Atorvastatin (Lipitor)
HMG-CoA reductase inhibitor for cholesterol management. Active metabolites (ortho- and para-hydroxy) are equipotent and account for ~70% of total inhibitory activity.
Projected serum levels — 20 mg, once daily
Maintenance schedule: 20 mg once daily (oral).
Modeled steady state after ~1 days: peak ≈ 1.0 mg, trough ≈ 0.005 mg body load. Population-based estimate over 15 days for a 20 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Statin
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 14 h
- Common dose
- 20 mg
- Suggested maximum
- 80 mg/day
- Reference dose range
- 5–80 mg (single dose)
- Suggested cadence
- once daily
- Validated against
- 40 mg oral — Cmax 0.027 mg/L at 1.5 h
Documented interactions
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contraindicated
Efavirenz (Sustiva) + Atorvastatin (Lipitor)
Efavirenz (Sustiva) inducer of CYP3A4 predicted to change Atorvastatin (Lipitor) AUC by ~0.16x
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contraindicated
Rifampin + Atorvastatin (Lipitor)
Rifampin inducer of CYP3A4 predicted to change Atorvastatin (Lipitor) AUC by ~0.16x
-
danger
Amlodipine (Norvasc) + Atorvastatin (Lipitor)
Amlodipine (Norvasc) reversible_inhibitor of CYP3A4 predicted to change Atorvastatin (Lipitor) AUC by ~2.07x
-
danger
Ashwagandha (KSM-66) + Atorvastatin (Lipitor)
Ashwagandha (KSM-66) reversible_inhibitor of CYP3A4 predicted to change Atorvastatin (Lipitor) AUC by ~2.07x
-
danger
Berberine + Atorvastatin (Lipitor)
Berberine reversible_inhibitor of CYP3A4 predicted to change Atorvastatin (Lipitor) AUC by ~2.07x
-
danger
Black Seed Oil (Nigella sativa / Thymoquinone) + Atorvastatin (Lipitor)
Black Seed Oil (Nigella sativa / Thymoquinone) reversible_inhibitor of CYP3A4 predicted to change Atorvastatin (Lipitor) AUC by ~2.07x
Serum checks 241 modeled interaction pairings for atorvastatin (lipitor) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations (ASCOT-LLA)
RCT of 10,305 patients found atorvastatin 10 mg reduced fatal and non-fatal stroke by 27% and total cardiovascular events by 21% in hypertensive patients with normal cholesterol.
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Intensive versus moderate lipid lowering with statins after acute coronary syndromes (PROVE IT-TIMI 22)
Landmark trial of 4,162 acute coronary syndrome patients found atorvastatin 80 mg reduced death and major cardiovascular events by 16% compared to pravastatin 40 mg.
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Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials
Meta-analysis of 26 statin trials found each 1 mmol/L LDL reduction reduced major vascular events by 22%, major coronary events by 24%, and stroke by 15%.
3 published studies referenced in the app, each with a plain-language summary.