Withdrawal Syndrome Following Cessation of Guanabenz Therapy
- 3 February 1979
- journal article
- research article
- Published by Wiley in The Journal of Clinical Pharmacology
- Vol. 19 (2-3) , 148-150
- https://doi.org/10.1002/j.1552-4604.1979.tb02472.x
Abstract
A withdrawal syndrome consisting of nervousness, palpitations, diaphoresis, and insomnia appeared in 3 patients within 16-48 h following discontinuation of guanabenz, a new centrally acting antihypertensive agent. A similar syndrome of sympathetic overactivity has been described with abrupt withdrawal of clonidine. Three of 4 patients treated with 48 mg/day but none of 20 other patients treated with 32 mg/day or less guanabenz developed this syndrome. None of the 3 patients developed hypertensive crisis, though 1 had a modest rise in the blood pressure above baseline levels. Guanabenz therapy apparently should not be discontinued abruptly and, when possible, the dosage should be limited to less than 48 mg/day.This publication has 9 references indexed in Scilit:
- CLONIDINE WITHDRAWAL IN HYPERTENSIONThe Lancet, 1977
- Guanabenz in essential hypertensionClinical Pharmacology & Therapeutics, 1977
- Guanabenz effects on blood pressure and noninvasive parameters of cardiac performance in patients with hypertensionClinical Pharmacology & Therapeutics, 1976
- The Intravenous Furosemide Test: A Simple Way to Evaluate Renin ResponsivenessAnnals of Internal Medicine, 1976
- Studies on the centrally mediated hypotensive activity of guanabenzEuropean Journal of Pharmacology, 1976
- Possible mechanism of the hypotensive action of 2,6-dichlorobenzylidene aminoguanidine: Evidence for central noradrenaline receptor stimulationEuropean Journal of Pharmacology, 1973
- Effects of Clonidine Withdrawal: Possible Mechanisms and Suggestions for ManagementBMJ, 1973
- Evidence for an α-sympathomimetic component in the effects of catapresan on vasomotor centres: Antagonism by piperoxaneEuropean Journal of Pharmacology, 1971
- Investigations into the mechanism of the hypotensive effect of 2-(2,6-dichlorphenylamino)-2-imidazoline-HClEuropean Journal of Pharmacology, 1967