simvastatin tablets is covered.pl.ob. 20 mg 30 pcs. (Simvastatin)

Packaging

30 pcs

Pharmacological action

The lipid-lowering agent obtained synthetically from the fermentation product Aspergillus terreus is an inactive lactone, undergoes hydrolysis in the body to form a hydroxy acid derivative. The active metabolite inhibits 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMG-CoA reductase), an enzyme that catalyzes the initial formation of mevalonate from HMG-CoA. Since the conversion of HMG-CoA to mevalonate is an early step in cholesterol synthesis, then the use of simvastatin does not cause the accumulation of potentially toxic sterols in the body. HMG-CoA is easily metabolized to acetyl-CoA, which is involved in many synthesis processes in the body.

Causes a decrease in plasma levels of triglycerides (TG), low density lipoproteins (LDL), very low density lipoproteins (VLDL) and total cholesterol (in cases of heterozygous familial and non-familial forms of hypercholesterolemia, with mixed hyperlipidemia, when there is an increased risk of cholesterol )

Increases the content of high density lipoproteins (HDL) and reduces the ratio of LDL / HDL and total cholesterol / HDL.

The onset of the manifestation of the effect is 2 weeks after the start of administration, the maximum therapeutic effect is achieved after 4-6 weeks. The action persists with continued treatment, upon termination of therapy, the cholesterol content gradually returns to its original level.

Indications

Primary type IIa and IIb hypercholesterolemia (with ineffective diet therapy in patients with an increased risk of coronary atherosclerosis), combined hypercholesterolemia and hypertriglyceridemia, hyperlipoproteinemia, which cannot be corrected by special diets.

Prevention of myocardial infarction (to slow the progression of coronary atherosclerosis), stroke and transient cerebrovascular disorders.

Contraindications

Hypersensitivity, liver failure, acute liver disease, increased activity of liver transaminases of unknown origin, pregnancy, lactation, age under 18 years (safety and efficacy have not been established).

Use during pregnancy and lactation

Simvastatin may have an adverse effect on the fetus and is contraindicated in pregnant women. There are several reports of the development of abnormalities in newborns whose mothers took Simvastatin.

Women of reproductive age taking Simvastatin should avoid conception. The use of simvastatin is not recommended in women of childbearing age who do not use contraceptives. If pregnancy does occur during treatment, Simvastatin should be canceled, and the woman should be warned of a possible danger to the fetus.

There are no data on the excretion of simvastatin with breast milk. If it is necessary to prescribe Simvastatin during breastfeeding, it should be borne in mind that many drugs are excreted in breast milk, and there is a risk of severe reactions, therefore breastfeeding while taking the drug is not recommended

Composition

1 tablet contains:

Active ingredient:

simvastatin 20 mg

of ancillary substances:

MCC

monohydrate lactose (milk sugar)

starch pregelatinized (starch 1500)

colloidal silicon dioxide (Aerosil)

ascorbic acid

butylhydroxyanisole

stearic acid, magnesium stearate



polyvinylalcohol

macrogol (polyethylene glycol)

dye iron oxide black

talc

dye iron oxide yellow

dye iron oxide red

titanium dioxide.

Dosage and administration

Inside, once a day, in the evening, with plenty of water, the drug should not be taken with food.

Before starting treatment with simvastatin, the patient should be prescribed a standard hypocholesterol diet, which must be followed throughout the course of treatment.

The recommended dose of simvastatin for the treatment of hypercholesterolemia varies from 10 to 80 mg once daily in the evening. The recommended starting dose for patients with hypercholesterolemia is 10 mg. The maximum daily dose is 80 mg.

Changes (selection) of the dose should be carried out at intervals of 4 weeks. In most patients, the optimal effect is achieved when taking the drug in doses up to 20 mg / day.

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients with which must be observed throughout the course of treatment.

The recommended dose of simvastatin for the treatment of hypercholesterolemia varies from 10 to 80 mg once daily in the evening. The recommended starting dose for patients with hypercholesterolemia is 10 mg. The maximum daily dose is 80 mg.

Changes (selection) of the dose should be carried out at intervals of 4 weeks. In most patients, the optimal effect is achieved when taking the drug in doses up to 20 mg / day.

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients with which must be observed throughout the course of treatment.

The recommended dose of simvastatin for the treatment of hypercholesterolemia varies from 10 to 80 mg once daily in the evening. The recommended starting dose for patients with hypercholesterolemia is 10 mg. The maximum daily dose is 80 mg.

Changes (selection) of the dose should be carried out at intervals of 4 weeks. In most patients, the optimal effect is achieved when taking the drug in doses up to 20 mg / day.

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients with The recommended starting dose for patients with hypercholesterolemia is 10 mg. The maximum daily dose is 80 mg.

Changes (selection) of the dose should be carried out at intervals of 4 weeks. In most patients, the optimal effect is achieved when taking the drug in doses up to 20 mg / day.

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients with The recommended starting dose for patients with hypercholesterolemia is 10 mg. The maximum daily dose is 80 mg.

Changes (selection) of the dose should be carried out at intervals of 4 weeks. In most patients, the optimal effect is achieved when taking the drug in doses up to 20 mg / day.

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients with

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients with

In patients with homozygous hereditary hypercholesterolemia, the recommended daily dose of Simvastatin is 40 mg once daily in the evening or 80 mg in 3 divided doses (20 mg in the morning, 20 mg in the afternoon and 40 mg in the evening).

In the treatment of patients withEffective doses of Simvastatin are 20–40 mg / day for ischemic heart disease or a high risk of coronary heart disease. Therefore, the recommended initial dose in such patients is 20 mg / day. Changes (selection) of the dose should be carried out at intervals of 4 weeks, if necessary, the dose can be increased to 40 mg / day. If the content of LDL

In elderly patients and patients with mild or moderate renal failure, a change in the dosage of the drug is not required.

In patients with chronic renal failure (Cl creatinine

For patients taking amiodarone or verapamil concomitantly with simvastatin, the daily dose should not exceed 20 mg.

Side effects of the

Digestive system: constipation, diarrhea, loss of appetite, flatulence, nausea, abdominal pain, pancreatitis, increased activity of ALT, AST, GGT, alkaline phosphatase.

From the side of the central nervous system and peripheral nervous system: headache, dizziness, muscle cramps, paresthesia, peripheral neuropathy.

From the cardiovascular system: transient arterial hypotension is possible.

From the musculoskeletal system: myalgia, myopathy, rhabdomyolysis, increased activity of CPK.

Allergic reactions: rarely - angioedema, lupus-like syndrome, vasculitis, thrombocytopenia, eosinophilia, increased ESR, arthritis, urticaria, fever, shortness of breath.

Dermatological reactions: photosensitivity, skin rash, itching, flushing of the skin, alopecia.

Other: anemia.

Drug Interaction

Cytostatics, antifungal agents (ketoconazole, itraconazole), fibrates, high doses of nicotinic acid, immunosuppressants, erythromycin, clarithromycin, telithromyces, HIV protease inhibitors, nefazodone increase the risk of myopathy.

Cyclosporine or danazol: the risk of myopathy / rhabdomyolysis increases with co-administration of cyclosporine or danazol with high doses of simvastatin.

Other lipid-lowering agents that can cause myopathy: The risk of developing myopathy increases with the co-administration of other lipid-lowering agents that are not potent CYP3A4 inhibitors but capable of causing myopathy in monotherapy. Such as gemfibrozil and other fibrates (except fenofibrate), as well as niacin (nicotinic acid) at a dose> 1 g / day.

Amiodarone and verapamil: The risk of developing myopathy increases with the co-administration of amiodarone or verapamil with high doses of simvastatin.

Diltiazem: the risk of myopathy is slightly increased in patients receiving diltiazem concomitantly with simvastatin 80 mg.

Simvastatin potentiates the effects of oral anticoagulants (eg, fenprocoumon, warfarin) and increases the risk of bleeding, which requires monitoring blood clotting before treatment, and often enough during the initial treatment period. Once a stable level of prothrombin time or International Normalized Attitude (MHO) is reached, its follow-up should be conducted at intervals recommended for patients receiving anticoagulation therapy. When changing the dosage or discontinuing simvastatin, prothrombin time or MHO should also be monitored according to the above schedule.

Simvastatin therapy does not cause changes in prothrombin time and bleeding risk in patients not taking anticoagulants. Increases the level of digoxin in blood plasma.

Colestyramine and colestipol reduce bioavailability (use of simvastatin is possible 4 h after administration of these drugs, with an additive effect noted).

Grapefruit juice contains one or more components that inhibit CYP3A4 and can increase the plasma concentration of CYP3A4 metabolised agents. The increase in the activity of HMG-CoA reductase inhibitors after the use of 250 ml of juice per day is minimal and has no clinical significance. However, consumption of a large volume of juice (more than 1 liter per day) when taking simvastatin significantly increases the level of inhibitory activity against HMG-CoA reductase in blood plasma. In this connection, it is necessary to avoid consuming grapefruit juice in large quantities.

Overdose

No specific symptoms were identified in any of the several known cases of overdose (maximum accepted dose of 450 mg).

Treatment: induce vomiting, accept activated charcoal. Symptomatic therapy. Functions of the liver and kidneys, the level of CPK in serum, should be monitored.

In the development of myopathy with rhabdomyolysis and acute renal failure (a rare but severe side effect), immediately discontinue the drug and introduce diuretic and sodium bicarbonate to the patient (intravenous infusion). If necessary, hemodialysis is indicated.

Rhabdomyolysis can cause hyperkalemia, which can be eliminated by intravenous administration of calcium chloride or gluconate calcium by infusing glucose with insulin, using potassium ion exchangers or, in severe cases, hemodialysis.

Storage conditions

In a dry, dark place at a temperature of no higher than 25 ° C.

Shelf suitability

3 Year

dosage form

dosage form

tablets

Vertex, Russia



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