Pravastatin vs Simvastatin
Medical Disclaimer: This content is for informational purposes only and does not constitute medical advice. Always consult your healthcare provider before starting, stopping, or changing any medication. Using this site does not create a doctor-patient relationship.
Drug information changes as the FDA updates labeling, and we cannot guarantee it is complete or current. Verify critical details with your pharmacist or physician.
Emergencies: If you think you may have a medical emergency, call 911 immediately. For a suspected overdose, call Poison Control at 1-800-222-1222. Report side effects to the FDA MedWatch program at fda.gov/medwatch or 1-800-FDA-1088.
See our Terms of Use and Editorial Policy.
Pravastatin (Pravachol) and simvastatin (Zocor) are both HMG-CoA reductase inhibitors (statins) used to lower LDL cholesterol and reduce cardiovascular risk [1][2]. While they share the same general mechanism, they differ in potency, drug interaction profile, and muscle-related side effect risk.
Simvastatin was one of the first statins available (approved 1991) and has extensive cardiovascular outcomes data from the landmark 4S and HPS trials [2][3]. Pravastatin was approved in 1991 as well and has outcomes data from the WOSCOPS and CARE trials [1][4].
A key distinction is their metabolism: simvastatin is extensively metabolized by CYP3A4, creating numerous drug interaction concerns, while pravastatin is not significantly metabolized by CYP enzymes, giving it a much cleaner interaction profile [1][2].
Pravastatin vs Simvastatin: Side-by-side comparison
| Category | Pravastatin | Simvastatin |
|---|---|---|
| Drug Class | HMG-CoA reductase inhibitor (statin) | HMG-CoA reductase inhibitor (statin) |
| Generic Name | Pravastatin sodium | Simvastatin |
| Brand Name | Pravachol | Zocor |
| FDA Approved For | Hyperlipidemia, CV risk reduction | Hyperlipidemia, CV risk reduction |
| LDL Reduction (40 mg) | 30-34% | 37-41% |
| CYP Metabolism | Minimal (not CYP3A4-dependent) | Extensive CYP3A4 metabolism |
| Drug Interactions | Few | Many (CYP3A4 inhibitors, CCBs, amiodarone) |
| Dosage Forms | Tablets (10, 20, 40, 80 mg) | Tablets (5, 10, 20, 40, 80 mg) |
| Typical Dose | 40 mg once daily | 20-40 mg once daily (evening) |
| Myopathy Risk | Lowest among statins | Higher, especially at 80 mg dose |
| Landmark Trials | WOSCOPS, CARE | 4S, HPS |
| Cost (Generic) | $5-$15/month | $4-$12/month |
Efficacy: How well does each drug work?
Both statins reduce LDL cholesterol, but simvastatin is more potent at comparable doses [2][3]. Simvastatin 40 mg reduces LDL by approximately 37-41%, while pravastatin 40 mg reduces LDL by approximately 30-34% [1][2]. Neither is as potent as atorvastatin or rosuvastatin.
Both have demonstrated cardiovascular outcomes benefits. The Scandinavian Simvastatin Survival Study (4S) showed simvastatin reduced total mortality by 30% and cardiovascular death by 42% in patients with coronary heart disease [3]. The Heart Protection Study (HPS) showed simvastatin reduced major vascular events by 25% [3].
Pravastatin reduced coronary events by 31% in the WOSCOPS primary prevention trial and by 24% in the CARE secondary prevention trial [4]. Both medications have solid evidence supporting their cardiovascular benefits.
Current guidelines generally recommend high-intensity statins (atorvastatin 40-80 mg or rosuvastatin 20-40 mg) for high-risk patients, which has shifted prescribing away from moderate-intensity statins like simvastatin and pravastatin [5].
Side effects comparison
Muscle-related side effects (myalgia, myopathy, rhabdomyolysis) are a concern with all statins, but the risk differs between these two [1][2].
Simvastatin at 80 mg carries a significantly elevated risk of myopathy (0.9% per year), leading the FDA to restrict this dose to patients already tolerating it for 12+ months [2]. At 40 mg, the risk is lower but still present. Simvastatin's CYP3A4 metabolism means numerous drugs can increase its blood levels and muscle risk: amiodarone, amlodipine, diltiazem, verapamil, strong CYP3A4 inhibitors (clarithromycin, ketoconazole, HIV protease inhibitors), and grapefruit juice [2].
Pravastatin has the lowest muscle-related side effect risk among commonly used statins [1]. It is not metabolized by CYP3A4, so the drug interaction concerns that plague simvastatin are largely absent [1]. This makes pravastatin particularly useful for patients on complex medication regimens.
Other shared statin side effects include elevated liver enzymes (rare), headache, GI upset, and a small increased risk of new-onset diabetes [1][2].
Cost comparison
Convenience and dosing
Both are once-daily medications typically taken in the evening (statins are slightly more effective when taken at night because cholesterol synthesis peaks overnight) [1][2]. Pravastatin can be taken without regard to food, while simvastatin should be taken in the evening [1][2]. Both are simple oral tablets.
Which is right for you?
In modern practice, both pravastatin and simvastatin have been largely superseded by atorvastatin and rosuvastatin for patients requiring significant LDL lowering [5].
Pravastatin remains useful for patients who need a statin with minimal drug interactions (e.g., patients on calcium channel blockers, amiodarone, or other CYP3A4-affecting drugs) and patients who have experienced muscle side effects with other statins [1].
Simvastatin remains appropriate for patients already stable on it at doses of 40 mg or less. The 80 mg dose should generally be avoided due to myopathy risk [2].
If more potent LDL lowering is needed, atorvastatin or rosuvastatin is typically preferred over increasing the dose of either pravastatin or simvastatin [5].
This information is for educational purposes only. Consult your healthcare provider for statin selection.
Frequently asked questions
References
- [Regulatory] Pravastatin (Pravachol) prescribing information. Bristol-Myers Squibb. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/019898s073lbl.pdf Accessed 2025-06-15.
- [Regulatory] Simvastatin (Zocor) prescribing information. Merck. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/019766s110lbl.pdf Accessed 2025-06-15.
- [Regulatory] Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease (4S). Lancet. 1994;344(8934):1383-1389. https://doi.org/10.1016/S0140-6736(94)90566-5 Accessed 2025-06-15.
- [Regulatory] Shepherd J, et al. Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia (WOSCOPS). N Engl J Med. 1995;333(20):1301-1307. https://doi.org/10.1056/NEJM199511163332001 Accessed 2025-06-15.
- [Regulatory] Grundy SM, et al. 2018 AHA/ACC guideline on the management of blood cholesterol. Circulation. 2019;139(25):e1082-e1143. https://doi.org/10.1161/CIR.0000000000000625 Accessed 2025-06-15.
- [Observational] GoodRx price comparison: pravastatin and simvastatin. https://www.goodrx.com Accessed 2025-06-15.
Written and fact-checked by PrescriptionDrugs.org Editorial Team
Last updated: