Omeprazole
Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.
| ID | DRUG-OMEPRAZOLE |
|---|---|
| Type | Drug |
| Aliases | LosecOmezOrtanolPrilosecОмепразол |
| Status | reviewed 2026-05-18 |
| Diseases | DIS-GASTRIC |
| Sources | SRC-NCCN-BCELL-2025 |
Drug Facts
| Class | Proton-pump inhibitor (PPI; substituted benzimidazole) |
|---|---|
| Mechanism | Prodrug that is acid-activated in the parietal cell secretory canaliculus to a sulfenamide cation, which forms a covalent disulfide bond with cysteine residues of the H+/K+-ATPase (proton pump) and irreversibly inhibits gastric acid secretion. New pump synthesis is required for recovery (≥24 h half-life of effect despite ~1 h plasma half-life). Cancer-prevention relevance: profound gastric acid suppression is required for H. pylori antimicrobial efficacy (clarithromycin and amoxicillin both require near-neutral gastric pH for stability and bactericidal activity) — PPI is the linchpin of triple / quadruple H. pylori eradication regimens. |
| Typical dosing | H. pylori eradication (component of triple therapy, adult): 20 mg PO BID × 14 days, taken 30-60 min before breakfast and dinner, with clarithromycin 500 mg BID + amoxicillin 1 g BID (or metronidazole 500 mg BID if penicillin-allergic). H. pylori quadruple (PBMT) therapy: 20 mg PO BID × 10-14 days with bismuth subcitrate + metronidazole + tetracycline. GERD / erosive esophagitis: 20-40 mg PO daily × 4-8 weeks. Duodenal ulcer: 20 mg PO daily × 4 weeks. Renal: no adjustment. Hepatic: reduce dose 50% in severe hepatic impairment (clearance ~⅓ normal). Long-term use carries risks (bone loss, B12 deficiency, hypomagnesemia, AKI, C. difficile) — limit duration where possible. |
| Ukraine registered | True |
| NSZU reimbursed | False |
| Ukraine last verified | 2026-05-18 |
Notes
STUB — v0.2 prevention-workstream authoring; pending two-Clinical-Co-Lead signoff per CHARTER §6.1 dev-mode. PPI is the linchpin of H. pylori triple and quadruple eradication therapy — without near-neutral gastric pH, clarithromycin is unstable and amoxicillin/tetracycline are less bactericidal. Standard 20 mg BID dose for 14 days in both triple and quadruple PBMT regimens. Critical interactions: clopidogrel (use pantoprazole instead), rilpivirine (contraindicated), high-dose methotrexate (hold), pH-dependent TKIs in oncology context (erlotinib, dasatinib, etc.). CYP2C19 poor metabolizer status (esp. Asian patients) → higher exposure and better H. pylori cure rates with standard doses; some experts dose PPI by genotype. Ukraine: cheap, OTC, ubiquitous, out-of-pocket. Long-term safety concerns (bone, B12, Mg, AKI, CDI, pneumonia) are largely irrelevant for a 14-day eradication course. Two-Co-Lead signoff queued for v0.2-A clinical review.
Used By
Access Pathways
AP-HP-ERADICATION-PHARMACY-OOP- H. pylori eradication (PPI + amox/clarithromycin / bismuth quadruple) — pharmacy out-of-p...
Regimens
REG-HP-BISMUTH-QUADRUPLE- Bismuth quadruple therapy (PBMT) — 14 daysREG-HP-PPI-CLAR-AMOX- PPI-clarithromycin-amoxicillin triple therapy — 14 days