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It is slightly soluble in water and freely soluble in alcohol,
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions).

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Bystolic may induce psychic and physical dependence of the morphine-type (?- opioid) (See WARNINGS).
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Do not drive or perform other possibly unsafe tasks until you know how you react to it.Do not drink
Bystolic has not been shown to cause histamine release. At therapeutic doses, Bystolic has no effect on heart rate,
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Bystolic is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4, as well as by conjugation of parent and metabolites.
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The volume of distribution of Bystolic was 2.6 and 2.9 liters/kg in male and female subjects, respectively,
Bystolic has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.

Bystolic had only slight thermoregulatory effects. Its use is thus unlikely to provoke hypothermia or to facilitate fever.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Bystolic and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Breast-feeding�Bystolic passes into breast milk and may cause unwanted effects in nursing babies.
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Bystolic has not been shown to cause histamine release. At therapeutic doses, Bystolic has no effect on heart rate, left-ventricular function or cardiac index.
Some people who use Bystolic for a long time without a break may develop a physical need to continue taking it.
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