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Hypotension, flushing, tachycardia, palpitation, and arrhythmia occurred at a rate of less than 1% and were considered possibly related to dipyridamole. The following adverse effects occurred at a rate equal to or greater than 1% in patients receiving aspirin-dipyridamole and more frequently than in the placebo group (treatment vs. HematologicHematologic side effects occurring at a rate equal to or greater than 1% in patients receiving aspirin-dipyridamole and more frequently than in the placebo group (treatment vs. OncologicOncologic adverse events occurring at a rate equal to or greater than 1% in patients receiving aspirin-dipyridamole and more frequently than in the placebo group were reported as unspecified neoplasms, 1. MetabolicMetabolic adverse events occurring at a rate of less than 1% and considered possibly related to either dipyridamole or aspirin included hyperglycemia and thirst.

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