In 2015, the FDA notified Janssen-Cilag, Risperdal’s manufacturer, that it must include what is known as a “black-box warning” on Risperdal labels, recommending that the product not be used to for treat seniors with dementia.
Since its introduction into the American market, Risperdal has been linked to a wide range of side effects, from blurred vision, dizziness or drowsiness and headaches to lethargy, indigestion and weight gain. Other side effects tied to use of Risperdal include:
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