Omeprazole, lansoprazole and pantoprazole are all mainly metabolised b
y the polymorphically expressed cytochrome P450 (CYP) isoform CYP2C19
(S-mephenytoin hydroxylase). All 3 proton pump inhibitors have a very
limited potential for drug interactions at the CYP level. Small effect
s on CYP reported for these compounds are usually of no clinical relev
ance. No dose related adverse effects have been identified, suggesting
that the small proportion of slow metabolisers is at no additional ri
sk for clinically important drug interactions. The absorption of some
compounds, e.g. benzylpenicillin (penicillin G), are altered during tr
eatment with proton pump inhibitors as a result of the increased intra
gastric pH. A synergy has been confirmed between omeprazole and amoxic
illin or clarithromycin in the antibacterial effect against Helicobact
er pylori.