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

PYREXIA ( 11 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 7 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
RASH ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
ACETONAEMIC VOMITING ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERPHOSPHATASAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
LEUKODERMA ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACNE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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