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HMG-CoA Reductase Inhibitor (Statin) Pregnancy: Contraindicated during pregnancy and breast-feeding. Women of child-bearing potential should use appropriate contraceptive measures; suspend treatment for the duration of pregnancy.

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.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 10 mg once daily (usual starting dose); range 10 mg to 80 mg once daily
Route: Oral
Frequency: Once daily
Max: 80 mg once daily
Prevention of cardiovascular disease: in the primary prevention trials the dose was 10 mg/day; higher doses may be necessary to attain LDL-cholesterol levels according to current guidelines. Dose individualised according to baseline LDL-C, goal of therapy and patient response; adjust at intervals of 4 weeks or more. Heterozygous familial hypercholesterolaemia: start 10 mg daily, adjust every 4 weeks to 40 mg daily, then to a maximum of 80 mg daily. Homozygous familial hypercholesterolaemia: 10 to 80 mg daily. May be taken at any time of day with or without food. Do not exceed 20 mg/day with elbasvir/grazoprevir or letermovir.

Dose adjustments

Renal

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.