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

BLOOD PRESSURE DECREASED ( 11 FDA reports)
INFUSION RELATED REACTION ( 7 FDA reports)
HEPATITIS C POSITIVE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
CHILLS ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
HEPATITIS B VIRUS TEST POSITIVE ( 2 FDA reports)
HEPATITIS B POSITIVE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FATIGUE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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