Substantially reduced atazanavir concentrations, leading to loss of antiviral effectiveness.
Proton pump inhibitors should be avoided in patients receiving atazanavir without ritonavir.
Source: G&G 14e · p1245-1266
Proton Pump Inhibitor · Antiulcer Agent
Proton pump inhibitors inhibit gastric acid secretion by blocking the hydrogen-potassium adenosine triphosphatase enzyme system (the ‘proton pump’) of the gastric parietal cell.
Manufacturer advises caution—no
Substantially reduced atazanavir concentrations, leading to loss of antiviral effectiveness.
Proton pump inhibitors should be avoided in patients receiving atazanavir without ritonavir.
Source: G&G 14e · p1245-1266
Reduced ledipasvir concentrations, potentially leading to treatment failure/relapse.
If PPIs must be used, their doses should not exceed the equivalent of 20 mg omeprazole once daily. Omeprazole must be administered simultaneously with LDV/SOF in the fasted state.
Source: G&G 14e · p1238, p1242
Reduced absorption and plasma concentrations of rilpivirine, potentially leading to loss of efficacy.
Should not be given with proton pump inhibitors.
Source: G&G 14e · p1245-1266
Reduced velpatasvir concentrations, potentially leading to treatment failure.
PPI doses should not exceed the equivalent of 20 mg omeprazole daily. SOF/VEL should be taken with food 4 hours prior to a PPI dose. Velpatasvir requires acidic gastric pH.
Source: G&G 14e · p1239, p1242
Increased risk of small intestine damage, despite reducing duodenal and gastric ulceration.
Consider the overall GI risk, including small intestine, when coadministering.
Source: G&G 14e · p834
Increased risk of small intestine damage, despite reducing duodenal and gastric ulceration.
Consider the overall GI risk, including small intestine, when coadministering.
Source: G&G 14e · p834
Altered bioavailability of ampicillin esters, potentially reducing their efficacy.
Not specified.
Source: G&G 14e · p1076
Increased risk of small intestine damage, despite reducing duodenal and gastric ulceration.
Consider the overall GI risk, including small intestine, when coadministering.
Source: G&G 14e · p834
Decreased plasma levels of azoles.
Source: Harrison 22e · p1742
Increased risk of small intestine damage, despite reducing duodenal and gastric ulceration.
Consider the overall GI risk, including small intestine, when coadministering.
Source: G&G 14e · p834
Increased risk of small intestine damage, despite reducing duodenal and gastric ulceration.
Consider the overall GI risk, including small intestine, when coadministering.
Source: G&G 14e · p834
Increased risk of small intestine damage, despite reducing duodenal and gastric ulceration.
Consider the overall GI risk, including small intestine, when coadministering.
Source: G&G 14e · p834
Continue into a citation-backed clinical answer with the drug context already attached.
Sources: BNF·Verified: 2026-05-13 · House clinical team