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

ENCEPHALOPATHY ( 15 FDA reports)
RENAL FAILURE ( 12 FDA reports)
CONVULSION ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
STATUS EPILEPTICUS ( 7 FDA reports)
OVERDOSE ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
DEATH ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)

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