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URBASON Safety Reports
Total URBASON reports: 1.URBASON FDA safety alerts: No.
Reported hospitalizations: 1.
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Physician from GERMANY reported URBASON problem on Nov 30, 2005. Male patient, 50 years of age, weighting 142.4 lb, was diagnosed with renal transplant and was treated with URBASON. After drug was administered, patient experienced the following problems/side effects: haematoma evacuation, haemoglobin decreased, haemorrhage, perineal haematoma, post procedural haemorrhage, suture insertion, wound dehiscence. URBASON dosage: 250 MG DAILY DOSE. During the same period patient was treated with CERTICAN, HEPARIN, MYFORTIC, NEORAL. Patient was hospitalized. Patient recovered.