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

MYOCARDIAL INFARCTION ( 3119 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1844 FDA reports)
CORONARY ARTERY DISEASE ( 1102 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1040 FDA reports)
CARDIAC DISORDER ( 704 FDA reports)
BLOOD GLUCOSE INCREASED ( 507 FDA reports)
DYSPNOEA ( 496 FDA reports)
CHEST PAIN ( 465 FDA reports)
NAUSEA ( 454 FDA reports)
CARDIOVASCULAR DISORDER ( 451 FDA reports)
MYOCARDIAL ISCHAEMIA ( 435 FDA reports)
WEIGHT INCREASED ( 394 FDA reports)
PAIN ( 344 FDA reports)
FATIGUE ( 323 FDA reports)
DIARRHOEA ( 300 FDA reports)
OEDEMA PERIPHERAL ( 296 FDA reports)
DIZZINESS ( 289 FDA reports)
HYPERTENSION ( 283 FDA reports)
DEATH ( 275 FDA reports)
WEIGHT DECREASED ( 268 FDA reports)
ATRIAL FIBRILLATION ( 251 FDA reports)
ASTHENIA ( 243 FDA reports)
DRUG INEFFECTIVE ( 228 FDA reports)
HEART INJURY ( 225 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 225 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 223 FDA reports)
INJURY ( 219 FDA reports)
CARDIAC FAILURE ( 218 FDA reports)
CARDIAC ARREST ( 205 FDA reports)
VOMITING ( 202 FDA reports)
OEDEMA ( 183 FDA reports)
CORONARY ARTERY BYPASS ( 182 FDA reports)
HEADACHE ( 177 FDA reports)
RENAL FAILURE ( 174 FDA reports)
ARTERIOSCLEROSIS ( 172 FDA reports)
CARDIOMYOPATHY ( 171 FDA reports)
DEPRESSION ( 168 FDA reports)
STENT PLACEMENT ( 168 FDA reports)
ANAEMIA ( 161 FDA reports)
DECREASED APPETITE ( 157 FDA reports)
ANXIETY ( 154 FDA reports)
ACUTE CORONARY SYNDROME ( 143 FDA reports)
ANGINA UNSTABLE ( 135 FDA reports)
FLUID RETENTION ( 133 FDA reports)
ARRHYTHMIA ( 127 FDA reports)
DIABETES MELLITUS ( 124 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 120 FDA reports)
VISION BLURRED ( 119 FDA reports)
BLOOD GLUCOSE DECREASED ( 117 FDA reports)
MALAISE ( 115 FDA reports)
HYPERLIPIDAEMIA ( 111 FDA reports)
ABDOMINAL PAIN UPPER ( 107 FDA reports)
PALPITATIONS ( 106 FDA reports)
PAIN IN EXTREMITY ( 105 FDA reports)
HYPOGLYCAEMIA ( 102 FDA reports)
ABDOMINAL PAIN ( 101 FDA reports)
ARTHRALGIA ( 100 FDA reports)
ANGINA PECTORIS ( 98 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 98 FDA reports)
PNEUMONIA ( 96 FDA reports)
RENAL FAILURE ACUTE ( 96 FDA reports)
BACK PAIN ( 95 FDA reports)
PULMONARY EMBOLISM ( 92 FDA reports)
CORONARY ARTERY OCCLUSION ( 90 FDA reports)
PULMONARY OEDEMA ( 90 FDA reports)
ABDOMINAL DISTENSION ( 84 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 84 FDA reports)
CONDITION AGGRAVATED ( 84 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 84 FDA reports)
HYPOAESTHESIA ( 84 FDA reports)
SWELLING ( 84 FDA reports)
AMNESIA ( 83 FDA reports)
CARDIOMEGALY ( 80 FDA reports)
HEART RATE IRREGULAR ( 79 FDA reports)
PANCREATITIS ( 79 FDA reports)
BLINDNESS ( 78 FDA reports)
MACULAR OEDEMA ( 78 FDA reports)
MYALGIA ( 78 FDA reports)
TREMOR ( 78 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 77 FDA reports)
COUGH ( 77 FDA reports)
MITRAL VALVE INCOMPETENCE ( 76 FDA reports)
FALL ( 75 FDA reports)
HYPERHIDROSIS ( 75 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 74 FDA reports)
RASH ( 72 FDA reports)
GAIT DISTURBANCE ( 71 FDA reports)
LOSS OF CONSCIOUSNESS ( 69 FDA reports)
VISUAL ACUITY REDUCED ( 69 FDA reports)
JOINT SWELLING ( 67 FDA reports)
MUSCLE SPASMS ( 67 FDA reports)
THROMBOSIS ( 67 FDA reports)
RESPIRATORY FAILURE ( 66 FDA reports)
HYPOTENSION ( 64 FDA reports)
CONSTIPATION ( 63 FDA reports)
HYPERGLYCAEMIA ( 62 FDA reports)
PLEURAL EFFUSION ( 62 FDA reports)
CHEST DISCOMFORT ( 61 FDA reports)
MUSCULAR WEAKNESS ( 61 FDA reports)
SYNCOPE ( 61 FDA reports)
CARDIO-RESPIRATORY ARREST ( 60 FDA reports)
INSOMNIA ( 60 FDA reports)
PARAESTHESIA ( 59 FDA reports)
PRURITUS ( 59 FDA reports)
SOMNOLENCE ( 59 FDA reports)
DYSPEPSIA ( 58 FDA reports)
TYPE 2 DIABETES MELLITUS ( 58 FDA reports)
ANOREXIA ( 56 FDA reports)
HEART RATE INCREASED ( 56 FDA reports)
PULMONARY HYPERTENSION ( 56 FDA reports)
VENTRICULAR TACHYCARDIA ( 56 FDA reports)
EMOTIONAL DISTRESS ( 55 FDA reports)
ADVERSE EVENT ( 52 FDA reports)
CARDIAC PACEMAKER INSERTION ( 52 FDA reports)
CONVULSION ( 52 FDA reports)
FEELING ABNORMAL ( 52 FDA reports)
STOMACH DISCOMFORT ( 51 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 49 FDA reports)
CONFUSIONAL STATE ( 49 FDA reports)
CORONARY ARTERY STENOSIS ( 48 FDA reports)
FLATULENCE ( 48 FDA reports)
HEPATIC FAILURE ( 47 FDA reports)
URINARY TRACT INFECTION ( 47 FDA reports)
BLOOD PRESSURE INCREASED ( 46 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 46 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 46 FDA reports)
PYREXIA ( 46 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 45 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 43 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 43 FDA reports)
DYSPNOEA EXERTIONAL ( 42 FDA reports)
DYSGEUSIA ( 41 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 41 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 40 FDA reports)
BLOOD CREATININE INCREASED ( 39 FDA reports)
SEPSIS ( 39 FDA reports)
VENTRICULAR FIBRILLATION ( 39 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 38 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 38 FDA reports)
DEHYDRATION ( 37 FDA reports)
DRUG INTERACTION ( 37 FDA reports)
HAEMOGLOBIN DECREASED ( 37 FDA reports)
PANCREATITIS ACUTE ( 37 FDA reports)
TREATMENT NONCOMPLIANCE ( 37 FDA reports)
VISUAL IMPAIRMENT ( 37 FDA reports)
SWELLING FACE ( 36 FDA reports)
ABASIA ( 35 FDA reports)
ASCITES ( 35 FDA reports)
URTICARIA ( 35 FDA reports)
BALANCE DISORDER ( 34 FDA reports)
CARDIAC OPERATION ( 34 FDA reports)
DEEP VEIN THROMBOSIS ( 34 FDA reports)
TACHYCARDIA ( 34 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 33 FDA reports)
RENAL DISORDER ( 33 FDA reports)
SUDDEN CARDIAC DEATH ( 33 FDA reports)
ABDOMINAL DISCOMFORT ( 32 FDA reports)
ALOPECIA ( 32 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 32 FDA reports)
CHOLELITHIASIS ( 32 FDA reports)
DIABETIC NEUROPATHY ( 32 FDA reports)
INTRACARDIAC THROMBUS ( 32 FDA reports)
BRADYCARDIA ( 31 FDA reports)
CEREBRAL INFARCTION ( 31 FDA reports)
FLUID OVERLOAD ( 31 FDA reports)
ILL-DEFINED DISORDER ( 31 FDA reports)
INJECTION SITE PAIN ( 31 FDA reports)
CARDIAC VALVE DISEASE ( 30 FDA reports)
CATHETERISATION CARDIAC ( 30 FDA reports)
HEPATIC CIRRHOSIS ( 30 FDA reports)
NASOPHARYNGITIS ( 30 FDA reports)
OBESITY ( 30 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 30 FDA reports)
ATELECTASIS ( 29 FDA reports)
CARDIOGENIC SHOCK ( 29 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 29 FDA reports)
ERUCTATION ( 29 FDA reports)
INCORRECT DOSE ADMINISTERED ( 29 FDA reports)
VERTIGO ( 29 FDA reports)
VISUAL DISTURBANCE ( 29 FDA reports)
CEREBROVASCULAR DISORDER ( 28 FDA reports)
ECONOMIC PROBLEM ( 28 FDA reports)
ERECTILE DYSFUNCTION ( 28 FDA reports)
HYPERKALAEMIA ( 28 FDA reports)
LACTIC ACIDOSIS ( 28 FDA reports)
NEUROPATHY PERIPHERAL ( 28 FDA reports)
ASTHMA ( 27 FDA reports)
ATRIAL FLUTTER ( 27 FDA reports)
CHILLS ( 27 FDA reports)
ERYTHEMA ( 27 FDA reports)
FLUSHING ( 27 FDA reports)
MEMORY IMPAIRMENT ( 27 FDA reports)
MULTI-ORGAN FAILURE ( 27 FDA reports)
NERVOUSNESS ( 27 FDA reports)
SICK SINUS SYNDROME ( 27 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 27 FDA reports)
HEPATIC STEATOSIS ( 26 FDA reports)
INFECTION ( 26 FDA reports)
ISCHAEMIC STROKE ( 26 FDA reports)
JAUNDICE ( 26 FDA reports)
LUNG DISORDER ( 26 FDA reports)
MEDICATION ERROR ( 26 FDA reports)
PERICARDIAL EFFUSION ( 26 FDA reports)
CATARACT ( 25 FDA reports)
DRUG EFFECT DECREASED ( 25 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 25 FDA reports)
EARLY SATIETY ( 25 FDA reports)
EYE DISORDER ( 25 FDA reports)
INCREASED APPETITE ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
RENAL FAILURE CHRONIC ( 25 FDA reports)
DIASTOLIC DYSFUNCTION ( 24 FDA reports)
GASTROINTESTINAL DISORDER ( 24 FDA reports)
HYPERCHOLESTEROLAEMIA ( 24 FDA reports)
HYPOXIA ( 24 FDA reports)
INJECTION SITE BRUISING ( 24 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 24 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 24 FDA reports)
LETHARGY ( 24 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 24 FDA reports)
LIVER INJURY ( 24 FDA reports)
SLEEP APNOEA SYNDROME ( 24 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 23 FDA reports)
DYSLIPIDAEMIA ( 23 FDA reports)
HEMIPARESIS ( 23 FDA reports)
HEPATIC ENZYME INCREASED ( 23 FDA reports)
HYPERTENSIVE HEART DISEASE ( 23 FDA reports)
OVERDOSE ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK ( 22 FDA reports)
DIABETIC KETOACIDOSIS ( 22 FDA reports)
FEELING COLD ( 22 FDA reports)
IRRITABILITY ( 22 FDA reports)
LEUKOPENIA ( 22 FDA reports)
MULTIPLE INJURIES ( 22 FDA reports)
PERIPHERAL COLDNESS ( 22 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
TRANSAMINASES INCREASED ( 22 FDA reports)
VASCULAR GRAFT ( 22 FDA reports)
ANEURYSM ( 21 FDA reports)
ARTERIAL DISORDER ( 21 FDA reports)
ARTHRITIS ( 21 FDA reports)
ARTHROPATHY ( 21 FDA reports)
CARDIAC MURMUR ( 21 FDA reports)
HYPERSENSITIVITY ( 21 FDA reports)
ISCHAEMIA ( 21 FDA reports)
LIVER DISORDER ( 21 FDA reports)
PRODUCT QUALITY ISSUE ( 21 FDA reports)
RESPIRATORY DISORDER ( 21 FDA reports)
SUICIDAL IDEATION ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
BRONCHITIS ( 20 FDA reports)
CAROTID ARTERY DISEASE ( 20 FDA reports)
DYSPHAGIA ( 20 FDA reports)
INFLUENZA LIKE ILLNESS ( 20 FDA reports)
PULMONARY CONGESTION ( 20 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
DIABETIC RETINOPATHY ( 19 FDA reports)
DIVERTICULITIS ( 19 FDA reports)
ENCEPHALOPATHY ( 19 FDA reports)
EYE SWELLING ( 19 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
HEMIPLEGIA ( 19 FDA reports)
NEPHROLITHIASIS ( 19 FDA reports)
NEUTROPENIA ( 19 FDA reports)
ORTHOPNOEA ( 19 FDA reports)
PARALYSIS ( 19 FDA reports)
RHABDOMYOLYSIS ( 19 FDA reports)
ACUTE PULMONARY OEDEMA ( 18 FDA reports)
ANGIOPLASTY ( 18 FDA reports)
AORTIC VALVE INCOMPETENCE ( 18 FDA reports)
COLD SWEAT ( 18 FDA reports)
COMA ( 18 FDA reports)
CONTUSION ( 18 FDA reports)
DISORIENTATION ( 18 FDA reports)
EJECTION FRACTION DECREASED ( 18 FDA reports)
FEAR ( 18 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
GENERALISED OEDEMA ( 18 FDA reports)
HYPOKALAEMIA ( 18 FDA reports)
MITRAL VALVE PROLAPSE ( 18 FDA reports)
MUSCULOSKELETAL PAIN ( 18 FDA reports)
RENAL INJURY ( 18 FDA reports)
STRESS ( 18 FDA reports)
SURGERY ( 18 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 18 FDA reports)
ANHEDONIA ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 17 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 17 FDA reports)
CIRCULATORY COLLAPSE ( 17 FDA reports)
FEELING HOT ( 17 FDA reports)
FOOT FRACTURE ( 17 FDA reports)
FRACTURE ( 17 FDA reports)
HEART RATE DECREASED ( 17 FDA reports)
HUNGER ( 17 FDA reports)
INJECTION SITE HAEMORRHAGE ( 17 FDA reports)
MENTAL DISORDER ( 17 FDA reports)
RETCHING ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
BLOOD BILIRUBIN INCREASED ( 16 FDA reports)
DENTAL CARIES ( 16 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 16 FDA reports)
DISABILITY ( 16 FDA reports)
DYSURIA ( 16 FDA reports)
FEELING JITTERY ( 16 FDA reports)
NECK PAIN ( 16 FDA reports)
NERVE INJURY ( 16 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 16 FDA reports)
PAIN IN JAW ( 16 FDA reports)
ABDOMINAL TENDERNESS ( 15 FDA reports)
ABORTION SPONTANEOUS ( 15 FDA reports)
AORTIC STENOSIS ( 15 FDA reports)
BLISTER ( 15 FDA reports)
CYANOSIS ( 15 FDA reports)
DEPRESSED MOOD ( 15 FDA reports)
DILATATION VENTRICULAR ( 15 FDA reports)
DRY MOUTH ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
HAEMATEMESIS ( 15 FDA reports)
HYPONATRAEMIA ( 15 FDA reports)
INJECTION SITE PRURITUS ( 15 FDA reports)
INJECTION SITE RASH ( 15 FDA reports)
OSTEOPENIA ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
RENAL CYST ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
VIITH NERVE PARALYSIS ( 15 FDA reports)
ANAEMIA MACROCYTIC ( 14 FDA reports)
AORTIC VALVE STENOSIS ( 14 FDA reports)
BREATH ODOUR ( 14 FDA reports)
DECREASED ACTIVITY ( 14 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 14 FDA reports)
DIVERTICULUM ( 14 FDA reports)
HAEMATURIA ( 14 FDA reports)
HIP FRACTURE ( 14 FDA reports)
INJECTION SITE IRRITATION ( 14 FDA reports)
LYMPHADENOPATHY ( 14 FDA reports)
MENTAL STATUS CHANGES ( 14 FDA reports)
METASTASES TO LIVER ( 14 FDA reports)
RASH GENERALISED ( 14 FDA reports)
RESTLESSNESS ( 14 FDA reports)
RETINAL HAEMORRHAGE ( 14 FDA reports)
ROAD TRAFFIC ACCIDENT ( 14 FDA reports)
SINUS BRADYCARDIA ( 14 FDA reports)
SKIN DISCOLOURATION ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 14 FDA reports)
ACUTE RESPIRATORY FAILURE ( 13 FDA reports)
AORTIC VALVE REPLACEMENT ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
CARDIAC FLUTTER ( 13 FDA reports)
DEMENTIA ( 13 FDA reports)
DRUG ADMINISTRATION ERROR ( 13 FDA reports)
DYSARTHRIA ( 13 FDA reports)
ELECTROLYTE IMBALANCE ( 13 FDA reports)
GASTRIC DISORDER ( 13 FDA reports)
GASTRITIS ( 13 FDA reports)
GINGIVAL BLEEDING ( 13 FDA reports)
IMPAIRED HEALING ( 13 FDA reports)
IRON DEFICIENCY ANAEMIA ( 13 FDA reports)
LACRIMATION INCREASED ( 13 FDA reports)
LACUNAR INFARCTION ( 13 FDA reports)
MIGRAINE ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
NEPHROPATHY ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
SINUSITIS ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
TINNITUS ( 13 FDA reports)
UPPER LIMB FRACTURE ( 13 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
AGITATION ( 12 FDA reports)
ANGIOPATHY ( 12 FDA reports)
ANKLE FRACTURE ( 12 FDA reports)
BLINDNESS UNILATERAL ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
BONE PAIN ( 12 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 12 FDA reports)
CAROTID ARTERY STENOSIS ( 12 FDA reports)
CELLULITIS ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
CORONARY ANGIOPLASTY ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
HAEMOPTYSIS ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 12 FDA reports)
MACULAR DEGENERATION ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
OPEN WOUND ( 12 FDA reports)
OROPHARYNGEAL PAIN ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
PERICARDITIS ( 12 FDA reports)
PROSTATE CANCER ( 12 FDA reports)
SPINAL OSTEOARTHRITIS ( 12 FDA reports)
URINARY INCONTINENCE ( 12 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 11 FDA reports)
APHASIA ( 11 FDA reports)
BLOOD ALBUMIN DECREASED ( 11 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 11 FDA reports)
DIABETIC COMA ( 11 FDA reports)
DRY SKIN ( 11 FDA reports)
HYPERTENSIVE CRISIS ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
MITRAL VALVE DISEASE ( 11 FDA reports)
MONOPLEGIA ( 11 FDA reports)
MOVEMENT DISORDER ( 11 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 11 FDA reports)
NOCTURIA ( 11 FDA reports)
OSTEOARTHRITIS ( 11 FDA reports)
PALLOR ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
POOR QUALITY SLEEP ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
SEPTIC SHOCK ( 11 FDA reports)
SUDDEN DEATH ( 11 FDA reports)
TOOTH FRACTURE ( 11 FDA reports)
UNEVALUABLE EVENT ( 11 FDA reports)
WHEEZING ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
CARDIAC FAILURE ACUTE ( 10 FDA reports)
DIPLOPIA ( 10 FDA reports)
DIVERTICULUM INTESTINAL ( 10 FDA reports)
DYSPHONIA ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
FAECES HARD ( 10 FDA reports)
HAEMORRHOIDS ( 10 FDA reports)
HEART VALVE INCOMPETENCE ( 10 FDA reports)
HOSPITALISATION ( 10 FDA reports)
HOT FLUSH ( 10 FDA reports)
HYPERPHAGIA ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
NASAL CONGESTION ( 10 FDA reports)
OESOPHAGITIS ( 10 FDA reports)
OFF LABEL USE ( 10 FDA reports)
PLEURISY ( 10 FDA reports)
PRURITUS GENERALISED ( 10 FDA reports)
PULMONARY FIBROSIS ( 10 FDA reports)
QUALITY OF LIFE DECREASED ( 10 FDA reports)
RALES ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
SCAR ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
WRIST FRACTURE ( 10 FDA reports)
ABDOMINAL PAIN LOWER ( 9 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 9 FDA reports)
BLOOD SODIUM DECREASED ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
COGNITIVE DISORDER ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DEVICE MALFUNCTION ( 9 FDA reports)
DIABETIC COMPLICATION ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
DYSPNOEA AT REST ( 9 FDA reports)
ENDOCARDITIS ( 9 FDA reports)
EXOSTOSIS ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
GALLBLADDER DISORDER ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HEPATIC NECROSIS ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
HYPOAESTHESIA FACIAL ( 9 FDA reports)
IMPAIRED DRIVING ABILITY ( 9 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 9 FDA reports)
IMPAIRED WORK ABILITY ( 9 FDA reports)
INJECTION SITE ERYTHEMA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
RASH ERYTHEMATOUS ( 9 FDA reports)
RHINORRHOEA ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
STEVENS-JOHNSON SYNDROME ( 9 FDA reports)
VITAMIN B12 DEFICIENCY ( 9 FDA reports)
VITREOUS DETACHMENT ( 9 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
AORTIC ANEURYSM ( 8 FDA reports)
AORTIC VALVE CALCIFICATION ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
BREAST CANCER ( 8 FDA reports)
CARDIAC ANEURYSM ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CARDIAC FAILURE CHRONIC ( 8 FDA reports)
CARDIAC HYPERTROPHY ( 8 FDA reports)
COLITIS ( 8 FDA reports)
COLLAPSE OF LUNG ( 8 FDA reports)
CRYING ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
EYE PAIN ( 8 FDA reports)
EYE PRURITUS ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HYPERSOMNIA ( 8 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 8 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LEFT ATRIAL DILATATION ( 8 FDA reports)
LIP SWELLING ( 8 FDA reports)
LOCAL SWELLING ( 8 FDA reports)
MICROCYTIC ANAEMIA ( 8 FDA reports)
MITRAL VALVE STENOSIS ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
OXYGEN SUPPLEMENTATION ( 8 FDA reports)
PANCREATITIS CHRONIC ( 8 FDA reports)
PAPILLOEDEMA ( 8 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
RESPIRATORY TRACT INFECTION ( 8 FDA reports)
RETINOPATHY ( 8 FDA reports)
RIGHT ATRIAL DILATATION ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
SWOLLEN TONGUE ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
UTERINE LEIOMYOMA ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ADRENAL DISORDER ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BONE FRAGMENTATION ( 7 FDA reports)
BREAST MASS ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
CEREBELLAR INFARCTION ( 7 FDA reports)
CHOLECYSTECTOMY ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DROOLING ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
ENTEROCOCCAL INFECTION ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
GASTROENTERITIS ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
LUNG NEOPLASM ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
METASTASES TO KIDNEY ( 7 FDA reports)
METASTASES TO PANCREAS ( 7 FDA reports)
MUSCLE TIGHTNESS ( 7 FDA reports)
MUSCULOSKELETAL DISORDER ( 7 FDA reports)
MYOSITIS ( 7 FDA reports)
NEUROENDOCRINE CARCINOMA ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
POLYMYALGIA RHEUMATICA ( 7 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 7 FDA reports)
RADIUS FRACTURE ( 7 FDA reports)
RASH PRURITIC ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
RESTLESS LEGS SYNDROME ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SUICIDE ATTEMPT ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
THALAMIC INFARCTION ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
TRAUMATIC LUNG INJURY ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
VITREOUS HAEMORRHAGE ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
AORTIC VALVE DISEASE ( 6 FDA reports)
ASPIRATION PLEURAL CAVITY ( 6 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BLADDER CANCER ( 6 FDA reports)
BLOOD DISORDER ( 6 FDA reports)
BREAST FIBROSIS ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
CHEMOTHERAPY ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CORONARY ARTERY REOCCLUSION ( 6 FDA reports)
CORONARY ARTERY THROMBOSIS ( 6 FDA reports)
DEAFNESS UNILATERAL ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
ETHMOID SINUS SURGERY ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
FAECES DISCOLOURED ( 6 FDA reports)
FIBROMYALGIA ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HEART VALVE REPLACEMENT ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
HEPATITIS C ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HEPATOTOXICITY ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
INJECTION SITE NODULE ( 6 FDA reports)
INJECTION SITE URTICARIA ( 6 FDA reports)
LIFE EXPECTANCY SHORTENED ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 6 FDA reports)
MASTECTOMY ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
METASTASES TO LYMPH NODES ( 6 FDA reports)
MITRAL VALVE SCLEROSIS ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
NON-CARDIAC CHEST PAIN ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PULMONARY VASCULAR DISORDER ( 6 FDA reports)
RADIOTHERAPY ( 6 FDA reports)
RESUSCITATION ( 6 FDA reports)
RETINAL TEAR ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
SINUS ANTROSTOMY ( 6 FDA reports)
SPINAL COMPRESSION FRACTURE ( 6 FDA reports)
STRESS FRACTURE ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
THIRST ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
VENTRICULAR DYSFUNCTION ( 6 FDA reports)
VENTRICULAR HYPERTROPHY ( 6 FDA reports)
VITH NERVE PARALYSIS ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ABNORMAL CLOTTING FACTOR ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD LACTIC ACID INCREASED ( 5 FDA reports)
BLOOD PRESSURE ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CHOKING ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
COR PULMONALE ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DISCOMFORT ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
FIBULA FRACTURE ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
ILEUS ( 5 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 5 FDA reports)
INTRACRANIAL ANEURYSM ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MITRAL VALVE CALCIFICATION ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NOCTURNAL DYSPNOEA ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
OPTIC DISC DISORDER ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SLUGGISHNESS ( 5 FDA reports)
SNORING ( 5 FDA reports)
TENDON RUPTURE ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
ULCER ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VITAMIN B12 DECREASED ( 5 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
AORTIC VALVE SCLEROSIS ( 4 FDA reports)
ASBESTOSIS ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
ATRIAL TACHYCARDIA ( 4 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BRAIN STEM STROKE ( 4 FDA reports)
BREAST CALCIFICATIONS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE ( 4 FDA reports)
DYSAESTHESIA ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
HAEMOCHROMATOSIS ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEMIVERTEBRA ( 4 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LACRIMATION DECREASED ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MELANOSIS ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NAIL INFECTION ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
ORAL TORUS ( 4 FDA reports)
ORCHIDECTOMY ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RESORPTION BONE INCREASED ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SELF-INJURIOUS IDEATION ( 4 FDA reports)
SENSORY LOSS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SOPOR ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
TERMINAL STATE ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD INSULIN DECREASED ( 3 FDA reports)
BLOOD IRON DECREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CARDIAC ABLATION ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIORENAL SYNDROME ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CYST ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRESSLER'S SYNDROME ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DUODENITIS ( 3 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ESSENTIAL HYPERTENSION ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GOUT ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIGAMENT RUPTURE ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NODULE ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
ONYCHOMADESIS ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATIC ENZYMES DECREASED ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCT DEPOSIT ( 3 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL TELANGIECTASIA ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
TOBACCO ABUSE ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRAUMATIC BRAIN INJURY ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CALCIUM DEFICIENCY ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COR PULMONALE CHRONIC ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DIABETIC RETINAL OEDEMA ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
ENCEPHALOMALACIA ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EXTRASKELETAL OSSIFICATION ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FIBROUS HISTIOCYTOMA ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HALITOSIS ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METATARSALGIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARYNGEAL OPERATION ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROSTATE INFECTION ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY VALVE DISEASE ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RHABDOMYOSARCOMA ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN FIBROSIS ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPLINTER HAEMORRHAGES ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TOXIC DILATATION OF COLON ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
URINARY BLADDER POLYP ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR REMODELING ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACRODERMATITIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANOVULATORY CYCLE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
AUDITORY RECRUITMENT ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE MARROW OEDEMA SYNDROME ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC IMAGING PROCEDURE ABNORMAL ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM HEAD ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYEBALL AVULSION ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HYDRAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPNOTHERAPY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSPIRATORY CAPACITY ABNORMAL ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL ABNORMAL ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTICOKINETIC NYSTAGMUS TESTS ABNORMAL ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS EXTERNA FUNGAL ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLARY TUMOUR OF RENAL PELVIS ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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