Simvastatin Krka – Simvastatin uses, dose and side effects

}

10 mg, 20 mg, and 40 mg film-coated tablet
simvastatin

What Simvastatin Krka is and what it is used for

Simvastatin Krka contains the active substance simvastatin. Simvastatin Krka is a drug used to lower the levels of total cholesterol in the blood, the “bad” cholesterol ( LDL – cholesterol ), and blood fats, so-called triglycerides. Simvastatin Krka also increases the levels of the “good” cholesterol ( HDL – cholesterol ). Simvastatin Krka belongs to a group of medicines called statins.

Cholesterol is one of several fats found in your blood. Your total cholesterol consists mainly of LDL and HDL cholesterol.

LDL cholesterol is often called the “bad” cholesterol because it causes fat storage in your vessel walls and forms plaque. This plaque storage can eventually lead to a narrowing of your vessels. This narrowing can reduce or block blood flow to important organs such as the heart and brain. Blockage of blood flow can result in a heart attack or stroke.

HDL cholesterol is often called the “good” cholesterol because it helps prevent the “bad” cholesterol from being stored in vessels and protects against heart disease.

Triglycerides are another type of fat in the blood that can increase the risk of heart disease.

You should continue with a cholesterol-lowering diet while you are taking this medicine.

Simvastatin Krka is used as a supplement to your cholesterol-lowering diet if you have:

  • elevated blood cholesterol levels (primary hypercholesterolemia ) or elevated blood fats (combined hyperlipidemia )
  • an inherited disease ( homozygous familial hypercholesterolemia ) that causes elevated cholesterol levels in the blood. You can also receive other treatments.
  • coronary heart disease or if you are at risk of developing coronary heart disease (because you have diabetes, previously had a stroke, or other vascular diseases). Treatment with Simvastatin Krka can lead to prolonged survival by reducing the risk of cardiovascular disease, regardless of the amount of cholesterol in your blood.

In most people, high cholesterol does not cause immediate symptoms. Your doctor can measure your cholesterol level with a simple blood test. Visit your doctor regularly, monitor your cholesterol levels, and discuss your goals with your doctor.

Simvastatin contained in Simvastatin Krka may also be approved for the treatment of other conditions not mentioned in this leaflet. Ask your doctor, pharmacist, or another healthcare professional if you have any further questions, and always follow their instructions.

What you need to know before you use Simvastatin Krka

Do not use Simvastatin Krka

  • if you are allergic to simvastatin or any of the other ingredients of this medicine (listed in section 6)
  • if you have liver problems
  • if you are pregnant or breastfeeding
  • if you are taking medicines containing one or more of the following active ingredients:
    • itraconazole, ketoconazole , posaconazole or voriconazole (used to treat fungal infections)
    • erythromycin, clarithromycin, or telithromycin (used to treat infections )
    • HIV protease inhibitors such as indinavir, nelfinavir, ritonavir and saquinavir ( HIV protease inhibitor used in HIV infections )
  • boceprevir or telaprevir (used to treat hepatitis C virus infection)
  • nefazodone (used to treat depression)
  • cobicistat
  • gemfibrozil (used to lower cholesterol)
  • cyclosporine (often used in organ transplant patients)
  • danazol (a synthetic hormone used to treat endometriosis, a condition in which the lining of the uterus grows outside the uterus)
  • if you are taking, or in the last 7 days, have taken a medicine called fusidic acid (used to treat bacterial infections ) either by mouth or by injection. The combination of fusidic acid and Simvastatin Krka can lead to severe muscle problems ( rhabdomyolysis ).

Do not take more than 40 mg Simvastatin Krka if you are taking lomitapide (used to treat a serious and rare genetic cholesterol condition).

Consult a doctor if you are unsure if your medicine is listed above.

Warnings and cautions

Tell your doctor:

  • about all your medical ailments, including allergies.
  • if you have high alcohol consumption.
  • if you have or have had any liver disease. Simvastatin Krka may not be the right medicine for you.
  • if you are going to have surgery. Discontinuation of treatment with Simvastatin Krka may need to be done for a short time.
  • if you are of Asian descent, then another dose may apply to you.

Your doctor should take a blood sample before you start taking Simvastatin Krka, and if you have any symptoms of liver problems during treatment with Simvastatin Krka. This blood test is taken to check your liver function.

Your doctor may also need to take a blood test to check your liver function after you start taking Simvastatin Krka.

During treatment with this medicine, your doctor will closely monitor you if you have diabetes or are at risk of developing diabetes. You are more likely to be at risk for diabetes if you have high blood sugar and blood fat levels, are overweight, and have high blood pressure.

Tell your doctor if you have any serious lung disease.

Contact a doctor immediately if you experience unexplained muscle aches, soreness, or weakness. The reason for this is that in rare cases, muscle problems can be serious and involve the breakdown of muscles with kidney damage as a result and in very rare cases, deaths have occurred.

The risk of muscle breakdown is greater at higher doses of Simvastatin Krka, this is especially true for a dose of 80 mg. The risk of muscle breakdown is also greater in some patients. Talk to your doctor if any of the following apply to you:

  • you have a high alcohol consumption
  • you have kidney problems
  • you have thyroid problems
  • you are 65 years or older
  • you are a woman
  • if you have ever had muscle problems during treatment with cholesterol-lowering drugs called “statins” or fibrates
  • you or a close relative has a hereditary muscle disease

Also, tell your doctor or pharmacist if you have persistent muscle weakness. Additional tests and medications may be needed to investigate and treat this.

Children and young people

The safety and efficacy of simvastatin have been studied in boys aged 10-17 years and in girls who have had menstruation for at least one year (see section 3). Simvastatin has not been studied in children under 10 years of age. For further information, consult a doctor.

Other medicines and Simvastatin Krka

It is especially important to tell your doctor if you are taking any of the following active ingredients. Taking Simvastatin Krka with any of these medicines may increase the risk of muscle problems (some of these have already been listed in the section above “Do not use Simvastatin Krka”).  

  • if you have to take fusidic acid by mouth to treat a bacterial infection, you must temporarily stop taking this medicine. Your doctor will tell you when it is safe to resume treatment with Simvastatin Krka. Taking Simvastatin Krka with fusidic acid may in rare cases lead to muscle weakness, tenderness, or pain ( rhabdomyolysis ). For more information on rhabdomyolysis, see section 4ciclosporin (often used by patients who have had an organ transplant)
  • danazol (a synthetic hormone used to treat endometriosis, a condition in which the lining of the uterus grows outside the uterus)
  • medicines containing an active substance such as itraconazole, ketoconazole, fluconazole, posaconazole, or voriconazole (used to treat fungal infections)
  • fibrates with an active ingredient such as gemfibrozil and bezafibrate (used to lower cholesterol)
  • erythromycin, clarithromycin, or telithromycin (used to treat bacterial infections )
  • HIV protease inhibitors such as indinavir, nelfinavir, ritonavir, and saquinavir (used to treat AIDS )
  • Hepatitis C medicines such as boceprevir, telaprevir, elbasvir, or grazoprevir (used to treat hepatitis C virus infection)
  • nefazodone (used to treat depression)
  • medicines containing the active substance cobicistat
  • amiodarone (used to treat irregular heartbeat)
  • verapamil, diltiazem, or amlodipine (used to treat high blood pressure, chest pain associated with cardiovascular disease or other heart problems)
  • lomitapide (used to treat a serious and rare genetic cholesterol condition)
  • daptomycin (a medicine used to treat complicated skin and soft tissue infections and bacteremia (presence of bacteria in the blood)). The risk of side effects affecting the muscles may be higher when this medicine is taken during treatment with simvastatin (eg Simvastatin Krka). Your doctor may decide to stop you from taking Simvastatin Krka for a while
  • colchicine (used in the treatment of gout ).
  • ticagrelor (antiplatelet drug).

Also tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. It is especially important to tell your doctor if you are taking medicines with any of the following active ingredients:

  • anticoagulants with an active ingredient such as warfarin, phenprocoumon, or acenocoumarol ( anticoagulants )
  • fenofibrate (also used to lower cholesterol)
  • niacin (also used to lower cholesterol)
  • rifampicin (used to treat tuberculosis )

Tell your doctor who is prescribing a new medicine that you are taking Simvastatin Krka.

Simvastatin Krka with food, drink, and alcohol

Grapefruit juice contains one or more substances that can affect the body’s breakdown of certain drugs, including Simvastatin Krka. Intake of grapefruit juice should be avoided.

Pregnancy, breastfeeding, and fertility

Do not use Simvastatin Krka if you are pregnant, trying to conceive, or think you may be pregnant. If you become pregnant during treatment with Simvastatin Krka, stop treatment immediately and contact your doctor.

Do not take Simvastatin Krka if you are breastfeeding as it is unknown if the medicine passes into breast milk.

Ask your doctor or pharmacist for advice before taking any medicine.

Driving and using machines

Simvastatin Krka is not expected to affect your ability to drive or use machines. However, keep in mind that some people get dizzy when they take Simvastatin Krka.

You are responsible for assessing whether you are fit to drive a motor vehicle or perform work that requires increased vigilance. One of the factors that can affect your ability in these respects is the use of drugs, due to their effects and/or side effects. Descriptions of these effects and side effects can be found in other sections. Read all the information in this leaflet for guidance. If you are not sure, talk to your doctor or pharmacist.

Simvastatin Krka contains lactose

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

How to use Simvastatin Krka

Your doctor will decide which dose is right for you depending on your symptoms, your current treatment, and your risk profile.

Always take this medicine exactly as your doctor or pharmacist has told you. Ask your doctor or pharmacist if you are unsure.

You should continue with a cholesterol-lowering diet while taking Simvastatin Krka.

Dosage:

The recommended dose is one Simvastatin Krka 10 mg, 20 mg, or 40 mg tablet once a day.

Adults:

The most common starting dose is 10 mg, 20 mg, or in some cases 40 mg daily. Your doctor may, after at least 4 weeks, need to adjust your dose to a maximum of 80 mg per day. Do not take more than 80 mg per day.

Your doctor may prescribe a lower dose for you, especially if you are taking certain medicines listed above or have certain kidney problems.

A dose of 80 mg is only recommended for adult patients with very high cholesterol levels and who are at high risk for cardiovascular disease and who have not achieved their treatment goals at lower doses.

Method of administration and duration of treatment:

Take Simvastatin Krka in the evening. Simvastatin Krka can be taken with or without food.

Continue to take Simvastatin Krka unless your doctor tells you to stop.

If your doctor has prescribed Simvastatin Krka together with another cholesterol-lowering medicine that contains bile acid sequestrants, you should take Simvastatin Krka at least 2 hours before or 4 hours after taking the bile acid sequestrant.

Use for children and adolescents

The recommended starting dose for children (10 – 17 years) is usually 10 mg in the evening. The maximum recommended dose is 40 mg daily.

If you use more Simvastatin Krka than you should  

If you have ingested too much medicine or if e.g. If a child has ingested the medicine by mistake, contact a doctor or hospital for risk assessment and advice.

If you forget to use Simvastatin Krka

Do not take a double dose to make up for a forgotten dose. Just take your usual dose of Simvastatin Krka at the time you usually take the next day.

If you stop using Simvastatin Krka

Talk to your doctor or pharmacist as your cholesterol levels may rise again.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

The following classification is 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)
  • Has been reported (occurs in an unknown number of users)

The following rare serious side effects have been reported.

If any of these serious side effects occur, stop taking your medicine and contact your doctor immediately or see an emergency department at the nearest hospital.

  • muscle aches, soreness, weakness, or cramps. In rare cases, muscle problems can be serious and involve the breakdown of muscles with kidney damage as a result, and in very rare cases, deaths have occurred.
  • hypersensitivity (allergic reactions) including:
    • swelling of the face, tongue, and throat, which may cause difficulty breathing ( angioedema )
    • severe muscle pain, usually in the shoulders and hips
    • rash with weakness in arms, legs, and neck muscles
    • joint pain or inflammation (rheumatic polymyalgia)
    • inflammation of blood vessels ( vasculitis )
    • bruising of unknown cause, skin rash, and swelling ( dermatomyositis ), hives, skin sensitivity to sun exposure, fever, redness
    • shortness of breath ( dyspnoea ) and general malaise
    • lupus-like disease picture (including rash, joint problems, and effects on blood cells )
  • inflammation of the liver with the following symptoms: the yellowish color of the skin and eyes, itching, dark-colored urine or pale stools, feeling of tiredness or weakness, loss of appetite, liver failure (very rare)
  • inflammation of the pancreas, often with severe abdominal pain.

The following side effects have been reported rarely:

  • low red blood cell count ( anemia )
  • numbness or weakness in the arms and legs
  • headache, “ant crawls”, dizziness
  • blurred vision and impaired vision
  • indigestion (abdominal pain, constipation, flatulence, dyspepsia, diarrhea, nausea, vomiting)
  • rash, itching, hair loss
  • weakness
  • difficulty sleeping (very rare)
  • poor memory (very rare), memory loss, confusion.

The following very rare serious side effects have been reported:

  • a severe allergic reaction that causes difficulty breathing or dizziness ( anaphylaxis )
  • rash that may occur on the skin or sores in the mouth (drug-related lichenoid rash)
  • muscle strain
  • gynecomastia (breast augmentation in men)

The following side effects have also been reported, but the frequency cannot be determined with available information (no known frequency):

  • erectile dysfunction
  • Depression
  • inflammation of the lungs that causes breathing problems including persistent cough and/or shortness of breath or fever
  • problems with tendons, sometimes aggravated by tendon rupture.

Additional possible side effects have been reported with certain statins:

  • sleep disorders, including nightmares
  • sexual problems
  • diabetes. This is more likely if you have high blood sugar and blood fat levels, are overweight, and have high blood pressure. Your doctor will check you while you are taking this medicine.
  • muscle pain, tenderness, or weakness which is persistent and which may not go away after stopping treatment with Simvastatin Krka (frequency not known)

Laboratory values

In some blood tests, elevations in liver function values ​​and a muscle enzyme (creatinine kinase) have been observed.

How to store Simvastatin Krka

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. The expiration date is the last day of the specified month.

Do not store above 30 ° C.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

Contents of the pack and other information

Content declaration

  • The active substance is simvastatin .Simvastatin Krka 10 mg: Each film-coated tablet contains 10 mg simvastatin .Simvastatin Krka 20 mg: Each film-coated tablet contains 20 mg simvastatin .Simvastatin Krka 40 mg: Each film-coated tablet contains 40 mg simvastatin .
  • The other ingredients (excipients) are pregelatinized starch, lactose monohydrate, microcrystalline cellulose (E460 (i)), butyl hydroxyanisole (E320), ascorbic acid (E300), maize starch, citric acid, magnesium stearate (E470b) (E470b) (, propylene glycol, titanium dioxide (E 171) in the film coating, (see section 2 “Simvastatin Krka contains lactose”).

What the medicine looks like and the contents of the pack

Simvastatin Krka 10 mg film-coated tablets are oval, white, marked “10” on one side, and have a score line on the other side. Tablet dimensions: approximately 9 x 4 mm. The tablet can be divided into equal doses.

Simvastatin Krka 20 mg film-coated tablets are oval, white, marked “20” on one side, and have a score line on the other side. Tablet dimensions: approximately 11 x 5 mm. The tablet can be divided into equal doses.

Simvastatin Krka 40 mg film-coated tablets are round, white, smooth on one side, and have a score line on the other side. Tablet dimensions: about 11 mm. The tablet can be divided into equal doses.

Simvastatin Krka 10 mg, 20 mg, and 40 mg film-coated tablets

Simvastatin Krka film-coated tablets are available in packs of 10, 20, 28, 30, 40, 50, 56, 60, 84, 98,100 and 100×1 film-coated tablets in (PVC / PE / PVDC / Al) blisters.

Simvastatin Krka 20 mg and 40 mg film-coated tablets

Simvastatin Krka film-coated tablets are supplied in packs of 250 film-coated tablets in a polyethylene (HDPE) tablet jar with a sealed polypropylene seal.

Not all pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Manufacturer

KRKA dd, Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia

Leave a Reply