Uncovering the Quality Deficiencies with Potentially Harmful Effects in Substandard and Falsified PDE-5 Inhibitors Seized by Belgian Controlling Agencies

Illicit PDE-5 inhibitors are frequently encountered by regulatory agencies. Self-medicating with substandard and falsified (SF) PDE-5 inhibitors could be dangerous as they are likely taken without any medical supervision and might be of poor quality which could result in adverse reactions. In order to provide an overview of the quality deficiencies present in recently seized illicit PDE-5 samples that may pose health risks, we set out to identify the products’ different chemical and/or biological risks. Our results indicate that 38% of the samples harbored a chemical risk including the signifi... Mehr ...

Verfasser: Celine Vanhee
Bram Jacobs
Marcella Mori
Angélique Kamugisha
Loïc Debehault
Michael Canfyn
Bart Ceyssens
Hans Van Der Meersch
Koenraad van Hoorde
Eric Deconinck
Marie Willocx
Dokumenttyp: Artikel
Erscheinungsdatum: 2023
Reihe/Periodikum: Forensic Sciences, Vol 3, Iss 31, Pp 426-451 (2023)
Verlag/Hrsg.: MDPI AG
Schlagwörter: mass spectrometry / microbiology / PDE-5 inhibitors / substandard drugs / Social pathology. Social and public welfare. Criminology / HV1-9960 / Analytical chemistry / QD71-142
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27310886
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://doi.org/10.3390/forensicsci3030031

Illicit PDE-5 inhibitors are frequently encountered by regulatory agencies. Self-medicating with substandard and falsified (SF) PDE-5 inhibitors could be dangerous as they are likely taken without any medical supervision and might be of poor quality which could result in adverse reactions. In order to provide an overview of the quality deficiencies present in recently seized illicit PDE-5 samples that may pose health risks, we set out to identify the products’ different chemical and/or biological risks. Our results indicate that 38% of the samples harbored a chemical risk including the significant exceedance of the maximum recommended dosage, a large heterogeneity in API content between the different tablets in the same package or blister and the presence of only 40% of the claimed dosage. Moreover, our results also demonstrate that 16 of the 32 samples were not compliant with the internationally set microbiological quality standards. Startlingly, two samples were severely contaminated with potentially pathogenic bacteria, which could result in a gastrointestinal illness upon oral intake.