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

CONVULSION ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
TREMOR ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
ASCITES ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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