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

TENDON RUPTURE ( 4285 FDA reports)
PAIN ( 3428 FDA reports)
TENDONITIS ( 3406 FDA reports)
ROTATOR CUFF SYNDROME ( 3341 FDA reports)
ARTHRALGIA ( 3150 FDA reports)
ANXIETY ( 3123 FDA reports)
PAIN IN EXTREMITY ( 2421 FDA reports)
NAUSEA ( 2368 FDA reports)
DYSPNOEA ( 2165 FDA reports)
DEPRESSION ( 2109 FDA reports)
ASTHENIA ( 1852 FDA reports)
FATIGUE ( 1825 FDA reports)
BACK PAIN ( 1711 FDA reports)
OEDEMA PERIPHERAL ( 1706 FDA reports)
ANAEMIA ( 1687 FDA reports)
INJURY ( 1665 FDA reports)
DIZZINESS ( 1611 FDA reports)
DIARRHOEA ( 1554 FDA reports)
PNEUMONIA ( 1502 FDA reports)
INSOMNIA ( 1498 FDA reports)
VOMITING ( 1435 FDA reports)
TENDON DISORDER ( 1427 FDA reports)
HYPOAESTHESIA ( 1341 FDA reports)
HEADACHE ( 1333 FDA reports)
PYREXIA ( 1331 FDA reports)
CHEST PAIN ( 1252 FDA reports)
FALL ( 1244 FDA reports)
OSTEOARTHRITIS ( 1201 FDA reports)
HYPERTENSION ( 1198 FDA reports)
MYALGIA ( 1189 FDA reports)
MENISCUS LESION ( 1172 FDA reports)
OSTEONECROSIS OF JAW ( 1155 FDA reports)
WEIGHT DECREASED ( 1109 FDA reports)
RENAL FAILURE ( 1107 FDA reports)
PARAESTHESIA ( 1104 FDA reports)
ABDOMINAL PAIN ( 1074 FDA reports)
NEUROPATHY PERIPHERAL ( 1052 FDA reports)
RASH ( 1038 FDA reports)
URINARY TRACT INFECTION ( 1033 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1017 FDA reports)
GAIT DISTURBANCE ( 1011 FDA reports)
JOINT INJURY ( 1009 FDA reports)
BURSITIS ( 969 FDA reports)
MUSCULOSKELETAL PAIN ( 966 FDA reports)
EMOTIONAL DISTRESS ( 962 FDA reports)
BONE DISORDER ( 946 FDA reports)
HYPOTENSION ( 917 FDA reports)
ATRIAL FIBRILLATION ( 911 FDA reports)
MUSCULAR WEAKNESS ( 908 FDA reports)
CONFUSIONAL STATE ( 898 FDA reports)
CONSTIPATION ( 862 FDA reports)
COUGH ( 858 FDA reports)
JOINT SWELLING ( 842 FDA reports)
DEHYDRATION ( 835 FDA reports)
DECREASED APPETITE ( 814 FDA reports)
OSTEOMYELITIS ( 808 FDA reports)
TENOSYNOVITIS ( 799 FDA reports)
PLEURAL EFFUSION ( 792 FDA reports)
PULMONARY EMBOLISM ( 785 FDA reports)
BRONCHITIS ( 784 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 754 FDA reports)
DEEP VEIN THROMBOSIS ( 752 FDA reports)
CEREBROVASCULAR ACCIDENT ( 745 FDA reports)
RENAL FAILURE ACUTE ( 719 FDA reports)
ANHEDONIA ( 718 FDA reports)
DYSPHAGIA ( 718 FDA reports)
PAIN IN JAW ( 718 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 706 FDA reports)
TENDON PAIN ( 694 FDA reports)
SPINAL OSTEOARTHRITIS ( 693 FDA reports)
MALAISE ( 693 FDA reports)
MUSCLE SPASMS ( 684 FDA reports)
CELLULITIS ( 680 FDA reports)
DRUG INEFFECTIVE ( 674 FDA reports)
PALPITATIONS ( 673 FDA reports)
TREMOR ( 667 FDA reports)
SWELLING ( 663 FDA reports)
DEATH ( 658 FDA reports)
INFECTION ( 647 FDA reports)
SINUSITIS ( 632 FDA reports)
MYOCARDIAL INFARCTION ( 617 FDA reports)
CARDIOMEGALY ( 607 FDA reports)
ATELECTASIS ( 602 FDA reports)
RESPIRATORY FAILURE ( 599 FDA reports)
SEPSIS ( 595 FDA reports)
THROMBOCYTOPENIA ( 585 FDA reports)
TOOTH EXTRACTION ( 584 FDA reports)
MITRAL VALVE INCOMPETENCE ( 576 FDA reports)
EPICONDYLITIS ( 574 FDA reports)
ERYTHEMA ( 570 FDA reports)
ARTHRITIS ( 556 FDA reports)
PLANTAR FASCIITIS ( 537 FDA reports)
CHOLELITHIASIS ( 527 FDA reports)
LIGAMENT RUPTURE ( 519 FDA reports)
NECK PAIN ( 514 FDA reports)
ECONOMIC PROBLEM ( 511 FDA reports)
PRURITUS ( 510 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 509 FDA reports)
METASTASES TO BONE ( 508 FDA reports)
OSTEONECROSIS ( 508 FDA reports)
SYNCOPE ( 505 FDA reports)
ABDOMINAL PAIN UPPER ( 501 FDA reports)
ARTHROPATHY ( 500 FDA reports)
FEELING ABNORMAL ( 500 FDA reports)
CORONARY ARTERY DISEASE ( 498 FDA reports)
CHILLS ( 491 FDA reports)
DIABETES MELLITUS ( 487 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 487 FDA reports)
IMPAIRED HEALING ( 486 FDA reports)
PANCYTOPENIA ( 484 FDA reports)
BONE PAIN ( 482 FDA reports)
OSTEOPENIA ( 482 FDA reports)
HYPOKALAEMIA ( 470 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 461 FDA reports)
BLOOD GLUCOSE INCREASED ( 455 FDA reports)
CONVULSION ( 450 FDA reports)
BURNING SENSATION ( 445 FDA reports)
TENDON INJURY ( 445 FDA reports)
CONTUSION ( 444 FDA reports)
HYPERHIDROSIS ( 443 FDA reports)
VISION BLURRED ( 442 FDA reports)
URTICARIA ( 441 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 438 FDA reports)
HEART RATE INCREASED ( 437 FDA reports)
ASTHMA ( 431 FDA reports)
STEVENS-JOHNSON SYNDROME ( 426 FDA reports)
ABASIA ( 423 FDA reports)
RENAL FAILURE CHRONIC ( 422 FDA reports)
DEFORMITY ( 420 FDA reports)
LOSS OF CONSCIOUSNESS ( 420 FDA reports)
HAEMOGLOBIN DECREASED ( 416 FDA reports)
TACHYCARDIA ( 416 FDA reports)
LYMPHADENOPATHY ( 408 FDA reports)
GASTRITIS ( 404 FDA reports)
HAEMORRHOIDS ( 401 FDA reports)
CARPAL TUNNEL SYNDROME ( 398 FDA reports)
HYPERSENSITIVITY ( 398 FDA reports)
DYSPEPSIA ( 395 FDA reports)
HYPERLIPIDAEMIA ( 393 FDA reports)
HALLUCINATION ( 391 FDA reports)
CONDITION AGGRAVATED ( 387 FDA reports)
OSTEOPOROSIS ( 387 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 385 FDA reports)
RENAL CYST ( 383 FDA reports)
STRESS ( 378 FDA reports)
SWELLING FACE ( 378 FDA reports)
WEIGHT INCREASED ( 376 FDA reports)
NEUTROPENIA ( 376 FDA reports)
CATARACT ( 374 FDA reports)
ABDOMINAL DISTENSION ( 372 FDA reports)
DENTAL CARIES ( 370 FDA reports)
UNEVALUABLE EVENT ( 368 FDA reports)
MENTAL STATUS CHANGES ( 359 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 357 FDA reports)
BLOOD PRESSURE INCREASED ( 354 FDA reports)
MUSCLE RUPTURE ( 352 FDA reports)
HYPOXIA ( 345 FDA reports)
CHEST DISCOMFORT ( 344 FDA reports)
EXOSTOSIS ( 344 FDA reports)
OEDEMA ( 344 FDA reports)
HIATUS HERNIA ( 336 FDA reports)
DIVERTICULUM ( 335 FDA reports)
LUNG INFILTRATION ( 333 FDA reports)
TOOTH DISORDER ( 333 FDA reports)
MULTIPLE INJURIES ( 332 FDA reports)
STAPHYLOCOCCAL INFECTION ( 330 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 329 FDA reports)
TINNITUS ( 327 FDA reports)
HAEMATURIA ( 326 FDA reports)
HYPONATRAEMIA ( 326 FDA reports)
CARDIAC DISORDER ( 323 FDA reports)
DRUG HYPERSENSITIVITY ( 321 FDA reports)
OROPHARYNGEAL PAIN ( 319 FDA reports)
SLEEP APNOEA SYNDROME ( 317 FDA reports)
AMNESIA ( 316 FDA reports)
DYSURIA ( 315 FDA reports)
FEAR ( 304 FDA reports)
DECREASED INTEREST ( 303 FDA reports)
BONE LESION ( 301 FDA reports)
DYSPNOEA EXERTIONAL ( 301 FDA reports)
ALOPECIA ( 299 FDA reports)
DISABILITY ( 299 FDA reports)
HERPES ZOSTER ( 294 FDA reports)
NEPHROLITHIASIS ( 294 FDA reports)
MEMORY IMPAIRMENT ( 289 FDA reports)
MULTIPLE MYELOMA ( 288 FDA reports)
RECTAL HAEMORRHAGE ( 287 FDA reports)
PLATELET COUNT DECREASED ( 286 FDA reports)
RIB FRACTURE ( 286 FDA reports)
BRADYCARDIA ( 284 FDA reports)
DRY MOUTH ( 283 FDA reports)
INFLAMMATION ( 281 FDA reports)
DRUG INTERACTION ( 279 FDA reports)
TOOTHACHE ( 279 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 279 FDA reports)
HEART RATE IRREGULAR ( 274 FDA reports)
HYPOPHAGIA ( 273 FDA reports)
NEOPLASM MALIGNANT ( 272 FDA reports)
PULMONARY HYPERTENSION ( 271 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 269 FDA reports)
NEURALGIA ( 269 FDA reports)
LETHARGY ( 264 FDA reports)
HAEMORRHAGE ( 263 FDA reports)
CARDIAC ARREST ( 262 FDA reports)
ARRHYTHMIA ( 261 FDA reports)
TOOTH ABSCESS ( 261 FDA reports)
VISUAL IMPAIRMENT ( 258 FDA reports)
BLOOD CREATININE INCREASED ( 258 FDA reports)
CHOLECYSTITIS CHRONIC ( 258 FDA reports)
BALANCE DISORDER ( 257 FDA reports)
DYSGEUSIA ( 256 FDA reports)
FEBRILE NEUTROPENIA ( 256 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 256 FDA reports)
MULTI-ORGAN FAILURE ( 255 FDA reports)
VERTIGO ( 255 FDA reports)
URINARY RETENTION ( 254 FDA reports)
SOMNOLENCE ( 254 FDA reports)
PRIMARY SEQUESTRUM ( 253 FDA reports)
VENTRICULAR TACHYCARDIA ( 253 FDA reports)
CHRONIC SINUSITIS ( 252 FDA reports)
PHYSICAL DISABILITY ( 252 FDA reports)
SLEEP DISORDER ( 251 FDA reports)
HYPOGLYCAEMIA ( 250 FDA reports)
PULMONARY OEDEMA ( 247 FDA reports)
EPISTAXIS ( 246 FDA reports)
SPINAL COMPRESSION FRACTURE ( 246 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 246 FDA reports)
TENOSYNOVITIS STENOSANS ( 245 FDA reports)
EAR PAIN ( 242 FDA reports)
SCOLIOSIS ( 242 FDA reports)
STOMATITIS ( 241 FDA reports)
GINGIVAL BLEEDING ( 240 FDA reports)
OBESITY ( 240 FDA reports)
POLLAKIURIA ( 240 FDA reports)
GALLBLADDER DISORDER ( 239 FDA reports)
RESTLESSNESS ( 239 FDA reports)
LEUKOCYTOSIS ( 238 FDA reports)
WHEEZING ( 238 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 237 FDA reports)
ARTERIOSCLEROSIS ( 237 FDA reports)
MENTAL DISORDER ( 236 FDA reports)
ORAL PAIN ( 236 FDA reports)
PSYCHOTIC DISORDER ( 235 FDA reports)
SCAR ( 235 FDA reports)
THROMBOSIS ( 234 FDA reports)
TOOTH LOSS ( 234 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 234 FDA reports)
ABDOMINAL DISCOMFORT ( 230 FDA reports)
CARDIOMYOPATHY ( 229 FDA reports)
GINGIVITIS ( 229 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 229 FDA reports)
SINUS TACHYCARDIA ( 229 FDA reports)
FOOT FRACTURE ( 228 FDA reports)
SPEECH DISORDER ( 228 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 227 FDA reports)
TRIGGER FINGER ( 227 FDA reports)
HAEMOPTYSIS ( 227 FDA reports)
ANOREXIA ( 226 FDA reports)
PERIARTHRITIS ( 226 FDA reports)
CANDIDIASIS ( 225 FDA reports)
NERVOUSNESS ( 225 FDA reports)
NASAL CONGESTION ( 224 FDA reports)
RENAL IMPAIRMENT ( 224 FDA reports)
LIGAMENT INJURY ( 223 FDA reports)
COLITIS ( 221 FDA reports)
HAEMATOCRIT DECREASED ( 221 FDA reports)
PERICARDIAL EFFUSION ( 221 FDA reports)
DEBRIDEMENT ( 220 FDA reports)
HYPOTHYROIDISM ( 220 FDA reports)
URINARY INCONTINENCE ( 220 FDA reports)
DISORIENTATION ( 219 FDA reports)
BLOOD PRESSURE DECREASED ( 218 FDA reports)
SKIN DISCOLOURATION ( 218 FDA reports)
ASCITES ( 216 FDA reports)
HYPERGLYCAEMIA ( 216 FDA reports)
JOINT EFFUSION ( 215 FDA reports)
TENDERNESS ( 215 FDA reports)
NIGHTMARE ( 214 FDA reports)
INFLUENZA ( 213 FDA reports)
RESPIRATORY DISTRESS ( 213 FDA reports)
SINUS DISORDER ( 213 FDA reports)
AGITATION ( 211 FDA reports)
COMPRESSION FRACTURE ( 210 FDA reports)
DEAFNESS ( 210 FDA reports)
HEPATIC STEATOSIS ( 210 FDA reports)
MOUTH ULCERATION ( 209 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 208 FDA reports)
IMPAIRED WORK ABILITY ( 208 FDA reports)
LOOSE TOOTH ( 207 FDA reports)
LUMBAR SPINAL STENOSIS ( 207 FDA reports)
LUNG DISORDER ( 207 FDA reports)
HEPATIC CYST ( 205 FDA reports)
METASTASES TO LIVER ( 205 FDA reports)
JOINT STIFFNESS ( 201 FDA reports)
METASTASES TO SPINE ( 201 FDA reports)
HYPERKALAEMIA ( 200 FDA reports)
LUNG NEOPLASM ( 200 FDA reports)
NIGHT SWEATS ( 200 FDA reports)
PANIC ATTACK ( 197 FDA reports)
TYPE 2 DIABETES MELLITUS ( 197 FDA reports)
JOINT DISLOCATION ( 196 FDA reports)
NERVOUS SYSTEM DISORDER ( 196 FDA reports)
CARDIO-RESPIRATORY ARREST ( 195 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 194 FDA reports)
HYPERCHOLESTEROLAEMIA ( 194 FDA reports)
SUICIDAL IDEATION ( 194 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 194 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 192 FDA reports)
PANCREATITIS ( 192 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 191 FDA reports)
MOBILITY DECREASED ( 191 FDA reports)
MUSCLE TWITCHING ( 191 FDA reports)
ABSCESS ( 190 FDA reports)
DISCOMFORT ( 190 FDA reports)
DYSPHONIA ( 190 FDA reports)
UNRESPONSIVE TO STIMULI ( 189 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 188 FDA reports)
EMOTIONAL DISORDER ( 188 FDA reports)
TOOTH INFECTION ( 187 FDA reports)
BONE DEBRIDEMENT ( 185 FDA reports)
LEUKOPENIA ( 184 FDA reports)
MUCOSAL INFLAMMATION ( 183 FDA reports)
BLOOD CALCIUM DECREASED ( 182 FDA reports)
MASS ( 182 FDA reports)
SPINAL COLUMN STENOSIS ( 182 FDA reports)
ANGINA PECTORIS ( 180 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 179 FDA reports)
PURULENT DISCHARGE ( 179 FDA reports)
BLOOD UREA INCREASED ( 178 FDA reports)
CEREBRAL ATROPHY ( 178 FDA reports)
GASTROENTERITIS ( 178 FDA reports)
TOOTH FRACTURE ( 178 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 178 FDA reports)
SYNOVITIS ( 177 FDA reports)
GINGIVAL PAIN ( 177 FDA reports)
FISTULA ( 176 FDA reports)
FUNGAL INFECTION ( 176 FDA reports)
MOVEMENT DISORDER ( 176 FDA reports)
THINKING ABNORMAL ( 176 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 175 FDA reports)
CARDIAC MURMUR ( 175 FDA reports)
GASTROINTESTINAL DISORDER ( 174 FDA reports)
JOINT SPRAIN ( 174 FDA reports)
SURGERY ( 174 FDA reports)
SYNOVIAL CYST ( 174 FDA reports)
DISEASE PROGRESSION ( 173 FDA reports)
FEMUR FRACTURE ( 173 FDA reports)
ABNORMAL BEHAVIOUR ( 172 FDA reports)
AORTIC VALVE INCOMPETENCE ( 172 FDA reports)
FIBROMYALGIA ( 172 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 172 FDA reports)
SKIN LESION ( 172 FDA reports)
CYST ( 171 FDA reports)
EMPHYSEMA ( 171 FDA reports)
CYSTITIS ( 170 FDA reports)
MALNUTRITION ( 170 FDA reports)
RHINORRHOEA ( 170 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 169 FDA reports)
HYPERCALCAEMIA ( 169 FDA reports)
ENDODONTIC PROCEDURE ( 168 FDA reports)
JAW OPERATION ( 168 FDA reports)
PRODUCTIVE COUGH ( 168 FDA reports)
SPLENOMEGALY ( 168 FDA reports)
OESOPHAGITIS ( 167 FDA reports)
RENAL INJURY ( 167 FDA reports)
ORAL INFECTION ( 166 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 165 FDA reports)
DISTURBANCE IN ATTENTION ( 164 FDA reports)
GOUT ( 164 FDA reports)
HEPATOMEGALY ( 164 FDA reports)
CARDIAC FAILURE ( 163 FDA reports)
DIVERTICULITIS ( 163 FDA reports)
ENCEPHALOPATHY ( 163 FDA reports)
OXYGEN SATURATION DECREASED ( 163 FDA reports)
HEPATIC ENZYME INCREASED ( 162 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 161 FDA reports)
EXPOSED BONE IN JAW ( 161 FDA reports)
EYE PAIN ( 161 FDA reports)
GENERALISED OEDEMA ( 161 FDA reports)
BLISTER ( 160 FDA reports)
DYSKINESIA ( 160 FDA reports)
TREATMENT NONCOMPLIANCE ( 160 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 159 FDA reports)
LIMB INJURY ( 158 FDA reports)
ORAL CANDIDIASIS ( 158 FDA reports)
DYSSTASIA ( 157 FDA reports)
FLANK PAIN ( 157 FDA reports)
GROIN PAIN ( 157 FDA reports)
BLOOD POTASSIUM DECREASED ( 156 FDA reports)
DYSARTHRIA ( 156 FDA reports)
HAEMATOCHEZIA ( 156 FDA reports)
LIGAMENT SPRAIN ( 156 FDA reports)
METASTASES TO LUNG ( 156 FDA reports)
PRESYNCOPE ( 156 FDA reports)
RASH GENERALISED ( 156 FDA reports)
RESPIRATORY DISORDER ( 156 FDA reports)
DRUG TOXICITY ( 155 FDA reports)
JAUNDICE ( 154 FDA reports)
MASTICATION DISORDER ( 153 FDA reports)
PATHOLOGICAL FRACTURE ( 153 FDA reports)
BONE DENSITY DECREASED ( 152 FDA reports)
HEPATIC FAILURE ( 152 FDA reports)
MIGRAINE ( 152 FDA reports)
OSTEOSCLEROSIS ( 152 FDA reports)
EJECTION FRACTION DECREASED ( 151 FDA reports)
FOOT DEFORMITY ( 151 FDA reports)
FACIAL PAIN ( 150 FDA reports)
ILL-DEFINED DISORDER ( 150 FDA reports)
MUSCLE ATROPHY ( 149 FDA reports)
CARDIAC VALVE DISEASE ( 148 FDA reports)
GINGIVAL DISORDER ( 148 FDA reports)
INFLUENZA LIKE ILLNESS ( 148 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 148 FDA reports)
NOCTURIA ( 148 FDA reports)
VISUAL ACUITY REDUCED ( 148 FDA reports)
SEPTIC SHOCK ( 147 FDA reports)
ANAPHYLACTIC REACTION ( 146 FDA reports)
CAROTID ARTERY STENOSIS ( 146 FDA reports)
HYDRONEPHROSIS ( 146 FDA reports)
LUMBAR RADICULOPATHY ( 146 FDA reports)
MYOSITIS ( 146 FDA reports)
FLUID OVERLOAD ( 145 FDA reports)
VIRAL INFECTION ( 145 FDA reports)
OSTEOLYSIS ( 144 FDA reports)
RASH PRURITIC ( 144 FDA reports)
RHEUMATOID ARTHRITIS ( 144 FDA reports)
SEQUESTRECTOMY ( 144 FDA reports)
FLATULENCE ( 142 FDA reports)
JOINT CREPITATION ( 142 FDA reports)
LIFE EXPECTANCY SHORTENED ( 142 FDA reports)
DECUBITUS ULCER ( 141 FDA reports)
ISCHAEMIA ( 141 FDA reports)
MUSCLE STRAIN ( 141 FDA reports)
IRRITABLE BOWEL SYNDROME ( 140 FDA reports)
KYPHOSIS ( 140 FDA reports)
PERIODONTAL DISEASE ( 139 FDA reports)
DIVERTICULUM INTESTINAL ( 138 FDA reports)
PARALYSIS ( 138 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 138 FDA reports)
CHOLECYSTECTOMY ( 137 FDA reports)
DEMENTIA ( 137 FDA reports)
LEFT ATRIAL DILATATION ( 137 FDA reports)
NODULE ( 137 FDA reports)
ROAD TRAFFIC ACCIDENT ( 137 FDA reports)
SKIN EXFOLIATION ( 137 FDA reports)
SKIN ULCER ( 137 FDA reports)
GINGIVAL SWELLING ( 136 FDA reports)
GLAUCOMA ( 136 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 136 FDA reports)
DENTURE WEARER ( 135 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 135 FDA reports)
PULMONARY CONGESTION ( 134 FDA reports)
SCIATICA ( 134 FDA reports)
SENSORY LOSS ( 134 FDA reports)
FLUID RETENTION ( 133 FDA reports)
ONYCHOMYCOSIS ( 133 FDA reports)
BLOOD GLUCOSE DECREASED ( 131 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 131 FDA reports)
DELIRIUM ( 131 FDA reports)
RASH ERYTHEMATOUS ( 131 FDA reports)
PERIODONTITIS ( 130 FDA reports)
PROTEINURIA ( 130 FDA reports)
PULMONARY FIBROSIS ( 130 FDA reports)
GINGIVAL ULCERATION ( 129 FDA reports)
CEREBRAL HAEMORRHAGE ( 128 FDA reports)
ORAL DISORDER ( 128 FDA reports)
PROTHROMBIN TIME PROLONGED ( 128 FDA reports)
SPONDYLOLISTHESIS ( 128 FDA reports)
SWOLLEN TONGUE ( 128 FDA reports)
COLONIC POLYP ( 127 FDA reports)
OSTEITIS ( 127 FDA reports)
PNEUMOTHORAX ( 127 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 126 FDA reports)
HOT FLUSH ( 126 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 126 FDA reports)
ERECTILE DYSFUNCTION ( 125 FDA reports)
RADICULOPATHY ( 125 FDA reports)
COAGULOPATHY ( 124 FDA reports)
DIPLOPIA ( 124 FDA reports)
PARANOIA ( 124 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 123 FDA reports)
BLINDNESS ( 123 FDA reports)
GASTRIC ULCER ( 122 FDA reports)
MUSCLE INJURY ( 122 FDA reports)
PERIPHERAL COLDNESS ( 122 FDA reports)
HAEMATOMA ( 121 FDA reports)
SPINAL DISORDER ( 121 FDA reports)
ATRIAL FLUTTER ( 120 FDA reports)
INTERSTITIAL LUNG DISEASE ( 120 FDA reports)
METABOLIC ACIDOSIS ( 119 FDA reports)
WALKING AID USER ( 118 FDA reports)
APHASIA ( 117 FDA reports)
NASOPHARYNGITIS ( 117 FDA reports)
AGEUSIA ( 116 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 116 FDA reports)
FEELING HOT ( 116 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 116 FDA reports)
ADVERSE DRUG REACTION ( 115 FDA reports)
HAEMATEMESIS ( 115 FDA reports)
HYPERKERATOSIS ( 115 FDA reports)
HYPOAESTHESIA ORAL ( 115 FDA reports)
OVERDOSE ( 115 FDA reports)
RHINITIS ALLERGIC ( 115 FDA reports)
SINUS CONGESTION ( 115 FDA reports)
FLUSHING ( 114 FDA reports)
DRY SKIN ( 113 FDA reports)
GINGIVAL INFECTION ( 113 FDA reports)
JAW FRACTURE ( 113 FDA reports)
BASAL CELL CARCINOMA ( 112 FDA reports)
BLOOD SODIUM DECREASED ( 112 FDA reports)
CHONDROPATHY ( 112 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 112 FDA reports)
PHARYNGITIS ( 112 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 112 FDA reports)
SINUS BRADYCARDIA ( 112 FDA reports)
CEREBRAL INFARCTION ( 111 FDA reports)
CHOLECYSTITIS ( 111 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 111 FDA reports)
MYOCARDIAL ISCHAEMIA ( 111 FDA reports)
ORTHOSTATIC HYPOTENSION ( 111 FDA reports)
RESTLESS LEGS SYNDROME ( 111 FDA reports)
CORONARY ARTERY OCCLUSION ( 110 FDA reports)
GASTRIC DISORDER ( 110 FDA reports)
HIP FRACTURE ( 110 FDA reports)
BODY TEMPERATURE INCREASED ( 109 FDA reports)
METASTATIC NEOPLASM ( 108 FDA reports)
COMA ( 107 FDA reports)
DYSLIPIDAEMIA ( 107 FDA reports)
AORTIC ANEURYSM ( 106 FDA reports)
HEPATITIS ( 106 FDA reports)
PROSTATOMEGALY ( 106 FDA reports)
WOUND DEHISCENCE ( 106 FDA reports)
ACUTE RESPIRATORY FAILURE ( 105 FDA reports)
BACTERAEMIA ( 105 FDA reports)
BEDRIDDEN ( 105 FDA reports)
JAW DISORDER ( 105 FDA reports)
LOBAR PNEUMONIA ( 105 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 105 FDA reports)
ABSCESS DRAINAGE ( 104 FDA reports)
ADVERSE EVENT ( 104 FDA reports)
CRYING ( 104 FDA reports)
VISUAL DISTURBANCE ( 104 FDA reports)
BACK DISORDER ( 103 FDA reports)
BLOOD BILIRUBIN INCREASED ( 103 FDA reports)
CARDIOVASCULAR DISORDER ( 103 FDA reports)
INGROWING NAIL ( 103 FDA reports)
ORTHOPNOEA ( 103 FDA reports)
PURULENCE ( 103 FDA reports)
AZOTAEMIA ( 102 FDA reports)
ODYNOPHAGIA ( 102 FDA reports)
SENSORY DISTURBANCE ( 102 FDA reports)
SKIN DISORDER ( 102 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 102 FDA reports)
FIBROSIS ( 101 FDA reports)
FRACTURE ( 101 FDA reports)
HEPATIC CIRRHOSIS ( 101 FDA reports)
MUSCLE TIGHTNESS ( 101 FDA reports)
PERONEAL NERVE PALSY ( 101 FDA reports)
PNEUMONIA ASPIRATION ( 101 FDA reports)
CERVICAL SPINAL STENOSIS ( 100 FDA reports)
OTITIS MEDIA ( 100 FDA reports)
THYROID NEOPLASM ( 100 FDA reports)
GINGIVAL RECESSION ( 99 FDA reports)
LACERATION ( 99 FDA reports)
DEVICE RELATED INFECTION ( 98 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 98 FDA reports)
FAILURE TO THRIVE ( 98 FDA reports)
INCORRECT DOSE ADMINISTERED ( 98 FDA reports)
ACTINOMYCOSIS ( 97 FDA reports)
DIFFICULTY IN WALKING ( 97 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 97 FDA reports)
POST PROCEDURAL COMPLICATION ( 97 FDA reports)
RENAL DISORDER ( 97 FDA reports)
HAEMANGIOMA ( 96 FDA reports)
MELAENA ( 96 FDA reports)
MUSCLE DISORDER ( 96 FDA reports)
RHINITIS ( 96 FDA reports)
ABSCESS JAW ( 95 FDA reports)
CEREBRAL ISCHAEMIA ( 95 FDA reports)
ILEUS ( 95 FDA reports)
ABNORMAL DREAMS ( 94 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 94 FDA reports)
MEDICATION ERROR ( 94 FDA reports)
PRURITUS GENERALISED ( 94 FDA reports)
RHABDOMYOLYSIS ( 94 FDA reports)
VENTRICULAR HYPERTROPHY ( 94 FDA reports)
VAGINAL INFECTION ( 93 FDA reports)
BONE MARROW FAILURE ( 93 FDA reports)
DRUG DEPENDENCE ( 93 FDA reports)
DRY EYE ( 92 FDA reports)
FAECAL INCONTINENCE ( 92 FDA reports)
ORAL CAVITY FISTULA ( 92 FDA reports)
PNEUMONITIS ( 92 FDA reports)
SENSITIVITY OF TEETH ( 92 FDA reports)
ASPIRATION ( 91 FDA reports)
COORDINATION ABNORMAL ( 91 FDA reports)
ESCHERICHIA INFECTION ( 91 FDA reports)
HYPOMAGNESAEMIA ( 91 FDA reports)
RETCHING ( 91 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 91 FDA reports)
SUICIDE ATTEMPT ( 90 FDA reports)
EATING DISORDER ( 90 FDA reports)
ECCHYMOSIS ( 90 FDA reports)
HEART RATE DECREASED ( 90 FDA reports)
MOUTH HAEMORRHAGE ( 90 FDA reports)
PHARYNGEAL OEDEMA ( 90 FDA reports)
QUALITY OF LIFE DECREASED ( 90 FDA reports)
RHONCHI ( 90 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 89 FDA reports)
DILATATION VENTRICULAR ( 89 FDA reports)
UTERINE LEIOMYOMA ( 89 FDA reports)
ANGER ( 88 FDA reports)
CHOLECYSTITIS ACUTE ( 88 FDA reports)
DIASTOLIC DYSFUNCTION ( 88 FDA reports)
PAIN OF SKIN ( 88 FDA reports)
SEBORRHOEIC KERATOSIS ( 88 FDA reports)
DENTAL OPERATION ( 87 FDA reports)
HYPOVOLAEMIA ( 87 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 87 FDA reports)
PROSTATE CANCER ( 87 FDA reports)
TARDIVE DYSKINESIA ( 87 FDA reports)
VENTRICULAR FIBRILLATION ( 86 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 86 FDA reports)
CARTILAGE INJURY ( 86 FDA reports)
EAR INFECTION ( 86 FDA reports)
IRRITABILITY ( 86 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 86 FDA reports)
ORAL HERPES ( 85 FDA reports)
ANGINA UNSTABLE ( 84 FDA reports)
BREAST CANCER RECURRENT ( 84 FDA reports)
COLITIS ULCERATIVE ( 84 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 84 FDA reports)
FEELING JITTERY ( 84 FDA reports)
LOCALISED INFECTION ( 84 FDA reports)
LUNG NEOPLASM MALIGNANT ( 84 FDA reports)
PLEURITIC PAIN ( 84 FDA reports)
ULCER ( 84 FDA reports)
GASTRITIS EROSIVE ( 83 FDA reports)
HEAD INJURY ( 83 FDA reports)
NERVE INJURY ( 83 FDA reports)
PLATELET COUNT INCREASED ( 83 FDA reports)
PSORIASIS ( 83 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 82 FDA reports)
DEPRESSED MOOD ( 82 FDA reports)
INFUSION RELATED REACTION ( 82 FDA reports)
PALLOR ( 82 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 81 FDA reports)
HEMIPARESIS ( 81 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 81 FDA reports)
MAJOR DEPRESSION ( 81 FDA reports)
PROCTALGIA ( 81 FDA reports)
STEM CELL TRANSPLANT ( 81 FDA reports)
ANAPHYLACTIC SHOCK ( 80 FDA reports)
CLOSTRIDIAL INFECTION ( 80 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 80 FDA reports)
FLUID INTAKE REDUCED ( 80 FDA reports)
GOITRE ( 80 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 80 FDA reports)
LYMPHOEDEMA ( 80 FDA reports)
OPEN WOUND ( 80 FDA reports)
PLASMACYTOMA ( 80 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 79 FDA reports)
CHROMATURIA ( 79 FDA reports)
CONJUNCTIVITIS ( 79 FDA reports)
DERMATITIS ( 79 FDA reports)
ORAL DISCOMFORT ( 79 FDA reports)
POLYNEUROPATHY ( 79 FDA reports)
STRESS FRACTURE ( 79 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 79 FDA reports)
AORTIC STENOSIS ( 78 FDA reports)
NO THERAPEUTIC RESPONSE ( 78 FDA reports)
ABDOMINAL PAIN LOWER ( 77 FDA reports)
FAECES DISCOLOURED ( 77 FDA reports)
HAND FRACTURE ( 77 FDA reports)
RALES ( 77 FDA reports)
SOFT TISSUE DISORDER ( 77 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 77 FDA reports)
BACTERIAL INFECTION ( 76 FDA reports)
BLINDNESS UNILATERAL ( 76 FDA reports)
COGNITIVE DISORDER ( 76 FDA reports)
DIABETIC NEUROPATHY ( 76 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 76 FDA reports)
GANGRENE ( 76 FDA reports)
LUNG CONSOLIDATION ( 76 FDA reports)
PELVIC FRACTURE ( 76 FDA reports)
PSEUDOMONAS INFECTION ( 76 FDA reports)
RASH MACULAR ( 76 FDA reports)
ANKLE FRACTURE ( 75 FDA reports)
BREAST CANCER METASTATIC ( 75 FDA reports)
HEPATIC LESION ( 75 FDA reports)
LIGAMENT DISORDER ( 75 FDA reports)
MICTURITION URGENCY ( 75 FDA reports)
PLASMACYTOSIS ( 75 FDA reports)
SINUS HEADACHE ( 75 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 74 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 74 FDA reports)
MUSCULOSKELETAL DISORDER ( 74 FDA reports)
PHOTOSENSITIVITY REACTION ( 74 FDA reports)
REFLUX OESOPHAGITIS ( 74 FDA reports)
SQUAMOUS CELL CARCINOMA ( 74 FDA reports)
THROAT TIGHTNESS ( 73 FDA reports)
BLOOD ALBUMIN DECREASED ( 73 FDA reports)
EYE DISORDER ( 73 FDA reports)
HAEMODIALYSIS ( 73 FDA reports)
INTESTINAL OBSTRUCTION ( 73 FDA reports)
PARAESTHESIA ORAL ( 73 FDA reports)
SICK SINUS SYNDROME ( 73 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 72 FDA reports)
EXCORIATION ( 72 FDA reports)
HYPOKINESIA ( 72 FDA reports)
INCONTINENCE ( 72 FDA reports)
PEPTIC ULCER ( 72 FDA reports)
DIALYSIS ( 71 FDA reports)
HYPOCALCAEMIA ( 71 FDA reports)
IMPAIRED DRIVING ABILITY ( 71 FDA reports)
SUBDURAL HAEMATOMA ( 71 FDA reports)
VASCULAR CALCIFICATION ( 71 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 70 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 70 FDA reports)
COLD SWEAT ( 70 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 70 FDA reports)
PANCREATITIS ACUTE ( 70 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 70 FDA reports)
RESPIRATORY ARREST ( 70 FDA reports)
BONE OPERATION ( 69 FDA reports)
BRONCHOPNEUMONIA ( 69 FDA reports)
COLON ADENOMA ( 69 FDA reports)
HERPES SIMPLEX ( 69 FDA reports)
HYPOALBUMINAEMIA ( 69 FDA reports)
LOCAL SWELLING ( 69 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 69 FDA reports)
ABSCESS ORAL ( 68 FDA reports)
BREAST MASS ( 68 FDA reports)
BREATH SOUNDS ABNORMAL ( 68 FDA reports)
ENTEROCOCCAL INFECTION ( 68 FDA reports)
MOOD SWINGS ( 68 FDA reports)
PLEURAL FIBROSIS ( 68 FDA reports)
PRODUCT QUALITY ISSUE ( 68 FDA reports)
TENDON CALCIFICATION ( 68 FDA reports)
UPPER LIMB FRACTURE ( 68 FDA reports)
SPINAL FRACTURE ( 67 FDA reports)
TRISMUS ( 67 FDA reports)
VASCULITIS ( 67 FDA reports)
ATAXIA ( 67 FDA reports)
GALLBLADDER ENLARGEMENT ( 67 FDA reports)
MITRAL VALVE PROLAPSE ( 67 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 67 FDA reports)
OCULAR HYPERAEMIA ( 67 FDA reports)
RADIOTHERAPY ( 67 FDA reports)
CARDIOGENIC SHOCK ( 66 FDA reports)
COLITIS ISCHAEMIC ( 66 FDA reports)
DEAFNESS NEUROSENSORY ( 66 FDA reports)
DYSTONIA ( 66 FDA reports)
EXERCISE TOLERANCE DECREASED ( 66 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 66 FDA reports)
INTENTIONAL DRUG MISUSE ( 66 FDA reports)
NEURITIS ( 66 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 66 FDA reports)
SINUS OPERATION ( 66 FDA reports)
SUBCUTANEOUS ABSCESS ( 66 FDA reports)
VAGINAL HAEMORRHAGE ( 65 FDA reports)
ACUTE SINUSITIS ( 65 FDA reports)
ANGIOPATHY ( 65 FDA reports)
BLOOD URINE PRESENT ( 65 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 65 FDA reports)
CYANOSIS ( 65 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 65 FDA reports)
LABORATORY TEST ABNORMAL ( 65 FDA reports)
LARYNGITIS ( 65 FDA reports)
PETECHIAE ( 65 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 65 FDA reports)
SHOCK ( 65 FDA reports)
AGGRESSION ( 64 FDA reports)
BIPOLAR DISORDER ( 64 FDA reports)
BREAST CANCER ( 64 FDA reports)
CHEST X-RAY ABNORMAL ( 64 FDA reports)
DISEASE RECURRENCE ( 64 FDA reports)
FACIAL BONES FRACTURE ( 64 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 64 FDA reports)
IRON DEFICIENCY ANAEMIA ( 64 FDA reports)
OSTEORADIONECROSIS ( 64 FDA reports)
OVARIAN CYST ( 64 FDA reports)
SPINAL CORD COMPRESSION ( 64 FDA reports)
UROSEPSIS ( 64 FDA reports)
FACET JOINT SYNDROME ( 63 FDA reports)
GYNAECOMASTIA ( 63 FDA reports)
MYELODYSPLASTIC SYNDROME ( 63 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 63 FDA reports)
RENAL TUBULAR NECROSIS ( 63 FDA reports)
SKIN LACERATION ( 63 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 62 FDA reports)
ATROPHY ( 62 FDA reports)
BILIARY DYSKINESIA ( 62 FDA reports)
BONE FRAGMENTATION ( 62 FDA reports)
DIABETIC KETOACIDOSIS ( 62 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 62 FDA reports)
LIP SWELLING ( 62 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 62 FDA reports)
NEOPLASM ( 62 FDA reports)
TONGUE ULCERATION ( 62 FDA reports)
VITREOUS FLOATERS ( 61 FDA reports)
FEELING COLD ( 61 FDA reports)
LIVER INJURY ( 61 FDA reports)
PULMONARY MASS ( 61 FDA reports)
BLOOD POTASSIUM INCREASED ( 60 FDA reports)
CHONDROMALACIA ( 60 FDA reports)
FACE OEDEMA ( 60 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 60 FDA reports)
MELANOCYTIC NAEVUS ( 60 FDA reports)
ORAL SURGERY ( 60 FDA reports)
SHOULDER PAIN ( 60 FDA reports)
SYNOVIAL RUPTURE ( 60 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 59 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 59 FDA reports)
TYPE 1 DIABETES MELLITUS ( 59 FDA reports)
ABDOMINAL HERNIA ( 59 FDA reports)
CERVICAL DYSPLASIA ( 59 FDA reports)
ESSENTIAL HYPERTENSION ( 59 FDA reports)
HUMERUS FRACTURE ( 59 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 59 FDA reports)
POOR QUALITY SLEEP ( 59 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 59 FDA reports)
SEROMA ( 59 FDA reports)
ANOSMIA ( 58 FDA reports)
ATRIOVENTRICULAR BLOCK ( 58 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 58 FDA reports)
CACHEXIA ( 58 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 58 FDA reports)
DECREASED ACTIVITY ( 58 FDA reports)
ELECTROLYTE IMBALANCE ( 58 FDA reports)
PELVIC PAIN ( 58 FDA reports)
SPINAL LAMINECTOMY ( 58 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 58 FDA reports)
TORSADE DE POINTES ( 58 FDA reports)
VENTRICULAR HYPOKINESIA ( 58 FDA reports)
VITAMIN D DEFICIENCY ( 58 FDA reports)
VITREOUS DETACHMENT ( 58 FDA reports)
TEMPERATURE INTOLERANCE ( 57 FDA reports)
WHEELCHAIR USER ( 57 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 57 FDA reports)
BLOOD CHLORIDE DECREASED ( 57 FDA reports)
CATARACT OPERATION ( 57 FDA reports)
GASTROINTESTINAL PAIN ( 57 FDA reports)
HOSPITALISATION ( 57 FDA reports)
NERVE COMPRESSION ( 57 FDA reports)
ADRENAL INSUFFICIENCY ( 56 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 56 FDA reports)
APPENDICITIS ( 56 FDA reports)
BRONCHOSPASM ( 56 FDA reports)
FAMILY STRESS ( 56 FDA reports)
GRAND MAL CONVULSION ( 56 FDA reports)
PALMAR FASCIITIS ( 56 FDA reports)
RASH MACULO-PAPULAR ( 56 FDA reports)
ABDOMINAL TENDERNESS ( 55 FDA reports)
DEVICE MALFUNCTION ( 55 FDA reports)
DRUG EFFECT DECREASED ( 55 FDA reports)
EAR DISORDER ( 55 FDA reports)
HYPOPHOSPHATAEMIA ( 55 FDA reports)
MALIGNANT MELANOMA ( 55 FDA reports)
MITRAL VALVE CALCIFICATION ( 55 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 55 FDA reports)
CORONARY ARTERY STENOSIS ( 54 FDA reports)
IMMUNE SYSTEM DISORDER ( 54 FDA reports)
NEUROGENIC BLADDER ( 54 FDA reports)
PHLEBITIS ( 54 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 54 FDA reports)
WOUND INFECTION ( 54 FDA reports)
THIRST ( 53 FDA reports)
BODY HEIGHT DECREASED ( 53 FDA reports)
CERVICOBRACHIAL SYNDROME ( 53 FDA reports)
EYE SWELLING ( 53 FDA reports)
HYPOACUSIS ( 53 FDA reports)
LIVER DISORDER ( 53 FDA reports)
MENTAL IMPAIRMENT ( 53 FDA reports)
PERIPHERAL ISCHAEMIA ( 53 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 53 FDA reports)
RENAL MASS ( 53 FDA reports)
ACCIDENTAL OVERDOSE ( 52 FDA reports)
ACNE ( 52 FDA reports)
CAROTID BRUIT ( 52 FDA reports)
ECZEMA ( 52 FDA reports)
GRANULOMA ( 52 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 52 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 52 FDA reports)
WOUND ( 52 FDA reports)
TONGUE DISCOLOURATION ( 51 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 51 FDA reports)
ACIDOSIS ( 51 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 51 FDA reports)
BONE LOSS ( 51 FDA reports)
BREATH ODOUR ( 51 FDA reports)
BRUXISM ( 51 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 51 FDA reports)
EYE IRRITATION ( 51 FDA reports)
HYPERTONIC BLADDER ( 51 FDA reports)
KIDNEY INFECTION ( 51 FDA reports)
LYMPHOMA ( 51 FDA reports)
APNOEA ( 50 FDA reports)
CARDIAC PACEMAKER INSERTION ( 50 FDA reports)
ENDOTRACHEAL INTUBATION ( 50 FDA reports)
EXTRASYSTOLES ( 50 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 50 FDA reports)
MACULAR DEGENERATION ( 50 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 50 FDA reports)
PHOTOPHOBIA ( 50 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 50 FDA reports)
PYELONEPHRITIS ( 50 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 50 FDA reports)
SKIN INDURATION ( 50 FDA reports)
SNORING ( 50 FDA reports)
SPUTUM DISCOLOURED ( 50 FDA reports)
THERMAL BURN ( 49 FDA reports)
THROAT IRRITATION ( 49 FDA reports)
TOOTH IMPACTED ( 49 FDA reports)
WRIST FRACTURE ( 49 FDA reports)
APPENDICECTOMY ( 49 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 49 FDA reports)
CALCULUS URETERIC ( 49 FDA reports)
EYELID PTOSIS ( 49 FDA reports)
INGUINAL HERNIA ( 49 FDA reports)
LIMB DISCOMFORT ( 49 FDA reports)
MEDICAL DEVICE COMPLICATION ( 49 FDA reports)
PULMONARY GRANULOMA ( 49 FDA reports)
PULMONARY INFARCTION ( 49 FDA reports)
SKIN BURNING SENSATION ( 49 FDA reports)
BONE EROSION ( 48 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 48 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 48 FDA reports)
METABOLIC ENCEPHALOPATHY ( 48 FDA reports)
METASTASES TO LYMPH NODES ( 48 FDA reports)
MULTIPLE SCLEROSIS ( 48 FDA reports)
NEUTROPHIL COUNT DECREASED ( 48 FDA reports)
PAROSMIA ( 48 FDA reports)
PROSTATE CANCER METASTATIC ( 48 FDA reports)
CATHETER PLACEMENT ( 47 FDA reports)
FORMICATION ( 47 FDA reports)
LACRIMATION INCREASED ( 47 FDA reports)
LUNG INFECTION ( 47 FDA reports)
NECK MASS ( 47 FDA reports)
NON-CARDIAC CHEST PAIN ( 47 FDA reports)
ORAL INTAKE REDUCED ( 47 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 47 FDA reports)
RESPIRATORY RATE INCREASED ( 47 FDA reports)
THYROID DISORDER ( 47 FDA reports)
TROPONIN INCREASED ( 47 FDA reports)
VEIN DISORDER ( 47 FDA reports)
WOUND DRAINAGE ( 47 FDA reports)
DEVICE FAILURE ( 46 FDA reports)
GLOSSODYNIA ( 46 FDA reports)
HAEMANGIOMA OF LIVER ( 46 FDA reports)
HIP ARTHROPLASTY ( 46 FDA reports)
MIDDLE INSOMNIA ( 46 FDA reports)
OCCULT BLOOD POSITIVE ( 46 FDA reports)
OLIGURIA ( 46 FDA reports)
OSTEITIS DEFORMANS ( 46 FDA reports)
PROSTATITIS ( 46 FDA reports)
SKIN HYPERPIGMENTATION ( 46 FDA reports)
BLADDER DISORDER ( 45 FDA reports)
CAROTID ARTERY DISEASE ( 45 FDA reports)
CHOKING ( 45 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 45 FDA reports)
HALLUCINATION, VISUAL ( 45 FDA reports)
ISCHAEMIC STROKE ( 45 FDA reports)
MOOD ALTERED ( 45 FDA reports)
MYELOMA RECURRENCE ( 45 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 45 FDA reports)
THROMBOCYTOSIS ( 45 FDA reports)
SUBCUTANEOUS NODULE ( 44 FDA reports)
VERTEBROPLASTY ( 44 FDA reports)
ASPIRATION PLEURAL CAVITY ( 44 FDA reports)
BACK INJURY ( 44 FDA reports)
BLOOD COUNT ABNORMAL ( 44 FDA reports)
ERUCTATION ( 44 FDA reports)
GINGIVAL ERYTHEMA ( 44 FDA reports)
INJECTION SITE ERYTHEMA ( 44 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 44 FDA reports)
OFF LABEL USE ( 44 FDA reports)
POOR DENTAL CONDITION ( 44 FDA reports)
PROCEDURAL PAIN ( 44 FDA reports)
PURPURA ( 44 FDA reports)
RADIUS FRACTURE ( 44 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 43 FDA reports)
BONE MARROW TRANSPLANT ( 43 FDA reports)
GINGIVAL OEDEMA ( 43 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 43 FDA reports)
INTESTINAL ISCHAEMIA ( 43 FDA reports)
MYOPATHY ( 43 FDA reports)
ONYCHOMADESIS ( 43 FDA reports)
POOR PERSONAL HYGIENE ( 43 FDA reports)
STOMACH DISCOMFORT ( 43 FDA reports)
TONGUE DISORDER ( 43 FDA reports)
VITAMIN D DECREASED ( 43 FDA reports)
TOE OPERATION ( 42 FDA reports)
BLOOD CULTURE POSITIVE ( 42 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 42 FDA reports)
CYSTOCELE ( 42 FDA reports)
DENTAL CARE ( 42 FDA reports)
DUODENITIS ( 42 FDA reports)
FIBULA FRACTURE ( 42 FDA reports)
FURUNCLE ( 42 FDA reports)
GASTROENTERITIS VIRAL ( 42 FDA reports)
HYPERAESTHESIA ( 42 FDA reports)
HYPERPARATHYROIDISM ( 42 FDA reports)
NEOPLASM PROGRESSION ( 42 FDA reports)
NEURODERMATITIS ( 42 FDA reports)
OEDEMA MOUTH ( 42 FDA reports)
OSTEOMYELITIS CHRONIC ( 42 FDA reports)
RENAL ATROPHY ( 42 FDA reports)
SOCIAL PROBLEM ( 42 FDA reports)
ACUTE PRERENAL FAILURE ( 41 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 41 FDA reports)
BREAST PAIN ( 41 FDA reports)
DENTAL FISTULA ( 41 FDA reports)
DYSPHEMIA ( 41 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 41 FDA reports)
FACIAL PALSY ( 41 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 41 FDA reports)
HEARING IMPAIRED ( 41 FDA reports)
HEPATOTOXICITY ( 41 FDA reports)
JOINT INSTABILITY ( 41 FDA reports)
LACUNAR INFARCTION ( 41 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 41 FDA reports)
PANIC DISORDER ( 41 FDA reports)
PERITONITIS ( 41 FDA reports)
POLYURIA ( 41 FDA reports)
TACHYPNOEA ( 41 FDA reports)
TOOTH REPAIR ( 40 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 40 FDA reports)
VENOUS THROMBOSIS ( 40 FDA reports)
BILE DUCT STONE ( 40 FDA reports)
CIRCULATORY COLLAPSE ( 40 FDA reports)
DERMAL CYST ( 40 FDA reports)
DRUG DOSE OMISSION ( 40 FDA reports)
EARLY SATIETY ( 40 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 40 FDA reports)
ENDOCARDITIS ( 40 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 40 FDA reports)
KLEBSIELLA INFECTION ( 40 FDA reports)
KNEE ARTHROPLASTY ( 40 FDA reports)
OCULAR ICTERUS ( 40 FDA reports)
OTITIS EXTERNA ( 40 FDA reports)
PROTEIN TOTAL DECREASED ( 40 FDA reports)
PULPITIS DENTAL ( 40 FDA reports)
RIGHT ATRIAL DILATATION ( 40 FDA reports)
SKIN ODOUR ABNORMAL ( 40 FDA reports)
SKIN TIGHTNESS ( 40 FDA reports)
ABDOMINAL ABSCESS ( 39 FDA reports)
ABSCESS LIMB ( 39 FDA reports)
APHTHOUS STOMATITIS ( 39 FDA reports)
BONE NEOPLASM MALIGNANT ( 39 FDA reports)
BONE SCAN ABNORMAL ( 39 FDA reports)
COSTOCHONDRITIS ( 39 FDA reports)
DILATATION ATRIAL ( 39 FDA reports)
DRUG INTOLERANCE ( 39 FDA reports)
ENTERITIS ( 39 FDA reports)
GASTRIC POLYPS ( 39 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 39 FDA reports)
HEPATIC MASS ( 39 FDA reports)
IMMOBILE ( 39 FDA reports)
INCISIONAL DRAINAGE ( 39 FDA reports)
LEG AMPUTATION ( 39 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 39 FDA reports)
LUNG HYPERINFLATION ( 39 FDA reports)
MYELOPATHY ( 39 FDA reports)
NECROSIS ( 39 FDA reports)
NEPHROPATHY ( 39 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 39 FDA reports)
RADICULAR PAIN ( 39 FDA reports)
SCAB ( 39 FDA reports)
SKIN HYPERTROPHY ( 39 FDA reports)
STRESS URINARY INCONTINENCE ( 39 FDA reports)
TRANSFUSION ( 39 FDA reports)
URINARY TRACT OBSTRUCTION ( 39 FDA reports)
VENTRICULAR DYSFUNCTION ( 39 FDA reports)
TRANSAMINASES INCREASED ( 38 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 38 FDA reports)
WEGENER'S GRANULOMATOSIS ( 38 FDA reports)
BONE NEOPLASM ( 38 FDA reports)
COLON CANCER ( 38 FDA reports)
CROHN'S DISEASE ( 38 FDA reports)
DRUG ADMINISTRATION ERROR ( 38 FDA reports)
DRUG RESISTANCE ( 38 FDA reports)
GRIP STRENGTH DECREASED ( 38 FDA reports)
HEMIPLEGIA ( 38 FDA reports)
HODGKIN'S DISEASE ( 38 FDA reports)
HYPERSOMNIA ( 38 FDA reports)
RESPIRATORY TRACT INFECTION ( 38 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 37 FDA reports)
BRONCHIECTASIS ( 37 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 37 FDA reports)
CERUMEN IMPACTION ( 37 FDA reports)
DYSPLASTIC NAEVUS ( 37 FDA reports)
GASTRODUODENITIS ( 37 FDA reports)
HEPATIC ENCEPHALOPATHY ( 37 FDA reports)
INCREASED TENDENCY TO BRUISE ( 37 FDA reports)
INTESTINAL PERFORATION ( 37 FDA reports)
MENINGIOMA ( 37 FDA reports)
NEPHRITIS INTERSTITIAL ( 37 FDA reports)
PANCREATIC CARCINOMA ( 37 FDA reports)
PHOTOPSIA ( 37 FDA reports)
RECTAL POLYP ( 37 FDA reports)
SKIN CANCER ( 37 FDA reports)
ALVEOLOPLASTY ( 36 FDA reports)
AORTIC DISORDER ( 36 FDA reports)
BLADDER CANCER ( 36 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 36 FDA reports)
CYSTITIS HAEMORRHAGIC ( 36 FDA reports)
DRUG ABUSE ( 36 FDA reports)
HAEMOLYTIC ANAEMIA ( 36 FDA reports)
HYPERNATRAEMIA ( 36 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 36 FDA reports)
HYSTERECTOMY ( 36 FDA reports)
IMMUNOSUPPRESSION ( 36 FDA reports)
NAIL DISORDER ( 36 FDA reports)
PSYCHIATRIC SYMPTOM ( 36 FDA reports)
THERAPY NON-RESPONDER ( 36 FDA reports)
WEIGHT BEARING DIFFICULTY ( 36 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 35 FDA reports)
TENSION HEADACHE ( 35 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 35 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 35 FDA reports)
APTYALISM ( 35 FDA reports)
CONNECTIVE TISSUE DISORDER ( 35 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 35 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 35 FDA reports)
GLOSSITIS ( 35 FDA reports)
HAEMOPHILUS INFECTION ( 35 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 35 FDA reports)
HEPATOCELLULAR DAMAGE ( 35 FDA reports)
HYPERTHYROIDISM ( 35 FDA reports)
HYPOAESTHESIA FACIAL ( 35 FDA reports)
INFUSION SITE ERYTHEMA ( 35 FDA reports)
INTERMITTENT CLAUDICATION ( 35 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 35 FDA reports)
LARGE INTESTINE PERFORATION ( 35 FDA reports)
OESOPHAGEAL SPASM ( 35 FDA reports)
PARAPROTEINAEMIA ( 35 FDA reports)
POST HERPETIC NEURALGIA ( 35 FDA reports)
PULMONARY HAEMORRHAGE ( 35 FDA reports)
SCLERODERMA ( 35 FDA reports)
SKELETAL INJURY ( 35 FDA reports)
SKIN ATROPHY ( 35 FDA reports)
SKIN PAPILLOMA ( 35 FDA reports)
SKIN WARM ( 35 FDA reports)
ANISOCYTOSIS ( 34 FDA reports)
AORTIC VALVE STENOSIS ( 34 FDA reports)
GINGIVAL EROSION ( 34 FDA reports)
HERNIA ( 34 FDA reports)
HYDROCEPHALUS ( 34 FDA reports)
MALOCCLUSION ( 34 FDA reports)
MECHANICAL VENTILATION ( 34 FDA reports)
MORTON'S NEUROMA ( 34 FDA reports)
PERICARDITIS ( 34 FDA reports)
RECTAL ABSCESS ( 34 FDA reports)
VENOUS INSUFFICIENCY ( 34 FDA reports)
WALKING DISABILITY ( 34 FDA reports)
STREPTOCOCCAL SEPSIS ( 33 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 33 FDA reports)
URINE OUTPUT DECREASED ( 33 FDA reports)
ANEURYSM ( 33 FDA reports)
AORTIC VALVE CALCIFICATION ( 33 FDA reports)
ATRIAL TACHYCARDIA ( 33 FDA reports)
BLADDER OBSTRUCTION ( 33 FDA reports)
BODY TEMPERATURE DECREASED ( 33 FDA reports)
DERMATITIS CONTACT ( 33 FDA reports)
EROSIVE OESOPHAGITIS ( 33 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 33 FDA reports)
FRACTURED SACRUM ( 33 FDA reports)
HERPES VIRUS INFECTION ( 33 FDA reports)
HYPERCOAGULATION ( 33 FDA reports)
HYPOTONIA ( 33 FDA reports)
LIGAMENT LAXITY ( 33 FDA reports)
LIP DRY ( 33 FDA reports)
PERSONALITY CHANGE ( 33 FDA reports)
PULSE ABSENT ( 33 FDA reports)
RESPIRATORY TRACT CONGESTION ( 33 FDA reports)
SKIN DEPIGMENTATION ( 33 FDA reports)
ACTINIC KERATOSIS ( 32 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 32 FDA reports)
AORTIC VALVE SCLEROSIS ( 32 FDA reports)
APHONIA ( 32 FDA reports)
AREFLEXIA ( 32 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 32 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 32 FDA reports)
BLOOD CHLORIDE INCREASED ( 32 FDA reports)
BULLOUS LUNG DISEASE ( 32 FDA reports)
CATHETER RELATED INFECTION ( 32 FDA reports)
CHORDAE TENDINAE RUPTURE ( 32 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 32 FDA reports)
DRUG ABUSER ( 32 FDA reports)
EYE INFECTION ( 32 FDA reports)
FACE INJURY ( 32 FDA reports)
FEAR OF DEATH ( 32 FDA reports)
HYPERPLASIA ( 32 FDA reports)
LARYNGEAL OEDEMA ( 32 FDA reports)
NEUTROPHIL COUNT INCREASED ( 32 FDA reports)
OESOPHAGEAL PAIN ( 32 FDA reports)
OESOPHAGEAL STENOSIS ( 32 FDA reports)
PATHOLOGICAL GAMBLING ( 32 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 32 FDA reports)
PNEUMONIA VIRAL ( 32 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 32 FDA reports)
RAYNAUD'S PHENOMENON ( 32 FDA reports)
SENSATION OF FOREIGN BODY ( 32 FDA reports)
UMBILICAL HERNIA ( 32 FDA reports)
VIITH NERVE PARALYSIS ( 32 FDA reports)
VISUAL FIELD DEFECT ( 32 FDA reports)
WOUND SECRETION ( 32 FDA reports)
TOOTH DEPOSIT ( 31 FDA reports)
VITAMIN B12 DEFICIENCY ( 31 FDA reports)
VOCAL CORD PARALYSIS ( 31 FDA reports)
ATRIAL SEPTAL DEFECT ( 31 FDA reports)
BONE SWELLING ( 31 FDA reports)
CLAVICLE FRACTURE ( 31 FDA reports)
ENCEPHALOMALACIA ( 31 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 31 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 31 FDA reports)
INJECTION SITE PAIN ( 31 FDA reports)
MAXILLOFACIAL OPERATION ( 31 FDA reports)
MEDICAL DEVICE REMOVAL ( 31 FDA reports)
MICTURITION DISORDER ( 31 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 31 FDA reports)
MYOCLONUS ( 31 FDA reports)
NASAL MUCOSAL DISORDER ( 31 FDA reports)
NEUTROPENIC SEPSIS ( 31 FDA reports)
RENAL CANCER ( 31 FDA reports)
RIGHT VENTRICULAR FAILURE ( 31 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 31 FDA reports)
ADENOCARCINOMA ( 30 FDA reports)
AGRANULOCYTOSIS ( 30 FDA reports)
CARDIOPULMONARY FAILURE ( 30 FDA reports)
DRUG ERUPTION ( 30 FDA reports)
ESCHERICHIA SEPSIS ( 30 FDA reports)
HILAR LYMPHADENOPATHY ( 30 FDA reports)
HYPERTENSIVE CRISIS ( 30 FDA reports)
HYPOVENTILATION ( 30 FDA reports)
JUGULAR VEIN DISTENSION ( 30 FDA reports)
LEUKAEMIA ( 30 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 30 FDA reports)
OSTEOCHONDROSIS ( 30 FDA reports)
POLYMYALGIA RHEUMATICA ( 30 FDA reports)
POSTURE ABNORMAL ( 30 FDA reports)
TOOTH INJURY ( 30 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 30 FDA reports)
TRIGEMINAL NEURALGIA ( 29 FDA reports)
ABDOMINAL MASS ( 29 FDA reports)
ADRENAL MASS ( 29 FDA reports)
ANOXIC ENCEPHALOPATHY ( 29 FDA reports)
APHAGIA ( 29 FDA reports)
BLEPHARITIS ( 29 FDA reports)
CATHETER REMOVAL ( 29 FDA reports)
CLOSTRIDIUM COLITIS ( 29 FDA reports)
CORONARY ARTERY BYPASS ( 29 FDA reports)
CUBITAL TUNNEL SYNDROME ( 29 FDA reports)
EDENTULOUS ( 29 FDA reports)
ERYTHEMA MULTIFORME ( 29 FDA reports)
FOLLICULITIS ( 29 FDA reports)
HALLUCINATION, AUDITORY ( 29 FDA reports)
HYPERTENSIVE HEART DISEASE ( 29 FDA reports)
HYPERTROPHY ( 29 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 29 FDA reports)
JOINT LOCK ( 29 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 29 FDA reports)
LOSS OF EMPLOYMENT ( 29 FDA reports)
MENINGITIS ( 29 FDA reports)
NEUROPATHY ( 29 FDA reports)
OTITIS MEDIA ACUTE ( 29 FDA reports)
POLYDIPSIA ( 29 FDA reports)
SEASONAL ALLERGY ( 29 FDA reports)
SJOGREN'S SYNDROME ( 29 FDA reports)
AFFECTIVE DISORDER ( 28 FDA reports)
AORTIC DILATATION ( 28 FDA reports)
BREAST RECONSTRUCTION ( 28 FDA reports)
CARBUNCLE ( 28 FDA reports)
CARDIAC FLUTTER ( 28 FDA reports)
CATHETERISATION CARDIAC ( 28 FDA reports)
CERVICAL CORD COMPRESSION ( 28 FDA reports)
CHOLESTASIS ( 28 FDA reports)
DEVICE RELATED SEPSIS ( 28 FDA reports)
DRUG PRESCRIBING ERROR ( 28 FDA reports)
FACIAL NEURALGIA ( 28 FDA reports)
HEART INJURY ( 28 FDA reports)
HYPERMETABOLISM ( 28 FDA reports)
IMMUNODEFICIENCY ( 28 FDA reports)
INADEQUATE ANALGESIA ( 28 FDA reports)
INTRACRANIAL ANEURYSM ( 28 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 28 FDA reports)
MYASTHENIA GRAVIS ( 28 FDA reports)
OPEN REDUCTION OF FRACTURE ( 28 FDA reports)
PANCREATITIS CHRONIC ( 28 FDA reports)
POLYP ( 28 FDA reports)
PROCTITIS ( 28 FDA reports)
RECTAL FISSURE ( 28 FDA reports)
SKIN FIBROSIS ( 28 FDA reports)
SOFT TISSUE INFLAMMATION ( 28 FDA reports)
TELANGIECTASIA ( 28 FDA reports)
VITREOUS HAEMORRHAGE ( 28 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 27 FDA reports)
TONSILLAR DISORDER ( 27 FDA reports)
WOUND COMPLICATION ( 27 FDA reports)
AORTIC CALCIFICATION ( 27 FDA reports)
BARRETT'S OESOPHAGUS ( 27 FDA reports)
BIOPSY BONE MARROW ( 27 FDA reports)
BLOOD TEST ABNORMAL ( 27 FDA reports)
BONE MARROW OEDEMA ( 27 FDA reports)
DEAFNESS BILATERAL ( 27 FDA reports)
DELUSION ( 27 FDA reports)
DIZZINESS POSTURAL ( 27 FDA reports)
EAR DISCOMFORT ( 27 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 27 FDA reports)
INITIAL INSOMNIA ( 27 FDA reports)
LIBIDO DECREASED ( 27 FDA reports)
LUMBAR SPINE FLATTENING ( 27 FDA reports)
METASTATIC PAIN ( 27 FDA reports)
MITRAL VALVE DISEASE ( 27 FDA reports)
NASAL SEPTUM DEVIATION ( 27 FDA reports)
ONYCHALGIA ( 27 FDA reports)
OROPHARYNGEAL PLAQUE ( 27 FDA reports)
PERIORBITAL OEDEMA ( 27 FDA reports)
PROTEIN URINE PRESENT ( 27 FDA reports)
RENAL PAIN ( 27 FDA reports)
SENSATION OF HEAVINESS ( 27 FDA reports)
ANGIONEUROTIC OEDEMA ( 26 FDA reports)
ATROPHIC VULVOVAGINITIS ( 26 FDA reports)
BACTERIAL TEST POSITIVE ( 26 FDA reports)
BILE DUCT OBSTRUCTION ( 26 FDA reports)
BLADDER CATHETERISATION ( 26 FDA reports)
BRAIN INJURY ( 26 FDA reports)
CHEILITIS ( 26 FDA reports)
COR PULMONALE ( 26 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 26 FDA reports)
ENTEROVESICAL FISTULA ( 26 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 26 FDA reports)
FULL BLOOD COUNT DECREASED ( 26 FDA reports)
GALLBLADDER INJURY ( 26 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 26 FDA reports)
HAEMODYNAMIC INSTABILITY ( 26 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 26 FDA reports)
HEPATITIS C ( 26 FDA reports)
INTERNAL INJURY ( 26 FDA reports)
LIGHT CHAIN ANALYSIS ( 26 FDA reports)
LIPASE INCREASED ( 26 FDA reports)
NARCOLEPSY ( 26 FDA reports)
OEDEMA MUCOSAL ( 26 FDA reports)
PARATHYROID TUMOUR BENIGN ( 26 FDA reports)
PROTEIN URINE ABSENT ( 26 FDA reports)
RESORPTION BONE INCREASED ( 26 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 26 FDA reports)
STENT PLACEMENT ( 26 FDA reports)
THROMBOPHLEBITIS ( 26 FDA reports)
TRACHEOBRONCHITIS ( 26 FDA reports)
URINE FLOW DECREASED ( 26 FDA reports)
THYROID ADENOMA ( 25 FDA reports)
URETHRAL STENOSIS ( 25 FDA reports)
VARICOSE VEIN ( 25 FDA reports)
ABORTION SPONTANEOUS ( 25 FDA reports)
CARDIAC TAMPONADE ( 25 FDA reports)
CULTURE URINE POSITIVE ( 25 FDA reports)
DEVICE OCCLUSION ( 25 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 25 FDA reports)
DRUG TOLERANCE ( 25 FDA reports)
EMBOLISM ( 25 FDA reports)
FIBRIN D DIMER INCREASED ( 25 FDA reports)
FORAMEN MAGNUM STENOSIS ( 25 FDA reports)
FOREIGN BODY ( 25 FDA reports)
INTENTIONAL OVERDOSE ( 25 FDA reports)
LIPOMA ( 25 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 25 FDA reports)
MACROGLOSSIA ( 25 FDA reports)
MENSTRUATION IRREGULAR ( 25 FDA reports)
MUCOSAL DRYNESS ( 25 FDA reports)
NASAL DISORDER ( 25 FDA reports)
OSTEOARTHROPATHY ( 25 FDA reports)
PARONYCHIA ( 25 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 25 FDA reports)
PSEUDOMONAL SEPSIS ( 25 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 25 FDA reports)
PUBIS FRACTURE ( 25 FDA reports)
RADIATION INJURY ( 25 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 25 FDA reports)
SINUS ARRHYTHMIA ( 25 FDA reports)
SKIN NEOPLASM EXCISION ( 25 FDA reports)
ABDOMINAL NEOPLASM ( 24 FDA reports)
ACCIDENT ( 24 FDA reports)
AUTOIMMUNE DISORDER ( 24 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 24 FDA reports)
BLOOD MAGNESIUM DECREASED ( 24 FDA reports)
BRAIN NEOPLASM ( 24 FDA reports)
BRONCHITIS CHRONIC ( 24 FDA reports)
CLAUSTROPHOBIA ( 24 FDA reports)
DIABETIC RETINOPATHY ( 24 FDA reports)
EXTRASKELETAL OSSIFICATION ( 24 FDA reports)
EYE HAEMORRHAGE ( 24 FDA reports)
FEMORAL NECK FRACTURE ( 24 FDA reports)
HAEMOLYSIS ( 24 FDA reports)
LACTOSE INTOLERANCE ( 24 FDA reports)
LIGAMENT PAIN ( 24 FDA reports)
MANIA ( 24 FDA reports)
MOTOR DYSFUNCTION ( 24 FDA reports)
NECK INJURY ( 24 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 24 FDA reports)
POOR VENOUS ACCESS ( 24 FDA reports)
RADIAL NERVE PALSY ( 24 FDA reports)
RENAL TUBULAR ACIDOSIS ( 24 FDA reports)
SEPSIS SYNDROME ( 24 FDA reports)
SEXUAL DYSFUNCTION ( 24 FDA reports)
SPINAL DECOMPRESSION ( 24 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 24 FDA reports)
TIBIA FRACTURE ( 24 FDA reports)
VARICES OESOPHAGEAL ( 24 FDA reports)
VENA CAVA THROMBOSIS ( 24 FDA reports)
VENTRICULAR ARRHYTHMIA ( 24 FDA reports)
SPINAL HAEMANGIOMA ( 23 FDA reports)
STASIS DERMATITIS ( 23 FDA reports)
STREPTOCOCCAL INFECTION ( 23 FDA reports)
THYROID CANCER ( 23 FDA reports)
THYROID CYST ( 23 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 23 FDA reports)
URINARY HESITATION ( 23 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 23 FDA reports)
ALCOHOL USE ( 23 FDA reports)
AMENORRHOEA ( 23 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 23 FDA reports)
ANXIETY DISORDER ( 23 FDA reports)
BLINDNESS TRANSIENT ( 23 FDA reports)
BREAST TENDERNESS ( 23 FDA reports)
BRONCHIAL SECRETION RETENTION ( 23 FDA reports)
CATHETER RELATED COMPLICATION ( 23 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 23 FDA reports)
COLLAPSE OF LUNG ( 23 FDA reports)
GRAFT VERSUS HOST DISEASE ( 23 FDA reports)
GRIEF REACTION ( 23 FDA reports)
INJECTION SITE REACTION ( 23 FDA reports)
JAUNDICE CHOLESTATIC ( 23 FDA reports)
LICHENOID KERATOSIS ( 23 FDA reports)
LIPIDS INCREASED ( 23 FDA reports)
LOWER LIMB FRACTURE ( 23 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 23 FDA reports)
MENORRHAGIA ( 23 FDA reports)
METASTASES TO SKIN ( 23 FDA reports)
MUSCLE CRAMP ( 23 FDA reports)
NEUROENDOCRINE CARCINOMA ( 23 FDA reports)
PARKINSONISM ( 23 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 23 FDA reports)
PRESBYOPIA ( 23 FDA reports)
PYELONEPHRITIS ACUTE ( 23 FDA reports)
RECTOCELE ( 23 FDA reports)
RESPIRATORY ACIDOSIS ( 23 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 23 FDA reports)
SERRATIA INFECTION ( 23 FDA reports)
SHOULDER ARTHROPLASTY ( 23 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 22 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 22 FDA reports)
BLADDER SPASM ( 22 FDA reports)
BLOOD DISORDER ( 22 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 22 FDA reports)
CARDIAC ANEURYSM ( 22 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 22 FDA reports)
COLECTOMY ( 22 FDA reports)
CONDUCTION DISORDER ( 22 FDA reports)
DYSAESTHESIA ( 22 FDA reports)
EOSINOPHILIA ( 22 FDA reports)
GINGIVAL HYPERPLASIA ( 22 FDA reports)
HEPATOSPLENOMEGALY ( 22 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 22 FDA reports)
HIP SURGERY ( 22 FDA reports)
HYPERACUSIS ( 22 FDA reports)
INTRAOCULAR LENS IMPLANT ( 22 FDA reports)
METASTASIS ( 22 FDA reports)
MYOPIA ( 22 FDA reports)
NERVE ROOT LESION ( 22 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 22 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 22 FDA reports)
ORTHOSIS USER ( 22 FDA reports)
PAPILLOMA ( 22 FDA reports)
PATELLA FRACTURE ( 22 FDA reports)
PORTAL HYPERTENSION ( 22 FDA reports)
PROCEDURAL COMPLICATION ( 22 FDA reports)
RESUSCITATION ( 22 FDA reports)
SACROILIITIS ( 22 FDA reports)
SCAN BONE MARROW ABNORMAL ( 22 FDA reports)
SKIN NECROSIS ( 22 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 22 FDA reports)
VASCULAR INSUFFICIENCY ( 22 FDA reports)
SUBGALEAL HAEMATOMA ( 21 FDA reports)
TENSION ( 21 FDA reports)
TONSILLITIS ( 21 FDA reports)
TUMOUR LYSIS SYNDROME ( 21 FDA reports)
URINE ODOUR ABNORMAL ( 21 FDA reports)
UTERINE CANCER ( 21 FDA reports)
VASCULAR PSEUDOANEURYSM ( 21 FDA reports)
ACUTE CORONARY SYNDROME ( 21 FDA reports)
ADRENAL DISORDER ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 21 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 21 FDA reports)
BENIGN COLONIC NEOPLASM ( 21 FDA reports)
BILIARY DILATATION ( 21 FDA reports)
BIPOLAR I DISORDER ( 21 FDA reports)
BLADDER CANCER RECURRENT ( 21 FDA reports)
BONE GRAFT ( 21 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 21 FDA reports)
CAROTID ARTERY OCCLUSION ( 21 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 21 FDA reports)
CHEST WALL MASS ( 21 FDA reports)
CREPITATIONS ( 21 FDA reports)
DENTAL IMPLANTATION ( 21 FDA reports)
DIVERTICULAR PERFORATION ( 21 FDA reports)
FAECALOMA ( 21 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 21 FDA reports)
FIBROMA ( 21 FDA reports)
FUNGAEMIA ( 21 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 21 FDA reports)
HEPATITIS ACUTE ( 21 FDA reports)
HYPERBILIRUBINAEMIA ( 21 FDA reports)
INCOHERENT ( 21 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 21 FDA reports)
INTRACARDIAC THROMBUS ( 21 FDA reports)
LICHEN PLANUS ( 21 FDA reports)
LUNG CANCER METASTATIC ( 21 FDA reports)
METAPLASIA ( 21 FDA reports)
OESOPHAGEAL DISORDER ( 21 FDA reports)
PARAPLEGIA ( 21 FDA reports)
PARKINSON'S DISEASE ( 21 FDA reports)
PNEUMONIA FUNGAL ( 21 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 21 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 21 FDA reports)
SEDATION ( 21 FDA reports)
BREAST LUMP REMOVAL ( 20 FDA reports)
BUNION ( 20 FDA reports)
CEREBELLAR INFARCTION ( 20 FDA reports)
CRYOTHERAPY ( 20 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 20 FDA reports)
EJECTION FRACTION ABNORMAL ( 20 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 20 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 20 FDA reports)
EYE MOVEMENT DISORDER ( 20 FDA reports)
FEELING OF DESPAIR ( 20 FDA reports)
FISTULA DISCHARGE ( 20 FDA reports)
FISTULA REPAIR ( 20 FDA reports)
ILIAC ARTERY THROMBOSIS ( 20 FDA reports)
INFARCTION ( 20 FDA reports)
ISCHAEMIC HEPATITIS ( 20 FDA reports)
MALIGNANT MELANOMA IN SITU ( 20 FDA reports)
MULTI-ORGAN DISORDER ( 20 FDA reports)
NERVE ROOT COMPRESSION ( 20 FDA reports)
OESOPHAGEAL ULCER ( 20 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 20 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 20 FDA reports)
PULMONARY CALCIFICATION ( 20 FDA reports)
QRS AXIS ABNORMAL ( 20 FDA reports)
SECRETION DISCHARGE ( 20 FDA reports)
SINUSITIS FUNGAL ( 20 FDA reports)
SKIN EROSION ( 20 FDA reports)
SYNCOPE VASOVAGAL ( 20 FDA reports)
TORTICOLLIS ( 20 FDA reports)
TREATMENT FAILURE ( 20 FDA reports)
TUMOUR INVASION ( 20 FDA reports)
URGE INCONTINENCE ( 20 FDA reports)
SPUTUM CULTURE POSITIVE ( 19 FDA reports)
SYSTEMIC CANDIDA ( 19 FDA reports)
TESTICULAR PAIN ( 19 FDA reports)
TESTICULAR TORSION ( 19 FDA reports)
TOE AMPUTATION ( 19 FDA reports)
ACUTE HEPATIC FAILURE ( 19 FDA reports)
ADDISON'S DISEASE ( 19 FDA reports)
ALVEOLAR OSTEITIS ( 19 FDA reports)
AORTIC THROMBOSIS ( 19 FDA reports)
APLASTIC ANAEMIA ( 19 FDA reports)
ARTHROPOD BITE ( 19 FDA reports)
AXILLARY MASS ( 19 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 19 FDA reports)
BLOOD CREATINE INCREASED ( 19 FDA reports)
BLOOD IRON DECREASED ( 19 FDA reports)
BONE MARROW DISORDER ( 19 FDA reports)
BREAST CANCER FEMALE ( 19 FDA reports)
BREAST DISORDER ( 19 FDA reports)
BUNDLE BRANCH BLOCK ( 19 FDA reports)
CATHETER SITE HAEMORRHAGE ( 19 FDA reports)
CEREBROVASCULAR DISORDER ( 19 FDA reports)
CYSTITIS INTERSTITIAL ( 19 FDA reports)
DEAFNESS UNILATERAL ( 19 FDA reports)
DRUG DISPENSING ERROR ( 19 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 19 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 19 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 19 FDA reports)
EPIGASTRIC DISCOMFORT ( 19 FDA reports)
EYE LASER SURGERY ( 19 FDA reports)
GASTROENTERITIS RADIATION ( 19 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 19 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 19 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 19 FDA reports)
JUGULAR VEIN THROMBOSIS ( 19 FDA reports)
LUDWIG ANGINA ( 19 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 19 FDA reports)
METASTASES TO PELVIS ( 19 FDA reports)
MONOCYTOSIS ( 19 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 19 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 19 FDA reports)
PATHOGEN RESISTANCE ( 19 FDA reports)
PITTING OEDEMA ( 19 FDA reports)
POST LAMINECTOMY SYNDROME ( 19 FDA reports)
PROCTOCOLITIS ( 19 FDA reports)
PULSE ABNORMAL ( 19 FDA reports)
SARCOIDOSIS ( 19 FDA reports)
SKIN NODULE ( 19 FDA reports)
SKIN REACTION ( 19 FDA reports)
ADENOMA BENIGN ( 18 FDA reports)
ANGIOEDEMA ( 18 FDA reports)
ANIMAL BITE ( 18 FDA reports)
ANORECTAL DISORDER ( 18 FDA reports)
APPENDICITIS PERFORATED ( 18 FDA reports)
BLOOD CREATININE DECREASED ( 18 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 18 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 18 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 18 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 18 FDA reports)
BONE TRIMMING ( 18 FDA reports)
BRAIN MASS ( 18 FDA reports)
CALCINOSIS ( 18 FDA reports)
CAPILLARY LEAK SYNDROME ( 18 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 18 FDA reports)
CENTRAL LINE INFECTION ( 18 FDA reports)
CHOLANGITIS ( 18 FDA reports)
COMMUNICATION DISORDER ( 18 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 18 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 18 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 18 FDA reports)
DEPERSONALISATION ( 18 FDA reports)
DYSPLASIA ( 18 FDA reports)
DYSTHYMIC DISORDER ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
EYELID OEDEMA ( 18 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 18 FDA reports)
FUNGAL SEPSIS ( 18 FDA reports)
GENITAL HERPES ( 18 FDA reports)
GLOMERULONEPHRITIS ( 18 FDA reports)
HAEMOTHORAX ( 18 FDA reports)
HEAD DISCOMFORT ( 18 FDA reports)
HERNIA REPAIR ( 18 FDA reports)
HICCUPS ( 18 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 18 FDA reports)
LIGAMENTITIS ( 18 FDA reports)
LOOSE BODY IN JOINT ( 18 FDA reports)
LYMPHOPENIA ( 18 FDA reports)
MASTITIS ( 18 FDA reports)
METASTASES TO THE MEDIASTINUM ( 18 FDA reports)
MIDDLE EAR EFFUSION ( 18 FDA reports)
MONOCYTE COUNT INCREASED ( 18 FDA reports)
MUCOSAL HAEMORRHAGE ( 18 FDA reports)
PELVIC HAEMATOMA ( 18 FDA reports)
PIGMENTATION DISORDER ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
PYURIA ( 18 FDA reports)
RETINAL HAEMORRHAGE ( 18 FDA reports)
ROSACEA ( 18 FDA reports)
SUNBURN ( 18 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 18 FDA reports)
VENA CAVA FILTER INSERTION ( 18 FDA reports)
VENOOCCLUSIVE DISEASE ( 18 FDA reports)
WEIGHT FLUCTUATION ( 18 FDA reports)
SPINAL FUSION ACQUIRED ( 17 FDA reports)
SPONDYLOLYSIS ( 17 FDA reports)
TOBACCO ABUSE ( 17 FDA reports)
UTERINE ENLARGEMENT ( 17 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 17 FDA reports)
X-RAY ABNORMAL ( 17 FDA reports)
ATRIAL THROMBOSIS ( 17 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 17 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 17 FDA reports)
BRAIN OEDEMA ( 17 FDA reports)
BURSA INJURY ( 17 FDA reports)
CAECITIS ( 17 FDA reports)
CHEST WALL PAIN ( 17 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 17 FDA reports)
COR PULMONALE CHRONIC ( 17 FDA reports)
DENTAL PULP DISORDER ( 17 FDA reports)
DIABETIC FOOT ( 17 FDA reports)
DIABETIC NEPHROPATHY ( 17 FDA reports)
DIPLEGIA ( 17 FDA reports)
DROP ATTACKS ( 17 FDA reports)
DRUG LEVEL INCREASED ( 17 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 17 FDA reports)
EAR HAEMORRHAGE ( 17 FDA reports)
FAT NECROSIS ( 17 FDA reports)
FRACTURE NONUNION ( 17 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 17 FDA reports)
GUILLAIN-BARRE SYNDROME ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HEPATIC ENZYME ABNORMAL ( 17 FDA reports)
HEPATITIS B ( 17 FDA reports)
HYPOTHERMIA ( 17 FDA reports)
ILIAC ARTERY STENOSIS ( 17 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 17 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 17 FDA reports)
JOINT CONTRACTURE ( 17 FDA reports)
LEUKOPLAKIA ORAL ( 17 FDA reports)
LYME DISEASE ( 17 FDA reports)
MASTOIDITIS ( 17 FDA reports)
MENOPAUSAL SYMPTOMS ( 17 FDA reports)
MITRAL VALVE STENOSIS ( 17 FDA reports)
NEOPLASM SKIN ( 17 FDA reports)
OCCULT BLOOD ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
ORAL DISCHARGE ( 17 FDA reports)
OVARIAN CANCER ( 17 FDA reports)
PANIC REACTION ( 17 FDA reports)
PERIODONTAL OPERATION ( 17 FDA reports)
PERIRECTAL ABSCESS ( 17 FDA reports)
PSYCHOLOGICAL TRAUMA ( 17 FDA reports)
RADICULITIS ( 17 FDA reports)
RENAL CELL CARCINOMA ( 17 FDA reports)
SINUS POLYP DEGENERATION ( 17 FDA reports)
SKIN IRRITATION ( 17 FDA reports)
SKIN PLAQUE ( 17 FDA reports)
ACCIDENT AT WORK ( 16 FDA reports)
ADRENAL NEOPLASM ( 16 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 16 FDA reports)
ANAL FISSURE ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
ARTERIAL DISORDER ( 16 FDA reports)
BILIARY COLIC ( 16 FDA reports)
BLOOD CALCIUM INCREASED ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 16 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 16 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 16 FDA reports)
BONE ABSCESS ( 16 FDA reports)
BONE CYST ( 16 FDA reports)
BREAKTHROUGH PAIN ( 16 FDA reports)
BREAST CYST ( 16 FDA reports)
CARDIAC OUTPUT DECREASED ( 16 FDA reports)
CHANGE OF BOWEL HABIT ( 16 FDA reports)
CHARLES BONNET SYNDROME ( 16 FDA reports)
COMPLETED SUICIDE ( 16 FDA reports)
CONCUSSION ( 16 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 16 FDA reports)
DIABETIC COMPLICATION ( 16 FDA reports)
DIAPHRAGMATIC HERNIA ( 16 FDA reports)
EAR NEOPLASM ( 16 FDA reports)
EUPHORIC MOOD ( 16 FDA reports)
EXTREMITY NECROSIS ( 16 FDA reports)
FOOD INTOLERANCE ( 16 FDA reports)
FRACTURE DISPLACEMENT ( 16 FDA reports)
GALLBLADDER POLYP ( 16 FDA reports)
GASTROINTESTINAL NECROSIS ( 16 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 16 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 16 FDA reports)
HAND DEFORMITY ( 16 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 16 FDA reports)
HEPATOJUGULAR REFLUX ( 16 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 16 FDA reports)
INCISION SITE BLISTER ( 16 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 16 FDA reports)
LOWER EXTREMITY MASS ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE ( 16 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 16 FDA reports)
NEPHROSCLEROSIS ( 16 FDA reports)
NEUROTOXICITY ( 16 FDA reports)
NODAL RHYTHM ( 16 FDA reports)
OVERWEIGHT ( 16 FDA reports)
PAPILLOEDEMA ( 16 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 16 FDA reports)
ROTATOR CUFF REPAIR ( 16 FDA reports)
SENSATION OF PRESSURE ( 16 FDA reports)
SICCA SYNDROME ( 16 FDA reports)
SINUS ANTROSTOMY ( 16 FDA reports)
SOFT TISSUE INFECTION ( 16 FDA reports)
SOMNAMBULISM ( 16 FDA reports)
SPINAL CORD DISORDER ( 16 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 16 FDA reports)
TEARFULNESS ( 16 FDA reports)
TRACHEITIS ( 16 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 16 FDA reports)
UTERINE HAEMORRHAGE ( 16 FDA reports)
VAGINITIS BACTERIAL ( 16 FDA reports)
SPLEEN DISORDER ( 15 FDA reports)
SPONDYLITIS ( 15 FDA reports)
SUDDEN DEATH ( 15 FDA reports)
TACHYARRHYTHMIA ( 15 FDA reports)
TONGUE INJURY ( 15 FDA reports)
ULNA FRACTURE ( 15 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 15 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 15 FDA reports)
VENOUS OCCLUSION ( 15 FDA reports)
VENTRICULAR DYSKINESIA ( 15 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 15 FDA reports)
ACUTE PULMONARY OEDEMA ( 15 FDA reports)
AMAUROSIS FUGAX ( 15 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 15 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 15 FDA reports)
ASTERIXIS ( 15 FDA reports)
BILIARY TRACT DISORDER ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 15 FDA reports)
BLOOD PRESSURE ABNORMAL ( 15 FDA reports)
BONE FISTULA ( 15 FDA reports)
BRONCHITIS ACUTE ( 15 FDA reports)
BURSA DISORDER ( 15 FDA reports)
CALCULUS URINARY ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 15 FDA reports)
CHEST WALL OPERATION ( 15 FDA reports)
COLON POLYPECTOMY ( 15 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 15 FDA reports)
DERMATITIS ALLERGIC ( 15 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 15 FDA reports)
GINGIVAL HYPERTROPHY ( 15 FDA reports)
HISTOPLASMOSIS ( 15 FDA reports)
HYDROURETER ( 15 FDA reports)
HYPOMANIA ( 15 FDA reports)
HYPOPNOEA ( 15 FDA reports)
ILEITIS ( 15 FDA reports)
INCISION SITE INFECTION ( 15 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 15 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 15 FDA reports)
INJECTION SITE PRURITUS ( 15 FDA reports)
INTESTINAL RESECTION ( 15 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 15 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 15 FDA reports)
LERICHE SYNDROME ( 15 FDA reports)
LYMPHADENITIS ( 15 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 15 FDA reports)
MENIERE'S DISEASE ( 15 FDA reports)
METABOLIC DISORDER ( 15 FDA reports)
MONARTHRITIS ( 15 FDA reports)
NEUROLOGICAL SYMPTOM ( 15 FDA reports)
OBSTRUCTION ( 15 FDA reports)
ORAL NEOPLASM ( 15 FDA reports)
PNEUMONIA KLEBSIELLA ( 15 FDA reports)
POLYARTHRITIS ( 15 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 15 FDA reports)
PREGNANCY ( 15 FDA reports)
PROCEDURAL HYPERTENSION ( 15 FDA reports)
RETINAL TEAR ( 15 FDA reports)
SALPINGO-OOPHORECTOMY ( 15 FDA reports)
SELF-MEDICATION ( 15 FDA reports)
SERUM SICKNESS ( 15 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 15 FDA reports)
SOFT TISSUE INJURY ( 15 FDA reports)
SOFT TISSUE MASS ( 15 FDA reports)
ANAEMIA POSTOPERATIVE ( 14 FDA reports)
APLASIA PURE RED CELL ( 14 FDA reports)
BASEDOW'S DISEASE ( 14 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 14 FDA reports)
BLADDER OPERATION ( 14 FDA reports)
BLEPHAROSPASM ( 14 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 14 FDA reports)
BREAST CANCER STAGE IV ( 14 FDA reports)
BRONCHIOLITIS ( 14 FDA reports)
BRONCHITIS VIRAL ( 14 FDA reports)
CARDIOVERSION ( 14 FDA reports)
CHOLECYSTITIS INFECTIVE ( 14 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 14 FDA reports)
DISSOCIATION ( 14 FDA reports)
DUODENAL POLYP ( 14 FDA reports)
ENTHESOPATHY ( 14 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 14 FDA reports)
GLIOSIS ( 14 FDA reports)
GOUTY ARTHRITIS ( 14 FDA reports)
HAEMARTHROSIS ( 14 FDA reports)
HAEMORRHAGIC ANAEMIA ( 14 FDA reports)
HEPATIC NECROSIS ( 14 FDA reports)
HEPATIC NEOPLASM ( 14 FDA reports)
HYDROCELE ( 14 FDA reports)
HYPERURICAEMIA ( 14 FDA reports)
ILEUS PARALYTIC ( 14 FDA reports)
IMPAIRED SELF-CARE ( 14 FDA reports)
INFECTIVE TENOSYNOVITIS ( 14 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 14 FDA reports)
INTESTINAL DILATATION ( 14 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 14 FDA reports)
KERATOMILEUSIS ( 14 FDA reports)
LACTIC ACIDOSIS ( 14 FDA reports)
LIVER TRANSPLANT REJECTION ( 14 FDA reports)
MULTIPLE ALLERGIES ( 14 FDA reports)
MUSCLE MASS ( 14 FDA reports)
MYELITIS TRANSVERSE ( 14 FDA reports)
MYOCARDITIS ( 14 FDA reports)
ONYCHOLYSIS ( 14 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 14 FDA reports)
OROANTRAL FISTULA ( 14 FDA reports)
OS TRIGONUM SYNDROME ( 14 FDA reports)
PANCREATIC INSUFFICIENCY ( 14 FDA reports)
PERFORMANCE STATUS DECREASED ( 14 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 14 FDA reports)
PLEURISY ( 14 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 14 FDA reports)
POLYPECTOMY ( 14 FDA reports)
PORTAL VEIN THROMBOSIS ( 14 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 14 FDA reports)
PROSTATE INFECTION ( 14 FDA reports)
RETINAL VEIN OCCLUSION ( 14 FDA reports)
SECONDARY SEQUESTRUM ( 14 FDA reports)
SINUS POLYP ( 14 FDA reports)
SNEEZING ( 14 FDA reports)
SPLENIC INFARCTION ( 14 FDA reports)
STERNAL FRACTURE ( 14 FDA reports)
TONGUE PARALYSIS ( 14 FDA reports)
TOXIC ENCEPHALOPATHY ( 14 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 14 FDA reports)
TRAUMATIC BRAIN INJURY ( 14 FDA reports)
UMBILICAL HERNIA REPAIR ( 14 FDA reports)
URETHRAL CARUNCLE ( 14 FDA reports)
URETHRAL OBSTRUCTION ( 14 FDA reports)
UVEITIS ( 14 FDA reports)
SUBDURAL HAEMORRHAGE ( 13 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 13 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 13 FDA reports)
TUBERCULOSIS ( 13 FDA reports)
ULCERATIVE KERATITIS ( 13 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 13 FDA reports)
URINE ANALYSIS ABNORMAL ( 13 FDA reports)
URINE KETONE BODY PRESENT ( 13 FDA reports)
UTERINE MASS ( 13 FDA reports)
UTERINE PROLAPSE ( 13 FDA reports)
VAGINAL DISCHARGE ( 13 FDA reports)
VOMITING PROJECTILE ( 13 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 13 FDA reports)
WRONG DRUG ADMINISTERED ( 13 FDA reports)
YELLOW SKIN ( 13 FDA reports)
ABNORMAL FAECES ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ADHESION ( 13 FDA reports)
AORTIC VALVE DISEASE ( 13 FDA reports)
ATHEROSCLEROSIS ( 13 FDA reports)
BETA GLOBULIN INCREASED ( 13 FDA reports)
BLOOD AMYLASE INCREASED ( 13 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 13 FDA reports)
BREAST CANCER IN SITU ( 13 FDA reports)
BREAST SWELLING ( 13 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 13 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 13 FDA reports)
COLOSTOMY ( 13 FDA reports)
CONGENITAL KNEE DEFORMITY ( 13 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 13 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 13 FDA reports)
EOSINOPHIL COUNT INCREASED ( 13 FDA reports)
EPIDIDYMITIS ( 13 FDA reports)
FAT TISSUE INCREASED ( 13 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 13 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 13 FDA reports)
GENERAL SYMPTOM ( 13 FDA reports)
GINGIVAL ABSCESS ( 13 FDA reports)
GLOMERULOSCLEROSIS ( 13 FDA reports)
GRAFT THROMBOSIS ( 13 FDA reports)
GRIMACING ( 13 FDA reports)
HEART VALVE INCOMPETENCE ( 13 FDA reports)
HELICOBACTER INFECTION ( 13 FDA reports)
HEPATORENAL SYNDROME ( 13 FDA reports)
HYPERPHOSPHATAEMIA ( 13 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 13 FDA reports)
ILIUM FRACTURE ( 13 FDA reports)
INFUSION SITE PRURITUS ( 13 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 13 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 13 FDA reports)
JOINT ARTHROPLASTY ( 13 FDA reports)
LARGE INTESTINAL ULCER ( 13 FDA reports)
LIP BLISTER ( 13 FDA reports)
LIP PAIN ( 13 FDA reports)
LYMPHANGITIS ( 13 FDA reports)
MALABSORPTION ( 13 FDA reports)
MEAN CELL VOLUME INCREASED ( 13 FDA reports)
METABOLIC SYNDROME ( 13 FDA reports)
METASTASES TO BONE MARROW ( 13 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 13 FDA reports)
NAIL DISCOLOURATION ( 13 FDA reports)
NEOPLASM RECURRENCE ( 13 FDA reports)
NO ADVERSE EVENT ( 13 FDA reports)
PAINFUL RESPIRATION ( 13 FDA reports)
PANCREATIC ENZYMES INCREASED ( 13 FDA reports)
PAROTITIS ( 13 FDA reports)
PARTNER STRESS ( 13 FDA reports)
PEAU D'ORANGE ( 13 FDA reports)
PERSONALITY DISORDER ( 13 FDA reports)
PICKWICKIAN SYNDROME ( 13 FDA reports)
PLEURAL DISORDER ( 13 FDA reports)
PLEURODESIS ( 13 FDA reports)
POLYCYSTIC OVARIES ( 13 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 13 FDA reports)
POSTNASAL DRIP ( 13 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 13 FDA reports)
PREMATURE BABY ( 13 FDA reports)
PROTEIN TOTAL INCREASED ( 13 FDA reports)
PULMONARY VASCULAR DISORDER ( 13 FDA reports)
RASH PAPULAR ( 13 FDA reports)
RENAL ARTERY STENOSIS ( 13 FDA reports)
RETINAL DETACHMENT ( 13 FDA reports)
RETINAL INFARCTION ( 13 FDA reports)
RETROPERITONEAL HAEMATOMA ( 13 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SERUM FERRITIN INCREASED ( 13 FDA reports)
SIALOADENITIS ( 13 FDA reports)
SKIN INJURY ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SMEAR CERVIX ABNORMAL ( 13 FDA reports)
ACETABULUM FRACTURE ( 12 FDA reports)
ADAMS-STOKES SYNDROME ( 12 FDA reports)
ANAL FISTULA ( 12 FDA reports)
ARTHROSCOPIC SURGERY ( 12 FDA reports)
BIOPSY GINGIVAL ( 12 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 12 FDA reports)
BLOOD PH DECREASED ( 12 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 12 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 12 FDA reports)
BONE DENSITY INCREASED ( 12 FDA reports)
CARDIAC FAILURE CHRONIC ( 12 FDA reports)
CATHETER SITE ERYTHEMA ( 12 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 12 FDA reports)
CERVICAL SPINE FLATTENING ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CYSTITIS NONINFECTIVE ( 12 FDA reports)
DENTAL DISCOMFORT ( 12 FDA reports)
DENTAL PLAQUE ( 12 FDA reports)
DUODENAL ULCER ( 12 FDA reports)
DYSGRAPHIA ( 12 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 12 FDA reports)
EMBOLIC STROKE ( 12 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 12 FDA reports)
ESCHERICHIA BACTERAEMIA ( 12 FDA reports)
EXTREMITY CONTRACTURE ( 12 FDA reports)
FEELING HOT AND COLD ( 12 FDA reports)
FLAT AFFECT ( 12 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 12 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 12 FDA reports)
GENERALISED ERYTHEMA ( 12 FDA reports)
HEART SOUNDS ABNORMAL ( 12 FDA reports)
HIV INFECTION ( 12 FDA reports)
HYPOPROTEINAEMIA ( 12 FDA reports)
IMMUNOGLOBULINS DECREASED ( 12 FDA reports)
IMPULSE-CONTROL DISORDER ( 12 FDA reports)
INJECTION SITE HAEMORRHAGE ( 12 FDA reports)
JOINT CAPSULE RUPTURE ( 12 FDA reports)
LABYRINTHITIS ( 12 FDA reports)
LAPAROTOMY ( 12 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 12 FDA reports)
LIMB DEFORMITY ( 12 FDA reports)
LIP HAEMORRHAGE ( 12 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 12 FDA reports)
MENOPAUSE ( 12 FDA reports)
METASTASES TO LARGE INTESTINE ( 12 FDA reports)
METATARSALGIA ( 12 FDA reports)
MONONEUROPATHY ( 12 FDA reports)
MOUTH CYST ( 12 FDA reports)
MUMPS ( 12 FDA reports)
MUSCLE CONTRACTURE ( 12 FDA reports)
MUSCLE FATIGUE ( 12 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 12 FDA reports)
NASAL SEPTAL OPERATION ( 12 FDA reports)
NEOPLASM PROSTATE ( 12 FDA reports)
NEPHRITIC SYNDROME ( 12 FDA reports)
NEUROMYOPATHY ( 12 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 12 FDA reports)
ORAL PUSTULE ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
OROPHARYNGEAL SWELLING ( 12 FDA reports)
OSTEOGENESIS IMPERFECTA ( 12 FDA reports)
OTITIS MEDIA CHRONIC ( 12 FDA reports)
PALATAL DISORDER ( 12 FDA reports)
PANCREATIC ATROPHY ( 12 FDA reports)
PANCREATIC DUCT DILATATION ( 12 FDA reports)
PARTIAL SEIZURES ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
PLASTIC SURGERY ( 12 FDA reports)
PNEUMOCONIOSIS ( 12 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 12 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 12 FDA reports)
POOR PERIPHERAL CIRCULATION ( 12 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 12 FDA reports)
POSTMENOPAUSE ( 12 FDA reports)
PRESBYOESOPHAGUS ( 12 FDA reports)
PROSTATIC DISORDER ( 12 FDA reports)
PUPIL FIXED ( 12 FDA reports)
RADIATION OESOPHAGITIS ( 12 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 12 FDA reports)
RENAL COLIC ( 12 FDA reports)
RESIDUAL URINE ( 12 FDA reports)
RETINAL DISORDER ( 12 FDA reports)
RHINALGIA ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 12 FDA reports)
RUBELLA ( 12 FDA reports)
SCARLET FEVER ( 12 FDA reports)
SKIN CANDIDA ( 12 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 12 FDA reports)
SPINAL CORD OEDEMA ( 12 FDA reports)
SPINAL OPERATION ( 12 FDA reports)
SPLENIC LESION ( 12 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 12 FDA reports)
SUFFOCATION FEELING ( 12 FDA reports)
TARSAL TUNNEL SYNDROME ( 12 FDA reports)
TUBERCULIN TEST POSITIVE ( 12 FDA reports)
URETERAL STENT INSERTION ( 12 FDA reports)
URINARY TRACT DISORDER ( 12 FDA reports)
URINE ABNORMALITY ( 12 FDA reports)
VASODILATATION ( 12 FDA reports)
VOCAL CORD THICKENING ( 12 FDA reports)
XEROSIS ( 12 FDA reports)
THROMBOSIS IN DEVICE ( 11 FDA reports)
THYROID MASS ( 11 FDA reports)
TIC ( 11 FDA reports)
TUMOUR MARKER INCREASED ( 11 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 11 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 11 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 11 FDA reports)
UTERINE DISORDER ( 11 FDA reports)
VASCULAR CAUTERISATION ( 11 FDA reports)
VOCAL CORD INFLAMMATION ( 11 FDA reports)
VULVOVAGINAL PRURITUS ( 11 FDA reports)
ADNEXA UTERI CYST ( 11 FDA reports)
ADNEXA UTERI MASS ( 11 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 11 FDA reports)
ALCOHOL ABUSE ( 11 FDA reports)
ANAL HAEMORRHAGE ( 11 FDA reports)
ANAPHYLACTOID REACTION ( 11 FDA reports)
ANURIA ( 11 FDA reports)
APATHY ( 11 FDA reports)
ARRESTED LABOUR ( 11 FDA reports)
ARTHRITIS BACTERIAL ( 11 FDA reports)
ASBESTOSIS ( 11 FDA reports)
ASPERGILLOSIS ( 11 FDA reports)
BACTERIAL DISEASE CARRIER ( 11 FDA reports)
BACTERIAL SEPSIS ( 11 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 11 FDA reports)
BLOOD SODIUM INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 11 FDA reports)
BREAST ABSCESS ( 11 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 11 FDA reports)
CATHETER SITE HAEMATOMA ( 11 FDA reports)
CELLULITIS ORBITAL ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
CHAPPED LIPS ( 11 FDA reports)
CHOREA ( 11 FDA reports)
CHROMATOPSIA ( 11 FDA reports)
CHRONIC FATIGUE SYNDROME ( 11 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 11 FDA reports)
CLUSTER HEADACHE ( 11 FDA reports)
CONVERSION DISORDER ( 11 FDA reports)
DEMYELINATION ( 11 FDA reports)
DEPENDENCE ( 11 FDA reports)
DERMATITIS ACNEIFORM ( 11 FDA reports)
DIABETIC COMA ( 11 FDA reports)
DRUG SCREEN POSITIVE ( 11 FDA reports)
EJACULATION DISORDER ( 11 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 11 FDA reports)
ENTEROBACTER INFECTION ( 11 FDA reports)
EXOPHTHALMOS ( 11 FDA reports)
EYE PRURITUS ( 11 FDA reports)
FACIAL OPERATION ( 11 FDA reports)
FACIAL PARESIS ( 11 FDA reports)
FEEDING TUBE COMPLICATION ( 11 FDA reports)
FINGER DEFORMITY ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
FRUSTRATION ( 11 FDA reports)
FUNGAL SKIN INFECTION ( 11 FDA reports)
GASTRITIS HAEMORRHAGIC ( 11 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 11 FDA reports)
HALLUCINATIONS, MIXED ( 11 FDA reports)
HEPATIC CALCIFICATION ( 11 FDA reports)
HOMICIDAL IDEATION ( 11 FDA reports)
IMPETIGO ( 11 FDA reports)
INFUSION SITE REACTION ( 11 FDA reports)
INFUSION SITE SWELLING ( 11 FDA reports)
JAW LESION EXCISION ( 11 FDA reports)
LARYNGEAL CYST ( 11 FDA reports)
LIVEDO RETICULARIS ( 11 FDA reports)
LIVER TRANSPLANT ( 11 FDA reports)
LOSS OF PROPRIOCEPTION ( 11 FDA reports)
LYMPH NODE PAIN ( 11 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 11 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 11 FDA reports)
MAGNESIUM DEFICIENCY ( 11 FDA reports)
MALIGNANT TUMOUR EXCISION ( 11 FDA reports)
MARROW HYPERPLASIA ( 11 FDA reports)
MASTECTOMY ( 11 FDA reports)
METASTASES TO ADRENALS ( 11 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 11 FDA reports)
METRORRHAGIA ( 11 FDA reports)
MIGRAINE WITH AURA ( 11 FDA reports)
MUCOSAL EROSION ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
MYOFASCITIS ( 11 FDA reports)
NAIL OPERATION ( 11 FDA reports)
NASAL SINUS CANCER ( 11 FDA reports)
NEUROFIBROMA ( 11 FDA reports)
NEUROSENSORY HYPOACUSIS ( 11 FDA reports)
NICOTINE DEPENDENCE ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER ( 11 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 11 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 11 FDA reports)
PCO2 INCREASED ( 11 FDA reports)
PERICARDIAL DISEASE ( 11 FDA reports)
PEYRONIE'S DISEASE ( 11 FDA reports)
PHYSICAL ASSAULT ( 11 FDA reports)
POLYCYTHAEMIA ( 11 FDA reports)
POSTOPERATIVE FEVER ( 11 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
RENAL ANEURYSM ( 11 FDA reports)
RENAL CANCER METASTATIC ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 11 FDA reports)
SCHIZOPHRENIA ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SMALL INTESTINE OPERATION ( 11 FDA reports)
AKATHISIA ( 10 FDA reports)
AMMONIA INCREASED ( 10 FDA reports)
ANORECTAL DISCOMFORT ( 10 FDA reports)
AORTIC VALVE REPLACEMENT ( 10 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 10 FDA reports)
ASTIGMATISM ( 10 FDA reports)
AUTOIMMUNE HEPATITIS ( 10 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 10 FDA reports)
BIOPSY BREAST ABNORMAL ( 10 FDA reports)
BLADDER DILATATION ( 10 FDA reports)
BLADDER MASS ( 10 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 10 FDA reports)
BLEEDING TIME PROLONGED ( 10 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 10 FDA reports)
BODY TINEA ( 10 FDA reports)
BRADYARRHYTHMIA ( 10 FDA reports)
BRAIN SCAN ABNORMAL ( 10 FDA reports)
BREAST CALCIFICATIONS ( 10 FDA reports)
BRONCHIAL OBSTRUCTION ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
CARDIAC ENZYMES INCREASED ( 10 FDA reports)
CARDIAC VALVE VEGETATION ( 10 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 10 FDA reports)
CEPHALHAEMATOMA ( 10 FDA reports)
CEREBRAL DISORDER ( 10 FDA reports)
CHEST TUBE INSERTION ( 10 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 10 FDA reports)
COLLATERAL CIRCULATION ( 10 FDA reports)
COMMINUTED FRACTURE ( 10 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 10 FDA reports)
CRANIAL NERVE DISORDER ( 10 FDA reports)
CRANIOSYNOSTOSIS ( 10 FDA reports)
CULTURE WOUND POSITIVE ( 10 FDA reports)
CYSTITIS KLEBSIELLA ( 10 FDA reports)
DENTAL NECROSIS ( 10 FDA reports)
DROOLING ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 10 FDA reports)
EMPYEMA ( 10 FDA reports)
ENDOMETRIAL CANCER ( 10 FDA reports)
EPIDERMAL NECROSIS ( 10 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 10 FDA reports)
EROSIVE DUODENITIS ( 10 FDA reports)
ERYTHEMA NODOSUM ( 10 FDA reports)
ETHMOID SINUS SURGERY ( 10 FDA reports)
FEMALE STERILISATION ( 10 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 10 FDA reports)
GAMMOPATHY ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GENERALISED ANXIETY DISORDER ( 10 FDA reports)
GRAFT INFECTION ( 10 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 10 FDA reports)
HEART RATE ABNORMAL ( 10 FDA reports)
HEMICEPHALALGIA ( 10 FDA reports)
HEPATIC FIBROSIS ( 10 FDA reports)
HEPATIC TRAUMA ( 10 FDA reports)
HYPERPHAGIA ( 10 FDA reports)
HYPERREFLEXIA ( 10 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 10 FDA reports)
HYPOCHLORAEMIA ( 10 FDA reports)
IMPLANT SITE THROMBOSIS ( 10 FDA reports)
INCISIONAL HERNIA ( 10 FDA reports)
INCREASED APPETITE ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
IRITIS ( 10 FDA reports)
KERATOACANTHOMA ( 10 FDA reports)
KNEE OPERATION ( 10 FDA reports)
LOSS OF CONTROL OF LEGS ( 10 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 10 FDA reports)
MACULE ( 10 FDA reports)
MALLORY-WEISS SYNDROME ( 10 FDA reports)
MEDIASTINUM NEOPLASM ( 10 FDA reports)
METASTASES TO KIDNEY ( 10 FDA reports)
MICTURITION FREQUENCY DECREASED ( 10 FDA reports)
MORGANELLA INFECTION ( 10 FDA reports)
MYODESOPSIA ( 10 FDA reports)
NASAL OBSTRUCTION ( 10 FDA reports)
NEPHRECTOMY ( 10 FDA reports)
NERVE BLOCK ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
NIGHT BLINDNESS ( 10 FDA reports)
ODONTOGENIC CYST ( 10 FDA reports)
ORGANISING PNEUMONIA ( 10 FDA reports)
PANCREATIC CYST ( 10 FDA reports)
PANCREATIC DISORDER ( 10 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 10 FDA reports)
PERIPHERAL NERVE INJURY ( 10 FDA reports)
PLAGIOCEPHALY ( 10 FDA reports)
PLEURECTOMY ( 10 FDA reports)
POST PROCEDURAL HAEMATOMA ( 10 FDA reports)
POST PROCEDURAL INFECTION ( 10 FDA reports)
POSTOPERATIVE INFECTION ( 10 FDA reports)
PROCEDURAL HYPOTENSION ( 10 FDA reports)
PROCEDURAL NAUSEA ( 10 FDA reports)
PRODUCT COUNTERFEIT ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 10 FDA reports)
PROTRUSION TONGUE ( 10 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 10 FDA reports)
PULMONARY TUBERCULOSIS ( 10 FDA reports)
RECTAL ULCER ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 10 FDA reports)
SCLERITIS ( 10 FDA reports)
SELF-INJURIOUS IDEATION ( 10 FDA reports)
SENILE OSTEOPOROSIS ( 10 FDA reports)
SHOULDER OPERATION ( 10 FDA reports)
SINUS ARREST ( 10 FDA reports)
SPINAL FUSION SURGERY ( 10 FDA reports)
SPONDYLOARTHROPATHY ( 10 FDA reports)
SUDDEN CARDIAC DEATH ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
TUNNEL VISION ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VENOUS THROMBOSIS LIMB ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
SPINAL CORD INJURY THORACIC ( 9 FDA reports)
STAG HORN CALCULUS ( 9 FDA reports)
STARING ( 9 FDA reports)
STATUS ASTHMATICUS ( 9 FDA reports)
STEATORRHOEA ( 9 FDA reports)
THROMBOTIC STROKE ( 9 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
TUMOUR EMBOLISM ( 9 FDA reports)
ULNAR NERVE INJURY ( 9 FDA reports)
UNDERDOSE ( 9 FDA reports)
UTEROVAGINAL PROLAPSE ( 9 FDA reports)
VENTRICULAR FAILURE ( 9 FDA reports)
WOUND TREATMENT ( 9 FDA reports)
ABDOMINAL ADHESIONS ( 9 FDA reports)
ACUTE LEUKAEMIA ( 9 FDA reports)
ADENOMYOSIS ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANAL PRURITUS ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANGIOMYOLIPOMA ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
ARTHROSCOPY ( 9 FDA reports)
BIOPSY BONE ( 9 FDA reports)
BLINDNESS CORTICAL ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BRAIN OPERATION ( 9 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 9 FDA reports)
CARDIORENAL SYNDROME ( 9 FDA reports)
CATHETER SEPSIS ( 9 FDA reports)
CEREBELLAR ATROPHY ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CHEST INJURY ( 9 FDA reports)
CHORIORETINAL DISORDER ( 9 FDA reports)
CHORIORETINOPATHY ( 9 FDA reports)
CLOSED HEAD INJURY ( 9 FDA reports)
COLONOSCOPY ABNORMAL ( 9 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 9 FDA reports)
CONGENITAL AORTIC ATRESIA ( 9 FDA reports)
CORONARY ANGIOPLASTY ( 9 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 9 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 9 FDA reports)
EATING DISORDER SYMPTOM ( 9 FDA reports)
EFFUSION ( 9 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 9 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
ENDOMETRIOSIS ( 9 FDA reports)
FOETAL MACROSOMIA ( 9 FDA reports)
FOOT OPERATION ( 9 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 9 FDA reports)
GASTRIC BYPASS ( 9 FDA reports)
GASTROINTESTINAL INFECTION ( 9 FDA reports)
HAEMOGLOBIN INCREASED ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HAIR COLOUR CHANGES ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HYPEROSMOLAR STATE ( 9 FDA reports)
HYPOGONADISM ( 9 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 9 FDA reports)
HYPOREFLEXIA ( 9 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 9 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 9 FDA reports)
INGROWN HAIR ( 9 FDA reports)
INJECTION SITE EXTRAVASATION ( 9 FDA reports)
INJECTION SITE RASH ( 9 FDA reports)
INTRA-UTERINE DEATH ( 9 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 9 FDA reports)
LIPID METABOLISM DISORDER ( 9 FDA reports)
LITHOTRIPSY ( 9 FDA reports)
MACROCYTOSIS ( 9 FDA reports)
MAMMOGRAM ABNORMAL ( 9 FDA reports)
MEDIASTINAL DISORDER ( 9 FDA reports)
MENINGITIS ASEPTIC ( 9 FDA reports)
METASTASES TO PANCREAS ( 9 FDA reports)
MOANING ( 9 FDA reports)
MUSCLE RIGIDITY ( 9 FDA reports)
MUSCLE SPASTICITY ( 9 FDA reports)
NASAL DISCOMFORT ( 9 FDA reports)
NEUTROPENIC COLITIS ( 9 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 9 FDA reports)
OOPHORECTOMY ( 9 FDA reports)
OSTEOCHONDRITIS ( 9 FDA reports)
OSTEOMYELITIS ACUTE ( 9 FDA reports)
OTORRHOEA ( 9 FDA reports)
OXYGEN SUPPLEMENTATION ( 9 FDA reports)
PANCREATIC MASS ( 9 FDA reports)
PANNICULITIS ( 9 FDA reports)
PARAPARESIS ( 9 FDA reports)
PARATHYROIDECTOMY ( 9 FDA reports)
PAROTID GLAND ENLARGEMENT ( 9 FDA reports)
PELVIC PROLAPSE ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERICARDIAL CYST ( 9 FDA reports)
PERIOSTITIS ( 9 FDA reports)
PNEUMOPERITONEUM ( 9 FDA reports)
POISONING ( 9 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 9 FDA reports)
PROCEDURAL VOMITING ( 9 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 9 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
RECTAL CANCER ( 9 FDA reports)
RED BLOOD CELL ABNORMALITY ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SHOULDER DEFORMITY ( 9 FDA reports)
SKIN FISSURES ( 9 FDA reports)
SLEEP TALKING ( 9 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ADJUSTMENT DISORDER ( 8 FDA reports)
ALCOHOLISM ( 8 FDA reports)
ALOPECIA AREATA ( 8 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 8 FDA reports)
APPETITE DISORDER ( 8 FDA reports)
ARTERIOSPASM CORONARY ( 8 FDA reports)
ASPHYXIA ( 8 FDA reports)
ASPIRATION JOINT ( 8 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 8 FDA reports)
AUTONOMIC NEUROPATHY ( 8 FDA reports)
AXONAL NEUROPATHY ( 8 FDA reports)
BASAL GANGLIA INFARCTION ( 8 FDA reports)
BENIGN GASTRIC NEOPLASM ( 8 FDA reports)
BLISTER INFECTED ( 8 FDA reports)
BLOOD BICARBONATE DECREASED ( 8 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 8 FDA reports)
BLOODY DISCHARGE ( 8 FDA reports)
BONE METABOLISM DISORDER ( 8 FDA reports)
BRADYPHRENIA ( 8 FDA reports)
BRAIN HERNIATION ( 8 FDA reports)
BREAST INFECTION ( 8 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CAROTID ARTERY ANEURYSM ( 8 FDA reports)
CATARACT NUCLEAR ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 8 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 8 FDA reports)
CSF TEST ABNORMAL ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 8 FDA reports)
EXCESSIVE EYE BLINKING ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
EYELID OPERATION ( 8 FDA reports)
FAILURE OF IMPLANT ( 8 FDA reports)
GASTRIC CANCER ( 8 FDA reports)
GASTRIC HAEMORRHAGE ( 8 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 8 FDA reports)
GINGIVECTOMY ( 8 FDA reports)
GUN SHOT WOUND ( 8 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 8 FDA reports)
HAEMOCHROMATOSIS ( 8 FDA reports)
HAEMORRHAGIC DIATHESIS ( 8 FDA reports)
HAIR GROWTH ABNORMAL ( 8 FDA reports)
HELICOBACTER TEST POSITIVE ( 8 FDA reports)
HOARSENESS ( 8 FDA reports)
HUNGER ( 8 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPERTENSIVE EMERGENCY ( 8 FDA reports)
HYPOVITAMINOSIS ( 8 FDA reports)
INFECTED SKIN ULCER ( 8 FDA reports)
INFECTIOUS PERITONITIS ( 8 FDA reports)
INFUSION SITE EXTRAVASATION ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 8 FDA reports)
IRON DEFICIENCY ( 8 FDA reports)
IRON METABOLISM DISORDER ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
KYPHOSCOLIOSIS ( 8 FDA reports)
LIMB OPERATION ( 8 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 8 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 8 FDA reports)
LOCALISED OEDEMA ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
MEDIASTINITIS ( 8 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 8 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
METASTASES TO CHEST WALL ( 8 FDA reports)
METASTASES TO EYE ( 8 FDA reports)
METASTASES TO STOMACH ( 8 FDA reports)
MICROANGIOPATHY ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MONOPLEGIA ( 8 FDA reports)
MUCOSAL ATROPHY ( 8 FDA reports)
NAIL DYSTROPHY ( 8 FDA reports)
NO ADVERSE EFFECT ( 8 FDA reports)
NODAL ARRHYTHMIA ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 8 FDA reports)
OBSTRUCTION GASTRIC ( 8 FDA reports)
OPEN FRACTURE ( 8 FDA reports)
OPIATES POSITIVE ( 8 FDA reports)
OROPHARYNGEAL BLISTERING ( 8 FDA reports)
OSTEOTOMY ( 8 FDA reports)
PANCREATITIS RELAPSING ( 8 FDA reports)
PARALYSIS FLACCID ( 8 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 8 FDA reports)
PCO2 DECREASED ( 8 FDA reports)
PELVIC DISCOMFORT ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PELVIC VENOUS THROMBOSIS ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 8 FDA reports)
POSTOPERATIVE ILEUS ( 8 FDA reports)
PRODUCT LABEL ISSUE ( 8 FDA reports)
PROSTATISM ( 8 FDA reports)
PROTEUS INFECTION ( 8 FDA reports)
PSORIATIC ARTHROPATHY ( 8 FDA reports)
PTERYGIUM ( 8 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 8 FDA reports)
PULSE PRESSURE DECREASED ( 8 FDA reports)
REHABILITATION THERAPY ( 8 FDA reports)
RELAPSING FEVER ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
RETINOPATHY ( 8 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 8 FDA reports)
SALIVARY HYPERSECRETION ( 8 FDA reports)
SALPINGITIS ( 8 FDA reports)
SCROTAL IRRITATION ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SEXUAL ABUSE ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
SUICIDAL BEHAVIOUR ( 8 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 8 FDA reports)
TENDINOUS CONTRACTURE ( 8 FDA reports)
TESTIS CANCER ( 8 FDA reports)
THORACOSTOMY ( 8 FDA reports)
THYROIDITIS ( 8 FDA reports)
TOBACCO USER ( 8 FDA reports)
TONGUE BLISTERING ( 8 FDA reports)
TRANSFUSION REACTION ( 8 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 8 FDA reports)
ULNAR TUNNEL SYNDROME ( 8 FDA reports)
URETERIC OBSTRUCTION ( 8 FDA reports)
VAGINAL PROLAPSE ( 8 FDA reports)
VENA CAVA INJURY ( 8 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 8 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 8 FDA reports)
SPLENIC CYST ( 7 FDA reports)
SPUTUM PURULENT ( 7 FDA reports)
STENT OCCLUSION ( 7 FDA reports)
STOMATOCYTES PRESENT ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 7 FDA reports)
SUPRAPUBIC PAIN ( 7 FDA reports)
TEETH BRITTLE ( 7 FDA reports)
TEMPORAL ARTERITIS ( 7 FDA reports)
TENDON OPERATION ( 7 FDA reports)
THORACIC CAVITY DRAINAGE ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 7 FDA reports)
TOE DEFORMITY ( 7 FDA reports)
TONGUE COATED ( 7 FDA reports)
TOOTH EROSION ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
TOXOPLASMOSIS ( 7 FDA reports)
TROPONIN I INCREASED ( 7 FDA reports)
TUMOUR FLARE ( 7 FDA reports)
URAEMIC ENCEPHALOPATHY ( 7 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
VITAMIN K DEFICIENCY ( 7 FDA reports)
VOCAL CORD CYST ( 7 FDA reports)
VOLVULUS ( 7 FDA reports)
VULVOVAGINAL DRYNESS ( 7 FDA reports)
ABDOMINAL INJURY ( 7 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 7 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 7 FDA reports)
ANAL ULCER ( 7 FDA reports)
APPARENT DEATH ( 7 FDA reports)
AUTOIMMUNE THYROIDITIS ( 7 FDA reports)
AZOOSPERMIA ( 7 FDA reports)
BACTERIA URINE ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BILE DUCT STENOSIS ( 7 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 7 FDA reports)
BLOOD MAGNESIUM INCREASED ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CAESAREAN SECTION ( 7 FDA reports)
CALCIPHYLAXIS ( 7 FDA reports)
CALCIUM DEFICIENCY ( 7 FDA reports)
CANDIDURIA ( 7 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 7 FDA reports)
CARCINOID TUMOUR ( 7 FDA reports)
CAROTID ARTERY ATHEROMA ( 7 FDA reports)
CERVICITIS ( 7 FDA reports)
CHEYNE-STOKES RESPIRATION ( 7 FDA reports)
CHOKING SENSATION ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
COMPULSIONS ( 7 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 7 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 7 FDA reports)
CONGENITAL ANOMALY ( 7 FDA reports)
CONJUNCTIVAL OEDEMA ( 7 FDA reports)
CORNEAL DYSTROPHY ( 7 FDA reports)
DERMATITIS BULLOUS ( 7 FDA reports)
DEVICE LEAKAGE ( 7 FDA reports)
DIABETIC MICROANGIOPATHY ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DYSMENORRHOEA ( 7 FDA reports)
EAR CONGESTION ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ENTEROCELE ( 7 FDA reports)
ERYTHEMA OF EYELID ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
ESCHAR ( 7 FDA reports)
EXPOSURE TO TOXIC AGENT ( 7 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 7 FDA reports)
EYE INJURY ( 7 FDA reports)
EYELID CYST ( 7 FDA reports)
FIBROUS HISTIOCYTOMA ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
FOREIGN BODY TRAUMA ( 7 FDA reports)
GALLBLADDER OPERATION ( 7 FDA reports)
GASTROSTOMY TUBE INSERTION ( 7 FDA reports)
GINGIVAL OPERATION ( 7 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HEMIANOPIA HOMONYMOUS ( 7 FDA reports)
HEPATIC CONGESTION ( 7 FDA reports)
HEPATIC INFARCTION ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HOMICIDE ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HOSTILITY ( 7 FDA reports)
HYPERTHERMIA ( 7 FDA reports)
HYPERVENTILATION ( 7 FDA reports)
HYPOCHROMASIA ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
IMPLANT SITE EFFUSION ( 7 FDA reports)
INFERTILITY ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
JOINT WARMTH ( 7 FDA reports)
LARYNGEAL DISORDER ( 7 FDA reports)
LARYNGEAL REPAIR ( 7 FDA reports)
LIPOATROPHY ( 7 FDA reports)
LORDOSIS ( 7 FDA reports)
LUNG ADENOCARCINOMA ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
LYMPHADENECTOMY ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MAMMOPLASTY ( 7 FDA reports)
MASS EXCISION ( 7 FDA reports)
METASTASES TO MENINGES ( 7 FDA reports)
METASTASES TO PLEURA ( 7 FDA reports)
MIXED INCONTINENCE ( 7 FDA reports)
MONOCLONAL GAMMOPATHY ( 7 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NASAL OEDEMA ( 7 FDA reports)
NEURALGIC AMYOTROPHY ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
NONSPECIFIC REACTION ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
ORAL FIBROMA ( 7 FDA reports)
ORAL PRURITUS ( 7 FDA reports)
OVARIAN ENLARGEMENT ( 7 FDA reports)
OVARIAN MASS ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PANCREATIC INJURY ( 7 FDA reports)
PERIPHERAL EMBOLISM ( 7 FDA reports)
PERITONEAL HAEMORRHAGE ( 7 FDA reports)
PHARYNGEAL ULCERATION ( 7 FDA reports)
PHOTODERMATOSIS ( 7 FDA reports)
PNEUMATOSIS INTESTINALIS ( 7 FDA reports)
POLYSUBSTANCE ABUSE ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
PRESCRIBED OVERDOSE ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PULMONARY TOXICITY ( 7 FDA reports)
RECALL PHENOMENON ( 7 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 7 FDA reports)
RESPIRATORY TRACT OEDEMA ( 7 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 7 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 7 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 7 FDA reports)
SKIN TURGOR DECREASED ( 7 FDA reports)
ABDOMINAL OPERATION ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
ACHLORHYDRIA ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
AGORAPHOBIA ( 6 FDA reports)
ALBUMIN URINE PRESENT ( 6 FDA reports)
AMINO ACID LEVEL INCREASED ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANGIOPLASTY ( 6 FDA reports)
ANION GAP INCREASED ( 6 FDA reports)
ANTISOCIAL BEHAVIOUR ( 6 FDA reports)
APHAKIA ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ARTERITIS ( 6 FDA reports)
ARTHROFIBROSIS ( 6 FDA reports)
ASTHENOPIA ( 6 FDA reports)
AURICULAR SWELLING ( 6 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 6 FDA reports)
B-CELL LYMPHOMA ( 6 FDA reports)
BABESIOSIS ( 6 FDA reports)
BACTEROIDES TEST POSITIVE ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 6 FDA reports)
BK VIRUS INFECTION ( 6 FDA reports)
BLADDER NEOPLASM ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BRAIN DEATH ( 6 FDA reports)
BREAST DISCHARGE ( 6 FDA reports)
BREAST OEDEMA ( 6 FDA reports)
BREAST OPERATION ( 6 FDA reports)
BRONCHIAL DISORDER ( 6 FDA reports)
BRONCHIAL HYPERACTIVITY ( 6 FDA reports)
CARBON DIOXIDE INCREASED ( 6 FDA reports)
CARDIAC OPERATION ( 6 FDA reports)
CATARACT CORTICAL ( 6 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHOLESTEROSIS ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
COLLAGEN DISORDER ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 6 FDA reports)
CRYOGLOBULINAEMIA ( 6 FDA reports)
CUTANEOUS SARCOIDOSIS ( 6 FDA reports)
CYSTIC FIBROSIS ( 6 FDA reports)
DEATH OF RELATIVE ( 6 FDA reports)
DENTAL TREATMENT ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DRY THROAT ( 6 FDA reports)
DUODENAL OBSTRUCTION ( 6 FDA reports)
DUPUYTREN'S CONTRACTURE ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
EMPTY SELLA SYNDROME ( 6 FDA reports)
ENCEPHALITIS VIRAL ( 6 FDA reports)
ENCHONDROMA ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENERGY INCREASED ( 6 FDA reports)
ENTEROBACTER SEPSIS ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EYE DISCHARGE ( 6 FDA reports)
EYE INFECTION VIRAL ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
EYELID INFECTION ( 6 FDA reports)
FACIAL WASTING ( 6 FDA reports)
FACTOR V LEIDEN MUTATION ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FOOD INTERACTION ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FRACTURE DELAYED UNION ( 6 FDA reports)
FUSOBACTERIUM INFECTION ( 6 FDA reports)
GALLBLADDER OEDEMA ( 6 FDA reports)
GALLBLADDER PAIN ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GASTROSTOMY ( 6 FDA reports)
GENITAL CANDIDIASIS ( 6 FDA reports)
GENITAL INFECTION FUNGAL ( 6 FDA reports)
GESTATIONAL DIABETES ( 6 FDA reports)
HAEMORRHOID OPERATION ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HYPERALBUMINAEMIA ( 6 FDA reports)
HYPERKINESIA ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOMETABOLISM ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
INFECTION MASKED ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
INFUSION SITE HAEMATOMA ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
INTESTINAL INFARCTION ( 6 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 6 FDA reports)
INTESTINAL STENOSIS ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
KERATITIS ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
LEUKOCYTURIA ( 6 FDA reports)
LISTLESS ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LUNG INJURY ( 6 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 6 FDA reports)
MENISCUS REMOVAL ( 6 FDA reports)
MICROALBUMINURIA ( 6 FDA reports)
MICROCYTIC ANAEMIA ( 6 FDA reports)
MICROCYTOSIS ( 6 FDA reports)
MIXED DEAFNESS ( 6 FDA reports)
MYCOPLASMA SEROLOGY ( 6 FDA reports)
MYOCARDIAL OEDEMA ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEPHROTIC SYNDROME ( 6 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 6 FDA reports)
OCCIPITAL NEURALGIA ( 6 FDA reports)
OESOPHAGEAL FISTULA ( 6 FDA reports)
ONYCHOCLASIS ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
OSTEOSARCOMA METASTATIC ( 6 FDA reports)
OSTEOSYNTHESIS ( 6 FDA reports)
PANCREATIC ENLARGEMENT ( 6 FDA reports)
PELVIC NEOPLASM ( 6 FDA reports)
PERICARDIAL DRAINAGE ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
PNEUMONIA LEGIONELLA ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POLYCHROMASIA ( 6 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 6 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 6 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 6 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 6 FDA reports)
PREMATURE LABOUR ( 6 FDA reports)
PROLONGED EXPIRATION ( 6 FDA reports)
PSEUDOHYPERKALAEMIA ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY HILUM MASS ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RADICAL MASTECTOMY ( 6 FDA reports)
RADICULITIS LUMBOSACRAL ( 6 FDA reports)
READING DISORDER ( 6 FDA reports)
RED MAN SYNDROME ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
ROULEAUX FORMATION ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SKIN BACTERIAL INFECTION ( 6 FDA reports)
SLEEP TERROR ( 6 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 6 FDA reports)
SPINAL CORD INJURY ( 6 FDA reports)
SPLENIC GRANULOMA ( 6 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 6 FDA reports)
STRESS INCONTINENCE ( 6 FDA reports)
THERAPY CESSATION ( 6 FDA reports)
THROAT CANCER ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
THYROGLOBULIN INCREASED ( 6 FDA reports)
TOXIC SHOCK SYNDROME ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRICUSPID VALVE DISEASE ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
URETERIC CANCER ( 6 FDA reports)
URETHRAL PAIN ( 6 FDA reports)
URINE CYTOLOGY ABNORMAL ( 6 FDA reports)
UTERINE PERFORATION ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VASECTOMY ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VERTIGO POSITIONAL ( 6 FDA reports)
VULVAL CANCER STAGE 0 ( 6 FDA reports)
VULVAR DYSPLASIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
SPEECH REHABILITATION ( 5 FDA reports)
SPHENOID SINUS OPERATION ( 5 FDA reports)
SPINAL CORPECTOMY ( 5 FDA reports)
SPLENIC ABSCESS ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
STENT REMOVAL ( 5 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 5 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
THERAPEUTIC PROCEDURE ( 5 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
UPPER EXTREMITY MASS ( 5 FDA reports)
URETERAL DISORDER ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 5 FDA reports)
UTERINE POLYP ( 5 FDA reports)
VENOUS STENOSIS ( 5 FDA reports)
VERBAL ABUSE ( 5 FDA reports)
VIRAEMIA ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
WEST NILE VIRAL INFECTION ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
X-RAY ( 5 FDA reports)
XANTHOPSIA ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
ACUTE PSYCHOSIS ( 5 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
AKINESIA ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
ANAL SPHINCTER ATONY ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ASEPTIC NECROSIS BONE ( 5 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 5 FDA reports)
BACTERIA STOOL IDENTIFIED ( 5 FDA reports)
BEHCET'S SYNDROME ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BLADDER DYSFUNCTION ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLAST CELL COUNT INCREASED ( 5 FDA reports)
BLOOD BICARBONATE INCREASED ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 5 FDA reports)
BONE DENSITOMETRY ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BRAIN DAMAGE ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BREAST HYPERPLASIA ( 5 FDA reports)
BREECH PRESENTATION ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
CARBON DIOXIDE DECREASED ( 5 FDA reports)
CARDIAC FIBRILLATION ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CAROTIDYNIA ( 5 FDA reports)
CEREBELLAR SYNDROME ( 5 FDA reports)
CEREBRAL CALCIFICATION ( 5 FDA reports)
CERVICAL POLYP ( 5 FDA reports)
CHOLESTATIC LIVER INJURY ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CLUBBING ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 5 FDA reports)
COMPULSIVE SHOPPING ( 5 FDA reports)
CONGENITAL SYPHILITIC OSTEOCHONDRITIS ( 5 FDA reports)
CONJUNCTIVITIS VIRAL ( 5 FDA reports)
CORNEAL ABRASION ( 5 FDA reports)
CRANIOCEREBRAL INJURY ( 5 FDA reports)
CRANIOTOMY ( 5 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DENTOFACIAL ANOMALY ( 5 FDA reports)
DIABETIC GASTROPARESIS ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 5 FDA reports)
DYSPHASIA ( 5 FDA reports)
DYSPHORIA ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
ENCEPHALITIS HERPES ( 5 FDA reports)
ENTEROBACTER BACTERAEMIA ( 5 FDA reports)
EYE INFLAMMATION ( 5 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 5 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
FEMORAL ARTERY OCCLUSION ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FLIGHT OF IDEAS ( 5 FDA reports)
FOOD ALLERGY ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
FRONTAL SINUS OPERATION ( 5 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 5 FDA reports)
FUNGAL RASH ( 5 FDA reports)
FUNGAL TEST POSITIVE ( 5 FDA reports)
GANGLION ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 5 FDA reports)
HAEMATOCRIT INCREASED ( 5 FDA reports)
HAEMATOSPERMIA ( 5 FDA reports)
HAEMORRHAGIC DISORDER ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEPATITIS A ( 5 FDA reports)
HORMONE THERAPY ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 5 FDA reports)
HYPERMETROPIA ( 5 FDA reports)
HYPERTRANSAMINASAEMIA ( 5 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 5 FDA reports)
HYPOCOAGULABLE STATE ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 5 FDA reports)
INCISION SITE COMPLICATION ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 5 FDA reports)
INFECTED CYST ( 5 FDA reports)
INFUSION SITE RASH ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 5 FDA reports)
INTESTINAL HAEMORRHAGE ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
IODINE ALLERGY ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 5 FDA reports)
LEUKOPLAKIA ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYMPH NODE PALPABLE ( 5 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 5 FDA reports)
MALIGNANT ASCITES ( 5 FDA reports)
MALIGNANT HYPERTENSION ( 5 FDA reports)
MANTLE CELL LYMPHOMA ( 5 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 5 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 5 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 5 FDA reports)
MONOPARESIS ( 5 FDA reports)
MUCOSAL NECROSIS ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
MUSCLE ENZYME INCREASED ( 5 FDA reports)
MUSCLE HYPERTROPHY ( 5 FDA reports)
MUSCLE SWELLING ( 5 FDA reports)
MYELOID LEUKAEMIA ( 5 FDA reports)
MYRINGOTOMY ( 5 FDA reports)
NASAL POLYPS ( 5 FDA reports)
NEGATIVE THOUGHTS ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEURODEGENERATIVE DISORDER ( 5 FDA reports)
NEUROGENIC BOWEL ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NOCTURNAL DYSPNOEA ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 5 FDA reports)
OESOPHAGEAL POLYP ( 5 FDA reports)
ORCHIDECTOMY ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
ORTHOSTATIC INTOLERANCE ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PARACENTESIS ( 5 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 5 FDA reports)
PERICARDIAL EXCISION ( 5 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 5 FDA reports)
PERIORBITAL HAEMATOMA ( 5 FDA reports)
PERITONITIS BACTERIAL ( 5 FDA reports)
PHARYNGEAL DISORDER ( 5 FDA reports)
PHLEBOTHROMBOSIS ( 5 FDA reports)
PNEUMOMEDIASTINUM ( 5 FDA reports)
PNEUMONIA NECROTISING ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POST-TRAUMATIC PAIN ( 5 FDA reports)
POSTOPERATIVE CONSTIPATION ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
PYELOCALIECTASIS ( 5 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 5 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RENAL OSTEODYSTROPHY ( 5 FDA reports)
RENAL STONE REMOVAL ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
RETINAL ARTERY OCCLUSION ( 5 FDA reports)
RHEUMATIC HEART DISEASE ( 5 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 5 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SIMPLE PARTIAL SEIZURES ( 5 FDA reports)
SINUS TARSI SYNDROME ( 5 FDA reports)
SKIN GRAFT ( 5 FDA reports)
SKIN INFECTION ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 4 FDA reports)
ABNORMAL WEIGHT GAIN ( 4 FDA reports)
ACROCHORDON ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
ADRENAL CARCINOMA ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
AMYLOIDOSIS ( 4 FDA reports)
ANASTOMOTIC COMPLICATION ( 4 FDA reports)
ANGIODYSPLASIA ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
APPLICATION SITE PAIN ( 4 FDA reports)
APPLICATION SITE PRURITUS ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 4 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 4 FDA reports)
ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
ASPIRATION BONE MARROW ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
BENIGN BONE NEOPLASM ( 4 FDA reports)
BINGE EATING ( 4 FDA reports)
BIOPSY BONE ABNORMAL ( 4 FDA reports)
BIOPSY STOMACH ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD URIC ACID DECREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BONE CANCER METASTATIC ( 4 FDA reports)
BONE INFARCTION ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 4 FDA reports)
CELLULITIS STREPTOCOCCAL ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
CLUMSINESS ( 4 FDA reports)
CORONARY ARTERY THROMBOSIS ( 4 FDA reports)
CORYNEBACTERIUM INFECTION ( 4 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 4 FDA reports)
CRYSTAL URINE PRESENT ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
CYSTITIS RADIATION ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
DACRYOCANALICULITIS ( 4 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 4 FDA reports)
DARK CIRCLES UNDER EYES ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DEVICE BREAKAGE ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DIZZINESS EXERTIONAL ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSLEXIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EAR PRURITUS ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 4 FDA reports)
EMBOLISM ARTERIAL ( 4 FDA reports)
EMBOLISM VENOUS ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EPIGLOTTIC OEDEMA ( 4 FDA reports)
EPIPHYSES PREMATURE FUSION ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
EYE BURNS ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FACE LIFT ( 4 FDA reports)
FAECES PALE ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FEBRILE INFECTION ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FOOT AMPUTATION ( 4 FDA reports)
GALACTORRHOEA ( 4 FDA reports)
GASTRIC CANCER RECURRENT ( 4 FDA reports)
GASTRIC VARICES ( 4 FDA reports)
GASTRITIS ATROPHIC ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 4 FDA reports)
GLOBULINS INCREASED ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
GRAVITATIONAL OEDEMA ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEMIANOPIA ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC SIDEROSIS ( 4 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 4 FDA reports)
HERPETIC STOMATITIS ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPHAEMA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
IMPAIRED FASTING GLUCOSE ( 4 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFUSION SITE IRRITATION ( 4 FDA reports)
INFUSION SITE PHLEBITIS ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
INNER EAR DISORDER ( 4 FDA reports)
INTERCEPTED MEDICATION ERROR ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 4 FDA reports)
JOINT INJECTION ( 4 FDA reports)
KAPOSI'S SARCOMA ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LACRIMATION DECREASED ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LAZINESS ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 4 FDA reports)
LOSS OF LIBIDO ( 4 FDA reports)
LOWER LIMB DEFORMITY ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 4 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MARITAL PROBLEM ( 4 FDA reports)
MEDICAL DIET ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MESENTERITIS ( 4 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 4 FDA reports)
METASTASES TO NECK ( 4 FDA reports)
MITRAL VALVE REPLACEMENT ( 4 FDA reports)
MITRAL VALVE SCLEROSIS ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MOUTH INJURY ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OBSTRUCTIVE UROPATHY ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
OPISTHOTONUS ( 4 FDA reports)
ORAL FUNGAL INFECTION ( 4 FDA reports)
OSTECTOMY ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PANCREATIC NEOPLASM ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PARADOXICAL DRUG REACTION ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 4 FDA reports)
PERIPHERAL PULSE DECREASED ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGEAL MASS ( 4 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
POST COITAL BLEEDING ( 4 FDA reports)
POST PROCEDURAL CELLULITIS ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PROCEDURAL SITE REACTION ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
RADIATION MUCOSITIS ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
SCAPULA FRACTURE ( 4 FDA reports)
SCIATIC NERVE NEUROPATHY ( 4 FDA reports)
SCLERODACTYLIA ( 4 FDA reports)
SCROTAL CYST ( 4 FDA reports)
SCROTAL SWELLING ( 4 FDA reports)
SELF ESTEEM DECREASED ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 4 FDA reports)
SKIN FLAP NECROSIS ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SMALL INTESTINAL RESECTION ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
SPLENIC ARTERY ANEURYSM ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
STEROID THERAPY ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SYSTOLIC DYSFUNCTION ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
TESTICULAR DISORDER ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THYROXINE FREE INCREASED ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TRACHEAL INJURY ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
UNEMPLOYMENT ( 4 FDA reports)
URINARY TRACT PAIN ( 4 FDA reports)
URINE COLOUR ABNORMAL ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UVULITIS ( 4 FDA reports)
UVULOPALATOPHARYNGOPLASTY ( 4 FDA reports)
VASCULAR OPERATION ( 4 FDA reports)
VENOUS INJURY ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VIRAL PHARYNGITIS ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VOCAL CORD DISORDER ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 4 FDA reports)
WEANING FAILURE ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WHITE BLOOD CELL DISORDER ( 4 FDA reports)
WHITE CLOT SYNDROME ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
ZINC DEFICIENCY ( 4 FDA reports)
SPERM COUNT ZERO ( 3 FDA reports)
STILLBIRTH ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TONIC CLONIC MOVEMENTS ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TRAUMATIC FRACTURE ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
URETHRITIS ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
UROSTOMY COMPLICATION ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VEIN DISCOLOURATION ( 3 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
WHITE BLOOD CELLS URINE ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ABSCESS NECK ( 3 FDA reports)
ACARODERMATITIS ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE POLYNEUROPATHY ( 3 FDA reports)
ADENOIDAL HYPERTROPHY ( 3 FDA reports)
ADVERSE REACTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
AORTITIS ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE HAEMATOMA ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 3 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 3 FDA reports)
ARTHRITIS REACTIVE ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BALANITIS ( 3 FDA reports)
BALANITIS CANDIDA ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 3 FDA reports)
BLADDER PROLAPSE ( 3 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD COPPER INCREASED ( 3 FDA reports)
BLOOD CREATININE ABNORMAL ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD IRON INCREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE FORMATION INCREASED ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 3 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST FIBROSIS ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHITIS FUNGAL ( 3 FDA reports)
BRONCHOPLEURAL FISTULA ( 3 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 3 FDA reports)
CAROTID ENDARTERECTOMY ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CERULOPLASMIN INCREASED ( 3 FDA reports)
CHONDROMATOSIS ( 3 FDA reports)
CHONDROSIS ( 3 FDA reports)
CHOREOATHETOSIS ( 3 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COGWHEEL RIGIDITY ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONGENITAL AORTIC STENOSIS ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYSTOPEXY ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELAYED ENGRAFTMENT ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DERMATOMYOSITIS ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
DYSPAREUNIA ( 3 FDA reports)
EJECTION FRACTION ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 3 FDA reports)
ENDOCERVICAL CURETTAGE ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXSANGUINATION ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FOREIGN BODY REACTION ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
FUSARIUM INFECTION ( 3 FDA reports)
GAIT DEVIATION ( 3 FDA reports)
GALLBLADDER PERFORATION ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENERAL NUTRITION DISORDER ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 3 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 3 FDA reports)
GRANULOCYTES MATURATION ARREST ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GRUNTING ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERMOBILITY SYNDROME ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
IMPACTED FRACTURE ( 3 FDA reports)
IMPLANT SITE EROSION ( 3 FDA reports)
IMPLANT SITE ERYTHEMA ( 3 FDA reports)
IMPLANT SITE INFECTION ( 3 FDA reports)
IMPLANT SITE PAIN ( 3 FDA reports)
INCISION SITE HAEMATOMA ( 3 FDA reports)
INCREASED BRONCHIAL SECRETION ( 3 FDA reports)
INFECTED SEBACEOUS CYST ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INJECTION SITE VESICLES ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTERTRIGO ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 3 FDA reports)
JOB DISSATISFACTION ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
LARYNGOSPASM ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIMB CRUSHING INJURY ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIPASE ABNORMAL ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
LISTERIOSIS ( 3 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LUNG OPERATION ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MACULAR ISCHAEMIA ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
METASTASES TO RETROPERITONEUM ( 3 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYCOBACTERIAL INFECTION ( 3 FDA reports)
MYOCARDIAL CALCIFICATION ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NODULE ON EXTREMITY ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORBITAL INFECTION ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PAIN EXACERBATED ( 3 FDA reports)
PANCREATIC ABSCESS ( 3 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 3 FDA reports)
PARANASAL CYST ( 3 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 3 FDA reports)
PENILE ULCERATION ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 3 FDA reports)
PHRENIC NERVE PARALYSIS ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONIA ASPERGILLUS ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST THROMBOTIC SYNDROME ( 3 FDA reports)
POSTPARTUM DEPRESSION ( 3 FDA reports)
PREALBUMIN DECREASED ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETROPERITONEAL ABSCESS ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 3 FDA reports)
SACCADIC EYE MOVEMENT ( 3 FDA reports)
SCAR PAIN ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SMOKER ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABORTION INFECTED ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACTINOMYCES TEST POSITIVE ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC BYPASS ( 2 FDA reports)
AORTIC VALVE PROLAPSE ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ATHERECTOMY ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATRIAL PRESSURE INCREASED ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
ATYPICAL MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN NEOPLASM OF SKIN ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BIOPSY HEART ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER PERFORATION ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD LACTIC ACID ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE OEDEMA ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BREAST CELLULITIS ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 2 FDA reports)
CARDIOMYOPATHY ACUTE ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CERVICAL GLAND TUBERCULOSIS ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHONDRITIS ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COITAL BLEEDING ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CUTANEOUS ANTHRAX ( 2 FDA reports)
CYP2D6 POLYMORPHISM ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEPENDENT RUBOR ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE STIMULATION ISSUE ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 2 FDA reports)
DISBACTERIOSIS ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
EMERGENCY CARE ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
EVANS SYNDROME ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FAMILIAL TREMOR ( 2 FDA reports)
FEAR OF PREGNANCY ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX PROPHYLAXIS ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
HAEMATOCRIT ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEART VALVE OPERATION ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC VEIN DILATATION ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATITIS B ANTIBODY ( 2 FDA reports)
HEPATITIS INFECTIOUS ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
ILEORECTAL FISTULA ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFLAMMATION LOCALISED ( 2 FDA reports)
INFUSION SITE BURNING ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE MASS ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INJECTION SITE CYST ( 2 FDA reports)
INJECTION SITE DERMATITIS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JAW INFLAMMATION ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT FLUID DRAINAGE ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LARYNGECTOMY ( 2 FDA reports)
LATERAL PATELLAR COMPRESSION SYNDROME ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIGAMENT CALCIFICATION ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG WEDGE RESECTION ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MALIGNANT MYOPIA ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEDICATION TAMPERING ( 2 FDA reports)
MELANODERMIA ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGOCELE ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
METASTATIC LYMPHOMA ( 2 FDA reports)
METATARSAL EXCISION ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYOCARDIAC ABSCESS ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEURILEMMOMA MALIGNANT ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALLANAESTHESIA ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARKINSONIAN GAIT ( 2 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIORBITAL CELLULITIS ( 2 FDA reports)
PERIORBITAL DISORDER ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PITYRIASIS RUBRA PILARIS ( 2 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONITIS CHEMICAL ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POSTPARTUM DISORDER ( 2 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATE TENDERNESS ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
RADIAL TUNNEL SYNDROME ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RADICULITIS CERVICAL ( 2 FDA reports)
RAOULTELLA TEST POSITIVE ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFLUX GASTRITIS ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RICKETS ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 2 FDA reports)
SALPINGOSTOMY ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SELF MUTILATION ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SICK RELATIVE ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SKIN GRAFT INFECTION ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SOFT TISSUE NEOPLASM ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINAL CORD INFECTION ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPOROTRICHOSIS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUDDEN ONSET OF SLEEP ( 2 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
TENDON SHEATH INCISION ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
TESTICULAR MASS ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THALASSAEMIA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THYROID PAIN ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 2 FDA reports)
TROCHANTERIC SYNDROME ( 2 FDA reports)
TROPONIN ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UMBILICAL HAEMORRHAGE ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEQUAL LIMB LENGTH ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URETHRAL SPASM ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE CERVIX STENOSIS ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VAGOTOMY ( 2 FDA reports)
VASCULAR COMPRESSION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VON WILLEBRAND'S DISEASE ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENOSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY ( 1 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYMBOLIC DYSFUNCTION ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TANNING ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON GRAFT ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TENONECTOMY ( 1 FDA reports)
TERMINAL DRIBBLING ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TETANY ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HAEMORRHAGE ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULOSIS OF PERIPHERAL LYMPH NODES ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
ULNAR NERVE PALSY ( 1 FDA reports)
UPPER AIRWAY NECROSIS ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 1 FDA reports)
URINARY TRACT INFECTION VIRAL ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
UROBILINOGEN URINE ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL OPERATION ( 1 FDA reports)
VAGINITIS ATROPHIC ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULAR SHUNT ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VEIN WALL HYPERTROPHY ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VIRAL TRACHEITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITREOUS LOSS ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL SCAN ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
X-RAY LIMB ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YAWNING ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABSCESS OF EYELID ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ADACTYLY ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADMINISTRATION SITE INFECTION ( 1 FDA reports)
ADRENAL GLAND INJURY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL DILATATION ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANKLE IMPINGEMENT ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY NEGATIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE URTICARIA ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROPOD-BORNE DISEASE ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ARTIFICIAL MENOPAUSE ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUTOPHONY ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN BREAST NEOPLASM ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY ADENOMA ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY PALATE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER FIBROSIS ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID PULSE INCREASED ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATHETER SITE EROSION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX OPERATION ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHEST X-RAY ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION MALE ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRANIAL NERVE INJURY ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOGENETIC ANALYSIS ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DANDY-WALKER SYNDROME ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE CAPTURING ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DIRECT INFECTION TRANSMISSION ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTIC CYST ( 1 FDA reports)
EPIPHYSEAL FRACTURE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHROPHAGOCYTOSIS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FAT INTOLERANCE ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER NAIL REMOVAL ( 1 FDA reports)
FLAT FEET ( 1 FDA reports)
FLUCTUANCE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL WARFARIN SYNDROME ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FROSTBITE ( 1 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOPHILIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEAL GANGRENE ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTION TRANSMISSION VIA PERSONAL CONTACT ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATITIS SCLEROSING ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABOUR ONSET DELAYED ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEMIERRE SYNDROME ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS EOSINOPHILIC ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIA SPUTUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 1 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARACENTESIS ABDOMEN ABNORMAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARMACOPHOBIA ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLACENTAL NECROSIS ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POROKERATOSIS ( 1 FDA reports)
PORTAL TRIADITIS ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE CARE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PROGRESSIVE BULBAR PALSY ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY TRICHOSPORONOSIS ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL CANCER RECURRENT ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY SIGHS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY SPASM ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALMONELLA TEST POSITIVE ( 1 FDA reports)
SALT CRAVING ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINUS CANCER METASTATIC ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)