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

FEBRILE BONE MARROW APLASIA ( 32 FDA reports)
MUCOSAL INFLAMMATION ( 31 FDA reports)
NEURALGIA ( 22 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 21 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 16 FDA reports)
RASH VESICULAR ( 13 FDA reports)
MYELITIS TRANSVERSE ( 12 FDA reports)
FIXED ERUPTION ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
FEBRILE NEUTROPENIA ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
PANCREATITIS ( 8 FDA reports)
PNEUMOTHORAX ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
TUMOUR NECROSIS ( 7 FDA reports)
VENOOCCLUSIVE DISEASE ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
VENTRICULAR ARRHYTHMIA ( 4 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOSARCOMA RECURRENT ( 1 FDA reports)
RICKETS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRISOMY 8 ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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