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

DIARRHOEA ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
VOMITING ( 10 FDA reports)
FATIGUE ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
DEHYDRATION ( 8 FDA reports)
NAUSEA ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
FALL ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
MALAISE ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FUSOBACTERIUM INFECTION ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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