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

DYSPNOEA ( 1240 FDA reports)
RENAL FAILURE ACUTE ( 1208 FDA reports)
HYPERKALAEMIA ( 1106 FDA reports)
ANAEMIA ( 920 FDA reports)
OEDEMA PERIPHERAL ( 913 FDA reports)
NAUSEA ( 894 FDA reports)
RENAL FAILURE ( 891 FDA reports)
DIARRHOEA ( 884 FDA reports)
ASTHENIA ( 850 FDA reports)
DRUG INTERACTION ( 812 FDA reports)
VOMITING ( 811 FDA reports)
FATIGUE ( 793 FDA reports)
CARDIAC FAILURE ( 780 FDA reports)
HYPOTENSION ( 770 FDA reports)
DEHYDRATION ( 765 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 746 FDA reports)
PAIN ( 743 FDA reports)
PYREXIA ( 742 FDA reports)
PNEUMONIA ( 714 FDA reports)
FALL ( 708 FDA reports)
DIZZINESS ( 692 FDA reports)
MALAISE ( 667 FDA reports)
HYPONATRAEMIA ( 665 FDA reports)
ANXIETY ( 583 FDA reports)
ASCITES ( 570 FDA reports)
CONDITION AGGRAVATED ( 560 FDA reports)
BLOOD CREATININE INCREASED ( 548 FDA reports)
ATRIAL FIBRILLATION ( 533 FDA reports)
PLEURAL EFFUSION ( 516 FDA reports)
DEATH ( 490 FDA reports)
PLATELET COUNT DECREASED ( 481 FDA reports)
CONFUSIONAL STATE ( 469 FDA reports)
DECREASED APPETITE ( 469 FDA reports)
HYPERTENSION ( 467 FDA reports)
BRADYCARDIA ( 465 FDA reports)
CHEST PAIN ( 463 FDA reports)
THROMBOCYTOPENIA ( 429 FDA reports)
RENAL IMPAIRMENT ( 427 FDA reports)
HEADACHE ( 426 FDA reports)
ABDOMINAL PAIN ( 420 FDA reports)
WEIGHT DECREASED ( 418 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 412 FDA reports)
HEPATIC ENCEPHALOPATHY ( 404 FDA reports)
BACK PAIN ( 403 FDA reports)
COUGH ( 400 FDA reports)
URINARY TRACT INFECTION ( 395 FDA reports)
RASH ( 387 FDA reports)
HAEMOGLOBIN DECREASED ( 370 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 370 FDA reports)
PAIN IN EXTREMITY ( 369 FDA reports)
MYOCARDIAL INFARCTION ( 368 FDA reports)
INJURY ( 367 FDA reports)
SYNCOPE ( 364 FDA reports)
BLOOD UREA INCREASED ( 361 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 360 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 357 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 349 FDA reports)
DEPRESSION ( 344 FDA reports)
WEIGHT INCREASED ( 343 FDA reports)
SOMNOLENCE ( 340 FDA reports)
ARTHRALGIA ( 332 FDA reports)
OEDEMA ( 331 FDA reports)
DRUG INEFFECTIVE ( 321 FDA reports)
HEPATIC FAILURE ( 321 FDA reports)
RESPIRATORY FAILURE ( 314 FDA reports)
INTERSTITIAL LUNG DISEASE ( 310 FDA reports)
SEPSIS ( 308 FDA reports)
CARDIAC ARREST ( 307 FDA reports)
BLOOD GLUCOSE INCREASED ( 303 FDA reports)
CARDIOMEGALY ( 302 FDA reports)
LIVER DISORDER ( 301 FDA reports)
CONSTIPATION ( 299 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 296 FDA reports)
PALPITATIONS ( 295 FDA reports)
LOSS OF CONSCIOUSNESS ( 289 FDA reports)
MULTI-ORGAN FAILURE ( 288 FDA reports)
HYPOKALAEMIA ( 286 FDA reports)
PRURITUS ( 285 FDA reports)
HYPOGLYCAEMIA ( 281 FDA reports)
PULMONARY HYPERTENSION ( 270 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 265 FDA reports)
ARRHYTHMIA ( 261 FDA reports)
BLOOD PRESSURE DECREASED ( 251 FDA reports)
ABDOMINAL PAIN UPPER ( 247 FDA reports)
MITRAL VALVE INCOMPETENCE ( 242 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 238 FDA reports)
BLOOD BILIRUBIN INCREASED ( 235 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 234 FDA reports)
DIABETES MELLITUS ( 233 FDA reports)
VENTRICULAR TACHYCARDIA ( 231 FDA reports)
GAIT DISTURBANCE ( 228 FDA reports)
ECONOMIC PROBLEM ( 227 FDA reports)
INSOMNIA ( 227 FDA reports)
MUSCLE SPASMS ( 225 FDA reports)
CEREBROVASCULAR ACCIDENT ( 224 FDA reports)
PULMONARY OEDEMA ( 224 FDA reports)
CARDIO-RESPIRATORY ARREST ( 221 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 220 FDA reports)
CARDIAC DISORDER ( 219 FDA reports)
HYPOAESTHESIA ( 214 FDA reports)
ABDOMINAL DISTENSION ( 213 FDA reports)
BLOOD POTASSIUM INCREASED ( 212 FDA reports)
HEPATIC CIRRHOSIS ( 211 FDA reports)
FEELING ABNORMAL ( 208 FDA reports)
CELLULITIS ( 204 FDA reports)
BRONCHITIS ( 199 FDA reports)
INFECTION ( 199 FDA reports)
BLOOD PRESSURE INCREASED ( 198 FDA reports)
CARDIOMYOPATHY ( 197 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 197 FDA reports)
ERYTHEMA ( 197 FDA reports)
UNEVALUABLE EVENT ( 195 FDA reports)
CORONARY ARTERY DISEASE ( 194 FDA reports)
EMOTIONAL DISTRESS ( 194 FDA reports)
TACHYCARDIA ( 193 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 190 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 189 FDA reports)
DISEASE PROGRESSION ( 188 FDA reports)
DEEP VEIN THROMBOSIS ( 186 FDA reports)
ANHEDONIA ( 184 FDA reports)
PANCYTOPENIA ( 181 FDA reports)
RENAL DISORDER ( 179 FDA reports)
ANOREXIA ( 178 FDA reports)
CHOLELITHIASIS ( 177 FDA reports)
HYPOXIA ( 176 FDA reports)
ENCEPHALOPATHY ( 175 FDA reports)
PULMONARY EMBOLISM ( 175 FDA reports)
JAUNDICE ( 174 FDA reports)
BLOOD SODIUM DECREASED ( 173 FDA reports)
EPISTAXIS ( 173 FDA reports)
HAEMORRHAGE ( 171 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 171 FDA reports)
RHABDOMYOLYSIS ( 171 FDA reports)
ASTHMA ( 170 FDA reports)
CHEST DISCOMFORT ( 170 FDA reports)
DYSPNOEA EXERTIONAL ( 170 FDA reports)
DYSPHONIA ( 169 FDA reports)
RENAL FAILURE CHRONIC ( 167 FDA reports)
VISION BLURRED ( 166 FDA reports)
HYPERHIDROSIS ( 165 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 165 FDA reports)
FLUID RETENTION ( 164 FDA reports)
HEART RATE INCREASED ( 164 FDA reports)
MYALGIA ( 163 FDA reports)
DYSPHAGIA ( 162 FDA reports)
OVERDOSE ( 162 FDA reports)
RIGHT VENTRICULAR FAILURE ( 162 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 162 FDA reports)
SEPTIC SHOCK ( 161 FDA reports)
MULTIPLE INJURIES ( 158 FDA reports)
MUSCULAR WEAKNESS ( 157 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 155 FDA reports)
HYPERGLYCAEMIA ( 153 FDA reports)
NEUTROPENIA ( 152 FDA reports)
CONVULSION ( 150 FDA reports)
TREMOR ( 150 FDA reports)
OSTEONECROSIS OF JAW ( 149 FDA reports)
CONTUSION ( 148 FDA reports)
NEUROPATHY PERIPHERAL ( 147 FDA reports)
PARAESTHESIA ( 147 FDA reports)
HAEMATOCRIT DECREASED ( 145 FDA reports)
OSTEOARTHRITIS ( 143 FDA reports)
DISORIENTATION ( 142 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 141 FDA reports)
EJECTION FRACTION DECREASED ( 141 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 140 FDA reports)
ATELECTASIS ( 139 FDA reports)
NASOPHARYNGITIS ( 139 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 138 FDA reports)
SINUSITIS ( 136 FDA reports)
VENTRICULAR FIBRILLATION ( 136 FDA reports)
ABDOMINAL DISCOMFORT ( 135 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 135 FDA reports)
GENERALISED OEDEMA ( 133 FDA reports)
PERICARDIAL EFFUSION ( 133 FDA reports)
RESPIRATORY DISTRESS ( 133 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 131 FDA reports)
LEUKOPENIA ( 130 FDA reports)
SHOCK ( 129 FDA reports)
SKIN ULCER ( 129 FDA reports)
BONE DISORDER ( 128 FDA reports)
OSTEOMYELITIS ( 128 FDA reports)
OXYGEN SATURATION DECREASED ( 128 FDA reports)
PROTHROMBIN TIME PROLONGED ( 127 FDA reports)
BLOOD POTASSIUM DECREASED ( 126 FDA reports)
MELAENA ( 126 FDA reports)
LETHARGY ( 124 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 121 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 121 FDA reports)
PULMONARY CONGESTION ( 120 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 119 FDA reports)
CEREBRAL INFARCTION ( 118 FDA reports)
HYPERLIPIDAEMIA ( 118 FDA reports)
INFLUENZA ( 118 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 117 FDA reports)
CARDIOGENIC SHOCK ( 117 FDA reports)
FLUID OVERLOAD ( 117 FDA reports)
CATARACT ( 116 FDA reports)
GASTRIC ULCER ( 116 FDA reports)
HAEMOPTYSIS ( 116 FDA reports)
MENTAL STATUS CHANGES ( 115 FDA reports)
STRESS ( 115 FDA reports)
FEAR ( 114 FDA reports)
PAIN IN JAW ( 114 FDA reports)
LUNG DISORDER ( 112 FDA reports)
CHILLS ( 111 FDA reports)
COMA ( 111 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 111 FDA reports)
TREATMENT NONCOMPLIANCE ( 111 FDA reports)
ALOPECIA ( 110 FDA reports)
TOOTHACHE ( 109 FDA reports)
BALANCE DISORDER ( 108 FDA reports)
CARDIAC MURMUR ( 108 FDA reports)
NECK PAIN ( 108 FDA reports)
HYPOPHAGIA ( 107 FDA reports)
METABOLIC ACIDOSIS ( 106 FDA reports)
RECTAL HAEMORRHAGE ( 106 FDA reports)
SURGERY ( 106 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 106 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 105 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 104 FDA reports)
AGRANULOCYTOSIS ( 103 FDA reports)
HAEMATOMA ( 103 FDA reports)
INCORRECT DOSE ADMINISTERED ( 103 FDA reports)
ORTHOPNOEA ( 103 FDA reports)
PANCREATITIS ( 103 FDA reports)
STAPHYLOCOCCAL INFECTION ( 103 FDA reports)
HEPATITIS ( 102 FDA reports)
ANGINA PECTORIS ( 101 FDA reports)
ARTHRITIS ( 100 FDA reports)
BONE PAIN ( 98 FDA reports)
CYTOLYTIC HEPATITIS ( 98 FDA reports)
HAEMATURIA ( 98 FDA reports)
HIATUS HERNIA ( 98 FDA reports)
OSTEONECROSIS ( 98 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 96 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 96 FDA reports)
GASTRITIS ( 96 FDA reports)
VERTIGO ( 96 FDA reports)
MUSCULOSKELETAL PAIN ( 95 FDA reports)
PURPURA ( 95 FDA reports)
GASTROENTERITIS ( 94 FDA reports)
THROMBOSIS ( 94 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 94 FDA reports)
COAGULOPATHY ( 93 FDA reports)
WHEEZING ( 93 FDA reports)
STOMATITIS ( 92 FDA reports)
HEPATIC ENZYME INCREASED ( 91 FDA reports)
RENAL INJURY ( 91 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 90 FDA reports)
DYSPEPSIA ( 90 FDA reports)
HYPERSENSITIVITY ( 90 FDA reports)
LUNG INFILTRATION ( 90 FDA reports)
NEOPLASM MALIGNANT ( 90 FDA reports)
NEUTROPHIL COUNT DECREASED ( 90 FDA reports)
STEVENS-JOHNSON SYNDROME ( 90 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 89 FDA reports)
HAEMODIALYSIS ( 89 FDA reports)
INFLAMMATION ( 89 FDA reports)
PRESYNCOPE ( 89 FDA reports)
SINUS BRADYCARDIA ( 89 FDA reports)
SWELLING ( 89 FDA reports)
BLOOD ALBUMIN DECREASED ( 88 FDA reports)
CARDIOVASCULAR DISORDER ( 88 FDA reports)
HYPOTHYROIDISM ( 87 FDA reports)
LYMPHADENOPATHY ( 87 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 87 FDA reports)
IMPAIRED HEALING ( 86 FDA reports)
SPEECH DISORDER ( 86 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 85 FDA reports)
DIALYSIS ( 85 FDA reports)
ABASIA ( 84 FDA reports)
HEPATOMEGALY ( 84 FDA reports)
RESPIRATORY ARREST ( 84 FDA reports)
ARTERIOSCLEROSIS ( 83 FDA reports)
DEVICE MALFUNCTION ( 83 FDA reports)
OFF LABEL USE ( 83 FDA reports)
AGITATION ( 82 FDA reports)
LACTIC ACIDOSIS ( 82 FDA reports)
PNEUMONIA ASPIRATION ( 82 FDA reports)
BLISTER ( 81 FDA reports)
DECREASED INTEREST ( 81 FDA reports)
HEART RATE IRREGULAR ( 81 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 81 FDA reports)
TOXIC SKIN ERUPTION ( 81 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 80 FDA reports)
SLEEP APNOEA SYNDROME ( 80 FDA reports)
JOINT SWELLING ( 79 FDA reports)
MYOCARDIAL ISCHAEMIA ( 79 FDA reports)
MEMORY IMPAIRMENT ( 78 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 78 FDA reports)
DELIRIUM ( 77 FDA reports)
DRUG ERUPTION ( 77 FDA reports)
DRY MOUTH ( 77 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 77 FDA reports)
PANCREATITIS ACUTE ( 77 FDA reports)
AMNESIA ( 76 FDA reports)
HEART RATE DECREASED ( 76 FDA reports)
HYPOVOLAEMIA ( 76 FDA reports)
PRODUCTIVE COUGH ( 76 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 76 FDA reports)
CHOLESTASIS ( 75 FDA reports)
TRANSAMINASES INCREASED ( 75 FDA reports)
DRUG HYPERSENSITIVITY ( 74 FDA reports)
ECZEMA ( 74 FDA reports)
HAEMATEMESIS ( 74 FDA reports)
HEPATIC STEATOSIS ( 74 FDA reports)
RALES ( 74 FDA reports)
SPLENOMEGALY ( 74 FDA reports)
AORTIC VALVE INCOMPETENCE ( 73 FDA reports)
ATRIOVENTRICULAR BLOCK ( 73 FDA reports)
HYPOAESTHESIA ORAL ( 73 FDA reports)
HYPOALBUMINAEMIA ( 73 FDA reports)
OBESITY ( 73 FDA reports)
ORTHOSTATIC HYPOTENSION ( 73 FDA reports)
HALLUCINATION ( 72 FDA reports)
METASTASES TO BONE ( 72 FDA reports)
ARTHROPATHY ( 71 FDA reports)
ELECTROLYTE IMBALANCE ( 71 FDA reports)
HERPES ZOSTER ( 71 FDA reports)
HYPERBILIRUBINAEMIA ( 71 FDA reports)
ILL-DEFINED DISORDER ( 71 FDA reports)
VISUAL ACUITY REDUCED ( 71 FDA reports)
ABSCESS ( 70 FDA reports)
BLOOD GLUCOSE DECREASED ( 70 FDA reports)
OROPHARYNGEAL PAIN ( 70 FDA reports)
FLUSHING ( 69 FDA reports)
MALNUTRITION ( 69 FDA reports)
OSTEOPENIA ( 69 FDA reports)
TOOTH EXTRACTION ( 69 FDA reports)
URINARY RETENTION ( 69 FDA reports)
GYNAECOMASTIA ( 68 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 68 FDA reports)
SUDDEN DEATH ( 68 FDA reports)
SWELLING FACE ( 68 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 67 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 67 FDA reports)
GOUT ( 67 FDA reports)
URINARY INCONTINENCE ( 67 FDA reports)
CIRCULATORY COLLAPSE ( 66 FDA reports)
TYPE 2 DIABETES MELLITUS ( 66 FDA reports)
UNRESPONSIVE TO STIMULI ( 66 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 66 FDA reports)
DYSARTHRIA ( 65 FDA reports)
GALLBLADDER DISORDER ( 65 FDA reports)
CEREBRAL HAEMORRHAGE ( 64 FDA reports)
CYANOSIS ( 64 FDA reports)
DEFORMITY ( 64 FDA reports)
DIVERTICULUM ( 64 FDA reports)
PROTEINURIA ( 64 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 64 FDA reports)
AZOTAEMIA ( 63 FDA reports)
FEBRILE NEUTROPENIA ( 63 FDA reports)
GASTROINTESTINAL DISORDER ( 63 FDA reports)
LIMB INJURY ( 63 FDA reports)
NEPHROTIC SYNDROME ( 63 FDA reports)
SINUS TACHYCARDIA ( 63 FDA reports)
HYPERURICAEMIA ( 62 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 62 FDA reports)
ACIDOSIS ( 61 FDA reports)
METASTASES TO LIVER ( 61 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 61 FDA reports)
AMMONIA INCREASED ( 60 FDA reports)
ANGINA UNSTABLE ( 60 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 60 FDA reports)
LEUKOCYTOSIS ( 60 FDA reports)
MENTAL DISORDER ( 60 FDA reports)
MOBILITY DECREASED ( 60 FDA reports)
OLIGURIA ( 60 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 60 FDA reports)
RIB FRACTURE ( 60 FDA reports)
ACUTE RESPIRATORY FAILURE ( 59 FDA reports)
ANURIA ( 59 FDA reports)
APHASIA ( 59 FDA reports)
ATRIAL FLUTTER ( 59 FDA reports)
BLOOD URIC ACID INCREASED ( 59 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 59 FDA reports)
NEPHROLITHIASIS ( 59 FDA reports)
VISUAL IMPAIRMENT ( 59 FDA reports)
IRON DEFICIENCY ANAEMIA ( 58 FDA reports)
MUCOSAL INFLAMMATION ( 58 FDA reports)
RASH ERYTHEMATOUS ( 58 FDA reports)
URINE OUTPUT DECREASED ( 58 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 57 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 57 FDA reports)
RESTLESSNESS ( 57 FDA reports)
URTICARIA ( 57 FDA reports)
DRUG TOXICITY ( 56 FDA reports)
SHOCK HAEMORRHAGIC ( 56 FDA reports)
CHOLECYSTITIS ( 55 FDA reports)
DEPRESSED MOOD ( 55 FDA reports)
DILATATION ATRIAL ( 55 FDA reports)
EOSINOPHILIA ( 55 FDA reports)
BACTERIAL INFECTION ( 54 FDA reports)
CEREBRAL ATROPHY ( 54 FDA reports)
DEMENTIA ( 54 FDA reports)
DIVERTICULUM INTESTINAL ( 54 FDA reports)
RHINORRHOEA ( 54 FDA reports)
BLOOD CHLORIDE DECREASED ( 53 FDA reports)
CARDIAC VALVE DISEASE ( 53 FDA reports)
DYSLIPIDAEMIA ( 53 FDA reports)
EAR PAIN ( 53 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 53 FDA reports)
SKIN EXFOLIATION ( 53 FDA reports)
THIRST ( 53 FDA reports)
ABNORMAL BEHAVIOUR ( 52 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 52 FDA reports)
BLOOD CALCIUM DECREASED ( 52 FDA reports)
CARDIAC FAILURE CHRONIC ( 52 FDA reports)
HOT FLUSH ( 52 FDA reports)
LUNG NEOPLASM ( 52 FDA reports)
OSTEOPOROSIS ( 52 FDA reports)
RENAL CYST ( 52 FDA reports)
DEAFNESS ( 51 FDA reports)
DEVICE RELATED INFECTION ( 51 FDA reports)
OESOPHAGITIS ( 51 FDA reports)
VARICES OESOPHAGEAL ( 51 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 50 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 50 FDA reports)
EATING DISORDER ( 50 FDA reports)
HIP FRACTURE ( 50 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 50 FDA reports)
NASAL CONGESTION ( 50 FDA reports)
RESPIRATORY DISORDER ( 50 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 50 FDA reports)
DIPLOPIA ( 49 FDA reports)
FACE OEDEMA ( 49 FDA reports)
MOUTH ULCERATION ( 49 FDA reports)
PHARYNGITIS ( 49 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 49 FDA reports)
SPINAL OSTEOARTHRITIS ( 49 FDA reports)
COGNITIVE DISORDER ( 48 FDA reports)
DILATATION VENTRICULAR ( 48 FDA reports)
HYPERAMMONAEMIA ( 48 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 48 FDA reports)
PULMONARY FIBROSIS ( 48 FDA reports)
ROTATOR CUFF SYNDROME ( 48 FDA reports)
TORSADE DE POINTES ( 48 FDA reports)
BURNING SENSATION ( 47 FDA reports)
FLATULENCE ( 47 FDA reports)
HEPATITIS FULMINANT ( 47 FDA reports)
HYPERNATRAEMIA ( 47 FDA reports)
LIPASE INCREASED ( 47 FDA reports)
ACUTE PRERENAL FAILURE ( 46 FDA reports)
ACUTE PULMONARY OEDEMA ( 46 FDA reports)
DERMATITIS ( 46 FDA reports)
HAEMORRHOIDS ( 46 FDA reports)
HEAD INJURY ( 46 FDA reports)
INTESTINAL OBSTRUCTION ( 46 FDA reports)
MEDICATION ERROR ( 46 FDA reports)
NERVOUS SYSTEM DISORDER ( 46 FDA reports)
DISABILITY ( 45 FDA reports)
DISTURBANCE IN ATTENTION ( 45 FDA reports)
FEELING COLD ( 45 FDA reports)
HEPATITIS ACUTE ( 45 FDA reports)
INJECTION SITE PAIN ( 45 FDA reports)
MULTIPLE MYELOMA ( 45 FDA reports)
PULMONARY MASS ( 45 FDA reports)
ADRENAL INSUFFICIENCY ( 44 FDA reports)
BLOOD AMYLASE INCREASED ( 44 FDA reports)
COLITIS ( 44 FDA reports)
DERMATITIS EXFOLIATIVE ( 44 FDA reports)
DIABETIC NEUROPATHY ( 44 FDA reports)
DYSGEUSIA ( 44 FDA reports)
DYSURIA ( 44 FDA reports)
FAILURE TO THRIVE ( 44 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 44 FDA reports)
PALLOR ( 44 FDA reports)
POLYURIA ( 44 FDA reports)
PRIMARY SEQUESTRUM ( 44 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 44 FDA reports)
BREAST PAIN ( 43 FDA reports)
HYPOCALCAEMIA ( 43 FDA reports)
POLLAKIURIA ( 43 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 43 FDA reports)
TENDERNESS ( 43 FDA reports)
TINNITUS ( 43 FDA reports)
TOOTH LOSS ( 43 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 42 FDA reports)
CARDIAC PACEMAKER INSERTION ( 42 FDA reports)
COLONIC POLYP ( 42 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 42 FDA reports)
DRUG INTOLERANCE ( 42 FDA reports)
DRY SKIN ( 42 FDA reports)
GLAUCOMA ( 42 FDA reports)
GOITRE ( 42 FDA reports)
HAEMATOCHEZIA ( 42 FDA reports)
NERVOUSNESS ( 42 FDA reports)
ORAL PAIN ( 42 FDA reports)
PEMPHIGOID ( 42 FDA reports)
PORTAL HYPERTENSION ( 42 FDA reports)
VARICOSE VEIN ( 42 FDA reports)
VENOUS INSUFFICIENCY ( 42 FDA reports)
VISUAL FIELD DEFECT ( 42 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 41 FDA reports)
CAROTID ARTERY STENOSIS ( 41 FDA reports)
ECCHYMOSIS ( 41 FDA reports)
EMPHYSEMA ( 41 FDA reports)
HEPATIC CONGESTION ( 41 FDA reports)
LABORATORY TEST ABNORMAL ( 41 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 41 FDA reports)
RASH MACULO-PAPULAR ( 41 FDA reports)
REFLUX OESOPHAGITIS ( 41 FDA reports)
ROAD TRAFFIC ACCIDENT ( 41 FDA reports)
SICK SINUS SYNDROME ( 41 FDA reports)
SLEEP DISORDER ( 41 FDA reports)
AGGRESSION ( 40 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 40 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 40 FDA reports)
BREAST CANCER ( 40 FDA reports)
CHEST X-RAY ABNORMAL ( 40 FDA reports)
DUODENAL ULCER ( 40 FDA reports)
HEPATITIS C ( 40 FDA reports)
INTESTINAL ISCHAEMIA ( 40 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 40 FDA reports)
SKIN LESION ( 40 FDA reports)
UTERINE LEIOMYOMA ( 40 FDA reports)
AORTIC ANEURYSM ( 39 FDA reports)
BACTERAEMIA ( 39 FDA reports)
BONE MARROW FAILURE ( 39 FDA reports)
CHOLECYSTITIS CHRONIC ( 39 FDA reports)
DYSKINESIA ( 39 FDA reports)
ENDOTRACHEAL INTUBATION ( 39 FDA reports)
EXOSTOSIS ( 39 FDA reports)
FUNGAL INFECTION ( 39 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 39 FDA reports)
MIGRAINE ( 39 FDA reports)
SERUM FERRITIN INCREASED ( 39 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 38 FDA reports)
CHROMATURIA ( 38 FDA reports)
CORONARY ARTERY STENOSIS ( 38 FDA reports)
DECUBITUS ULCER ( 38 FDA reports)
DISCOMFORT ( 38 FDA reports)
EPILEPSY ( 38 FDA reports)
GINGIVAL BLEEDING ( 38 FDA reports)
ILEUS ( 38 FDA reports)
LOBAR PNEUMONIA ( 38 FDA reports)
NEURALGIA ( 38 FDA reports)
PERITONITIS ( 38 FDA reports)
SKIN DISORDER ( 38 FDA reports)
VENTRICULAR HYPERTROPHY ( 38 FDA reports)
BURSITIS ( 37 FDA reports)
DISEASE RECURRENCE ( 37 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 37 FDA reports)
EOSINOPHIL COUNT INCREASED ( 37 FDA reports)
HYPERKERATOSIS ( 37 FDA reports)
HYPERTHYROIDISM ( 37 FDA reports)
POST PROCEDURAL COMPLICATION ( 37 FDA reports)
SCAR ( 37 FDA reports)
SPONDYLOLISTHESIS ( 37 FDA reports)
SUBDURAL HAEMATOMA ( 37 FDA reports)
VIRAL INFECTION ( 37 FDA reports)
VITREOUS FLOATERS ( 37 FDA reports)
AORTIC STENOSIS ( 36 FDA reports)
CORONARY ARTERY OCCLUSION ( 36 FDA reports)
ERECTILE DYSFUNCTION ( 36 FDA reports)
FEMUR FRACTURE ( 36 FDA reports)
HALLUCINATION, VISUAL ( 36 FDA reports)
HYPERTHERMIA ( 36 FDA reports)
HYPOPHOSPHATAEMIA ( 36 FDA reports)
IMPAIRED WORK ABILITY ( 36 FDA reports)
INFLUENZA LIKE ILLNESS ( 36 FDA reports)
NECROSIS ( 36 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 36 FDA reports)
OSTEITIS ( 36 FDA reports)
PATHOLOGICAL FRACTURE ( 36 FDA reports)
PERITONITIS BACTERIAL ( 36 FDA reports)
SINUS DISORDER ( 36 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 35 FDA reports)
CONJUNCTIVITIS ( 35 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 35 FDA reports)
EMOTIONAL DISORDER ( 35 FDA reports)
HYPERCALCAEMIA ( 35 FDA reports)
HYPOMAGNESAEMIA ( 35 FDA reports)
LEFT ATRIAL DILATATION ( 35 FDA reports)
MASS ( 35 FDA reports)
PROTEIN TOTAL DECREASED ( 35 FDA reports)
ANAPHYLACTIC SHOCK ( 34 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 34 FDA reports)
BREATH SOUNDS ABNORMAL ( 34 FDA reports)
INCONTINENCE ( 34 FDA reports)
JOINT INJURY ( 34 FDA reports)
PIGMENTATION DISORDER ( 34 FDA reports)
RASH PRURITIC ( 34 FDA reports)
BONE LESION ( 33 FDA reports)
CREPITATIONS ( 33 FDA reports)
DRUG LEVEL INCREASED ( 33 FDA reports)
FAECAL INCONTINENCE ( 33 FDA reports)
GASTRIC HAEMORRHAGE ( 33 FDA reports)
INFUSION RELATED REACTION ( 33 FDA reports)
INTRACARDIAC THROMBUS ( 33 FDA reports)
NEPHROGENIC ANAEMIA ( 33 FDA reports)
PERIODONTAL DISEASE ( 33 FDA reports)
PNEUMONITIS ( 33 FDA reports)
RASH GENERALISED ( 33 FDA reports)
TOOTH FRACTURE ( 33 FDA reports)
VENTRICULAR HYPOKINESIA ( 33 FDA reports)
CANDIDIASIS ( 32 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 32 FDA reports)
COMPRESSION FRACTURE ( 32 FDA reports)
FAECES DISCOLOURED ( 32 FDA reports)
HEPATORENAL SYNDROME ( 32 FDA reports)
IRRITABILITY ( 32 FDA reports)
IRRITABLE BOWEL SYNDROME ( 32 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 32 FDA reports)
MYOPATHY ( 32 FDA reports)
PNEUMOTHORAX ( 32 FDA reports)
SCOLIOSIS ( 32 FDA reports)
VASODILATATION ( 32 FDA reports)
ASPIRATION ( 31 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 31 FDA reports)
BLOOD CALCIUM INCREASED ( 31 FDA reports)
BONE DENSITY DECREASED ( 31 FDA reports)
CONDUCTION DISORDER ( 31 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 31 FDA reports)
HEPATITIS CHOLESTATIC ( 31 FDA reports)
INJECTION SITE HAEMORRHAGE ( 31 FDA reports)
INTERMITTENT CLAUDICATION ( 31 FDA reports)
INTESTINAL PERFORATION ( 31 FDA reports)
NIGHT SWEATS ( 31 FDA reports)
PNEUMONIA BACTERIAL ( 31 FDA reports)
RASH PAPULAR ( 31 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 31 FDA reports)
SUICIDAL IDEATION ( 31 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 31 FDA reports)
ABDOMINAL PAIN LOWER ( 30 FDA reports)
ACCIDENTAL OVERDOSE ( 30 FDA reports)
ATAXIA ( 30 FDA reports)
CATHETERISATION CARDIAC ( 30 FDA reports)
DIABETIC RETINOPATHY ( 30 FDA reports)
DIVERTICULITIS ( 30 FDA reports)
ESCHERICHIA INFECTION ( 30 FDA reports)
HAEMODYNAMIC INSTABILITY ( 30 FDA reports)
HAEMOTHORAX ( 30 FDA reports)
INJECTION SITE ERYTHEMA ( 30 FDA reports)
METASTASES TO LUNG ( 30 FDA reports)
PERICARDITIS ( 30 FDA reports)
PETECHIAE ( 30 FDA reports)
PHLEBITIS ( 30 FDA reports)
PROSTATE CANCER ( 30 FDA reports)
PSORIASIS ( 30 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 30 FDA reports)
VISUAL DISTURBANCE ( 30 FDA reports)
ANGIOPATHY ( 29 FDA reports)
APNOEA ( 29 FDA reports)
BLINDNESS ( 29 FDA reports)
BRONCHOPNEUMONIA ( 29 FDA reports)
CAROTID ARTERY DISEASE ( 29 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 29 FDA reports)
DRY EYE ( 29 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 29 FDA reports)
ERYTHEMA MULTIFORME ( 29 FDA reports)
HAEMOLYTIC ANAEMIA ( 29 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 29 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 29 FDA reports)
OESOPHAGEAL ULCER ( 29 FDA reports)
SQUAMOUS CELL CARCINOMA ( 29 FDA reports)
TACHYPNOEA ( 29 FDA reports)
VITREOUS HAEMORRHAGE ( 29 FDA reports)
ANGIOEDEMA ( 28 FDA reports)
BLINDNESS UNILATERAL ( 28 FDA reports)
BLOOD IRON DECREASED ( 28 FDA reports)
CATHETER RELATED INFECTION ( 28 FDA reports)
CEREBRAL ISCHAEMIA ( 28 FDA reports)
CHEILITIS ( 28 FDA reports)
FIBROSIS ( 28 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 28 FDA reports)
HEPATIC CYST ( 28 FDA reports)
HEPATIC LESION ( 28 FDA reports)
HYPERVENTILATION ( 28 FDA reports)
LIFE EXPECTANCY SHORTENED ( 28 FDA reports)
LOCALISED INFECTION ( 28 FDA reports)
LUNG NEOPLASM MALIGNANT ( 28 FDA reports)
MICROCYTIC ANAEMIA ( 28 FDA reports)
ORAL CANDIDIASIS ( 28 FDA reports)
ORAL DISORDER ( 28 FDA reports)
ORAL INTAKE REDUCED ( 28 FDA reports)
PARKINSONISM ( 28 FDA reports)
PHOTOPSIA ( 28 FDA reports)
RASH MACULAR ( 28 FDA reports)
RHINITIS ALLERGIC ( 28 FDA reports)
SPINAL COLUMN STENOSIS ( 28 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 28 FDA reports)
THROMBOPHLEBITIS ( 28 FDA reports)
AORTIC VALVE STENOSIS ( 27 FDA reports)
AUTOIMMUNE HEPATITIS ( 27 FDA reports)
BRADYARRHYTHMIA ( 27 FDA reports)
BRONCHITIS CHRONIC ( 27 FDA reports)
BRONCHOSPASM ( 27 FDA reports)
CARDIAC FAILURE ACUTE ( 27 FDA reports)
CARPAL TUNNEL SYNDROME ( 27 FDA reports)
CYSTITIS ( 27 FDA reports)
DERMATITIS BULLOUS ( 27 FDA reports)
DIASTOLIC DYSFUNCTION ( 27 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 27 FDA reports)
DYSSTASIA ( 27 FDA reports)
GINGIVITIS ( 27 FDA reports)
HAEMOLYSIS ( 27 FDA reports)
HAEMORRHAGIC DIATHESIS ( 27 FDA reports)
HEMIPARESIS ( 27 FDA reports)
LEFT VENTRICULAR FAILURE ( 27 FDA reports)
MUSCLE HAEMORRHAGE ( 27 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 27 FDA reports)
PERIPHERAL COLDNESS ( 27 FDA reports)
PLEURAL FIBROSIS ( 27 FDA reports)
PYELONEPHRITIS ( 27 FDA reports)
RHEUMATOID ARTHRITIS ( 27 FDA reports)
SCIATICA ( 27 FDA reports)
SKIN DISCOLOURATION ( 27 FDA reports)
SPINAL COMPRESSION FRACTURE ( 27 FDA reports)
BLOOD CREATINE INCREASED ( 26 FDA reports)
BUNDLE BRANCH BLOCK ( 26 FDA reports)
CATARACT OPERATION ( 26 FDA reports)
COLORECTAL CANCER ( 26 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 26 FDA reports)
DRUG DOSE OMISSION ( 26 FDA reports)
ENTEROCOCCAL INFECTION ( 26 FDA reports)
FIBROMYALGIA ( 26 FDA reports)
HOSPITALISATION ( 26 FDA reports)
INFARCTION ( 26 FDA reports)
JOINT EFFUSION ( 26 FDA reports)
LACERATION ( 26 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 26 FDA reports)
LYMPHADENITIS ( 26 FDA reports)
LYMPHOMA ( 26 FDA reports)
METASTASES TO LYMPH NODES ( 26 FDA reports)
NEOPLASM PROGRESSION ( 26 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 26 FDA reports)
RENAL TUBULAR NECROSIS ( 26 FDA reports)
RESPIRATORY TRACT INFECTION ( 26 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 26 FDA reports)
THYROID DISORDER ( 26 FDA reports)
VIITH NERVE PARALYSIS ( 26 FDA reports)
BLOOD SODIUM INCREASED ( 25 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 25 FDA reports)
COLD SWEAT ( 25 FDA reports)
DRUG ADMINISTRATION ERROR ( 25 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 25 FDA reports)
FAECALOMA ( 25 FDA reports)
FRACTURE ( 25 FDA reports)
GRANULOCYTOPENIA ( 25 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 25 FDA reports)
HEARING IMPAIRED ( 25 FDA reports)
HEPATIC NEOPLASM ( 25 FDA reports)
HYPERCAPNIA ( 25 FDA reports)
HYPERCHOLESTEROLAEMIA ( 25 FDA reports)
HYPERTENSIVE HEART DISEASE ( 25 FDA reports)
HYPOKINESIA ( 25 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 25 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 25 FDA reports)
IRON DEFICIENCY ( 25 FDA reports)
METABOLIC ALKALOSIS ( 25 FDA reports)
NO THERAPEUTIC RESPONSE ( 25 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 25 FDA reports)
THERAPY NON-RESPONDER ( 25 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 25 FDA reports)
TOOTH DISORDER ( 25 FDA reports)
TUMOUR LYSIS SYNDROME ( 25 FDA reports)
VENTRICULAR DYSFUNCTION ( 25 FDA reports)
WOUND DRAINAGE ( 25 FDA reports)
ANEURYSM ( 24 FDA reports)
ATRIAL TACHYCARDIA ( 24 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 24 FDA reports)
DIFFICULTY IN WALKING ( 24 FDA reports)
DRUG EFFECT DECREASED ( 24 FDA reports)
EXCORIATION ( 24 FDA reports)
FEELING HOT ( 24 FDA reports)
GASTRITIS EROSIVE ( 24 FDA reports)
GRAND MAL CONVULSION ( 24 FDA reports)
HEPATOCELLULAR INJURY ( 24 FDA reports)
HEPATOTOXICITY ( 24 FDA reports)
HYPOTHERMIA ( 24 FDA reports)
HYPOVOLAEMIC SHOCK ( 24 FDA reports)
LIGAMENT SPRAIN ( 24 FDA reports)
LIMB DISCOMFORT ( 24 FDA reports)
LOOSE TOOTH ( 24 FDA reports)
LUNG INFECTION ( 24 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 24 FDA reports)
MYELODYSPLASTIC SYNDROME ( 24 FDA reports)
ONYCHOMYCOSIS ( 24 FDA reports)
PULMONARY HAEMORRHAGE ( 24 FDA reports)
RASH PUSTULAR ( 24 FDA reports)
SINUS CONGESTION ( 24 FDA reports)
THYROID NEOPLASM ( 24 FDA reports)
WOUND DEHISCENCE ( 24 FDA reports)
ACUTE CORONARY SYNDROME ( 23 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 23 FDA reports)
BLADDER CANCER ( 23 FDA reports)
BLADDER MASS ( 23 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 23 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 23 FDA reports)
CACHEXIA ( 23 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 23 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 23 FDA reports)
HEMIPLEGIA ( 23 FDA reports)
HYPOGLYCAEMIC COMA ( 23 FDA reports)
ILEUS PARALYTIC ( 23 FDA reports)
LUNG CONSOLIDATION ( 23 FDA reports)
MENTAL IMPAIRMENT ( 23 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 23 FDA reports)
MUSCLE STRAIN ( 23 FDA reports)
MYOCLONUS ( 23 FDA reports)
NIGHTMARE ( 23 FDA reports)
PRODUCT QUALITY ISSUE ( 23 FDA reports)
PULSE ABSENT ( 23 FDA reports)
RESPIRATORY ACIDOSIS ( 23 FDA reports)
RETINAL HAEMORRHAGE ( 23 FDA reports)
RHONCHI ( 23 FDA reports)
TENOSYNOVITIS ( 23 FDA reports)
TROPONIN INCREASED ( 23 FDA reports)
VASCULITIS ( 23 FDA reports)
VITAMIN D DEFICIENCY ( 23 FDA reports)
WOUND INFECTION ( 23 FDA reports)
APPENDICITIS ( 22 FDA reports)
BLOOD URINE PRESENT ( 22 FDA reports)
BREAST MASS ( 22 FDA reports)
CHOLECYSTECTOMY ( 22 FDA reports)
COSTOCHONDRITIS ( 22 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 22 FDA reports)
ESCHERICHIA SEPSIS ( 22 FDA reports)
EXERCISE TOLERANCE DECREASED ( 22 FDA reports)
FRACTURE NONUNION ( 22 FDA reports)
HEPATOCELLULAR DAMAGE ( 22 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 22 FDA reports)
INTENTIONAL DRUG MISUSE ( 22 FDA reports)
ISCHAEMIA ( 22 FDA reports)
LACUNAR INFARCTION ( 22 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 22 FDA reports)
MYDRIASIS ( 22 FDA reports)
ONYCHOCLASIS ( 22 FDA reports)
PERIODONTITIS ( 22 FDA reports)
PHARYNGEAL OEDEMA ( 22 FDA reports)
SKIN ATROPHY ( 22 FDA reports)
SKIN LACERATION ( 22 FDA reports)
SUICIDE ATTEMPT ( 22 FDA reports)
SYNOVIAL CYST ( 22 FDA reports)
TENDON RUPTURE ( 22 FDA reports)
TENDONITIS ( 22 FDA reports)
TOOTH ABSCESS ( 22 FDA reports)
ADVERSE DRUG REACTION ( 21 FDA reports)
BASAL CELL CARCINOMA ( 21 FDA reports)
BODY TEMPERATURE INCREASED ( 21 FDA reports)
BONE EROSION ( 21 FDA reports)
DECREASED ACTIVITY ( 21 FDA reports)
DENTAL CARIES ( 21 FDA reports)
DIABETIC NEPHROPATHY ( 21 FDA reports)
EMBOLIC STROKE ( 21 FDA reports)
FEMORAL NECK FRACTURE ( 21 FDA reports)
GANGRENE ( 21 FDA reports)
GENERALISED ERYTHEMA ( 21 FDA reports)
GINGIVAL PAIN ( 21 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 21 FDA reports)
HEPATITIS B ( 21 FDA reports)
HYDROCELE ( 21 FDA reports)
HYDRONEPHROSIS ( 21 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 21 FDA reports)
JAUNDICE CHOLESTATIC ( 21 FDA reports)
MOUTH HAEMORRHAGE ( 21 FDA reports)
MUCOSAL ULCERATION ( 21 FDA reports)
NECK INJURY ( 21 FDA reports)
NOCTURIA ( 21 FDA reports)
ORAL CAVITY FISTULA ( 21 FDA reports)
PARONYCHIA ( 21 FDA reports)
PROTEIN TOTAL INCREASED ( 21 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 21 FDA reports)
PRURIGO ( 21 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 21 FDA reports)
RESTLESS LEGS SYNDROME ( 21 FDA reports)
TACHYARRHYTHMIA ( 21 FDA reports)
ABNORMAL DREAMS ( 20 FDA reports)
ADVERSE EVENT ( 20 FDA reports)
ASTERIXIS ( 20 FDA reports)
CHOKING ( 20 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 20 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 20 FDA reports)
ENDODONTIC PROCEDURE ( 20 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 20 FDA reports)
GASTRIC DISORDER ( 20 FDA reports)
GASTROENTERITIS VIRAL ( 20 FDA reports)
HYPERSOMNIA ( 20 FDA reports)
INJECTION SITE REACTION ( 20 FDA reports)
ISCHAEMIC STROKE ( 20 FDA reports)
LIVER CARCINOMA RUPTURED ( 20 FDA reports)
PARALYSIS ( 20 FDA reports)
PROTEIN URINE PRESENT ( 20 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 20 FDA reports)
QRS AXIS ABNORMAL ( 20 FDA reports)
RESPIRATORY TRACT CONGESTION ( 20 FDA reports)
RESUSCITATION ( 20 FDA reports)
SINOATRIAL BLOCK ( 20 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 20 FDA reports)
UPPER LIMB FRACTURE ( 20 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
BEDRIDDEN ( 19 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 19 FDA reports)
BLOOD CULTURE POSITIVE ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 19 FDA reports)
BREAST CANCER FEMALE ( 19 FDA reports)
CARDIOPULMONARY FAILURE ( 19 FDA reports)
CAROTID BRUIT ( 19 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 19 FDA reports)
DYSPNOEA EXACERBATED ( 19 FDA reports)
EDENTULOUS ( 19 FDA reports)
ENTEROCOLITIS ( 19 FDA reports)
EYELID OEDEMA ( 19 FDA reports)
FACE INJURY ( 19 FDA reports)
FAMILY STRESS ( 19 FDA reports)
FLANK PAIN ( 19 FDA reports)
GLOSSODYNIA ( 19 FDA reports)
INJECTION SITE HAEMATOMA ( 19 FDA reports)
LIP SWELLING ( 19 FDA reports)
LYMPHOPENIA ( 19 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 19 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 19 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 19 FDA reports)
NON-CARDIAC CHEST PAIN ( 19 FDA reports)
OPEN WOUND ( 19 FDA reports)
PARACENTESIS ( 19 FDA reports)
PERIPHERAL ISCHAEMIA ( 19 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 19 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 19 FDA reports)
PRURITUS GENERALISED ( 19 FDA reports)
RENAL CELL CARCINOMA ( 19 FDA reports)
SKIN NECROSIS ( 19 FDA reports)
STENOTROPHOMONAS INFECTION ( 19 FDA reports)
SUDDEN CARDIAC DEATH ( 19 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 19 FDA reports)
ACUTE HEPATIC FAILURE ( 18 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 18 FDA reports)
ANGER ( 18 FDA reports)
ARTERIAL STENOSIS ( 18 FDA reports)
BLADDER DISORDER ( 18 FDA reports)
BONE LOSS ( 18 FDA reports)
BONE OPERATION ( 18 FDA reports)
BREAST TENDERNESS ( 18 FDA reports)
CORONARY ANGIOPLASTY ( 18 FDA reports)
CROHN'S DISEASE ( 18 FDA reports)
CRYING ( 18 FDA reports)
ECZEMA ASTEATOTIC ( 18 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 18 FDA reports)
EYE SWELLING ( 18 FDA reports)
EYELID PTOSIS ( 18 FDA reports)
FLUID INTAKE REDUCED ( 18 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 18 FDA reports)
HUMERUS FRACTURE ( 18 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 18 FDA reports)
JAW DISORDER ( 18 FDA reports)
JAW OPERATION ( 18 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 18 FDA reports)
LOWER LIMB FRACTURE ( 18 FDA reports)
LUMBAR SPINAL STENOSIS ( 18 FDA reports)
MOVEMENT DISORDER ( 18 FDA reports)
MUSCLE RIGIDITY ( 18 FDA reports)
NO ADVERSE EVENT ( 18 FDA reports)
PORTAL VEIN THROMBOSIS ( 18 FDA reports)
RADICULOPATHY ( 18 FDA reports)
RADIOTHERAPY ( 18 FDA reports)
RETCHING ( 18 FDA reports)
SINUS ARREST ( 18 FDA reports)
SPINAL COLUMN INJURY ( 18 FDA reports)
STAPHYLOMA ( 18 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 18 FDA reports)
SWOLLEN TONGUE ( 18 FDA reports)
TOBACCO USER ( 18 FDA reports)
TRACHEAL DEVIATION ( 18 FDA reports)
VENOUS THROMBOSIS ( 18 FDA reports)
ANAEMIA MACROCYTIC ( 17 FDA reports)
ANKLE FRACTURE ( 17 FDA reports)
AORTIC VALVE SCLEROSIS ( 17 FDA reports)
APATHY ( 17 FDA reports)
APLASIA PURE RED CELL ( 17 FDA reports)
ATRIAL SEPTAL DEFECT ( 17 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 17 FDA reports)
CARDIAC OUTPUT DECREASED ( 17 FDA reports)
COLON ADENOMA ( 17 FDA reports)
CULTURE URINE POSITIVE ( 17 FDA reports)
DERMATITIS CONTACT ( 17 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 17 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 17 FDA reports)
ENDOCARDITIS ( 17 FDA reports)
EROSIVE OESOPHAGITIS ( 17 FDA reports)
HAEMANGIOMA ( 17 FDA reports)
HYPERPLASIA ( 17 FDA reports)
HYPOTONIA ( 17 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
LYMPHOEDEMA ( 17 FDA reports)
METABOLIC ENCEPHALOPATHY ( 17 FDA reports)
METABOLIC SYNDROME ( 17 FDA reports)
METASTASES TO SPINE ( 17 FDA reports)
METRORRHAGIA ( 17 FDA reports)
MIOSIS ( 17 FDA reports)
NASAL SEPTUM DEVIATION ( 17 FDA reports)
NEUTROPHIL COUNT INCREASED ( 17 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 17 FDA reports)
OSTEOSCLEROSIS ( 17 FDA reports)
PSEUDOMONAS INFECTION ( 17 FDA reports)
PULMONARY TUBERCULOSIS ( 17 FDA reports)
SEASONAL ALLERGY ( 17 FDA reports)
TENDON INJURY ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 17 FDA reports)
TRISMUS ( 17 FDA reports)
WALKING AID USER ( 17 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 16 FDA reports)
APLASTIC ANAEMIA ( 16 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 16 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 16 FDA reports)
BRAIN OEDEMA ( 16 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
CHOLANGITIS ( 16 FDA reports)
COMA HEPATIC ( 16 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 16 FDA reports)
FACIAL PAIN ( 16 FDA reports)
GASTRIC CANCER ( 16 FDA reports)
GINGIVAL RECESSION ( 16 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 16 FDA reports)
GROIN PAIN ( 16 FDA reports)
HICCUPS ( 16 FDA reports)
MITRAL VALVE DISEASE ( 16 FDA reports)
MONOCYTE COUNT INCREASED ( 16 FDA reports)
ORAL HERPES ( 16 FDA reports)
PARAESTHESIA ORAL ( 16 FDA reports)
PELVIC FRACTURE ( 16 FDA reports)
PHYSICAL DISABILITY ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
PLEURITIC PAIN ( 16 FDA reports)
PO2 DECREASED ( 16 FDA reports)
SENSATION OF HEAVINESS ( 16 FDA reports)
SENSORY DISTURBANCE ( 16 FDA reports)
STENT PLACEMENT ( 16 FDA reports)
THROMBOSIS IN DEVICE ( 16 FDA reports)
ULCER ( 16 FDA reports)
VASCULAR PURPURA ( 16 FDA reports)
ABDOMINAL TENDERNESS ( 15 FDA reports)
ACNE ( 15 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 15 FDA reports)
CERUMEN IMPACTION ( 15 FDA reports)
COR PULMONALE ( 15 FDA reports)
CORONARY ARTERY BYPASS ( 15 FDA reports)
CYST ( 15 FDA reports)
ESSENTIAL HYPERTENSION ( 15 FDA reports)
GINGIVAL INFECTION ( 15 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 15 FDA reports)
HEPATOSPLENOMEGALY ( 15 FDA reports)
HYPERCOAGULATION ( 15 FDA reports)
HYPERTENSIVE CRISIS ( 15 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 15 FDA reports)
JAW FRACTURE ( 15 FDA reports)
JOINT STIFFNESS ( 15 FDA reports)
JUGULAR VEIN DISTENSION ( 15 FDA reports)
LARGE INTESTINE PERFORATION ( 15 FDA reports)
LIVER INJURY ( 15 FDA reports)
MARROW HYPERPLASIA ( 15 FDA reports)
MOTOR DYSFUNCTION ( 15 FDA reports)
NEPHROPATHY ( 15 FDA reports)
NIKOLSKY'S SIGN ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER ( 15 FDA reports)
OCCULT BLOOD POSITIVE ( 15 FDA reports)
OESOPHAGEAL DISORDER ( 15 FDA reports)
OOPHORECTOMY ( 15 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 15 FDA reports)
ORGAN FAILURE ( 15 FDA reports)
OTITIS EXTERNA ( 15 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 15 FDA reports)
PROSTATITIS ( 15 FDA reports)
RESPIRATORY DEPRESSION ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
TENDON DISORDER ( 15 FDA reports)
UMBILICAL HERNIA ( 15 FDA reports)
URINARY HESITATION ( 15 FDA reports)
URINE OUTPUT INCREASED ( 15 FDA reports)
VENTRICULAR FAILURE ( 15 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 15 FDA reports)
WOUND ( 15 FDA reports)
ANXIETY DISORDER ( 14 FDA reports)
ASPIRATION JOINT ( 14 FDA reports)
BACK DISORDER ( 14 FDA reports)
BLOOD LACTIC ACID INCREASED ( 14 FDA reports)
BLOOD MAGNESIUM DECREASED ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
BREAST ENLARGEMENT ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CARDIORENAL SYNDROME ( 14 FDA reports)
CARDIOVERSION ( 14 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 14 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 14 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 14 FDA reports)
COORDINATION ABNORMAL ( 14 FDA reports)
DIABETIC KETOACIDOSIS ( 14 FDA reports)
DIZZINESS POSTURAL ( 14 FDA reports)
DRUG DEPENDENCE ( 14 FDA reports)
DRUG RESISTANCE ( 14 FDA reports)
DUODENITIS ( 14 FDA reports)
EPIDIDYMITIS ( 14 FDA reports)
ERYSIPELAS ( 14 FDA reports)
GASTROINTESTINAL PAIN ( 14 FDA reports)
HAEMORRHAGIC ANAEMIA ( 14 FDA reports)
HAEMORRHAGIC ASCITES ( 14 FDA reports)
HELICOBACTER INFECTION ( 14 FDA reports)
HYPOCHLORAEMIA ( 14 FDA reports)
HYPOPROTEINAEMIA ( 14 FDA reports)
HYPOVENTILATION ( 14 FDA reports)
INJECTION SITE MASS ( 14 FDA reports)
KLEBSIELLA INFECTION ( 14 FDA reports)
MANIA ( 14 FDA reports)
MITRAL VALVE CALCIFICATION ( 14 FDA reports)
MUSCLE ATROPHY ( 14 FDA reports)
NODAL RHYTHM ( 14 FDA reports)
OCULAR HYPERAEMIA ( 14 FDA reports)
OSTEOLYSIS ( 14 FDA reports)
OVARIAN ADHESION ( 14 FDA reports)
PANIC ATTACK ( 14 FDA reports)
PELVIC ADHESIONS ( 14 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 14 FDA reports)
PERITONEAL HAEMORRHAGE ( 14 FDA reports)
PLATELET COUNT INCREASED ( 14 FDA reports)
POLYNEUROPATHY ( 14 FDA reports)
PROTHROMBIN TIME SHORTENED ( 14 FDA reports)
PSYCHOMOTOR RETARDATION ( 14 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 14 FDA reports)
PURULENT DISCHARGE ( 14 FDA reports)
RETINAL DETACHMENT ( 14 FDA reports)
RETROPERITONEAL HAEMATOMA ( 14 FDA reports)
SERRATIA BACTERAEMIA ( 14 FDA reports)
SINUS HEADACHE ( 14 FDA reports)
SPINAL FRACTURE ( 14 FDA reports)
SPUTUM CULTURE POSITIVE ( 14 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 14 FDA reports)
TOOTH INFECTION ( 14 FDA reports)
X-RAY ABNORMAL ( 14 FDA reports)
ABSCESS JAW ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 13 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 13 FDA reports)
AORTIC VALVE DISEASE ( 13 FDA reports)
APPLICATION SITE ERYTHEMA ( 13 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 13 FDA reports)
BONE SWELLING ( 13 FDA reports)
CANCER PAIN ( 13 FDA reports)
CARDIAC ASTHMA ( 13 FDA reports)
CARDIAC FLUTTER ( 13 FDA reports)
COLITIS ISCHAEMIC ( 13 FDA reports)
DELUSION ( 13 FDA reports)
DERMATITIS ALLERGIC ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 13 FDA reports)
EMBOLISM ( 13 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 13 FDA reports)
EXTRASYSTOLES ( 13 FDA reports)
FOOT DEFORMITY ( 13 FDA reports)
FRACTURED SACRUM ( 13 FDA reports)
GASTROINTESTINAL INFECTION ( 13 FDA reports)
HEART DISEASE CONGENITAL ( 13 FDA reports)
HEPATIC NECROSIS ( 13 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 13 FDA reports)
IATROGENIC INJURY ( 13 FDA reports)
INCREASED TENDENCY TO BRUISE ( 13 FDA reports)
INTESTINAL HAEMORRHAGE ( 13 FDA reports)
LARYNGEAL OEDEMA ( 13 FDA reports)
MACULAR DEGENERATION ( 13 FDA reports)
MITRAL VALVE PROLAPSE ( 13 FDA reports)
MOOD SWINGS ( 13 FDA reports)
MYOCARDITIS ( 13 FDA reports)
NODULE ( 13 FDA reports)
OESOPHAGEAL STENOSIS ( 13 FDA reports)
ORAL NEOPLASM ( 13 FDA reports)
PATHOGEN RESISTANCE ( 13 FDA reports)
PEPTIC ULCER ( 13 FDA reports)
PHOTOSENSITIVITY REACTION ( 13 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 13 FDA reports)
PROCEDURAL COMPLICATION ( 13 FDA reports)
RESPIRATORY RATE INCREASED ( 13 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
SINUS ARRHYTHMIA ( 13 FDA reports)
SKIN FRAGILITY ( 13 FDA reports)
SOCIAL PROBLEM ( 13 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 13 FDA reports)
THROMBOCYTOPENIC PURPURA ( 13 FDA reports)
TONGUE ULCERATION ( 13 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 13 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 13 FDA reports)
VEIN PAIN ( 13 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
XEROSIS ( 13 FDA reports)
ADENOCARCINOMA ( 12 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 12 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 12 FDA reports)
BLOOD URIC ACID DECREASED ( 12 FDA reports)
BREAST INFLAMMATION ( 12 FDA reports)
BRONCHIOLITIS ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
CLOSTRIDIAL INFECTION ( 12 FDA reports)
COMPLETED SUICIDE ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
CUTANEOUS VASCULITIS ( 12 FDA reports)
DERMAL CYST ( 12 FDA reports)
DERMATITIS ACNEIFORM ( 12 FDA reports)
ENCEPHALOMALACIA ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
EYE DISORDER ( 12 FDA reports)
EYE PAIN ( 12 FDA reports)
FEELING JITTERY ( 12 FDA reports)
FURUNCLE ( 12 FDA reports)
GASTROINTESTINAL INJURY ( 12 FDA reports)
GLOSSITIS ( 12 FDA reports)
HEART SOUNDS ABNORMAL ( 12 FDA reports)
HEPATIC FIBROSIS ( 12 FDA reports)
HERPES VIRUS INFECTION ( 12 FDA reports)
INGUINAL HERNIA ( 12 FDA reports)
INJECTION SITE INDURATION ( 12 FDA reports)
INJECTION SITE PRURITUS ( 12 FDA reports)
INTRAOCULAR LENS IMPLANT ( 12 FDA reports)
ISCHAEMIC HEPATITIS ( 12 FDA reports)
LABILE HYPERTENSION ( 12 FDA reports)
LIBIDO DECREASED ( 12 FDA reports)
LIP ULCERATION ( 12 FDA reports)
MEAN CELL VOLUME INCREASED ( 12 FDA reports)
MEGACOLON ( 12 FDA reports)
MUSCLE TWITCHING ( 12 FDA reports)
PANCREATIC CARCINOMA ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 12 FDA reports)
PITTING OEDEMA ( 12 FDA reports)
POSTOPERATIVE INFECTION ( 12 FDA reports)
PREGNANCY ( 12 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 12 FDA reports)
PROTEUS INFECTION ( 12 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 12 FDA reports)
SPINAL DISORDER ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 12 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 12 FDA reports)
TRANSFUSION ( 12 FDA reports)
TYPE 1 DIABETES MELLITUS ( 12 FDA reports)
URETERIC OBSTRUCTION ( 12 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 12 FDA reports)
ABDOMINAL ADHESIONS ( 11 FDA reports)
ABDOMINAL NEOPLASM ( 11 FDA reports)
ACTINOMYCOSIS ( 11 FDA reports)
ALCOHOLIC LIVER DISEASE ( 11 FDA reports)
APPENDIX DISORDER ( 11 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 11 FDA reports)
BACK INJURY ( 11 FDA reports)
BACTERIAL TEST POSITIVE ( 11 FDA reports)
BILIARY DILATATION ( 11 FDA reports)
BLOOD BICARBONATE DECREASED ( 11 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 11 FDA reports)
BLOOD DISORDER ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 11 FDA reports)
BODY TEMPERATURE DECREASED ( 11 FDA reports)
BONE MARROW DEPRESSION ( 11 FDA reports)
BREAST CALCIFICATIONS ( 11 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 11 FDA reports)
CIRRHOSIS ALCOHOLIC ( 11 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 11 FDA reports)
DENTAL FISTULA ( 11 FDA reports)
DRUG PRESCRIBING ERROR ( 11 FDA reports)
FAT NECROSIS ( 11 FDA reports)
FEMORAL ARTERY OCCLUSION ( 11 FDA reports)
FIBRIN D DIMER INCREASED ( 11 FDA reports)
FOOT FRACTURE ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 11 FDA reports)
INCREASED APPETITE ( 11 FDA reports)
INTRACRANIAL ANEURYSM ( 11 FDA reports)
JOINT DISLOCATION ( 11 FDA reports)
KIDNEY INFECTION ( 11 FDA reports)
KLEBSIELLA TEST POSITIVE ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 11 FDA reports)
LUNG TRANSPLANT ( 11 FDA reports)
MECHANICAL VENTILATION ( 11 FDA reports)
METASTASES TO OVARY ( 11 FDA reports)
METASTASES TO PERITONEUM ( 11 FDA reports)
MIDDLE INSOMNIA ( 11 FDA reports)
MYOSITIS ( 11 FDA reports)
NEPHROSCLEROSIS ( 11 FDA reports)
NEUROLOGICAL SYMPTOM ( 11 FDA reports)
NEUROPATHY ( 11 FDA reports)
ODYNOPHAGIA ( 11 FDA reports)
ORAL INFECTION ( 11 FDA reports)
ORAL SURGERY ( 11 FDA reports)
PELVIC PAIN ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
PROCEDURAL PAIN ( 11 FDA reports)
RENAL ARTERY STENOSIS ( 11 FDA reports)
RETICULOCYTE COUNT INCREASED ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SKIN BURNING SENSATION ( 11 FDA reports)
SKIN FIBROSIS ( 11 FDA reports)
SKIN INDURATION ( 11 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 11 FDA reports)
SUBMANDIBULAR MASS ( 11 FDA reports)
THROAT TIGHTNESS ( 11 FDA reports)
TONGUE INJURY ( 11 FDA reports)
TONSILLITIS ( 11 FDA reports)
UTERINE HAEMORRHAGE ( 11 FDA reports)
WEIGHT BEARING DIFFICULTY ( 11 FDA reports)
ABDOMINAL MASS ( 10 FDA reports)
ABORTION INDUCED ( 10 FDA reports)
ABSCESS DRAINAGE ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
ACUTE SINUSITIS ( 10 FDA reports)
ADHESIOLYSIS ( 10 FDA reports)
ALVEOLOPLASTY ( 10 FDA reports)
AMYLOIDOSIS ( 10 FDA reports)
ANAPHYLACTIC REACTION ( 10 FDA reports)
BLOOD CREATININE DECREASED ( 10 FDA reports)
BLOOD PH DECREASED ( 10 FDA reports)
BLOOD UREA DECREASED ( 10 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 10 FDA reports)
BREAST NEOPLASM ( 10 FDA reports)
BRONCHITIS ACUTE ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 10 FDA reports)
CHOLECYSTITIS ACUTE ( 10 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 10 FDA reports)
CLONIC CONVULSION ( 10 FDA reports)
COLITIS ULCERATIVE ( 10 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 10 FDA reports)
DEMYELINATION ( 10 FDA reports)
DRUG ABUSE ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
FACTOR V LEIDEN MUTATION ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GASTROINTESTINAL PERFORATION ( 10 FDA reports)
GINGIVAL ULCERATION ( 10 FDA reports)
GOUTY ARTHRITIS ( 10 FDA reports)
HALO VISION ( 10 FDA reports)
HEART TRANSPLANT ( 10 FDA reports)
HEPATORENAL FAILURE ( 10 FDA reports)
HERNIA ( 10 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 10 FDA reports)
HYPERPARATHYROIDISM ( 10 FDA reports)
HYPOACUSIS ( 10 FDA reports)
HYSTERECTOMY ( 10 FDA reports)
IMMOBILE ( 10 FDA reports)
INCOHERENT ( 10 FDA reports)
INGUINAL MASS ( 10 FDA reports)
INJECTION SITE SWELLING ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 10 FDA reports)
KNEE ARTHROPLASTY ( 10 FDA reports)
LIP EROSION ( 10 FDA reports)
LIVER ABSCESS ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
LOCAL SWELLING ( 10 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
MENIERE'S DISEASE ( 10 FDA reports)
MENSTRUATION IRREGULAR ( 10 FDA reports)
MICROCYTOSIS ( 10 FDA reports)
MITRAL VALVE REPLACEMENT ( 10 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 10 FDA reports)
OCULAR HYPERTENSION ( 10 FDA reports)
OXYGEN SUPPLEMENTATION ( 10 FDA reports)
PNEUMOMEDIASTINUM ( 10 FDA reports)
POLYCYTHAEMIA ( 10 FDA reports)
POSTNASAL DRIP ( 10 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 10 FDA reports)
PSYCHOTIC DISORDER ( 10 FDA reports)
PYURIA ( 10 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 10 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 10 FDA reports)
RHINITIS ( 10 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 10 FDA reports)
SCLERODERMA ( 10 FDA reports)
SKIN HYPERPIGMENTATION ( 10 FDA reports)
SKIN HYPERTROPHY ( 10 FDA reports)
SKIN TIGHTNESS ( 10 FDA reports)
SNORING ( 10 FDA reports)
SOFT TISSUE INFLAMMATION ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
STATUS EPILEPTICUS ( 10 FDA reports)
STOMACH DISCOMFORT ( 10 FDA reports)
SUPERINFECTION ( 10 FDA reports)
TARDIVE DYSKINESIA ( 10 FDA reports)
TIBIA FRACTURE ( 10 FDA reports)
TUMOUR EMBOLISM ( 10 FDA reports)
ULCER HAEMORRHAGE ( 10 FDA reports)
WRIST FRACTURE ( 10 FDA reports)
ABSCESS ORAL ( 9 FDA reports)
ADRENAL NEOPLASM ( 9 FDA reports)
AORTIC CALCIFICATION ( 9 FDA reports)
AORTIC THROMBOSIS ( 9 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 9 FDA reports)
BACTERIAL DISEASE CARRIER ( 9 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 9 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BILIARY DYSKINESIA ( 9 FDA reports)
BLOOD COUNT ABNORMAL ( 9 FDA reports)
BLOOD TEST ABNORMAL ( 9 FDA reports)
BRADYKINESIA ( 9 FDA reports)
BREAST SWELLING ( 9 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATHETER REMOVAL ( 9 FDA reports)
CENTRAL LINE INFECTION ( 9 FDA reports)
CEREBELLAR INFARCTION ( 9 FDA reports)
CHEYNE-STOKES RESPIRATION ( 9 FDA reports)
CHRONIC HEPATIC FAILURE ( 9 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 9 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 9 FDA reports)
COLITIS COLLAGENOUS ( 9 FDA reports)
COLON CANCER ( 9 FDA reports)
COLOSTOMY ( 9 FDA reports)
DIABETIC GASTROPARESIS ( 9 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
EMBOLISM ARTERIAL ( 9 FDA reports)
ENDOMETRIAL ATROPHY ( 9 FDA reports)
EOSINOPHILIC PNEUMONIA ( 9 FDA reports)
EPIDIDYMAL CYST ( 9 FDA reports)
EYE OPERATION ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 9 FDA reports)
FIBROUS HISTIOCYTOMA ( 9 FDA reports)
GALLOP RHYTHM PRESENT ( 9 FDA reports)
GASTRIC POLYPS ( 9 FDA reports)
GASTROINTESTINAL NECROSIS ( 9 FDA reports)
GLIOSIS ( 9 FDA reports)
GRANULOCYTE COUNT DECREASED ( 9 FDA reports)
HEAT EXHAUSTION ( 9 FDA reports)
HYPERLACTACIDAEMIA ( 9 FDA reports)
HYPERSPLENISM ( 9 FDA reports)
HYPOGEUSIA ( 9 FDA reports)
IMMUNODEFICIENCY ( 9 FDA reports)
IMPETIGO ( 9 FDA reports)
INJECTION SITE RASH ( 9 FDA reports)
INJECTION SITE WARMTH ( 9 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 9 FDA reports)
INTESTINAL ULCER ( 9 FDA reports)
KYPHOSIS ( 9 FDA reports)
LABILE BLOOD PRESSURE ( 9 FDA reports)
LEUKOENCEPHALOPATHY ( 9 FDA reports)
LIVEDO RETICULARIS ( 9 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 9 FDA reports)
LYMPHANGITIS ( 9 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 9 FDA reports)
MICTURITION URGENCY ( 9 FDA reports)
MONONEURITIS ( 9 FDA reports)
MOOD ALTERED ( 9 FDA reports)
MOUTH INJURY ( 9 FDA reports)
NASAL ODOUR ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NEPHROPATHY TOXIC ( 9 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 9 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 9 FDA reports)
ORAL FUNGAL INFECTION ( 9 FDA reports)
OTITIS MEDIA ( 9 FDA reports)
OVARIAN CANCER ( 9 FDA reports)
OVARIAN CYST ( 9 FDA reports)
PAROTID GLAND ENLARGEMENT ( 9 FDA reports)
PHOTOPHOBIA ( 9 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 9 FDA reports)
PROCTALGIA ( 9 FDA reports)
PULMONARY THROMBOSIS ( 9 FDA reports)
RAYNAUD'S PHENOMENON ( 9 FDA reports)
RENAL ATROPHY ( 9 FDA reports)
RHEUMATIC FEVER ( 9 FDA reports)
SALIVARY GLAND PAIN ( 9 FDA reports)
SCAN ABNORMAL ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKIN PAPILLOMA ( 9 FDA reports)
SKIN REACTION ( 9 FDA reports)
SPINAL HAEMANGIOMA ( 9 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 9 FDA reports)
STREPTOCOCCAL SEPSIS ( 9 FDA reports)
STUPOR ( 9 FDA reports)
SUBCUTANEOUS ABSCESS ( 9 FDA reports)
SUBILEUS ( 9 FDA reports)
TERMINAL STATE ( 9 FDA reports)
THERAPEUTIC PROCEDURE ( 9 FDA reports)
THORACOTOMY ( 9 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 9 FDA reports)
TOBACCO ABUSE ( 9 FDA reports)
TONGUE COATED ( 9 FDA reports)
TREATMENT FAILURE ( 9 FDA reports)
UNDERDOSE ( 9 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 9 FDA reports)
VARICELLA ( 9 FDA reports)
VARICOCELE ( 9 FDA reports)
VASCULAR CAUTERISATION ( 9 FDA reports)
VEIN DISORDER ( 9 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 9 FDA reports)
ABDOMINAL OPERATION ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ADDISON'S DISEASE ( 8 FDA reports)
ANGIONEUROTIC OEDEMA ( 8 FDA reports)
AORTIC DISSECTION ( 8 FDA reports)
APHTHOUS STOMATITIS ( 8 FDA reports)
ARTERIAL THROMBOSIS ( 8 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 8 FDA reports)
BIOPSY BONE ABNORMAL ( 8 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 8 FDA reports)
BIPOLAR DISORDER ( 8 FDA reports)
BRADYPNOEA ( 8 FDA reports)
BRAIN HERNIATION ( 8 FDA reports)
BRAIN INJURY ( 8 FDA reports)
BREAST CYST ( 8 FDA reports)
CALCIPHYLAXIS ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CAROTID ARTERY OCCLUSION ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CHRONIC SINUSITIS ( 8 FDA reports)
CITROBACTER INFECTION ( 8 FDA reports)
CLAVICLE FRACTURE ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 8 FDA reports)
CONCUSSION ( 8 FDA reports)
CUSHING'S SYNDROME ( 8 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 8 FDA reports)
DENTAL PULP DISORDER ( 8 FDA reports)
DEVICE DISLOCATION ( 8 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 8 FDA reports)
DRUG ABUSER ( 8 FDA reports)
DYSPAREUNIA ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
EJECTION FRACTION ABNORMAL ( 8 FDA reports)
EPIGASTRIC DISCOMFORT ( 8 FDA reports)
EXANTHEM ( 8 FDA reports)
EYE INFECTION ( 8 FDA reports)
GASTROENTERITIS RADIATION ( 8 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 8 FDA reports)
HAEMOBILIA ( 8 FDA reports)
HAEMOGLOBIN INCREASED ( 8 FDA reports)
HEPATIC PAIN ( 8 FDA reports)
HEPATITIS TOXIC ( 8 FDA reports)
HEPATOJUGULAR REFLUX ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
HYPERMAGNESAEMIA ( 8 FDA reports)
HYPERPHOSPHATAEMIA ( 8 FDA reports)
HYPOPERFUSION ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
INTESTINAL MASS ( 8 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
JOINT SPRAIN ( 8 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 8 FDA reports)
LEUKAEMIA ( 8 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 8 FDA reports)
MASTECTOMY ( 8 FDA reports)
MASTOIDITIS ( 8 FDA reports)
METABOLIC DISORDER ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE ( 8 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 8 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 8 FDA reports)
ORAL MUCOSA EROSION ( 8 FDA reports)
ORAL NEOPLASM BENIGN ( 8 FDA reports)
ORAL TORUS ( 8 FDA reports)
OVERWEIGHT ( 8 FDA reports)
PANNICULITIS ( 8 FDA reports)
PARALYSIS FLACCID ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PERFORMANCE STATUS DECREASED ( 8 FDA reports)
PERONEAL NERVE PALSY ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 8 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
PYOTHORAX ( 8 FDA reports)
QUADRIPLEGIA ( 8 FDA reports)
RENAL MASS ( 8 FDA reports)
RENAL TUBULAR DISORDER ( 8 FDA reports)
RENIN INCREASED ( 8 FDA reports)
RETINOPATHY ( 8 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 8 FDA reports)
SALIVARY HYPERSECRETION ( 8 FDA reports)
SALPINGITIS ( 8 FDA reports)
SNEEZING ( 8 FDA reports)
SUDDEN HEARING LOSS ( 8 FDA reports)
SUNBURN ( 8 FDA reports)
TONGUE NEOPLASM ( 8 FDA reports)
TUBERCULOUS PLEURISY ( 8 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 8 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
VENOUS THROMBOSIS LIMB ( 8 FDA reports)
VOCAL CORD POLYP ( 8 FDA reports)
WALKING DISABILITY ( 8 FDA reports)
WOUND HAEMORRHAGE ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
ABDOMINAL HERNIA ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
AFFECTIVE DISORDER ( 7 FDA reports)
AKINESIA ( 7 FDA reports)
ALCOHOL ABUSE ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 7 FDA reports)
ANGIOPLASTY ( 7 FDA reports)
APALLIC SYNDROME ( 7 FDA reports)
APHONIA ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 7 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 7 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 7 FDA reports)
BIOPSY LIVER ABNORMAL ( 7 FDA reports)
BLADDER SPASM ( 7 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 7 FDA reports)
BLOOD CHLORIDE INCREASED ( 7 FDA reports)
BLOOD CORTISOL INCREASED ( 7 FDA reports)
BLOOD PH INCREASED ( 7 FDA reports)
BLOOD UREA ABNORMAL ( 7 FDA reports)
BONE FRAGMENTATION ( 7 FDA reports)
CARDIAC VALVE VEGETATION ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
CATHETER PLACEMENT ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CEREBELLAR SYNDROME ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
CHOLANGIOGRAM ( 7 FDA reports)
CHRONIC HEPATITIS ( 7 FDA reports)
CLUBBING ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
DEBRIDEMENT ( 7 FDA reports)
DEVICE FAILURE ( 7 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 7 FDA reports)
DISUSE SYNDROME ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
ELECTROLYTE DEPLETION ( 7 FDA reports)
ENDOPHTHALMITIS ( 7 FDA reports)
ENTERITIS INFECTIOUS ( 7 FDA reports)
ERUCTATION ( 7 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 7 FDA reports)
EYE ROLLING ( 7 FDA reports)
FEBRILE BONE MARROW APLASIA ( 7 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 7 FDA reports)
GASTRIC MUCOSAL LESION ( 7 FDA reports)
GASTRIC VARICES ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HAEMORRHAGIC STROKE ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HEART TRANSPLANT REJECTION ( 7 FDA reports)
HEART VALVE INCOMPETENCE ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 7 FDA reports)
HEPATIC TRAUMA ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HYPERTONIA ( 7 FDA reports)
HYPERVOLAEMIA ( 7 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 7 FDA reports)
ICHTHYOSIS ( 7 FDA reports)
IMPAIRED DRIVING ABILITY ( 7 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
INCREASED BRONCHIAL SECRETION ( 7 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 7 FDA reports)
INFUSION SITE PRURITUS ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 7 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 7 FDA reports)
IRON OVERLOAD ( 7 FDA reports)
JOINT LOCK ( 7 FDA reports)
KIDNEY SMALL ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
MALIGNANT HYPERTENSION ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MASTICATION DISORDER ( 7 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 7 FDA reports)
MULTIPLE SCLEROSIS ( 7 FDA reports)
MUSCLE CRAMP ( 7 FDA reports)
MYCOSIS FUNGOIDES ( 7 FDA reports)
NIPPLE PAIN ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 7 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
ORAL FIBROMA ( 7 FDA reports)
ORAL MUCOSA ATROPHY ( 7 FDA reports)
ORTHODONTIC APPLIANCE USER ( 7 FDA reports)
PARAPROTEINAEMIA ( 7 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 7 FDA reports)
PHARYNGEAL DISORDER ( 7 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 7 FDA reports)
PLASMACYTOSIS ( 7 FDA reports)
PNEUMONIA VIRAL ( 7 FDA reports)
POISONING ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POLYMYOSITIS ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 7 FDA reports)
PSEUDOMONAL SEPSIS ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
QUALITY OF LIFE DECREASED ( 7 FDA reports)
RESPIRATORY RATE DECREASED ( 7 FDA reports)
SCROTAL OEDEMA ( 7 FDA reports)
SEPTIC EMBOLUS ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
STASIS DERMATITIS ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
THALASSAEMIA BETA ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TRAUMATIC HAEMATOMA ( 7 FDA reports)
TRIGGER FINGER ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
URINE ANALYSIS ABNORMAL ( 7 FDA reports)
UVEITIS ( 7 FDA reports)
VASCULAR GRAFT ( 7 FDA reports)
VASOPLEGIA SYNDROME ( 7 FDA reports)
VITAMIN B12 DEFICIENCY ( 7 FDA reports)
WEIGHT LOSS POOR ( 7 FDA reports)
ABDOMINAL ABSCESS ( 6 FDA reports)
AGEUSIA ( 6 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 6 FDA reports)
ANAEMIA MEGALOBLASTIC ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ANGIOKERATOMA ( 6 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 6 FDA reports)
ANTIBODY TEST POSITIVE ( 6 FDA reports)
APPLICATION SITE PRURITUS ( 6 FDA reports)
ARTERIAL DISORDER ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BILE DUCT CANCER ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BLOOD CREATININE ABNORMAL ( 6 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 6 FDA reports)
BLOOD OSMOLARITY DECREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 6 FDA reports)
BLOOD TRYPSIN INCREASED ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BRAIN STEM INFARCTION ( 6 FDA reports)
BRONCHIAL OBSTRUCTION ( 6 FDA reports)
BURNS SECOND DEGREE ( 6 FDA reports)
CALCULUS URETERIC ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CARDIAC ANEURYSM ( 6 FDA reports)
CARDIAC OPERATION ( 6 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CERVICOBRACHIAL SYNDROME ( 6 FDA reports)
CHOLANGIOLITIS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
COARCTATION OF THE AORTA ( 6 FDA reports)
COLLAGEN DISORDER ( 6 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 6 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 6 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 6 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 6 FDA reports)
DIABETIC FOOT ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
EAR DISCOMFORT ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
EYE HAEMORRHAGE ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
FIBRIN DECREASED ( 6 FDA reports)
FOLATE DEFICIENCY ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 6 FDA reports)
GASTROINTESTINAL EROSION ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 6 FDA reports)
GINGIVAL SWELLING ( 6 FDA reports)
GLOMERULONEPHRITIS ( 6 FDA reports)
GLUCOSE URINE PRESENT ( 6 FDA reports)
HAEMANGIOMA OF LIVER ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HEPATIC MASS ( 6 FDA reports)
HEPATIC VEIN STENOSIS ( 6 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 6 FDA reports)
HEPATOBILIARY DISEASE ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
HYPERALDOSTERONISM ( 6 FDA reports)
HYPOCOAGULABLE STATE ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
IMPAIRED SELF-CARE ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 6 FDA reports)
INCISION SITE HAEMORRHAGE ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
INTENTIONAL MISUSE ( 6 FDA reports)
IRITIS ( 6 FDA reports)
JUGULAR VEIN THROMBOSIS ( 6 FDA reports)
LARGE INTESTINE CARCINOMA ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LOSS OF EMPLOYMENT ( 6 FDA reports)
MALIGNANT ASCITES ( 6 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 6 FDA reports)
MASTITIS ( 6 FDA reports)
MEDICATION RESIDUE ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
MENOMETRORRHAGIA ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
METASTATIC NEOPLASM ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MITRAL VALVE STENOSIS ( 6 FDA reports)
MOUTH BREATHING ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 6 FDA reports)
MULTIPLE FRACTURES ( 6 FDA reports)
MUSCLE DISORDER ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
NEURODEGENERATIVE DISORDER ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NEUROMYOPATHY ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OPEN ANGLE GLAUCOMA ( 6 FDA reports)
ORAL DISCOMFORT ( 6 FDA reports)
ORAL MUCOSAL ERUPTION ( 6 FDA reports)
OXYGEN SATURATION ABNORMAL ( 6 FDA reports)
PAIN OF SKIN ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PANCREATIC ENZYMES INCREASED ( 6 FDA reports)
PANCREATIC INSUFFICIENCY ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PCO2 DECREASED ( 6 FDA reports)
PERIORBITAL HAEMATOMA ( 6 FDA reports)
PERIORBITAL OEDEMA ( 6 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 6 FDA reports)
POLYP ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PULMONARY TOXICITY ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PYLORIC STENOSIS ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RADIUS FRACTURE ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
RESPIRATORY TRACT IRRITATION ( 6 FDA reports)
RETINOPATHY HYPERTENSIVE ( 6 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SCLEROMALACIA ( 6 FDA reports)
SEDATION ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
SKIN INJURY ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
SOPOR ( 6 FDA reports)
SPINAL CORD DISORDER ( 6 FDA reports)
SPLENIC ABSCESS ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
THYROIDITIS ( 6 FDA reports)
TONGUE BLACK HAIRY ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TONGUE DISORDER ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
TUMOUR HAEMORRHAGE ( 6 FDA reports)
URINARY TRACT OBSTRUCTION ( 6 FDA reports)
VASCULAR CALCIFICATION ( 6 FDA reports)
VASCULITIS NECROTISING ( 6 FDA reports)
ABDOMINAL INFECTION ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ACCIDENT AT HOME ( 5 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ADAMS-STOKES SYNDROME ( 5 FDA reports)
ADENOMA BENIGN ( 5 FDA reports)
ADRENAL CARCINOMA ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ALCOHOLISM ( 5 FDA reports)
ALVEOLITIS ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANAL EROSION ( 5 FDA reports)
ANAL FISSURE ( 5 FDA reports)
ANASTOMOTIC ULCER ( 5 FDA reports)
ANISOCYTOSIS ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
ANTI-INSULIN ANTIBODY ( 5 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 5 FDA reports)
ANTICHOLINERGIC SYNDROME ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 5 FDA reports)
ANTINUCLEAR ANTIBODY ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
AUTOIMMUNE THYROIDITIS ( 5 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 5 FDA reports)
BARRETT'S OESOPHAGUS ( 5 FDA reports)
BASOPHIL COUNT DECREASED ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 5 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOODY AIRWAY DISCHARGE ( 5 FDA reports)
BONE MARROW DISORDER ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BREATH SOUNDS DECREASED ( 5 FDA reports)
BRONCHIAL INFECTION ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BUTTOCK PAIN ( 5 FDA reports)
CARDIAC CIRRHOSIS ( 5 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 5 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 5 FDA reports)
CATHETER SITE HAEMORRHAGE ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CERVICAL DYSPLASIA ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHANGE OF BOWEL HABIT ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHOLESTATIC LIVER INJURY ( 5 FDA reports)
CHONDROCALCINOSIS ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
CLEFT PALATE ( 5 FDA reports)
CLOSED FRACTURE MANIPULATION ( 5 FDA reports)
COLLAPSE OF LUNG ( 5 FDA reports)
COMPLEX PARTIAL SEIZURES ( 5 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 5 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 5 FDA reports)
CORNEAL ABRASION ( 5 FDA reports)
CROUP INFECTIOUS ( 5 FDA reports)
CUSHINGOID ( 5 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 5 FDA reports)
DIURETIC THERAPY ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
DRUG-INDUCED LIVER INJURY ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
ENTEROCUTANEOUS FISTULA ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
EXSANGUINATION ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FISTULA ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
FUNGAL DNA TEST POSITIVE ( 5 FDA reports)
GALACTORRHOEA ( 5 FDA reports)
GALLBLADDER OEDEMA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 5 FDA reports)
GASTRIC PERFORATION ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GASTRODUODENAL ULCER ( 5 FDA reports)
GAZE PALSY ( 5 FDA reports)
GINGIVAL ERYTHEMA ( 5 FDA reports)
GLOBULINS INCREASED ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLYCOSURIA ( 5 FDA reports)
HAEMORRHAGIC DISORDER ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HEPATIC ATROPHY ( 5 FDA reports)
HISTIOCYTOSIS ( 5 FDA reports)
HYPERCHLORAEMIA ( 5 FDA reports)
HYPERCREATININAEMIA ( 5 FDA reports)
HYPERGLOBULINAEMIA ( 5 FDA reports)
HYPERKINESIA ( 5 FDA reports)
HYPERPROLACTINAEMIA ( 5 FDA reports)
HYPERTONIC BLADDER ( 5 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INFUSION SITE PAIN ( 5 FDA reports)
INJECTION SITE IRRITATION ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
KNEE OPERATION ( 5 FDA reports)
LARGE INTESTINAL ULCER ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LUNG ADENOCARCINOMA ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
LYMPH NODE FIBROSIS ( 5 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 5 FDA reports)
LYMPHOCYTOSIS ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MARASMUS ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
MENINGIOMA ( 5 FDA reports)
MENSTRUAL DISORDER ( 5 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 5 FDA reports)
MONOCYTE COUNT DECREASED ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARTNER STRESS ( 5 FDA reports)
PEMPHIGUS ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PERNICIOUS ANAEMIA ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PLEURODESIS ( 5 FDA reports)
POOR PERSONAL HYGIENE ( 5 FDA reports)
POST PROCEDURAL INFECTION ( 5 FDA reports)
PRESCRIBED OVERDOSE ( 5 FDA reports)
PRODUCT ADHESION ISSUE ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULSE ABNORMAL ( 5 FDA reports)
PUPIL FIXED ( 5 FDA reports)
PUPILS UNEQUAL ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RECTAL PROLAPSE ( 5 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 5 FDA reports)
REHABILITATION THERAPY ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
SCAB ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SCROTAL ULCER ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SEXUAL DYSFUNCTION ( 5 FDA reports)
SKIN INFECTION ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
SOFT TISSUE DISORDER ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SOMNAMBULISM ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
SYNCOPE VASOVAGAL ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
THINKING ABNORMAL ( 5 FDA reports)
THYROXINE FREE INCREASED ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
TUMOUR NECROSIS ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
URINE SODIUM DECREASED ( 5 FDA reports)
UTERINE DISORDER ( 5 FDA reports)
VENOUS STASIS ( 5 FDA reports)
VITAMIN D DECREASED ( 5 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMBLYOPIA ( 4 FDA reports)
AMYLASE INCREASED ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANASTOMOTIC STENOSIS ( 4 FDA reports)
ANGIOGRAM ( 4 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APPARENT DEATH ( 4 FDA reports)
APPLICATION SITE IRRITATION ( 4 FDA reports)
ARM AMPUTATION ( 4 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ASTHMATIC CRISIS ( 4 FDA reports)
ATOPY ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
BLADDER PAIN ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD INSULIN INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BREAST DISCOMFORT ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BRONCHOPNEUMOPATHY ( 4 FDA reports)
BUNION ( 4 FDA reports)
CANDIDA PNEUMONIA ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC AMYLOIDOSIS ( 4 FDA reports)
CARDIAC HYPERTROPHY ( 4 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 4 FDA reports)
CATHETER SITE ERYTHEMA ( 4 FDA reports)
CATHETER SITE OEDEMA ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CELL MARKER INCREASED ( 4 FDA reports)
CELLULITIS STREPTOCOCCAL ( 4 FDA reports)
CEREBRAL MICROANGIOPATHY ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLESTEROSIS ( 4 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 4 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
CYTOTOXIC OEDEMA ( 4 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG INTERACTION POTENTIATION ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
DUODENAL ULCER PERFORATION ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 4 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FANCONI SYNDROME ACQUIRED ( 4 FDA reports)
FEAR OF PREGNANCY ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FOETAL DISORDER ( 4 FDA reports)
FOOD INTERACTION ( 4 FDA reports)
FOOT OPERATION ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
FRUSTRATION ( 4 FDA reports)
FULL BLOOD COUNT DECREASED ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 4 FDA reports)
GASTROINTESTINAL OEDEMA ( 4 FDA reports)
GILBERT'S SYNDROME ( 4 FDA reports)
GINGIVAL DISORDER ( 4 FDA reports)
GINGIVAL GRAFT ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HAPTOGLOBIN INCREASED ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC HYDROTHORAX ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 4 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HOMOCYSTINAEMIA ( 4 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPOAESTHESIA FACIAL ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 4 FDA reports)
HYPOVITAMINOSIS ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
ILIAC ARTERY STENOSIS ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
INTRAPERICARDIAL THROMBOSIS ( 4 FDA reports)
KYPHOSCOLIOSIS ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEIOMYOSARCOMA ( 4 FDA reports)
LICHENOID KERATOSIS ( 4 FDA reports)
LIP OEDEMA ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 4 FDA reports)
LUMBAR RADICULOPATHY ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
MACULAR OEDEMA ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
METAPLASIA ( 4 FDA reports)
MICROCOCCUS INFECTION ( 4 FDA reports)
MIXED HEPATOCELLULAR CHOLANGIOCARCINOMA ( 4 FDA reports)
MIXED LIVER INJURY ( 4 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NAIL DISCOLOURATION ( 4 FDA reports)
NAIL DISORDER ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
ORCHITIS ( 4 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
PACEMAKER COMPLICATION ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERITONEAL DIALYSIS ( 4 FDA reports)
PERITONEAL EFFUSION ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 4 FDA reports)
PLATELET DISORDER ( 4 FDA reports)
PLEUROTHOTONUS ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POLYCYSTIC OVARIES ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROCEDURAL NAUSEA ( 4 FDA reports)
PROCEDURAL VOMITING ( 4 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
PULMONARY ARTERY DILATATION ( 4 FDA reports)
PULMONARY HILUM MASS ( 4 FDA reports)
PULMONARY SEPSIS ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
READING DISORDER ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 4 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 4 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
SENSATION OF PRESSURE ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN NEOPLASM EXCISION ( 4 FDA reports)
SKIN SWELLING ( 4 FDA reports)
SKULL FRACTURE ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SPLENIC INJURY ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
SUBACUTE ENDOCARDITIS ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
TEARFULNESS ( 4 FDA reports)
TENSION ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
THORACIC CAVITY DRAINAGE ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TUBERCULIN TEST POSITIVE ( 4 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
URINARY TRACT DISORDER ( 4 FDA reports)
URINE CYTOLOGY ABNORMAL ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
UTERINE CANCER ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VITAMIN K DEFICIENCY ( 4 FDA reports)
VITREOUS DETACHMENT ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
VOLUME BLOOD DECREASED ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
WRONG DRUG ADMINISTERED ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ACANTHOSIS NIGRICANS ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ADRENOCORTICAL CARCINOMA ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
ALVEOLAR PROTEINOSIS ( 3 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANAL STENOSIS ( 3 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 3 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
AORTIC DISORDER ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ASCITES INFECTION ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILE DUCT STENT REMOVAL ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 3 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BLOOD URIC ACID ABNORMAL ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE DEBRIDEMENT ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CANDIDA TEST POSITIVE ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARCINOID TUMOUR PULMONARY ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC DISCOMFORT ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 3 FDA reports)
CARDIAC SEPTAL DEFECT ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 3 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CRYOGLOBULINAEMIA ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CYANOSIS CENTRAL ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DECREASED VENTRICULAR PRELOAD ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEVICE OCCLUSION ( 3 FDA reports)
DIAPHRAGMATIC DISORDER ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DRAIN REMOVAL ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG INTERACTION INHIBITION ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DYSPONESIS ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
ELEVATED MOOD ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENDOCARDITIS CANDIDA ( 3 FDA reports)
ENDOCRINE DISORDER ( 3 FDA reports)
ENTEROBACTER BACTERAEMIA ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EXTRAVASATION ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EXTUBATION ( 3 FDA reports)
FACIAL BONES FRACTURE ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
FANCONI SYNDROME ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 3 FDA reports)
GENITAL HERPES ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GLOBULIN ABNORMAL ( 3 FDA reports)
GOUTY TOPHUS ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC INFARCTION ( 3 FDA reports)
HIGH FREQUENCY ABLATION ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
IMPULSIVE BEHAVIOUR ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFUSION SITE NECROSIS ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE URTICARIA ( 3 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 3 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
JUDGEMENT IMPAIRED ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LIMB MALFORMATION ( 3 FDA reports)
LIPASE ABNORMAL ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LOSS OF LIBIDO ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG INJURY ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEASLES ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
MESENTERIC OCCLUSION ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MITRAL VALVE DISEASE MIXED ( 3 FDA reports)
MITRAL VALVE REPAIR ( 3 FDA reports)
MITRAL VALVE SCLEROSIS ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOGLOBINAEMIA ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NIPPLE SWELLING ( 3 FDA reports)
NODAL OSTEOARTHRITIS ( 3 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OBSTRUCTION ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OEDEMATOUS PANCREATITIS ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PANCOAST'S SYNDROME ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PATELLA FRACTURE ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PEAU D'ORANGE ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIARTICULAR DISORDER ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL HAEMATOMA ( 3 FDA reports)
PERITONEAL INFECTION ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHARYNGEAL MASS ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PLASMAPHERESIS ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
POLYARTHRITIS ( 3 FDA reports)
POOR DENTAL CONDITION ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 3 FDA reports)
PREVENTIVE SURGERY ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
PUTAMEN HAEMORRHAGE ( 3 FDA reports)
PYOMETRA ( 3 FDA reports)
RADICULAR PAIN ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RECTOCELE ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
RENAL ISCHAEMIA ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RETINAL ARTERY OCCLUSION ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
RHEUMATIC HEART DISEASE ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
SALPINGECTOMY ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
SCROTAL ABSCESS ( 3 FDA reports)
SCROTAL DISORDER ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SKIN DYSTROPHY ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STARING ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SURFACTANT PROTEIN INCREASED ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TONSILLAR INFLAMMATION ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
VACCINATION COMPLICATION ( 3 FDA reports)
VARICOSE ULCERATION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR OPERATION ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VENOUS PRESSURE INCREASED ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 3 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 3 FDA reports)
VERTIGO POSITIONAL ( 3 FDA reports)
VIRAL SKIN INFECTION ( 3 FDA reports)
VITAMIN B1 DEFICIENCY ( 3 FDA reports)
VITAMIN B6 DEFICIENCY ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACID FAST STAIN POSITIVE ( 2 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACTIVATION SYNDROME ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
ALOPECIA EFFLUVIUM ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMAUROSIS FUGAX ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANDROGEN DEFICIENCY ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
AORTIC INTRAMURAL HAEMATOMA ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL CATHETERISATION ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BACTERIAL TOXAEMIA ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BENIGN MESENTERIC NEOPLASM ( 2 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
BILE DUCT CANCER STAGE IV ( 2 FDA reports)
BILE OUTPUT ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD GONADOTROPHIN DECREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BONE SCAN ABNORMAL ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN STEM ISCHAEMIA ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BREAST HYPERPLASIA ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
C-REACTIVE PROTEIN ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CALCIFICATION OF MUSCLE ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC OUTPUT INCREASED ( 2 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CEREBELLAR HAEMATOMA ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL MALARIA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CERVIX CARCINOMA STAGE III ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CHYLOTHORAX ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 2 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 2 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREATININE URINE DECREASED ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRYOGLOBULINS PRESENT ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CULTURE WOUND POSITIVE ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DENTURE WEARER ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DERMO-HYPODERMITIS ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE ISSUE ( 2 FDA reports)
DEVICE PACING ISSUE ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DEVICE STIMULATION ISSUE ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR INFECTION VIRAL ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ERYTHEMA INDURATUM ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EXTRASKELETAL OSSIFICATION ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FABRY'S DISEASE ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FATTY LIVER ALCOHOLIC ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GALLBLADDER ABSCESS ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL DISCHARGE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
GLUCOSE URINE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HBV DNA INCREASED ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEPATIC ARTERY EMBOLISM ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS B ANTIBODY ABNORMAL ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSPICE CARE ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERCORTICOIDISM ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSION NEONATAL ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTRANSAMINASAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPHYSITIS ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILEITIS ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INBORN ERROR OF METABOLISM ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFUSION SITE ABSCESS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRACRANIAL INJURY ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
ISOLATED ADRENOCORTICOTROPIC HORMONE DEFICIENCY ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JAUNDICE ACHOLURIC ( 2 FDA reports)
JOINT FLUID DRAINAGE ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KIDNEY DUPLEX ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LISTERIA ENCEPHALITIS ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPH NODE PALPABLE ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
MARFAN'S SYNDROME ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEDIASTINUM NEOPLASM ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENOPAUSE ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 2 FDA reports)
METASTASES TO LARGE INTESTINE ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOCARDIAL CALCIFICATION ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCCUPATIONAL EXPOSURE TO DUST ( 2 FDA reports)
OESOPHAGEAL NEOPLASM ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
OESOPHAGEAL PAIN ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OTITIS MEDIA ACUTE ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PATHOLOGICAL GAMBLING ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PENILE ABSCESS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIODONTAL OPERATION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHLEBITIS INFECTIVE ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PITUITARY ENLARGEMENT ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLASMA CELL DISORDER ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PLATELET COUNT NORMAL ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLIOMYELITIS ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POLYTRAUMATISM ( 2 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL DIARRHOEA ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 2 FDA reports)
PULMONARY VEIN STENOSIS ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL SALT-WASTING SYNDROME ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROGRADE EJACULATION ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RHYTHM IDIOVENTRICULAR ( 2 FDA reports)
SALMONELLA BACTERAEMIA ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SIGNET-RING CELL CARCINOMA ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SILICOSIS ( 2 FDA reports)
SINUS ANTROSTOMY ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPLENORENAL SHUNT ( 2 FDA reports)
SPONDYLITIC MYELOPATHY ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
SPUTUM PURULENT ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THROMBOENDARTERECTOMY ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROID OPERATION ( 2 FDA reports)
TIC ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIFASCICULAR BLOCK ( 2 FDA reports)
TROPONIN ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TUMOUR RUPTURE ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
URETHRAL DISCHARGE ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URETHRAL NEOPLASM ( 2 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE POTASSIUM INCREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VALVULOPLASTY CARDIAC ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULOPERITONEAL SHUNT MALFUNCTION ( 2 FDA reports)
VIRAL CARDIOMYOPATHY ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN C DECREASED ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
VULVAL ULCERATION ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CYST ( 1 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 1 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALCOHOLIC PSYCHOSIS ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTIC VALVE REPAIR ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERASCITES ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BASOPHIL COUNT ABNORMAL ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY HEART ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER IRRIGATION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER PROLAPSE ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD THROMBOPLASTIN ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
CALCIFICATION PANCREATIC DUCT ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL DISCHARGE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMA NEONATAL ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTATIN C INCREASED ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC BULLOSIS ( 1 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER REPAIR ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECTOPIC ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EISENMENGER'S SYNDROME ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
END STAGE AIDS ( 1 FDA reports)
END-TIDAL CO2 DECREASED ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC PUSTULOSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FAILURE TO CAPTURE ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEMINISATION ACQUIRED ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GINGIVECTOMY ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLUCAGONOMA ( 1 FDA reports)
GONADAL DYSGENESIS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTE COUNT ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA CONGENITAL ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART AND LUNG TRANSPLANT ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC ANGIOSARCOMA ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOBLASTOMA ( 1 FDA reports)
HEPATOPULMONARY SYNDROME ( 1 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILIAC VEIN OCCLUSION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAUNDICE HEPATOCELLULAR ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT STABILISATION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME ABNORMAL ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 1 FDA reports)
LUPUS HEPATITIS ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANDIBULAR PROSTHESIS USER ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO MOUTH ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHRITIS AUTOIMMUNE ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
ONCOCYTOMA ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISCS BLURRED ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PEPTOSTREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERFORATED DUODENAL ULCER REPAIR ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMA VISCOSITY ABNORMAL ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA MORAXELLA ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PORTAL HYPERTENSIVE ENTEROPATHY ( 1 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SEX HORMONE BINDING GLOBULIN INCREASED ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC INFECTION BACTERIAL ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STRANGULATED HERNIA REPAIR ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRACLAVICULAR RETRACTION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
TETANUS ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC HYPOTHERMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYMOMA MALIGNANT ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROID NODULE REMOVAL ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TOXOCARIASIS ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
URTICARIA PIGMENTOSA ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL HYPERPLASIA ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR REMODELING ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE PRURITUS ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOLVULUS OF SMALL 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 MYCOTIC INFECTION ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)

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