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

BLOOD CREATININE INCREASED ( 101 FDA reports)
RENAL IMPAIRMENT ( 57 FDA reports)
DECREASED APPETITE ( 56 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 56 FDA reports)
PYREXIA ( 56 FDA reports)
VOMITING ( 56 FDA reports)
MALAISE ( 54 FDA reports)
INTERSTITIAL LUNG DISEASE ( 51 FDA reports)
ANAEMIA ( 49 FDA reports)
CEREBRAL INFARCTION ( 49 FDA reports)
PLATELET COUNT DECREASED ( 48 FDA reports)
BLOOD UREA INCREASED ( 42 FDA reports)
BLOOD URIC ACID INCREASED ( 42 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 39 FDA reports)
HAEMOGLOBIN DECREASED ( 39 FDA reports)
CARDIAC FAILURE ( 38 FDA reports)
PNEUMONIA ( 38 FDA reports)
BLOOD PRESSURE DECREASED ( 37 FDA reports)
HYPOGLYCAEMIA ( 37 FDA reports)
RENAL FAILURE ACUTE ( 37 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 36 FDA reports)
LOSS OF CONSCIOUSNESS ( 36 FDA reports)
DIARRHOEA ( 35 FDA reports)
DIZZINESS ( 35 FDA reports)
HYPERKALAEMIA ( 35 FDA reports)
NAUSEA ( 35 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 34 FDA reports)
HYPERTENSION ( 34 FDA reports)
BLOOD PRESSURE INCREASED ( 33 FDA reports)
BRADYCARDIA ( 33 FDA reports)
RHABDOMYOLYSIS ( 33 FDA reports)
RENAL FAILURE ( 32 FDA reports)
FALL ( 31 FDA reports)
NEPHROTIC SYNDROME ( 30 FDA reports)
BLOOD GLUCOSE INCREASED ( 29 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 29 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 27 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 26 FDA reports)
RENAL FAILURE CHRONIC ( 26 FDA reports)
THROMBOCYTOPENIA ( 26 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 25 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 25 FDA reports)
COUGH ( 23 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 23 FDA reports)
DYSPNOEA ( 22 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 22 FDA reports)
LIVER DISORDER ( 22 FDA reports)
OEDEMA PERIPHERAL ( 22 FDA reports)
SEPSIS ( 22 FDA reports)
DEATH ( 21 FDA reports)
HYPERGLYCAEMIA ( 21 FDA reports)
RASH ( 21 FDA reports)
HYPOAESTHESIA ( 20 FDA reports)
HYPONATRAEMIA ( 20 FDA reports)
NEPHROGENIC ANAEMIA ( 20 FDA reports)
PLEURAL EFFUSION ( 20 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 19 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 19 FDA reports)
DRUG ERUPTION ( 19 FDA reports)
ASTHENIA ( 18 FDA reports)
CARDIO-RESPIRATORY ARREST ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 17 FDA reports)
INFECTION ( 17 FDA reports)
METABOLIC ACIDOSIS ( 17 FDA reports)
ANGINA PECTORIS ( 16 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 16 FDA reports)
HYPOKALAEMIA ( 16 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 16 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
CONVULSION ( 15 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 15 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 15 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
DYSARTHRIA ( 14 FDA reports)
NEUTROPHIL COUNT DECREASED ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
BLOOD POTASSIUM INCREASED ( 13 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
ERYTHEMA ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
GOUT ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
OSTEOARTHRITIS ( 13 FDA reports)
RENAL DISORDER ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 12 FDA reports)
ANOREXIA ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
FEELING COLD ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
JAUNDICE ( 12 FDA reports)
NEUTROPENIA ( 12 FDA reports)
PRURITUS ( 12 FDA reports)
STOMATITIS ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
ASCITES ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
HAEMATOCRIT DECREASED ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
OXYGEN SATURATION DECREASED ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
URINE OUTPUT DECREASED ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 10 FDA reports)
BONE MARROW FAILURE ( 10 FDA reports)
COLON ADENOMA ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
DISEASE PROGRESSION ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 10 FDA reports)
HEPATIC FAILURE ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
MELAENA ( 10 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
COLONIC POLYP ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
DIALYSIS ( 9 FDA reports)
ERYTHEMA MULTIFORME ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
NEPHRITIS ( 9 FDA reports)
PARKINSONISM ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
PAIN ( 8 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 8 FDA reports)
RENAL CELL CARCINOMA ( 8 FDA reports)
SHOCK ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
AGRANULOCYTOSIS ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
CELL MARKER INCREASED ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DYSLALIA ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
METASTASES TO LIVER ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
OLIGOHYDRAMNIOS ( 7 FDA reports)
POLYHYDRAMNIOS ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
THREATENED LABOUR ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
CARDIAC FAILURE ACUTE ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIABETIC NEPHROPATHY ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYPOCALCAEMIA ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
KIDNEY ENLARGEMENT ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
SWELLING ( 6 FDA reports)
TUBERCULOUS PLEURISY ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ABDOMINAL NEOPLASM ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 5 FDA reports)
ANGIOMYOLIPOMA ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 5 FDA reports)
BLOOD URIC ACID ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
CHOLANGITIS ACUTE ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
DIABETIC ENTEROPATHY ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
ELECTROLYTE IMBALANCE ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEAT ILLNESS ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
ILEUS ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SERONEGATIVE ARTHRITIS ( 5 FDA reports)
SUDDEN HEARING LOSS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC PACEMAKER INSERTION ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 4 FDA reports)
EXTRACORPOREAL SHOCK WAVE THERAPY ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FRACTURED COCCYX ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
INJURY ASPHYXIATION ( 4 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LARGE INTESTINE CARCINOMA ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LUMBAR SPINAL STENOSIS ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PRE-ECLAMPSIA ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
SCROTAL SWELLING ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
SPINAL CORD INJURY CERVICAL ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VENTRICULAR FLUTTER ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLOOD AMYLASE ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IMPLANT SITE EXTRAVASATION ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 3 FDA reports)
PENILE OEDEMA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PERITONITIS SCLEROSING ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RAYNAUD'S PHENOMENON ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL FAILURE NEONATAL ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SURFACTANT PROTEIN INCREASED ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
AUTOANTIBODY POSITIVE ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS ( 2 FDA reports)
FISTULA ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GALLSTONES IN BILE DUCT REMOVAL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTEIN TOTAL ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TACITURNITY ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URINE NITROGEN ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CAROTID ANEURYSM RUPTURE ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRUCTOSAMINE INCREASED ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use