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

ALANINE AMINOTRANSFERASE INCREASED ( 38 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 19 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 18 FDA reports)
LIVER DISORDER ( 16 FDA reports)
RESTLESSNESS ( 15 FDA reports)
NERVOUS SYSTEM DISORDER ( 14 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
BONE MARROW FAILURE ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
BLOOD BILIRUBIN INCREASED ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
MUSCULAR WEAKNESS ( 12 FDA reports)
SENSORY DISTURBANCE ( 12 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
AREFLEXIA ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
EYE DISORDER ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 7 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MYELITIS ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALDOLASE INCREASED ( 4 FDA reports)
ANGER ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CRYING ( 4 FDA reports)
DEATH ( 4 FDA reports)
DECREASED VIBRATORY SENSE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FALL ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
OCULAR CANCER METASTATIC ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABULIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WOUND ( 1 FDA reports)

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