CYP2D6: How This Enzyme Affects Your Medications and Supplements
When you take a pill, your body doesn’t just absorb it and call it a day. It has to break it down—and one of the most important tools for that job is an enzyme called CYP2D6, a liver enzyme responsible for metabolizing about 25% of all prescription drugs. Also known as cytochrome P450 2D6, it’s the reason why two people taking the same dose of the same drug can have completely different results. Some people process drugs too fast, so the medicine never works. Others process it too slow, so it builds up and causes side effects. This isn’t about how much you weigh or what you ate—it’s about your genes.
CYP2D6 doesn’t work alone. It’s part of a system that handles antidepressants like fluoxetine, painkillers like codeine, beta-blockers like metoprolol, and even some anti-nausea drugs. If your CYP2D6 activity is low, codeine won’t turn into morphine, so your pain won’t improve. If it’s超高, you might clear the drug too quickly and need a higher dose. And here’s the kicker: over 100 medications are affected by this one enzyme. That’s why drug interactions aren’t just about mixing pills—they’re about how your body handles them at a genetic level. You can’t see CYP2D6, but its impact shows up in your symptoms, your side effects, and sometimes, your hospital visits.
That’s why knowing your CYP2D6 status matters. If you’ve had bad reactions to meds, or if your doctor keeps adjusting your dose without results, it might not be trial and error—it could be your enzyme. Genetic tests for CYP2D6 are available and becoming more common, especially in psychiatry and pain management. Even if you haven’t been tested, understanding this enzyme helps you ask better questions. Ask your pharmacist: "Is this drug processed by CYP2D6?" Ask your doctor: "Could my genes be affecting how this works?" You’re not just taking a pill—you’re interacting with your biology.
The posts below dive into real cases where CYP2D6 plays a hidden role: why some people get dizzy on antidepressants, why certain statins cause muscle pain in some but not others, how supplements like St. John’s wort can throw off drug levels, and why generic medications sometimes seem to fail even when they’re chemically identical. These aren’t random stories—they’re all tied to how your body breaks things down. What you’re about to read isn’t theory. It’s what’s happening inside millions of people every day, right now, without them knowing why.
Genetic Variations and Drug Metabolism: How Your DNA Affects Medications
Dec 5, 2025, Posted by Mike Clayton
Your genes affect how your body processes medications. Pharmacogenomics uses DNA testing to match drugs to your biology - reducing side effects and improving treatment success. Here’s how it works and who benefits most.
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