Abstract
Nonsteroidal anti-inflammatory drug (NSAID)-induced gastrointestinal toxicity is associated with morbidity and mortality, and given the very wide use of NSAIDs, is problematic and costly to society. Several options are now available to minimize gastrointestinal toxicity from NSAIDs. These options include the proton pump inhibitors, misoprostil, double-dose H2-receptor blockers and the COX-2 selective NSAIDs. No head-to-head clinical trials have compared these options. The effectiveness of these strategies to minimize NSAID-induced gastrointestinal toxicity is summarized. In addition, their associated adverse effect profiles and costs are compared.
MeSH terms
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Administration, Oral
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Anti-Inflammatory Agents, Non-Steroidal / adverse effects*
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Anti-Ulcer Agents / therapeutic use
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Clinical Trials as Topic
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Cyclooxygenase Inhibitors / adverse effects
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Cyclooxygenase Inhibitors / therapeutic use
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Drug Administration Schedule
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Drug Therapy, Combination
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Gastrointestinal Diseases / chemically induced*
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Gastrointestinal Diseases / prevention & control*
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Histamine H2 Antagonists / therapeutic use
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Humans
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Misoprostol / therapeutic use
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Proton Pumps / therapeutic use
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Anti-Ulcer Agents
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Cyclooxygenase Inhibitors
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Histamine H2 Antagonists
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Proton Pumps
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Misoprostol