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

THROMBOCYTOPENIA ( 164 FDA reports)
MYOCARDIAL INFARCTION ( 57 FDA reports)
DEATH ( 44 FDA reports)
HAEMORRHAGE ( 40 FDA reports)
CEREBRAL HAEMORRHAGE ( 38 FDA reports)
HAEMOGLOBIN DECREASED ( 37 FDA reports)
CARDIOGENIC SHOCK ( 36 FDA reports)
CORONARY ARTERY STENOSIS ( 25 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 24 FDA reports)
HAEMATOMA ( 22 FDA reports)
RENAL FAILURE ( 22 FDA reports)
CARDIAC FAILURE ( 17 FDA reports)
HAEMATOCRIT DECREASED ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
PAIN ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 14 FDA reports)
INJURY ( 13 FDA reports)
POST PROCEDURAL COMPLICATION ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
ANXIETY ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
PETECHIAE ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
THROMBOSIS IN DEVICE ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 10 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
FEAR ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
VOMITING ( 9 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CHILLS ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
CORONARY ARTERY OCCLUSION ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
STRESS ( 7 FDA reports)
ANHEDONIA ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CATHETER SITE HAEMORRHAGE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
TROPONIN T INCREASED ( 6 FDA reports)
UNEVALUABLE EVENT ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
BASILAR ARTERY THROMBOSIS ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
SPLENIC HAEMORRHAGE ( 5 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
VENTRICULAR ARRHYTHMIA ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
EXTRADURAL HAEMATOMA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RALES ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
VASCULAR INJURY ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC CAPILLARITIS ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET AGGREGATION INHIBITION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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