
Dementa5 mg
Ziska Pharmaceuticals Ltd.
Memantine Hydrochloride is an FDA-approved and guideline-supported treatment for the following: Established/FDA-approved use Treatment of moderate to severe dementia of the Alzheimer's type…
Memantine Hydrochloride is an FDA-approved and guideline-supported treatment for the following:
Memantine Hydrochloride provides symptomatic benefit only; it does not stop or reverse the underlying neurodegenerative disease process, and the overall magnitude of clinical benefit is generally modest.
| Week | Dose |
|---|---|
| Week 1 | 5 mg once daily |
| Week 2 | 5 mg twice daily (10 mg/day) |
| Week 3 | 5 mg in the morning and 10 mg in the evening (15 mg/day) |
| Week 4 onward | 10 mg twice daily (20 mg/day, target maintenance dose) |
The minimum recommended interval between dose increases is one week, based on individual tolerability. Memantine Hydrochloride may be taken with or without food. If using the extended-release capsule formulation, the target maintenance dose is 28 mg once daily, titrated over several weeks in a similar stepwise manner; capsules may be swallowed whole or opened and sprinkled on applesauce.
Safety and efficacy of Memantine Hydrochloride have not been established in pediatric patients; it is not recommended for use in children.
In patients with severe renal impairment, a reduced target dose of 5 mg twice daily (immediate-release) is recommended. See Use in Special Populations for further detail.
No dosage adjustment is generally required in mild to moderate hepatic impairment; use with caution in severe hepatic impairment.
Adverse effects of Memantine Hydrochloride are generally mild.
Memantine Hydrochloride is contraindicated in patients with known hypersensitivity to memantine hydrochloride or to any excipient in the formulation.
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