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

ASTHENIA ( 22 FDA reports)
HYPONATRAEMIA ( 22 FDA reports)
DYSPNOEA ( 21 FDA reports)
HYPOKALAEMIA ( 18 FDA reports)
CONSTIPATION ( 14 FDA reports)
BONE PAIN ( 13 FDA reports)
INFECTION ( 13 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
BACK PAIN ( 12 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 11 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
OEDEMA ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
SPINAL CORD COMPRESSION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LYMPHANGITIS ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEATH ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
COMA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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