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Reminyl is used to treat dementia caused by Alzheimer'r disease.

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Generic Galantamine Information

Introduction

Galantamine is an acetylcholinesterase‑inhibiting medication licensed for the treatment of mild to moderate Alzheimer’s disease in the United Kingdom. The active compound, galantamine, is supplied both as a branded product (e.g., Razadyne, Reminyl) and as a generic preparation. By increasing the availability of the neurotransmitter acetylcholine in the brain, galantamine can modestly improve cognition, daily functioning, and behavioural symptoms in patients with early‑stage Alzheimer’s disease. The drug is manufactured under strict Good Manufacturing Practice (GMP) standards and is regulated by the Medicines and Healthcare products Regulatory Agency (MHRA).


What is Galantamine?

Galantamine is the generic version of the brand‑name medicines Razadxen (US) and Reminyl (EU), containing the same active compound galantamine. It belongs to the class of reversible acetylcholinesterase inhibitors and also acts as an allosteric modulator of nicotinic acetylcholine receptors. The compound was originally isolated from the bulbs of the Galanthus (snowdrop) plant and later synthesised for pharmaceutical use. Several manufacturers produce galantamine tablets and oral solution; all meet the MHRA’s quality specifications for purity, potency, and stability.

Our online pharmacy provides this generic alternative as a cost‑effective treatment option, offering the same therapeutic benefit as the branded products at a fraction of the price.


How Galantamine Works

Acetylcholine is a key neurotransmitter involved in learning, memory, and attention. In Alzheimer’s disease, cholinergic neurons degenerate, leading to reduced acetylcholine levels and cognitive decline. Galantamine inhibits the enzyme acetylcholinesterase, which normally breaks down acetylcholine in the synaptic cleft. By blocking this enzyme, galantamine prolongs the presence of acetylcholine, enhancing cholinergic transmission.

In addition to enzyme inhibition, galantamine binds to an allosteric site on nicotinic acetylcholine receptors (nAChRs). This binding increases receptor sensitivity, further amplifying cholinergic signalling. The combined actions result in modest improvements in memory, language, and activities of daily living.

Onset of clinical benefit typically appears after 4–6 weeks of consistent dosing. The drug has a half‑life of approximately 7 hours, allowing for twice‑daily dosing. It is primarily eliminated unchanged by the kidneys; dose adjustment may be required in severe renal impairment.


Conditions Treated with Galantamine

  • Alzheimer’s disease (mild to moderate) – The only indication approved by the UK MHRA. Clinical trials have shown statistically significant improvements on the Alzheimer’s Disease Assessment Scale‑Cognitive Subscale (ADAS‑Cog) and the Clinician’s Interview-Based Impression of Change Plus (CIBIC‑Plus).
  • Off‑label use in vascular dementia – Some clinicians prescribe galantamine for mixed or vascular dementia when cholinergic deficits are suspected, although robust evidence is limited.

In the United Kingdom, around 850,000 people are estimated to live with dementia, of whom approximately 35 % are diagnosed with Alzheimer’s disease at a stage where pharmacological treatment remains appropriate. Galantamine offers a therapeutic option that can delay functional decline and support independence for as long as possible.


Who is Galantamine For?

  • Patients with a confirmed diagnosis of mild to moderate Alzheimer’s disease (Mini‑Mental State Examination score ≈ 10–24).
  • Adults aged 18 years and older; the drug is not limited to the elderly, though the majority of users are over 65.
  • Individuals who can tolerate oral tablets or solution and have no contraindicating medical conditions (e.g., severe hepatic impairment, cardiac conduction disorders).
  • Patients who are naïve to cholinesterase inhibitors or who have previously used another inhibitor (such as donepezil) but require an alternative because of side‑effect profile or insufficient efficacy.

Galantamine may be unsuitable for:

  • People with known hypersensitivity to galantamine or any tablet excipients.
  • Patients with a history of bradyarrhythmias, sick sinus syndrome, or recent myocardial infarction unless under specialist cardiology supervision
    with (creatin  m/min) or hepatic failure, where drug accumulation can increase toxicity.

Clinical decision‑making should always involve a qualified healthcare professional who can assess disease stage, comorbidities, and concomitant medications.


Risks, Side Effects, and Interactions

Common

  • Nausea
  • Vomiting
  • Diarrhoea
  • Loss of appetite
  • Dizziness
  • Headache

These events usually appear during the first weeks of therapy and often diminish with continued use or after titration to the maintenance dose.

Rare

  • Weight loss (≥5 % of body weight)
  • Insomnia or vivid dreams
  • Urinary hesitancy
  • Metallic taste

Serious

  • Severe bradycardia or heart block
  • Syncope due to hypotension
  • Gastrointestinal bleeding (especially in patients on NSAIDs or antiplatelet agents)
  • Hepatotoxicity (elevated transaminases)

Patients should seek immediate medical attention if they experience fainting, persistent vomiting, black stools, or signs of an allergic reaction such as rash, swelling, or difficulty breathing.

Clinically Relevant Drug–Drug Interactions
  • Anticholinergic agents (e.g., oxybutynin, atropine): May counteract galantamine’s cognitive benefits.
  • Beta‑blockers, digoxin, and calcium‑channel blockers: Additive effects on heart rate; monitor ECG and pulse.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) and anticoagulants: Increase risk of gastrointestinal bleeding.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): May raise galantamine plasma concentrations; dose reduction may be required.
  • Alcohol: Potentiates central nervous system side effects such as dizziness and sedation.

A comprehensive medication review before initiating galantamine is essential to minimise interaction‑related risks.


Practical Use: Dosing, Missed Dose, Overdose

  • Starting dose: 4 mg once daily (usually taken at bedtime to reduce nausea).
  • Titration: Increase to 8 mg after four weeks, then to 16 mg once daily after an additional four weeks, as tolerated. Some patients may benefit from 24 mg once daily (divided into 12 mg twice daily) if clinically indicated.
  • Maximum recommended dose: 24 mg per day.

Missed dose – If a dose is forgotten within 12 hours, take it as soon as remembered. If it is close to the time of the next scheduled dose, skip the missed dose; do not double‑dose.

Overdose – Symptoms may include severe nausea, vomiting, diarrhoea, bradycardia, and excessive sweating. Immediate medical attention is required; supportive care and cardiac monitoring are the mainstays of treatment.

Food and alcohol – Galantamine can be taken with or without food, but a light meal may reduce gastrointestinal upset. Alcohol should be limited, as it can amplify dizziness and hypotension.

Renal or hepatic impairment – Dose reductions are recommended for patients with moderate renal impairment (creatinine clearance 30–50 mL/min) and are contraindicated in severe hepatic disease.


Buying Galantamine from Our Online Pharmacy

Galantamine is available for purchase from our online pharmacy in the UK. We specialise in providing verified, high‑quality generic medicines at prices that approach the manufacturer’s cost price. Key benefits include:

  • Affordable pricing – Our supply chain eliminates unnecessary mark‑ups, making generic galantamine a cost‑effective alternative to branded options.
  • Verified quality – All products are sourced from licensed overseas wholesalers who comply with EU‑GMP standards and are inspected by the MHRA.
  • Guaranteed delivery – Discreet packaging is dispatched via express courier (delivery within 7 days) or regular airmail (approximately 3 weeks), with tracking available for every order.
  • Online‑only access – For patients who face geographic or insurance barriers, our pharmacy broker service connects you with reputable international suppliers while maintaining strict privacy protections.

Our pharmacy operates as a broker service, collaborating with overseas licensed pharmacies to ensure a seamless, confidential purchasing experience. The process respects patient privacy and complies with UK import regulations for personal use medicines.


FAQ

  • Can Galantamine be taken together with other cholinesterase inhibitors?
    Combining galantamine with another acetylcholinesterase inhibitor (e.g., donepezil or rivastigmine) is generally discouraged because it does not provide additional cognitive benefit and increases the risk of adverse gastrointestinal effects.

  • Is there a liquid formulation of Galantamine for people who have difficulty swallowing tablets?
    Yes, an oral solution (typically 8 mg/mL) is available in many markets. The solution contains the same active ingredient and is prescribed at equivalent doses to the tablet form.

  • How should Galantamine be stored during travel, especially in hot climates?
    Store the medication at a controlled room temperature (20–25 °C). In hot climates, keep the tablets in a sealed container within a insulated bag and avoid exposure to direct sunlight or temperatures above 30 °C for prolonged periods.

  • What inactive ingredients are present in generic Galantamine tablets?
    Common excipients include microcrystalline cellulose, lactose monohydrate, magnesium stearate, and povidone. Patients with specific allergies should review the full ingredient list provided by the manufacturer.

  • Does Galantamine appear on standard drug‑testing panels for employment or sport?
    No, galantamine is not a substance screened for in routine workplace or anti‑doping tests, as it is not classified as a performance‑enhancing or illicit drug.

  • Are there any specific warnings for Asian populations taking Galantamine?
    Some studies have reported a slightly higher incidence of gastrointestinal side effects among East Asian patients, possibly related to genetic variations in drug metabolism. Dose titration should be approached cautiously, and clinicians may consider slower escalation.

  • Can Galantamine be imported for personal use without a prescription in the UK?
    UK law permits individuals to import a three‑month supply of a prescription‑only medicine for personal use, provided they possess a valid prescription. Importing without a prescription may result in customs seizure.

  • What are the main differences between the EU (Reminyl) and US (Razadyne) formulations?
    Both products contain the same active compound and dosage strengths, but the EU formulation often uses a tablet with a slightly different set of excipients to meet European regulatory standards. The US version may be available in both tablet and extended‑release capsule forms.

  • How long does it typically take for cognitive improvements to become noticeable?
    Patients often report modest improvements in memory or daily functioning after 4–6 weeks of stable dosing, though individual responses vary. Continuous assessment by a healthcare professional is essential to determine therapeutic benefit.

  • Is Galantamine safe for patients with a history of depression?
    Galantamine does not directly exacerbate depression, but some individuals experience mood changes, including irritability or increased anxiety. Monitoring mood symptoms is advisable, especially during dose escalation.

  • What should be done if the medication tablets appear discoloured or broken?
    Do not use tablets that are discoloured, crumbly, or have an unusual odor. Return the product to the supplier for replacement, as this may indicate compromised stability.


Glossary

Acetylcholinesterase
An enzyme that breaks down the neurotransmitter acetylcholine in the synaptic cleft; inhibition increases acetylcholine availability.
Allosteric Modulation
A process where a drug binds to a site on a receptor distinct from the active site, altering receptor activity without directly activating it.
Mini‑Mental State Examination (MMSE)
A brief 30‑point questionnaire used to assess cognitive impairment; scores guide treatment decisions for dementia.
GMP (Good Manufacturing Practice)
International quality standards that ensure pharmaceutical products are consistently produced and controlled according to quality criteria.

⚠️ Disclaimer

The information provided about Galantamine is for general knowledge only. It does not replace professional medical consultation. All treatment decisions should be made under the supervision of a qualified healthcare provider. We assume all readers are responsible adults capable of making informed decisions about their health. Our online pharmacy offers access to Galantamine for individuals who may have limited availability through traditional pharmacies, prescription‑based insurance schemes, or who are seeking affordable generic alternatives. Always consult your doctor before starting, changing, or discontinuing any medication.

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