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Review Vaseretic Safety Reports submitted to FDA

Total Vaseretic reports: 2.
Vaseretic FDA safety alerts: 2001 2002 2003 2004 2005 2006 2007 2008 .
   Reported hospitalizations: 1.
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FDA Reported Vaseretic Side Effects:
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Vaseretic Side Effects Report #5674207-X
Physician from reported VASERETIC problem on Mar 11, 2008. Male patient, 56 years of age, was diagnosed with hypertension and was treated with VASERETIC. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, blood creatinine increased, blood triglycerides increased, blood urea increased, cardiovascular disorder, headache, hypertension, low density lipoprotein increased, metabolic disorder. VASERETIC dosage: unknown. During the same period patient was treated with NORVASC, LIPITOR, CRESTOR, EZETROL, CALCIUM CHANNEL BLOCKERS, DIOVAN, DIURETICS, DIOVAN HCT. Patient recovered.

Vaseretic Side Effects Report #5738487-4
VASERETIC problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 24, 2008. Female patient, weighting 163.0 lb, was diagnosed with blood pressure and was treated with VASERETIC. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood pressure increased, cataract, cystitis, dizziness, ear infection, joint swelling, oedema peripheral. VASERETIC dosage: (1 DF QD 10/25 MG TABLET ORAL). During the same period patient was treated with TOPROL, PRANDIN, METFORMIN. Patient was hospitalized. Patient recovered.


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blood cholesterol increased, blood creatinine increased, blood triglycerides increased, blood urea increased, cardiovascular disorder, headache, hypertension, low density lipoprotein increased, metabolic disorder, , %drugN% was diagnosed with hypertension and %drugN% was diagnosed with blood pressure and