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

PYREXIA ( 75 FDA reports)
CARDIAC FAILURE ( 65 FDA reports)
CONDITION AGGRAVATED ( 52 FDA reports)
PLATELET COUNT DECREASED ( 46 FDA reports)
DYSPNOEA ( 41 FDA reports)
RENAL FAILURE ( 41 FDA reports)
RENAL IMPAIRMENT ( 40 FDA reports)
PLEURAL EFFUSION ( 39 FDA reports)
PULMONARY OEDEMA ( 37 FDA reports)
RESPIRATORY FAILURE ( 37 FDA reports)
BLOOD BILIRUBIN INCREASED ( 33 FDA reports)
INFANTILE APNOEIC ATTACK ( 29 FDA reports)
PNEUMONIA ( 29 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 28 FDA reports)
HAEMOGLOBIN DECREASED ( 28 FDA reports)
ACIDOSIS ( 27 FDA reports)
ASCITES ( 26 FDA reports)
CEREBRAL INFARCTION ( 26 FDA reports)
MYOCARDIAL INFARCTION ( 26 FDA reports)
VOMITING ( 26 FDA reports)
APNOEIC ATTACK ( 25 FDA reports)
BLOOD POTASSIUM DECREASED ( 25 FDA reports)
DRUG INEFFECTIVE ( 25 FDA reports)
ANAEMIA ( 23 FDA reports)
BLOOD PRESSURE DECREASED ( 23 FDA reports)
CARDIAC ARREST ( 23 FDA reports)
HYPERTENSION ( 23 FDA reports)
NAUSEA ( 23 FDA reports)
RASH ( 23 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 22 FDA reports)
DIZZINESS ( 22 FDA reports)
SHOCK ( 21 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 20 FDA reports)
CHILLS ( 20 FDA reports)
DIARRHOEA ( 20 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 20 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 20 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 19 FDA reports)
CONSTIPATION ( 19 FDA reports)
PAIN IN EXTREMITY ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 18 FDA reports)
HERPES ZOSTER ( 18 FDA reports)
INTERSTITIAL LUNG DISEASE ( 18 FDA reports)
OXYGEN SATURATION DECREASED ( 18 FDA reports)
PAIN ( 18 FDA reports)
POST PROCEDURAL COMPLICATION ( 18 FDA reports)
RHABDOMYOLYSIS ( 18 FDA reports)
BLOOD PRESSURE INCREASED ( 17 FDA reports)
BRADYCARDIA ( 17 FDA reports)
LEG AMPUTATION ( 17 FDA reports)
OROPHARYNGEAL PAIN ( 17 FDA reports)
PREMATURE BABY ( 17 FDA reports)
PRIAPISM ( 17 FDA reports)
PURULENCE ( 17 FDA reports)
GENERALISED OEDEMA ( 16 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 16 FDA reports)
HEPATITIS ( 16 FDA reports)
HYPOTENSION ( 16 FDA reports)
MALAISE ( 16 FDA reports)
OEDEMA ( 16 FDA reports)
PANCREATIC ENZYMES INCREASED ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
SKIN ULCER ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
CAESAREAN SECTION ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
POST HERPETIC NEURALGIA ( 14 FDA reports)
PULMONARY CONGESTION ( 14 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
DIALYSIS ( 13 FDA reports)
ERYTHEMA ( 13 FDA reports)
HYPOXIA ( 13 FDA reports)
INFECTION ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
PREGNANCY ( 13 FDA reports)
CANCER PAIN ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
CONVULSION ( 12 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
LIVER DISORDER ( 12 FDA reports)
NEONATAL APNOEIC ATTACK ( 12 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 12 FDA reports)
RESPIRATORY ARREST ( 12 FDA reports)
VENTRICULAR FIBRILLATION ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
APNOEA ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
DEATH ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
NEONATAL DISORDER ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
STAPHYLOCOCCAL INFECTION ( 11 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
FALL ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HEPATIC ENCEPHALOPATHY ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
INFUSION RELATED REACTION ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
RESPIRATORY RATE INCREASED ( 10 FDA reports)
SUBACUTE HEPATIC FAILURE ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
HAEMATOMA ( 9 FDA reports)
LUNG INFECTION ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 9 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
URINE OUTPUT DECREASED ( 9 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
ANGINA PECTORIS ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
COMA ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
PAINFUL ERECTION ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PO2 DECREASED ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 7 FDA reports)
ANOREXIA ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BURSITIS ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 7 FDA reports)
COUGH ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HAEMORRHAGIC DIATHESIS ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
NEUROBLASTOMA RECURRENT ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PERIPHERAL ISCHAEMIA ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CYSTITIS VIRAL ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NEONATAL HYPONATRAEMIA ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PARESIS ( 6 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BASILAR ARTERY OCCLUSION ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CAROTID ARTERY THROMBOSIS ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HEPATIC ARTERY STENOSIS ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
PENILE PAIN ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
VENOUS THROMBOSIS ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BLOOD CREATININE DECREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CONVULSION NEONATAL ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
FAT EMBOLISM ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
INCISIONAL HERNIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PERIOSTITIS HYPERTROPHIC ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SCAR ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STRESS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC INDEX DECREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 3 FDA reports)
CYST ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DEVICE FAILURE ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
ENDOTOXIC SHOCK ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GRAFT DYSFUNCTION ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCISIONAL HERNIA REPAIR ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJURY ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NECROSIS ISCHAEMIC ( 3 FDA reports)
NEUTROPENIC INFECTION ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PEYRONIE'S DISEASE ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POOR PERIPHERAL CIRCULATION ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PULMONARY ARTERY ATRESIA ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENA CAVA FILTER INSERTION ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BASE EXCESS NEGATIVE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHYLOTHORAX ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
EBSTEIN'S ANOMALY ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEVER NEONATAL ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LYMPHATIC DUCT RUPTURE ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEONATAL CARDIAC FAILURE ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PCO2 INCREASED ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RALES ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS SUPPURATIVE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 1 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFUSE VASCULITIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 1 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECTOPIA CORDIS ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE NEONATAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPATIC ARTERY EMBOLISM ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOPLAKIA OESOPHAGEAL ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OEDEMA NEONATAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAOESOPHAGEAL ABSCESS ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PENILE CELLULITIS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYSTEMIC-PULMONARY ARTERY SHUNT ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENIPUNCTURE SITE THROMBOSIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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