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

FEBRILE NEUTROPENIA ( 9 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
OFF LABEL USE ( 5 FDA reports)
VITRITIS ( 4 FDA reports)
HYPOPYON ( 4 FDA reports)
CORNEAL OEDEMA ( 4 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
PSEUDOMONAS PSEUDOMALLEI INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use