A Guide to Most Common Cholesterol Medications


A Guide to Most Common Cholesterol Medications

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 💊


 

1

Atorvastatin

Cholesterol Medications

  • 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

 


Highly recommend online Marketing tool from SEMRUSH

Cholesterol Medications


 

2

Lovastatin

Cholesterol Medications

 

  • 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

Highly Recommend this Hydrossential Serum: Amazing for your SkinCholesterol Medications

 


3

Pravastatin

Cholesterol Medications

  • 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


4

Rosuvastatin

Cholesterol Medications

  • 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

 


5

Simvastatin

Cholesterol Medications

  • 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

 


Read More


Related Readings:

Copyright ©: All content on FADIC Website, including medical opinion and any other health-related information, and drug Informtation is for informational purposes only