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

DYSPNOEA ( 4107 FDA reports)
ATRIAL FIBRILLATION ( 4092 FDA reports)
PAIN ( 3947 FDA reports)
NAUSEA ( 3630 FDA reports)
DIZZINESS ( 3592 FDA reports)
ECONOMIC PROBLEM ( 3475 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3309 FDA reports)
ASTHENIA ( 3147 FDA reports)
ANXIETY ( 2916 FDA reports)
FATIGUE ( 2821 FDA reports)
INJURY ( 2673 FDA reports)
HYPOTENSION ( 2664 FDA reports)
VOMITING ( 2606 FDA reports)
MULTIPLE INJURIES ( 2434 FDA reports)
RENAL FAILURE ( 2302 FDA reports)
DIARRHOEA ( 2284 FDA reports)
FALL ( 2267 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2254 FDA reports)
OEDEMA PERIPHERAL ( 2067 FDA reports)
ANAEMIA ( 2055 FDA reports)
BRADYCARDIA ( 2012 FDA reports)
PNEUMONIA ( 2009 FDA reports)
RENAL FAILURE ACUTE ( 1970 FDA reports)
CHEST PAIN ( 1886 FDA reports)
HYPERTENSION ( 1797 FDA reports)
DEATH ( 1686 FDA reports)
MYOCARDIAL INFARCTION ( 1629 FDA reports)
WEIGHT DECREASED ( 1611 FDA reports)
DEHYDRATION ( 1534 FDA reports)
CONFUSIONAL STATE ( 1501 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1456 FDA reports)
PALPITATIONS ( 1435 FDA reports)
CARDIAC FAILURE ( 1421 FDA reports)
MALAISE ( 1380 FDA reports)
UNEVALUABLE EVENT ( 1364 FDA reports)
BACK PAIN ( 1355 FDA reports)
PLEURAL EFFUSION ( 1334 FDA reports)
DRUG INTERACTION ( 1326 FDA reports)
HEADACHE ( 1320 FDA reports)
CARDIAC ARREST ( 1313 FDA reports)
DECREASED APPETITE ( 1269 FDA reports)
PYREXIA ( 1263 FDA reports)
CONDITION AGGRAVATED ( 1252 FDA reports)
URINARY TRACT INFECTION ( 1231 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1229 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1218 FDA reports)
COUGH ( 1196 FDA reports)
SYNCOPE ( 1184 FDA reports)
DEPRESSION ( 1173 FDA reports)
CARDIOMEGALY ( 1157 FDA reports)
PAIN IN EXTREMITY ( 1140 FDA reports)
ANHEDONIA ( 1127 FDA reports)
CARDIAC DISORDER ( 1104 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1093 FDA reports)
ABDOMINAL PAIN ( 1092 FDA reports)
CORONARY ARTERY DISEASE ( 1081 FDA reports)
BLOOD GLUCOSE INCREASED ( 1073 FDA reports)
ARRHYTHMIA ( 1060 FDA reports)
ARTHRALGIA ( 1042 FDA reports)
HYPERKALAEMIA ( 981 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 976 FDA reports)
EMOTIONAL DISTRESS ( 969 FDA reports)
LOSS OF CONSCIOUSNESS ( 941 FDA reports)
RESPIRATORY FAILURE ( 934 FDA reports)
SEPSIS ( 927 FDA reports)
PULMONARY HYPERTENSION ( 902 FDA reports)
INSOMNIA ( 900 FDA reports)
VENTRICULAR TACHYCARDIA ( 891 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 877 FDA reports)
CARDIOMYOPATHY ( 860 FDA reports)
HEART RATE IRREGULAR ( 856 FDA reports)
TACHYCARDIA ( 815 FDA reports)
DRUG INEFFECTIVE ( 804 FDA reports)
SURGERY ( 803 FDA reports)
PULMONARY OEDEMA ( 796 FDA reports)
CHEST DISCOMFORT ( 789 FDA reports)
GAIT DISTURBANCE ( 772 FDA reports)
HEART RATE INCREASED ( 770 FDA reports)
HAEMOGLOBIN DECREASED ( 764 FDA reports)
BLOOD CREATININE INCREASED ( 751 FDA reports)
THROMBOCYTOPENIA ( 733 FDA reports)
BRONCHITIS ( 721 FDA reports)
CONSTIPATION ( 719 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 719 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 718 FDA reports)
CARDIAC MURMUR ( 712 FDA reports)
HYPERHIDROSIS ( 710 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 710 FDA reports)
RENAL IMPAIRMENT ( 694 FDA reports)
WEIGHT INCREASED ( 682 FDA reports)
HEART RATE DECREASED ( 681 FDA reports)
ABDOMINAL PAIN UPPER ( 668 FDA reports)
ILL-DEFINED DISORDER ( 659 FDA reports)
MULTI-ORGAN FAILURE ( 654 FDA reports)
SOMNOLENCE ( 654 FDA reports)
PARAESTHESIA ( 652 FDA reports)
FEELING ABNORMAL ( 646 FDA reports)
DIABETES MELLITUS ( 642 FDA reports)
RASH ( 642 FDA reports)
BLOOD PRESSURE DECREASED ( 639 FDA reports)
RENAL FAILURE CHRONIC ( 632 FDA reports)
VISION BLURRED ( 629 FDA reports)
HYPOKALAEMIA ( 625 FDA reports)
OEDEMA ( 622 FDA reports)
HYPONATRAEMIA ( 615 FDA reports)
LETHARGY ( 606 FDA reports)
OVERDOSE ( 600 FDA reports)
DYSPNOEA EXERTIONAL ( 599 FDA reports)
HYPERLIPIDAEMIA ( 595 FDA reports)
HYPOAESTHESIA ( 590 FDA reports)
CARDIO-RESPIRATORY ARREST ( 583 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 577 FDA reports)
ATELECTASIS ( 576 FDA reports)
BLOOD UREA INCREASED ( 565 FDA reports)
FEAR ( 565 FDA reports)
DYSPHAGIA ( 561 FDA reports)
CONTUSION ( 556 FDA reports)
CONVULSION ( 554 FDA reports)
MENTAL STATUS CHANGES ( 553 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 545 FDA reports)
BLOOD PRESSURE INCREASED ( 544 FDA reports)
ATRIAL FLUTTER ( 543 FDA reports)
EJECTION FRACTION DECREASED ( 540 FDA reports)
EMOTIONAL DISORDER ( 535 FDA reports)
TREATMENT NONCOMPLIANCE ( 526 FDA reports)
CELLULITIS ( 516 FDA reports)
RECTAL HAEMORRHAGE ( 514 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 511 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 508 FDA reports)
MENTAL DISORDER ( 503 FDA reports)
PRURITUS ( 501 FDA reports)
MUSCULAR WEAKNESS ( 499 FDA reports)
OSTEOARTHRITIS ( 499 FDA reports)
TREMOR ( 499 FDA reports)
ANGINA PECTORIS ( 491 FDA reports)
HAEMORRHAGE ( 486 FDA reports)
VENTRICULAR FIBRILLATION ( 485 FDA reports)
VISUAL IMPAIRMENT ( 482 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 473 FDA reports)
HYPOXIA ( 463 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 462 FDA reports)
SINUSITIS ( 460 FDA reports)
ABDOMINAL DISTENSION ( 459 FDA reports)
HYPOGLYCAEMIA ( 455 FDA reports)
MUSCLE SPASMS ( 447 FDA reports)
DYSPEPSIA ( 443 FDA reports)
PRESYNCOPE ( 441 FDA reports)
STRESS ( 441 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 440 FDA reports)
MYOCARDIAL ISCHAEMIA ( 438 FDA reports)
MYALGIA ( 435 FDA reports)
EPISTAXIS ( 431 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 430 FDA reports)
MUSCULOSKELETAL PAIN ( 429 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 428 FDA reports)
ANOREXIA ( 427 FDA reports)
DEEP VEIN THROMBOSIS ( 424 FDA reports)
AORTIC VALVE INCOMPETENCE ( 423 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 423 FDA reports)
SLEEP APNOEA SYNDROME ( 422 FDA reports)
INFECTION ( 417 FDA reports)
ERYTHEMA ( 416 FDA reports)
DISORIENTATION ( 414 FDA reports)
UNRESPONSIVE TO STIMULI ( 414 FDA reports)
HAEMATURIA ( 411 FDA reports)
PLATELET COUNT DECREASED ( 410 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 402 FDA reports)
BALANCE DISORDER ( 397 FDA reports)
PROTHROMBIN TIME PROLONGED ( 391 FDA reports)
WHEEZING ( 391 FDA reports)
ASTHMA ( 383 FDA reports)
PULMONARY CONGESTION ( 376 FDA reports)
ORTHOPNOEA ( 369 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 368 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 365 FDA reports)
CHOLELITHIASIS ( 365 FDA reports)
NEUROPATHY PERIPHERAL ( 365 FDA reports)
HYPERGLYCAEMIA ( 363 FDA reports)
RENAL INJURY ( 363 FDA reports)
HYPOTHYROIDISM ( 361 FDA reports)
SPINAL OSTEOARTHRITIS ( 360 FDA reports)
BLOOD POTASSIUM INCREASED ( 358 FDA reports)
CHILLS ( 357 FDA reports)
HAEMATOCRIT DECREASED ( 353 FDA reports)
HALLUCINATION ( 353 FDA reports)
SOCIAL PROBLEM ( 352 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 351 FDA reports)
DRUG TOXICITY ( 350 FDA reports)
SINUS BRADYCARDIA ( 348 FDA reports)
PULMONARY EMBOLISM ( 347 FDA reports)
STAPHYLOCOCCAL INFECTION ( 345 FDA reports)
ARTERIOSCLEROSIS ( 341 FDA reports)
FLUSHING ( 341 FDA reports)
HAEMORRHOIDS ( 340 FDA reports)
CARDIOGENIC SHOCK ( 337 FDA reports)
GASTRITIS ( 337 FDA reports)
PERICARDIAL EFFUSION ( 337 FDA reports)
ABDOMINAL DISCOMFORT ( 335 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 330 FDA reports)
ABASIA ( 328 FDA reports)
JOINT SWELLING ( 327 FDA reports)
SICK SINUS SYNDROME ( 327 FDA reports)
BLOOD POTASSIUM DECREASED ( 325 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 322 FDA reports)
RESPIRATORY DISTRESS ( 322 FDA reports)
DILATATION VENTRICULAR ( 321 FDA reports)
OSTEONECROSIS OF JAW ( 318 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 318 FDA reports)
SINUS TACHYCARDIA ( 318 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 315 FDA reports)
COAGULOPATHY ( 315 FDA reports)
NECK PAIN ( 315 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 309 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 307 FDA reports)
DIVERTICULUM ( 307 FDA reports)
ASCITES ( 306 FDA reports)
DYSURIA ( 304 FDA reports)
VERTIGO ( 300 FDA reports)
BONE DISORDER ( 299 FDA reports)
DISEASE PROGRESSION ( 299 FDA reports)
RENAL CYST ( 298 FDA reports)
MELAENA ( 297 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 295 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 294 FDA reports)
FLUID RETENTION ( 293 FDA reports)
LEUKOCYTOSIS ( 292 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 291 FDA reports)
LEFT ATRIAL DILATATION ( 291 FDA reports)
METABOLIC ACIDOSIS ( 291 FDA reports)
PANCYTOPENIA ( 290 FDA reports)
OSTEOMYELITIS ( 287 FDA reports)
DEFORMITY ( 286 FDA reports)
PRODUCTIVE COUGH ( 284 FDA reports)
AGITATION ( 283 FDA reports)
PRODUCT QUALITY ISSUE ( 281 FDA reports)
COLONIC POLYP ( 280 FDA reports)
AORTIC STENOSIS ( 279 FDA reports)
ARTHRITIS ( 277 FDA reports)
HAEMATOMA ( 277 FDA reports)
INCORRECT DOSE ADMINISTERED ( 277 FDA reports)
AMNESIA ( 276 FDA reports)
MEMORY IMPAIRMENT ( 276 FDA reports)
SWELLING ( 276 FDA reports)
DEMENTIA ( 275 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 274 FDA reports)
SEPTIC SHOCK ( 273 FDA reports)
SKIN ULCER ( 272 FDA reports)
HAEMOPTYSIS ( 272 FDA reports)
OBESITY ( 272 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 271 FDA reports)
RENAL DISORDER ( 271 FDA reports)
HYPOPHAGIA ( 267 FDA reports)
FLUID OVERLOAD ( 266 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 265 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 265 FDA reports)
URINARY INCONTINENCE ( 265 FDA reports)
MEDICATION ERROR ( 264 FDA reports)
BLOOD BILIRUBIN INCREASED ( 263 FDA reports)
RIGHT VENTRICULAR FAILURE ( 263 FDA reports)
SPEECH DISORDER ( 261 FDA reports)
IMPAIRED HEALING ( 261 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 260 FDA reports)
CATARACT ( 260 FDA reports)
HAEMODIALYSIS ( 260 FDA reports)
OROPHARYNGEAL PAIN ( 260 FDA reports)
LUNG DISORDER ( 257 FDA reports)
OXYGEN SATURATION DECREASED ( 256 FDA reports)
DIALYSIS ( 255 FDA reports)
MOBILITY DECREASED ( 254 FDA reports)
PAIN IN JAW ( 254 FDA reports)
POLLAKIURIA ( 254 FDA reports)
HEPATIC ENZYME INCREASED ( 252 FDA reports)
MALNUTRITION ( 249 FDA reports)
DELIRIUM ( 246 FDA reports)
DYSARTHRIA ( 245 FDA reports)
GASTRIC ULCER ( 242 FDA reports)
GOUT ( 241 FDA reports)
FAMILY STRESS ( 240 FDA reports)
NEPHROLITHIASIS ( 240 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 238 FDA reports)
ACUTE RESPIRATORY FAILURE ( 236 FDA reports)
CARDIAC VALVE DISEASE ( 235 FDA reports)
LUNG INFILTRATION ( 235 FDA reports)
ANGINA UNSTABLE ( 233 FDA reports)
BLOOD SODIUM DECREASED ( 232 FDA reports)
CAROTID ARTERY STENOSIS ( 231 FDA reports)
HEPATIC FAILURE ( 231 FDA reports)
COMA ( 229 FDA reports)
HIATUS HERNIA ( 229 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 226 FDA reports)
TYPE 2 DIABETES MELLITUS ( 225 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 224 FDA reports)
RESPIRATORY ARREST ( 223 FDA reports)
VENTRICULAR HYPOKINESIA ( 223 FDA reports)
RALES ( 222 FDA reports)
ORTHOSTATIC HYPOTENSION ( 221 FDA reports)
HEAD INJURY ( 220 FDA reports)
HAEMATOCHEZIA ( 219 FDA reports)
CYSTITIS ( 216 FDA reports)
CEREBRAL ATROPHY ( 215 FDA reports)
RHABDOMYOLYSIS ( 215 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 214 FDA reports)
THROMBOSIS ( 214 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 212 FDA reports)
NEUTROPENIA ( 212 FDA reports)
LEFT VENTRICULAR FAILURE ( 211 FDA reports)
GASTROINTESTINAL DISORDER ( 210 FDA reports)
ATRIOVENTRICULAR BLOCK ( 209 FDA reports)
PALLOR ( 209 FDA reports)
RIB FRACTURE ( 209 FDA reports)
TORSADE DE POINTES ( 208 FDA reports)
CARDIAC PACEMAKER INSERTION ( 208 FDA reports)
LOBAR PNEUMONIA ( 208 FDA reports)
CEREBRAL HAEMORRHAGE ( 206 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 206 FDA reports)
SHOCK ( 204 FDA reports)
CORONARY ARTERY OCCLUSION ( 202 FDA reports)
CYANOSIS ( 202 FDA reports)
URINARY RETENTION ( 201 FDA reports)
EMPHYSEMA ( 200 FDA reports)
HYPERCHOLESTEROLAEMIA ( 200 FDA reports)
FLANK PAIN ( 199 FDA reports)
INFLUENZA LIKE ILLNESS ( 197 FDA reports)
SUDDEN DEATH ( 196 FDA reports)
SUBDURAL HAEMATOMA ( 195 FDA reports)
AORTIC ANEURYSM ( 195 FDA reports)
CEREBRAL ISCHAEMIA ( 195 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 194 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 194 FDA reports)
FLATULENCE ( 193 FDA reports)
TOOTH EXTRACTION ( 192 FDA reports)
HAEMATEMESIS ( 190 FDA reports)
JAUNDICE ( 190 FDA reports)
PULSE ABSENT ( 190 FDA reports)
HIP FRACTURE ( 189 FDA reports)
PNEUMONIA ASPIRATION ( 189 FDA reports)
DYSLIPIDAEMIA ( 188 FDA reports)
BLOOD GLUCOSE DECREASED ( 187 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 185 FDA reports)
CEREBRAL INFARCTION ( 185 FDA reports)
INTERSTITIAL LUNG DISEASE ( 185 FDA reports)
NERVOUSNESS ( 185 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 185 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 184 FDA reports)
SKIN DISCOLOURATION ( 183 FDA reports)
GASTRITIS EROSIVE ( 182 FDA reports)
LIVER DISORDER ( 182 FDA reports)
NASOPHARYNGITIS ( 181 FDA reports)
ALOPECIA ( 180 FDA reports)
DRY MOUTH ( 180 FDA reports)
VISUAL ACUITY REDUCED ( 180 FDA reports)
NASAL CONGESTION ( 178 FDA reports)
OSTEOPENIA ( 178 FDA reports)
APHASIA ( 176 FDA reports)
DILATATION ATRIAL ( 176 FDA reports)
GENERALISED OEDEMA ( 176 FDA reports)
PANCREATITIS ( 176 FDA reports)
DRUG LEVEL INCREASED ( 175 FDA reports)
NODAL RHYTHM ( 175 FDA reports)
DECUBITUS ULCER ( 173 FDA reports)
HYPOVOLAEMIA ( 173 FDA reports)
MUSCLE TWITCHING ( 172 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 172 FDA reports)
METASTASES TO BONE ( 171 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 171 FDA reports)
INFLAMMATION ( 170 FDA reports)
OSTEONECROSIS ( 170 FDA reports)
HYPERSENSITIVITY ( 169 FDA reports)
LYMPHADENOPATHY ( 169 FDA reports)
OSTEOPOROSIS ( 169 FDA reports)
PULMONARY FIBROSIS ( 167 FDA reports)
DIPLOPIA ( 166 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 166 FDA reports)
DYSGEUSIA ( 165 FDA reports)
HERPES ZOSTER ( 165 FDA reports)
URTICARIA ( 165 FDA reports)
SWELLING FACE ( 164 FDA reports)
CARDIOVASCULAR DISORDER ( 162 FDA reports)
DYSPHONIA ( 162 FDA reports)
LABORATORY TEST ABNORMAL ( 162 FDA reports)
MITRAL VALVE CALCIFICATION ( 161 FDA reports)
ROAD TRAFFIC ACCIDENT ( 161 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 160 FDA reports)
INTRACARDIAC THROMBUS ( 160 FDA reports)
AZOTAEMIA ( 159 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 159 FDA reports)
FAILURE TO THRIVE ( 159 FDA reports)
GASTROENTERITIS ( 159 FDA reports)
BLOOD CALCIUM DECREASED ( 158 FDA reports)
NOCTURIA ( 158 FDA reports)
OESOPHAGITIS ( 157 FDA reports)
CORONARY ARTERY STENOSIS ( 156 FDA reports)
MULTIPLE MYELOMA ( 156 FDA reports)
BREATH SOUNDS ABNORMAL ( 155 FDA reports)
DIASTOLIC DYSFUNCTION ( 155 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 154 FDA reports)
HEMIPARESIS ( 154 FDA reports)
POST PROCEDURAL COMPLICATION ( 154 FDA reports)
RHEUMATOID ARTHRITIS ( 154 FDA reports)
URINE OUTPUT DECREASED ( 154 FDA reports)
ATRIAL TACHYCARDIA ( 153 FDA reports)
DIVERTICULITIS ( 153 FDA reports)
MASS ( 153 FDA reports)
IRON DEFICIENCY ANAEMIA ( 152 FDA reports)
DEAFNESS ( 151 FDA reports)
HYDRONEPHROSIS ( 151 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 151 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 151 FDA reports)
CIRCULATORY COLLAPSE ( 150 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 149 FDA reports)
RESTLESSNESS ( 149 FDA reports)
SPINAL COMPRESSION FRACTURE ( 149 FDA reports)
SLEEP DISORDER ( 148 FDA reports)
COLD SWEAT ( 148 FDA reports)
EAR PAIN ( 148 FDA reports)
HYPOMAGNESAEMIA ( 148 FDA reports)
BONE PAIN ( 146 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 146 FDA reports)
ANURIA ( 145 FDA reports)
LUNG NEOPLASM ( 144 FDA reports)
VENTRICULAR HYPERTROPHY ( 144 FDA reports)
RHINORRHOEA ( 143 FDA reports)
HEPATIC STEATOSIS ( 143 FDA reports)
ECCHYMOSIS ( 142 FDA reports)
IMPAIRED WORK ABILITY ( 142 FDA reports)
INTERMITTENT CLAUDICATION ( 142 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 141 FDA reports)
CHOLECYSTITIS ( 141 FDA reports)
ENCEPHALOPATHY ( 141 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 141 FDA reports)
RHINITIS ALLERGIC ( 140 FDA reports)
TENDERNESS ( 140 FDA reports)
SKIN EXFOLIATION ( 139 FDA reports)
VARICOSE VEIN ( 139 FDA reports)
DRUG HYPERSENSITIVITY ( 139 FDA reports)
HYPERTENSIVE HEART DISEASE ( 139 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 138 FDA reports)
CARDIAC FLUTTER ( 138 FDA reports)
DISCOMFORT ( 138 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 138 FDA reports)
NEOPLASM MALIGNANT ( 136 FDA reports)
BLOOD CHLORIDE DECREASED ( 135 FDA reports)
OFF LABEL USE ( 135 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 134 FDA reports)
HEPATOMEGALY ( 134 FDA reports)
AORTIC VALVE SCLEROSIS ( 132 FDA reports)
DYSSTASIA ( 132 FDA reports)
ERECTILE DYSFUNCTION ( 132 FDA reports)
BLOOD ALBUMIN DECREASED ( 131 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 131 FDA reports)
COLITIS ( 131 FDA reports)
JOINT INJURY ( 131 FDA reports)
SCAR ( 131 FDA reports)
SKIN LESION ( 131 FDA reports)
RASH PRURITIC ( 130 FDA reports)
MYELODYSPLASTIC SYNDROME ( 130 FDA reports)
HOT FLUSH ( 129 FDA reports)
TINNITUS ( 129 FDA reports)
VISUAL DISTURBANCE ( 129 FDA reports)
ROTATOR CUFF SYNDROME ( 128 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 128 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 127 FDA reports)
DISTURBANCE IN ATTENTION ( 126 FDA reports)
FEBRILE NEUTROPENIA ( 126 FDA reports)
HYPOCALCAEMIA ( 126 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 125 FDA reports)
FAECES DISCOLOURED ( 125 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 125 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 124 FDA reports)
PERIPHERAL COLDNESS ( 124 FDA reports)
ABNORMAL BEHAVIOUR ( 123 FDA reports)
ANAL FISSURE ( 123 FDA reports)
PANIC ATTACK ( 123 FDA reports)
SPINAL COLUMN STENOSIS ( 123 FDA reports)
APLASIA PURE RED CELL ( 122 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 122 FDA reports)
CONDUCTION DISORDER ( 122 FDA reports)
DISEASE RECURRENCE ( 122 FDA reports)
CHEST X-RAY ABNORMAL ( 121 FDA reports)
EXTRASYSTOLES ( 121 FDA reports)
ISCHAEMIA ( 121 FDA reports)
BLISTER ( 120 FDA reports)
IRRITABILITY ( 119 FDA reports)
LIMB INJURY ( 119 FDA reports)
CANDIDIASIS ( 118 FDA reports)
DEVICE RELATED INFECTION ( 118 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 118 FDA reports)
HEPATITIS ( 118 FDA reports)
LEUKOPENIA ( 118 FDA reports)
LOSS OF EMPLOYMENT ( 118 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 118 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 118 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 118 FDA reports)
ARTHROPATHY ( 117 FDA reports)
DECREASED INTEREST ( 117 FDA reports)
BLINDNESS UNILATERAL ( 116 FDA reports)
LACERATION ( 116 FDA reports)
SPLENOMEGALY ( 115 FDA reports)
VIRAL INFECTION ( 115 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 114 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 113 FDA reports)
PARTNER STRESS ( 113 FDA reports)
RASH ERYTHEMATOUS ( 113 FDA reports)
AGGRESSION ( 112 FDA reports)
BLINDNESS ( 112 FDA reports)
COMPLETED SUICIDE ( 112 FDA reports)
FEELING HOT ( 112 FDA reports)
HYPERSOMNIA ( 111 FDA reports)
ABDOMINAL TENDERNESS ( 110 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 110 FDA reports)
DIABETIC NEUROPATHY ( 110 FDA reports)
INCONTINENCE ( 110 FDA reports)
DRUG EFFECT DECREASED ( 109 FDA reports)
TOOTHACHE ( 109 FDA reports)
UROSEPSIS ( 108 FDA reports)
COGNITIVE DISORDER ( 108 FDA reports)
EXERCISE TOLERANCE DECREASED ( 108 FDA reports)
PLEURAL FIBROSIS ( 108 FDA reports)
ACUTE PRERENAL FAILURE ( 107 FDA reports)
BURNING SENSATION ( 107 FDA reports)
ATAXIA ( 106 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 106 FDA reports)
NERVOUS SYSTEM DISORDER ( 106 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 105 FDA reports)
CARPAL TUNNEL SYNDROME ( 105 FDA reports)
EXCORIATION ( 105 FDA reports)
HYPOPNOEA ( 105 FDA reports)
RESPIRATORY TRACT INFECTION ( 105 FDA reports)
RIGHT ATRIAL DILATATION ( 105 FDA reports)
VENTRICULAR DYSFUNCTION ( 105 FDA reports)
TROPONIN INCREASED ( 104 FDA reports)
BURSITIS ( 104 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 104 FDA reports)
HEPATIC CIRRHOSIS ( 104 FDA reports)
HYPERTHYROIDISM ( 104 FDA reports)
PULMONARY MASS ( 104 FDA reports)
ATRIAL SEPTAL DEFECT ( 103 FDA reports)
BLOOD URINE PRESENT ( 103 FDA reports)
NO THERAPEUTIC RESPONSE ( 103 FDA reports)
REFRACTORY ANAEMIA ( 103 FDA reports)
RENAL TUBULAR NECROSIS ( 103 FDA reports)
RESPIRATORY RATE INCREASED ( 102 FDA reports)
GANGRENE ( 101 FDA reports)
ISCHAEMIC STROKE ( 101 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 100 FDA reports)
ASPIRATION ( 100 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 100 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 100 FDA reports)
INFLUENZA ( 100 FDA reports)
LACTIC ACIDOSIS ( 100 FDA reports)
PERIPHERAL ISCHAEMIA ( 100 FDA reports)
WOUND INFECTION ( 100 FDA reports)
TACHYPNOEA ( 99 FDA reports)
ULCER ( 99 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 99 FDA reports)
APNOEA ( 99 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 99 FDA reports)
CREPITATIONS ( 99 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 99 FDA reports)
ORAL INTAKE REDUCED ( 99 FDA reports)
BACTERAEMIA ( 98 FDA reports)
EATING DISORDER ( 98 FDA reports)
GASTRIC DISORDER ( 98 FDA reports)
VAGINAL ABSCESS ( 98 FDA reports)
STOMATITIS ( 97 FDA reports)
SUICIDAL IDEATION ( 97 FDA reports)
BASAL CELL CARCINOMA ( 97 FDA reports)
DRUG INTOLERANCE ( 97 FDA reports)
DYSKINESIA ( 97 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 97 FDA reports)
ILEUS ( 97 FDA reports)
OCCULT BLOOD POSITIVE ( 97 FDA reports)
COLITIS ISCHAEMIC ( 96 FDA reports)
DRY SKIN ( 96 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 96 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 95 FDA reports)
HEPATIC CONGESTION ( 95 FDA reports)
IRRITABLE BOWEL SYNDROME ( 95 FDA reports)
PHYSICAL DISABILITY ( 95 FDA reports)
BRONCHOSPASM ( 94 FDA reports)
DECREASED ACTIVITY ( 94 FDA reports)
HOSPITALISATION ( 94 FDA reports)
PEPTIC ULCER ( 94 FDA reports)
ACUTE PULMONARY OEDEMA ( 93 FDA reports)
CACHEXIA ( 93 FDA reports)
DENTAL CARIES ( 93 FDA reports)
HALLUCINATION, VISUAL ( 93 FDA reports)
TOOTH LOSS ( 93 FDA reports)
VENOUS INSUFFICIENCY ( 92 FDA reports)
CHOLECYSTITIS ACUTE ( 92 FDA reports)
FISTULA ( 92 FDA reports)
ACCIDENTAL OVERDOSE ( 91 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 91 FDA reports)
FIBROSIS ( 91 FDA reports)
QUALITY OF LIFE DECREASED ( 91 FDA reports)
ACUTE CORONARY SYNDROME ( 90 FDA reports)
DEPRESSED MOOD ( 90 FDA reports)
HYPOKINESIA ( 90 FDA reports)
JOINT EFFUSION ( 90 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 90 FDA reports)
ADVERSE DRUG REACTION ( 89 FDA reports)
MITRAL VALVE STENOSIS ( 89 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 89 FDA reports)
RHONCHI ( 89 FDA reports)
WOUND ( 89 FDA reports)
RETCHING ( 88 FDA reports)
DRUG DOSE OMISSION ( 88 FDA reports)
ELECTROLYTE IMBALANCE ( 88 FDA reports)
FEMUR FRACTURE ( 88 FDA reports)
ACIDOSIS ( 87 FDA reports)
AGRANULOCYTOSIS ( 87 FDA reports)
CAROTID BRUIT ( 87 FDA reports)
PNEUMONITIS ( 87 FDA reports)
TACHYARRHYTHMIA ( 87 FDA reports)
RESPIRATORY DISORDER ( 86 FDA reports)
BRONCHOPNEUMONIA ( 86 FDA reports)
CARDIAC FAILURE ACUTE ( 86 FDA reports)
CRYING ( 86 FDA reports)
GALLBLADDER DISORDER ( 86 FDA reports)
MIGRAINE ( 86 FDA reports)
PROTEINURIA ( 86 FDA reports)
HEART TRANSPLANT ( 85 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 85 FDA reports)
LUNG NEOPLASM MALIGNANT ( 85 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 85 FDA reports)
VENTRICULAR ARRHYTHMIA ( 85 FDA reports)
RASH GENERALISED ( 84 FDA reports)
ANGIOEDEMA ( 84 FDA reports)
AORTIC VALVE CALCIFICATION ( 84 FDA reports)
DIVERTICULUM INTESTINAL ( 84 FDA reports)
HYPOALBUMINAEMIA ( 84 FDA reports)
MASTICATION DISORDER ( 84 FDA reports)
NIGHT SWEATS ( 84 FDA reports)
AORTIC VALVE STENOSIS ( 83 FDA reports)
FAECAL INCONTINENCE ( 83 FDA reports)
FEELING COLD ( 83 FDA reports)
GLAUCOMA ( 83 FDA reports)
HEART INJURY ( 83 FDA reports)
JAW FRACTURE ( 83 FDA reports)
NEURALGIA ( 83 FDA reports)
PROTEIN TOTAL DECREASED ( 83 FDA reports)
STEVENS-JOHNSON SYNDROME ( 83 FDA reports)
WALKING AID USER ( 83 FDA reports)
SWOLLEN TONGUE ( 82 FDA reports)
BLOOD CULTURE POSITIVE ( 82 FDA reports)
CATARACT OPERATION ( 82 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 82 FDA reports)
GINGIVAL BLEEDING ( 82 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 82 FDA reports)
MITRAL VALVE DISEASE ( 82 FDA reports)
ABDOMINAL PAIN LOWER ( 81 FDA reports)
BRADYARRHYTHMIA ( 81 FDA reports)
BUNDLE BRANCH BLOCK ( 81 FDA reports)
EXOSTOSIS ( 81 FDA reports)
INTESTINAL ISCHAEMIA ( 81 FDA reports)
KYPHOSIS ( 81 FDA reports)
LEG AMPUTATION ( 81 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 81 FDA reports)
MOVEMENT DISORDER ( 81 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 81 FDA reports)
STOMACH DISCOMFORT ( 81 FDA reports)
SUICIDE ATTEMPT ( 81 FDA reports)
UTERINE CANCER ( 81 FDA reports)
TOOTH DISORDER ( 80 FDA reports)
ABSCESS ( 80 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 80 FDA reports)
KLEBSIELLA INFECTION ( 80 FDA reports)
MITRAL VALVE PROLAPSE ( 80 FDA reports)
GYNAECOMASTIA ( 79 FDA reports)
HEART RATE ABNORMAL ( 79 FDA reports)
JOINT STIFFNESS ( 79 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 79 FDA reports)
OLIGURIA ( 79 FDA reports)
PHARYNGITIS ( 79 FDA reports)
SKIN HYPERTROPHY ( 79 FDA reports)
RESTLESS LEGS SYNDROME ( 78 FDA reports)
HEPATIC CYST ( 78 FDA reports)
METABOLIC ENCEPHALOPATHY ( 78 FDA reports)
MUCOSAL INFLAMMATION ( 78 FDA reports)
ONYCHOMYCOSIS ( 78 FDA reports)
ORAL CANDIDIASIS ( 78 FDA reports)
COR PULMONALE ( 77 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 77 FDA reports)
JUGULAR VEIN DISTENSION ( 77 FDA reports)
LIFE EXPECTANCY SHORTENED ( 77 FDA reports)
RENAL CANCER ( 77 FDA reports)
SKIN INDURATION ( 77 FDA reports)
THROAT IRRITATION ( 77 FDA reports)
CATHETERISATION CARDIAC ( 76 FDA reports)
NODAL ARRHYTHMIA ( 76 FDA reports)
PHOTOPHOBIA ( 76 FDA reports)
PSYCHOTIC DISORDER ( 76 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 75 FDA reports)
DIZZINESS POSTURAL ( 75 FDA reports)
INTESTINAL OBSTRUCTION ( 75 FDA reports)
PANCREATITIS ACUTE ( 75 FDA reports)
CYST ( 74 FDA reports)
DISABILITY ( 74 FDA reports)
METASTASES TO LUNG ( 74 FDA reports)
OSTEOLYSIS ( 74 FDA reports)
TUBERCULIN TEST POSITIVE ( 74 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 74 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 73 FDA reports)
BREAST CANCER ( 73 FDA reports)
DRUG ADMINISTRATION ERROR ( 73 FDA reports)
FRACTURE ( 73 FDA reports)
MACULAR DEGENERATION ( 73 FDA reports)
CULTURE URINE POSITIVE ( 72 FDA reports)
DEBRIDEMENT ( 72 FDA reports)
EYE PAIN ( 72 FDA reports)
GLOSSODYNIA ( 72 FDA reports)
HYPOACUSIS ( 72 FDA reports)
PSEUDOMONAS INFECTION ( 72 FDA reports)
SINUS HEADACHE ( 72 FDA reports)
TOOTH FRACTURE ( 72 FDA reports)
SUBDURAL HAEMORRHAGE ( 71 FDA reports)
ENDOCARDITIS ( 71 FDA reports)
ESSENTIAL HYPERTENSION ( 71 FDA reports)
HYPOTHERMIA ( 71 FDA reports)
INGUINAL HERNIA ( 71 FDA reports)
JAW DISORDER ( 71 FDA reports)
LUNG INFECTION ( 71 FDA reports)
PNEUMOTHORAX ( 71 FDA reports)
PURPURA ( 71 FDA reports)
CHROMATURIA ( 70 FDA reports)
ENDOTRACHEAL INTUBATION ( 70 FDA reports)
EYE DISORDER ( 70 FDA reports)
MENSTRUATION IRREGULAR ( 70 FDA reports)
PROSTATOMEGALY ( 70 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 70 FDA reports)
ANOXIC ENCEPHALOPATHY ( 69 FDA reports)
EMBOLIC STROKE ( 69 FDA reports)
HEPATOTOXICITY ( 69 FDA reports)
MAJOR DEPRESSION ( 69 FDA reports)
PETECHIAE ( 69 FDA reports)
CLOSTRIDIAL INFECTION ( 68 FDA reports)
ENTEROCOCCAL INFECTION ( 68 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 68 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 68 FDA reports)
SKIN LACERATION ( 68 FDA reports)
WRONG DRUG ADMINISTERED ( 68 FDA reports)
SKIN DISORDER ( 67 FDA reports)
THIRST ( 67 FDA reports)
ADVERSE EVENT ( 67 FDA reports)
LUMBAR SPINAL STENOSIS ( 67 FDA reports)
BLOOD CREATINE INCREASED ( 66 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 66 FDA reports)
SINUS CONGESTION ( 66 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 66 FDA reports)
SKIN HYPERPIGMENTATION ( 65 FDA reports)
GROIN PAIN ( 65 FDA reports)
JOINT DISLOCATION ( 65 FDA reports)
MUSCLE STRAIN ( 65 FDA reports)
POLYCYSTIC OVARIES ( 65 FDA reports)
POLYP ( 65 FDA reports)
ANGER ( 64 FDA reports)
AORTIC VALVE DISEASE ( 64 FDA reports)
CAROTID ARTERY DISEASE ( 64 FDA reports)
CHOLESTASIS ( 64 FDA reports)
CONJUNCTIVITIS ( 64 FDA reports)
COORDINATION ABNORMAL ( 64 FDA reports)
DRY EYE ( 64 FDA reports)
ERUCTATION ( 64 FDA reports)
FUNGAL INFECTION ( 64 FDA reports)
HAEMODYNAMIC INSTABILITY ( 64 FDA reports)
HYPERCALCAEMIA ( 64 FDA reports)
PURULENT DISCHARGE ( 64 FDA reports)
SINUS ARRHYTHMIA ( 64 FDA reports)
SUDDEN CARDIAC DEATH ( 64 FDA reports)
UPPER LIMB FRACTURE ( 64 FDA reports)
VIITH NERVE PARALYSIS ( 64 FDA reports)
DIABETIC RETINOPATHY ( 63 FDA reports)
EYE HAEMORRHAGE ( 63 FDA reports)
FIBROMYALGIA ( 63 FDA reports)
GRAND MAL CONVULSION ( 63 FDA reports)
HAIR GROWTH ABNORMAL ( 63 FDA reports)
MYOCLONUS ( 63 FDA reports)
BACTERIAL INFECTION ( 62 FDA reports)
CARDIAC FAILURE CHRONIC ( 62 FDA reports)
DIFFICULTY IN WALKING ( 62 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 62 FDA reports)
HAEMORRHAGIC ANAEMIA ( 62 FDA reports)
MENTAL IMPAIRMENT ( 62 FDA reports)
PARKINSONISM ( 62 FDA reports)
QRS AXIS ABNORMAL ( 62 FDA reports)
SINUS DISORDER ( 62 FDA reports)
BONE MARROW FAILURE ( 61 FDA reports)
CHOLECYSTECTOMY ( 61 FDA reports)
CORONARY ARTERY BYPASS ( 61 FDA reports)
MULTIPLE DRUG OVERDOSE ( 61 FDA reports)
POLYURIA ( 61 FDA reports)
CEREBROVASCULAR DISORDER ( 60 FDA reports)
DISSOCIATION ( 60 FDA reports)
INFERTILITY ( 60 FDA reports)
INFUSION RELATED REACTION ( 60 FDA reports)
KNEE ARTHROPLASTY ( 60 FDA reports)
LYMPHOMA ( 60 FDA reports)
RASH MACULAR ( 60 FDA reports)
RENAL ARTERY STENOSIS ( 60 FDA reports)
SNORING ( 60 FDA reports)
THYROID DISORDER ( 60 FDA reports)
SCOLIOSIS ( 59 FDA reports)
SKIN FIBROSIS ( 59 FDA reports)
BLOOD PRESSURE ABNORMAL ( 59 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 59 FDA reports)
CALCULUS URETERIC ( 59 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 59 FDA reports)
COMPRESSION FRACTURE ( 59 FDA reports)
DELUSION ( 59 FDA reports)
DEVICE FAILURE ( 59 FDA reports)
MOUTH HAEMORRHAGE ( 59 FDA reports)
OESOPHAGEAL ULCER ( 59 FDA reports)
PYELONEPHRITIS ( 59 FDA reports)
BEDRIDDEN ( 58 FDA reports)
BRONCHIECTASIS ( 58 FDA reports)
CARDIAC DEATH ( 58 FDA reports)
DEVICE MALFUNCTION ( 58 FDA reports)
HYPERBILIRUBINAEMIA ( 58 FDA reports)
LOOSE TOOTH ( 58 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 58 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 58 FDA reports)
SKIN TIGHTNESS ( 58 FDA reports)
THERAPY NON-RESPONDER ( 58 FDA reports)
RESUSCITATION ( 57 FDA reports)
TEMPERATURE INTOLERANCE ( 57 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 57 FDA reports)
BODY TEMPERATURE INCREASED ( 57 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 57 FDA reports)
DUODENITIS ( 57 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 57 FDA reports)
INJECTION SITE PAIN ( 57 FDA reports)
MEDIASTINITIS ( 57 FDA reports)
BLOOD URIC ACID INCREASED ( 56 FDA reports)
FACIAL PALSY ( 56 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 56 FDA reports)
RESPIRATORY ACIDOSIS ( 55 FDA reports)
VISUAL FIELD DEFECT ( 55 FDA reports)
WRIST FRACTURE ( 55 FDA reports)
ABDOMINAL HERNIA ( 55 FDA reports)
ACUTE SINUSITIS ( 55 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 55 FDA reports)
CHOKING ( 55 FDA reports)
EPIDIDYMITIS ( 55 FDA reports)
HYPOTONIA ( 55 FDA reports)
POLYNEUROPATHY ( 55 FDA reports)
ACTINIC KERATOSIS ( 54 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 54 FDA reports)
ESCHERICHIA INFECTION ( 54 FDA reports)
GASTROENTERITIS VIRAL ( 54 FDA reports)
GOITRE ( 54 FDA reports)
MEDICAL DEVICE COMPLICATION ( 54 FDA reports)
METASTASES TO LIVER ( 54 FDA reports)
PELVIC FRACTURE ( 54 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 54 FDA reports)
POOR QUALITY SLEEP ( 54 FDA reports)
PRIMARY SEQUESTRUM ( 54 FDA reports)
AORTIC CALCIFICATION ( 53 FDA reports)
DIABETIC NEPHROPATHY ( 53 FDA reports)
FACIAL PAIN ( 53 FDA reports)
HYPERCAPNIA ( 53 FDA reports)
LACUNAR INFARCTION ( 53 FDA reports)
LIMB DISCOMFORT ( 53 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 53 FDA reports)
SKIN WARM ( 53 FDA reports)
SPINAL FRACTURE ( 53 FDA reports)
STENT PLACEMENT ( 53 FDA reports)
THROMBOPHLEBITIS ( 53 FDA reports)
TOXIC SKIN ERUPTION ( 53 FDA reports)
SEDATION ( 52 FDA reports)
SHOCK HAEMORRHAGIC ( 52 FDA reports)
VAGINAL HAEMORRHAGE ( 52 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 52 FDA reports)
EXPOSED BONE IN JAW ( 52 FDA reports)
GOUTY ARTHRITIS ( 52 FDA reports)
MECHANICAL VENTILATION ( 52 FDA reports)
MEDICATION RESIDUE ( 52 FDA reports)
ORAL PAIN ( 52 FDA reports)
PHARYNGEAL OEDEMA ( 52 FDA reports)
AORTIC DISSECTION ( 51 FDA reports)
CARDIOVERSION ( 51 FDA reports)
CERUMEN IMPACTION ( 51 FDA reports)
CYTOLYTIC HEPATITIS ( 51 FDA reports)
EMBOLISM ( 51 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 51 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 51 FDA reports)
HYPOAESTHESIA ORAL ( 51 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 51 FDA reports)
INCOHERENT ( 51 FDA reports)
LIP SWELLING ( 51 FDA reports)
LIPOMA ( 51 FDA reports)
LYMPHOEDEMA ( 51 FDA reports)
MUSCLE ATROPHY ( 51 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 51 FDA reports)
ORAL DISCOMFORT ( 51 FDA reports)
ORAL DISORDER ( 51 FDA reports)
PROCTALGIA ( 51 FDA reports)
PROSTATE CANCER ( 51 FDA reports)
SENSATION OF HEAVINESS ( 51 FDA reports)
SKIN BURNING SENSATION ( 51 FDA reports)
SKIN NECROSIS ( 51 FDA reports)
RETROPERITONEAL HAEMATOMA ( 50 FDA reports)
APATHY ( 50 FDA reports)
BACK INJURY ( 50 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 50 FDA reports)
CARDIOPULMONARY FAILURE ( 50 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 50 FDA reports)
GASTRIC POLYPS ( 50 FDA reports)
HEPATIC NECROSIS ( 50 FDA reports)
HIP ARTHROPLASTY ( 50 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 50 FDA reports)
LIVEDO RETICULARIS ( 50 FDA reports)
MOOD SWINGS ( 50 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 50 FDA reports)
PROCEDURAL COMPLICATION ( 50 FDA reports)
PRURITUS GENERALISED ( 50 FDA reports)
ABNORMAL DREAMS ( 49 FDA reports)
ANAPHYLACTIC REACTION ( 49 FDA reports)
BLADDER CANCER ( 49 FDA reports)
BREAST PAIN ( 49 FDA reports)
CARDIAC OPERATION ( 49 FDA reports)
DERMATITIS ( 49 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 49 FDA reports)
ENDODONTIC PROCEDURE ( 49 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 49 FDA reports)
MICTURITION URGENCY ( 49 FDA reports)
MYOPATHY ( 49 FDA reports)
PARANOIA ( 49 FDA reports)
PERITONITIS ( 49 FDA reports)
RADICULOPATHY ( 49 FDA reports)
SKIN CANCER ( 49 FDA reports)
SPUTUM DISCOLOURED ( 49 FDA reports)
RESPIRATORY TRACT CONGESTION ( 48 FDA reports)
TENDONITIS ( 48 FDA reports)
TOOTH ABSCESS ( 48 FDA reports)
BACK DISORDER ( 48 FDA reports)
DERMAL CYST ( 48 FDA reports)
FACE INJURY ( 48 FDA reports)
FACE OEDEMA ( 48 FDA reports)
HEART VALVE INCOMPETENCE ( 48 FDA reports)
METASTASES TO SPINE ( 48 FDA reports)
PLEURITIC PAIN ( 48 FDA reports)
ADRENAL INSUFFICIENCY ( 47 FDA reports)
ANGIOPATHY ( 47 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 47 FDA reports)
CAESAREAN SECTION ( 47 FDA reports)
GINGIVITIS ( 47 FDA reports)
HAEMOTHORAX ( 47 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 47 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 47 FDA reports)
NEPHROSCLEROSIS ( 47 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 47 FDA reports)
RASH MACULO-PAPULAR ( 47 FDA reports)
SENSORY DISTURBANCE ( 47 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 46 FDA reports)
X-RAY ABNORMAL ( 46 FDA reports)
ALCOHOL USE ( 46 FDA reports)
BLOOD SODIUM INCREASED ( 46 FDA reports)
BRAIN OEDEMA ( 46 FDA reports)
BREAST CANCER FEMALE ( 46 FDA reports)
BRONCHITIS CHRONIC ( 46 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 46 FDA reports)
DISEASE COMPLICATION ( 46 FDA reports)
DRUG ERUPTION ( 46 FDA reports)
ECZEMA ( 46 FDA reports)
ISCHAEMIC HEPATITIS ( 46 FDA reports)
LOCALISED INFECTION ( 46 FDA reports)
PSORIASIS ( 46 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 45 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 45 FDA reports)
ANAPHYLACTIC SHOCK ( 45 FDA reports)
ANEURYSM ( 45 FDA reports)
AORTIC DILATATION ( 45 FDA reports)
BLOOD MAGNESIUM DECREASED ( 45 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 45 FDA reports)
DRUG DEPENDENCE ( 45 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 45 FDA reports)
HEPATIC ENCEPHALOPATHY ( 45 FDA reports)
NODULE ( 45 FDA reports)
ODYNOPHAGIA ( 45 FDA reports)
PARALYSIS ( 45 FDA reports)
PERICARDITIS ( 45 FDA reports)
PHOTOPSIA ( 45 FDA reports)
PNEUMONIA BACTERIAL ( 45 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 45 FDA reports)
SERUM FERRITIN INCREASED ( 45 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 44 FDA reports)
THINKING ABNORMAL ( 44 FDA reports)
TREATMENT FAILURE ( 44 FDA reports)
AGEUSIA ( 44 FDA reports)
BONE LESION ( 44 FDA reports)
DUODENAL ULCER ( 44 FDA reports)
HAEMORRHAGIC STROKE ( 44 FDA reports)
HUMERUS FRACTURE ( 44 FDA reports)
HYPOPHOSPHATAEMIA ( 44 FDA reports)
HYPOREFLEXIA ( 44 FDA reports)
INCREASED TENDENCY TO BRUISE ( 44 FDA reports)
LOCAL SWELLING ( 44 FDA reports)
MYOSITIS ( 44 FDA reports)
ORGAN FAILURE ( 44 FDA reports)
PERIODONTAL DISEASE ( 44 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 44 FDA reports)
PREMATURE BABY ( 44 FDA reports)
PULMONARY HAEMORRHAGE ( 44 FDA reports)
ATROPHY ( 43 FDA reports)
CARDIAC OUTPUT DECREASED ( 43 FDA reports)
EOSINOPHILIA ( 43 FDA reports)
FACIAL BONES FRACTURE ( 43 FDA reports)
HEART SOUNDS ABNORMAL ( 43 FDA reports)
HEMIPLEGIA ( 43 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 43 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 43 FDA reports)
MOUTH ULCERATION ( 43 FDA reports)
NEPHROPATHY ( 43 FDA reports)
ORCHITIS ( 43 FDA reports)
PHLEBITIS ( 43 FDA reports)
TRANSAMINASES INCREASED ( 43 FDA reports)
SCIATICA ( 42 FDA reports)
SEROTONIN SYNDROME ( 42 FDA reports)
APHAGIA ( 42 FDA reports)
BIPOLAR DISORDER ( 42 FDA reports)
CERVICAL SPINAL STENOSIS ( 42 FDA reports)
ENDOMETRIAL CANCER ( 42 FDA reports)
FLUID INTAKE REDUCED ( 42 FDA reports)
MUSCLE HAEMORRHAGE ( 42 FDA reports)
NEUTROPHIL COUNT DECREASED ( 42 FDA reports)
NON-CARDIAC CHEST PAIN ( 42 FDA reports)
POOR PERIPHERAL CIRCULATION ( 42 FDA reports)
AORTIC VALVE REPLACEMENT ( 41 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 41 FDA reports)
CYSTOCELE ( 41 FDA reports)
DENTAL OPERATION ( 41 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 41 FDA reports)
EYE SWELLING ( 41 FDA reports)
HAEMOLYSIS ( 41 FDA reports)
HALO VISION ( 41 FDA reports)
HEPATIC NEOPLASM ( 41 FDA reports)
HYPERPARATHYROIDISM ( 41 FDA reports)
HYPERTHERMIA ( 41 FDA reports)
HYPERURICAEMIA ( 41 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 41 FDA reports)
JOINT CONTRACTURE ( 41 FDA reports)
LARYNGITIS ( 41 FDA reports)
METASTASES TO LYMPH NODES ( 41 FDA reports)
OSTEOSCLEROSIS ( 41 FDA reports)
TONGUE DISORDER ( 41 FDA reports)
TUBERCULOSIS ( 40 FDA reports)
BLADDER DISORDER ( 40 FDA reports)
COAGULATION TIME PROLONGED ( 40 FDA reports)
GASTRIC HAEMORRHAGE ( 40 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 40 FDA reports)
INTENTIONAL DRUG MISUSE ( 40 FDA reports)
JOINT SPRAIN ( 40 FDA reports)
OESOPHAGEAL STENOSIS ( 40 FDA reports)
PARAESTHESIA ORAL ( 40 FDA reports)
PATHOLOGICAL FRACTURE ( 40 FDA reports)
PIGMENTATION DISORDER ( 40 FDA reports)
PLATELET COUNT INCREASED ( 40 FDA reports)
PROTEIN URINE PRESENT ( 40 FDA reports)
BODY TEMPERATURE DECREASED ( 39 FDA reports)
CATHETER RELATED INFECTION ( 39 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 39 FDA reports)
CENTRAL LINE INFECTION ( 39 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 39 FDA reports)
EPIGASTRIC DISCOMFORT ( 39 FDA reports)
FOOT FRACTURE ( 39 FDA reports)
GINGIVAL SWELLING ( 39 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 39 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 39 FDA reports)
PERIPHERAL EMBOLISM ( 39 FDA reports)
PLEURISY ( 39 FDA reports)
POLYCYTHAEMIA ( 39 FDA reports)
SPONDYLOLISTHESIS ( 39 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 39 FDA reports)
TOBACCO USER ( 39 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 39 FDA reports)
RASH PAPULAR ( 38 FDA reports)
SOFT TISSUE DISORDER ( 38 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 38 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 38 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 38 FDA reports)
BRAIN INJURY ( 38 FDA reports)
BREAST CANCER METASTATIC ( 38 FDA reports)
CARDIAC ENZYMES INCREASED ( 38 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 38 FDA reports)
CLOSTRIDIUM COLITIS ( 38 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 38 FDA reports)
EAR DISCOMFORT ( 38 FDA reports)
HAEMOLYTIC ANAEMIA ( 38 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 38 FDA reports)
HYPERVENTILATION ( 38 FDA reports)
LIVER INJURY ( 38 FDA reports)
LUNG CONSOLIDATION ( 38 FDA reports)
MIDDLE INSOMNIA ( 38 FDA reports)
PHOTOSENSITIVITY REACTION ( 38 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 37 FDA reports)
DRUG ABUSE ( 37 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 37 FDA reports)
FURUNCLE ( 37 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 37 FDA reports)
INJECTION SITE HAEMORRHAGE ( 37 FDA reports)
INTENTIONAL OVERDOSE ( 37 FDA reports)
MENISCUS LESION ( 37 FDA reports)
MOTOR DYSFUNCTION ( 37 FDA reports)
OCULAR HYPERAEMIA ( 37 FDA reports)
OSTEITIS ( 37 FDA reports)
RETINAL HAEMORRHAGE ( 37 FDA reports)
THROAT TIGHTNESS ( 37 FDA reports)
UMBILICAL HERNIA ( 37 FDA reports)
VASCULITIS ( 37 FDA reports)
VITREOUS FLOATERS ( 37 FDA reports)
SUBCUTANEOUS ABSCESS ( 36 FDA reports)
TONGUE ULCERATION ( 36 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 36 FDA reports)
COLON ADENOMA ( 36 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 36 FDA reports)
EROSIVE OESOPHAGITIS ( 36 FDA reports)
FEMORAL NECK FRACTURE ( 36 FDA reports)
LUMBAR RADICULOPATHY ( 36 FDA reports)
METASTATIC NEOPLASM ( 36 FDA reports)
PROTHROMBIN TIME SHORTENED ( 36 FDA reports)
PULSE PRESSURE DECREASED ( 36 FDA reports)
BLOOD CALCIUM INCREASED ( 35 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 35 FDA reports)
BREAST MASS ( 35 FDA reports)
CAROTID ARTERY OCCLUSION ( 35 FDA reports)
DRUG LEVEL DECREASED ( 35 FDA reports)
EYE IRRITATION ( 35 FDA reports)
GINGIVAL RECESSION ( 35 FDA reports)
HEARING IMPAIRED ( 35 FDA reports)
HEPATIC LESION ( 35 FDA reports)
HEPATOSPLENOMEGALY ( 35 FDA reports)
HYPOAESTHESIA FACIAL ( 35 FDA reports)
KIDNEY INFECTION ( 35 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 35 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 35 FDA reports)
PROSTATE CANCER METASTATIC ( 35 FDA reports)
PUPIL FIXED ( 35 FDA reports)
REFLUX OESOPHAGITIS ( 35 FDA reports)
SKIN PLAQUE ( 35 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 35 FDA reports)
RADIUS FRACTURE ( 34 FDA reports)
RENAL ATROPHY ( 34 FDA reports)
SINUS ARREST ( 34 FDA reports)
SPLENIC INFARCTION ( 34 FDA reports)
SPONDYLOLYSIS ( 34 FDA reports)
TONGUE DISCOLOURATION ( 34 FDA reports)
URINARY TRACT DISORDER ( 34 FDA reports)
ANXIETY DISORDER ( 34 FDA reports)
BLOOD CHLORIDE INCREASED ( 34 FDA reports)
BONE NEOPLASM MALIGNANT ( 34 FDA reports)
CLAUSTROPHOBIA ( 34 FDA reports)
DRUG PRESCRIBING ERROR ( 34 FDA reports)
EFFUSION ( 34 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 34 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 34 FDA reports)
FIBRIN D DIMER INCREASED ( 34 FDA reports)
HAEMORRHAGIC DIATHESIS ( 34 FDA reports)
HYDROCELE ( 34 FDA reports)
HYPERTENSIVE CRISIS ( 34 FDA reports)
LISTLESS ( 34 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 34 FDA reports)
NOCTURNAL DYSPNOEA ( 34 FDA reports)
PAIN OF SKIN ( 34 FDA reports)
PERITONITIS BACTERIAL ( 34 FDA reports)
ACCIDENT ( 33 FDA reports)
BLOOD TEST ABNORMAL ( 33 FDA reports)
CATHETER RELATED COMPLICATION ( 33 FDA reports)
DERMATITIS BULLOUS ( 33 FDA reports)
DERMATITIS EXFOLIATIVE ( 33 FDA reports)
DYSAESTHESIA ( 33 FDA reports)
ENCEPHALOMALACIA ( 33 FDA reports)
ERYTHEMA MULTIFORME ( 33 FDA reports)
HALLUCINATIONS, MIXED ( 33 FDA reports)
HYPERNATRAEMIA ( 33 FDA reports)
ILEUS PARALYTIC ( 33 FDA reports)
LIPASE INCREASED ( 33 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 33 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 33 FDA reports)
OBSTRUCTIVE UROPATHY ( 33 FDA reports)
OSTEORADIONECROSIS ( 33 FDA reports)
POLYDIPSIA ( 33 FDA reports)
POLYMYALGIA RHEUMATICA ( 33 FDA reports)
RASH PUSTULAR ( 33 FDA reports)
RENAL COLIC ( 33 FDA reports)
RENAL MASS ( 33 FDA reports)
RHINITIS ( 33 FDA reports)
TIBIA FRACTURE ( 33 FDA reports)
TRANSFUSION ( 33 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 33 FDA reports)
VASCULAR CALCIFICATION ( 33 FDA reports)
SENSORY LOSS ( 32 FDA reports)
VASCULAR GRAFT OCCLUSION ( 32 FDA reports)
ABNORMAL FAECES ( 32 FDA reports)
AMMONIA INCREASED ( 32 FDA reports)
ANGIOPLASTY ( 32 FDA reports)
CERVICOBRACHIAL SYNDROME ( 32 FDA reports)
CHOLECYSTITIS CHRONIC ( 32 FDA reports)
ESCHERICHIA TEST POSITIVE ( 32 FDA reports)
HEART DISEASE CONGENITAL ( 32 FDA reports)
HYPERCOAGULATION ( 32 FDA reports)
INITIAL INSOMNIA ( 32 FDA reports)
INTRA-UTERINE DEATH ( 32 FDA reports)
JAUNDICE CHOLESTATIC ( 32 FDA reports)
MITRAL VALVE REPLACEMENT ( 32 FDA reports)
NEPHROGENIC ANAEMIA ( 32 FDA reports)
PARKINSON'S DISEASE ( 32 FDA reports)
PITTING OEDEMA ( 32 FDA reports)
POSTPARTUM DISORDER ( 32 FDA reports)
PREGNANCY ( 32 FDA reports)
PROSTATITIS ( 32 FDA reports)
APPENDICECTOMY ( 31 FDA reports)
BLEPHARITIS ( 31 FDA reports)
BONE DENSITY DECREASED ( 31 FDA reports)
CARDIAC ANEURYSM ( 31 FDA reports)
COLON CANCER ( 31 FDA reports)
COMMUNICATION DISORDER ( 31 FDA reports)
GINGIVAL ULCERATION ( 31 FDA reports)
GRANULOMA ( 31 FDA reports)
HEPATIC ENZYME ABNORMAL ( 31 FDA reports)
HEPATOCELLULAR INJURY ( 31 FDA reports)
HYPOVENTILATION ( 31 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 31 FDA reports)
LACRIMATION INCREASED ( 31 FDA reports)
OPEN REDUCTION OF FRACTURE ( 31 FDA reports)
ORAL INFECTION ( 31 FDA reports)
OTITIS EXTERNA ( 31 FDA reports)
PROTEIN TOTAL INCREASED ( 31 FDA reports)
RENAL CELL CARCINOMA ( 31 FDA reports)
SENSATION OF FOREIGN BODY ( 31 FDA reports)
SKIN ATROPHY ( 31 FDA reports)
SPINAL DISORDER ( 31 FDA reports)
TOE AMPUTATION ( 31 FDA reports)
WHEELCHAIR USER ( 31 FDA reports)
SKIN IRRITATION ( 30 FDA reports)
SPUTUM CULTURE POSITIVE ( 30 FDA reports)
STASIS DERMATITIS ( 30 FDA reports)
STEM CELL TRANSPLANT ( 30 FDA reports)
STRESS URINARY INCONTINENCE ( 30 FDA reports)
TROPONIN I INCREASED ( 30 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 30 FDA reports)
ANOGENITAL WARTS ( 30 FDA reports)
BLOOD CREATININE DECREASED ( 30 FDA reports)
BLOOD IRON DECREASED ( 30 FDA reports)
BLOOD PH DECREASED ( 30 FDA reports)
CORONARY ARTERY THROMBOSIS ( 30 FDA reports)
COSTOCHONDRITIS ( 30 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 30 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 30 FDA reports)
GASTROINTESTINAL INFECTION ( 30 FDA reports)
HYDROCEPHALUS ( 30 FDA reports)
JAW OPERATION ( 30 FDA reports)
LARGE INTESTINE PERFORATION ( 30 FDA reports)
LIBIDO DECREASED ( 30 FDA reports)
LOWER LIMB FRACTURE ( 30 FDA reports)
MUSCLE CRAMP ( 30 FDA reports)
NERVE INJURY ( 30 FDA reports)
NEUROGENIC BLADDER ( 30 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 30 FDA reports)
POSTNASAL DRIP ( 30 FDA reports)
PULSE ABNORMAL ( 30 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 29 FDA reports)
BLOOD AMYLASE INCREASED ( 29 FDA reports)
BLOOD DISORDER ( 29 FDA reports)
BODY HEIGHT DECREASED ( 29 FDA reports)
CARDIAC FIBRILLATION ( 29 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 29 FDA reports)
DEAFNESS BILATERAL ( 29 FDA reports)
DEATH OF RELATIVE ( 29 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 29 FDA reports)
EYELID PTOSIS ( 29 FDA reports)
GALLOP RHYTHM PRESENT ( 29 FDA reports)
GINGIVAL DISORDER ( 29 FDA reports)
HELICOBACTER INFECTION ( 29 FDA reports)
HEPATOJUGULAR REFLUX ( 29 FDA reports)
METABOLIC SYNDROME ( 29 FDA reports)
MUSCLE DISORDER ( 29 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 29 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 29 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 29 FDA reports)
SYNOVITIS ( 29 FDA reports)
TERMINAL STATE ( 29 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 29 FDA reports)
THROMBOSIS IN DEVICE ( 29 FDA reports)
TOOTH INJURY ( 29 FDA reports)
TOXIC ENCEPHALOPATHY ( 29 FDA reports)
VITREOUS HAEMORRHAGE ( 29 FDA reports)
STREPTOCOCCAL SEPSIS ( 28 FDA reports)
THYROID NEOPLASM ( 28 FDA reports)
URETERIC OBSTRUCTION ( 28 FDA reports)
UTERINE LEIOMYOMA ( 28 FDA reports)
VASODILATATION ( 28 FDA reports)
VITREOUS DETACHMENT ( 28 FDA reports)
WOUND SECRETION ( 28 FDA reports)
ARTHRITIS BACTERIAL ( 28 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 28 FDA reports)
BRAIN DEATH ( 28 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 28 FDA reports)
HEPATITIS CHOLESTATIC ( 28 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 28 FDA reports)
MENORRHAGIA ( 28 FDA reports)
MUSCULOSKELETAL DISORDER ( 28 FDA reports)
NEOPLASM PROGRESSION ( 28 FDA reports)
NON-SMALL CELL LUNG CANCER ( 28 FDA reports)
PELVIC PAIN ( 28 FDA reports)
PREMATURE LABOUR ( 28 FDA reports)
PULMONARY VALVE STENOSIS ( 28 FDA reports)
APPENDICITIS ( 27 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 27 FDA reports)
EJECTION FRACTION ABNORMAL ( 27 FDA reports)
FAECALOMA ( 27 FDA reports)
HAEMARTHROSIS ( 27 FDA reports)
HYPERKINESIA ( 27 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 27 FDA reports)
INGROWING NAIL ( 27 FDA reports)
MOOD ALTERED ( 27 FDA reports)
MYDRIASIS ( 27 FDA reports)
NECROSIS ( 27 FDA reports)
PANCREATIC DISORDER ( 27 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 27 FDA reports)
SCAB ( 27 FDA reports)
SKIN PAPILLOMA ( 27 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 27 FDA reports)
THERMAL BURN ( 27 FDA reports)
ULCER HAEMORRHAGE ( 27 FDA reports)
UNEMPLOYMENT ( 27 FDA reports)
VASCULAR GRAFT ( 27 FDA reports)
RENAL PAIN ( 26 FDA reports)
RESPIRATORY DEPRESSION ( 26 FDA reports)
RETINAL DISORDER ( 26 FDA reports)
SEQUESTRECTOMY ( 26 FDA reports)
SPINAL CORD COMPRESSION ( 26 FDA reports)
TEARFULNESS ( 26 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 26 FDA reports)
VERTEBROPLASTY ( 26 FDA reports)
WITHDRAWAL SYNDROME ( 26 FDA reports)
XANTHOPSIA ( 26 FDA reports)
ABDOMINAL ADHESIONS ( 26 FDA reports)
ACROCHORDON ( 26 FDA reports)
ANKLE FRACTURE ( 26 FDA reports)
APPARENT DEATH ( 26 FDA reports)
BLINDNESS TRANSIENT ( 26 FDA reports)
BONE DEBRIDEMENT ( 26 FDA reports)
CARDIAC TAMPONADE ( 26 FDA reports)
CHRONIC SINUSITIS ( 26 FDA reports)
DEAFNESS NEUROSENSORY ( 26 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 26 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 26 FDA reports)
DRUG LEVEL FLUCTUATING ( 26 FDA reports)
FEAR OF DEATH ( 26 FDA reports)
FEELING JITTERY ( 26 FDA reports)
HYSTERECTOMY ( 26 FDA reports)
ILIAC ARTERY STENOSIS ( 26 FDA reports)
IMMOBILE ( 26 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 26 FDA reports)
JOINT CREPITATION ( 26 FDA reports)
NIGHTMARE ( 26 FDA reports)
OESOPHAGEAL PAIN ( 26 FDA reports)
OTITIS MEDIA ( 26 FDA reports)
PERICARDIAL HAEMORRHAGE ( 26 FDA reports)
POISONING ( 26 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 26 FDA reports)
ABSCESS NECK ( 25 FDA reports)
ADHESION ( 25 FDA reports)
AFFECTIVE DISORDER ( 25 FDA reports)
AKINESIA ( 25 FDA reports)
ALCOHOL ABUSE ( 25 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 25 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 25 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 25 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 25 FDA reports)
CEREBELLAR ATROPHY ( 25 FDA reports)
CEREBRAL HAEMATOMA ( 25 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 25 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 25 FDA reports)
DROOLING ( 25 FDA reports)
DRUG DISPENSING ERROR ( 25 FDA reports)
DYSPNOEA EXACERBATED ( 25 FDA reports)
EROSIVE DUODENITIS ( 25 FDA reports)
FIBULA FRACTURE ( 25 FDA reports)
GALLBLADDER POLYP ( 25 FDA reports)
GINGIVAL INFECTION ( 25 FDA reports)
HALLUCINATION, AUDITORY ( 25 FDA reports)
HYPOPERFUSION ( 25 FDA reports)
IATROGENIC INJURY ( 25 FDA reports)
LABILE HYPERTENSION ( 25 FDA reports)
LOCALISED OEDEMA ( 25 FDA reports)
MALIGNANT HYPERTENSION ( 25 FDA reports)
MUSCLE CONTRACTURE ( 25 FDA reports)
PERONEAL NERVE PALSY ( 25 FDA reports)
PNEUMONIA KLEBSIELLA ( 25 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 25 FDA reports)
SNEEZING ( 25 FDA reports)
TESTICULAR SWELLING ( 25 FDA reports)
TOOTH INFECTION ( 25 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 25 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 25 FDA reports)
RETINAL DETACHMENT ( 24 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 24 FDA reports)
URINE ODOUR ABNORMAL ( 24 FDA reports)
WEIGHT FLUCTUATION ( 24 FDA reports)
ABSCESS DRAINAGE ( 24 FDA reports)
ASBESTOSIS ( 24 FDA reports)
BACTERIAL TEST POSITIVE ( 24 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 24 FDA reports)
BLOOD COUNT ABNORMAL ( 24 FDA reports)
BUNION ( 24 FDA reports)
CANDIDURIA ( 24 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 24 FDA reports)
CYSTITIS INTERSTITIAL ( 24 FDA reports)
DENTAL DISCOMFORT ( 24 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 24 FDA reports)
HEPATOCELLULAR DAMAGE ( 24 FDA reports)
INJECTION SITE ERYTHEMA ( 24 FDA reports)
OPEN WOUND ( 24 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 24 FDA reports)
PO2 DECREASED ( 24 FDA reports)
PULMONARY GRANULOMA ( 24 FDA reports)
PULMONARY THROMBOSIS ( 24 FDA reports)
ABSCESS LIMB ( 23 FDA reports)
ACCIDENTAL EXPOSURE ( 23 FDA reports)
ADDISON'S DISEASE ( 23 FDA reports)
ANAL FISTULA ( 23 FDA reports)
APPETITE DISORDER ( 23 FDA reports)
AREFLEXIA ( 23 FDA reports)
ARTHRITIS INFECTIVE ( 23 FDA reports)
B-CELL LYMPHOMA ( 23 FDA reports)
BILIARY COLIC ( 23 FDA reports)
CLAVICLE FRACTURE ( 23 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 23 FDA reports)
EATING DISORDER SYMPTOM ( 23 FDA reports)
HAEMOGLOBIN INCREASED ( 23 FDA reports)
HEPATITIS FULMINANT ( 23 FDA reports)
HYPOPROTEINAEMIA ( 23 FDA reports)
INFARCTION ( 23 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 23 FDA reports)
LIGAMENT SPRAIN ( 23 FDA reports)
LUNG HYPERINFLATION ( 23 FDA reports)
MEAN CELL VOLUME INCREASED ( 23 FDA reports)
NEUROPATHY ( 23 FDA reports)
PROCEDURAL PAIN ( 23 FDA reports)
RESPIRATION ABNORMAL ( 23 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 23 FDA reports)
ROSACEA ( 23 FDA reports)
SEBORRHOEIC KERATOSIS ( 23 FDA reports)
SKIN FISSURES ( 23 FDA reports)
STRIDOR ( 23 FDA reports)
TENDON RUPTURE ( 23 FDA reports)
TRACHEOSTOMY ( 23 FDA reports)
TRAUMATIC LUNG INJURY ( 23 FDA reports)
UNDERDOSE ( 23 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 23 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 23 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 23 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 22 FDA reports)
SCHIZOPHRENIA ( 22 FDA reports)
STREPTOCOCCAL INFECTION ( 22 FDA reports)
TARDIVE DYSKINESIA ( 22 FDA reports)
TESTICULAR PAIN ( 22 FDA reports)
TOBACCO ABUSE ( 22 FDA reports)
TRAUMATIC HAEMATOMA ( 22 FDA reports)
TYPE 1 DIABETES MELLITUS ( 22 FDA reports)
VASCULAR PSEUDOANEURYSM ( 22 FDA reports)
WOUND DRAINAGE ( 22 FDA reports)
ABDOMINAL MASS ( 22 FDA reports)
ANGIONEUROTIC OEDEMA ( 22 FDA reports)
ASPIRATION PLEURAL CAVITY ( 22 FDA reports)
ASTERIXIS ( 22 FDA reports)
AUTOIMMUNE DISORDER ( 22 FDA reports)
BIOPSY CHEST WALL ABNORMAL ( 22 FDA reports)
CAROTID ARTERY ANEURYSM ( 22 FDA reports)
CEREBELLAR INFARCTION ( 22 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 22 FDA reports)
DIABETIC ULCER ( 22 FDA reports)
DUODENAL ULCER PERFORATION ( 22 FDA reports)
EPILEPSY ( 22 FDA reports)
EXPOSURE TO TOXIC AGENT ( 22 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 22 FDA reports)
FEMORAL ARTERY OCCLUSION ( 22 FDA reports)
FOOD INTERACTION ( 22 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 22 FDA reports)
GENERALISED ANXIETY DISORDER ( 22 FDA reports)
HEART VALVE REPLACEMENT ( 22 FDA reports)
HEPATITIS ACUTE ( 22 FDA reports)
HEPATITIS C ( 22 FDA reports)
HEPATORENAL SYNDROME ( 22 FDA reports)
HUNGER ( 22 FDA reports)
HYPOGLYCAEMIC COMA ( 22 FDA reports)
HYPOGONADISM ( 22 FDA reports)
METAPLASIA ( 22 FDA reports)
MONOPLEGIA ( 22 FDA reports)
MULTIPLE FRACTURES ( 22 FDA reports)
MYELOMA RECURRENCE ( 22 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 22 FDA reports)
OVARIAN CYST ( 22 FDA reports)
PERIORBITAL HAEMATOMA ( 22 FDA reports)
PERIORBITAL OEDEMA ( 22 FDA reports)
PORTAL HYPERTENSION ( 22 FDA reports)
POSTURE ABNORMAL ( 22 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 22 FDA reports)
PULMONARY VASCULAR DISORDER ( 22 FDA reports)
ANIMAL BITE ( 21 FDA reports)
AORTIC DISORDER ( 21 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 21 FDA reports)
BLOOD UREA ABNORMAL ( 21 FDA reports)
BONE MARROW DISORDER ( 21 FDA reports)
BRONCHIAL SECRETION RETENTION ( 21 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 21 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 21 FDA reports)
CHOKING SENSATION ( 21 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 21 FDA reports)
COAGULATION TEST ABNORMAL ( 21 FDA reports)
CORNEAL ABRASION ( 21 FDA reports)
DERMATITIS ATOPIC ( 21 FDA reports)
DERMATITIS CONTACT ( 21 FDA reports)
DEVICE DISLOCATION ( 21 FDA reports)
DIABETIC GASTROPARESIS ( 21 FDA reports)
ENTEROBACTER INFECTION ( 21 FDA reports)
ENURESIS ( 21 FDA reports)
EXTREMITY NECROSIS ( 21 FDA reports)
FOOD INTOLERANCE ( 21 FDA reports)
FOOT DEFORMITY ( 21 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 21 FDA reports)
INTRAOCULAR LENS IMPLANT ( 21 FDA reports)
NYSTAGMUS ( 21 FDA reports)
ORAL HERPES ( 21 FDA reports)
PERITONEAL DIALYSIS ( 21 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 21 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 21 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 21 FDA reports)
PULMONARY HILUM MASS ( 21 FDA reports)
RADIATION INJURY ( 21 FDA reports)
RECTAL POLYP ( 21 FDA reports)
RENAL INFARCT ( 21 FDA reports)
RENAL ISCHAEMIA ( 21 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 21 FDA reports)
SCLERODERMA ( 21 FDA reports)
SEPSIS SYNDROME ( 21 FDA reports)
TENDON DISORDER ( 21 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 21 FDA reports)
URINARY HESITATION ( 21 FDA reports)
SHOULDER OPERATION ( 20 FDA reports)
SKIN HAEMORRHAGE ( 20 FDA reports)
STUPOR ( 20 FDA reports)
TENOSYNOVITIS ( 20 FDA reports)
VASCULAR PURPURA ( 20 FDA reports)
VENOUS THROMBOSIS ( 20 FDA reports)
ABSCESS JAW ( 20 FDA reports)
BILIARY DILATATION ( 20 FDA reports)
BLOOD UREA DECREASED ( 20 FDA reports)
BRAIN HERNIATION ( 20 FDA reports)
CENTRAL OBESITY ( 20 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 20 FDA reports)
CEREBRAL DISORDER ( 20 FDA reports)
COARCTATION OF THE AORTA ( 20 FDA reports)
CONCUSSION ( 20 FDA reports)
CULTURE WOUND POSITIVE ( 20 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 20 FDA reports)
ESCHERICHIA SEPSIS ( 20 FDA reports)
FACIAL PARESIS ( 20 FDA reports)
GINGIVAL PAIN ( 20 FDA reports)
HEAD DISCOMFORT ( 20 FDA reports)
HICCUPS ( 20 FDA reports)
HYDROPNEUMOTHORAX ( 20 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 20 FDA reports)
INJECTION SITE HAEMATOMA ( 20 FDA reports)
LONG QT SYNDROME ( 20 FDA reports)
METABOLIC DISORDER ( 20 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 20 FDA reports)
MUSCLE RIGIDITY ( 20 FDA reports)
MUSCLE TIGHTNESS ( 20 FDA reports)
NASAL SEPTUM DEVIATION ( 20 FDA reports)
OESOPHAGEAL DISORDER ( 20 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 20 FDA reports)
PRE-ECLAMPSIA ( 20 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 20 FDA reports)
PULMONARY TOXICITY ( 20 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 20 FDA reports)
ADENOMA BENIGN ( 19 FDA reports)
AMAUROSIS FUGAX ( 19 FDA reports)
BARRETT'S OESOPHAGUS ( 19 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 19 FDA reports)
BIOPSY BONE ABNORMAL ( 19 FDA reports)
BLOOD MAGNESIUM INCREASED ( 19 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 19 FDA reports)
EDENTULOUS ( 19 FDA reports)
EMPTY SELLA SYNDROME ( 19 FDA reports)
HEPATIC FIBROSIS ( 19 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 19 FDA reports)
INTESTINAL DILATATION ( 19 FDA reports)
LIP DISORDER ( 19 FDA reports)
MASTOIDITIS ( 19 FDA reports)
METABOLIC ALKALOSIS ( 19 FDA reports)
MULTIPLE ALLERGIES ( 19 FDA reports)
NEOPLASM ( 19 FDA reports)
OSTEITIS DEFORMANS ( 19 FDA reports)
PERIRECTAL ABSCESS ( 19 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 19 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 19 FDA reports)
SEROMA ( 19 FDA reports)
SHOULDER ARTHROPLASTY ( 19 FDA reports)
TELANGIECTASIA ( 19 FDA reports)
URINE ANALYSIS ABNORMAL ( 19 FDA reports)
VARICES OESOPHAGEAL ( 19 FDA reports)
VASCULAR DEMENTIA ( 19 FDA reports)
RHEUMATIC HEART DISEASE ( 18 FDA reports)
SCOTOMA ( 18 FDA reports)
SCRATCH ( 18 FDA reports)
SPINAL DEFORMITY ( 18 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 18 FDA reports)
TRICUSPID VALVE DISEASE ( 18 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 18 FDA reports)
VENTRICULAR FAILURE ( 18 FDA reports)
VITAMIN D DEFICIENCY ( 18 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 18 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 18 FDA reports)
ANAEMIA POSTOPERATIVE ( 18 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 18 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 18 FDA reports)
BILE DUCT STONE ( 18 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 18 FDA reports)
BLOOD OSMOLARITY DECREASED ( 18 FDA reports)
BONE MARROW DEPRESSION ( 18 FDA reports)
CALCULUS URINARY ( 18 FDA reports)
CARDIAC HYPERTROPHY ( 18 FDA reports)
CARDIAC VALVE ABSCESS ( 18 FDA reports)
CARDIORENAL SYNDROME ( 18 FDA reports)
CATATONIA ( 18 FDA reports)
CHOLANGITIS ( 18 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 18 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 18 FDA reports)
DIABETIC KETOACIDOSIS ( 18 FDA reports)
ECLAMPSIA ( 18 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 18 FDA reports)
EYE INJURY ( 18 FDA reports)
FACET JOINT SYNDROME ( 18 FDA reports)
FLAT AFFECT ( 18 FDA reports)
FORMICATION ( 18 FDA reports)
HAND FRACTURE ( 18 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 18 FDA reports)
HYPERKERATOSIS ( 18 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 18 FDA reports)
IMPAIRED DRIVING ABILITY ( 18 FDA reports)
IMPAIRED SELF-CARE ( 18 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 18 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 18 FDA reports)
LIVE BIRTH ( 18 FDA reports)
LUNG CANCER METASTATIC ( 18 FDA reports)
MANIA ( 18 FDA reports)
METASTASIS ( 18 FDA reports)
MUSCULAR DYSTROPHY ( 18 FDA reports)
MYELOPATHY ( 18 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 18 FDA reports)
NECK MASS ( 18 FDA reports)
NEUTROPENIC SEPSIS ( 18 FDA reports)
PATHOGEN RESISTANCE ( 18 FDA reports)
PSYCHIATRIC SYMPTOM ( 18 FDA reports)
PURULENCE ( 18 FDA reports)
APHONIA ( 17 FDA reports)
ARTERIAL INSUFFICIENCY ( 17 FDA reports)
ARTERIAL THROMBOSIS ( 17 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 17 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 17 FDA reports)
BRONCHITIS ACUTE ( 17 FDA reports)
CATHETER SITE INFECTION ( 17 FDA reports)
DEAFNESS UNILATERAL ( 17 FDA reports)
DRUG INTERACTION POTENTIATION ( 17 FDA reports)
EYELID OEDEMA ( 17 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 17 FDA reports)
FOREIGN BODY ( 17 FDA reports)
GENERALISED ERYTHEMA ( 17 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 17 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 17 FDA reports)
HEPATITIS TOXIC ( 17 FDA reports)
HERNIA ( 17 FDA reports)
HERNIA REPAIR ( 17 FDA reports)
HYPERTONIA ( 17 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 17 FDA reports)
INTESTINAL PERFORATION ( 17 FDA reports)
INTRACRANIAL ANEURYSM ( 17 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 17 FDA reports)
MENINGITIS ( 17 FDA reports)
MICROANGIOPATHY ( 17 FDA reports)
MUCOSAL DRYNESS ( 17 FDA reports)
MYOCARDIAL FIBROSIS ( 17 FDA reports)
NEPHRITIS INTERSTITIAL ( 17 FDA reports)
NEUROLOGICAL SYMPTOM ( 17 FDA reports)
NODAL OSTEOARTHRITIS ( 17 FDA reports)
OEDEMA MOUTH ( 17 FDA reports)
OESOPHAGEAL SPASM ( 17 FDA reports)
ORAL DISCHARGE ( 17 FDA reports)
PACEMAKER COMPLICATION ( 17 FDA reports)
PCO2 DECREASED ( 17 FDA reports)
PEDAL PULSE DECREASED ( 17 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 17 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 17 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 17 FDA reports)
PNEUMONIA VIRAL ( 17 FDA reports)
PROCTITIS ( 17 FDA reports)
PYURIA ( 17 FDA reports)
RASH VESICULAR ( 17 FDA reports)
RETINOPATHY ( 17 FDA reports)
SALIVARY HYPERSECRETION ( 17 FDA reports)
SCROTAL ABSCESS ( 17 FDA reports)
SLUGGISHNESS ( 17 FDA reports)
SMALL FOR DATES BABY ( 17 FDA reports)
TONGUE OEDEMA ( 17 FDA reports)
TRAUMATIC BRAIN INJURY ( 17 FDA reports)
TRIGEMINAL NEURALGIA ( 17 FDA reports)
URGE INCONTINENCE ( 17 FDA reports)
URINARY TRACT OBSTRUCTION ( 17 FDA reports)
URINE ABNORMALITY ( 17 FDA reports)
WOUND HAEMORRHAGE ( 17 FDA reports)
RENAL TUBULAR ACIDOSIS ( 16 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 16 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 16 FDA reports)
SKELETAL INJURY ( 16 FDA reports)
SKIN INFECTION ( 16 FDA reports)
SKIN REACTION ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 16 FDA reports)
SYNCOPE VASOVAGAL ( 16 FDA reports)
SYSTEMIC CANDIDA ( 16 FDA reports)
TACHYCARDIA PAROXYSMAL ( 16 FDA reports)
TONIC CONVULSION ( 16 FDA reports)
URINE KETONE BODY PRESENT ( 16 FDA reports)
UVEITIS ( 16 FDA reports)
VERTIGO POSITIONAL ( 16 FDA reports)
VOCAL CORD DISORDER ( 16 FDA reports)
VOCAL CORD PARALYSIS ( 16 FDA reports)
WOUND DEHISCENCE ( 16 FDA reports)
ABSCESS ORAL ( 16 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 16 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 16 FDA reports)
APPENDICITIS PERFORATED ( 16 FDA reports)
ATRIAL THROMBOSIS ( 16 FDA reports)
AUTONOMIC NEUROPATHY ( 16 FDA reports)
BLADDER NEOPLASM ( 16 FDA reports)
BONE SCAN ABNORMAL ( 16 FDA reports)
BRAIN NEOPLASM ( 16 FDA reports)
CARBON DIOXIDE INCREASED ( 16 FDA reports)
CHEILITIS ( 16 FDA reports)
CHEYNE-STOKES RESPIRATION ( 16 FDA reports)
COLOUR BLINDNESS ( 16 FDA reports)
CYSTITIS HAEMORRHAGIC ( 16 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 16 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 16 FDA reports)
DRY THROAT ( 16 FDA reports)
EYE PRURITUS ( 16 FDA reports)
FANCONI SYNDROME ( 16 FDA reports)
GLOMERULONEPHRITIS ( 16 FDA reports)
GRAFT VERSUS HOST DISEASE ( 16 FDA reports)
HELICOBACTER GASTRITIS ( 16 FDA reports)
HYPERAESTHESIA ( 16 FDA reports)
HYPOCOAGULABLE STATE ( 16 FDA reports)
IMPETIGO ( 16 FDA reports)
INFECTIOUS PERITONITIS ( 16 FDA reports)
INTESTINAL POLYP ( 16 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 16 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 16 FDA reports)
KYPHOSCOLIOSIS ( 16 FDA reports)
MIOSIS ( 16 FDA reports)
MITRAL VALVE SCLEROSIS ( 16 FDA reports)
NO ADVERSE EVENT ( 16 FDA reports)
OCCULT BLOOD ( 16 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 16 FDA reports)
OROPHARYNGEAL BLISTERING ( 16 FDA reports)
OTITIS MEDIA CHRONIC ( 16 FDA reports)
PANCREATIC CYST ( 16 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 16 FDA reports)
POST PROCEDURAL INFECTION ( 16 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 15 FDA reports)
ADRENAL ADENOMA ( 15 FDA reports)
ANORECTAL DISCOMFORT ( 15 FDA reports)
ANOSMIA ( 15 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 15 FDA reports)
APPLICATION SITE PRURITUS ( 15 FDA reports)
ARTERIAL DISORDER ( 15 FDA reports)
ASPIRATION JOINT ( 15 FDA reports)
BONE MARROW OEDEMA ( 15 FDA reports)
BONE MARROW TRANSPLANT ( 15 FDA reports)
BRAIN SCAN ABNORMAL ( 15 FDA reports)
CALCINOSIS ( 15 FDA reports)
CATARACT NUCLEAR ( 15 FDA reports)
CHROMATOPSIA ( 15 FDA reports)
COMMINUTED FRACTURE ( 15 FDA reports)
CONGENITAL ANOMALY ( 15 FDA reports)
CORONARY ARTERY SURGERY ( 15 FDA reports)
DERMATITIS ALLERGIC ( 15 FDA reports)
DIABETIC FOOT ( 15 FDA reports)
EAR DISORDER ( 15 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 15 FDA reports)
EOSINOPHIL COUNT INCREASED ( 15 FDA reports)
GINGIVAL OPERATION ( 15 FDA reports)
GLOSSITIS ( 15 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 15 FDA reports)
HEPATIC INFARCTION ( 15 FDA reports)
HIGH FREQUENCY ABLATION ( 15 FDA reports)
HILAR LYMPHADENOPATHY ( 15 FDA reports)
HOARSENESS ( 15 FDA reports)
HYDROPS FOETALIS ( 15 FDA reports)
HYPERPHOSPHATAEMIA ( 15 FDA reports)
HYPERTONIC BLADDER ( 15 FDA reports)
HYPOVOLAEMIC SHOCK ( 15 FDA reports)
INNER EAR DISORDER ( 15 FDA reports)
ISCHAEMIC NEPHROPATHY ( 15 FDA reports)
LABILE BLOOD PRESSURE ( 15 FDA reports)
LABORATORY TEST INTERFERENCE ( 15 FDA reports)
LARGE INTESTINAL ULCER ( 15 FDA reports)
LEUKAEMIA ( 15 FDA reports)
LOSS OF CONTROL OF LEGS ( 15 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 15 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 15 FDA reports)
MICROCYTIC ANAEMIA ( 15 FDA reports)
MULTIPLE SCLEROSIS ( 15 FDA reports)
OBSTRUCTION ( 15 FDA reports)
OPERATIVE HAEMORRHAGE ( 15 FDA reports)
ORAL CAVITY FISTULA ( 15 FDA reports)
OXYGEN SUPPLEMENTATION ( 15 FDA reports)
PEMPHIGOID ( 15 FDA reports)
PERFORMANCE STATUS DECREASED ( 15 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 15 FDA reports)
POSTOPERATIVE ILEUS ( 15 FDA reports)
PSEUDODEMENTIA ( 15 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 15 FDA reports)
SERRATIA INFECTION ( 15 FDA reports)
SPLENIC ABSCESS ( 15 FDA reports)
STRABISMUS ( 15 FDA reports)
SYNOVIAL CYST ( 15 FDA reports)
THERAPEUTIC PROCEDURE ( 15 FDA reports)
TINEA PEDIS ( 15 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 15 FDA reports)
XEROSIS ( 15 FDA reports)
REGURGITATION ( 14 FDA reports)
SENSATION OF PRESSURE ( 14 FDA reports)
SERRATIA BACTERAEMIA ( 14 FDA reports)
SKIN INJURY ( 14 FDA reports)
SKIN TURGOR DECREASED ( 14 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 14 FDA reports)
STATUS EPILEPTICUS ( 14 FDA reports)
SURGICAL PROCEDURE REPEATED ( 14 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 14 FDA reports)
ACNE ( 14 FDA reports)
ACTINOMYCOSIS ( 14 FDA reports)
ALCOHOLIC LIVER DISEASE ( 14 FDA reports)
ATRIAL HYPERTROPHY ( 14 FDA reports)
BLOOD BICARBONATE DECREASED ( 14 FDA reports)
BONE GRAFT ( 14 FDA reports)
BUNION OPERATION ( 14 FDA reports)
CARBON DIOXIDE DECREASED ( 14 FDA reports)
CARDIOTOXICITY ( 14 FDA reports)
CATHETER SITE HAEMORRHAGE ( 14 FDA reports)
CHANGE OF BOWEL HABIT ( 14 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 14 FDA reports)
CULTURE POSITIVE ( 14 FDA reports)
DENTAL FISTULA ( 14 FDA reports)
DEVICE RELATED SEPSIS ( 14 FDA reports)
DIABETIC COMPLICATION ( 14 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 14 FDA reports)
EXFOLIATIVE RASH ( 14 FDA reports)
EYE INFECTION ( 14 FDA reports)
GASTROENTERITIS RADIATION ( 14 FDA reports)
HIDRADENITIS ( 14 FDA reports)
HOSPICE CARE ( 14 FDA reports)
HYPERPLASIA ( 14 FDA reports)
IMPLANT SITE HAEMATOMA ( 14 FDA reports)
INCREASED APPETITE ( 14 FDA reports)
INFUSION SITE INFECTION ( 14 FDA reports)
INJECTION SITE PRURITUS ( 14 FDA reports)
LABYRINTHITIS ( 14 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 14 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 14 FDA reports)
NASAL ULCER ( 14 FDA reports)
NEPHROTIC SYNDROME ( 14 FDA reports)
NERVE COMPRESSION ( 14 FDA reports)
NEUROSENSORY HYPOACUSIS ( 14 FDA reports)
NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 14 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 14 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 14 FDA reports)
OSTEOMYELITIS ACUTE ( 14 FDA reports)
OSTEOPOROTIC FRACTURE ( 14 FDA reports)
PANCREATIC CARCINOMA ( 14 FDA reports)
PARTIAL SEIZURES ( 14 FDA reports)
PERSONALITY CHANGE ( 14 FDA reports)
PNEUMOPERITONEUM ( 14 FDA reports)
POST PROCEDURAL HAEMATOMA ( 14 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 14 FDA reports)
PYELONEPHRITIS ACUTE ( 14 FDA reports)
ABDOMINAL ABSCESS ( 13 FDA reports)
ACUTE HEPATIC FAILURE ( 13 FDA reports)
ADNEXA UTERI MASS ( 13 FDA reports)
ALVEOLITIS ( 13 FDA reports)
ANAEMIA MACROCYTIC ( 13 FDA reports)
ANOXIA ( 13 FDA reports)
AORTIC THROMBOSIS ( 13 FDA reports)
APNOEIC ATTACK ( 13 FDA reports)
ARTERIAL STENOSIS ( 13 FDA reports)
AUTOIMMUNE HEPATITIS ( 13 FDA reports)
AUTOIMMUNE THYROIDITIS ( 13 FDA reports)
BASEDOW'S DISEASE ( 13 FDA reports)
BLEEDING TIME PROLONGED ( 13 FDA reports)
BLOOD LACTIC ACID INCREASED ( 13 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 13 FDA reports)
BREAST TENDERNESS ( 13 FDA reports)
CAROTIDYNIA ( 13 FDA reports)
CEREBRAL HYPOPERFUSION ( 13 FDA reports)
CHEST INJURY ( 13 FDA reports)
COLLAPSE OF LUNG ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 13 FDA reports)
EMPYEMA ( 13 FDA reports)
ERYTHEMA OF EYELID ( 13 FDA reports)
EXPIRED DRUG ADMINISTERED ( 13 FDA reports)
EYE MOVEMENT DISORDER ( 13 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 13 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
HAEMANGIOMA ( 13 FDA reports)
HAEMATOCRIT INCREASED ( 13 FDA reports)
HERPES SIMPLEX ( 13 FDA reports)
HERPES VIRUS INFECTION ( 13 FDA reports)
HERPES ZOSTER OTICUS ( 13 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 13 FDA reports)
HYPERTROPHY ( 13 FDA reports)
INCISION SITE COMPLICATION ( 13 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 13 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 13 FDA reports)
IRITIS ( 13 FDA reports)
IRON DEFICIENCY ( 13 FDA reports)
JUDGEMENT IMPAIRED ( 13 FDA reports)
KNEE OPERATION ( 13 FDA reports)
LUNG ADENOCARCINOMA ( 13 FDA reports)
MAMMOGRAM ABNORMAL ( 13 FDA reports)
MASTECTOMY ( 13 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 13 FDA reports)
MEDIASTINAL MASS ( 13 FDA reports)
MENINGIOMA ( 13 FDA reports)
METASTASES TO PELVIS ( 13 FDA reports)
NAIL DISCOLOURATION ( 13 FDA reports)
NEURODERMATITIS ( 13 FDA reports)
NEUROTOXICITY ( 13 FDA reports)
NONSPECIFIC REACTION ( 13 FDA reports)
OLIGOHYDRAMNIOS ( 13 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 13 FDA reports)
ORTHOSTATIC INTOLERANCE ( 13 FDA reports)
PCO2 INCREASED ( 13 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 13 FDA reports)
PLANTAR FASCIITIS ( 13 FDA reports)
PLEURAL CALCIFICATION ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 13 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 13 FDA reports)
RADIATION OESOPHAGITIS ( 13 FDA reports)
RADIOTHERAPY ( 13 FDA reports)
RETROPERITONEAL NEOPLASM ( 13 FDA reports)
RHEUMATIC FEVER ( 13 FDA reports)
SARCOIDOSIS ( 13 FDA reports)
SCROTAL OEDEMA ( 13 FDA reports)
SECRETION DISCHARGE ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SEXUAL DYSFUNCTION ( 13 FDA reports)
SKIN HYPOPIGMENTATION ( 13 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 13 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 13 FDA reports)
THROAT LESION ( 13 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 13 FDA reports)
THYROID CYST ( 13 FDA reports)
TOOTH IMPACTED ( 13 FDA reports)
TRIGGER FINGER ( 13 FDA reports)
VITAMIN B12 DEFICIENCY ( 13 FDA reports)
VULVOVAGINAL DRYNESS ( 13 FDA reports)
WALKING DISABILITY ( 13 FDA reports)
SELF-MEDICATION ( 12 FDA reports)
SHOULDER PAIN ( 12 FDA reports)
SPUTUM PURULENT ( 12 FDA reports)
STARING ( 12 FDA reports)
SUPERINFECTION ( 12 FDA reports)
TEMPORAL ARTERITIS ( 12 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
ULCERATIVE KERATITIS ( 12 FDA reports)
VASCULITIC RASH ( 12 FDA reports)
VITAMIN D DECREASED ( 12 FDA reports)
VOCAL CORD THICKENING ( 12 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 12 FDA reports)
ACNE PUSTULAR ( 12 FDA reports)
ACUTE LEUKAEMIA ( 12 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
ADVERSE REACTION ( 12 FDA reports)
ANAL SKIN TAGS ( 12 FDA reports)
APPENDIX DISORDER ( 12 FDA reports)
ARTHROPOD BITE ( 12 FDA reports)
ASPERGILLOSIS ( 12 FDA reports)
AXILLARY PAIN ( 12 FDA reports)
BACTERIAL SEPSIS ( 12 FDA reports)
BLADDER MASS ( 12 FDA reports)
BLOOD BLISTER ( 12 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 12 FDA reports)
BLOOD PH INCREASED ( 12 FDA reports)
BONE CYST ( 12 FDA reports)
BOWEL SOUNDS ABNORMAL ( 12 FDA reports)
BREAST CALCIFICATIONS ( 12 FDA reports)
BREAST OEDEMA ( 12 FDA reports)
BREAST PROSTHESIS USER ( 12 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 12 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 12 FDA reports)
CEREBRAL MICROANGIOPATHY ( 12 FDA reports)
CLUBBING ( 12 FDA reports)
CORONARY ANGIOPLASTY ( 12 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 12 FDA reports)
DIVERTICULAR PERFORATION ( 12 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 12 FDA reports)
ENDARTERECTOMY ( 12 FDA reports)
ENDOCARDITIS BACTERIAL ( 12 FDA reports)
ENDOPHTHALMITIS ( 12 FDA reports)
ENTEROCOLITIS ( 12 FDA reports)
FAECES HARD ( 12 FDA reports)
FEEDING DISORDER ( 12 FDA reports)
FOOT AMPUTATION ( 12 FDA reports)
GALLBLADDER OPERATION ( 12 FDA reports)
GASTROINTESTINAL ULCER ( 12 FDA reports)
GENITAL CANDIDIASIS ( 12 FDA reports)
HELICOBACTER TEST POSITIVE ( 12 FDA reports)
HORDEOLUM ( 12 FDA reports)
HYDROTHORAX ( 12 FDA reports)
HYPOCHLORAEMIA ( 12 FDA reports)
HYPOCHROMIC ANAEMIA ( 12 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
IMMUNOSUPPRESSION ( 12 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 12 FDA reports)
INADEQUATE ANALGESIA ( 12 FDA reports)
INGUINAL HERNIA REPAIR ( 12 FDA reports)
INJECTION SITE IRRITATION ( 12 FDA reports)
INJECTION SITE SWELLING ( 12 FDA reports)
INTENTIONAL SELF-INJURY ( 12 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 12 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 12 FDA reports)
LIP OEDEMA ( 12 FDA reports)
LUNG LOBECTOMY ( 12 FDA reports)
MACROCYTOSIS ( 12 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 12 FDA reports)
MICTURITION DISORDER ( 12 FDA reports)
MOANING ( 12 FDA reports)
MULTI-ORGAN DISORDER ( 12 FDA reports)
MUSCLE FATIGUE ( 12 FDA reports)
MYOCARDITIS ( 12 FDA reports)
NAIL DISORDER ( 12 FDA reports)
NEPHRITIC SYNDROME ( 12 FDA reports)
NEPHROPATHY TOXIC ( 12 FDA reports)
ORTHOSIS USER ( 12 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
PHARYNGEAL DISORDER ( 12 FDA reports)
PNEUMONIA HAEMOPHILUS ( 12 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 12 FDA reports)
PROCEDURAL HYPOTENSION ( 12 FDA reports)
ABORTION INDUCED ( 11 FDA reports)
AFFECT LABILITY ( 11 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 11 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 11 FDA reports)
AORTIC BYPASS ( 11 FDA reports)
ARTERIOSPASM CORONARY ( 11 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 11 FDA reports)
ARTERIOVENOUS MALFORMATION ( 11 FDA reports)
ATHEROSCLEROSIS ( 11 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 11 FDA reports)
BODY TINEA ( 11 FDA reports)
BONE LOSS ( 11 FDA reports)
BONE SWELLING ( 11 FDA reports)
BRAIN STEM INFARCTION ( 11 FDA reports)
BREAST HAEMATOMA ( 11 FDA reports)
BURNS SECOND DEGREE ( 11 FDA reports)
CALCIPHYLAXIS ( 11 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 11 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CEREBRAL THROMBOSIS ( 11 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 11 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 11 FDA reports)
COLITIS ULCERATIVE ( 11 FDA reports)
CONTRAST MEDIA REACTION ( 11 FDA reports)
CUTANEOUS VASCULITIS ( 11 FDA reports)
DIAPHRAGMATIC HERNIA ( 11 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 11 FDA reports)
DYSMORPHISM ( 11 FDA reports)
DYSPAREUNIA ( 11 FDA reports)
DYSPNOEA AT REST ( 11 FDA reports)
DYSTONIA ( 11 FDA reports)
EAR CONGESTION ( 11 FDA reports)
ENTEROCOCCAL SEPSIS ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
GASTROINTESTINAL NECROSIS ( 11 FDA reports)
GRAVITATIONAL OEDEMA ( 11 FDA reports)
HAEMANGIOMA OF LIVER ( 11 FDA reports)
HAEMORRHAGE URINARY TRACT ( 11 FDA reports)
HYPERALBUMINAEMIA ( 11 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 11 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 11 FDA reports)
IMMUNE SYSTEM DISORDER ( 11 FDA reports)
INJECTION SITE REACTION ( 11 FDA reports)
KLEBSIELLA TEST POSITIVE ( 11 FDA reports)
LARYNGEAL OEDEMA ( 11 FDA reports)
LICHENOID KERATOSIS ( 11 FDA reports)
LOGORRHOEA ( 11 FDA reports)
LYMPHANGITIS ( 11 FDA reports)
MALIGNANT MELANOMA ( 11 FDA reports)
MICROALBUMINURIA ( 11 FDA reports)
MITRAL VALVE REPAIR ( 11 FDA reports)
MUSCLE NECROSIS ( 11 FDA reports)
NAIL DYSTROPHY ( 11 FDA reports)
NARCOLEPSY ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 11 FDA reports)
OBSTRUCTION GASTRIC ( 11 FDA reports)
OPEN FRACTURE ( 11 FDA reports)
ORAL TORUS ( 11 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 11 FDA reports)
OVARIAN ADHESION ( 11 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 11 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 11 FDA reports)
PAPILLOMA VIRAL INFECTION ( 11 FDA reports)
PATHOLOGICAL GAMBLING ( 11 FDA reports)
PELVIC ADHESIONS ( 11 FDA reports)
PERITONEAL HAEMORRHAGE ( 11 FDA reports)
PHARYNGEAL ERYTHEMA ( 11 FDA reports)
PLASMACYTOMA ( 11 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 11 FDA reports)
POSTURING ( 11 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 11 FDA reports)
PROTEUS INFECTION ( 11 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 11 FDA reports)
PULMONARY INFARCTION ( 11 FDA reports)
PULPITIS DENTAL ( 11 FDA reports)
RESPIRATORY ALKALOSIS ( 11 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 11 FDA reports)
RETINAL TEAR ( 11 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 11 FDA reports)
SALIVARY GLAND CANCER ( 11 FDA reports)
SALPINGITIS ( 11 FDA reports)
SEASONAL ALLERGY ( 11 FDA reports)
SENILE DEMENTIA ( 11 FDA reports)
SINOATRIAL BLOCK ( 11 FDA reports)
SINOBRONCHITIS ( 11 FDA reports)
SPINAL FUSION SURGERY ( 11 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 11 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 11 FDA reports)
THALAMIC INFARCTION ( 11 FDA reports)
TOXIC NODULAR GOITRE ( 11 FDA reports)
TRISMUS ( 11 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 11 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 11 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 11 FDA reports)
URINE FLOW DECREASED ( 11 FDA reports)
VASOSPASM ( 11 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
WOUND COMPLICATION ( 11 FDA reports)
X-RAY ( 11 FDA reports)
RAYNAUD'S PHENOMENON ( 10 FDA reports)
RENAL ABSCESS ( 10 FDA reports)
RESPIRATORY RATE DECREASED ( 10 FDA reports)
RETINAL ARTERY OCCLUSION ( 10 FDA reports)
RETINOPATHY OF PREMATURITY ( 10 FDA reports)
RHYTHM IDIOVENTRICULAR ( 10 FDA reports)
RIB DEFORMITY ( 10 FDA reports)
SCROTAL INFECTION ( 10 FDA reports)
SCROTAL SWELLING ( 10 FDA reports)
SEBORRHOEIC DERMATITIS ( 10 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 10 FDA reports)
SOFT TISSUE INJURY ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
SUFFOCATION FEELING ( 10 FDA reports)
TALIPES ( 10 FDA reports)
TENDON INJURY ( 10 FDA reports)
TENSION HEADACHE ( 10 FDA reports)
TESTICULAR ATROPHY ( 10 FDA reports)
THROMBECTOMY ( 10 FDA reports)
TINEA VERSICOLOUR ( 10 FDA reports)
TRACHEITIS ( 10 FDA reports)
TUMOUR INVASION ( 10 FDA reports)
TUMOUR LYSIS SYNDROME ( 10 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 10 FDA reports)
ACINETOBACTER INFECTION ( 10 FDA reports)
ACUTE ABDOMEN ( 10 FDA reports)
ANAESTHETIC COMPLICATION ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
AORTIC ATHEROSCLEROSIS ( 10 FDA reports)
APPLICATION SITE ERYTHEMA ( 10 FDA reports)
ATRIAL PRESSURE INCREASED ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 10 FDA reports)
BACTERIA URINE IDENTIFIED ( 10 FDA reports)
BLADDER PROLAPSE ( 10 FDA reports)
BONE FRAGMENTATION ( 10 FDA reports)
BREAST DISORDER ( 10 FDA reports)
BREATH ODOUR ( 10 FDA reports)
CARDIAC SEPTAL DEFECT ( 10 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 10 FDA reports)
CIRRHOSIS ALCOHOLIC ( 10 FDA reports)
CLUMSINESS ( 10 FDA reports)
COAGULATION FACTOR DECREASED ( 10 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 10 FDA reports)
DENTAL CARE ( 10 FDA reports)
DENTAL PLAQUE ( 10 FDA reports)
DIAGNOSTIC PROCEDURE ( 10 FDA reports)
DRUG EFFECT INCREASED ( 10 FDA reports)
DUODENAL POLYP ( 10 FDA reports)
EARLY SATIETY ( 10 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 10 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 10 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 10 FDA reports)
EPIDIDYMAL CYST ( 10 FDA reports)
ERYSIPELAS ( 10 FDA reports)
EXTREMITY CONTRACTURE ( 10 FDA reports)
EYE ROLLING ( 10 FDA reports)
FEELING DRUNK ( 10 FDA reports)
FUNGAEMIA ( 10 FDA reports)
FUSOBACTERIUM INFECTION ( 10 FDA reports)
GASTRODUODENITIS ( 10 FDA reports)
GRANULOCYTOPENIA ( 10 FDA reports)
HAEMATOMA INFECTION ( 10 FDA reports)
HAEMORRHAGIC DISORDER ( 10 FDA reports)
HEART VALVE STENOSIS ( 10 FDA reports)
HELLP SYNDROME ( 10 FDA reports)
HYPERMETABOLISM ( 10 FDA reports)
HYPERTENSIVE EMERGENCY ( 10 FDA reports)
INCISION SITE HAEMORRHAGE ( 10 FDA reports)
INTERVERTEBRAL DISCITIS ( 10 FDA reports)
INTESTINAL INFARCTION ( 10 FDA reports)
LAZINESS ( 10 FDA reports)
LIMB CRUSHING INJURY ( 10 FDA reports)
LUNG TRANSPLANT ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 10 FDA reports)
MENISCAL DEGENERATION ( 10 FDA reports)
MESENTERIC OCCLUSION ( 10 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 10 FDA reports)
NASAL DISCOMFORT ( 10 FDA reports)
NEUROMA ( 10 FDA reports)
NEUTROPHILIA ( 10 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 10 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 10 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 10 FDA reports)
ONYCHOLYSIS ( 10 FDA reports)
OPTIC NERVE DISORDER ( 10 FDA reports)
OVARIAN CANCER ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PANCREATITIS NECROTISING ( 10 FDA reports)
PAPILLOEDEMA ( 10 FDA reports)
PEAU D'ORANGE ( 10 FDA reports)
PLATELET DISORDER ( 10 FDA reports)
PROTEIN URINE ( 10 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 10 FDA reports)
PSYCHOMOTOR RETARDATION ( 10 FDA reports)
PUPILLARY DISORDER ( 10 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 9 FDA reports)
ACUTE LUNG INJURY ( 9 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 9 FDA reports)
ALVEOLITIS ALLERGIC ( 9 FDA reports)
ANKYLOSING SPONDYLITIS ( 9 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
AORTIC VALVE DISEASE MIXED ( 9 FDA reports)
APALLIC SYNDROME ( 9 FDA reports)
ASTIGMATISM ( 9 FDA reports)
AXILLARY MASS ( 9 FDA reports)
BALANITIS CANDIDA ( 9 FDA reports)
BASAL GANGLION DEGENERATION ( 9 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 9 FDA reports)
BEZOAR ( 9 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 9 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 9 FDA reports)
BONE NEOPLASM ( 9 FDA reports)
BREAST CANCER RECURRENT ( 9 FDA reports)
CARDIAC VALVE VEGETATION ( 9 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
CATHETER SEPSIS ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
COLONOSCOPY ABNORMAL ( 9 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 9 FDA reports)
DEVELOPMENTAL DELAY ( 9 FDA reports)
DIABETIC COMA ( 9 FDA reports)
DIET REFUSAL ( 9 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 9 FDA reports)
DRUG TOLERANCE ( 9 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 9 FDA reports)
DYSPLASIA ( 9 FDA reports)
EAR INFECTION ( 9 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 9 FDA reports)
ENDOSCOPY ( 9 FDA reports)
EPIDERMOLYSIS ( 9 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 9 FDA reports)
FOETAL HEART RATE ABNORMAL ( 9 FDA reports)
FULL BLOOD COUNT DECREASED ( 9 FDA reports)
GALLBLADDER ENLARGEMENT ( 9 FDA reports)
GASTRITIS ATROPHIC ( 9 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 9 FDA reports)
GRIEF REACTION ( 9 FDA reports)
GRIP STRENGTH DECREASED ( 9 FDA reports)
HEMIANOPIA ( 9 FDA reports)
HEMIANOPIA HOMONYMOUS ( 9 FDA reports)
HEPATORENAL FAILURE ( 9 FDA reports)
HYPERAEMIA ( 9 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 9 FDA reports)
INDURATION ( 9 FDA reports)
INJECTION SITE DISCOLOURATION ( 9 FDA reports)
LUNG INJURY ( 9 FDA reports)
MAGNESIUM DEFICIENCY ( 9 FDA reports)
MALABSORPTION ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MALLORY-WEISS SYNDROME ( 9 FDA reports)
MARROW HYPERPLASIA ( 9 FDA reports)
METAMORPHOPSIA ( 9 FDA reports)
ONYCHOMADESIS ( 9 FDA reports)
OOPHORECTOMY ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
PARACENTESIS ( 9 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 9 FDA reports)
PARANEOPLASTIC SYNDROME ( 9 FDA reports)
PARATHYROID TUMOUR BENIGN ( 9 FDA reports)
PARONYCHIA ( 9 FDA reports)
PAROTITIS ( 9 FDA reports)
PATELLA FRACTURE ( 9 FDA reports)
PELVIC MASS ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PERIPHERAL PULSE DECREASED ( 9 FDA reports)
PERITONEAL EFFUSION ( 9 FDA reports)
POLYARTHRITIS ( 9 FDA reports)
PORTAL VEIN THROMBOSIS ( 9 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 9 FDA reports)
PROSTATIC DISORDER ( 9 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 9 FDA reports)
PUPILS UNEQUAL ( 9 FDA reports)
RECTAL ULCER ( 9 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SPIDER VEIN ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 9 FDA reports)
SYSTOLIC DYSFUNCTION ( 9 FDA reports)
TETANY ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
TONGUE DRY ( 9 FDA reports)
TRICHOMONIASIS ( 9 FDA reports)
TROPONIN T INCREASED ( 9 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 9 FDA reports)
URINE OUTPUT INCREASED ( 9 FDA reports)
UTERINE POLYP ( 9 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 9 FDA reports)
VENOUS STENOSIS ( 9 FDA reports)
WEIGHT ABNORMAL ( 9 FDA reports)
WEIGHT BEARING DIFFICULTY ( 9 FDA reports)
WOUND NECROSIS ( 9 FDA reports)
RADIATION PNEUMONITIS ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 8 FDA reports)
ROTATOR CUFF REPAIR ( 8 FDA reports)
SCHAMBERG'S DISEASE ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SOFT TISSUE NECROSIS ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 8 FDA reports)
SUBDURAL HYGROMA ( 8 FDA reports)
TENOSYNOVITIS STENOSANS ( 8 FDA reports)
TESTICULAR DISORDER ( 8 FDA reports)
THORACIC CAVITY DRAINAGE ( 8 FDA reports)
TOOTH EROSION ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 8 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 8 FDA reports)
URINE CYTOLOGY ABNORMAL ( 8 FDA reports)
VAGINAL DISCHARGE ( 8 FDA reports)
VASCULAR INSUFFICIENCY ( 8 FDA reports)
VASCULAR OCCLUSION ( 8 FDA reports)
VASCULAR RUPTURE ( 8 FDA reports)
VENTRICULAR DYSKINESIA ( 8 FDA reports)
ABDOMINAL INFECTION ( 8 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 8 FDA reports)
AMPUTATION ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
ANTIBODY TEST POSITIVE ( 8 FDA reports)
APGAR SCORE LOW ( 8 FDA reports)
APHTHOUS STOMATITIS ( 8 FDA reports)
APPLICATION SITE RASH ( 8 FDA reports)
ARM AMPUTATION ( 8 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 8 FDA reports)
ATROPHIC VULVOVAGINITIS ( 8 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 8 FDA reports)
BALANOPOSTHITIS ( 8 FDA reports)
BLOOD BICARBONATE INCREASED ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 8 FDA reports)
BLOODY DISCHARGE ( 8 FDA reports)
BONE CANCER METASTATIC ( 8 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 8 FDA reports)
BRADYCARDIA FOETAL ( 8 FDA reports)
BRADYKINESIA ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
BRAIN ABSCESS ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BRAIN MIDLINE SHIFT ( 8 FDA reports)
BRUXISM ( 8 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 8 FDA reports)
CANCER PAIN ( 8 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 8 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 8 FDA reports)
CARDIAC ABLATION ( 8 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 8 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
CHRONIC HEPATIC FAILURE ( 8 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 8 FDA reports)
COLON NEOPLASM ( 8 FDA reports)
COMA SCALE ABNORMAL ( 8 FDA reports)
COOMBS TEST POSITIVE ( 8 FDA reports)
COR PULMONALE CHRONIC ( 8 FDA reports)
CORNEAL REFLEX DECREASED ( 8 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 8 FDA reports)
DENTAL PULP DISORDER ( 8 FDA reports)
DERMATITIS ACNEIFORM ( 8 FDA reports)
DIZZINESS EXERTIONAL ( 8 FDA reports)
DRUG ABUSER ( 8 FDA reports)
DRUG RESISTANCE ( 8 FDA reports)
DRUG THERAPY ( 8 FDA reports)
EX-TOBACCO USER ( 8 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 8 FDA reports)
FACIAL WASTING ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
FOETAL DEATH ( 8 FDA reports)
FRACTURED COCCYX ( 8 FDA reports)
FUNGAL SKIN INFECTION ( 8 FDA reports)
GASTRIC ULCER PERFORATION ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 8 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 8 FDA reports)
GIARDIASIS ( 8 FDA reports)
GLOBULINS INCREASED ( 8 FDA reports)
GLUCOSE URINE PRESENT ( 8 FDA reports)
GOUTY TOPHUS ( 8 FDA reports)
GRAFT INFECTION ( 8 FDA reports)
HAEMOGLOBIN ABNORMAL ( 8 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 8 FDA reports)
HAND DEFORMITY ( 8 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 8 FDA reports)
HYPERTHERMIA MALIGNANT ( 8 FDA reports)
HYPOPARATHYROIDISM ( 8 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 8 FDA reports)
INCREASED BRONCHIAL SECRETION ( 8 FDA reports)
INFECTED SKIN ULCER ( 8 FDA reports)
INFERIOR VENA CAVA DILATATION ( 8 FDA reports)
INJECTION SITE BURNING ( 8 FDA reports)
INSULIN RESISTANCE ( 8 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 8 FDA reports)
INTERTRIGO ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
JAW LESION EXCISION ( 8 FDA reports)
JUGULAR VEIN THROMBOSIS ( 8 FDA reports)
LEUKOCYTURIA ( 8 FDA reports)
LIPID METABOLISM DISORDER ( 8 FDA reports)
LIPIDS INCREASED ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
LYMPHOPENIA ( 8 FDA reports)
MARITAL PROBLEM ( 8 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 8 FDA reports)
MENOPAUSE ( 8 FDA reports)
METASTASES TO PLEURA ( 8 FDA reports)
MIXED HYPERLIPIDAEMIA ( 8 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 8 FDA reports)
MYASTHENIA GRAVIS ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 8 FDA reports)
NECK INJURY ( 8 FDA reports)
NIKOLSKY'S SIGN ( 8 FDA reports)
OEDEMA GENITAL ( 8 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 8 FDA reports)
OPTIC NEUROPATHY ( 8 FDA reports)
OROPHARYNGEAL SWELLING ( 8 FDA reports)
PANCREATITIS CHRONIC ( 8 FDA reports)
PANIC REACTION ( 8 FDA reports)
PARAPLEGIA ( 8 FDA reports)
PAROSMIA ( 8 FDA reports)
PELVIC HAEMATOMA ( 8 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 8 FDA reports)
PERSONALITY DISORDER ( 8 FDA reports)
PICKWICKIAN SYNDROME ( 8 FDA reports)
PLATELET COUNT ABNORMAL ( 8 FDA reports)
PNEUMOCONIOSIS ( 8 FDA reports)
POPLITEAL PULSE DECREASED ( 8 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 8 FDA reports)
POTENTIATING DRUG INTERACTION ( 8 FDA reports)
PROSTATISM ( 8 FDA reports)
PRURIGO ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
PULMONARY TUBERCULOSIS ( 8 FDA reports)
ABDOMEN CRUSHING ( 7 FDA reports)
ACCIDENT AT WORK ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 7 FDA reports)
ADJUSTMENT DISORDER ( 7 FDA reports)
AKATHISIA ( 7 FDA reports)
ALLERGY TO CHEMICALS ( 7 FDA reports)
ANAL SPHINCTER ATONY ( 7 FDA reports)
ANGIOMYOLIPOMA ( 7 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 7 FDA reports)
APICAL GRANULOMA ( 7 FDA reports)
APPLICATION SITE IRRITATION ( 7 FDA reports)
ARTERIAL BYPASS OPERATION ( 7 FDA reports)
ARTERITIS ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
AV DISSOCIATION ( 7 FDA reports)
BILE DUCT CANCER ( 7 FDA reports)
BLADDER OBSTRUCTION ( 7 FDA reports)
BLAST CELL COUNT INCREASED ( 7 FDA reports)
BLOOD CREATININE ABNORMAL ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 7 FDA reports)
BLOOD IRON INCREASED ( 7 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 7 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 7 FDA reports)
BONE FORMATION INCREASED ( 7 FDA reports)
BREAST CELLULITIS ( 7 FDA reports)
BREAST CYST ( 7 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 7 FDA reports)
BRONCHIAL OBSTRUCTION ( 7 FDA reports)
BRONCHIOLITIS ( 7 FDA reports)
BRONCHITIS BACTERIAL ( 7 FDA reports)
BRONCHITIS VIRAL ( 7 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 7 FDA reports)
BULLOUS LUNG DISEASE ( 7 FDA reports)
BURNS THIRD DEGREE ( 7 FDA reports)
CALCULUS BLADDER ( 7 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 7 FDA reports)
CHEST WALL PAIN ( 7 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 7 FDA reports)
COLONOSCOPY ( 7 FDA reports)
COMA HEPATIC ( 7 FDA reports)
COMPLEX PARTIAL SEIZURES ( 7 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 7 FDA reports)
CONJUNCTIVAL ABRASION ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
CORONARY ARTERY ANEURYSM ( 7 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 7 FDA reports)
CORONARY ARTERY EMBOLISM ( 7 FDA reports)
CRANIOTOMY ( 7 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
CYST REMOVAL ( 7 FDA reports)
DEFAECATION URGENCY ( 7 FDA reports)
DIABETIC EYE DISEASE ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 7 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 7 FDA reports)
ESCHERICHIA BACTERAEMIA ( 7 FDA reports)
EXSANGUINATION ( 7 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 7 FDA reports)
EXTRADURAL ABSCESS ( 7 FDA reports)
FAECES PALE ( 7 FDA reports)
FISTULA DISCHARGE ( 7 FDA reports)
FOAMING AT MOUTH ( 7 FDA reports)
FOOD POISONING ( 7 FDA reports)
FRACTURE DISPLACEMENT ( 7 FDA reports)
GASTRIC DILATATION ( 7 FDA reports)
GASTROINTESTINAL EROSION ( 7 FDA reports)
HEART TRANSPLANT REJECTION ( 7 FDA reports)
HEPATIC CANCER METASTATIC ( 7 FDA reports)
HODGKIN'S DISEASE ( 7 FDA reports)
HOMOCYSTINAEMIA ( 7 FDA reports)
HYPEROSMOLAR STATE ( 7 FDA reports)
IMPAIRED FASTING GLUCOSE ( 7 FDA reports)
IMPLANT SITE INFECTION ( 7 FDA reports)
INCISION SITE HAEMATOMA ( 7 FDA reports)
INFECTED SEBACEOUS CYST ( 7 FDA reports)
INJECTION SITE BRUISING ( 7 FDA reports)
INJECTION SITE MASS ( 7 FDA reports)
INTENTION TREMOR ( 7 FDA reports)
INTESTINAL MASS ( 7 FDA reports)
LEGAL PROBLEM ( 7 FDA reports)
LIP PAIN ( 7 FDA reports)
LOCALISED OSTEOARTHRITIS ( 7 FDA reports)
LUPUS-LIKE SYNDROME ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 7 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 7 FDA reports)
MEDIASTINAL DISORDER ( 7 FDA reports)
MELANOCYTIC NAEVUS ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 7 FDA reports)
MUCOSAL DISCOLOURATION ( 7 FDA reports)
MUCOSAL ULCERATION ( 7 FDA reports)
MUSCLE RUPTURE ( 7 FDA reports)
MUSCLE SPASTICITY ( 7 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 7 FDA reports)
MYOGLOBINURIA ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEOPLASM PROSTATE ( 7 FDA reports)
NEPHRECTOMY ( 7 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
OEDEMA MUCOSAL ( 7 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 7 FDA reports)
OPEN ANGLE GLAUCOMA ( 7 FDA reports)
OPPORTUNISTIC INFECTION ( 7 FDA reports)
OPTIC NEURITIS ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
OSTEOMYELITIS CHRONIC ( 7 FDA reports)
OXYGEN SATURATION ABNORMAL ( 7 FDA reports)
PANNICULITIS ( 7 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 7 FDA reports)
PHONOPHOBIA ( 7 FDA reports)
PIGMENTED NAEVUS ( 7 FDA reports)
PLEURAL DISORDER ( 7 FDA reports)
PRODUCT SIZE ISSUE ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 7 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 7 FDA reports)
PULMONARY HYPOPLASIA ( 7 FDA reports)
PULMONARY MALFORMATION ( 7 FDA reports)
PULMONARY VALVE CALCIFICATION ( 7 FDA reports)
QUADRIPLEGIA ( 7 FDA reports)
RADICULITIS ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
RECURRENT CANCER ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RENAL HAEMORRHAGE ( 7 FDA reports)
RENAL TUBULAR DISORDER ( 7 FDA reports)
RETINAL VEIN OCCLUSION ( 7 FDA reports)
RETINOPATHY HYPERTENSIVE ( 7 FDA reports)
RETROGRADE AMNESIA ( 7 FDA reports)
SALIVA ALTERED ( 7 FDA reports)
SIMPLE PARTIAL SEIZURES ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKULL FRACTURE ( 7 FDA reports)
SLEEP WALKING ( 7 FDA reports)
SPINAL LAMINECTOMY ( 7 FDA reports)
SPUTUM ABNORMAL ( 7 FDA reports)
STENT OCCLUSION ( 7 FDA reports)
STRESS INCONTINENCE ( 7 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 7 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 7 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 7 FDA reports)
SUPRAPUBIC PAIN ( 7 FDA reports)
SWEAT DISCOLOURATION ( 7 FDA reports)
THROMBOCYTHAEMIA ( 7 FDA reports)
THYROIDECTOMY ( 7 FDA reports)
THYROXINE FREE INCREASED ( 7 FDA reports)
TONSILLAR DISORDER ( 7 FDA reports)
TONSILLECTOMY ( 7 FDA reports)
TRACHEAL INJURY ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 7 FDA reports)
TUNNEL VISION ( 7 FDA reports)
UNDERWEIGHT ( 7 FDA reports)
URINE LEUKOCYTE ESTERASE ( 7 FDA reports)
URINE SODIUM DECREASED ( 7 FDA reports)
VASCULAR BYPASS GRAFT ( 7 FDA reports)
VEIN DISORDER ( 7 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 7 FDA reports)
WEANING FAILURE ( 7 FDA reports)
READING DISORDER ( 6 FDA reports)
RECTOCELE ( 6 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
RENAL LIPOMATOSIS ( 6 FDA reports)
RENAL NEOPLASM ( 6 FDA reports)
RENAL TRANSPLANT ( 6 FDA reports)
RENAL VESSEL DISORDER ( 6 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 6 FDA reports)
RETINAL SCAR ( 6 FDA reports)
RETINITIS ( 6 FDA reports)
RHEUMATOID FACTOR INCREASED ( 6 FDA reports)
SACROILIITIS ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SARCOMA ( 6 FDA reports)
SCLERODACTYLIA ( 6 FDA reports)
SCROTAL PAIN ( 6 FDA reports)
SEPTIC EMBOLUS ( 6 FDA reports)
SINUS RHYTHM ( 6 FDA reports)
SKIN CANCER METASTATIC ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN NODULE ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SKIN SWELLING ( 6 FDA reports)
SMALL INTESTINE CARCINOMA ( 6 FDA reports)
SOPOR ( 6 FDA reports)
SPINAL COLUMN INJURY ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
SPLENIC ARTERY ANEURYSM ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
SPUTUM INCREASED ( 6 FDA reports)
STENOTROPHOMONAS INFECTION ( 6 FDA reports)
TACHYCARDIA FOETAL ( 6 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 6 FDA reports)
TENDON PAIN ( 6 FDA reports)
TENSION ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
THROAT CANCER ( 6 FDA reports)
TONSILLAR HYPERTROPHY ( 6 FDA reports)
TRACHEAL STENOSIS ( 6 FDA reports)
TRANSFUSION REACTION ( 6 FDA reports)
TRANSPLANT ( 6 FDA reports)
TRICUSPID VALVE REPAIR ( 6 FDA reports)
TRISOMY 21 ( 6 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
URAEMIC ENCEPHALOPATHY ( 6 FDA reports)
URETHRAL MEATUS STENOSIS ( 6 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
UTERINE FIBROSIS ( 6 FDA reports)
VASOCONSTRICTION ( 6 FDA reports)
VIRAL CARDIOMYOPATHY ( 6 FDA reports)
VITAL CAPACITY DECREASED ( 6 FDA reports)
VOCAL CORD PARESIS ( 6 FDA reports)
VULVOVAGINAL PRURITUS ( 6 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 6 FDA reports)
WOUND DEBRIDEMENT ( 6 FDA reports)
ABDOMINAL HAEMATOMA ( 6 FDA reports)
ABDOMINAL SEPSIS ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
ADRENAL DISORDER ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
ALBUMIN URINE PRESENT ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANEURYSM RUPTURED ( 6 FDA reports)
ANGIOGRAM ABNORMAL ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
APPLICATION SITE VESICLES ( 6 FDA reports)
APRAXIA ( 6 FDA reports)
ARCUS LIPOIDES ( 6 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 6 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
BACTERIURIA ( 6 FDA reports)
BASILAR ARTERY OCCLUSION ( 6 FDA reports)
BENIGN COLONIC NEOPLASM ( 6 FDA reports)
BILE DUCT OBSTRUCTION ( 6 FDA reports)
BILIARY DYSKINESIA ( 6 FDA reports)
BILIARY TRACT DISORDER ( 6 FDA reports)
BITE ( 6 FDA reports)
BLADDER DISCOMFORT ( 6 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
BLEPHAROSPASM ( 6 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 6 FDA reports)
BLOOD PRESSURE ( 6 FDA reports)
BLOOD SODIUM ( 6 FDA reports)
BONE OPERATION ( 6 FDA reports)
BOVINE TUBERCULOSIS ( 6 FDA reports)
CARDIAC AMYLOIDOSIS ( 6 FDA reports)
CARDIAC INFECTION ( 6 FDA reports)
CAT SCRATCH DISEASE ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CATHETER SITE DISCHARGE ( 6 FDA reports)
CELL MARKER INCREASED ( 6 FDA reports)
CEREBELLAR HAEMATOMA ( 6 FDA reports)
CEREBELLAR HAEMORRHAGE ( 6 FDA reports)
CEREBELLAR ISCHAEMIA ( 6 FDA reports)
CERVICAL CYST ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHRONIC FATIGUE SYNDROME ( 6 FDA reports)
COCCYDYNIA ( 6 FDA reports)
COELIAC ARTERY OCCLUSION ( 6 FDA reports)
COLON CANCER RECURRENT ( 6 FDA reports)
COLONIC HAEMORRHAGE ( 6 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 6 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 6 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
CUTANEOUS SARCOIDOSIS ( 6 FDA reports)
CYSTITIS ESCHERICHIA ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DEATH NEONATAL ( 6 FDA reports)
DELAYED SLEEP PHASE ( 6 FDA reports)
DEMYELINATION ( 6 FDA reports)
DEPENDENT RUBOR ( 6 FDA reports)
DEPERSONALISATION ( 6 FDA reports)
DEVICE BREAKAGE ( 6 FDA reports)
DEVICE LEAKAGE ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 6 FDA reports)
DYSPHEMIA ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 6 FDA reports)
ENTERITIS ( 6 FDA reports)
ENTEROBACTER PNEUMONIA ( 6 FDA reports)
ENTEROVESICAL FISTULA ( 6 FDA reports)
EXANTHEM ( 6 FDA reports)
EXTRASKELETAL OSSIFICATION ( 6 FDA reports)
EYE INFECTION FUNGAL ( 6 FDA reports)
EYE OEDEMA ( 6 FDA reports)
FACTOR VIII DEFICIENCY ( 6 FDA reports)
FAECAL VOLUME INCREASED ( 6 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 6 FDA reports)
FOETAL GROWTH RESTRICTION ( 6 FDA reports)
FOOD ALLERGY ( 6 FDA reports)
FOOT OPERATION ( 6 FDA reports)
GAMMOPATHY ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 6 FDA reports)
GINGIVAL HYPERPLASIA ( 6 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 6 FDA reports)
GRAFT DYSFUNCTION ( 6 FDA reports)
GRAFT THROMBOSIS ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
GUN SHOT WOUND ( 6 FDA reports)
HAIR COLOUR CHANGES ( 6 FDA reports)
HAIR TEXTURE ABNORMAL ( 6 FDA reports)
HAPTOGLOBIN DECREASED ( 6 FDA reports)
HEART BLOCK CONGENITAL ( 6 FDA reports)
HERNIA OBSTRUCTIVE ( 6 FDA reports)
HYPERREFLEXIA ( 6 FDA reports)
HYPOLIPIDAEMIA ( 6 FDA reports)
HYPOVITAMINOSIS ( 6 FDA reports)
ILEAL STENOSIS ( 6 FDA reports)
ILIAC ARTERY OCCLUSION ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
IMPLANT SITE DISCHARGE ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INTRACRANIAL HAEMATOMA ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
LARGE INTESTINE CARCINOMA ( 6 FDA reports)
LENTIGO ( 6 FDA reports)
LICHEN PLANUS ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LIP DRY ( 6 FDA reports)
LITHOTRIPSY ( 6 FDA reports)
LOSS OF PROPRIOCEPTION ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUNG CREPITATION ( 6 FDA reports)
MACROCEPHALY ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MANTLE CELL LYMPHOMA ( 6 FDA reports)
MARASMUS ( 6 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 6 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 6 FDA reports)
METASTASES TO PERITONEUM ( 6 FDA reports)
METASTATIC LYMPHOMA ( 6 FDA reports)
MUCOUS MEMBRANE DISORDER ( 6 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MYXOEDEMA ( 6 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 6 FDA reports)
NERVE ROOT COMPRESSION ( 6 FDA reports)
NICOTINE DEPENDENCE ( 6 FDA reports)
NOONAN SYNDROME ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 6 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 6 FDA reports)
OESOPHAGEAL MASS ( 6 FDA reports)
OPTIC ATROPHY ( 6 FDA reports)
ORAL FUNGAL INFECTION ( 6 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 6 FDA reports)
PAINFUL RESPIRATION ( 6 FDA reports)
PANCREATIC MASS ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PEMPHIGUS ( 6 FDA reports)
PENILE OEDEMA ( 6 FDA reports)
PERFORATED ULCER ( 6 FDA reports)
PERICARDITIS CONSTRICTIVE ( 6 FDA reports)
PERITONEAL ADHESIONS ( 6 FDA reports)
PLASMA VISCOSITY DECREASED ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POST-TRAUMATIC PAIN ( 6 FDA reports)
POSTOPERATIVE FEVER ( 6 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 6 FDA reports)
PRODUCT FORMULATION ISSUE ( 6 FDA reports)
PRODUCT TASTE ABNORMAL ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 6 FDA reports)
PUBIS FRACTURE ( 6 FDA reports)
PYELOCALIECTASIS ( 6 FDA reports)
QUADRIPARESIS ( 6 FDA reports)
ABDOMINAL WALL DISORDER ( 5 FDA reports)
ACHLORHYDRIA ( 5 FDA reports)
ADRENOMEGALY ( 5 FDA reports)
AGNOSIA ( 5 FDA reports)
AGONAL RHYTHM ( 5 FDA reports)
ALCOHOL POISONING ( 5 FDA reports)
ALDOLASE INCREASED ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANDROGEN DEFICIENCY ( 5 FDA reports)
ANTICOAGULANT THERAPY ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC VALVE REPAIR ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
APPLICATION SITE HAEMATOMA ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
BACTERIA URINE ( 5 FDA reports)
BENIGN COLONIC POLYP ( 5 FDA reports)
BENIGN NEOPLASM ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BIOPSY LIVER ABNORMAL ( 5 FDA reports)
BLADDER CATHETERISATION ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 5 FDA reports)
BODY MASS INDEX DECREASED ( 5 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 5 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREATH SOUNDS DECREASED ( 5 FDA reports)
BRONCHOSCOPY ABNORMAL ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIAC CIRRHOSIS ( 5 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 5 FDA reports)
CARDIOPULMONARY BYPASS ( 5 FDA reports)
CAROTID ARTERY ATHEROMA ( 5 FDA reports)
CAROTID ARTERY STENT INSERTION ( 5 FDA reports)
CAROTID ENDARTERECTOMY ( 5 FDA reports)
CATHETER REMOVAL ( 5 FDA reports)
CATHETER SITE ERYTHEMA ( 5 FDA reports)
CATHETER SITE PAIN ( 5 FDA reports)
CATHETER SITE SWELLING ( 5 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
CERVIX DISORDER ( 5 FDA reports)
CHAPPED LIPS ( 5 FDA reports)
CHEMOTHERAPY ( 5 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 5 FDA reports)
CHYLOTHORAX ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
CLEFT PALATE ( 5 FDA reports)
CLONUS ( 5 FDA reports)
COAGULATION TIME ABNORMAL ( 5 FDA reports)
COLECTOMY ( 5 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
CORNEAL DISORDER ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
CORRECTIVE LENS USER ( 5 FDA reports)
CSF TEST ABNORMAL ( 5 FDA reports)
CUTIS LAXA ( 5 FDA reports)
DELUSION OF REPLACEMENT ( 5 FDA reports)
DEPRESSIVE SYMPTOM ( 5 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
DIVORCED ( 5 FDA reports)
DRUG INTERACTION INHIBITION ( 5 FDA reports)
DRUG LEVEL CHANGED ( 5 FDA reports)
DUODENAL PERFORATION ( 5 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 5 FDA reports)
EMBOLISM ARTERIAL ( 5 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 5 FDA reports)
ENTHESOPATHY ( 5 FDA reports)
ESCHAR ( 5 FDA reports)
EUPHORIC MOOD ( 5 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 5 FDA reports)
EXTRAVASATION ( 5 FDA reports)
EYE OPERATION ( 5 FDA reports)
FAT NECROSIS ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FOETAL DISORDER ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
GALLBLADDER OEDEMA ( 5 FDA reports)
GASTRIC INFECTION ( 5 FDA reports)
GASTRIC MUCOSAL LESION ( 5 FDA reports)
GASTRITIS HAEMORRHAGIC ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GASTROINTESTINAL OEDEMA ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GENITAL BURNING SENSATION ( 5 FDA reports)
GINGIVAL BLISTER ( 5 FDA reports)
GLIOBLASTOMA ( 5 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 5 FDA reports)
GLOMERULOSCLEROSIS ( 5 FDA reports)
GRAFT COMPLICATION ( 5 FDA reports)
GRUNTING ( 5 FDA reports)
HAEMATOMA EVACUATION ( 5 FDA reports)
HAEMATOTOXICITY ( 5 FDA reports)
HAEMOPHILUS INFECTION ( 5 FDA reports)
HAEMORRHAGIC INFARCTION ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEART VALVE CALCIFICATION ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HIP SURGERY ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOGONADISM MALE ( 5 FDA reports)
HYPOTRICHOSIS ( 5 FDA reports)
IDIOPATHIC URTICARIA ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
ILIAC ARTERY THROMBOSIS ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INCISION SITE ERYTHEMA ( 5 FDA reports)
INCISION SITE PAIN ( 5 FDA reports)
INCORRECT STORAGE OF DRUG ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INJECTION SITE SCAR ( 5 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 5 FDA reports)
INTESTINAL HAEMORRHAGE ( 5 FDA reports)
INVESTIGATION ABNORMAL ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
JOINT WARMTH ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
KLEBSIELLA BACTERAEMIA ( 5 FDA reports)
LARYNGEAL STENOSIS ( 5 FDA reports)
LESION EXCISION ( 5 FDA reports)
LIGAMENT DISORDER ( 5 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
LYMPHADENECTOMY ( 5 FDA reports)
MARFAN'S SYNDROME ( 5 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 5 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 5 FDA reports)
MEDICAL DIET ( 5 FDA reports)
MEGAKARYOCYTES ( 5 FDA reports)
MESENTERIC ARTERY STENOSIS ( 5 FDA reports)
MESOTHELIOMA ( 5 FDA reports)
METASTATIC GASTRIC CANCER ( 5 FDA reports)
MITRAL VALVE DISEASE MIXED ( 5 FDA reports)
MONARTHRITIS ( 5 FDA reports)
MOUTH INJURY ( 5 FDA reports)
MYOCARDIAL CALCIFICATION ( 5 FDA reports)
MYOPIA ( 5 FDA reports)
MYXOEDEMA COMA ( 5 FDA reports)
NASAL OEDEMA ( 5 FDA reports)
NEAR DROWNING ( 5 FDA reports)
NEONATAL DISORDER ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
NOSOCOMIAL INFECTION ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OESOPHAGEAL CARCINOMA ( 5 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 5 FDA reports)
ORBITAL CYST ( 5 FDA reports)
PACEMAKER GENERATED RHYTHM ( 5 FDA reports)
PAIN EXACERBATED ( 5 FDA reports)
PANCREATIC ATROPHY ( 5 FDA reports)
PANCREATITIS RELAPSING ( 5 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 5 FDA reports)
PERIARTHRITIS ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PHOTODERMATOSIS ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POST PROCEDURAL PAIN ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 5 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 5 FDA reports)
PROCEDURAL NAUSEA ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PROPOFOL INFUSION SYNDROME ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC ADENOMA ( 5 FDA reports)
PROSTATIC OPERATION ( 5 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 5 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 5 FDA reports)
PSYCHOLOGICAL TRAUMA ( 5 FDA reports)
PSYCHOMOTOR AGITATION ( 5 FDA reports)
PSYCHOSOMATIC DISEASE ( 5 FDA reports)
PULMONARY CAVITATION ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
RADIATION NEUROPATHY ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
RECTAL PROLAPSE ( 5 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
RENOVASCULAR HYPERTENSION ( 5 FDA reports)
RETICULOCYTE COUNT INCREASED ( 5 FDA reports)
RETINAL ARTERY THROMBOSIS ( 5 FDA reports)
ROTAVIRUS INFECTION ( 5 FDA reports)
SALPINGECTOMY ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SIGMOIDOSCOPY ( 5 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 5 FDA reports)
SKIN DESQUAMATION ( 5 FDA reports)
SOMATOFORM DISORDER ( 5 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 5 FDA reports)
SPIROMETRY ABNORMAL ( 5 FDA reports)
SPLENIC HAEMORRHAGE ( 5 FDA reports)
SPLINTER HAEMORRHAGES ( 5 FDA reports)
STEROID THERAPY ( 5 FDA reports)
STOOL ANALYSIS ABNORMAL ( 5 FDA reports)
STRESS FRACTURE ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
SUBSTANCE ABUSE ( 5 FDA reports)
SUDDEN HEARING LOSS ( 5 FDA reports)
SUTURE INSERTION ( 5 FDA reports)
TESTICULAR APPENDAGE TORSION ( 5 FDA reports)
THYROID MASS ( 5 FDA reports)
THYROIDITIS ( 5 FDA reports)
THYROIDITIS CHRONIC ( 5 FDA reports)
TONGUE INJURY ( 5 FDA reports)
TONGUE PRURITUS ( 5 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 5 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 5 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 5 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 5 FDA reports)
URETERAL DISORDER ( 5 FDA reports)
UTERINE HAEMORRHAGE ( 5 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 5 FDA reports)
VEIN PAIN ( 5 FDA reports)
VESTIBULAR NEURONITIS ( 5 FDA reports)
VITAMIN B12 DECREASED ( 5 FDA reports)
WEGENER'S GRANULOMATOSIS ( 5 FDA reports)
WEIGHT GAIN POOR ( 5 FDA reports)
WOUND DECOMPOSITION ( 5 FDA reports)
X-RAY LIMB ABNORMAL ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RECTAL LESION ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RENAL HAEMATOMA ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETINAL ANEURYSM ( 4 FDA reports)
RETINAL DEGENERATION ( 4 FDA reports)
RIB EXCISION ( 4 FDA reports)
SELF-INJURIOUS IDEATION ( 4 FDA reports)
SERRATIA TEST POSITIVE ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
SHUNT THROMBOSIS ( 4 FDA reports)
SIGHT DISABILITY ( 4 FDA reports)
SKIN CANDIDA ( 4 FDA reports)
SKIN FRAGILITY ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SPINAL DECOMPRESSION ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUBRETINAL FIBROSIS ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 4 FDA reports)
TABLET ISSUE ( 4 FDA reports)
TACHYPHRENIA ( 4 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 4 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 4 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 4 FDA reports)
THERAPY CESSATION ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THROMBOTIC STROKE ( 4 FDA reports)
THYMOMA ( 4 FDA reports)
THYROTOXIC CRISIS ( 4 FDA reports)
TINEA CRURIS ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TOXICOLOGIC TEST NORMAL ( 4 FDA reports)
TRAUMATIC FRACTURE ( 4 FDA reports)
TRICUSPID VALVE STENOSIS ( 4 FDA reports)
ULNA FRACTURE ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
URETHRAL PAIN ( 4 FDA reports)
URETHRITIS ( 4 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
UTERINE PERFORATION ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VAGINAL INFECTION ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VARICOSE ULCERATION ( 4 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
VENOUS PRESSURE JUGULAR ( 4 FDA reports)
VENOUS THROMBOSIS LIMB ( 4 FDA reports)
VENTRICULAR FLUTTER ( 4 FDA reports)
VESTIBULAR DISORDER ( 4 FDA reports)
VIBRATION TEST ABNORMAL ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VITAMIN K INCREASED ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
VOLVULUS OF BOWEL ( 4 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 4 FDA reports)
VULVOVAGINAL ERYTHEMA ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 4 FDA reports)
XEROPHTHALMIA ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 4 FDA reports)
AIR EMBOLISM ( 4 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 4 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 4 FDA reports)
AMYLASE INCREASED ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAL PRURITUS ( 4 FDA reports)
ANGIOGRAM ( 4 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC OCCLUSION ( 4 FDA reports)
APPENDICEAL ABSCESS ( 4 FDA reports)
APPLICATION SITE DISCHARGE ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 4 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
AXONAL NEUROPATHY ( 4 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BASAL GANGLIA INFARCTION ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BILE DUCT STENOSIS ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLADDER DISTENSION ( 4 FDA reports)
BLADDER NECK OBSTRUCTION ( 4 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLOOD OESTROGEN INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 4 FDA reports)
BLOOD PROLACTIN INCREASED ( 4 FDA reports)
BLUE TOE SYNDROME ( 4 FDA reports)
BONE MARROW TOXICITY ( 4 FDA reports)
BRAIN CONTUSION ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BRAIN TUMOUR OPERATION ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST INDURATION ( 4 FDA reports)
BREAST NEOPLASM ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BRONCHIAL INFECTION ( 4 FDA reports)
BRONCHOPNEUMOPATHY ( 4 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 4 FDA reports)
BURSA DISORDER ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARDIAC ASTHMA ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC MONITORING ( 4 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 4 FDA reports)
CELLULITIS ORBITAL ( 4 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 4 FDA reports)
CHEST CRUSHING ( 4 FDA reports)
CHOLINERGIC SYNDROME ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
COAGULATION TIME SHORTENED ( 4 FDA reports)
COCCIDIOIDOMYCOSIS ( 4 FDA reports)
COELIAC DISEASE ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
COLON CANCER STAGE III ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 4 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CONGENITAL NEUROPATHY ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 4 FDA reports)
CONSTRICTED AFFECT ( 4 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 4 FDA reports)
CONVERSION DISORDER ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CRANIOCEREBRAL INJURY ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DERMOID CYST ( 4 FDA reports)
DEVICE STIMULATION ISSUE ( 4 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 4 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DUODENAL NEOPLASM ( 4 FDA reports)
DYSENTERY ( 4 FDA reports)
DYSPHASIA ( 4 FDA reports)
EAR PRURITUS ( 4 FDA reports)
ECTOPIC PREGNANCY ( 4 FDA reports)
EISENMENGER'S SYNDROME ( 4 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ENDOCARDIAL FIBROSIS ( 4 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHROMELALGIA ( 4 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXOPHTHALMOS ( 4 FDA reports)
EXPLORATIVE LAPAROTOMY ( 4 FDA reports)
EXTERNAL EAR DISORDER ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
EYELID FUNCTION DISORDER ( 4 FDA reports)
FAILURE TO CAPTURE ( 4 FDA reports)
FAMILIAL TREMOR ( 4 FDA reports)
FEAR OF WEIGHT GAIN ( 4 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 4 FDA reports)
FEMORAL ARTERY ANEURYSM ( 4 FDA reports)
FIXED ERUPTION ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FRACTURE REDUCTION ( 4 FDA reports)
FRACTURED SACRUM ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GALLSTONE ILEUS ( 4 FDA reports)
GAMMA RADIATION THERAPY ( 4 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 4 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 4 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 4 FDA reports)
HAEMOCHROMATOSIS ( 4 FDA reports)
HEAT RASH ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HEPATIC HAEMORRHAGE ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
HEPATIC VEIN THROMBOSIS ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HYDROCELE MALE INFECTED ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
HYPERALDOSTERONISM ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERPHAGIA ( 4 FDA reports)
HYPERPHOSPHATASAEMIA ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 4 FDA reports)
HYPOPROTHROMBINAEMIA ( 4 FDA reports)
HYPOTONIC URINARY BLADDER ( 4 FDA reports)
IMPLANT SITE EXTRAVASATION ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INFECTION MASKED ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INFUSION SITE CELLULITIS ( 4 FDA reports)
INFUSION SITE HAEMATOMA ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INHALATION THERAPY ( 4 FDA reports)
INJECTION SITE ABSCESS ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 4 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
IRON METABOLISM DISORDER ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
KAPOSI'S SARCOMA ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 4 FDA reports)
LARYNGECTOMY ( 4 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 4 FDA reports)
LEUKAEMIA PLASMACYTIC ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIP HAEMORRHAGE ( 4 FDA reports)
LIPOMATOSIS ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MACULAR SCAR ( 4 FDA reports)
MANDIBULECTOMY ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MENINGITIS LISTERIA ( 4 FDA reports)
METASTASES TO ADRENALS ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MORNING GLORY SYNDROME ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 4 FDA reports)
MUTISM ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NEPHRITIS AUTOIMMUNE ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 4 FDA reports)
NITRITE URINE ABSENT ( 4 FDA reports)
NO ADVERSE EFFECT ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
NONINFECTIOUS PERITONITIS ( 4 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
OESOPHAGEAL DISCOMFORT ( 4 FDA reports)
OESOPHAGEAL OEDEMA ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
OLIGODENDROGLIOMA ( 4 FDA reports)
ONYCHALGIA ( 4 FDA reports)
ONYCHOCLASIS ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORAL SOFT TISSUE DISORDER ( 4 FDA reports)
ORTHOSTATIC HYPERTENSION ( 4 FDA reports)
OVARIAN DISORDER ( 4 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 4 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 4 FDA reports)
PALATAL OEDEMA ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PARAPARESIS ( 4 FDA reports)
PENILE HAEMORRHAGE ( 4 FDA reports)
PERICARDIAL EXCISION ( 4 FDA reports)
PERICARDIAL RUB ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL DISORDER ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
POLYP COLORECTAL ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
PORTAL VEIN OCCLUSION ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
POST PROCEDURAL SWELLING ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
POVERTY OF THOUGHT CONTENT ( 4 FDA reports)
PRESBYACUSIS ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PROCEDURAL DIZZINESS ( 4 FDA reports)
PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PROLONGED EXPIRATION ( 4 FDA reports)
PROSTATE CANCER STAGE II ( 4 FDA reports)
PULMONARY ARTERY DILATATION ( 4 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACETABULUM FRACTURE ( 3 FDA reports)
ACQUIRED MACROGLOSSIA ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADAMS-STOKES SYNDROME ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
ANGIOSARCOMA ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC ANEURYSM REPAIR ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE REACTION ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
ARACHNOID CYST ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ARTERIAL REPAIR ( 3 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASPIRATION TRACHEAL ( 3 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 3 FDA reports)
AUTOMATISM ( 3 FDA reports)
AXILLARY VEIN THROMBOSIS ( 3 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BETA GLOBULIN ABNORMAL ( 3 FDA reports)
BICUSPID AORTIC VALVE ( 3 FDA reports)
BILIRUBIN CONJUGATED ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIOPSY KIDNEY ( 3 FDA reports)
BIPOLAR I DISORDER ( 3 FDA reports)
BLADDER INJURY ( 3 FDA reports)
BLADDER NEOPLASM SURGERY ( 3 FDA reports)
BLEPHARAL PAPILLOMA ( 3 FDA reports)
BLINDNESS CORTICAL ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATINE DECREASED ( 3 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 3 FDA reports)
BLOOD FOLATE INCREASED ( 3 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 3 FDA reports)
BLOOD POTASSIUM ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 3 FDA reports)
BLOOD URINE ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BREAST OPERATION ( 3 FDA reports)
BREECH DELIVERY ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHOSCOPY ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CARDIAC INDEX DECREASED ( 3 FDA reports)
CARDIAC MYXOMA ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARPUS CURVUS ( 3 FDA reports)
CATHETER SITE OEDEMA ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 3 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CERVICAL MYELOPATHY ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHILD ABUSE ( 3 FDA reports)
CHORDAE TENDINAE RUPTURE ( 3 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLEFT LIP AND PALATE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COLONIC OBSTRUCTION ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL TRANSPLANT ( 3 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CRYOTHERAPY ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
CYSTITIS RADIATION ( 3 FDA reports)
CYSTOSCOPY ( 3 FDA reports)
DECREASED EYE CONTACT ( 3 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 3 FDA reports)
DENTAL TREATMENT ( 3 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEVICE ELECTRICAL FINDING ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC FOOT INFECTION ( 3 FDA reports)
DIABETIC GANGRENE ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DISINHIBITION ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DRESSLER'S SYNDROME ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
ECHOCARDIOGRAM ( 3 FDA reports)
ELECTROCARDIOGRAM ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENDOCRINE DISORDER ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
EXECUTIVE DYSFUNCTION ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EYE INFECTION INTRAOCULAR ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FEMORAL NERVE PALSY ( 3 FDA reports)
FEMORAL PULSE DECREASED ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
GALLBLADDER FISTULA ( 3 FDA reports)
GASTRIC HYPOMOTILITY ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENDER IDENTITY DISORDER ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GENITAL HERPES ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GINGIVAL ERYTHEMA ( 3 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GRIMACING ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMANGIOBLASTOMA ( 3 FDA reports)
HAEMATOCRIT ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMOSTASIS ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HEART AND LUNG TRANSPLANT ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATIC VEIN DILATATION ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 3 FDA reports)
HIP DYSPLASIA ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERSPLENISM ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPOALDOSTERONISM ( 3 FDA reports)
HYPOCHROMASIA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOPITUITARISM ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
ILEAL GANGRENE ( 3 FDA reports)
IMPLANT SITE ERYTHEMA ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INFECTION PARASITIC ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INFUSION SITE PHLEBITIS ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE THROMBOSIS ( 3 FDA reports)
INJECTION SITE WARMTH ( 3 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
JOINT FLUID DRAINAGE ( 3 FDA reports)
KERATOPATHY ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LERICHE SYNDROME ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LISTERIOSIS ( 3 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
LYMPHOHISTIOCYTOSIS ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEDIASTINAL FIBROSIS ( 3 FDA reports)
MEDICAL DEVICE PAIN ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENINGIOMA BENIGN ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
MENTAL DISABILITY ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MOTION SICKNESS ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYELOBLASTOMA ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 3 FDA reports)
OESOPHAGEAL DILATATION ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL PERFORATION ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL SURGERY ( 3 FDA reports)
ORBITAL OEDEMA ( 3 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 3 FDA reports)
OVERSENSING ( 3 FDA reports)
PALATAL DISORDER ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PANCREATIC NEOPLASM ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PARKINSONIAN GAIT ( 3 FDA reports)
PASSIVE SMOKING ( 3 FDA reports)
PENILE SWELLING ( 3 FDA reports)
PERIANAL ERYTHEMA ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERIDIVERTICULITIS ( 3 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 3 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 3 FDA reports)
PERITONITIS SCLEROSING ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHAEHYPHOMYCOSIS ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHLEBOLITH ( 3 FDA reports)
PHOTOCOAGULATION ( 3 FDA reports)
PLASMAPHERESIS ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PLEURAL ADHESION ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMONIA INFLUENZAL ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
POLYCYTHAEMIA VERA ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POOR PERSONAL HYGIENE ( 3 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 3 FDA reports)
POSITIVE ROMBERGISM ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
POST PROCEDURAL PNEUMONIA ( 3 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCEDURAL VOMITING ( 3 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 3 FDA reports)
PRODUCT DOSAGE FORM ISSUE ( 3 FDA reports)
PROSTATE INFECTION ( 3 FDA reports)
PROSTRATION ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
PTERYGIUM ( 3 FDA reports)
PULMONARY FUNCTION TEST ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PURPURA SENILE ( 3 FDA reports)
PUTAMEN HAEMORRHAGE ( 3 FDA reports)
PYELONEPHRITIS CHRONIC ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RECTAL CANCER STAGE 0 ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 3 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 3 FDA reports)
RENAL OSTEODYSTROPHY ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RETINITIS PIGMENTOSA ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 3 FDA reports)
SALIVARY GLAND DISORDER ( 3 FDA reports)
SCAN ABDOMEN ABNORMAL ( 3 FDA reports)
SCLERAL DISCOLOURATION ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
SCROTAL HAEMATOCOELE ( 3 FDA reports)
SCROTAL VARICOSE VEINS ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SINUS OPERATION ( 3 FDA reports)
SKIN BLEEDING ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SLEEP TERROR ( 3 FDA reports)
SMALL INTESTINE GANGRENE ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SOFT TISSUE INFLAMMATION ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL X-RAY ABNORMAL ( 3 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 3 FDA reports)
STERNOTOMY ( 3 FDA reports)
STOMACH MASS ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
STROKE IN EVOLUTION ( 3 FDA reports)
SUBDURAL EMPYEMA ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
SUTURE REMOVAL ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
TIC ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH REPAIR ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TRACHEAL HAEMORRHAGE ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
URETERIC DILATATION ( 3 FDA reports)
URETHRAL DISORDER ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URETHRAL STENOSIS ( 3 FDA reports)
URINARY CASTS PRESENT ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINE CALCIUM INCREASED ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VICTIM OF HOMICIDE ( 3 FDA reports)
VIRAL SKIN INFECTION ( 3 FDA reports)
VISUAL BRIGHTNESS ( 3 FDA reports)
VISUAL PATHWAY DISORDER ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VITREOUS DEGENERATION ( 3 FDA reports)
WEIGHT LOSS POOR ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
RADIAL PULSE INCREASED ( 2 FDA reports)
RASH PAPULOSQUAMOUS ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY DEPTH DECREASED ( 2 FDA reports)
RESPIRATORY FATIGUE ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RIFT VALLEY FEVER ( 2 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SEBACEOUS CYST EXCISION ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SICKLE CELL TRAIT ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SILICOSIS ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SKULL MALFORMATION ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL CORD INJURY THORACIC ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPINAL MENINGEAL CYST ( 2 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC CALCIFICATION ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SWEATING FEVER ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TESTICULAR TORSION ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THROMBOEMBOLECTOMY ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
THYMOMA MALIGNANT ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL DEVIATION ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRIGEMINAL PALSY ( 2 FDA reports)
TROPONIN ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TYPE IIA HYPERLIPIDAEMIA ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URETHRAL NEOPLASM ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URETHRAL SPASM ( 2 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINE AMYLASE INCREASED ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINOMA ( 2 FDA reports)
UROGRAM ABNORMAL ( 2 FDA reports)
URTICARIA CHRONIC ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VASCULAR SKIN DISORDER ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VERTEBRAL INJURY ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VITAMIN A INCREASED ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
VOLVULUS OF SMALL BOWEL ( 2 FDA reports)
VOMITING IN PREGNANCY ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 2 FDA reports)
WOUND INFECTION FUNGAL ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
XANTHOMA ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACANTHOLYSIS ( 2 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 2 FDA reports)
ACINETOBACTER BACTERAEMIA ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 2 FDA reports)
ALLERGY TO ARTHROPOD STING ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
AMPUTATION STUMP PAIN ( 2 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL SPASM ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANASTOMOTIC COMPLICATION ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANORECTAL STENOSIS ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTISOCIAL BEHAVIOUR ( 2 FDA reports)
AORTA HYPOPLASIA ( 2 FDA reports)
AORTIC SURGERY ( 2 FDA reports)
AORTOGRAM ABNORMAL ( 2 FDA reports)
APHAKIA ( 2 FDA reports)
APOPTOSIS ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ATHERECTOMY ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
AUTOANTIBODY POSITIVE ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL TEST ( 2 FDA reports)
BACTERIAL TOXAEMIA ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASOPHIL COUNT DECREASED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BED REST ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BENIGN GASTRIC NEOPLASM ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BILE DUCT STENT INSERTION ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BIOPSY STOMACH ABNORMAL ( 2 FDA reports)
BLADDER DIVERTICULUM ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLADDER SPASM ( 2 FDA reports)
BLEEDING TIME SHORTENED ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 2 FDA reports)
BLOOD ETHANOL INCREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BLOOD TRIGLYCERIDES ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRAIN STEM THROMBOSIS ( 2 FDA reports)
BREAST DISORDER FEMALE ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
BRONCHITIS MORAXELLA ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 2 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIAC PSEUDOANEURYSM ( 2 FDA reports)
CARDIAC STRESS TEST ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIOPLEGIA ( 2 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 2 FDA reports)
CAROTID PULSE INCREASED ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 2 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
CHEMICAL CYSTITIS ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHONDROMALACIA ( 2 FDA reports)
CHOREA ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CLUSTER HEADACHE ( 2 FDA reports)
COELIAC ARTERY STENOSIS ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COLOSTOMY CLOSURE ( 2 FDA reports)
COMA URAEMIC ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONGENITAL HEARING DISORDER ( 2 FDA reports)
CONGENITAL HYDROCEPHALUS ( 2 FDA reports)
CONGENITAL INFECTION ( 2 FDA reports)
CONJUNCTIVAL PALLOR ( 2 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL DEGENERATION ( 2 FDA reports)
CORNEAL DYSTROPHY ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY DILATATION ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
CREATININE URINE INCREASED ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CROSS SENSITIVITY REACTION ( 2 FDA reports)
CRYOGLOBULINAEMIA ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
CYTOLOGY ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DECREASED VIBRATORY SENSE ( 2 FDA reports)
DEFIBRILLATION THRESHOLD INCREASED ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DEVICE BATTERY ISSUE ( 2 FDA reports)
DEVICE CAPTURING ISSUE ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE INTOLERANCE ( 2 FDA reports)
DEVICE LEAD DAMAGE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DEVICE PACING ISSUE ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DIPHTHERIA ( 2 FDA reports)
DISABLED RELATIVE ( 2 FDA reports)
DISEASE PRODROMAL STAGE ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DIURETIC THERAPY ( 2 FDA reports)
DOUBLE VESSEL BYPASS GRAFT ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUODENAL FISTULA ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTRIC SHOCK ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ELEVATED PACING THRESHOLD ( 2 FDA reports)
EMBOLISM VENOUS ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDOCARDIAL DISEASE ( 2 FDA reports)
ENDOCARDITIS CANDIDA ( 2 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENZYME INDUCTION ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPIGLOTTIC CARCINOMA ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESSENTIAL TREMOR ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FAECAL VOLUME DECREASED ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FEELINGS OF WORTHLESSNESS ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMORAL PULSE ABNORMAL ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOETAL CARDIAC DISORDER ( 2 FDA reports)
FONTANELLE BULGING ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FRUCTOSAMINE INCREASED ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL ENDOCARDITIS ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GAIT DEVIATION ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENITAL SWELLING ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN S DECREASED ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMORRHAGIC ASCITES ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HANGNAIL ( 2 FDA reports)
HEART VALVE OPERATION ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
HERNIA DIAPHRAGMATIC REPAIR ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HYALOSIS ASTEROID ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPHAEMA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
HYPOZINCAEMIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE STINGING ( 2 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL OPERATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 2 FDA reports)
IRIDOCELE ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LARGE INTESTINAL STRICTURE ( 2 FDA reports)
LARYNGOSCOPY ABNORMAL ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LID LAG ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPOEDEMA ( 2 FDA reports)
LIPOGRANULOMA ( 2 FDA reports)
LISTERIA ENCEPHALITIS ( 2 FDA reports)
LIVER INDURATION ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOOSE BODY IN JOINT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ( 2 FDA reports)
LOW TURNOVER OSTEOPATHY ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG HERNIA ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
LYMPHANGIECTASIA INTESTINAL ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACROANGIOPATHY ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALFORMATION VENOUS ( 2 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 2 FDA reports)
MALIGNANT MYOPIA ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MEDICAL DEVICE SITE REACTION ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MENINGIOMA MALIGNANT ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS COCCIDIOIDES ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEOLOGISM ( 2 FDA reports)
NEONATAL ANURIA ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEURILEMMOMA MALIGNANT ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
NOCTIPHOBIA ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NOSE DEFORMITY ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OCCIPITAL NEURALGIA ( 2 FDA reports)
OCCUPATIONAL EXPOSURE TO DUST ( 2 FDA reports)
OCULAR DYSMETRIA ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
OPTIC NERVE INFARCTION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM BENIGN ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEOARTHRITIS GENERALISED ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 2 FDA reports)
PACHYMENINGITIS ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARANASAL CYST ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARESIS CRANIAL NERVE ( 2 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 2 FDA reports)
PAST-POINTING ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PENILE OPERATION ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERICARDITIS INFECTIVE ( 2 FDA reports)
PERINEAL CYST ( 2 FDA reports)
PERIORBITAL DISORDER ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONEAL LESION ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHOSPHENES ( 2 FDA reports)
PLEURAL INFECTION ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POOR DENTAL CONDITION ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
PRADER-WILLI SYNDROME ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT SHAPE ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROSTATE TENDERNESS ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOPOLYP ( 2 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 2 FDA reports)
PULMONARY ARTERY STENOSIS ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY CALCIFICATION ( 2 FDA reports)
PULMONARY EOSINOPHILIA ( 2 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 2 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PULMONARY VALVE DISEASE ( 2 FDA reports)
PULMONARY VALVE REPLACEMENT ( 2 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 2 FDA reports)
PULMONARY VEIN OCCLUSION ( 2 FDA reports)
PULMONARY VEIN STENOSIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL EXPLORATION ( 1 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL TRANSPOSITION ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CORTEX ATROPHY ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE ABSENT ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALDOLASE DECREASED ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALPHA GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-PROTHROMBIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
AORTO-ILIAC ARTERIAL STENOSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA 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)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASPLENIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATHEROSCLEROSIS PROPHYLAXIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL RUPTURE ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
BACTERIAL DIARRHOEA ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BALLOON ATRIAL SEPTOSTOMY ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY BREAST NORMAL ( 1 FDA reports)
BIOPSY CARTILAGE ABNORMAL ( 1 FDA reports)
BIOPSY CERVIX ABNORMAL ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD COPPER DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E DECREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FISTULA ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOMA EXCISION ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC PACEMAKER EVALUATION ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ANGIOPLASTY ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID SINUS SYNDROME ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBELLAR HYPOPLASIA ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL ATAXIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLEDOCHOENTEROSTOMY ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROIDAL COLOBOMA ( 1 FDA reports)
CHOROIDAL HAEMORRHAGE ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
COAGULATION DISORDER NEONATAL ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COMPLEMENT FACTOR ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 1 FDA reports)
CONGENITAL CORNEAL ANOMALY ( 1 FDA reports)
CONGENITAL EYELID MALFORMATION ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL OPTIC NERVE ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONTACT LENS COMPLICATION ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL CYST ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
COX-MAZE PROCEDURE ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRONKHITE-CANADA SYNDROME ( 1 FDA reports)
CROSSMATCH COMPATIBLE ( 1 FDA reports)
CROSSMATCH INCOMPATIBLE ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTATIN C INCREASED ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS MYOCARDITIS ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED FONTANELLE CLOSURE ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIGITAL ULCER ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DUST INHALATION PNEUMOPATHY ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR DEFORMITY ACQUIRED ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMBOLECTOMY ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPITHELIOMA ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXTERNAL EAR LESION EXCISION ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER HYPOPLASIA ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURED ZYGOMATIC ARCH ELEVATION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GALLBLADDER OBSTRUCTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE NORMAL ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OCCULT BLOOD POSITIVE ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRINOMA ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRANULOCYTE COUNT ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROSS MOTOR DELAY ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HALLUCINATION, GUSTATORY ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAND DERMATITIS ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CANCER STAGE I ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE TYPE STAGE UNSPECIFIED ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOMOSEXUALITY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYDROXYCORTICOSTEROIDS INCREASED ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPONATRAEMIC SYNDROME ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPLASTIC ANAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
IDIOPATHIC LENTICULAR MUCOCUTANEOUS PIGMENTATION ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEAL FISTULA ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE IRRITATION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA SYNDROME ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE PUSTULE ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL CONGESTION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL STOMA SITE BLEEDING ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
IVTH NERVE PARESIS ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LID MARGIN DISCHARGE ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LIVING ALONE ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOW INCOME ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
LYMPHOMA TRANSFORMATION ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA IN SITU ( 1 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL GLAND ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO OESOPHAGUS ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROBIOLOGY TEST ABNORMAL ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOYAMOYA DISEASE ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MURDER ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
MYRINGITIS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEEDLE BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
NEONATAL CARDIAC FAILURE ( 1 FDA reports)
NEONATAL CHOLESTASIS ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEUROBORRELIOSIS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING THORACIC ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OFFICE VISIT ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORBITAL PSEUDOTUMOUR ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OSTEOCALCIN INCREASED ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCOAST'S TUMOUR ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANEL-REACTIVE ANTIBODY INCREASED ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROTID ABSCESS ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC MUSCLES INADEQUATE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERIORBITAL HAEMORRHAGE ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CANCER METASTATIC ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOBIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PIGMENT NEPHROPATHY ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLANTAR FASCIAL FIBROMATOSIS ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLASMA CELLS DECREASED ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POIKILODERMA ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTPARTUM HYPOPITUITARISM ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY AIR LEAKAGE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERY ANEURYSM ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS NORMAL ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL ARTERY DISSECTION ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINAL ANOMALY CONGENITAL ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL OPERATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINITIS VIRAL ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
SACRAL HYPOPLASIA ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCAPULA FRACTURE ( 1 FDA reports)
SCHISTOSOMIASIS ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLERAL PIGMENTATION ( 1 FDA reports)
SCLEREMA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCROTAL HAEMATOMA ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OPERATION ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SHUNT ANEURYSM ( 1 FDA reports)
SHUNT BLOOD FLOW EXCESSIVE ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SITUS AMBIGUOUS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKELETAL MUSCLE ENZYMES ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST NEGATIVE ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRAVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TACITURNITY ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TENONECTOMY ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTICULAR HYPERTROPHY ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) STAGE II ( 1 FDA reports)
TETANUS ( 1 FDA reports)
TETRALOGY OF FALLOT REPAIR ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBIN TIME SHORTENED ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOENDARTERECTOMY ( 1 FDA reports)
THROMBOSIS PROPHYLAXIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TINEL'S SIGN ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL FISTULA REPAIR ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANS-SEXUALISM ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRIGEMINAL NERVE ABLATION ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR LOCAL INVASION ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 1 FDA reports)
ULTRASOUND ABDOMEN NORMAL ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ABNORMAL ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND CHEST ( 1 FDA reports)
UPPER AIRWAY NECROSIS ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
URATE NEPHROPATHY ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE CALCIUM ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE CHLORIDE INCREASED ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE HAEMATOMA ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS OPERATION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VICTIM OF CHILD ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL TRACHEITIS ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)