G. Wiedermann et al., ADVERSE EVENTS AFTER ORAL VACCINATION AGAINST CHOLERA WITH CVD103-HGR, Wiener Klinische Wochenschrift, 110(10), 1998, pp. 376-378
The goal of the present study was to evaluate the tolerability and acc
eptability of an oral cholera vaccine (CVD103HgR) in individuals prepa
ring for travel to countries endemic for cholera. 2545 Austrian travel
ers between 6 months and 81.5 years of age received a single dose of C
VD103HgR and were asked to complete a questionnaire for documentation
of adverse events during a 7 day period post immunisation. Events were
recorded regardless of whether they were caused by concomitant vaccin
ations or other factors and thus, a causative relationship was not nec
essarily present. Despite this drawback and the possibility of overrep
orting, this study has proven a low frequency in side effects and the
good tolerability of CVD103HgR. Occasional gastrointestinal side effec
ts (15% diarrhea, 8.1% nausea, 1.1% vomiting) were seen and were of mi
ld character and probably a consequence of associated intake of sodium
bicarbonate buffer. Other events (7% skin eruptions, 2.7% fever) were
mild and considered as harmless (or not vaccine related). The results
show that the oral cholera vaccine CVD103HgR was well tolerated and a
ccepted by travelers.