat severe and rare genetic cholesterol disorders)
If any of the above situations occur, the medicine should not be taken, but the doctor should be consulted to discuss treatment.
The safety and efficacy of Simvagen have been studied in boys aged 10-17 and girls who have started menstruating at least one year earlier (see "How to use Simvagen").
No studies have been conducted on simvastatin in children under the age of 10. To obtain additional information, you should consult a doctor
Before starting simvastatin, the doctor will perform blood tests to check liver function.
The doctor may order blood tests to assess liver function after starting simvastatin.
After starting simvastatin, the doctor will order regular blood tests to check the effectiveness of the medicine.
During simvastatin treatment, patients with diabetes or patients at risk of diabetes will be under constant observation by the doctor. The increased risk of developing diabetes applies to patients with high levels of sugars and fats in the blood, patients who are overweight, and patients with high blood pressure.
In rare cases, deaths have been reported.
The risk of muscle damage is higher in patients taking Simvagen in high doses, especially at a dose of 80 mg. The risk of muscle damage is higher in a certain group of patients.
You should discuss with your doctor:
You should inform your doctor or pharmacist if you experience persistent muscle weakness. Additional tests may be necessary to diagnose and treat the condition.
If you have breathing difficulties or a persistent cough, you should consult a doctor.
If you are to undergo surgery, it may be necessary to stop taking simvastatin for a short time.
Many medicines affect the action of simvastatin. You should tell your doctor about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take, including those available without a prescription, herbal preparations, and dietary supplements.
Taking simvastatin with any of these medicines can increase the risk of muscle problems (some of which are listed in the "When not to use Simvagen" section).
If you need to take fusidic acid orally for bacterial infections, you should temporarily stop taking this medicine. The doctor will decide when it is safe to return to taking Simvagen. Concurrent use of Simvagen with fusidic acid can rarely lead to muscle weakness, tenderness, or pain (rhabdomyolysis). More information on rhabdomyolysis can be found in section 4.
You should also tell your doctor if you are taking niacin (nicotinic acid) or products containing niacin, if you are from China.
Grapefruit juice can affect the action of simvastatin in the body. You should not drink grapefruit juice while taking simvastatin.
DO NOTtake Simvagen if you are pregnant, planning to become pregnant, or suspect you may be pregnant. If you become pregnant while taking Simvagen, you should STOPtreatment and immediately consult your doctor.
You should not take Simvagen while breastfeeding, as it is not known whether the medicine passes into breast milk.
Before taking any medicine, you should consult a doctor or pharmacist.
Simvagen does not affect the ability to drive or use machines.
Simvagen can cause dizziness, and before driving or using machines, you should make sure that such symptoms do not occur.
If you have previously been diagnosed with intolerance to some sugars, you should consult your doctor before taking this medicine.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means the medicine is "sodium-free".
This medicine should always be used as directed by your doctor or pharmacist. If you are unsure, you should consult your doctor or pharmacist. The dose of the medicine will be determined by your doctor based on blood test results.
You should remember to follow a low-fat diet and maintain physical activity.
The recommended dose is 20 mg to 40 mg and should be taken in the evening. The doctor may increase the dose used every 4 weeks. The maximum dose is 80 mg. The doctor will determine the appropriate dose for each patient based on their condition, current treatment, and individual risk profile.
You should not stop taking Simvagen unless your doctor advises you to do so.
The recommended initial dose is 10 mg to 20 mg and should be taken in the evening. The doctor may increase the dose used every 4 weeks. The maximum dose is 80 mg.
The recommended initial dose is 40 mg and should be taken in the evening.
A dose of 80 mg is recommended only for adult patients with very high cholesterol levels in the blood and a high risk of developing heart disease, who have not achieved the target cholesterol level with lower doses.
The recommended initial dose for children aged 10-17 is 10 mg. This dose should usually be taken in the evening. If necessary, the dose can be increased, up to a maximum of 40 mg.
Some patients may need a lower dose, especially if they are also taking medicines such as fibrates or niacin and have kidney problems.
During simvastatin treatment, the doctor may recommend taking a medicine called cholestyramine. This medicine may affect the action of simvastatin. Simvastatin should be taken 2 hours before or 4 hours after taking cholestyramine.
The medicine should be swallowed with a large amount of water. The medicine can be taken with or without food.
The 20 mg tablet can be divided into equal doses.
If you take a higher dose of Simvagen than recommended, you should immediately consult a doctor or go to the emergency room of the nearest hospital. You should bring the packaging of the medicine with you.
If you miss a dose of the medicine, you should take it as soon as you remember, unless it is almost time for the next dose. You should not take a double dose to make up for the missed dose.
The doctor will determine how long you should take the medicine. DO NOTsuddenly stop taking the medicine without consulting your doctor, as your cholesterol levels may increase again.
If you have any further doubts about using this medicine, you should consult your doctor or pharmacist.
Like all medicines, Simvagen can cause side effects, although not everybody gets them.
The list of side effects below is not intended to alarm you, but it is important to know what to do if they occur.
Other possible side effects:
Rare (may affect up to 1 in 1000 people):
Very rare (may affect up to 1 in 10,000 people)
Unknown (frequency cannot be estimated from available data):
You should discuss with your doctor if you experience weakness in your arms or legs, worsening after periods of activity, double vision, or drooping eyelids, difficulty swallowing, or shortness of breath.
Additionally, side effects that have occurred with the use of some statins include:
If you experience any side effects, including any side effects not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety Monitoring, 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, you can help provide more information on the safety of this medicine.
The medicine should be stored out of sight and reach of children.
There are no special storage instructions for the medicine.
Do not use this medicine after the expiration date stated on the packaging/bottle/blister pack after: EXP. The expiration date refers to the last day of the specified month.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Simvagen is available in the form of coated tablets in two different doses containing 20 mg or 40 mg of simvastatin as the active substance.
Each coated tablet also contains ascorbic acid, butylhydroxyanisole (E320), citric acid monohydrate, lactose monohydrate (see section 2 "Simvagen contains lactose"), magnesium stearate, microcrystalline cellulose, maize starch, sodium lauryl sulfate, hypromellose, talc, hydroxypropyl cellulose, titanium dioxide (E171), macrogol, iron oxide red (E172), and iron oxide yellow (E172).
Simvagen 20 mg coated tablets: dark brown, oval, biconvex coated tablets with beveled edges, with the inscription "SV3" on one side and a dividing line on the other side. The tablet can be divided into equal doses.
Simvagen 40 mg coated tablets: pink, oval, biconvex coated tablets with beveled edges, with the inscription "SV4" on one side and the inscription "M" on the other side.
Simvagen coated tablets are packaged in plastic bottles or blister packs containing 28 or 30 tablets.
Simvagen 20 mg tablets are also packaged in blister packs containing 84 tablets.
Not all pack sizes may be marketed.
Viatris Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
DUBLIN
Ireland
McDermott Laboratories Ltd. trading as Gerard Laboratories, 35/36 Baldoyle Industrial Estate, Grange Road Dublin 13, Ireland
Mylan Hungary Kft., H-2900, Komárom, Mylan utca 1, Hungary
Mylan Germany GmbH, Zweigniederlassung Bad Homburg v. d. Hoehe, Benzstrasse 1, Bad Homburg
To obtain more detailed information about the medicine and its names in the Member States of the European Economic Area, you should contact the local representative of the marketing authorization holder:
Tel: +48 22 546 64 00
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.