Rabeprazole 20mg Injection

Rabeprazole injection suppresses stomach acid when a proton-pump inhibitor is required and oral treatment is unsuitable. It is used in selected acid-related disorders under an injectable-product protocol.
A clinician reconstitutes and administers the product intravenously according to its label. It must not be self-injected or taken by mouth. Oral acid-suppression treatment can be resumed when clinically suitable.
Inhibition of gastric H+/K+-ATPase blocks the final step of acid secretion by parietal cells.
Headache, diarrhoea, nausea, abdominal discomfort and injection-site reactions can occur.
Persistent bleeding, swallowing difficulty or unexplained weight loss needs investigation. Longer exposure can affect magnesium and B12; short-term injection should not automatically become indefinite treatment.
Maintains acid suppression when swallowing or oral administration is temporarily unsuitable.
No. Injectable and oral formulations are prepared differently.
No. Diluent, compatibility and stability instructions are product-specific.
No. It inhibits new acid secretion rather than directly neutralising existing acid.
An injection may no longer be needed once oral therapy is feasible.
No. Eradication requires an appropriate combination with antibiotics.
It is an emergency; acid suppression alone does not establish control of gastrointestinal bleeding.
Yes. Extended proton-pump-inhibitor exposure can require laboratory review.
Usually not. The indication and suitability of oral treatment should be assessed.
Proton pump: the gastric H + /K + -ATPase enzyme. Parietal cell: an acid-producing stomach cell. Reconstitution: preparation of powder with the specified diluent., AR: Rabeprazole حقن, FR: Rabeprazole, PT: Rabeprazole injeção, ES: Rabeprazole inyección, RU: Rabeprazole инъекция, ID: Rabeprazole injeksi, VI: Rabeprazole thuốc tiêm, MS: Rabeprazole suntikan, TL: Rabeprazole iniksyon, ZH-SG: Rabeprazole 注射剂
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Rabeprazole 20mg Injection