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

FALL ( 10645 FDA reports)
PAIN ( 6503 FDA reports)
PAIN IN EXTREMITY ( 6434 FDA reports)
NAUSEA ( 5969 FDA reports)
DIZZINESS ( 5954 FDA reports)
ARTHRALGIA ( 5794 FDA reports)
ASTHENIA ( 5601 FDA reports)
FATIGUE ( 5286 FDA reports)
BACK PAIN ( 5274 FDA reports)
MALAISE ( 4596 FDA reports)
MUSCLE SPASMS ( 4380 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3844 FDA reports)
HEADACHE ( 3668 FDA reports)
FEELING ABNORMAL ( 3577 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3551 FDA reports)
DYSPNOEA ( 3349 FDA reports)
INJECTION SITE HAEMATOMA ( 3255 FDA reports)
GAIT DISTURBANCE ( 3063 FDA reports)
INJECTION SITE ERYTHEMA ( 3006 FDA reports)
PNEUMONIA ( 2972 FDA reports)
INJECTION SITE PAIN ( 2955 FDA reports)
BONE PAIN ( 2634 FDA reports)
WEIGHT DECREASED ( 2604 FDA reports)
VOMITING ( 2584 FDA reports)
HOSPITALISATION ( 2557 FDA reports)
HIP FRACTURE ( 2532 FDA reports)
DRUG DOSE OMISSION ( 2503 FDA reports)
CONTUSION ( 2492 FDA reports)
DIARRHOEA ( 2455 FDA reports)
OEDEMA PERIPHERAL ( 2441 FDA reports)
CONSTIPATION ( 2430 FDA reports)
DEATH ( 2192 FDA reports)
MUSCULAR WEAKNESS ( 1933 FDA reports)
BLOOD CALCIUM INCREASED ( 1808 FDA reports)
LOSS OF CONSCIOUSNESS ( 1769 FDA reports)
BALANCE DISORDER ( 1765 FDA reports)
MYALGIA ( 1607 FDA reports)
ARTHRITIS ( 1571 FDA reports)
CHEST PAIN ( 1555 FDA reports)
HEART RATE INCREASED ( 1494 FDA reports)
MEMORY IMPAIRMENT ( 1464 FDA reports)
INSOMNIA ( 1463 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1454 FDA reports)
SPINAL FRACTURE ( 1435 FDA reports)
URINARY TRACT INFECTION ( 1410 FDA reports)
ABDOMINAL PAIN UPPER ( 1376 FDA reports)
FEMUR FRACTURE ( 1376 FDA reports)
COUGH ( 1374 FDA reports)
TREMOR ( 1366 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1360 FDA reports)
MYOCARDIAL INFARCTION ( 1357 FDA reports)
DEHYDRATION ( 1351 FDA reports)
DECREASED APPETITE ( 1323 FDA reports)
HYPOAESTHESIA ( 1306 FDA reports)
ARTHROPATHY ( 1301 FDA reports)
ANXIETY ( 1254 FDA reports)
PYREXIA ( 1223 FDA reports)
NASOPHARYNGITIS ( 1179 FDA reports)
BLOOD PRESSURE INCREASED ( 1163 FDA reports)
ANAEMIA ( 1126 FDA reports)
SOMNOLENCE ( 1116 FDA reports)
MEDICATION ERROR ( 1100 FDA reports)
MOBILITY DECREASED ( 1098 FDA reports)
UPPER LIMB FRACTURE ( 1095 FDA reports)
SURGERY ( 1076 FDA reports)
PELVIC FRACTURE ( 1073 FDA reports)
HEAD INJURY ( 1051 FDA reports)
NECK PAIN ( 1050 FDA reports)
HYPERTENSION ( 1042 FDA reports)
BONE DISORDER ( 1041 FDA reports)
DRUG INEFFECTIVE ( 1040 FDA reports)
JOINT SWELLING ( 1036 FDA reports)
WEIGHT INCREASED ( 1029 FDA reports)
BRONCHITIS ( 1017 FDA reports)
BONE DENSITY DECREASED ( 1011 FDA reports)
ABDOMINAL PAIN ( 1005 FDA reports)
PRURITUS ( 990 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 979 FDA reports)
CARDIAC DISORDER ( 959 FDA reports)
MUSCULOSKELETAL PAIN ( 957 FDA reports)
RASH ( 952 FDA reports)
NERVOUSNESS ( 927 FDA reports)
RIB FRACTURE ( 924 FDA reports)
ERYTHEMA ( 911 FDA reports)
CONFUSIONAL STATE ( 886 FDA reports)
PALPITATIONS ( 884 FDA reports)
BACK DISORDER ( 879 FDA reports)
MOVEMENT DISORDER ( 856 FDA reports)
ATRIAL FIBRILLATION ( 845 FDA reports)
ABDOMINAL DISCOMFORT ( 844 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 844 FDA reports)
BLOOD PRESSURE DECREASED ( 821 FDA reports)
LIMB INJURY ( 811 FDA reports)
HYPOTENSION ( 808 FDA reports)
DEPRESSION ( 807 FDA reports)
WRIST FRACTURE ( 795 FDA reports)
CONDITION AGGRAVATED ( 794 FDA reports)
HYPERSENSITIVITY ( 793 FDA reports)
INFECTION ( 789 FDA reports)
MUSCLE CRAMP ( 780 FDA reports)
THROMBOSIS ( 780 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 768 FDA reports)
HYPERHIDROSIS ( 756 FDA reports)
VISUAL IMPAIRMENT ( 752 FDA reports)
HAEMORRHAGE ( 718 FDA reports)
CATARACT ( 702 FDA reports)
ABASIA ( 700 FDA reports)
INTENTIONAL DRUG MISUSE ( 694 FDA reports)
PARAESTHESIA ( 692 FDA reports)
VISUAL ACUITY REDUCED ( 691 FDA reports)
HIP ARTHROPLASTY ( 672 FDA reports)
OSTEOARTHRITIS ( 667 FDA reports)
ABDOMINAL DISTENSION ( 666 FDA reports)
JOINT INJURY ( 658 FDA reports)
FEAR ( 655 FDA reports)
KNEE ARTHROPLASTY ( 655 FDA reports)
SINUSITIS ( 654 FDA reports)
FOOT FRACTURE ( 642 FDA reports)
RENAL FAILURE ( 641 FDA reports)
VERTIGO ( 641 FDA reports)
VITAMIN D DECREASED ( 640 FDA reports)
NEPHROLITHIASIS ( 638 FDA reports)
IMPAIRED HEALING ( 634 FDA reports)
OSTEOPOROSIS ( 633 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 632 FDA reports)
ASTHMA ( 619 FDA reports)
DYSPEPSIA ( 610 FDA reports)
CYSTITIS ( 605 FDA reports)
INFLUENZA ( 604 FDA reports)
LUNG DISORDER ( 602 FDA reports)
CONVULSION ( 600 FDA reports)
DYSSTASIA ( 590 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 590 FDA reports)
OVERDOSE ( 573 FDA reports)
DISCOMFORT ( 570 FDA reports)
LOWER LIMB FRACTURE ( 557 FDA reports)
ALOPECIA ( 556 FDA reports)
ROAD TRAFFIC ACCIDENT ( 556 FDA reports)
STRESS ( 553 FDA reports)
COMPRESSION FRACTURE ( 549 FDA reports)
SYNCOPE ( 543 FDA reports)
LIMB DISCOMFORT ( 538 FDA reports)
BREAST CANCER ( 537 FDA reports)
SPINAL COMPRESSION FRACTURE ( 532 FDA reports)
HYPERCALCAEMIA ( 529 FDA reports)
VISION BLURRED ( 529 FDA reports)
ARRHYTHMIA ( 514 FDA reports)
FRACTURE ( 514 FDA reports)
INTESTINAL OBSTRUCTION ( 489 FDA reports)
CHEST DISCOMFORT ( 486 FDA reports)
CHILLS ( 486 FDA reports)
ANKLE FRACTURE ( 481 FDA reports)
SPEECH DISORDER ( 477 FDA reports)
AMNESIA ( 471 FDA reports)
DRY MOUTH ( 470 FDA reports)
DYSPHAGIA ( 470 FDA reports)
DYSPHONIA ( 470 FDA reports)
GASTROINTESTINAL DISORDER ( 469 FDA reports)
SPINAL DISORDER ( 462 FDA reports)
BODY HEIGHT DECREASED ( 453 FDA reports)
FLATULENCE ( 449 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 443 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 435 FDA reports)
ILL-DEFINED DISORDER ( 435 FDA reports)
FEELING HOT ( 432 FDA reports)
HEART RATE IRREGULAR ( 426 FDA reports)
BLOOD GLUCOSE INCREASED ( 418 FDA reports)
DYSGEUSIA ( 417 FDA reports)
CARDIAC FAILURE ( 411 FDA reports)
EXOSTOSIS ( 411 FDA reports)
SWELLING ( 411 FDA reports)
SLEEP DISORDER ( 405 FDA reports)
RESPIRATORY FAILURE ( 404 FDA reports)
JOINT DISLOCATION ( 401 FDA reports)
BURNING SENSATION ( 400 FDA reports)
KIDNEY INFECTION ( 394 FDA reports)
PULMONARY EMBOLISM ( 393 FDA reports)
INFLUENZA LIKE ILLNESS ( 392 FDA reports)
EMPHYSEMA ( 391 FDA reports)
HERPES ZOSTER ( 391 FDA reports)
EYE DISORDER ( 387 FDA reports)
MIGRAINE ( 387 FDA reports)
BLOOD POTASSIUM DECREASED ( 386 FDA reports)
SPINAL COLUMN STENOSIS ( 378 FDA reports)
POST PROCEDURAL COMPLICATION ( 377 FDA reports)
DIFFICULTY IN WALKING ( 374 FDA reports)
VIRAL INFECTION ( 373 FDA reports)
RHEUMATOID ARTHRITIS ( 371 FDA reports)
HYPOACUSIS ( 368 FDA reports)
OFF LABEL USE ( 367 FDA reports)
DIVERTICULITIS ( 366 FDA reports)
HOT FLUSH ( 366 FDA reports)
SEPSIS ( 361 FDA reports)
CHOLELITHIASIS ( 359 FDA reports)
HAND FRACTURE ( 353 FDA reports)
PANCREATITIS ( 351 FDA reports)
HIATUS HERNIA ( 349 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 346 FDA reports)
INJECTION SITE REACTION ( 342 FDA reports)
OROPHARYNGEAL PAIN ( 340 FDA reports)
STAPHYLOCOCCAL INFECTION ( 337 FDA reports)
CELLULITIS ( 336 FDA reports)
NEOPLASM MALIGNANT ( 335 FDA reports)
LUNG NEOPLASM MALIGNANT ( 331 FDA reports)
LETHARGY ( 330 FDA reports)
NERVE COMPRESSION ( 330 FDA reports)
ANOREXIA ( 328 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 327 FDA reports)
ADVERSE EVENT ( 326 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 325 FDA reports)
ADVERSE DRUG REACTION ( 324 FDA reports)
PULMONARY OEDEMA ( 324 FDA reports)
INJECTION SITE DISCOLOURATION ( 320 FDA reports)
HAEMOGLOBIN DECREASED ( 316 FDA reports)
SWELLING FACE ( 316 FDA reports)
TACHYCARDIA ( 312 FDA reports)
DIABETES MELLITUS ( 306 FDA reports)
LUNG INFECTION ( 306 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 301 FDA reports)
RHINORRHOEA ( 297 FDA reports)
MASS ( 296 FDA reports)
FLUID RETENTION ( 295 FDA reports)
EATING DISORDER ( 294 FDA reports)
HEARING IMPAIRED ( 293 FDA reports)
MULTIPLE MYELOMA ( 293 FDA reports)
RENAL DISORDER ( 293 FDA reports)
GASTRIC DISORDER ( 292 FDA reports)
STOMACH DISCOMFORT ( 291 FDA reports)
POLLAKIURIA ( 289 FDA reports)
ACCIDENTAL OVERDOSE ( 288 FDA reports)
BLOOD CALCIUM DECREASED ( 288 FDA reports)
RECTAL HAEMORRHAGE ( 287 FDA reports)
HUMERUS FRACTURE ( 286 FDA reports)
DEEP VEIN THROMBOSIS ( 283 FDA reports)
OXYGEN SATURATION DECREASED ( 281 FDA reports)
SKIN DISORDER ( 280 FDA reports)
CORONARY ARTERY OCCLUSION ( 279 FDA reports)
DISORIENTATION ( 279 FDA reports)
SKIN DISCOLOURATION ( 279 FDA reports)
INJURY ( 278 FDA reports)
FEMORAL NECK FRACTURE ( 277 FDA reports)
FEELING COLD ( 276 FDA reports)
BLOOD GLUCOSE DECREASED ( 270 FDA reports)
BLOOD SODIUM DECREASED ( 270 FDA reports)
NERVOUS SYSTEM DISORDER ( 270 FDA reports)
PAIN IN JAW ( 270 FDA reports)
URTICARIA ( 270 FDA reports)
HEART RATE DECREASED ( 268 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 266 FDA reports)
INFLAMMATION ( 264 FDA reports)
CARDIAC ARREST ( 263 FDA reports)
RESPIRATORY DISORDER ( 262 FDA reports)
SKIN INJURY ( 261 FDA reports)
HAEMATOCHEZIA ( 260 FDA reports)
DEVICE FAILURE ( 259 FDA reports)
DEMENTIA ( 258 FDA reports)
MACULAR DEGENERATION ( 255 FDA reports)
RETCHING ( 254 FDA reports)
GROIN PAIN ( 253 FDA reports)
SCOLIOSIS ( 253 FDA reports)
INJECTION SITE PRURITUS ( 252 FDA reports)
PROCEDURAL PAIN ( 252 FDA reports)
NERVE INJURY ( 251 FDA reports)
URINARY INCONTINENCE ( 248 FDA reports)
OSTEONECROSIS ( 245 FDA reports)
THYROID DISORDER ( 245 FDA reports)
ANGINA PECTORIS ( 244 FDA reports)
INCORRECT STORAGE OF DRUG ( 244 FDA reports)
PLEURAL EFFUSION ( 244 FDA reports)
ROTATOR CUFF SYNDROME ( 244 FDA reports)
DYSKINESIA ( 243 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 243 FDA reports)
BLISTER ( 241 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 240 FDA reports)
INJECTION SITE SWELLING ( 238 FDA reports)
INJECTION SITE MASS ( 237 FDA reports)
INJECTION SITE RASH ( 237 FDA reports)
MEDICAL DEVICE COMPLICATION ( 236 FDA reports)
BLINDNESS ( 235 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 235 FDA reports)
PRESYNCOPE ( 234 FDA reports)
RENAL IMPAIRMENT ( 234 FDA reports)
SPINAL OSTEOARTHRITIS ( 234 FDA reports)
HYPOPHAGIA ( 233 FDA reports)
SENSORY DISTURBANCE ( 233 FDA reports)
GASTRITIS ( 229 FDA reports)
LACERATION ( 228 FDA reports)
DEVICE DISLOCATION ( 226 FDA reports)
DYSURIA ( 225 FDA reports)
MUSCULOSKELETAL DISORDER ( 225 FDA reports)
NASAL CONGESTION ( 225 FDA reports)
CORONARY ARTERY DISEASE ( 222 FDA reports)
DRUG INTERACTION ( 222 FDA reports)
FLUSHING ( 222 FDA reports)
JAW DISORDER ( 222 FDA reports)
HIP SURGERY ( 220 FDA reports)
MUSCLE DISORDER ( 219 FDA reports)
NEUROPATHY PERIPHERAL ( 217 FDA reports)
STRESS FRACTURE ( 217 FDA reports)
OSTEOMYELITIS ( 216 FDA reports)
APHASIA ( 215 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 215 FDA reports)
SCIATICA ( 215 FDA reports)
TIBIA FRACTURE ( 215 FDA reports)
INJECTION SITE BURNING ( 214 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 212 FDA reports)
BACK INJURY ( 211 FDA reports)
EPISTAXIS ( 211 FDA reports)
FIBROMYALGIA ( 210 FDA reports)
TOOTH DISORDER ( 210 FDA reports)
PRURITUS GENERALISED ( 209 FDA reports)
ACCIDENT ( 206 FDA reports)
BLOOD TEST ABNORMAL ( 204 FDA reports)
BURSITIS ( 204 FDA reports)
DEVICE BREAKAGE ( 204 FDA reports)
RASH PRURITIC ( 204 FDA reports)
NEURALGIA ( 203 FDA reports)
RENAL FAILURE ACUTE ( 203 FDA reports)
GASTROENTERITIS VIRAL ( 201 FDA reports)
DEPRESSED MOOD ( 200 FDA reports)
LABORATORY TEST ABNORMAL ( 200 FDA reports)
JOINT STIFFNESS ( 198 FDA reports)
CONCUSSION ( 195 FDA reports)
BLINDNESS UNILATERAL ( 194 FDA reports)
COLITIS ( 194 FDA reports)
DYSARTHRIA ( 193 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 192 FDA reports)
NO ADVERSE EVENT ( 192 FDA reports)
PATHOLOGICAL FRACTURE ( 192 FDA reports)
VISUAL DISTURBANCE ( 192 FDA reports)
WOUND ( 191 FDA reports)
GLAUCOMA ( 191 FDA reports)
INCORRECT DOSE ADMINISTERED ( 191 FDA reports)
INJECTION SITE IRRITATION ( 191 FDA reports)
MIDDLE INSOMNIA ( 191 FDA reports)
STENT PLACEMENT ( 191 FDA reports)
COLON CANCER ( 190 FDA reports)
SPINAL FUSION SURGERY ( 190 FDA reports)
CARDIAC PACEMAKER INSERTION ( 188 FDA reports)
NODULE ( 188 FDA reports)
HYPOKINESIA ( 186 FDA reports)
COMA ( 185 FDA reports)
BACTERIAL INFECTION ( 184 FDA reports)
RASH MACULAR ( 184 FDA reports)
HERNIA ( 182 FDA reports)
MUSCLE TIGHTNESS ( 182 FDA reports)
EMOTIONAL DISTRESS ( 181 FDA reports)
BLOOD MAGNESIUM DECREASED ( 180 FDA reports)
HAEMATOMA ( 180 FDA reports)
LARYNGITIS ( 179 FDA reports)
EAR PAIN ( 178 FDA reports)
GALLBLADDER DISORDER ( 178 FDA reports)
GASTROINTESTINAL INFECTION ( 178 FDA reports)
DECREASED ACTIVITY ( 177 FDA reports)
PRODUCTIVE COUGH ( 177 FDA reports)
CLOSTRIDIAL INFECTION ( 176 FDA reports)
POSTURE ABNORMAL ( 176 FDA reports)
HYPERSOMNIA ( 175 FDA reports)
LYMPHOMA ( 175 FDA reports)
BLOOD URINE PRESENT ( 174 FDA reports)
SKIN CANCER ( 174 FDA reports)
VERTEBROPLASTY ( 174 FDA reports)
PULMONARY FIBROSIS ( 173 FDA reports)
DRUG HYPERSENSITIVITY ( 172 FDA reports)
PULMONARY HYPERTENSION ( 172 FDA reports)
SINUS DISORDER ( 172 FDA reports)
WEIGHT BEARING DIFFICULTY ( 172 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 171 FDA reports)
STOMATITIS ( 171 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 170 FDA reports)
MENTAL IMPAIRMENT ( 170 FDA reports)
BLOOD PRESSURE ABNORMAL ( 169 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 169 FDA reports)
PARKINSON'S DISEASE ( 169 FDA reports)
TINNITUS ( 169 FDA reports)
CEREBRAL HAEMORRHAGE ( 167 FDA reports)
CRYING ( 167 FDA reports)
FACIAL BONES FRACTURE ( 167 FDA reports)
THROAT IRRITATION ( 167 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 166 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 165 FDA reports)
BLOOD DISORDER ( 164 FDA reports)
HAEMORRHOIDS ( 163 FDA reports)
NEOPLASM ( 163 FDA reports)
TOOTH FRACTURE ( 162 FDA reports)
KNEE OPERATION ( 161 FDA reports)
CARDIAC OPERATION ( 160 FDA reports)
CAROTID ARTERY OCCLUSION ( 160 FDA reports)
DIZZINESS POSTURAL ( 159 FDA reports)
EYE PAIN ( 159 FDA reports)
FRACTURE NONUNION ( 158 FDA reports)
MICTURITION URGENCY ( 158 FDA reports)
CALCINOSIS ( 157 FDA reports)
SCRATCH ( 157 FDA reports)
INJECTION SITE BRUISING ( 156 FDA reports)
SCREAMING ( 156 FDA reports)
GOUT ( 154 FDA reports)
INJECTION SITE NODULE ( 154 FDA reports)
CLAVICLE FRACTURE ( 153 FDA reports)
FLANK PAIN ( 153 FDA reports)
BLOOD CREATININE INCREASED ( 152 FDA reports)
DRY SKIN ( 152 FDA reports)
HAEMATURIA ( 152 FDA reports)
DRUG PRESCRIBING ERROR ( 151 FDA reports)
HYPONATRAEMIA ( 151 FDA reports)
LYMPHADENOPATHY ( 151 FDA reports)
MUSCLE ATROPHY ( 151 FDA reports)
CATARACT OPERATION ( 150 FDA reports)
SCAR ( 150 FDA reports)
WALKING AID USER ( 150 FDA reports)
VITAMIN D DEFICIENCY ( 149 FDA reports)
LOCALISED INFECTION ( 149 FDA reports)
INJECTION SITE STINGING ( 148 FDA reports)
INJECTION SITE URTICARIA ( 148 FDA reports)
CARDIAC MURMUR ( 147 FDA reports)
JOINT EFFUSION ( 147 FDA reports)
PATELLA FRACTURE ( 147 FDA reports)
RENAL CYST ( 147 FDA reports)
TOOTH INJURY ( 147 FDA reports)
HYPOKALAEMIA ( 146 FDA reports)
MUSCLE STRAIN ( 146 FDA reports)
ABNORMAL BEHAVIOUR ( 145 FDA reports)
TREATMENT NONCOMPLIANCE ( 143 FDA reports)
MULTIPLE FRACTURES ( 142 FDA reports)
NIGHT SWEATS ( 142 FDA reports)
BREAST MASS ( 141 FDA reports)
GASTROENTERITIS ( 141 FDA reports)
ULCER ( 141 FDA reports)
BASAL CELL CARCINOMA ( 140 FDA reports)
FIBULA FRACTURE ( 140 FDA reports)
ANGIOPATHY ( 139 FDA reports)
INJECTION SITE DISCOMFORT ( 138 FDA reports)
LIGAMENT SPRAIN ( 138 FDA reports)
BODY TEMPERATURE INCREASED ( 137 FDA reports)
DEVICE MISUSE ( 137 FDA reports)
DYSPNOEA EXERTIONAL ( 137 FDA reports)
FRACTURED SACRUM ( 137 FDA reports)
SPINAL COLUMN INJURY ( 137 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 137 FDA reports)
APHONIA ( 136 FDA reports)
CARDIAC VALVE DISEASE ( 136 FDA reports)
GASTRIC ULCER ( 136 FDA reports)
PLATELET COUNT DECREASED ( 136 FDA reports)
EXCORIATION ( 135 FDA reports)
SCAB ( 135 FDA reports)
ORAL PAIN ( 134 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 134 FDA reports)
BEDRIDDEN ( 133 FDA reports)
LIVER DISORDER ( 133 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 133 FDA reports)
SNEEZING ( 133 FDA reports)
CHOKING ( 132 FDA reports)
RESPIRATORY TRACT INFECTION ( 132 FDA reports)
COGNITIVE DISORDER ( 131 FDA reports)
EXTRASYSTOLES ( 131 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 131 FDA reports)
ONYCHOCLASIS ( 131 FDA reports)
NAIL DISORDER ( 129 FDA reports)
CHOLECYSTECTOMY ( 127 FDA reports)
SKIN LACERATION ( 127 FDA reports)
AORTIC ANEURYSM ( 126 FDA reports)
DISTURBANCE IN ATTENTION ( 126 FDA reports)
FAECES DISCOLOURED ( 126 FDA reports)
RESTLESS LEGS SYNDROME ( 126 FDA reports)
SENSATION OF HEAVINESS ( 126 FDA reports)
CARPAL TUNNEL SYNDROME ( 125 FDA reports)
RADIUS FRACTURE ( 125 FDA reports)
VAGINAL HAEMORRHAGE ( 125 FDA reports)
PERIORBITAL HAEMATOMA ( 123 FDA reports)
URINARY RETENTION ( 123 FDA reports)
BLADDER CANCER ( 122 FDA reports)
BREAST CANCER FEMALE ( 122 FDA reports)
OSTEOPENIA ( 122 FDA reports)
URINE ODOUR ABNORMAL ( 122 FDA reports)
DISABILITY ( 121 FDA reports)
GALLBLADDER OPERATION ( 121 FDA reports)
PNEUMONIA ASPIRATION ( 120 FDA reports)
EXPIRED DRUG ADMINISTERED ( 119 FDA reports)
IRRITABLE BOWEL SYNDROME ( 119 FDA reports)
HYPOGLYCAEMIA ( 118 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 118 FDA reports)
FACE INJURY ( 117 FDA reports)
JOINT CREPITATION ( 117 FDA reports)
LUMBAR SPINAL STENOSIS ( 117 FDA reports)
PROSTATE CANCER ( 117 FDA reports)
BLADDER PROLAPSE ( 116 FDA reports)
CARDIOVASCULAR DISORDER ( 116 FDA reports)
ELECTROLYTE IMBALANCE ( 116 FDA reports)
HYPOTHYROIDISM ( 116 FDA reports)
PROCEDURAL COMPLICATION ( 116 FDA reports)
BREAST PAIN ( 115 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 115 FDA reports)
DEVICE RELATED INFECTION ( 115 FDA reports)
HEPATIC ENZYME INCREASED ( 115 FDA reports)
IRRITABILITY ( 115 FDA reports)
SHOULDER ARTHROPLASTY ( 115 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 115 FDA reports)
BLOOD IRON DECREASED ( 114 FDA reports)
CYST ( 114 FDA reports)
DIVERTICULUM ( 114 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 114 FDA reports)
MITRAL VALVE INCOMPETENCE ( 114 FDA reports)
OSTEONECROSIS OF JAW ( 114 FDA reports)
SKIN ULCER ( 114 FDA reports)
THIRST ( 114 FDA reports)
UNRESPONSIVE TO STIMULI ( 114 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 113 FDA reports)
HEAD DISCOMFORT ( 113 FDA reports)
BREAST CANCER IN SITU ( 112 FDA reports)
VEIN DISORDER ( 112 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 112 FDA reports)
BLOOD POTASSIUM INCREASED ( 111 FDA reports)
DENTAL CARIES ( 111 FDA reports)
FOOT DEFORMITY ( 111 FDA reports)
MENTAL STATUS CHANGES ( 111 FDA reports)
MULTI-ORGAN FAILURE ( 111 FDA reports)
SWOLLEN TONGUE ( 111 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 110 FDA reports)
MALNUTRITION ( 110 FDA reports)
THINKING ABNORMAL ( 110 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 109 FDA reports)
BRONCHOPNEUMONIA ( 109 FDA reports)
HALLUCINATION ( 109 FDA reports)
HEMIPARESIS ( 109 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 109 FDA reports)
BLADDER DISORDER ( 108 FDA reports)
CEREBRAL INFARCTION ( 108 FDA reports)
MALIGNANT MELANOMA ( 108 FDA reports)
FOOT OPERATION ( 107 FDA reports)
HEART VALVE INCOMPETENCE ( 107 FDA reports)
METASTASES TO BONE ( 107 FDA reports)
PELVIC PAIN ( 107 FDA reports)
AGITATION ( 105 FDA reports)
OESOPHAGEAL DISORDER ( 105 FDA reports)
LUNG NEOPLASM ( 104 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 104 FDA reports)
TOOTH ABSCESS ( 104 FDA reports)
NEUROLOGICAL SYMPTOM ( 103 FDA reports)
UNDERDOSE ( 103 FDA reports)
DIPLOPIA ( 102 FDA reports)
SPINAL OPERATION ( 102 FDA reports)
TOOTH INFECTION ( 102 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 101 FDA reports)
MULTIPLE ALLERGIES ( 101 FDA reports)
PIGMENTATION DISORDER ( 101 FDA reports)
CARDIOMEGALY ( 100 FDA reports)
MENTAL DISORDER ( 100 FDA reports)
EYE HAEMORRHAGE ( 99 FDA reports)
FUNGAL INFECTION ( 99 FDA reports)
HAEMOPTYSIS ( 99 FDA reports)
THYROID NEOPLASM ( 99 FDA reports)
RASH ERYTHEMATOUS ( 98 FDA reports)
SENSORY LOSS ( 98 FDA reports)
COLD SWEAT ( 97 FDA reports)
JOINT SPRAIN ( 97 FDA reports)
MUSCLE INJURY ( 97 FDA reports)
PARALYSIS ( 97 FDA reports)
SECRETION DISCHARGE ( 97 FDA reports)
SPINAL DEFORMITY ( 97 FDA reports)
ULCER HAEMORRHAGE ( 97 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 96 FDA reports)
CATHETERISATION CARDIAC ( 96 FDA reports)
INCOHERENT ( 96 FDA reports)
SCIATIC NERVE INJURY ( 96 FDA reports)
LIMB OPERATION ( 95 FDA reports)
SKIN EXFOLIATION ( 95 FDA reports)
PANCREATIC CARCINOMA ( 94 FDA reports)
DEVICE ISSUE ( 93 FDA reports)
EYE SWELLING ( 93 FDA reports)
INGUINAL HERNIA ( 93 FDA reports)
TOOTH EXTRACTION ( 93 FDA reports)
VASCULAR INJURY ( 93 FDA reports)
VASCULAR OCCLUSION ( 93 FDA reports)
WHEEZING ( 92 FDA reports)
CHEST WALL PAIN ( 92 FDA reports)
COORDINATION ABNORMAL ( 92 FDA reports)
EAR INFECTION ( 92 FDA reports)
EYELID DISORDER ( 92 FDA reports)
GENERALISED OEDEMA ( 92 FDA reports)
GINGIVAL PAIN ( 92 FDA reports)
HYPERLIPIDAEMIA ( 92 FDA reports)
MUSCLE TWITCHING ( 92 FDA reports)
DEAFNESS ( 91 FDA reports)
DRY EYE ( 91 FDA reports)
EMOTIONAL DISORDER ( 91 FDA reports)
INCREASED APPETITE ( 91 FDA reports)
TOOTHACHE ( 90 FDA reports)
VISUAL FIELD DEFECT ( 90 FDA reports)
CROHN'S DISEASE ( 89 FDA reports)
DEVICE MALFUNCTION ( 89 FDA reports)
ERUCTATION ( 89 FDA reports)
ABDOMINAL PAIN LOWER ( 88 FDA reports)
CALCIUM DEFICIENCY ( 88 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 88 FDA reports)
ISCHAEMIC STROKE ( 88 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 88 FDA reports)
PALLOR ( 88 FDA reports)
PHARYNGEAL OEDEMA ( 88 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 88 FDA reports)
APPENDICITIS ( 87 FDA reports)
DRUG INTOLERANCE ( 87 FDA reports)
KYPHOSIS ( 87 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 87 FDA reports)
RASH GENERALISED ( 87 FDA reports)
UTERINE CANCER ( 87 FDA reports)
VARICOSE VEIN ( 87 FDA reports)
VENOUS INJURY ( 86 FDA reports)
ARTERIOSCLEROSIS ( 86 FDA reports)
EAR DISCOMFORT ( 86 FDA reports)
HAEMATOCRIT DECREASED ( 86 FDA reports)
OEDEMA ( 86 FDA reports)
OSTEITIS DEFORMANS ( 86 FDA reports)
PLEURISY ( 86 FDA reports)
RENAL FAILURE CHRONIC ( 86 FDA reports)
SUICIDAL IDEATION ( 86 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 85 FDA reports)
COLITIS ULCERATIVE ( 85 FDA reports)
INCREASED TENDENCY TO BRUISE ( 85 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 85 FDA reports)
PYELONEPHRITIS ( 85 FDA reports)
SINUS CONGESTION ( 85 FDA reports)
SUBDURAL HAEMATOMA ( 85 FDA reports)
TENDON DISORDER ( 85 FDA reports)
ANGER ( 84 FDA reports)
EAR DISORDER ( 84 FDA reports)
HAEMATEMESIS ( 84 FDA reports)
ORTHOSTATIC HYPOTENSION ( 84 FDA reports)
POOR QUALITY SLEEP ( 84 FDA reports)
ACCIDENTAL NEEDLE STICK ( 83 FDA reports)
ACNE ( 83 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 83 FDA reports)
BLOOD UREA INCREASED ( 83 FDA reports)
ESCHERICHIA INFECTION ( 83 FDA reports)
FEELING JITTERY ( 83 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 83 FDA reports)
INTRACRANIAL ANEURYSM ( 83 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 83 FDA reports)
HYPERGLYCAEMIA ( 82 FDA reports)
METASTATIC NEOPLASM ( 82 FDA reports)
PERICARDIAL EFFUSION ( 82 FDA reports)
RESPIRATORY DISTRESS ( 82 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 81 FDA reports)
CHOLECYSTITIS ( 81 FDA reports)
PHLEBITIS ( 81 FDA reports)
HYPOXIA ( 80 FDA reports)
SKELETAL INJURY ( 80 FDA reports)
TEMPORAL ARTERITIS ( 80 FDA reports)
BLOOD COUNT ABNORMAL ( 79 FDA reports)
PERIPHERAL COLDNESS ( 79 FDA reports)
GOITRE ( 78 FDA reports)
STERNAL FRACTURE ( 78 FDA reports)
TENDON RUPTURE ( 78 FDA reports)
ANEURYSM ( 77 FDA reports)
HEPATITIS ( 77 FDA reports)
LACRIMATION INCREASED ( 77 FDA reports)
RESPIRATORY ARREST ( 77 FDA reports)
THROMBOCYTOPENIA ( 77 FDA reports)
GASTRIC HAEMORRHAGE ( 76 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 76 FDA reports)
POLYP ( 76 FDA reports)
SLEEP APNOEA SYNDROME ( 76 FDA reports)
TENDERNESS ( 76 FDA reports)
WOUND INFECTION ( 76 FDA reports)
WOUND DRAINAGE ( 75 FDA reports)
BONE EROSION ( 75 FDA reports)
BONE OPERATION ( 75 FDA reports)
BRADYCARDIA ( 75 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 75 FDA reports)
OPEN WOUND ( 75 FDA reports)
PULMONARY CONGESTION ( 75 FDA reports)
RESPIRATORY TRACT CONGESTION ( 75 FDA reports)
ACUTE RESPIRATORY FAILURE ( 74 FDA reports)
APHAGIA ( 74 FDA reports)
DRY THROAT ( 74 FDA reports)
ECZEMA ( 74 FDA reports)
FAECAL INCONTINENCE ( 74 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 74 FDA reports)
HYSTERECTOMY ( 74 FDA reports)
INCONTINENCE ( 74 FDA reports)
PLATELET COUNT INCREASED ( 73 FDA reports)
RENAL PAIN ( 73 FDA reports)
CREPITATIONS ( 72 FDA reports)
METASTASES TO LIVER ( 72 FDA reports)
POST PROCEDURAL INFECTION ( 72 FDA reports)
PUBIS FRACTURE ( 72 FDA reports)
SPONDYLOLISTHESIS ( 72 FDA reports)
LOCAL SWELLING ( 71 FDA reports)
MULTIPLE SCLEROSIS ( 71 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 71 FDA reports)
COLONIC POLYP ( 70 FDA reports)
MENISCUS LESION ( 70 FDA reports)
OPTIC ATROPHY ( 70 FDA reports)
RASH PAPULAR ( 70 FDA reports)
TRANSFUSION ( 70 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 70 FDA reports)
ABNORMAL SENSATION IN EYE ( 69 FDA reports)
DELIRIUM ( 69 FDA reports)
ECCHYMOSIS ( 69 FDA reports)
ENTEROCOCCAL INFECTION ( 69 FDA reports)
INCISION SITE COMPLICATION ( 69 FDA reports)
OEDEMA MOUTH ( 69 FDA reports)
PANCREATIC DISORDER ( 69 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 69 FDA reports)
SUDDEN DEATH ( 69 FDA reports)
THERMAL BURN ( 69 FDA reports)
APPETITE DISORDER ( 68 FDA reports)
DRUG ADMINISTRATION ERROR ( 68 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 68 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 68 FDA reports)
LIGAMENT INJURY ( 68 FDA reports)
LOWER EXTREMITY MASS ( 68 FDA reports)
LYMPH NODE PAIN ( 68 FDA reports)
MYOCARDIAL ISCHAEMIA ( 68 FDA reports)
SKIN LESION ( 68 FDA reports)
SKIN MASS ( 68 FDA reports)
TENDONITIS ( 68 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 68 FDA reports)
WOUND SECRETION ( 68 FDA reports)
VIITH NERVE PARALYSIS ( 67 FDA reports)
WOUND HAEMORRHAGE ( 67 FDA reports)
ASPIRATION ( 67 FDA reports)
CHONDROPATHY ( 67 FDA reports)
DECUBITUS ULCER ( 67 FDA reports)
HYPOTONIA ( 67 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 66 FDA reports)
CAROTID ARTERY STENOSIS ( 66 FDA reports)
COLONOSCOPY ( 66 FDA reports)
PANIC REACTION ( 66 FDA reports)
RESTLESSNESS ( 66 FDA reports)
UTERINE LEIOMYOMA ( 66 FDA reports)
ABDOMINAL HERNIA ( 65 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 65 FDA reports)
FAECES HARD ( 65 FDA reports)
GRAND MAL CONVULSION ( 65 FDA reports)
PNEUMOTHORAX ( 65 FDA reports)
BRAIN NEOPLASM ( 64 FDA reports)
FEEDING DISORDER ( 64 FDA reports)
AORTIC STENOSIS ( 63 FDA reports)
BREAST CALCIFICATIONS ( 63 FDA reports)
HERNIA REPAIR ( 63 FDA reports)
INJECTION SITE EXTRAVASATION ( 63 FDA reports)
INJECTION SITE STREAKING ( 63 FDA reports)
INTERSTITIAL LUNG DISEASE ( 63 FDA reports)
NON-CARDIAC CHEST PAIN ( 63 FDA reports)
RADICULOPATHY ( 63 FDA reports)
RETINAL HAEMORRHAGE ( 63 FDA reports)
STRESS CARDIOMYOPATHY ( 63 FDA reports)
WEGENER'S GRANULOMATOSIS ( 63 FDA reports)
ABNORMAL DREAMS ( 62 FDA reports)
APPENDICECTOMY ( 62 FDA reports)
CARDIAC FLUTTER ( 62 FDA reports)
SCLERODERMA ( 62 FDA reports)
ARTHROPOD BITE ( 61 FDA reports)
GINGIVAL SWELLING ( 61 FDA reports)
HEPATIC CIRRHOSIS ( 61 FDA reports)
SENSATION OF PRESSURE ( 61 FDA reports)
SLUGGISHNESS ( 61 FDA reports)
THROMBOPHLEBITIS ( 61 FDA reports)
ATELECTASIS ( 60 FDA reports)
DERMAL CYST ( 60 FDA reports)
GASTRIC CANCER ( 60 FDA reports)
JAUNDICE ( 60 FDA reports)
LIMB DEFORMITY ( 60 FDA reports)
MOTOR DYSFUNCTION ( 60 FDA reports)
THROAT TIGHTNESS ( 60 FDA reports)
AGGRESSION ( 59 FDA reports)
ARTERIAL DISORDER ( 59 FDA reports)
AXILLARY PAIN ( 59 FDA reports)
CHROMATURIA ( 59 FDA reports)
FEAR OF FALLING ( 59 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 59 FDA reports)
HEART RATE ABNORMAL ( 59 FDA reports)
INJECTION SITE WARMTH ( 59 FDA reports)
MEDICAL DEVICE REMOVAL ( 59 FDA reports)
OVARIAN CANCER ( 59 FDA reports)
PHARYNGITIS ( 59 FDA reports)
POLYMYALGIA RHEUMATICA ( 59 FDA reports)
POOR PERIPHERAL CIRCULATION ( 59 FDA reports)
SCOTOMA ( 59 FDA reports)
VASCULITIS ( 59 FDA reports)
CARDIO-RESPIRATORY ARREST ( 58 FDA reports)
CYSTOCELE ( 58 FDA reports)
ENDODONTIC PROCEDURE ( 58 FDA reports)
FAILURE TO THRIVE ( 58 FDA reports)
HEMIPLEGIA ( 58 FDA reports)
LOOSE TOOTH ( 58 FDA reports)
LUMBAR HERNIA ( 58 FDA reports)
OESOPHAGEAL STENOSIS ( 58 FDA reports)
RHINITIS ( 58 FDA reports)
SEDATION ( 58 FDA reports)
TENDON INJURY ( 58 FDA reports)
BONE NEOPLASM MALIGNANT ( 57 FDA reports)
HYPERKALAEMIA ( 57 FDA reports)
IMMUNE SYSTEM DISORDER ( 57 FDA reports)
IRON DEFICIENCY ANAEMIA ( 57 FDA reports)
NECROSIS ( 57 FDA reports)
OCULAR HYPERAEMIA ( 57 FDA reports)
PUBIC RAMI FRACTURE ( 57 FDA reports)
RECTAL PROLAPSE ( 57 FDA reports)
RESPIRATORY RATE DECREASED ( 57 FDA reports)
APATHY ( 56 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 56 FDA reports)
BRONCHIECTASIS ( 56 FDA reports)
BUNION ( 56 FDA reports)
COAGULOPATHY ( 56 FDA reports)
EYE OPERATION ( 56 FDA reports)
FRACTURE DELAYED UNION ( 56 FDA reports)
FRACTURED COCCYX ( 56 FDA reports)
HYPERCHOLESTEROLAEMIA ( 56 FDA reports)
JOINT ARTHROPLASTY ( 56 FDA reports)
LEUKAEMIA ( 56 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 56 FDA reports)
MOUTH ULCERATION ( 56 FDA reports)
ORAL INTAKE REDUCED ( 56 FDA reports)
PULMONARY THROMBOSIS ( 56 FDA reports)
RAYNAUD'S PHENOMENON ( 56 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 56 FDA reports)
THROAT CANCER ( 56 FDA reports)
AORTIC VALVE INCOMPETENCE ( 55 FDA reports)
COLLAPSE OF LUNG ( 55 FDA reports)
EPILEPSY ( 55 FDA reports)
HYPERTHYROIDISM ( 55 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 55 FDA reports)
INFECTED CYST ( 55 FDA reports)
RETINAL DISORDER ( 55 FDA reports)
URINARY TRACT OBSTRUCTION ( 55 FDA reports)
URINE ABNORMALITY ( 55 FDA reports)
BILE DUCT OBSTRUCTION ( 54 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 54 FDA reports)
BONE FRAGMENTATION ( 54 FDA reports)
BREAST SWELLING ( 54 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 54 FDA reports)
EYE IRRITATION ( 54 FDA reports)
FRUSTRATION ( 54 FDA reports)
HICCUPS ( 54 FDA reports)
HYPERPARATHYROIDISM ( 54 FDA reports)
LACUNAR INFARCTION ( 54 FDA reports)
LIMB ASYMMETRY ( 54 FDA reports)
OBSTRUCTION ( 54 FDA reports)
PRODUCT QUALITY ISSUE ( 54 FDA reports)
SHOULDER PAIN ( 54 FDA reports)
BUTTOCK PAIN ( 53 FDA reports)
CORONARY ARTERY BYPASS ( 53 FDA reports)
FACIAL PAIN ( 53 FDA reports)
LOSS OF CONTROL OF LEGS ( 53 FDA reports)
PAIN EXACERBATED ( 53 FDA reports)
PAPILLOEDEMA ( 53 FDA reports)
PERIODONTAL DISEASE ( 53 FDA reports)
PERONEAL NERVE PALSY ( 53 FDA reports)
BLOOD CALCIUM ABNORMAL ( 52 FDA reports)
BONE DENSITY ABNORMAL ( 52 FDA reports)
BONE FORMATION INCREASED ( 52 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 52 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 52 FDA reports)
HYPOAESTHESIA ORAL ( 52 FDA reports)
LIGAMENT RUPTURE ( 52 FDA reports)
MYELODYSPLASTIC SYNDROME ( 52 FDA reports)
NECK INJURY ( 52 FDA reports)
UNEVALUABLE EVENT ( 52 FDA reports)
UTERINE DISORDER ( 52 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 51 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 51 FDA reports)
GLOSSODYNIA ( 51 FDA reports)
HAIR GROWTH ABNORMAL ( 51 FDA reports)
HEPATIC FAILURE ( 51 FDA reports)
INTENTIONAL OVERDOSE ( 51 FDA reports)
MELAENA ( 51 FDA reports)
MITRAL VALVE PROLAPSE ( 51 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 51 FDA reports)
SKIN REACTION ( 51 FDA reports)
SPINAL PAIN ( 51 FDA reports)
WHEELCHAIR USER ( 51 FDA reports)
ADVERSE REACTION ( 50 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 50 FDA reports)
BONE MARROW DISORDER ( 50 FDA reports)
DERMATITIS ( 50 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 50 FDA reports)
FINGER DEFORMITY ( 50 FDA reports)
GINGIVITIS ( 50 FDA reports)
GRIP STRENGTH DECREASED ( 50 FDA reports)
MALABSORPTION ( 50 FDA reports)
MOUTH INJURY ( 50 FDA reports)
OLIGURIA ( 50 FDA reports)
OPTIC NERVE DISORDER ( 50 FDA reports)
SEPTIC SHOCK ( 50 FDA reports)
BLOOD URIC ACID INCREASED ( 49 FDA reports)
COLITIS ISCHAEMIC ( 49 FDA reports)
DYSGRAPHIA ( 49 FDA reports)
HAIR TEXTURE ABNORMAL ( 49 FDA reports)
HUNGER ( 49 FDA reports)
OVARIAN CYST ( 49 FDA reports)
PAIN OF SKIN ( 49 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 49 FDA reports)
SARCOMA ( 49 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 49 FDA reports)
TENSION ( 49 FDA reports)
VENOUS OCCLUSION ( 49 FDA reports)
WOUND COMPLICATION ( 49 FDA reports)
ANAESTHETIC COMPLICATION ( 48 FDA reports)
CARDIOMYOPATHY ( 48 FDA reports)
DRUG EFFECT DECREASED ( 48 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 48 FDA reports)
HEPATIC STEATOSIS ( 48 FDA reports)
HYPERTENSIVE CRISIS ( 48 FDA reports)
IMMOBILE ( 48 FDA reports)
JAW FRACTURE ( 48 FDA reports)
METASTASES TO SPINE ( 48 FDA reports)
OSTEOPOROTIC FRACTURE ( 48 FDA reports)
RENAL NEOPLASM ( 48 FDA reports)
SKIN HAEMORRHAGE ( 48 FDA reports)
SPINAL LAMINECTOMY ( 48 FDA reports)
SPONDYLITIS ( 48 FDA reports)
SQUAMOUS CELL CARCINOMA ( 48 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 47 FDA reports)
BIPOLAR DISORDER ( 47 FDA reports)
BREAST TENDERNESS ( 47 FDA reports)
EXERCISE TOLERANCE DECREASED ( 47 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 47 FDA reports)
INJECTION SITE DYSAESTHESIA ( 47 FDA reports)
INNER EAR DISORDER ( 47 FDA reports)
OPEN FRACTURE ( 47 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 47 FDA reports)
PHOTOPHOBIA ( 47 FDA reports)
POSTOPERATIVE ADHESION ( 47 FDA reports)
SHOULDER OPERATION ( 47 FDA reports)
ADRENAL INSUFFICIENCY ( 46 FDA reports)
APTYALISM ( 46 FDA reports)
ASCITES ( 46 FDA reports)
AUTOIMMUNE DISORDER ( 46 FDA reports)
CARTILAGE INJURY ( 46 FDA reports)
DISEASE RECURRENCE ( 46 FDA reports)
INTESTINAL PERFORATION ( 46 FDA reports)
LARGE INTESTINE PERFORATION ( 46 FDA reports)
LISTLESS ( 46 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 46 FDA reports)
MUSCLE FATIGUE ( 46 FDA reports)
OESOPHAGEAL PAIN ( 46 FDA reports)
ORTHOSIS USER ( 46 FDA reports)
PERIODONTITIS ( 46 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 46 FDA reports)
RETINAL TEAR ( 46 FDA reports)
SKIN ATROPHY ( 46 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 46 FDA reports)
UNDERWEIGHT ( 46 FDA reports)
UTERINE PROLAPSE ( 46 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 45 FDA reports)
CEREBRAL ISCHAEMIA ( 45 FDA reports)
EROSIVE OESOPHAGITIS ( 45 FDA reports)
FOOD POISONING ( 45 FDA reports)
GINGIVAL DISORDER ( 45 FDA reports)
INFARCTION ( 45 FDA reports)
METASTASES TO LYMPH NODES ( 45 FDA reports)
OSTEOLYSIS ( 45 FDA reports)
PETIT MAL EPILEPSY ( 45 FDA reports)
TOOTH LOSS ( 45 FDA reports)
BLINDNESS TRANSIENT ( 44 FDA reports)
BRADYPHRENIA ( 44 FDA reports)
BRONCHITIS CHRONIC ( 44 FDA reports)
CHOLECYSTITIS INFECTIVE ( 44 FDA reports)
GINGIVAL INFECTION ( 44 FDA reports)
HERPES SIMPLEX ( 44 FDA reports)
LUNG CANCER METASTATIC ( 44 FDA reports)
OESOPHAGITIS ( 44 FDA reports)
OSTEOCHONDROSIS ( 44 FDA reports)
PANCREATITIS ACUTE ( 44 FDA reports)
PERITONITIS ( 44 FDA reports)
POLYDIPSIA ( 44 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 44 FDA reports)
AORTIC CALCIFICATION ( 43 FDA reports)
CEREBRAL THROMBOSIS ( 43 FDA reports)
CIRCULATORY COLLAPSE ( 43 FDA reports)
COLONIC OBSTRUCTION ( 43 FDA reports)
EYELID PTOSIS ( 43 FDA reports)
GENERAL SYMPTOM ( 43 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 43 FDA reports)
INJECTION SITE INDURATION ( 43 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 43 FDA reports)
INVESTIGATION ( 43 FDA reports)
LIMB CRUSHING INJURY ( 43 FDA reports)
MONOPLEGIA ( 43 FDA reports)
NOSOCOMIAL INFECTION ( 43 FDA reports)
SKIN SWELLING ( 43 FDA reports)
TERMINAL STATE ( 43 FDA reports)
ACUTE PULMONARY OEDEMA ( 42 FDA reports)
CEREBROVASCULAR DISORDER ( 42 FDA reports)
CERUMEN IMPACTION ( 42 FDA reports)
DENTAL OPERATION ( 42 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 42 FDA reports)
DUODENAL ULCER ( 42 FDA reports)
HEPATITIS C ( 42 FDA reports)
IMPAIRED DRIVING ABILITY ( 42 FDA reports)
LIPOMA ( 42 FDA reports)
NOCTURIA ( 42 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 42 FDA reports)
SOFT TISSUE INJURY ( 42 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 41 FDA reports)
BODY TEMPERATURE DECREASED ( 41 FDA reports)
CARDIAC FIBRILLATION ( 41 FDA reports)
HAND DEFORMITY ( 41 FDA reports)
METASTASIS ( 41 FDA reports)
SPLENOMEGALY ( 41 FDA reports)
ULNA FRACTURE ( 41 FDA reports)
VENOUS INSUFFICIENCY ( 41 FDA reports)
ABSCESS ( 40 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 40 FDA reports)
DUODENITIS ( 40 FDA reports)
FLUID INTAKE REDUCED ( 40 FDA reports)
INITIAL INSOMNIA ( 40 FDA reports)
LOW TURNOVER OSTEOPATHY ( 40 FDA reports)
LUMBAR RADICULOPATHY ( 40 FDA reports)
NO THERAPEUTIC RESPONSE ( 40 FDA reports)
OSTEITIS ( 40 FDA reports)
PARATHYROID DISORDER ( 40 FDA reports)
PERSONALITY CHANGE ( 40 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 40 FDA reports)
RESORPTION BONE INCREASED ( 40 FDA reports)
SEROMA ( 40 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 40 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 39 FDA reports)
ARTHRITIS INFECTIVE ( 39 FDA reports)
BLADDER PAIN ( 39 FDA reports)
BLOOD BLISTER ( 39 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 39 FDA reports)
BRAIN INJURY ( 39 FDA reports)
LOCALISED OEDEMA ( 39 FDA reports)
ORAL DISORDER ( 39 FDA reports)
RETINAL DETACHMENT ( 39 FDA reports)
SKULL FRACTURE ( 39 FDA reports)
SPUTUM DISCOLOURED ( 39 FDA reports)
THERAPY NON-RESPONDER ( 39 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 39 FDA reports)
URINE ANALYSIS ABNORMAL ( 39 FDA reports)
ADDISON'S DISEASE ( 38 FDA reports)
BONE FISSURE ( 38 FDA reports)
CERVICAL SPINAL STENOSIS ( 38 FDA reports)
CYANOSIS ( 38 FDA reports)
DEAFNESS UNILATERAL ( 38 FDA reports)
DISEASE PROGRESSION ( 38 FDA reports)
HAIR COLOUR CHANGES ( 38 FDA reports)
ODYNOPHAGIA ( 38 FDA reports)
PARANOIA ( 38 FDA reports)
PNEUMONITIS ( 38 FDA reports)
PROSTATE CANCER METASTATIC ( 38 FDA reports)
PROSTATIC OPERATION ( 38 FDA reports)
PROTEIN TOTAL INCREASED ( 38 FDA reports)
PULSE ABNORMAL ( 38 FDA reports)
PULSE ABSENT ( 38 FDA reports)
SINUS TACHYCARDIA ( 38 FDA reports)
SJOGREN'S SYNDROME ( 38 FDA reports)
SKIN WRINKLING ( 38 FDA reports)
STRESS SYMPTOMS ( 38 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 38 FDA reports)
URINARY TRACT DISORDER ( 38 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 37 FDA reports)
EMBOLISM ( 37 FDA reports)
EYE INJURY ( 37 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 37 FDA reports)
INJECTION SITE INJURY ( 37 FDA reports)
OSTEOMALACIA ( 37 FDA reports)
PANIC ATTACK ( 37 FDA reports)
PHOTOPSIA ( 37 FDA reports)
POST PROCEDURAL OEDEMA ( 37 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 37 FDA reports)
RALES ( 37 FDA reports)
SOFT TISSUE DISORDER ( 37 FDA reports)
THYROIDECTOMY ( 37 FDA reports)
TRIGGER FINGER ( 37 FDA reports)
VITREOUS DETACHMENT ( 37 FDA reports)
ATRIOVENTRICULAR BLOCK ( 36 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 36 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 36 FDA reports)
BREAST CANCER METASTATIC ( 36 FDA reports)
DIPLEGIA ( 36 FDA reports)
EYELID FUNCTION DISORDER ( 36 FDA reports)
GASTROINTESTINAL PAIN ( 36 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 36 FDA reports)
HELICOBACTER INFECTION ( 36 FDA reports)
HYPERKERATOSIS ( 36 FDA reports)
PULMONARY MASS ( 36 FDA reports)
RENAL CANCER ( 36 FDA reports)
SUBCUTANEOUS NODULE ( 36 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 36 FDA reports)
URINE COLOUR ABNORMAL ( 36 FDA reports)
URINE OUTPUT INCREASED ( 36 FDA reports)
ABNORMAL FAECES ( 35 FDA reports)
AGEUSIA ( 35 FDA reports)
BONE GRAFT ( 35 FDA reports)
DERMATITIS CONTACT ( 35 FDA reports)
EYELID OEDEMA ( 35 FDA reports)
GASTROINTESTINAL CARCINOMA ( 35 FDA reports)
HYPOVOLAEMIA ( 35 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 35 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 35 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 35 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 35 FDA reports)
LEUKOCYTOSIS ( 35 FDA reports)
LUNG ADENOCARCINOMA ( 35 FDA reports)
LYMPHOEDEMA ( 35 FDA reports)
NEUROPATHY ( 35 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 35 FDA reports)
PROSTHESIS IMPLANTATION ( 35 FDA reports)
PULPITIS DENTAL ( 35 FDA reports)
URINE OUTPUT DECREASED ( 35 FDA reports)
BLOOD CHLORIDE DECREASED ( 34 FDA reports)
CENTRAL OBESITY ( 34 FDA reports)
DEVICE OCCLUSION ( 34 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 34 FDA reports)
GASTROINTESTINAL NECROSIS ( 34 FDA reports)
HYPOCALCAEMIA ( 34 FDA reports)
LEG AMPUTATION ( 34 FDA reports)
LOBAR PNEUMONIA ( 34 FDA reports)
METABOLIC DISORDER ( 34 FDA reports)
ORAL CANDIDIASIS ( 34 FDA reports)
ORAL HERPES ( 34 FDA reports)
POOR DENTAL CONDITION ( 34 FDA reports)
PSEUDOMONAS INFECTION ( 34 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 34 FDA reports)
RHINITIS ALLERGIC ( 34 FDA reports)
SENSITIVITY OF TEETH ( 34 FDA reports)
SHOCK ( 34 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 34 FDA reports)
STREPTOCOCCAL INFECTION ( 34 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 34 FDA reports)
THROMBOCYTOSIS ( 34 FDA reports)
TROPONIN INCREASED ( 34 FDA reports)
WEIGHT FLUCTUATION ( 34 FDA reports)
VASCULAR CALCIFICATION ( 33 FDA reports)
VULVOVAGINAL PAIN ( 33 FDA reports)
WOUND DEHISCENCE ( 33 FDA reports)
AORTIC VALVE DISEASE ( 33 FDA reports)
BONE DEBRIDEMENT ( 33 FDA reports)
BONE NEOPLASM ( 33 FDA reports)
CARDIAC ENZYMES INCREASED ( 33 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 33 FDA reports)
GROWING PAINS ( 33 FDA reports)
HAEMANGIOMA ( 33 FDA reports)
HEPATIC PAIN ( 33 FDA reports)
HYDRONEPHROSIS ( 33 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 33 FDA reports)
PAROSMIA ( 33 FDA reports)
PERICARDITIS ( 33 FDA reports)
PERIPHERAL NERVE OPERATION ( 33 FDA reports)
SALIVARY HYPERSECRETION ( 33 FDA reports)
SURGICAL PROCEDURE REPEATED ( 33 FDA reports)
SYNOVITIS ( 33 FDA reports)
TOE OPERATION ( 33 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 33 FDA reports)
TYPE 2 DIABETES MELLITUS ( 33 FDA reports)
BONE CYST ( 32 FDA reports)
COCCYDYNIA ( 32 FDA reports)
DEVICE COMPONENT ISSUE ( 32 FDA reports)
ENTERITIS ( 32 FDA reports)
EYE INFECTION ( 32 FDA reports)
FACE OEDEMA ( 32 FDA reports)
GINGIVAL RECESSION ( 32 FDA reports)
INJECTION SITE VESICLES ( 32 FDA reports)
LOOSE STOOLS ( 32 FDA reports)
MASTICATION DISORDER ( 32 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 32 FDA reports)
MOTION SICKNESS ( 32 FDA reports)
OESOPHAGEAL CARCINOMA ( 32 FDA reports)
ORAL DISCOMFORT ( 32 FDA reports)
REHABILITATION THERAPY ( 32 FDA reports)
SOFT TISSUE INFECTION ( 32 FDA reports)
TONGUE DISORDER ( 32 FDA reports)
VITAMIN D ABNORMAL ( 32 FDA reports)
VASODILATATION ( 31 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 31 FDA reports)
APPENDICITIS PERFORATED ( 31 FDA reports)
BIOPSY PROSTATE ( 31 FDA reports)
CACHEXIA ( 31 FDA reports)
COLECTOMY ( 31 FDA reports)
DELUSION ( 31 FDA reports)
EYE LASER SURGERY ( 31 FDA reports)
EYE MOVEMENT DISORDER ( 31 FDA reports)
FACIAL NEURALGIA ( 31 FDA reports)
FOOD CRAVING ( 31 FDA reports)
GINGIVAL BLEEDING ( 31 FDA reports)
HYDROCEPHALUS ( 31 FDA reports)
HYPERTHERMIA ( 31 FDA reports)
MOOD ALTERED ( 31 FDA reports)
MUSCLE RIGIDITY ( 31 FDA reports)
NONSPECIFIC REACTION ( 31 FDA reports)
ORAL FUNGAL INFECTION ( 31 FDA reports)
ORAL INFECTION ( 31 FDA reports)
POLYURIA ( 31 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 31 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 31 FDA reports)
PRESCRIBED OVERDOSE ( 31 FDA reports)
PURULENCE ( 31 FDA reports)
RENAL COLIC ( 31 FDA reports)
SICK SINUS SYNDROME ( 31 FDA reports)
SPINAL CLAUDICATION ( 31 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 31 FDA reports)
THERAPEUTIC PROCEDURE ( 31 FDA reports)
UROSEPSIS ( 31 FDA reports)
UTERINE ENLARGEMENT ( 31 FDA reports)
ASPHYXIA ( 30 FDA reports)
CALCULUS URINARY ( 30 FDA reports)
DIALYSIS ( 30 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 30 FDA reports)
FACIAL PALSY ( 30 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 30 FDA reports)
HAEMORRHAGIC STROKE ( 30 FDA reports)
HYPERAESTHESIA ( 30 FDA reports)
INCORRECT PRODUCT STORAGE ( 30 FDA reports)
LIVER INJURY ( 30 FDA reports)
MELANOCYTIC NAEVUS ( 30 FDA reports)
NIGHT CRAMPS ( 30 FDA reports)
PROCTALGIA ( 30 FDA reports)
SPINAL CORD COMPRESSION ( 30 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 30 FDA reports)
THYROID CANCER ( 30 FDA reports)
VASCULAR GRAFT ( 30 FDA reports)
X-RAY ABNORMAL ( 29 FDA reports)
ABDOMINAL ADHESIONS ( 29 FDA reports)
ACUTE STRESS DISORDER ( 29 FDA reports)
AORTIC VALVE REPLACEMENT ( 29 FDA reports)
AORTIC VALVE STENOSIS ( 29 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 29 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 29 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 29 FDA reports)
CHEMOTHERAPY ( 29 FDA reports)
DIVERTICULUM INTESTINAL ( 29 FDA reports)
FORMICATION ( 29 FDA reports)
HYPERCAPNIA ( 29 FDA reports)
HYPOAESTHESIA EYE ( 29 FDA reports)
HYPOAESTHESIA FACIAL ( 29 FDA reports)
MALOCCLUSION ( 29 FDA reports)
MECHANICAL VENTILATION ( 29 FDA reports)
PRODUCT TASTE ABNORMAL ( 29 FDA reports)
RECTOCELE ( 29 FDA reports)
RENAL TUBULAR DISORDER ( 29 FDA reports)
TYPE 1 DIABETES MELLITUS ( 29 FDA reports)
ABDOMINAL TENDERNESS ( 28 FDA reports)
ADENOCARCINOMA ( 28 FDA reports)
ANAEMIA POSTOPERATIVE ( 28 FDA reports)
BONE SCAN ABNORMAL ( 28 FDA reports)
BREAST CANCER STAGE I ( 28 FDA reports)
EYE DISCHARGE ( 28 FDA reports)
FAECALOMA ( 28 FDA reports)
HAEMOGLOBIN ABNORMAL ( 28 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 28 FDA reports)
LATEX ALLERGY ( 28 FDA reports)
LUNG INFILTRATION ( 28 FDA reports)
METASTASES TO LUNG ( 28 FDA reports)
NEUROMA ( 28 FDA reports)
PELVIC MASS ( 28 FDA reports)
POLYARTHRITIS ( 28 FDA reports)
PROTEIN URINE PRESENT ( 28 FDA reports)
SCAPULA FRACTURE ( 28 FDA reports)
SCAR EXCISION ( 28 FDA reports)
SKIN BURNING SENSATION ( 28 FDA reports)
SKIN DISCOMFORT ( 28 FDA reports)
SKIN IRRITATION ( 28 FDA reports)
UTERINE HAEMORRHAGE ( 28 FDA reports)
VITAMIN D INCREASED ( 28 FDA reports)
VITAMIN B12 DEFICIENCY ( 27 FDA reports)
ACUTE CORONARY SYNDROME ( 27 FDA reports)
BLOOD ALBUMIN DECREASED ( 27 FDA reports)
BREAST CANCER RECURRENT ( 27 FDA reports)
BREAST DISCOMFORT ( 27 FDA reports)
CALCULUS URETERIC ( 27 FDA reports)
CANDIDIASIS ( 27 FDA reports)
COLLAGEN DISORDER ( 27 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 27 FDA reports)
DENTAL CARE ( 27 FDA reports)
ERYSIPELAS ( 27 FDA reports)
GASTRIC DILATATION ( 27 FDA reports)
HEPATIC ENZYME ABNORMAL ( 27 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 27 FDA reports)
HYPOTRICHOSIS ( 27 FDA reports)
INJECTION SITE SCAB ( 27 FDA reports)
MYASTHENIA GRAVIS ( 27 FDA reports)
ONYCHOMADESIS ( 27 FDA reports)
PEPTIC ULCER ( 27 FDA reports)
PERIARTHRITIS ( 27 FDA reports)
URETHRAL CARBUNCLE ( 27 FDA reports)
URINE CALCIUM INCREASED ( 27 FDA reports)
UTERINE POLYP ( 27 FDA reports)
ABDOMINAL RIGIDITY ( 26 FDA reports)
ABDOMINAL WALL DISORDER ( 26 FDA reports)
ANGIOEDEMA ( 26 FDA reports)
BLADDER OPERATION ( 26 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 26 FDA reports)
BONE LOSS ( 26 FDA reports)
BREAST DISORDER ( 26 FDA reports)
BREAST ENLARGEMENT ( 26 FDA reports)
BRONCHOSPASM ( 26 FDA reports)
CARDIOGENIC SHOCK ( 26 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 26 FDA reports)
COLON ADENOMA ( 26 FDA reports)
COLON OPERATION ( 26 FDA reports)
CREST SYNDROME ( 26 FDA reports)
DEFORMITY ( 26 FDA reports)
EJECTION FRACTION DECREASED ( 26 FDA reports)
EYE PRURITUS ( 26 FDA reports)
FLUID OVERLOAD ( 26 FDA reports)
FOOD AVERSION ( 26 FDA reports)
HYDROMETRA ( 26 FDA reports)
HYPOVITAMINOSIS ( 26 FDA reports)
IMMUNODEFICIENCY ( 26 FDA reports)
INJECTION SITE DERMATITIS ( 26 FDA reports)
ITCHING SCAR ( 26 FDA reports)
MOUTH HAEMORRHAGE ( 26 FDA reports)
OCULAR DISCOMFORT ( 26 FDA reports)
OESOPHAGEAL SPASM ( 26 FDA reports)
OESOPHAGEAL ULCER ( 26 FDA reports)
POST-TRAUMATIC PAIN ( 26 FDA reports)
PSORIASIS ( 26 FDA reports)
PSYCHOTIC DISORDER ( 26 FDA reports)
RENAL MASS ( 26 FDA reports)
SENSATION OF FOREIGN BODY ( 26 FDA reports)
SYNCOPE VASOVAGAL ( 26 FDA reports)
VEIN PAIN ( 26 FDA reports)
VENTRICULAR HYPERTROPHY ( 26 FDA reports)
VOMITING PROJECTILE ( 26 FDA reports)
WEIGHT GAIN POOR ( 26 FDA reports)
VOCAL CORD DISORDER ( 25 FDA reports)
ABDOMINAL INFECTION ( 25 FDA reports)
APPENDIX DISORDER ( 25 FDA reports)
ASEPTIC NECROSIS BONE ( 25 FDA reports)
BLADDER NEOPLASM ( 25 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 25 FDA reports)
CARDIOPULMONARY FAILURE ( 25 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 25 FDA reports)
DUODENAL ULCER PERFORATION ( 25 FDA reports)
FIBROSIS ( 25 FDA reports)
FOREARM FRACTURE ( 25 FDA reports)
FULL BLOOD COUNT DECREASED ( 25 FDA reports)
HERNIA HIATUS REPAIR ( 25 FDA reports)
HOSPICE CARE ( 25 FDA reports)
ILEUS ( 25 FDA reports)
INTESTINAL POLYP ( 25 FDA reports)
INTESTINAL RESECTION ( 25 FDA reports)
MAMMOGRAM ABNORMAL ( 25 FDA reports)
NEGATIVE THOUGHTS ( 25 FDA reports)
NEOPLASM SKIN ( 25 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 25 FDA reports)
PROTHROMBIN TIME PROLONGED ( 25 FDA reports)
SINUS HEADACHE ( 25 FDA reports)
VAGINAL DISCHARGE ( 25 FDA reports)
ALCOHOL INTOLERANCE ( 24 FDA reports)
AMMONIA ( 24 FDA reports)
ANDROGENS ABNORMAL ( 24 FDA reports)
ANHEDONIA ( 24 FDA reports)
ANKLE OPERATION ( 24 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 24 FDA reports)
ATAXIA ( 24 FDA reports)
ATROPHY ( 24 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 24 FDA reports)
BONE LESION ( 24 FDA reports)
BONE SARCOMA ( 24 FDA reports)
CHEILITIS ( 24 FDA reports)
CHRONIC SINUSITIS ( 24 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 24 FDA reports)
DECREASED INTEREST ( 24 FDA reports)
DYSPHEMIA ( 24 FDA reports)
ECONOMIC PROBLEM ( 24 FDA reports)
FOOD INTOLERANCE ( 24 FDA reports)
GLOSSITIS ( 24 FDA reports)
INJECTION SITE COLDNESS ( 24 FDA reports)
JOINT ADHESION ( 24 FDA reports)
LACTOSE INTOLERANCE ( 24 FDA reports)
LIP SWELLING ( 24 FDA reports)
PHARYNGEAL DISORDER ( 24 FDA reports)
PROSTATOMEGALY ( 24 FDA reports)
RASH PUSTULAR ( 24 FDA reports)
SYNOVIAL CYST ( 24 FDA reports)
THYROID CYST ( 24 FDA reports)
URINE FLOW DECREASED ( 24 FDA reports)
ADENOCARCINOMA PANCREAS ( 23 FDA reports)
ATRIAL FLUTTER ( 23 FDA reports)
BRAIN SCAN ABNORMAL ( 23 FDA reports)
CEREBRAL ATROPHY ( 23 FDA reports)
CHEST INJURY ( 23 FDA reports)
DIVERTICULAR PERFORATION ( 23 FDA reports)
DRUG DISPENSING ERROR ( 23 FDA reports)
FAMILY STRESS ( 23 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 23 FDA reports)
HAIR DISORDER ( 23 FDA reports)
HEART VALVE CALCIFICATION ( 23 FDA reports)
HYPERTROPHY BREAST ( 23 FDA reports)
IATROGENIC INJURY ( 23 FDA reports)
IMMUNOSUPPRESSION ( 23 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 23 FDA reports)
IRON DEFICIENCY ( 23 FDA reports)
LEUKOPENIA ( 23 FDA reports)
MONOPARESIS ( 23 FDA reports)
SCAN BONE MARROW ABNORMAL ( 23 FDA reports)
URETHRAL DISORDER ( 23 FDA reports)
URINARY BLADDER POLYP ( 23 FDA reports)
VOCAL CORD PARALYSIS ( 23 FDA reports)
VARICELLA ( 22 FDA reports)
WAGNER'S DISEASE ( 22 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 22 FDA reports)
BLOOD URINE ( 22 FDA reports)
BRONCHIAL DISORDER ( 22 FDA reports)
CALCULUS BLADDER ( 22 FDA reports)
CARDIAC STRESS TEST ( 22 FDA reports)
CORNEAL DISORDER ( 22 FDA reports)
CORONARY ARTERY STENOSIS ( 22 FDA reports)
EAR CONGESTION ( 22 FDA reports)
ENDOCRINE DISORDER ( 22 FDA reports)
GANGRENE ( 22 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 22 FDA reports)
INCISIONAL HERNIA ( 22 FDA reports)
INTESTINAL ISCHAEMIA ( 22 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 22 FDA reports)
LYMPHADENECTOMY ( 22 FDA reports)
MITRAL VALVE DISEASE ( 22 FDA reports)
MUSCLE RUPTURE ( 22 FDA reports)
NO ADVERSE DRUG EFFECT ( 22 FDA reports)
OTITIS EXTERNA ( 22 FDA reports)
POST PROCEDURAL HAEMATOMA ( 22 FDA reports)
POST PROCEDURAL PAIN ( 22 FDA reports)
PYODERMA GANGRENOSUM ( 22 FDA reports)
RETINAL INJURY ( 22 FDA reports)
SEASONAL ALLERGY ( 22 FDA reports)
ADENOMA BENIGN ( 21 FDA reports)
AORTIC VALVE CALCIFICATION ( 21 FDA reports)
APHTHOUS STOMATITIS ( 21 FDA reports)
BENIGN NEOPLASM ( 21 FDA reports)
BREATH ODOUR ( 21 FDA reports)
BUNION OPERATION ( 21 FDA reports)
BURSA DISORDER ( 21 FDA reports)
CARBON DIOXIDE INCREASED ( 21 FDA reports)
COELIAC DISEASE ( 21 FDA reports)
COLON NEOPLASM ( 21 FDA reports)
COLOSTOMY ( 21 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 21 FDA reports)
DENTAL DISCOMFORT ( 21 FDA reports)
GASTRIC OPERATION ( 21 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 21 FDA reports)
LABILE BLOOD PRESSURE ( 21 FDA reports)
LIP DRY ( 21 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 21 FDA reports)
NARCOLEPSY ( 21 FDA reports)
OSTEOMYELITIS CHRONIC ( 21 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 21 FDA reports)
PANCREATIC CYST ( 21 FDA reports)
PLEURITIC PAIN ( 21 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 21 FDA reports)
RENAL CELL CARCINOMA ( 21 FDA reports)
ROTATOR CUFF REPAIR ( 21 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 21 FDA reports)
SIALOADENITIS ( 21 FDA reports)
SKIN INFECTION ( 21 FDA reports)
SKIN TIGHTNESS ( 21 FDA reports)
SUICIDE ATTEMPT ( 21 FDA reports)
TUBERCULOSIS ( 21 FDA reports)
VERTIGO POSITIONAL ( 21 FDA reports)
WEIGHT CONTROL ( 21 FDA reports)
WRIST SURGERY ( 21 FDA reports)
VASCULAR RUPTURE ( 20 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
ABDOMINAL OPERATION ( 20 FDA reports)
ANAPHYLACTIC REACTION ( 20 FDA reports)
ANGINA UNSTABLE ( 20 FDA reports)
ANOSMIA ( 20 FDA reports)
APNOEA ( 20 FDA reports)
ASTHMATIC CRISIS ( 20 FDA reports)
BILIARY COLIC ( 20 FDA reports)
BILIARY DILATATION ( 20 FDA reports)
BLOOD CULTURE POSITIVE ( 20 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 20 FDA reports)
BRAIN OEDEMA ( 20 FDA reports)
BURNS SECOND DEGREE ( 20 FDA reports)
CALCIUM IONISED INCREASED ( 20 FDA reports)
CHOKING SENSATION ( 20 FDA reports)
COSTOCHONDRITIS ( 20 FDA reports)
CULTURE URINE POSITIVE ( 20 FDA reports)
DERMATITIS ALLERGIC ( 20 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 20 FDA reports)
ENDOMETRIAL CANCER ( 20 FDA reports)
FEELING DRUNK ( 20 FDA reports)
GASTRIC INFECTION ( 20 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 20 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 20 FDA reports)
GASTROINTESTINAL ULCER ( 20 FDA reports)
HAEMOGLOBIN INCREASED ( 20 FDA reports)
HEPATIC CYST ( 20 FDA reports)
HYPERTRICHOSIS ( 20 FDA reports)
HYPOMAGNESAEMIA ( 20 FDA reports)
JOINT CONTRACTURE ( 20 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 20 FDA reports)
LIPASE INCREASED ( 20 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 20 FDA reports)
MAMMOPLASTY ( 20 FDA reports)
MENINGITIS ( 20 FDA reports)
NASAL DRYNESS ( 20 FDA reports)
NEUTROPENIA ( 20 FDA reports)
ONYCHOMYCOSIS ( 20 FDA reports)
RECTAL CANCER ( 20 FDA reports)
SINUS BRADYCARDIA ( 20 FDA reports)
SKIN NODULE ( 20 FDA reports)
SKIN ODOUR ABNORMAL ( 20 FDA reports)
SPIDER VEIN ( 20 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 20 FDA reports)
TONGUE DISCOLOURATION ( 20 FDA reports)
TRAUMATIC HAEMATOMA ( 20 FDA reports)
TREATMENT FAILURE ( 20 FDA reports)
ABDOMINAL MASS ( 19 FDA reports)
ABSCESS INTESTINAL ( 19 FDA reports)
ACUTE SINUSITIS ( 19 FDA reports)
ADHESION ( 19 FDA reports)
ANAL HAEMORRHAGE ( 19 FDA reports)
ASTHENOPIA ( 19 FDA reports)
ATRIAL SEPTAL DEFECT ( 19 FDA reports)
BLOOD AMYLASE INCREASED ( 19 FDA reports)
BONE MARROW FAILURE ( 19 FDA reports)
BONE MARROW OEDEMA ( 19 FDA reports)
CALCIPHYLAXIS ( 19 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 19 FDA reports)
CAROTID BRUIT ( 19 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 19 FDA reports)
CLUMSINESS ( 19 FDA reports)
COMMUNICATION DISORDER ( 19 FDA reports)
DISLOCATION OF VERTEBRA ( 19 FDA reports)
ENCEPHALOPATHY ( 19 FDA reports)
GRANULOMA ( 19 FDA reports)
HAEMORRHAGIC ANAEMIA ( 19 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 19 FDA reports)
INTESTINAL MASS ( 19 FDA reports)
JOINT INSTABILITY ( 19 FDA reports)
JOINT LOCK ( 19 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 19 FDA reports)
LARGE INTESTINAL ULCER ( 19 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 19 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 19 FDA reports)
MUCOSAL INFLAMMATION ( 19 FDA reports)
MYOSITIS ( 19 FDA reports)
NAIL GROWTH ABNORMAL ( 19 FDA reports)
NERVE BLOCK ( 19 FDA reports)
NEUTROPHIL COUNT INCREASED ( 19 FDA reports)
NIGHTMARE ( 19 FDA reports)
OESOPHAGEAL ACHALASIA ( 19 FDA reports)
PNEUMONIA BACTERIAL ( 19 FDA reports)
POLYP COLORECTAL ( 19 FDA reports)
RASH MACULO-PAPULAR ( 19 FDA reports)
SPINAL CORD INJURY ( 19 FDA reports)
SUFFOCATION FEELING ( 19 FDA reports)
URETHRAL ATROPHY ( 19 FDA reports)
URETHRAL OBSTRUCTION ( 19 FDA reports)
VAGUS NERVE DISORDER ( 19 FDA reports)
VENTRICULAR TACHYCARDIA ( 19 FDA reports)
WALKING DISABILITY ( 18 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 18 FDA reports)
ANGIOGRAM ( 18 FDA reports)
ANKYLOSING SPONDYLITIS ( 18 FDA reports)
BREAST INDURATION ( 18 FDA reports)
BREAST MICROCALCIFICATION ( 18 FDA reports)
BRONCHIAL CARCINOMA ( 18 FDA reports)
BRONCHITIS ACUTE ( 18 FDA reports)
BRONCHITIS VIRAL ( 18 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 18 FDA reports)
CAROTID ARTERY DISEASE ( 18 FDA reports)
COAGULATION TIME PROLONGED ( 18 FDA reports)
CORRECTIVE LENS USER ( 18 FDA reports)
CYSTOPEXY ( 18 FDA reports)
DARK CIRCLES UNDER EYES ( 18 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 18 FDA reports)
FEELING HOT AND COLD ( 18 FDA reports)
FEMORAL ARTERY OCCLUSION ( 18 FDA reports)
HALLUCINATION, AUDITORY ( 18 FDA reports)
HEPATIC ENCEPHALOPATHY ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
HERPES VIRUS INFECTION ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 18 FDA reports)
INTESTINAL HAEMORRHAGE ( 18 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 18 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 18 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 18 FDA reports)
LIGAMENT DISORDER ( 18 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 18 FDA reports)
NEOPLASM PROGRESSION ( 18 FDA reports)
NODULE ON EXTREMITY ( 18 FDA reports)
PANCREATIC NEOPLASM ( 18 FDA reports)
PROCEDURAL HAEMORRHAGE ( 18 FDA reports)
PROTEIN TOTAL DECREASED ( 18 FDA reports)
QUALITY OF LIFE DECREASED ( 18 FDA reports)
RENAL HAEMORRHAGE ( 18 FDA reports)
SKIN STRIAE ( 18 FDA reports)
SKIN WARM ( 18 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 18 FDA reports)
URINE PHOSPHATE INCREASED ( 18 FDA reports)
ACCIDENT AT HOME ( 17 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 17 FDA reports)
ANAPHYLACTIC SHOCK ( 17 FDA reports)
ANGIOPLASTY ( 17 FDA reports)
ANURIA ( 17 FDA reports)
ARTERITIS ( 17 FDA reports)
ARTHRITIS BACTERIAL ( 17 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 17 FDA reports)
ATROPHIC VULVOVAGINITIS ( 17 FDA reports)
BENIGN LUNG NEOPLASM ( 17 FDA reports)
BILE DUCT STONE ( 17 FDA reports)
BLADDER DISCOMFORT ( 17 FDA reports)
BRAIN CONTUSION ( 17 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 17 FDA reports)
CEMENTOPLASTY ( 17 FDA reports)
DIABETIC NEUROPATHY ( 17 FDA reports)
DIASTOLIC DYSFUNCTION ( 17 FDA reports)
ENCEPHALITIS ( 17 FDA reports)
ENDOTRACHEAL INTUBATION ( 17 FDA reports)
EYE REDNESS ( 17 FDA reports)
FAILURE OF IMPLANT ( 17 FDA reports)
FEAR OF NEEDLES ( 17 FDA reports)
FOREIGN BODY TRAUMA ( 17 FDA reports)
FRACTURE MALUNION ( 17 FDA reports)
GASTRIC PERFORATION ( 17 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 17 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 17 FDA reports)
HEPATIC NEOPLASM ( 17 FDA reports)
HOARSENESS ( 17 FDA reports)
ILIAC ARTERY OCCLUSION ( 17 FDA reports)
INCISION SITE HAEMORRHAGE ( 17 FDA reports)
INJECTION SITE INFLAMMATION ( 17 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 17 FDA reports)
JOINT DESTRUCTION ( 17 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 17 FDA reports)
NASAL ULCER ( 17 FDA reports)
NEOPLASM RECURRENCE ( 17 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 17 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 17 FDA reports)
PARTIAL SEIZURES ( 17 FDA reports)
PELVIC DISCOMFORT ( 17 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 17 FDA reports)
SKIN PAPILLOMA ( 17 FDA reports)
STOMACH MASS ( 17 FDA reports)
STRESS URINARY INCONTINENCE ( 17 FDA reports)
THERAPY CESSATION ( 17 FDA reports)
TRACHEOSTOMY ( 17 FDA reports)
VITAMIN A DEFICIENCY ( 17 FDA reports)
WEIGHT LOSS POOR ( 17 FDA reports)
VENTRICULAR FIBRILLATION ( 16 FDA reports)
VITAMIN C DEFICIENCY ( 16 FDA reports)
VOLVULUS ( 16 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 16 FDA reports)
ABSCESS LIMB ( 16 FDA reports)
ADRENAL DISORDER ( 16 FDA reports)
ANOREXIA NERVOSA ( 16 FDA reports)
AUTOIMMUNE THYROIDITIS ( 16 FDA reports)
CALCIUM METABOLISM DISORDER ( 16 FDA reports)
DRUG LEVEL INCREASED ( 16 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 16 FDA reports)
FOREIGN BODY ( 16 FDA reports)
GASTRIC PH DECREASED ( 16 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 16 FDA reports)
HAEMORRHAGE URINARY TRACT ( 16 FDA reports)
HYPERALDOSTERONISM ( 16 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 16 FDA reports)
IMPAIRED SELF-CARE ( 16 FDA reports)
KNEE DEFORMITY ( 16 FDA reports)
MACULAR HOLE ( 16 FDA reports)
NAIL BED BLEEDING ( 16 FDA reports)
NECK MASS ( 16 FDA reports)
NON-SMALL CELL LUNG CANCER ( 16 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 16 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 16 FDA reports)
ORGANISING PNEUMONIA ( 16 FDA reports)
PAINFUL RESPIRATION ( 16 FDA reports)
PERTUSSIS ( 16 FDA reports)
PLASMACYTOMA ( 16 FDA reports)
PNEUMONIA FUNGAL ( 16 FDA reports)
POLYMEDICATION ( 16 FDA reports)
POST POLIO SYNDROME ( 16 FDA reports)
POST PROCEDURAL DISCOMFORT ( 16 FDA reports)
PULMONARY HAEMORRHAGE ( 16 FDA reports)
RECTAL TENESMUS ( 16 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 16 FDA reports)
SPINAL CORD DISORDER ( 16 FDA reports)
UMBILICAL HERNIA ( 16 FDA reports)
URINARY TRACT PAIN ( 16 FDA reports)
ABSCESS ORAL ( 15 FDA reports)
ANIMAL SCRATCH ( 15 FDA reports)
APPARENT DEATH ( 15 FDA reports)
BIOPSY TONGUE ABNORMAL ( 15 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 15 FDA reports)
BRONCHIAL SECRETION RETENTION ( 15 FDA reports)
CALCIFICATION OF MUSCLE ( 15 FDA reports)
CARCINOID TUMOUR PULMONARY ( 15 FDA reports)
CATHETER RELATED INFECTION ( 15 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 15 FDA reports)
CHONDROSARCOMA ( 15 FDA reports)
COLITIS MICROSCOPIC ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
CRANIAL NERVE DISORDER ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
DERMATITIS EXFOLIATIVE ( 15 FDA reports)
DRUG LEVEL DECREASED ( 15 FDA reports)
DYSLEXIA ( 15 FDA reports)
DYSPNOEA EXACERBATED ( 15 FDA reports)
EMPYEMA ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
GASTRIC MUCOSAL LESION ( 15 FDA reports)
GASTRITIS EROSIVE ( 15 FDA reports)
GASTRODUODENITIS ( 15 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 15 FDA reports)
GINGIVAL ERYTHEMA ( 15 FDA reports)
GINGIVAL ULCERATION ( 15 FDA reports)
HEART VALVE REPLACEMENT ( 15 FDA reports)
HYPOMETABOLISM ( 15 FDA reports)
INCISION SITE PAIN ( 15 FDA reports)
INGUINAL HERNIA REPAIR ( 15 FDA reports)
INJECTION ( 15 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 15 FDA reports)
INTRACARDIAC THROMBUS ( 15 FDA reports)
JOINT WARMTH ( 15 FDA reports)
LIFE EXPECTANCY SHORTENED ( 15 FDA reports)
MENINGIOMA ( 15 FDA reports)
MOOD SWINGS ( 15 FDA reports)
MYCOSIS FUNGOIDES ( 15 FDA reports)
N-TELOPEPTIDE URINE INCREASED ( 15 FDA reports)
NAIL DISCOLOURATION ( 15 FDA reports)
OCULAR NEOPLASM ( 15 FDA reports)
ORAL SURGERY ( 15 FDA reports)
OSTEOTOMY ( 15 FDA reports)
PANCREATIC DUCT DILATATION ( 15 FDA reports)
PHARYNGEAL ERYTHEMA ( 15 FDA reports)
PHOTOSENSITIVITY REACTION ( 15 FDA reports)
PINEAL GLAND CYST ( 15 FDA reports)
PROCEDURAL NAUSEA ( 15 FDA reports)
SARCOIDOSIS ( 15 FDA reports)
SPONDYLOARTHROPATHY ( 15 FDA reports)
SURGICAL FAILURE ( 15 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 15 FDA reports)
VAGINAL INFECTION ( 15 FDA reports)
VERTEBRAL INJURY ( 15 FDA reports)
VERTEBRAL WEDGING ( 15 FDA reports)
VITAMIN B12 INCREASED ( 15 FDA reports)
WART EXCISION ( 15 FDA reports)
VARICOSE ULCERATION ( 14 FDA reports)
VENTRICULAR DYSFUNCTION ( 14 FDA reports)
VITREOUS FLOATERS ( 14 FDA reports)
ABDOMINAL NEOPLASM ( 14 FDA reports)
ACETABULUM FRACTURE ( 14 FDA reports)
ADENOMYOSIS ( 14 FDA reports)
AFFECT LABILITY ( 14 FDA reports)
ANIMAL BITE ( 14 FDA reports)
AORTIC DISSECTION ( 14 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 14 FDA reports)
BASEDOW'S DISEASE ( 14 FDA reports)
BIOPSY BONE ABNORMAL ( 14 FDA reports)
BLOOD BILIRUBIN INCREASED ( 14 FDA reports)
CARDIAC FAILURE CHRONIC ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
CHOLECYSTITIS ACUTE ( 14 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 14 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 14 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 14 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 14 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 14 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 14 FDA reports)
FRACTURE DISPLACEMENT ( 14 FDA reports)
HYPERVENTILATION ( 14 FDA reports)
HYPOTHERMIA ( 14 FDA reports)
HYPOVENTILATION ( 14 FDA reports)
ILEUS PARALYTIC ( 14 FDA reports)
ILIUM FRACTURE ( 14 FDA reports)
INFESTATION ( 14 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 14 FDA reports)
INTESTINAL INFARCTION ( 14 FDA reports)
LABYRINTHITIS ( 14 FDA reports)
LAZINESS ( 14 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 14 FDA reports)
METABOLIC ACIDOSIS ( 14 FDA reports)
MICTURITION DISORDER ( 14 FDA reports)
MITRAL VALVE CALCIFICATION ( 14 FDA reports)
MONONUCLEOSIS SYNDROME ( 14 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 14 FDA reports)
MUSCLE HAEMORRHAGE ( 14 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 14 FDA reports)
MYOCARDIAL RUPTURE ( 14 FDA reports)
MYOPATHY ( 14 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 14 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 14 FDA reports)
ONYCHORRHEXIS ( 14 FDA reports)
PARAESTHESIA ORAL ( 14 FDA reports)
PARATHYROID TUMOUR BENIGN ( 14 FDA reports)
POLYMYOSITIS ( 14 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 14 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
SKIN FRAGILITY ( 14 FDA reports)
SOMNAMBULISM ( 14 FDA reports)
SUTURE INSERTION ( 14 FDA reports)
TOE AMPUTATION ( 14 FDA reports)
TONGUE INJURY ( 14 FDA reports)
ACCIDENT AT WORK ( 13 FDA reports)
ADNEXA UTERI MASS ( 13 FDA reports)
ANION GAP INCREASED ( 13 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 13 FDA reports)
AORTIC DISORDER ( 13 FDA reports)
ARTERIAL GRAFT ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
BACTERAEMIA ( 13 FDA reports)
BARRETT'S OESOPHAGUS ( 13 FDA reports)
BED REST ( 13 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 13 FDA reports)
BLOOD SODIUM ABNORMAL ( 13 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 13 FDA reports)
BONE SWELLING ( 13 FDA reports)
BREAST CANCER STAGE II ( 13 FDA reports)
BRUXISM ( 13 FDA reports)
BURNOUT SYNDROME ( 13 FDA reports)
CATHETER RELATED COMPLICATION ( 13 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 13 FDA reports)
COLON CANCER METASTATIC ( 13 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 13 FDA reports)
CORNEAL ABRASION ( 13 FDA reports)
DEAFNESS TRANSITORY ( 13 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 13 FDA reports)
DROOLING ( 13 FDA reports)
EMBOLIC STROKE ( 13 FDA reports)
ENDOCARDITIS ( 13 FDA reports)
FAECES PALE ( 13 FDA reports)
GAMMOPATHY ( 13 FDA reports)
GASTRECTOMY ( 13 FDA reports)
HALLUCINATION, VISUAL ( 13 FDA reports)
HERNIAL EVENTRATION ( 13 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
INCISION SITE INFECTION ( 13 FDA reports)
INGROWING NAIL ( 13 FDA reports)
ISCHAEMIA ( 13 FDA reports)
KIDNEY MALROTATION ( 13 FDA reports)
LYME DISEASE ( 13 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 13 FDA reports)
MENIERE'S DISEASE ( 13 FDA reports)
MIGRAINE WITH AURA ( 13 FDA reports)
MONARTHRITIS ( 13 FDA reports)
NAIL PIGMENTATION ( 13 FDA reports)
NEURITIS ( 13 FDA reports)
NO ADVERSE EFFECT ( 13 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 13 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 13 FDA reports)
OXYGEN SUPPLEMENTATION ( 13 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 13 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 13 FDA reports)
POSTOPERATIVE INFECTION ( 13 FDA reports)
PROTEINURIA ( 13 FDA reports)
PSEUDARTHROSIS ( 13 FDA reports)
PSYCHIATRIC SYMPTOM ( 13 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 13 FDA reports)
RETINAL VEIN OCCLUSION ( 13 FDA reports)
RIB DEFORMITY ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
SEBORRHOEIC KERATOSIS ( 13 FDA reports)
STARING ( 13 FDA reports)
SUDDEN ONSET OF SLEEP ( 13 FDA reports)
SUTURE RELATED COMPLICATION ( 13 FDA reports)
TEMPERATURE INTOLERANCE ( 13 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 13 FDA reports)
TONSILLAR DISORDER ( 13 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 13 FDA reports)
TUMOUR MARKER INCREASED ( 13 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 13 FDA reports)
URINE CALCIUM DECREASED ( 13 FDA reports)
WHIPLASH INJURY ( 13 FDA reports)
VASCULAR INSUFFICIENCY ( 12 FDA reports)
VITAMIN B12 DECREASED ( 12 FDA reports)
ADRENAL MASS ( 12 FDA reports)
AMMONIA INCREASED ( 12 FDA reports)
ARTERIAL STENOSIS ( 12 FDA reports)
ARTERIAL STENT INSERTION ( 12 FDA reports)
AURA ( 12 FDA reports)
BILE DUCT CANCER ( 12 FDA reports)
BILIARY TRACT DISORDER ( 12 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 12 FDA reports)
BLOOD IRON INCREASED ( 12 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
CHAPPED LIPS ( 12 FDA reports)
CHONDROCALCINOSIS ( 12 FDA reports)
CORNEAL DYSTROPHY ( 12 FDA reports)
CORONARY ARTERY THROMBOSIS ( 12 FDA reports)
DEPENDENCE ( 12 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 12 FDA reports)
DRUG ABUSE ( 12 FDA reports)
ENCHONDROMA ( 12 FDA reports)
ENTROPION ( 12 FDA reports)
FIBROMA ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
GALLSTONE ILEUS ( 12 FDA reports)
GRIEF REACTION ( 12 FDA reports)
H1N1 INFLUENZA ( 12 FDA reports)
HAEMORRHOID OPERATION ( 12 FDA reports)
IMPAIRED WORK ABILITY ( 12 FDA reports)
INADEQUATE ANALGESIA ( 12 FDA reports)
INFECTED SKIN ULCER ( 12 FDA reports)
INFECTIOUS PERITONITIS ( 12 FDA reports)
INFUSION RELATED REACTION ( 12 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 12 FDA reports)
INTESTINAL OPERATION ( 12 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 12 FDA reports)
LIP PAIN ( 12 FDA reports)
LOWER LIMB DEFORMITY ( 12 FDA reports)
LUNG TRANSPLANT ( 12 FDA reports)
MACULOPATHY ( 12 FDA reports)
MASTECTOMY ( 12 FDA reports)
MEDICAL DEVICE CHANGE ( 12 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 12 FDA reports)
OPERATIVE HAEMORRHAGE ( 12 FDA reports)
ORAL TORUS ( 12 FDA reports)
OSTEOCALCIN INCREASED ( 12 FDA reports)
PANCREATIC INJURY ( 12 FDA reports)
PARAPARESIS ( 12 FDA reports)
PARATHYROID TUMOUR ( 12 FDA reports)
PERNICIOUS ANAEMIA ( 12 FDA reports)
PITTING OEDEMA ( 12 FDA reports)
POLYNEUROPATHY ( 12 FDA reports)
PULSE PRESSURE DECREASED ( 12 FDA reports)
PYURIA ( 12 FDA reports)
RECTAL SPASM ( 12 FDA reports)
RETINAL TOXICITY ( 12 FDA reports)
SHOULDER DEFORMITY ( 12 FDA reports)
SHUNT MALFUNCTION ( 12 FDA reports)
SPINAL ROD INSERTION ( 12 FDA reports)
SPLEEN DISORDER ( 12 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 12 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 12 FDA reports)
AMENORRHOEA ( 11 FDA reports)
ANORECTAL DISCOMFORT ( 11 FDA reports)
ARACHNOIDITIS ( 11 FDA reports)
B-CELL LYMPHOMA ( 11 FDA reports)
BENIGN BONE NEOPLASM ( 11 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 11 FDA reports)
BIOPSY BREAST ( 11 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 11 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 11 FDA reports)
CAROTID ARTERY ANEURYSM ( 11 FDA reports)
CEREBRAL HAEMATOMA ( 11 FDA reports)
CEREBRAL PALSY ( 11 FDA reports)
CERVIX CARCINOMA ( 11 FDA reports)
CHOLELITHOTOMY ( 11 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 11 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 11 FDA reports)
CORNEAL TRANSPLANT ( 11 FDA reports)
DIABETIC COMA ( 11 FDA reports)
DIABETIC RETINOPATHY ( 11 FDA reports)
DIET REFUSAL ( 11 FDA reports)
DILATATION ATRIAL ( 11 FDA reports)
DRUG LEVEL FLUCTUATING ( 11 FDA reports)
EAR HAEMORRHAGE ( 11 FDA reports)
ELECTROLYTE DEPLETION ( 11 FDA reports)
ENDOMETRIOSIS ( 11 FDA reports)
EXTRADURAL HAEMATOMA ( 11 FDA reports)
GALLBLADDER PAIN ( 11 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 11 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 11 FDA reports)
HEPATIC HAEMORRHAGE ( 11 FDA reports)
HORMONE LEVEL ABNORMAL ( 11 FDA reports)
ILEOSTOMY ( 11 FDA reports)
INJECTION SITE JOINT REDNESS ( 11 FDA reports)
JOINT HYPEREXTENSION ( 11 FDA reports)
KIDNEY ENLARGEMENT ( 11 FDA reports)
LORDOSIS ( 11 FDA reports)
MACULAR OEDEMA ( 11 FDA reports)
MEAN CELL VOLUME INCREASED ( 11 FDA reports)
MYOCLONUS ( 11 FDA reports)
NAIL INFECTION ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NERVE ROOT INJURY ( 11 FDA reports)
OPTIC NEURITIS ( 11 FDA reports)
PACEMAKER COMPLICATION ( 11 FDA reports)
PANCREATIC ENZYMES INCREASED ( 11 FDA reports)
PATELLA REPLACEMENT ( 11 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 11 FDA reports)
PIRIFORMIS SYNDROME ( 11 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 11 FDA reports)
PULSE PRESSURE INCREASED ( 11 FDA reports)
PUPILS UNEQUAL ( 11 FDA reports)
PURPURA ( 11 FDA reports)
RADIOTHERAPY ( 11 FDA reports)
RASH VESICULAR ( 11 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 11 FDA reports)
REFLUX OESOPHAGITIS ( 11 FDA reports)
RENAL ARTERY STENOSIS ( 11 FDA reports)
RENAL INJURY ( 11 FDA reports)
SKIN CHAPPED ( 11 FDA reports)
SUDDEN CARDIAC DEATH ( 11 FDA reports)
TEARFULNESS ( 11 FDA reports)
TERMINAL INSOMNIA ( 11 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 11 FDA reports)
TRANSAMINASES INCREASED ( 11 FDA reports)
TRANSPLANT ( 11 FDA reports)
URETERIC OBSTRUCTION ( 11 FDA reports)
VENOUS THROMBOSIS ( 11 FDA reports)
VULVAL CANCER ( 11 FDA reports)
VOCAL CORD NEOPLASM ( 10 FDA reports)
WHITE BLOOD CELL DISORDER ( 10 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 10 FDA reports)
WOUND CLOSURE ( 10 FDA reports)
ACCOMMODATION DISORDER ( 10 FDA reports)
ACTINIC KERATOSIS ( 10 FDA reports)
ANAEMIA MACROCYTIC ( 10 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 10 FDA reports)
ANAL CANCER ( 10 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
AORTIC ANEURYSM RUPTURE ( 10 FDA reports)
AORTIC RUPTURE ( 10 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 10 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 10 FDA reports)
BENIGN OVARIAN TUMOUR ( 10 FDA reports)
BILIARY NEOPLASM ( 10 FDA reports)
BIOPSY ( 10 FDA reports)
BIOPSY BLOOD VESSEL ( 10 FDA reports)
BLADDER DYSFUNCTION ( 10 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 10 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 10 FDA reports)
BOWEL SOUNDS ABNORMAL ( 10 FDA reports)
BRAIN HYPOXIA ( 10 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 10 FDA reports)
BREAST CYST ( 10 FDA reports)
BREAST NEOPLASM ( 10 FDA reports)
CLOSTRIDIUM COLITIS ( 10 FDA reports)
COITAL BLEEDING ( 10 FDA reports)
COMMINUTED FRACTURE ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
DERMATITIS ATOPIC ( 10 FDA reports)
DEVICE MIGRATION ( 10 FDA reports)
DIAPHRAGMATIC DISORDER ( 10 FDA reports)
ENCHONDROMATOSIS ( 10 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 10 FDA reports)
ENTEROCELE ( 10 FDA reports)
ESSENTIAL HYPERTENSION ( 10 FDA reports)
FISTULA ( 10 FDA reports)
FISTULA DISCHARGE ( 10 FDA reports)
FOAMING AT MOUTH ( 10 FDA reports)
FOREIGN BODY IN EYE ( 10 FDA reports)
GENITAL PRURITUS FEMALE ( 10 FDA reports)
HAEMOLYTIC ANAEMIA ( 10 FDA reports)
HEAT ILLNESS ( 10 FDA reports)
HIGH FREQUENCY ABLATION ( 10 FDA reports)
HYPERCALCIURIA ( 10 FDA reports)
HYPERURICAEMIA ( 10 FDA reports)
INFECTED BUNION ( 10 FDA reports)
INFUSION SITE PAIN ( 10 FDA reports)
INJECTION SITE HYPERTROPHY ( 10 FDA reports)
INJECTION SITE OEDEMA ( 10 FDA reports)
INTERMITTENT CLAUDICATION ( 10 FDA reports)
INTRAOCULAR MELANOMA ( 10 FDA reports)
JOINT SURGERY ( 10 FDA reports)
LARYNGEAL CANCER ( 10 FDA reports)
LEUKOPLAKIA ORAL ( 10 FDA reports)
LIMB IMMOBILISATION ( 10 FDA reports)
LIP NEOPLASM ( 10 FDA reports)
METRORRHAGIA ( 10 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 10 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 10 FDA reports)
NASAL DISCOMFORT ( 10 FDA reports)
NIGHT BLINDNESS ( 10 FDA reports)
NUCHAL RIGIDITY ( 10 FDA reports)
OROPHARYNGEAL SWELLING ( 10 FDA reports)
OVARIAN CANCER METASTATIC ( 10 FDA reports)
PANCREATITIS CHRONIC ( 10 FDA reports)
PARATHYROIDECTOMY ( 10 FDA reports)
PCO2 INCREASED ( 10 FDA reports)
PERFORATED ULCER ( 10 FDA reports)
POISONING ( 10 FDA reports)
POST LAMINECTOMY SYNDROME ( 10 FDA reports)
PROCEDURAL SITE REACTION ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 10 FDA reports)
RED BLOOD CELL ABNORMALITY ( 10 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 10 FDA reports)
RESPIRATION ABNORMAL ( 10 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 10 FDA reports)
SKIN NECROSIS ( 10 FDA reports)
SPINAL HAEMANGIOMA ( 10 FDA reports)
SPLINTER ( 10 FDA reports)
SPONDYLOLYSIS ( 10 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 10 FDA reports)
SUDDEN HEARING LOSS ( 10 FDA reports)
THROMBOSIS PROPHYLAXIS ( 10 FDA reports)
TONGUE COATED ( 10 FDA reports)
TONGUE OEDEMA ( 10 FDA reports)
UPPER EXTREMITY MASS ( 10 FDA reports)
URETHRAL PAIN ( 10 FDA reports)
ABDOMINAL WALL NEOPLASM ( 9 FDA reports)
ACUTE LEUKAEMIA ( 9 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ANION GAP DECREASED ( 9 FDA reports)
ARTHRODESIS ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
BACTERIAL DISEASE CARRIER ( 9 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BLEPHARITIS ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 9 FDA reports)
BLOOD SODIUM ( 9 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 9 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 9 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
CAUDA EQUINA SYNDROME ( 9 FDA reports)
CHANGE OF BOWEL HABIT ( 9 FDA reports)
CHEST CRUSHING ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 9 FDA reports)
COLON CANCER STAGE III ( 9 FDA reports)
CONJUNCTIVITIS VIRAL ( 9 FDA reports)
CONVERSION DISORDER ( 9 FDA reports)
CORNEAL DEGENERATION ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 9 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 9 FDA reports)
DRUG TOXICITY ( 9 FDA reports)
DURAL TEAR ( 9 FDA reports)
DYSPAREUNIA ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
EYE ALLERGY ( 9 FDA reports)
EYE ROLLING ( 9 FDA reports)
FIBRIN D DIMER INCREASED ( 9 FDA reports)
FROSTBITE ( 9 FDA reports)
FUNGAL SKIN INFECTION ( 9 FDA reports)
GENERALISED ERYTHEMA ( 9 FDA reports)
HAEMANGIOMA OF LIVER ( 9 FDA reports)
HEPATITIS B ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HERNIA PAIN ( 9 FDA reports)
HIRSUTISM ( 9 FDA reports)
HYPERCHLORHYDRIA ( 9 FDA reports)
HYPERTENSIVE HEART DISEASE ( 9 FDA reports)
IGA NEPHROPATHY ( 9 FDA reports)
INTERNAL HERNIA ( 9 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 9 FDA reports)
IODINE ALLERGY ( 9 FDA reports)
LASER THERAPY ( 9 FDA reports)
LENS DISORDER ( 9 FDA reports)
LIGAMENT LAXITY ( 9 FDA reports)
LIP HAEMORRHAGE ( 9 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 9 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
MYELOPATHY ( 9 FDA reports)
NAIL DISCOMFORT ( 9 FDA reports)
NEPHROPATHY ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 9 FDA reports)
NEUROLOGICAL INFECTION ( 9 FDA reports)
NEUTROPHIL COUNT DECREASED ( 9 FDA reports)
NIPPLE DISORDER ( 9 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 9 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 9 FDA reports)
OVARIAN ENLARGEMENT ( 9 FDA reports)
OXYGEN SATURATION INCREASED ( 9 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 9 FDA reports)
PANCREATIC MASS ( 9 FDA reports)
PERICARDITIS LUPUS ( 9 FDA reports)
PNEUMONIA KLEBSIELLA ( 9 FDA reports)
POLYCYTHAEMIA VERA ( 9 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 9 FDA reports)
RENAL ARTERY OCCLUSION ( 9 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 9 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 9 FDA reports)
SINUS ARRHYTHMIA ( 9 FDA reports)
SKIN HYPERTROPHY ( 9 FDA reports)
SMALL INTESTINE CARCINOMA ( 9 FDA reports)
SOFT TISSUE INFLAMMATION ( 9 FDA reports)
SPIDER NAEVUS ( 9 FDA reports)
SPINAL FUSION ACQUIRED ( 9 FDA reports)
SPLENIC ARTERY ANEURYSM ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
TETANY ( 9 FDA reports)
TOE DEFORMITY ( 9 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 9 FDA reports)
TRISMUS ( 9 FDA reports)
UNEQUAL LIMB LENGTH ( 9 FDA reports)
URETERIC CANCER ( 9 FDA reports)
VARICOPHLEBITIS ( 9 FDA reports)
WRONG DRUG ADMINISTERED ( 9 FDA reports)
VASCULAR ACCESS COMPLICATION ( 8 FDA reports)
VENOUS OPERATION ( 8 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 8 FDA reports)
VULVOVAGINAL DISCOMFORT ( 8 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 8 FDA reports)
WITHDRAWAL SYNDROME ( 8 FDA reports)
ACOUSTIC NEUROMA ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 8 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
AORTIC DILATATION ( 8 FDA reports)
ARTERIOSPASM CORONARY ( 8 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 8 FDA reports)
BENIGN NEOPLASM OF SKIN ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BLADDER CANCER RECURRENT ( 8 FDA reports)
BLADDER DILATATION ( 8 FDA reports)
BLADDER SPASM ( 8 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
BLEPHAROSPASM ( 8 FDA reports)
BLOOD CREATININE ABNORMAL ( 8 FDA reports)
BLOOD CREATININE DECREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BLOOD POTASSIUM ( 8 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 8 FDA reports)
BRAIN OPERATION ( 8 FDA reports)
BREATH SOUNDS ABNORMAL ( 8 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 8 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 8 FDA reports)
CAROTID ARTERY ATHEROMA ( 8 FDA reports)
CARTILAGE NEOPLASM ( 8 FDA reports)
CHONDROMA ( 8 FDA reports)
CRUSH INJURY ( 8 FDA reports)
DENTAL FISTULA ( 8 FDA reports)
DENTAL PLAQUE ( 8 FDA reports)
DEVICE DIFFICULT TO USE ( 8 FDA reports)
DIABETIC ULCER ( 8 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
EATING DISORDER SYMPTOM ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
EXTRASKELETAL OSSIFICATION ( 8 FDA reports)
EYE OPERATION COMPLICATION ( 8 FDA reports)
FAT TISSUE INCREASED ( 8 FDA reports)
GALLBLADDER ENLARGEMENT ( 8 FDA reports)
GALLBLADDER PERFORATION ( 8 FDA reports)
GASTRIC POLYPS ( 8 FDA reports)
GASTROINTESTINAL NEOPLASM ( 8 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 8 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 8 FDA reports)
GROIN ABSCESS ( 8 FDA reports)
HEPATIC INFECTION ( 8 FDA reports)
HEPATIC MASS ( 8 FDA reports)
HYPERTONIC BLADDER ( 8 FDA reports)
HYPERVITAMINOSIS ( 8 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 8 FDA reports)
INFLAMMATION OF WOUND ( 8 FDA reports)
INJECTION SITE PUSTULE ( 8 FDA reports)
INJECTION SITE ULCER ( 8 FDA reports)
INTESTINAL FISTULA ( 8 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 8 FDA reports)
JAW OPERATION ( 8 FDA reports)
JOINT FLUID DRAINAGE ( 8 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 8 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 8 FDA reports)
MEDICAL DEVICE PAIN ( 8 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
MONOCYTE COUNT INCREASED ( 8 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
NECK DEFORMITY ( 8 FDA reports)
NECK SURGERY ( 8 FDA reports)
NEPHRECTOMY ( 8 FDA reports)
NEUROPATHIC ARTHROPATHY ( 8 FDA reports)
NIPPLE PAIN ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
OCULAR VASCULAR DISORDER ( 8 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 8 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 8 FDA reports)
OESOPHAGEAL PERFORATION ( 8 FDA reports)
OESOPHAGEAL RUPTURE ( 8 FDA reports)
ONCOLOGIC COMPLICATION ( 8 FDA reports)
ORGAN FAILURE ( 8 FDA reports)
OSTEOSARCOMA LOCALISED ( 8 FDA reports)
PAPILLARY THYROID CANCER ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
PARVOVIRUS INFECTION ( 8 FDA reports)
PEMPHIGOID ( 8 FDA reports)
PERIORBITAL OEDEMA ( 8 FDA reports)
PHOTODERMATOSIS ( 8 FDA reports)
PILOERECTION ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
PLASMAPHERESIS ( 8 FDA reports)
POLIOMYELITIS ( 8 FDA reports)
POOR PERSONAL HYGIENE ( 8 FDA reports)
POSTNASAL DRIP ( 8 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 8 FDA reports)
PURULENT DISCHARGE ( 8 FDA reports)
RENAL SURGERY ( 8 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 8 FDA reports)
RETINAL ARTERY OCCLUSION ( 8 FDA reports)
SACROILIITIS ( 8 FDA reports)
SALIVARY GLAND CANCER ( 8 FDA reports)
SKIN FISSURES ( 8 FDA reports)
SPINAL CORD OPERATION ( 8 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 8 FDA reports)
STENT REMOVAL ( 8 FDA reports)
STRABISMUS ( 8 FDA reports)
THROAT LESION ( 8 FDA reports)
THYROID ADENOMA ( 8 FDA reports)
THYROID MASS ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TOOTH REPAIR ( 8 FDA reports)
TRACHEAL DISORDER ( 8 FDA reports)
TRACHEOBRONCHITIS ( 8 FDA reports)
TRANSPLANT REJECTION ( 8 FDA reports)
TRAUMATIC BRAIN INJURY ( 8 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 8 FDA reports)
URINARY HESITATION ( 8 FDA reports)
URINE CALCIUM ( 8 FDA reports)
VAGINAL CANCER ( 8 FDA reports)
ABSCESS JAW ( 7 FDA reports)
ACID BASE BALANCE ABNORMAL ( 7 FDA reports)
ALVEOLITIS ALLERGIC ( 7 FDA reports)
AMMONIA ABNORMAL ( 7 FDA reports)
AMPUTATION ( 7 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 7 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
AORTIC SURGERY ( 7 FDA reports)
APALLIC SYNDROME ( 7 FDA reports)
ARTERIAL BYPASS OPERATION ( 7 FDA reports)
ARTERIAL HAEMORRHAGE ( 7 FDA reports)
ARTERIAL STENOSIS LIMB ( 7 FDA reports)
ASTIGMATISM ( 7 FDA reports)
AVERSION ( 7 FDA reports)
BEHCET'S SYNDROME ( 7 FDA reports)
BLEPHAROPLASTY ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DIFFERENCE OF EXTREMITIES ( 7 FDA reports)
BREAKTHROUGH PAIN ( 7 FDA reports)
BREAST CANCER STAGE III ( 7 FDA reports)
BREAST CANCER STAGE IV ( 7 FDA reports)
BREAST INFECTION ( 7 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 7 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 7 FDA reports)
CERVICAL MYELOPATHY ( 7 FDA reports)
CHOLECYSTITIS CHRONIC ( 7 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 7 FDA reports)
COAGULATION TEST ABNORMAL ( 7 FDA reports)
CONDUCTION DISORDER ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 7 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
DAYDREAMING ( 7 FDA reports)
DENTAL TREATMENT ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
EARLY MORNING AWAKENING ( 7 FDA reports)
ERYTHEMA NODOSUM ( 7 FDA reports)
EXCITABILITY ( 7 FDA reports)
EXOPHTHALMOS ( 7 FDA reports)
EXTRAVASATION ( 7 FDA reports)
EYE INFLAMMATION ( 7 FDA reports)
EYE OEDEMA ( 7 FDA reports)
FACIAL ASYMMETRY ( 7 FDA reports)
GALLBLADDER CANCER ( 7 FDA reports)
GASTROINTESTINAL SURGERY ( 7 FDA reports)
GENITAL DISCOMFORT ( 7 FDA reports)
GENITAL INFECTION VIRAL ( 7 FDA reports)
GENITAL PAIN ( 7 FDA reports)
GINGIVAL INJURY ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
HAEMATOCRIT INCREASED ( 7 FDA reports)
HEART INJURY ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HERNIA OBSTRUCTIVE ( 7 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 7 FDA reports)
HORMONE THERAPY ( 7 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 7 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 7 FDA reports)
INTERVERTEBRAL DISC INJURY ( 7 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 7 FDA reports)
KERATITIS HERPETIC ( 7 FDA reports)
LIP DISORDER ( 7 FDA reports)
LIP ULCERATION ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 7 FDA reports)
LUNG INJURY ( 7 FDA reports)
LUNG OPERATION ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
LUPUS PNEUMONITIS ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 7 FDA reports)
MALLORY-WEISS SYNDROME ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 7 FDA reports)
MEDICAL DEVICE SITE REACTION ( 7 FDA reports)
MESENTERITIS ( 7 FDA reports)
METASTASES TO STOMACH ( 7 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 7 FDA reports)
MYCOBACTERIAL INFECTION ( 7 FDA reports)
MYELOFIBROSIS ( 7 FDA reports)
NEURILEMMOMA MALIGNANT ( 7 FDA reports)
OBESITY ( 7 FDA reports)
OESOPHAGEAL INFECTION ( 7 FDA reports)
OESOPHAGEAL INJURY ( 7 FDA reports)
OESOPHAGEAL OEDEMA ( 7 FDA reports)
OSTEOCHONDRITIS ( 7 FDA reports)
PAIN MANAGEMENT ( 7 FDA reports)
PAROTID GLAND ENLARGEMENT ( 7 FDA reports)
PERIORBITAL CELLULITIS ( 7 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 7 FDA reports)
PNEUMONIA VIRAL ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
POTENTIATING DRUG INTERACTION ( 7 FDA reports)
PROSTATIC DISORDER ( 7 FDA reports)
PSORIATIC ARTHROPATHY ( 7 FDA reports)
PULMONARY GRANULOMA ( 7 FDA reports)
PULMONARY TUBERCULOSIS ( 7 FDA reports)
RASH SCALY ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RETINAL VASCULAR DISORDER ( 7 FDA reports)
ROSACEA ( 7 FDA reports)
SCIATIC NERVE NEUROPATHY ( 7 FDA reports)
SEBORRHOEA ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SMALL INTESTINAL PERFORATION ( 7 FDA reports)
STENT OCCLUSION ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
THROMBOTIC STROKE ( 7 FDA reports)
TOOTH DISCOLOURATION ( 7 FDA reports)
TOXIC SHOCK SYNDROME ( 7 FDA reports)
TRAUMATIC LUNG INJURY ( 7 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 7 FDA reports)
VAGINAL BURNING SENSATION ( 7 FDA reports)
VAGINAL PROLAPSE ( 7 FDA reports)
VARICOSE VEIN OPERATION ( 7 FDA reports)
VASCULAR BYPASS GRAFT ( 7 FDA reports)
VASOCONSTRICTION ( 7 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 7 FDA reports)
VESTIBULAR NEURONITIS ( 7 FDA reports)
VIRAL PERICARDITIS ( 7 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 7 FDA reports)
YELLOW SKIN ( 7 FDA reports)
VASCULAR HEADACHE ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VOCAL CORD PARESIS ( 6 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 6 FDA reports)
WEST NILE VIRAL INFECTION ( 6 FDA reports)
WOUND TREATMENT ( 6 FDA reports)
ABDOMINAL ABSCESS ( 6 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 6 FDA reports)
ABSCESS NECK ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
ADRENAL NEOPLASM ( 6 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 6 FDA reports)
ANAL DISCOMFORT ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ANGIONEUROTIC OEDEMA ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 6 FDA reports)
ARTERIAL RUPTURE ( 6 FDA reports)
ARTERIAL SPASM ( 6 FDA reports)
ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
ARTHROFIBROSIS ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
ASTERIXIS ( 6 FDA reports)
AUTOIMMUNE HEPATITIS ( 6 FDA reports)
BENIGN BREAST NEOPLASM ( 6 FDA reports)
BIFASCICULAR BLOCK ( 6 FDA reports)
BLOOD CREATINE INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 6 FDA reports)
BLOOD VISCOSITY INCREASED ( 6 FDA reports)
BONE DENSITY INCREASED ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BRAIN STEM THROMBOSIS ( 6 FDA reports)
BREAST FIBROMA ( 6 FDA reports)
BREAST HYPERPLASIA ( 6 FDA reports)
BREAST INJURY ( 6 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 6 FDA reports)
CAPILLARY DISORDER ( 6 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 6 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 6 FDA reports)
CARDIAC ABLATION ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CAROTID SINUS MASSAGE ( 6 FDA reports)
CATHETER SITE HAEMATOMA ( 6 FDA reports)
CENTRAL LINE INFECTION ( 6 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 6 FDA reports)
CHRONIC LEUKAEMIA ( 6 FDA reports)
COLON CANCER RECURRENT ( 6 FDA reports)
COLON CANCER STAGE I ( 6 FDA reports)
COLON CANCER STAGE II ( 6 FDA reports)
COMPLEX PARTIAL SEIZURES ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 6 FDA reports)
CREATININE URINE INCREASED ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
CYSTITIS ESCHERICHIA ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DEPRESSIVE SYMPTOM ( 6 FDA reports)
DEVICE LEAD DAMAGE ( 6 FDA reports)
DUODENAL PERFORATION ( 6 FDA reports)
DUODENAL STENOSIS ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 6 FDA reports)
ENCEPHALOMALACIA ( 6 FDA reports)
ENDOMETRIAL CANCER STAGE IV ( 6 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 6 FDA reports)
EPICONDYLITIS ( 6 FDA reports)
EPIDURAL ANAESTHESIA ( 6 FDA reports)
EPIGASTRIC DISCOMFORT ( 6 FDA reports)
EXERCISE LACK OF ( 6 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 6 FDA reports)
FAECAL VOLUME INCREASED ( 6 FDA reports)
FEMORAL HERNIA ( 6 FDA reports)
FOOD ALLERGY ( 6 FDA reports)
FUNGAL OESOPHAGITIS ( 6 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
GASTROINTESTINAL PERFORATION ( 6 FDA reports)
GASTROSTOMY TUBE INSERTION ( 6 FDA reports)
GINGIVAL BLISTER ( 6 FDA reports)
GRAFT HAEMORRHAGE ( 6 FDA reports)
HAEMATOMA INFECTION ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HEAT RASH ( 6 FDA reports)
HEAT STROKE ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HEPATITIS VIRAL ( 6 FDA reports)
HILAR LYMPHADENOPATHY ( 6 FDA reports)
HYPOGEUSIA ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
INFLAMMATORY MARKER INCREASED ( 6 FDA reports)
INJECTION SITE PARAESTHESIA ( 6 FDA reports)
INJECTION SITE SCAR ( 6 FDA reports)
INTESTINAL DILATATION ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 6 FDA reports)
LARYNGEAL POLYP ( 6 FDA reports)
LEFT VENTRICULAR FAILURE ( 6 FDA reports)
LIMB SALVAGE THERAPY ( 6 FDA reports)
LIP INJURY ( 6 FDA reports)
LUPUS NEPHRITIS ( 6 FDA reports)
MACROCYTOSIS ( 6 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 6 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
MENSTRUAL DISORDER ( 6 FDA reports)
METABOLIC ENCEPHALOPATHY ( 6 FDA reports)
METASTASES TO PLEURA ( 6 FDA reports)
METASTATIC CARCINOID TUMOUR ( 6 FDA reports)
MULTIMORBIDITY ( 6 FDA reports)
NASAL POLYPS ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
OPTIC NERVE INJURY ( 6 FDA reports)
ORTHOPNOEA ( 6 FDA reports)
OVERWEIGHT ( 6 FDA reports)
PAINFUL DEFAECATION ( 6 FDA reports)
PATHOGEN RESISTANCE ( 6 FDA reports)
PEDAL PULSE DECREASED ( 6 FDA reports)
PELVIC FLOOR REPAIR ( 6 FDA reports)
PERITONITIS BACTERIAL ( 6 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 6 FDA reports)
PLEURAL FIBROSIS ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
PRECANCEROUS CELLS PRESENT ( 6 FDA reports)
PRIMITIVE NEUROECTODERMAL TUMOUR ( 6 FDA reports)
PROTEIN TOTAL ABNORMAL ( 6 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 6 FDA reports)
QUADRIPLEGIA ( 6 FDA reports)
RADIAL NERVE INJURY ( 6 FDA reports)
RADIATION SKIN INJURY ( 6 FDA reports)
RADICULAR PAIN ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
RECURRENT CANCER ( 6 FDA reports)
REGURGITATION ( 6 FDA reports)
RENAL ANEURYSM ( 6 FDA reports)
RENAL TRANSPLANT ( 6 FDA reports)
RETINAL DEGENERATION ( 6 FDA reports)
RETINITIS ( 6 FDA reports)
SALMONELLOSIS ( 6 FDA reports)
SCAR PAIN ( 6 FDA reports)
SELF-MEDICATION ( 6 FDA reports)
SENILE DEMENTIA ( 6 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 6 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 6 FDA reports)
SPINAL CORD INJURY CERVICAL ( 6 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
THIRST DECREASED ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
THROMBOSIS IN DEVICE ( 6 FDA reports)
THYROID GLAND CANCER ( 6 FDA reports)
TRANSFUSION REACTION ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRIGEMINAL NEURALGIA ( 6 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
URETHRAL STENOSIS ( 6 FDA reports)
UTERINE MASS ( 6 FDA reports)
VACCINATION COMPLICATION ( 6 FDA reports)
VAGINAL DISORDER ( 6 FDA reports)
ABDOMINAL INJURY ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
ALCOHOLISM ( 5 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 5 FDA reports)
ALLERGY TO ARTHROPOD STING ( 5 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 5 FDA reports)
ANEURYSM REPAIR ( 5 FDA reports)
ANEURYSM RUPTURED ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 5 FDA reports)
AORTIC ATHEROSCLEROSIS ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
ARACHNOID CYST ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
ARTERIAL THROMBOSIS ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ARTICULAR CALCIFICATION ( 5 FDA reports)
ASPIRATION BRONCHIAL ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
ATROPHY OF GLOBE ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BACTERIAL TEST POSITIVE ( 5 FDA reports)
BACTERIURIA ( 5 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BILIARY CIRRHOSIS ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BITE ( 5 FDA reports)
BLADDER MASS ( 5 FDA reports)
BLEEDING TIME PROLONGED ( 5 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 5 FDA reports)
BLOOD CALCIUM ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BODY FAT DISORDER ( 5 FDA reports)
BURN INFECTION ( 5 FDA reports)
BUTTERFLY RASH ( 5 FDA reports)
CAPILLARY FRAGILITY ( 5 FDA reports)
CARCINOMA IN SITU ( 5 FDA reports)
CARDIAC ANEURYSM ( 5 FDA reports)
CARDIAC DEATH ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CATARACT NUCLEAR ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 5 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 5 FDA reports)
COLONIC HAEMORRHAGE ( 5 FDA reports)
COLONOSCOPY ABNORMAL ( 5 FDA reports)
COLOSTOMY CLOSURE ( 5 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 5 FDA reports)
CORNEAL DEPOSITS ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CROUP INFECTIOUS ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DIALYSIS DEVICE INSERTION ( 5 FDA reports)
DISEASE COMPLICATION ( 5 FDA reports)
DYSKINESIA OESOPHAGEAL ( 5 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 5 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 5 FDA reports)
EPENDYMOMA BENIGN ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER OBSTRUCTION ( 5 FDA reports)
GALLBLADDER OEDEMA ( 5 FDA reports)
GASTRIC BYPASS ( 5 FDA reports)
GASTRIC VOLVULUS ( 5 FDA reports)
GASTROENTERITIS NOROVIRUS ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
GINGIVAL DISCOLOURATION ( 5 FDA reports)
GLIOBLASTOMA MULTIFORME ( 5 FDA reports)
GLOBAL AMNESIA ( 5 FDA reports)
HEMIANOPIA ( 5 FDA reports)
HEPATIC VEIN OCCLUSION ( 5 FDA reports)
HIV TEST POSITIVE ( 5 FDA reports)
HODGKIN'S DISEASE ( 5 FDA reports)
HYPERMETROPIA ( 5 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERREFLEXIA ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOCHROMIC ANAEMIA ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
IMMUNOGLOBULINS DECREASED ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFLAMMATION LOCALISED ( 5 FDA reports)
INFUSION ( 5 FDA reports)
INFUSION SITE BRUISING ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INFUSION SITE EXTRAVASATION ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
INVESTIGATION ABNORMAL ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
KERATITIS ( 5 FDA reports)
LABILE HYPERTENSION ( 5 FDA reports)
LEIOMYOMA ( 5 FDA reports)
LESION EXCISION ( 5 FDA reports)
LEUKOARAIOSIS ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LIGAMENT PAIN ( 5 FDA reports)
LIGAMENTITIS ( 5 FDA reports)
LIP AND/OR ORAL CAVITY CANCER RECURRENT ( 5 FDA reports)
LIPOHYPERTROPHY ( 5 FDA reports)
LIVER TRANSPLANT REJECTION ( 5 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 5 FDA reports)
MASTOIDITIS ( 5 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 5 FDA reports)
MESENTERIC OCCLUSION ( 5 FDA reports)
METASTASES TO ADRENALS ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MIDDLE EAR EFFUSION ( 5 FDA reports)
MITRAL VALVE REPAIR ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
NAIL INJURY ( 5 FDA reports)
NECROTISING COLITIS ( 5 FDA reports)
NEEDLE ISSUE ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
NEUTROPHIL COUNT ( 5 FDA reports)
NO ADVERSE DRUG REACTION ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
NODAL OSTEOARTHRITIS ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 5 FDA reports)
OBSTRUCTION GASTRIC ( 5 FDA reports)
OBSTRUCTIVE UROPATHY ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
OESOPHAGEAL DILATATION ( 5 FDA reports)
ORTHOSTATIC HYPERTENSION ( 5 FDA reports)
OSTEOMA ( 5 FDA reports)
OVARIAN EPITHELIAL CANCER ( 5 FDA reports)
OVARIAN NEOPLASM ( 5 FDA reports)
PANCREATIC CALCIFICATION ( 5 FDA reports)
PANCREATOLITHIASIS ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PANNICULITIS LOBULAR ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PARKINSONIAN CRISIS ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
PHAEOCHROMOCYTOMA ( 5 FDA reports)
PHOBIA ( 5 FDA reports)
PHYSICAL DISABILITY ( 5 FDA reports)
PNEUMONECTOMY ( 5 FDA reports)
POOR VENOUS ACCESS ( 5 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
PRURITUS GENITAL ( 5 FDA reports)
PSEUDOCYST ( 5 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
PYELONEPHRITIS ACUTE ( 5 FDA reports)
RADICULITIS ( 5 FDA reports)
RADICULITIS LUMBOSACRAL ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
READING DISORDER ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 5 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 5 FDA reports)
REMOVAL OF INERT MATTER FROM SKIN OR SUBCUTANEOUS TISSUE ( 5 FDA reports)
RENAL CANCER METASTATIC ( 5 FDA reports)
RENAL STONE REMOVAL ( 5 FDA reports)
RETINAL OEDEMA ( 5 FDA reports)
SACRAL PAIN ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SKIN DEGENERATIVE DISORDER ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
SMALL INTESTINE OPERATION ( 5 FDA reports)
SMOKER ( 5 FDA reports)
SPASMODIC DYSPHONIA ( 5 FDA reports)
SPINAL CORD NEOPLASM ( 5 FDA reports)
SPINAL DECOMPRESSION ( 5 FDA reports)
SPLENIC INJURY ( 5 FDA reports)
STRIDOR ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
THERAPY REGIMEN CHANGED ( 5 FDA reports)
THERMOANAESTHESIA ( 5 FDA reports)
TONGUE ERUPTION ( 5 FDA reports)
TONGUE NEOPLASM ( 5 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 5 FDA reports)
TRAUMATIC ARTHROPATHY ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
URETHRAL DILATATION ( 5 FDA reports)
URETHRAL PROLAPSE ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
UTERINE OPERATION ( 5 FDA reports)
VAGINAL ERYTHEMA ( 5 FDA reports)
VASCULAR OPERATION ( 5 FDA reports)
VOLUME BLOOD DECREASED ( 5 FDA reports)
WHOLE BLOOD TRANSFUSION ( 5 FDA reports)
WRIST DEFORMITY ( 5 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 5 FDA reports)
VASCULAR DEMENTIA ( 4 FDA reports)
VASCULAR PSEUDOANEURYSM ( 4 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 4 FDA reports)
VESTIBULAR DISORDER ( 4 FDA reports)
VOLVULUS OF BOWEL ( 4 FDA reports)
ABDOMINAL HAEMATOMA ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ACCIDENTAL DEATH ( 4 FDA reports)
ADNEXA UTERI PAIN ( 4 FDA reports)
ADRENAL CYST ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANOXIA ( 4 FDA reports)
AORTIC VALVE REPAIR ( 4 FDA reports)
APPLICATION SITE ODOUR ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
AXILLARY MASS ( 4 FDA reports)
AXILLARY VEIN THROMBOSIS ( 4 FDA reports)
BARTHOLIN'S CYST ( 4 FDA reports)
BENIGN NEOPLASM OF EYELID ( 4 FDA reports)
BENIGN RENAL NEOPLASM ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 4 FDA reports)
BODY DYSMORPHIC DISORDER ( 4 FDA reports)
BONE FORMATION DECREASED ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BREAST HAEMORRHAGE ( 4 FDA reports)
CALLUS FORMATION DELAYED ( 4 FDA reports)
CARCINOMA IN SITU OF EYE ( 4 FDA reports)
CARDIAC MYXOMA ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CAST APPLICATION ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CHONDROMALACIA ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 4 FDA reports)
COAGULATION TIME SHORTENED ( 4 FDA reports)
COLORECTAL CANCER ( 4 FDA reports)
COLORECTAL CANCER METASTATIC ( 4 FDA reports)
COMPLICATED FRACTURE ( 4 FDA reports)
COMPLICATED MIGRAINE ( 4 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 4 FDA reports)
CORNEAL PERFORATION ( 4 FDA reports)
CORONARY ARTERY ANEURYSM ( 4 FDA reports)
CORONARY ARTERY DISSECTION ( 4 FDA reports)
CORONARY ARTERY SURGERY ( 4 FDA reports)
CRANIOPLASTY ( 4 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 4 FDA reports)
CRYSTAL URINE PRESENT ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CYSTITIS BACTERIAL ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 4 FDA reports)
DENTAL NECROSIS ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMATOFIBROSARCOMA ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DUODENAL POLYP ( 4 FDA reports)
DYSENTERY ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
EFFUSION ( 4 FDA reports)
ELBOW OPERATION ( 4 FDA reports)
EMBOLISM ARTERIAL ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 4 FDA reports)
ENDOMETRIAL DISORDER ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EUSTACHIAN TUBE DISORDER ( 4 FDA reports)
EVANS SYNDROME ( 4 FDA reports)
EVENTRATION PROCEDURE ( 4 FDA reports)
EXPLORATORY OPERATION ( 4 FDA reports)
EYE DEGENERATIVE DISORDER ( 4 FDA reports)
EYELID MARGIN CRUSTING ( 4 FDA reports)
FACIAL SPASM ( 4 FDA reports)
FAECALURIA ( 4 FDA reports)
FALLOPIAN TUBE CANCER ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FLUID IMBALANCE ( 4 FDA reports)
FOOT AMPUTATION ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FRACTURE PAIN ( 4 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 4 FDA reports)
GANGLION ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTRIC NEOPLASM ( 4 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 4 FDA reports)
GENITAL BURNING SENSATION ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
GINGIVAL EROSION ( 4 FDA reports)
GLOBULINS INCREASED ( 4 FDA reports)
GOUTY ARTHRITIS ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HANGNAIL ( 4 FDA reports)
HANGOVER ( 4 FDA reports)
HEART TRANSPLANT ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEPATIC ARTERY ANEURYSM ( 4 FDA reports)
HEPATIC ARTERY OCCLUSION ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HORNER'S SYNDROME ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 4 FDA reports)
IMPAIRED FASTING GLUCOSE ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INJECTION SITE ANAESTHESIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 4 FDA reports)
INTESTINAL ATRESIA ( 4 FDA reports)
INTESTINAL STRANGULATION ( 4 FDA reports)
INTRACRANIAL HAEMATOMA ( 4 FDA reports)
INTRACRANIAL HYPOTENSION ( 4 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 4 FDA reports)
JUDGEMENT IMPAIRED ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
KYPHOSCOLIOSIS ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIP BLISTER ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LOCALISED SKIN REACTION ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
LYMPH NODE CANCER METASTATIC ( 4 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MAMMOGRAM ( 4 FDA reports)
MANIA ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 4 FDA reports)
METASTASES TO CHEST WALL ( 4 FDA reports)
METASTASES TO PERITONEUM ( 4 FDA reports)
METASTASES TO SALIVARY GLAND ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MUSCLE SPASTICITY ( 4 FDA reports)
MYELOID LEUKAEMIA ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
MYOPIA ( 4 FDA reports)
NAIL AVULSION ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 4 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 4 FDA reports)
NYSTAGMUS ( 4 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 4 FDA reports)
OESOPHAGEAL NEOPLASM ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ONYCHALGIA ( 4 FDA reports)
ORTHOPEDIC PROCEDURE ( 4 FDA reports)
OSTEOGENESIS IMPERFECTA ( 4 FDA reports)
OSTEOSARCOMA METASTATIC ( 4 FDA reports)
OTITIS MEDIA ACUTE ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
PAIN THRESHOLD DECREASED ( 4 FDA reports)
PANCREATIC ENLARGEMENT ( 4 FDA reports)
PANCREATITIS VIRAL ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PARAPROTEINAEMIA ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 4 FDA reports)
PELVIC HAEMATOMA ( 4 FDA reports)
PELVIC NEOPLASM ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PERIODONTAL OPERATION ( 4 FDA reports)
PERIPROSTHETIC FRACTURE ( 4 FDA reports)
PHLEBOTHROMBOSIS ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PITUITARY TUMOUR BENIGN ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 4 FDA reports)
PRIMARY HYPOTHYROIDISM ( 4 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PUNCTURE SITE INFECTION ( 4 FDA reports)
RADIATION ASSOCIATED PAIN ( 4 FDA reports)
RADIATION INJURY ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RHEUMATOID LUNG ( 4 FDA reports)
SALIVA ALTERED ( 4 FDA reports)
SALIVARY GLAND CALCULUS ( 4 FDA reports)
SALIVARY GLAND PAIN ( 4 FDA reports)
SALMONELLA SEPSIS ( 4 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 4 FDA reports)
SCOLIOSIS SURGERY ( 4 FDA reports)
SEBACEOUS ADENOMA ( 4 FDA reports)
SENSATION OF BLOCK IN EAR ( 4 FDA reports)
SERUM FERRITIN INCREASED ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SIDEROBLASTIC ANAEMIA ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SKIN HYPOPIGMENTATION ( 4 FDA reports)
SKIN OPERATION ( 4 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 4 FDA reports)
SMALL CELL LUNG CANCER LIMITED STAGE ( 4 FDA reports)
SMALL INTESTINAL RESECTION ( 4 FDA reports)
SMALL INTESTINE ULCER ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SOFT TISSUE NEOPLASM ( 4 FDA reports)
SPINAL X-RAY ABNORMAL ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STAPHYLOMA ( 4 FDA reports)
STARVATION ( 4 FDA reports)
STRESS ULCER ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SUCROSE INTOLERANCE ( 4 FDA reports)
SUPERINFECTION LUNG ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THORACIC CAVITY DRAINAGE ( 4 FDA reports)
THORACIC HAEMORRHAGE ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TOOTH RESORPTION ( 4 FDA reports)
TRACHEAL DIVERTICULUM ( 4 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 4 FDA reports)
TRAUMATIC ARTHRITIS ( 4 FDA reports)
TRAUMATIC FRACTURE ( 4 FDA reports)
TROPONIN ( 4 FDA reports)
ULCERATIVE KERATITIS ( 4 FDA reports)
UMBILICAL MALFORMATION ( 4 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 4 FDA reports)
URETERAL DISORDER ( 4 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URINARY TRACT OPERATION ( 4 FDA reports)
URINE PHOSPHATE DECREASED ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 3 FDA reports)
ABNORMAL CHEST SOUND ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACROCHORDON ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ADRENAL CARCINOMA ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALLERGIC BRONCHITIS ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ANAL POLYP ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL CATHETERISATION ( 3 FDA reports)
ASTROCYTOMA MALIGNANT ( 3 FDA reports)
ATYPICAL FEMUR FRACTURE ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
AUTONOMIC NEUROPATHY ( 3 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 3 FDA reports)
BACTERIA URINE IDENTIFIED ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 3 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 3 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 3 FDA reports)
BIOPSY BONE ( 3 FDA reports)
BIOPSY COLON ABNORMAL ( 3 FDA reports)
BIOPSY LYMPH GLAND ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLADDER PAPILLOMA ( 3 FDA reports)
BLADDER REPAIR ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BLOOD ZINC DECREASED ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BONE CANCER METASTATIC ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE METABOLISM DISORDER ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN NEOPLASM BENIGN ( 3 FDA reports)
BREAST ATROPHY ( 3 FDA reports)
BREAST ENGORGEMENT ( 3 FDA reports)
BREAST OPERATION ( 3 FDA reports)
BREAST RECONSTRUCTION ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
BURSITIS INFECTIVE ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARBON MONOXIDE POISONING ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC DISCOMFORT ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 3 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 3 FDA reports)
CAROTID ARTERY BYPASS ( 3 FDA reports)
CATABOLIC STATE ( 3 FDA reports)
CATARACT OPERATION COMPLICATION ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CEREBELLAR TUMOUR ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL CYST ( 3 FDA reports)
CERVICITIS ( 3 FDA reports)
CHEMICAL INJURY ( 3 FDA reports)
CHOLECYSTOSTOMY ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 4 ( 3 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLUBBING ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
COLECTOMY TOTAL ( 3 FDA reports)
COLON INJURY ( 3 FDA reports)
COLON POLYPECTOMY ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CRYPTOCOCCOSIS ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DEFICIENCY ANAEMIA ( 3 FDA reports)
DEVICE POWER SOURCE ISSUE ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIABETIC GANGRENE ( 3 FDA reports)
DIAPHRAGMALGIA ( 3 FDA reports)
DIAPHRAGMATIC RUPTURE ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DROWNING ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRY GANGRENE ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
EAR INJURY ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ELECTRIC SHOCK ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EMERGENCY CARE ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
ENDOSCOPY ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EWING'S SARCOMA ( 3 FDA reports)
EXFOLIATIVE RASH ( 3 FDA reports)
EYE NAEVUS ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FIBROUS HISTIOCYTOMA ( 3 FDA reports)
FINE MOTOR DELAY ( 3 FDA reports)
FORAMINOTOMY ( 3 FDA reports)
FRACTURED ISCHIUM ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
GASTRIC FISTULA ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROENTERITIS BACTERIAL ( 3 FDA reports)
GASTROINTESTINAL FISTULA ( 3 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GENERALISED ANXIETY DISORDER ( 3 FDA reports)
GENITAL PROLAPSE ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEART ALTERNATION ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEART VALVE STENOSIS ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HEPATIC CALCIFICATION ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HERPES OPHTHALMIC ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HOUSE DUST ALLERGY ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPERVITAMINOSIS D ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
INCISION SITE CELLULITIS ( 3 FDA reports)
INCISION SITE OEDEMA ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFECTION PARASITIC ( 3 FDA reports)
INFUSION SITE IRRITATION ( 3 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
INJECTION SITE DESQUAMATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTESTINAL PROLAPSE ( 3 FDA reports)
INTESTINAL STENOSIS ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LUNG CREPITATION ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MADAROSIS ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 3 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 3 FDA reports)
MASS EXCISION ( 3 FDA reports)
MASTOID ABSCESS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MEDICATION RESIDUE ( 3 FDA reports)
MEDULLARY THYROID CANCER ( 3 FDA reports)
MENINGIOMA BENIGN ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METAPLASIA ( 3 FDA reports)
METASTASES TO ABDOMINAL WALL ( 3 FDA reports)
METASTASES TO MUSCLE ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
NAIL BED DISORDER ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUROFIBROMA ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 3 FDA reports)
OCULAR FISTULA ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL NEOPLASM ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 3 FDA reports)
OSTEOSCLEROSIS ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
PAIN TRAUMA ACTIVATED ( 3 FDA reports)
PALATAL DISORDER ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERIPHLEBITIS ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
POST PROCEDURAL DRAINAGE ( 3 FDA reports)
POSTOPERATIVE FEVER ( 3 FDA reports)
POSTOPERATIVE THROMBOSIS ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PRESBYOESOPHAGUS ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROSTATE CANCER STAGE I ( 3 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
PSEUDOMYXOMA PERITONEI ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY SEQUESTRATION ( 3 FDA reports)
PUNCTURE SITE REACTION ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RECTAL CANCER METASTATIC ( 3 FDA reports)
RECTAL POLYP ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
RETINAL ARTERY EMBOLISM ( 3 FDA reports)
RETINAL DYSTROPHY ( 3 FDA reports)
RETINAL OPERATION ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
SARCOMA OF SKIN ( 3 FDA reports)
SCAN ABNORMAL ( 3 FDA reports)
SELECTIVE IGG SUBCLASS DEFICIENCY ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SEXUAL ASSAULT VICTIM ( 3 FDA reports)
SHORT-BOWEL SYNDROME ( 3 FDA reports)
SICKLE CELL ANAEMIA ( 3 FDA reports)
SILICOSIS ( 3 FDA reports)
SINUS PAIN ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN LESION EXCISION ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STEROID THERAPY ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
SYNOVIAL RUPTURE ( 3 FDA reports)
SYRINGOMYELIA ( 3 FDA reports)
SYSTEMIC SCLEROSIS ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TERMINAL DRIBBLING ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TOOTH EROSION ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRACHEAL OEDEMA ( 3 FDA reports)
TRANSAMINASES ABNORMAL ( 3 FDA reports)
TRANSITIONAL CELL CANCER OF RENAL PELVIS AND URETER METASTATIC ( 3 FDA reports)
TRAUMATIC SHOCK ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
ULNAR NERVE INJURY ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
URETERIC CANCER METASTATIC ( 3 FDA reports)
URETHRAL CANCER METASTATIC ( 3 FDA reports)
URETHRAL INJURY ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE MALPOSITION ( 3 FDA reports)
VAGINAL CYST ( 3 FDA reports)
VASCULAR ENCEPHALOPATHY ( 3 FDA reports)
VASCULAR FRAGILITY ( 3 FDA reports)
VEIN DISCOLOURATION ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VERTEBRAL COLUMN MASS ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VIRAL MYOCARDITIS ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
WHITE BLOOD CELLS URINE ( 3 FDA reports)
WOUND HAEMATOMA ( 3 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VARICOSE VEIN RUPTURED ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VESSEL PERFORATION ( 2 FDA reports)
VICTIM OF CRIME ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN E DECREASED ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOLVULUS OF SMALL BOWEL ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
X-RAY WITH CONTRAST UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL WALL CYST ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACARIASIS ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACROCHORDON EXCISION ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
AEROPHAGIA ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AGRAPHIA ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
AMINO ACID LEVEL ABNORMAL ( 2 FDA reports)
AMYLOIDOMA ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANAL PROLAPSE ( 2 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANALGESIC INTERVENTION SUPPORTIVE THERAPY ( 2 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC BYPASS ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 2 FDA reports)
ARTERIAL FIBROSIS ( 2 FDA reports)
ARTERIOGRAM ( 2 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASTROCYTOMA ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA LOW GRADE ( 2 FDA reports)
BACK CRUSHING ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 2 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BILE OUTPUT DECREASED ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BIOPSY HEART ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY VAGINA ( 2 FDA reports)
BIRTH MARK ( 2 FDA reports)
BLADDER HYPERTROPHY ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLADDER NECK SUSPENSION ( 2 FDA reports)
BLADDER SPHINCTER ATONY ( 2 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD GASTRIN INCREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD IRON ABNORMAL ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOODY AIRWAY DISCHARGE ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE DENSITOMETRY ( 2 FDA reports)
BONE GIANT CELL TUMOUR ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST NECROSIS ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRUCELLOSIS ( 2 FDA reports)
BULBAR PALSY ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CANALITH REPOSITIONING PROCEDURE ( 2 FDA reports)
CANDIDA OSTEOMYELITIS ( 2 FDA reports)
CARDIAC PACEMAKER REMOVAL ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CAROTID BODY TUMOUR ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CAUTERY TO NOSE ( 2 FDA reports)
CELLS IN URINE ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL MALARIA ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHEST WALL MASS ( 2 FDA reports)
CHEST WALL OPERATION ( 2 FDA reports)
CHOLANGIOGRAM ( 2 FDA reports)
CHORIORETINAL DISORDER ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COLLAGEN ANTIGEN TYPE 1 ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COLORECTAL CANCER RECURRENT ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 2 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONTRALATERAL BREAST CANCER ( 2 FDA reports)
CONVALESCENT ( 2 FDA reports)
CORNEAL GRAFT REJECTION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CRYOTHERAPY ( 2 FDA reports)
CRYSTALLURIA ( 2 FDA reports)
CSF SHUNT OPERATION ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYSTIC LYMPHANGIOMA ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYSTOCELE REPAIR ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEATH OF SIBLING ( 2 FDA reports)
DEATH OF SPOUSE ( 2 FDA reports)
DENGUE FEVER ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEVICE DEPLOYMENT ISSUE ( 2 FDA reports)
DEVICE THERAPY ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISLOCATION OF STERNUM ( 2 FDA reports)
DISORDER OF ORBIT ( 2 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG THERAPY CHANGED ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DRY SOCKET ( 2 FDA reports)
DUODENAL OBSTRUCTION ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ECHINOCOCCIASIS ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EPITHELIOID SARCOMA ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
EXERCISE CAPACITY DECREASED ( 2 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYEBALL RUPTURE ( 2 FDA reports)
EYELASH THICKENING ( 2 FDA reports)
EYELID CYST ( 2 FDA reports)
EYELID PAIN ( 2 FDA reports)
FACETECTOMY ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GASTRIC ATONY ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRIC POLYPECTOMY ( 2 FDA reports)
GASTRIC ULCER HELICOBACTER ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS ATROPHIC ( 2 FDA reports)
GASTRITIS VIRAL ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENITAL DISCHARGE ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL INFECTION FEMALE ( 2 FDA reports)
GENITAL LESION ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 2 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 2 FDA reports)
GOODPASTURE'S SYNDROME ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMANGIOPERICYTOMA ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HAMARTOMA ( 2 FDA reports)
HEAD BANGING ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HETEROPLASIA ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HOSTILITY ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERINSULINISM ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
HYPERMOBILITY SYNDROME ( 2 FDA reports)
HYPERSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMMUNOGLOBULINS ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCISION SITE HYPOAESTHESIA ( 2 FDA reports)
INCISIONAL DRAINAGE ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INJECTION SITE JOINT PAIN ( 2 FDA reports)
INJECTION SITE JOINT SWELLING ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL POLYPECTOMY ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
LACTATION DISORDER ( 2 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGEAL VENTRICLE PROLAPSE ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LESION OF SCIATIC NERVE ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUMBAR SPINE FLATTENING ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 2 FDA reports)
LUPUS VASCULITIS ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHORRHOEA ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MASTOCYTOSIS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENISCUS REMOVAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO PHARYNX ( 2 FDA reports)
METASTASES TO SKIN ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MINERAL DEFICIENCY ( 2 FDA reports)
MINERAL SUPPLEMENTATION ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUELLER'S MIXED TUMOUR ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 2 FDA reports)
MYOCARDIAL STRAIN ( 2 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 2 FDA reports)
NAIL RIDGING ( 2 FDA reports)
NARCOTIC INTOXICATION ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NEOPLASM OF THYMUS ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROSURGERY ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
NUTRITIONAL SUPPORT ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 2 FDA reports)
OESOPHAGEAL POLYP ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OOPHORECTOMY BILATERAL ( 2 FDA reports)
OPTIC NERVE INFARCTION ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOARTHROPATHY ( 2 FDA reports)
OSTEOCALCIN DECREASED ( 2 FDA reports)
OSTEOCHONDROMA ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OSTEOPATHIC TREATMENT ( 2 FDA reports)
OSTEOPETROSIS ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PANCREATIC CARCINOMA RECURRENT ( 2 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PELVIC DEFORMITY ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIPROSTHETIC OSTEOLYSIS ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERONEAL NERVE PALSY POSTOPERATIVE ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGEAL INJURY ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHLEBECTOMY ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PIGMENTED NAEVUS ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLASMA VISCOSITY DECREASED ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLEURAL NEOPLASM ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
POLYARTERITIS NODOSA ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POLYPOIDAL CHOROIDAL VASCULOPATHY ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL CONSTIPATION ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PRESBYACUSIS ( 2 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATE CANCER STAGE II ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDOMONAS BRONCHITIS ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY RADIATION INJURY ( 2 FDA reports)
PULMONARY SARCOIDOSIS ( 2 FDA reports)
PULMONARY VALVE STENOSIS ( 2 FDA reports)
PYELECTASIA ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RADICULOTOMY ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
REDUCED BLADDER CAPACITY ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CYST RUPTURED ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
REPETITIVE STRAIN INJURY ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL VASCULAR OCCLUSION ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHEUMATOID FACTOR DECREASED ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SCAN WITH CONTRAST ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SELF ESTEEM DECREASED ( 2 FDA reports)
SENILE OSTEOPOROSIS ( 2 FDA reports)
SENSORY LEVEL ABNORMAL ( 2 FDA reports)
SERONEGATIVE ARTHRITIS ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SKULL X-RAY ABNORMAL ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SNAKE BITE ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPINAL CORPECTOMY ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPINOCEREBELLAR ATAXIA ( 2 FDA reports)
SPORTS INJURY ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 2 FDA reports)
STAG HORN CALCULUS ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STENT MALFUNCTION ( 2 FDA reports)
STENT-GRAFT MALFUNCTION ( 2 FDA reports)
STIFF-MAN SYNDROME ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SUPERINFECTION BACTERIAL ( 2 FDA reports)
SUPPORTIVE CARE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 2 FDA reports)
SYNOVIAL SARCOMA ( 2 FDA reports)
SYNOVIORTHESIS ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID CANCER METASTATIC ( 2 FDA reports)
TONGUE CANCER METASTATIC ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH DEPOSIT ( 2 FDA reports)
TRACHEAL OPERATION ( 2 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TRAUMATIC TOOTH DISPLACEMENT ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYPHOID FEVER ( 2 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 2 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC INJURY ( 2 FDA reports)
URETHRAL DISCHARGE ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
URINE POTASSIUM DECREASED ( 2 FDA reports)
UROGENITAL HAEMORRHAGE ( 2 FDA reports)
UROGENITAL PROLAPSE ( 2 FDA reports)
UTERINE NEOPLASM ( 2 FDA reports)
UTEROVAGINAL PROLAPSE ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL OPERATION ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 1 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCESSORY CARDIAC PATHWAY ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACRAL LENTIGINOUS MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE NORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TEST ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANKLE RECONSTRUCTION ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANASTOMOSIS ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRITIS VIRAL ( 1 FDA reports)
ARTIFICIAL BLADDER IMPLANTATION ( 1 FDA reports)
ARTIFICIAL URINARY SPHINCTER IMPLANT ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL DIARRHOEA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 1 FDA reports)
BENIGN EAR NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BENIGN VASCULAR NEOPLASM ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BLADDER CALCULUS REMOVAL ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLADDER POLYPECTOMY ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTICOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST FIBROSIS ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREAST PROSTHESIS REMOVAL ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
C-TELOPEPTIDE ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC REHABILITATION THERAPY ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CERVIX CARCINOMA STAGE IV ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHEST X-RAY ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CLAMPING OF BLOOD VESSEL ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COCCYGECTOMY ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COGAN'S SYNDROME ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CORNEAL INFECTION ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRANIAL NERVE OPERATION ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUPULOLITHIASIS ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTIC FIBROSIS ( 1 FDA reports)
CYSTINE URINE PRESENT ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYSTOSARCOMA PHYLLODES ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEGENERATION OF UTERINE FIBROID ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DELUSIONAL PERCEPTION ( 1 FDA reports)
DEMENTIA WITH LEWY BODIES ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL EXAMINATION ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE COLOUR ISSUE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE EXTRUSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE INFUSION ISSUE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIVERTICULITIS OESOPHAGEAL ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOLICHOCOLON ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
EAR CANAL INJURY ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECHOCARDIOGRAM NORMAL ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELDERLY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMERGENCY CARE EXAMINATION ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOMETRIAL ADENOMA ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL METAPLASIA ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIC COLITIS ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFECTION INTRAOCULAR ( 1 FDA reports)
EYE PROSTHESIS INSERTION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FALLOPIAN TUBE CANCER METASTATIC ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FAMILIAL MEDITERRANEAN FEVER ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FASTING ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FIBROMATOSIS ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FINGER CRUSHING ( 1 FDA reports)
FISTULA REPAIR ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC DYSPLASIA ( 1 FDA reports)
GASTRIC STAPLING ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROINTESTINAL INJURY ( 1 FDA reports)
GASTROINTESTINAL MUCOCOELE ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROSTOMY CLOSURE ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GENITALIA EXTERNAL PAINFUL ( 1 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLUCOCORTICOIDS DECREASED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMANGIOBLASTOMA ( 1 FDA reports)
HAEMATOLOGY TEST ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEAD LAG ABNORMAL ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIATUS HERNIA, OBSTRUCTIVE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV ANTIBODY POSITIVE ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HORDEOLUM ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPOCALCIURIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOGLOBULIN THERAPY ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANT SITE CALCIFICATION ( 1 FDA reports)
IMPLANT SITE CYST ( 1 FDA reports)
IMPLANT SITE THROMBOSIS ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLAMMATION OF LACRIMAL PASSAGE ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE CALCIFICATION ( 1 FDA reports)
INJECTION SITE JOINT WARMTH ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IRIS VASCULAR DISORDER ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISOIMMUNISATION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT PROSTHESIS USER ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE II ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEAD URINE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOSARCOMA RECURRENT ( 1 FDA reports)
LEMMEL'S SYNDROME ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKAEMIA MONOCYTIC ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
MACRODACTYLY ( 1 FDA reports)
MACULAR RUPTURE ( 1 FDA reports)
MALIGNANT LYMPHOID NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT MIDDLE EAR NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO OESOPHAGUS ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MIKULICZ'S DISEASE ( 1 FDA reports)
MILIA ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MIXED HYPERLIPIDAEMIA ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE INCISION ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOGLOBIN BLOOD ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NAEVUS CELL NAEVUS ( 1 FDA reports)
NAIL GROWTH CESSATION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NASAL CYST REMOVAL ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIPPLE NEOPLASM ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODDING OF HEAD ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIA ( 1 FDA reports)
NOROVIRUS TEST POSITIVE ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
OCCIPITAL NEURALGIA ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
OSTEOCALCIN ( 1 FDA reports)
OSTEOMA CUTIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE III ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAGET'S DISEASE OF SKIN ( 1 FDA reports)
PALINDROMIC RHEUMATISM ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALPATORY FINDING ABNORMAL ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICORONITIS ( 1 FDA reports)
PERINEOPLASTY ( 1 FDA reports)
PERINEURIAL CYST ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL CYST ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PH BODY FLUID ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PHYSICAL EXAMINATION ( 1 FDA reports)
PIGMENTARY GLAUCOMA ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTAL NEOPLASM ( 1 FDA reports)
PLAGUE ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMASTECTOMY LYMPHOEDEMA SYNDROME ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCOLLAGEN TYPE I C-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROLAPSE REPAIR ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN TOTAL ( 1 FDA reports)
PROTEIN URINE ABSENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PSEUDOHYPOPARATHYROIDISM ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PUNCTATE KERATOSIS ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADICAL CYSTECTOMY ( 1 FDA reports)
RADIOISOTOPE SCAN ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL ADENOMA ( 1 FDA reports)
RECTAL CANCER STAGE 0 ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETINAL NEOPLASM ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SARCOMA UTERUS ( 1 FDA reports)
SCAN LYMPH NODES ( 1 FDA reports)
SCHISTOSOMIASIS ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL MENINGEAL CYST ( 1 FDA reports)
SPINAL X-RAY ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC INFECTION BACTERIAL ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SYMPHYSIOLYSIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TENDON GRAFT ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE CYST ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE NEOPLASM BENIGN ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH IMPACTED ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOSTOMY INFECTION ( 1 FDA reports)
TRACTION ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYMPANOSCLEROSIS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULTRASOUND BLADDER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ( 1 FDA reports)
UNDIFFERENTIATED SARCOMA ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL NEOPLASM ( 1 FDA reports)
URETHRAL OPERATION ( 1 FDA reports)
URETHRAL STENT INSERTION ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER EXCISION ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT CARCINOMA IN SITU ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION VIRAL ( 1 FDA reports)
URINARY TRACT INFLAMMATION ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE PROLAPSE REPAIR ( 1 FDA reports)
VAGINAL CANCER RECURRENT ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VAGINAL OEDEMA ( 1 FDA reports)
VAGINAL POLYP ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VALVULOPLASTY CARDIAC ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASECTOMY ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENIPUNCTURE SITE BRUISE ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 1 FDA reports)
VERTIGO LABYRINTHINE ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESICOURETERAL REFLUX SURGERY ( 1 FDA reports)
VESTIBULAR ATAXIA ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIRAL LABYRINTHITIS ( 1 FDA reports)
VIRAL TONSILLITIS ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN B12 ABNORMAL ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VULVAL CANCER STAGE I ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVAL NEOPLASM ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WHIPPLE'S DISEASE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use