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

BLOOD PRESSURE INCREASED ( 38 FDA reports)
BLOOD CREATININE INCREASED ( 31 FDA reports)
DYSPNOEA ( 28 FDA reports)
RENAL FAILURE ( 23 FDA reports)
DEATH ( 22 FDA reports)
HYPERTENSION ( 21 FDA reports)
BLOOD GLUCOSE INCREASED ( 20 FDA reports)
ANGINA PECTORIS ( 19 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 18 FDA reports)
VOMITING ( 18 FDA reports)
DIARRHOEA ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
CEREBRAL INFARCTION ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
HYPERKALAEMIA ( 11 FDA reports)
HYPOGLYCAEMIA ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PORTAL VEIN THROMBOSIS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
RENAL IMPAIRMENT ( 10 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 10 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
ORTHOSTATIC INTOLERANCE ( 8 FDA reports)
PAIN ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
FALL ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
HAEMORRHAGIC INFARCTION ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HISTIOCYTOSIS ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INJURY ( 4 FDA reports)
LARGE INTESTINE CARCINOMA ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
STRESS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CREATININE URINE INCREASED ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LOCALISED OEDEMA ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
FACIAL SPASM ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEAR ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OOPHORITIS ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THIRST ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREATH SOUNDS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTOPIA CORDIS ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RECTAL CANCER RECURRENT ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SOLITARY KIDNEY SECONDARY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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