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

HYPOREFLEXIA ( 13 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 9 FDA reports)
GUILLAIN-BARRE SYNDROME ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
AREFLEXIA ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NEUROTOXICITY ( 5 FDA reports)
QUADRIPLEGIA ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
VESTIBULAR DISORDER ( 5 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
ATAXIA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACUTE POLYNEUROPATHY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA REFRACTORY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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