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

ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
SHOCK ( 6 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RASH ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
DEATH ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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