Next Article in Journal
The Future of Prenatal Diagnosis and Screening
Next Article in Special Issue
Hyponatremia in Patients with Spontaneous Intracerebral Hemorrhage
Previous Article in Journal / Special Issue
Physiopathological, Epidemiological, Clinical and Therapeutic Aspects of Exercise-Associated Hyponatremia
Open AccessReview

Review of Tolvaptan’s Pharmacokinetic and Pharmacodynamic Properties and Drug Interactions

1
Division of Pharmacotherapy and Experimental Therapeutics (DPET), UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, CB# 7569 Rm 3212 Kerr Hall, Chapel Hill, NC 27599-7569, USA
2
Cardiovascular Team Lead Pharmacist, Department of Pharmacy, Rex Hospital, Raleigh, NC 27607, USA
3
Division of Cardiology, UNC Heart and Vascular, University of North Carolina at Chapel Hill, CB# 7569 Rm 3212 Kerr Hall, Chapel Hill, NC 27599-7569, USA
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
J. Clin. Med. 2014, 3(4), 1276-1290; https://doi.org/10.3390/jcm3041276
Received: 22 August 2014 / Revised: 15 October 2014 / Accepted: 24 October 2014 / Published: 12 November 2014
(This article belongs to the Special Issue Hyponatremia: Advances in Diagnosis and Management)
Tolvaptan is an arginine vasopressin (AVP) antagonist that acts to increase excretion of free water (aquaresis) in patients without introducing electrolyte abnormalities or worsening renal function. It works via blockade of vasopressin-2 receptors at the renal collecting duct. Since the approval of tolvaptan for the treatment of hypervolemic and euvolemic hyponatremia in 2009, new studies have been reported to better characterize its pharmacokinetic and pharmacodynamic profile of tolvaptan. This paper is a review of both these clinical studies, as well as previous literature, in order to help guide appropriate clinical use of tolvaptan in patients. With appropriate monitoring of serum sodium, tolvaptan may be safely dose escalated from 15 mg once daily to a maximum effective dose of 60 mg once daily for multiple days, to achieve optimal aqauretic effects. In terms of drug interactions, co-administration of moderate to potent CYP3A4 inhibitors and inducers should be avoided. Tolvaptan should also be co-administered with caution and proper monitoring in the presence of P-glycoprotein substrate and strong inhibitors. Co-administration of tolvaptan with diuretic therapy did not appear to alter the aquaretic effect of tolvaptan; and was shown to be safe and well tolerated. View Full-Text
Keywords: tolvaptan; pharmacokinetic; pharmacodynamic; arginine vasopressin; aquaretic; CYP3A4; digoxin; heart failure; hyponatremia tolvaptan; pharmacokinetic; pharmacodynamic; arginine vasopressin; aquaretic; CYP3A4; digoxin; heart failure; hyponatremia
MDPI and ACS Style

Bhatt, P.R.; McNeely, E.B.; Lin, T.E.; Adams, K.F., Jr.; Patterson, J.H. Review of Tolvaptan’s Pharmacokinetic and Pharmacodynamic Properties and Drug Interactions. J. Clin. Med. 2014, 3, 1276-1290.

Show more citation formats Show less citations formats

Article Access Map by Country/Region

1
Only visits after 24 November 2015 are recorded.
Back to TopTop