Effect of Aspirin Pretreatment or Slow Dose Titration on Flushing and Gastrointestinal Events in Healthy Volunteers Receiving Delayed-release Dimethyl Fumarate.
暂无分享,去创建一个
[1] R. Gold,et al. Clinical Significance of Gastrointestinal and Flushing Events in Patients with Multiple Sclerosis Treated with Delayed-Release Dimethyl Fumarate. , 2015, International journal of MS care.
[2] M. Hutchinson,et al. Managing flushing and gastrointestinal events associated with delayed-release dimethyl fumarate: Experiences of an international panel. , 2014, Multiple sclerosis and related disorders.
[3] I. Nestorov,et al. Tolerability and pharmacokinetics of delayed-release dimethyl fumarate administered with and without aspirin in healthy volunteers. , 2013, Clinical therapeutics.
[4] D. Arnold,et al. Placebo-controlled phase 3 study of oral BG-12 for relapsing multiple sclerosis. , 2012, The New England journal of medicine.
[5] David H. Miller,et al. Placebo-controlled phase 3 study of oral BG-12 or glatiramer in multiple sclerosis. , 2012, The New England journal of medicine.
[6] M. Gönen,et al. Reliability of adverse symptom event reporting by clinicians , 2012, Quality of Life Research.
[7] W. Rief,et al. Lessons learned from placebo groups in antidepressant trials , 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.
[8] T. Jacobson. A "hot" topic in dyslipidemia management--"how to beat a flush": optimizing niacin tolerability to promote long-term treatment adherence and coronary disease prevention. , 2010, Mayo Clinic proceedings.
[9] Ludwig Kappos,et al. Efficacy and safety of oral fumarate in patients with relapsing-remitting multiple sclerosis: a multicentre, randomised, double-blind, placebo-controlled phase IIb study , 2008, The Lancet.
[10] Serguei V. S. Pakhomov,et al. Agreement between patient-reported symptoms and their documentation in the medical record. , 2008, The American journal of managed care.
[11] J. Paolini,et al. Measuring flushing symptoms with extended-release niacin using the flushing symptom questionnaire©: results from a randomised placebo-controlled clinical trial , 2008, International journal of clinical practice.
[12] G. Geisslinger,et al. PGD2 metabolism in plasma: kinetics and relationship with bioactivity on DP1 and CRTH2 receptors. , 2007, Biochemical pharmacology.
[13] N. Santanello,et al. Validation of a questionnaire to assess niacin-induced cutaneous flushing , 2007, Current medical research and opinion.
[14] J. Morrow,et al. Quantification of F2-isoprostanes as a biomarker of oxidative stress , 2007, Nature Protocols.
[15] A. Avins,et al. Brief Communication: Better Ways To Question Patients about Adverse Medical Events , 2006, Annals of Internal Medicine.
[16] S. Tepper,et al. Assessment of Adverse Events Associated With Triptans—Methods of Assessment Influence the Results , 2004, Headache.
[17] J. Morrow,et al. Simplification of the mass spectrometric assay for the major urinary metabolite of prostaglandin D2. , 1993, Journal of chromatography.
[18] B. Gandevia,et al. DECLARATION OF HELSINKI. , 1964, The Medical journal of Australia.
[19] H. Zimmerman. Hepatotoxicity: The adverse effects of drugs and other chemicals on the liver , 1978 .