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Revia

Revia
In stock
50mg
from 68,78 £
Strength
Pack size — the bigger the pack, the cheaper the tablet
82,53 £68,78 £
6,88 £ per tablet

In brief

  • In our pharmacy you can buy Revia without a prescription, with delivery in 9–21 days throughout the United Kingdom. Discreet and anonymous packaging.
  • Revia (naltrexone hydrochloride) is used to prevent relapse in opioid dependence and to reduce craving in alcohol dependence; it works as an opioid receptor antagonist (competitive mu‑opioid receptor blocker) and is used as part of medication‑assisted treatment (MAT).
  • The usual dose is 50 mg orally once daily for adults; an extended‑release injectable formulation (Vivitrol) is given as 380 mg intramuscularly every 4 weeks.
  • Form of administration: oral film‑coated, scored 50 mg tablets (blisters or bottles) or a prolonged‑release 380 mg IM injection (powder for reconstitution, single‑use vial administered by a healthcare professional).
  • Onset time: oral naltrexone begins to take effect within 30–60 minutes (peak concentrations ~1–2 hours); the injectable formulation releases drug gradually with therapeutic levels reached over the first days.
  • Duration of action: a single 50 mg oral dose has effects for about 24 hours; the extended‑release IM injection provides effect for approximately 4 weeks.
  • Alcohol warning: although used to treat alcohol dependence, avoid heavy drinking and be aware of liver risk — naltrexone is not recommended in acute hepatitis or severe hepatic impairment and regular liver function monitoring is advised.
  • The most common side effect is nausea; other frequent side effects include headache, insomnia, joint or muscle pain, anxiety, fatigue and loss of appetite.
  • Would you like to try “revia” without a prescription?

Basic Revia Information

  • INN (International Nonproprietary Name): Naltrexone hydrochloride
  • Brand Names Available In United Kingdom: Revia (USA, Europe); Vivitrol (Global); Naltrexona (Spain, Latin America); Depade (USA) — availability by brand in the United Kingdom not specified in source data
  • ATC Code: N07BB04
  • Forms And Dosages: Oral tablet 50 mg (film-coated, scored; blisters or bottles); prolonged‑release injection 380 mg vial for intramuscular use (powder for reconstitution, single‑use)
  • Manufacturers In United Kingdom: Generics supplied by manufacturers active in EU/UK markets include Teva, Sandoz and Accord Healthcare (local UK manufacturer listings not specified)
  • Registration Status In United Kingdom: Not specified in source data; EU/EMA approval and USA/FDA approvals are referenced
  • OTC / Rx Classification: Prescription Only (Rx)

Latest Research Highlights (UK & EU 2022–2025)

Worried that naltrexone is either oversold or not offered where it helps most?

Recent UK and EU evaluations from 2022–2024 have reinforced naltrexone’s role in relapse prevention for alcohol and opioid use disorders while refining safety and delivery questions.

Meta‑analyses and pragmatic trials report modest but clinically meaningful reductions in heavy drinking days and alcohol craving versus placebo, with the largest effects when medication is combined with psychosocial interventions.

For opioid dependence, oral naltrexone performs best in highly selected, highly motivated and opioid‑abstinent cohorts.

Extended‑release injectable naltrexone (380 mg IM, Vivitrol) is associated with improved adherence and lower re‑admission rates in several European observational studies.

Safety signals in recent work emphasise hepatotoxicity risk at high cumulative doses and the potential for precipitated withdrawal if the drug is started before adequate opioid abstinence.

UK service evaluations across NHS trusts (2022–24) note practical barriers such as initiation delays around inpatient detox timing and limited access to monthly injectable clinics.

Research highlights health‑inequality effects with marginalised populations less likely to access extended‑release options.

Outcome Direction Notes
Heavy Drinking Days Reduced Greatest reduction when combined with counselling
Opioid Readmissions Lower With Injectable Observed in EU cohort studies for Vivitrol 380 mg IM
Serious Hepatic Events Rare But Noted Risk increases with high cumulative dosing

Clinical Effectiveness In The UK

Do patients actually do better on naltrexone in NHS practice?

Naltrexone is used primarily for alcohol dependence and for relapse prevention after detoxification from opioids in UK services.

Clinical audits across several NHS trusts show adherent patients report reduced craving, fewer heavy drinking days and fewer alcohol‑related A&E visits where medication is combined with community counselling and mutual‑help referrals.

Oral naltrexone’s real‑world effectiveness for opioid use disorder is limited by adherence problems.

Injectable 380 mg IM (Vivitrol) provides better continuity and is associated with reduced overdose‑related readmissions in cohort studies, although availability across NHS regions varies.

Safety monitoring with baseline and periodic liver function tests is standard practice and improves patient selection and outcomes.

Cost‑effectiveness work by local commissioning groups shows generic oral naltrexone is inexpensive compared with other options, while branded extended‑release injections are costlier and often provided via specific pathways.

Outcome Oral Naltrexone Injectable Naltrexone (380 mg IM)
Adherence Variable Improved
Readmission Rates Mixed Lower in some cohorts
Cost Lower Higher

Indications And Expanded Uses

Is naltrexone only for alcohol and opioid problems?

MHRA‑ and NICE‑aligned practice recognises naltrexone hydrochloride primarily for alcohol dependence and for relapse prevention in opioid dependence after confirmed detoxification.

Off‑label uses seen in specialist NHS or private clinics include adjunctive treatment for some behavioural addictions and experimental low‑dose protocols for binge‑eating disorder, but these remain investigational and require specialist oversight.

Protocols consistently require documented opioid abstinence, typically 7–10 days, before initiation to avoid precipitated withdrawal.

Extended‑release 380 mg intramuscular injections are chosen when adherence is a known problem, while oral 50 mg tablets remain the daily standard for many patients.

Use in pregnancy is decided case‑by‑case with attention to risks from opioid withdrawal and limited safety data; lactation guidance varies and specialist advice is needed.

  • MHRA/NICE‑Recognised Uses: Alcohol dependence; relapse prevention after opioid detoxification.
  • Off‑Label/Investigational: Behavioural addictions in specialist settings; low‑dose protocols for binge‑eating disorder under supervision.

Composition And Brand Landscape

Which brands and formulations will the pharmacist actually see?

The active ingredient is naltrexone hydrochloride (INN) and the ATC code is N07BB04 for drugs used in alcohol dependence.

The UK market is dominated by generic oral 50 mg tablets produced by manufacturers active in EU/UK markets such as Teva, Sandoz and Accord Healthcare.

Revia was the original branded tablet but is discontinued in many regions; Vivitrol by Alkermes supplies the 380 mg prolonged‑release intramuscular formulation internationally and remains available.

Packaging for tablets generally comprises film‑coated, scored tablets in blister packs or bottles, while injectables are supplied as single‑use vials containing powder for reconstitution.

Brand Form Manufacturer Availability
Revia 50 mg Tablets Originally Mallinckrodt Discontinued in many regions
Generic Naltrexone 50 mg Tablets Teva, Sandoz, Accord Healthcare Widely available
Vivitrol 380 mg IM Injection Alkermes Available

Contraindications And Special Precautions

What could make naltrexone unsafe for someone?

Absolute contraindications are recent or current opioid use due to the risk of precipitated withdrawal, acute hepatitis or severe hepatic impairment, and known hypersensitivity to naltrexone or excipients.

Relative contraindications that require close monitoring include moderate hepatic or renal impairment and a history of severe depression or suicidal ideation, given reports of mood‑related adverse effects.

Practical precautions in UK practice include baseline liver function tests and periodic monitoring thereafter, urine or other opioid screening to verify abstinence before initiation, and clear counselling about the blockade of opioid analgesia.

Patients should be warned about dose‑related dizziness or fatigue and advised on driving and safety implications.

Pharmacists must explain emergency plans for acute pain management because naltrexone blocks opioid analgesia and document routes for non‑opioid strategies or specialist supervised opioid analgesia if required.

  • Checklist For Contraindications: Recent opioid use; acute hepatitis; severe hepatic impairment; known hypersensitivity.
  • Pre‑Initiation Screening: Baseline LFTs; opioid testing; mood assessment; informed consent documented.

Dosage Guidelines

How should naltrexone be dosed and what if a dose is missed?

The standard adult oral dose is 50 mg once daily for alcohol dependence and relapse prevention, while extended‑release intramuscular injections are 380 mg every four weeks.

NHS protocols commonly recommend an individualised duration, often a minimum of 3–6 months for alcohol dependence and ongoing specialist review for some opioid‑dependent patients.

Initiation rules require confirmation of opioid abstinence, usually 7–10 days after last opioid use, to avoid precipitated withdrawal.

Children under 18 are not recommended to use naltrexone owing to lack of established safety and efficacy data.

Elderly patients require careful monitoring of renal and hepatic function and clinical judgement about dosing, although routine dose reductions are not specified.

For hepatic impairment avoid use in acute hepatitis or liver failure and consider lower dosing plus more frequent LFTs in moderate disease.

Population Typical Dose Notes
Adults (Alcohol) 50 mg PO daily Minimum 3–6 months
Adults (Opioid Relapse Prevention) 50 mg PO daily or 380 mg IM monthly Initiate only after 7–10 days opioid‑free
Children & Adolescents Not Recommended Safety not established

Interactions Overview

Will this drug clash with other medicines I take?

The principal pharmacological interaction is with opioids, where antagonism can cause precipitated withdrawal and will block opioid analgesia.

There are no major food interactions of clinical significance, but patients should avoid heavy alcohol consumption during early treatment because of added liver risk.

Concomitant use with other hepatotoxic medications increases liver risk and clinicians should review statins, high‑dose paracetamol, and other hepatically metabolised agents when prescribing.

MHRA Yellow Card reports have flagged elevated liver enzymes and mood changes; a full medication review including OTC products and herbal remedies is essential before starting naltrexone.

Pharmacists should coordinate with GPs and hospital teams to document non‑opioid analgesia pathways for emergencies and ensure there are no gaps in care that might expose the patient to unblocked opioids.

  • High‑Risk Interactions: Opioids (precipitated withdrawal/blocking analgesia); hepatotoxic drugs (increased liver risk).
  • Practical Steps: Check full medication list; advise on paracetamol limits; report suspected interaction reactions via Yellow Card.

Cultural Perceptions And Patient Habits In The UK

What do people in the UK actually think about taking naltrexone?

Patient forums and peer support groups report mixed attitudes—many patients value the reduction in craving and sense of control, while others worry about blocking opioid analgesia and the stigma of medication‑assisted treatment.

Trust in pharmacists is high in the UK, and patients commonly ask pharmacy teams at Boots, LloydsPharmacy or independent pharmacies for side‑effect advice and adherence support.

NHS 111, local trust web pages and the NHS App are often your first stop for questions about treatment and repeat prescriptions.

Shared decision‑making is expected, with strong patient preference for psychosocial support alongside medication, and there is notable regional variance in access to injectable clinics, especially in more deprived areas.

Community pharmacy adherence programmes and peer‑led community initiatives improve uptake and persistence with treatment in many areas.

  • Common Patient Concerns: Will it block pain relief; will it help with cravings; how often must I attend clinic for injectables?
  • Pharmacist Counselling Prompts: Explain blockade of opioids; remind about LFT monitoring; signpost local counselling and recovery groups.

Availability And Pricing Patterns (UK)

How easy is it to get naltrexone and what will it cost me?

Oral generic naltrexone 50 mg tablets are widely available on NHS prescription and through major pharmacy chains, and registered online pharmacies can dispense to NHS‑registered patients with electronic prescriptions.

Revia as a branded tablet is largely discontinued, while Vivitrol 380 mg IM remains available but is used selectively because of cost and clinic infrastructure needs.

Prescription charges in England apply unless the patient is exempt and this affects out‑of‑pocket cost, while Scotland, Wales and Northern Ireland use different prescription cost structures, often meaning no charge.

Private purchase of injectables or clinic‑delivered services can incur additional fees on top of the medicine cost owing to administration and clinic resource use.

In our online pharmacy, revia is available without a prescription, with discreet delivery to United Kingdom in 9‑21 days.

Form NHS Availability Typical Cost (NHS vs Private)
Oral 50 mg Tablet (Generic) Widely Available Low (NHS prescription charge where applicable); low cost privately
Injection 380 mg IM (Vivitrol) Available Selectively Higher; private clinic fees likely

Comparable Medicines And Prescribing Preferences

How does naltrexone stack up against other options?

For alcohol dependence, common NHS alternatives are acamprosate and disulfiram, with choice depending on comorbidity, drinking pattern and likely adherence.

Acamprosate is suited to maintenance after detox and has minimal hepatic burden, while disulfiram provides aversive therapy that needs supervised adherence and may suit a motivated, supervised patient.

For opioid dependence, agonist maintenance with methadone or buprenorphine is first‑line for many patients because it reduces cravings and overdose risk under supervision.

Naltrexone’s advantages are that it blocks opioid effects, reduces alcohol cravings in many patients, and has no abuse potential.

Its drawbacks are hepatotoxicity risk, blockade of opioid analgesia and adherence challenges with daily oral dosing; these factors guide whether antagonist or agonist therapy is preferred.

Drug Indication Advantage Drawback
Naltrexone Alcohol, Opioid Relapse Prevention Blocks opioids, reduces craving Hepatic risk; blocks analgesia; adherence
Methadone / Buprenorphine Opioid Dependence Reduces withdrawal and overdose risk Requires supervised dispensing; agonist effects
Acamprosate Alcohol Dependence Low hepatic burden Requires abstinence at start

Frequently Asked Questions

Q1: Can I start naltrexone straight after my last opioid use?

A: No. Initiate only after 7–10 days opioid‑free for most opiates, and longer after long‑acting opioids, to avoid precipitated withdrawal; verify with testing and clinical history.

Q2: Will naltrexone affect emergency pain relief?

A: Yes. Naltrexone blocks opioid analgesia; inform GPs and emergency services, carry a card advising non‑opioid pain strategies and plan for specialist managed high‑dose opioid analgesia if needed.

Q3: What monitoring is needed?

A: Baseline liver function tests and periodic repeats, mood screening and adherence checks; report adverse effects via the MHRA Yellow Card system.

Q4: Can I drink alcohol while on naltrexone?

A: The medicine reduces craving and heavy drinking but does not make drinking safe; counsel on reduced tolerance and ongoing liver risks and combine medication with psychosocial support.

  1. Emergency Analgesia Steps: Notify GP; carry a treatment card; in emergencies, inform ambulance/ED staff that opioid antagonism may require specialist pain management.

Guidelines For Proper Use

What should pharmacists do at the point of dispensing?

Use a standardised checklist to confirm indication and informed consent, verify opioid abstinence with documented tests and perform baseline LFTs before initiation.

Discuss common side effects such as nausea, headache, insomnia and mood changes, and explain when to seek help or stop the medicine.

For injectables ensure correct cold‑chain handling, clinic scheduling every four weeks and accurate administration records.

Advise on missed‑dose rules: take a missed tablet as soon as remembered unless it is close to the next dose, and do not double up.

Storage guidance for tablets is 20–25°C and protect from moisture and excess heat; injections should be refrigerated and used per reconstitution instructions.

Emphasise referral to IAPT, local alcohol services or community recovery groups and give the patient a written information card about emergency analgesia steps.

Activity When Who
Baseline LFTs Before initiation Prescriber / GP
Opioid Screening Before initiation Prescriber / Clinic
Periodic LFTs & Mood Checks As per local protocol GP / Pharmacist

Delivery Across United Kingdom

City Region Delivery time
London Greater London 9-14 days
Birmingham West Midlands 9-14 days
Manchester Greater Manchester 9-14 days
Glasgow Scotland 9-14 days
Leeds West Yorkshire 9-14 days
Bristol South West England 9-14 days
Edinburgh Scotland 9-14 days
Liverpool Merseyside 9-14 days
Sheffield South Yorkshire 9-14 days
Newcastle Upon Tyne North East England 9-14 days
Cardiff Wales 9-14 days
Belfast Northern Ireland 9-14 days
Coventry West Midlands 14-21 days
Plymouth Devon 14-21 days

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