Atorvastatin
Brand names: Lipitor
Atorvastatin is a synthetic HMG-CoA reductase inhibitor (statin) used for lipid lowering and cardiovascular risk reduction in primary and secondary prevention, including atherosclerotic vascular disease.
Adult dose
Dose adjustments
No adjustment of dose is required.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance or to any of the excipients
- Active liver disease or unexplained persistent elevations of serum transaminases exceeding 3 times the upper limit of normal
- Pregnancy, breast-feeding, and women of child-bearing potential not using appropriate contraceptive measures
- Treatment with the hepatitis C antivirals glecaprevir/pibrentasvir
Side effects
- Nasopharyngitis
- Headache
- Constipation, flatulence, dyspepsia, nausea, diarrhoea
- Myalgia, arthralgia, pain in extremity, muscle spasms, back pain
- Hyperglycaemia
Interactions
- Elbasvir/grazoprevir or letermovir: do not exceed atorvastatin 20 mg/day
- Letermovir co-administered with ciclosporin: use of atorvastatin not recommended
- Glecaprevir/pibrentasvir: contraindicated
- CYP3A4 and transporter (OATP1B1/1B3, P-gp, BCRP) inhibitors: increased atorvastatin exposure and risk of myopathy/rhabdomyolysis
Clinical monograph
How it works
It competitively inhibits HMG-CoA reductase, the rate-limiting enzyme of hepatic cholesterol synthesis, upregulating LDL receptors and lowering circulating LDL-cholesterol, with additional plaque-stabilising and anti-inflammatory effects.
Prescribing in practice
- Advise patients to report unexplained muscle pain, tenderness or weakness promptly, as statins can rarely cause myopathy or rhabdomyolysis; check creatine kinase if symptoms occur and review interacting drugs.
- It is metabolised by CYP3A4, so interactions with macrolides, azole antifungals, certain calcium-channel blockers and grapefruit juice can raise concentrations and myopathy risk.
- Atorvastatin is contraindicated in active liver disease and in pregnancy and breast-feeding.
Monitoring
Check baseline lipids, liver transaminases and a baseline creatine kinase where indicated, with transaminases rechecked within the first months of treatment per current prescribing references.
Counselling the patient
- Can be taken at any time of day, with or without food.
- Report unexplained muscle pain or weakness.
- Continue a healthy diet and lifestyle alongside treatment.
Evidence & guidelines
Large outcome trials and meta-analyses establish that atorvastatin lowers cardiovascular events across the spectrum of vascular risk, underpinning its use in NICE lipid-modification guidance.
Reference: NICE NG238; ASCOT-LLA trial; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Framingham Risk Score · Cardiovascular Risk
- ACC/AHA Pooled Cohort Equations — ASCVD Risk · Cardiovascular Risk
- PREVENT Cardiovascular Risk Calculator (AHA/ACC 2023) · Cardiovascular Risk
- Reynolds Risk Score for Women · Cardiovascular Risk
- SCORE2 — 10-Year CVD Risk (Age 40–69) · Cardiovascular Risk
- SCORE2-OP — 5/10-Year CVD Risk (Age ≥ 70) · Cardiovascular Risk
- Peripheral Arterial Disease · NICE NG19 2012 / ESVS 2017
- Carotid Artery Disease · NICE CG68 / ESVS 2018
- Varicose Veins Management · NICE CG168 2013
- Venous Leg Ulcer Management · NICE NG204 2022
- Acute Heart Failure · ESC 2021 Heart Failure Guidelines; NICE NG106
- NSTEMI / Unstable Angina · ESC 2020 NSTEMI Guidelines; NICE NG185