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Drug Safety|November 2, 2013
Profiling cumulative proportional reporting ratios of drug-induced liver injury in the FDA Adverse Event Reporting System (FAERS) databaseAllen D Brinker, Jenna Lyndly, Joseph Tonning, et al.
Drug Safety|July 16, 2014
A comparison of active adverse event surveillance systems worldwideYu-Lin Huang, Jinhee Moon, Jodi B Segal
Drug Safety|April 22, 2016
Pharmacokinetics, Efficacy, and Safety of Hepatitis C Virus Drugs in Patients with Liver and/or Renal ImpairmentElise J Smolders, Clara T M M de Kanter, Bart van Hoek, et al.
Drug Safety|July 27, 2017
Drug-Induced Dental Caries: A Disproportionality Analysis Using Data from VigiBaseEmilie Patras de Campaigno, Inès Kebir, Jean-Louis Montastruc, et al.
Drug Safety|August 7, 2017
Channeling in the Use of Nonprescription Paracetamol and Ibuprofen in an Electronic Medical Records Database: Evidence and ImplicationsRachel B Weinstein, Patrick Ryan, Jesse A Berlin, et al.
Drug Safety|October 28, 2017
Neuropsychiatric Events Associated with Leukotriene-Modifying Agents: A Systematic ReviewSharon W Y Law, Angel Y S Wong, Shweta Anand, et al.
Drug Safety|August 26, 2017
From Big Data to Smart Data for Pharmacovigilance: The Role of Healthcare Databases and Other Emerging SourcesGianluca Trifirò, Janet Sultana, Andrew Bate
Drug Safety|August 18, 2017
A New Erice Report Considering the Safety of Medicines in the 21st CenturyIvor Ralph Edwards
Drug Safety|December 10, 2015
Tools for Assessing Potential Significance of Pharmacist Interventions: A Systematic ReviewThi-Ha Vo, Bruno Charpiat, Claire Catoire, et al.
Drug Safety|May 20, 2016
Benefit and Risk of Tofacitinib in the Treatment of Rheumatoid Arthritis: A Focus on Herpes ZosterKunihiro Yamaoka
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