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Generic Reminyl ( Galantamine )
Reminyl (galantamine hydrobromide) is a cholinergic agent indicated for the symptomatic treatment of mild to moderate dementia of the Alzheimer's type. It functions as a selective, reversible, and competitive inhibitor of acetylcholinesterase, the enzyme responsible for the breakdown of acetylcholine in the synaptic cleft. In addition, galantamine enhances the intrinsic action of acetylcholine on nicotinic receptors through allosteric modulation, a dual mechanism of action that is thought to augment cholinergic neurotransmission in the cerebral cortex and hippocampus, thereby improving cognitive function, global functioning, and activities of daily living in affected patients.
Usual adult dose: The recommended starting dose is 4 mg twice daily (8 mg per day), taken with morning and evening meals to minimize gastrointestinal side effects. After a minimum of 4 weeks of treatment, the dose may be increased to the maintenance dose of 8 mg twice daily (16 mg per day), provided the starting dose is well tolerated. Following an additional minimum of 4 weeks at 8 mg twice daily, a further dose escalation to 12 mg twice daily (24 mg per day) may be considered for patients who demonstrate inadequate clinical response and tolerate the lower doses. The maximum recommended dose is 12 mg twice daily (24 mg per day). Dose increases should be based on clinical assessment of tolerability and response. For patients with moderate hepatic or renal impairment, dose adjustments may be required. Treatment should be periodically reassessed, and discontinuation should be considered when evidence of a therapeutic effect is no longer present.
Dosage form: Film-coated tablets: 4 mg (off-white, circular, biconvex) and 8 mg (pink, circular, biconvex). An oral solution (4 mg/mL) is also available for patients who have difficulty swallowing or require flexible dose titration. The scored tablets allow for dose adjustments where necessary.
Onset of action: Galantamine is rapidly absorbed after oral administration, with peak plasma concentrations occurring approximately 1 hour after dosing. While acetylcholinesterase inhibition begins shortly after administration, measurable clinical improvement in cognitive function and global status is typically observed within 4 to 12 weeks of initiating therapy at the target maintenance dose. Therapeutic benefits are gradual and require consistent long-term treatment.
Duration of action: The elimination half-life of galantamine is approximately 7 to 8 hours, supporting twice-daily administration with maintenance of acetylcholinesterase inhibition over a 24-hour period when taken morning and evening. Steady-state plasma concentrations are achieved within 3 to 7 days of repeat dosing.
Alcohol recommendation: Alcohol consumption should be avoided or minimized during treatment with Reminyl. Alcohol may exacerbate the gastrointestinal side effects of galantamine, including nausea, vomiting, and diarrhea, and may potentiate central nervous system depressant effects such as sedation and dizziness. Concurrent use of alcohol and galantamine may also impair cognitive function, which is particularly concerning in patients being treated for dementia. Patients and caregivers should be advised to limit alcohol intake accordingly.
Most common side effects: Nausea, vomiting, diarrhea, anorexia, dizziness, headache, and weight loss. Gastrointestinal adverse effects are the most frequently reported, occurring predominantly during the dose-escalation phase and generally diminishing with continued treatment. Taking galantamine with meals significantly reduces the incidence and severity of gastrointestinal intolerance. Cholinergically mediated side effects such as bradycardia and syncope have been reported and require caution in patients with underlying cardiac conduction disorders. Serious skin reactions, including Stevens-Johnson syndrome, have been reported rarely.
Would you like to learn more about Reminyl (Galantamine) for the treatment of Alzheimer's dementia?
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