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

THROMBOCYTOPENIA ( 13 FDA reports)
VOMITING ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
ANAEMIA ( 11 FDA reports)
HEADACHE ( 10 FDA reports)
HAEMATEMESIS ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
EPISTAXIS ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 9 FDA reports)
ELECTROLYTE IMBALANCE ( 9 FDA reports)
HORNER'S SYNDROME ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
TALIPES ( 5 FDA reports)
RETROGNATHIA ( 5 FDA reports)
BRACHYCEPHALY ( 5 FDA reports)
CEREBELLAR HYPOPLASIA ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
OESOPHAGEAL ATRESIA ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PNEUMONITIS ( 3 FDA reports)
FALL ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
DEATH ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
SURGERY ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)

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