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Review Ikorel Safety Reports submitted to FDA

Total Ikorel reports: 2.
Ikorel FDA safety alerts: No.
   Reported hospitalizations: 2.
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FDA Reported Ikorel Side Effects:
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Ikorel Side Effects Report #5564344-2
Consumer or non-health professional from FRANCE reported IKOREL problem on Dec 10, 2007. Male patient, 80 years of age, was treated with IKOREL. After drug was administered, patient experienced the following problems/side effects: angina unstable, blood creatinine increased, dehydration, fluid replacement, hyperthyroidism, hyponatraemia, hypotension, loss of consciousness, malaise. IKOREL dosage: 40 MG, QD. During the same period patient was treated with SERETIDE DISKUS, BRONCHOKOD, LASIX, ISOPTIN, CORDARONE, NITRODERM. Patient was hospitalized. Patient recovered.

Ikorel Side Effects Report #5530518-X
IKOREL problem was reported by a Consumer or non-health professional from on Nov 19, 2007. Male patient, 80 years of age, was treated with IKOREL. After drug was administered, patient experienced the following problems/side effects: dehydration, hyperthyroidism, hyponatraemia, hypotension, renal failure. IKOREL dosage: unknown. During the same period patient was treated with LASIX, CORDARONE, NITRODERM, ISOPTIN, SERETIDE, BRONCHOKOD. Patient was hospitalized. Patient recovered.


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angina unstable, blood creatinine increased, dehydration, fluid replacement, hyperthyroidism, hyponatraemia, hypotension, loss of consciousness, malaise, , %drugN% %drugN%