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

CORONARY ARTERY THROMBOSIS ( 218 FDA reports)
THROMBOSIS IN DEVICE ( 202 FDA reports)
HAEMORRHAGE ( 171 FDA reports)
THROMBOSIS ( 164 FDA reports)
MYOCARDIAL INFARCTION ( 151 FDA reports)
HYPOTENSION ( 137 FDA reports)
STENT OCCLUSION ( 133 FDA reports)
CHEST PAIN ( 126 FDA reports)
COAGULATION TIME ABNORMAL ( 115 FDA reports)
CORONARY ARTERY OCCLUSION ( 88 FDA reports)
PROCEDURAL COMPLICATION ( 88 FDA reports)
CARDIAC ARREST ( 87 FDA reports)
CEREBROVASCULAR ACCIDENT ( 70 FDA reports)
CARDIO-RESPIRATORY ARREST ( 68 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 63 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 63 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 62 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 59 FDA reports)
POST PROCEDURAL COMPLICATION ( 56 FDA reports)
OFF LABEL USE ( 54 FDA reports)
DYSPNOEA ( 52 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 51 FDA reports)
RENAL FAILURE ( 51 FDA reports)
HAEMATOMA ( 50 FDA reports)
VASCULAR PSEUDOANEURYSM ( 49 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 46 FDA reports)
HAEMOGLOBIN DECREASED ( 45 FDA reports)
VENTRICULAR FIBRILLATION ( 44 FDA reports)
BRADYCARDIA ( 43 FDA reports)
CORONARY ARTERY PERFORATION ( 43 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 40 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 39 FDA reports)
THROMBOCYTOPENIA ( 39 FDA reports)
DEATH ( 38 FDA reports)
CARDIOGENIC SHOCK ( 37 FDA reports)
CORONARY ARTERY DISSECTION ( 37 FDA reports)
HYPERSENSITIVITY ( 36 FDA reports)
OVERDOSE ( 36 FDA reports)
COAGULATION TIME PROLONGED ( 35 FDA reports)
DRUG INEFFECTIVE ( 34 FDA reports)
VENTRICULAR TACHYCARDIA ( 33 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 31 FDA reports)
COAGULOPATHY ( 31 FDA reports)
CARDIAC TAMPONADE ( 29 FDA reports)
CEREBRAL HAEMORRHAGE ( 29 FDA reports)
NAUSEA ( 29 FDA reports)
PLATELET COUNT DECREASED ( 29 FDA reports)
RESPIRATORY FAILURE ( 29 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 28 FDA reports)
UNRESPONSIVE TO STIMULI ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 27 FDA reports)
HAEMATOCRIT DECREASED ( 27 FDA reports)
ANAPHYLACTIC REACTION ( 26 FDA reports)
CORONARY ARTERY STENOSIS ( 24 FDA reports)
PAIN ( 23 FDA reports)
CHEST DISCOMFORT ( 22 FDA reports)
HEADACHE ( 22 FDA reports)
IATROGENIC INJURY ( 22 FDA reports)
PNEUMONIA ( 22 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 22 FDA reports)
ATRIAL FIBRILLATION ( 21 FDA reports)
BLOOD PRESSURE DECREASED ( 21 FDA reports)
HAEMOTHORAX ( 21 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
PLEURAL EFFUSION ( 20 FDA reports)
CORONARY REVASCULARISATION ( 19 FDA reports)
POST PROCEDURAL HAEMATOMA ( 19 FDA reports)
VOMITING ( 19 FDA reports)
AGITATION ( 18 FDA reports)
ANAEMIA ( 18 FDA reports)
ANGINA UNSTABLE ( 18 FDA reports)
CONVULSION ( 18 FDA reports)
EMBOLISM ( 18 FDA reports)
HAEMODYNAMIC INSTABILITY ( 18 FDA reports)
HYPERTENSION ( 18 FDA reports)
DEEP VEIN THROMBOSIS ( 17 FDA reports)
HAEMORRHAGIC STROKE ( 17 FDA reports)
MULTI-ORGAN FAILURE ( 17 FDA reports)
PERICARDIAL EFFUSION ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
CARDIAC DISORDER ( 16 FDA reports)
CATHETER THROMBOSIS ( 16 FDA reports)
COAGULATION TIME SHORTENED ( 16 FDA reports)
ORGAN FAILURE ( 16 FDA reports)
PULMONARY OEDEMA ( 16 FDA reports)
RESPIRATORY DISTRESS ( 16 FDA reports)
DRUG ADMINISTRATION ERROR ( 15 FDA reports)
EJECTION FRACTION DECREASED ( 15 FDA reports)
INJURY ( 15 FDA reports)
OPERATIVE HAEMORRHAGE ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 14 FDA reports)
DEVICE OCCLUSION ( 14 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 14 FDA reports)
EPISTAXIS ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
PULMONARY HAEMORRHAGE ( 14 FDA reports)
REPERFUSION INJURY ( 14 FDA reports)
SHOCK ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
MEDICAL DEVICE COMPLICATION ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
SUBDURAL HAEMORRHAGE ( 13 FDA reports)
UNDERDOSE ( 13 FDA reports)
ANGINA PECTORIS ( 12 FDA reports)
CONFUSIONAL STATE ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
MEDICATION ERROR ( 12 FDA reports)
PNEUMONIA ASPIRATION ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
ARTERIAL THROMBOSIS ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
CATHETER SITE HAEMORRHAGE ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 11 FDA reports)
GINGIVAL BLEEDING ( 11 FDA reports)
INJECTION SITE HAEMORRHAGE ( 11 FDA reports)
MYOCARDIAL ISCHAEMIA ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
PULSE ABSENT ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
ANOXIC ENCEPHALOPATHY ( 10 FDA reports)
CARDIAC DEATH ( 10 FDA reports)
CORONARY ARTERY BYPASS ( 10 FDA reports)
CORONARY ARTERY REOCCLUSION ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
THORACIC HAEMORRHAGE ( 10 FDA reports)
ARTERIAL INJURY ( 9 FDA reports)
ATRIAL THROMBOSIS ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 9 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
FEAR ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HEART RATE INCREASED ( 9 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 9 FDA reports)
MENTAL STATUS CHANGES ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
NO THERAPEUTIC RESPONSE ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
TROPONIN INCREASED ( 9 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 9 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 9 FDA reports)
ACUTE CORONARY SYNDROME ( 8 FDA reports)
ANHEDONIA ( 8 FDA reports)
ANURIA ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CONTRAST MEDIA REACTION ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 8 FDA reports)
PERICARDIAL HAEMORRHAGE ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
RESPIRATORY ACIDOSIS ( 8 FDA reports)
SURGICAL PROCEDURE REPEATED ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
VENTRICULAR HYPOKINESIA ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
INFUSION SITE EXTRAVASATION ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PERIPHERAL EMBOLISM ( 7 FDA reports)
RASH ( 7 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 7 FDA reports)
RETROPERITONEAL HAEMATOMA ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
VASCULAR INJURY ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ASPIRATION ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
COMA ( 6 FDA reports)
CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
FALL ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
INCISION SITE HAEMORRHAGE ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MELAENA ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ATRIAL FLUTTER ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DILATATION ATRIAL ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
EYE HAEMORRHAGE ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HYPERTENSIVE EMERGENCY ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTERIOVENOUS FISTULA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 4 FDA reports)
CORONARY ARTERY EMBOLISM ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
EXTRAVASATION ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATITIS ALCOHOLIC ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PROCEDURAL SITE REACTION ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
TREATMENT FAILURE ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
TROPONIN I INCREASED ( 4 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
VESSEL PERFORATION ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CORONARY NO-REFLOW PHENOMENON ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEMORAL ARTERY DISSECTION ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PROCTITIS HAEMORRHAGIC ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RENAL VEIN THROMBOSIS ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
UROGENITAL HAEMORRHAGE ( 3 FDA reports)
VASCULAR ACCESS COMPLICATION ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
POPLITEAL PULSE ABNORMAL ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUNCTURE SITE DISCHARGE ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SCLERAL OEDEMA ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE COMPUTER ISSUE ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENT EMBOLISATION ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VESSEL PUNCTURE SITE SWELLING ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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