Drug class
Antihyperlipidemics HMGCo-A Reductase Inhibitors (Statins)
Antihyperlipidemics: HMG-CoA reductase inhibitors, commonly referred to as statins, are a foundational class of lipid-lowering therapeutic agents. Read more about Antihyperlipidemics HMGCo-A Reductase Inhibitors (Statins)
195 drugs in this class 87 manufacturers
Drugs in Antihyperlipidemics HMGCo-A Reductase Inhibitors (Statins)
LOVASTATIN
PRAVASTATIN SODIUM
ROSUVASTATIN CALCIUM
SIMVASTATIN
PRAVASTATIN SODIUM
ROSUVASTATIN CALCIUM
ROSUVASTATIN CALCIUM
ATORVASTATIN CALCIUM
Antihyperlipidemics: HMG-CoA reductase inhibitors, commonly referred to as statins, are a foundational class of lipid-lowering therapeutic agents.
They function by competitively inhibiting 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme in hepatic cholesterol biosynthesis, which triggers an upregulation of hepatic low-density lipoprotein (LDL) receptors and accelerates the clearance of circulating atherogenic lipoproteins.
Clinically, these medications are primarily prescribed to treat primary hyperlipidemia and mixed dyslipidemia, as well as for the primary and secondary prevention of atherosclerotic cardiovascular disease, including myocardial infarction and ischemic stroke.
-
nih.gov
Antihyperlipidemics: HMG-CoA reductase inhibitors, commonly referred to as statins, are a foundational class of lipid-lowering therapeutic agents Clinically, these medications are primarily prescribed to treat primary hyperlipidemia and mixed dyslipidemia, as well as for the primary and secondary prevention of atherosclerotic cardiovascular disease, including myocardial infarction and ischemic stroke
-
nih.gov
Antihyperlipidemics: HMG-CoA reductase inhibitors, commonly referred to as statins, are a foundational class of lipid-lowering therapeutic agents They function by competitively inhibiting 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme in hepatic cholesterol biosynthesis, which triggers an upregulation of hepatic low-density lipoprotein (LDL) receptors and accelerates the clearance of circulating atherogenic lipoproteins
-
nih.gov
They function by competitively inhibiting 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme in hepatic cholesterol biosynthesis, which triggers an upregulation of hepatic low-density lipoprotein (LDL) receptors and accelerates the clearance of circulating atherogenic lipoproteins
-
nih.gov
Clinically, these medications are primarily prescribed to treat primary hyperlipidemia and mixed dyslipidemia, as well as for the primary and secondary prevention of atherosclerotic cardiovascular disease, including myocardial infarction and ischemic stroke
-
nih.gov
Clinically, these medications are primarily prescribed to treat primary hyperlipidemia and mixed dyslipidemia, as well as for the primary and secondary prevention of atherosclerotic cardiovascular disease, including myocardial infarction and ischemic stroke
Sign in to follow this class
Following a drug class requires a free Physicians Office Resource account.