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

RENAL FAILURE ACUTE ( 77 FDA reports)
HYPOGLYCAEMIA ( 67 FDA reports)
PYREXIA ( 55 FDA reports)
MYOCARDIAL INFARCTION ( 45 FDA reports)
DYSPNOEA ( 44 FDA reports)
OEDEMA PERIPHERAL ( 44 FDA reports)
NAUSEA ( 37 FDA reports)
VOMITING ( 37 FDA reports)
DIARRHOEA ( 36 FDA reports)
RENAL FAILURE ( 36 FDA reports)
ASTHENIA ( 33 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 31 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 31 FDA reports)
BLOOD GLUCOSE INCREASED ( 31 FDA reports)
CARDIAC FAILURE ( 31 FDA reports)
BLOOD CREATININE INCREASED ( 30 FDA reports)
DRUG INTERACTION ( 30 FDA reports)
FALL ( 30 FDA reports)
PAIN ( 30 FDA reports)
PNEUMONIA ( 30 FDA reports)
DIZZINESS ( 29 FDA reports)
ATRIAL FIBRILLATION ( 27 FDA reports)
WEIGHT DECREASED ( 26 FDA reports)
ANAEMIA ( 24 FDA reports)
CORONARY ARTERY DISEASE ( 24 FDA reports)
FATIGUE ( 24 FDA reports)
HEADACHE ( 24 FDA reports)
HYPERTENSION ( 24 FDA reports)
MALAISE ( 24 FDA reports)
CHEST PAIN ( 23 FDA reports)
ARTHRALGIA ( 22 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
HYPERGLYCAEMIA ( 22 FDA reports)
LACTIC ACIDOSIS ( 22 FDA reports)
HYPERKALAEMIA ( 21 FDA reports)
MYALGIA ( 21 FDA reports)
RHABDOMYOLYSIS ( 21 FDA reports)
ABDOMINAL PAIN ( 20 FDA reports)
ABDOMINAL PAIN UPPER ( 20 FDA reports)
CONVULSION ( 20 FDA reports)
CYTOLYTIC HEPATITIS ( 20 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 20 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 20 FDA reports)
PRURITUS ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
CARDIAC ARREST ( 19 FDA reports)
DISORIENTATION ( 19 FDA reports)
HYPONATRAEMIA ( 19 FDA reports)
BRADYCARDIA ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
DEHYDRATION ( 17 FDA reports)
PANCREATITIS ACUTE ( 17 FDA reports)
WEIGHT INCREASED ( 17 FDA reports)
BLOOD GLUCOSE DECREASED ( 16 FDA reports)
CONSTIPATION ( 16 FDA reports)
DIABETES MELLITUS ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
HYPOTENSION ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
ANXIETY ( 15 FDA reports)
BACK PAIN ( 15 FDA reports)
CARDIOMEGALY ( 15 FDA reports)
METABOLIC ACIDOSIS ( 15 FDA reports)
CARDIO-RESPIRATORY ARREST ( 14 FDA reports)
RENAL FAILURE CHRONIC ( 14 FDA reports)
ANGINA PECTORIS ( 13 FDA reports)
DEPRESSION ( 13 FDA reports)
HAEMATURIA ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
OEDEMA ( 13 FDA reports)
RASH ( 13 FDA reports)
RASH MACULO-PAPULAR ( 13 FDA reports)
VENTRICULAR FIBRILLATION ( 13 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
CARDIOMYOPATHY ( 12 FDA reports)
CEREBRAL INFARCTION ( 12 FDA reports)
CORONARY ARTERY STENOSIS ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 12 FDA reports)
HEPATITIS CHOLESTATIC ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
HYPERLIPIDAEMIA ( 12 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
COUGH ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 11 FDA reports)
HAEMATOCRIT DECREASED ( 11 FDA reports)
HEPATIC STEATOSIS ( 11 FDA reports)
HEPATITIS ( 11 FDA reports)
HYPOGLYCAEMIC COMA ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
ASCITES ( 10 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
DEATH ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
DISTURBANCE IN ATTENTION ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
BLADDER CANCER ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
PERICARDIAL EFFUSION ( 9 FDA reports)
PNEUMATOSIS INTESTINALIS ( 9 FDA reports)
PURPURA ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
STEVENS-JOHNSON SYNDROME ( 9 FDA reports)
SUBDURAL HAEMATOMA ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
AGRANULOCYTOSIS ( 8 FDA reports)
ATELECTASIS ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
COMA ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
INFECTION ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 8 FDA reports)
LIPASE INCREASED ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
VASCULAR PURPURA ( 8 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 7 FDA reports)
COAGULATION TIME PROLONGED ( 7 FDA reports)
DISCOMFORT ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
INJURY ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
MECHANICAL VENTILATION ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
NEPHROLITHIASIS ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PRESYNCOPE ( 7 FDA reports)
PSEUDOLYMPHOMA ( 7 FDA reports)
PULMONARY HYPERTENSION ( 7 FDA reports)
RASH MACULAR ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
TREMOR ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ANGIOEDEMA ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
DIABETIC GASTROPARESIS ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PLEURAL MESOTHELIOMA ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
UNRESPONSIVE TO STIMULI ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
AUTONOMIC NEUROPATHY ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 5 FDA reports)
CAROTIDYNIA ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DIABETIC RETINOPATHY ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DYSCHEZIA ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENDOMETRIAL CANCER ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
GOITRE ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NEURODEGENERATIVE DISORDER ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SURGERY ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TEMPORAL ARTERITIS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BLOOD URIC ACID ABNORMAL ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CEREBELLAR SYNDROME ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CORONARY ARTERY REOCCLUSION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MACROGLOSSIA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SWELLING ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TENSION ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 2 FDA reports)
AORTIC BRUIT ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOSCOPY ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEAR OF NEEDLES ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLOMUS TUMOUR ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERCOAGULATION ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
KERATOLYSIS EXFOLIATIVA ACQUIRED ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BONE LESION EXCISION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEAL ULCER PERFORATION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
ISOLATED ADRENOCORTICOTROPIC HORMONE DEFICIENCY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARACENTESIS ABDOMEN ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT BLISTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAR ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
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STRESS ( 1 FDA reports)
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STRIDOR ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
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TESTICULAR PAIN ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
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THYROID DISORDER ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
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VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
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VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
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VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIBRIO TEST POSITIVE ( 1 FDA reports)
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WOUND COMPLICATION ( 1 FDA reports)
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