Acute Stress Ulcer and Acute Gastric Mucosal Lesions Clinical Trial
Official title:
Lansoprazole Intravenous 30 mg Specified Drug-use Survey [Acute Stress Ulcer and Acute Gastric Mucosal Lesions]
The purpose of this survey is to evaluate the safety (that is, frequency of adverse events) and efficacy (that is, hemostatic effect, rate of rebleeding after confirmation of hemostasis) of administration of lansoprazole intravenous 30 milligram (mg) (Takepron Intravenous 30 mg ) to a large number of participants with acute stress ulcer or acute gastric mucosal lesion in daily medical practice.
This survey was designed to evaluate the safety (that is, frequency of adverse events) and
efficacy (i.e., hemostatic effect, rate of rebleeding after confirmation of hemostasis) of
administration of lansoprazole intravenous 30 mg (Takepron Intravenous 30 mg) to a large
number of participants with acute stress ulcer or acute gastric mucosal lesion in daily
medical practice.
For adults, 30 mg of lansoprazole is typically mixed in physiological saline (JP) or 5
percent (%) glucose solution for injection (JP) and administered twice daily by drip
infusion or dissolved in 20 mL of physiological saline (JP) or 5% glucose solution for
injection (JP) and administered twice daily by direct slow intravenous injection.
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Observational Model: Cohort, Time Perspective: Prospective