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Reminyl (Galantamine Hydrobromide) - Summary

 
 



REMINYL SUMMARY

REMINYL® (galantamine hydrobromide) is a reversible, competitive acetylcholinesterase inhibitor.

REMINYL® (galantamine hydrobromide) is indicated for the treatment of mild to moderate dementia of the Alzheimer's type.


See all Reminyl indications & dosage >>

NEWS HIGHLIGHTS

Media Articles Related to Reminyl (Galantamine)

Medical News Today: Why are scientists redefining Alzheimer's disease?
Source: Featured Health News from Medical News Today [2017.07.20]
The traditional view that protein buildup in the brain causes Alzheimer's disease is being challenged, and new evidence brings hope of novel drug targets.

Why are scientists redefining Alzheimer's disease?
Source: Genetics News From Medical News Today [2017.07.20]
The traditional view that protein buildup in the brain causes Alzheimer's disease is being challenged, and new evidence brings hope of novel drug targets.

Sleep disorders may predict Alzheimer's disease
Source: Public Health News From Medical News Today [2017.07.06]
New research finds biological markers for Alzheimer's disease in the spinal fluid of people who report poor sleep quality or who have trouble sleeping.

Alzheimer's disease patients with psychosis more likely to be misdiagnosed, study suggests
Source: Medical Devices / Diagnostics News From Medical News Today [2017.07.04]
People with Alzheimer's disease who experience psychosis - including delusions and hallucinations - are five times more likely to be misdiagnosed with dementia with Lewy bodies compared to patients...

Alzheimer's Disease
Source: MedicineNet Encephalitis and Meningitis Specialty [2017.06.01]
Title: Alzheimer's Disease
Category: Symptoms and Signs
Created: 8/5/2014 12:00:00 AM
Last Editorial Review: 6/1/2017 12:00:00 AM

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Published Studies Related to Reminyl (Galantamine)

Efficacy and safety of donepezil, galantamine, rivastigmine, and memantine for the treatment of Alzheimer's disease: a systematic review and meta-analysis. [2014]
rivastigmine, and memantine for the treatment of AD... CONCLUSIONS: Cholinesterase inhibitors and memantine are able to stabilize or

The prediction of response to galantamine treatment in patients with mild to moderate Alzheimer's disease. [2014]
The prediction of efficacy in long-term treatment of acetylcholinesterase inhibitors (AChEIs) is a major clinical issue, although no consistently strong predictive factors have emerged thus far... Patients who show improvement of episodic memory function during the first 4 weeks of galantamine administration may be likely to particularly benefit from galantamine treatment.

Long-term response to galantamine in relation to short-term efficacy data: pooled analysis in patients with mild to moderate Alzheimer's disease. [2011.03]
BACKGROUND: This analysis aimed to identify an operational, clinically relevant definition of response achieved in short-term clinical trials to support the identification of patients with Alzheimer's disease (AD) who would benefit most from long-term galantamine therapy... CONCLUSIONS: Patients who demonstrate improvement, stability, or limited cognitive decline 2-5 months after reaching maintenance doses of galantamine are more likely to experience continued benefit from long-term galantamine therapy.

Galantamine improves sustained attention in chronic cocaine users. [2011.02]
Chronic cocaine users are known to have cognitive deficits that are predictive of poor treatment response. Whether these deficits improve with medications targeting specific cognitive functions has not been examined in previous studies.

Galantamine augmentation of long-acting injectable risperidone for cognitive impairments in chronic schizophrenia. [2011.02]
CONCLUSION: Galantamine showed no ameliorative effects on cognitive measures in this 6month, double-blind study of patients with schizophrenia treated with an assured and stable antipsychotic medication delivery system. Galantamine may not be an appropriate augmentation agent for cognitive impairments in patients with schizophrenia at the dose used. Copyright (c) 2010 Elsevier B.V. All rights reserved.

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Clinical Trials Related to Reminyl (Galantamine)

Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Dose in Healthy Subjects Under Fed Conditions [Completed]
The objective of this study was to compare the rate and extent of absorption of Purepac, a subsidiary of Alpharma Inc., U. S.A., galantamine and Janssen Pharmaceutica Products, L. P., U. S.A. (Reminyl),galantamine, administered as a 1 x 4 mg tablet, under fed conditions.

Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Dose in Healthy Subjects Under Fasting Conditions [Completed]
The objective of this study was to compare the rate and extent of absorption of Purepac, a subsidiary of Alpharma Inc., U. S.A., galantamine and Janssen Pharmaceutica Products, L. P., U. S.A. (Reminyl),galantamine, administered as a 1 x 4 mg tablet, under fasting conditions.

Galantamine Bioequivalence Study of Dr. Reddy's Under Fasting Condition [Completed]

Galantamine Bioequivalence Study of Dr. Reddy's Under Fed Condition [Completed]

A Study to Show That the Change of Attention Measure is Correlated With the Changes of Caregiver's Burden After Treatment With Galantamine in Patients With Alzheimer's Disease [Completed]
The purpose of this study is to demonstrate that the change of attention measure is correlated with the changes of caregiver's burden after treatment with galantamine.

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Page last updated: 2017-07-20

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