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Atorvastatin is Dragon Pharma's formulation of the most potent widely available statin at 40mg per tablet β HMG-CoA reductase inhibitor that reduces LDL cholesterol by 39-60% depending on dose. In the context of AAS use, Atorvastatin addresses one of the most clinically significant and consistently underappreciated cardiovascular risks of anabolic steroid cycles: the dramatic deterioration of the LDL/HDL ratio that virtually all AAS produce to varying degrees.
Also searched as: Atorvastatin 40mg, Lipitor 40mg, statin cholesterol AAS cycle, Atorvastatin Dragon Pharma.
The cardiovascular risk from AAS is frequently discussed in terms of blood pressure and cardiac hypertrophy, but cholesterol dysregulation is equally significant and often less proactively managed:
Atorvastatin is not just any statin β it is consistently among the most potent LDL-lowering statins available:
| Statin | LDL Reduction at Standard Dose | Notes |
|---|---|---|
| Atorvastatin 40mg | ~39β60% | Most potent widely available statin at this dose |
| Rosuvastatin 20mg | ~45β55% | Comparable to Atorvastatin; less hepatic metabolism |
| Simvastatin 40mg | ~35β45% | Older statin; more drug interactions |
| Pravastatin 40mg | ~25β35% | Least hepatically metabolised; weakest LDL reduction |
In the AAS context, where LDL elevation can be acute and significant, Atorvastatin's potent LDL reduction at 40mg makes it the most practical choice for meaningful lipid management during a cycle. At 10mg, some statin effect is achieved; at 40mg, the LDL reduction is clinically meaningful enough to partially counteract AAS-driven elevation.
A critical practical consideration that competitor content consistently overlooks for the AAS audience:
| AAS Category | HDL Effect | LDL Effect | Atorvastatin Priority |
|---|---|---|---|
| Oral 17-AA (Dbol, Winstrol, Anadrol) | -40 to -70% | Significant increase | High β most acute lipid deterioration |
| Trenbolone (any ester) | -30 to -50% | Moderate increase | High β no estrogen cardioprotection |
| Testosterone (supraphysiological) | -15 to -25% | Mild-moderate increase | Moderate |
| Nandrolone Decanoate | -20 to -35% | Mild increase | Moderate |
| Boldenone (EQ) | -10 to -20% | Minimal increase | Lower β generally milder lipid effects |
| Protocol | Dose | Timing | Notes |
|---|---|---|---|
| On-cycle lipid management | 10β40 mg/day | Evening (Atorvastatin peak effect at night) | 10mg with oral AAS; 40mg with injectables |
| Post-cycle lipid normalisation | 20β40 mg/day | Evening | Continue 4-8 weeks post-cycle until lipids normalise |
Atorvastatin is typically taken in the evening β cholesterol synthesis peaks at night and evening dosing maximises its inhibitory effect. At 40mg per tablet, the Dragon Pharma formulation can be split for 10-20mg doses during oral AAS phases where a lower statin load is preferred. Blood lipid testing before, during and after cycling is strongly recommended β lipid panels are inexpensive and provide the only reliable measure of actual cardiovascular risk management.