key: cord-0779833-k5vswy4a authors: Persico, Amelia L; Wegrzyn, Erica L; Fudin, Jeffrey; Schatman, Michael E title: Fentalogues date: 2020-08-20 journal: J Pain Res DOI: 10.2147/jpr.s265901 sha: 2b5792cac63c3598065e676e06a8937d67e678d7 doc_id: 779833 cord_uid: k5vswy4a nan The implication of this rescheduling is to mitigate circumvention of regulatory controls by those who manufacture illicit FRS and streamline prosecution of those who synthesize clandestine FRS without reliance on the Analogue Act. 6 Established in 1988, the Analogue Act provides that all analogues of schedule I substances be treated as schedule I substances themselves, a key consideration with over 20 illicit fentanyl analogues identified as of June 2018 and new compounds frequently being synthesized. 7 The DEA identified illicit fentanyl and other synthetic opioids as the most lethal category of opioids used in the US in the 2018 national threat assessment. 8 In fact, the very limited diversion of pharmaceutical (licit) fentanyl that occurs is noted to mostly be for small-scale personal use and street sales while illicit fentanyl analogues are trafficked into the US from China and Mexico and are considered to be the primary cause of the high rate of fentanylassociated overdose deaths in the US, often due to central nervous system depression secondary to additive pharmacologic activity when combined with heroin with which these FRSs are frequently laced. 8 Non-pharmaceutical fentanyl products that have been chemically altered into new products are often created in unregulated, clandestine laboratories and can be tainted with toxic adulterants. 8, 9 Alarmingly, some legitimate laboratories have been found to also be manufacturing illicit fentanyl analogues in addition to their legitimate manufacture of pharmaceutical grade medication. 3 Often, these products have been manipulated to increase potency, some hundreds to thousands of times more potent than licit fentanyl, resulting in more addicting and potentially lethal substances. 7 These fentanyl analogues are DEA Schedule I substances, deemed not to have any therapeutic indication while also presenting the strongest potential for abuse and associated morbidity and mortality. 8 Further, they have not been studied in humans, and potency data is generally lacking. 7, 8 Given the specific qualities and extreme hazard associated with nonpharmaceutical, illicit fentanyl analogues, we propose that specific terminology be used going forward in reference to these chemicals, ie "fentalogues". Notably, while preparing this editorial, consideration was given to multiple spellings of "fentalogue" including "fentanylogue", "fentylogue", and "fentanilogue". However, reference to "fentalogues" was identified in a recent publication by Sofalvi et al in reference to novel fentanyl analogues, and it therefore was decided to select this spelling to maintain consistency in the literature. 10 As Bettinger et al noted, the distinction between licit and illicit fentanyl is an essential public health interest due to its potential to stigmatize legitimate patients. 7 Use of the term "fentalogue" to differentiate illicit, non-pharmaceutical fentanyl analogues from licit prescription fentanyl can also allow for precise documentation and increased accuracy in reporting of an often "murky" distinction. The stigmatization of the roughly 20 million Americans reliant upon prescription opioids in order to maintain some semblance of quality of life has been brutal and highly unnecessary. The lives of these unfortunate patients are difficult enough, and conflating licit and illicit opioids only serves to make their plight worse. Although our recommendation to begin referring to illicit fentanyl products as "fentalogues" is highly symbolic, our hope is that it will serve as a reminder to the media, legislators, and the general public that iatrogenic addiction among legitimate chronic pain sufferers is estimated at 2-8% with a tendency towards the lower endthis needs to be clearly and strongly delineated from those suffering from opioid use disorders. 11 Disclosure Dr Jeffrey Fudin is speaker for Abbott Laboratories, Acutis Diagnostics, Inc.; advisory board, speakers bureau, and/or consulting for AcelRx Pharmaceuticals, BioDelivery Sciences International, Daiichi Sankyo, Firstox Laboratories, GlaxoSmithKline (GSK), Human Half-Cell, Inc., Quest Diagnostics, Scilex Pharmaceuticals, and Salix Pharmaceuticals, outside the submitted work. Dr Erica Wegrzyn reports personal fees from Remitigate LLC, outside the submitted work. Dr Amelia L Persico is currently affiliated to Valor Healthcare, Kingston, NY, USA. The authors report no other conflicts of interest in this work. The American chronic pain crisis and the media: about time to get it right? The fentanyl family: a distinguished medical history tainted by abuse Drug Enforcement Administration. Counterfeit Prescription Pills Containing Fentanyls: A Global Threat Provisional drug overdose death counts Analogue act. 1988. (DEA) Title 21 Section 813 Understanding the differences between pharmaceutical and illicit fentanyl and their analogues could save the opioid crisis 2018 national drug threat assessment report The emerging role of toxic adulterants in street drugs in the US illicit opioid crisis Unique structural/stereo-isomer and isobar analysis of novel fentanyl analogues in postmortem and DUID whole blood by UHPLC-MS-MS Opioid abuse in chronic pain-misconceptions and mitigation strategies The Journal of Pain Research is an international, peer reviewed, open access, online journal that welcomes laboratory and clinical findings in the fields of pain research and the prevention and management of pain. Original research, reviews, symposium reports, hypothesis formation and commentaries are all considered for publication. The manuscript management system is completely online and includes a very quick and fair peer-review system, which is all easy to use. 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