1.1. Adults
Maximum daily adult doses for PPIs when prescribed as acute and maintenance therapy, as well as components of combination treatments, are summarized in Tables 1-4. Dosages exceeding these recommended values will be reviewed.
Drug Name | Dosage Form/Strength | Treatment Indication | Maximum Recommended Dosage |
---|---|---|---|
dexlansoprazole (Dexilant) | 30 mg, 60 mg delayed- release capsules | erosive esophagitis (EE) | 60 mg/day |
gastroesophageal reflux disease (GERD) - nonerosive | 30 mg/day | ||
esomeprazole magnesium (Nexium®, generics) | 20 mg, 40 mg delayed-release capsules; 2.5 mg, 5 mg, 10 mg, 20 mg, 40 mg delayed-release powder for suspension | EE | 40 mg/day |
GERD - nonerosive | 20 mg/day | ||
Helicobacter pylori eradication | 40 mg/day* | ||
heartburn | 20 mg/day | ||
hypersecretory conditions | 240 mg/day in divided doses | ||
lansoprazole (Prevacid®, generics) | 15 mg, 30 mg delayed-release capsules, 15 mg, 30 mg orally disintegrating tablets | duodenal ulcer | 15 mg/day |
EE | 30 mg/day | ||
gastric ulcer | 30 mg/day | ||
GERD - nonerosive | 15 mg/day | ||
H. pylori eradication | 90 mg/day (in divided doses)* | ||
heartburn | 15 mg/day | ||
hypersecretory conditions | 180 mg/day in divided doses | ||
NSAID-associated gastric ulcer | 30 mg/day | ||
omeprazole (Prilosec®, generics) | 10 mg, 20 mg, 20.6 mg, 40 mg delayed-release capsule; 20 mg delayed-release orally disintegrating tablet | duodenal ulcer | 20 mg/day |
EE | 20 mg/day | ||
gastric ulcer | 40 mg/day | ||
GERD - nonerosive | 20 mg/day | ||
heartburn | 20 mg/day | ||
H. pylori eradication |
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hypersecretory conditions | 360 mg/day in divided doses | ||
omeprazole magnesium (Prilosec®) | 2.5 mg, 10 mg packet with delayed-release granules for suspension, 20.6 mg delayed-release capsule | duodenal ulcer | 20 mg/day |
EE | 20 mg/day | ||
gastric ulcer | 40 mg/day | ||
GERD - nonerosive | 20 mg/day | ||
H. pylori eradication |
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||
hypersecretory conditions | 360 mg/day in divided doses | ||
pantoprazole (Protonix®, generics) | 20 mg, 40 mg delayed-release tablets; 40 mg delayed-release granules for suspension | EE | 40 mg/day |
hypersecretory conditions | 240 mg/day in divided doses | ||
rabeprazole (Aciphex®, generics) | 20 mg delayed-release tablet; 5 mg, 10 mg delayed-release sprinkle capsule | duodenal ulcer | 20 mg/day |
EE | 20 mg/day | ||
GERD - nonerosive | 20 mg/day | ||
H. pylori eradication | 40 mg/day in divided doses* | ||
hypersecretory conditions | 120 mg/day in divided doses |
Legend:
- *Per ACG Guidelines, PPI dosing may be doubled depending on the regimen used for H. Pylori eradication12
Drug Name | Dosage Form/Strength | Treatment Indication | Maximum Recommended Dosage |
---|---|---|---|
omeprazole/ sodium bicarbonate (Zegerid®, generics) | 20 mg/1100 mg, 40 mg/1100 mg capsules; 20 mg/1680 mg, 40 mg/1680 mg packets for suspension | duodenal ulcer | 20 mg/day (as mg of omeprazole) |
EE | 20 mg/day (as mg of omeprazole) | ||
gastric ulcer | 40 mg/day (as mg of omeprazole) | ||
GERD - nonerosive | 20 mg/day (as mg of omeprazole) | ||
heartburn | 20 mg/day (as mg of omeprazole) | ||
upper GI bleed risk reduction in critically ill (suspension only) | Day 1: 80 mg (in divided doses); Days 2-14: 40 mg/day (as mg of omeprazole) |
Drug Name | Dosage Form/Strength | Treatment Indication | Maximum Recommended Dosage |
---|---|---|---|
dexlansoprazole (Dexilant) | 30 mg, 60 mg delayed- release capsules | erosive esophagitis (EE) | 30 mg/day |
heartburn | 30 mg/day | ||
esomeprazole magnesium (Nexium®, generics) | 20 mg, 40 mg delayed-release capsules; 2.5 mg, 5 mg, 10 mg, 20 mg, 40 mg delayed-release powder for suspension | EE | 20 mg/day |
hypersecretory conditions | 240 mg/day in divided doses | ||
risk reduction of NSAID-associated gastric ulcer | 40 mg/day | ||
lansoprazole (Prevacid®, generics) | 15 mg, 30 mg delayed-release capsules, 15 mg, 30 mg orally disintegrating tablets | duodenal ulcer | 15 mg/day |
EE | 15 mg/day | ||
hypersecretory conditions | 180 mg/day in divided doses | ||
hypersecretory conditions | 180 mg/day in divided doses | ||
risk reduction of NSAID-associated gastric ulcer | 15 mg/day | ||
omeprazole (Prilosec®, generics) | 10 mg, 20 mg, 40 mg delayed-release capsule; 20 mg delayed-release orally disintegrating tablet | EE | 20 mg/day |
hypersecretory conditions | 360 mg/day in divided doses | ||
omeprazole magnesium (Prilosec®) | 2.5 mg, 10 mg packet with delayed-release granules for suspension | EE | 20 mg/day |
hypersecretory conditions | 360 mg/day in divided doses | ||
pantoprazole (Protonix®, generics) | 20 mg, 40 mg delayed-release tablets; 40 mg delayed-release granules for suspension | EE | 40 mg/day |
hypersecretory conditions | 240 mg/day in divided doses | ||
rabeprazole (Aciphex®, generics) | 20 mg delayed-release tablet; 5 mg, 10 mg delayed-release sprinkle capsule | EE | 20 mg/day |
hypersecretory conditions | 120 mg/day in divided doses |
Drug Name | Dosage Form/Strength | Treatment Indication | Maximum Recommended Dosage |
---|---|---|---|
esomeprazole/ naproxen (Vimovo®, generics) | 20 mg immediate-release/375 mg delayed-release, 20 mg immediate-release/500 mg delayed-release tablets | prevention of NSAID-associated gastric ulcer in patients with osteoarthritis, rheumatoid arthritis, ankylosing spondylitis | 40 mg/1000 mg/day in divided doses |
omeprazole/ sodium bicarbonate (Zegerid®, generics) | 20 mg/1100 mg, 40 mg/1100 mg capsules; 20 mg/1680 mg, 40 mg/1680 mg packets for suspension | EE | 20 mg/day (as mg of omeprazole) |