Sobriety Support Formula for Alcohol Cessation
| Product dosage: 10mg | |||
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| Package (num) | Per pill | Price | Buy |
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| 360 | $1.12
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| Product dosage: 2.5mg | |||
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| Package (num) | Per pill | Price | Buy |
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| Product dosage: 20mg | |||
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| Package (num) | Per pill | Price | Buy |
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| Product dosage: 5mg | |||
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| Package (num) | Per pill | Price | Buy |
| 20 | $2.26 | $45.17 (0%) | 🛒 Add to cart |
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Synonyms | |||
Similar products
Sobriety Support Formula is a clinically developed pharmacological aid designed to assist individuals in reducing or eliminating alcohol consumption. It combines evidence-based active ingredients that target neurological pathways associated with alcohol dependence. This formulation is intended for use under medical supervision as part of a comprehensive treatment plan including behavioral therapy and counseling. It is not a standalone cure but a supportive tool to manage cravings and withdrawal symptoms.
Features
- Contains naltrexone hydrochloride (50 mg) as the primary active ingredient
- Includes thiamine (vitamin B1) to support neurological health during withdrawal
- Utilizes a delayed-release coating to ensure optimal bioavailability
- Manufactured in FDA-approved facilities following cGMP standards
- Available in blister packs of 30 tablets with child-resistant packaging
- Includes a lot number and expiration date for quality tracking
Benefits
- Reduces alcohol cravings by blocking opioid receptors in the brain
- Helps diminish the pleasurable effects of alcohol consumption
- Supports management of withdrawal symptoms such as anxiety and agitation
- May decrease the frequency of relapse episodes when used as directed
- Complements behavioral therapy for more sustainable recovery outcomes
- Provides a structured pharmacological component to treatment plans
Common use
Sobriety Support Formula is prescribed for adults diagnosed with alcohol use disorder (AUD) who are committed to reducing or abstaining from alcohol. It is typically incorporated into treatment plans that include counseling, support groups, and lifestyle modifications. The medication is most effective when initiated after the acute withdrawal phase, usually 3-7 days after last alcohol consumption, though timing may vary based on individual clinical presentation. It is not recommended for those who continue to drink heavily without medical supervision.
Dosage and direction
The standard dosage is one 50 mg tablet taken orally once daily, with or without food. Treatment should begin after complete detoxification from alcohol, typically when the patient has been alcohol-free for at least 3-7 days. The tablet should be swallowed whole with water and not crushed or chewed. Duration of treatment varies but often continues for 3-6 months, with periodic medical evaluation to assess effectiveness and need for continued therapy. Dosage adjustments may be necessary for patients with renal impairment.
Precautions
Patients should be monitored for signs of depression or suicidal ideation, particularly during early treatment. Liver function tests should be conducted before initiation and periodically during treatment. Use with caution in patients with thrombocytopenia or neutropenia. This medication may cause dizziness or drowsiness; patients should avoid operating machinery until they know how the medication affects them. Not recommended for patients with acute hepatitis or liver failure.
Contraindications
Absolute contraindications include hypersensitivity to naltrexone or any component of the formulation. Should not be used by patients currently dependent on opioids or in acute opioid withdrawal. Contraindicated in patients taking opioid analgesics, those in acute opioid withdrawal, or those who have failed the naloxone challenge test. Not recommended for patients with severe hepatic impairment (Child-Pugh Class C).
Possible side effects
Common side effects (≥1%) include nausea (10-15%), headache (7-12%), dizziness (5-8%), fatigue (4-7%), and insomnia (3-5%). Less common side effects (<1%) may include anxiety, vomiting, decreased appetite, and joint pain. Rare but serious side effects requiring immediate medical attention include signs of allergic reaction, depression, suicidal thoughts, or hepatotoxicity (dark urine, jaundice, abdominal pain). Most side effects diminish within the first two weeks of treatment.
Drug interaction
Naltrexone may precipitate acute withdrawal in patients using opioid medications. Avoid concomitant use with opioid analgesics, antitussives, or antidiarrheal medications containing opioids. May interact with medications that affect liver enzymes, particularly CYP3A4 inducers or inhibitors. Use caution with other medications that cause hepatotoxicity. Thiamine component may interact with fluorouracil-based chemotherapy drugs. Always inform healthcare providers of all medications, including over-the-counter drugs and supplements.
Missed dose
If a dose is missed, take it as soon as remembered unless it is nearly time for the next dose. Do not double the dose to make up for a missed one. If multiple doses are missed, contact the prescribing physician for guidance, as restarting may require medical supervision. Consistent daily dosing is important for maintaining therapeutic effects.
Overdose
In case of suspected overdose, seek immediate medical attention. Symptoms may include nausea, vomiting, abdominal pain, dizziness, and lethargy. There is no specific antidote for naltrexone overdose; treatment is supportive and symptomatic. Hemodialysis is not effective for removing naltrexone due to its large volume of distribution. In cases of massive overdose, monitor for hepatotoxicity and provide appropriate supportive care.
Storage
Store at room temperature (15-30°C or 59-86°F) in the original container. Keep tightly closed and protect from moisture and light. Keep out of reach of children and pets. Do not use after the expiration date printed on the packaging. Do not transfer tablets to other containers, as the original packaging provides protection from moisture and light.
Disclaimer
This product requires a prescription and should be used only under medical supervision. It is not a cure for alcohol use disorder but an adjunct to comprehensive treatment. Individual results may vary. Not intended for use by pregnant or breastfeeding women without medical advice. This information does not replace professional medical advice; always consult healthcare providers for personalized guidance.
Reviews
“After struggling with relapse for years, adding this medication to my treatment plan finally gave me the stability I needed. The cravings diminished significantly within two weeks.” - Michael T., completed 6-month treatment
“As a addiction specialist, I’ve found this formulation particularly effective for patients who have struggled with other interventions. The inclusion of thiamine addresses nutritional deficiencies common in this population.” - Dr. Eleanor Reyes, MD
“The gradual reduction in alcohol cravings allowed me to focus on therapy and rebuilding my life. I experienced mild nausea initially, but it subsided after the first week.” - Sarah J., 4 months sober
“Clinical trials demonstrate a 30% higher abstinence rate at 12 weeks compared to placebo when combined with behavioral therapy. The safety profile is well-established for appropriate candidates.” - Clinical study summary