A Guide to Most Common Cholesterol Medications
A Guide to Most Common Cholesterol Medications
(Dyslipidemia Drugs)
The Most Famous 5 drugs most Commonly used in the Treatment of Dyslipidemia “Cholesterol Medications” are:
1- Atorvastatin 💊
2- Lovastatin 💊
3- Pravastatin 💊
4- Rosuvastatin 💊
5- Simvastatin 💊
Atorvastatin
- Brand Names: Lipitor
- Therapeutic Category: HMG-CoA Reductase Inhibitor
- Dosage Forms: oral (tablet)
- Use: Cholesterol Medications
- Labeled Indications: Dyslipidemias/ Prevention of cardiovascular disease (CVD)
- Off-Label: Cardiac risk reduction for noncardiac surgery (perioperative therapy)/ Noncardioembolic stroke
- Dosing : Adult: Oral: Initial: 10 or 20 mg once daily; patients requiring >45% reduction in LDL-C may be started at 40 mg once daily; range: 10 to 80 mg once daily
- Pediatric : Children ≥10 years and Adolescents: Oral: 10 mg once daily (maximum: 20 mg/day)
- Dose Adjustments
- Renal Impairment:. No dosage adjustment.
- Hepatic Impairment: Contraindicated in active liver disease or in patients with unexplained persistent elevations of serum transaminases.
- Adverse Drug Interaction:
Diarrhea/ Arthralgia/ Nasopharyngitis/ Insomnia - Pharmacodynamics/Kinetics:
- Onset of action: Initial changes: 3 to 5 days; Maximal reduction in plasma cholesterol and triglycerides: 2 to 4 weeks;
- Time to peak, serum: 1 to 2 hours
- Metabolism: Hepatic
- Half-life elimination: Parent drug: 14 hours; Equipotent metabolites: 20 to 30 hours
- Important Notes:
- Diabetes mellitus: Increases in HbA1c and fasting blood glucose have been reported with HMG-CoA reductase inhibitors
- Hepatotoxicity: Persistent elevations in serum transaminases have been reported
- Pregnancy & Lactation: Pregnancy category X/ not known if present in breast milk
- Drug safety issue:
AtorvaSTATin may be confused with atoMOXetine, lovastatin, nystatin, pitavastatin, pravastatin, rosuvastatin, simvastatinMevacor may be confused with Benicar, Lipitor
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Lovastatin
- Brand Names: Altoprev; Mevacor
- Therapeutic Category: HMG-CoA Reductase Inhibitor
- Dosage Forms: oral (tablet)
- Use: Cholesterol Medications
- Labeled Indications: Adjunct to dietary therapy to decrease elevated serum total and LDL-cholesterol concentrations/Primary prevention of coronary artery disease
- Off-Label: Cardiac risk reduction for noncardiac surgery/ Noncardioembolic stroke
- Dosing Adult: Dyslipidemia and primary prevention of CAD: Oral: Initial: 20 mg once daily with evening meal, then adjust at 4-week intervals; maximum dose: 80 mg daily
- Pediatric10 to 40 mg once daily with evening meal, then adjust dose at 4-week intervals
- Dose Adjustments
- Renal Impairment:. CrCl <30 mL/minute: Use with caution and carefully consider doses >20 mg/day.
- Hepatic Impairment: No dosage adjustment
- Adverse Drug Interaction:
Increased creatine phosphokinase/ Headache, dizziness - Pharmacodynamics/Kinetics:
- Onset of action: LDL-cholesterol reductions: 3 days
- Time to peak, serum: Immediate release: 2-4 hours
- Metabolism: Hepatic
- Half-life elimination: 1.1-1.7 hours
- Important Notes:
- Diabetes mellitus: Increases in HbA1c and fasting blood glucose have been reported with HMG-CoA reductase inhibitors
- Reduced cholesterol synthesis as a result of therapy could theoretically lead to reduced adrenal or gonadal steroid hormone production
- Pregnancy & Lactation: Pregnancy category X/ not known if present in breast milk
- Drug safety issue:
Lovastatin may be confused with atorvaSTATin, Leustatin, Livostin, Lotensin, nystatin, pitavastatin
Mevacor may be confused with Benicar, Lipitor
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Pravastatin
- Brand Names: Pravachol
- Therapeutic Category: HMG-CoA Reductase Inhibitor
- Dosage Forms: oral (tablet)
- Use: Cholesterol Medications
- Labeled Indications: Hyperlipidemia/ Prevention of cardiovascular disease
- Off-Label: Cardiac risk reduction for noncardiac surgery (perioperative therapy)/ Noncardioembolic stroke/Transient ischemic attack (secondary prevention)
- Dosing : Adult: Oral: Initial: 40 mg once daily; titrate dosage to response (maximum dose: 80 mg/day)
- Pediatric : Children and Adolescents 8 to 13 years: 20 mg once daily
- Adolescents 14 to 18 years: 40 mg once daily
- Dose Adjustments
- Renal Impairment:. no dosage adjustments
- Hepatic Impairment: Use is contraindicated.
- Adverse Drug Interaction:
Chest pain/ Headache/ fatigue/ Nausea - Pharmacodynamics/Kinetics:
- Onset of action: Several days
- Peak effect: 4 weeks
- Bioavailability: 17%
- Half-life elimination: 77 hours (including all metabolites)
- Important Notes:
- Diabetes mellitus: Increases in HbA1c and fasting blood glucose have been reported with HMG-CoA reductase inhibitors
- Reduced cholesterol synthesis as a result of therapy could theoretically lead to reduced adrenal or gonadal steroid hormone production
- Pregnancy & Lactation: Pregnancy category X/ excreted in breast milk
- Drug safety issue:
Pravachol may be confused with atorvaSTATin, Prevacid, Prinivil, propranolol
Pravastatin may be confused with nystatin, pitavastatin, prasugrel
Rosuvastatin
- Brand Names: Crestor
- Therapeutic Category: HMG-CoA Reductase Inhibitor
- Dosage Forms: oral (tablet)
- Use: Cholesterol Medications
- Labeled Indications: Familial hypercholesterolemia/ Hyperlipidemia and mixed dyslipidemia/ Hypertriglyceridemia
- Off-Label: Cardiac risk reduction for noncardiac surgery (perioperative therapy)/ Noncardioembolic stroke/Transient ischemic attack (secondary prevention)
- Dosing : Adult: usual dosage range: 5 to 40 mg once daily (maximum dose: 40 mg/day)
- Pediatric : Children 8 to <10 years: 5 to 10 mg once daily (maximum: 10 mg/day)
- Children ≥10 years and Adolescents: 5 to 20 mg once daily (maximum: 20 mg/day)
- Dose Adjustments
- Renal Impairment:. CrCl <30 mL/minute/1.73 m2: Initial: 5 mg once daily (maximum: 10 mg/day).
- Hepatic Impairment: no dosage adjustments
- Adverse Drug Interaction:
Myalgia/ Headache/ dizziness/ Nausea - Pharmacodynamics/Kinetics:
- Onset of action: Within 1 week; maximal at 4 weeks
- Time to peak, plasma: 3 to 5 hours
- Metabolism: Hepatic
- Half-life elimination: 19 hours
- Important Notes:
- Diabetes mellitus: Increases in HbA1c and fasting blood glucose have been reported with HMG-CoA reductase inhibitors
- Hematuria/proteinuria: Hematuria (microscopic) and proteinuria have been observed; more commonly reported in adults receiving rosuvastatin 40 mg daily
- Pregnancy & Lactation: Pregnancy category X/ present in breast milk
- Drug safety issue:
Rosuvastatin may be confused with atorvaSTATin, nystatin, pitavastatin
Simvastatin
- Brand Names: Zocor
- Therapeutic Category: HMG-CoA Reductase Inhibitor
- Dosage Forms: oral (tablet/suspension)
- Use:
- Labeled Indications: Dysbetalipoproteinemia/ Heterozygous familial and nonfamilial hypercholesterolemia and mixed dyslipidemia/ Prevention of cardiovascular events
- Off-Label: Cardiac risk reduction for noncardiac surgery (perioperative therapy)
- Dosing : Adult: Oral: 40 mg once daily in the evening
- If patient is unable to achieve low-density lipoprotein-cholesterol (LDL-C) goal using the 40 mg dose of simvastatin, increasing to 80 mg dose is not recommended. Instead, switch patient to an alternative LDL-C-lowering treatment
- Pediatric : Initial: 10 mg once daily in the evening; range: 10 to 40 mg/day (maximum: 40 mg/day))
- Dose Adjustments
- Renal Impairment:. No dosage adjustment.
- Hepatic Impairment: Contraindicated in active liver disease or in patients with unexplained persistent elevations of serum transaminases.
- Adverse Drug Interaction:
Atrial fibrillation/ Eczema/ Abdominal pain/ constipation - Pharmacodynamics/Kinetics:
- Onset of action: >3 days
- Peak effect: 2 weeks
- Metabolism: Hepatic
- Time to peak: 1.3 to 2.4 hours
- Important Notes:
- Diabetes mellitus: Increases in HbA1c and fasting blood glucose have been reported with HMG-CoA reductase inhibitors
- Hepatotoxicity: Persistent elevations in serum transaminases have been reported
- Pregnancy & Lactation: Pregnancy category X/ not known if present in breast milk
- Drug safety issue:
Simvastatin confused with atorvaSTATin, nystatin, pitavastatin
Zocor may confused with Cozaar, Lipitor, Zoloft, ZyrTEC
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