Ask your doctor or pharmacist if you have any questions.Take galantamine with a full glass of water.
The only event with an incidence of ≥0.5% in placebo patients was nausea (17, 0.7%).In the 5 open-label studies, 103 (7.1%) patients (N=1454) discontinued due to an adverse reaction.

The Percentages of Randomized Patients Who Completed the Study Were: Placebo 90%, 24-32 mg/day 67%.Call your doctor for medical advice about side effects. After i.v. A further increase to 12 mg twice a day (24 mg/day) should be attempted after a minimum of 4 weeks at 8 mg twice a day (16 mg/day).Dosage increases should be based upon assessment of clinical benefit and tolerability of the previous dose.Galantamine tablets should be administered twice a day, preferably with morning and evening meals.Patients and caregivers should be advised to ensure adequate fluid intake during treatment.

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Galantamine is a type of alkaloid which was first used for cure of polio. Follow the directions on your prescription label.Store galantamine at room temperature away from moisture and heat.Before taking Reminyl  (Galantamine), tell your doctor if you are allergic to any drugs, or if you have urination problems, heart disease, a heart rhythm disorder, stomach ulcers or bleeding, a seizure disorder, kidney disease, liver disease, or asthma.Do not use this medication if you are allergic to galantamine. There were no statistically significant differences between the 16 mg/day and 24 mg/day dose groups.In a study of 26 weeks duration, 636 patients were randomized to either a dose of 24 mg or 32 mg of Galantamine per day, or to placebo, each given in two divided doses. In whole blood, Galantamine is mainly distributed to blood cells (52.7%). Tell your doctor if you are pregnant or plan to become pregnant.It is not known whether galantamine passes into breast milk or if it could affect the nursing baby. Genetic Implication.

Exposure to Galantamine would be expected to increase further with increasing degree of hepatic impairment Following a single 8 mg dose of Galantamine tablets, AUC increased by 37% and 67% in patients with moderate and severe renal impairment, respectively, compared with normal volunteers Approximately 7% of the normal population has a genetic variation that leads to reduced levels of activity of CYP2D6 isozyme. The present invention relates to a method of forming a film. Side Effects. Study Flashcards On Compounding look alike/sound alike at

If therapy has been interrupted for more than three days, the patient should be restarted with the lowest dose and then re-titrated to an appropriate dosage Advise patients and caregivers to ensure adequate fluid intake during treatment Advise patients and caregivers that the most frequent adverse events associated with use of the drug can be minimized by following the recommended dosage and administration.This product's label may have been updated. Select one or more newsletters to continue.

Both treatments were statistically significantly superior to placebo, but were not significantly different from each other.Figure 5 illustrates the cumulative percentages of patients from each of the three treatment groups who had attained at least the measure of improvement in ADAS-cog score shown on the X-axis.

This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. The differences vs. the 8 mg/day treatment for the 16 and 24 mg/day treatments were 0.26 and 0.29, respectively.

All rights reserved. Three change scores (10-point, 7-point and 4-point reductions) and no change in score from baseline have been identified for illustrative purposes, and the percent of patients in each group achieving that result is shown in the inset table.The curves demonstrate that both patients assigned to Galantamine and placebo have a wide range of responses, but that the Galantamine group is more likely to show the greater improvement.Figure 12 is a histogram of the percentage distribution of CIBIC-plus scores attained by patients assigned to each of the two treatment groups who completed 13 weeks of treatment. The patients in the active treatment arm of the study were maintained at either 24 mg/day or 32 mg/day at the discretion of the investigator.Figure 10 illustrates the time course for the change from baseline in ADAS-cog scores for both dose groups over the 13 weeks of the study.

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