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PMID: 3421267 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Pharmacodynamics and tolerance of oral sustained release ritodrine.

American journal of obstetrics and gynecology ·Vol. 159 ·No. 3 ·1988-09-00 ·Pages 690-5

Witter FR, Benedetti TJ, Petty BG, Feldman AM, Traill TA, Anderson J

Abstract

A new oral sustained release formulation of ritodrine was tested for patient tolerance in this open study. The doses tested were 120 mg/day, 240 mg/day, and 360 mg/day. No objective toxicity was seen at any level. Doses of 120 mg/day and 240 mg/day were well-tolerated. Of the subjects who received the 360 mg/day dose, most tolerated it well.

MeSH Terms
Administration, Oral Adolescent Adult Delayed-Action Preparations Female Heart Rate, Fetal/drug effects Hemodynamics/drug effects Humans Obstetric Labor, Premature/prevention & control Pregnancy Ritodrine/administration & dosage,adverse effects,pharmacokinetics
Chemicals
Delayed-Action Preparations Ritodrine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Witter F R
Johns Hopkins University School of Medicine, Department of Gynecology and Obstetrics, Baltimore, MD 21205.
Benedetti T J
Petty B G
Feldman A M
Traill T A
Anderson J
Article Info
Journal
American journal of obstetrics and gynecology
Abbr.
Am J Obstet Gynecol
ISSN
0002-9378
Published
1988-09-00
Pages
690-5
Language
English
Region
United States
NLM ID
0370476
Subset
IM
Grants
NCRR NIH HHS · RR0035 · United States
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