Evidence for benefits and risks of tadalafil as a non-prescription medicine: review and evaluation using the Group Delphi technique to achieve consensus amongst clinical experts

An evidence-based consensus meeting was held with urologists, a pharmacist and a cardiologist to perform a structured benefit-risk analysis of reclassifying tadalafil, a phosphodiesterase type 5 (PDE5) inhibitor for treatment of erectile dysfunction (ED), to be available without prescription in Germ...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Kurt Miller (Autore), Uwe May (Autore), Wolf-Dietrich Beecken (Autore), Georgios Hatzichristodoulou (Autore), Michael Böhm (Autore), Stefan Fink (Autore)
Natura: Libro
Pubblicazione: Frontiers Media S.A., 2023-10-01T00:00:00Z.
Soggetti:
Accesso online:Connect to this object online.
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_cbd36f2815c04b41b7c11af8a38d2d05
042 |a dc 
100 1 0 |a Kurt Miller  |e author 
700 1 0 |a Uwe May  |e author 
700 1 0 |a Wolf-Dietrich Beecken  |e author 
700 1 0 |a Georgios Hatzichristodoulou  |e author 
700 1 0 |a Michael Böhm  |e author 
700 1 0 |a Stefan Fink  |e author 
245 0 0 |a Evidence for benefits and risks of tadalafil as a non-prescription medicine: review and evaluation using the Group Delphi technique to achieve consensus amongst clinical experts 
260 |b Frontiers Media S.A.,   |c 2023-10-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2023.1254706 
520 |a An evidence-based consensus meeting was held with urologists, a pharmacist and a cardiologist to perform a structured benefit-risk analysis of reclassifying tadalafil, a phosphodiesterase type 5 (PDE5) inhibitor for treatment of erectile dysfunction (ED), to be available without prescription in Germany. As per the Brass process endorsed by regulatory authorities, an evidence-based Brass value tree was developed, which identified the incremental benefits and risks that should be considered above the safety and efficacy evidence required for prescription medicines. During the Group Delphi consensus meeting, the expert panel rated the likelihood and clinical impact of each benefit and risk on a scale of 0 (none) to 3 (high). Overall attribute scores were calculated from the product of the mean likelihood and mean clinical impact scores giving a possible score of 0-9. The overall benefit attribute scores ranged from 2.8 to 5.4. The overall risk attribute scores ranged from 0.2 to 2.2 though most were 1.0 or less (3 or more is generally considered to be of concern). On balance, the independent meeting scored the benefits of reclassification of tadalafil higher than the risks and considered the risk mitigation strategies of the packaging label and patient information leaflet (PIL) sufficient. 
546 |a EN 
690 |a erectile dysfunction 
690 |a non-prescription 
690 |a phosphodiesterase type 5 inhibitor (PDE5 inhibitor) 
690 |a reclassification 
690 |a tadalafil 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 14 (2023) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2023.1254706/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/cbd36f2815c04b41b7c11af8a38d2d05  |z Connect to this object online.