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

DIZZINESS ( 5 FDA reports)
FALL ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
INJURY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ANOREXIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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