Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 1984 Aug;26(2):160-3.
doi: 10.1128/AAC.26.2.160.

Furazolidone versus ampicillin in the treatment of traveler's diarrhea

Clinical Trial

Furazolidone versus ampicillin in the treatment of traveler's diarrhea

H L DuPont et al. Antimicrob Agents Chemother. 1984 Aug.

Abstract

Ninety-four U.S. students who acquired diarrhea in Mexico were treated with furazolidone (47 subjects) or ampicillin (47 subjects) on a double-blind random basis. Of 47 students, 26 (55%) who received furazolidone (100 mg four times daily for 5 days) recovered from illness within 48 h after initiation of therapy, in contrast to 15 of 47 (32%) who received ampicillin (500 mg four times daily for 5 days) (P less than 0.05). Altogether, 74% of students treated with furazolidone and 49% of those receiving ampicillin were well within 72 h (P less than 0.05). When furazolidone was compared with ampicillin, clinical illness was shortened on the average from 65 to 61 h for enterotoxigenic Escherichia coli diarrhea, from 83 to 58 h for shigellosis, from 82 to 51 h for diarrhea unassociated with a detectable agent, and from 72 to 57 h for all cases irrespective of etiology. Although not dramatically effective in the current trial, the broad spectrum of activity of furazolidone is of interest. Because of in vitro activity against Campylobacter strains and known effectiveness in treating giardiasis, furazolidone should be considered in therapy for diarrhea of unknown etiology in certain settings when laboratory processing of stools for etiological agent is not feasible.

PubMed Disclaimer

References

    1. Lancet. 1968 Feb 17;1(7538):332-3 - PubMed
    1. Am J Ment Defic. 1968 Sep;73(2):214-7 - PubMed
    1. JAMA. 1968 Dec 16;206(12):2745 - PubMed
    1. J Trop Med Hyg. 1970 Jan;73(1):15-8 - PubMed
    1. Bull World Health Organ. 1970;43(3):373-8 - PubMed

Publication types