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Tadalafil dosage 60 mg or divided into 4 doses at least 36 hours apart or a total daily dose of 60 mg or divided into 4 doses at least 36 hours apart. It may be necessary to have the patient periodically assessed for improvement. The invention additionally provides an oral dosage form for administration of divalproex sodium including a capsule or tablet, delayed release a transdermal patch, an intravenous solution, a nasal spray, transdermal system or a rectal suppository. It is preferable to use a delayed release tablet or dose-form in the treatment of patients with severe congestive heart failure. In preferred embodiment dosed on a three, six, nine, 12 or 15 week schedule, the tablet is dissolved and administered as single dose. If the maximum daily dose is desired to be reduced, the tablet is dissolved and dose repeated on the following day. Alternatively, tablet may be dissolved in water only with added flavoring. Suitable flavors of the present invention include, but are not limited to, strawberry, peach, chocolate, cherry and strawberry flavoring, mango, apple orange and cherry, grape, apple, pear, pineapple, orange, peach, grape and strawberry. Other flavors may be mixed in the quantity of up to 1% the tablet with water. capsule or may also be taken as a delayed release tablet. If desired, the oral dosage form may include an aerosol. The aerosol can be designed to have a pungent, acidic, foul tasting, smelling odor or any other that may be desired by the patient. It also may have any flavor desired. Aerosol inhalants are preferred as these provide for less painful administration of the dose and provide potential for faster relief of symptoms. The oral dose may be administered in one or more formulations. This is desirable because for patients with severe complications it may be difficult to achieve effective therapeutic doses. However, the invention does not intend to be limited one specific formulation, but to broadly design the composition of compositions for administration to the patient and incorporate any desired therapeutic advantage for treating the same. composition, dosage form, application method and dosing schedule are not limited as to choice or modification desired by the person of ordinary skill in the art of pharmaceutical composition present invention. SUMMARY OF THE INVENTION As shown in FIG. 1, the present invention provides a transdermal delivery system for treating patients with congestive heart failure. The invention further provides a transdermal formulation containing divalproex sodium as the active ingredient to treat patients with congestive heart failure. The invention also provides a transdermal dosage form containing composition incorporating a comprising divalproex sodium as the active ingredient. invention further provides a transdermal dosage form with different levels of divalproex sodium. The invention further provides for design to achieve desired therapeutic effect in each dose of the composition. For example, a patient may receive transdermal formulation 20 mg, 50 100 mg or 200 dosed at 20, 50 and 100 minutes, resp