Esonix M 20 mg is a proton pump inhibitor (PPI) formulated to effectively suppress gastric acid secretion. It is used in the treatment and prevention of various acid-related gastrointestinal disorders. By providing prolonged inhibition of gastric acid production, Esonix M 20 mg helps relieve symptoms, promotes healing of damaged mucosa, and reduces the risk of ulcer recurrence in patients requiring acid suppression therapy.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Esonix M 20 mg is indicated for the treatment of:
Gastroesophageal Reflux Disease (GERD)
Healing of erosive esophagitis
Maintenance of healing of erosive esophagitis
Symptomatic GERD
Reduction of NSAID-associated gastric ulcers
Helicobacter pylori eradication as part of triple therapy
Zollinger–Ellison syndrome
Proton Pump Inhibitor
Esonix M 20 mg suppresses gastric acid secretion by irreversibly inhibiting the H⁺/K⁺-ATPase enzyme system located on the secretory surface of gastric parietal cells. It covalently binds to sulfhydryl groups of cysteine residues on the proton pump, thereby blocking the final step of acid production. This mechanism results in inhibition of both basal and stimulated acid secretion, regardless of the stimulus. Because acid secretion resumes only after new enzyme synthesis, the antisecretory effect of Esonix M 20 mg lasts longer than 24 hours.
Tablet or Capsule
Healing of Erosive Esophagitis
20 mg or 40 mg once daily for 4–8 weeks
An additional 4–8 weeks may be considered if healing is incomplete
Maintenance of Healing of Erosive Esophagitis
20 mg once daily
Controlled studies did not extend beyond 6 months
Symptomatic GERD
20 mg once daily for 4 weeks
Treatment may be extended for another 4 weeks if symptoms persist
H. pylori Eradication (Triple Therapy)
Esonix M 20 mg: 20 mg twice daily for 10 days
Amoxicillin: 1000 mg twice daily for 10 days
Clarithromycin: 500 mg twice daily for 10 days
Injection (IV Use)
20 mg or 40 mg once daily by slow intravenous injection (minimum 3 minutes) or intravenous infusion (10–30 minutes) in GERD with erosive esophagitis
Intravenous Infusion Preparation
Reconstitute one vial with 5 ml of 0.9% sodium chloride
Further dilute to a final volume of 50 ml (final concentration: 0.8 mg/ml)
Administration
20 mg dose: Withdraw 25 ml and infuse over 10–30 minutes
10 mg dose: Withdraw 12.5 ml and infuse over 10–30 minutes
Esonix M 20 mg selectively inhibits the cytochrome P450 mono-oxygenase system
Clinically significant drug interactions have not been commonly reported
Reduction in gastric acid may affect vitamin B12 absorption and gastric bacterial colonization
Possible interaction with oral combined contraceptives cannot be fully excluded
Known hypersensitivity to Esonix M 20 mg or any component of the formulation
Reported side effects include:
Headache
Diarrhea
Abdominal pain
Esonix M 20 mg is classified as US FDA Pregnancy Category C. It should be avoided during pregnancy and lactation unless the potential benefits outweigh the possible risks to the fetus or infant.
Malignancy should be excluded in patients with suspected gastric ulcer before initiating therapy
When used with antibiotics, consult the prescribing information of the respective antibacterial agents
Store in a dry place
Protect from light and heat
Keep out of reach of children
For injection, reconstitute the vial with 5 ml of 0.9% sodium chloride for intravenous use. The resulting solution should be clear and colorless to slightly yellow before administration.
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