Deriving harmonised permitted daily exposures (PDEs) for paracetamol (acetaminophen) CAS #: 103-90-2.

Acceptable daily exposure (ADE) CAS RN 103-90-2 Cleaning validation Cross contamination Health-based exposure limit (HBEL) Multipurpose manufacturing facility Paracetamol (acetaminophen) Permitted daily exposure (PDE) Residual carry-over

Journal

Regulatory toxicology and pharmacology : RTP
ISSN: 1096-0295
Titre abrégé: Regul Toxicol Pharmacol
Pays: Netherlands
ID NLM: 8214983

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 10 02 2020
revised: 19 05 2020
accepted: 28 05 2020
pubmed: 12 6 2020
medline: 26 3 2021
entrez: 12 6 2020
Statut: ppublish

Résumé

In the pharmaceutical industry, cleaning criteria are required for multipurpose manufacturing facilities. These Health Based Exposure Limits (HBELs), also called permitted daily exposures (PDEs) values, are derived from toxicological and pharmacological evaluation of the active pharmaceutical ingredients (APIs). The purpose of this publication is to show an example of how authors from different companies evaluate a generic drug, paracetamol, and discuss different approaches and relevance of the nonclinical studies for deriving PDEs. PDE limits of 25 mg/day for the oral route, and 20 mg/day for the intravenous (i.v.) and inhalation (inhal.) routes, respectively, were established herein. However, it has been already recognised that there are acceptable differences in the PDE calculations, which may be based on data accessibility, company-specific science-policy decisions or expert judgments. These differences can cause up to a 3-fold lower or higher values. If unnecessarily high factors are applied, this would result in a very conservative PDE value and unneeded additional cleaning and higher manufacturing costs. The PDE values presented are considered to be protective against adverse and pharmacological effects observed in clinical trials and in this case, a very long postmarketing period of paracetamol.

Identifiants

pubmed: 32522580
pii: S0273-2300(20)30118-5
doi: 10.1016/j.yrtph.2020.104692
pii:
doi:

Substances chimiques

Analgesics 0
Acetaminophen 362O9ITL9D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104692

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kamila Gromek (K)

GlaxoSmithKline, United Kingdom. Electronic address: kamila.x.gromek@gsk.com.

William Hawkins (W)

GlaxoSmithKline, United Kingdom. Electronic address: william.a.hawkins@gsk.com.

Tanja Bernier (T)

Abbott, United States. Electronic address: tanja.bernier@abbott.com.

Claudia Sehner (C)

Boehringer Ingelheim, Germany. Electronic address: claudia.sehner@boehringer-ingelheim.com.

Eva Zeller (E)

Boehringer Ingelheim, Germany. Electronic address: eva_2.zeller@boehringer-ingelheim.com.

Markus Schwind (M)

Sanofi, France. Electronic address: markus.Schwind@sanofi.com.

Thomas Pfister (T)

Roche, Switzerland. Electronic address: thomas.pfister.tp1@roche.com.

Martin Kohan (M)

Astra Zeneca, United Kingdom. Electronic address: martin.kohan@astrazeneca.com.

Osahon Osadolor (O)

Novartis, Switzerland. Electronic address: osahon.osadolor@novartis.com.

Milica Glogovac (M)

Novartis, Switzerland. Electronic address: milica.glogovac@novartis.com.

Gregor Tuschl (G)

Merck Healthcare KGaA, Germany. Electronic address: gregor.tuschl@merckgroup.com.

David G Dolan (DG)

Amgen Inc., United States. Electronic address: ddolan@amgen.com.

Ester Lovsin Barle (E)

Takeda, Switzerland. Electronic address: ester.lovsin-barle@takeda.com.

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