Please choose an event type to view the corresponding MedsFacts report:

AFFECT LABILITY ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
CRYING ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
RESTLESSNESS ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
AGITATION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
PARESIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)

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