Tolerability of Azithromycin as Malaria Prophylaxis in Adults in Northeast Papua, Indonesia

Author:

Taylor Walter R.12,Richie Thomas L.1,Fryauff David J.1,Ohrt Colin3,Picarima Helena1,Tang Douglas4,Murphy Gerald S.1,Widjaja Hendra1,Braitman David5,Tjitra Emiliana6,Ganjar Asep7,Jones Trevor R.1,Basri Hasan1,Berman Josh3

Affiliation:

1. U.S. Naval Medical Research Unit No. 2

2. Department of Tropical Medicine, Tulane University School of Public Health, New Orleans, Louisiana

3. Division of Experimental Therapeutics

4. Division of Biometrics, Walter Reed Army Institute of Research, Washington, D.C.

5. U.S. Army Medical Materiel Development Activity, Fort Detrick, Maryland

6. Centre for Health Research and Development, National Institutes of Health, Jakarta

7. District Military Health Services, Jayapura, Papua, Indonesia

Abstract

ABSTRACT Drug tolerability affects compliance. We evaluated the tolerability levels of azithromycin (750-mg loading dose plus 250 mg/day; n = 148 subjects), doxycycline (100 mg/day; n = 75), and placebo ( n = 77) as prophylaxis against malaria in Indonesian adults over 20 weeks. Self-reported and elicited symptoms, health perception, hearing, hematology, and biochemistry were assessed. The loading dose was well tolerated. The frequencies (number per person-years [p-yr]) of all daily reported symptoms were similar in the three arms of the study: 40.2/p-yr for azithromycin, 39.7/p-yr for doxycycline, and 38.2/p-yr for placebo. Relative to those who received placebo, azithromycin recipients complained more often of heartburn (rate ratio = 10.5 [95% confidence interval, 2.8 to 88.1]), paresthesia (2.03 [1.08 to 4.24]), and mild (1.55 [1.01 to 2.48]) and severe (11.2 [1.34 to ∞]) itching but less often of fever (0.21 [0.09 to 0.49]) and tinnitus (0.09 [0.04 to 0.21]). Azithromycin recipients showed no evidence of clinical hearing loss or hematologic, hepatic, or renal toxicity. One azithromycin recipient developed an erythematous rash. Daily azithromycin was well tolerated by these Indonesian adults during 20 weeks of treatment.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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