Source: Health Products Regulatory Authority (IE) Revision Year: 2021 Publisher: Rowa Pharmaceuticals Limited, Newtown, Bantry, Co. Cork, Ireland
Razole is indicated in:
The recommended oral dose for both active duodenal ulcer and active benign gastric ulcer is 20 mg to be taken once daily in the morning.
Most patients with active duodenal ulcer heal within four weeks. However, some patients may require an additional four weeks of treatment to achieve healing. Most patients with benign active gastric ulcer heal within six weeks. However again some patients may require an additional six weeks of treatment to achieve healing.
The recommended oral dose for this condition is 20 mg to be taken once daily for four to eight weeks.
For long-term management, a maintenance dose is 20 mg or 10 mg once daily can be used, depending upon patient response.
10 mg once daily in patients without oesophagitis. If symptom control has not been achieved during 4 weeks, the patient should be further investigated. Once the symptoms have resolved, subsequent symptom control can be achieved using an on-demand regimen taking 10 mg once daily when needed.
The recommended adult starting dose is 60 mg once a day. The dose may be titrated upwards to 120 mg/day based on individual patient needs. Single daily doses up to 100 mg/day may be given. 120 mg dose may require divided doses, 60 mg twice daily. Treatment should continue for as long as clinically indicated.
Patients with H. pylori infection should be treated with eradication therapy. The following combination given for 7 days is recommended.
Rabeprazole sodium gastro-resistant tablets 20 mg twice daily + clarithromycin 500 mg twice daily and amoxicillin 1 gram twice daily.
For indications requiring once daily treatment, Razole gastro-resistant tablets should be taken in the morning, before eating; and although neither the time of day nor food intake was shown to have any effect on rabeprazole sodium activity, this regimen will facilitate treatment compliance.
No dosage adjustment is necessary for patients with renal or hepatic impairment.
See section 4.4 in the treatment of patients with severe hepatic impairment.
Razole is not recommended for use in children, as there is no experience of its use in this group.
For oral use.
Patients should be cautioned that Razole gastro-resistant tablets should not be chewed or crushed, but should be swallowed whole.
Experience to date with deliberate or accidental overdose is limited. The established exposure has not exceeded 60 mg twice daily, or 160 mg once daily. Effects are generally minimal, representative of the known adverse event profile and reversible without further medical intervention. No specific antidote is known. Rabeprazole sodium is extensively protein bound and is therefore not easy to dialyse. As in any case of overdose, treatment should be symptomatic and general supportive measures should be utilised.
3 years.
Do not store above 25°C. Store in the original package.
Aluminium/aluminium blisters in a cardboard carton.
1, 5, 7, 14, 15, 25, 28, 30, 50, 56, 75, 98 or 120 gastro-resistant tablets.
Not all pack sizes may be marketed.
No special requirements.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
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