The reported adverse events in Memantine hydrochloride trials reflect experience gained under closely monitored conditions in a highly selected patient population. In actual practice or in other clinical trials, these frequency estimates may not apply, as the conditions of use, reporting behavior and the types of patients treated may differ. Table below lists treatment-emergent signs and symptoms that were reported in at least 2% of patients in placebo-controlled dementia trials and for which the rate of occurrence was greater for patients treated with Memantine than for those treated with placebo. No adverse event occurred at a frequency of at least 5% and twice the placebo rate. See Table 2.
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