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4% (11/2677) patients, who received placebo and Prevacid, respectively, had enzyme elevations greater than three times the upper limit of normal range at the final treatment visit. Ask your health care provider if Prevacid Powder Packet may interact with other medicines that you take. The incidence of diarrhea was similar between patients who received placebo and patients who received 15 mg and 30 mg of Prevacid, but higher in the patients who received 60 mg of Prevacid (2. It is not known if Prevacid Powder Packet is found in breast milk. If there is a recurrence of erosive esophagitis an additional 8-week course of Prevacid may be considered. Adverse reactions that have occurred have been limited to those that had been previously reported with Prevacid, amoxicillin, or clarithromycin. Be sure your doctor and lab personnel know you are taking Prevacid Powder Packet. The adverse reaction profiles for Prevacid Delayed-Release Capsules and Prevacid for Delayed-Release Oral Suspension are similar. None of these patients who received Prevacid reported jaundice at any time during the study. Prevacid is a member of the drug class proton pump inhibitors. The nonerosive GERD patients received Prevacid 15 mg daily for 8 weeks and the EE patients received Prevacid 30 mg daily for 8 to 12 weeks.

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