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KELNOR Safety Reports

Total KELNOR reports: 1.
KELNOR FDA safety alerts: No.
   Reported hospitalizations: 1.
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Health Professional from UNITED STATES reported KELNOR problem on Sept 04, 2007. Female patient, weighting 154.3 lb, was diagnosed with oral contraception and was treated with KELNOR. After drug was administered, patient experienced the following problems/side effects: jaundice cholestatic. KELNOR dosage: unknown. Patient was hospitalized. Patient recovered.

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