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

DYSPNOEA ( 1997 FDA reports)
NAUSEA ( 1928 FDA reports)
DIARRHOEA ( 1538 FDA reports)
VOMITING ( 1534 FDA reports)
DIZZINESS ( 1514 FDA reports)
RENAL FAILURE ACUTE ( 1423 FDA reports)
FATIGUE ( 1404 FDA reports)
ANAEMIA ( 1313 FDA reports)
ASTHENIA ( 1309 FDA reports)
OEDEMA PERIPHERAL ( 1292 FDA reports)
HYPOTENSION ( 1266 FDA reports)
PNEUMONIA ( 1264 FDA reports)
HYPERTENSION ( 1246 FDA reports)
PAIN ( 1187 FDA reports)
FALL ( 1165 FDA reports)
PYREXIA ( 1146 FDA reports)
DRUG INEFFECTIVE ( 1119 FDA reports)
HEADACHE ( 1117 FDA reports)
DRUG INTERACTION ( 1032 FDA reports)
MALAISE ( 1031 FDA reports)
RENAL FAILURE ( 991 FDA reports)
CHEST PAIN ( 920 FDA reports)
WEIGHT DECREASED ( 845 FDA reports)
ABDOMINAL PAIN ( 835 FDA reports)
DEHYDRATION ( 803 FDA reports)
PAIN IN EXTREMITY ( 800 FDA reports)
PRURITUS ( 794 FDA reports)
ARTHRALGIA ( 785 FDA reports)
BLOOD CREATININE INCREASED ( 761 FDA reports)
RASH ( 761 FDA reports)
BLOOD PRESSURE INCREASED ( 750 FDA reports)
HAEMOGLOBIN DECREASED ( 726 FDA reports)
COUGH ( 716 FDA reports)
CONFUSIONAL STATE ( 712 FDA reports)
DECREASED APPETITE ( 692 FDA reports)
DEATH ( 674 FDA reports)
ATRIAL FIBRILLATION ( 668 FDA reports)
PLEURAL EFFUSION ( 657 FDA reports)
BACK PAIN ( 650 FDA reports)
MYALGIA ( 642 FDA reports)
CEREBROVASCULAR ACCIDENT ( 622 FDA reports)
URINARY TRACT INFECTION ( 612 FDA reports)
LOSS OF CONSCIOUSNESS ( 609 FDA reports)
BLOOD GLUCOSE INCREASED ( 608 FDA reports)
FLUSHING ( 607 FDA reports)
SYNCOPE ( 605 FDA reports)
INSOMNIA ( 591 FDA reports)
RENAL IMPAIRMENT ( 586 FDA reports)
SEPSIS ( 582 FDA reports)
SOMNOLENCE ( 581 FDA reports)
CONSTIPATION ( 581 FDA reports)
MYOCARDIAL INFARCTION ( 574 FDA reports)
ANXIETY ( 572 FDA reports)
COMPLETED SUICIDE ( 555 FDA reports)
HYPONATRAEMIA ( 554 FDA reports)
RESPIRATORY FAILURE ( 523 FDA reports)
BRADYCARDIA ( 521 FDA reports)
HYPERKALAEMIA ( 518 FDA reports)
PARAESTHESIA ( 515 FDA reports)
CARDIAC ARREST ( 509 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 496 FDA reports)
RHABDOMYOLYSIS ( 489 FDA reports)
ERYTHEMA ( 488 FDA reports)
DEPRESSION ( 487 FDA reports)
ABDOMINAL PAIN UPPER ( 485 FDA reports)
MUSCULAR WEAKNESS ( 480 FDA reports)
THROMBOCYTOPENIA ( 477 FDA reports)
CONDITION AGGRAVATED ( 475 FDA reports)
GAIT DISTURBANCE ( 467 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 461 FDA reports)
OVERDOSE ( 459 FDA reports)
MUSCLE SPASMS ( 457 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 451 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 442 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 433 FDA reports)
CARDIAC FAILURE ( 432 FDA reports)
PLATELET COUNT DECREASED ( 430 FDA reports)
HYPOKALAEMIA ( 422 FDA reports)
CONVULSION ( 417 FDA reports)
TREMOR ( 413 FDA reports)
PULMONARY EMBOLISM ( 402 FDA reports)
VISION BLURRED ( 394 FDA reports)
FEELING ABNORMAL ( 393 FDA reports)
HYPOAESTHESIA ( 392 FDA reports)
RENAL FAILURE CHRONIC ( 372 FDA reports)
DYSPHAGIA ( 371 FDA reports)
INTERSTITIAL LUNG DISEASE ( 369 FDA reports)
PALPITATIONS ( 364 FDA reports)
PULMONARY OEDEMA ( 359 FDA reports)
WEIGHT INCREASED ( 357 FDA reports)
DIABETES MELLITUS ( 357 FDA reports)
BLOOD PRESSURE DECREASED ( 355 FDA reports)
HYPOGLYCAEMIA ( 348 FDA reports)
ANGINA PECTORIS ( 347 FDA reports)
PANCYTOPENIA ( 344 FDA reports)
CHEST DISCOMFORT ( 331 FDA reports)
JOINT SWELLING ( 330 FDA reports)
LETHARGY ( 330 FDA reports)
BLOOD UREA INCREASED ( 327 FDA reports)
HYPERHIDROSIS ( 327 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 325 FDA reports)
METABOLIC ACIDOSIS ( 321 FDA reports)
CHILLS ( 319 FDA reports)
OEDEMA ( 315 FDA reports)
TACHYCARDIA ( 310 FDA reports)
NEUTROPENIA ( 309 FDA reports)
INFECTION ( 305 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 301 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 294 FDA reports)
CELLULITIS ( 289 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 288 FDA reports)
HEART RATE INCREASED ( 286 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 285 FDA reports)
CORONARY ARTERY DISEASE ( 284 FDA reports)
DEEP VEIN THROMBOSIS ( 278 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 278 FDA reports)
ANGIOEDEMA ( 275 FDA reports)
HAEMODIALYSIS ( 275 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 274 FDA reports)
HYPERSENSITIVITY ( 270 FDA reports)
MULTI-ORGAN FAILURE ( 259 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 256 FDA reports)
BRONCHITIS ( 256 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 254 FDA reports)
EPISTAXIS ( 252 FDA reports)
RECTAL HAEMORRHAGE ( 251 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 249 FDA reports)
HYPOXIA ( 249 FDA reports)
BALANCE DISORDER ( 248 FDA reports)
ABDOMINAL DISTENSION ( 247 FDA reports)
DRY MOUTH ( 245 FDA reports)
ALOPECIA ( 244 FDA reports)
DISEASE PROGRESSION ( 244 FDA reports)
DYSARTHRIA ( 243 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 242 FDA reports)
INJURY ( 242 FDA reports)
DELIRIUM ( 239 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 239 FDA reports)
CONTUSION ( 236 FDA reports)
MEMORY IMPAIRMENT ( 233 FDA reports)
HYPERGLYCAEMIA ( 232 FDA reports)
MENTAL STATUS CHANGES ( 232 FDA reports)
ABDOMINAL DISCOMFORT ( 230 FDA reports)
ASTHMA ( 230 FDA reports)
MUSCULOSKELETAL PAIN ( 230 FDA reports)
DYSPEPSIA ( 229 FDA reports)
DRUG TOXICITY ( 228 FDA reports)
HAEMATEMESIS ( 227 FDA reports)
HEPATIC ENZYME INCREASED ( 227 FDA reports)
ARRHYTHMIA ( 226 FDA reports)
SEPTIC SHOCK ( 226 FDA reports)
SWELLING FACE ( 226 FDA reports)
DISORIENTATION ( 221 FDA reports)
FEELING HOT ( 220 FDA reports)
HAEMORRHAGE ( 220 FDA reports)
CARDIO-RESPIRATORY ARREST ( 217 FDA reports)
CEREBRAL INFARCTION ( 216 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 216 FDA reports)
CARDIAC DISORDER ( 215 FDA reports)
SWELLING ( 214 FDA reports)
URTICARIA ( 212 FDA reports)
GASTRITIS ( 211 FDA reports)
PROTEINURIA ( 210 FDA reports)
VISUAL ACUITY REDUCED ( 210 FDA reports)
BLOOD SODIUM DECREASED ( 208 FDA reports)
OROPHARYNGEAL PAIN ( 206 FDA reports)
SWOLLEN TONGUE ( 205 FDA reports)
VISUAL IMPAIRMENT ( 205 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 204 FDA reports)
HAEMATOCRIT DECREASED ( 203 FDA reports)
OFF LABEL USE ( 203 FDA reports)
CHOLELITHIASIS ( 199 FDA reports)
MELAENA ( 199 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 198 FDA reports)
HERPES ZOSTER ( 198 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 198 FDA reports)
BLOOD POTASSIUM DECREASED ( 197 FDA reports)
PRODUCT QUALITY ISSUE ( 197 FDA reports)
DYSGEUSIA ( 196 FDA reports)
CIRCULATORY COLLAPSE ( 194 FDA reports)
COMA ( 194 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 192 FDA reports)
RENAL DISORDER ( 192 FDA reports)
CYSTITIS ( 191 FDA reports)
PANCREATITIS ( 191 FDA reports)
FEBRILE NEUTROPENIA ( 189 FDA reports)
HAEMORRHOIDS ( 189 FDA reports)
LACTIC ACIDOSIS ( 189 FDA reports)
BLOOD BILIRUBIN INCREASED ( 187 FDA reports)
HALLUCINATION ( 187 FDA reports)
NEUROPATHY PERIPHERAL ( 187 FDA reports)
AMNESIA ( 185 FDA reports)
OSTEOARTHRITIS ( 185 FDA reports)
HAEMATURIA ( 184 FDA reports)
HAEMOPTYSIS ( 184 FDA reports)
SUICIDE ATTEMPT ( 184 FDA reports)
AGITATION ( 183 FDA reports)
LIVER DISORDER ( 183 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 181 FDA reports)
MYOCARDIAL ISCHAEMIA ( 181 FDA reports)
WHEEZING ( 181 FDA reports)
CATARACT ( 180 FDA reports)
HEART RATE DECREASED ( 180 FDA reports)
APLASIA PURE RED CELL ( 178 FDA reports)
ASCITES ( 177 FDA reports)
LIP SWELLING ( 177 FDA reports)
HYPERTENSIVE CRISIS ( 176 FDA reports)
SPEECH DISORDER ( 176 FDA reports)
UNRESPONSIVE TO STIMULI ( 175 FDA reports)
JAUNDICE ( 175 FDA reports)
INCORRECT DOSE ADMINISTERED ( 174 FDA reports)
ANOREXIA ( 172 FDA reports)
MOBILITY DECREASED ( 172 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 171 FDA reports)
SHOCK ( 171 FDA reports)
VERTIGO ( 171 FDA reports)
LEFT VENTRICULAR FAILURE ( 169 FDA reports)
CARDIOMEGALY ( 168 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 168 FDA reports)
ARTHRITIS ( 167 FDA reports)
DRUG HYPERSENSITIVITY ( 167 FDA reports)
HYPOCALCAEMIA ( 167 FDA reports)
IMPAIRED HEALING ( 166 FDA reports)
HYPOTHYROIDISM ( 164 FDA reports)
MUSCLE TWITCHING ( 164 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 164 FDA reports)
ABASIA ( 163 FDA reports)
LEUKOPENIA ( 163 FDA reports)
SINUSITIS ( 162 FDA reports)
UNEVALUABLE EVENT ( 159 FDA reports)
BONE PAIN ( 159 FDA reports)
DRUG DOSE OMISSION ( 159 FDA reports)
NASOPHARYNGITIS ( 159 FDA reports)
DRUG ERUPTION ( 157 FDA reports)
COLONIC POLYP ( 156 FDA reports)
ANAPHYLACTIC REACTION ( 155 FDA reports)
GASTRIC ULCER ( 155 FDA reports)
HAEMATOCHEZIA ( 155 FDA reports)
INTENTIONAL OVERDOSE ( 155 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 155 FDA reports)
STAPHYLOCOCCAL INFECTION ( 155 FDA reports)
STOMATITIS ( 155 FDA reports)
NERVOUSNESS ( 154 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 153 FDA reports)
GASTRITIS EROSIVE ( 153 FDA reports)
BURNING SENSATION ( 152 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 149 FDA reports)
HYPOMAGNESAEMIA ( 149 FDA reports)
URINARY INCONTINENCE ( 149 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 147 FDA reports)
DYSPNOEA EXERTIONAL ( 147 FDA reports)
FLATULENCE ( 146 FDA reports)
INJECTION SITE PAIN ( 146 FDA reports)
LEUKOCYTOSIS ( 146 FDA reports)
RESPIRATORY DISTRESS ( 146 FDA reports)
SKIN ULCER ( 146 FDA reports)
RESPIRATORY ARREST ( 144 FDA reports)
BLOOD POTASSIUM INCREASED ( 144 FDA reports)
PNEUMONIA ASPIRATION ( 143 FDA reports)
INFLAMMATION ( 142 FDA reports)
PANCREATITIS ACUTE ( 142 FDA reports)
BLISTER ( 140 FDA reports)
THROMBOSIS ( 139 FDA reports)
OSTEONECROSIS OF JAW ( 138 FDA reports)
ATELECTASIS ( 137 FDA reports)
ECONOMIC PROBLEM ( 136 FDA reports)
FLUID RETENTION ( 136 FDA reports)
HEMIPARESIS ( 136 FDA reports)
NECK PAIN ( 136 FDA reports)
PULMONARY FIBROSIS ( 135 FDA reports)
SUICIDAL IDEATION ( 135 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 134 FDA reports)
HYPERLIPIDAEMIA ( 134 FDA reports)
BLOOD GLUCOSE DECREASED ( 133 FDA reports)
OSTEOMYELITIS ( 132 FDA reports)
OSTEOPOROSIS ( 132 FDA reports)
TREATMENT NONCOMPLIANCE ( 131 FDA reports)
RESTLESSNESS ( 130 FDA reports)
HAEMATOMA ( 130 FDA reports)
PERICARDIAL EFFUSION ( 130 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 129 FDA reports)
LUNG DISORDER ( 129 FDA reports)
ORTHOSTATIC HYPOTENSION ( 129 FDA reports)
RASH GENERALISED ( 129 FDA reports)
RIGHT VENTRICULAR FAILURE ( 128 FDA reports)
SKIN EXFOLIATION ( 128 FDA reports)
CARDIOGENIC SHOCK ( 128 FDA reports)
DIALYSIS ( 128 FDA reports)
NEOPLASM MALIGNANT ( 128 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 127 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 127 FDA reports)
VENTRICULAR TACHYCARDIA ( 127 FDA reports)
URINARY RETENTION ( 126 FDA reports)
RASH ERYTHEMATOUS ( 125 FDA reports)
CEREBRAL HAEMORRHAGE ( 124 FDA reports)
DYSURIA ( 124 FDA reports)
HOT FLUSH ( 123 FDA reports)
OXYGEN SATURATION DECREASED ( 123 FDA reports)
RHEUMATOID ARTHRITIS ( 123 FDA reports)
DYSKINESIA ( 122 FDA reports)
GOUT ( 122 FDA reports)
INFLUENZA LIKE ILLNESS ( 122 FDA reports)
MITRAL VALVE INCOMPETENCE ( 122 FDA reports)
PALLOR ( 122 FDA reports)
ENCEPHALOPATHY ( 121 FDA reports)
FEELING COLD ( 120 FDA reports)
HEAD INJURY ( 120 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 120 FDA reports)
PRURITUS GENERALISED ( 120 FDA reports)
SKIN DISCOLOURATION ( 119 FDA reports)
DYSPHONIA ( 119 FDA reports)
EMOTIONAL DISTRESS ( 119 FDA reports)
NEUTROPHIL COUNT DECREASED ( 119 FDA reports)
ANHEDONIA ( 118 FDA reports)
HIATUS HERNIA ( 118 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 118 FDA reports)
SLEEP DISORDER ( 118 FDA reports)
TINNITUS ( 117 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 117 FDA reports)
DRY SKIN ( 117 FDA reports)
FAECES DISCOLOURED ( 117 FDA reports)
OESOPHAGITIS ( 117 FDA reports)
GENERALISED OEDEMA ( 116 FDA reports)
POLLAKIURIA ( 115 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 115 FDA reports)
TRANSAMINASES INCREASED ( 115 FDA reports)
ABNORMAL BEHAVIOUR ( 114 FDA reports)
LUNG INFILTRATION ( 113 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 113 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 113 FDA reports)
RASH PRURITIC ( 112 FDA reports)
VARICOSE VEIN ( 112 FDA reports)
ANAL FISSURE ( 112 FDA reports)
ANURIA ( 112 FDA reports)
ARTHROPATHY ( 112 FDA reports)
CAROTID ARTERY STENOSIS ( 112 FDA reports)
COLITIS ( 112 FDA reports)
HEPATIC STEATOSIS ( 112 FDA reports)
LYMPHADENOPATHY ( 112 FDA reports)
MEDICATION ERROR ( 112 FDA reports)
PSORIASIS ( 111 FDA reports)
DISTURBANCE IN ATTENTION ( 110 FDA reports)
EYE SWELLING ( 110 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 109 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 109 FDA reports)
FEAR ( 109 FDA reports)
INTESTINAL OBSTRUCTION ( 109 FDA reports)
MENTAL DISORDER ( 109 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 109 FDA reports)
SPINAL OSTEOARTHRITIS ( 108 FDA reports)
BLOOD ALBUMIN DECREASED ( 108 FDA reports)
HEART RATE IRREGULAR ( 108 FDA reports)
AGGRESSION ( 107 FDA reports)
REFRACTORY ANAEMIA ( 107 FDA reports)
SINUS TACHYCARDIA ( 107 FDA reports)
GASTROENTERITIS ( 106 FDA reports)
HEPATIC FAILURE ( 106 FDA reports)
INTENTIONAL DRUG MISUSE ( 105 FDA reports)
PULMONARY CONGESTION ( 104 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 104 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 104 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 104 FDA reports)
FLUID OVERLOAD ( 103 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 103 FDA reports)
MULTIPLE DRUG OVERDOSE ( 103 FDA reports)
NIGHTMARE ( 103 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 102 FDA reports)
CORONARY ARTERY OCCLUSION ( 101 FDA reports)
DRUG EFFECT DECREASED ( 101 FDA reports)
HEPATITIS ( 101 FDA reports)
INFLUENZA ( 101 FDA reports)
PERITONITIS ( 101 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 101 FDA reports)
PHARYNGEAL OEDEMA ( 101 FDA reports)
HIP FRACTURE ( 100 FDA reports)
HYPOPNOEA ( 100 FDA reports)
SUDDEN DEATH ( 100 FDA reports)
FEMUR FRACTURE ( 99 FDA reports)
APHASIA ( 98 FDA reports)
PULMONARY HYPERTENSION ( 98 FDA reports)
SINUS BRADYCARDIA ( 98 FDA reports)
VAGINAL ABSCESS ( 98 FDA reports)
RENAL TUBULAR NECROSIS ( 97 FDA reports)
STEVENS-JOHNSON SYNDROME ( 97 FDA reports)
HALLUCINATION, VISUAL ( 97 FDA reports)
MUCOSAL INFLAMMATION ( 96 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 96 FDA reports)
SKIN BURNING SENSATION ( 96 FDA reports)
STRESS ( 96 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 95 FDA reports)
DYSSTASIA ( 95 FDA reports)
NEOPLASM PROGRESSION ( 95 FDA reports)
OLIGURIA ( 95 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 94 FDA reports)
ILEUS ( 94 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 94 FDA reports)
URINE OUTPUT DECREASED ( 94 FDA reports)
VASCULITIS ( 93 FDA reports)
ARTERIOSCLEROSIS ( 93 FDA reports)
BONE MARROW FAILURE ( 93 FDA reports)
ALVEOLITIS ( 92 FDA reports)
BLINDNESS ( 92 FDA reports)
CHROMATURIA ( 92 FDA reports)
DRUG LEVEL INCREASED ( 92 FDA reports)
CARDIAC MURMUR ( 91 FDA reports)
HYPOPHAGIA ( 91 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 90 FDA reports)
MYOPATHY ( 90 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 89 FDA reports)
BRONCHOPNEUMONIA ( 89 FDA reports)
DRUG ADMINISTRATION ERROR ( 89 FDA reports)
GINGIVAL BLEEDING ( 89 FDA reports)
INJECTION SITE ERYTHEMA ( 89 FDA reports)
MALNUTRITION ( 89 FDA reports)
OSTEONECROSIS ( 89 FDA reports)
PARKINSONISM ( 89 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 89 FDA reports)
VENTRICULAR FIBRILLATION ( 89 FDA reports)
DEPRESSED MOOD ( 88 FDA reports)
ECZEMA ( 88 FDA reports)
EPILEPSY ( 87 FDA reports)
MULTIPLE MYELOMA ( 87 FDA reports)
NEPHROLITHIASIS ( 87 FDA reports)
ABNORMAL DREAMS ( 86 FDA reports)
BONE DISORDER ( 86 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 86 FDA reports)
IRRITABILITY ( 86 FDA reports)
NEPHROTIC SYNDROME ( 86 FDA reports)
CHOLESTASIS ( 85 FDA reports)
DEMENTIA ( 85 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 85 FDA reports)
PRODUCTIVE COUGH ( 85 FDA reports)
OBESITY ( 84 FDA reports)
HYPOALBUMINAEMIA ( 83 FDA reports)
PNEUMONITIS ( 83 FDA reports)
SURGERY ( 83 FDA reports)
ROAD TRAFFIC ACCIDENT ( 82 FDA reports)
DIPLOPIA ( 82 FDA reports)
ILL-DEFINED DISORDER ( 82 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 82 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 82 FDA reports)
NASAL CONGESTION ( 82 FDA reports)
PROSTATE CANCER ( 82 FDA reports)
EYE PAIN ( 81 FDA reports)
MYOSITIS ( 81 FDA reports)
RHINORRHOEA ( 81 FDA reports)
TYPE 2 DIABETES MELLITUS ( 81 FDA reports)
PROTHROMBIN TIME PROLONGED ( 80 FDA reports)
RASH MACULAR ( 80 FDA reports)
ATRIAL FLUTTER ( 80 FDA reports)
BLOOD CALCIUM DECREASED ( 80 FDA reports)
CHOLECYSTITIS ( 80 FDA reports)
GRAND MAL CONVULSION ( 80 FDA reports)
HYPERCHOLESTEROLAEMIA ( 80 FDA reports)
MYOCLONUS ( 80 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 79 FDA reports)
HAEMOLYTIC ANAEMIA ( 79 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 79 FDA reports)
NO THERAPEUTIC RESPONSE ( 79 FDA reports)
CRYING ( 78 FDA reports)
POISONING ( 78 FDA reports)
BREAST CANCER ( 77 FDA reports)
COGNITIVE DISORDER ( 77 FDA reports)
EMPHYSEMA ( 77 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 77 FDA reports)
PANIC ATTACK ( 77 FDA reports)
SKIN LESION ( 77 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 77 FDA reports)
THROAT IRRITATION ( 77 FDA reports)
RASH MACULO-PAPULAR ( 76 FDA reports)
RESTLESS LEGS SYNDROME ( 76 FDA reports)
SUBDURAL HAEMATOMA ( 76 FDA reports)
CORONARY ARTERY STENOSIS ( 76 FDA reports)
PRESYNCOPE ( 76 FDA reports)
COAGULOPATHY ( 75 FDA reports)
FACE OEDEMA ( 75 FDA reports)
ISCHAEMIC STROKE ( 75 FDA reports)
OSTEOPENIA ( 75 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 75 FDA reports)
DIVERTICULITIS ( 74 FDA reports)
EXOSTOSIS ( 74 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 74 FDA reports)
LUNG NEOPLASM ( 74 FDA reports)
PAIN IN JAW ( 74 FDA reports)
SEDATION ( 74 FDA reports)
NEPHROPATHY TOXIC ( 73 FDA reports)
ORAL PAIN ( 73 FDA reports)
ATRIOVENTRICULAR BLOCK ( 72 FDA reports)
CEREBRAL ATROPHY ( 72 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 72 FDA reports)
RESPIRATORY DISORDER ( 72 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 72 FDA reports)
UROSEPSIS ( 71 FDA reports)
VENTRICULAR HYPERTROPHY ( 71 FDA reports)
DISCOMFORT ( 71 FDA reports)
DIVERTICULUM ( 71 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 71 FDA reports)
GLAUCOMA ( 71 FDA reports)
INJECTION SITE HAEMATOMA ( 71 FDA reports)
NIGHT SWEATS ( 71 FDA reports)
ATAXIA ( 70 FDA reports)
CEREBRAL ISCHAEMIA ( 70 FDA reports)
ERECTILE DYSFUNCTION ( 70 FDA reports)
HUMERUS FRACTURE ( 70 FDA reports)
HYPERURICAEMIA ( 70 FDA reports)
PERIPHERAL COLDNESS ( 70 FDA reports)
RENAL CYST ( 70 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 70 FDA reports)
TORSADE DE POINTES ( 70 FDA reports)
RIB FRACTURE ( 69 FDA reports)
SINUS DISORDER ( 69 FDA reports)
SKIN TIGHTNESS ( 69 FDA reports)
ANGINA UNSTABLE ( 69 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 69 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 69 FDA reports)
CARDIOVASCULAR DISORDER ( 68 FDA reports)
DIABETIC RETINOPATHY ( 68 FDA reports)
HYPOTHERMIA ( 68 FDA reports)
POST PROCEDURAL COMPLICATION ( 68 FDA reports)
SCAR ( 68 FDA reports)
SKIN DISORDER ( 68 FDA reports)
SLEEP APNOEA SYNDROME ( 68 FDA reports)
RENAL INJURY ( 67 FDA reports)
TACHYPNOEA ( 67 FDA reports)
BRONCHOSPASM ( 67 FDA reports)
EJECTION FRACTION DECREASED ( 67 FDA reports)
METASTASES TO LUNG ( 67 FDA reports)
ACCIDENTAL OVERDOSE ( 66 FDA reports)
ENTEROCOCCAL INFECTION ( 66 FDA reports)
FIBROSIS ( 66 FDA reports)
HEPATIC ENCEPHALOPATHY ( 66 FDA reports)
RALES ( 66 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 65 FDA reports)
ACUTE RESPIRATORY FAILURE ( 65 FDA reports)
BURSITIS ( 65 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 65 FDA reports)
EYE DISORDER ( 65 FDA reports)
INFUSION RELATED REACTION ( 65 FDA reports)
LARYNGEAL OEDEMA ( 65 FDA reports)
ACIDOSIS ( 64 FDA reports)
DISEASE RECURRENCE ( 64 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 64 FDA reports)
JOINT STIFFNESS ( 64 FDA reports)
LOCAL SWELLING ( 64 FDA reports)
MOUTH ULCERATION ( 64 FDA reports)
NERVOUS SYSTEM DISORDER ( 64 FDA reports)
PLATELET COUNT INCREASED ( 64 FDA reports)
PURPURA ( 64 FDA reports)
PYELONEPHRITIS ( 64 FDA reports)
TOOTH ABSCESS ( 64 FDA reports)
TRANSPLANT REJECTION ( 64 FDA reports)
TOOTH DISORDER ( 63 FDA reports)
TOXIC SKIN ERUPTION ( 63 FDA reports)
BODY TEMPERATURE INCREASED ( 63 FDA reports)
DRUG INTOLERANCE ( 63 FDA reports)
MULTIPLE INJURIES ( 63 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 63 FDA reports)
AORTIC ANEURYSM ( 62 FDA reports)
CARDIOMYOPATHY ( 62 FDA reports)
HOSPITALISATION ( 62 FDA reports)
HYPERCALCAEMIA ( 62 FDA reports)
TOOTH EXTRACTION ( 62 FDA reports)
PSYCHOTIC DISORDER ( 61 FDA reports)
RESPIRATORY RATE INCREASED ( 61 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 61 FDA reports)
COLITIS ISCHAEMIC ( 61 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 61 FDA reports)
EYELID OEDEMA ( 61 FDA reports)
GINGIVAL HYPERPLASIA ( 61 FDA reports)
LUNG NEOPLASM MALIGNANT ( 61 FDA reports)
MIGRAINE ( 61 FDA reports)
PARALYSIS ( 61 FDA reports)
BRAIN OEDEMA ( 60 FDA reports)
EOSINOPHILIA ( 60 FDA reports)
GASTROINTESTINAL DISORDER ( 60 FDA reports)
METASTASES TO BONE ( 60 FDA reports)
MIDDLE INSOMNIA ( 60 FDA reports)
MOOD ALTERED ( 60 FDA reports)
NOCTURIA ( 60 FDA reports)
AGRANULOCYTOSIS ( 59 FDA reports)
ANGER ( 59 FDA reports)
AZOTAEMIA ( 59 FDA reports)
EATING DISORDER ( 59 FDA reports)
EMOTIONAL DISORDER ( 59 FDA reports)
ERUCTATION ( 59 FDA reports)
LOBAR PNEUMONIA ( 59 FDA reports)
MICTURITION URGENCY ( 59 FDA reports)
NEURALGIA ( 59 FDA reports)
ACUTE CORONARY SYNDROME ( 58 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 58 FDA reports)
DIVERTICULUM INTESTINAL ( 58 FDA reports)
ELECTROLYTE IMBALANCE ( 58 FDA reports)
GINGIVITIS ( 58 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 58 FDA reports)
MOVEMENT DISORDER ( 58 FDA reports)
RESPIRATORY TRACT INFECTION ( 58 FDA reports)
SKIN HYPERTROPHY ( 57 FDA reports)
ANAPHYLACTIC SHOCK ( 57 FDA reports)
COLD SWEAT ( 57 FDA reports)
DECUBITUS ULCER ( 57 FDA reports)
ERYTHEMA MULTIFORME ( 57 FDA reports)
MYELODYSPLASTIC SYNDROME ( 57 FDA reports)
NO ADVERSE EVENT ( 57 FDA reports)
ANGIONEUROTIC OEDEMA ( 56 FDA reports)
DERMATITIS ( 56 FDA reports)
DUODENAL ULCER ( 56 FDA reports)
GLOSSODYNIA ( 56 FDA reports)
HEPATOMEGALY ( 56 FDA reports)
HYPOKINESIA ( 56 FDA reports)
HYPOVOLAEMIA ( 56 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 56 FDA reports)
PERIPHERAL ISCHAEMIA ( 56 FDA reports)
RASH PAPULAR ( 56 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 55 FDA reports)
ULCER ( 55 FDA reports)
BLOOD AMYLASE INCREASED ( 55 FDA reports)
CANDIDIASIS ( 55 FDA reports)
IRON DEFICIENCY ANAEMIA ( 55 FDA reports)
JOINT INJURY ( 55 FDA reports)
METASTASES TO LIVER ( 55 FDA reports)
PEPTIC ULCER ( 55 FDA reports)
ANKLE FRACTURE ( 54 FDA reports)
DERMATOMYOSITIS ( 54 FDA reports)
DEVICE RELATED INFECTION ( 54 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 54 FDA reports)
HALLUCINATION, AUDITORY ( 54 FDA reports)
HEMIPLEGIA ( 54 FDA reports)
HYDRONEPHROSIS ( 54 FDA reports)
NEPHROPATHY ( 54 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 54 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 54 FDA reports)
SEROTONIN SYNDROME ( 54 FDA reports)
SICK SINUS SYNDROME ( 54 FDA reports)
ROTATOR CUFF SYNDROME ( 53 FDA reports)
UPPER LIMB FRACTURE ( 53 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 53 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 52 FDA reports)
INJECTION SITE HAEMORRHAGE ( 52 FDA reports)
PHOTOSENSITIVITY REACTION ( 52 FDA reports)
WITHDRAWAL SYNDROME ( 52 FDA reports)
VIRAL INFECTION ( 51 FDA reports)
ACUTE PULMONARY OEDEMA ( 51 FDA reports)
BLOOD CHLORIDE DECREASED ( 51 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 51 FDA reports)
MENTAL IMPAIRMENT ( 51 FDA reports)
MUSCLE ATROPHY ( 51 FDA reports)
PNEUMOTHORAX ( 51 FDA reports)
BLOOD PRESSURE ABNORMAL ( 50 FDA reports)
DEFORMITY ( 50 FDA reports)
DENTAL CARIES ( 50 FDA reports)
ESCHERICHIA INFECTION ( 50 FDA reports)
FLANK PAIN ( 50 FDA reports)
OSTEITIS ( 50 FDA reports)
SKIN INDURATION ( 50 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 50 FDA reports)
TUMOUR LYSIS SYNDROME ( 49 FDA reports)
WOUND INFECTION ( 49 FDA reports)
AGEUSIA ( 49 FDA reports)
BACTERIAL INFECTION ( 49 FDA reports)
DYSLIPIDAEMIA ( 49 FDA reports)
ECCHYMOSIS ( 49 FDA reports)
INFARCTION ( 49 FDA reports)
LACUNAR INFARCTION ( 49 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 49 FDA reports)
PERITONITIS BACTERIAL ( 49 FDA reports)
PROTEIN TOTAL DECREASED ( 49 FDA reports)
BLOOD MAGNESIUM DECREASED ( 48 FDA reports)
COORDINATION ABNORMAL ( 48 FDA reports)
CYANOSIS ( 48 FDA reports)
GINGIVAL SWELLING ( 48 FDA reports)
INCOHERENT ( 48 FDA reports)
ORGAN FAILURE ( 48 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 48 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 48 FDA reports)
RETCHING ( 48 FDA reports)
TARDIVE DYSKINESIA ( 48 FDA reports)
PULSE ABSENT ( 47 FDA reports)
RENAL CELL CARCINOMA ( 47 FDA reports)
RHINITIS ALLERGIC ( 47 FDA reports)
TENDONITIS ( 47 FDA reports)
BLADDER CANCER ( 47 FDA reports)
BLOOD CREATINE INCREASED ( 47 FDA reports)
CARPAL TUNNEL SYNDROME ( 47 FDA reports)
CHOKING ( 47 FDA reports)
DRY EYE ( 47 FDA reports)
GALLBLADDER DISORDER ( 47 FDA reports)
GINGIVAL PAIN ( 47 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 47 FDA reports)
LUNG INFECTION ( 47 FDA reports)
PETECHIAE ( 47 FDA reports)
BLOOD URIC ACID INCREASED ( 46 FDA reports)
CHOLECYSTITIS ACUTE ( 46 FDA reports)
DERMATITIS EXFOLIATIVE ( 46 FDA reports)
DRUG DEPENDENCE ( 46 FDA reports)
GASTRIC DISORDER ( 46 FDA reports)
LACRIMATION INCREASED ( 46 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 46 FDA reports)
ORTHOPNOEA ( 46 FDA reports)
TROPONIN INCREASED ( 46 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 45 FDA reports)
TENDERNESS ( 45 FDA reports)
BLOOD URINE PRESENT ( 45 FDA reports)
CLOSTRIDIAL INFECTION ( 45 FDA reports)
ORAL CANDIDIASIS ( 45 FDA reports)
PLEURISY ( 45 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 44 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 44 FDA reports)
BASAL CELL CARCINOMA ( 44 FDA reports)
CYTOLYTIC HEPATITIS ( 44 FDA reports)
EOSINOPHIL COUNT INCREASED ( 44 FDA reports)
FOOT FRACTURE ( 44 FDA reports)
HAEMORRHAGIC ANAEMIA ( 44 FDA reports)
HAEMORRHAGIC STROKE ( 44 FDA reports)
HEPATITIS C ( 44 FDA reports)
MACULAR DEGENERATION ( 44 FDA reports)
PERICARDITIS ( 44 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 44 FDA reports)
RENAL ARTERY STENOSIS ( 44 FDA reports)
RESPIRATORY TRACT CONGESTION ( 44 FDA reports)
SHOCK HAEMORRHAGIC ( 44 FDA reports)
WRONG DRUG ADMINISTERED ( 44 FDA reports)
PSEUDOMONAS INFECTION ( 43 FDA reports)
STENT PLACEMENT ( 43 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 43 FDA reports)
COLON CANCER ( 43 FDA reports)
FAILURE TO THRIVE ( 43 FDA reports)
HYPOACUSIS ( 43 FDA reports)
INTESTINAL PERFORATION ( 43 FDA reports)
KNEE ARTHROPLASTY ( 43 FDA reports)
LIPASE INCREASED ( 43 FDA reports)
ACCIDENTAL EXPOSURE ( 42 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 42 FDA reports)
APHAGIA ( 42 FDA reports)
BREATH SOUNDS ABNORMAL ( 42 FDA reports)
CONJUNCTIVITIS ( 42 FDA reports)
EXCORIATION ( 42 FDA reports)
FAECALOMA ( 42 FDA reports)
ISCHAEMIA ( 42 FDA reports)
LYMPHOCELE ( 42 FDA reports)
METABOLIC ENCEPHALOPATHY ( 42 FDA reports)
NEUTROPHIL COUNT INCREASED ( 42 FDA reports)
OEDEMA MOUTH ( 42 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 42 FDA reports)
SENSORY DISTURBANCE ( 42 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 42 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 42 FDA reports)
RETINAL HAEMORRHAGE ( 41 FDA reports)
ADVERSE EVENT ( 41 FDA reports)
BACTERAEMIA ( 41 FDA reports)
BLOOD CALCIUM INCREASED ( 41 FDA reports)
DIZZINESS POSTURAL ( 41 FDA reports)
GOITRE ( 41 FDA reports)
HICCUPS ( 41 FDA reports)
INJECTION SITE SWELLING ( 41 FDA reports)
LIMB DISCOMFORT ( 41 FDA reports)
PANCREATIC CARCINOMA ( 41 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 40 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 40 FDA reports)
HEPATIC CIRRHOSIS ( 40 FDA reports)
HYPERTHYROIDISM ( 40 FDA reports)
INCONTINENCE ( 40 FDA reports)
LABORATORY TEST ABNORMAL ( 40 FDA reports)
OCULAR HYPERAEMIA ( 40 FDA reports)
POLYNEUROPATHY ( 40 FDA reports)
PROTEIN URINE PRESENT ( 40 FDA reports)
SPINAL COMPRESSION FRACTURE ( 40 FDA reports)
TOOTH LOSS ( 40 FDA reports)
ABORTION SPONTANEOUS ( 39 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 39 FDA reports)
AORTIC CALCIFICATION ( 39 FDA reports)
AORTIC DISSECTION ( 39 FDA reports)
DIASTOLIC DYSFUNCTION ( 39 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 39 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 39 FDA reports)
HYPERTENSIVE EMERGENCY ( 39 FDA reports)
LYMPHOMA ( 39 FDA reports)
ORAL INTAKE REDUCED ( 39 FDA reports)
OROPHARYNGEAL BLISTERING ( 39 FDA reports)
PAIN OF SKIN ( 39 FDA reports)
PHOTOPHOBIA ( 39 FDA reports)
PROCEDURAL COMPLICATION ( 39 FDA reports)
BODY TEMPERATURE DECREASED ( 38 FDA reports)
COMA SCALE ABNORMAL ( 38 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 38 FDA reports)
DILATATION VENTRICULAR ( 38 FDA reports)
EAR PAIN ( 38 FDA reports)
HYPERTENSIVE HEART DISEASE ( 38 FDA reports)
HYPOPHOSPHATAEMIA ( 38 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 38 FDA reports)
JOINT DISLOCATION ( 38 FDA reports)
NEOPLASM ( 38 FDA reports)
ODYNOPHAGIA ( 38 FDA reports)
PARAESTHESIA ORAL ( 38 FDA reports)
PHARYNGITIS ( 38 FDA reports)
SPLENOMEGALY ( 38 FDA reports)
VISUAL DISTURBANCE ( 38 FDA reports)
SENSATION OF HEAVINESS ( 37 FDA reports)
ABDOMINAL PAIN LOWER ( 37 FDA reports)
ACUTE HEPATIC FAILURE ( 37 FDA reports)
ASPIRATION ( 37 FDA reports)
CARDIAC VALVE DISEASE ( 37 FDA reports)
DIABETIC NEPHROPATHY ( 37 FDA reports)
ENDOCARDITIS ( 37 FDA reports)
EXPOSED BONE IN JAW ( 37 FDA reports)
EXTRASYSTOLES ( 37 FDA reports)
FORMICATION ( 37 FDA reports)
FUNGAL INFECTION ( 37 FDA reports)
GANGRENE ( 37 FDA reports)
HYPERSOMNIA ( 37 FDA reports)
ILEUS PARALYTIC ( 37 FDA reports)
LACERATION ( 37 FDA reports)
LIVER INJURY ( 37 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 37 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 37 FDA reports)
PEMPHIGOID ( 37 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 37 FDA reports)
ADRENAL INSUFFICIENCY ( 36 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 36 FDA reports)
BLOOD SODIUM INCREASED ( 36 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 36 FDA reports)
CROHN'S DISEASE ( 36 FDA reports)
DRUG DISPENSING ERROR ( 36 FDA reports)
DYSTONIA ( 36 FDA reports)
EYE PRURITUS ( 36 FDA reports)
FAECAL INCONTINENCE ( 36 FDA reports)
HAEMOLYSIS ( 36 FDA reports)
HEPATITIS ACUTE ( 36 FDA reports)
HEPATOTOXICITY ( 36 FDA reports)
HYDROCEPHALUS ( 36 FDA reports)
HYPERBILIRUBINAEMIA ( 36 FDA reports)
NYSTAGMUS ( 36 FDA reports)
PARANOIA ( 36 FDA reports)
PELVIC FRACTURE ( 36 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 36 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 36 FDA reports)
SPINAL FRACTURE ( 36 FDA reports)
STATUS EPILEPTICUS ( 36 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 36 FDA reports)
VAGINAL HAEMORRHAGE ( 36 FDA reports)
SCIATICA ( 35 FDA reports)
THYROID CANCER ( 35 FDA reports)
VISUAL FIELD DEFECT ( 35 FDA reports)
ACUTE PRERENAL FAILURE ( 35 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 35 FDA reports)
FEMORAL NECK FRACTURE ( 35 FDA reports)
GASTRIC HAEMORRHAGE ( 35 FDA reports)
HAEMODYNAMIC INSTABILITY ( 35 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 35 FDA reports)
ORAL DISORDER ( 35 FDA reports)
OSTEOLYSIS ( 35 FDA reports)
CARDIAC FAILURE ACUTE ( 34 FDA reports)
CEREBRAL DISORDER ( 34 FDA reports)
CHEST X-RAY ABNORMAL ( 34 FDA reports)
CORONARY ARTERY BYPASS ( 34 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 34 FDA reports)
DELUSION ( 34 FDA reports)
DROOLING ( 34 FDA reports)
DUODENITIS ( 34 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 34 FDA reports)
ENTERITIS ( 34 FDA reports)
GASTROINTESTINAL PERFORATION ( 34 FDA reports)
GINGIVAL INFECTION ( 34 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 34 FDA reports)
IMPAIRED WORK ABILITY ( 34 FDA reports)
KIDNEY INFECTION ( 34 FDA reports)
MECHANICAL VENTILATION ( 34 FDA reports)
MOOD SWINGS ( 34 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 34 FDA reports)
NEUTROPENIC SEPSIS ( 34 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 34 FDA reports)
POLYURIA ( 34 FDA reports)
RENAL PAIN ( 34 FDA reports)
SKIN PLAQUE ( 34 FDA reports)
TENDON RUPTURE ( 34 FDA reports)
THYROID DISORDER ( 34 FDA reports)
TOOTHACHE ( 34 FDA reports)
WOUND ( 34 FDA reports)
SKIN NECROSIS ( 33 FDA reports)
STOMACH DISCOMFORT ( 33 FDA reports)
ADVERSE DRUG REACTION ( 33 FDA reports)
ANOSMIA ( 33 FDA reports)
APATHY ( 33 FDA reports)
APNOEA ( 33 FDA reports)
BLINDNESS UNILATERAL ( 33 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 33 FDA reports)
BONE DENSITY DECREASED ( 33 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 33 FDA reports)
DEVICE FAILURE ( 33 FDA reports)
DIABETIC NEUROPATHY ( 33 FDA reports)
DRUG PRESCRIBING ERROR ( 33 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 33 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 33 FDA reports)
ESSENTIAL HYPERTENSION ( 33 FDA reports)
GROIN PAIN ( 33 FDA reports)
HEPATITIS CHOLESTATIC ( 33 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 33 FDA reports)
INJECTION SITE REACTION ( 33 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 33 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 33 FDA reports)
MIOSIS ( 33 FDA reports)
NODULE ( 33 FDA reports)
PATHOLOGICAL FRACTURE ( 33 FDA reports)
PERFORMANCE STATUS DECREASED ( 33 FDA reports)
ABSCESS ( 32 FDA reports)
AORTIC VALVE INCOMPETENCE ( 32 FDA reports)
BREAST PAIN ( 32 FDA reports)
BRONCHIECTASIS ( 32 FDA reports)
CARDIOPULMONARY FAILURE ( 32 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 32 FDA reports)
ERYSIPELAS ( 32 FDA reports)
FRACTURE ( 32 FDA reports)
IRRITABLE BOWEL SYNDROME ( 32 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 32 FDA reports)
MASS ( 32 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 32 FDA reports)
POOR PERIPHERAL CIRCULATION ( 32 FDA reports)
RENAL ATROPHY ( 32 FDA reports)
RETINAL DETACHMENT ( 32 FDA reports)
TACHYARRHYTHMIA ( 32 FDA reports)
THINKING ABNORMAL ( 32 FDA reports)
URINARY HESITATION ( 32 FDA reports)
RENAL CANCER ( 31 FDA reports)
SELF-MEDICATION ( 31 FDA reports)
SUDDEN CARDIAC DEATH ( 31 FDA reports)
THIRST ( 31 FDA reports)
THROMBOSIS IN DEVICE ( 31 FDA reports)
TIBIA FRACTURE ( 31 FDA reports)
VENTRICULAR HYPOKINESIA ( 31 FDA reports)
ALCOHOL USE ( 31 FDA reports)
AORTIC STENOSIS ( 31 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 31 FDA reports)
BRADYARRHYTHMIA ( 31 FDA reports)
CARDIAC HYPERTROPHY ( 31 FDA reports)
CAROTID ARTERY OCCLUSION ( 31 FDA reports)
DEVICE MALFUNCTION ( 31 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 31 FDA reports)
ENTEROCOLITIS ( 31 FDA reports)
EYE IRRITATION ( 31 FDA reports)
GASTROINTESTINAL PAIN ( 31 FDA reports)
IMPAIRED DRIVING ABILITY ( 31 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 31 FDA reports)
JOINT CONTRACTURE ( 31 FDA reports)
MEDICATION RESIDUE ( 31 FDA reports)
NODAL RHYTHM ( 31 FDA reports)
PARKINSON'S DISEASE ( 31 FDA reports)
ANEURYSM ( 30 FDA reports)
APPENDICITIS ( 30 FDA reports)
BACK DISORDER ( 30 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 30 FDA reports)
CEREBROVASCULAR DISORDER ( 30 FDA reports)
DERMATITIS BULLOUS ( 30 FDA reports)
DISABILITY ( 30 FDA reports)
DRUG ABUSE ( 30 FDA reports)
EOSINOPHILIC PNEUMONIA ( 30 FDA reports)
GLUCOSE URINE PRESENT ( 30 FDA reports)
HYPERVENTILATION ( 30 FDA reports)
IMMOBILE ( 30 FDA reports)
INJECTION SITE PRURITUS ( 30 FDA reports)
KLEBSIELLA INFECTION ( 30 FDA reports)
MULTIPLE FRACTURES ( 30 FDA reports)
MUSCLE TIGHTNESS ( 30 FDA reports)
MUSCULOSKELETAL DISORDER ( 30 FDA reports)
PERIODONTAL DISEASE ( 30 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 30 FDA reports)
SERUM FERRITIN INCREASED ( 30 FDA reports)
SKIN FIBROSIS ( 30 FDA reports)
SKIN HYPERPIGMENTATION ( 30 FDA reports)
STRESS FRACTURE ( 30 FDA reports)
THERAPY NON-RESPONDER ( 30 FDA reports)
THROAT TIGHTNESS ( 30 FDA reports)
RAYNAUD'S PHENOMENON ( 29 FDA reports)
SPINAL COLUMN STENOSIS ( 29 FDA reports)
WRIST FRACTURE ( 29 FDA reports)
ANGIOPATHY ( 29 FDA reports)
APLASTIC ANAEMIA ( 29 FDA reports)
ASPHYXIA ( 29 FDA reports)
BLOOD PH DECREASED ( 29 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 29 FDA reports)
COLITIS ULCERATIVE ( 29 FDA reports)
DECREASED ACTIVITY ( 29 FDA reports)
DIABETIC KETOACIDOSIS ( 29 FDA reports)
EMBOLISM ( 29 FDA reports)
FEELING JITTERY ( 29 FDA reports)
GASTROINTESTINAL INFECTION ( 29 FDA reports)
HERNIA ( 29 FDA reports)
HYPERAESTHESIA ( 29 FDA reports)
HYPOAESTHESIA ORAL ( 29 FDA reports)
HYPOTONIA ( 29 FDA reports)
IMPAIRED SELF-CARE ( 29 FDA reports)
INTENTIONAL MISUSE ( 29 FDA reports)
LOCALISED INFECTION ( 29 FDA reports)
LUNG CONSOLIDATION ( 29 FDA reports)
MUSCLE DISORDER ( 29 FDA reports)
NEPHROGENIC ANAEMIA ( 29 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 28 FDA reports)
BLOOD CULTURE POSITIVE ( 28 FDA reports)
BODY HEIGHT DECREASED ( 28 FDA reports)
BREAST MASS ( 28 FDA reports)
CARDIAC PACEMAKER INSERTION ( 28 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 28 FDA reports)
COMPRESSION FRACTURE ( 28 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 28 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 28 FDA reports)
FIBULA FRACTURE ( 28 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 28 FDA reports)
HEPATOCELLULAR INJURY ( 28 FDA reports)
HYPERNATRAEMIA ( 28 FDA reports)
INFECTIOUS PERITONITIS ( 28 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 28 FDA reports)
JOINT SPRAIN ( 28 FDA reports)
MENINGITIS ( 28 FDA reports)
NECROSIS ( 28 FDA reports)
RESPIRATORY DEPRESSION ( 28 FDA reports)
SNEEZING ( 28 FDA reports)
SQUAMOUS CELL CARCINOMA ( 28 FDA reports)
TOOTH FRACTURE ( 28 FDA reports)
PULMONARY HAEMORRHAGE ( 27 FDA reports)
PULMONARY TUBERCULOSIS ( 27 FDA reports)
RENAL TUBULAR DISORDER ( 27 FDA reports)
SKIN FISSURES ( 27 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 27 FDA reports)
SNORING ( 27 FDA reports)
TETANY ( 27 FDA reports)
BLOOD LACTIC ACID INCREASED ( 27 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 27 FDA reports)
CEREBRAL HAEMATOMA ( 27 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 27 FDA reports)
EXERCISE TOLERANCE DECREASED ( 27 FDA reports)
EXPIRED DRUG ADMINISTERED ( 27 FDA reports)
FEMORAL ARTERY OCCLUSION ( 27 FDA reports)
HEPATOCELLULAR DAMAGE ( 27 FDA reports)
HYPOVENTILATION ( 27 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 27 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 27 FDA reports)
INTESTINAL ISCHAEMIA ( 27 FDA reports)
JAUNDICE CHOLESTATIC ( 27 FDA reports)
LUMBAR SPINAL STENOSIS ( 27 FDA reports)
MASTICATION DISORDER ( 27 FDA reports)
OCCULT BLOOD POSITIVE ( 27 FDA reports)
OESOPHAGEAL ULCER ( 27 FDA reports)
ORAL INFECTION ( 27 FDA reports)
PERIORBITAL OEDEMA ( 27 FDA reports)
PHLEBITIS ( 27 FDA reports)
PLEURAL FIBROSIS ( 27 FDA reports)
ARTERIOSPASM CORONARY ( 26 FDA reports)
BEDRIDDEN ( 26 FDA reports)
CACHEXIA ( 26 FDA reports)
CARDIOTOXICITY ( 26 FDA reports)
CEREBELLAR HAEMORRHAGE ( 26 FDA reports)
CHOLECYSTITIS CHRONIC ( 26 FDA reports)
DEAFNESS ( 26 FDA reports)
DERMATITIS ACNEIFORM ( 26 FDA reports)
ESCHERICHIA SEPSIS ( 26 FDA reports)
EYE HAEMORRHAGE ( 26 FDA reports)
FISTULA ( 26 FDA reports)
HAEMORRHAGIC DIATHESIS ( 26 FDA reports)
HYPOGLYCAEMIC COMA ( 26 FDA reports)
LYMPHOPENIA ( 26 FDA reports)
MUSCLE RUPTURE ( 26 FDA reports)
OVARIAN CYST ( 26 FDA reports)
PELVIC PAIN ( 26 FDA reports)
PERIODONTITIS ( 26 FDA reports)
PERSONALITY CHANGE ( 26 FDA reports)
POOR QUALITY SLEEP ( 26 FDA reports)
PSYCHOMOTOR RETARDATION ( 26 FDA reports)
RENAL TRANSPLANT ( 26 FDA reports)
THROMBOCYTOSIS ( 26 FDA reports)
TOOTH INFECTION ( 26 FDA reports)
TRISMUS ( 26 FDA reports)
TUBERCULOSIS ( 26 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 26 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 25 FDA reports)
TEARFULNESS ( 25 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 25 FDA reports)
ABDOMINAL TENDERNESS ( 25 FDA reports)
ABSCESS LIMB ( 25 FDA reports)
ANGIOPLASTY ( 25 FDA reports)
BLOOD DISORDER ( 25 FDA reports)
CATARACT OPERATION ( 25 FDA reports)
CHOLANGITIS ( 25 FDA reports)
CULTURE URINE POSITIVE ( 25 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 25 FDA reports)
EPIGLOTTIC OEDEMA ( 25 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 25 FDA reports)
EXTREMITY CONTRACTURE ( 25 FDA reports)
FIBRIN D DIMER INCREASED ( 25 FDA reports)
GRAFT VERSUS HOST DISEASE ( 25 FDA reports)
HYPERKERATOSIS ( 25 FDA reports)
HYPOPERFUSION ( 25 FDA reports)
JAW DISORDER ( 25 FDA reports)
JOINT EFFUSION ( 25 FDA reports)
LEG AMPUTATION ( 25 FDA reports)
MENINGIOMA ( 25 FDA reports)
MONOPLEGIA ( 25 FDA reports)
OPEN WOUND ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
ORAL HERPES ( 25 FDA reports)
ABNORMAL SENSATION IN EYE ( 24 FDA reports)
AMMONIA INCREASED ( 24 FDA reports)
ANAPHYLACTOID REACTION ( 24 FDA reports)
ANORECTAL DISCOMFORT ( 24 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 24 FDA reports)
APPLICATION SITE ERYTHEMA ( 24 FDA reports)
ARTERIOVENOUS MALFORMATION ( 24 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 24 FDA reports)
CATHETER RELATED INFECTION ( 24 FDA reports)
CATHETERISATION CARDIAC ( 24 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 24 FDA reports)
CHOKING SENSATION ( 24 FDA reports)
CONDUCTION DISORDER ( 24 FDA reports)
CREPITATIONS ( 24 FDA reports)
CYST ( 24 FDA reports)
DEAFNESS UNILATERAL ( 24 FDA reports)
EXTREMITY NECROSIS ( 24 FDA reports)
FACET JOINT SYNDROME ( 24 FDA reports)
FACIAL PALSY ( 24 FDA reports)
GASTRIC CANCER ( 24 FDA reports)
GASTROENTERITIS VIRAL ( 24 FDA reports)
GRANULOCYTOPENIA ( 24 FDA reports)
GUILLAIN-BARRE SYNDROME ( 24 FDA reports)
HEPATORENAL SYNDROME ( 24 FDA reports)
INITIAL INSOMNIA ( 24 FDA reports)
LARGE INTESTINAL ULCER ( 24 FDA reports)
LISTLESS ( 24 FDA reports)
MUSCLE HAEMORRHAGE ( 24 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 24 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 24 FDA reports)
PURULENT DISCHARGE ( 24 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 24 FDA reports)
STREPTOCOCCAL INFECTION ( 24 FDA reports)
TONGUE OEDEMA ( 24 FDA reports)
VITAMIN D DECREASED ( 24 FDA reports)
REFLUX OESOPHAGITIS ( 23 FDA reports)
SKIN INFECTION ( 23 FDA reports)
SOMNAMBULISM ( 23 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 23 FDA reports)
THYROID NEOPLASM ( 23 FDA reports)
TOOTH INJURY ( 23 FDA reports)
TROPONIN I INCREASED ( 23 FDA reports)
VITAMIN D DEFICIENCY ( 23 FDA reports)
APHONIA ( 23 FDA reports)
ARTHRITIS BACTERIAL ( 23 FDA reports)
BIPOLAR DISORDER ( 23 FDA reports)
BLADDER DISORDER ( 23 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 23 FDA reports)
BONE EROSION ( 23 FDA reports)
ENDOTRACHEAL INTUBATION ( 23 FDA reports)
FACIAL PAIN ( 23 FDA reports)
FLUID INTAKE REDUCED ( 23 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 23 FDA reports)
HAEMOTHORAX ( 23 FDA reports)
HEPATITIS TOXIC ( 23 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 23 FDA reports)
HOSTILITY ( 23 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 23 FDA reports)
INCREASED APPETITE ( 23 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 23 FDA reports)
LEUKOENCEPHALOPATHY ( 23 FDA reports)
MACULAR OEDEMA ( 23 FDA reports)
MENISCUS LESION ( 23 FDA reports)
METASTASES TO SPINE ( 23 FDA reports)
NEPHRITIS INTERSTITIAL ( 23 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 23 FDA reports)
PLEURITIC PAIN ( 23 FDA reports)
ACCIDENT ( 22 FDA reports)
ANGIODYSPLASIA ( 22 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 22 FDA reports)
DERMAL CYST ( 22 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 22 FDA reports)
EAR INFECTION ( 22 FDA reports)
FIBROMYALGIA ( 22 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 22 FDA reports)
GENERALISED ERYTHEMA ( 22 FDA reports)
HEPATIC CYST ( 22 FDA reports)
HEPATIC NECROSIS ( 22 FDA reports)
HEPATIC PAIN ( 22 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 22 FDA reports)
LARGE INTESTINE PERFORATION ( 22 FDA reports)
LOCALISED OEDEMA ( 22 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 22 FDA reports)
METASTASES TO LYMPH NODES ( 22 FDA reports)
MUSCLE STRAIN ( 22 FDA reports)
OESOPHAGEAL CARCINOMA ( 22 FDA reports)
OSTEOMALACIA ( 22 FDA reports)
PIGMENTATION DISORDER ( 22 FDA reports)
PNEUMONIA BACTERIAL ( 22 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 22 FDA reports)
PROCEDURAL PAIN ( 22 FDA reports)
SENSATION OF FOREIGN BODY ( 22 FDA reports)
SINUS ARRHYTHMIA ( 22 FDA reports)
SKIN CANCER ( 22 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 22 FDA reports)
SPUTUM CULTURE POSITIVE ( 22 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 22 FDA reports)
VENTRICULAR ARRHYTHMIA ( 22 FDA reports)
VIITH NERVE PARALYSIS ( 22 FDA reports)
VITREOUS DETACHMENT ( 22 FDA reports)
YELLOW SKIN ( 22 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 21 FDA reports)
PULMONARY GRANULOMA ( 21 FDA reports)
RASH PUSTULAR ( 21 FDA reports)
SCOTOMA ( 21 FDA reports)
SEROSITIS ( 21 FDA reports)
SKIN HAEMORRHAGE ( 21 FDA reports)
TONGUE DISORDER ( 21 FDA reports)
TRANSPLANT FAILURE ( 21 FDA reports)
URINE COLOUR ABNORMAL ( 21 FDA reports)
VAGINAL INFECTION ( 21 FDA reports)
AREFLEXIA ( 21 FDA reports)
BLOOD BICARBONATE DECREASED ( 21 FDA reports)
CHEILITIS ( 21 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 21 FDA reports)
GLOMERULONEPHRITIS ( 21 FDA reports)
HEAD DISCOMFORT ( 21 FDA reports)
HERPES SIMPLEX ( 21 FDA reports)
HYPOAESTHESIA FACIAL ( 21 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 21 FDA reports)
MANIA ( 21 FDA reports)
MOUTH HAEMORRHAGE ( 21 FDA reports)
NEPHRITIS ( 21 FDA reports)
NEUROLOGICAL SYMPTOM ( 21 FDA reports)
NEUROTOXICITY ( 21 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 21 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 21 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 21 FDA reports)
PARONYCHIA ( 21 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 21 FDA reports)
PERONEAL NERVE PALSY ( 21 FDA reports)
POLYP ( 21 FDA reports)
PREGNANCY ( 21 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 20 FDA reports)
APPLICATION SITE RASH ( 20 FDA reports)
BACK INJURY ( 20 FDA reports)
BACTERIAL SEPSIS ( 20 FDA reports)
BLOOD CREATININE DECREASED ( 20 FDA reports)
BLOOD OSMOLARITY DECREASED ( 20 FDA reports)
BONE LESION ( 20 FDA reports)
BONE NEOPLASM MALIGNANT ( 20 FDA reports)
CHOLECYSTECTOMY ( 20 FDA reports)
DECREASED INTEREST ( 20 FDA reports)
ENCEPHALITIS ( 20 FDA reports)
FACIAL PARESIS ( 20 FDA reports)
FOOT DEFORMITY ( 20 FDA reports)
GLOSSITIS ( 20 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 20 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 20 FDA reports)
LIMB INJURY ( 20 FDA reports)
LUPUS NEPHRITIS ( 20 FDA reports)
MALIGNANT MELANOMA ( 20 FDA reports)
MENORRHAGIA ( 20 FDA reports)
MULTI-ORGAN DISORDER ( 20 FDA reports)
MULTIPLE SCLEROSIS ( 20 FDA reports)
PERITONEAL HAEMORRHAGE ( 20 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 20 FDA reports)
PROCTALGIA ( 20 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 20 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 20 FDA reports)
SARCOIDOSIS ( 20 FDA reports)
SCAB ( 20 FDA reports)
SCHIZOPHRENIA ( 20 FDA reports)
TESTICULAR SWELLING ( 20 FDA reports)
UTERINE LEIOMYOMA ( 20 FDA reports)
VITREOUS HAEMORRHAGE ( 20 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 19 FDA reports)
RETROPERITONEAL HAEMATOMA ( 19 FDA reports)
SCREAMING ( 19 FDA reports)
SINUS ARREST ( 19 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 19 FDA reports)
UTERINE HAEMORRHAGE ( 19 FDA reports)
APHTHOUS STOMATITIS ( 19 FDA reports)
BILE DUCT STONE ( 19 FDA reports)
BILIARY DILATATION ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 19 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 19 FDA reports)
BONE MARROW TOXICITY ( 19 FDA reports)
COMMUNICATION DISORDER ( 19 FDA reports)
DERMATITIS CONTACT ( 19 FDA reports)
DIABETIC FOOT INFECTION ( 19 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 19 FDA reports)
EMBOLIC STROKE ( 19 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 19 FDA reports)
HEART VALVE INCOMPETENCE ( 19 FDA reports)
HEMIANOPIA HOMONYMOUS ( 19 FDA reports)
HILAR LYMPHADENOPATHY ( 19 FDA reports)
INGUINAL HERNIA ( 19 FDA reports)
INJECTION SITE IRRITATION ( 19 FDA reports)
LINEAR IGA DISEASE ( 19 FDA reports)
LOW TURNOVER OSTEOPATHY ( 19 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 19 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 19 FDA reports)
MUSCLE FATIGUE ( 19 FDA reports)
NECK MASS ( 19 FDA reports)
NEPHROSCLEROSIS ( 19 FDA reports)
POLYDIPSIA ( 19 FDA reports)
PRIMARY SEQUESTRUM ( 19 FDA reports)
ACROCHORDON ( 18 FDA reports)
AORTIC DISORDER ( 18 FDA reports)
APPLICATION SITE PRURITUS ( 18 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 18 FDA reports)
AURICULAR SWELLING ( 18 FDA reports)
BARRETT'S OESOPHAGUS ( 18 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 18 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 18 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 18 FDA reports)
BRAIN DEATH ( 18 FDA reports)
BRAIN INJURY ( 18 FDA reports)
BREATH ODOUR ( 18 FDA reports)
BRUXISM ( 18 FDA reports)
CARDIAC FAILURE CHRONIC ( 18 FDA reports)
CAROTID BRUIT ( 18 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 18 FDA reports)
CYSTITIS HAEMORRHAGIC ( 18 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 18 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 18 FDA reports)
DERMATITIS ALLERGIC ( 18 FDA reports)
DRUG RESISTANCE ( 18 FDA reports)
DRY THROAT ( 18 FDA reports)
GYNAECOMASTIA ( 18 FDA reports)
HELICOBACTER INFECTION ( 18 FDA reports)
HYPERAMMONAEMIA ( 18 FDA reports)
IMMUNE SYSTEM DISORDER ( 18 FDA reports)
INCREASED TENDENCY TO BRUISE ( 18 FDA reports)
INJECTION SITE MASS ( 18 FDA reports)
INJECTION SITE RASH ( 18 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 18 FDA reports)
MACULAR HOLE ( 18 FDA reports)
MALLORY-WEISS SYNDROME ( 18 FDA reports)
OCULAR ICTERUS ( 18 FDA reports)
OESOPHAGEAL STENOSIS ( 18 FDA reports)
ORAL DISCHARGE ( 18 FDA reports)
PITTING OEDEMA ( 18 FDA reports)
PSEUDOLYMPHOMA ( 18 FDA reports)
PULSE ABNORMAL ( 18 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 18 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 18 FDA reports)
PYELONEPHRITIS ACUTE ( 18 FDA reports)
SINUS CONGESTION ( 18 FDA reports)
SKIN WARM ( 18 FDA reports)
SLEEP TERROR ( 18 FDA reports)
THALAMUS HAEMORRHAGE ( 18 FDA reports)
VENOUS THROMBOSIS ( 18 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 17 FDA reports)
RHINITIS ( 17 FDA reports)
SENSORY LOSS ( 17 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 17 FDA reports)
SOCIAL PROBLEM ( 17 FDA reports)
TOE AMPUTATION ( 17 FDA reports)
TRANSFUSION ( 17 FDA reports)
TRAUMATIC HAEMATOMA ( 17 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 17 FDA reports)
URINE ODOUR ABNORMAL ( 17 FDA reports)
VERTIGO POSITIONAL ( 17 FDA reports)
WEGENER'S GRANULOMATOSIS ( 17 FDA reports)
WOUND HAEMORRHAGE ( 17 FDA reports)
XEROSIS ( 17 FDA reports)
ACNE ( 17 FDA reports)
ACUTE SINUSITIS ( 17 FDA reports)
AKATHISIA ( 17 FDA reports)
ANDROGENETIC ALOPECIA ( 17 FDA reports)
BLOOD IRON DECREASED ( 17 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 17 FDA reports)
BONE FRAGMENTATION ( 17 FDA reports)
CAESAREAN SECTION ( 17 FDA reports)
CARDIAC FLUTTER ( 17 FDA reports)
CONCUSSION ( 17 FDA reports)
CRYSTALLURIA ( 17 FDA reports)
DIVERTICULAR PERFORATION ( 17 FDA reports)
DRUG LEVEL DECREASED ( 17 FDA reports)
EAR DISCOMFORT ( 17 FDA reports)
ENTERECTOMY ( 17 FDA reports)
EYELID PTOSIS ( 17 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 17 FDA reports)
FOLLICULITIS ( 17 FDA reports)
GASTRIC POLYPS ( 17 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 17 FDA reports)
HIP ARTHROPLASTY ( 17 FDA reports)
INTRACARDIAC THROMBUS ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 17 FDA reports)
MEDICAL DEVICE COMPLICATION ( 17 FDA reports)
METASTATIC NEOPLASM ( 17 FDA reports)
MITRAL VALVE CALCIFICATION ( 17 FDA reports)
MYDRIASIS ( 17 FDA reports)
NAIL DISORDER ( 17 FDA reports)
NOSOCOMIAL INFECTION ( 17 FDA reports)
OESOPHAGEAL PAIN ( 17 FDA reports)
OTITIS EXTERNA ( 17 FDA reports)
PERIPHERAL EMBOLISM ( 17 FDA reports)
PORTAL VEIN THROMBOSIS ( 17 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 16 FDA reports)
ANION GAP INCREASED ( 16 FDA reports)
APTYALISM ( 16 FDA reports)
ARTHROPOD BITE ( 16 FDA reports)
BONE DEBRIDEMENT ( 16 FDA reports)
BONE NEOPLASM ( 16 FDA reports)
BRADYPHRENIA ( 16 FDA reports)
BREAST CANCER RECURRENT ( 16 FDA reports)
CATHETER SITE INFECTION ( 16 FDA reports)
CELL MARKER INCREASED ( 16 FDA reports)
CHANGE OF BOWEL HABIT ( 16 FDA reports)
CUSHING'S SYNDROME ( 16 FDA reports)
DIFFICULTY IN WALKING ( 16 FDA reports)
DILATATION ATRIAL ( 16 FDA reports)
DISSEMINATED TUBERCULOSIS ( 16 FDA reports)
DRUG EFFECT INCREASED ( 16 FDA reports)
DUODENAL ULCER PERFORATION ( 16 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 16 FDA reports)
ESCHERICHIA BACTERAEMIA ( 16 FDA reports)
FACIAL BONES FRACTURE ( 16 FDA reports)
FINGER DEFORMITY ( 16 FDA reports)
FRACTURED SACRUM ( 16 FDA reports)
FUNGAL SKIN INFECTION ( 16 FDA reports)
GRAFT DYSFUNCTION ( 16 FDA reports)
HAIR COLOUR CHANGES ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HODGKIN'S DISEASE ( 16 FDA reports)
HYPOREFLEXIA ( 16 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 16 FDA reports)
INTERVERTEBRAL DISCITIS ( 16 FDA reports)
INTESTINAL DILATATION ( 16 FDA reports)
INTRA-UTERINE DEATH ( 16 FDA reports)
IRON DEFICIENCY ( 16 FDA reports)
LARYNGITIS ( 16 FDA reports)
LIVEDO RETICULARIS ( 16 FDA reports)
LOOSE TOOTH ( 16 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 16 FDA reports)
MENOPAUSAL SYMPTOMS ( 16 FDA reports)
METABOLIC ALKALOSIS ( 16 FDA reports)
METABOLIC DISORDER ( 16 FDA reports)
NASAL DISCOMFORT ( 16 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 16 FDA reports)
PRIAPISM ( 16 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 16 FDA reports)
PULMONARY THROMBOSIS ( 16 FDA reports)
RETINAL VEIN OCCLUSION ( 16 FDA reports)
SCLERODERMA ( 16 FDA reports)
SCOLIOSIS ( 16 FDA reports)
SEASONAL ALLERGY ( 16 FDA reports)
SKIN OEDEMA ( 16 FDA reports)
STUPOR ( 16 FDA reports)
TRIGEMINAL NEURALGIA ( 16 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 16 FDA reports)
UTERINE CANCER ( 16 FDA reports)
WALKING AID USER ( 16 FDA reports)
PSYCHIATRIC SYMPTOM ( 15 FDA reports)
QUADRIPLEGIA ( 15 FDA reports)
RADICULOPATHY ( 15 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 15 FDA reports)
RENAL INFARCT ( 15 FDA reports)
RESORPTION BONE INCREASED ( 15 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 15 FDA reports)
RETINAL ARTERY OCCLUSION ( 15 FDA reports)
SEROMA ( 15 FDA reports)
SKIN IRRITATION ( 15 FDA reports)
SKIN LACERATION ( 15 FDA reports)
STRIDOR ( 15 FDA reports)
SUBCUTANEOUS ABSCESS ( 15 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 15 FDA reports)
URINARY TRACT OBSTRUCTION ( 15 FDA reports)
VASCULAR GRAFT ( 15 FDA reports)
VASCULITIC RASH ( 15 FDA reports)
WOUND SECRETION ( 15 FDA reports)
ABDOMINAL MASS ( 15 FDA reports)
APPENDICECTOMY ( 15 FDA reports)
ARTERIAL THROMBOSIS ( 15 FDA reports)
AUTOIMMUNE HEPATITIS ( 15 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 15 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 15 FDA reports)
BILE DUCT OBSTRUCTION ( 15 FDA reports)
BLEPHARITIS ( 15 FDA reports)
BREAST TENDERNESS ( 15 FDA reports)
CARDIAC ENZYMES INCREASED ( 15 FDA reports)
CARDIAC OUTPUT DECREASED ( 15 FDA reports)
CARDIAC TAMPONADE ( 15 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 15 FDA reports)
CHONDROCALCINOSIS ( 15 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 15 FDA reports)
CHRONIC SINUSITIS ( 15 FDA reports)
DIABETIC COMA ( 15 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 15 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 15 FDA reports)
ENDODONTIC PROCEDURE ( 15 FDA reports)
EYE MOVEMENT DISORDER ( 15 FDA reports)
FEMORAL ARTERY EMBOLISM ( 15 FDA reports)
FRACTURE NONUNION ( 15 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 15 FDA reports)
GINGIVAL HYPERTROPHY ( 15 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 15 FDA reports)
HAND FRACTURE ( 15 FDA reports)
HEARING IMPAIRED ( 15 FDA reports)
HEPATITIS FULMINANT ( 15 FDA reports)
HEPATOSPLENOMEGALY ( 15 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 15 FDA reports)
INADEQUATE ANALGESIA ( 15 FDA reports)
INTERMITTENT CLAUDICATION ( 15 FDA reports)
INTESTINAL POLYP ( 15 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 15 FDA reports)
INTRACRANIAL ANEURYSM ( 15 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 15 FDA reports)
LEUKOCYTURIA ( 15 FDA reports)
LIP PAIN ( 15 FDA reports)
LUMBAR RADICULOPATHY ( 15 FDA reports)
LYMPHOEDEMA ( 15 FDA reports)
MICROALBUMINURIA ( 15 FDA reports)
MICTURITION DISORDER ( 15 FDA reports)
MITRAL VALVE DISEASE ( 15 FDA reports)
MOTOR DYSFUNCTION ( 15 FDA reports)
NODULE ON EXTREMITY ( 15 FDA reports)
NON-CARDIAC CHEST PAIN ( 15 FDA reports)
OVARIAN CANCER ( 15 FDA reports)
PARAPLEGIA ( 15 FDA reports)
PARATHYROIDECTOMY ( 15 FDA reports)
PNEUMONIA KLEBSIELLA ( 15 FDA reports)
POISONING DELIBERATE ( 15 FDA reports)
POLYARTHRITIS ( 15 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 15 FDA reports)
POSTOPERATIVE ILEUS ( 15 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 14 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 14 FDA reports)
AORTIC VALVE DISEASE ( 14 FDA reports)
APRAXIA ( 14 FDA reports)
ARTHRITIS INFECTIVE ( 14 FDA reports)
ASTERIXIS ( 14 FDA reports)
ATROPHY ( 14 FDA reports)
BLOOD CHLORIDE INCREASED ( 14 FDA reports)
BLOOD COUNT ABNORMAL ( 14 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 14 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 14 FDA reports)
BLOOD PROLACTIN INCREASED ( 14 FDA reports)
BRAIN NEOPLASM ( 14 FDA reports)
CATHETER SITE HAEMORRHAGE ( 14 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 14 FDA reports)
CHOREA ( 14 FDA reports)
DEMYELINATION ( 14 FDA reports)
DEVICE OCCLUSION ( 14 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 14 FDA reports)
DRUG SCREEN POSITIVE ( 14 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 14 FDA reports)
ENCEPHALITIS VIRAL ( 14 FDA reports)
EYE LASER SURGERY ( 14 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 14 FDA reports)
FOREIGN BODY ( 14 FDA reports)
FULL BLOOD COUNT DECREASED ( 14 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 14 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 14 FDA reports)
GRANULOMA ( 14 FDA reports)
HAEMARTHROSIS ( 14 FDA reports)
HEPATIC CONGESTION ( 14 FDA reports)
HIP SURGERY ( 14 FDA reports)
HYPERPARATHYROIDISM ( 14 FDA reports)
HYPERPHOSPHATAEMIA ( 14 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 14 FDA reports)
INJECTION SITE DISCOLOURATION ( 14 FDA reports)
INJECTION SITE EXTRAVASATION ( 14 FDA reports)
IRITIS ( 14 FDA reports)
JAW FRACTURE ( 14 FDA reports)
LEFT ATRIAL DILATATION ( 14 FDA reports)
MALIGNANT HYPERTENSION ( 14 FDA reports)
METASTASIS ( 14 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 14 FDA reports)
NERVE INJURY ( 14 FDA reports)
NEUTROPHILIA ( 14 FDA reports)
ONYCHOMYCOSIS ( 14 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 14 FDA reports)
PHOTOPSIA ( 14 FDA reports)
POOR DENTAL CONDITION ( 14 FDA reports)
POST PROCEDURAL HAEMATOMA ( 14 FDA reports)
PUPIL FIXED ( 14 FDA reports)
QUADRIPARESIS ( 14 FDA reports)
RENAL HAEMORRHAGE ( 14 FDA reports)
RESUSCITATION ( 14 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 14 FDA reports)
SKIN REACTION ( 14 FDA reports)
SPINAL DISORDER ( 14 FDA reports)
SPUTUM DISCOLOURED ( 14 FDA reports)
STEM CELL TRANSPLANT ( 14 FDA reports)
SUBILEUS ( 14 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 14 FDA reports)
TOXIC ENCEPHALOPATHY ( 14 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 14 FDA reports)
TUMOUR HAEMORRHAGE ( 14 FDA reports)
UNDERDOSE ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 14 FDA reports)
PULMONARY MASS ( 13 FDA reports)
QRS AXIS ABNORMAL ( 13 FDA reports)
RESPIRATORY ACIDOSIS ( 13 FDA reports)
SCAN BONE MARROW ABNORMAL ( 13 FDA reports)
SEXUAL DYSFUNCTION ( 13 FDA reports)
SKIN ATROPHY ( 13 FDA reports)
SKIN NODULE ( 13 FDA reports)
STRESS URINARY INCONTINENCE ( 13 FDA reports)
THROMBOCYTOPENIC PURPURA ( 13 FDA reports)
THROMBOPHLEBITIS ( 13 FDA reports)
TRIGGER FINGER ( 13 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 13 FDA reports)
VASCULAR CALCIFICATION ( 13 FDA reports)
VASODILATATION ( 13 FDA reports)
VENTRICULAR DYSFUNCTION ( 13 FDA reports)
VITAMIN B12 DEFICIENCY ( 13 FDA reports)
ADRENAL NEOPLASM ( 13 FDA reports)
AFFECT LABILITY ( 13 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 13 FDA reports)
ANAEMIA POSTOPERATIVE ( 13 FDA reports)
ANASTOMOTIC LEAK ( 13 FDA reports)
ARTERIAL DISORDER ( 13 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 13 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 13 FDA reports)
BILE DUCT CANCER ( 13 FDA reports)
BIPOLAR I DISORDER ( 13 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 13 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 13 FDA reports)
BLOOD CREATININE ABNORMAL ( 13 FDA reports)
BLOOD TEST ABNORMAL ( 13 FDA reports)
BLOOD UREA DECREASED ( 13 FDA reports)
BRAIN HERNIATION ( 13 FDA reports)
BRONCHITIS CHRONIC ( 13 FDA reports)
CALCINOSIS ( 13 FDA reports)
CALCIPHYLAXIS ( 13 FDA reports)
COELIAC DISEASE ( 13 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 13 FDA reports)
CUSHINGOID ( 13 FDA reports)
DIABETIC COMPLICATION ( 13 FDA reports)
DYSGRAPHIA ( 13 FDA reports)
EFFUSION ( 13 FDA reports)
EUPHORIC MOOD ( 13 FDA reports)
EXFOLIATIVE RASH ( 13 FDA reports)
EXTRADURAL ABSCESS ( 13 FDA reports)
FACIAL NEURALGIA ( 13 FDA reports)
FAECES HARD ( 13 FDA reports)
FAMILY STRESS ( 13 FDA reports)
FOOD INTERACTION ( 13 FDA reports)
HAEMANGIOMA ( 13 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 13 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 13 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 13 FDA reports)
IATROGENIC INJURY ( 13 FDA reports)
INAPPROPRIATE AFFECT ( 13 FDA reports)
JEALOUS DELUSION ( 13 FDA reports)
KNEE OPERATION ( 13 FDA reports)
METASTASES TO PERITONEUM ( 13 FDA reports)
MULTIPLE ALLERGIES ( 13 FDA reports)
NEPHRECTOMY ( 13 FDA reports)
OESOPHAGEAL DISORDER ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
PALATAL DISORDER ( 13 FDA reports)
PAROSMIA ( 13 FDA reports)
PENILE OEDEMA ( 13 FDA reports)
PERICARDIAL HAEMORRHAGE ( 13 FDA reports)
PITUITARY TUMOUR BENIGN ( 13 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 13 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 13 FDA reports)
ABDOMINAL ABSCESS ( 12 FDA reports)
ABDOMINAL ADHESIONS ( 12 FDA reports)
ABNORMAL FAECES ( 12 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 12 FDA reports)
ACUTE ABDOMEN ( 12 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 12 FDA reports)
ADRENAL ADENOMA ( 12 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
ARTERIAL STENOSIS ( 12 FDA reports)
ASPERGILLOSIS ( 12 FDA reports)
ASTHENOPIA ( 12 FDA reports)
B-CELL LYMPHOMA ( 12 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 12 FDA reports)
BILOMA ( 12 FDA reports)
BONE LOSS ( 12 FDA reports)
BONE MARROW DISORDER ( 12 FDA reports)
BRADYKINESIA ( 12 FDA reports)
BREAST CANCER METASTATIC ( 12 FDA reports)
CAPILLARY LEAK SYNDROME ( 12 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 12 FDA reports)
CERVICAL SPINAL STENOSIS ( 12 FDA reports)
DEBRIDEMENT ( 12 FDA reports)
DENTAL OPERATION ( 12 FDA reports)
DIAPHRAGMATIC HERNIA ( 12 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 12 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 12 FDA reports)
ERYTHEMA NODOSUM ( 12 FDA reports)
ESCHAR ( 12 FDA reports)
FOAMING AT MOUTH ( 12 FDA reports)
GASTRITIS ATROPHIC ( 12 FDA reports)
GASTRITIS HAEMORRHAGIC ( 12 FDA reports)
GRIP STRENGTH DECREASED ( 12 FDA reports)
HAEMOGLOBIN INCREASED ( 12 FDA reports)
HAIR TEXTURE ABNORMAL ( 12 FDA reports)
HEPATIC HAEMATOMA ( 12 FDA reports)
HEPATITIS B ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
HYSTERECTOMY ( 12 FDA reports)
INCORRECT STORAGE OF DRUG ( 12 FDA reports)
INJECTION SITE NODULE ( 12 FDA reports)
JUGULAR VEIN THROMBOSIS ( 12 FDA reports)
KLEBSIELLA SEPSIS ( 12 FDA reports)
LIMB OPERATION ( 12 FDA reports)
LIP DRY ( 12 FDA reports)
LIVER TRANSPLANT ( 12 FDA reports)
LUNG CANCER METASTATIC ( 12 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 12 FDA reports)
LYMPHADENITIS ( 12 FDA reports)
MENINGITIS BACTERIAL ( 12 FDA reports)
METABOLIC SYNDROME ( 12 FDA reports)
MUCOUS MEMBRANE DISORDER ( 12 FDA reports)
MUSCLE CONTRACTURE ( 12 FDA reports)
MUSCLE RIGIDITY ( 12 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 12 FDA reports)
NERVE COMPRESSION ( 12 FDA reports)
OPTIC DISC DISORDER ( 12 FDA reports)
OTITIS MEDIA ( 12 FDA reports)
PANCREATITIS CHRONIC ( 12 FDA reports)
PANCREATITIS NECROTISING ( 12 FDA reports)
PERIARTHRITIS ( 12 FDA reports)
PERITONEAL DIALYSIS ( 12 FDA reports)
PLEUROPERICARDITIS ( 12 FDA reports)
PNEUMONIA VIRAL ( 12 FDA reports)
POSTURE ABNORMAL ( 12 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 12 FDA reports)
PROSTATIC DISORDER ( 12 FDA reports)
PROTEIN TOTAL INCREASED ( 12 FDA reports)
PSORIATIC ARTHROPATHY ( 12 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 12 FDA reports)
RESPIRATORY ALKALOSIS ( 12 FDA reports)
SALIVARY HYPERSECRETION ( 12 FDA reports)
SENSATION OF PRESSURE ( 12 FDA reports)
SOPOR ( 12 FDA reports)
SPLENIC LESION ( 12 FDA reports)
SYNCOPE VASOVAGAL ( 12 FDA reports)
SYNOVITIS ( 12 FDA reports)
TONGUE BLISTERING ( 12 FDA reports)
TROPONIN T INCREASED ( 12 FDA reports)
VASCULAR PSEUDOANEURYSM ( 12 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 12 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 12 FDA reports)
VOCAL CORD PARALYSIS ( 12 FDA reports)
RHONCHI ( 11 FDA reports)
SKIN PAPILLOMA ( 11 FDA reports)
SKIN SWELLING ( 11 FDA reports)
SPONDYLOLISTHESIS ( 11 FDA reports)
SUBDURAL HAEMORRHAGE ( 11 FDA reports)
SURFACTANT PROTEIN INCREASED ( 11 FDA reports)
TEMPORAL ARTERITIS ( 11 FDA reports)
TESTICULAR PAIN ( 11 FDA reports)
THORACIC CAVITY DRAINAGE ( 11 FDA reports)
THROMBOCYTHAEMIA ( 11 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 11 FDA reports)
UMBILICAL HERNIA ( 11 FDA reports)
URINE KETONE BODY PRESENT ( 11 FDA reports)
VASCULAR GRAFT COMPLICATION ( 11 FDA reports)
VASCULAR PURPURA ( 11 FDA reports)
WHITE BLOOD CELL DISORDER ( 11 FDA reports)
ACCELERATED HYPERTENSION ( 11 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
ANOREXIA NERVOSA ( 11 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 11 FDA reports)
BLOOD MAGNESIUM INCREASED ( 11 FDA reports)
BREAST DISORDER ( 11 FDA reports)
BRONCHITIS ACUTE ( 11 FDA reports)
CARDIAC FIBRILLATION ( 11 FDA reports)
CONTRAST MEDIA REACTION ( 11 FDA reports)
DEAFNESS NEUROSENSORY ( 11 FDA reports)
DEVICE DISLOCATION ( 11 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 11 FDA reports)
DYSAESTHESIA ( 11 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 11 FDA reports)
ENTERITIS INFECTIOUS ( 11 FDA reports)
FEELING OF DESPAIR ( 11 FDA reports)
FOOD POISONING ( 11 FDA reports)
GASTRODUODENITIS ( 11 FDA reports)
GENERAL SYMPTOM ( 11 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 11 FDA reports)
HAEMATOMA INFECTION ( 11 FDA reports)
HEART DISEASE CONGENITAL ( 11 FDA reports)
HELICOBACTER TEST POSITIVE ( 11 FDA reports)
HEPATIC ENZYME ABNORMAL ( 11 FDA reports)
HEPATIC HAEMORRHAGE ( 11 FDA reports)
HERPES VIRUS INFECTION ( 11 FDA reports)
HYPERCOAGULATION ( 11 FDA reports)
HYPERPYREXIA ( 11 FDA reports)
HYPOMANIA ( 11 FDA reports)
HYPOVOLAEMIC SHOCK ( 11 FDA reports)
INHIBITORY DRUG INTERACTION ( 11 FDA reports)
INJECTION SITE INDURATION ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 11 FDA reports)
JUGULAR VEIN DISTENSION ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LIBIDO INCREASED ( 11 FDA reports)
LIGAMENT SPRAIN ( 11 FDA reports)
LIP OEDEMA ( 11 FDA reports)
LIPIDS INCREASED ( 11 FDA reports)
LOSS OF LIBIDO ( 11 FDA reports)
LUNG HYPERINFLATION ( 11 FDA reports)
MACROCYTOSIS ( 11 FDA reports)
MERALGIA PARAESTHETICA ( 11 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 11 FDA reports)
MUSCLE SPASTICITY ( 11 FDA reports)
NEUROGENIC BLADDER ( 11 FDA reports)
NODAL ARRHYTHMIA ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER ( 11 FDA reports)
OSTEITIS DEFORMANS ( 11 FDA reports)
PANCREATIC ATROPHY ( 11 FDA reports)
PANCREATIC PSEUDOCYST ( 11 FDA reports)
PANIC REACTION ( 11 FDA reports)
PCO2 INCREASED ( 11 FDA reports)
PELVIC ABSCESS ( 11 FDA reports)
PO2 DECREASED ( 11 FDA reports)
POLYCYTHAEMIA ( 11 FDA reports)
ABORTION INDUCED ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 10 FDA reports)
ADENOMYOSIS ( 10 FDA reports)
ANAL HAEMORRHAGE ( 10 FDA reports)
APPETITE DISORDER ( 10 FDA reports)
ATRIAL TACHYCARDIA ( 10 FDA reports)
BLEEDING TIME PROLONGED ( 10 FDA reports)
BLOOD BICARBONATE INCREASED ( 10 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 10 FDA reports)
BONE OPERATION ( 10 FDA reports)
BRAIN CONTUSION ( 10 FDA reports)
BREAST CANCER FEMALE ( 10 FDA reports)
CALCULUS URETERIC ( 10 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 10 FDA reports)
CATHETER RELATED COMPLICATION ( 10 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 10 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 10 FDA reports)
CEREBELLAR HAEMANGIOMA ( 10 FDA reports)
CEREBELLAR SYNDROME ( 10 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 10 FDA reports)
CHAPPED LIPS ( 10 FDA reports)
CHOLESTATIC LIVER INJURY ( 10 FDA reports)
CHORIORETINOPATHY ( 10 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 10 FDA reports)
CORONARY ANGIOPLASTY ( 10 FDA reports)
CORONARY ARTERY RESTENOSIS ( 10 FDA reports)
CORONARY ARTERY THROMBOSIS ( 10 FDA reports)
CRYOGLOBULINAEMIA ( 10 FDA reports)
CYSTITIS NONINFECTIVE ( 10 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 10 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 10 FDA reports)
DIABETIC EYE DISEASE ( 10 FDA reports)
DIABETIC MICROANGIOPATHY ( 10 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 10 FDA reports)
DIPLEGIA ( 10 FDA reports)
DISTRACTIBILITY ( 10 FDA reports)
DYSPNOEA AT REST ( 10 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
GLOMERULOSCLEROSIS ( 10 FDA reports)
HAEMATOCRIT INCREASED ( 10 FDA reports)
HEART RATE ABNORMAL ( 10 FDA reports)
HELICOBACTER GASTRITIS ( 10 FDA reports)
HEMIANOPIA ( 10 FDA reports)
HISTOPLASMOSIS ( 10 FDA reports)
ILEOSTOMY ( 10 FDA reports)
INJECTION SITE INFECTION ( 10 FDA reports)
INJECTION SITE URTICARIA ( 10 FDA reports)
INJECTION SITE WARMTH ( 10 FDA reports)
INTESTINAL INFARCTION ( 10 FDA reports)
IRON OVERLOAD ( 10 FDA reports)
ISCHAEMIC HEPATITIS ( 10 FDA reports)
KIDNEY FIBROSIS ( 10 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 10 FDA reports)
LIBIDO DECREASED ( 10 FDA reports)
LICHEN PLANUS ( 10 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 10 FDA reports)
LUPUS-LIKE SYNDROME ( 10 FDA reports)
MALOCCLUSION ( 10 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 10 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 10 FDA reports)
MENINGITIS ENTEROCOCCAL ( 10 FDA reports)
MICROANGIOPATHY ( 10 FDA reports)
MUSCLE NECROSIS ( 10 FDA reports)
MYELOFIBROSIS ( 10 FDA reports)
MYOCARDIAL FIBROSIS ( 10 FDA reports)
NEPHROCALCINOSIS ( 10 FDA reports)
NIPPLE EXUDATE BLOODY ( 10 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 10 FDA reports)
OROANTRAL FISTULA ( 10 FDA reports)
ORTHOSTATIC HYPERTENSION ( 10 FDA reports)
OSTEOSYNTHESIS ( 10 FDA reports)
OTITIS MEDIA ACUTE ( 10 FDA reports)
PANOPHTHALMITIS ( 10 FDA reports)
PAPULE ( 10 FDA reports)
PARAPARESIS ( 10 FDA reports)
PCO2 DECREASED ( 10 FDA reports)
PELVIC MASS ( 10 FDA reports)
PENILE PAIN ( 10 FDA reports)
PETIT MAL EPILEPSY ( 10 FDA reports)
PO2 INCREASED ( 10 FDA reports)
POLYMYALGIA RHEUMATICA ( 10 FDA reports)
POST HERPETIC NEURALGIA ( 10 FDA reports)
POST PROCEDURAL INFECTION ( 10 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 10 FDA reports)
POTENTIATING DRUG INTERACTION ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
PROCEDURAL HYPOTENSION ( 10 FDA reports)
PRODUCT ADHESION ISSUE ( 10 FDA reports)
PULPITIS DENTAL ( 10 FDA reports)
RECTAL CANCER ( 10 FDA reports)
RENAL ARTERY OCCLUSION ( 10 FDA reports)
RENAL NEOPLASM ( 10 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 10 FDA reports)
RETINITIS ( 10 FDA reports)
SCRATCH ( 10 FDA reports)
SINUS HEADACHE ( 10 FDA reports)
SKELETAL INJURY ( 10 FDA reports)
SLEEP TALKING ( 10 FDA reports)
SPINAL CORD DISORDER ( 10 FDA reports)
SPUTUM PURULENT ( 10 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 10 FDA reports)
STRONGYLOIDIASIS ( 10 FDA reports)
SYNOVIAL CYST ( 10 FDA reports)
TERMINAL STATE ( 10 FDA reports)
TRANSFUSION REACTION ( 10 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 10 FDA reports)
UVEITIS ( 10 FDA reports)
VESTIBULAR DISORDER ( 10 FDA reports)
VOMITING PROJECTILE ( 10 FDA reports)
WEIGHT BEARING DIFFICULTY ( 10 FDA reports)
PULMONARY TOXICITY ( 9 FDA reports)
PUSTULAR PSORIASIS ( 9 FDA reports)
RADIUS FRACTURE ( 9 FDA reports)
REFLEXES ABNORMAL ( 9 FDA reports)
RENAL ARTERIOSCLEROSIS ( 9 FDA reports)
RENAL COLIC ( 9 FDA reports)
RENAL TUBULAR ACIDOSIS ( 9 FDA reports)
RETINAL DISORDER ( 9 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 9 FDA reports)
SHOCK HYPOGLYCAEMIC ( 9 FDA reports)
SJOGREN'S SYNDROME ( 9 FDA reports)
SKIN CHAPPED ( 9 FDA reports)
SKIN MASS ( 9 FDA reports)
SLUGGISHNESS ( 9 FDA reports)
SPINAL CORD COMPRESSION ( 9 FDA reports)
STENT OCCLUSION ( 9 FDA reports)
STRESS CARDIOMYOPATHY ( 9 FDA reports)
SUNBURN ( 9 FDA reports)
TESTICULAR NEOPLASM ( 9 FDA reports)
TONGUE DISCOLOURATION ( 9 FDA reports)
TONGUE ULCERATION ( 9 FDA reports)
TRAUMATIC LUNG INJURY ( 9 FDA reports)
TUBERCULOUS PLEURISY ( 9 FDA reports)
TUMOUR PAIN ( 9 FDA reports)
ULCER HAEMORRHAGE ( 9 FDA reports)
URETERIC OBSTRUCTION ( 9 FDA reports)
URETHRAL STENOSIS ( 9 FDA reports)
URINE FLOW DECREASED ( 9 FDA reports)
UTERINE DISORDER ( 9 FDA reports)
VASCULAR OCCLUSION ( 9 FDA reports)
WOUND DEHISCENCE ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
ACTINIC KERATOSIS ( 9 FDA reports)
ADENOCARCINOMA ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
ARTERIAL BYPASS OPERATION ( 9 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 9 FDA reports)
BLADDER PROLAPSE ( 9 FDA reports)
BRAIN STEM HAEMORRHAGE ( 9 FDA reports)
BREAST CANCER STAGE I ( 9 FDA reports)
BUNDLE BRANCH BLOCK ( 9 FDA reports)
BURNS SECOND DEGREE ( 9 FDA reports)
CARBON DIOXIDE INCREASED ( 9 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 9 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
CEREBRAL THROMBOSIS ( 9 FDA reports)
CLOSTRIDIUM COLITIS ( 9 FDA reports)
COLORECTAL CANCER ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
COR PULMONALE ( 9 FDA reports)
DERMOID CYST ( 9 FDA reports)
DEVICE BREAKAGE ( 9 FDA reports)
DIABETIC GASTROPARESIS ( 9 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 9 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 9 FDA reports)
EMBOLISM ARTERIAL ( 9 FDA reports)
ENCEPHALOMALACIA ( 9 FDA reports)
ENDOMETRIAL CANCER ( 9 FDA reports)
ENDOPHTHALMITIS ( 9 FDA reports)
EROSIVE DUODENITIS ( 9 FDA reports)
EROSIVE OESOPHAGITIS ( 9 FDA reports)
ESCHERICHIA TEST POSITIVE ( 9 FDA reports)
FUNGAEMIA ( 9 FDA reports)
GINGIVAL ATROPHY ( 9 FDA reports)
GINGIVAL DISORDER ( 9 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 9 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HAEMORRHAGE URINARY TRACT ( 9 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 9 FDA reports)
HAEMORRHAGIC INFARCTION ( 9 FDA reports)
HAEMOSTASIS ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEPATIC FIBROSIS ( 9 FDA reports)
HEPATIC INFARCTION ( 9 FDA reports)
HEPATIC MASS ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HUNGER ( 9 FDA reports)
HYPERACUSIS ( 9 FDA reports)
HYPERMETROPIA ( 9 FDA reports)
HYPERPLASIA ( 9 FDA reports)
HYPERREFLEXIA ( 9 FDA reports)
IMMUNODEFICIENCY ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 9 FDA reports)
INTESTINAL RESECTION ( 9 FDA reports)
KAPOSI'S SARCOMA ( 9 FDA reports)
LACTOSE INTOLERANCE ( 9 FDA reports)
LARYNGEAL CANCER ( 9 FDA reports)
LICHENOID KERATOSIS ( 9 FDA reports)
LIP EROSION ( 9 FDA reports)
MAJOR DEPRESSION ( 9 FDA reports)
METAPLASIA ( 9 FDA reports)
METASTATIC GASTRIC CANCER ( 9 FDA reports)
MITRAL VALVE PROLAPSE ( 9 FDA reports)
NAIL DISCOLOURATION ( 9 FDA reports)
NEUROMUSCULAR BLOCKADE ( 9 FDA reports)
NEUROPATHY ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 9 FDA reports)
OBSTRUCTIVE UROPATHY ( 9 FDA reports)
ORAL MUCOSA EROSION ( 9 FDA reports)
OSTEOSCLEROSIS ( 9 FDA reports)
OVARIAN EPITHELIAL CANCER ( 9 FDA reports)
PANCREATIC MASS ( 9 FDA reports)
PAPILLOEDEMA ( 9 FDA reports)
PAROTITIS ( 9 FDA reports)
PARTIAL SEIZURES ( 9 FDA reports)
PEDAL PULSE DECREASED ( 9 FDA reports)
PENILE SWELLING ( 9 FDA reports)
PERSECUTORY DELUSION ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
PLASMAPHERESIS ( 9 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 9 FDA reports)
POLYARTERITIS NODOSA ( 9 FDA reports)
PRODUCT COUNTERFEIT ( 9 FDA reports)
ABDOMINAL HERNIA ( 8 FDA reports)
ACINETOBACTER INFECTION ( 8 FDA reports)
ACUTE LUNG INJURY ( 8 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 8 FDA reports)
ADENOVIRUS INFECTION ( 8 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 8 FDA reports)
ALVEOLITIS ALLERGIC ( 8 FDA reports)
AMAUROSIS ( 8 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 8 FDA reports)
ANAL ABSCESS ( 8 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 8 FDA reports)
ANTIBODY TEST POSITIVE ( 8 FDA reports)
ANXIETY DISORDER ( 8 FDA reports)
APPARENT LIFE THREATENING EVENT ( 8 FDA reports)
APPLICATION SITE IRRITATION ( 8 FDA reports)
APPLICATION SITE VESICLES ( 8 FDA reports)
ARTERIAL HAEMORRHAGE ( 8 FDA reports)
ATRIAL THROMBOSIS ( 8 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 8 FDA reports)
AUTOIMMUNE DISORDER ( 8 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 8 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 8 FDA reports)
BK VIRUS INFECTION ( 8 FDA reports)
BLOOD CORTISOL INCREASED ( 8 FDA reports)
BLOOD OSMOLARITY INCREASED ( 8 FDA reports)
BREAST SWELLING ( 8 FDA reports)
CANCER PAIN ( 8 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
COMA HEPATIC ( 8 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 8 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 8 FDA reports)
CREATININE URINE INCREASED ( 8 FDA reports)
CUTANEOUS VASCULITIS ( 8 FDA reports)
DEFAECATION URGENCY ( 8 FDA reports)
DENTURE WEARER ( 8 FDA reports)
DEVICE RELATED SEPSIS ( 8 FDA reports)
DIABETIC FOOT ( 8 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
DYSPHORIA ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
EMPYEMA ( 8 FDA reports)
ENCEPHALITIS HERPES ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
ENZYME ABNORMALITY ( 8 FDA reports)
EYE DISCHARGE ( 8 FDA reports)
FACIAL NERVE DISORDER ( 8 FDA reports)
FAECES PALE ( 8 FDA reports)
FEAR OF DEATH ( 8 FDA reports)
FEELING DRUNK ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 8 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 8 FDA reports)
GASTROINTESTINAL NECROSIS ( 8 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 8 FDA reports)
GRANULOCYTE COUNT DECREASED ( 8 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 8 FDA reports)
HORMONE LEVEL ABNORMAL ( 8 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 8 FDA reports)
HYPERVOLAEMIA ( 8 FDA reports)
HYPHAEMA ( 8 FDA reports)
IMPLANT SITE INFECTION ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INFLAMMATORY MARKER INCREASED ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
LABYRINTHITIS ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LIVER TENDERNESS ( 8 FDA reports)
LIVER TRANSPLANT REJECTION ( 8 FDA reports)
LUNG ADENOCARCINOMA ( 8 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 8 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 8 FDA reports)
LYMPHOCYTOSIS ( 8 FDA reports)
MACULOPATHY ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
MEAN CELL VOLUME INCREASED ( 8 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 8 FDA reports)
METASTASES TO MENINGES ( 8 FDA reports)
METHAEMOGLOBINAEMIA ( 8 FDA reports)
MUSCLE CRAMP ( 8 FDA reports)
MUSCLE INJURY ( 8 FDA reports)
NASAL SEPTUM DEVIATION ( 8 FDA reports)
NECK INJURY ( 8 FDA reports)
NEOPLASM SKIN ( 8 FDA reports)
OLIGOHYDRAMNIOS ( 8 FDA reports)
ORAL FIBROMA ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
ORGANISING PNEUMONIA ( 8 FDA reports)
PARACENTESIS ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 8 FDA reports)
PHARYNGEAL ERYTHEMA ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 8 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 8 FDA reports)
PSEUDODEMENTIA ( 8 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 8 FDA reports)
RENAL TUBULAR ATROPHY ( 8 FDA reports)
RESPIRATION ABNORMAL ( 8 FDA reports)
RETINAL OEDEMA ( 8 FDA reports)
RETINOPATHY ( 8 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 8 FDA reports)
SKIN TURGOR DECREASED ( 8 FDA reports)
SKULL FRACTURE ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 8 FDA reports)
SUFFOCATION FEELING ( 8 FDA reports)
SYNOVIAL DISORDER ( 8 FDA reports)
SYSTOLIC DYSFUNCTION ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
THERAPY REGIMEN CHANGED ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
TREATMENT FAILURE ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
URETERAL NECROSIS ( 8 FDA reports)
VAGINAL DISCHARGE ( 8 FDA reports)
VASCULAR STENOSIS ( 8 FDA reports)
VASCULITIS NECROTISING ( 8 FDA reports)
VENOUS THROMBOSIS LIMB ( 8 FDA reports)
VENTRICULAR FAILURE ( 8 FDA reports)
WHITE BLOOD CELL COUNT ( 8 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 7 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 7 FDA reports)
PURPURA SENILE ( 7 FDA reports)
RASH VESICULAR ( 7 FDA reports)
RENAL MASS ( 7 FDA reports)
RETINAL ARTERY THROMBOSIS ( 7 FDA reports)
SCHAMBERG'S DISEASE ( 7 FDA reports)
SCLERODERMA RENAL CRISIS ( 7 FDA reports)
SECRETION DISCHARGE ( 7 FDA reports)
SINOATRIAL BLOCK ( 7 FDA reports)
SKIN EROSION ( 7 FDA reports)
SKIN INFLAMMATION ( 7 FDA reports)
SKIN WRINKLING ( 7 FDA reports)
SPUTUM INCREASED ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
SUDDEN ONSET OF SLEEP ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
TACHYPHRENIA ( 7 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 7 FDA reports)
THROMBOTIC STROKE ( 7 FDA reports)
THYROIDITIS ( 7 FDA reports)
ULCERATIVE KERATITIS ( 7 FDA reports)
URETERIC STENOSIS ( 7 FDA reports)
URETHRITIS ( 7 FDA reports)
URGE INCONTINENCE ( 7 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 7 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 7 FDA reports)
URINE PHOSPHORUS INCREASED ( 7 FDA reports)
VASOCONSTRICTION ( 7 FDA reports)
VEIN DISORDER ( 7 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 7 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
YAWNING ( 7 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
ABDOMINAL SEPSIS ( 7 FDA reports)
ABSCESS JAW ( 7 FDA reports)
ACHLORHYDRIA ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
ADVERSE REACTION ( 7 FDA reports)
AMINOACIDURIA ( 7 FDA reports)
ANAL ULCER ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 7 FDA reports)
AORTIC ANEURYSM RUPTURE ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 7 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
BACTERIAL TEST POSITIVE ( 7 FDA reports)
BIOPSY LIVER ABNORMAL ( 7 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 7 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 7 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BONE SWELLING ( 7 FDA reports)
BRADYPNOEA ( 7 FDA reports)
BREAST CYST ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BURNS THIRD DEGREE ( 7 FDA reports)
CARBON DIOXIDE DECREASED ( 7 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 7 FDA reports)
CEREBRAL HYPOPERFUSION ( 7 FDA reports)
CHEST INJURY ( 7 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
CITROBACTER INFECTION ( 7 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 7 FDA reports)
COAGULATION TEST ABNORMAL ( 7 FDA reports)
COLECTOMY ( 7 FDA reports)
COLITIS COLLAGENOUS ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
CONJUNCTIVAL OEDEMA ( 7 FDA reports)
COR PULMONALE CHRONIC ( 7 FDA reports)
CORONARY ARTERY SURGERY ( 7 FDA reports)
CRYSTAL URINE PRESENT ( 7 FDA reports)
CSF PROTEIN INCREASED ( 7 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 7 FDA reports)
DENGUE FEVER ( 7 FDA reports)
DEPERSONALISATION ( 7 FDA reports)
DERMATITIS ATOPIC ( 7 FDA reports)
DERMATITIS PSORIASIFORM ( 7 FDA reports)
DIARRHOEA INFECTIOUS ( 7 FDA reports)
DUODENAL NEOPLASM ( 7 FDA reports)
EJACULATION DELAYED ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 7 FDA reports)
EOSINOPHIL COUNT DECREASED ( 7 FDA reports)
EPIDIDYMITIS ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
EYE ALLERGY ( 7 FDA reports)
FANCONI SYNDROME ( 7 FDA reports)
FOETAL DISTRESS SYNDROME ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
FUNGAL SEPSIS ( 7 FDA reports)
GALACTORRHOEA ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 7 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 7 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 7 FDA reports)
GASTROINTESTINAL EROSION ( 7 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 7 FDA reports)
GASTROSTOMY TUBE INSERTION ( 7 FDA reports)
GOUTY ARTHRITIS ( 7 FDA reports)
GRIMACING ( 7 FDA reports)
HAEMATOMA EVACUATION ( 7 FDA reports)
HAEMOGLOBINURIA ( 7 FDA reports)
HAEMORRHAGE CONTROL ( 7 FDA reports)
HAEMORRHAGIC DISORDER ( 7 FDA reports)
HALLUCINATIONS, MIXED ( 7 FDA reports)
HAND DEFORMITY ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 7 FDA reports)
HYPERTONIA ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 7 FDA reports)
HYPOPROTEINAEMIA ( 7 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
INFUSION SITE SWELLING ( 7 FDA reports)
JC VIRUS INFECTION ( 7 FDA reports)
JOINT ARTHROPLASTY ( 7 FDA reports)
JUDGEMENT IMPAIRED ( 7 FDA reports)
KETOACIDOSIS ( 7 FDA reports)
KIDNEY ENLARGEMENT ( 7 FDA reports)
LIPOMA ( 7 FDA reports)
LUNG ABSCESS ( 7 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 7 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MEAN CELL VOLUME DECREASED ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MONONEUROPATHY ( 7 FDA reports)
MONOPARESIS ( 7 FDA reports)
MYASTHENIA GRAVIS ( 7 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 7 FDA reports)
MYOCARDITIS ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NECROTISING FASCIITIS ( 7 FDA reports)
NEURITIS ( 7 FDA reports)
NIKOLSKY'S SIGN ( 7 FDA reports)
NOCARDIOSIS ( 7 FDA reports)
NORMAL NEWBORN ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
OESOPHAGITIS ULCERATIVE ( 7 FDA reports)
ONYCHOCLASIS ( 7 FDA reports)
ONYCHOLYSIS ( 7 FDA reports)
OPEN FRACTURE ( 7 FDA reports)
OPTIC NEURITIS ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
ORAL NEOPLASM ( 7 FDA reports)
OVARIAN CANCER METASTATIC ( 7 FDA reports)
PANCREATIC NEOPLASM ( 7 FDA reports)
PELVIC NEOPLASM ( 7 FDA reports)
PERNICIOUS ANAEMIA ( 7 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 7 FDA reports)
PNEUMONIA LEGIONELLA ( 7 FDA reports)
POSTICTAL STATE ( 7 FDA reports)
POSTOPERATIVE INFECTION ( 7 FDA reports)
PRE-ECLAMPSIA ( 7 FDA reports)
PRODUCT ODOUR ABNORMAL ( 7 FDA reports)
PROSTATE CANCER METASTATIC ( 7 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 6 FDA reports)
ACTINOMYCOSIS ( 6 FDA reports)
ACUTE PSYCHOSIS ( 6 FDA reports)
ACUTE STRESS DISORDER ( 6 FDA reports)
AFFECTIVE DISORDER ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ALBUMIN URINE PRESENT ( 6 FDA reports)
ALVEOLITIS FIBROSING ( 6 FDA reports)
AMBLYOPIA ( 6 FDA reports)
ANAESTHETIC COMPLICATION ( 6 FDA reports)
ANAL PRURITUS ( 6 FDA reports)
ANGIOGRAM ( 6 FDA reports)
ANKLE OPERATION ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
APLASIA ( 6 FDA reports)
APPLICATION SITE BURN ( 6 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 6 FDA reports)
AXONAL NEUROPATHY ( 6 FDA reports)
BICYTOPENIA ( 6 FDA reports)
BILIARY COLIC ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BIOPSY BONE MARROW ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 6 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 6 FDA reports)
BLOOD URINE ( 6 FDA reports)
BRAIN COMPRESSION ( 6 FDA reports)
BRAIN SCAN ABNORMAL ( 6 FDA reports)
BREAST ENLARGEMENT ( 6 FDA reports)
BRONCHIAL DISORDER ( 6 FDA reports)
CALCIUM IONISED DECREASED ( 6 FDA reports)
CALCIUM METABOLISM DISORDER ( 6 FDA reports)
CANDIDA SEPSIS ( 6 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 6 FDA reports)
CAROTID ARTERY STENT INSERTION ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CEREBELLAR INFARCTION ( 6 FDA reports)
CHROMATOPSIA ( 6 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 6 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 6 FDA reports)
CLAVICLE FRACTURE ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CRANIOCEREBRAL INJURY ( 6 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
DENTAL IMPLANTATION ( 6 FDA reports)
DERMATOSIS ( 6 FDA reports)
DISEASE COMPLICATION ( 6 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 6 FDA reports)
DRUG TOLERANCE INCREASED ( 6 FDA reports)
DYSENTERY ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
DYSPLASIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 6 FDA reports)
ELECTROLYTE DEPLETION ( 6 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 6 FDA reports)
ENTEROCOCCAL SEPSIS ( 6 FDA reports)
ENURESIS ( 6 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 6 FDA reports)
EYELID DISORDER ( 6 FDA reports)
FRACTURED COCCYX ( 6 FDA reports)
FUNGAL OESOPHAGITIS ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 6 FDA reports)
GASTRECTOMY ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTRIC ULCER PERFORATION ( 6 FDA reports)
GASTROENTERITIS RADIATION ( 6 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 6 FDA reports)
GENITAL RASH ( 6 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 6 FDA reports)
GRAFT THROMBOSIS ( 6 FDA reports)
HAEMATOSPERMIA ( 6 FDA reports)
HAEMOPHILUS INFECTION ( 6 FDA reports)
HAIR GROWTH ABNORMAL ( 6 FDA reports)
HEPATIC ISCHAEMIA ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HERNIA OBSTRUCTIVE ( 6 FDA reports)
HERNIA REPAIR ( 6 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INHALATION THERAPY ( 6 FDA reports)
INTENTIONAL SELF-INJURY ( 6 FDA reports)
INVESTIGATION ( 6 FDA reports)
IRIS NEOPLASM ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEUKAEMIA ( 6 FDA reports)
LEUKAEMIA RECURRENT ( 6 FDA reports)
LIP BLISTER ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 6 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
MALIGNANT ASCITES ( 6 FDA reports)
MASTOIDITIS ( 6 FDA reports)
MENIERE'S DISEASE ( 6 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 6 FDA reports)
MIXED LIVER INJURY ( 6 FDA reports)
MUCOSAL DRYNESS ( 6 FDA reports)
MYELOPATHY ( 6 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 6 FDA reports)
NASAL POLYPS ( 6 FDA reports)
NEPHRITIC SYNDROME ( 6 FDA reports)
NEPHROBLASTOMA ( 6 FDA reports)
NEUROENDOCRINE TUMOUR ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OCCULT BLOOD ( 6 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 6 FDA reports)
OEDEMA GENITAL ( 6 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PARAKERATOSIS ( 6 FDA reports)
PARESIS ( 6 FDA reports)
PAST-POINTING ( 6 FDA reports)
PATELLA FRACTURE ( 6 FDA reports)
PENIS DISORDER ( 6 FDA reports)
PERIORBITAL HAEMATOMA ( 6 FDA reports)
PHAEOCHROMOCYTOMA ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
PNEUMONIA MYCOPLASMAL ( 6 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
POST PROCEDURAL BILE LEAK ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
PSEUDOMONAL SEPSIS ( 6 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 6 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
PYOTHORAX ( 6 FDA reports)
RED BLOOD CELL ABNORMALITY ( 6 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
RENIN INCREASED ( 6 FDA reports)
REPETITIVE SPEECH ( 6 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
RETICULOCYTE COUNT DECREASED ( 6 FDA reports)
RHINALGIA ( 6 FDA reports)
RHYTHM IDIOVENTRICULAR ( 6 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 6 FDA reports)
SCROTAL SWELLING ( 6 FDA reports)
SEBORRHOEIC KERATOSIS ( 6 FDA reports)
SIALOADENITIS ( 6 FDA reports)
SLEEP-RELATED EATING DISORDER ( 6 FDA reports)
SOFT TISSUE DISORDER ( 6 FDA reports)
SOFT TISSUE NECROSIS ( 6 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 6 FDA reports)
STREPTOCOCCAL SEPSIS ( 6 FDA reports)
TARSAL TUNNEL SYNDROME ( 6 FDA reports)
TENDON PAIN ( 6 FDA reports)
TENSION ( 6 FDA reports)
THERAPEUTIC EMBOLISATION ( 6 FDA reports)
THERAPY CESSATION ( 6 FDA reports)
TOBACCO USER ( 6 FDA reports)
TONGUE COATED ( 6 FDA reports)
TONGUE DRY ( 6 FDA reports)
TOOTH EROSION ( 6 FDA reports)
TRACHEOBRONCHITIS ( 6 FDA reports)
TUBERCULIN TEST POSITIVE ( 6 FDA reports)
TUMOUR MARKER INCREASED ( 6 FDA reports)
TUMOUR RUPTURE ( 6 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
URINOMA ( 6 FDA reports)
VENIPUNCTURE SITE SWELLING ( 6 FDA reports)
VENOUS OCCLUSION ( 6 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VOCAL CORD DISORDER ( 6 FDA reports)
VULVOVAGINAL DRYNESS ( 6 FDA reports)
WEIGHT ABNORMAL ( 6 FDA reports)
WEIGHT LOSS POOR ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PSEUDOPORPHYRIA ( 5 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RED BLOOD CELLS URINE ( 5 FDA reports)
RENAL CANCER METASTATIC ( 5 FDA reports)
RENAL ISCHAEMIA ( 5 FDA reports)
RENAL LYMPHOCELE ( 5 FDA reports)
RESPIRATORY TRACT IRRITATION ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RETINOPATHY HYPERTENSIVE ( 5 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 5 FDA reports)
SHOULDER ARTHROPLASTY ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SINUSITIS FUNGAL ( 5 FDA reports)
SKIN ODOUR ABNORMAL ( 5 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SPINAL FUSION SURGERY ( 5 FDA reports)
SPINAL OPERATION ( 5 FDA reports)
SPINAL PAIN ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 5 FDA reports)
STRESS ULCER ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
SUBCUTANEOUS NODULE ( 5 FDA reports)
SUBRETINAL FIBROSIS ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
SYNOVECTOMY ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
TERMINAL INSOMNIA ( 5 FDA reports)
THALAMIC INFARCTION ( 5 FDA reports)
THERAPEUTIC PROCEDURE ( 5 FDA reports)
THYROXINE FREE DECREASED ( 5 FDA reports)
TOBACCO ABUSE ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TONIC CONVULSION ( 5 FDA reports)
TONSIL CANCER ( 5 FDA reports)
TONSILLAR DISORDER ( 5 FDA reports)
TONSILLECTOMY ( 5 FDA reports)
TOXIC OPTIC NEUROPATHY ( 5 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
URINE OUTPUT INCREASED ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
UTERINE ENLARGEMENT ( 5 FDA reports)
UTERINE MALPOSITION ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 5 FDA reports)
VASCULITIS CEREBRAL ( 5 FDA reports)
VENA CAVA FILTER INSERTION ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
VESICAL FISTULA ( 5 FDA reports)
VITAMIN B12 DECREASED ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
VULVOVAGINAL PRURITUS ( 5 FDA reports)
WEIGHT GAIN POOR ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ACCOMMODATION DISORDER ( 5 FDA reports)
ADENOCARCINOMA PANCREAS ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ADNEXA UTERI CYST ( 5 FDA reports)
ADRENAL DISORDER ( 5 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ALBUMINURIA ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ALCOHOLIC LIVER DISEASE ( 5 FDA reports)
ALCOHOLISM ( 5 FDA reports)
ANGIOSARCOMA ( 5 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
AORTIC ANEURYSM REPAIR ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
AORTIC VALVE STENOSIS ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ASPIRATION BONE MARROW ( 5 FDA reports)
ASTHMATIC CRISIS ( 5 FDA reports)
ATROPHIC VULVOVAGINITIS ( 5 FDA reports)
BACILLUS INFECTION ( 5 FDA reports)
BACTERIAL PYELONEPHRITIS ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BILIARY CIRRHOSIS ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLADDER DILATATION ( 5 FDA reports)
BLADDER NEOPLASM ( 5 FDA reports)
BLEPHAROSPASM ( 5 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BONE INFARCTION ( 5 FDA reports)
BOVINE TUBERCULOSIS ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BRAIN STEM ISCHAEMIA ( 5 FDA reports)
BREAST CANCER IN SITU ( 5 FDA reports)
BREAST CANCER STAGE II ( 5 FDA reports)
CALCULUS URINARY ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 5 FDA reports)
CEREBRAL ARTERY STENOSIS ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHEST WALL MASS ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
COLLAPSE OF LUNG ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
COMPLEX PARTIAL SEIZURES ( 5 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 5 FDA reports)
DEATH OF RELATIVE ( 5 FDA reports)
DEVICE INTERACTION ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DNA ANTIBODY POSITIVE ( 5 FDA reports)
DRAIN REMOVAL ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 5 FDA reports)
DRUG EFFECT DELAYED ( 5 FDA reports)
DRUG LEVEL FLUCTUATING ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
EAR CONGESTION ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
EAR NEOPLASM ( 5 FDA reports)
EAR OPERATION ( 5 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 5 FDA reports)
ENDOSCOPY ( 5 FDA reports)
ENERGY INCREASED ( 5 FDA reports)
EPIDERMAL NECROSIS ( 5 FDA reports)
EPIGASTRIC DISCOMFORT ( 5 FDA reports)
EPIGLOTTITIS ( 5 FDA reports)
EXCESSIVE EYE BLINKING ( 5 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
EYE ROLLING ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FEBRILE INFECTION ( 5 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 5 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FLOPPY IRIS SYNDROME ( 5 FDA reports)
FLUID IMBALANCE ( 5 FDA reports)
FOLATE DEFICIENCY ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER OEDEMA ( 5 FDA reports)
GASTRODUODENAL ULCER ( 5 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 5 FDA reports)
GASTROINTESTINAL CARCINOMA ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 5 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 5 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 5 FDA reports)
GRAVITATIONAL OEDEMA ( 5 FDA reports)
HAEMATOCRIT ABNORMAL ( 5 FDA reports)
HAEMATOTOXICITY ( 5 FDA reports)
HAEMOGLOBIN ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HANGOVER ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HEPATITIS A ( 5 FDA reports)
HEPATOBILIARY DISEASE ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HEPATORENAL FAILURE ( 5 FDA reports)
HEREDITARY ANGIOEDEMA ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
HIRSUTISM ( 5 FDA reports)
HYDROPNEUMOTHORAX ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERPHOSPHATASAEMIA ( 5 FDA reports)
HYPERSPLENISM ( 5 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 5 FDA reports)
HYPERTRICHOSIS ( 5 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 5 FDA reports)
HYPERTROPHY ( 5 FDA reports)
HYPOVITAMINOSIS ( 5 FDA reports)
IIIRD NERVE PARALYSIS ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INCISIONAL HERNIA ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 5 FDA reports)
INCORRECT PRODUCT STORAGE ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 5 FDA reports)
INFECTIVE ANEURYSM ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 5 FDA reports)
INTESTINAL FISTULA ( 5 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 5 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 5 FDA reports)
INTRACRANIAL HAEMATOMA ( 5 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 5 FDA reports)
ITCHING SCAR ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
KIDNEY SMALL ( 5 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
LEUKAEMOID REACTION ( 5 FDA reports)
LIPOSARCOMA ( 5 FDA reports)
LONG QT SYNDROME ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
LYMPHOCYTIC INFILTRATION ( 5 FDA reports)
MACROGLOSSIA ( 5 FDA reports)
MALIGNANT PITUITARY TUMOUR ( 5 FDA reports)
MARASMUS ( 5 FDA reports)
MASTITIS ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 5 FDA reports)
MESENTERITIS ( 5 FDA reports)
METASTASES TO ADRENALS ( 5 FDA reports)
MOANING ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 5 FDA reports)
MYELOMA RECURRENCE ( 5 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 5 FDA reports)
NAIL PIGMENTATION ( 5 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA ( 5 FDA reports)
NEUTROPENIC INFECTION ( 5 FDA reports)
NEUTROPHIL COUNT ( 5 FDA reports)
NIPPLE SWELLING ( 5 FDA reports)
NITRITOID REACTION ( 5 FDA reports)
NONSPECIFIC REACTION ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
OBSTRUCTION GASTRIC ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
OSTEORADIONECROSIS ( 5 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 5 FDA reports)
PAINFUL RESPIRATION ( 5 FDA reports)
PALMAR ERYTHEMA ( 5 FDA reports)
PANCREATIC CYST ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PARADOXICAL DRUG REACTION ( 5 FDA reports)
PELVIC HAEMATOMA ( 5 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 5 FDA reports)
PERIPHERAL NERVE OPERATION ( 5 FDA reports)
PERITONEAL EFFLUENT LEUKOCYTE COUNT INCREASED ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PITUITARY TUMOUR RECURRENT ( 5 FDA reports)
PLATELET COUNT ABNORMAL ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PNEUMOMEDIASTINUM ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PRODUCT TASTE ABNORMAL ( 5 FDA reports)
PROSTATIC OPERATION ( 5 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ADAMS-STOKES SYNDROME ( 4 FDA reports)
AIR EMBOLISM ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANIMAL SCRATCH ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
AORTIC DISSECTION RUPTURE ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
AORTITIS ( 4 FDA reports)
APPLICATION SITE EXFOLIATION ( 4 FDA reports)
APPLICATION SITE PAIN ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ARTERIAL STENT INSERTION ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 4 FDA reports)
ATYPICAL FEMUR FRACTURE ( 4 FDA reports)
BENIGN NEOPLASM ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BILIARY TRACT INFECTION ( 4 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 4 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BLOOD URIC ACID DECREASED ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 4 FDA reports)
BODY FAT DISORDER ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE DENSITY ABNORMAL ( 4 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 4 FDA reports)
BONE METABOLISM DISORDER ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 4 FDA reports)
BREAST CALCIFICATIONS ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CAROTID ARTERY DISEASE ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CENTRAL LINE INFECTION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM FUNCTION TEST ABNORMAL ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CERVICAL MYELOPATHY ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHARLES BONNET SYNDROME ( 4 FDA reports)
CHOLINERGIC SYNDROME ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CNS VENTRICULITIS ( 4 FDA reports)
COLON CANCER METASTATIC ( 4 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 4 FDA reports)
CONJUNCTIVAL DISORDER ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORNEAL TRANSPLANT ( 4 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CYSTOCELE ( 4 FDA reports)
CYSTOID MACULAR OEDEMA ( 4 FDA reports)
DEAFNESS BILATERAL ( 4 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
DEVICE INEFFECTIVE ( 4 FDA reports)
DEVICE LEAKAGE ( 4 FDA reports)
DIAPHRAGMATIC DISORDER ( 4 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DISSOCIATIVE FUGUE ( 4 FDA reports)
DRUG CLEARANCE DECREASED ( 4 FDA reports)
DRUG INTERACTION POTENTIATION ( 4 FDA reports)
DRUG-INDUCED LIVER INJURY ( 4 FDA reports)
DYSCHEZIA ( 4 FDA reports)
EAR HAEMORRHAGE ( 4 FDA reports)
EAR TUBE INSERTION ( 4 FDA reports)
ECTROPION ( 4 FDA reports)
ECZEMA ASTEATOTIC ( 4 FDA reports)
ECZEMA NUMMULAR ( 4 FDA reports)
EJACULATION DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
ENTEROCOLITIS BACTERIAL ( 4 FDA reports)
ERYTHEMA ELEVATUM DIUTINUM ( 4 FDA reports)
ERYTHEMA OF EYELID ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXTRAVASATION ( 4 FDA reports)
EYE BURNS ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
FACTOR VIII INHIBITION ( 4 FDA reports)
FLASHBACK ( 4 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 4 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
FUNGAL PERITONITIS ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 4 FDA reports)
GASTRIC MUCOSAL LESION ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTRIC PH DECREASED ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 4 FDA reports)
GASTROINTESTINAL NEOPLASM ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GASTROINTESTINAL ULCER ( 4 FDA reports)
GINGIVAL ERYTHEMA ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GINGIVAL ULCERATION ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLOBAL AMNESIA ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
GRAFT LOSS ( 4 FDA reports)
GROWTH HORMONE DEFICIENCY ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMORRHAGIC CYST ( 4 FDA reports)
HBV DNA INCREASED ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC CANCER METASTATIC ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HEPATOBLASTOMA ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HIGH FREQUENCY ABLATION ( 4 FDA reports)
HIV TEST POSITIVE ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERLACTACIDAEMIA ( 4 FDA reports)
HYPERPROTEINAEMIA ( 4 FDA reports)
HYPERSEXUALITY ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
ILIAC ARTERY STENOSIS ( 4 FDA reports)
ILIAC ARTERY THROMBOSIS ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INCISION SITE ABSCESS ( 4 FDA reports)
INCLUSION BODY MYOSITIS ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INFECTIVE SPONDYLITIS ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INNER EAR DISORDER ( 4 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 4 FDA reports)
INTESTINAL MASS ( 4 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
IRON METABOLISM DISORDER ( 4 FDA reports)
JOINT WARMTH ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KLEBSIELLA TEST POSITIVE ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LAGOPHTHALMOS ( 4 FDA reports)
LAPAROSCOPIC SURGERY ( 4 FDA reports)
LEUKOARAIOSIS ( 4 FDA reports)
LIGAMENT RUPTURE ( 4 FDA reports)
LIMB CRUSHING INJURY ( 4 FDA reports)
LIP DISORDER ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LIVER CARCINOMA RUPTURED ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MASS EXCISION ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MELANOCYTIC NAEVUS ( 4 FDA reports)
MENINGISM ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
MENTAL RETARDATION ( 4 FDA reports)
MESENTERIC OCCLUSION ( 4 FDA reports)
MESENTERIC PANNICULITIS ( 4 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 4 FDA reports)
METASTASES TO PLEURA ( 4 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MILK-ALKALI SYNDROME ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MOUTH INJURY ( 4 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOPATHY TOXIC ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
MYXOEDEMA COMA ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NARCOLEPSY ( 4 FDA reports)
NEAR DROWNING ( 4 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 4 FDA reports)
NECROSIS ISCHAEMIC ( 4 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEOPLASM RECURRENCE ( 4 FDA reports)
NEOVASCULARISATION ( 4 FDA reports)
NEPHROANGIOSCLEROSIS ( 4 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NIGHT BLINDNESS ( 4 FDA reports)
NITRITOID CRISIS ( 4 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 4 FDA reports)
OESOPHAGEAL MASS ( 4 FDA reports)
ON AND OFF PHENOMENON ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
ONYCHOPHAGIA ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OTITIS MEDIA CHRONIC ( 4 FDA reports)
OVARIAN NEOPLASM ( 4 FDA reports)
PANCREATOLITHIASIS ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARASOMNIA ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PERICARDIAL DRAINAGE ( 4 FDA reports)
PERITONEAL TUBERCULOSIS ( 4 FDA reports)
PERITONITIS SCLEROSING ( 4 FDA reports)
PERIVASCULAR DERMATITIS ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 4 FDA reports)
PHARYNGEAL ULCERATION ( 4 FDA reports)
PILONIDAL CYST ( 4 FDA reports)
PLASMACYTOMA ( 4 FDA reports)
PLEOCYTOSIS ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 4 FDA reports)
POST PROCEDURAL URINE LEAK ( 4 FDA reports)
POSTOPERATIVE ADHESION ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
POSTRENAL FAILURE ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PRECANCEROUS SKIN LESION ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PSEUDOALDOSTERONISM ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PUTAMEN HAEMORRHAGE ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
REFLUX GASTRITIS ( 4 FDA reports)
RENAL ARTERY THROMBOSIS ( 4 FDA reports)
RENAL HAEMATOMA ( 4 FDA reports)
RENAL HYPERTENSION ( 4 FDA reports)
RENAL LIPOMATOSIS ( 4 FDA reports)
RETINAL VASCULAR DISORDER ( 4 FDA reports)
RETROGRADE AMNESIA ( 4 FDA reports)
RETROPERITONEAL FIBROSIS ( 4 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SELF-INJURIOUS IDEATION ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SHUNT MALFUNCTION ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SINUS POLYP ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SMALL INTESTINE ULCER ( 4 FDA reports)
SOMATIC DELUSION ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 4 FDA reports)
SYSTEMIC MYCOSIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 4 FDA reports)
THROMBOSIS PROPHYLAXIS ( 4 FDA reports)
THYROID CYST ( 4 FDA reports)
TONGUE HAEMORRHAGE ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TRAUMATIC FRACTURE ( 4 FDA reports)
TRAUMATIC LIVER INJURY ( 4 FDA reports)
TRICHORRHEXIS ( 4 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 4 FDA reports)
TUNNEL VISION ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 4 FDA reports)
URAEMIC ENCEPHALOPATHY ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URINARY FISTULA ( 4 FDA reports)
URINE SODIUM INCREASED ( 4 FDA reports)
UTERINE NEOPLASM ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
UTERINE PROLAPSE ( 4 FDA reports)
VAGINAL ODOUR ( 4 FDA reports)
VARICOSE ULCERATION ( 4 FDA reports)
VASCULAR DEMENTIA ( 4 FDA reports)
VASCULAR GRAFT OCCLUSION ( 4 FDA reports)
VASCULAR INJURY ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
PRURIGO ( 3 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 3 FDA reports)
PSYCHOLOGICAL TRAUMA ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
PULMONARY SEPSIS ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
RADIATION ASSOCIATED PAIN ( 3 FDA reports)
RADIOTHERAPY ( 3 FDA reports)
READING DISORDER ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RECTAL PERFORATION ( 3 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RENAL ANEURYSM ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL GRAFT LOSS ( 3 FDA reports)
RENAL STONE REMOVAL ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RENIN DECREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RIGHT ATRIAL DILATATION ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
SCAN ABNORMAL ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SENILE DEMENTIA ( 3 FDA reports)
SENSATION OF BLOOD FLOW ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SERONEGATIVE ARTHRITIS ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
SMALL INTESTINE CARCINOMA ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
STARING ( 3 FDA reports)
STRANGURY ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUPERFICIAL INJURY OF EYE ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SUTURE RELATED COMPLICATION ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
TENOSYNOVITIS STENOSANS ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
THYROID OPERATION ( 3 FDA reports)
THYROTOXIC CRISIS ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TRANCE ( 3 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 3 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 3 FDA reports)
URINE OSMOLARITY INCREASED ( 3 FDA reports)
URINE POTASSIUM INCREASED ( 3 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
UTERINE MASS ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASODILATION PROCEDURE ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VIBRATION TEST ABNORMAL ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VITAL CAPACITY DECREASED ( 3 FDA reports)
VITAMIN A DEFICIENCY ( 3 FDA reports)
VITAMIN C DECREASED ( 3 FDA reports)
VOGT-KOYANAGI-HARADA SYNDROME ( 3 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 3 FDA reports)
WITHDRAWAL HYPERTENSION ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ABULIA ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACID FAST BACILLI INFECTION ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ADDISON'S DISEASE ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADRENAL CYST ( 3 FDA reports)
ADRENALECTOMY ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AIDS RETINOPATHY ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 3 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 3 FDA reports)
ANOSOGNOSIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTISOCIAL BEHAVIOUR ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
AORTIC VALVE DISEASE MIXED ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
APPLICATION SITE DISCHARGE ( 3 FDA reports)
APPLICATION SITE DISCOMFORT ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
APPLICATION SITE SCAR ( 3 FDA reports)
ARTERIAL SPASM ( 3 FDA reports)
ARTERIOGRAM CORONARY ( 3 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ASPERGILLOSIS ORAL ( 3 FDA reports)
ATRIAL HYPERTROPHY ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
AUTOMATISM ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
BACTERIAL TOXAEMIA ( 3 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BASE EXCESS INCREASED ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BED REST ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILE DUCT STENT INSERTION ( 3 FDA reports)
BILIARY SPHINCTEROTOMY ( 3 FDA reports)
BIOPSY PROSTATE ( 3 FDA reports)
BLADDER CANCER RECURRENT ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 3 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIFFERENCE OF EXTREMITIES ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE GRAFT ( 3 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 3 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 3 FDA reports)
BRACHIAL PLEXOPATHY ( 3 FDA reports)
BRAIN CANCER METASTATIC ( 3 FDA reports)
BRAIN NEOPLASM BENIGN ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST CANCER STAGE III ( 3 FDA reports)
BREAST DISCOMFORT ( 3 FDA reports)
BREAST INFLAMMATION ( 3 FDA reports)
BREAST INJURY ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHOPLEURAL FISTULA ( 3 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 3 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 3 FDA reports)
BUNION OPERATION ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CAPILLARITIS ( 3 FDA reports)
CARDIAC ABLATION ( 3 FDA reports)
CARDIAC ANEURYSM ( 3 FDA reports)
CARDIAC INDEX DECREASED ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CAROTID ARTERY BYPASS ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CD4/CD8 RATIO INCREASED ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL FUNGAL INFECTION ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEMICAL POISONING ( 3 FDA reports)
CHOLANGITIS SCLEROSING ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CIRCUMORAL OEDEMA ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLD AGGLUTININS ( 3 FDA reports)
COLITIS MICROSCOPIC ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
COMMINUTED FRACTURE ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 3 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
COOMBS TEST POSITIVE ( 3 FDA reports)
COPPER DEFICIENCY ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL DYSTROPHY ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
COSTOCHONDRITIS ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
CYSTIC LYMPHANGIOMA ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DACRYOCYSTORHINOSTOMY ( 3 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 3 FDA reports)
DELUSIONAL DISORDER, JEALOUS TYPE ( 3 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 3 FDA reports)
ECHOCARDIOGRAM ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
EMBOLISM VENOUS ( 3 FDA reports)
ENDOSCOPY SMALL INTESTINE ( 3 FDA reports)
ERYTHROPENIA ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXTRASKELETAL OSSIFICATION ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEMORAL BRUIT ( 3 FDA reports)
FIBROMA ( 3 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 3 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FRACTURE DISPLACEMENT ( 3 FDA reports)
FRACTURE MALUNION ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GALLBLADDER INJURY ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 3 FDA reports)
GENITAL HERPES ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GESTATIONAL HYPERTENSION ( 3 FDA reports)
GLOBULINS DECREASED ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLOSSOPTOSIS ( 3 FDA reports)
GRANULOCYTOSIS ( 3 FDA reports)
GRANULOMA ANNULARE ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
GROIN INFECTION ( 3 FDA reports)
GUTTATE PSORIASIS ( 3 FDA reports)
HAEMANGIOMA OF SKIN ( 3 FDA reports)
HAEMOBILIA ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEART VALVE CALCIFICATION ( 3 FDA reports)
HEAT ILLNESS ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 3 FDA reports)
HEPATITIS E ( 3 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 3 FDA reports)
HIDRADENITIS ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HORDEOLUM ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HYPERALDOSTERONISM ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERCREATININAEMIA ( 3 FDA reports)
HYPERINSULINAEMIA ( 3 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOPITUITARISM ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCISION SITE HAEMATOMA ( 3 FDA reports)
INCISION SITE INFECTION ( 3 FDA reports)
INCISIONAL DRAINAGE ( 3 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
INJECTION SITE ABSCESS ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 3 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 3 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL HAEMORRHAGE ( 3 FDA reports)
INTESTINAL PROLAPSE ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRACARDIAC MASS ( 3 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 3 FDA reports)
INTUBATION COMPLICATION ( 3 FDA reports)
JAW OPERATION ( 3 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
KYPHOSCOLIOSIS ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LACRIMAL DUCT PROCEDURE ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LASER THERAPY ( 3 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 3 FDA reports)
LEUKAEMIA PLASMACYTIC ( 3 FDA reports)
LEUKOPLAKIA ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LIPASE DECREASED ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 3 FDA reports)
LOCHIAL INFECTION ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOW BIRTH WEIGHT BABY ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LUNG CREPITATION ( 3 FDA reports)
LUNG INJURY ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPH NODE TUBERCULOSIS ( 3 FDA reports)
LYMPHANGIECTASIA ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 3 FDA reports)
MALIGNANT ANORECTAL NEOPLASM ( 3 FDA reports)
MALIGNANT RENAL HYPERTENSION ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MINERAL DEFICIENCY ( 3 FDA reports)
MONARTHRITIS ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCORMYCOSIS ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 3 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYOGLOBINURIA ( 3 FDA reports)
MYOTONIA ( 3 FDA reports)
NARCOTIC INTOXICATION ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NEPHROSTOMY ( 3 FDA reports)
NEURAL TUBE DEFECT ( 3 FDA reports)
NEUROFIBROMATOSIS ( 3 FDA reports)
NEUROGLYCOPENIA ( 3 FDA reports)
NEUROMA ( 3 FDA reports)
NEUROMYELITIS OPTICA ( 3 FDA reports)
NIPPLE INFECTION ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OESOPHAGEAL FISTULA ( 3 FDA reports)
OESOPHAGEAL PERFORATION ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
ORTHOSIS USER ( 3 FDA reports)
OSMOLAR GAP ABNORMAL ( 3 FDA reports)
OSTEOMYELITIS CHRONIC ( 3 FDA reports)
OSTEOPETROSIS ( 3 FDA reports)
OVARIAN TORSION ( 3 FDA reports)
PANCREAS LIPOMATOSIS ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARAGANGLION NEOPLASM ( 3 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
PEAU D'ORANGE ( 3 FDA reports)
PELVIC FLUID COLLECTION ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PERIORBITAL ABSCESS ( 3 FDA reports)
PERIOSTITIS ( 3 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PHARYNGEAL LESION ( 3 FDA reports)
PHLEBITIS INFECTIVE ( 3 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 3 FDA reports)
PITUITARY TUMOUR ( 3 FDA reports)
PLANTAR ERYTHEMA ( 3 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PLEURAL INFECTION BACTERIAL ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYCYTHAEMIA VERA ( 3 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 3 FDA reports)
POLYPECTOMY ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 3 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PREGNANCY TEST NEGATIVE ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 3 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
17-HYDROXYPROGESTERONE INCREASED ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACETONAEMIA ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALOPECIA TOTALIS ( 2 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 2 FDA reports)
ALVEOLAR SOFT PART SARCOMA ( 2 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANAL NEOPLASM ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANGIOLIPOMA ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTERIOR CHAMBER FLARE ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APICAL GRANULOMA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE INFECTION ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARTERIAL CATHETERISATION ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASOCIAL BEHAVIOUR ( 2 FDA reports)
ASTEATOSIS ( 2 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 2 FDA reports)
ATHERECTOMY ( 2 FDA reports)
AURICULAR PERICHONDRITIS ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BARIATRIC GASTRIC BALLOON INSERTION ( 2 FDA reports)
BAROTITIS MEDIA ( 2 FDA reports)
BASAL GANGLIA INFARCTION ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASE EXCESS DECREASED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BETA GLOBULIN INCREASED ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY LUNG ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLADDER ABLATION ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER POLYPECTOMY ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD ELASTASE INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD HIV RNA DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 2 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD THROMBIN ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BUNION ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
BURSA CALCIFICATION ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CALCIUM IONISED ABNORMAL ( 2 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 2 FDA reports)
CAPSULE PHYSICAL ISSUE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC ENZYMES ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIOPULMONARY BYPASS ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CAROTID PULSE INCREASED ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CIRCUMCISION ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CLEAR CELL SARCOMA OF THE KIDNEY ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COLPOCELE ( 2 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
CONDYLOMA ACUMINATUM ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 2 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONTRACTED BLADDER ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL STRIAE ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORONARY BYPASS THROMBOSIS ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYTOKINE RELEASE SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
CYTOREDUCTIVE SURGERY ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELIVERY ( 2 FDA reports)
DEMENTIA WITH LEWY BODIES ( 2 FDA reports)
DENTAL PLAQUE ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DEVICE CONNECTION ISSUE ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 2 FDA reports)
DUBIN-JOHNSON SYNDROME ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSPLASTIC NAEVUS ( 2 FDA reports)
DYSSOMNIA ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ECTROPION OF CERVIX ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
ENTEROVESICAL FISTULA ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIGLOTTIC CARCINOMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ERGOT POISONING ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
ERYTHROLEUKAEMIA ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTERNAL EAR INFLAMMATION ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FACTOR V INHIBITION ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEAR OF WEIGHT GAIN ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FISTULA REPAIR ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GALLBLADDER NECROSIS ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GALLSTONE ILEUS ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC CANCER STAGE III ( 2 FDA reports)
GASTRIC FISTULA ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC LAVAGE ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENITAL CANDIDIASIS ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GRAM STAIN ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMICEPHALALGIA ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 2 FDA reports)
HEPATIC ARTERY ANEURYSM ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATIC SIDEROSIS ( 2 FDA reports)
HEPATIC VEIN STENOSIS ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HISTIOCYTOSIS ( 2 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYDROCHOLECYSTIS ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERADRENALISM ( 2 FDA reports)
HYPERADRENOCORTICISM ( 2 FDA reports)
HYPERCALCIURIA ( 2 FDA reports)
HYPERCHROMASIA ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
HYPOPHARYNGEAL CANCER ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
INCISION SITE CELLULITIS ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 2 FDA reports)
IRIS ADHESIONS ( 2 FDA reports)
IRIS ATROPHY ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
ISCHAEMIC LIMB PAIN ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 2 FDA reports)
KETOSIS ( 2 FDA reports)
LABIA ENLARGED ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 2 FDA reports)
LID LAG ( 2 FDA reports)
LIGAMENT OPERATION ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUMBAR SPINE FLATTENING ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MAMMOPLASTY ( 2 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEDICAL OBSERVATION ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL NECROSIS ( 2 FDA reports)
MULTI-VITAMIN DEFICIENCY ( 2 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NASAL VESTIBULITIS ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NELSON'S SYNDROME ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROFIBROMA ( 2 FDA reports)
NEUROGENIC SHOCK ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULAR TOXICITY ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ONYCHALGIA ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OVARIAN GERM CELL CANCER STAGE III ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANCREATECTOMY ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PANCREATIC FISTULA ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PAPILLARY MUSCLE DISORDER ( 2 FDA reports)
PARANEOPLASTIC SYNDROME ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERINEPHRIC EFFUSION ( 2 FDA reports)
PERIPHERAL NERVE INJURY ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERIPHERAL REVASCULARISATION ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PERIPORTAL OEDEMA ( 2 FDA reports)
PERITONEAL ADHESIONS DIVISION ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERITONEAL LESION ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PIGMENTATION LIP ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLASMA CELL DISORDER ( 2 FDA reports)
PLEURAL RUB ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POSTPARTUM HAEMORRHAGE ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
POVERTY OF THOUGHT CONTENT ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PROSTATE CANCER STAGE II ( 2 FDA reports)
PROSTATIC CALCIFICATION ( 2 FDA reports)
PSEUDO LYMPHOMA ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY SARCOIDOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PYELECTASIA ( 2 FDA reports)
PYOGENIC GRANULOMA ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFLUX LARYNGITIS ( 2 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 2 FDA reports)
RENAL ADENOMA ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL SALT-WASTING SYNDROME ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL DEPOSITS ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINAL OPERATION ( 2 FDA reports)
REYE'S SYNDROME ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
RHINITIS SEASONAL ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCAN ABDOMEN ABNORMAL ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 2 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 2 FDA reports)
SCLERAL HAEMORRHAGE ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SECONDARY HYPERTHYROIDISM ( 2 FDA reports)
SEPTIC ARTHRITIS STREPTOBACILLUS ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SERUM SEROTONIN INCREASED ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SHUNT THROMBOSIS ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SKIN WOUND ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP PARALYSIS ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMOKER ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL CORD PARALYSIS ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUBDURAL EMPYEMA ( 2 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TABLET ISSUE ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRANSPLANT ABSCESS ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIGEMINAL NERVE DISORDER ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL MEATUS STENOSIS ( 2 FDA reports)
URETHRECTOMY ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE MAGNESIUM DECREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
UROSTOMY ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
UTERINE CERVIX STENOSIS ( 2 FDA reports)
UTERINE HYPOTONUS ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VERTEBRAL ARTERY HYPOPLASIA ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN C DEFICIENCY ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VOCAL CORD POLYP ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 2 FDA reports)
WART EXCISION ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WOUND EVISCERATION ( 2 FDA reports)
WOUND INFECTION FUNGAL ( 2 FDA reports)
XERODERMA ( 2 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY AIR LEAKAGE ( 1 FDA reports)
PULMONARY FISTULA ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULSE WAVEFORM ABNORMAL ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELOCYSTITIS ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RABIES ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED CELL FRAGMENTATION SYNDROME ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REFRACTORY ANAEMIA WITH EXCESS BLASTS IN TRANSFORMATION ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL INFECTION ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHESUS INCOMPATIBILITY ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCIATIC NERVE PALSY ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTIC NECROSIS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SERUM PROCOLLAGEN TYPE I N-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE VESSEL BYPASS GRAFT ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SLIPPING RIB SYNDROME ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SOMATOFORM DISORDER NEUROLOGIC ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STROKE IN EVOLUTION ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SURGICAL HAEMOSTASIS ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACITURNITY ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TEMPERATURE PERCEPTION TEST ABNORMAL ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENSILON TEST ABNORMAL ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THALASSAEMIA ALPHA ( 1 FDA reports)
THERAPEUTIC AGENT URINE POSITIVE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROXINE FREE ABNORMAL ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE ABSCESS ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URAEMIC ACIDOSIS ( 1 FDA reports)
URATE NEPHROPATHY ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERECTOMY ( 1 FDA reports)
URETERIC OPERATION ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL DILATION PROCEDURE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINE ELECTROLYTES INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE URIC ACID ABNORMAL ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
VACTERL SYNDROME ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR CAUTERISATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS HAEMORRHAGE ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR REMODELING ( 1 FDA reports)
VERTEBROPLASTY ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIBRIO TEST POSITIVE ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAMIN B1 DEFICIENCY ( 1 FDA reports)
VITAMIN B1 INCREASED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL CANCER STAGE II ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL HAEMORRHAGE ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)
ZINC SULPHATE TURBIDITY INCREASED ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INDUCED COMPLETE ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACRODERMATITIS ENTEROPATHICA ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTINOMYCES TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENERGIC SYNDROME ( 1 FDA reports)
ADRENOGENITAL SYNDROME ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALDOSTERONE URINE INCREASED ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC BAND SYNDROME ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGINA BULLOSA HAEMORRHAGICA ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANGIOGRAM CEREBRAL ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMATOMA ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACILLARY ANGIOMATOSIS ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL DIARRHOEA ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARTONELLOSIS ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA 2 MICROGLOBULIN DECREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 1 FDA reports)
BILATERAL ORCHIDECTOMY ( 1 FDA reports)
BILE CULTURE POSITIVE ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY BILE DUCT ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 1 FDA reports)
BIOPSY THYROID GLAND ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALCOHOL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE ABNORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE ABNORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD METHANOL INCREASED ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INFECTION ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST OPERATION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOMALACIA ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIUM PHOSPHATE PRODUCT INCREASED ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC VALVE SCLEROSIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CARDIOVASCULAR EVENT PROPHYLAXIS ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERULOPLASMIN INCREASED ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVIX CARCINOMA STAGE I ( 1 FDA reports)
CERVIX INFLAMMATION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC LEUKAEMIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLPOSUSPENSION ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFLUENT AND RETICULATE PAPILLOMATOSIS ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL CEREBRAL CYST ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS DIRECT TEST NEGATIVE ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL EXFOLIATION ( 1 FDA reports)
CORNEAL IMPLANT ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL OPACITY CONGENITAL ( 1 FDA reports)
CORONA VIRUS INFECTION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORTISOL FREE URINE DECREASED ( 1 FDA reports)
CORTISOL FREE URINE INCREASED ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CRYSTAL URINE ABSENT ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS PERMANENT ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEFICIENCY OF BILE SECRETION ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED SLEEP PHASE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC MACROANGIOPATHY ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISTRIBUTIVE SHOCK ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULITIS MECKEL'S ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR IRRIGATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECG P WAVE INVERTED ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECTOPIA CORDIS ( 1 FDA reports)
ECTOPIC ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM RR INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROOCULOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMATOUS PYELONEPHRITIS ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALITIS ALLERGIC ( 1 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
ENZYME LEVEL INCREASED ( 1 FDA reports)
EOSINOPHIL CATIONIC PROTEIN INCREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPULIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROID SERIES ABNORMAL ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXCHANGE BLOOD TRANSFUSION ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBRIN ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 1 FDA reports)
FLUOROSIS ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL MONITORING ABNORMAL ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GASTRIC ADENOMA ( 1 FDA reports)
GASTRIC CANCER STAGE 0 ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS PSEUDOMONAS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL GANGRENE ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOGEN STORAGE DISORDER ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOPERFUSION ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAIR METAL TEST ABNORMAL ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELICOBACTER SEPSIS ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HIGH GRADE B-CELL LYMPHOMA BURKITT-LIKE LYMPHOMA ( 1 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOTELORISM OF ORBIT ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOLOGY TEST ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL ( 1 FDA reports)
IMMUNOTACTOID GLOMERULONEPHRITIS ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE INDURATION ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFECTED LYMPHOCELE ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE FIBROSIS ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE EROSION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJURY CORNEAL ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCEPTED DRUG PRESCRIBING ERROR ( 1 FDA reports)
INTERMEDIATE UVEITIS ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR LENS IMPLANT ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JAPAN COMA SCALE ABNORMAL ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JUVENILE CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
KIDNEY ANASTOMOSIS ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KINESITHERAPY ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
LARYNGEAL RHEUMATOID ARTHRITIS ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOCELE ( 1 FDA reports)
LATERAL MEDULLARY SYNDROME ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE DECREASED ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP HAEMATOMA ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOW SET EARS ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUPUS MYOCARDITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MAMMARY DUCT ECTASIA ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL CYST ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTALLY LATE DEVELOPER ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO MUSCLE ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO OESOPHAGUS ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTASES TO THYROID ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL ENZYME DEFICIENCY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MODERATE MENTAL RETARDATION ( 1 FDA reports)
MORAXELLA TEST POSITIVE ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE FIBROSIS ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MYALGIA INTERCOSTAL ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN URINE ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL CAVITY MASS ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEISSERIA TEST POSITIVE ( 1 FDA reports)
NEOPLASM OF ORBIT ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHROURETERECTOMY ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NEUROPSYCHIATRIC SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIA SEPSIS ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NOROVIRUS TEST POSITIVE ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OCCUPATIONAL PROBLEM ENVIRONMENTAL ( 1 FDA reports)
OCCUPATIONAL THERAPY ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE III ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL IRRITATION ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OOPHORECTOMY BILATERAL ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORBITAL GRANULOMA ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORBITAL PSEUDOTUMOUR ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PALINDROMIC RHEUMATISM ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS ISLET CELL TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA RESECTABLE ( 1 FDA reports)
PANCREATIC FISTULA REPAIR ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PARADOXICAL PRESSOR RESPONSE ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID HAEMORRHAGE ( 1 FDA reports)
PARATHYROID REIMPLANTATION ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE ADHESION ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL NERVE PARESIS ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL EFFLUENT ERYTHROCYTE COUNT INCREASED ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERITONSILLITIS ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHOTODYNAMIC THERAPY ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYSTIC LIVER DISEASE ( 1 FDA reports)
POLYGLANDULAR AUTOIMMUNE SYNDROME TYPE II ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORTAL VEIN PHLEBITIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL DIZZINESS ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCOLLAGEN TYPE I C-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN URINE ABSENT ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)

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