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Mysoline Safety Reports
Total Mysoline reports: 5.Mysoline FDA safety alerts: No.
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Reported Mysoline Side Effects: schizophrenia, musculoskeletal stiffness, insomnia, hypotonia, hypoaesthesia, hand deformity, crying, asthenia, aphonia, activities of daily living impaired, tremor.
Mysoline Usage.
Mysoline Side Effects Report #5341605-3
Physician from UNITED STATES reported MYSOLINE problem on May 29, 2007. Female patient, 20 years of age, weighting 148.0 lb, was diagnosed with rett's disorder and was treated with MYSOLINE. After drug was administered, patient experienced the following problems/side effects: rett's disorder. MYSOLINE dosage: 250MG/ML ORAL. Patient recovered.
Mysoline Side Effects Report #5066324-2
MYSOLINE problem was reported by a Pharmacist from UNITED STATES on July 11, 2006. Male patient, 58 years of age, was diagnosed with tremor and was treated with MYSOLINE. After drug was administered, patient experienced the following problems/side effects: schizophrenia. MYSOLINE dosage: 50 MG QDAY PO. During the same period patient was treated with WARFARIN. Patient recovered.
Mysoline Side Effects Report #5112884-2
Physician from UNITED STATES reported MYSOLINE problem on Sept 21, 2006. Female patient, 76 years of age, weighting 217.0 lb, was diagnosed with essential tremor and was treated with MYSOLINE. After drug was administered, patient experienced the following problems/side effects: dizziness, gait disturbance, speech disorder, tremor. MYSOLINE dosage: 50 MG TID ORAL. Patient recovered.
Mysoline Side Effects Report #5122925-4
MYSOLINE problem was reported by a Pharmacist from UNITED STATES on Sept 19, 2006. Male patient, 58 years of age, was diagnosed with tremor and was treated with MYSOLINE. After drug was administered, patient experienced the following problems/side effects: schizophrenia. MYSOLINE dosage: 50 MG QDAY PO. During the same period patient was treated with WARFARIN. Patient recovered.
Mysoline Side Effects Report #5424841-7
Consumer or non-health professional from UNITED STATES reported MYSOLINE problem on Aug 06, 2007. Female patient, 75 years of age, weighting 175.0 lb, was diagnosed with essential tremor and was treated with MYSOLINE. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, aphonia, asthenia, crying, hand deformity, hypoaesthesia, hypotonia, insomnia, musculoskeletal stiffness. MYSOLINE dosage: (250 MG QD ORAL), (250 MG QD ORAL), (350 MG QD ORAL). During the same period patient was treated with PLAVIX, TOPAMAX, HYZAAR, CRESTOR, KLONOPIN. Patient recovered.