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

SEPSIS ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
RASH ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
FALL ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use