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Unlike adrenaline and noradrenaline, PHE is not a catecholamine and is not influenced by the enzyme 0-methyltransferase; therefore, it is more stable and has a prolonged effect.

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The method of administering the pharmaceutical composition of the present invention may be used to treat a variety of diseases, illnesses and conditions for which the CNS active agents of the present invention might be prescribed when used alone, or in combination with other therapies.

The term “suspension tablets” as used herein refers to compressed tablets which rapidly disintegrate after they are placed in water, and are readily dispersible to form a suspension containing a precise dosage of the CNS active agent, PHE and GUA.

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