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Naltrexone (oral and IM depot)

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDDRUG-NALTREXONE-PO
TypeDrug
Aliases
DepadeNaltrexoneReViaVivitrol (IM depot)Налтрексон (пероральний і депо-IM)
Statusreviewed 2026-05-18 | pending_clinical_signoff
DiseasesNone declared
SourcesSRC-NCCN-BCELL-2025

Drug Facts

ClassOpioid receptor antagonist (μ, κ, δ)
MechanismCompetitive antagonist at opioid receptors. In alcohol use disorder (AUD), blocks endogenous opioid-mediated reward signaling triggered by alcohol ingestion → reduces craving and heavy-drinking days. First-line FDA-approved AUD pharmacotherapy (alongside acamprosate and disulfiram). Also FDA-approved for opioid use disorder (block opioid effect — requires opioid-free interval first).
Typical dosingAUD: PO: 50 mg once daily (some protocols use 25 mg × 1-2 days to assess tolerance, then escalate); can extend to 100 mg if needed. IM depot (Vivitrol): 380 mg deep IM gluteal every 4 weeks; preferred if adherence is a concern. Verify opioid-free for ≥7-10 days before first IM dose (precipitated withdrawal otherwise).
Ukraine registeredTrue
NSZU reimbursedFalse
Ukraine last verified2026-05-18

Warnings

Notes

STUB — v0.2 prevention-workstream authoring; pending two-Clinical-Co-Lead signoff per CHARTER §6.1 dev-mode. First-line AUD pharmacotherapy (NIAAA + APA). Both oral and IM depot superior to placebo at reducing heavy-drinking days; IM depot preferred when adherence challenging. Critical: must be opioid-free ≥7-10 days before initiation. Alcohol cessation/reduction is a cancer-prevention intervention (HCC, CRC, esophageal SCC, breast). Source cited (SRC-NCCN-BCELL-2025) is closest in-KB until NIAAA/APA AUD sources land in source-stub workstream.

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