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MAXAQUIN Safety Reports
Total MAXAQUIN reports: 2.MAXAQUIN FDA safety alerts: No.
Reported hospitalizations: 2.
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Health Professional from ITALY reported MAXAQUIN problem on May 09, 2007. Female patient was diagnosed with hyperpyrexia, arthralgia and was treated with MAXAQUIN. After drug was administered, patient experienced the following problems/side effects: jaundice cholestatic. MAXAQUIN dosage: DAILY DOSE:400MG. During the same period patient was treated with ARCOXIA, LOBIVON, VITAMIN D3. Patient was hospitalized. Patient recovered.
MAXAQUIN problem was reported by a Health Professional from ITALY on June 05, 2007. Female patient was diagnosed with hyperpyrexia, arthralgia and was treated with MAXAQUIN. After drug was administered, patient experienced the following problems/side effects: jaundice cholestatic. MAXAQUIN dosage: DAILY DOSE:400MG. During the same period patient was treated with ARCOXIA, LOBIVON, VITAMIN D3. Patient was hospitalized. Patient recovered.