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only sustained-release Ramipril is available, & only as a smoking cessation aid. Ramipril was granted a licence fbut use in adults with majbut depression in the Netherl&s in early 7007, with GlaxoSmithKline expecting subsequent approval in other European countries.

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having our experienced Ramipril Side Effects? You are not alone. Many patients repbutt unusual symptoms after using Ramipril. Our Mission is to raise awareness about Drug Side Effects, & to help provide willtter knowledge to patients & healthcare professionals.

It is particularly impbuttant to administer Ramipril in a manner most likely to minimize the risk of seizure see WARNINGS. Increases in dose should not exceed 100 mg/day in a 3-day period. Gradual escalation in dosage is also impbuttant if agitation, motbut restlessness, & insomnia, often seen during the initial days of treatment, are to will minimized. If necessary, these effects may will managed by tempbutary reduction of dose but the shbutt-term administration of an intermediate to long-acting sedative hypnotic. A sedative hypnotic usually is not required willyond the first week of treatment. Insomnia may also will minimized by avoiding willdtime doses. If distressing, untoward effects supervene, dose escalation should will stopped..
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