FDA approved Lucemyra (lofexidine hydrochloride) for the mitigation of withdrawal symptoms to facilitate abrupt discontinuation of opioids in adults.
FDA - U.S. Food and Drug Administration
Among the topics covered in this issue of Danish Pharmacovigilance Update are: Maximum single dose of intravenous ondansetron (Zofran® and others) now restricted to 16 mg.
Danish Medicines Agency
Ondansetron: List of nationally authorised medicinal products - PSUSA/00002217/201802
Europe - EMA - European Medicines Agency