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DAYPRO Safety Reports

Total DAYPRO reports: 2.
DAYPRO FDA safety alerts: No.
   Reported hospitalizations: 2.
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Health Professional from UNITED STATES reported DAYPRO problem on Jan 26, 2007. Male patient, weighting 175.0 lb, was diagnosed with pain and was treated with DAYPRO. After drug was administered, patient experienced the following problems/side effects: asthenia, gastritis, gastrointestinal haemorrhage, shock, syncope. DAYPRO dosage: unknown. During the same period patient was treated with CRESTOR, TOPROL, ASPIRIN, MOTRIN. Patient was hospitalized. Patient recovered.

DAYPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2006. Female patient, 80 years of age, was diagnosed with osteoarthritis, urinary incontinence and was treated with DAYPRO. After drug was administered, patient experienced the following problems/side effects: colitis ulcerative, condition aggravated, haematochezia, irritable bowel syndrome. DAYPRO dosage: 1200 MG (600 MG,2 IN 1 D),ORAL. During the same period patient was treated with OXYBUTYNIN CHLORIDE, IBUPROFEN, DITROPAN, ROBINUL, PROCHLORPERAZINE MALEATE. Patient was hospitalized. Patient recovered.

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