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

ASTHENIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
VOMITING ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
MALAISE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
RASH ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INFLAMMATION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID C-CELL HYPERPLASIA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)

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