J P W Heaton
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
J P W Heaton has a total of 2 co-authors. Here are the top co-authors by number of shared publications:
D J Sleep
Abbott International, Abbott Park, IL, USA
1 shared publicationJ Dean
The Salisbury Clinic, Plymouth, UK
1 shared publication
Latest Publications
- 1 February 2002
- Published by Springer Nature in International Journal Of Impotence Research
- Vol. 14 (1) , 61-64
Sequential administration enhances the effect of apomorphine SL in men with erectile dysfunction
The response to Uprima® (apomorphine sublingual, (apo SL)) has been well documented in conventional clinical trials. Apo SL produces a predictable, consistent and durable response across a wide variety of patients. The positive reinforcement of a successful outcome should further support clinical benefit. Apo SL with its rapid onset affords a greater opportunity for spontaneity, which can be an important factor in influencing patient choice. It is recognised that patient counselling and the setting of realistic expectations are vital to a successful outcome. The impact of persisting with sequential treatment on outcome has been calculated from the clinical data. While apo SL is effective de novo in 50% of single doses, additional benefit is observed with repeat dosing. Full benefit may not be achieved until four or more treatments have been taken in an optimal setting. The data also confirm that 3 mg has superior activity. Patients should therefore be encouraged to try a minimum of 4 doses at 3 mg.
- 1 February 2002
- Published by Springer Nature in International Journal Of Impotence Research
- Vol. 14 (1) , 61-64
Sequential administration enhances the effect of apomorphine SL in men with erectile dysfunction
The response to Uprima® (apomorphine sublingual, (apo SL)) has been well documented in conventional clinical trials. Apo SL produces a predictable, consistent and durable response across a wide variety of patients. The positive reinforcement of a successful outcome should further support clinical benefit. Apo SL with its rapid onset affords a greater opportunity for spontaneity, which can be an important factor in influencing patient choice. It is recognised that patient counselling and the setting of realistic expectations are vital to a successful outcome. The impact of persisting with sequential treatment on outcome has been calculated from the clinical data. While apo SL is effective de novo in 50% of single doses, additional benefit is observed with repeat dosing. Full benefit may not be achieved until four or more treatments have been taken in an optimal setting. The data also confirm that 3 mg has superior activity. Patients should therefore be encouraged to try a minimum of 4 doses at 3 mg.