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

RENAL FAILURE ACUTE ( 174 FDA reports)
DRUG INTERACTION ( 135 FDA reports)
FALL ( 132 FDA reports)
ANAEMIA ( 113 FDA reports)
RENAL FAILURE ( 110 FDA reports)
MALAISE ( 105 FDA reports)
PYREXIA ( 94 FDA reports)
THROMBOCYTOPENIA ( 89 FDA reports)
DYSPNOEA ( 87 FDA reports)
HYPOTENSION ( 68 FDA reports)
ASTHENIA ( 67 FDA reports)
HYPONATRAEMIA ( 67 FDA reports)
PRURITUS ( 65 FDA reports)
CONFUSIONAL STATE ( 64 FDA reports)
HYPERKALAEMIA ( 60 FDA reports)
DIARRHOEA ( 57 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 57 FDA reports)
CHOLESTASIS ( 56 FDA reports)
CYTOLYTIC HEPATITIS ( 54 FDA reports)
HAEMATOMA ( 54 FDA reports)
OEDEMA PERIPHERAL ( 54 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 52 FDA reports)
ORTHOSTATIC HYPOTENSION ( 52 FDA reports)
HYPERTENSION ( 51 FDA reports)
VOMITING ( 51 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 49 FDA reports)
DEHYDRATION ( 48 FDA reports)
BLOOD CREATININE INCREASED ( 47 FDA reports)
TOXIC SKIN ERUPTION ( 46 FDA reports)
BRADYCARDIA ( 39 FDA reports)
CARDIAC FAILURE ( 39 FDA reports)
COMA ( 38 FDA reports)
EOSINOPHILIA ( 38 FDA reports)
LUNG DISORDER ( 36 FDA reports)
OVERDOSE ( 36 FDA reports)
LOSS OF CONSCIOUSNESS ( 35 FDA reports)
NAUSEA ( 35 FDA reports)
AGRANULOCYTOSIS ( 34 FDA reports)
ATRIAL FIBRILLATION ( 34 FDA reports)
CEREBROVASCULAR ACCIDENT ( 33 FDA reports)
RHABDOMYOLYSIS ( 33 FDA reports)
ABDOMINAL PAIN ( 32 FDA reports)
HYPOGLYCAEMIA ( 32 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
CARDIAC ARREST ( 29 FDA reports)
FATIGUE ( 28 FDA reports)
DISORIENTATION ( 27 FDA reports)
HEADACHE ( 27 FDA reports)
MYALGIA ( 27 FDA reports)
SYNCOPE ( 27 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 26 FDA reports)
HYPOKALAEMIA ( 26 FDA reports)
LEUKOPENIA ( 26 FDA reports)
RASH ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
ANURIA ( 25 FDA reports)
MYOCARDIAL INFARCTION ( 25 FDA reports)
NEUTROPENIA ( 25 FDA reports)
RASH MACULO-PAPULAR ( 25 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 24 FDA reports)
CONVULSION ( 24 FDA reports)
WEIGHT DECREASED ( 24 FDA reports)
ABDOMINAL PAIN UPPER ( 23 FDA reports)
COUGH ( 23 FDA reports)
HAEMOGLOBIN DECREASED ( 23 FDA reports)
PULMONARY FIBROSIS ( 23 FDA reports)
TACHYCARDIA ( 23 FDA reports)
BLOOD UREA INCREASED ( 22 FDA reports)
DERMATITIS EXFOLIATIVE ( 22 FDA reports)
FACE OEDEMA ( 22 FDA reports)
HEPATITIS CHOLESTATIC ( 22 FDA reports)
INTERSTITIAL LUNG DISEASE ( 22 FDA reports)
PULMONARY EMBOLISM ( 22 FDA reports)
PURPURA ( 21 FDA reports)
SEPSIS ( 21 FDA reports)
SOMNOLENCE ( 21 FDA reports)
TREMOR ( 21 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 20 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 20 FDA reports)
CHEST PAIN ( 20 FDA reports)
CONDITION AGGRAVATED ( 20 FDA reports)
HEPATIC FAILURE ( 20 FDA reports)
HYPERHIDROSIS ( 20 FDA reports)
HYPOXIA ( 20 FDA reports)
JAUNDICE ( 20 FDA reports)
MUSCULAR WEAKNESS ( 20 FDA reports)
PYELONEPHRITIS ( 20 FDA reports)
URINARY TRACT INFECTION ( 20 FDA reports)
ACUTE PULMONARY OEDEMA ( 19 FDA reports)
AGITATION ( 19 FDA reports)
ANOREXIA ( 19 FDA reports)
BLOOD PRESSURE INCREASED ( 19 FDA reports)
DECREASED APPETITE ( 19 FDA reports)
DIZZINESS ( 19 FDA reports)
LACTIC ACIDOSIS ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 18 FDA reports)
ERYTHEMA ( 18 FDA reports)
INFLAMMATION ( 18 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 17 FDA reports)
DEATH ( 17 FDA reports)
GAIT DISTURBANCE ( 17 FDA reports)
RASH ERYTHEMATOUS ( 17 FDA reports)
RASH PUSTULAR ( 17 FDA reports)
ANGINA PECTORIS ( 16 FDA reports)
ARTHRALGIA ( 16 FDA reports)
BRONCHITIS ( 16 FDA reports)
CHILLS ( 16 FDA reports)
ENCEPHALOPATHY ( 16 FDA reports)
MUSCLE HAEMORRHAGE ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
SHOCK ( 16 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
HAEMODIALYSIS ( 15 FDA reports)
HEPATOMEGALY ( 15 FDA reports)
LEUKOCYTOSIS ( 15 FDA reports)
MELAENA ( 15 FDA reports)
PANCYTOPENIA ( 15 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
PROTEINURIA ( 15 FDA reports)
RESPIRATORY DISTRESS ( 15 FDA reports)
URTICARIA ( 15 FDA reports)
ACCIDENTAL OVERDOSE ( 14 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
ANXIETY ( 14 FDA reports)
DEPRESSION ( 14 FDA reports)
ISCHAEMIC STROKE ( 14 FDA reports)
MEMORY IMPAIRMENT ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
TRANSAMINASES INCREASED ( 14 FDA reports)
ANAPHYLACTIC SHOCK ( 13 FDA reports)
BLOOD PRESSURE DECREASED ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
HOT FLUSH ( 13 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 13 FDA reports)
NEPHROTIC SYNDROME ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
PYELONEPHRITIS ACUTE ( 13 FDA reports)
RESPIRATORY DISORDER ( 13 FDA reports)
SUBDURAL HAEMATOMA ( 13 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
APLASTIC ANAEMIA ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
CEREBELLAR SYNDROME ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
OXYGEN SATURATION DECREASED ( 12 FDA reports)
PERITONITIS ( 12 FDA reports)
RALES ( 12 FDA reports)
RASH MACULAR ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
SKIN LESION ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
VASCULAR PURPURA ( 12 FDA reports)
BLOOD BILIRUBIN INCREASED ( 11 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
DELIRIUM ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
DYSPHAGIA ( 11 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 11 FDA reports)
HEPATITIS FULMINANT ( 11 FDA reports)
HEPATOCELLULAR INJURY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
LUNG INFECTION ( 11 FDA reports)
LYMPHOPENIA ( 11 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
ORTHOPNOEA ( 11 FDA reports)
PALLOR ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
SKIN EXFOLIATION ( 11 FDA reports)
AGGRESSION ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 10 FDA reports)
BACK PAIN ( 10 FDA reports)
CEREBRAL HAEMORRHAGE ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
DYSKINESIA ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
ERYSIPELAS ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HALLUCINATION ( 10 FDA reports)
HEMIPLEGIA ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
SUDDEN DEATH ( 10 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 9 FDA reports)
CYANOSIS ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
HALLUCINATION, AUDITORY ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
LEFT VENTRICULAR FAILURE ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
MALNUTRITION ( 9 FDA reports)
MIOSIS ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
PANCREATITIS ( 9 FDA reports)
PANCREATITIS NECROTISING ( 9 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
STEVENS-JOHNSON SYNDROME ( 9 FDA reports)
TROPONIN INCREASED ( 9 FDA reports)
URETERIC STENOSIS ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
APHASIA ( 8 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 8 FDA reports)
CANDIDIASIS ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DIFFICULTY IN WALKING ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
GENERALISED OEDEMA ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HAEMORRHAGE ( 8 FDA reports)
HEPATIC ENZYME INCREASED ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HYPOCHLORAEMIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
MENINGITIS ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
PAIN ( 8 FDA reports)
PRURIGO ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 8 FDA reports)
TRANSPLANT REJECTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
AFFECTIVE DISORDER ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 7 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
CEREBRAL ATROPHY ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
DERMATITIS ( 7 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
HEPATIC STEATOSIS ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
HYPOTONIA ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYOCLONUS ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
WOUND ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHROMATOPSIA ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
FEBRILE BONE MARROW APLASIA ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FLUID OVERLOAD ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GOUT ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 6 FDA reports)
INFECTION ( 6 FDA reports)
JAUNDICE CHOLESTATIC ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
NEPHRITIS INTERSTITIAL ( 6 FDA reports)
NEPHROANGIOSCLEROSIS ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
PERITONITIS SCLEROSING ( 6 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 6 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
SKIN NECROSIS ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
WRIST FRACTURE ( 6 FDA reports)
ACIDOSIS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ANOGENITAL DYSPLASIA ( 5 FDA reports)
APATHY ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BLADDER CATHETERISATION ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
CREPITATIONS ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
ERYTHROSIS ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GUILLAIN-BARRE SYNDROME ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
IMPETIGO ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
INTRACRANIAL HAEMATOMA ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
POLYURIA ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
SKIN HAEMORRHAGE ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
AKINESIA ( 4 FDA reports)
ASPIRATION BONE MARROW ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
ERUCTATION ( 4 FDA reports)
ERYTHROPENIA ( 4 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERLACTACIDAEMIA ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VASCULITIS NECROTISING ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
CORNEAL ABSCESS ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENDOCARDITIS CANDIDA ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OPSOCLONUS MYOCLONUS ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SERUM FERRITIN DECREASED ( 3 FDA reports)
SODIUM RETENTION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ACANTHOLYSIS ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEVICE DISLOCATION ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EYE OEDEMA ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ARTERY STENOSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HISTAMINE LEVEL INCREASED ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
ICHTHYOSIS ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LARYNGEAL DYSPNOEA ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUTISM ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL FUNGAL INFECTION ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATROPHIC GLOSSITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER NECK OPERATION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERITIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL MALARIA ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGENITAL SKIN DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDURITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL INFECTION ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MANIA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PAO2/FIO2 RATIO DECREASED ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSIOTHERAPY CHEST ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCIATIC NERVE PALSY ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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