KERLONE Safety Questions, KERLONE Answers
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KERLONE Safety Reports
Total KERLONE reports: 3.KERLONE FDA safety alerts: No.
Reported hospitalizations: 1.
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Health Professional from FRANCE reported KERLONE problem on Dec 27, 2006. Male patient, weighting 5.73 lb, was treated with KERLONE. After drug was administered, patient experienced the following problems/side effects: bradycardia foetal, caesarean section, foetal distress syndrome, foetal growth retardation, hypoglycaemia neonatal, meconium stain, tricuspid valve incompetence. KERLONE dosage: unknown. Patient was hospitalized. Patient recovered.
KERLONE problem was reported by a Health Professional from FRANCE on Jan 15, 2007. Female patient, 64 years of age, weighting 125.7 lb, was diagnosed with depression and was treated with KERLONE. After drug was administered, patient experienced the following problems/side effects: retinal artery occlusion, visual acuity reduced. KERLONE dosage: 10 MG. During the same period patient was treated with RIVOTRIL, PIASCLEDINE, ARTHROTEC, PROZAC. Patient recovered.
Physician from FRANCE reported KERLONE problem on July 02, 2007. Female patient, 60 years of age, was diagnosed with atrial fibrillation and was treated with KERLONE. After drug was administered, patient experienced the following problems/side effects: hallucinations, mixed. KERLONE dosage: unknown. Patient recovered.