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CIMETIDINE PREVENTS RECURRENCE. AND COMPLICATIONS OF PEPTIC ULCER In 68 patients with chronic peptic ulcer, cimetidine 400mg bid significantly reduced the recurrence rate. Six of 32 who received cimetidine had a recurrent ulcer within 7 months compared with 30 of 36 within 4 months in the placebo group. None of the cimetidine group had complications; whereas 4 did in the placebo group. Only I cimetidine-treated patient underwent surgery compared with 15 who received placebo. Compared with placebo. cimetidine significantly reduced pain, antacid consumption, absenteeism, . and the frequency of other symptoms. The Gimetidine.g roup. sho.wedno ..signs gastric-acid secretion either 2 days or 3.5 months after stopping long-term (1 year) treatment. Cimetidine given long-term was found -to· be-reasonablY safe: . Reversible liver damage was the only probable serious side-effect and occurred in only I patient. I &demar, G. and Walan, A.: Lancet I: 403(25 Feb 1978) INPHARMA 18th March. ·1978 p12

CIMETIDINE PREVENTS RECURRENCE AND COMPLICATIONS OF PEPTIC ULCER

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Page 1: CIMETIDINE PREVENTS RECURRENCE AND COMPLICATIONS OF PEPTIC ULCER

CIMETIDINE PREVENTS RECURRENCE. AND COMPLICATIONS OF PEPTIC ULCER

In 68 patients with chronic peptic ulcer, cimetidine 400mg bid significantly reduced the recurrence rate. Six of 32 who received cimetidine had a recurrent ulcer within 7 months compared with 30 of 36 within 4 months in the placebo group. None of the cimetidine group had complications; whereas 4 did in the placebo group. Only I cimetidine-treated patient underwent surgery compared with 15 who received placebo. Compared with placebo. cimetidine significantly reduced pain, antacid consumption, absenteeism, . and the frequency of other symptoms. The Gimetidine.g roup. sho.wedno ..signs Qfr~.Qo~I1d gastric-acid secretion either 2 days or 3.5 months after stopping long-term (1 year) treatment. Cimetidine given long-term was found -to·be-reasonablY safe: . Reversible liver damage was the only probable serious side-effect and occurred in only I patient.

I &demar, G. and Walan, A.: Lancet I: 403(25 Feb 1978)

INPHARMA 18th March. ·1978 p12