Background: Omeprazole causes irreversible inhibition of the hydrogen/
potassium adenosine triphosphatase enzyme, leading to a marked reducti
on in both acid secretion and volume of gastric juice. Reported side-e
ffects include nausea, vomiting, diarrhoea, constipation, and headache
. We report the development of dry mouth during omeprazole therapy. Me
thods: We have identified six patients taking omeprazole for more than
6 weeks who complained of a dry mouth. Salivary production was measur
ed as whole salivary Bow produced over a 10-min period spat into a col
lecting vessel and as 5% citric acid-stimulated parotid salivary flow
collected with a Lashley cup device placed over the parotid duct. Flow
rates were evaluated both during and after cessation of treatment. Sa
liva produced was then cultured for microbes. Results: Four of the six
had subnormal parotid or whole salivary flow rates on treatment that
recovered after stopping treatment. The increase after treatment was m
arked in four. Significant amounts of Candida albicans grew from the s
aliva of the three patients with the lowest salivary flows; one saliva
also grew Staphylococcus aureus. Conclusion: Salivary flow is reduced
in some patients treated with omeprazole, returning to normal after c
essation of treatment. This reduction may predispose to opportunistic
infection, particularly in the edentulous.