Index of drugs

hypercholesterolemia: supplementation of dietary therapy in order to lower elevated total cholesterol, LDL cholesterol, apolipoprotein B and triglycerides in adults, adolescents and children aged 10 years or older with primary hypercholesterolaemia, including heterozygous familial hypercholesterolaemia or mixed (hyperlipidemia) hyperlipidemia - corresponding to type hyperlipidemia IIa and IIb according to Fredrickson's classification, in the case of insufficient response to the use of diet and other non-pharmacological methods of treatment. The drug is also used to lower total cholesterol and LDL-cholesterol in patients with homozygous familial hypercholesterolemia, as added therapy to other lipid-lowering therapy (eg LDL cholesterol apheresis) or when such therapy is not available.Prevention of cardiovascular diseases: Prevention of cardiovascular events in adult patients at risk of the first event being assessed as high, along with activities aimed at reducing other risk factors.

1 tabl powl. contains 10 mg, 20 mg, 40 mg or 80 mg of Atorvastatin (as Calcium salt); Table. powl. contain contains lactose. 1 tabl for chewing and chewing contains 5 mg or 10 mg of atorvastatin (in the form of calcium salt); Table. chewing and chewing contains aspartame.

A selective, competitive inhibitor of HMG-CoA reductase - an enzyme limiting the rate of cholesterol synthesis, catalyzing the conversion of 3-hydroxy-3-methylglutaryl-coenzyme A to mevalonate - a precursor of sterols, including cholesterol. Atorvastatin reduces blood cholesterol and lipoprotein levels by inhibiting HMG-CoA reductase, which in turn inhibits cholesterol biosynthesis in the liver and leads to an increase in the number of LDL receptors on the surface of the hepatocytes cell membrane, thereby increasing the uptake and catabolism of LDL. It reduces the production of LDL and the amount of LDL particles, induces a significant and sustained increase in LDL receptor activity and preferably changes the quality of circulating LDL molecules. It reduces LDL (LDL-C) cholesterol in patients with homozygous familial hypercholesterolaemia who have not generally responded to lipid-lowering therapy. Atorvastatin reduces total cholesterol (by 30-46%), LDL-C (by 41-61%), apolipoprotein B (by 34-50%) and triglycerides (by 14-33%) and increases HDL-C and apolipoprotein A1. Atorvastatin is rapidly absorbed from the gastrointestinal tract, reaching C_max after 1-2 h. The absolute bioavailability is about 12%, and the systemic activity inhibiting HMG-CoA reductase is about 30%. Plasma proteins are more than 98% bound. It is metabolized in the liver by cytochrome P-450 3A4 to ortho- and parahydroxylated derivatives and various β-oxidation products that are further metabolised by glucuronidation. About 70% of the HMG-CoA reductase inhibitory activity is attributed to active metabolites. The drug is mainly excreted in the bile. Medium T_0,5 is approximately 14 h. The half-life of HMG-CoA reductase inhibitors is 20-30 h due to the effect of active metabolites. Renal failure does not affect the concentration of atorvastatin and its active metabolites in the blood or its effectiveness. The concentration of atorvastatin and its active metabolites in the blood is significantly increased (C_max approximately 16 times and AUC approximately 11 times) in patients with chronic alcohol-related liver injury (Childs-Pugh B).

Hypersensitivity to atorvastatin or any of the excipients. Active liver disease or unexplained, permanently elevated blood aminotransferase levels exceeding the upper limit of normal (ULN) 3-fold. Pregnancy. Breastfeeding period. Women of childbearing potential not using effective methods of contraception.

Atorvastatin should be used with caution in patients with predisposing factors for myopathy or rhabdomyolysis such as: renal dysfunction, hypothyroidism, muscle disease or history of hereditary muscular diseases, signs of muscle damage following the use of another HMG-CoA reductase inhibitor or fibrates , history of liver disease and / or large amounts of alcohol, age> 70 years, situations in which blood levels may increase (eg patients with a polymorphism in the OATP1B1 - SLCO1B1 c.521CC gene - greater exposure to atorvastatin).The risk of myopathy may also be increased if atorvastatin interacts with other drugs (pharmacokinetic or pharmacodynamic interactions, see also interactions). In patients with an increased risk of myopathy, the risks and benefits of treatment should be considered and patients should be monitored during treatment; before initiation of therapy, creatine kinase (CK) activity should be determined. If the CK activity is significantly increased during the first determination (> 5 x ULN), follow-up should be performed after 5-7 days. Treatment should not be initiated if the control CK> 5 x ULN. If unexplained muscle pain, muscle weakness or muscle spasms occur during treatment with Atorvastatin, especially when accompanied by malaise or fever, CK activity should be determined. Treatment should be discontinued if CK activity is significantly increased (> 5 times ULN) or if the muscle symptoms are severe and cause discomfort during daily activities (even if CK activity ≤5 times ULN). Once the clinical symptoms have subsided and CK levels are reduced to normal, re-use of atorvastatin or another HMG-CoA inhibitor at the lowest dose may be considered with close observation of the patient. Treatment with atorvastatin must be discontinued if there is a significant increase in CK (> 10 x ULN) or when rhabdomyolysis occurs or is suspected. Very rare cases of immunological necrotizing myopathy (IMNM) have been reported, which are clinically characterized by permanent weakness of the proximal muscles and elevated CK levels during or after withdrawal of statins. Liver check-ups should be performed prior to initiation of therapy and liver function should be monitored during therapy. Patients who develop signs or symptoms of liver damage should undergo liver function tests. If transaminase elevation is detected, the patient should be monitored until resolution of the disorder. In the case of persistent elevation of aminotransferases, greater than 3-fold of GGN, it is recommended to reduce the dose of the drug or its discontinuation. The drug should be used with caution in patients who are abusing alcohol and / or have a history of liver disease. In patients without a history of coronary artery disease who have recently undergone a stroke or a transient ischemic attack, haemorrhagic strokes have been more frequent in patients treated with atorvastatin 80 mg, compared to the placebo group. Increased risk has been observed mainly in patients with pre-existing hemorrhagic stroke or lacunar infarction - in these patients, the potential risk of haemorrhagic stroke should be carefully considered before initiating treatment with atorvastatin 80 mg. If the patient is suspected of developing interstitial lung disease (manifested by dyspnoea, dry cough, general deterioration of health - fatigue, weight loss, fever), statin therapy should be discontinued. Statins can cause an increase in blood Glucose and in some patients at risk for developing diabetes can cause hyperglycaemia, which requires proper diabetes care. However, this risk should not be a reason for discontinuation of statin therapy, because the benefits of reducing the risk of vascular disorders due to the use of statins are greater. Patients at risk (with a fasting glucose level of 5.6-6.9 mmol / l, BMI> 30 kg / m², increased triglycerides, hypertension) should be monitored both clinically and biochemically in accordance with national guidelines. There is limited experience in the use of atorvastatin in children aged 6-10 years, therefore the medicine is not recommended for use in children <10 years of age. There are no studies on the effects of the medicine on the development of children. Due to the lactose content, the tablets are powl. should not be used in patients with rare hereditary galactose intolerance, lactase deficiency (Lapp type) or malabsorption of glucose-galactose. Due to the content of aspartame, tabl. chewing and chewing may be harmful for people with phenylketonuria.

Use during pregnancy and breast-feeding is contraindicated. Patients of childbearing age should use effective methods of contraception.

Common: rhinitis, allergic reactions, hyperglycemia, headache, sore throat and larynx, nosebleeds, constipation, bloating, indigestion, nausea, diarrhea, myalgia, joint pain, limb pain, muscle cramps, swollen joints , back pain, abnormal liver function tests, increased blood creatine kinase. Uncommon: hypoglycaemia, weight gain, anorexia, nightmares, insomnia, dizziness, paresthesia, hypoesthesia, dysgeusia, amnesia, blurred vision, tinnitus, vomiting, pain in the upper and lower abdomen, belching in the return of gastric contents , pancreatitis, hepatitis, urticaria, pruritus, rash, alopecia, neck pain, muscular fatigue, malaise, weakness, chest pain, peripheral edema, fatigue, fever, white blood cells in the urine. Rare: thrombocytopenia, peripheral neuropathy, blurred vision, cholestasis, angioneurotic edema, bladder rash (including erythema multiforme, Stevens-Johnson syndrome and toxic epidermal necrolysis), myopathy, myositis, rhabdomyolysis, tendon problems sometimes complicated by tendon rupture. Very rare: anaphylaxis, hearing loss, liver failure, gynecomastia. During the use of atorvastatin, an increase in serum transaminases was observed (these changes were usually mild and transient and did not require discontinuation of therapy). Clinically important (> 3 times ULN) increase in blood transaminases occurred in 0.8% of patients (it was dose-dependent and reversible in all patients). Increased CK activity in the blood (> 3 times above ULN) was noted in 2.5% of patients. A 10-fold increase in CK activity occurred in 0.4% of patients.Children. Common: headache, abdominal pain, increased ALT, increased creatine phosphokinase in the blood. Based on the available data, it can be expected that the frequency, type and severity of side effects in children will be the same as in adult patients. Data on long-term safety in children are limited. During treatment with some statins, the following side effects have been reported: sexual dysfunction, depression, isolated cases of interstitial lung disease (especially during long-term treatment), diabetes mellitus.

Orally. The dose should be adjusted individually depending on the purpose of treatment, LDL-cholesterol before treatment and patient's response to treatment. Before and during the treatment, the patient should use a standard low cholesterol diet. The usual starting dose is 10 mg once a day. Dose modifications should be made every 4 weeks or less frequently. The maximum dose is 80 mg once a day.Primary hypercholesterolemia and mixed hyperlipidemia: 10 mg once a day; efficacy is observed within 2 weeks and the maximum response is usually achieved within 4 weeks and is maintained during long-term treatment.Heterozygous familial hypercholesterolaemia: the recommended starting dose is 10 mg once a day; dose changes should be made every 4 weeks to achieve a 40 mg dose once a day; then the dose can be either increased to a maximum dose of 80 mg once a day or atorvastatin 40 mg once a day in combination with bile acid sequestrants.Homozygous familial hypercholesterolaemia: 10-80 mg once a day as adjunctive therapy for other lipid-lowering therapy (eg LDL cholesterol apheresis) or when such treatments are not available.Prevention of cardiovascular diseases: 10 mg once a day; to get the recommended LDL-cholesterol level, higher doses may be necessary.Special groups of patients. There is no need to change the dosage in patients with renal insufficiency and in the elderly.Children from 10 years. Hypercholesterolemia: the use of the preparation should be under the control of specialist physicians experienced in the treatment of hyperlipidemia in children; Regularly assess the health of patients in terms of treatment effectiveness. The recommended starting dose is 10 mg daily, the dose may be increased to 20 mg daily, depending on the response to treatment and tolerability. Data regarding the safety of children at doses above 20 mg (corresponding to approximately 0.5 mg / kg) are limited.Way of giving. The daily dose of atorvastatin is given as a single dose only. The preparation can be taken at any time of the day, regardless of meals. Table. chewing and chewing can be chewed or swallowed whole with water.