Naltrexone — Nutrient Depletion & Health Patterns

Also known as: Naltrexone / Low Dose Naltrexone — LDN (ReVia, Vivitrol, Contrave)

Drug Class: Opioid antagonist / Immunomodulator (LDN)

Full opioid antagonist used at standard doses (50mg/day) for alcohol use disorder and opioid use disorder. At ultra-low doses (1.5–4.5mg/day) used off-label as 'Low Dose Naltrexone' (LDN) for autoimmune conditions, fibromyalgia, Crohn's disease, MS, chronic pain, and mood disorders. LDN's mechanism differs from standard dosing — it transiently blocks opioid receptors causing a rebound increase in endorphin production and modulates microglia to reduce neuroinflammation.

Nutrients That Naltrexone May Deplete

Long-term use of Naltrexone is associated with lower levels of the following nutrients based on peer-reviewed clinical research. WePattern surfaces these patterns from its clinical Knowledge Graph.

Common Side Effects of Naltrexone

Key Drug Interactions — Naltrexone

Naltrexone has 5 documented drug-drug interactions in WePattern's Pattern Health Intelligence database. Key interactions include:

Frequently Asked Questions

Does Naltrexone deplete nutrients?

Yes. Naltrexone has been associated with depletion of Endorphins (endogenous opioid peptides — rebound effect is therapeutic at LDN doses), Vitamin D, Magnesium based on clinical research. WePattern maps these relationships from peer-reviewed sources.

What nutrients does Naltrexone deplete?

Naltrexone is associated with lower levels of: Endorphins (endogenous opioid peptides — rebound effect is therapeutic at LDN doses), Vitamin D, Magnesium. These depletions can develop over weeks to months of regular use.

What are the side effects of Naltrexone?

Common side effects associated with Naltrexone include: Standard dose (50mg): Nausea (most common early), headache, fatigue, sleep disturbances, loss of appetite; LDN (1.5–4.5mg): Vivid dreams or sleep disturbances (most common early side effect), transient nausea; Liver toxicity risk (standard doses — baseline liver function required); Precipitation of opioid withdrawal (if opioids present in system at initiation); Depression (rare — opioid system modulation).

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