HMG-CoA reductase inhibitor (statin)

Atorvastatin

Inhibits HMG-CoA reductase, reducing hepatic cholesterol synthesis, upregulating LDL receptors and lowering LDL cholesterol; also stabilises plaque through pleiotropic anti-inflammatory effects.

ATC C10AA05OralLast reviewed 2026-08-20

Brands

Lipitor · Atorva · Storvas

Adult dosing

Maximum 80 mg/day
IndicationDoseRouteFrequency
Secondary prevention / ACS (high intensity)80 mgOralOnce daily
Primary prevention20 mgMax 80 mg once dailyOralOnce daily
With a CYP3A4 inhibitor10-20 mgCap the dose or choose pravastatinOralOnce daily

Older adults: No dose change, but review interacting drugs and muscle symptoms.

Paediatric dosing

Always confirm the weight and the local paediatric formulary
IndicationDoseRouteFrequency
Heterozygous familial hypercholesterolaemia, 10 years and older10 mgMax 20 mg once daily (higher only in specialist care)OralOnce daily

Renal adjustment

Move the slider to the patient's eGFR
60 mL/min/1.73 m²
no changeAny eGFR

No adjustment — biliary elimination

Prefer atorvastatin over rosuvastatin in advanced CKD

  • Any eGFRNo adjustment — biliary elimination

Hepatic adjustment

  • Active liver disease or ALT above 3× upper limitDo not use
  • Stable fatty liverUsual dose; statins are not contraindicated

Practical notes

The things that go wrong at the bedside
  • Any time of day is acceptable — the half-life is long, unlike simvastatin.
  • Check lipids 8-12 weeks after starting or changing dose, aiming for a ≥ 50% LDL reduction.

DrZep structured dosing table (demo dataset, formulary-aligned) · DrZep. Confirm every dose against your local formulary and the patient's weight, renal function and comorbidities.

Indications

  • Secondary prevention after ACS, stroke or peripheral arterial disease
  • Primary prevention with elevated cardiovascular risk
  • Familial hypercholesterolaemia
  • Diabetes with additional risk factors

Dosing summary

High intensity (secondary prevention)
40-80 mg once daily
Moderate intensity
10-20 mg once daily
Target
LDL reduction ≥ 50% and LDL < 1.4 mmol/L in very high risk

Organ adjustment

Renal

All stages including dialysis
No dose adjustment (hepatic elimination); benefit is limited in dialysis patients

Hepatic

Transaminases < 3× ULN
May continue with monitoring
Active liver disease or unexplained persistent transaminases > 3× ULN
Contraindicated

Monitoring

  1. 1Lipid profile 8-12 weeks after starting or changing dose
  2. 2Baseline liver enzymes; recheck if symptomatic
  3. 3Creatine kinase only if muscle symptoms occur
  4. 4HbA1c in those at diabetes risk

Contraindications & cautions

Do not use / use with care

  • Active liver disease
  • Pregnancy and breastfeeding
  • Previous statin-related rhabdomyolysis

Pregnancy & lactation

Pregnancy
Avoid; stop before conception. Recent regulatory reviews are less absolute, but discontinue unless a specialist advises otherwise.
Lactation
Avoid.

Interactions

  • Clarithromycin, itraconazole, ritonavir (CYP3A4 inhibitors)Raised statin levels and myopathy riskmajor
  • CiclosporinMarkedly raised atorvastatin exposuremajor
  • GemfibrozilRhabdomyolysis risk — avoid the combinationmajor
  • Grapefruit juice (large quantities)Increased exposuremoderate
  • Amiodarone, diltiazem, verapamilIncreased statin levels — consider a lower dosemoderate

Adverse effects

Common

  • Myalgia
  • Headache
  • Dyspepsia
  • Mild transaminase elevation

Serious

  • Rhabdomyolysis
  • Immune-mediated necrotising myopathy
  • Hepatotoxicity
  • Small increase in new-onset diabetes

Toxicity & overdose

Recognise and treat

  • Rhabdomyolysis: proximal myalgia, weakness, dark urine, CK > 10× ULN — stop the statin, hydrate and monitor renal function and potassium

Alternatives

  • Rosuvastatin
  • Ezetimibe (add-on or intolerance)
  • PCSK9 inhibitor or inclisiran
  • Bempedoic acid

Demo monograph for educational use. Always confirm dose, route and interactions against your national formulary and the product label before prescribing.

DrZep v0.1

Demo content. Educational decision support only. Verify every dose, citation and recommendation against your national formulary and the primary source before clinical use.