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

INTERNATIONAL NORMALISED RATIO INCREASED ( 11 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
ANAEMIA ( 7 FDA reports)
OVERDOSE ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
AGITATION ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COMA ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FALL ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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