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

SUPRAVENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
WEIGHT GAIN POOR ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 11 FDA reports)
HYPOTONIA ( 11 FDA reports)
ATRIAL SEPTAL DEFECT ( 11 FDA reports)
ATRIAL TACHYCARDIA ( 11 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CARDIAC MURMUR ( 11 FDA reports)
CARDIOMEGALY ( 11 FDA reports)
CEREBRAL PALSY ( 11 FDA reports)
RESPIRATORY DEPTH INCREASED ( 11 FDA reports)
FAILURE TO THRIVE ( 11 FDA reports)
DEVELOPMENTAL DELAY ( 11 FDA reports)
PREMATURE BABY ( 11 FDA reports)
NEUROMYOPATHY ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
EATING DISORDER ( 11 FDA reports)
DYSPNOEA EXERTIONAL ( 11 FDA reports)
DYSMORPHISM ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
THROMBOCYTOPENIA ( 10 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 10 FDA reports)
NEUTROPENIA ( 9 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 8 FDA reports)
SPASTIC DIPLEGIA ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 4 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
POISONING ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
DEATH ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)

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