Примери за използване на Neosimva на Английски и техните преводи на Български
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Neosimva is indicated for the treatment of.
Special considerations for treatment Neosimva.
Neosimva is contraindicated during pregnancy.
Patients with mild to moderate hypercholesterolemia can be treated with an initial dose of 10 mg Neosimva.
Do not take Neosimva under the following conditions.
The risk of myopathy/ rhabdomyolysis is increased by concomitant administration of Neosimva following medications.
Neosimva ratios decreased LDL/ FTOL and total cholesterol/ HDL.
Diltiazem: Patients taking concomitant Neosimva and Diltiazem 80 mg have a slightly increased risk of myopathy.
Neosimva is effective alone or in combination with bile acid sequestrants.
Active liver diseases orunexplained transaminase increases are contraindications to the use of Neosimva.
Neosimva dosage ranges from 5 to 80 mg per day taken once daily in the evening.
Diltiazem: The risk of myopathy is increased slightly in patients Diltiazem,who simultaneously accept Neosimva 80 mg.
Neosimva generally well tolerated, the majority of the known side effects are mild and transient.
There is no evidence to suggest that taking Neosimva would affect your ability to drive or use machines.
Neosimva treatment should be discontinued during pregnancy or until it is established that the woman is not pregnant.
In patients with coronary artery disease and hypercholesterolemia, Neosimva been shown to slow the progression of coronary atherosclerosis, incl.
Neosimva is indicated for the treatment of patients with primary disbetalipoproteinemiya(Fredrickson type III hyperlipidemia);
Cyclosporine: The risk of myopathy/ rhabdomyolysis is increased by concomitant administration of cyclosporine,especially with high doses Neosimva.
In patients taking Neosimva with Amiodarone or Verapamil, the dose should not exceed 20 mg daily.
Amiodarone or Verapamil:The risk of myopathy/ rhabdomyolysis is increased by concomitant use of higher doses Neosimva c Amiodarone or Verapamil.
Neosimva should be used in addition to other cholesterol-lowering treatments(eg LDL apheresis) in these patients or if such treatments do not exist.
Because many drugs are excreted in human milk andbecause of the potential for serious side effects women receiving Neosimva, should not breastfeed.
The recommended dosage for patients with homozygous familial hypercholesterolemia is Neosimva 40 mg daily in the evening or 80 mg daily in 3 divided doses- 20 mg, 20 mg, and an evening dose of 40 mg.
Neosimva is also indicated in addition to diet and other measures nedietichni for the treatment of patients with homozygous familial hypercholesterolemia to reduce elevated total-C, LDL-C, apo-B.
The patient should be placed on a standard cholesterol-lowering diet before applying Neosimva and adhering to this diet should be continued during treatment with Neosimva.
In patients with diabetes, Neosimva been shown to reduce the risk of developing complications from the large peripheral vessels(peripheral revascularization procedures, amputations of the lower limbs or feet ulkusi).
Patients taking Cyclosporine, Gemfibrozil, other fibrates(except Fenofibrate) or Niacin(nicotinic acid) in lipid lowering doses(>1g daily) in combination with Neosimva, the dose should not exceed 10 mg daily.
Patients at high risk of CHD(with or without hyperlipidaemia), ie in patients with diabetes, history of stroke or other cerebrovascular disease, peripheral vascular disease orwith known coronary artery disease, Neosimva is indicated for.
Patients at high risk of CHD(with or without hyperlipidaemia), ie patients with diabetes, history of stroke or other cerebrovascular disease, peripheral vascular disease or with known coronary artery disease,the usual starting dose is 40 mg Neosimva once daily in the evening.