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

PAIN ( 1952 FDA reports)
RENAL FAILURE ( 1644 FDA reports)
ANXIETY ( 1567 FDA reports)
INJURY ( 1427 FDA reports)
UNEVALUABLE EVENT ( 1352 FDA reports)
FEAR ( 1220 FDA reports)
EMOTIONAL DISTRESS ( 1132 FDA reports)
RENAL INJURY ( 1059 FDA reports)
RENAL IMPAIRMENT ( 996 FDA reports)
STRESS ( 984 FDA reports)
ANHEDONIA ( 885 FDA reports)
DEATH ( 819 FDA reports)
NAUSEA ( 811 FDA reports)
MYOCARDIAL INFARCTION ( 769 FDA reports)
DIZZINESS ( 754 FDA reports)
MULTI-ORGAN FAILURE ( 734 FDA reports)
FLUSHING ( 718 FDA reports)
DEPRESSION ( 707 FDA reports)
DYSPNOEA ( 700 FDA reports)
DRUG INEFFECTIVE ( 648 FDA reports)
CEREBROVASCULAR ACCIDENT ( 629 FDA reports)
ASTHENIA ( 573 FDA reports)
FATIGUE ( 572 FDA reports)
DRUG INTERACTION ( 550 FDA reports)
HEADACHE ( 546 FDA reports)
RENAL FAILURE ACUTE ( 535 FDA reports)
VOMITING ( 533 FDA reports)
PRURITUS ( 528 FDA reports)
FALL ( 475 FDA reports)
DIARRHOEA ( 465 FDA reports)
PNEUMONIA ( 453 FDA reports)
HYPOTENSION ( 445 FDA reports)
CHEST PAIN ( 424 FDA reports)
PAIN IN EXTREMITY ( 409 FDA reports)
PYREXIA ( 393 FDA reports)
BLOOD GLUCOSE INCREASED ( 389 FDA reports)
OEDEMA PERIPHERAL ( 381 FDA reports)
MYALGIA ( 378 FDA reports)
MALAISE ( 369 FDA reports)
PARAESTHESIA ( 340 FDA reports)
HYPERTENSION ( 335 FDA reports)
ANAEMIA ( 332 FDA reports)
INSOMNIA ( 331 FDA reports)
CONFUSIONAL STATE ( 324 FDA reports)
DEHYDRATION ( 313 FDA reports)
HAEMOGLOBIN DECREASED ( 304 FDA reports)
CONDITION AGGRAVATED ( 303 FDA reports)
ARTHRALGIA ( 300 FDA reports)
ATRIAL FIBRILLATION ( 298 FDA reports)
RASH ( 296 FDA reports)
WEIGHT DECREASED ( 295 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 281 FDA reports)
FEELING ABNORMAL ( 280 FDA reports)
BACK PAIN ( 274 FDA reports)
SOMNOLENCE ( 272 FDA reports)
SYNCOPE ( 265 FDA reports)
BLOOD PRESSURE INCREASED ( 263 FDA reports)
GAIT DISTURBANCE ( 258 FDA reports)
HYPERHIDROSIS ( 248 FDA reports)
MUSCULAR WEAKNESS ( 246 FDA reports)
CONSTIPATION ( 243 FDA reports)
ANGIOEDEMA ( 242 FDA reports)
WEIGHT INCREASED ( 242 FDA reports)
LOSS OF CONSCIOUSNESS ( 240 FDA reports)
FEELING HOT ( 239 FDA reports)
THROMBOCYTOPENIA ( 238 FDA reports)
ABDOMINAL PAIN UPPER ( 233 FDA reports)
MUSCLE SPASMS ( 233 FDA reports)
ABDOMINAL PAIN ( 225 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 222 FDA reports)
RHABDOMYOLYSIS ( 211 FDA reports)
BLOOD CREATININE INCREASED ( 209 FDA reports)
CARDIAC ARREST ( 209 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 208 FDA reports)
ERYTHEMA ( 205 FDA reports)
VISION BLURRED ( 204 FDA reports)
SEPSIS ( 203 FDA reports)
URINARY TRACT INFECTION ( 203 FDA reports)
COUGH ( 201 FDA reports)
CARDIAC FAILURE ( 200 FDA reports)
CONTUSION ( 198 FDA reports)
CARDIAC DISORDER ( 190 FDA reports)
HYPOAESTHESIA ( 190 FDA reports)
TREMOR ( 188 FDA reports)
CONVULSION ( 187 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 186 FDA reports)
HEART RATE INCREASED ( 186 FDA reports)
RESPIRATORY FAILURE ( 183 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 182 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 180 FDA reports)
NERVOUSNESS ( 178 FDA reports)
ANGINA PECTORIS ( 177 FDA reports)
HYPOGLYCAEMIA ( 176 FDA reports)
HAEMORRHAGE ( 174 FDA reports)
BRADYCARDIA ( 170 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 169 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 166 FDA reports)
COMPLETED SUICIDE ( 164 FDA reports)
ANOREXIA ( 160 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 159 FDA reports)
BURNING SENSATION ( 156 FDA reports)
CHILLS ( 156 FDA reports)
PALPITATIONS ( 155 FDA reports)
DECREASED APPETITE ( 153 FDA reports)
HYPONATRAEMIA ( 153 FDA reports)
AGITATION ( 151 FDA reports)
CORONARY ARTERY DISEASE ( 149 FDA reports)
HYPERSENSITIVITY ( 149 FDA reports)
MEMORY IMPAIRMENT ( 148 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 147 FDA reports)
PULMONARY EMBOLISM ( 147 FDA reports)
URTICARIA ( 146 FDA reports)
BALANCE DISORDER ( 145 FDA reports)
PLEURAL EFFUSION ( 143 FDA reports)
TACHYCARDIA ( 139 FDA reports)
BLOOD PRESSURE DECREASED ( 134 FDA reports)
AMNESIA ( 133 FDA reports)
DIABETES MELLITUS ( 133 FDA reports)
OVERDOSE ( 131 FDA reports)
MELAENA ( 130 FDA reports)
EPISTAXIS ( 128 FDA reports)
DRUG TOXICITY ( 125 FDA reports)
DYSGEUSIA ( 124 FDA reports)
CORONARY ARTERY OCCLUSION ( 123 FDA reports)
CHEST DISCOMFORT ( 122 FDA reports)
COMA ( 121 FDA reports)
HAEMATEMESIS ( 121 FDA reports)
DRY MOUTH ( 119 FDA reports)
INFECTION ( 118 FDA reports)
BLOOD UREA INCREASED ( 117 FDA reports)
DISORIENTATION ( 117 FDA reports)
HAEMATOCRIT DECREASED ( 117 FDA reports)
THROMBOSIS ( 117 FDA reports)
HYPERKALAEMIA ( 116 FDA reports)
PULMONARY OEDEMA ( 115 FDA reports)
HYPOKALAEMIA ( 113 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 112 FDA reports)
OEDEMA ( 108 FDA reports)
CARDIOGENIC SHOCK ( 107 FDA reports)
CEREBRAL HAEMORRHAGE ( 107 FDA reports)
DYSPHAGIA ( 107 FDA reports)
GASTRITIS ( 107 FDA reports)
LETHARGY ( 107 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 107 FDA reports)
ABDOMINAL DISTENSION ( 106 FDA reports)
DYSPEPSIA ( 106 FDA reports)
ARRHYTHMIA ( 103 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 103 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 103 FDA reports)
ABASIA ( 102 FDA reports)
MYOCARDIAL ISCHAEMIA ( 102 FDA reports)
PLATELET COUNT DECREASED ( 99 FDA reports)
MOBILITY DECREASED ( 97 FDA reports)
SWELLING FACE ( 97 FDA reports)
VERTIGO ( 97 FDA reports)
SWELLING ( 96 FDA reports)
DRUG HYPERSENSITIVITY ( 96 FDA reports)
BLOOD BILIRUBIN INCREASED ( 95 FDA reports)
FLATULENCE ( 95 FDA reports)
HAEMOPTYSIS ( 95 FDA reports)
JOINT SWELLING ( 95 FDA reports)
MENTAL DISORDER ( 95 FDA reports)
PANCYTOPENIA ( 95 FDA reports)
ALOPECIA ( 94 FDA reports)
MEDICATION ERROR ( 93 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 92 FDA reports)
CIRCULATORY COLLAPSE ( 91 FDA reports)
HOT FLUSH ( 91 FDA reports)
SUICIDAL IDEATION ( 91 FDA reports)
VISUAL ACUITY REDUCED ( 91 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 90 FDA reports)
ARTHRITIS ( 88 FDA reports)
GASTRIC ULCER ( 88 FDA reports)
HAEMATOMA ( 88 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 88 FDA reports)
DISTURBANCE IN ATTENTION ( 85 FDA reports)
HAEMATURIA ( 84 FDA reports)
JAUNDICE ( 84 FDA reports)
SPEECH DISORDER ( 84 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 82 FDA reports)
HAEMATOCHEZIA ( 82 FDA reports)
MUSCULOSKELETAL PAIN ( 82 FDA reports)
DYSARTHRIA ( 81 FDA reports)
NEUTROPENIA ( 81 FDA reports)
RECTAL HAEMORRHAGE ( 81 FDA reports)
ABDOMINAL DISCOMFORT ( 80 FDA reports)
DISABILITY ( 80 FDA reports)
MENTAL STATUS CHANGES ( 80 FDA reports)
DRUG EFFECT DECREASED ( 79 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 79 FDA reports)
HAEMODIALYSIS ( 79 FDA reports)
HYPERGLYCAEMIA ( 79 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 79 FDA reports)
VENTRICULAR TACHYCARDIA ( 78 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 78 FDA reports)
METABOLIC ACIDOSIS ( 78 FDA reports)
MITRAL VALVE INCOMPETENCE ( 78 FDA reports)
SLEEP DISORDER ( 77 FDA reports)
NEUROPATHY PERIPHERAL ( 76 FDA reports)
BLOOD POTASSIUM DECREASED ( 75 FDA reports)
AGGRESSION ( 74 FDA reports)
NASOPHARYNGITIS ( 74 FDA reports)
DISEASE PROGRESSION ( 73 FDA reports)
FEAR OF DEATH ( 73 FDA reports)
HALLUCINATION ( 73 FDA reports)
OSTEOARTHRITIS ( 73 FDA reports)
CORONARY ARTERY STENOSIS ( 72 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 72 FDA reports)
POST PROCEDURAL COMPLICATION ( 72 FDA reports)
RENAL DISORDER ( 72 FDA reports)
BLOOD SODIUM DECREASED ( 71 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 71 FDA reports)
IRRITABILITY ( 71 FDA reports)
NECK PAIN ( 71 FDA reports)
CHOLELITHIASIS ( 70 FDA reports)
HEART RATE DECREASED ( 70 FDA reports)
HEPATIC FAILURE ( 70 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 69 FDA reports)
CARDIO-RESPIRATORY ARREST ( 68 FDA reports)
EYE SWELLING ( 68 FDA reports)
ACCIDENTAL EXPOSURE ( 67 FDA reports)
DEEP VEIN THROMBOSIS ( 67 FDA reports)
HEPATIC ENZYME INCREASED ( 67 FDA reports)
INTERSTITIAL LUNG DISEASE ( 67 FDA reports)
ABNORMAL DREAMS ( 66 FDA reports)
SUICIDE ATTEMPT ( 66 FDA reports)
URINARY RETENTION ( 66 FDA reports)
SEPTIC SHOCK ( 65 FDA reports)
SKIN BURNING SENSATION ( 65 FDA reports)
TINNITUS ( 65 FDA reports)
CATARACT ( 65 FDA reports)
ABNORMAL BEHAVIOUR ( 64 FDA reports)
BLOOD GLUCOSE DECREASED ( 64 FDA reports)
DELIRIUM ( 64 FDA reports)
HYPOTHYROIDISM ( 64 FDA reports)
LACTIC ACIDOSIS ( 64 FDA reports)
POLLAKIURIA ( 64 FDA reports)
SCAR ( 64 FDA reports)
RENAL FAILURE CHRONIC ( 62 FDA reports)
THROMBOSIS IN DEVICE ( 62 FDA reports)
INJECTION SITE PAIN ( 62 FDA reports)
PRURITUS GENERALISED ( 62 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 61 FDA reports)
INCORRECT DOSE ADMINISTERED ( 61 FDA reports)
ORGAN FAILURE ( 61 FDA reports)
APHASIA ( 60 FDA reports)
FAECES DISCOLOURED ( 60 FDA reports)
MULTIPLE DRUG OVERDOSE ( 60 FDA reports)
OXYGEN SATURATION DECREASED ( 60 FDA reports)
PALLOR ( 60 FDA reports)
RESPIRATORY ARREST ( 60 FDA reports)
SHOCK ( 59 FDA reports)
VENTRICULAR FIBRILLATION ( 59 FDA reports)
BLISTER ( 59 FDA reports)
CEREBRAL INFARCTION ( 59 FDA reports)
DIFFICULTY IN WALKING ( 59 FDA reports)
DRY SKIN ( 59 FDA reports)
HALLUCINATION, VISUAL ( 59 FDA reports)
LIVER DISORDER ( 59 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 59 FDA reports)
BLOOD POTASSIUM INCREASED ( 58 FDA reports)
PROTHROMBIN TIME PROLONGED ( 58 FDA reports)
RESTLESSNESS ( 58 FDA reports)
SINUSITIS ( 57 FDA reports)
SWOLLEN TONGUE ( 57 FDA reports)
DUODENAL ULCER ( 57 FDA reports)
HEART RATE IRREGULAR ( 57 FDA reports)
INFLUENZA LIKE ILLNESS ( 57 FDA reports)
PERICARDIAL EFFUSION ( 57 FDA reports)
ADVERSE EVENT ( 56 FDA reports)
BRONCHITIS ( 56 FDA reports)
GASTROINTESTINAL DISORDER ( 56 FDA reports)
LEUKOPENIA ( 56 FDA reports)
GASTRITIS EROSIVE ( 55 FDA reports)
ANGINA UNSTABLE ( 54 FDA reports)
HYPOXIA ( 54 FDA reports)
IMPAIRED HEALING ( 54 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 54 FDA reports)
NERVOUS SYSTEM DISORDER ( 54 FDA reports)
PANCREATITIS ( 54 FDA reports)
SKIN DISCOLOURATION ( 54 FDA reports)
WHEEZING ( 54 FDA reports)
RASH ERYTHEMATOUS ( 53 FDA reports)
STEVENS-JOHNSON SYNDROME ( 53 FDA reports)
URINARY INCONTINENCE ( 53 FDA reports)
BONE PAIN ( 53 FDA reports)
EMOTIONAL DISORDER ( 53 FDA reports)
ERECTILE DYSFUNCTION ( 53 FDA reports)
HEPATITIS ( 52 FDA reports)
INFLAMMATION ( 52 FDA reports)
ISCHAEMIC STROKE ( 52 FDA reports)
MIGRAINE ( 52 FDA reports)
ROAD TRAFFIC ACCIDENT ( 52 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 52 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 51 FDA reports)
UNRESPONSIVE TO STIMULI ( 51 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 51 FDA reports)
CARDIAC MURMUR ( 51 FDA reports)
DISEASE RECURRENCE ( 51 FDA reports)
DYSSTASIA ( 51 FDA reports)
OESOPHAGITIS ( 51 FDA reports)
BLINDNESS ( 50 FDA reports)
CELLULITIS ( 50 FDA reports)
DIPLOPIA ( 50 FDA reports)
DYSKINESIA ( 50 FDA reports)
HEPATIC STEATOSIS ( 50 FDA reports)
SINUS TACHYCARDIA ( 50 FDA reports)
STOMACH DISCOMFORT ( 49 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 49 FDA reports)
HEMIPARESIS ( 49 FDA reports)
INTENTIONAL OVERDOSE ( 49 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 49 FDA reports)
ACUTE CORONARY SYNDROME ( 48 FDA reports)
AORTIC ANEURYSM ( 48 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 48 FDA reports)
CARDIOMEGALY ( 48 FDA reports)
ILL-DEFINED DISORDER ( 48 FDA reports)
STENT PLACEMENT ( 48 FDA reports)
TREATMENT NONCOMPLIANCE ( 48 FDA reports)
VISUAL IMPAIRMENT ( 48 FDA reports)
RASH GENERALISED ( 47 FDA reports)
BLOOD ALBUMIN DECREASED ( 47 FDA reports)
CHROMATURIA ( 47 FDA reports)
COLITIS ( 47 FDA reports)
DYSURIA ( 47 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 47 FDA reports)
FLUID RETENTION ( 47 FDA reports)
HIATUS HERNIA ( 47 FDA reports)
LUNG NEOPLASM MALIGNANT ( 47 FDA reports)
PSYCHIATRIC SYMPTOM ( 47 FDA reports)
PULMONARY FIBROSIS ( 47 FDA reports)
ANAPHYLACTIC REACTION ( 46 FDA reports)
DYSPNOEA EXERTIONAL ( 46 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 46 FDA reports)
HEAD INJURY ( 46 FDA reports)
HEPATOMEGALY ( 46 FDA reports)
MOVEMENT DISORDER ( 46 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 46 FDA reports)
PULMONARY HYPERTENSION ( 46 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 46 FDA reports)
STAPHYLOCOCCAL INFECTION ( 45 FDA reports)
VISUAL DISTURBANCE ( 45 FDA reports)
AGEUSIA ( 45 FDA reports)
ATELECTASIS ( 45 FDA reports)
GASTROENTERITIS ( 45 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 45 FDA reports)
PROSTATE CANCER ( 45 FDA reports)
HAEMORRHOIDS ( 44 FDA reports)
LUNG DISORDER ( 44 FDA reports)
NEOPLASM MALIGNANT ( 44 FDA reports)
PANIC ATTACK ( 44 FDA reports)
PNEUMONIA ASPIRATION ( 44 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 44 FDA reports)
RHEUMATOID ARTHRITIS ( 43 FDA reports)
SUBDURAL HAEMATOMA ( 43 FDA reports)
HERPES ZOSTER ( 43 FDA reports)
INFLUENZA ( 43 FDA reports)
CARDIAC TAMPONADE ( 42 FDA reports)
ENCEPHALOPATHY ( 42 FDA reports)
EPILEPSY ( 42 FDA reports)
SKIN ULCER ( 42 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 41 FDA reports)
COAGULOPATHY ( 41 FDA reports)
DIVERTICULITIS ( 41 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 41 FDA reports)
FEBRILE NEUTROPENIA ( 41 FDA reports)
GASTRIC DISORDER ( 41 FDA reports)
INJECTION SITE ERYTHEMA ( 41 FDA reports)
ORTHOSTATIC HYPOTENSION ( 41 FDA reports)
OSTEOPOROSIS ( 41 FDA reports)
ASTHMA ( 40 FDA reports)
ATRIAL FLUTTER ( 40 FDA reports)
ECCHYMOSIS ( 40 FDA reports)
NO ADVERSE EVENT ( 40 FDA reports)
PLATELET COUNT INCREASED ( 40 FDA reports)
RESPIRATORY DISTRESS ( 40 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 40 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 39 FDA reports)
THINKING ABNORMAL ( 39 FDA reports)
ANAPHYLACTIC SHOCK ( 39 FDA reports)
ARTERIOSCLEROSIS ( 39 FDA reports)
BODY TEMPERATURE INCREASED ( 39 FDA reports)
DIALYSIS ( 39 FDA reports)
EJECTION FRACTION DECREASED ( 39 FDA reports)
LYMPHADENOPATHY ( 39 FDA reports)
MENTAL IMPAIRMENT ( 39 FDA reports)
MYOPATHY ( 39 FDA reports)
CARDIOVASCULAR DISORDER ( 38 FDA reports)
COGNITIVE DISORDER ( 38 FDA reports)
CYANOSIS ( 38 FDA reports)
DISCOMFORT ( 38 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 38 FDA reports)
HYPOCALCAEMIA ( 38 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 38 FDA reports)
LUNG INFILTRATION ( 38 FDA reports)
MUSCLE DISORDER ( 38 FDA reports)
NEPHROLITHIASIS ( 38 FDA reports)
PANCREATITIS ACUTE ( 38 FDA reports)
SKIN EXFOLIATION ( 38 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 37 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 37 FDA reports)
TRANSAMINASES INCREASED ( 37 FDA reports)
ATAXIA ( 37 FDA reports)
COORDINATION ABNORMAL ( 37 FDA reports)
CRYING ( 37 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 37 FDA reports)
EATING DISORDER ( 37 FDA reports)
EYE DISORDER ( 37 FDA reports)
MUSCLE ATROPHY ( 37 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 37 FDA reports)
BLINDNESS UNILATERAL ( 36 FDA reports)
CAROTID ARTERY STENOSIS ( 36 FDA reports)
CORONARY ARTERY BYPASS ( 36 FDA reports)
DEMENTIA ( 36 FDA reports)
EYE PAIN ( 36 FDA reports)
GRAND MAL CONVULSION ( 36 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 36 FDA reports)
MUSCLE TWITCHING ( 36 FDA reports)
MYOSITIS ( 36 FDA reports)
PAIN IN JAW ( 36 FDA reports)
RASH MACULAR ( 36 FDA reports)
SENSORY DISTURBANCE ( 36 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 35 FDA reports)
BONE DISORDER ( 35 FDA reports)
CANDIDIASIS ( 35 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 35 FDA reports)
IMPAIRED DRIVING ABILITY ( 35 FDA reports)
LEUKOCYTOSIS ( 35 FDA reports)
ASCITES ( 34 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 34 FDA reports)
FEELING COLD ( 34 FDA reports)
HIP FRACTURE ( 34 FDA reports)
HYPERLIPIDAEMIA ( 34 FDA reports)
HYPERTENSIVE CRISIS ( 34 FDA reports)
ORAL INTAKE REDUCED ( 34 FDA reports)
OSTEOMYELITIS ( 34 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 34 FDA reports)
PERITONITIS ( 34 FDA reports)
RASH PRURITIC ( 34 FDA reports)
SLEEP APNOEA SYNDROME ( 34 FDA reports)
TACHYPNOEA ( 34 FDA reports)
SURGERY ( 33 FDA reports)
TENDERNESS ( 33 FDA reports)
VASCULITIS ( 33 FDA reports)
CEREBRAL ISCHAEMIA ( 33 FDA reports)
CHOLESTASIS ( 33 FDA reports)
DRUG INTOLERANCE ( 33 FDA reports)
DYSPHONIA ( 33 FDA reports)
JOINT STIFFNESS ( 33 FDA reports)
MIDDLE INSOMNIA ( 33 FDA reports)
ANGIONEUROTIC OEDEMA ( 32 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 32 FDA reports)
DIVERTICULUM ( 32 FDA reports)
HEMIPLEGIA ( 32 FDA reports)
HYPOKINESIA ( 32 FDA reports)
PERIPHERAL COLDNESS ( 32 FDA reports)
PSYCHOTIC DISORDER ( 32 FDA reports)
RESPIRATORY DISORDER ( 32 FDA reports)
RESPIRATORY RATE INCREASED ( 32 FDA reports)
SEROTONIN SYNDROME ( 32 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 32 FDA reports)
RHINORRHOEA ( 31 FDA reports)
SKIN HYPERTROPHY ( 31 FDA reports)
ANGER ( 31 FDA reports)
AORTIC VALVE INCOMPETENCE ( 31 FDA reports)
ARTHROPATHY ( 31 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 31 FDA reports)
FUNGAL INFECTION ( 31 FDA reports)
NIGHTMARE ( 31 FDA reports)
PRESYNCOPE ( 31 FDA reports)
AGRANULOCYTOSIS ( 30 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 30 FDA reports)
BEDRIDDEN ( 30 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 30 FDA reports)
BLOOD URINE PRESENT ( 30 FDA reports)
BRAIN OEDEMA ( 30 FDA reports)
EYE HAEMORRHAGE ( 30 FDA reports)
FIBROMYALGIA ( 30 FDA reports)
GASTRIC HAEMORRHAGE ( 30 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 30 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 30 FDA reports)
NASAL CONGESTION ( 30 FDA reports)
OSTEONECROSIS ( 30 FDA reports)
SENSATION OF HEAVINESS ( 30 FDA reports)
VISUAL FIELD DEFECT ( 30 FDA reports)
SKIN LESION ( 29 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 29 FDA reports)
ANGIOPLASTY ( 29 FDA reports)
BACTERIAL INFECTION ( 29 FDA reports)
BODY HEIGHT DECREASED ( 29 FDA reports)
CHOLECYSTITIS ( 29 FDA reports)
DEPRESSED MOOD ( 29 FDA reports)
EYE IRRITATION ( 29 FDA reports)
HYPERCALCAEMIA ( 29 FDA reports)
HYPERCHOLESTEROLAEMIA ( 29 FDA reports)
HYPOVOLAEMIA ( 29 FDA reports)
NIGHT SWEATS ( 29 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 29 FDA reports)
OROPHARYNGEAL PAIN ( 29 FDA reports)
ANURIA ( 28 FDA reports)
BLOOD CALCIUM DECREASED ( 28 FDA reports)
CARDIOMYOPATHY ( 28 FDA reports)
COLD SWEAT ( 28 FDA reports)
DELUSION ( 28 FDA reports)
DRUG ERUPTION ( 28 FDA reports)
DRY EYE ( 28 FDA reports)
INTESTINAL OBSTRUCTION ( 28 FDA reports)
NEURALGIA ( 28 FDA reports)
PEPTIC ULCER ( 28 FDA reports)
PERICARDIAL HAEMORRHAGE ( 28 FDA reports)
SENSORY LOSS ( 28 FDA reports)
SINUS BRADYCARDIA ( 28 FDA reports)
SKIN DISORDER ( 28 FDA reports)
VIRAL INFECTION ( 28 FDA reports)
RASH MACULO-PAPULAR ( 27 FDA reports)
STOMATITIS ( 27 FDA reports)
THERAPY NON-RESPONDER ( 27 FDA reports)
TOOTH EXTRACTION ( 27 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 27 FDA reports)
DEAFNESS ( 27 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 27 FDA reports)
DRUG LEVEL INCREASED ( 27 FDA reports)
DRUG RESISTANCE ( 27 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 27 FDA reports)
ECZEMA ( 27 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 27 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 27 FDA reports)
FACE OEDEMA ( 27 FDA reports)
GOUT ( 27 FDA reports)
HYPOPHAGIA ( 27 FDA reports)
INJECTION SITE HAEMORRHAGE ( 27 FDA reports)
INTENTIONAL DRUG MISUSE ( 27 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 27 FDA reports)
NOCTURIA ( 27 FDA reports)
PARALYSIS ( 27 FDA reports)
POLYURIA ( 27 FDA reports)
PSORIASIS ( 27 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 27 FDA reports)
ACUTE HEPATIC FAILURE ( 26 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 26 FDA reports)
CEREBRAL ATROPHY ( 26 FDA reports)
DUODENITIS ( 26 FDA reports)
GLAUCOMA ( 26 FDA reports)
HAEMODYNAMIC INSTABILITY ( 26 FDA reports)
HAEMORRHAGIC STROKE ( 26 FDA reports)
HEPATOTOXICITY ( 26 FDA reports)
MOUTH HAEMORRHAGE ( 26 FDA reports)
PURPURA ( 26 FDA reports)
SEDATION ( 26 FDA reports)
THROAT TIGHTNESS ( 25 FDA reports)
VENTRICULAR HYPERTROPHY ( 25 FDA reports)
ACIDOSIS ( 25 FDA reports)
BLOOD PRESSURE ABNORMAL ( 25 FDA reports)
BODY TEMPERATURE DECREASED ( 25 FDA reports)
BRONCHOPNEUMONIA ( 25 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 25 FDA reports)
FEMUR FRACTURE ( 25 FDA reports)
FLUID OVERLOAD ( 25 FDA reports)
GENERALISED OEDEMA ( 25 FDA reports)
GRANULOCYTOPENIA ( 25 FDA reports)
HEPATIC NECROSIS ( 25 FDA reports)
KNEE ARTHROPLASTY ( 25 FDA reports)
LIP SWELLING ( 25 FDA reports)
LIPASE INCREASED ( 25 FDA reports)
LOCALISED INFECTION ( 25 FDA reports)
MYOCLONUS ( 25 FDA reports)
OLIGURIA ( 25 FDA reports)
PROCEDURAL COMPLICATION ( 25 FDA reports)
PROTEINURIA ( 25 FDA reports)
CARDIAC OPERATION ( 24 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 24 FDA reports)
HEPATIC CIRRHOSIS ( 24 FDA reports)
MUCOSAL INFLAMMATION ( 24 FDA reports)
OCULAR HYPERAEMIA ( 24 FDA reports)
PERIORBITAL OEDEMA ( 24 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 24 FDA reports)
PRODUCTIVE COUGH ( 24 FDA reports)
RENAL CYST ( 24 FDA reports)
SKIN INDURATION ( 24 FDA reports)
TENDON RUPTURE ( 24 FDA reports)
RETINAL HAEMORRHAGE ( 23 FDA reports)
SKIN TIGHTNESS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK ( 23 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 23 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 23 FDA reports)
BREAST CANCER ( 23 FDA reports)
EXOSTOSIS ( 23 FDA reports)
EXTRASYSTOLES ( 23 FDA reports)
HYPOAESTHESIA ORAL ( 23 FDA reports)
HYPOTONIA ( 23 FDA reports)
LUNG INFECTION ( 23 FDA reports)
METASTASES TO LIVER ( 23 FDA reports)
MYELODYSPLASTIC SYNDROME ( 23 FDA reports)
NO THERAPEUTIC RESPONSE ( 23 FDA reports)
OFF LABEL USE ( 23 FDA reports)
PHARYNGEAL OEDEMA ( 23 FDA reports)
POLYNEUROPATHY ( 23 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 22 FDA reports)
CARPAL TUNNEL SYNDROME ( 22 FDA reports)
COLITIS ISCHAEMIC ( 22 FDA reports)
COLON CANCER ( 22 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 22 FDA reports)
DRUG ADMINISTRATION ERROR ( 22 FDA reports)
DRUG DEPENDENCE ( 22 FDA reports)
FIBROSIS ( 22 FDA reports)
GINGIVAL BLEEDING ( 22 FDA reports)
HYPERSOMNIA ( 22 FDA reports)
INITIAL INSOMNIA ( 22 FDA reports)
INJECTION SITE IRRITATION ( 22 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 22 FDA reports)
LYMPHOMA ( 22 FDA reports)
MIOSIS ( 22 FDA reports)
MOOD ALTERED ( 22 FDA reports)
MOUTH ULCERATION ( 22 FDA reports)
MUSCLE CRAMP ( 22 FDA reports)
MUSCLE TIGHTNESS ( 22 FDA reports)
PERIPHERAL ISCHAEMIA ( 22 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 22 FDA reports)
RALES ( 22 FDA reports)
RIGHT VENTRICULAR FAILURE ( 22 FDA reports)
SUDDEN DEATH ( 22 FDA reports)
VENTRICULAR DYSFUNCTION ( 22 FDA reports)
STENT OCCLUSION ( 21 FDA reports)
TYPE 2 DIABETES MELLITUS ( 21 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 21 FDA reports)
CARDIOPULMONARY FAILURE ( 21 FDA reports)
CHOLECYSTECTOMY ( 21 FDA reports)
CYSTITIS ( 21 FDA reports)
EMPHYSEMA ( 21 FDA reports)
ENDOCARDITIS ( 21 FDA reports)
IMPAIRED WORK ABILITY ( 21 FDA reports)
NEUROPATHY ( 21 FDA reports)
OSTEOPENIA ( 21 FDA reports)
PAROSMIA ( 21 FDA reports)
PNEUMONITIS ( 21 FDA reports)
PRODUCT QUALITY ISSUE ( 21 FDA reports)
PULMONARY CONGESTION ( 21 FDA reports)
ABDOMINAL TENDERNESS ( 20 FDA reports)
ACCIDENTAL OVERDOSE ( 20 FDA reports)
BASAL CELL CARCINOMA ( 20 FDA reports)
BLOOD CREATINE INCREASED ( 20 FDA reports)
BRADYARRHYTHMIA ( 20 FDA reports)
BRONCHOSPASM ( 20 FDA reports)
CATARACT OPERATION ( 20 FDA reports)
DERMATITIS ( 20 FDA reports)
DRUG DOSE OMISSION ( 20 FDA reports)
FACIAL PALSY ( 20 FDA reports)
FEELING JITTERY ( 20 FDA reports)
GENERALISED ERYTHEMA ( 20 FDA reports)
HAEMORRHAGIC ANAEMIA ( 20 FDA reports)
HEPATOCELLULAR DAMAGE ( 20 FDA reports)
HYPERVENTILATION ( 20 FDA reports)
HYPOGLYCAEMIC COMA ( 20 FDA reports)
INCISION SITE HAEMORRHAGE ( 20 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 20 FDA reports)
LEFT VENTRICULAR FAILURE ( 20 FDA reports)
LOBAR PNEUMONIA ( 20 FDA reports)
MALNUTRITION ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MUSCLE STRAIN ( 20 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 20 FDA reports)
NEUTROPHIL COUNT INCREASED ( 20 FDA reports)
OSTEONECROSIS OF JAW ( 20 FDA reports)
PARKINSON'S DISEASE ( 20 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 20 FDA reports)
RESPIRATORY TRACT INFECTION ( 20 FDA reports)
RIB FRACTURE ( 20 FDA reports)
SPINAL OSTEOARTHRITIS ( 20 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 20 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 20 FDA reports)
TOOTH DISORDER ( 20 FDA reports)
TORSADE DE POINTES ( 20 FDA reports)
VASCULAR OCCLUSION ( 20 FDA reports)
RENAL TUBULAR NECROSIS ( 19 FDA reports)
RETCHING ( 19 FDA reports)
SPINAL COLUMN STENOSIS ( 19 FDA reports)
STATUS EPILEPTICUS ( 19 FDA reports)
TROPONIN INCREASED ( 19 FDA reports)
ULCER ( 19 FDA reports)
ALCOHOL USE ( 19 FDA reports)
APATHY ( 19 FDA reports)
ASPIRATION ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 19 FDA reports)
BILIARY TRACT DISORDER ( 19 FDA reports)
BIPOLAR DISORDER ( 19 FDA reports)
BLOOD URIC ACID INCREASED ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
ELECTROLYTE IMBALANCE ( 19 FDA reports)
EYE PRURITUS ( 19 FDA reports)
HEPATITIS ACUTE ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
HYPOALBUMINAEMIA ( 19 FDA reports)
HYPOMAGNESAEMIA ( 19 FDA reports)
HYPOTHERMIA ( 19 FDA reports)
INJECTION SITE HAEMATOMA ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
LABORATORY TEST ABNORMAL ( 19 FDA reports)
MUSCLE INJURY ( 19 FDA reports)
NEOPLASM PROGRESSION ( 19 FDA reports)
ORAL PAIN ( 19 FDA reports)
PROTEIN TOTAL DECREASED ( 19 FDA reports)
PROTEIN URINE PRESENT ( 19 FDA reports)
ADVERSE DRUG REACTION ( 18 FDA reports)
BLOOD CHLORIDE DECREASED ( 18 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 18 FDA reports)
CEREBROVASCULAR DISORDER ( 18 FDA reports)
COLONIC POLYP ( 18 FDA reports)
DEAFNESS UNILATERAL ( 18 FDA reports)
DECUBITUS ULCER ( 18 FDA reports)
DIABETIC KETOACIDOSIS ( 18 FDA reports)
DYSPNOEA EXACERBATED ( 18 FDA reports)
FEELING DRUNK ( 18 FDA reports)
GALLBLADDER DISORDER ( 18 FDA reports)
GINGIVAL DISORDER ( 18 FDA reports)
GINGIVAL PAIN ( 18 FDA reports)
HAEMORRHAGIC DIATHESIS ( 18 FDA reports)
HEARING IMPAIRED ( 18 FDA reports)
HIP ARTHROPLASTY ( 18 FDA reports)
ILEUS ( 18 FDA reports)
INCONTINENCE ( 18 FDA reports)
LACRIMATION INCREASED ( 18 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 18 FDA reports)
METASTASES TO BONE ( 18 FDA reports)
METASTASES TO LUNG ( 18 FDA reports)
METASTASES TO LYMPH NODES ( 18 FDA reports)
MYDRIASIS ( 18 FDA reports)
OBESITY ( 18 FDA reports)
OEDEMA MOUTH ( 18 FDA reports)
PELVIC FRACTURE ( 18 FDA reports)
PHOTOSENSITIVITY REACTION ( 18 FDA reports)
RESPIRATORY DEPRESSION ( 18 FDA reports)
RESTLESS LEGS SYNDROME ( 18 FDA reports)
SPINAL FRACTURE ( 18 FDA reports)
SUDDEN CARDIAC DEATH ( 18 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 18 FDA reports)
SHOCK HAEMORRHAGIC ( 17 FDA reports)
SKIN HAEMORRHAGE ( 17 FDA reports)
SYNCOPE VASOVAGAL ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
TOOTHACHE ( 17 FDA reports)
VENTRICULAR HYPOKINESIA ( 17 FDA reports)
ACUTE PULMONARY OEDEMA ( 17 FDA reports)
ANGIOPATHY ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 17 FDA reports)
BREAST CANCER FEMALE ( 17 FDA reports)
CAESAREAN SECTION ( 17 FDA reports)
CLOSTRIDIAL INFECTION ( 17 FDA reports)
DILATATION ATRIAL ( 17 FDA reports)
EOSINOPHILIA ( 17 FDA reports)
FACIAL PAIN ( 17 FDA reports)
GANGRENE ( 17 FDA reports)
GLOSSODYNIA ( 17 FDA reports)
INCREASED TENDENCY TO BRUISE ( 17 FDA reports)
INTESTINAL HAEMORRHAGE ( 17 FDA reports)
IRON DEFICIENCY ANAEMIA ( 17 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 17 FDA reports)
MACULAR DEGENERATION ( 17 FDA reports)
MOOD SWINGS ( 17 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 17 FDA reports)
PARANOIA ( 17 FDA reports)
PETECHIAE ( 17 FDA reports)
POOR PERIPHERAL CIRCULATION ( 17 FDA reports)
PULMONARY HAEMORRHAGE ( 17 FDA reports)
PURULENT DISCHARGE ( 17 FDA reports)
BLOOD IRON DECREASED ( 16 FDA reports)
BLOOD PH DECREASED ( 16 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 16 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 16 FDA reports)
BURSITIS ( 16 FDA reports)
CATHETER SITE HAEMORRHAGE ( 16 FDA reports)
COLITIS ULCERATIVE ( 16 FDA reports)
CORONARY ARTERY THROMBOSIS ( 16 FDA reports)
DILATATION VENTRICULAR ( 16 FDA reports)
EAR PAIN ( 16 FDA reports)
ENTEROCOCCAL INFECTION ( 16 FDA reports)
EOSINOPHIL COUNT INCREASED ( 16 FDA reports)
EYE MOVEMENT DISORDER ( 16 FDA reports)
FAECAL INCONTINENCE ( 16 FDA reports)
FLANK PAIN ( 16 FDA reports)
HALLUCINATION, AUDITORY ( 16 FDA reports)
HEPATIC ENCEPHALOPATHY ( 16 FDA reports)
HYPERAESTHESIA ( 16 FDA reports)
LARYNGEAL OEDEMA ( 16 FDA reports)
LISTLESS ( 16 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
MEDICATION RESIDUE ( 16 FDA reports)
MICTURITION URGENCY ( 16 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 16 FDA reports)
PAPILLOEDEMA ( 16 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
PULSE ABSENT ( 16 FDA reports)
RASH PAPULAR ( 16 FDA reports)
REYE'S SYNDROME ( 16 FDA reports)
SINUS DISORDER ( 16 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 16 FDA reports)
URINE OUTPUT DECREASED ( 16 FDA reports)
WOUND ( 16 FDA reports)
RENAL PAIN ( 15 FDA reports)
ROTATOR CUFF SYNDROME ( 15 FDA reports)
TACHYARRHYTHMIA ( 15 FDA reports)
TENDONITIS ( 15 FDA reports)
THIRST ( 15 FDA reports)
TONGUE DISORDER ( 15 FDA reports)
TOXIC SKIN ERUPTION ( 15 FDA reports)
ULCER HAEMORRHAGE ( 15 FDA reports)
VASCULAR GRAFT ( 15 FDA reports)
ABDOMINAL PAIN LOWER ( 15 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 15 FDA reports)
APLASTIC ANAEMIA ( 15 FDA reports)
ASPERGILLOSIS ( 15 FDA reports)
BLOOD DISORDER ( 15 FDA reports)
BLOOD TEST ABNORMAL ( 15 FDA reports)
CARDIAC PACEMAKER INSERTION ( 15 FDA reports)
CARDIAC VALVE DISEASE ( 15 FDA reports)
CONJUNCTIVITIS ( 15 FDA reports)
CREPITATIONS ( 15 FDA reports)
DERMATITIS EXFOLIATIVE ( 15 FDA reports)
DIZZINESS POSTURAL ( 15 FDA reports)
ERUCTATION ( 15 FDA reports)
EXCORIATION ( 15 FDA reports)
EXERCISE TOLERANCE DECREASED ( 15 FDA reports)
FEMORAL ARTERY OCCLUSION ( 15 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 15 FDA reports)
HAEMOLYSIS ( 15 FDA reports)
HAEMORRHAGE URINARY TRACT ( 15 FDA reports)
HELICOBACTER INFECTION ( 15 FDA reports)
HYPERTHYROIDISM ( 15 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 15 FDA reports)
HYPOREFLEXIA ( 15 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 15 FDA reports)
INFUSION RELATED REACTION ( 15 FDA reports)
INJECTION SITE REACTION ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
JOINT INJURY ( 15 FDA reports)
LEG AMPUTATION ( 15 FDA reports)
LIMB INJURY ( 15 FDA reports)
LOWER LIMB FRACTURE ( 15 FDA reports)
LYMPHOPENIA ( 15 FDA reports)
MULTIPLE SCLEROSIS ( 15 FDA reports)
ORAL SURGERY ( 15 FDA reports)
PNEUMOTHORAX ( 15 FDA reports)
PSYCHOLOGICAL TRAUMA ( 15 FDA reports)
AORTIC VALVE DISEASE ( 14 FDA reports)
BRADYPHRENIA ( 14 FDA reports)
BRAIN INJURY ( 14 FDA reports)
CARDIAC ANEURYSM ( 14 FDA reports)
CARDIAC FAILURE ACUTE ( 14 FDA reports)
CAROTID ARTERY OCCLUSION ( 14 FDA reports)
CATHETER RELATED COMPLICATION ( 14 FDA reports)
CHOLANGITIS ( 14 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
DECREASED INTEREST ( 14 FDA reports)
DEVICE RELATED INFECTION ( 14 FDA reports)
DIABETIC NEPHROPATHY ( 14 FDA reports)
DIVERTICULUM INTESTINAL ( 14 FDA reports)
DRUG SCREEN POSITIVE ( 14 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 14 FDA reports)
EXTRADURAL HAEMATOMA ( 14 FDA reports)
FEMORAL NECK FRACTURE ( 14 FDA reports)
FOOT FRACTURE ( 14 FDA reports)
FRACTURE ( 14 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 14 FDA reports)
HAEMOLYTIC ANAEMIA ( 14 FDA reports)
HEPATITIS CHOLESTATIC ( 14 FDA reports)
HEPATITIS FULMINANT ( 14 FDA reports)
INFARCTION ( 14 FDA reports)
JOINT EFFUSION ( 14 FDA reports)
LIMB DISCOMFORT ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
NERVE COMPRESSION ( 14 FDA reports)
NEUTROPHIL COUNT DECREASED ( 14 FDA reports)
NON-CARDIAC CHEST PAIN ( 14 FDA reports)
PAIN OF SKIN ( 14 FDA reports)
PCO2 DECREASED ( 14 FDA reports)
PERSONALITY CHANGE ( 14 FDA reports)
PHOTOPHOBIA ( 14 FDA reports)
PLEURITIC PAIN ( 14 FDA reports)
PRIMARY SEQUESTRUM ( 14 FDA reports)
PSEUDOMONAS INFECTION ( 14 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 14 FDA reports)
RECTAL CANCER ( 14 FDA reports)
REFLUX OESOPHAGITIS ( 14 FDA reports)
RHINITIS ( 14 FDA reports)
SCRATCH ( 14 FDA reports)
SELF-INJURIOUS IDEATION ( 14 FDA reports)
SKIN FIBROSIS ( 14 FDA reports)
SKIN IRRITATION ( 14 FDA reports)
SPLENOMEGALY ( 14 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 14 FDA reports)
SUBDURAL HAEMORRHAGE ( 14 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 14 FDA reports)
THYROID NEOPLASM ( 14 FDA reports)
VENTRICULAR ARRHYTHMIA ( 14 FDA reports)
WALKING AID USER ( 14 FDA reports)
SELF-MEDICATION ( 13 FDA reports)
SENILE DEMENTIA ( 13 FDA reports)
SKIN LACERATION ( 13 FDA reports)
SPLENIC HAEMORRHAGE ( 13 FDA reports)
SURGICAL PROCEDURE REPEATED ( 13 FDA reports)
THROMBOCYTHAEMIA ( 13 FDA reports)
THYROID DISORDER ( 13 FDA reports)
TUBERCULOSIS ( 13 FDA reports)
VASCULAR PSEUDOANEURYSM ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
ABSCESS ( 13 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ANEURYSM ( 13 FDA reports)
ANOSMIA ( 13 FDA reports)
ARTERIOSPASM CORONARY ( 13 FDA reports)
BACK DISORDER ( 13 FDA reports)
BLADDER DISORDER ( 13 FDA reports)
BLINDNESS TRANSIENT ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
BLOOD SODIUM INCREASED ( 13 FDA reports)
BREATH SOUNDS ABNORMAL ( 13 FDA reports)
CORONARY ARTERY SURGERY ( 13 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 13 FDA reports)
DERMATOMYOSITIS ( 13 FDA reports)
DEVICE FAILURE ( 13 FDA reports)
DEVICE MALFUNCTION ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
EMBOLISM ( 13 FDA reports)
FOOT DEFORMITY ( 13 FDA reports)
HEPATITIS B ( 13 FDA reports)
HEPATITIS TOXIC ( 13 FDA reports)
HYPERAMMONAEMIA ( 13 FDA reports)
IMMUNE SYSTEM DISORDER ( 13 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 13 FDA reports)
JOINT CONTRACTURE ( 13 FDA reports)
LACUNAR INFARCTION ( 13 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 13 FDA reports)
MANIA ( 13 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 13 FDA reports)
MUSCLE RIGIDITY ( 13 FDA reports)
NERVE INJURY ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
PARAESTHESIA ORAL ( 13 FDA reports)
PROTHROMBIN TIME SHORTENED ( 13 FDA reports)
ACNE ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 12 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 12 FDA reports)
AZOTAEMIA ( 12 FDA reports)
BLADDER CANCER ( 12 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 12 FDA reports)
BONE MARROW FAILURE ( 12 FDA reports)
CARDIAC FLUTTER ( 12 FDA reports)
CEREBRAL HAEMATOMA ( 12 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 12 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
DRY THROAT ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 12 FDA reports)
EYELID OEDEMA ( 12 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 12 FDA reports)
HYPERNATRAEMIA ( 12 FDA reports)
HYPERURICAEMIA ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
INTRACARDIAC THROMBUS ( 12 FDA reports)
ISCHAEMIA ( 12 FDA reports)
JAUNDICE CHOLESTATIC ( 12 FDA reports)
JAW DISORDER ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
LUMBAR SPINAL STENOSIS ( 12 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 12 FDA reports)
METABOLIC DISORDER ( 12 FDA reports)
MULTIPLE MYELOMA ( 12 FDA reports)
NEPHROPATHY TOXIC ( 12 FDA reports)
PEMPHIGOID ( 12 FDA reports)
PERICARDITIS ( 12 FDA reports)
PRESCRIBED OVERDOSE ( 12 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 12 FDA reports)
RENAL INFARCT ( 12 FDA reports)
SALIVARY HYPERSECRETION ( 12 FDA reports)
SEXUAL DYSFUNCTION ( 12 FDA reports)
SKIN HYPERPIGMENTATION ( 12 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 12 FDA reports)
TOE AMPUTATION ( 12 FDA reports)
TOOTH INFECTION ( 12 FDA reports)
UROSEPSIS ( 12 FDA reports)
URTICARIA GENERALISED ( 12 FDA reports)
VAGINAL HAEMORRHAGE ( 12 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 12 FDA reports)
WHEELCHAIR USER ( 12 FDA reports)
WRONG DRUG ADMINISTERED ( 12 FDA reports)
RESPIRATORY THERAPY ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
RHONCHI ( 11 FDA reports)
SERUM FERRITIN INCREASED ( 11 FDA reports)
SKIN REACTION ( 11 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 11 FDA reports)
SPLENIC INFARCTION ( 11 FDA reports)
TENDON INJURY ( 11 FDA reports)
UNDERDOSE ( 11 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 11 FDA reports)
VENOUS OCCLUSION ( 11 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 11 FDA reports)
WEIGHT FLUCTUATION ( 11 FDA reports)
WOUND DEHISCENCE ( 11 FDA reports)
X-RAY ABNORMAL ( 11 FDA reports)
ABORTION SPONTANEOUS ( 11 FDA reports)
ACUTE ABDOMEN ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 11 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 11 FDA reports)
ARTERIAL DISORDER ( 11 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 11 FDA reports)
BACTERAEMIA ( 11 FDA reports)
BILE DUCT CANCER ( 11 FDA reports)
BLOOD AMYLASE INCREASED ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
BLOOD CULTURE POSITIVE ( 11 FDA reports)
BLOOD MAGNESIUM DECREASED ( 11 FDA reports)
BRAIN HERNIATION ( 11 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 11 FDA reports)
CHEST X-RAY ABNORMAL ( 11 FDA reports)
CHOKING ( 11 FDA reports)
COMMUNICATION DISORDER ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 11 FDA reports)
CORONARY ANGIOPLASTY ( 11 FDA reports)
CORONARY ARTERY ANEURYSM ( 11 FDA reports)
DENTAL CARIES ( 11 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 11 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DYSAESTHESIA ( 11 FDA reports)
DYSTONIA ( 11 FDA reports)
EAR INFECTION ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 11 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 11 FDA reports)
EMBOLIC STROKE ( 11 FDA reports)
ERYSIPELAS ( 11 FDA reports)
EUPHORIC MOOD ( 11 FDA reports)
EXTREMITY CONTRACTURE ( 11 FDA reports)
EYE INFLAMMATION ( 11 FDA reports)
FISTULA ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
FRUSTRATION ( 11 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 11 FDA reports)
HEPATIC CONGESTION ( 11 FDA reports)
HEPATIC LESION ( 11 FDA reports)
HYPERREFLEXIA ( 11 FDA reports)
HYPERTENSIVE HEART DISEASE ( 11 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 11 FDA reports)
INCOHERENT ( 11 FDA reports)
INGUINAL HERNIA ( 11 FDA reports)
INJECTION SITE BURNING ( 11 FDA reports)
KLEBSIELLA INFECTION ( 11 FDA reports)
LARGE INTESTINE PERFORATION ( 11 FDA reports)
LIBIDO DECREASED ( 11 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 11 FDA reports)
MITRAL VALVE DISEASE ( 11 FDA reports)
MUSCLE HAEMORRHAGE ( 11 FDA reports)
NEUROLOGICAL SYMPTOM ( 11 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 11 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 11 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 11 FDA reports)
PANCREATIC CARCINOMA ( 11 FDA reports)
PARESIS ( 11 FDA reports)
PARKINSONISM ( 11 FDA reports)
PHLEBITIS ( 11 FDA reports)
PROSTATITIS ( 11 FDA reports)
PROTEIN TOTAL INCREASED ( 11 FDA reports)
PUPIL FIXED ( 11 FDA reports)
ANKLE FRACTURE ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
AORTIC STENOSIS ( 10 FDA reports)
AREFLEXIA ( 10 FDA reports)
ARTHRITIS BACTERIAL ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 10 FDA reports)
AUTOIMMUNE HEPATITIS ( 10 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 10 FDA reports)
BLEEDING TIME PROLONGED ( 10 FDA reports)
BLOOD CALCIUM INCREASED ( 10 FDA reports)
BLOOD URINE ( 10 FDA reports)
BRAIN DEATH ( 10 FDA reports)
BRAIN STEM SYNDROME ( 10 FDA reports)
COMPARTMENT SYNDROME ( 10 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 10 FDA reports)
CYTOLYTIC HEPATITIS ( 10 FDA reports)
DECREASED ACTIVITY ( 10 FDA reports)
DIABETIC NEUROPATHY ( 10 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 10 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
FEELING GUILTY ( 10 FDA reports)
FOOD INTERACTION ( 10 FDA reports)
FORMICATION ( 10 FDA reports)
GASTROENTERITIS VIRAL ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GROIN PAIN ( 10 FDA reports)
HEPATIC CYST ( 10 FDA reports)
HYDROCEPHALUS ( 10 FDA reports)
HYPOVENTILATION ( 10 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 10 FDA reports)
INADEQUATE ANALGESIA ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 10 FDA reports)
INJECTION SITE SWELLING ( 10 FDA reports)
INTERMITTENT CLAUDICATION ( 10 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 10 FDA reports)
LABYRINTHITIS ( 10 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 10 FDA reports)
LOOSE TOOTH ( 10 FDA reports)
LUNG CONSOLIDATION ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
LYMPHOEDEMA ( 10 FDA reports)
MACULAR OEDEMA ( 10 FDA reports)
MASS ( 10 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 10 FDA reports)
MENINGITIS ( 10 FDA reports)
NECROSIS ( 10 FDA reports)
NON-SMALL CELL LUNG CANCER ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
PERIPHERAL EMBOLISM ( 10 FDA reports)
PERONEAL NERVE PALSY ( 10 FDA reports)
PERSONALITY DISORDER ( 10 FDA reports)
PETIT MAL EPILEPSY ( 10 FDA reports)
PIGMENTATION DISORDER ( 10 FDA reports)
POLYP ( 10 FDA reports)
POOR QUALITY SLEEP ( 10 FDA reports)
PROCTALGIA ( 10 FDA reports)
PULMONARY GRANULOMA ( 10 FDA reports)
PURULENCE ( 10 FDA reports)
PYELONEPHRITIS ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 10 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 10 FDA reports)
SINUS CONGESTION ( 10 FDA reports)
SNEEZING ( 10 FDA reports)
SOPOR ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 10 FDA reports)
TENDON DISORDER ( 10 FDA reports)
TENSION ( 10 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 10 FDA reports)
TONGUE DISCOLOURATION ( 10 FDA reports)
TOOTH LOSS ( 10 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 10 FDA reports)
WITHDRAWAL SYNDROME ( 10 FDA reports)
QRS AXIS ABNORMAL ( 9 FDA reports)
QUADRIPLEGIA ( 9 FDA reports)
RASH PUSTULAR ( 9 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 9 FDA reports)
SCHIZOPHRENIA ( 9 FDA reports)
SINUS ARRHYTHMIA ( 9 FDA reports)
SPUTUM CULTURE POSITIVE ( 9 FDA reports)
SPUTUM DISCOLOURED ( 9 FDA reports)
URINE ANALYSIS ABNORMAL ( 9 FDA reports)
URINE COLOUR ABNORMAL ( 9 FDA reports)
VASCULAR BYPASS GRAFT ( 9 FDA reports)
AORTIC DISSECTION ( 9 FDA reports)
AORTIC VALVE SCLEROSIS ( 9 FDA reports)
ATHEROSCLEROSIS ( 9 FDA reports)
BARRETT'S OESOPHAGUS ( 9 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BLOOD BICARBONATE DECREASED ( 9 FDA reports)
BLOOD CREATININE DECREASED ( 9 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 9 FDA reports)
BREAST CANCER METASTATIC ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 9 FDA reports)
CARDIOVERSION ( 9 FDA reports)
CAROTID ARTERY DISEASE ( 9 FDA reports)
CATHETERISATION CARDIAC ( 9 FDA reports)
CHONDROPATHY ( 9 FDA reports)
CONDUCTION DISORDER ( 9 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 9 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 9 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 9 FDA reports)
DEMYELINATION ( 9 FDA reports)
DENTAL OPERATION ( 9 FDA reports)
DEPENDENCE ( 9 FDA reports)
DERMATITIS CONTACT ( 9 FDA reports)
ECONOMIC PROBLEM ( 9 FDA reports)
ENURESIS ( 9 FDA reports)
EXTREMITY NECROSIS ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
GALLBLADDER OPERATION ( 9 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 9 FDA reports)
GUILLAIN-BARRE SYNDROME ( 9 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 9 FDA reports)
HEPATOCELLULAR INJURY ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HYPERTONIA ( 9 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
INJECTION SITE NODULE ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
KIDNEY INFECTION ( 9 FDA reports)
KOUNIS SYNDROME ( 9 FDA reports)
MALIGNANT HYPERTENSION ( 9 FDA reports)
MALIGNANT MELANOMA ( 9 FDA reports)
MASTICATION DISORDER ( 9 FDA reports)
METRORRHAGIA ( 9 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 9 FDA reports)
NODULE ( 9 FDA reports)
NYSTAGMUS ( 9 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 9 FDA reports)
OPERATIVE HAEMORRHAGE ( 9 FDA reports)
OVARIAN ADENOMA ( 9 FDA reports)
PERFORMANCE STATUS DECREASED ( 9 FDA reports)
POLYDIPSIA ( 9 FDA reports)
POLYMYOSITIS ( 9 FDA reports)
POST PROCEDURAL HAEMATOMA ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 9 FDA reports)
PREMATURE BABY ( 9 FDA reports)
PULMONARY MASS ( 9 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 8 FDA reports)
ACUTE PRERENAL FAILURE ( 8 FDA reports)
ANAL FISTULA ( 8 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 8 FDA reports)
APNOEA ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BACK INJURY ( 8 FDA reports)
BLOOD COUNT ABNORMAL ( 8 FDA reports)
BONE MARROW DEPRESSION ( 8 FDA reports)
BREAST MASS ( 8 FDA reports)
BREAST PAIN ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 8 FDA reports)
CEREBELLAR HAEMORRHAGE ( 8 FDA reports)
CEREBRAL THROMBOSIS ( 8 FDA reports)
CHOKING SENSATION ( 8 FDA reports)
COMA HEPATIC ( 8 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 8 FDA reports)
CORONARY ARTERY RESTENOSIS ( 8 FDA reports)
DEAFNESS NEUROSENSORY ( 8 FDA reports)
DERMATITIS ALLERGIC ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DIVERTICULAR PERFORATION ( 8 FDA reports)
DROOLING ( 8 FDA reports)
DRUG ABUSER ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
EPICONDYLITIS ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
EROSIVE OESOPHAGITIS ( 8 FDA reports)
ESCHERICHIA INFECTION ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
FAT EMBOLISM ( 8 FDA reports)
GASTROINTESTINAL INFECTION ( 8 FDA reports)
GASTROINTESTINAL ULCER ( 8 FDA reports)
GINGIVITIS ( 8 FDA reports)
GLUCOSE URINE PRESENT ( 8 FDA reports)
HAEMATOCRIT INCREASED ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HAIR TEXTURE ABNORMAL ( 8 FDA reports)
HALLUCINATIONS, MIXED ( 8 FDA reports)
HEART RATE ABNORMAL ( 8 FDA reports)
HEPATIC MASS ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HERNIA ( 8 FDA reports)
HERNIA REPAIR ( 8 FDA reports)
HOARSENESS ( 8 FDA reports)
HUNGER ( 8 FDA reports)
HYPERBILIRUBINAEMIA ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
HYPOAESTHESIA FACIAL ( 8 FDA reports)
HYPOVOLAEMIC SHOCK ( 8 FDA reports)
IMMUNODEFICIENCY ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LIP OEDEMA ( 8 FDA reports)
LIVER TRANSPLANT REJECTION ( 8 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 8 FDA reports)
MALLORY-WEISS SYNDROME ( 8 FDA reports)
MENISCUS LESION ( 8 FDA reports)
METASTASIS ( 8 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 8 FDA reports)
METASTATIC NEOPLASM ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
MUSCULOSKELETAL DISORDER ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
ODYNOPHAGIA ( 8 FDA reports)
OEDEMA MUCOSAL ( 8 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 8 FDA reports)
OPTIC ATROPHY ( 8 FDA reports)
ORAL DISCOMFORT ( 8 FDA reports)
PARAPLEGIA ( 8 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
PLEURAL FIBROSIS ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 8 FDA reports)
POSTOPERATIVE INFECTION ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
QUALITY OF LIFE DECREASED ( 8 FDA reports)
RADIUS FRACTURE ( 8 FDA reports)
RAYNAUD'S PHENOMENON ( 8 FDA reports)
RESPIRATORY ALKALOSIS ( 8 FDA reports)
RETINAL DISORDER ( 8 FDA reports)
RETINAL VEIN OCCLUSION ( 8 FDA reports)
SCIATICA ( 8 FDA reports)
SCOTOMA ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SICK SINUS SYNDROME ( 8 FDA reports)
SINUS HEADACHE ( 8 FDA reports)
SKIN CANCER ( 8 FDA reports)
SKIN NECROSIS ( 8 FDA reports)
SNORING ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
TOOTH ABSCESS ( 8 FDA reports)
UPPER LIMB FRACTURE ( 8 FDA reports)
VIITH NERVE PARALYSIS ( 8 FDA reports)
WRIST FRACTURE ( 8 FDA reports)
REGURGITATION ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
SCAB ( 7 FDA reports)
SEQUESTRECTOMY ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
SKIN FLAP NECROSIS ( 7 FDA reports)
SKIN WRINKLING ( 7 FDA reports)
SKULL FRACTURE ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
STREPTOCOCCAL SEPSIS ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
SYNOVITIS ( 7 FDA reports)
TEMPORAL ARTERITIS ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
TUMOUR LYSIS SYNDROME ( 7 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 7 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 7 FDA reports)
URETHRAL HAEMORRHAGE ( 7 FDA reports)
VASCULAR CALCIFICATION ( 7 FDA reports)
VASOCONSTRICTION ( 7 FDA reports)
VASOSPASM ( 7 FDA reports)
VULVOVAGINAL PRURITUS ( 7 FDA reports)
WOUND INFECTION ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
YELLOW SKIN ( 7 FDA reports)
ABSCESS JAW ( 7 FDA reports)
ACCIDENT ( 7 FDA reports)
ALVEOLITIS ALLERGIC ( 7 FDA reports)
ANAEMIA MACROCYTIC ( 7 FDA reports)
ANEURYSM RUPTURED ( 7 FDA reports)
ARTERIAL THROMBOSIS ( 7 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 7 FDA reports)
BONE LESION ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
CACHEXIA ( 7 FDA reports)
CATHETER RELATED INFECTION ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
CERVICAL SPINAL STENOSIS ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHRONIC HEPATITIS ( 7 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
CORONARY ARTERY DISSECTION ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
DECEREBRATION ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DRUG LEVEL FLUCTUATING ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 7 FDA reports)
ENTEROCOLITIS ( 7 FDA reports)
ESSENTIAL HYPERTENSION ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
FACIAL PARESIS ( 7 FDA reports)
FAECALOMA ( 7 FDA reports)
FAILURE TO THRIVE ( 7 FDA reports)
FEEDING DISORDER ( 7 FDA reports)
FOOD ALLERGY ( 7 FDA reports)
GASTRIC MUCOSAL LESION ( 7 FDA reports)
GASTRIC ULCER PERFORATION ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
GYNAECOMASTIA ( 7 FDA reports)
HAEMOGLOBIN ( 7 FDA reports)
HEART INJURY ( 7 FDA reports)
HEART TRANSPLANT REJECTION ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HEPATIC HAEMORRHAGE ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HICCUPS ( 7 FDA reports)
HYPERPHOSPHATAEMIA ( 7 FDA reports)
HYPHAEMA ( 7 FDA reports)
HYPOTRICHOSIS ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
IMPAIRED SELF-CARE ( 7 FDA reports)
INJECTION SITE PRURITUS ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
JAW OPERATION ( 7 FDA reports)
JOINT ARTHROPLASTY ( 7 FDA reports)
JUGULAR VEIN DISTENSION ( 7 FDA reports)
LABILE BLOOD PRESSURE ( 7 FDA reports)
LIP DRY ( 7 FDA reports)
LIVER INJURY ( 7 FDA reports)
MAJOR DEPRESSION ( 7 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 7 FDA reports)
MEDICAL DEVICE COMPLICATION ( 7 FDA reports)
MENIERE'S DISEASE ( 7 FDA reports)
MITRAL VALVE PROLAPSE ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
MYOPIA ( 7 FDA reports)
NEPHROGENIC ANAEMIA ( 7 FDA reports)
NEPHROPATHY ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
OESOPHAGEAL DISORDER ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 7 FDA reports)
OROPHARYNGEAL SWELLING ( 7 FDA reports)
ORTHOPNOEA ( 7 FDA reports)
OSTEOSYNTHESIS ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PCO2 INCREASED ( 7 FDA reports)
PERIODONTAL DISEASE ( 7 FDA reports)
PERIODONTITIS ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
POLYARTHRITIS ( 7 FDA reports)
POOR PERSONAL HYGIENE ( 7 FDA reports)
PORTAL VEIN THROMBOSIS ( 7 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 7 FDA reports)
PROTEUS INFECTION ( 7 FDA reports)
ABDOMINAL HERNIA ( 6 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ABNORMAL SENSATION IN EYE ( 6 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
ADRENOGENITAL SYNDROME ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ALVEOLITIS FIBROSING ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ANISOCYTOSIS ( 6 FDA reports)
ANXIETY DISORDER ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
AORTIC DISORDER ( 6 FDA reports)
ARTERIAL HAEMORRHAGE ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 6 FDA reports)
BLOOD LACTIC ACID INCREASED ( 6 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 6 FDA reports)
BLOODY DISCHARGE ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
CALCULUS URETERIC ( 6 FDA reports)
CARDIAC ASTHMA ( 6 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 6 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 6 FDA reports)
COLLAPSE OF LUNG ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 6 FDA reports)
CYST ( 6 FDA reports)
DENTAL FISTULA ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DRUG INTERACTION POTENTIATION ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DYSLIPIDAEMIA ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
EJACULATION DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 6 FDA reports)
EMBOLISM ARTERIAL ( 6 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 6 FDA reports)
ENDOTRACHEAL INTUBATION ( 6 FDA reports)
ENTEROVESICAL FISTULA ( 6 FDA reports)
ERECTION INCREASED ( 6 FDA reports)
EROSIVE DUODENITIS ( 6 FDA reports)
EXANTHEM ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FOAMING AT MOUTH ( 6 FDA reports)
FRACTURED SACRUM ( 6 FDA reports)
FULL BLOOD COUNT DECREASED ( 6 FDA reports)
FURUNCLE ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
GASTRIC PERFORATION ( 6 FDA reports)
GASTRIC POLYPS ( 6 FDA reports)
GASTRITIS HAEMORRHAGIC ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GOITRE ( 6 FDA reports)
GRAFT THROMBOSIS ( 6 FDA reports)
HAEMOGLOBIN INCREASED ( 6 FDA reports)
HEAD DISCOMFORT ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATITIS C ( 6 FDA reports)
HERPES VIRUS INFECTION ( 6 FDA reports)
HOSTILITY ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPOPHOSPHATAEMIA ( 6 FDA reports)
ILIAC ARTERY STENOSIS ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
INDURATION ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
INJECTION SITE RASH ( 6 FDA reports)
INTRA-UTERINE DEATH ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
LEFT ATRIAL DILATATION ( 6 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LUNG ABSCESS ( 6 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 6 FDA reports)
MECHANICAL VENTILATION ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
METABOLIC SYNDROME ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MUCOSAL HAEMORRHAGE ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 6 FDA reports)
MUSCLE CONTRACTURE ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MYOCARDIAL RUPTURE ( 6 FDA reports)
NAIL DISORDER ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
NEUTROPHILIA ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 6 FDA reports)
OCULAR VASCULAR DISORDER ( 6 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 6 FDA reports)
OESOPHAGITIS ULCERATIVE ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
OSTEOMYELITIS CHRONIC ( 6 FDA reports)
OSTEOTOMY ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PEAU D'ORANGE ( 6 FDA reports)
PERIORBITAL HAEMATOMA ( 6 FDA reports)
PERITONEAL HAEMORRHAGE ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
PHYSICAL DISABILITY ( 6 FDA reports)
PLASMACYTOMA ( 6 FDA reports)
PO2 INCREASED ( 6 FDA reports)
POISONING ( 6 FDA reports)
POLYMYALGIA RHEUMATICA ( 6 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 6 FDA reports)
POST PROCEDURAL PAIN ( 6 FDA reports)
POSTURE ABNORMAL ( 6 FDA reports)
PULSE PRESSURE DECREASED ( 6 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 6 FDA reports)
PUPILS UNEQUAL ( 6 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SKIN WARM ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 6 FDA reports)
SOFT TISSUE INJURY ( 6 FDA reports)
SPLINTER HAEMORRHAGES ( 6 FDA reports)
SPONTANEOUS HAEMATOMA ( 6 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 6 FDA reports)
STREPTOCOCCAL INFECTION ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
SUPERINFECTION ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 6 FDA reports)
TONGUE HAEMORRHAGE ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 6 FDA reports)
TUMOUR NECROSIS ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
URINE KETONE BODY PRESENT ( 6 FDA reports)
UTERINE CANCER ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VITAMIN D DECREASED ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RESPIRATORY RATE DECREASED ( 5 FDA reports)
RESPIRATORY TRACT CONGESTION ( 5 FDA reports)
RHINITIS ALLERGIC ( 5 FDA reports)
SCOLIOSIS ( 5 FDA reports)
SENSATION OF PRESSURE ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
SPUTUM RETENTION ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 5 FDA reports)
STUPOR ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
TELANGIECTASIA ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 5 FDA reports)
TRAUMATIC HAEMATOMA ( 5 FDA reports)
TRAUMATIC HAEMORRHAGE ( 5 FDA reports)
TRIGEMINAL NEURALGIA ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
URINARY HESITATION ( 5 FDA reports)
URINE ABNORMALITY ( 5 FDA reports)
UTERINE LEIOMYOMA ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VASCULAR STENOSIS ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL MASS ( 5 FDA reports)
ACQUIRED HAEMOPHILIA ( 5 FDA reports)
ACTINIC KERATOSIS ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
ALBUMIN URINE PRESENT ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
AMPUTATION ( 5 FDA reports)
ANASTOMOTIC COMPLICATION ( 5 FDA reports)
ANORGASMIA ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 5 FDA reports)
AORTIC OCCLUSION ( 5 FDA reports)
APHAGIA ( 5 FDA reports)
APHONIA ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
APRAXIA ( 5 FDA reports)
ARTERIAL BYPASS OPERATION ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BENIGN RENAL NEOPLASM ( 5 FDA reports)
BILIARY COLIC ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
BLOOD OSMOLARITY INCREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
BRAIN NEOPLASM ( 5 FDA reports)
BRAIN SCAN ABNORMAL ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BREAST TENDERNESS ( 5 FDA reports)
BRONCHIAL INFECTION ( 5 FDA reports)
BRONCHITIS CHRONIC ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CARBON DIOXIDE DECREASED ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CEREBELLAR SYNDROME ( 5 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 5 FDA reports)
CERUMEN IMPACTION ( 5 FDA reports)
CHAPPED LIPS ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 5 FDA reports)
CLONUS ( 5 FDA reports)
CLOSTRIDIUM COLITIS ( 5 FDA reports)
CONTRAST MEDIA REACTION ( 5 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
DETOXIFICATION ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIABETIC COMPLICATION ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
DYSENTERY ( 5 FDA reports)
EJACULATION FAILURE ( 5 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 5 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 5 FDA reports)
EXPIRED DRUG ADMINISTERED ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
FAILURE OF IMPLANT ( 5 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 5 FDA reports)
FOETAL CARDIAC DISORDER ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
FOOD POISONING ( 5 FDA reports)
FOOT AMPUTATION ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 5 FDA reports)
GASTRIC INFECTION ( 5 FDA reports)
GASTROENTERITIS RADIATION ( 5 FDA reports)
GASTROINTESTINAL NEOPLASM ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GINGIVAL ULCERATION ( 5 FDA reports)
HAEMATOMA INFECTION ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAIR GROWTH ABNORMAL ( 5 FDA reports)
HAND FRACTURE ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPOCHROMASIA ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
IMPLANT SITE INFECTION ( 5 FDA reports)
IMPRISONMENT ( 5 FDA reports)
INCISION SITE COMPLICATION ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INJECTION SITE INDURATION ( 5 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
INTESTINAL POLYP ( 5 FDA reports)
IRIS DISORDER ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
ISCHAEMIC HEPATITIS ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
LARYNGITIS ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
METAPLASIA ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MORBID THOUGHTS ( 5 FDA reports)
MUCOSAL DRYNESS ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MUSCLE SWELLING ( 5 FDA reports)
MYELOFIBROSIS ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
NASAL DISCOMFORT ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 5 FDA reports)
NEURODERMATITIS ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
NICOTINE DEPENDENCE ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OPTIC NERVE INJURY ( 5 FDA reports)
ORAL FUNGAL INFECTION ( 5 FDA reports)
OSTEITIS ( 5 FDA reports)
OVERWEIGHT ( 5 FDA reports)
PACEMAKER COMPLICATION ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PANIC REACTION ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PERIANAL ABSCESS ( 5 FDA reports)
PERIARTHRITIS ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
PLEUROTHOTONUS ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
POSTINFARCTION ANGINA ( 5 FDA reports)
POSTOPERATIVE ILEUS ( 5 FDA reports)
PROCEDURAL PAIN ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PROSTATE CANCER RECURRENT ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PROSTATISM ( 5 FDA reports)
PROTEIN URINE ( 5 FDA reports)
PULMONARY HILUM MASS ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
PYELONEPHRITIS ACUTE ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABDOMINAL WALL INFECTION ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ALDOLASE INCREASED ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ALLERGY TO CHEMICALS ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAESTHETIC COMPLICATION ( 4 FDA reports)
ANTEROGRADE AMNESIA ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
AORTIC CALCIFICATION ( 4 FDA reports)
APPENDICECTOMY ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
AURA ( 4 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BIOPSY BREAST ABNORMAL ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD TRIGLYCERIDES ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN STEM ISCHAEMIA ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BREAST SWELLING ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARDIAC HYPERTROPHY ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CHOROIDAL HAEMORRHAGE ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
COUGH DECREASED ( 4 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DEMENTIA WITH LEWY BODIES ( 4 FDA reports)
DENTAL TREATMENT ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
DYSMENORRHOEA ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
DYSTROPHIC CALCIFICATION ( 4 FDA reports)
EAR PRURITUS ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FACTOR VIII DEFICIENCY ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
FOETAL HEART RATE ABNORMAL ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL INJURY ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENERAL SYMPTOM ( 4 FDA reports)
GINGIVAL INFECTION ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GLIOBLASTOMA MULTIFORME ( 4 FDA reports)
GLOBAL AMNESIA ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HAEMATOCRIT ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEARING AID USER ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC HAEMATOMA ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATORENAL FAILURE ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HISTOLOGY ABNORMAL ( 4 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HOSPITALISATION ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERCHROMIC ANAEMIA ( 4 FDA reports)
HYPERCOAGULATION ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPERLACTACIDAEMIA ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPERPARATHYROIDISM ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
IMMUNOGLOBULINS INCREASED ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INJECTION SITE BRUISING ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
KNEE OPERATION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEUKOCYTURIA ( 4 FDA reports)
LICHENOID KERATOSIS ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LIMB OPERATION ( 4 FDA reports)
LIP DISORDER ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
MALABSORPTION ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
MESENTERIC OCCLUSION ( 4 FDA reports)
MESOTHELIOMA ( 4 FDA reports)
METASTASES TO ADRENALS ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
MICTURITION DISORDER ( 4 FDA reports)
MIDDLE LOBE SYNDROME ( 4 FDA reports)
MIGRAINE WITH AURA ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MONARTHRITIS ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MULTIPLE ALLERGIES ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 4 FDA reports)
NASAL INFLAMMATION ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEURITIS ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
ORAL HERPES ( 4 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PHANTOM PAIN ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PNEUMOPERICARDIUM ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
POSTPARTUM HAEMORRHAGE ( 4 FDA reports)
POTENTIATING DRUG INTERACTION ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
PROSTATE CANCER METASTATIC ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PROSTHESIS IMPLANTATION ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
RADICULOPATHY ( 4 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 4 FDA reports)
RETINAL ARTERY OCCLUSION ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RETINAL VASCULAR DISORDER ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SEBORRHOEIC KERATOSIS ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEPTIC EMBOLUS ( 4 FDA reports)
SEROMA ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SLEEP WALKING ( 4 FDA reports)
SMOKER ( 4 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 4 FDA reports)
SOMNAMBULISM ( 4 FDA reports)
SPINAL CORD HAEMORRHAGE ( 4 FDA reports)
STOOL PH DECREASED ( 4 FDA reports)
SYNOVIAL CYST ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
TENDON PAIN ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
TETANY ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
THROMBOLYSIS ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
THYROIDITIS ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE CYST ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TOXIC SHOCK SYNDROME ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER REGIONAL ( 4 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 4 FDA reports)
URINE FLOW DECREASED ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
URINOMA ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VASCULAR INJURY ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VITRECTOMY ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
WEST NILE VIRAL INFECTION ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
YAWNING ( 4 FDA reports)
PYURIA ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RADICULITIS CERVICAL ( 3 FDA reports)
RADICULITIS LUMBOSACRAL ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
REPETITIVE SPEECH ( 3 FDA reports)
RETINAL ARTERY EMBOLISM ( 3 FDA reports)
RETINAL DEPOSITS ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RETROGRADE AMNESIA ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
ROULEAUX FORMATION ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SERRATIA BACTERAEMIA ( 3 FDA reports)
SHUNT OCCLUSION ( 3 FDA reports)
SINOATRIAL BLOCK ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN NEOPLASM EXCISION ( 3 FDA reports)
SKIN ODOUR ABNORMAL ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL CORD INFARCTION ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SPINAL LAMINECTOMY ( 3 FDA reports)
SPINAL OPERATION ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SURGICAL STAPLING ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TACHYCARDIA FOETAL ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THYROXINE DECREASED ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
URETHRAL INJURY ( 3 FDA reports)
URETHRAL STRICTURE ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINE CALCIUM INCREASED ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VASCULAR ENCEPHALOPATHY ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VENTRICULAR ASYSTOLE ( 3 FDA reports)
VISUAL BRIGHTNESS ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WOUND COMPLICATION ( 3 FDA reports)
ABDOMINAL ABSCESS ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL CHEST SOUND ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACANTHOLYSIS ( 3 FDA reports)
ACCOMMODATION DISORDER ( 3 FDA reports)
ACTINOMYCOSIS ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
AGORAPHOBIA ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANIMAL BITE ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANORECTAL OPERATION ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 3 FDA reports)
APPLICATION SITE PAIN ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL STENT INSERTION ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATRIAL TACHYCARDIA ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BITE ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLADDER TAMPONADE ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD ALCOHOL INCREASED ( 3 FDA reports)
BLOOD AMYLASE DECREASED ( 3 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BLOOD URIC ACID DECREASED ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BRAIN STEM STROKE ( 3 FDA reports)
BREAST CYST ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
BUNION ( 3 FDA reports)
BURNS SECOND DEGREE ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CATARACT OPERATION COMPLICATION ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
COLITIS MICROSCOPIC ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
COMPLICATED FRACTURE ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 3 FDA reports)
COOMBS TEST POSITIVE ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORONARY ARTERY REOCCLUSION ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CRANIOPHARYNGIOMA ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CUTANEOUS VASCULITIS ( 3 FDA reports)
CYSTOCELE ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DROP ATTACKS ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DUODENAL OBSTRUCTION ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
EAR INJURY ( 3 FDA reports)
ECZEMA NUMMULAR ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXERCISE TEST ABNORMAL ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EYE ALLERGY ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FEELING HOT AND COLD ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
GASTRIC ATONY ( 3 FDA reports)
GASTRIC ULCER HELICOBACTER ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GASTROSTOMY ( 3 FDA reports)
GENERAL ANAESTHESIA ( 3 FDA reports)
GROIN INFECTION ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMATOMA EVACUATION ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HEART TRANSPLANT ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATITIS VIRAL ( 3 FDA reports)
HEPATOBLASTOMA ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERNIA OBSTRUCTIVE ( 3 FDA reports)
HISTIOCYTOSIS ( 3 FDA reports)
HISTOPLASMOSIS ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPOCAPNIA ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
ILIAC ARTERY OCCLUSION ( 3 FDA reports)
ILIAC ARTERY THROMBOSIS ( 3 FDA reports)
IMPLANT SITE DISCHARGE ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTESTINAL MASS ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
JAW LESION EXCISION ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JOINT STABILISATION ( 3 FDA reports)
KAWASAKI'S DISEASE ( 3 FDA reports)
KERATOSIS FOLLICULAR ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LERICHE SYNDROME ( 3 FDA reports)
LIFE EXPECTANCY SHORTENED ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
MECHANICAL ILEUS ( 3 FDA reports)
MEDIASTINUM NEOPLASM ( 3 FDA reports)
MEDICAL DEVICE REMOVAL ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
METASTATIC UTERINE CANCER ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
MICROALBUMINURIA ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MORTON'S NEUROMA ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYASTHENIA GRAVIS ( 3 FDA reports)
MYASTHENIC SYNDROME ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 3 FDA reports)
MYOGLOBINURIA ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NASAL OPERATION ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESOPHAGEAL SPASM ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
OROPHARYNGEAL PLAQUE ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OVARIAN CYST ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PELVIC HAEMATOMA ( 3 FDA reports)
PENILE PAIN ( 3 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
POLYCHROMASIA ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYMERASE CHAIN REACTION ( 3 FDA reports)
POLYSUBSTANCE ABUSE ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POST PROCEDURAL VOMITING ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROSTATIC ADENOMA ( 3 FDA reports)
PSEUDODEMENTIA ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSEUDOPORPHYRIA ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY RADIATION INJURY ( 3 FDA reports)
ABDOMINAL INFECTION ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 2 FDA reports)
ALVEOLAR PROTEINOSIS ( 2 FDA reports)
AMBLYOPIA STRABISMIC ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL NEOPLASM ( 2 FDA reports)
ANAL PRURITUS ( 2 FDA reports)
ANAL SPHINCTER ATONY ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANION GAP ABNORMAL ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANTERIOR CHAMBER DISORDER ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
AORTO-DUODENAL FISTULA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE DISCHARGE ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARRHYTHMIA NEONATAL ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTOMATIC BLADDER ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 2 FDA reports)
BENIGN PERITONEAL NEOPLASM ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD CAFFEINE INCREASED ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY MASS INDEX DECREASED ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRACHYCEPHALY ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST RECONSTRUCTION ( 2 FDA reports)
BREATH SOUNDS DECREASED ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CAMPTODACTYLY CONGENITAL ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONAL EVOLUTION ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLOBOMA ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
CONNECTIVE TISSUE DISORDER ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CONUS MEDULLARIS SYNDROME ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIAL NERVE INFECTION ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIET NONCOMPLIANCE ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DIFFUSE AXONAL INJURY ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSLOGIA ( 2 FDA reports)
DYSSOMNIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ELECTIVE SURGERY ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXCESSIVE EXERCISE ( 2 FDA reports)
EXCHANGE BLOOD TRANSFUSION ( 2 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
FACTOR XIII DEFICIENCY ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEMORAL ARTERY DISSECTION ( 2 FDA reports)
FEMORAL NERVE INJURY ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER EMPYEMA ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GLYCOGEN STORAGE DISORDER ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEAD BANGING ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATIC SIDEROSIS ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS E ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HERPETIC STOMATITIS ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HOMOSEXUALITY ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
INCISIONAL HERNIA REPAIR ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INFECTIOUS DISEASE CARRIER ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE SCAB ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTESTINAL STOMA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
KARNOFSKY SCALE WORSENED ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
LARYNGITIS BACTERIAL ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOSS OF BLADDER SENSATION ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE COUNT ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MALE ORGASMIC DISORDER ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MEDIAN NERVE INJURY ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTASES TO STOMACH ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MINOR COGNITIVE MOTOR DISORDER ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MOANING ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NELSON'S SYNDROME ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEONATAL HYPOXIA ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEUROGLYCOPENIA ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NEUROMUSCULAR BLOCKADE ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NIPPLE SWELLING ( 2 FDA reports)
NITRITOID CRISIS ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
OPTIC NERVE INFARCTION ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOARTHROPATHY ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OVERSENSING ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PALLANAESTHESIA ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERFORATED DUODENAL ULCER REPAIR ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIORBITAL ABSCESS ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL HAEMATOMA ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PH URINE DECREASED ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHARYNGEAL HAEMATOMA ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POST PROCEDURAL BILE LEAK ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL SEPSIS ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRESBYOPIA ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROSTATIC CALCIFICATION ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDOPOLYPOSIS ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYOMYOSITIS ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIATION ASSOCIATED PAIN ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL CYST RUPTURED ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL LYMPHOCELE ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
REOCCLUSION ( 2 FDA reports)
REPERFUSION ARRHYTHMIA ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SERUM SEROTONIN INCREASED ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SMALL CELL CARCINOMA ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 2 FDA reports)
SPINAL CORD OPERATION ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPLENIC HAEMATOMA ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SUPRAPUBIC PAIN ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
TESTICULAR HAEMORRHAGE ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYROID OPERATION ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TIC ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TUBO-OVARIAN ABSCESS ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
URAEMIC ENCEPHALOPATHY ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URINARY FISTULA ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS RECANALISATION ( 2 FDA reports)
VERBAL ABUSE ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VULVOVAGINAL ERYTHEMA ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WOUND CLOSURE ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RADIOULNAR SYNOSTOSIS ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH PSORIAFORM ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCLERAL OPERATION ( 1 FDA reports)
SEBACEOUS GLAND DISORDER ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SECONDARY HYPOTHYROIDISM ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN VOLUME ABNORMAL ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 1 FDA reports)
SHUNT BLOOD FLOW EXCESSIVE ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINGLE VESSEL BYPASS GRAFT ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN CYST EXCISION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 1 FDA reports)
SPINAL LIGAMENT OPERATION ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STENT EMBOLISATION ( 1 FDA reports)
STENT-GRAFT MALFUNCTION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRANGURY ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SYMPATHECTOMY ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST DECREASED ( 1 FDA reports)
TENDON SHEATH LESION EXCISION ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC HYPOTHERMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBIN TIME SHORTENED ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID HAEMORRHAGE ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTH REPAIR ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC DILATATION OF COLON ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UBIQUINONE DECREASED ( 1 FDA reports)
ULTRASOUND KIDNEY ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL PAPILLOMA ( 1 FDA reports)
URETHRAL PERFORATION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT MALFORMATION ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VAGINAL OPERATION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS STASIS RETINOPATHY ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR CISTERNOSTOMY ( 1 FDA reports)
VENTRICULAR DRAINAGE ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN K INCREASED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WORD SALAD ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL CYST ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENOCORTICAL CARCINOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY ( 1 FDA reports)
ANTI-SS-B ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE MIXED ( 1 FDA reports)
AORTO-ILIAC ARTERIAL STENOSIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTERITIS CORONARY ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASHERMAN'S SYNDROME ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA STAGE IV ( 1 FDA reports)
BABINSKI REFLEX TEST ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN MESOTHELIOMA ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY LIP ( 1 FDA reports)
BIOPSY RECTUM ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER CANCER STAGE II ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLADDER CATHETER PERMANENT ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD COPPER ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE OPERATION ( 1 FDA reports)
BORDERLINE OVARIAN TUMOUR ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVASCULAR EVENT PROPHYLAXIS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL DECOMPRESSION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR OPERATION ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHORDOMA ( 1 FDA reports)
CHOROIDAL EFFUSION ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLINODACTYLY ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMPLEMENT FACTOR C1 DECREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL NEOPLASM ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTRAINDICATION TO VACCINATION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CSF PRESSURE ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DELAYED SLEEP PHASE ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DENTAL CARE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELDER ABUSE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROPHORESIS ( 1 FDA reports)
ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENLARGED CEREBRAL PERIVASCULAR SPACES ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCLYSIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILS URINE ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIDIDYMAL CYST ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPLORATORY OPERATION ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACE LIFT ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL HEMIPLEGIC MIGRAINE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRITIS FUNGAL ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GENDER IDENTITY DISORDER ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIAL SCAR ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATINURIA ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOGLOBINOPATHY ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATION, GUSTATORY ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HAND DERMATITIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC INFECTION BACTERIAL ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMUNISATION REACTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG THERAPY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INNER EAR INFLAMMATION ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
ITCHING SCAR ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LENTICULAR PIGMENTATION ( 1 FDA reports)
LEUKAEMIC INFILTRATION ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LITHOTRIPSY ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA RECURRENT ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LUPUS VASCULITIS ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
LYMPHOMA TRANSFORMATION ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT NEOPLASM OF CORNEA ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGIOMA MALIGNANT ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CHEMICAL ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASES TO THORAX ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUMPS ANTIBODY TEST POSITIVE ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FIBROSIS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NITRITOID REACTION ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NODULAR VASCULITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
ORAL MUCOSA ATROPHY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OVERWORK ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PAINFUL RESPONSE TO NORMAL STIMULI ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC LEAK ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLARY MUSCLE HAEMORRHAGE ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL PRESSOR RESPONSE ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARASPINAL ABSCESS ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE BULBAR PALSY ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE INFECTION ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use