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Repaglinide Safety Reports submitted to FDA

Total Repaglinide reports: 2.
Repaglinide FDA safety alerts: 2003 .
   Reported hospitalizations: 2.
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Reported Repaglinide Side Effects: renal failure acute, anuria, anaemia, vision blurred, urinary tract infection, renal failure, hyperkalaemia, dizziness, diplopia, blood glucose decreased.
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Repaglinide Side Effects Report #5066642-8
Pharmacist from UNITED STATES reported REPAGLINIDE problem on July 19, 2006. Male patient, 70 years of age, weighting 148.4 lb, was diagnosed with diabetes mellitus and was treated with REPAGLINIDE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, diplopia, dizziness, hyperkalaemia, renal failure, urinary tract infection, vision blurred. REPAGLINIDE dosage: unknown. Patient was hospitalized. Patient recovered.

Repaglinide Side Effects Report #5447276-X
REPAGLINIDE problem was reported by a Health Professional from FRANCE on Aug 28, 2007. Male patient, 71 years of age, was treated with REPAGLINIDE. After drug was administered, patient experienced the following problems/side effects: anaemia, anuria, renal failure acute. REPAGLINIDE dosage: .5 MG, TID. During the same period patient was treated with IRBESARTAN, STAGID, LASILIX, POTASSIUM CHLORIDE, BURINEX. Patient was hospitalized. Patient recovered.


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blood glucose decreased, diplopia, dizziness, hyperkalaemia, renal failure, urinary tract infection, vision blurred, was diagnosed with diabetes mellitus and