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

ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
ORAL CANDIDIASIS ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
VAGINAL CANDIDIASIS ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
CITROBACTER INFECTION ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
ASPIRATION ( 3 FDA reports)
CHOKING ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GENITAL CANDIDIASIS ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INFANTILE ASTHMA ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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